Please choose an event type to view the corresponding MedsFacts report:

DYSPNOEA ( 13522 FDA reports)
NAUSEA ( 12650 FDA reports)
DIZZINESS ( 11600 FDA reports)
FATIGUE ( 10270 FDA reports)
FLUSHING ( 9994 FDA reports)
MYOCARDIAL INFARCTION ( 9976 FDA reports)
PAIN ( 9964 FDA reports)
ASTHENIA ( 9609 FDA reports)
CHEST PAIN ( 9213 FDA reports)
DIARRHOEA ( 8825 FDA reports)
FALL ( 8492 FDA reports)
VOMITING ( 8253 FDA reports)
HEADACHE ( 8010 FDA reports)
ANAEMIA ( 7819 FDA reports)
ANXIETY ( 7409 FDA reports)
HYPERTENSION ( 7401 FDA reports)
OEDEMA PERIPHERAL ( 7231 FDA reports)
HYPOTENSION ( 7072 FDA reports)
CEREBROVASCULAR ACCIDENT ( 6908 FDA reports)
PNEUMONIA ( 6898 FDA reports)
PAIN IN EXTREMITY ( 6516 FDA reports)
PRURITUS ( 6506 FDA reports)
DRUG INEFFECTIVE ( 6371 FDA reports)
ARTHRALGIA ( 6039 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 6005 FDA reports)
BACK PAIN ( 5997 FDA reports)
PYREXIA ( 5953 FDA reports)
DEPRESSION ( 5780 FDA reports)
RENAL FAILURE ACUTE ( 5759 FDA reports)
ATRIAL FIBRILLATION ( 5696 FDA reports)
WEIGHT DECREASED ( 5688 FDA reports)
BLOOD GLUCOSE INCREASED ( 5598 FDA reports)
MALAISE ( 5151 FDA reports)
CORONARY ARTERY DISEASE ( 5130 FDA reports)
RENAL FAILURE ( 4998 FDA reports)
PARAESTHESIA ( 4987 FDA reports)
DEHYDRATION ( 4930 FDA reports)
ABDOMINAL PAIN ( 4864 FDA reports)
COUGH ( 4583 FDA reports)
CONSTIPATION ( 4491 FDA reports)
CONFUSIONAL STATE ( 4401 FDA reports)
RASH ( 4350 FDA reports)
MYALGIA ( 4311 FDA reports)
HAEMOGLOBIN DECREASED ( 4197 FDA reports)
URINARY TRACT INFECTION ( 4175 FDA reports)
INSOMNIA ( 4160 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 4135 FDA reports)
SYNCOPE ( 4031 FDA reports)
DEATH ( 4029 FDA reports)
DRUG INTERACTION ( 3975 FDA reports)
INJURY ( 3959 FDA reports)
ERYTHEMA ( 3775 FDA reports)
DECREASED APPETITE ( 3713 FDA reports)
LOSS OF CONSCIOUSNESS ( 3680 FDA reports)
HYPOAESTHESIA ( 3586 FDA reports)
GAIT DISTURBANCE ( 3566 FDA reports)
ABDOMINAL PAIN UPPER ( 3503 FDA reports)
BLOOD PRESSURE INCREASED ( 3486 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 3373 FDA reports)
HYPERHIDROSIS ( 3357 FDA reports)
FEELING ABNORMAL ( 3314 FDA reports)
MUSCLE SPASMS ( 3280 FDA reports)
FEELING HOT ( 3164 FDA reports)
BLOOD CREATININE INCREASED ( 3159 FDA reports)
WEIGHT INCREASED ( 3147 FDA reports)
PLEURAL EFFUSION ( 3125 FDA reports)
SOMNOLENCE ( 3113 FDA reports)
ANGINA PECTORIS ( 3048 FDA reports)
MUSCULAR WEAKNESS ( 3045 FDA reports)
TREMOR ( 3030 FDA reports)
THROMBOCYTOPENIA ( 3010 FDA reports)
PALPITATIONS ( 3007 FDA reports)
CONDITION AGGRAVATED ( 2977 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2941 FDA reports)
SEPSIS ( 2809 FDA reports)
CARDIAC DISORDER ( 2807 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2777 FDA reports)
CONTUSION ( 2759 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2747 FDA reports)
CARDIAC ARREST ( 2723 FDA reports)
DIABETES MELLITUS ( 2710 FDA reports)
VISION BLURRED ( 2707 FDA reports)
CHEST DISCOMFORT ( 2696 FDA reports)
CARDIAC FAILURE ( 2687 FDA reports)
CONVULSION ( 2681 FDA reports)
RESPIRATORY FAILURE ( 2642 FDA reports)
DYSPEPSIA ( 2618 FDA reports)
OSTEOARTHRITIS ( 2617 FDA reports)
DYSPHAGIA ( 2577 FDA reports)
PULMONARY EMBOLISM ( 2569 FDA reports)
EMOTIONAL DISTRESS ( 2544 FDA reports)
HAEMORRHAGE ( 2495 FDA reports)
DEEP VEIN THROMBOSIS ( 2470 FDA reports)
BRADYCARDIA ( 2408 FDA reports)
RHABDOMYOLYSIS ( 2405 FDA reports)
BRONCHITIS ( 2369 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2358 FDA reports)
OSTEONECROSIS OF JAW ( 2324 FDA reports)
INFECTION ( 2294 FDA reports)
HYPOGLYCAEMIA ( 2286 FDA reports)
HEART RATE INCREASED ( 2275 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2259 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2212 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2196 FDA reports)
PLATELET COUNT DECREASED ( 2194 FDA reports)
NEUROPATHY PERIPHERAL ( 2174 FDA reports)
CHILLS ( 2154 FDA reports)
EPISTAXIS ( 2095 FDA reports)
CELLULITIS ( 2084 FDA reports)
HYPONATRAEMIA ( 2054 FDA reports)
BLOOD PRESSURE DECREASED ( 2038 FDA reports)
HYPERLIPIDAEMIA ( 2032 FDA reports)
TACHYCARDIA ( 2006 FDA reports)
RENAL IMPAIRMENT ( 1995 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1980 FDA reports)
HYPOKALAEMIA ( 1961 FDA reports)
CORONARY ARTERY OCCLUSION ( 1953 FDA reports)
OEDEMA ( 1936 FDA reports)
BONE DISORDER ( 1924 FDA reports)
CARDIOMEGALY ( 1922 FDA reports)
SINUSITIS ( 1917 FDA reports)
URTICARIA ( 1911 FDA reports)
RECTAL HAEMORRHAGE ( 1888 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1878 FDA reports)
ABDOMINAL DISCOMFORT ( 1863 FDA reports)
GASTRITIS ( 1852 FDA reports)
RENAL FAILURE CHRONIC ( 1837 FDA reports)
PULMONARY OEDEMA ( 1833 FDA reports)
ABDOMINAL DISTENSION ( 1822 FDA reports)
CATARACT ( 1808 FDA reports)
BALANCE DISORDER ( 1800 FDA reports)
HYPERKALAEMIA ( 1796 FDA reports)
THROMBOSIS ( 1782 FDA reports)
ARRHYTHMIA ( 1778 FDA reports)
AMNESIA ( 1768 FDA reports)
HYPERSENSITIVITY ( 1762 FDA reports)
ATELECTASIS ( 1755 FDA reports)
CHOLELITHIASIS ( 1708 FDA reports)
OSTEOMYELITIS ( 1704 FDA reports)
MUSCULOSKELETAL PAIN ( 1694 FDA reports)
HAEMATURIA ( 1689 FDA reports)
LETHARGY ( 1678 FDA reports)
MEMORY IMPAIRMENT ( 1675 FDA reports)
ARTHRITIS ( 1673 FDA reports)
HAEMATOCRIT DECREASED ( 1650 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1647 FDA reports)
SPINAL OSTEOARTHRITIS ( 1636 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1627 FDA reports)
BLOOD UREA INCREASED ( 1625 FDA reports)
OVERDOSE ( 1620 FDA reports)
PANCYTOPENIA ( 1613 FDA reports)
ANGINA UNSTABLE ( 1611 FDA reports)
JOINT SWELLING ( 1604 FDA reports)
ANHEDONIA ( 1603 FDA reports)
SWELLING ( 1589 FDA reports)
DYSPNOEA EXERTIONAL ( 1565 FDA reports)
MENTAL STATUS CHANGES ( 1563 FDA reports)
NECK PAIN ( 1547 FDA reports)
PANCREATITIS ( 1530 FDA reports)
BURNING SENSATION ( 1530 FDA reports)
ASTHMA ( 1522 FDA reports)
NEUTROPENIA ( 1514 FDA reports)
MULTI-ORGAN FAILURE ( 1509 FDA reports)
MELAENA ( 1503 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1501 FDA reports)
DRY MOUTH ( 1497 FDA reports)
HYPERGLYCAEMIA ( 1485 FDA reports)
PAIN IN JAW ( 1483 FDA reports)
HAEMATEMESIS ( 1478 FDA reports)
OSTEOPOROSIS ( 1440 FDA reports)
VENTRICULAR TACHYCARDIA ( 1437 FDA reports)
CEREBRAL INFARCTION ( 1413 FDA reports)
ECONOMIC PROBLEM ( 1409 FDA reports)
HAEMATOCHEZIA ( 1401 FDA reports)
BLOOD GLUCOSE DECREASED ( 1397 FDA reports)
DIVERTICULUM ( 1396 FDA reports)
ARTERIOSCLEROSIS ( 1386 FDA reports)
VERTIGO ( 1381 FDA reports)
GASTRIC ULCER ( 1380 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1374 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1371 FDA reports)
SKIN BURNING SENSATION ( 1369 FDA reports)
DRUG HYPERSENSITIVITY ( 1367 FDA reports)
HOT FLUSH ( 1362 FDA reports)
SWELLING FACE ( 1357 FDA reports)
HALLUCINATION ( 1354 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1348 FDA reports)
HIATUS HERNIA ( 1347 FDA reports)
HEART RATE IRREGULAR ( 1326 FDA reports)
IMPAIRED HEALING ( 1326 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1324 FDA reports)
AGITATION ( 1320 FDA reports)
OSTEONECROSIS ( 1304 FDA reports)
HAEMORRHOIDS ( 1300 FDA reports)
HYPOXIA ( 1263 FDA reports)
DYSARTHRIA ( 1262 FDA reports)
ANOREXIA ( 1260 FDA reports)
SPEECH DISORDER ( 1253 FDA reports)
DISORIENTATION ( 1250 FDA reports)
CEREBRAL HAEMORRHAGE ( 1242 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1232 FDA reports)
HAEMATOMA ( 1227 FDA reports)
UNEVALUABLE EVENT ( 1221 FDA reports)
NASOPHARYNGITIS ( 1217 FDA reports)
DYSGEUSIA ( 1212 FDA reports)
BONE PAIN ( 1211 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1208 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1202 FDA reports)
OSTEOPENIA ( 1199 FDA reports)
OFF LABEL USE ( 1193 FDA reports)
CORONARY ARTERY STENOSIS ( 1192 FDA reports)
ALOPECIA ( 1181 FDA reports)
SLEEP APNOEA SYNDROME ( 1181 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1179 FDA reports)
PULMONARY HYPERTENSION ( 1178 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1174 FDA reports)
DYSURIA ( 1174 FDA reports)
STRESS ( 1170 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1166 FDA reports)
ABASIA ( 1160 FDA reports)
WHEEZING ( 1155 FDA reports)
INJECTION SITE PAIN ( 1154 FDA reports)
NERVOUSNESS ( 1153 FDA reports)
POLLAKIURIA ( 1136 FDA reports)
VISUAL IMPAIRMENT ( 1136 FDA reports)
ARTHROPATHY ( 1127 FDA reports)
VISUAL ACUITY REDUCED ( 1124 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1123 FDA reports)
OROPHARYNGEAL PAIN ( 1113 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1112 FDA reports)
CARDIAC MURMUR ( 1098 FDA reports)
HERPES ZOSTER ( 1096 FDA reports)
NEPHROLITHIASIS ( 1094 FDA reports)
LIVER DISORDER ( 1078 FDA reports)
MOBILITY DECREASED ( 1078 FDA reports)
CARDIOMYOPATHY ( 1076 FDA reports)
HAEMOPTYSIS ( 1072 FDA reports)
TINNITUS ( 1069 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1068 FDA reports)
DYSPHONIA ( 1059 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1059 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1051 FDA reports)
HYPOTHYROIDISM ( 1043 FDA reports)
TOOTH EXTRACTION ( 1042 FDA reports)
RENAL CYST ( 1039 FDA reports)
ERECTILE DYSFUNCTION ( 1033 FDA reports)
SLEEP DISORDER ( 1029 FDA reports)
SUICIDAL IDEATION ( 1024 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1019 FDA reports)
FLATULENCE ( 1016 FDA reports)
TREATMENT NONCOMPLIANCE ( 1007 FDA reports)
RENAL DISORDER ( 1005 FDA reports)
COMA ( 993 FDA reports)
UNRESPONSIVE TO STIMULI ( 992 FDA reports)
DRUG DOSE OMISSION ( 991 FDA reports)
HEPATIC ENZYME INCREASED ( 990 FDA reports)
INJECTION SITE HAEMORRHAGE ( 988 FDA reports)
MULTIPLE MYELOMA ( 972 FDA reports)
INFLUENZA LIKE ILLNESS ( 960 FDA reports)
INCORRECT DOSE ADMINISTERED ( 959 FDA reports)
FAECES DISCOLOURED ( 959 FDA reports)
VENTRICULAR FIBRILLATION ( 958 FDA reports)
URINARY RETENTION ( 943 FDA reports)
DRUG TOXICITY ( 943 FDA reports)
URINARY INCONTINENCE ( 941 FDA reports)
HEPATIC STEATOSIS ( 940 FDA reports)
ROTATOR CUFF SYNDROME ( 934 FDA reports)
DISEASE PROGRESSION ( 933 FDA reports)
FEAR ( 933 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 929 FDA reports)
LUNG DISORDER ( 927 FDA reports)
RIB FRACTURE ( 926 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 925 FDA reports)
CAROTID ARTERY STENOSIS ( 925 FDA reports)
BLOOD BILIRUBIN INCREASED ( 922 FDA reports)
LYMPHADENOPATHY ( 921 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 918 FDA reports)
ANGIOEDEMA ( 912 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 911 FDA reports)
DIVERTICULITIS ( 910 FDA reports)
FLUID RETENTION ( 910 FDA reports)
MULTIPLE INJURIES ( 910 FDA reports)
ORTHOSTATIC HYPOTENSION ( 910 FDA reports)
SINUS BRADYCARDIA ( 909 FDA reports)
GOUT ( 909 FDA reports)
HEART RATE DECREASED ( 908 FDA reports)
JAUNDICE ( 906 FDA reports)
OXYGEN SATURATION DECREASED ( 899 FDA reports)
PERICARDIAL EFFUSION ( 897 FDA reports)
EJECTION FRACTION DECREASED ( 891 FDA reports)
NEOPLASM MALIGNANT ( 888 FDA reports)
BLOOD POTASSIUM DECREASED ( 881 FDA reports)
PRODUCT QUALITY ISSUE ( 880 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 879 FDA reports)
SEPTIC SHOCK ( 878 FDA reports)
SKIN ULCER ( 877 FDA reports)
APHASIA ( 872 FDA reports)
DELIRIUM ( 864 FDA reports)
COLONIC POLYP ( 854 FDA reports)
ROAD TRAFFIC ACCIDENT ( 850 FDA reports)
RESPIRATORY DISTRESS ( 849 FDA reports)
PANCREATITIS ACUTE ( 836 FDA reports)
METABOLIC ACIDOSIS ( 833 FDA reports)
BLOOD SODIUM DECREASED ( 832 FDA reports)
HEAD INJURY ( 831 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 830 FDA reports)
MEDICATION ERROR ( 830 FDA reports)
SKIN DISCOLOURATION ( 826 FDA reports)
DEFORMITY ( 826 FDA reports)
CARDIOVASCULAR DISORDER ( 822 FDA reports)
LEUKOCYTOSIS ( 818 FDA reports)
LEUKOPENIA ( 816 FDA reports)
FEBRILE NEUTROPENIA ( 814 FDA reports)
COMPLETED SUICIDE ( 810 FDA reports)
HYPOPHAGIA ( 808 FDA reports)
INFLAMMATION ( 803 FDA reports)
MIGRAINE ( 801 FDA reports)
DIPLOPIA ( 797 FDA reports)
POST PROCEDURAL COMPLICATION ( 787 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 783 FDA reports)
DENTAL CARIES ( 783 FDA reports)
BURSITIS ( 774 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 774 FDA reports)
SWOLLEN TONGUE ( 774 FDA reports)
PALLOR ( 773 FDA reports)
CARDIOGENIC SHOCK ( 772 FDA reports)
FEMUR FRACTURE ( 771 FDA reports)
GASTROINTESTINAL DISORDER ( 768 FDA reports)
HEMIPARESIS ( 762 FDA reports)
PULMONARY CONGESTION ( 760 FDA reports)
RASH PRURITIC ( 758 FDA reports)
HIP FRACTURE ( 758 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 756 FDA reports)
LUNG NEOPLASM ( 756 FDA reports)
OESOPHAGITIS ( 750 FDA reports)
METASTASES TO BONE ( 749 FDA reports)
INFLUENZA ( 748 FDA reports)
LUNG INFILTRATION ( 747 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 747 FDA reports)
ATRIAL FLUTTER ( 746 FDA reports)
SURGERY ( 740 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 739 FDA reports)
AORTIC VALVE INCOMPETENCE ( 737 FDA reports)
PRESYNCOPE ( 736 FDA reports)
TOOTHACHE ( 735 FDA reports)
BLOOD POTASSIUM INCREASED ( 732 FDA reports)
COGNITIVE DISORDER ( 732 FDA reports)
RHINORRHOEA ( 730 FDA reports)
DRUG EFFECT DECREASED ( 729 FDA reports)
ADVERSE EVENT ( 728 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 723 FDA reports)
SHOCK ( 721 FDA reports)
RESTLESSNESS ( 719 FDA reports)
COLITIS ( 718 FDA reports)
TOOTH DISORDER ( 716 FDA reports)
EXOSTOSIS ( 715 FDA reports)
HEPATIC FAILURE ( 714 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 712 FDA reports)
STOMATITIS ( 712 FDA reports)
BLINDNESS ( 710 FDA reports)
DRY SKIN ( 709 FDA reports)
RASH GENERALISED ( 708 FDA reports)
DISTURBANCE IN ATTENTION ( 703 FDA reports)
ILL-DEFINED DISORDER ( 701 FDA reports)
PRURITUS GENERALISED ( 701 FDA reports)
SINUS TACHYCARDIA ( 699 FDA reports)
ASCITES ( 699 FDA reports)
RASH ERYTHEMATOUS ( 696 FDA reports)
NOCTURIA ( 695 FDA reports)
BLISTER ( 695 FDA reports)
PRODUCTIVE COUGH ( 694 FDA reports)
NASAL CONGESTION ( 691 FDA reports)
DYSKINESIA ( 691 FDA reports)
ACUTE CORONARY SYNDROME ( 690 FDA reports)
EMPHYSEMA ( 689 FDA reports)
EYE PAIN ( 686 FDA reports)
SPINAL COLUMN STENOSIS ( 683 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 682 FDA reports)
DUODENAL ULCER ( 680 FDA reports)
MENTAL DISORDER ( 680 FDA reports)
CARPAL TUNNEL SYNDROME ( 679 FDA reports)
HAEMODIALYSIS ( 678 FDA reports)
CIRCULATORY COLLAPSE ( 677 FDA reports)
ANAPHYLACTIC REACTION ( 676 FDA reports)
FLUID OVERLOAD ( 676 FDA reports)
DEAFNESS ( 675 FDA reports)
RHEUMATOID ARTHRITIS ( 674 FDA reports)
PNEUMONIA ASPIRATION ( 670 FDA reports)
SCAR ( 670 FDA reports)
SKIN LESION ( 669 FDA reports)
VIRAL INFECTION ( 669 FDA reports)
AGGRESSION ( 668 FDA reports)
OBESITY ( 667 FDA reports)
PROTHROMBIN TIME PROLONGED ( 665 FDA reports)
GASTROENTERITIS ( 662 FDA reports)
CHROMATURIA ( 661 FDA reports)
SKIN EXFOLIATION ( 661 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 660 FDA reports)
INJECTION SITE ERYTHEMA ( 658 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 657 FDA reports)
GASTRIC HAEMORRHAGE ( 653 FDA reports)
BREAST CANCER ( 652 FDA reports)
COAGULOPATHY ( 652 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 648 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 648 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 648 FDA reports)
VENTRICULAR HYPERTROPHY ( 647 FDA reports)
IRRITABILITY ( 646 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 645 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 642 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 638 FDA reports)
RESPIRATORY ARREST ( 638 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 633 FDA reports)
PROSTATE CANCER ( 623 FDA reports)
DEMENTIA ( 621 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 620 FDA reports)
IRON DEFICIENCY ANAEMIA ( 615 FDA reports)
NIGHT SWEATS ( 612 FDA reports)
AORTIC ANEURYSM ( 608 FDA reports)
DECREASED INTEREST ( 607 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 605 FDA reports)
THROMBOSIS IN DEVICE ( 603 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 598 FDA reports)
TOOTH ABSCESS ( 596 FDA reports)
ISCHAEMIC STROKE ( 594 FDA reports)
PSORIASIS ( 594 FDA reports)
FEELING COLD ( 593 FDA reports)
GASTRIC DISORDER ( 588 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 588 FDA reports)
ABNORMAL BEHAVIOUR ( 585 FDA reports)
RENAL INJURY ( 580 FDA reports)
SUICIDE ATTEMPT ( 577 FDA reports)
DYSLIPIDAEMIA ( 574 FDA reports)
GINGIVAL BLEEDING ( 569 FDA reports)
BONE LESION ( 567 FDA reports)
HYPOCALCAEMIA ( 564 FDA reports)
THROAT IRRITATION ( 564 FDA reports)
TOOTH LOSS ( 564 FDA reports)
CYSTITIS ( 563 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 563 FDA reports)
ACUTE RESPIRATORY FAILURE ( 559 FDA reports)
VISUAL DISTURBANCE ( 559 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 557 FDA reports)
ENCEPHALOPATHY ( 557 FDA reports)
INJECTION SITE BRUISING ( 556 FDA reports)
DISCOMFORT ( 555 FDA reports)
NERVOUS SYSTEM DISORDER ( 553 FDA reports)
LACTIC ACIDOSIS ( 552 FDA reports)
BASAL CELL CARCINOMA ( 552 FDA reports)
HYPOVOLAEMIA ( 551 FDA reports)
CEREBRAL ATROPHY ( 550 FDA reports)
SKIN DISORDER ( 550 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 547 FDA reports)
GLAUCOMA ( 547 FDA reports)
RASH MACULAR ( 546 FDA reports)
DYSSTASIA ( 545 FDA reports)
ORAL PAIN ( 544 FDA reports)
PANIC ATTACK ( 542 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 541 FDA reports)
MOUTH ULCERATION ( 541 FDA reports)
JOINT INJURY ( 538 FDA reports)
SPINAL COMPRESSION FRACTURE ( 538 FDA reports)
SUDDEN DEATH ( 538 FDA reports)
SUBDURAL HAEMATOMA ( 536 FDA reports)
SINUS DISORDER ( 534 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 533 FDA reports)
PROTEINURIA ( 532 FDA reports)
BLOOD URINE PRESENT ( 531 FDA reports)
CEREBRAL ISCHAEMIA ( 530 FDA reports)
PULMONARY FIBROSIS ( 530 FDA reports)
CANDIDIASIS ( 529 FDA reports)
GASTRITIS EROSIVE ( 526 FDA reports)
NEUTROPHIL COUNT DECREASED ( 524 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 523 FDA reports)
RHINITIS ALLERGIC ( 523 FDA reports)
HYPOACUSIS ( 522 FDA reports)
STOMACH DISCOMFORT ( 519 FDA reports)
BLOOD CALCIUM DECREASED ( 518 FDA reports)
LUMBAR SPINAL STENOSIS ( 517 FDA reports)
HEPATITIS ( 515 FDA reports)
PRIMARY SEQUESTRUM ( 512 FDA reports)
DIALYSIS ( 510 FDA reports)
STEVENS-JOHNSON SYNDROME ( 508 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 507 FDA reports)
INJECTION SITE HAEMATOMA ( 506 FDA reports)
LACUNAR INFARCTION ( 506 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 505 FDA reports)
STENT PLACEMENT ( 504 FDA reports)
ULCER ( 503 FDA reports)
LACERATION ( 499 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 499 FDA reports)
MIDDLE INSOMNIA ( 496 FDA reports)
BONE DENSITY DECREASED ( 495 FDA reports)
COMPRESSION FRACTURE ( 493 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 493 FDA reports)
EMOTIONAL DISORDER ( 491 FDA reports)
MOVEMENT DISORDER ( 488 FDA reports)
SCOLIOSIS ( 488 FDA reports)
IRRITABLE BOWEL SYNDROME ( 486 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 485 FDA reports)
EYE SWELLING ( 483 FDA reports)
CARDIAC VALVE DISEASE ( 482 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 481 FDA reports)
LUNG NEOPLASM MALIGNANT ( 481 FDA reports)
INTESTINAL OBSTRUCTION ( 479 FDA reports)
EAR PAIN ( 479 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 479 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 478 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 478 FDA reports)
MASS ( 477 FDA reports)
MYOPATHY ( 474 FDA reports)
TOOTH FRACTURE ( 474 FDA reports)
ABNORMAL DREAMS ( 472 FDA reports)
BLINDNESS UNILATERAL ( 472 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 471 FDA reports)
PHARYNGEAL OEDEMA ( 470 FDA reports)
ISCHAEMIA ( 468 FDA reports)
LIMB INJURY ( 468 FDA reports)
DIFFICULTY IN WALKING ( 468 FDA reports)
DIABETIC NEUROPATHY ( 466 FDA reports)
EYE DISORDER ( 466 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 466 FDA reports)
HYPOMAGNESAEMIA ( 464 FDA reports)
NEURALGIA ( 464 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 462 FDA reports)
ERUCTATION ( 462 FDA reports)
TENDONITIS ( 461 FDA reports)
ABSCESS ( 460 FDA reports)
CHOLECYSTITIS ( 460 FDA reports)
DIVERTICULUM INTESTINAL ( 458 FDA reports)
MALNUTRITION ( 458 FDA reports)
COLD SWEAT ( 456 FDA reports)
HALLUCINATION, VISUAL ( 456 FDA reports)
BODY TEMPERATURE INCREASED ( 454 FDA reports)
LIP SWELLING ( 454 FDA reports)
AORTIC STENOSIS ( 453 FDA reports)
FIBROMYALGIA ( 452 FDA reports)
ILEUS ( 452 FDA reports)
ECCHYMOSIS ( 451 FDA reports)
PURULENT DISCHARGE ( 451 FDA reports)
JOINT STIFFNESS ( 448 FDA reports)
DILATATION VENTRICULAR ( 448 FDA reports)
EYE HAEMORRHAGE ( 448 FDA reports)
DRY EYE ( 445 FDA reports)
GENERALISED OEDEMA ( 445 FDA reports)
CYANOSIS ( 444 FDA reports)
DEPRESSED MOOD ( 444 FDA reports)
BLOOD ALBUMIN DECREASED ( 442 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 442 FDA reports)
CYST ( 441 FDA reports)
GALLBLADDER DISORDER ( 440 FDA reports)
RESPIRATORY DISORDER ( 440 FDA reports)
SCIATICA ( 440 FDA reports)
RESTLESS LEGS SYNDROME ( 439 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 439 FDA reports)
FOOT FRACTURE ( 439 FDA reports)
VASCULITIS ( 438 FDA reports)
ABDOMINAL PAIN LOWER ( 436 FDA reports)
JAW DISORDER ( 436 FDA reports)
TENDERNESS ( 435 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 434 FDA reports)
MYELODYSPLASTIC SYNDROME ( 432 FDA reports)
MYOSITIS ( 432 FDA reports)
NON-CARDIAC CHEST PAIN ( 431 FDA reports)
PLATELET COUNT INCREASED ( 430 FDA reports)
RENAL TUBULAR NECROSIS ( 429 FDA reports)
FLANK PAIN ( 428 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 427 FDA reports)
DILATATION ATRIAL ( 426 FDA reports)
DISABILITY ( 426 FDA reports)
ATRIOVENTRICULAR BLOCK ( 425 FDA reports)
HYPERCALCAEMIA ( 425 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 424 FDA reports)
PHYSICAL DISABILITY ( 423 FDA reports)
DECUBITUS ULCER ( 423 FDA reports)
INTENTIONAL DRUG MISUSE ( 421 FDA reports)
NIGHTMARE ( 421 FDA reports)
PATHOLOGICAL FRACTURE ( 421 FDA reports)
MUCOSAL INFLAMMATION ( 420 FDA reports)
SICK SINUS SYNDROME ( 419 FDA reports)
AZOTAEMIA ( 419 FDA reports)
GRAND MAL CONVULSION ( 418 FDA reports)
BACK DISORDER ( 416 FDA reports)
VENTRICULAR DYSFUNCTION ( 416 FDA reports)
OSTEOLYSIS ( 416 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 415 FDA reports)
EATING DISORDER ( 415 FDA reports)
BACTERIAL INFECTION ( 414 FDA reports)
MACULAR DEGENERATION ( 412 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 412 FDA reports)
COORDINATION ABNORMAL ( 411 FDA reports)
METASTASES TO LIVER ( 410 FDA reports)
THROAT TIGHTNESS ( 410 FDA reports)
VENTRICULAR HYPOKINESIA ( 408 FDA reports)
DISEASE RECURRENCE ( 405 FDA reports)
HEPATOMEGALY ( 405 FDA reports)
ORTHOPNOEA ( 403 FDA reports)
LIMB DISCOMFORT ( 401 FDA reports)
VAGINAL HAEMORRHAGE ( 401 FDA reports)
BLADDER CANCER ( 401 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 400 FDA reports)
AGEUSIA ( 399 FDA reports)
PEPTIC ULCER ( 398 FDA reports)
HERNIA ( 396 FDA reports)
FISTULA ( 394 FDA reports)
TOOTH INFECTION ( 393 FDA reports)
URINE OUTPUT DECREASED ( 393 FDA reports)
CAROTID ARTERY OCCLUSION ( 391 FDA reports)
LOOSE TOOTH ( 391 FDA reports)
PERIPHERAL COLDNESS ( 391 FDA reports)
RASH MACULO-PAPULAR ( 391 FDA reports)
OCULAR HYPERAEMIA ( 389 FDA reports)
RETCHING ( 389 FDA reports)
UPPER LIMB FRACTURE ( 389 FDA reports)
DRUG INTOLERANCE ( 389 FDA reports)
GROIN PAIN ( 389 FDA reports)
DRUG ADMINISTRATION ERROR ( 388 FDA reports)
HYPERSOMNIA ( 386 FDA reports)
HYDRONEPHROSIS ( 384 FDA reports)
BRONCHOPNEUMONIA ( 383 FDA reports)
ELECTROLYTE IMBALANCE ( 382 FDA reports)
PNEUMONITIS ( 382 FDA reports)
DRUG ERUPTION ( 381 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 380 FDA reports)
ECZEMA ( 380 FDA reports)
PERITONITIS ( 380 FDA reports)
RASH PAPULAR ( 378 FDA reports)
COLON CANCER ( 378 FDA reports)
GINGIVITIS ( 378 FDA reports)
PNEUMOTHORAX ( 377 FDA reports)
MUSCLE ATROPHY ( 375 FDA reports)
DIASTOLIC DYSFUNCTION ( 375 FDA reports)
INTENTIONAL OVERDOSE ( 373 FDA reports)
TROPONIN INCREASED ( 372 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 371 FDA reports)
ORAL CANDIDIASIS ( 370 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 370 FDA reports)
LOBAR PNEUMONIA ( 369 FDA reports)
ADVERSE DRUG REACTION ( 367 FDA reports)
HOSPITALISATION ( 367 FDA reports)
INTERMITTENT CLAUDICATION ( 364 FDA reports)
SPINAL FRACTURE ( 363 FDA reports)
THYROID DISORDER ( 363 FDA reports)
MENTAL IMPAIRMENT ( 362 FDA reports)
EXPOSED BONE IN JAW ( 362 FDA reports)
FACE OEDEMA ( 362 FDA reports)
MUSCLE STRAIN ( 360 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 358 FDA reports)
MUSCLE TWITCHING ( 357 FDA reports)
PERIODONTITIS ( 356 FDA reports)
PSYCHOTIC DISORDER ( 356 FDA reports)
CORONARY ARTERY BYPASS ( 356 FDA reports)
FUNGAL INFECTION ( 356 FDA reports)
CORONARY ARTERY THROMBOSIS ( 355 FDA reports)
COLITIS ISCHAEMIC ( 354 FDA reports)
FAILURE TO THRIVE ( 354 FDA reports)
DUODENITIS ( 353 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 352 FDA reports)
BONE MARROW FAILURE ( 352 FDA reports)
OSTEITIS ( 352 FDA reports)
TACHYPNOEA ( 351 FDA reports)
HYPOAESTHESIA ORAL ( 351 FDA reports)
EXCORIATION ( 350 FDA reports)
SINUS CONGESTION ( 349 FDA reports)
INCONTINENCE ( 348 FDA reports)
JOINT DISLOCATION ( 348 FDA reports)
LEFT VENTRICULAR FAILURE ( 348 FDA reports)
LOCALISED INFECTION ( 348 FDA reports)
GINGIVAL DISORDER ( 348 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 347 FDA reports)
PETECHIAE ( 346 FDA reports)
ATAXIA ( 346 FDA reports)
RADICULOPATHY ( 345 FDA reports)
LEFT ATRIAL DILATATION ( 344 FDA reports)
MENISCUS LESION ( 344 FDA reports)
SKIN INDURATION ( 344 FDA reports)
ANGIOPATHY ( 344 FDA reports)
IMPAIRED WORK ABILITY ( 344 FDA reports)
INFUSION RELATED REACTION ( 343 FDA reports)
SENSORY DISTURBANCE ( 341 FDA reports)
ANAPHYLACTIC SHOCK ( 339 FDA reports)
BRONCHOSPASM ( 339 FDA reports)
UROSEPSIS ( 338 FDA reports)
ORAL DISORDER ( 338 FDA reports)
RESPIRATORY RATE INCREASED ( 337 FDA reports)
HEPATIC CYST ( 336 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 336 FDA reports)
HEMIPLEGIA ( 335 FDA reports)
MYOCLONUS ( 335 FDA reports)
LACRIMATION INCREASED ( 331 FDA reports)
HYPOKINESIA ( 331 FDA reports)
CATHETERISATION CARDIAC ( 329 FDA reports)
CEREBROVASCULAR DISORDER ( 329 FDA reports)
CHOLESTASIS ( 329 FDA reports)
DERMATITIS ( 329 FDA reports)
FAECAL INCONTINENCE ( 329 FDA reports)
MITRAL VALVE PROLAPSE ( 329 FDA reports)
SKIN TIGHTNESS ( 326 FDA reports)
SKIN LACERATION ( 325 FDA reports)
EXTRASYSTOLES ( 325 FDA reports)
CATARACT OPERATION ( 324 FDA reports)
SHOCK HAEMORRHAGIC ( 324 FDA reports)
MICTURITION URGENCY ( 322 FDA reports)
LUNG INFECTION ( 321 FDA reports)
JOINT EFFUSION ( 320 FDA reports)
PHARYNGITIS ( 320 FDA reports)
SKIN HYPERTROPHY ( 320 FDA reports)
ANGER ( 320 FDA reports)
CARDIAC PACEMAKER INSERTION ( 319 FDA reports)
RALES ( 319 FDA reports)
POOR QUALITY SLEEP ( 318 FDA reports)
BACTERAEMIA ( 318 FDA reports)
BLOOD CALCIUM INCREASED ( 318 FDA reports)
CAROTID ARTERY DISEASE ( 318 FDA reports)
GINGIVAL PAIN ( 318 FDA reports)
GOITRE ( 318 FDA reports)
HEPATIC CIRRHOSIS ( 318 FDA reports)
EOSINOPHILIA ( 317 FDA reports)
CHOKING ( 316 FDA reports)
TENDON RUPTURE ( 316 FDA reports)
OCCULT BLOOD POSITIVE ( 315 FDA reports)
MULTIPLE SCLEROSIS ( 314 FDA reports)
OSTEOSCLEROSIS ( 314 FDA reports)
INCREASED TENDENCY TO BRUISE ( 313 FDA reports)
PULSE ABSENT ( 313 FDA reports)
ACTINIC KERATOSIS ( 313 FDA reports)
ANKLE FRACTURE ( 313 FDA reports)
ACCIDENTAL OVERDOSE ( 311 FDA reports)
GYNAECOMASTIA ( 311 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 310 FDA reports)
MASTICATION DISORDER ( 309 FDA reports)
CONJUNCTIVITIS ( 309 FDA reports)
BONE DEBRIDEMENT ( 308 FDA reports)
EPILEPSY ( 308 FDA reports)
PARKINSON'S DISEASE ( 308 FDA reports)
SPLENOMEGALY ( 308 FDA reports)
EYE IRRITATION ( 307 FDA reports)
HAEMORRHAGIC STROKE ( 307 FDA reports)
ASPIRATION ( 306 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 306 FDA reports)
FEELING JITTERY ( 306 FDA reports)
PROCEDURAL COMPLICATION ( 306 FDA reports)
RESPIRATORY TRACT INFECTION ( 306 FDA reports)
ACIDOSIS ( 305 FDA reports)
ACUTE PULMONARY OEDEMA ( 305 FDA reports)
ANGIONEUROTIC OEDEMA ( 305 FDA reports)
GENERALISED ERYTHEMA ( 305 FDA reports)
GLOSSODYNIA ( 305 FDA reports)
AGRANULOCYTOSIS ( 304 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 304 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 303 FDA reports)
DRUG DEPENDENCE ( 303 FDA reports)
BODY HEIGHT DECREASED ( 302 FDA reports)
HYPERTENSIVE CRISIS ( 302 FDA reports)
FIBROSIS ( 300 FDA reports)
DIABETIC RETINOPATHY ( 299 FDA reports)
SEDATION ( 297 FDA reports)
WRIST FRACTURE ( 297 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 296 FDA reports)
METASTASES TO LUNG ( 296 FDA reports)
PURPURA ( 295 FDA reports)
KYPHOSIS ( 294 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 294 FDA reports)
ENDODONTIC PROCEDURE ( 293 FDA reports)
LABORATORY TEST ABNORMAL ( 293 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 293 FDA reports)
ORAL INTAKE REDUCED ( 292 FDA reports)
BACK INJURY ( 290 FDA reports)
DEBRIDEMENT ( 290 FDA reports)
EYELID OEDEMA ( 289 FDA reports)
KNEE ARTHROPLASTY ( 288 FDA reports)
SQUAMOUS CELL CARCINOMA ( 288 FDA reports)
PERIODONTAL DISEASE ( 287 FDA reports)
SKIN CANCER ( 287 FDA reports)
CRYING ( 287 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 287 FDA reports)
DIABETIC KETOACIDOSIS ( 286 FDA reports)
HEARING IMPAIRED ( 286 FDA reports)
FACIAL PAIN ( 285 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 285 FDA reports)
OESOPHAGEAL ULCER ( 285 FDA reports)
PHOTOPHOBIA ( 285 FDA reports)
CARDIAC TAMPONADE ( 282 FDA reports)
CHRONIC SINUSITIS ( 281 FDA reports)
NO THERAPEUTIC RESPONSE ( 280 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 279 FDA reports)
PERIPHERAL ISCHAEMIA ( 279 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 279 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 278 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 277 FDA reports)
LIPASE INCREASED ( 277 FDA reports)
MUSCLE TIGHTNESS ( 276 FDA reports)
PARAESTHESIA ORAL ( 276 FDA reports)
NEOPLASM PROGRESSION ( 275 FDA reports)
PARANOIA ( 275 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 275 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 273 FDA reports)
SPONDYLOLISTHESIS ( 273 FDA reports)
NO ADVERSE EVENT ( 272 FDA reports)
FOOT DEFORMITY ( 272 FDA reports)
INTESTINAL ISCHAEMIA ( 271 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 271 FDA reports)
MOUTH HAEMORRHAGE ( 270 FDA reports)
THERAPY NON-RESPONDER ( 270 FDA reports)
DRUG LEVEL INCREASED ( 270 FDA reports)
ESCHERICHIA INFECTION ( 270 FDA reports)
CHOLECYSTECTOMY ( 269 FDA reports)
TRANSAMINASES INCREASED ( 269 FDA reports)
ULCER HAEMORRHAGE ( 267 FDA reports)
WOUND ( 267 FDA reports)
VISUAL FIELD DEFECT ( 266 FDA reports)
VITREOUS FLOATERS ( 266 FDA reports)
ANURIA ( 266 FDA reports)
HYPERTHYROIDISM ( 266 FDA reports)
PARALYSIS ( 265 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 264 FDA reports)
THINKING ABNORMAL ( 263 FDA reports)
BREAST PAIN ( 263 FDA reports)
CHEST X-RAY ABNORMAL ( 263 FDA reports)
UTERINE LEIOMYOMA ( 263 FDA reports)
WOUND INFECTION ( 263 FDA reports)
WRONG DRUG ADMINISTERED ( 262 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 262 FDA reports)
BARRETT'S OESOPHAGUS ( 262 FDA reports)
CORONARY ARTERY RESTENOSIS ( 262 FDA reports)
HIP ARTHROPLASTY ( 261 FDA reports)
METASTASES TO SPINE ( 261 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 261 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 260 FDA reports)
WALKING AID USER ( 259 FDA reports)
NODULE ( 258 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 257 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 257 FDA reports)
VENOUS INSUFFICIENCY ( 256 FDA reports)
BREAST CANCER FEMALE ( 255 FDA reports)
KIDNEY INFECTION ( 253 FDA reports)
MUSCLE CRAMP ( 253 FDA reports)
SENSATION OF HEAVINESS ( 253 FDA reports)
WOUND DEHISCENCE ( 253 FDA reports)
ABDOMINAL HERNIA ( 252 FDA reports)
OLIGURIA ( 252 FDA reports)
ANEURYSM ( 249 FDA reports)
DIZZINESS POSTURAL ( 249 FDA reports)
GANGRENE ( 249 FDA reports)
HYPERTENSIVE HEART DISEASE ( 249 FDA reports)
CHOLECYSTITIS CHRONIC ( 248 FDA reports)
PERICARDITIS ( 248 FDA reports)
RETINAL HAEMORRHAGE ( 248 FDA reports)
LOCAL SWELLING ( 247 FDA reports)
MUSCLE DISORDER ( 246 FDA reports)
TORSADE DE POINTES ( 246 FDA reports)
MOOD SWINGS ( 245 FDA reports)
BLOOD CHLORIDE DECREASED ( 245 FDA reports)
BLOOD PRESSURE ABNORMAL ( 245 FDA reports)
GASTROENTERITIS VIRAL ( 245 FDA reports)
HAEMORRHAGIC ANAEMIA ( 245 FDA reports)
HEPATOTOXICITY ( 245 FDA reports)
ACUTE SINUSITIS ( 244 FDA reports)
CARDIAC FLUTTER ( 244 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 244 FDA reports)
FRACTURE ( 244 FDA reports)
ONYCHOMYCOSIS ( 244 FDA reports)
SEBORRHOEIC KERATOSIS ( 244 FDA reports)
LIFE EXPECTANCY SHORTENED ( 243 FDA reports)
MULTIPLE DRUG OVERDOSE ( 243 FDA reports)
PELVIC FRACTURE ( 243 FDA reports)
COLITIS ULCERATIVE ( 243 FDA reports)
FACIAL PALSY ( 242 FDA reports)
OEDEMA MOUTH ( 242 FDA reports)
INJECTION SITE REACTION ( 241 FDA reports)
LOWER LIMB FRACTURE ( 241 FDA reports)
PAIN OF SKIN ( 241 FDA reports)
HAEMOLYTIC ANAEMIA ( 241 FDA reports)
PELVIC PAIN ( 240 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 240 FDA reports)
MAJOR DEPRESSION ( 239 FDA reports)
CERUMEN IMPACTION ( 239 FDA reports)
DELUSION ( 239 FDA reports)
EYELID PTOSIS ( 239 FDA reports)
HYPOALBUMINAEMIA ( 238 FDA reports)
INFARCTION ( 238 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 238 FDA reports)
POLYP ( 237 FDA reports)
UMBILICAL HERNIA ( 237 FDA reports)
VIITH NERVE PARALYSIS ( 237 FDA reports)
HYPERKERATOSIS ( 237 FDA reports)
INTRACARDIAC THROMBUS ( 236 FDA reports)
NEUTROPHIL COUNT INCREASED ( 236 FDA reports)
PROTEIN URINE PRESENT ( 236 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 235 FDA reports)
THIRST ( 235 FDA reports)
DEVICE RELATED INFECTION ( 235 FDA reports)
ESSENTIAL HYPERTENSION ( 234 FDA reports)
BRAIN OEDEMA ( 233 FDA reports)
CARDIAC OPERATION ( 233 FDA reports)
DEVICE FAILURE ( 233 FDA reports)
LYMPHOEDEMA ( 233 FDA reports)
METASTATIC NEOPLASM ( 233 FDA reports)
TARDIVE DYSKINESIA ( 233 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 232 FDA reports)
JOINT SPRAIN ( 232 FDA reports)
TYPE 1 DIABETES MELLITUS ( 232 FDA reports)
BREATH SOUNDS ABNORMAL ( 232 FDA reports)
BONE LOSS ( 230 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 230 FDA reports)
NECROSIS ( 230 FDA reports)
REFLUX OESOPHAGITIS ( 230 FDA reports)
STRESS FRACTURE ( 230 FDA reports)
POLYURIA ( 229 FDA reports)
SKIN HYPERPIGMENTATION ( 229 FDA reports)
CHOLECYSTITIS ACUTE ( 229 FDA reports)
HEPATITIS ACUTE ( 229 FDA reports)
BLADDER DISORDER ( 228 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 228 FDA reports)
HUMERUS FRACTURE ( 228 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 228 FDA reports)
INGUINAL HERNIA ( 227 FDA reports)
PERONEAL NERVE PALSY ( 226 FDA reports)
HAND FRACTURE ( 226 FDA reports)
CROHN'S DISEASE ( 225 FDA reports)
PULMONARY MASS ( 225 FDA reports)
SPINAL DISORDER ( 225 FDA reports)
INJECTION SITE PRURITUS ( 224 FDA reports)
ENTEROCOCCAL INFECTION ( 224 FDA reports)
ACUTE PRERENAL FAILURE ( 223 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 223 FDA reports)
MOOD ALTERED ( 223 FDA reports)
ORAL DISCOMFORT ( 223 FDA reports)
RENAL PAIN ( 223 FDA reports)
SUDDEN CARDIAC DEATH ( 223 FDA reports)
BIPOLAR DISORDER ( 222 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 222 FDA reports)
BEDRIDDEN ( 221 FDA reports)
DIABETIC NEPHROPATHY ( 221 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 221 FDA reports)
HAEMORRHAGIC DIATHESIS ( 221 FDA reports)
NERVE COMPRESSION ( 221 FDA reports)
VASCULAR PSEUDOANEURYSM ( 221 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 220 FDA reports)
LIBIDO DECREASED ( 220 FDA reports)
SEQUESTRECTOMY ( 220 FDA reports)
PULMONARY HAEMORRHAGE ( 219 FDA reports)
BREAST MASS ( 219 FDA reports)
EOSINOPHIL COUNT INCREASED ( 219 FDA reports)
GINGIVAL INFECTION ( 219 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 219 FDA reports)
EMBOLISM ( 218 FDA reports)
VITAMIN D DEFICIENCY ( 218 FDA reports)
OPEN WOUND ( 218 FDA reports)
SYNOVIAL CYST ( 218 FDA reports)
MITRAL VALVE CALCIFICATION ( 217 FDA reports)
POLYNEUROPATHY ( 217 FDA reports)
PYELONEPHRITIS ( 217 FDA reports)
PLASMACYTOSIS ( 216 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 216 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 216 FDA reports)
HAEMODYNAMIC INSTABILITY ( 215 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 215 FDA reports)
PANCREATIC CARCINOMA ( 214 FDA reports)
CAROTID BRUIT ( 214 FDA reports)
CLOSTRIDIAL INFECTION ( 214 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 214 FDA reports)
ERYTHEMA MULTIFORME ( 214 FDA reports)
NEUROPATHY ( 213 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 213 FDA reports)
MUSCLE HAEMORRHAGE ( 211 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 210 FDA reports)
DERMAL CYST ( 209 FDA reports)
JAW FRACTURE ( 209 FDA reports)
LYMPHOMA ( 208 FDA reports)
CERVICAL SPINAL STENOSIS ( 208 FDA reports)
EROSIVE OESOPHAGITIS ( 208 FDA reports)
CYTOLYTIC HEPATITIS ( 207 FDA reports)
PARKINSONISM ( 207 FDA reports)
VITREOUS HAEMORRHAGE ( 207 FDA reports)
LARYNGEAL OEDEMA ( 206 FDA reports)
RENAL ARTERY STENOSIS ( 206 FDA reports)
ABORTION SPONTANEOUS ( 205 FDA reports)
HYPERURICAEMIA ( 205 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 205 FDA reports)
APHAGIA ( 204 FDA reports)
HEART INJURY ( 204 FDA reports)
AORTIC VALVE SCLEROSIS ( 203 FDA reports)
BLOOD MAGNESIUM DECREASED ( 203 FDA reports)
BLOOD URIC ACID INCREASED ( 203 FDA reports)
GINGIVAL RECESSION ( 203 FDA reports)
SCAB ( 203 FDA reports)
SENSORY LOSS ( 203 FDA reports)
SHOULDER PAIN ( 203 FDA reports)
APNOEA ( 202 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 202 FDA reports)
LIVER INJURY ( 201 FDA reports)
INJECTION SITE SWELLING ( 200 FDA reports)
RHINITIS ( 200 FDA reports)
GINGIVAL SWELLING ( 200 FDA reports)
AORTIC CALCIFICATION ( 199 FDA reports)
APLASIA PURE RED CELL ( 199 FDA reports)
BRONCHIECTASIS ( 199 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 199 FDA reports)
NERVE INJURY ( 198 FDA reports)
DERMATITIS EXFOLIATIVE ( 198 FDA reports)
ANOSMIA ( 197 FDA reports)
BLOOD DISORDER ( 197 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 197 FDA reports)
INCOHERENT ( 197 FDA reports)
SKIN WARM ( 196 FDA reports)
STENT OCCLUSION ( 196 FDA reports)
RETINAL DETACHMENT ( 195 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 195 FDA reports)
HYPOPHOSPHATAEMIA ( 195 FDA reports)
HICCUPS ( 194 FDA reports)
THYROID NEOPLASM ( 194 FDA reports)
MEDICAL DEVICE COMPLICATION ( 193 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 193 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 192 FDA reports)
DRUG ABUSE ( 192 FDA reports)
HYPOTONIA ( 192 FDA reports)
ANXIETY DISORDER ( 191 FDA reports)
BODY TEMPERATURE DECREASED ( 191 FDA reports)
FAECALOMA ( 191 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 190 FDA reports)
EAR INFECTION ( 188 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 188 FDA reports)
INJECTION SITE IRRITATION ( 187 FDA reports)
PHLEBITIS ( 187 FDA reports)
RIGHT VENTRICULAR FAILURE ( 187 FDA reports)
SEROTONIN SYNDROME ( 187 FDA reports)
BLEPHARITIS ( 187 FDA reports)
CARDIAC FAILURE ACUTE ( 187 FDA reports)
HEPATOCELLULAR DAMAGE ( 186 FDA reports)
IMPAIRED DRIVING ABILITY ( 186 FDA reports)
OCULAR ICTERUS ( 186 FDA reports)
SNEEZING ( 186 FDA reports)
WITHDRAWAL SYNDROME ( 186 FDA reports)
EYE PRURITUS ( 185 FDA reports)
INCREASED APPETITE ( 185 FDA reports)
QUALITY OF LIFE DECREASED ( 185 FDA reports)
RESPIRATORY TRACT CONGESTION ( 185 FDA reports)
JAW OPERATION ( 184 FDA reports)
ABDOMINAL TENDERNESS ( 184 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 184 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 183 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 183 FDA reports)
METASTASES TO LYMPH NODES ( 183 FDA reports)
NEPHROPATHY ( 183 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 183 FDA reports)
ORAL INFECTION ( 182 FDA reports)
VARICOSE VEIN ( 182 FDA reports)
GENERALISED ANXIETY DISORDER ( 182 FDA reports)
ADRENAL INSUFFICIENCY ( 181 FDA reports)
INITIAL INSOMNIA ( 181 FDA reports)
TENDON DISORDER ( 181 FDA reports)
APPENDICITIS ( 180 FDA reports)
BLOOD CREATINE INCREASED ( 180 FDA reports)
GRANULOMA ( 180 FDA reports)
HEPATITIS C ( 180 FDA reports)
ACTINOMYCOSIS ( 179 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 179 FDA reports)
NEPHROTIC SYNDROME ( 179 FDA reports)
SEASONAL ALLERGY ( 179 FDA reports)
LARGE INTESTINE PERFORATION ( 178 FDA reports)
NASAL SEPTUM DEVIATION ( 178 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 178 FDA reports)
HEPATIC ENCEPHALOPATHY ( 178 FDA reports)
HYPOAESTHESIA FACIAL ( 178 FDA reports)
BONE NEOPLASM MALIGNANT ( 177 FDA reports)
CAESAREAN SECTION ( 177 FDA reports)
DEAFNESS UNILATERAL ( 177 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 177 FDA reports)
METABOLIC ENCEPHALOPATHY ( 177 FDA reports)
PSEUDOMONAS INFECTION ( 177 FDA reports)
SNORING ( 177 FDA reports)
PLEURAL FIBROSIS ( 176 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 176 FDA reports)
ANGIOPLASTY ( 175 FDA reports)
PROSTATOMEGALY ( 175 FDA reports)
SKIN FIBROSIS ( 175 FDA reports)
ATHEROSCLEROSIS ( 174 FDA reports)
BLOOD AMYLASE INCREASED ( 174 FDA reports)
HALLUCINATION, AUDITORY ( 174 FDA reports)
ACNE ( 173 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 173 FDA reports)
MELANOCYTIC NAEVUS ( 173 FDA reports)
OESOPHAGEAL DISORDER ( 173 FDA reports)
RADIUS FRACTURE ( 173 FDA reports)
VITAMIN D DECREASED ( 173 FDA reports)
BLINDNESS TRANSIENT ( 172 FDA reports)
MANIA ( 172 FDA reports)
LEG AMPUTATION ( 171 FDA reports)
MALIGNANT MELANOMA ( 171 FDA reports)
NEPHROSCLEROSIS ( 171 FDA reports)
VENTRICULAR ARRHYTHMIA ( 171 FDA reports)
MOTOR DYSFUNCTION ( 170 FDA reports)
PROTEIN TOTAL DECREASED ( 170 FDA reports)
DECREASED ACTIVITY ( 170 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 170 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 169 FDA reports)
PANIC DISORDER ( 169 FDA reports)
SPINAL CORD COMPRESSION ( 169 FDA reports)
SINUS HEADACHE ( 168 FDA reports)
VASCULAR CALCIFICATION ( 168 FDA reports)
CREPITATIONS ( 168 FDA reports)
HEPATIC LESION ( 168 FDA reports)
ACUTE HEPATIC FAILURE ( 167 FDA reports)
FEMORAL NECK FRACTURE ( 167 FDA reports)
HYPERVENTILATION ( 167 FDA reports)
HYPOTHERMIA ( 167 FDA reports)
JOINT CONTRACTURE ( 167 FDA reports)
PLEURISY ( 167 FDA reports)
PROSTATITIS ( 167 FDA reports)
SOFT TISSUE DISORDER ( 167 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 166 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 166 FDA reports)
SEXUAL DYSFUNCTION ( 166 FDA reports)
APPLICATION SITE ERYTHEMA ( 166 FDA reports)
BLOOD IRON DECREASED ( 166 FDA reports)
COSTOCHONDRITIS ( 166 FDA reports)
DEVICE MALFUNCTION ( 166 FDA reports)
APATHY ( 165 FDA reports)
ATRIAL TACHYCARDIA ( 165 FDA reports)
LARYNGITIS ( 165 FDA reports)
LUMBAR RADICULOPATHY ( 165 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 165 FDA reports)
VITAMIN B12 DEFICIENCY ( 165 FDA reports)
APHONIA ( 164 FDA reports)
FORMICATION ( 164 FDA reports)
BREATH ODOUR ( 163 FDA reports)
DEAFNESS NEUROSENSORY ( 163 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 162 FDA reports)
EXERCISE TOLERANCE DECREASED ( 162 FDA reports)
INTESTINAL PERFORATION ( 162 FDA reports)
INTRACRANIAL ANEURYSM ( 162 FDA reports)
JAUNDICE CHOLESTATIC ( 162 FDA reports)
PERICARDIAL HAEMORRHAGE ( 162 FDA reports)
RADIOTHERAPY ( 162 FDA reports)
SKIN HAEMORRHAGE ( 162 FDA reports)
RETROPERITONEAL HAEMATOMA ( 161 FDA reports)
ABSCESS ORAL ( 161 FDA reports)
CARDIAC ENZYMES INCREASED ( 161 FDA reports)
EMBOLIC STROKE ( 161 FDA reports)
HAEMANGIOMA ( 161 FDA reports)
ENDOCARDITIS ( 160 FDA reports)
HYPERPARATHYROIDISM ( 160 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 160 FDA reports)
MEDICATION RESIDUE ( 160 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 159 FDA reports)
ORGAN FAILURE ( 159 FDA reports)
SYNOVITIS ( 159 FDA reports)
VITREOUS DETACHMENT ( 159 FDA reports)
ARTERIAL STENOSIS ( 159 FDA reports)
BONE FRAGMENTATION ( 158 FDA reports)
GASTROINTESTINAL PAIN ( 158 FDA reports)
HELICOBACTER INFECTION ( 158 FDA reports)
ILEUS PARALYTIC ( 158 FDA reports)
PHOTOSENSITIVITY REACTION ( 158 FDA reports)
TACHYARRHYTHMIA ( 158 FDA reports)
PATHOLOGICAL GAMBLING ( 157 FDA reports)
THROMBOPHLEBITIS ( 157 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 157 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 156 FDA reports)
DERMATITIS CONTACT ( 156 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 156 FDA reports)
PLEURITIC PAIN ( 156 FDA reports)
STEM CELL TRANSPLANT ( 156 FDA reports)
FRACTURED SACRUM ( 155 FDA reports)
PURULENCE ( 154 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 153 FDA reports)
TENSION HEADACHE ( 153 FDA reports)
TOXIC SKIN ERUPTION ( 153 FDA reports)
WOUND SECRETION ( 153 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 152 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 152 FDA reports)
LIGAMENT SPRAIN ( 152 FDA reports)
ORAL SURGERY ( 152 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 152 FDA reports)
PERITONITIS BACTERIAL ( 152 FDA reports)
SPUTUM DISCOLOURED ( 151 FDA reports)
TONGUE DISORDER ( 151 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 151 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 150 FDA reports)
GASTROINTESTINAL ULCER ( 150 FDA reports)
MONOPLEGIA ( 150 FDA reports)
TOE AMPUTATION ( 150 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 149 FDA reports)
NEUTROPENIC SEPSIS ( 149 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 149 FDA reports)
BLOOD CULTURE POSITIVE ( 149 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 149 FDA reports)
COLON ADENOMA ( 149 FDA reports)
DENTURE WEARER ( 149 FDA reports)
EAR DISCOMFORT ( 148 FDA reports)
HAEMOLYSIS ( 148 FDA reports)
OVARIAN CYST ( 148 FDA reports)
PLASMACYTOMA ( 148 FDA reports)
SERUM FERRITIN INCREASED ( 148 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 148 FDA reports)
MACULAR OEDEMA ( 147 FDA reports)
MENORRHAGIA ( 147 FDA reports)
ATRIAL SEPTAL DEFECT ( 147 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 147 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 147 FDA reports)
ALCOHOL USE ( 146 FDA reports)
AREFLEXIA ( 146 FDA reports)
ARTERIAL DISORDER ( 146 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 146 FDA reports)
VASCULAR GRAFT ( 146 FDA reports)
ACCIDENT ( 145 FDA reports)
ARTERIOSPASM CORONARY ( 145 FDA reports)
BLOOD COUNT ABNORMAL ( 145 FDA reports)
CARDIAC FAILURE CHRONIC ( 145 FDA reports)
HEPATIC NECROSIS ( 145 FDA reports)
HYPERBILIRUBINAEMIA ( 145 FDA reports)
HYPERNATRAEMIA ( 145 FDA reports)
ORAL HERPES ( 145 FDA reports)
PREGNANCY ( 145 FDA reports)
PROCEDURAL PAIN ( 145 FDA reports)
SOCIAL PROBLEM ( 145 FDA reports)
SENSATION OF FOREIGN BODY ( 144 FDA reports)
EAR DISORDER ( 144 FDA reports)
HEPATITIS CHOLESTATIC ( 143 FDA reports)
COLLAPSE OF LUNG ( 142 FDA reports)
DRUG PRESCRIBING ERROR ( 142 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 142 FDA reports)
LARGE INTESTINAL ULCER ( 142 FDA reports)
MITRAL VALVE DISEASE ( 142 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 142 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 142 FDA reports)
NEPHROPATHY TOXIC ( 141 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 141 FDA reports)
FACET JOINT SYNDROME ( 141 FDA reports)
ANAEMIA POSTOPERATIVE ( 140 FDA reports)
BRONCHITIS ACUTE ( 140 FDA reports)
DYSAESTHESIA ( 140 FDA reports)
EXPIRED DRUG ADMINISTERED ( 140 FDA reports)
VASCULAR OCCLUSION ( 140 FDA reports)
KLEBSIELLA INFECTION ( 140 FDA reports)
MUSCLE RIGIDITY ( 140 FDA reports)
ODYNOPHAGIA ( 140 FDA reports)
ORAL CAVITY FISTULA ( 140 FDA reports)
OTITIS EXTERNA ( 140 FDA reports)
POST PROCEDURAL HAEMATOMA ( 140 FDA reports)
RETINAL VEIN OCCLUSION ( 140 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 139 FDA reports)
TONGUE DISCOLOURATION ( 139 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 139 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 139 FDA reports)
URINE ODOUR ABNORMAL ( 138 FDA reports)
CERVICOBRACHIAL SYNDROME ( 138 FDA reports)
FACIAL BONES FRACTURE ( 138 FDA reports)
AFFECTIVE DISORDER ( 137 FDA reports)
AORTIC VALVE STENOSIS ( 137 FDA reports)
APHTHOUS STOMATITIS ( 137 FDA reports)
CONDUCTION DISORDER ( 137 FDA reports)
DENTAL FISTULA ( 137 FDA reports)
EPIGASTRIC DISCOMFORT ( 137 FDA reports)
HYPOVOLAEMIC SHOCK ( 137 FDA reports)
SKIN PAPILLOMA ( 137 FDA reports)
PROCTALGIA ( 136 FDA reports)
RHONCHI ( 135 FDA reports)
CEREBRAL HAEMATOMA ( 135 FDA reports)
FAMILY STRESS ( 135 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 134 FDA reports)
FIBRIN D DIMER INCREASED ( 134 FDA reports)
LUNG CONSOLIDATION ( 134 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 134 FDA reports)
PNEUMONIA BACTERIAL ( 134 FDA reports)
POST HERPETIC NEURALGIA ( 134 FDA reports)
SKIN NECROSIS ( 134 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 134 FDA reports)
STRIDOR ( 134 FDA reports)
MUSCULOSKELETAL DISORDER ( 133 FDA reports)
NECK INJURY ( 133 FDA reports)
THROMBOCYTOSIS ( 133 FDA reports)
APLASTIC ANAEMIA ( 133 FDA reports)
BUNDLE BRANCH BLOCK ( 133 FDA reports)
CATHETER RELATED COMPLICATION ( 133 FDA reports)
HYPOGLYCAEMIC COMA ( 133 FDA reports)
WHEELCHAIR USER ( 133 FDA reports)
NEPHRITIS INTERSTITIAL ( 132 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 132 FDA reports)
OTITIS MEDIA ( 132 FDA reports)
PERIORBITAL OEDEMA ( 132 FDA reports)
POLYMYALGIA RHEUMATICA ( 132 FDA reports)
PRESCRIBED OVERDOSE ( 132 FDA reports)
PROSTATIC DISORDER ( 132 FDA reports)
SINUS ARRHYTHMIA ( 132 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 132 FDA reports)
TENSION ( 132 FDA reports)
TRISMUS ( 132 FDA reports)
FACE INJURY ( 132 FDA reports)
FOREIGN BODY ( 132 FDA reports)
DRUG DISPENSING ERROR ( 131 FDA reports)
GASTRIC POLYPS ( 131 FDA reports)
LIPOMA ( 131 FDA reports)
MUSCLE INJURY ( 131 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 131 FDA reports)
OESOPHAGEAL STENOSIS ( 131 FDA reports)
PANCREATITIS CHRONIC ( 131 FDA reports)
PREMATURE BABY ( 130 FDA reports)
TEMPERATURE INTOLERANCE ( 130 FDA reports)
TIBIA FRACTURE ( 130 FDA reports)
ABSCESS JAW ( 130 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 130 FDA reports)
ADRENAL MASS ( 130 FDA reports)
DEVICE OCCLUSION ( 130 FDA reports)
GRANULOCYTOPENIA ( 130 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 129 FDA reports)
IMMUNOSUPPRESSION ( 129 FDA reports)
RESPIRATORY ACIDOSIS ( 129 FDA reports)
POLYDIPSIA ( 128 FDA reports)
SYNCOPE VASOVAGAL ( 128 FDA reports)
ABNORMAL FAECES ( 128 FDA reports)
CONCUSSION ( 128 FDA reports)
GASTRIC CANCER ( 128 FDA reports)
HYPOVENTILATION ( 128 FDA reports)
AORTIC VALVE DISEASE ( 127 FDA reports)
DRY THROAT ( 127 FDA reports)
SENSITIVITY OF TEETH ( 127 FDA reports)
LOCALISED OEDEMA ( 126 FDA reports)
MALLORY-WEISS SYNDROME ( 126 FDA reports)
NEUROGENIC BLADDER ( 126 FDA reports)
NEUROLOGICAL SYMPTOM ( 126 FDA reports)
PERSONALITY CHANGE ( 126 FDA reports)
POSTNASAL DRIP ( 126 FDA reports)
SKIN ATROPHY ( 126 FDA reports)
SKIN INFECTION ( 126 FDA reports)
X-RAY ABNORMAL ( 126 FDA reports)
ABNORMAL SENSATION IN EYE ( 126 FDA reports)
BILE DUCT STONE ( 126 FDA reports)
BRADYARRHYTHMIA ( 126 FDA reports)
CACHEXIA ( 126 FDA reports)
DYSTONIA ( 126 FDA reports)
FIBULA FRACTURE ( 126 FDA reports)
CHOLANGITIS ( 125 FDA reports)
BLOOD BICARBONATE DECREASED ( 124 FDA reports)
BLOOD CHLORIDE INCREASED ( 124 FDA reports)
CARDIAC ANEURYSM ( 124 FDA reports)
ENTERITIS ( 124 FDA reports)
HYPERAESTHESIA ( 124 FDA reports)
INADEQUATE ANALGESIA ( 124 FDA reports)
LYMPHOPENIA ( 124 FDA reports)
NEOPLASM ( 124 FDA reports)
SUBCUTANEOUS ABSCESS ( 124 FDA reports)
METABOLIC SYNDROME ( 123 FDA reports)
MYDRIASIS ( 123 FDA reports)
ESCHERICHIA SEPSIS ( 123 FDA reports)
HYDROCEPHALUS ( 123 FDA reports)
APPLICATION SITE PRURITUS ( 122 FDA reports)
GASTRITIS HAEMORRHAGIC ( 122 FDA reports)
HEART VALVE INCOMPETENCE ( 122 FDA reports)
TROPONIN I INCREASED ( 122 FDA reports)
VENOUS OCCLUSION ( 122 FDA reports)
MENINGIOMA ( 121 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 121 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 120 FDA reports)
SKIN IRRITATION ( 120 FDA reports)
TEMPORAL ARTERITIS ( 120 FDA reports)
AORTIC DILATATION ( 120 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 120 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 120 FDA reports)
BLOOD SODIUM INCREASED ( 120 FDA reports)
BRAIN INJURY ( 120 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 120 FDA reports)
DERMATITIS ALLERGIC ( 120 FDA reports)
EYE INFECTION ( 120 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 120 FDA reports)
WOUND DRAINAGE ( 120 FDA reports)
INTRAOCULAR LENS IMPLANT ( 119 FDA reports)
PROSTATE CANCER METASTATIC ( 119 FDA reports)
ABSCESS DRAINAGE ( 119 FDA reports)
BLOOD PH DECREASED ( 118 FDA reports)
MARROW HYPERPLASIA ( 118 FDA reports)
POOR DENTAL CONDITION ( 118 FDA reports)
RETINAL ARTERY OCCLUSION ( 118 FDA reports)
SKIN PLAQUE ( 118 FDA reports)
POOR PERIPHERAL CIRCULATION ( 117 FDA reports)
PULMONARY GRANULOMA ( 117 FDA reports)
SLUGGISHNESS ( 117 FDA reports)
STREPTOCOCCAL INFECTION ( 117 FDA reports)
TRANSFUSION ( 117 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 117 FDA reports)
BRONCHITIS CHRONIC ( 117 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 117 FDA reports)
EROSIVE DUODENITIS ( 117 FDA reports)
HERPES VIRUS INFECTION ( 117 FDA reports)
DRUG RESISTANCE ( 116 FDA reports)
GALLBLADDER OPERATION ( 116 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 116 FDA reports)
LUNG HYPERINFLATION ( 116 FDA reports)
MUSCLE FATIGUE ( 116 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 116 FDA reports)
TONGUE ULCERATION ( 116 FDA reports)
STRESS SYMPTOMS ( 115 FDA reports)
URINARY HESITATION ( 115 FDA reports)
GASTROINTESTINAL NECROSIS ( 115 FDA reports)
HYPERTONIC BLADDER ( 115 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 114 FDA reports)
BRAIN NEOPLASM ( 114 FDA reports)
HEPATOCELLULAR INJURY ( 114 FDA reports)
RETINOPATHY ( 114 FDA reports)
SOMNAMBULISM ( 114 FDA reports)
RECTAL POLYP ( 113 FDA reports)
TOOTH IMPACTED ( 113 FDA reports)
UNDERDOSE ( 113 FDA reports)
ABSCESS LIMB ( 113 FDA reports)
ANAEMIA MACROCYTIC ( 113 FDA reports)
BRAIN HERNIATION ( 113 FDA reports)
BREAST CANCER METASTATIC ( 113 FDA reports)
HYPERCOAGULATION ( 113 FDA reports)
BREAST TENDERNESS ( 112 FDA reports)
CEREBELLAR INFARCTION ( 112 FDA reports)
COAGULATION TIME PROLONGED ( 112 FDA reports)
DRUG ABUSER ( 112 FDA reports)
PSYCHIATRIC SYMPTOM ( 112 FDA reports)
PULMONARY THROMBOSIS ( 112 FDA reports)
SEBORRHOEIC DERMATITIS ( 112 FDA reports)
SUBDURAL HAEMORRHAGE ( 112 FDA reports)
INJECTION SITE MASS ( 111 FDA reports)
LABYRINTHITIS ( 111 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 111 FDA reports)
PITTING OEDEMA ( 111 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 111 FDA reports)
TONGUE OEDEMA ( 111 FDA reports)
ATROPHY ( 111 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 111 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 111 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 111 FDA reports)
HYPERPLASIA ( 110 FDA reports)
LIVEDO RETICULARIS ( 110 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 110 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 110 FDA reports)
RENAL ATROPHY ( 110 FDA reports)
SELF-MEDICATION ( 110 FDA reports)
SKIN FISSURES ( 110 FDA reports)
METABOLIC DISORDER ( 109 FDA reports)
PULPITIS DENTAL ( 109 FDA reports)
TUBERCULOSIS ( 109 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 109 FDA reports)
VERTIGO POSITIONAL ( 109 FDA reports)
ASTIGMATISM ( 109 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 109 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 109 FDA reports)
CATHETER SITE HAEMORRHAGE ( 109 FDA reports)
CHRONIC FATIGUE SYNDROME ( 109 FDA reports)
CALCULUS URETERIC ( 108 FDA reports)
DENTAL OPERATION ( 108 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 108 FDA reports)
FACIAL PARESIS ( 108 FDA reports)
HEPATIC CONGESTION ( 108 FDA reports)
HEPATITIS FULMINANT ( 108 FDA reports)
HYSTERECTOMY ( 108 FDA reports)
LIPIDS INCREASED ( 108 FDA reports)
NAIL DISORDER ( 108 FDA reports)
THYROID CANCER ( 108 FDA reports)
URINE FLOW DECREASED ( 108 FDA reports)
EYE MOVEMENT DISORDER ( 107 FDA reports)
INTENTIONAL MISUSE ( 107 FDA reports)
STRESS URINARY INCONTINENCE ( 107 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 106 FDA reports)
RAYNAUD'S PHENOMENON ( 106 FDA reports)
VASCULAR GRAFT OCCLUSION ( 106 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 106 FDA reports)
BONE EROSION ( 106 FDA reports)
CARDIOPULMONARY FAILURE ( 106 FDA reports)
DERMATITIS BULLOUS ( 106 FDA reports)
DIABETIC FOOT ( 106 FDA reports)
DISSOCIATION ( 106 FDA reports)
ENDOTRACHEAL INTUBATION ( 105 FDA reports)
MIOSIS ( 105 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 105 FDA reports)
PHOTOPSIA ( 105 FDA reports)
SALIVARY HYPERSECRETION ( 105 FDA reports)
INJECTION SITE EXTRAVASATION ( 104 FDA reports)
OESOPHAGEAL SPASM ( 104 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 104 FDA reports)
PRESBYOPIA ( 104 FDA reports)
ARTHRITIS BACTERIAL ( 104 FDA reports)
DRUG SCREEN POSITIVE ( 104 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 104 FDA reports)
GOUTY ARTHRITIS ( 104 FDA reports)
HUNGER ( 104 FDA reports)
DUODENAL ULCER PERFORATION ( 103 FDA reports)
FURUNCLE ( 103 FDA reports)
GINGIVAL ULCERATION ( 103 FDA reports)
INJECTION SITE RASH ( 103 FDA reports)
ISCHAEMIC HEPATITIS ( 103 FDA reports)
LOW TURNOVER OSTEOPATHY ( 103 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 103 FDA reports)
SKIN REACTION ( 103 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 102 FDA reports)
PCO2 DECREASED ( 102 FDA reports)
PLANTAR FASCIITIS ( 102 FDA reports)
QRS AXIS ABNORMAL ( 102 FDA reports)
AUTOIMMUNE HEPATITIS ( 102 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 102 FDA reports)
CLAVICLE FRACTURE ( 102 FDA reports)
COLITIS COLLAGENOUS ( 102 FDA reports)
HYPHAEMA ( 102 FDA reports)
VEIN DISORDER ( 102 FDA reports)
VENOUS THROMBOSIS ( 102 FDA reports)
WOUND HAEMORRHAGE ( 102 FDA reports)
LEUKAEMIA ( 101 FDA reports)
NON-SMALL CELL LUNG CANCER ( 101 FDA reports)
URINE COLOUR ABNORMAL ( 101 FDA reports)
APPENDICECTOMY ( 101 FDA reports)
COMPARTMENT SYNDROME ( 101 FDA reports)
CULTURE URINE POSITIVE ( 101 FDA reports)
FLUID INTAKE REDUCED ( 101 FDA reports)
HEAD DISCOMFORT ( 101 FDA reports)
IMMOBILE ( 101 FDA reports)
ANAL HAEMORRHAGE ( 100 FDA reports)
CARDIAC DEATH ( 100 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 100 FDA reports)
CORONARY ANGIOPLASTY ( 100 FDA reports)
EARLY SATIETY ( 100 FDA reports)
HAEMOTHORAX ( 100 FDA reports)
HERPES SIMPLEX ( 100 FDA reports)
HYPERPHOSPHATAEMIA ( 100 FDA reports)
MYELOMA RECURRENCE ( 100 FDA reports)
NASAL POLYPS ( 100 FDA reports)
NEPHROGENIC ANAEMIA ( 99 FDA reports)
NODAL RHYTHM ( 99 FDA reports)
RASH PUSTULAR ( 99 FDA reports)
AORTIC DISORDER ( 99 FDA reports)
CYSTOCELE ( 99 FDA reports)
GASTROINTESTINAL INFECTION ( 99 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 99 FDA reports)
BRAIN DEATH ( 98 FDA reports)
BREAST CANCER IN SITU ( 98 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 98 FDA reports)
INJECTION SITE INDURATION ( 98 FDA reports)
INJECTION SITE NODULE ( 98 FDA reports)
OSTEORADIONECROSIS ( 98 FDA reports)
PANCREATIC DISORDER ( 98 FDA reports)
PAPILLOEDEMA ( 98 FDA reports)
RENAL CELL CARCINOMA ( 98 FDA reports)
ROSACEA ( 98 FDA reports)
TRANSPLANT REJECTION ( 98 FDA reports)
PARAPLEGIA ( 97 FDA reports)
POLYTRAUMATISM ( 97 FDA reports)
PYURIA ( 97 FDA reports)
RESORPTION BONE INCREASED ( 97 FDA reports)
TENDON INJURY ( 97 FDA reports)
ENCEPHALITIS ( 97 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 96 FDA reports)
DEMYELINATION ( 96 FDA reports)
INGROWING NAIL ( 96 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 96 FDA reports)
METAPLASIA ( 95 FDA reports)
RENAL HAEMORRHAGE ( 95 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 95 FDA reports)
ACCIDENTAL EXPOSURE ( 95 FDA reports)
ALCOHOLISM ( 95 FDA reports)
ARTHROPOD BITE ( 95 FDA reports)
CLOSTRIDIUM COLITIS ( 95 FDA reports)
EXTREMITY CONTRACTURE ( 95 FDA reports)
AUTONOMIC NEUROPATHY ( 94 FDA reports)
BREAST CYST ( 94 FDA reports)
BUNION ( 94 FDA reports)
CHEILITIS ( 94 FDA reports)
EYE DISCHARGE ( 94 FDA reports)
FEMORAL ARTERY OCCLUSION ( 94 FDA reports)
FULL BLOOD COUNT DECREASED ( 94 FDA reports)
HYPERMETROPIA ( 94 FDA reports)
MENINGITIS ( 94 FDA reports)
PORTAL VEIN THROMBOSIS ( 94 FDA reports)
SCHIZOPHRENIA ( 94 FDA reports)
SKELETAL INJURY ( 94 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 94 FDA reports)
INJECTION SITE URTICARIA ( 93 FDA reports)
METASTASIS ( 93 FDA reports)
NYSTAGMUS ( 93 FDA reports)
OESOPHAGEAL PAIN ( 93 FDA reports)
PREMATURE LABOUR ( 93 FDA reports)
TENOSYNOVITIS ( 93 FDA reports)
THERMAL BURN ( 93 FDA reports)
DIABETIC COMPLICATION ( 93 FDA reports)
FRACTURE NONUNION ( 93 FDA reports)
HODGKIN'S DISEASE ( 93 FDA reports)
BLEEDING TIME PROLONGED ( 92 FDA reports)
CEREBELLAR HAEMORRHAGE ( 92 FDA reports)
HYPOREFLEXIA ( 92 FDA reports)
VASODILATATION ( 92 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 92 FDA reports)
OROPHARYNGEAL BLISTERING ( 92 FDA reports)
PERFORMANCE STATUS DECREASED ( 92 FDA reports)
STATUS EPILEPTICUS ( 92 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 92 FDA reports)
LABILE BLOOD PRESSURE ( 91 FDA reports)
MACROCYTOSIS ( 91 FDA reports)
PAROTITIS ( 91 FDA reports)
PSORIATIC ARTHROPATHY ( 91 FDA reports)
TOOTH INJURY ( 91 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 91 FDA reports)
ENTEROCOLITIS ( 91 FDA reports)
EPICONDYLITIS ( 91 FDA reports)
ACROCHORDON ( 90 FDA reports)
ADENOCARCINOMA ( 90 FDA reports)
AMMONIA INCREASED ( 90 FDA reports)
ANOXIC ENCEPHALOPATHY ( 90 FDA reports)
BONE SCAN ABNORMAL ( 90 FDA reports)
HAEMOGLOBIN INCREASED ( 90 FDA reports)
HAEMORRHAGE URINARY TRACT ( 90 FDA reports)
INTESTINAL HAEMORRHAGE ( 90 FDA reports)
OPERATIVE HAEMORRHAGE ( 90 FDA reports)
TRACHEOBRONCHITIS ( 90 FDA reports)
WEIGHT FLUCTUATION ( 90 FDA reports)
ADJUSTMENT DISORDER ( 89 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 89 FDA reports)
DIVERTICULAR PERFORATION ( 89 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 89 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 89 FDA reports)
PO2 DECREASED ( 89 FDA reports)
METRORRHAGIA ( 88 FDA reports)
TRIGGER FINGER ( 88 FDA reports)
VERTEBROPLASTY ( 88 FDA reports)
AUTOIMMUNE DISORDER ( 88 FDA reports)
BLOOD TEST ABNORMAL ( 88 FDA reports)
CHOKING SENSATION ( 88 FDA reports)
DERMATOMYOSITIS ( 88 FDA reports)
DROOLING ( 88 FDA reports)
DRUG LEVEL DECREASED ( 88 FDA reports)
EXTREMITY NECROSIS ( 88 FDA reports)
IATROGENIC INJURY ( 88 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 87 FDA reports)
ALVEOLITIS ( 87 FDA reports)
AORTIC VALVE REPLACEMENT ( 87 FDA reports)
HOMICIDAL IDEATION ( 87 FDA reports)
IMMUNE SYSTEM DISORDER ( 87 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 87 FDA reports)
RETINAL TEAR ( 87 FDA reports)
SINUS ARREST ( 87 FDA reports)
TUMOUR LYSIS SYNDROME ( 87 FDA reports)
VAGINAL INFECTION ( 87 FDA reports)
UTERINE POLYP ( 86 FDA reports)
VENOUS THROMBOSIS LIMB ( 86 FDA reports)
BRAIN STEM INFARCTION ( 86 FDA reports)
COELIAC DISEASE ( 86 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 86 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 86 FDA reports)
NASAL DISCOMFORT ( 86 FDA reports)
NODAL ARRHYTHMIA ( 86 FDA reports)
OVARIAN CANCER ( 86 FDA reports)
POLYARTHRITIS ( 86 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 86 FDA reports)
LISTLESS ( 85 FDA reports)
MACULOPATHY ( 85 FDA reports)
OVERWEIGHT ( 85 FDA reports)
RENAL TRANSPLANT ( 85 FDA reports)
RESPIRATORY DEPRESSION ( 85 FDA reports)
BILIARY DILATATION ( 85 FDA reports)
BONE OPERATION ( 85 FDA reports)
DYSGRAPHIA ( 85 FDA reports)
FEELING DRUNK ( 85 FDA reports)
HERNIA REPAIR ( 85 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 84 FDA reports)
BREAST CALCIFICATIONS ( 84 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 84 FDA reports)
ESSENTIAL TREMOR ( 84 FDA reports)
EXTRADURAL HAEMATOMA ( 84 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 84 FDA reports)
PERIARTHRITIS ( 84 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 84 FDA reports)
SCRATCH ( 84 FDA reports)
MECHANICAL VENTILATION ( 83 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 83 FDA reports)
SPINAL FUSION SURGERY ( 83 FDA reports)
SPUTUM CULTURE POSITIVE ( 83 FDA reports)
ABDOMINAL ABSCESS ( 83 FDA reports)
AKATHISIA ( 83 FDA reports)
BLADDER OBSTRUCTION ( 83 FDA reports)
CHANGE OF BOWEL HABIT ( 83 FDA reports)
CHEST WALL PAIN ( 83 FDA reports)
GINGIVAL OEDEMA ( 83 FDA reports)
GUILLAIN-BARRE SYNDROME ( 83 FDA reports)
HAEMANGIOMA OF LIVER ( 83 FDA reports)
AORTIC ANEURYSM RUPTURE ( 82 FDA reports)
APPLICATION SITE RASH ( 82 FDA reports)
BACTERIAL SEPSIS ( 82 FDA reports)
BLOOD LACTIC ACID INCREASED ( 82 FDA reports)
BRUXISM ( 82 FDA reports)
CALCINOSIS ( 82 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 82 FDA reports)
GINGIVAL ERYTHEMA ( 82 FDA reports)
HEPATIC NEOPLASM ( 82 FDA reports)
KNEE OPERATION ( 82 FDA reports)
MYOCARDITIS ( 82 FDA reports)
OPTIC NEURITIS ( 82 FDA reports)
PAROSMIA ( 82 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 82 FDA reports)
RESUSCITATION ( 82 FDA reports)
TINEA PEDIS ( 82 FDA reports)
URINARY TRACT DISORDER ( 82 FDA reports)
IRON DEFICIENCY ( 81 FDA reports)
MEAN CELL VOLUME INCREASED ( 81 FDA reports)
SCLERODERMA ( 81 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 81 FDA reports)
STRESS INCONTINENCE ( 81 FDA reports)
URINE ANALYSIS ABNORMAL ( 81 FDA reports)
CARDIOVERSION ( 81 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 81 FDA reports)
COR PULMONALE ( 81 FDA reports)
HYPOGONADISM ( 81 FDA reports)
ANAPHYLACTOID REACTION ( 80 FDA reports)
AORTIC VALVE CALCIFICATION ( 80 FDA reports)
ARTERIAL THROMBOSIS ( 80 FDA reports)
BILE DUCT OBSTRUCTION ( 80 FDA reports)
BILIARY COLIC ( 80 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 80 FDA reports)
HYPERREFLEXIA ( 80 FDA reports)
UTERINE CANCER ( 80 FDA reports)
MULTIPLE FRACTURES ( 80 FDA reports)
MYASTHENIA GRAVIS ( 80 FDA reports)
NASAL DRYNESS ( 80 FDA reports)
POSTURE ABNORMAL ( 80 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 80 FDA reports)
SINUS OPERATION ( 80 FDA reports)
SJOGREN'S SYNDROME ( 80 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 79 FDA reports)
MULTIPLE ALLERGIES ( 79 FDA reports)
PANCREATITIS NECROTISING ( 79 FDA reports)
PEMPHIGOID ( 79 FDA reports)
PIGMENTATION DISORDER ( 79 FDA reports)
POISONING ( 79 FDA reports)
POLYMYOSITIS ( 79 FDA reports)
SARCOIDOSIS ( 79 FDA reports)
BLOOD CREATININE DECREASED ( 79 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 79 FDA reports)
EYE INFLAMMATION ( 79 FDA reports)
FOLLICULITIS ( 79 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 79 FDA reports)
HEART RATE ABNORMAL ( 79 FDA reports)
B-CELL LYMPHOMA ( 78 FDA reports)
CATHETER RELATED INFECTION ( 78 FDA reports)
CEREBRAL DISORDER ( 78 FDA reports)
CERVICAL MYELOPATHY ( 78 FDA reports)
EDENTULOUS ( 78 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 78 FDA reports)
GASTROINTESTINAL PERFORATION ( 78 FDA reports)
GINGIVAL EROSION ( 78 FDA reports)
INDURATION ( 78 FDA reports)
MONOCYTE COUNT INCREASED ( 78 FDA reports)
MYELOPATHY ( 78 FDA reports)
TEARFULNESS ( 78 FDA reports)
TESTICULAR PAIN ( 78 FDA reports)
MYOGLOBINURIA ( 77 FDA reports)
MYOPIA ( 77 FDA reports)
PERIPHERAL EMBOLISM ( 77 FDA reports)
POSTOPERATIVE ILEUS ( 77 FDA reports)
RENAL MASS ( 77 FDA reports)
SCOTOMA ( 77 FDA reports)
STUPOR ( 77 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 77 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 77 FDA reports)
HEPATITIS B ( 77 FDA reports)
VARICES OESOPHAGEAL ( 77 FDA reports)
VASCULAR DEMENTIA ( 77 FDA reports)
YELLOW SKIN ( 77 FDA reports)
JOINT CREPITATION ( 76 FDA reports)
MENOPAUSE ( 76 FDA reports)
MICROCYTIC ANAEMIA ( 76 FDA reports)
ADENOMA BENIGN ( 76 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 76 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 76 FDA reports)
CORONARY ARTERY SURGERY ( 76 FDA reports)
FISTULA DISCHARGE ( 76 FDA reports)
HEPATITIS TOXIC ( 76 FDA reports)
APPLICATION SITE IRRITATION ( 75 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 75 FDA reports)
ARTHRITIS INFECTIVE ( 75 FDA reports)
BRADYPHRENIA ( 75 FDA reports)
BREAST CANCER RECURRENT ( 75 FDA reports)
FAECES HARD ( 75 FDA reports)
INCISIONAL HERNIA ( 75 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 75 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 75 FDA reports)
LOSS OF EMPLOYMENT ( 75 FDA reports)
OBSTRUCTION ( 75 FDA reports)
PERIORBITAL HAEMATOMA ( 75 FDA reports)
PULMONARY INFARCTION ( 75 FDA reports)
SECRETION DISCHARGE ( 75 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 74 FDA reports)
OBSTRUCTIVE UROPATHY ( 74 FDA reports)
SOPOR ( 74 FDA reports)
TOBACCO ABUSE ( 74 FDA reports)
TRAUMATIC HAEMATOMA ( 74 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 74 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 74 FDA reports)
CHOLECYSTITIS INFECTIVE ( 74 FDA reports)
AKINESIA ( 73 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 73 FDA reports)
CALCULUS URINARY ( 73 FDA reports)
DEMENTIA WITH LEWY BODIES ( 73 FDA reports)
DIABETIC GASTROPARESIS ( 73 FDA reports)
EXFOLIATIVE RASH ( 73 FDA reports)
FAECES PALE ( 73 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 73 FDA reports)
INTENTIONAL SELF-INJURY ( 73 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 73 FDA reports)
RENAL CANCER ( 73 FDA reports)
SUNBURN ( 73 FDA reports)
MICTURITION DISORDER ( 72 FDA reports)
OPTIC NERVE CUPPING ( 72 FDA reports)
PROCEDURAL HYPOTENSION ( 72 FDA reports)
PROTEIN TOTAL INCREASED ( 72 FDA reports)
RENAL COLIC ( 72 FDA reports)
TRIGEMINAL NEURALGIA ( 72 FDA reports)
AMAUROSIS FUGAX ( 72 FDA reports)
AORTIC DISSECTION ( 72 FDA reports)
BONE MARROW OEDEMA ( 72 FDA reports)
BONE SWELLING ( 72 FDA reports)
DEAFNESS BILATERAL ( 72 FDA reports)
BLADDER SPASM ( 71 FDA reports)
DIABETIC COMA ( 71 FDA reports)
ERYSIPELAS ( 71 FDA reports)
GASTRIC ULCER PERFORATION ( 71 FDA reports)
HYDROCELE ( 71 FDA reports)
INFECTIOUS PERITONITIS ( 71 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 71 FDA reports)
PROCTITIS ( 71 FDA reports)
PULSE ABNORMAL ( 71 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 71 FDA reports)
TOXIC ENCEPHALOPATHY ( 71 FDA reports)
UVEITIS ( 71 FDA reports)
ANAL FISSURE ( 70 FDA reports)
CERVICAL DYSPLASIA ( 70 FDA reports)
COMMUNICATION DISORDER ( 70 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 70 FDA reports)
HAIR GROWTH ABNORMAL ( 70 FDA reports)
HILAR LYMPHADENOPATHY ( 70 FDA reports)
HYPERTONIA ( 70 FDA reports)
INJECTION SITE DISCOLOURATION ( 70 FDA reports)
IRITIS ( 70 FDA reports)
MALIGNANT HYPERTENSION ( 70 FDA reports)
MENINGITIS ASEPTIC ( 70 FDA reports)
PROTHROMBIN TIME SHORTENED ( 70 FDA reports)
RETINAL DISORDER ( 70 FDA reports)
SINUS POLYP ( 70 FDA reports)
TOBACCO USER ( 70 FDA reports)
JUGULAR VEIN DISTENSION ( 69 FDA reports)
LARYNGOSPASM ( 69 FDA reports)
METABOLIC ALKALOSIS ( 69 FDA reports)
MIGRAINE WITH AURA ( 69 FDA reports)
NEURODERMATITIS ( 69 FDA reports)
OLFACTORY NERVE DISORDER ( 69 FDA reports)
PARTIAL SEIZURES ( 69 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 69 FDA reports)
SEPSIS SYNDROME ( 69 FDA reports)
THALAMUS HAEMORRHAGE ( 69 FDA reports)
UTERINE HAEMORRHAGE ( 69 FDA reports)
WOUND COMPLICATION ( 69 FDA reports)
ASPERGILLOSIS ( 69 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 69 FDA reports)
HEART DISEASE CONGENITAL ( 69 FDA reports)
HEPATORENAL SYNDROME ( 69 FDA reports)
BACTERIAL TEST POSITIVE ( 68 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 68 FDA reports)
DEVICE DISLOCATION ( 68 FDA reports)
ENCEPHALOMALACIA ( 68 FDA reports)
FEAR OF DEATH ( 68 FDA reports)
GASTRODUODENITIS ( 68 FDA reports)
HYPERTHERMIA ( 68 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 68 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 68 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 68 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 68 FDA reports)
SPONDYLOSIS ( 68 FDA reports)
THROMBOCYTHAEMIA ( 68 FDA reports)
MASTECTOMY ( 67 FDA reports)
MENIERE'S DISEASE ( 67 FDA reports)
MONOCLONAL GAMMOPATHY ( 67 FDA reports)
OROANTRAL FISTULA ( 67 FDA reports)
PANIC REACTION ( 67 FDA reports)
PATELLA FRACTURE ( 67 FDA reports)
PORTAL HYPERTENSION ( 67 FDA reports)
RADICULAR PAIN ( 67 FDA reports)
SKIN SWELLING ( 67 FDA reports)
SOFT TISSUE INFECTION ( 67 FDA reports)
AFFECT LABILITY ( 67 FDA reports)
BOWEN'S DISEASE ( 67 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 67 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 67 FDA reports)
FLAT AFFECT ( 67 FDA reports)
GRAFT THROMBOSIS ( 67 FDA reports)
HAEMATOCRIT INCREASED ( 67 FDA reports)
HEPATIC FIBROSIS ( 67 FDA reports)
HYPERCAPNIA ( 67 FDA reports)
ABDOMINAL RIGIDITY ( 66 FDA reports)
ABSCESS NECK ( 66 FDA reports)
AMYLOIDOSIS ( 66 FDA reports)
APPETITE DISORDER ( 66 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 66 FDA reports)
BREAST HYPERPLASIA ( 66 FDA reports)
CANCER PAIN ( 66 FDA reports)
CEREBRAL THROMBOSIS ( 66 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 66 FDA reports)
INFECTED SKIN ULCER ( 66 FDA reports)
LYMPHADENITIS ( 66 FDA reports)
MASTOIDITIS ( 66 FDA reports)
NOSOCOMIAL INFECTION ( 66 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 66 FDA reports)
POST PROCEDURAL INFECTION ( 66 FDA reports)
URINARY TRACT OBSTRUCTION ( 66 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 66 FDA reports)
VULVOVAGINAL DRYNESS ( 66 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 65 FDA reports)
BLADDER NEOPLASM ( 65 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 65 FDA reports)
CEREBRAL ARTERY STENOSIS ( 65 FDA reports)
EAR HAEMORRHAGE ( 65 FDA reports)
HAIR TEXTURE ABNORMAL ( 65 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 65 FDA reports)
HIP SURGERY ( 65 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 65 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 65 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 65 FDA reports)
MUSCLE RUPTURE ( 65 FDA reports)
OPTIC ATROPHY ( 65 FDA reports)
PULMONARY VASCULAR DISORDER ( 65 FDA reports)
PUPILS UNEQUAL ( 65 FDA reports)
SCREAMING ( 65 FDA reports)
SPONDYLOLYSIS ( 65 FDA reports)
SURGICAL PROCEDURE REPEATED ( 65 FDA reports)
THROAT CANCER ( 65 FDA reports)
TOURETTE'S DISORDER ( 65 FDA reports)
LIMB OPERATION ( 64 FDA reports)
RECTOCELE ( 64 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 64 FDA reports)
SEROMA ( 64 FDA reports)
SKIN ODOUR ABNORMAL ( 64 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 64 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 64 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 64 FDA reports)
ASPIRATION PLEURAL CAVITY ( 64 FDA reports)
BLOODY DISCHARGE ( 64 FDA reports)
CARDIAC FIBRILLATION ( 64 FDA reports)
CARDIAC OUTPUT DECREASED ( 64 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 64 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 64 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 64 FDA reports)
FOOD POISONING ( 64 FDA reports)
HAEMARTHROSIS ( 64 FDA reports)
HEARING DISABILITY ( 64 FDA reports)
HOARSENESS ( 64 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 63 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 63 FDA reports)
BRONCHIOLITIS ( 63 FDA reports)
CLAUSTROPHOBIA ( 63 FDA reports)
EXOPHTHALMOS ( 63 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 63 FDA reports)
FRUSTRATION ( 63 FDA reports)
GRIP STRENGTH DECREASED ( 63 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 63 FDA reports)
MICROALBUMINURIA ( 63 FDA reports)
MUSCLE SPASTICITY ( 63 FDA reports)
PANCREATIC CYST ( 63 FDA reports)
PANCREATIC NEOPLASM ( 63 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 63 FDA reports)
PUPIL FIXED ( 63 FDA reports)
PYELONEPHRITIS ACUTE ( 63 FDA reports)
RESPIRATORY ALKALOSIS ( 63 FDA reports)
RIGHT ATRIAL DILATATION ( 63 FDA reports)
INCISION SITE HAEMORRHAGE ( 62 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 62 FDA reports)
LUPUS-LIKE SYNDROME ( 62 FDA reports)
MICROANGIOPATHY ( 62 FDA reports)
MUCOSAL DRYNESS ( 62 FDA reports)
NECK MASS ( 62 FDA reports)
ORAL FUNGAL INFECTION ( 62 FDA reports)
PAPULE ( 62 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 62 FDA reports)
RECTAL CANCER ( 62 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 62 FDA reports)
TETANY ( 62 FDA reports)
TONGUE INJURY ( 62 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 62 FDA reports)
URINE OUTPUT INCREASED ( 62 FDA reports)
ABDOMINAL MASS ( 62 FDA reports)
ARTERIAL HAEMORRHAGE ( 62 FDA reports)
ARTERIOVENOUS MALFORMATION ( 62 FDA reports)
BLOOD BLISTER ( 62 FDA reports)
EJECTION FRACTION ABNORMAL ( 62 FDA reports)
FOREIGN BODY TRAUMA ( 62 FDA reports)
FRACTURE DELAYED UNION ( 62 FDA reports)
GLOBAL AMNESIA ( 62 FDA reports)
HEMIANOPIA HOMONYMOUS ( 62 FDA reports)
HEPATOSPLENOMEGALY ( 62 FDA reports)
HYPERAMMONAEMIA ( 62 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 61 FDA reports)
BILE DUCT STENOSIS ( 61 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 61 FDA reports)
CARTILAGE INJURY ( 61 FDA reports)
HAEMOGLOBIN ABNORMAL ( 61 FDA reports)
HELICOBACTER GASTRITIS ( 61 FDA reports)
LIGAMENT INJURY ( 61 FDA reports)
MUSCLE CONTRACTURE ( 61 FDA reports)
NOCTURNAL DYSPNOEA ( 61 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 61 FDA reports)
RESPIRATION ABNORMAL ( 61 FDA reports)
REYE'S SYNDROME ( 61 FDA reports)
ROTATOR CUFF REPAIR ( 61 FDA reports)
LACTOSE INTOLERANCE ( 60 FDA reports)
MALABSORPTION ( 60 FDA reports)
PARAPROTEINAEMIA ( 60 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 60 FDA reports)
ADRENAL DISORDER ( 60 FDA reports)
AORTIC ATHEROSCLEROSIS ( 60 FDA reports)
BLOOD UREA DECREASED ( 60 FDA reports)
BREAST SWELLING ( 60 FDA reports)
CHONDROPATHY ( 60 FDA reports)
CONTRAST MEDIA REACTION ( 60 FDA reports)
ERYTHEMA NODOSUM ( 60 FDA reports)
EYE NAEVUS ( 60 FDA reports)
GALLBLADDER POLYP ( 60 FDA reports)
VOCAL CORD DISORDER ( 60 FDA reports)
INJECTION SITE WARMTH ( 59 FDA reports)
INTESTINAL DILATATION ( 59 FDA reports)
LIGAMENT DISORDER ( 59 FDA reports)
LIP DRY ( 59 FDA reports)
MYOCARDIAL RUPTURE ( 59 FDA reports)
OESOPHAGEAL RUPTURE ( 59 FDA reports)
PARONYCHIA ( 59 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 59 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 59 FDA reports)
POSTOPERATIVE INFECTION ( 59 FDA reports)
RADICULITIS LUMBOSACRAL ( 59 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 59 FDA reports)
ASTHENOPIA ( 59 FDA reports)
BILIARY DYSKINESIA ( 59 FDA reports)
BRADYKINESIA ( 59 FDA reports)
BRAIN SCAN ABNORMAL ( 59 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 59 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 59 FDA reports)
HAND DEFORMITY ( 59 FDA reports)
ANIMAL BITE ( 58 FDA reports)
BLOOD PH INCREASED ( 58 FDA reports)
BONE MARROW DEPRESSION ( 58 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 58 FDA reports)
COLONOSCOPY ( 58 FDA reports)
COMPLEX PARTIAL SEIZURES ( 58 FDA reports)
DEFAECATION URGENCY ( 58 FDA reports)
DENTAL PLAQUE ( 58 FDA reports)
FOOD INTOLERANCE ( 58 FDA reports)
LABILE HYPERTENSION ( 58 FDA reports)
MITRAL VALVE STENOSIS ( 58 FDA reports)
NASAL DISORDER ( 58 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 58 FDA reports)
PNEUMONIA VIRAL ( 58 FDA reports)
RESPIRATORY RATE DECREASED ( 58 FDA reports)
SPINAL LAMINECTOMY ( 58 FDA reports)
THROMBOCYTOPENIC PURPURA ( 58 FDA reports)
TROPONIN T INCREASED ( 58 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 57 FDA reports)
URINE ABNORMALITY ( 57 FDA reports)
ABDOMINAL ADHESIONS ( 57 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 57 FDA reports)
BLADDER PROLAPSE ( 57 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 57 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 57 FDA reports)
HEART TRANSPLANT REJECTION ( 57 FDA reports)
HYPERPHAGIA ( 57 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 57 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 56 FDA reports)
ATROPHIC VULVOVAGINITIS ( 56 FDA reports)
CARDIAC HYPERTROPHY ( 56 FDA reports)
DEVICE BREAKAGE ( 56 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 56 FDA reports)
DYSPNOEA EXACERBATED ( 56 FDA reports)
ENDOMETRIAL CANCER ( 56 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 56 FDA reports)
HEPATIC ENZYME ABNORMAL ( 56 FDA reports)
HYPOPERFUSION ( 56 FDA reports)
ILIAC ARTERY STENOSIS ( 56 FDA reports)
WEGENER'S GRANULOMATOSIS ( 56 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 56 FDA reports)
MORTON'S NEUROMA ( 56 FDA reports)
NEUTROPHILIA ( 56 FDA reports)
OESOPHAGEAL CARCINOMA ( 56 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 56 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 56 FDA reports)
OROPHARYNGEAL SWELLING ( 56 FDA reports)
PAINFUL RESPIRATION ( 56 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 56 FDA reports)
PERITONEAL HAEMORRHAGE ( 56 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 56 FDA reports)
RENAL TUBULAR DISORDER ( 56 FDA reports)
SOFT TISSUE INFLAMMATION ( 56 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 56 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 56 FDA reports)
URETERIC OBSTRUCTION ( 56 FDA reports)
LICHEN PLANUS ( 55 FDA reports)
OROPHARYNGEAL PLAQUE ( 55 FDA reports)
OSTEITIS DEFORMANS ( 55 FDA reports)
PERSONALITY DISORDER ( 55 FDA reports)
PLATELET DISORDER ( 55 FDA reports)
PRINZMETAL ANGINA ( 55 FDA reports)
SMALL INTESTINE ULCER ( 55 FDA reports)
APPENDICITIS PERFORATED ( 55 FDA reports)
APRAXIA ( 55 FDA reports)
COLON POLYPECTOMY ( 55 FDA reports)
CONVERSION DISORDER ( 55 FDA reports)
EAR CONGESTION ( 55 FDA reports)
EYELID DISORDER ( 55 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 55 FDA reports)
HYPOCHLORAEMIA ( 55 FDA reports)
ARTERIOVENOUS FISTULA ( 54 FDA reports)
CONGENITAL ANOMALY ( 54 FDA reports)
DRUG TOLERANCE ( 54 FDA reports)
DYSLALIA ( 54 FDA reports)
DYSPHEMIA ( 54 FDA reports)
EFFUSION ( 54 FDA reports)
EJACULATION DISORDER ( 54 FDA reports)
EMPYEMA ( 54 FDA reports)
EYE OPERATION ( 54 FDA reports)
FRACTURE DISPLACEMENT ( 54 FDA reports)
HANGOVER ( 54 FDA reports)
IMPAIRED SELF-CARE ( 54 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 54 FDA reports)
NEURITIS ( 54 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 54 FDA reports)
ORAL DISCHARGE ( 54 FDA reports)
PHARYNGEAL ERYTHEMA ( 54 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 54 FDA reports)
STREPTOCOCCAL SEPSIS ( 54 FDA reports)
URINE KETONE BODY PRESENT ( 54 FDA reports)
UTERINE DISORDER ( 54 FDA reports)
ABSCESS INTESTINAL ( 53 FDA reports)
APPLICATION SITE REACTION ( 53 FDA reports)
ARTERIAL RUPTURE ( 53 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 53 FDA reports)
BLOOD URINE ( 53 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 53 FDA reports)
CALCULUS BLADDER ( 53 FDA reports)
CARDIOTOXICITY ( 53 FDA reports)
DYSPHORIA ( 53 FDA reports)
DYSTHYMIC DISORDER ( 53 FDA reports)
EOSINOPHILIC PNEUMONIA ( 53 FDA reports)
ESCHERICHIA BACTERAEMIA ( 53 FDA reports)
FOOT AMPUTATION ( 53 FDA reports)
GLUCOSE URINE PRESENT ( 53 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 53 FDA reports)
HYPERMETABOLISM ( 53 FDA reports)
HYPOCHROMIC ANAEMIA ( 53 FDA reports)
INTESTINAL POLYP ( 53 FDA reports)
LIMB CRUSHING INJURY ( 53 FDA reports)
LOSS OF LIBIDO ( 53 FDA reports)
OTORRHOEA ( 53 FDA reports)
RADIATION INJURY ( 53 FDA reports)
RASH VESICULAR ( 53 FDA reports)
STRESS CARDIOMYOPATHY ( 53 FDA reports)
TONGUE BITING ( 53 FDA reports)
URGE INCONTINENCE ( 53 FDA reports)
INTRA-UTERINE DEATH ( 52 FDA reports)
NECROTISING FASCIITIS ( 52 FDA reports)
PETIT MAL EPILEPSY ( 52 FDA reports)
TONGUE HAEMORRHAGE ( 52 FDA reports)
TRANSPLANT FAILURE ( 52 FDA reports)
VESICAL FISTULA ( 52 FDA reports)
WEIGHT BEARING DIFFICULTY ( 52 FDA reports)
AORTIC THROMBOSIS ( 52 FDA reports)
APPENDIX DISORDER ( 52 FDA reports)
APPLICATION SITE PAIN ( 52 FDA reports)
BILE DUCT CANCER ( 52 FDA reports)
BIOPSY ( 52 FDA reports)
CATHETER PLACEMENT ( 52 FDA reports)
COCCYDYNIA ( 52 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 52 FDA reports)
EUPHORIC MOOD ( 52 FDA reports)
GRAVITATIONAL OEDEMA ( 52 FDA reports)
HEPATIC MASS ( 52 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 52 FDA reports)
IMPETIGO ( 52 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 51 FDA reports)
BIPOLAR I DISORDER ( 51 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 51 FDA reports)
BREAST DISORDER ( 51 FDA reports)
BREAST ENLARGEMENT ( 51 FDA reports)
CATARACT NUCLEAR ( 51 FDA reports)
COLONOSCOPY ABNORMAL ( 51 FDA reports)
DENTOFACIAL FUNCTIONAL DISORDER ( 51 FDA reports)
DERMATITIS ACNEIFORM ( 51 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 51 FDA reports)
ERYTHEMA OF EYELID ( 51 FDA reports)
FOAMING AT MOUTH ( 51 FDA reports)
GLOSSITIS ( 51 FDA reports)
INNER EAR DISORDER ( 51 FDA reports)
KETOACIDOSIS ( 51 FDA reports)
KYPHOSCOLIOSIS ( 51 FDA reports)
LOCALISED OSTEOARTHRITIS ( 51 FDA reports)
MUCOSAL HAEMORRHAGE ( 51 FDA reports)
ORAL TORUS ( 51 FDA reports)
POLYPECTOMY ( 51 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 51 FDA reports)
SACROILIITIS ( 51 FDA reports)
INCISIONAL DRAINAGE ( 50 FDA reports)
JOINT INSTABILITY ( 50 FDA reports)
JOINT LOCK ( 50 FDA reports)
MASTITIS ( 50 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 50 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 50 FDA reports)
NEUROPATHIC ARTHROPATHY ( 50 FDA reports)
OPEN REDUCTION OF FRACTURE ( 50 FDA reports)
PARTNER STRESS ( 50 FDA reports)
PROSTATIC OBSTRUCTION ( 50 FDA reports)
SIALOADENITIS ( 50 FDA reports)
SUBILEUS ( 50 FDA reports)
THROMBOTIC STROKE ( 50 FDA reports)
TOOTH DISCOLOURATION ( 50 FDA reports)
TOOTH REPAIR ( 50 FDA reports)
TREATMENT FAILURE ( 50 FDA reports)
APTYALISM ( 50 FDA reports)
CARBON DIOXIDE DECREASED ( 50 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 50 FDA reports)
EYE INJURY ( 50 FDA reports)
FEAR OF EATING ( 50 FDA reports)
GENERAL SYMPTOM ( 50 FDA reports)
HALLUCINATIONS, MIXED ( 50 FDA reports)
HEART VALVE REPLACEMENT ( 50 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 50 FDA reports)
VAGINAL DISCHARGE ( 50 FDA reports)
LUNG CANCER METASTATIC ( 49 FDA reports)
MALOCCLUSION ( 49 FDA reports)
MENOPAUSAL SYMPTOMS ( 49 FDA reports)
MONARTHRITIS ( 49 FDA reports)
OPTIC NEUROPATHY ( 49 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 49 FDA reports)
SCROTAL SWELLING ( 49 FDA reports)
SHOULDER ARTHROPLASTY ( 49 FDA reports)
STARING ( 49 FDA reports)
STASIS DERMATITIS ( 49 FDA reports)
TENDON PAIN ( 49 FDA reports)
TRAUMATIC BRAIN INJURY ( 49 FDA reports)
ANORECTAL DISCOMFORT ( 49 FDA reports)
BONE NEOPLASM ( 49 FDA reports)
BRAIN STEM HAEMORRHAGE ( 49 FDA reports)
BREAKTHROUGH PAIN ( 49 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 49 FDA reports)
CHAPPED LIPS ( 49 FDA reports)
EJACULATION FAILURE ( 49 FDA reports)
EPIDIDYMITIS ( 49 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 49 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 49 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 49 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 49 FDA reports)
IMMUNODEFICIENCY ( 49 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 48 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 48 FDA reports)
BLADDER CATHETERISATION ( 48 FDA reports)
BRAIN STEM SYNDROME ( 48 FDA reports)
CARDIAC VALVE SCLEROSIS ( 48 FDA reports)
CHOREA ( 48 FDA reports)
FEELING OF DESPAIR ( 48 FDA reports)
FINGER DEFORMITY ( 48 FDA reports)
LONG QT SYNDROME ( 48 FDA reports)
LYMPHOCYTOSIS ( 48 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 48 FDA reports)
NASAL OEDEMA ( 48 FDA reports)
NICOTINE DEPENDENCE ( 48 FDA reports)
OVARIAN MASS ( 48 FDA reports)
PARAPARESIS ( 48 FDA reports)
PNEUMONIA KLEBSIELLA ( 48 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 48 FDA reports)
PRE-ECLAMPSIA ( 48 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 48 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 48 FDA reports)
IRON OVERLOAD ( 47 FDA reports)
LIGAMENT RUPTURE ( 47 FDA reports)
MAMMOGRAM ABNORMAL ( 47 FDA reports)
PANCREATIC ATROPHY ( 47 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 47 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 47 FDA reports)
PCO2 INCREASED ( 47 FDA reports)
PENIS DISORDER ( 47 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 47 FDA reports)
SPINAL CORD DISORDER ( 47 FDA reports)
SPLENIC INFARCTION ( 47 FDA reports)
SPLENIC RUPTURE ( 47 FDA reports)
SPONDYLOARTHROPATHY ( 47 FDA reports)
ABORTION INDUCED ( 47 FDA reports)
ACUTE ABDOMEN ( 47 FDA reports)
ATRIAL THROMBOSIS ( 47 FDA reports)
BONE GRAFT ( 47 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 47 FDA reports)
COLONIC STENOSIS ( 47 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 47 FDA reports)
ACUTE LEUKAEMIA ( 46 FDA reports)
ADHESION ( 46 FDA reports)
ASPHYXIA ( 46 FDA reports)
AUTOIMMUNE THYROIDITIS ( 46 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 46 FDA reports)
BREAST LUMP REMOVAL ( 46 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 46 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 46 FDA reports)
DEPENDENCE ( 46 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 46 FDA reports)
FUNGAL SKIN INFECTION ( 46 FDA reports)
GASTRIC PERFORATION ( 46 FDA reports)
GASTROENTERITIS RADIATION ( 46 FDA reports)
GINGIVAL HYPERPLASIA ( 46 FDA reports)
HEMIANOPIA ( 46 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 46 FDA reports)
WALKING DISABILITY ( 46 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 46 FDA reports)
MENSTRUATION IRREGULAR ( 46 FDA reports)
MUCOSAL EROSION ( 46 FDA reports)
MULTI-ORGAN DISORDER ( 46 FDA reports)
PINGUECULA ( 46 FDA reports)
PULSE PRESSURE DECREASED ( 46 FDA reports)
PYELOCALIECTASIS ( 46 FDA reports)
REFLUX GASTRITIS ( 46 FDA reports)
SENSATION OF PRESSURE ( 46 FDA reports)
SKIN GRAFT ( 46 FDA reports)
SPINAL HAEMANGIOMA ( 46 FDA reports)
TELANGIECTASIA ( 46 FDA reports)
THYROID CYST ( 46 FDA reports)
TONGUE COATED ( 46 FDA reports)
TOOTH DEPOSIT ( 46 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 46 FDA reports)
URETHRAL STENOSIS ( 46 FDA reports)
LUNG ADENOCARCINOMA ( 45 FDA reports)
MAXILLOFACIAL OPERATION ( 45 FDA reports)
MUSCLE NECROSIS ( 45 FDA reports)
NEPHROCALCINOSIS ( 45 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 45 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 45 FDA reports)
PANCREATIC MASS ( 45 FDA reports)
PERIRECTAL ABSCESS ( 45 FDA reports)
PLATELET COUNT ABNORMAL ( 45 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 45 FDA reports)
SMALL INTESTINAL PERFORATION ( 45 FDA reports)
SPUTUM INCREASED ( 45 FDA reports)
TOOTH EROSION ( 45 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 45 FDA reports)
AMPUTATION ( 45 FDA reports)
ARTERIAL BYPASS OPERATION ( 45 FDA reports)
BASEDOW'S DISEASE ( 45 FDA reports)
BONE CYST ( 45 FDA reports)
CENTRAL LINE INFECTION ( 45 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 45 FDA reports)
COLECTOMY ( 45 FDA reports)
DIAPHRAGMATIC DISORDER ( 45 FDA reports)
DYSTROPHIC CALCIFICATION ( 45 FDA reports)
ENZYME ABNORMALITY ( 45 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 45 FDA reports)
FAT EMBOLISM ( 45 FDA reports)
GINGIVAL ABSCESS ( 45 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 45 FDA reports)
HEPATIC CANCER METASTATIC ( 45 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 45 FDA reports)
ALVEOLOPLASTY ( 44 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 44 FDA reports)
BLADDER CANCER RECURRENT ( 44 FDA reports)
BREAST DISCHARGE ( 44 FDA reports)
BUTTOCK PAIN ( 44 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 44 FDA reports)
DERMATOPHYTOSIS ( 44 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 44 FDA reports)
ENTEROBACTER INFECTION ( 44 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 44 FDA reports)
HEART TRANSPLANT ( 44 FDA reports)
HYPOGEUSIA ( 44 FDA reports)
LOSS OF CONTROL OF LEGS ( 44 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 44 FDA reports)
OCCULT BLOOD ( 44 FDA reports)
PARESIS ( 44 FDA reports)
PO2 INCREASED ( 44 FDA reports)
PRODUCT ADHESION ISSUE ( 44 FDA reports)
PROSTATE CANCER RECURRENT ( 44 FDA reports)
REGURGITATION ( 44 FDA reports)
SERUM SICKNESS ( 44 FDA reports)
SICCA SYNDROME ( 44 FDA reports)
SKIN NEOPLASM EXCISION ( 44 FDA reports)
SPINAL DEFORMITY ( 44 FDA reports)
SPUTUM PURULENT ( 44 FDA reports)
VASCULAR BYPASS GRAFT ( 44 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 44 FDA reports)
XEROSIS ( 44 FDA reports)
VESTIBULAR DISORDER ( 43 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 43 FDA reports)
AMENORRHOEA ( 43 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 43 FDA reports)
BLOOD IRON INCREASED ( 43 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 43 FDA reports)
CARDIORENAL SYNDROME ( 43 FDA reports)
DYSPHASIA ( 43 FDA reports)
EMBOLISM ARTERIAL ( 43 FDA reports)
HAEMATOCRIT ABNORMAL ( 43 FDA reports)
HEART SOUNDS ABNORMAL ( 43 FDA reports)
HYPERCHLORHYDRIA ( 43 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 43 FDA reports)
INCISION SITE INFECTION ( 43 FDA reports)
LICHENOID KERATOSIS ( 43 FDA reports)
LIP BLISTER ( 43 FDA reports)
NEUROTOXICITY ( 43 FDA reports)
NIPPLE PAIN ( 43 FDA reports)
OCULAR VASCULAR DISORDER ( 43 FDA reports)
OESOPHAGITIS ULCERATIVE ( 43 FDA reports)
ORAL FIBROMA ( 43 FDA reports)
OSTEOCHONDROSIS ( 43 FDA reports)
PERITONEAL DISORDER ( 43 FDA reports)
POISONING DELIBERATE ( 43 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 43 FDA reports)
PROTEUS INFECTION ( 43 FDA reports)
REFRACTORY ANAEMIA ( 43 FDA reports)
SPLENIC GRANULOMA ( 43 FDA reports)
SUFFOCATION FEELING ( 43 FDA reports)
INCISION SITE COMPLICATION ( 42 FDA reports)
JUGULAR VEIN THROMBOSIS ( 42 FDA reports)
LIP PAIN ( 42 FDA reports)
NERVE ROOT LESION ( 42 FDA reports)
ONYCHOCLASIS ( 42 FDA reports)
PELVIC HAEMATOMA ( 42 FDA reports)
POLYCYTHAEMIA ( 42 FDA reports)
POOR PERSONAL HYGIENE ( 42 FDA reports)
PULMONARY TOXICITY ( 42 FDA reports)
QUADRIPLEGIA ( 42 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 42 FDA reports)
TESTICULAR SWELLING ( 42 FDA reports)
VASCULAR ANOMALY ( 42 FDA reports)
ACETABULUM FRACTURE ( 42 FDA reports)
ARTERIAL INJURY ( 42 FDA reports)
BLOOD BICARBONATE INCREASED ( 42 FDA reports)
CARDIAC ABLATION ( 42 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 42 FDA reports)
CAROTID ARTERY ATHEROMA ( 42 FDA reports)
COMA SCALE ABNORMAL ( 42 FDA reports)
CUBITAL TUNNEL SYNDROME ( 42 FDA reports)
ENDOCARDITIS BACTERIAL ( 42 FDA reports)
EYE ROLLING ( 42 FDA reports)
FINGER AMPUTATION ( 42 FDA reports)
FOOD ALLERGY ( 42 FDA reports)
GALLBLADDER ENLARGEMENT ( 42 FDA reports)
GLYCOSURIA ( 42 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 42 FDA reports)
HYPERTROPHY ( 42 FDA reports)
HYPOCOAGULABLE STATE ( 42 FDA reports)
HYPOPROTEINAEMIA ( 42 FDA reports)
APPARENT DEATH ( 41 FDA reports)
BLEPHAROSPASM ( 41 FDA reports)
BLOOD CREATININE ABNORMAL ( 41 FDA reports)
CLUSTER HEADACHE ( 41 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 41 FDA reports)
DIABETIC FOOT INFECTION ( 41 FDA reports)
EYE OEDEMA ( 41 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 41 FDA reports)
HOSTILITY ( 41 FDA reports)
HYPERSEXUALITY ( 41 FDA reports)
HYPERTENSIVE EMERGENCY ( 41 FDA reports)
IMMUNOGLOBULINS DECREASED ( 41 FDA reports)
MACULAR HOLE ( 41 FDA reports)
MESOTHELIOMA ( 41 FDA reports)
MIDDLE EAR EFFUSION ( 41 FDA reports)
NEUROMYOPATHY ( 41 FDA reports)
PANCREATIC PSEUDOCYST ( 41 FDA reports)
PEAU D'ORANGE ( 41 FDA reports)
PHARYNGEAL DISORDER ( 41 FDA reports)
PNEUMONIA FUNGAL ( 41 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 41 FDA reports)
RETINOPATHY HYPERTENSIVE ( 41 FDA reports)
SUDDEN ONSET OF SLEEP ( 41 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 41 FDA reports)
ULCERATIVE KERATITIS ( 41 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 41 FDA reports)
UTERINE ENLARGEMENT ( 41 FDA reports)
VULVOVAGINAL PAIN ( 41 FDA reports)
VAGINITIS BACTERIAL ( 40 FDA reports)
VOCAL CORD PARALYSIS ( 40 FDA reports)
APPLICATION SITE VESICLES ( 40 FDA reports)
BILIARY TRACT DISORDER ( 40 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 40 FDA reports)
CORONARY ARTERY REOCCLUSION ( 40 FDA reports)
CYSTITIS INTERSTITIAL ( 40 FDA reports)
DENTAL IMPLANTATION ( 40 FDA reports)
DEVELOPMENTAL DELAY ( 40 FDA reports)
ENERGY INCREASED ( 40 FDA reports)
H1N1 INFLUENZA ( 40 FDA reports)
LYMPHADENECTOMY ( 40 FDA reports)
MENSTRUAL DISORDER ( 40 FDA reports)
NEOPLASM SKIN ( 40 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 40 FDA reports)
ORTHOSIS USER ( 40 FDA reports)
OSTEOMYELITIS ACUTE ( 40 FDA reports)
PARATHYROID DISORDER ( 40 FDA reports)
RENAL INFARCT ( 40 FDA reports)
STERNAL FRACTURE ( 40 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 40 FDA reports)
TIC ( 40 FDA reports)
INJECTION SITE INFECTION ( 39 FDA reports)
LIP OEDEMA ( 39 FDA reports)
MEAN CELL VOLUME DECREASED ( 39 FDA reports)
NARCOLEPSY ( 39 FDA reports)
NARCOTIC INTOXICATION ( 39 FDA reports)
NEOPLASM RECURRENCE ( 39 FDA reports)
NEPHRITIS ( 39 FDA reports)
ORGANISING PNEUMONIA ( 39 FDA reports)
PNEUMONIA LEGIONELLA ( 39 FDA reports)
POST PROCEDURAL PAIN ( 39 FDA reports)
POTENTIATING DRUG INTERACTION ( 39 FDA reports)
PSYCHOMOTOR RETARDATION ( 39 FDA reports)
RECTAL ULCER ( 39 FDA reports)
SKIN MASS ( 39 FDA reports)
SKIN NODULE ( 39 FDA reports)
SLEEP TERROR ( 39 FDA reports)
SPONDYLITIS ( 39 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 39 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 39 FDA reports)
ACCELERATED HYPERTENSION ( 39 FDA reports)
ANAL FISTULA ( 39 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 39 FDA reports)
BENIGN COLONIC NEOPLASM ( 39 FDA reports)
BENIGN NEOPLASM ( 39 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 39 FDA reports)
BLADDER PAIN ( 39 FDA reports)
BLOOD MAGNESIUM INCREASED ( 39 FDA reports)
BRAIN CONTUSION ( 39 FDA reports)
CARTILAGE ATROPHY ( 39 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 39 FDA reports)
CUTANEOUS VASCULITIS ( 39 FDA reports)
DIAPHRAGMATIC HERNIA ( 39 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 39 FDA reports)
GLIOSIS ( 39 FDA reports)
ADVERSE REACTION ( 38 FDA reports)
ALCOHOL ABUSE ( 38 FDA reports)
ALCOHOLIC LIVER DISEASE ( 38 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 38 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 38 FDA reports)
ARTERIAL STENT INSERTION ( 38 FDA reports)
BLADDER MASS ( 38 FDA reports)
BONE MARROW DISORDER ( 38 FDA reports)
BRAIN DAMAGE ( 38 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 38 FDA reports)
CEREBELLAR SYNDROME ( 38 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 38 FDA reports)
CHONDROCALCINOSIS ( 38 FDA reports)
COMMINUTED FRACTURE ( 38 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 38 FDA reports)
CUSHINGOID ( 38 FDA reports)
DEPRESSIVE SYMPTOM ( 38 FDA reports)
DISEASE COMPLICATION ( 38 FDA reports)
DYSPAREUNIA ( 38 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 38 FDA reports)
EYE LASER SURGERY ( 38 FDA reports)
FAT NECROSIS ( 38 FDA reports)
HAEMOCHROMATOSIS ( 38 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 38 FDA reports)
HAEMOPHILUS INFECTION ( 38 FDA reports)
ILIAC ARTERY OCCLUSION ( 38 FDA reports)
VASCULAR INSUFFICIENCY ( 38 FDA reports)
WOUND DEBRIDEMENT ( 38 FDA reports)
IMPULSIVE BEHAVIOUR ( 38 FDA reports)
LIMB ASYMMETRY ( 38 FDA reports)
LUNG ABSCESS ( 38 FDA reports)
OPTIC NERVE DISORDER ( 38 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 38 FDA reports)
PHLEBITIS SUPERFICIAL ( 38 FDA reports)
PULMONARY TUBERCULOSIS ( 38 FDA reports)
RADICULITIS ( 38 FDA reports)
INCORRECT STORAGE OF DRUG ( 37 FDA reports)
INGUINAL HERNIA REPAIR ( 37 FDA reports)
LIP EROSION ( 37 FDA reports)
LIVER TRANSPLANT REJECTION ( 37 FDA reports)
MITRAL VALVE SCLEROSIS ( 37 FDA reports)
MOUTH INJURY ( 37 FDA reports)
MYOCARDIAL FIBROSIS ( 37 FDA reports)
PANCREATITIS RELAPSING ( 37 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 37 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 37 FDA reports)
PRURIGO ( 37 FDA reports)
READING DISORDER ( 37 FDA reports)
RENAL ISCHAEMIA ( 37 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 37 FDA reports)
SKIN CANDIDA ( 37 FDA reports)
SKIN WRINKLING ( 37 FDA reports)
SPLEEN DISORDER ( 37 FDA reports)
SUBCUTANEOUS NODULE ( 37 FDA reports)
THORACOTOMY ( 37 FDA reports)
ACCIDENTAL NEEDLE STICK ( 37 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 37 FDA reports)
BACTERIA URINE IDENTIFIED ( 37 FDA reports)
BIOPSY BREAST ABNORMAL ( 37 FDA reports)
BOWEL SOUNDS ABNORMAL ( 37 FDA reports)
CHEST INJURY ( 37 FDA reports)
CLONUS ( 37 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 37 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 37 FDA reports)
ACCIDENT AT WORK ( 36 FDA reports)
ADDISON'S DISEASE ( 36 FDA reports)
ADENOCARCINOMA PANCREAS ( 36 FDA reports)
ADENOMYOSIS ( 36 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 36 FDA reports)
ANGIOMYOLIPOMA ( 36 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 36 FDA reports)
BODY DYSMORPHIC DISORDER ( 36 FDA reports)
CATHETER SEPSIS ( 36 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 36 FDA reports)
COLITIS MICROSCOPIC ( 36 FDA reports)
CONNECTIVE TISSUE DISORDER ( 36 FDA reports)
COR PULMONALE CHRONIC ( 36 FDA reports)
CORNEAL ABRASION ( 36 FDA reports)
CORONARY ARTERY DISSECTION ( 36 FDA reports)
CORONARY REVASCULARISATION ( 36 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 36 FDA reports)
DYSPLASTIC NAEVUS ( 36 FDA reports)
ENDOMETRIOSIS ( 36 FDA reports)
ENURESIS ( 36 FDA reports)
FOOD AVERSION ( 36 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 36 FDA reports)
GASTRITIS ATROPHIC ( 36 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 36 FDA reports)
INJECTION SITE BURNING ( 36 FDA reports)
INJECTION SITE DISCOMFORT ( 36 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 36 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 36 FDA reports)
NODULE ON EXTREMITY ( 36 FDA reports)
OBSTRUCTION GASTRIC ( 36 FDA reports)
OPEN ANGLE GLAUCOMA ( 36 FDA reports)
OSTEOPOROTIC FRACTURE ( 36 FDA reports)
OTITIS MEDIA ACUTE ( 36 FDA reports)
PERIODONTAL INFECTION ( 36 FDA reports)
PRODUCT TASTE ABNORMAL ( 36 FDA reports)
PUSTULAR PSORIASIS ( 36 FDA reports)
SALIVARY GLAND DISORDER ( 36 FDA reports)
SELF-INJURIOUS IDEATION ( 36 FDA reports)
SPINAL COLUMN INJURY ( 36 FDA reports)
SPLENIC CALCIFICATION ( 36 FDA reports)
THROMBOEMBOLIC STROKE ( 36 FDA reports)
LIVER TRANSPLANT ( 35 FDA reports)
LOOSE STOOLS ( 35 FDA reports)
LUNG INJURY ( 35 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 35 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 35 FDA reports)
MONONEURITIS ( 35 FDA reports)
PATHOGEN RESISTANCE ( 35 FDA reports)
POST THROMBOTIC SYNDROME ( 35 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 35 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 35 FDA reports)
RADICULAR SYNDROME ( 35 FDA reports)
REFLUX LARYNGITIS ( 35 FDA reports)
RENAL ARTERY OCCLUSION ( 35 FDA reports)
RETINAL ISCHAEMIA ( 35 FDA reports)
SKIN INJURY ( 35 FDA reports)
SKULL FRACTURE ( 35 FDA reports)
SLEEP TALKING ( 35 FDA reports)
STOMATITIS NECROTISING ( 35 FDA reports)
STRABISMUS ( 35 FDA reports)
TENOSYNOVITIS STENOSANS ( 35 FDA reports)
TERMINAL STATE ( 35 FDA reports)
THYROIDECTOMY ( 35 FDA reports)
TOE DEFORMITY ( 35 FDA reports)
TONSILLAR DISORDER ( 35 FDA reports)
TRANSFUSION REACTION ( 35 FDA reports)
ALBUMIN URINE PRESENT ( 35 FDA reports)
ANEURYSM RUPTURED ( 35 FDA reports)
APPLICATION SITE BURN ( 35 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 35 FDA reports)
ASEPTIC NECROSIS BONE ( 35 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 35 FDA reports)
CENTRAL OBESITY ( 35 FDA reports)
CHONDROMALACIA ( 35 FDA reports)
DRUG INTERACTION POTENTIATION ( 35 FDA reports)
ESCHAR ( 35 FDA reports)
FOETAL GROWTH RESTRICTION ( 35 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 35 FDA reports)
GAZE PALSY ( 35 FDA reports)
VASCULAR GRAFT COMPLICATION ( 35 FDA reports)
WHIPLASH INJURY ( 35 FDA reports)
INTESTINAL ULCER ( 34 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 34 FDA reports)
LIP ULCERATION ( 34 FDA reports)
LOGORRHOEA ( 34 FDA reports)
MENINGITIS VIRAL ( 34 FDA reports)
MITRAL VALVE REPAIR ( 34 FDA reports)
MUCOUS MEMBRANE DISORDER ( 34 FDA reports)
NEPHRECTOMY ( 34 FDA reports)
PARATHYROID TUMOUR BENIGN ( 34 FDA reports)
PENILE PAIN ( 34 FDA reports)
SHOULDER OPERATION ( 34 FDA reports)
SOFT TISSUE MASS ( 34 FDA reports)
THYROIDITIS ( 34 FDA reports)
TONSILLITIS ( 34 FDA reports)
TUMOUR FLARE ( 34 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 34 FDA reports)
ACCOMMODATION DISORDER ( 34 FDA reports)
ANISOCYTOSIS ( 34 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 34 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 34 FDA reports)
CARBON DIOXIDE INCREASED ( 34 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 34 FDA reports)
DERMATITIS ATOPIC ( 34 FDA reports)
DERMOID CYST ( 34 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 34 FDA reports)
DIPLEGIA ( 34 FDA reports)
FOETAL GROWTH RETARDATION ( 34 FDA reports)
FOOT OPERATION ( 34 FDA reports)
GASTROINTESTINAL CARCINOMA ( 34 FDA reports)
GRIEF REACTION ( 34 FDA reports)
HAEMATOSPERMIA ( 34 FDA reports)
HAIR COLOUR CHANGES ( 34 FDA reports)
HEAT RASH ( 34 FDA reports)
HEPATIC INFARCTION ( 34 FDA reports)
HORDEOLUM ( 34 FDA reports)
ABDOMINAL HAEMATOMA ( 33 FDA reports)
ABDOMINAL INFECTION ( 33 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 33 FDA reports)
ANGIODYSPLASIA ( 33 FDA reports)
AORTIC BRUIT ( 33 FDA reports)
ARTHROPOD STING ( 33 FDA reports)
ASBESTOSIS ( 33 FDA reports)
ASTERIXIS ( 33 FDA reports)
AXILLARY PAIN ( 33 FDA reports)
BACTERIAL DISEASE CARRIER ( 33 FDA reports)
BENIGN BREAST NEOPLASM ( 33 FDA reports)
BIOPSY BONE ABNORMAL ( 33 FDA reports)
BLADDER DYSFUNCTION ( 33 FDA reports)
BLADDER OPERATION ( 33 FDA reports)
BULIMIA NERVOSA ( 33 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 33 FDA reports)
CHROMATOPSIA ( 33 FDA reports)
CORNEAL DISORDER ( 33 FDA reports)
CUTIS LAXA ( 33 FDA reports)
DEVICE RELATED SEPSIS ( 33 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 33 FDA reports)
ENDOMETRIAL DISORDER ( 33 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 33 FDA reports)
FEEDING DISORDER ( 33 FDA reports)
GENITAL RASH ( 33 FDA reports)
GROIN ABSCESS ( 33 FDA reports)
HYDROPNEUMOTHORAX ( 33 FDA reports)
HYPERACUSIS ( 33 FDA reports)
HYPERKINESIA ( 33 FDA reports)
HYPERVOLAEMIA ( 33 FDA reports)
HYPOPARATHYROIDISM ( 33 FDA reports)
HYPOPNOEA ( 33 FDA reports)
VASCULAR INJURY ( 33 FDA reports)
VOMITING PROJECTILE ( 33 FDA reports)
LIPODYSTROPHY ACQUIRED ( 33 FDA reports)
MEDIASTINAL HAEMATOMA ( 33 FDA reports)
MONOPARESIS ( 33 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 33 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 33 FDA reports)
OLIGOHYDRAMNIOS ( 33 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 33 FDA reports)
PELVIC MASS ( 33 FDA reports)
POSTURING ( 33 FDA reports)
RADIATION PNEUMONITIS ( 33 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 33 FDA reports)
RETICULOCYTE COUNT INCREASED ( 33 FDA reports)
SUICIDAL BEHAVIOUR ( 33 FDA reports)
THERAPEUTIC PROCEDURE ( 33 FDA reports)
THERAPY CESSATION ( 33 FDA reports)
INTESTINAL INFARCTION ( 32 FDA reports)
JUDGEMENT IMPAIRED ( 32 FDA reports)
LIBIDO INCREASED ( 32 FDA reports)
MEGACOLON ( 32 FDA reports)
METASTASES TO SPLEEN ( 32 FDA reports)
ORCHITIS ( 32 FDA reports)
OSTEOMYELITIS CHRONIC ( 32 FDA reports)
PALATAL DISORDER ( 32 FDA reports)
PAROTID GLAND ENLARGEMENT ( 32 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 32 FDA reports)
PNEUMATOSIS INTESTINALIS ( 32 FDA reports)
POLYP COLORECTAL ( 32 FDA reports)
RECURRENT CANCER ( 32 FDA reports)
RENAL NEOPLASM ( 32 FDA reports)
RETINAL OEDEMA ( 32 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 32 FDA reports)
SCAN MYOCARDIAL PERFUSION ( 32 FDA reports)
SKIN TURGOR DECREASED ( 32 FDA reports)
SYNOVIAL RUPTURE ( 32 FDA reports)
URETHRITIS ( 32 FDA reports)
ACUTE PSYCHOSIS ( 32 FDA reports)
ADRENAL ADENOMA ( 32 FDA reports)
ANAL PRURITUS ( 32 FDA reports)
ANION GAP INCREASED ( 32 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 32 FDA reports)
BLOOD ALBUMIN INCREASED ( 32 FDA reports)
BURNS SECOND DEGREE ( 32 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 32 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 32 FDA reports)
CHRONIC HEPATITIS ( 32 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 32 FDA reports)
EATING DISORDER SYMPTOM ( 32 FDA reports)
EOSINOPHIL COUNT DECREASED ( 32 FDA reports)
EXTRAOCULAR MUSCLE DISORDER ( 32 FDA reports)
FACIAL NEURALGIA ( 32 FDA reports)
GALLOP RHYTHM PRESENT ( 32 FDA reports)
GAMMOPATHY ( 32 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 32 FDA reports)
GLOMERULOSCLEROSIS ( 32 FDA reports)
HAEMOGLOBINURIA ( 32 FDA reports)
VASCULAR RUPTURE ( 32 FDA reports)
VENOUS STENOSIS ( 32 FDA reports)
VITAMIN B12 DECREASED ( 32 FDA reports)
URTICARIA GENERALISED ( 31 FDA reports)
VASCULAR STENOSIS ( 31 FDA reports)
VASCULITIC RASH ( 31 FDA reports)
VENOUS STASIS ( 31 FDA reports)
IMPULSE-CONTROL DISORDER ( 31 FDA reports)
INFUSION SITE PAIN ( 31 FDA reports)
LEUKOENCEPHALOPATHY ( 31 FDA reports)
LIP DISORDER ( 31 FDA reports)
MALIGNANT MELANOMA IN SITU ( 31 FDA reports)
MONOCYTOSIS ( 31 FDA reports)
MUCOSAL ULCERATION ( 31 FDA reports)
MYELITIS TRANSVERSE ( 31 FDA reports)
NASAL MUCOSAL DISORDER ( 31 FDA reports)
ONYCHOMADESIS ( 31 FDA reports)
OTITIS MEDIA CHRONIC ( 31 FDA reports)
PSEUDOMONAL SEPSIS ( 31 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 31 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 31 FDA reports)
RENAL OSTEODYSTROPHY ( 31 FDA reports)
SCAPULA FRACTURE ( 31 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 31 FDA reports)
SUDDEN HEARING LOSS ( 31 FDA reports)
THYROID MASS ( 31 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 31 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 31 FDA reports)
ADNEXA UTERI MASS ( 31 FDA reports)
ALCOHOL POISONING ( 31 FDA reports)
ALVEOLAR OSTEITIS ( 31 FDA reports)
ANOGENITAL WARTS ( 31 FDA reports)
ANTIBODY TEST POSITIVE ( 31 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 31 FDA reports)
ARTERIAL INSUFFICIENCY ( 31 FDA reports)
AXILLARY MASS ( 31 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 31 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 31 FDA reports)
BONE FORMATION INCREASED ( 31 FDA reports)
CEREBELLAR ATROPHY ( 31 FDA reports)
CEREBRAL HYPOPERFUSION ( 31 FDA reports)
CLUMSINESS ( 31 FDA reports)
COLONIC OBSTRUCTION ( 31 FDA reports)
COLOSTOMY ( 31 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 31 FDA reports)
DEVICE LEAKAGE ( 31 FDA reports)
DISSEMINATED TUBERCULOSIS ( 31 FDA reports)
DYSPLASIA ( 31 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 31 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 31 FDA reports)
ENCEPHALITIS HERPES ( 31 FDA reports)
GANGLION ( 31 FDA reports)
GASTROINTESTINAL INJURY ( 31 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 31 FDA reports)
HYPOTRICHOSIS ( 31 FDA reports)
ABDOMINAL SYMPTOM ( 30 FDA reports)
ANAL SPHINCTER ATONY ( 30 FDA reports)
ANASTOMOTIC ULCER ( 30 FDA reports)
ANORECTAL DISORDER ( 30 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 30 FDA reports)
BLADDER DILATATION ( 30 FDA reports)
BONE TRIMMING ( 30 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 30 FDA reports)
CEREBRAL CALCIFICATION ( 30 FDA reports)
CHOLESTATIC LIVER INJURY ( 30 FDA reports)
CLEFT LIP AND PALATE ( 30 FDA reports)
COAGULATION TIME ABNORMAL ( 30 FDA reports)
COLON CANCER METASTATIC ( 30 FDA reports)
COLON NEOPLASM ( 30 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 30 FDA reports)
DRUG EFFECT INCREASED ( 30 FDA reports)
EMBOLISM VENOUS ( 30 FDA reports)
ENTEROVESICAL FISTULA ( 30 FDA reports)
EXTRAVASATION ( 30 FDA reports)
GLOMERULONEPHRITIS ( 30 FDA reports)
HAEMORRHOID OPERATION ( 30 FDA reports)
HEAT STROKE ( 30 FDA reports)
HYPERTROPHY BREAST ( 30 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 30 FDA reports)
UTERINE PROLAPSE ( 30 FDA reports)
VASOSPASM ( 30 FDA reports)
VOLVULUS ( 30 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 30 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 30 FDA reports)
INTENTION TREMOR ( 30 FDA reports)
KERATOACANTHOMA ( 30 FDA reports)
KIDNEY FIBROSIS ( 30 FDA reports)
LENTIGO ( 30 FDA reports)
LEUKOCYTURIA ( 30 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 30 FDA reports)
LOSS OF BLADDER SENSATION ( 30 FDA reports)
MONOCYTE COUNT DECREASED ( 30 FDA reports)
MYOPATHY TOXIC ( 30 FDA reports)
NIGHT BLINDNESS ( 30 FDA reports)
NIKOLSKY'S SIGN ( 30 FDA reports)
NODAL OSTEOARTHRITIS ( 30 FDA reports)
OCCIPITAL NEURALGIA ( 30 FDA reports)
PELVIC ABSCESS ( 30 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 30 FDA reports)
PERITONEAL DIALYSIS ( 30 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 30 FDA reports)
PHYSICAL ASSAULT ( 30 FDA reports)
PLEURODESIS ( 30 FDA reports)
PRESBYOESOPHAGUS ( 30 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 30 FDA reports)
SERUM FERRITIN DECREASED ( 30 FDA reports)
SMALL FOR DATES BABY ( 30 FDA reports)
SUPERINFECTION ( 30 FDA reports)
THALAMIC INFARCTION ( 30 FDA reports)
TONIC CLONIC MOVEMENTS ( 30 FDA reports)
ULNA FRACTURE ( 30 FDA reports)
URETERAL DISORDER ( 30 FDA reports)
JOINT ARTHROPLASTY ( 29 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 29 FDA reports)
METASTASES TO ABDOMINAL WALL ( 29 FDA reports)
METASTASES TO MENINGES ( 29 FDA reports)
METASTASES TO THE MEDIASTINUM ( 29 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 29 FDA reports)
MIXED LIVER INJURY ( 29 FDA reports)
MOANING ( 29 FDA reports)
MORBID THOUGHTS ( 29 FDA reports)
MYOPATHY STEROID ( 29 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 29 FDA reports)
OBSESSIVE THOUGHTS ( 29 FDA reports)
OCULAR HYPERTENSION ( 29 FDA reports)
ONYCHALGIA ( 29 FDA reports)
ORAL SOFT TISSUE DISORDER ( 29 FDA reports)
PAPILLOMA ( 29 FDA reports)
PERFORATED ULCER ( 29 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 29 FDA reports)
RASH MORBILLIFORM ( 29 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 29 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 29 FDA reports)
THYROID ADENOMA ( 29 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 29 FDA reports)
TRICUSPID VALVE DISEASE ( 29 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 29 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 29 FDA reports)
ANGIOGRAM ( 29 FDA reports)
ASPIRATION JOINT ( 29 FDA reports)
BLOOD OSMOLARITY DECREASED ( 29 FDA reports)
BREAST CANCER STAGE I ( 29 FDA reports)
CAECITIS ( 29 FDA reports)
CATATONIA ( 29 FDA reports)
CSF TEST ABNORMAL ( 29 FDA reports)
CYSTITIS HAEMORRHAGIC ( 29 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 29 FDA reports)
DROP ATTACKS ( 29 FDA reports)
DRUG-INDUCED LIVER INJURY ( 29 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 29 FDA reports)
FEELING HOT AND COLD ( 29 FDA reports)
GASTROINTESTINAL EROSION ( 29 FDA reports)
HEAT EXHAUSTION ( 29 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 29 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 29 FDA reports)
HYPOMANIA ( 29 FDA reports)
VULVOVAGINAL PRURITUS ( 29 FDA reports)
WEIGHT LOSS POOR ( 29 FDA reports)
VITAMIN B12 INCREASED ( 28 FDA reports)
VULVOVAGINAL DISCOMFORT ( 28 FDA reports)
INCREASED BRONCHIAL SECRETION ( 28 FDA reports)
INFECTED SEBACEOUS CYST ( 28 FDA reports)
INTESTINAL RESECTION ( 28 FDA reports)
KERATITIS ( 28 FDA reports)
KIDNEY ENLARGEMENT ( 28 FDA reports)
LOWER EXTREMITY MASS ( 28 FDA reports)
MEDIASTINITIS ( 28 FDA reports)
MITRAL VALVE REPLACEMENT ( 28 FDA reports)
MUMPS ( 28 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 28 FDA reports)
NO ADVERSE EFFECT ( 28 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 28 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 28 FDA reports)
OPPORTUNISTIC INFECTION ( 28 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 28 FDA reports)
PERINEURIAL CYST ( 28 FDA reports)
POST LAMINECTOMY SYNDROME ( 28 FDA reports)
PRIMARY HYPOGONADISM ( 28 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 28 FDA reports)
QUADRIPARESIS ( 28 FDA reports)
RADICULAR CYST ( 28 FDA reports)
RENAL VESSEL DISORDER ( 28 FDA reports)
RHINITIS SEASONAL ( 28 FDA reports)
SINUS POLYP DEGENERATION ( 28 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 28 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 28 FDA reports)
THORACOSTOMY ( 28 FDA reports)
TINEA CRURIS ( 28 FDA reports)
TONGUE DRY ( 28 FDA reports)
TUMOUR HAEMORRHAGE ( 28 FDA reports)
UMBILICAL HERNIA REPAIR ( 28 FDA reports)
ACCIDENT AT HOME ( 28 FDA reports)
ASTEATOSIS ( 28 FDA reports)
AURA ( 28 FDA reports)
BACTERIURIA ( 28 FDA reports)
BIFASCICULAR BLOCK ( 28 FDA reports)
BIOPSY BONE ( 28 FDA reports)
BLOOD GASES ABNORMAL ( 28 FDA reports)
BONE MARROW TRANSPLANT ( 28 FDA reports)
BRONCHIAL OBSTRUCTION ( 28 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 28 FDA reports)
CERVICAL CORD COMPRESSION ( 28 FDA reports)
CERVICITIS ( 28 FDA reports)
CHEST TUBE INSERTION ( 28 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 28 FDA reports)
CORONARY OSTIAL STENOSIS ( 28 FDA reports)
CULTURE POSITIVE ( 28 FDA reports)
CYSTITIS NONINFECTIVE ( 28 FDA reports)
DEATH OF RELATIVE ( 28 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 28 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 28 FDA reports)
DYSPNOEA AT REST ( 28 FDA reports)
ENDOPHTHALMITIS ( 28 FDA reports)
ENTEROCUTANEOUS FISTULA ( 28 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 28 FDA reports)
GRAFT COMPLICATION ( 28 FDA reports)
HALO VISION ( 28 FDA reports)
HYPERMAGNESAEMIA ( 28 FDA reports)
ADRENAL NEOPLASM ( 27 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 27 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 27 FDA reports)
ALVEOLITIS ALLERGIC ( 27 FDA reports)
AMYLASE INCREASED ( 27 FDA reports)
ARTERITIS ( 27 FDA reports)
BELLIGERENCE ( 27 FDA reports)
BENIGN TUMOUR EXCISION ( 27 FDA reports)
BICYTOPENIA ( 27 FDA reports)
BLUE TOE SYNDROME ( 27 FDA reports)
BONE DENSITY INCREASED ( 27 FDA reports)
BRAIN CANCER METASTATIC ( 27 FDA reports)
CALCIUM DEFICIENCY ( 27 FDA reports)
CARDIAC ASTHMA ( 27 FDA reports)
CAROTID ARTERY DISSECTION ( 27 FDA reports)
COLON OPERATION ( 27 FDA reports)
CYST RUPTURE ( 27 FDA reports)
DENTAL DISCOMFORT ( 27 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 27 FDA reports)
FEELINGS OF WORTHLESSNESS ( 27 FDA reports)
FUNGAEMIA ( 27 FDA reports)
GALLBLADDER INJURY ( 27 FDA reports)
GRANULOMA ANNULARE ( 27 FDA reports)
HIGH FREQUENCY ABLATION ( 27 FDA reports)
HORNER'S SYNDROME ( 27 FDA reports)
HYPERAEMIA ( 27 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 27 FDA reports)
IN-STENT ARTERIAL RESTENOSIS ( 27 FDA reports)
INFUSION SITE REACTION ( 27 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 27 FDA reports)
LENS DISORDER ( 27 FDA reports)
LIP EXFOLIATION ( 27 FDA reports)
MASS EXCISION ( 27 FDA reports)
METASTASES TO ADRENALS ( 27 FDA reports)
MYCOSIS FUNGOIDES ( 27 FDA reports)
NERVE ROOT COMPRESSION ( 27 FDA reports)
NONSPECIFIC REACTION ( 27 FDA reports)
PANCREATIC ENZYMES INCREASED ( 27 FDA reports)
PLACENTAL INSUFFICIENCY ( 27 FDA reports)
POLYCYTHAEMIA VERA ( 27 FDA reports)
POSTICTAL STATE ( 27 FDA reports)
POSTOPERATIVE FEVER ( 27 FDA reports)
RADIAL NERVE PALSY ( 27 FDA reports)
REBOUND EFFECT ( 27 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 27 FDA reports)
RETROGRADE EJACULATION ( 27 FDA reports)
RHEUMATIC FEVER ( 27 FDA reports)
SHOCK HYPOGLYCAEMIC ( 27 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 27 FDA reports)
TUBERCULIN TEST POSITIVE ( 27 FDA reports)
TUMOUR MARKER INCREASED ( 27 FDA reports)
TUNNEL VISION ( 27 FDA reports)
MAMMOPLASTY ( 26 FDA reports)
MEDICAL DEVICE REMOVAL ( 26 FDA reports)
MUCOUS STOOLS ( 26 FDA reports)
NAEVUS FLAMMEUS ( 26 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 26 FDA reports)
OSTEOMALACIA ( 26 FDA reports)
PALMAR ERYTHEMA ( 26 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 26 FDA reports)
PERNICIOUS ANAEMIA ( 26 FDA reports)
PLEURAL DISORDER ( 26 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 26 FDA reports)
PNEUMOPERITONEUM ( 26 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 26 FDA reports)
PULMONARY AIR LEAKAGE ( 26 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 26 FDA reports)
RENAL TUBULAR ACIDOSIS ( 26 FDA reports)
RETINAL EXUDATES ( 26 FDA reports)
RHEUMATOID FACTOR INCREASED ( 26 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 26 FDA reports)
SEPTIC EMBOLUS ( 26 FDA reports)
SKIN EROSION ( 26 FDA reports)
SKIN FRAGILITY ( 26 FDA reports)
T-CELL LYMPHOMA ( 26 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 26 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 26 FDA reports)
ABDOMINAL NEOPLASM ( 26 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 26 FDA reports)
ANKYLOSING SPONDYLITIS ( 26 FDA reports)
APPLICATION SITE DISCOLOURATION ( 26 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 26 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 26 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 26 FDA reports)
BOVINE TUBERCULOSIS ( 26 FDA reports)
BRAIN STEM STROKE ( 26 FDA reports)
BREAST ABSCESS ( 26 FDA reports)
CANDIDURIA ( 26 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 26 FDA reports)
CAROTID ARTERY ANEURYSM ( 26 FDA reports)
COARCTATION OF THE AORTA ( 26 FDA reports)
COLORECTAL CANCER ( 26 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 26 FDA reports)
CSF PROTEIN INCREASED ( 26 FDA reports)
CULTURE WOUND POSITIVE ( 26 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 26 FDA reports)
GALLBLADDER PAIN ( 26 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 26 FDA reports)
GRAFT DYSFUNCTION ( 26 FDA reports)
GRANULOCYTE COUNT DECREASED ( 26 FDA reports)
HOSPICE CARE ( 26 FDA reports)
HYDROURETER ( 26 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 26 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 26 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 26 FDA reports)
VASCULAR PURPURA ( 26 FDA reports)
VITH NERVE PARALYSIS ( 26 FDA reports)
VULVAL DISORDER ( 26 FDA reports)
YAWNING ( 26 FDA reports)
VASCULITIS CEREBRAL ( 25 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 25 FDA reports)
VESSEL PUNCTURE SITE HAEMORRHAGE ( 25 FDA reports)
WOUND ABSCESS ( 25 FDA reports)
INFUSION SITE ERYTHEMA ( 25 FDA reports)
KLEBSIELLA SEPSIS ( 25 FDA reports)
MIXED HYPERLIPIDAEMIA ( 25 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 25 FDA reports)
MYELOFIBROSIS ( 25 FDA reports)
NASAL ULCER ( 25 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 25 FDA reports)
NEURODEGENERATIVE DISORDER ( 25 FDA reports)
NEUROGENIC BOWEL ( 25 FDA reports)
OEDEMA MUCOSAL ( 25 FDA reports)
ORAL MUCOSAL BLISTERING ( 25 FDA reports)
ORTHOPEDIC PROCEDURE ( 25 FDA reports)
OVARIAN ADENOMA ( 25 FDA reports)
OVARIAN DISORDER ( 25 FDA reports)
PALATAL OEDEMA ( 25 FDA reports)
PENILE HAEMORRHAGE ( 25 FDA reports)
PERIODONTAL OPERATION ( 25 FDA reports)
PLASMAPHERESIS ( 25 FDA reports)
PSYCHOLOGICAL TRAUMA ( 25 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 25 FDA reports)
SENILE DEMENTIA ( 25 FDA reports)
SKIN CHAPPED ( 25 FDA reports)
SMEAR CERVIX ABNORMAL ( 25 FDA reports)
SOFT TISSUE INJURY ( 25 FDA reports)
STEATORRHOEA ( 25 FDA reports)
SUBRETINAL FIBROSIS ( 25 FDA reports)
SYSTOLIC DYSFUNCTION ( 25 FDA reports)
TRAUMATIC HAEMORRHAGE ( 25 FDA reports)
APALLIC SYNDROME ( 25 FDA reports)
AURICULAR SWELLING ( 25 FDA reports)
BLOOD CHOLESTEROL ( 25 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 25 FDA reports)
CAPILLARY LEAK SYNDROME ( 25 FDA reports)
CARBUNCLE ( 25 FDA reports)
CAROTID ARTERY THROMBOSIS ( 25 FDA reports)
CAROTID ENDARTERECTOMY ( 25 FDA reports)
CHOROIDAL DETACHMENT ( 25 FDA reports)
COAGULATION TEST ABNORMAL ( 25 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 25 FDA reports)
DENTAL CARE ( 25 FDA reports)
DERMATITIS PSORIASIFORM ( 25 FDA reports)
DRUG LEVEL FLUCTUATING ( 25 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 25 FDA reports)
EXTRASKELETAL OSSIFICATION ( 25 FDA reports)
HAEMATOMA INFECTION ( 25 FDA reports)
HEPATIC TRAUMA ( 25 FDA reports)
ANALGESIC ASTHMA SYNDROME ( 24 FDA reports)
APICAL GRANULOMA ( 24 FDA reports)
ARTHROSCOPIC SURGERY ( 24 FDA reports)
BALANITIS ( 24 FDA reports)
BENIGN BONE NEOPLASM ( 24 FDA reports)
BONE GIANT CELL TUMOUR ( 24 FDA reports)
BREAST NECROSIS ( 24 FDA reports)
CALCIPHYLAXIS ( 24 FDA reports)
CATHETER SITE HAEMATOMA ( 24 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 24 FDA reports)
CORONARY ARTERY EMBOLISM ( 24 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 24 FDA reports)
ESCHERICHIA TEST POSITIVE ( 24 FDA reports)
FIBROMA ( 24 FDA reports)
FLASHBACK ( 24 FDA reports)
FOOD CRAVING ( 24 FDA reports)
GASTRODUODENAL ULCER ( 24 FDA reports)
GASTROSTOMY TUBE INSERTION ( 24 FDA reports)
GENITAL HAEMORRHAGE ( 24 FDA reports)
HAIR DISORDER ( 24 FDA reports)
HEART VALVE INSUFFICIENCY ( 24 FDA reports)
HORMONE LEVEL ABNORMAL ( 24 FDA reports)
HYPERPYREXIA ( 24 FDA reports)
VENTRICULAR FAILURE ( 24 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 24 FDA reports)
INTERVERTEBRAL DISCITIS ( 24 FDA reports)
INTESTINAL STENOSIS ( 24 FDA reports)
INTUBATION ( 24 FDA reports)
KNEE DEFORMITY ( 24 FDA reports)
LABORATORY TEST INTERFERENCE ( 24 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 24 FDA reports)
LEUKAEMIA PLASMACYTIC ( 24 FDA reports)
LIMB DEFORMITY ( 24 FDA reports)
LYMPHOCELE ( 24 FDA reports)
LYMPHOCYTIC INFILTRATION ( 24 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 24 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 24 FDA reports)
METASTASES TO PERITONEUM ( 24 FDA reports)
MOTION SICKNESS ( 24 FDA reports)
NECROSIS ISCHAEMIC ( 24 FDA reports)
NEGATIVE THOUGHTS ( 24 FDA reports)
NEUROMA ( 24 FDA reports)
NEUTROPENIC COLITIS ( 24 FDA reports)
PAROTIDECTOMY ( 24 FDA reports)
PEDAL PULSE DECREASED ( 24 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 24 FDA reports)
PLACENTAL INFARCTION ( 24 FDA reports)
PROCEDURAL SITE REACTION ( 24 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 24 FDA reports)
RED BLOOD CELL MORPHOLOGY ABNORMAL ( 24 FDA reports)
SALIVARY GLAND MASS ( 24 FDA reports)
SHUNT MALFUNCTION ( 24 FDA reports)
SOFT TISSUE NECROSIS ( 24 FDA reports)
SPIDER VEIN ( 24 FDA reports)
SPINAL CLAUDICATION ( 24 FDA reports)
SPINAL HAEMATOMA ( 24 FDA reports)
TRACHEOSTOMY ( 24 FDA reports)
UMBILICAL CORD ABNORMALITY ( 24 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 24 FDA reports)
INFUSION SITE SWELLING ( 23 FDA reports)
KELOID SCAR ( 23 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 23 FDA reports)
MARITAL PROBLEM ( 23 FDA reports)
MELANOSIS COLI ( 23 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 23 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 23 FDA reports)
NAIL DISCOLOURATION ( 23 FDA reports)
NIGHT CRAMPS ( 23 FDA reports)
NORMAL NEWBORN ( 23 FDA reports)
OESTROGEN DEFICIENCY ( 23 FDA reports)
PAIN EXACERBATED ( 23 FDA reports)
PLEURAL CALCIFICATION ( 23 FDA reports)
PRIAPISM ( 23 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 23 FDA reports)
PULMONARY HILUM MASS ( 23 FDA reports)
PYLORIC STENOSIS ( 23 FDA reports)
RETINAL ARTERY THROMBOSIS ( 23 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 23 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 23 FDA reports)
SALIVA ALTERED ( 23 FDA reports)
SMALL INTESTINAL ULCER HAEMORRHAGE ( 23 FDA reports)
SPINAL DECOMPRESSION ( 23 FDA reports)
SUBMANDIBULAR MASS ( 23 FDA reports)
THROAT LESION ( 23 FDA reports)
TONGUE PARALYSIS ( 23 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 23 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 23 FDA reports)
AMBLYOPIA ( 23 FDA reports)
ANAESTHETIC COMPLICATION ( 23 FDA reports)
ANGIOGRAM ABNORMAL ( 23 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 23 FDA reports)
BRAIN MASS ( 23 FDA reports)
BREAST RECONSTRUCTION ( 23 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 23 FDA reports)
BRONCHITIS BACTERIAL ( 23 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 23 FDA reports)
CEREBRAL CYST ( 23 FDA reports)
CHEMICAL POISONING ( 23 FDA reports)
CHEYNE-STOKES RESPIRATION ( 23 FDA reports)
CLUBBING ( 23 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 23 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 23 FDA reports)
DIABETES INSIPIDUS ( 23 FDA reports)
DIABETIC ULCER ( 23 FDA reports)
DRESSLER'S SYNDROME ( 23 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 23 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 23 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 23 FDA reports)
GASTRIC DILATATION ( 23 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 23 FDA reports)
GRAFT INFECTION ( 23 FDA reports)
GUN SHOT WOUND ( 23 FDA reports)
HAEMORRHAGIC DISORDER ( 23 FDA reports)
HYPOCHONDRIASIS ( 23 FDA reports)
ILIAC ARTERY THROMBOSIS ( 23 FDA reports)
IMPAIRED FASTING GLUCOSE ( 23 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 23 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 22 FDA reports)
INFUSION SITE EXTRAVASATION ( 22 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 22 FDA reports)
JAW LESION EXCISION ( 22 FDA reports)
LEUKOPLAKIA ORAL ( 22 FDA reports)
LIVER ABSCESS ( 22 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 22 FDA reports)
MEDIASTINAL DISORDER ( 22 FDA reports)
METASTASES TO THORAX ( 22 FDA reports)
METASTATIC PAIN ( 22 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 22 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 22 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 22 FDA reports)
OCULAR DISCOMFORT ( 22 FDA reports)
ORAL NEOPLASM ( 22 FDA reports)
OXYGEN SATURATION ABNORMAL ( 22 FDA reports)
OXYGEN SUPPLEMENTATION ( 22 FDA reports)
PAINFUL DEFAECATION ( 22 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 22 FDA reports)
PLEUROTHOTONUS ( 22 FDA reports)
PNEUMOPERICARDIUM ( 22 FDA reports)
PULMONARY CALCIFICATION ( 22 FDA reports)
RADICULITIS CERVICAL ( 22 FDA reports)
RED BLOOD CELL ABNORMALITY ( 22 FDA reports)
RESIDUAL URINE ( 22 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 22 FDA reports)
RHEUMATIC HEART DISEASE ( 22 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 22 FDA reports)
RHINALGIA ( 22 FDA reports)
SCROTAL OEDEMA ( 22 FDA reports)
SIGMOIDITIS ( 22 FDA reports)
SIMPLE PARTIAL SEIZURES ( 22 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 22 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 22 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 22 FDA reports)
TACHYPHRENIA ( 22 FDA reports)
TRACHEAL HAEMORRHAGE ( 22 FDA reports)
TRAUMATIC INTRACRANIAL HAEMORRHAGE ( 22 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 22 FDA reports)
URETHRAL PAIN ( 22 FDA reports)
ANTI-INSULIN ANTIBODY POSITIVE ( 22 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 22 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 22 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 22 FDA reports)
ARTERIOVENOUS GRAFT SITE INFECTION ( 22 FDA reports)
BASAL GANGLIA INFARCTION ( 22 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 22 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 22 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 22 FDA reports)
BONE ABSCESS ( 22 FDA reports)
BREAST PROSTHESIS USER ( 22 FDA reports)
BRONCHIAL CARCINOMA ( 22 FDA reports)
BRONCHIAL DISORDER ( 22 FDA reports)
BRONCHIAL SECRETION RETENTION ( 22 FDA reports)
CARDIAC DISCOMFORT ( 22 FDA reports)
CATHETER SITE INFECTION ( 22 FDA reports)
CHORIOAMNIONITIS ( 22 FDA reports)
COGWHEEL RIGIDITY ( 22 FDA reports)
COLON CANCER RECURRENT ( 22 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 22 FDA reports)
CORNEAL OEDEMA ( 22 FDA reports)
CYST REMOVAL ( 22 FDA reports)
DELIRIUM TREMENS ( 22 FDA reports)
DENTAL PROSTHESIS USER ( 22 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 22 FDA reports)
DYSMENORRHOEA ( 22 FDA reports)
ENTHESOPATHY ( 22 FDA reports)
FANCONI SYNDROME ( 22 FDA reports)
FASCIITIS ( 22 FDA reports)
FEMORAL ARTERY ANEURYSM ( 22 FDA reports)
FIBROADENOMA OF BREAST ( 22 FDA reports)
FULGURATION ( 22 FDA reports)
GASTRIC INFECTION ( 22 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 22 FDA reports)
GLARE ( 22 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 22 FDA reports)
HEPATIC PAIN ( 22 FDA reports)
HYPERLACTACIDAEMIA ( 22 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 22 FDA reports)
ABDOMINAL HERNIA OBSTRUCTIVE ( 21 FDA reports)
ANASTOMOTIC LEAK ( 21 FDA reports)
ANKLE OPERATION ( 21 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 21 FDA reports)
BARTHOLIN'S CYST ( 21 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 21 FDA reports)
BLADDER DISCOMFORT ( 21 FDA reports)
BREAST OPERATION ( 21 FDA reports)
BURN OESOPHAGEAL ( 21 FDA reports)
CALCIUM METABOLISM DISORDER ( 21 FDA reports)
CATHETER THROMBOSIS ( 21 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 21 FDA reports)
CEREBRAL MICROANGIOPATHY ( 21 FDA reports)
CHEMOTHERAPY ( 21 FDA reports)
COLON CANCER STAGE III ( 21 FDA reports)
CUSHING'S SYNDROME ( 21 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 21 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 21 FDA reports)
DEPRESSION SUICIDAL ( 21 FDA reports)
DIARRHOEA INFECTIOUS ( 21 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 21 FDA reports)
DUPUYTREN'S CONTRACTURE ( 21 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 21 FDA reports)
EPIGLOTTITIS ( 21 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 21 FDA reports)
FOLATE DEFICIENCY ( 21 FDA reports)
FOOD INTERACTION ( 21 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 21 FDA reports)
GASTROINTESTINAL NEOPLASM ( 21 FDA reports)
GINGIVAL HYPERTROPHY ( 21 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 21 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 21 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 21 FDA reports)
VASCULITIS NECROTISING ( 21 FDA reports)
VIRAL MYOCARDITIS ( 21 FDA reports)
WOUND DECOMPOSITION ( 21 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 21 FDA reports)
INAPPROPRIATE AFFECT ( 21 FDA reports)
INTRADUCTAL PAPILLOMA OF BREAST ( 21 FDA reports)
KAPOSI'S SARCOMA ( 21 FDA reports)
LIP DISCOLOURATION ( 21 FDA reports)
LIPIDS ABNORMAL ( 21 FDA reports)
LOOSE BODY IN JOINT ( 21 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 21 FDA reports)
MASKED FACIES ( 21 FDA reports)
METHAEMOGLOBINAEMIA ( 21 FDA reports)
NAIL DYSTROPHY ( 21 FDA reports)
NEOPLASM PROSTATE ( 21 FDA reports)
OPEN FRACTURE ( 21 FDA reports)
OVARIAN CANCER RECURRENT ( 21 FDA reports)
PANCREATIC INSUFFICIENCY ( 21 FDA reports)
PERIRENAL HAEMATOMA ( 21 FDA reports)
PNEUMONIA INFLUENZAL ( 21 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 21 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 21 FDA reports)
QUADRUPLE VESSEL BYPASS GRAFT ( 21 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 21 FDA reports)
SCAN ABNORMAL ( 21 FDA reports)
SERRATIA INFECTION ( 21 FDA reports)
SKIN HYPOPIGMENTATION ( 21 FDA reports)
SLEEP WALKING ( 21 FDA reports)
SOMATOFORM DISORDER ( 21 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 21 FDA reports)
THERAPY REGIMEN CHANGED ( 21 FDA reports)
TONSILLECTOMY ( 21 FDA reports)
TORTICOLLIS ( 21 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 21 FDA reports)
URINARY BLADDER POLYP ( 21 FDA reports)
INFECTED CYST ( 20 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 20 FDA reports)
KETONURIA ( 20 FDA reports)
KOUNIS SYNDROME ( 20 FDA reports)
LARYNGEAL CANCER ( 20 FDA reports)
LIP HAEMORRHAGE ( 20 FDA reports)
LYMPHANGITIS ( 20 FDA reports)
MAMMOGRAM ( 20 FDA reports)
MANTLE CELL LYMPHOMA ( 20 FDA reports)
PACEMAKER COMPLICATION ( 20 FDA reports)
PEMPHIGUS ( 20 FDA reports)
PENILE OEDEMA ( 20 FDA reports)
PERIANAL ABSCESS ( 20 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 20 FDA reports)
PHLEBOLITH ( 20 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 20 FDA reports)
PLATELET AGGREGATION INCREASED ( 20 FDA reports)
POIKILOCYTOSIS ( 20 FDA reports)
POOR VENOUS ACCESS ( 20 FDA reports)
POSTPERICARDIOTOMY SYNDROME ( 20 FDA reports)
PROCEDURAL HYPERTENSION ( 20 FDA reports)
PROTRUSION TONGUE ( 20 FDA reports)
RASH SCALY ( 20 FDA reports)
RENAL ARTERIOSCLEROSIS ( 20 FDA reports)
SCARLET FEVER ( 20 FDA reports)
SEMEN VOLUME DECREASED ( 20 FDA reports)
SKIN OEDEMA ( 20 FDA reports)
SPUTUM RETENTION ( 20 FDA reports)
STOOL ANALYSIS ABNORMAL ( 20 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 20 FDA reports)
ALCOHOL INTERACTION ( 20 FDA reports)
ALDOLASE INCREASED ( 20 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 20 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 20 FDA reports)
ARTERIOVENOUS FISTULA OCCLUSION ( 20 FDA reports)
BLOOD CORTISOL DECREASED ( 20 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 20 FDA reports)
BONE MARROW TOXICITY ( 20 FDA reports)
BRAIN MIDLINE SHIFT ( 20 FDA reports)
BRONCHOPLEURAL FISTULA ( 20 FDA reports)
BUNION OPERATION ( 20 FDA reports)
CARDIAC VALVE ABSCESS ( 20 FDA reports)
CATHETER REMOVAL ( 20 FDA reports)
CERVIX CARCINOMA ( 20 FDA reports)
CONJUNCTIVAL OEDEMA ( 20 FDA reports)
CORONARY ARTERY ANEURYSM ( 20 FDA reports)
CORONARY ARTERY PERFORATION ( 20 FDA reports)
CYANOPSIA ( 20 FDA reports)
CYST ASPIRATION ( 20 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 20 FDA reports)
DIABETIC VASCULAR DISORDER ( 20 FDA reports)
DISLOCATION OF VERTEBRA ( 20 FDA reports)
DRUG TOLERANCE DECREASED ( 20 FDA reports)
EMPTY SELLA SYNDROME ( 20 FDA reports)
FEELING OF RELAXATION ( 20 FDA reports)
FIBROUS HISTIOCYTOMA ( 20 FDA reports)
FUNGAL RASH ( 20 FDA reports)
GASTRIC MUCOSAL LESION ( 20 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 20 FDA reports)
GRAFT VERSUS HOST DISEASE ( 20 FDA reports)
HAEMATOTOXICITY ( 20 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 20 FDA reports)
HISTOPLASMOSIS ( 20 FDA reports)
IIIRD NERVE PARALYSIS ( 20 FDA reports)
VARICELLA ( 20 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 20 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 20 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 20 FDA reports)
WHITE BLOOD CELL DISORDER ( 20 FDA reports)
VESTIBULAR NEURONITIS ( 19 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 19 FDA reports)
WEIGHT GAIN POOR ( 19 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 19 FDA reports)
INHALATION THERAPY ( 19 FDA reports)
LACRIMATION DECREASED ( 19 FDA reports)
LESION EXCISION ( 19 FDA reports)
LOW DENSITY LIPOPROTEIN ABNORMAL ( 19 FDA reports)
MADAROSIS ( 19 FDA reports)
METAMORPHOPSIA ( 19 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 19 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 19 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 19 FDA reports)
NEUTROPENIC INFECTION ( 19 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 19 FDA reports)
ORAL MUCOSA EROSION ( 19 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 19 FDA reports)
PARAKERATOSIS ( 19 FDA reports)
PELVIC FLOOR MUSCLE WEAKNESS ( 19 FDA reports)
PHIMOSIS ( 19 FDA reports)
PHOTODERMATOSIS ( 19 FDA reports)
PHYSIOTHERAPY ( 19 FDA reports)
PITUITARY TUMOUR ( 19 FDA reports)
PITUITARY TUMOUR BENIGN ( 19 FDA reports)
PLEURAL HAEMORRHAGE ( 19 FDA reports)
POLYCYSTIC OVARIES ( 19 FDA reports)
PUBIS FRACTURE ( 19 FDA reports)
RECTAL ABSCESS ( 19 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 19 FDA reports)
RETINAL ARTERY EMBOLISM ( 19 FDA reports)
RETINAL VEIN THROMBOSIS ( 19 FDA reports)
RHYTHM IDIOVENTRICULAR ( 19 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 19 FDA reports)
SCIATIC NERVE INJURY ( 19 FDA reports)
SOCIAL PHOBIA ( 19 FDA reports)
SPINAL CORD HAEMORRHAGE ( 19 FDA reports)
SUPRAVENTRICULAR TACHYARRHYTHMIA ( 19 FDA reports)
SYSTEMIC CANDIDA ( 19 FDA reports)
SYSTOLIC HYPERTENSION ( 19 FDA reports)
TERATOGENICITY ( 19 FDA reports)
TERMINAL INSOMNIA ( 19 FDA reports)
TONGUE BLISTERING ( 19 FDA reports)
TOXIC SHOCK SYNDROME ( 19 FDA reports)
ACANTHOSIS ( 19 FDA reports)
ADNEXA UTERI CYST ( 19 FDA reports)
APPLICATION SITE DISCHARGE ( 19 FDA reports)
APPLICATION SITE SCAB ( 19 FDA reports)
ARTERIAL RESTENOSIS ( 19 FDA reports)
ARTERY DISSECTION ( 19 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 19 FDA reports)
ATRIAL NATRIURETIC PEPTIDE INCREASED ( 19 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 19 FDA reports)
BODY MASS INDEX DECREASED ( 19 FDA reports)
BREAST CELLULITIS ( 19 FDA reports)
BREAST DISCOMFORT ( 19 FDA reports)
BREAST INFECTION ( 19 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 19 FDA reports)
CARDIAC SEPTAL DEFECT ( 19 FDA reports)
CAROTID INTIMA-MEDIA THICKNESS INCREASED ( 19 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 19 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 19 FDA reports)
DRUG TOLERANCE INCREASED ( 19 FDA reports)
ECHOCARDIOGRAM ( 19 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 19 FDA reports)
GALLBLADDER PERFORATION ( 19 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 19 FDA reports)
GLOBULINS INCREASED ( 19 FDA reports)
GRIMACING ( 19 FDA reports)
HELICOBACTER TEST POSITIVE ( 19 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 19 FDA reports)
HYPOGLYCAEMIC ENCEPHALOPATHY ( 19 FDA reports)
ILEAL ULCER ( 19 FDA reports)
ABDOMINAL WALL ABSCESS ( 18 FDA reports)
ACTINIC ELASTOSIS ( 18 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 18 FDA reports)
ADMINISTRATION SITE INFECTION ( 18 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 18 FDA reports)
ARTERIAL REPAIR ( 18 FDA reports)
ARTERIOGRAM CORONARY ( 18 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 18 FDA reports)
BACTERIA URINE ( 18 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 18 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 18 FDA reports)
BLEEDING TIME ABNORMAL ( 18 FDA reports)
BLOOD FOLATE INCREASED ( 18 FDA reports)
BONE FORMATION DECREASED ( 18 FDA reports)
BORDERLINE GLAUCOMA ( 18 FDA reports)
BRAIN COMPRESSION ( 18 FDA reports)
BREAST NEOPLASM ( 18 FDA reports)
CERVIX INFLAMMATION ( 18 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 18 FDA reports)
CHYLOTHORAX ( 18 FDA reports)
CLEFT PALATE ( 18 FDA reports)
CLOSED HEAD INJURY ( 18 FDA reports)
COLON CANCER STAGE IV ( 18 FDA reports)
CONJUNCTIVAL ABRASION ( 18 FDA reports)
CRANIOCEREBRAL INJURY ( 18 FDA reports)
DIABETIC EYE DISEASE ( 18 FDA reports)
DIET REFUSAL ( 18 FDA reports)
EAR PRURITUS ( 18 FDA reports)
ENCEPHALITIS VIRAL ( 18 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 18 FDA reports)
ENTEROCOCCAL SEPSIS ( 18 FDA reports)
ERECTION INCREASED ( 18 FDA reports)
FEBRILE INFECTION ( 18 FDA reports)
FEELING GUILTY ( 18 FDA reports)
FOREARM FRACTURE ( 18 FDA reports)
GASTRIC VARICES ( 18 FDA reports)
GENITAL HERPES ( 18 FDA reports)
HIDRADENITIS ( 18 FDA reports)
HIGH DENSITY LIPOPROTEIN ABNORMAL ( 18 FDA reports)
HIV INFECTION ( 18 FDA reports)
HOMICIDE ( 18 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 18 FDA reports)
HYPERPATHIA ( 18 FDA reports)
ILLUSION ( 18 FDA reports)
UTERINE DILATION AND CURETTAGE ( 18 FDA reports)
VARICOCELE ( 18 FDA reports)
VASCULAR ENCEPHALOPATHY ( 18 FDA reports)
VASOCONSTRICTION ( 18 FDA reports)
VENA CAVA THROMBOSIS ( 18 FDA reports)
VENTRICULAR DYSKINESIA ( 18 FDA reports)
VERTEBRAL WEDGING ( 18 FDA reports)
VITRECTOMY ( 18 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 18 FDA reports)
WOUND INFECTION BACTERIAL ( 18 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 18 FDA reports)
INCISION SITE PAIN ( 18 FDA reports)
INJECTION SITE ABSCESS ( 18 FDA reports)
INJECTION SITE CELLULITIS ( 18 FDA reports)
INJECTION SITE ULCER ( 18 FDA reports)
INJURY ASPHYXIATION ( 18 FDA reports)
INJURY CORNEAL ( 18 FDA reports)
INSULIN RESISTANCE ( 18 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 18 FDA reports)
LARGE INTESTINE CARCINOMA ( 18 FDA reports)
LARYNGOCELE ( 18 FDA reports)
LUNG LOBECTOMY ( 18 FDA reports)
MALIGNANT TUMOUR EXCISION ( 18 FDA reports)
MEIBOMIANITIS ( 18 FDA reports)
MICTURITION FREQUENCY DECREASED ( 18 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 18 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 18 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 18 FDA reports)
OPHTHALMOPLEGIA ( 18 FDA reports)
OPTIC NERVE INJURY ( 18 FDA reports)
PANCREATIC CALCIFICATION ( 18 FDA reports)
PANCREATIC NECROSIS ( 18 FDA reports)
PHAEOCHROMOCYTOMA ( 18 FDA reports)
PILONIDAL CYST ( 18 FDA reports)
POSTRENAL FAILURE ( 18 FDA reports)
PROTEIN URINE ( 18 FDA reports)
PSEUDOCYST ( 18 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 18 FDA reports)
RADIATION SKIN INJURY ( 18 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 18 FDA reports)
RECTAL PROLAPSE ( 18 FDA reports)
RECTAL TENESMUS ( 18 FDA reports)
RENAL ABSCESS ( 18 FDA reports)
RENAL ARTERY THROMBOSIS ( 18 FDA reports)
RETINAL VASCULAR DISORDER ( 18 FDA reports)
SCLERITIS ( 18 FDA reports)
SHUNT THROMBOSIS ( 18 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 18 FDA reports)
SKIN OPERATION ( 18 FDA reports)
SMOKER ( 18 FDA reports)
SPINAL OPERATION ( 18 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 18 FDA reports)
SYMPATHETIC POSTERIOR CERVICAL SYNDROME ( 18 FDA reports)
TONIC CONVULSION ( 18 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 18 FDA reports)
ULNAR NERVE INJURY ( 18 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 18 FDA reports)
URETHRAL CARUNCLE ( 18 FDA reports)
INADEQUATE DIET ( 17 FDA reports)
INJECTION SITE VESICLES ( 17 FDA reports)
KIDNEY SMALL ( 17 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 17 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 17 FDA reports)
MACULAR SCAR ( 17 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 17 FDA reports)
MESENTERIC OCCLUSION ( 17 FDA reports)
MORGANELLA INFECTION ( 17 FDA reports)
MUSCLE SWELLING ( 17 FDA reports)
MUTISM ( 17 FDA reports)
NEUROFIBROMA ( 17 FDA reports)
NEUROSIS ( 17 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 17 FDA reports)
OEDEMA GENITAL ( 17 FDA reports)
ORAL PRURITUS ( 17 FDA reports)
PANCREATIC DUCT STENOSIS ( 17 FDA reports)
PERICARDIAL DISEASE ( 17 FDA reports)
PERONEAL MUSCULAR ATROPHY ( 17 FDA reports)
PILOERECTION ( 17 FDA reports)
PLASTIC SURGERY ( 17 FDA reports)
PLATELET TRANSFUSION ( 17 FDA reports)
PNEUMOCOCCAL INFECTION ( 17 FDA reports)
POLYSUBSTANCE ABUSE ( 17 FDA reports)
PRODUCT ODOUR ABNORMAL ( 17 FDA reports)
PSOAS ABSCESS ( 17 FDA reports)
PULMONARY ARTERY DILATATION ( 17 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 17 FDA reports)
RETINAL DEGENERATION ( 17 FDA reports)
RHEUMATOID NODULE ( 17 FDA reports)
SCAN BONE MARROW ABNORMAL ( 17 FDA reports)
SINUS ANTROSTOMY ( 17 FDA reports)
SINUS RHYTHM ( 17 FDA reports)
SINUSITIS FUNGAL ( 17 FDA reports)
SLOW RESPONSE TO STIMULI ( 17 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 17 FDA reports)
SPERMATOZOA PROGRESSIVE MOTILITY DECREASED ( 17 FDA reports)
SPLENIC VEIN THROMBOSIS ( 17 FDA reports)
STRESS ULCER ( 17 FDA reports)
SURGICAL FAILURE ( 17 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 17 FDA reports)
TEETH BRITTLE ( 17 FDA reports)
TINEL'S SIGN ( 17 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 17 FDA reports)
UPPER EXTREMITY MASS ( 17 FDA reports)
URETERAL STENT INSERTION ( 17 FDA reports)
ABDOMINAL SEPSIS ( 17 FDA reports)
AGNOSIA ( 17 FDA reports)
AGORAPHOBIA ( 17 FDA reports)
ANORGASMIA ( 17 FDA reports)
ANOXIA ( 17 FDA reports)
AORTIC ANEURYSM REPAIR ( 17 FDA reports)
APPLICATION SITE URTICARIA ( 17 FDA reports)
BENCE JONES PROTEIN URINE PRESENT ( 17 FDA reports)
BILIARY SEPSIS ( 17 FDA reports)
BIOPSY SKIN ABNORMAL ( 17 FDA reports)
BLOOD CORTISOL ABNORMAL ( 17 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 17 FDA reports)
CRANIAL NERVE DISORDER ( 17 FDA reports)
CREATININE URINE INCREASED ( 17 FDA reports)
DIABETIC RETINAL OEDEMA ( 17 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 17 FDA reports)
DIEULAFOY'S VASCULAR MALFORMATION ( 17 FDA reports)
DIZZINESS EXERTIONAL ( 17 FDA reports)
DRY GANGRENE ( 17 FDA reports)
ECZEMA ASTEATOTIC ( 17 FDA reports)
ENDOSCOPY ( 17 FDA reports)
ENGRAFTMENT SYNDROME ( 17 FDA reports)
EXTRADURAL ABSCESS ( 17 FDA reports)
FACIAL WASTING ( 17 FDA reports)
FAT TISSUE INCREASED ( 17 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 17 FDA reports)
GASTRIC NEOPLASM ( 17 FDA reports)
GASTRIC PH DECREASED ( 17 FDA reports)
GASTROINTESTINAL OEDEMA ( 17 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 17 FDA reports)
HEPATITIS A ( 17 FDA reports)
HYPEROSMOLAR STATE ( 17 FDA reports)
HYPOVITAMINOSIS ( 17 FDA reports)
VENOOCCLUSIVE DISEASE ( 17 FDA reports)
VIRAL LOAD INCREASED ( 17 FDA reports)
VEIN PAIN ( 16 FDA reports)
VITREOUS DEGENERATION ( 16 FDA reports)
INFLAMMATORY MARKER INCREASED ( 16 FDA reports)
INJECTION SITE STINGING ( 16 FDA reports)
INTESTINAL MASS ( 16 FDA reports)
INTRACRANIAL HAEMATOMA ( 16 FDA reports)
JAUNDICE ACHOLURIC ( 16 FDA reports)
LASER THERAPY ( 16 FDA reports)
LIP INJURY ( 16 FDA reports)
LYMPH GLAND INFECTION ( 16 FDA reports)
LYMPH NODE PAIN ( 16 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 16 FDA reports)
MECHANICAL URTICARIA ( 16 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 16 FDA reports)
MEDIASTINAL MASS ( 16 FDA reports)
MENINGITIS BACTERIAL ( 16 FDA reports)
MENISCUS REMOVAL ( 16 FDA reports)
MICROCYTOSIS ( 16 FDA reports)
MOUTH BREATHING ( 16 FDA reports)
MYODESOPSIA ( 16 FDA reports)
NIPPLE DISORDER ( 16 FDA reports)
NO ADVERSE DRUG EFFECT ( 16 FDA reports)
OESOPHAGEAL MUCOSAL HYPERPLASIA ( 16 FDA reports)
ORBITAL OEDEMA ( 16 FDA reports)
OROPHARYNGEAL SPASM ( 16 FDA reports)
ORTHOSTATIC INTOLERANCE ( 16 FDA reports)
PANNICULITIS ( 16 FDA reports)
PARACENTESIS ( 16 FDA reports)
PARALYSIS FLACCID ( 16 FDA reports)
PARANEOPLASTIC SYNDROME ( 16 FDA reports)
PECTUS EXCAVATUM ( 16 FDA reports)
PEPTIC ULCER PERFORATION ( 16 FDA reports)
PHARYNX DISCOMFORT ( 16 FDA reports)
PLASMA CELLS INCREASED ( 16 FDA reports)
PNEUMOCOCCAL SEPSIS ( 16 FDA reports)
PNEUMONIA MYCOPLASMAL ( 16 FDA reports)
POSTPARTUM HAEMORRHAGE ( 16 FDA reports)
PROCEDURAL NAUSEA ( 16 FDA reports)
PROCEDURAL VOMITING ( 16 FDA reports)
PROSTATECTOMY ( 16 FDA reports)
PROSTATIC OPERATION ( 16 FDA reports)
PUTAMEN HAEMORRHAGE ( 16 FDA reports)
RADIATION OESOPHAGITIS ( 16 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 16 FDA reports)
RENAL TUBULAR ATROPHY ( 16 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 16 FDA reports)
RUBELLA ( 16 FDA reports)
SALMONELLOSIS ( 16 FDA reports)
SELF ESTEEM DECREASED ( 16 FDA reports)
SHIFT TO THE LEFT ( 16 FDA reports)
SPERMATOZOA PROGRESSIVE MOTILITY ABNORMAL ( 16 FDA reports)
SPUTUM ABNORMAL ( 16 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 16 FDA reports)
SUPRAPUBIC PAIN ( 16 FDA reports)
TONSILLAR HYPERTROPHY ( 16 FDA reports)
TRAUMATIC LUNG INJURY ( 16 FDA reports)
TUMOUR EXCISION ( 16 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 16 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 16 FDA reports)
URETERIC CANCER ( 16 FDA reports)
URETHRAL HAEMORRHAGE ( 16 FDA reports)
URETHRAL OBSTRUCTION ( 16 FDA reports)
URINE BILIRUBIN INCREASED ( 16 FDA reports)
ABSCESS SOFT TISSUE ( 16 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 16 FDA reports)
ALBUMINURIA ( 16 FDA reports)
ALLERGIC SINUSITIS ( 16 FDA reports)
AMAUROSIS ( 16 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 16 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 16 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 16 FDA reports)
AORTIC BYPASS ( 16 FDA reports)
ASPIRATION BONE MARROW ( 16 FDA reports)
ATRIAL HYPERTROPHY ( 16 FDA reports)
BASOSQUAMOUS CARCINOMA ( 16 FDA reports)
BEREAVEMENT ( 16 FDA reports)
BIOPSY BONE MARROW ( 16 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 16 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 16 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 16 FDA reports)
BONE LESION EXCISION ( 16 FDA reports)
BRAIN HYPOXIA ( 16 FDA reports)
BRAIN STEM ISCHAEMIA ( 16 FDA reports)
BULLOUS LUNG DISEASE ( 16 FDA reports)
BURNS THIRD DEGREE ( 16 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 16 FDA reports)
CARCINOID TUMOUR ( 16 FDA reports)
CARDIAC STRESS TEST ( 16 FDA reports)
CATARACT CORTICAL ( 16 FDA reports)
CITROBACTER INFECTION ( 16 FDA reports)
COLLAGEN DISORDER ( 16 FDA reports)
CORNEAL DEPOSITS ( 16 FDA reports)
CRANIOTOMY ( 16 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 16 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 16 FDA reports)
DEVICE INTERACTION ( 16 FDA reports)
DEVICE MISUSE ( 16 FDA reports)
DYSLEXIA ( 16 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 16 FDA reports)
ENDARTERECTOMY ( 16 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 16 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 16 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 16 FDA reports)
EYE EXCISION ( 16 FDA reports)
FEAR OF DISEASE ( 16 FDA reports)
FEMORAL ARTERY EMBOLISM ( 16 FDA reports)
FOREIGN BODY ASPIRATION ( 16 FDA reports)
GAMBLING ( 16 FDA reports)
GINGIVAL ATROPHY ( 16 FDA reports)
HAEMOGLOBIN ( 16 FDA reports)
HEPATOJUGULAR REFLUX ( 16 FDA reports)
ILIOTIBIAL BAND SYNDROME ( 16 FDA reports)
ABDOMINAL WALL DISORDER ( 15 FDA reports)
ABORTION ( 15 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 15 FDA reports)
ACUTE LUNG INJURY ( 15 FDA reports)
ALKALOSIS ( 15 FDA reports)
ANTI-INSULIN ANTIBODY INCREASED ( 15 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 15 FDA reports)
AORTIC OCCLUSION ( 15 FDA reports)
APNOEIC ATTACK ( 15 FDA reports)
ARACHNOID CYST ( 15 FDA reports)
BEHCET'S SYNDROME ( 15 FDA reports)
BLADDER INJURY ( 15 FDA reports)
BLOOD ALCOHOL INCREASED ( 15 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 15 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 15 FDA reports)
BLOOD PRESSURE ( 15 FDA reports)
BONE FISTULA ( 15 FDA reports)
BONE METABOLISM DISORDER ( 15 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 15 FDA reports)
BREAST CANCER STAGE II ( 15 FDA reports)
BREAST CANCER STAGE III ( 15 FDA reports)
BREATH SOUNDS DECREASED ( 15 FDA reports)
BRONCHIAL HAEMORRHAGE ( 15 FDA reports)
BRONCHITIS VIRAL ( 15 FDA reports)
BULBAR PALSY ( 15 FDA reports)
CARDIAC PERFORATION ( 15 FDA reports)
CAROTID BODY TUMOUR ( 15 FDA reports)
CHEST WALL MASS ( 15 FDA reports)
CHLOASMA ( 15 FDA reports)
CORNEAL DYSTROPHY ( 15 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 15 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 15 FDA reports)
DUODENAL POLYP ( 15 FDA reports)
ELEVATED MOOD ( 15 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 15 FDA reports)
ERYTHRODERMIC PSORIASIS ( 15 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 15 FDA reports)
EYELIDS PRURITUS ( 15 FDA reports)
FAILURE OF IMPLANT ( 15 FDA reports)
FEAR OF FALLING ( 15 FDA reports)
FLOPPY IRIS SYNDROME ( 15 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 15 FDA reports)
GENITAL BURNING SENSATION ( 15 FDA reports)
GLIOBLASTOMA ( 15 FDA reports)
GLIOBLASTOMA MULTIFORME ( 15 FDA reports)
HAPTOGLOBIN DECREASED ( 15 FDA reports)
HYPERALBUMINAEMIA ( 15 FDA reports)
HYPERTRICHOSIS ( 15 FDA reports)
HYPOMETABOLISM ( 15 FDA reports)
HYPOSMIA ( 15 FDA reports)
ILEAL PERFORATION ( 15 FDA reports)
VARICOSE ULCERATION ( 15 FDA reports)
VOCAL CORD THICKENING ( 15 FDA reports)
WOUND TREATMENT ( 15 FDA reports)
INFECTED DERMAL CYST ( 15 FDA reports)
INJECTION SITE NECROSIS ( 15 FDA reports)
INJECTION SITE PAPULE ( 15 FDA reports)
IRIDOCELE ( 15 FDA reports)
JOINT WARMTH ( 15 FDA reports)
KLEBSIELLA TEST POSITIVE ( 15 FDA reports)
LAZINESS ( 15 FDA reports)
LEUKOARAIOSIS ( 15 FDA reports)
LIFE SUPPORT ( 15 FDA reports)
LISTERIOSIS ( 15 FDA reports)
LITHOTRIPSY ( 15 FDA reports)
LYME DISEASE ( 15 FDA reports)
MARASMUS ( 15 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 15 FDA reports)
METATARSUS PRIMUS VARUS ( 15 FDA reports)
MONONEUROPATHY ( 15 FDA reports)
NASAL ODOUR ( 15 FDA reports)
NASAL SEPTUM DISORDER ( 15 FDA reports)
NEUROPATHIC PAIN ( 15 FDA reports)
NOCARDIOSIS ( 15 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 15 FDA reports)
OESOPHAGEAL DISCOMFORT ( 15 FDA reports)
OESOPHAGEAL PERFORATION ( 15 FDA reports)
OOPHORECTOMY ( 15 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 15 FDA reports)
PANCREATOLITHIASIS ( 15 FDA reports)
PARKINSONIAN GAIT ( 15 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 15 FDA reports)
PHARYNGEAL ULCERATION ( 15 FDA reports)
POST PROCEDURAL FISTULA ( 15 FDA reports)
PREMATURE DELIVERY ( 15 FDA reports)
PROSTATIC CALCIFICATION ( 15 FDA reports)
PROSTATISM ( 15 FDA reports)
PRURITUS GENITAL ( 15 FDA reports)
PSEUDOPORPHYRIA ( 15 FDA reports)
PUPILLARY DISORDER ( 15 FDA reports)
PYOGENIC GRANULOMA ( 15 FDA reports)
RENAL CANCER METASTATIC ( 15 FDA reports)
REPERFUSION ARRHYTHMIA ( 15 FDA reports)
RETINAL PIGMENT EPITHELIAL TEAR ( 15 FDA reports)
SARCOMA ( 15 FDA reports)
SKIN DEPIGMENTATION ( 15 FDA reports)
SPINAL CORD INJURY ( 15 FDA reports)
SPLEEN CONGESTION ( 15 FDA reports)
SPLENIC CYST ( 15 FDA reports)
STERNOTOMY ( 15 FDA reports)
SUTURE RELATED COMPLICATION ( 15 FDA reports)
SYNOVIAL DISORDER ( 15 FDA reports)
SYPHILIS ( 15 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 15 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 15 FDA reports)
TUMOUR NECROSIS ( 15 FDA reports)
TWIN PREGNANCY ( 15 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 15 FDA reports)
URAEMIC ENCEPHALOPATHY ( 15 FDA reports)
INHIBITORY DRUG INTERACTION ( 14 FDA reports)
INTUBATION COMPLICATION ( 14 FDA reports)
IRIS DISORDER ( 14 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 14 FDA reports)
IRON METABOLISM DISORDER ( 14 FDA reports)
IVTH NERVE PARALYSIS ( 14 FDA reports)
LIGHT CHAIN DISEASE ( 14 FDA reports)
LUNG OPERATION ( 14 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 14 FDA reports)
MERALGIA PARAESTHETICA ( 14 FDA reports)
MESENTERIC ARTERY STENOSIS ( 14 FDA reports)
METASTASES TO NASAL SINUSES ( 14 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 14 FDA reports)
NAIL GROWTH ABNORMAL ( 14 FDA reports)
NEUTRALISING ANTIBODIES POSITIVE ( 14 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 14 FDA reports)
OESOPHAGEAL MASS ( 14 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 14 FDA reports)
OSTECTOMY ( 14 FDA reports)
PENILE SWELLING ( 14 FDA reports)
PERIDIVERTICULAR ABSCESS ( 14 FDA reports)
PIRIFORMIS SYNDROME ( 14 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 14 FDA reports)
POST CONCUSSION SYNDROME ( 14 FDA reports)
POSTOPERATIVE ADHESION ( 14 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 14 FDA reports)
PRODUCT COUNTERFEIT ( 14 FDA reports)
PROGRESSIVE SUPRANUCLEAR PALSY ( 14 FDA reports)
PROSTATE INFECTION ( 14 FDA reports)
PROTEUS TEST POSITIVE ( 14 FDA reports)
PULMONARY SARCOIDOSIS ( 14 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 14 FDA reports)
RENAL PAPILLARY NECROSIS ( 14 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 14 FDA reports)
RETINAL VASCULAR OCCLUSION ( 14 FDA reports)
RETINITIS ( 14 FDA reports)
RETROGRADE AMNESIA ( 14 FDA reports)
RHEUMATOID LUNG ( 14 FDA reports)
SCHAMBERG'S DISEASE ( 14 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 14 FDA reports)
SHUNT OCCLUSION ( 14 FDA reports)
SINOATRIAL BLOCK ( 14 FDA reports)
SKIN TEST POSITIVE ( 14 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 14 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 14 FDA reports)
SPLENECTOMY ( 14 FDA reports)
STARVATION ( 14 FDA reports)
STEAL SYNDROME ( 14 FDA reports)
SUBCLAVIAN STEAL SYNDROME ( 14 FDA reports)
SUBSTANCE ABUSE ( 14 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 14 FDA reports)
TONGUE HAEMATOMA ( 14 FDA reports)
TRAUMATIC FRACTURE ( 14 FDA reports)
TRICHORRHEXIS ( 14 FDA reports)
UNDERWEIGHT ( 14 FDA reports)
URETERIC STENOSIS ( 14 FDA reports)
URINARY CASTS ( 14 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 14 FDA reports)
ABSCESS MANAGEMENT ( 14 FDA reports)
ACCIDENTAL DEATH ( 14 FDA reports)
ADJUSTMENT DISORDER WITH MIXED ANXIETY AND DEPRESSED MOOD ( 14 FDA reports)
AGITATED DEPRESSION ( 14 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 14 FDA reports)
ANDROGEN DEFICIENCY ( 14 FDA reports)
APPLICATION SITE EXFOLIATION ( 14 FDA reports)
APPLICATION SITE HAEMATOMA ( 14 FDA reports)
ASTHMATIC CRISIS ( 14 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 14 FDA reports)
BREAST MICROCALCIFICATION ( 14 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 14 FDA reports)
CALCIUM IONISED INCREASED ( 14 FDA reports)
CARDIAC VALVE VEGETATION ( 14 FDA reports)
CAROTID ARTERY STENT INSERTION ( 14 FDA reports)
CEREBELLAR ISCHAEMIA ( 14 FDA reports)
CHOLESTEROSIS ( 14 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 14 FDA reports)
COCCIDIOIDOMYCOSIS ( 14 FDA reports)
COLONIC FISTULA ( 14 FDA reports)
COLONIC HAEMATOMA ( 14 FDA reports)
COLOUR BLINDNESS ( 14 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 14 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 14 FDA reports)
CROUP INFECTIOUS ( 14 FDA reports)
CRYOGLOBULINAEMIA ( 14 FDA reports)
CULTURE STOOL POSITIVE ( 14 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 14 FDA reports)
DIABETIC MICROANGIOPATHY ( 14 FDA reports)
DRUG EFFECT DELAYED ( 14 FDA reports)
DRUG LEVEL CHANGED ( 14 FDA reports)
DUODENAL STENOSIS ( 14 FDA reports)
EARLY MORNING AWAKENING ( 14 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 14 FDA reports)
EPIDERMAL NECROSIS ( 14 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 14 FDA reports)
EUSTACHIAN TUBE DISORDER ( 14 FDA reports)
EXANTHEM ( 14 FDA reports)
EXCESSIVE EYE BLINKING ( 14 FDA reports)
EYELID OPERATION ( 14 FDA reports)
FACIAL ASYMMETRY ( 14 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 14 FDA reports)
GASTRIC BYPASS ( 14 FDA reports)
GLOBULINS DECREASED ( 14 FDA reports)
GLYCOSYLATED HAEMOGLOBIN DECREASED ( 14 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 14 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 14 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 14 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 14 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 14 FDA reports)
HYPERINSULINAEMIA ( 14 FDA reports)
HYPERPARATHYROIDISM PRIMARY ( 14 FDA reports)
HYPOCAPNIA ( 14 FDA reports)
HYPOCHROMASIA ( 14 FDA reports)
ILEAL STENOSIS ( 14 FDA reports)
ILEITIS ( 14 FDA reports)
URTICARIA PAPULAR ( 14 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 14 FDA reports)
VENTRICLE RUPTURE ( 14 FDA reports)
VISUAL BRIGHTNESS ( 14 FDA reports)
VITAL CAPACITY DECREASED ( 14 FDA reports)
VOCAL CORD POLYP ( 14 FDA reports)
VULVAL CANCER ( 14 FDA reports)
WEANING FAILURE ( 14 FDA reports)
URINE SODIUM INCREASED ( 13 FDA reports)
VASCULAR OPERATION ( 13 FDA reports)
VENOUS INJURY ( 13 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 13 FDA reports)
WATER INTOXICATION ( 13 FDA reports)
XANTHOPSIA ( 13 FDA reports)
INCISION SITE HAEMATOMA ( 13 FDA reports)
INFUSION SITE HAEMORRHAGE ( 13 FDA reports)
INJECTION SITE OEDEMA ( 13 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 13 FDA reports)
INVESTIGATION ABNORMAL ( 13 FDA reports)
IRIDOCYCLITIS ( 13 FDA reports)
IRIS ADHESIONS ( 13 FDA reports)
JOINT HYPEREXTENSION ( 13 FDA reports)
LEIOMYOMA ( 13 FDA reports)
LEUKOPLAKIA ( 13 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 13 FDA reports)
LINEAR IGA DISEASE ( 13 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 13 FDA reports)
LUPUS NEPHRITIS ( 13 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 13 FDA reports)
MACULE ( 13 FDA reports)
MAGNESIUM DEFICIENCY ( 13 FDA reports)
METASTASES TO BLADDER ( 13 FDA reports)
METASTASES TO PANCREAS ( 13 FDA reports)
MOUTH CYST ( 13 FDA reports)
MUCOSAL DISCOLOURATION ( 13 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 13 FDA reports)
MUSCLE ABSCESS ( 13 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 13 FDA reports)
MYOPERICARDITIS ( 13 FDA reports)
NAIL PITTING ( 13 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 13 FDA reports)
NASOPHARYNGEAL DISORDER ( 13 FDA reports)
NEUROMUSCULAR BLOCKADE ( 13 FDA reports)
NEUTROPHIL COUNT ( 13 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 13 FDA reports)
OEDEMATOUS PANCREATITIS ( 13 FDA reports)
ORTHOSTATIC HYPERTENSION ( 13 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 13 FDA reports)
PARADOXICAL DRUG REACTION ( 13 FDA reports)
PERICARDITIS CONSTRICTIVE ( 13 FDA reports)
PERSECUTORY DELUSION ( 13 FDA reports)
PHONOPHOBIA ( 13 FDA reports)
PICKWICKIAN SYNDROME ( 13 FDA reports)
PNEUMOCONIOSIS ( 13 FDA reports)
POLYCHROMASIA ( 13 FDA reports)
POST PROCEDURAL MYOCARDIAL INFARCTION ( 13 FDA reports)
POSTERIOR CAPSULOTOMY ( 13 FDA reports)
PROSTATIC HAEMORRHAGE ( 13 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 13 FDA reports)
PSEUDOMONAS BRONCHITIS ( 13 FDA reports)
PTERYGIUM ( 13 FDA reports)
PUBIC RAMI FRACTURE ( 13 FDA reports)
PULMONARY CAVITATION ( 13 FDA reports)
RASH PAPULOSQUAMOUS ( 13 FDA reports)
REACTIVE PSYCHOSIS ( 13 FDA reports)
RECTAL DISCHARGE ( 13 FDA reports)
RENAL CYST HAEMORRHAGE ( 13 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 13 FDA reports)
RESPIRATORY TRACT IRRITATION ( 13 FDA reports)
RETICULOCYTE COUNT DECREASED ( 13 FDA reports)
RETINAL INJURY ( 13 FDA reports)
RETINAL MELANOMA ( 13 FDA reports)
RETROPERITONEAL FIBROSIS ( 13 FDA reports)
SALIVARY GLAND CANCER ( 13 FDA reports)
SCLERAL DISORDER ( 13 FDA reports)
SENILE OSTEOPOROSIS ( 13 FDA reports)
SKIN LESION EXCISION ( 13 FDA reports)
SKULL FRACTURED BASE ( 13 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 13 FDA reports)
SPINAL EPIDURAL HAEMORRHAGE ( 13 FDA reports)
SPLENIC LESION ( 13 FDA reports)
SPONTANEOUS PENILE ERECTION ( 13 FDA reports)
STENT EMBOLISATION ( 13 FDA reports)
STENT MALFUNCTION ( 13 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 13 FDA reports)
THYROID GLAND CANCER ( 13 FDA reports)
THYROXINE DECREASED ( 13 FDA reports)
TUMOUR INVASION ( 13 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 13 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 13 FDA reports)
URETHRAL DILATATION ( 13 FDA reports)
URINARY SEDIMENT PRESENT ( 13 FDA reports)
ABDOMINAL OPERATION ( 13 FDA reports)
ABNORMAL CLOTTING FACTOR ( 13 FDA reports)
AEROMONA INFECTION ( 13 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 13 FDA reports)
ALLERGIC COUGH ( 13 FDA reports)
ALVEOLITIS FIBROSING ( 13 FDA reports)
ANION GAP DECREASED ( 13 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST ( 13 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 13 FDA reports)
APPLICATION SITE DERMATITIS ( 13 FDA reports)
ARTERIAL SPASM ( 13 FDA reports)
ARTERIAL STENOSIS LIMB ( 13 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 13 FDA reports)
ARTERIOVENOUS SHUNT OPERATION ( 13 FDA reports)
ARTHROSCOPY ( 13 FDA reports)
AXILLARY VEIN THROMBOSIS ( 13 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 13 FDA reports)
BENIGN LUNG NEOPLASM ( 13 FDA reports)
BIOPSY GINGIVAL ( 13 FDA reports)
BK VIRUS INFECTION ( 13 FDA reports)
BLADDER IRRITATION ( 13 FDA reports)
BLOOD CALCIUM ABNORMAL ( 13 FDA reports)
BLOOD GLUCOSE ( 13 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 13 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 13 FDA reports)
BLOOD PROLACTIN INCREASED ( 13 FDA reports)
BLOOD VISCOSITY INCREASED ( 13 FDA reports)
BODY MASS INDEX INCREASED ( 13 FDA reports)
BONE ATROPHY ( 13 FDA reports)
BONE DENSITOMETRY ( 13 FDA reports)
BRADYPNOEA ( 13 FDA reports)
BRONCHIAL INFECTION ( 13 FDA reports)
CAPILLARY DISORDER ( 13 FDA reports)
CARDIAC AMYLOIDOSIS ( 13 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 13 FDA reports)
CATHETER SITE RELATED REACTION ( 13 FDA reports)
CAUDA EQUINA SYNDROME ( 13 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 13 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 13 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 13 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 13 FDA reports)
CIRRHOSIS ALCOHOLIC ( 13 FDA reports)
COMPLICATIONS OF TRANSPLANTED HEART ( 13 FDA reports)
CONGENITAL ATRIAL SEPTAL DEFECT ( 13 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 13 FDA reports)
CORNEAL OPACITY ( 13 FDA reports)
CRACKLES LUNG ( 13 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 13 FDA reports)
CRYPTORCHISM ( 13 FDA reports)
DEAFNESS TRANSITORY ( 13 FDA reports)
DROWNING ( 13 FDA reports)
ECZEMA NUMMULAR ( 13 FDA reports)
ELECTROCARDIOGRAM PQ INTERVAL PROLONGED ( 13 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 13 FDA reports)
ENANTHEMA ( 13 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 13 FDA reports)
ENTERITIS INFECTIOUS ( 13 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 13 FDA reports)
EPIDIDYMAL CYST ( 13 FDA reports)
FOETAL DISORDER ( 13 FDA reports)
GALACTORRHOEA ( 13 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 13 FDA reports)
GINGIVECTOMY ( 13 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 13 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 13 FDA reports)
HEPATITIS E ( 13 FDA reports)
HERNIA HIATUS REPAIR ( 13 FDA reports)
HIRSUTISM ( 13 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 13 FDA reports)
HYPERCALCIURIA ( 13 FDA reports)
HYPERTRANSAMINASAEMIA ( 13 FDA reports)
HYPERVIGILANCE ( 13 FDA reports)
ILIUM FRACTURE ( 13 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 12 FDA reports)
ADAMS-STOKES SYNDROME ( 12 FDA reports)
ALLODYNIA ( 12 FDA reports)
ANAL SKIN TAGS ( 12 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 12 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 12 FDA reports)
APPLICATION SITE DRYNESS ( 12 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 12 FDA reports)
AUTOIMMUNE INNER EAR DISEASE ( 12 FDA reports)
BACTERIAL TEST ( 12 FDA reports)
BILIARY CIRRHOSIS ( 12 FDA reports)
BIOPSY BREAST ( 12 FDA reports)
BIOPSY LIVER ABNORMAL ( 12 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 12 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 12 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 12 FDA reports)
CAMPYLOBACTER GASTROENTERITIS ( 12 FDA reports)
CANDIDA SEPSIS ( 12 FDA reports)
CAUSTIC INJURY ( 12 FDA reports)
CEREBELLAR ATAXIA ( 12 FDA reports)
CEREBROSCLEROSIS ( 12 FDA reports)
CHOLINERGIC SYNDROME ( 12 FDA reports)
CHOROIDAL DYSTROPHY ( 12 FDA reports)
COMPRESSION STOCKINGS APPLICATION ( 12 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 12 FDA reports)
CORNEAL TRANSPLANT ( 12 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 12 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 12 FDA reports)
CYST DRAINAGE ( 12 FDA reports)
DIABETIC GANGRENE ( 12 FDA reports)
DISINHIBITION ( 12 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 12 FDA reports)
DUODENAL PERFORATION ( 12 FDA reports)
ELECTRIC SHOCK ( 12 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 12 FDA reports)
EPIDERMAL NAEVUS ( 12 FDA reports)
ERYTHEMA INFECTIOSUM ( 12 FDA reports)
ERYTHROMELALGIA ( 12 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 12 FDA reports)
EYE REDNESS ( 12 FDA reports)
FAECAL VOLUME INCREASED ( 12 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 12 FDA reports)
FEBRILE CONVULSION ( 12 FDA reports)
FEEDING TUBE COMPLICATION ( 12 FDA reports)
FOETAL CARDIAC DISORDER ( 12 FDA reports)
FOREIGN BODY IN EYE ( 12 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 12 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA HAEMORRHAGIC ( 12 FDA reports)
GENITAL EROSION ( 12 FDA reports)
GESTATIONAL DIABETES ( 12 FDA reports)
GLUCOSE TOLERANCE TEST ABNORMAL ( 12 FDA reports)
HELLP SYNDROME ( 12 FDA reports)
HEPATIC CALCIFICATION ( 12 FDA reports)
HERNIA OBSTRUCTIVE ( 12 FDA reports)
HIP DYSPLASIA ( 12 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 12 FDA reports)
HYPERPROTEINAEMIA ( 12 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 12 FDA reports)
ICHTHYOSIS ( 12 FDA reports)
URINE OSMOLARITY DECREASED ( 12 FDA reports)
UTERINE ATROPHY ( 12 FDA reports)
VAGINAL DISORDER ( 12 FDA reports)
VARICOSE VEIN OPERATION ( 12 FDA reports)
VASCULAR PROCEDURE COMPLICATION ( 12 FDA reports)
VENTRICULAR TACHYARRHYTHMIA ( 12 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 12 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 12 FDA reports)
VITREOUS OPACITIES ( 12 FDA reports)
IMPLANT SITE EFFUSION ( 12 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 12 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 12 FDA reports)
INJECTION SITE SCAR ( 12 FDA reports)
INTRA-AORTIC BALLOON PLACEMENT ( 12 FDA reports)
JOINT ANKYLOSIS ( 12 FDA reports)
KLEBSIELLA BACTERAEMIA ( 12 FDA reports)
LACTOBACILLUS INFECTION ( 12 FDA reports)
LICHENIFICATION ( 12 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 12 FDA reports)
MENINGITIS NONINFECTIVE ( 12 FDA reports)
MYCOBACTERIAL INFECTION ( 12 FDA reports)
MYELITIS ( 12 FDA reports)
MYOGLOBIN URINE PRESENT ( 12 FDA reports)
NEUROENDOCRINE CARCINOMA ( 12 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 12 FDA reports)
ONYCHOLYSIS ( 12 FDA reports)
ORAL MUCOSA ATROPHY ( 12 FDA reports)
OSTEOARTHROPATHY ( 12 FDA reports)
OSTEOSARCOMA METASTATIC ( 12 FDA reports)
OVARIAN FAILURE ( 12 FDA reports)
PANCREATIC ABSCESS ( 12 FDA reports)
PELVIC DEFORMITY ( 12 FDA reports)
PELVIC FLUID COLLECTION ( 12 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 12 FDA reports)
PERIPHERAL NERVE INJURY ( 12 FDA reports)
PHOSPHORUS METABOLISM DISORDER ( 12 FDA reports)
PIGMENTARY GLAUCOMA ( 12 FDA reports)
PLEURAL ADHESION ( 12 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 12 FDA reports)
POSITIVE ROMBERGISM ( 12 FDA reports)
POST PROCEDURAL BILE LEAK ( 12 FDA reports)
POST PROCEDURAL NAUSEA ( 12 FDA reports)
POST-TRAUMATIC PAIN ( 12 FDA reports)
POSTOPERATIVE THORACIC PROCEDURE COMPLICATION ( 12 FDA reports)
PROCEDURAL HAEMORRHAGE ( 12 FDA reports)
PSYCHOSOMATIC DISEASE ( 12 FDA reports)
PULMONARY MYCOSIS ( 12 FDA reports)
RADICULITIS BRACHIAL ( 12 FDA reports)
RADIOTHERAPY TO BRAIN ( 12 FDA reports)
REFLEX SYMPATHETIC DYSTROPHY ( 12 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 12 FDA reports)
SALIVARY GLAND ADENOMA ( 12 FDA reports)
SCLERAL OPERATION ( 12 FDA reports)
SECONDARY HYPOGONADISM ( 12 FDA reports)
SELF MUTILATION ( 12 FDA reports)
SINUS PAIN ( 12 FDA reports)
SKIN DISCOMFORT ( 12 FDA reports)
SLEEP-RELATED EATING DISORDER ( 12 FDA reports)
SPLINT APPLICATION ( 12 FDA reports)
SPONTANEOUS HAEMATOMA ( 12 FDA reports)
STILLBIRTH ( 12 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 12 FDA reports)
SYRINGOMYELIA ( 12 FDA reports)
TABLET PHYSICAL ISSUE ( 12 FDA reports)
TACHYCARDIA PAROXYSMAL ( 12 FDA reports)
TESTICULAR ATROPHY ( 12 FDA reports)
THROMBECTOMY ( 12 FDA reports)
THYROTOXIC CRISIS ( 12 FDA reports)
THYROXINE FREE DECREASED ( 12 FDA reports)
TONSIL CANCER ( 12 FDA reports)
TRAUMATIC RENAL INJURY ( 12 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 11 FDA reports)
INCREASED VENTRICULAR AFTERLOAD ( 11 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 11 FDA reports)
INSULIN C-PEPTIDE INCREASED ( 11 FDA reports)
INVESTIGATION ( 11 FDA reports)
LENTIGO MALIGNA STAGE UNSPECIFIED ( 11 FDA reports)
LERICHE SYNDROME ( 11 FDA reports)
LEUCINE AMINOPEPTIDASE INCREASED ( 11 FDA reports)
LORDOSIS ( 11 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 11 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 11 FDA reports)
MANDIBULAR PROSTHESIS USER ( 11 FDA reports)
MECHANICAL ILEUS ( 11 FDA reports)
MEDICAL DIET ( 11 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 11 FDA reports)
MENISCAL DEGENERATION ( 11 FDA reports)
METASTATIC GASTRIC CANCER ( 11 FDA reports)
MONONEUROPATHY MULTIPLEX ( 11 FDA reports)
MYOCLONIC EPILEPSY ( 11 FDA reports)
NAIL HYPERTROPHY ( 11 FDA reports)
NAIL INFECTION ( 11 FDA reports)
NASAL OBSTRUCTION ( 11 FDA reports)
NEUROENDOCRINE TUMOUR ( 11 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 11 FDA reports)
OESOPHAGEAL DILATATION ( 11 FDA reports)
OESOPHAGEAL INJURY ( 11 FDA reports)
OESOPHAGEAL NEOPLASM ( 11 FDA reports)
OLIGODENDROGLIOMA ( 11 FDA reports)
ON AND OFF PHENOMENON ( 11 FDA reports)
OOPHORECTOMY BILATERAL ( 11 FDA reports)
OPTIC DISC HAEMORRHAGE ( 11 FDA reports)
OSTEOGENESIS IMPERFECTA ( 11 FDA reports)
OSTEOSYNTHESIS ( 11 FDA reports)
PARAPSORIASIS ( 11 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 11 FDA reports)
PELVIC VENOUS THROMBOSIS ( 11 FDA reports)
PENILE PROSTHESIS INSERTION ( 11 FDA reports)
PERIPARTUM CARDIOMYOPATHY ( 11 FDA reports)
PHLEBOTHROMBOSIS ( 11 FDA reports)
PLACENTA PRAEVIA ( 11 FDA reports)
PNEUMONIA HAEMOPHILUS ( 11 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 11 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 11 FDA reports)
POST PROCEDURAL DISCHARGE ( 11 FDA reports)
POSTOPERATIVE ABSCESS ( 11 FDA reports)
POUCHITIS ( 11 FDA reports)
PRODUCT FORMULATION ISSUE ( 11 FDA reports)
PRODUCT PACKAGING ISSUE ( 11 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 11 FDA reports)
PULMONARY SEPSIS ( 11 FDA reports)
PULMONARY VALVE STENOSIS ( 11 FDA reports)
REGURGITATION OF FOOD ( 11 FDA reports)
REOCCLUSION ( 11 FDA reports)
REPETITIVE SPEECH ( 11 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 11 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 11 FDA reports)
SALIVARY GLAND CALCULUS ( 11 FDA reports)
SALIVARY GLAND NEOPLASM ( 11 FDA reports)
SALIVARY GLAND PAIN ( 11 FDA reports)
SCROTAL ABSCESS ( 11 FDA reports)
SENSATION OF BLOOD FLOW ( 11 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 11 FDA reports)
SKIN BACTERIAL INFECTION ( 11 FDA reports)
SKIN FLAP NECROSIS ( 11 FDA reports)
SKIN GRAFT FAILURE ( 11 FDA reports)
SLEEP ATTACKS ( 11 FDA reports)
SMALL INTESTINAL STENOSIS ( 11 FDA reports)
SPLENIC ABSCESS ( 11 FDA reports)
SPLENIC HAEMORRHAGE ( 11 FDA reports)
SPONDYLOLISTHESIS ACQUIRED ( 11 FDA reports)
SPONDYLOPATHY TRAUMATIC ( 11 FDA reports)
SUBGALEAL HAEMATOMA ( 11 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 11 FDA reports)
SUTURE REMOVAL ( 11 FDA reports)
TENDON SHEATH LESION EXCISION ( 11 FDA reports)
THYROXINE FREE INCREASED ( 11 FDA reports)
TINEA INFECTION ( 11 FDA reports)
TOXIC NODULAR GOITRE ( 11 FDA reports)
TRACHEAL DISORDER ( 11 FDA reports)
TRANSPLANT ( 11 FDA reports)
TYPE I HYPERSENSITIVITY ( 11 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 11 FDA reports)
ACINETOBACTER INFECTION ( 11 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 11 FDA reports)
ANASTOMOTIC STENOSIS ( 11 FDA reports)
ANOMALOUS PULMONARY VENOUS CONNECTION ( 11 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 11 FDA reports)
APGAR SCORE LOW ( 11 FDA reports)
ARTERIOSCLEROTIC RETINOPATHY ( 11 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 11 FDA reports)
BACTERIA STOOL IDENTIFIED ( 11 FDA reports)
BACTERIAL CULTURE POSITIVE ( 11 FDA reports)
BILIARY ANASTOMOSIS COMPLICATION ( 11 FDA reports)
BINOCULAR EYE MOVEMENT DISORDER ( 11 FDA reports)
BLADDER CANCER STAGE II ( 11 FDA reports)
BLADDER NECK OBSTRUCTION ( 11 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 11 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 11 FDA reports)
BLOOD INSULIN INCREASED ( 11 FDA reports)
BLOOD OSMOLARITY INCREASED ( 11 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 11 FDA reports)
BONE CALLUS EXCESSIVE ( 11 FDA reports)
BONE DENSITY ABNORMAL ( 11 FDA reports)
BRAIN ABSCESS ( 11 FDA reports)
BREAST HAEMATOMA ( 11 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 11 FDA reports)
BURSITIS INFECTIVE ( 11 FDA reports)
CARBON MONOXIDE DIFFUSING CAPACITY DECREASED ( 11 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 11 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 11 FDA reports)
CELLULITIS ORBITAL ( 11 FDA reports)
CENTRAL NERVOUS SYSTEM NEOPLASM ( 11 FDA reports)
CEREBELLAR HAEMATOMA ( 11 FDA reports)
CEREBRAL HAEMORRHAGE TRAUMATIC ( 11 FDA reports)
CERULOPLASMIN DECREASED ( 11 FDA reports)
CHOLANGITIS ACUTE ( 11 FDA reports)
CHOROIDAL HAEMORRHAGE ( 11 FDA reports)
CIRCUMORAL OEDEMA ( 11 FDA reports)
COGNITIVE DETERIORATION ( 11 FDA reports)
COLONIC HAEMORRHAGE ( 11 FDA reports)
COMPLICATED MIGRAINE ( 11 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 11 FDA reports)
COMPULSIVE SHOPPING ( 11 FDA reports)
CONFUSION POSTOPERATIVE ( 11 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 11 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 11 FDA reports)
CREUTZFELDT-JAKOB DISEASE ( 11 FDA reports)
CRITICAL ILLNESS POLYNEUROPATHY ( 11 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 11 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 11 FDA reports)
DENTAL TREATMENT ( 11 FDA reports)
DEPERSONALISATION ( 11 FDA reports)
DUODENAL OBSTRUCTION ( 11 FDA reports)
ENEMA ADMINISTRATION ( 11 FDA reports)
ENTEROBACTER PNEUMONIA ( 11 FDA reports)
EXPOSURE TO TOXIC AGENT ( 11 FDA reports)
EYEBALL RUPTURE ( 11 FDA reports)
EYELID FUNCTION DISORDER ( 11 FDA reports)
FALLOT'S TETRALOGY ( 11 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 11 FDA reports)
FLIGHT OF IDEAS ( 11 FDA reports)
FRACTURED COCCYX ( 11 FDA reports)
FUNGAL OESOPHAGITIS ( 11 FDA reports)
FUNGAL PERITONITIS ( 11 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ( 11 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 11 FDA reports)
GASTROINTESTINAL TOXICITY ( 11 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 11 FDA reports)
HAEMATOMA EVACUATION ( 11 FDA reports)
HAEMOBILIA ( 11 FDA reports)
HAEMORRHAGIC INFARCTION ( 11 FDA reports)
HAEMOSIDEROSIS ( 11 FDA reports)
HALLUCINATION, TACTILE ( 11 FDA reports)
HAPTOGLOBIN INCREASED ( 11 FDA reports)
HEAD AND NECK CANCER ( 11 FDA reports)
HEPATIC ATROPHY ( 11 FDA reports)
HEPATITIS VIRAL ( 11 FDA reports)
HEPATORENAL FAILURE ( 11 FDA reports)
HOMOCYSTINAEMIA ( 11 FDA reports)
HYPERAMYLASAEMIA ( 11 FDA reports)
HYPOPITUITARISM ( 11 FDA reports)
ILIAC VEIN OCCLUSION ( 11 FDA reports)
IMPATIENCE ( 11 FDA reports)
VAGINAL MYCOSIS ( 11 FDA reports)
VAGINITIS ( 11 FDA reports)
VARICOSE VEIN RUPTURED ( 11 FDA reports)
VENTRICULAR ASYSTOLE ( 11 FDA reports)
VENTRICULAR FLUTTER ( 11 FDA reports)
VIRAL PERICARDITIS ( 11 FDA reports)
WANDERING PACEMAKER ( 11 FDA reports)
URINE OUTPUT ( 10 FDA reports)
VASCULAR COMPRESSION ( 10 FDA reports)
VASCULAR HEADACHE ( 10 FDA reports)
VENOUS HAEMORRHAGE ( 10 FDA reports)
VERTEBRAL INJURY ( 10 FDA reports)
VIRAL LABYRINTHITIS ( 10 FDA reports)
VOLUME BLOOD DECREASED ( 10 FDA reports)
WHITE BLOOD CELL COUNT ( 10 FDA reports)
WHITE CLOT SYNDROME ( 10 FDA reports)
WOUND EVISCERATION ( 10 FDA reports)
WOUND NECROSIS ( 10 FDA reports)
WOUND SEPSIS ( 10 FDA reports)
X-RAY ( 10 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 10 FDA reports)
INJECTION SITE INFLAMMATION ( 10 FDA reports)
INTERCAPILLARY GLOMERULOSCLEROSIS ( 10 FDA reports)
INTERVERTEBRAL DISC INJURY ( 10 FDA reports)
ISCHAEMIC ULCER ( 10 FDA reports)
JAUNDICE NEONATAL ( 10 FDA reports)
KERATOSIS OBTURANS ( 10 FDA reports)
KUSSMAUL RESPIRATION ( 10 FDA reports)
LARYNGOTRACHEAL OEDEMA ( 10 FDA reports)
LDL/HDL RATIO ( 10 FDA reports)
LEARNING DISORDER ( 10 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 10 FDA reports)
LIPID METABOLISM DISORDER ( 10 FDA reports)
LIPOGRANULOMA ( 10 FDA reports)
LOSS OF PROPRIOCEPTION ( 10 FDA reports)
LUNG CREPITATION ( 10 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 10 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 10 FDA reports)
MEGAKARYOCYTES INCREASED ( 10 FDA reports)
MENINGEAL DISORDER ( 10 FDA reports)
MENISCUS OPERATION ( 10 FDA reports)
MENOMETRORRHAGIA ( 10 FDA reports)
METASTASES TO KIDNEY ( 10 FDA reports)
MICROVASCULAR ANGINA ( 10 FDA reports)
MIGRAINE WITHOUT AURA ( 10 FDA reports)
MOTOR NEURONE DISEASE ( 10 FDA reports)
MUSCULAR DYSTROPHY ( 10 FDA reports)
MYCOBACTERIUM KANSASII INFECTION ( 10 FDA reports)
MYOMECTOMY ( 10 FDA reports)
MYOSCLEROSIS ( 10 FDA reports)
NASAL CAVITY CANCER ( 10 FDA reports)
NASAL SINUS DRAINAGE ( 10 FDA reports)
NEONATAL DISORDER ( 10 FDA reports)
NEOVASCULARISATION ( 10 FDA reports)
NEUROGLYCOPENIA ( 10 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 10 FDA reports)
OESOPHAGEAL OEDEMA ( 10 FDA reports)
OESOPHAGEAL POLYP ( 10 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 10 FDA reports)
OLIGOMENORRHOEA ( 10 FDA reports)
ORTHODONTIC APPLIANCE USER ( 10 FDA reports)
OVARIAN CYST RUPTURED ( 10 FDA reports)
PANCREAS TRANSPLANT ( 10 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 10 FDA reports)
PARANASAL SINUS DISCOMFORT ( 10 FDA reports)
PEDAL PULSE ABNORMAL ( 10 FDA reports)
PERICARDIAL RUB ( 10 FDA reports)
PERINEAL ABSCESS ( 10 FDA reports)
PERIPHERAL PULSE DECREASED ( 10 FDA reports)
PERITONEAL EFFUSION ( 10 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 10 FDA reports)
PIGMENTED NAEVUS ( 10 FDA reports)
PLACENTAL DISORDER ( 10 FDA reports)
POST PROCEDURAL OEDEMA ( 10 FDA reports)
POSTPARTUM DISORDER ( 10 FDA reports)
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME ( 10 FDA reports)
PRECANCEROUS CELLS PRESENT ( 10 FDA reports)
PRECEREBRAL ARTERY OCCLUSION ( 10 FDA reports)
PROCTITIS ULCERATIVE ( 10 FDA reports)
PROSTATE CANCER STAGE IV ( 10 FDA reports)
PROTEIN S DECREASED ( 10 FDA reports)
PSEUDODEMENTIA ( 10 FDA reports)
PULMONARY EOSINOPHILIA ( 10 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 10 FDA reports)
PYOTHORAX ( 10 FDA reports)
RADIAL PULSE ABNORMAL ( 10 FDA reports)
RATHKE'S CLEFT CYST ( 10 FDA reports)
RENAL HAEMATOMA ( 10 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 10 FDA reports)
RETICULOCYTOSIS ( 10 FDA reports)
RETINAL ANEURYSM ( 10 FDA reports)
REVERSIBLE AIRWAYS OBSTRUCTION ( 10 FDA reports)
RIB DEFORMITY ( 10 FDA reports)
SCINTILLATING SCOTOMA ( 10 FDA reports)
SEBORRHOEA ( 10 FDA reports)
SENSORIMOTOR DISORDER ( 10 FDA reports)
SEXUAL ABUSE ( 10 FDA reports)
SPINAL CORD INJURY CERVICAL ( 10 FDA reports)
STROKE IN EVOLUTION ( 10 FDA reports)
SUBDURAL HYGROMA ( 10 FDA reports)
SUPERINFECTION BACTERIAL ( 10 FDA reports)
SUTURE RUPTURE ( 10 FDA reports)
TEMPERATURE REGULATION DISORDER ( 10 FDA reports)
TESTICULAR DISORDER ( 10 FDA reports)
TESTIS CANCER ( 10 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO INCREASED ( 10 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 10 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 10 FDA reports)
TRIGONITIS ( 10 FDA reports)
ULTRASOUND ANTENATAL SCREEN ABNORMAL ( 10 FDA reports)
UNEMPLOYMENT ( 10 FDA reports)
URETERIC DILATATION ( 10 FDA reports)
URINARY TRACT OPERATION ( 10 FDA reports)
ABDOMINAL WALL INFECTION ( 10 FDA reports)
ACANTHOSIS NIGRICANS ( 10 FDA reports)
ACCELERATED IDIOVENTRICULAR RHYTHM ( 10 FDA reports)
ACID BASE BALANCE ABNORMAL ( 10 FDA reports)
ACUTE PHOSPHATE NEPHROPATHY ( 10 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 10 FDA reports)
ALLERGY TO ANIMAL ( 10 FDA reports)
AMYOTROPHY ( 10 FDA reports)
ANASTOMOTIC ULCER HAEMORRHAGE ( 10 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 10 FDA reports)
AORTIC EMBOLUS ( 10 FDA reports)
AORTIC RUPTURE ( 10 FDA reports)
ARTHRODESIS ( 10 FDA reports)
AUTOANTIBODY POSITIVE ( 10 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 10 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 10 FDA reports)
BASILAR ARTERY STENOSIS ( 10 FDA reports)
BASOPHIL COUNT DECREASED ( 10 FDA reports)
BASOPHIL COUNT INCREASED ( 10 FDA reports)
BILIARY CYST ( 10 FDA reports)
BIOPSY BLADDER ABNORMAL ( 10 FDA reports)
BIOPSY LYMPH GLAND ( 10 FDA reports)
BLADDER TAMPONADE ( 10 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 10 FDA reports)
BLOOD FOLATE DECREASED ( 10 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 10 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 10 FDA reports)
BLOOD SODIUM ABNORMAL ( 10 FDA reports)
BLOOD UREA ABNORMAL ( 10 FDA reports)
BLOOD URIC ACID DECREASED ( 10 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 10 FDA reports)
BREAST FIBROSIS ( 10 FDA reports)
BREAST HAEMORRHAGE ( 10 FDA reports)
BREAST OEDEMA ( 10 FDA reports)
BRONCHOSCOPY ABNORMAL ( 10 FDA reports)
BURSA DISORDER ( 10 FDA reports)
CANDIDA PNEUMONIA ( 10 FDA reports)
CARBOHYDRATE ANTIGEN 27.29 INCREASED ( 10 FDA reports)
CELL DEATH ( 10 FDA reports)
CELL MARKER INCREASED ( 10 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 10 FDA reports)
CHOLANGIOGRAM ( 10 FDA reports)
COAGULATION TIME SHORTENED ( 10 FDA reports)
COLON INJURY ( 10 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 10 FDA reports)
COMA HEPATIC ( 10 FDA reports)
CONGENITAL TRICUSPID VALVE ATRESIA ( 10 FDA reports)
CORNEAL SCAR ( 10 FDA reports)
CORYNEBACTERIUM INFECTION ( 10 FDA reports)
CYSTOSCOPY ( 10 FDA reports)
DANDRUFF ( 10 FDA reports)
DEREALISATION ( 10 FDA reports)
DIHYDROTESTOSTERONE DECREASED ( 10 FDA reports)
DISSEMINATED CYTOMEGALOVIRAL INFECTION ( 10 FDA reports)
DIVERTICULUM DUODENAL ( 10 FDA reports)
DRUG INTERACTION INHIBITION ( 10 FDA reports)
DRUG NAME CONFUSION ( 10 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 10 FDA reports)
EAR NEOPLASM ( 10 FDA reports)
EAR TUBE INSERTION ( 10 FDA reports)
ENDOCRINE DISORDER ( 10 FDA reports)
ENTEROCELE ( 10 FDA reports)
EOSINOPHILIC MYOCARDITIS ( 10 FDA reports)
EPHELIDES ( 10 FDA reports)
EXERCISE TEST ABNORMAL ( 10 FDA reports)
EYE INFECTION VIRAL ( 10 FDA reports)
FISTULA REPAIR ( 10 FDA reports)
GALLBLADDER OBSTRUCTION ( 10 FDA reports)
GASTRITIS HYPERTROPHIC ( 10 FDA reports)
GASTROOESOPHAGITIS ( 10 FDA reports)
GASTROSTOMY ( 10 FDA reports)
GENITAL PRURITUS FEMALE ( 10 FDA reports)
GLIOMA ( 10 FDA reports)
GOUTY TOPHUS ( 10 FDA reports)
HEART VALVE OPERATION ( 10 FDA reports)
HEAT ILLNESS ( 10 FDA reports)
HEMICEPHALALGIA ( 10 FDA reports)
HEREDITARY ANGIOEDEMA ( 10 FDA reports)
ABDOMINAL WALL HAEMORRHAGE ( 9 FDA reports)
ACANTHOLYSIS ( 9 FDA reports)
ACUTE STRESS DISORDER ( 9 FDA reports)
ADRENAL HAEMORRHAGE ( 9 FDA reports)
ADRENOMEGALY ( 9 FDA reports)
ALBUMIN GLOBULIN RATIO INCREASED ( 9 FDA reports)
ALLERGIC RESPIRATORY DISEASE ( 9 FDA reports)
ALLERGY TO CHEMICALS ( 9 FDA reports)
ANEURYSM REPAIR ( 9 FDA reports)
ANHIDROSIS ( 9 FDA reports)
ANION GAP ABNORMAL ( 9 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 9 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 9 FDA reports)
APPARENT LIFE THREATENING EVENT ( 9 FDA reports)
ARACHNOIDITIS ( 9 FDA reports)
ATYPICAL FEMUR FRACTURE ( 9 FDA reports)
BENIGN GASTROINTESTINAL NEOPLASM ( 9 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 9 FDA reports)
BEREAVEMENT REACTION ( 9 FDA reports)
BIOPSY LIP ( 9 FDA reports)
BIOPSY MUCOSA ABNORMAL ( 9 FDA reports)
BITE ( 9 FDA reports)
BLADDER HYPERTROPHY ( 9 FDA reports)
BLADDER PERFORATION ( 9 FDA reports)
BLINDNESS CORTICAL ( 9 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 9 FDA reports)
BLOOD LUTEINISING HORMONE DECREASED ( 9 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 9 FDA reports)
BONE CANCER METASTATIC ( 9 FDA reports)
BRAIN NATRIURETIC PEPTIDE ABNORMAL ( 9 FDA reports)
BREAST PROSTHESIS REMOVAL ( 9 FDA reports)
BRONCHIAL HYPERACTIVITY ( 9 FDA reports)
BRONCHOSTENOSIS ( 9 FDA reports)
BURNING MOUTH SYNDROME ( 9 FDA reports)
CALCULUS URETHRAL ( 9 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 9 FDA reports)
CARDIAC INFECTION ( 9 FDA reports)
CARDIAC PSEUDOANEURYSM ( 9 FDA reports)
CAROTIDYNIA ( 9 FDA reports)
CATARACT OPERATION COMPLICATION ( 9 FDA reports)
CATHETER SITE DISCHARGE ( 9 FDA reports)
CATHETER SITE SWELLING ( 9 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 9 FDA reports)
CERVICAL NEURITIS ( 9 FDA reports)
CERVIX DISORDER ( 9 FDA reports)
CHOROIDAL EFFUSION ( 9 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 9 FDA reports)
CLONIC CONVULSION ( 9 FDA reports)
CORNEAL EROSION ( 9 FDA reports)
COUNTERFEIT DRUG ADMINISTERED ( 9 FDA reports)
CYSTIC FIBROSIS PANCREATIC ( 9 FDA reports)
DARK CIRCLES UNDER EYES ( 9 FDA reports)
DAYDREAMING ( 9 FDA reports)
DENTAL CLEANING ( 9 FDA reports)
DENTAL NECROSIS ( 9 FDA reports)
DIABETIC HYPERGLYCAEMIC COMA ( 9 FDA reports)
DISBACTERIOSIS ( 9 FDA reports)
DOUBLE OUTLET RIGHT VENTRICLE ( 9 FDA reports)
DREAMY STATE ( 9 FDA reports)
DRUG CLEARANCE DECREASED ( 9 FDA reports)
DRUG EFFECT PROLONGED ( 9 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 9 FDA reports)
DYSENTERY ( 9 FDA reports)
DYSKINESIA OESOPHAGEAL ( 9 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 9 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 9 FDA reports)
ELECTROLYTE DEPLETION ( 9 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 9 FDA reports)
EOSINOPHILIC COLITIS ( 9 FDA reports)
EPIGLOTTIC OEDEMA ( 9 FDA reports)
EXAGGERATED STARTLE RESPONSE ( 9 FDA reports)
EXPOSURE DURING BREAST FEEDING ( 9 FDA reports)
EXPOSURE TO CHEMICAL POLLUTION ( 9 FDA reports)
EYELID MARGIN CRUSTING ( 9 FDA reports)
FACIAL NERVE DISORDER ( 9 FDA reports)
FACIAL SPASM ( 9 FDA reports)
FAILURE TO ANASTOMOSE ( 9 FDA reports)
FLUID IMBALANCE ( 9 FDA reports)
FLUID REPLACEMENT ( 9 FDA reports)
FOETAL DEATH ( 9 FDA reports)
GALLBLADDER CANCER ( 9 FDA reports)
GALLBLADDER OEDEMA ( 9 FDA reports)
GASTRIC ULCER HELICOBACTER ( 9 FDA reports)
GASTROENTERITIS HELICOBACTER ( 9 FDA reports)
GASTROENTERITIS NOROVIRUS ( 9 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 9 FDA reports)
GENITAL PAIN ( 9 FDA reports)
GIARDIASIS ( 9 FDA reports)
GILBERT'S SYNDROME ( 9 FDA reports)
GINGIVAL BLISTER ( 9 FDA reports)
GRUNTING ( 9 FDA reports)
HAEMORRHAGE CORONARY ARTERY ( 9 FDA reports)
HETEROPHORIA ( 9 FDA reports)
HYPERVISCOSITY SYNDROME ( 9 FDA reports)
HYPOCHOLESTEROLAEMIA ( 9 FDA reports)
HYPOPYON ( 9 FDA reports)
IDIOPATHIC URTICARIA ( 9 FDA reports)
ILEOSTOMY ( 9 FDA reports)
IMMUNOGLOBULINS INCREASED ( 9 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 9 FDA reports)
VAGINAL BURNING SENSATION ( 9 FDA reports)
VENTRICULAR SEPTAL DEFECT REPAIR ( 9 FDA reports)
WEST NILE VIRAL INFECTION ( 9 FDA reports)
WISDOM TEETH REMOVAL ( 9 FDA reports)
WRIST SURGERY ( 9 FDA reports)
INFUSION SITE PRURITUS ( 9 FDA reports)
INJECTION SITE SCAB ( 9 FDA reports)
INTERCOSTAL NEURALGIA ( 9 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 9 FDA reports)
INTESTINAL HAEMATOMA ( 9 FDA reports)
IRON BINDING CAPACITY TOTAL INCREASED ( 9 FDA reports)
JOINT SURGERY ( 9 FDA reports)
LATEX ALLERGY ( 9 FDA reports)
LENTICULAR OPACITIES ( 9 FDA reports)
LIP NEOPLASM BENIGN ( 9 FDA reports)
LIPOATROPHY ( 9 FDA reports)
LOW BIRTH WEIGHT BABY ( 9 FDA reports)
LYMPHATIC DISORDER ( 9 FDA reports)
MACULAR ISCHAEMIA ( 9 FDA reports)
MALABSORPTION FROM INJECTION SITE ( 9 FDA reports)
MALIGNANT FIBROUS HISTIOCYTOMA ( 9 FDA reports)
MALIGNANT URINARY TRACT NEOPLASM ( 9 FDA reports)
MEAN PLATELET VOLUME INCREASED ( 9 FDA reports)
MEASLES ( 9 FDA reports)
MENINGIOMA BENIGN ( 9 FDA reports)
MENINGISM ( 9 FDA reports)
MENINGOENCEPHALITIS BACTERIAL ( 9 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 9 FDA reports)
METASTASES TO REPRODUCTIVE ORGAN ( 9 FDA reports)
METASTATIC CARCINOID TUMOUR ( 9 FDA reports)
MODIFIED RADICAL MASTECTOMY ( 9 FDA reports)
MUSCLE ENZYME INCREASED ( 9 FDA reports)
MUSCLE MASS ( 9 FDA reports)
MYASTHENIC SYNDROME ( 9 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 9 FDA reports)
MYOCARDIAL CALCIFICATION ( 9 FDA reports)
NUCHAL RIGIDITY ( 9 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 9 FDA reports)
OESOPHAGEAL FOOD IMPACTION ( 9 FDA reports)
ORCHIDECTOMY ( 9 FDA reports)
ORGASM ABNORMAL ( 9 FDA reports)
OVARIAN ATROPHY ( 9 FDA reports)
OVARIAN CANCER METASTATIC ( 9 FDA reports)
PANCREAS TRANSPLANT REJECTION ( 9 FDA reports)
PANCREATIC DUCT DILATATION ( 9 FDA reports)
PAPILLARY THYROID CANCER ( 9 FDA reports)
PARVOVIRUS B19 SEROLOGY POSITIVE ( 9 FDA reports)
PERIORBITAL CELLULITIS ( 9 FDA reports)
PERIPHERAL NERVE LESION ( 9 FDA reports)
PERTUSSIS ( 9 FDA reports)
PHANTOM PAIN ( 9 FDA reports)
PNEUMONIA NECROTISING ( 9 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 9 FDA reports)
POLYMYALGIA ( 9 FDA reports)
POST PROCEDURAL DISCOMFORT ( 9 FDA reports)
POST-TRAUMATIC AMNESTIC DISORDER ( 9 FDA reports)
POSTOPERATIVE THROMBOSIS ( 9 FDA reports)
PRESSURE OF SPEECH ( 9 FDA reports)
PROCALCITONIN INCREASED ( 9 FDA reports)
PROSTATIC ADENOMA ( 9 FDA reports)
PROSTATIC PAIN ( 9 FDA reports)
PROTEIN TOTAL ABNORMAL ( 9 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 9 FDA reports)
PYODERMA ( 9 FDA reports)
RECTAL FISTULA REPAIR ( 9 FDA reports)
RECTOCELE REPAIR ( 9 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 9 FDA reports)
REFLEXES ABNORMAL ( 9 FDA reports)
RENAL AND PANCREAS TRANSPLANT REJECTION ( 9 FDA reports)
RENAL ARTERY STENT PLACEMENT ( 9 FDA reports)
RESPIRATORY MUSCLE WEAKNESS ( 9 FDA reports)
RETROPERITONEAL NEOPLASM ( 9 FDA reports)
SCAN ABDOMEN ABNORMAL ( 9 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 9 FDA reports)
SEXUALLY TRANSMITTED DISEASE ( 9 FDA reports)
SKIN INFLAMMATION ( 9 FDA reports)
SKIN ULCER HAEMORRHAGE ( 9 FDA reports)
SKULL MALFORMATION ( 9 FDA reports)
SMALL INTESTINAL RESECTION ( 9 FDA reports)
SPIDER NAEVUS ( 9 FDA reports)
SPONDYLITIC MYELOPATHY ( 9 FDA reports)
SUBACUTE ENDOCARDITIS ( 9 FDA reports)
TALIPES ( 9 FDA reports)
TESTICULAR MASS ( 9 FDA reports)
THROMBOLYSIS ( 9 FDA reports)
THYROID PAIN ( 9 FDA reports)
TOXOPLASMOSIS ( 9 FDA reports)
TROPONIN ( 9 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 9 FDA reports)
URETHRAL FISTULA ( 9 FDA reports)
IMPLANT SITE HAEMATOMA ( 8 FDA reports)
INCISION SITE OEDEMA ( 8 FDA reports)
INDIFFERENCE ( 8 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 8 FDA reports)
INFUSION SITE HAEMATOMA ( 8 FDA reports)
INSULIN-LIKE GROWTH FACTOR INCREASED ( 8 FDA reports)
INTERVENTRICULAR SEPTUM RUPTURE ( 8 FDA reports)
INTESTINAL OPERATION ( 8 FDA reports)
INTRAOCULAR PRESSURE DECREASED ( 8 FDA reports)
INTUSSUSCEPTION ( 8 FDA reports)
IODINE ALLERGY ( 8 FDA reports)
IRIS HYPERPIGMENTATION ( 8 FDA reports)
JOINT DESTRUCTION ( 8 FDA reports)
JOINT PROSTHESIS USER ( 8 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 8 FDA reports)
LABELLED DRUG-FOOD INTERACTION MEDICATION ERROR ( 8 FDA reports)
LACTESCENT SERUM ( 8 FDA reports)
LAPAROTOMY ( 8 FDA reports)
LARYNGEAL DISORDER ( 8 FDA reports)
LIPOMA EXCISION ( 8 FDA reports)
MALFORMATION VENOUS ( 8 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 8 FDA reports)
MAMMARY DUCT ECTASIA ( 8 FDA reports)
MANDIBULECTOMY ( 8 FDA reports)
MASTOCYTOSIS ( 8 FDA reports)
MESOTHELIOMA MALIGNANT ( 8 FDA reports)
METASTASES TO BONE MARROW ( 8 FDA reports)
MICROTIA ( 8 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 8 FDA reports)
MITOCHONDRIAL CYTOPATHY ( 8 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 8 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 8 FDA reports)
MYELOID MATURATION ARREST ( 8 FDA reports)
NASAL INFLAMMATION ( 8 FDA reports)
NASAL SEPTUM PERFORATION ( 8 FDA reports)
NECROTISING OESOPHAGITIS ( 8 FDA reports)
NEONATAL ASPIRATION ( 8 FDA reports)
NEPHRITIC SYNDROME ( 8 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 8 FDA reports)
NERVE BLOCK ( 8 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 8 FDA reports)
NODULAR REGENERATIVE HYPERPLASIA ( 8 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE I ( 8 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ( 8 FDA reports)
OESOPHAGEAL IRRITATION ( 8 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 8 FDA reports)
OPTIC DISC DISORDER ( 8 FDA reports)
OPTIC NERVE SHEATH HAEMORRHAGE ( 8 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 8 FDA reports)
OSTEOMYELITIS BACTERIAL ( 8 FDA reports)
OVARIAN ENLARGEMENT ( 8 FDA reports)
OVARIAN HAEMORRHAGE ( 8 FDA reports)
OVERGROWTH BACTERIAL ( 8 FDA reports)
PANCREAS INFECTION ( 8 FDA reports)
PANCREAS LIPOMATOSIS ( 8 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 8 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 8 FDA reports)
PERICARDIAL DRAINAGE ( 8 FDA reports)
PERITONEAL CARCINOMA ( 8 FDA reports)
PERITONEAL CLOUDY EFFLUENT ( 8 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 8 FDA reports)
PHARYNGEAL ABSCESS ( 8 FDA reports)
PHLEBOSCLEROSIS ( 8 FDA reports)
PLATYBASIA ( 8 FDA reports)
PLEOCYTOSIS ( 8 FDA reports)
PLEURAL DECORTICATION ( 8 FDA reports)
PNEUMATOSIS ( 8 FDA reports)
PNEUMOMEDIASTINUM ( 8 FDA reports)
PNEUMONITIS CHEMICAL ( 8 FDA reports)
PORPHYRIA NON-ACUTE ( 8 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 8 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 8 FDA reports)
PROCTOCOLITIS ( 8 FDA reports)
PSEUDOENDOPHTHALMITIS ( 8 FDA reports)
PSEUDOLYMPHOMA ( 8 FDA reports)
PSEUDOPHAKIA ( 8 FDA reports)
REACTION TO AZO-DYES ( 8 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 8 FDA reports)
RED BLOOD CELLS URINE ( 8 FDA reports)
REFRACTION DISORDER ( 8 FDA reports)
REHABILITATION THERAPY ( 8 FDA reports)
RESPIRATORY DEPTH DECREASED ( 8 FDA reports)
RETINAL VASCULITIS ( 8 FDA reports)
RETINOBLASTOMA ( 8 FDA reports)
RETINOGRAM ABNORMAL ( 8 FDA reports)
ROULEAUX FORMATION ( 8 FDA reports)
SALPINGITIS ( 8 FDA reports)
SCLERAL DISCOLOURATION ( 8 FDA reports)
SCROTAL DISORDER ( 8 FDA reports)
SECONDARY HYPERTENSION ( 8 FDA reports)
SERONEGATIVE ARTHRITIS ( 8 FDA reports)
SERRATIA BACTERAEMIA ( 8 FDA reports)
SERRATIA SEPSIS ( 8 FDA reports)
SICKLE CELL ANAEMIA ( 8 FDA reports)
SKIN BLEEDING ( 8 FDA reports)
SKULL X-RAY ABNORMAL ( 8 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 8 FDA reports)
SOMATIC DELUSION ( 8 FDA reports)
SPLENIC ARTERY ANEURYSM ( 8 FDA reports)
SPLINTER ( 8 FDA reports)
SPLINTER HAEMORRHAGES ( 8 FDA reports)
STATUS ASTHMATICUS ( 8 FDA reports)
STENOTROPHOMONAS INFECTION ( 8 FDA reports)
STRESS AT WORK ( 8 FDA reports)
TENDINOUS CONTRACTURE ( 8 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 8 FDA reports)
THOUGHT BLOCKING ( 8 FDA reports)
THROMBIN TIME PROLONGED ( 8 FDA reports)
THYROXINE INCREASED ( 8 FDA reports)
TONGUE BLACK HAIRY ( 8 FDA reports)
TONGUE EXFOLIATION ( 8 FDA reports)
TONGUE GEOGRAPHIC ( 8 FDA reports)
TRACHEITIS ( 8 FDA reports)
TRANSFERRIN SATURATION INCREASED ( 8 FDA reports)
TRI-IODOTHYRONINE FREE INCREASED ( 8 FDA reports)
URETHRAL MEATUS STENOSIS ( 8 FDA reports)
URETHRAL POLYP ( 8 FDA reports)
ABDOMINAL CAVITY DRAINAGE ( 8 FDA reports)
ABDOMINAL REBOUND TENDERNESS ( 8 FDA reports)
ACARODERMATITIS ( 8 FDA reports)
ACHLORHYDRIA ( 8 FDA reports)
ACQUIRED HAEMOPHILIA ( 8 FDA reports)
ACQUIRED PORPHYRIA ( 8 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 8 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 8 FDA reports)
ADRENAL CYST ( 8 FDA reports)
ANAL ABSCESS ( 8 FDA reports)
ANAL CANDIDIASIS ( 8 FDA reports)
ANAL STENOSIS ( 8 FDA reports)
ANAPHYLACTOID SHOCK ( 8 FDA reports)
ANTISOCIAL BEHAVIOUR ( 8 FDA reports)
ANTITHROMBIN III DECREASED ( 8 FDA reports)
AORTITIS ( 8 FDA reports)
APLASIA ( 8 FDA reports)
APPLICATION SITE SWELLING ( 8 FDA reports)
ARTERIOGRAM CAROTID ABNORMAL ( 8 FDA reports)
ASPIRATION BRONCHIAL ( 8 FDA reports)
AURICULAR PERICHONDRITIS ( 8 FDA reports)
AUTOMATIC BLADDER ( 8 FDA reports)
AXONAL NEUROPATHY ( 8 FDA reports)
BACILLUS INFECTION ( 8 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 8 FDA reports)
BASAL GANGLION DEGENERATION ( 8 FDA reports)
BASE EXCESS DECREASED ( 8 FDA reports)
BASE EXCESS INCREASED ( 8 FDA reports)
BENIGN VASCULAR NEOPLASM ( 8 FDA reports)
BETA GLOBULIN INCREASED ( 8 FDA reports)
BIOPSY THYMUS GLAND ABNORMAL ( 8 FDA reports)
BLADDER NECK OPERATION ( 8 FDA reports)
BLISTER INFECTED ( 8 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 8 FDA reports)
BLOOD CREATININE ( 8 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE DECREASED ( 8 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 8 FDA reports)
BLOOD PARATHYROID HORMONE ABNORMAL ( 8 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 8 FDA reports)
BLOOD PRESSURE SYSTOLIC ABNORMAL ( 8 FDA reports)
BODY FAT DISORDER ( 8 FDA reports)
BODY TINEA ( 8 FDA reports)
BOTULISM ( 8 FDA reports)
BREAST DISORDER FEMALE ( 8 FDA reports)
BRONCHIAL FISTULA ( 8 FDA reports)
BRUGADA SYNDROME ( 8 FDA reports)
CARBON MONOXIDE POISONING ( 8 FDA reports)
CARDIOMYOPATHY ALCOHOLIC ( 8 FDA reports)
CAROTID ARTERY BYPASS ( 8 FDA reports)
CAROTID ARTERY INSUFFICIENCY ( 8 FDA reports)
CATHETER SITE ERYTHEMA ( 8 FDA reports)
CATHETER SITE PAIN ( 8 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 8 FDA reports)
CEREBROVASCULAR STENOSIS ( 8 FDA reports)
CERVICAL CYST ( 8 FDA reports)
CHOLANGITIS CHRONIC ( 8 FDA reports)
CHOLELITHIASIS OBSTRUCTIVE ( 8 FDA reports)
CHOREOATHETOSIS ( 8 FDA reports)
COELIAC ARTERY STENOSIS ( 8 FDA reports)
COLON CANCER STAGE II ( 8 FDA reports)
COLORECTAL CANCER METASTATIC ( 8 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 8 FDA reports)
CONGENITAL GASTRIC ANOMALY ( 8 FDA reports)
CONGENITAL TERATOMA ( 8 FDA reports)
CONTRAST MEDIA ALLERGY ( 8 FDA reports)
CRANIAL NERVE PARALYSIS ( 8 FDA reports)
CULTURE ( 8 FDA reports)
CUTANEOUS SARCOIDOSIS ( 8 FDA reports)
CYSTITIS GLANDULARIS ( 8 FDA reports)
CYSTOPEXY ( 8 FDA reports)
CYTOKINE RELEASE SYNDROME ( 8 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 8 FDA reports)
DELUSIONAL PERCEPTION ( 8 FDA reports)
DENTOFACIAL ANOMALY ( 8 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 8 FDA reports)
DIURETIC THERAPY ( 8 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 8 FDA reports)
DUODENAL FISTULA ( 8 FDA reports)
DYSMORPHISM ( 8 FDA reports)
ECLAMPSIA ( 8 FDA reports)
ECTROPION ( 8 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 8 FDA reports)
ENCEPHALITIS POST MEASLES ( 8 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 8 FDA reports)
EPIDERMOLYSIS ( 8 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 8 FDA reports)
EUTHYROID SICK SYNDROME ( 8 FDA reports)
EXERCISE LACK OF ( 8 FDA reports)
EXPLORATIVE LAPAROTOMY ( 8 FDA reports)
EXTERNAL EAR DISORDER ( 8 FDA reports)
EXTUBATION ( 8 FDA reports)
EYE ALLERGY ( 8 FDA reports)
EYE PROSTHESIS INSERTION ( 8 FDA reports)
FACE LIFT ( 8 FDA reports)
FACTOR VIII DEFICIENCY ( 8 FDA reports)
FEMORAL BRUIT ( 8 FDA reports)
FIBROUS DYSPLASIA OF BONE ( 8 FDA reports)
FIXED ERUPTION ( 8 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 8 FDA reports)
FRACTURE MALUNION ( 8 FDA reports)
FUNGAL SEPSIS ( 8 FDA reports)
GASTRECTOMY ( 8 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 8 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 8 FDA reports)
GASTROINTESTINAL TELANGIECTASIA ( 8 FDA reports)
GINGIVAL GRAFT ( 8 FDA reports)
HAEMORRHAGIC ASCITES ( 8 FDA reports)
HALLUCINATION, OLFACTORY ( 8 FDA reports)
HEPATIC HAEMATOMA ( 8 FDA reports)
HEPATIC HAEMORRHAGE ( 8 FDA reports)
HEPATIC ISCHAEMIA ( 8 FDA reports)
HEPATIC SIDEROSIS ( 8 FDA reports)
HEPATOBILIARY DISEASE ( 8 FDA reports)
HERPES ZOSTER DISSEMINATED ( 8 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 8 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 8 FDA reports)
HOFFMANN'S SIGN ( 8 FDA reports)
HYPERADRENALISM ( 8 FDA reports)
HYPERGLOBULINAEMIA ( 8 FDA reports)
HYPERPROLACTINAEMIA ( 8 FDA reports)
HYPOGONADISM MALE ( 8 FDA reports)
HYPOLIPIDAEMIA ( 8 FDA reports)
VAGINAL EROSION ( 8 FDA reports)
VAGINAL PROLAPSE ( 8 FDA reports)
VAGINAL ULCERATION ( 8 FDA reports)
VASCULAR ACCESS COMPLICATION ( 8 FDA reports)
VASCULAR BYPASS DYSFUNCTION ( 8 FDA reports)
VASCULAR PSEUDOANEURYSM RUPTURED ( 8 FDA reports)
VENTRICULAR INTERNAL DIAMETER ABNORMAL ( 8 FDA reports)
VERBAL ABUSE ( 8 FDA reports)
VIRAL CARDIOMYOPATHY ( 8 FDA reports)
VIRAL RASH ( 8 FDA reports)
VITAMIN K DEFICIENCY ( 8 FDA reports)
VULVAL ULCERATION ( 8 FDA reports)
VULVITIS ( 8 FDA reports)
VULVOVAGINAL ERYTHEMA ( 8 FDA reports)
VULVOVAGINITIS ( 8 FDA reports)
X-RAY LIMB ABNORMAL ( 8 FDA reports)
URINE OSMOLARITY INCREASED ( 7 FDA reports)
URINE SODIUM DECREASED ( 7 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 7 FDA reports)
UTERINE CYST ( 7 FDA reports)
UVULITIS ( 7 FDA reports)
VAGINAL CANDIDIASIS ( 7 FDA reports)
VAGINAL LESION ( 7 FDA reports)
VAGINAL ODOUR ( 7 FDA reports)
VAGINAL PAIN ( 7 FDA reports)
VASCULAR RESISTANCE SYSTEMIC DECREASED ( 7 FDA reports)
VASCULAR RESISTANCE SYSTEMIC INCREASED ( 7 FDA reports)
VASCULAR SHUNT ( 7 FDA reports)
VENA CAVA FILTER INSERTION ( 7 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 7 FDA reports)
VIRAL DIARRHOEA ( 7 FDA reports)
VITAMIN D INCREASED ( 7 FDA reports)
VITREOUS DISORDER ( 7 FDA reports)
VOMITING IN PREGNANCY ( 7 FDA reports)
WEIGHT ABNORMAL ( 7 FDA reports)
WRIST DEFORMITY ( 7 FDA reports)
IMPLANT SITE INFECTION ( 7 FDA reports)
IMPLANT SITE REACTION ( 7 FDA reports)
IMPRISONMENT ( 7 FDA reports)
INCISIONAL HERNIA REPAIR ( 7 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 7 FDA reports)
INCORRECT PRODUCT STORAGE ( 7 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 7 FDA reports)
INFERTILITY ( 7 FDA reports)
INFUSION SITE WARMTH ( 7 FDA reports)
INJECTION SITE DISCHARGE ( 7 FDA reports)
INTERTRIGO ( 7 FDA reports)
INTESTINAL ADENOCARCINOMA ( 7 FDA reports)
INTESTINAL DIAPHRAGM DISEASE ( 7 FDA reports)
INTESTINAL FISTULA ( 7 FDA reports)
INTRACRANIAL HYPOTENSION ( 7 FDA reports)
ISCHAEMIC NEPHROPATHY ( 7 FDA reports)
ITCHING SCAR ( 7 FDA reports)
JEALOUS DELUSION ( 7 FDA reports)
JOB DISSATISFACTION ( 7 FDA reports)
JOINT ABSCESS ( 7 FDA reports)
JOINT INJECTION ( 7 FDA reports)
KETOSIS ( 7 FDA reports)
LABIA ENLARGED ( 7 FDA reports)
LEIOMYOSARCOMA METASTATIC ( 7 FDA reports)
LEUKOERYTHROBLASTIC ANAEMIA ( 7 FDA reports)
LIPASE DECREASED ( 7 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 7 FDA reports)
LOCKED-IN SYNDROME ( 7 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 7 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE III ( 7 FDA reports)
LYMPH NODE CALCIFICATION ( 7 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 7 FDA reports)
LYMPHOMATOID PAPULOSIS ( 7 FDA reports)
MENTAL RETARDATION ( 7 FDA reports)
METABOLIC FUNCTION TEST ABNORMAL ( 7 FDA reports)
METASTASES TO LARGE INTESTINE ( 7 FDA reports)
METASTATIC BRONCHIAL CARCINOMA ( 7 FDA reports)
MITRAL VALVE ATRESIA ( 7 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 7 FDA reports)
MYOFASCIAL SPASM ( 7 FDA reports)
MYOGLOBINAEMIA ( 7 FDA reports)
NAIL AVULSION ( 7 FDA reports)
NAIL BED TENDERNESS ( 7 FDA reports)
NASAL OPERATION ( 7 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 7 FDA reports)
OBESITY SURGERY ( 7 FDA reports)
OESOPHAGEAL ACHALASIA ( 7 FDA reports)
ORAL HAIRY LEUKOPLAKIA ( 7 FDA reports)
OSCILLOPSIA ( 7 FDA reports)
OSTEOPETROSIS ( 7 FDA reports)
OSTEOTOMY ( 7 FDA reports)
OTITIS EXTERNA FUNGAL ( 7 FDA reports)
OTOTOXICITY ( 7 FDA reports)
OVARIAN NEOPLASM ( 7 FDA reports)
OVERLAP SYNDROME ( 7 FDA reports)
PALPABLE PURPURA ( 7 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 7 FDA reports)
PANOPHTHALMITIS ( 7 FDA reports)
PAROTID ABSCESS ( 7 FDA reports)
PARVOVIRUS INFECTION ( 7 FDA reports)
PENILE ULCERATION ( 7 FDA reports)
PEPTOSTREPTOCOCCUS INFECTION ( 7 FDA reports)
PERCUSSION TEST ABNORMAL ( 7 FDA reports)
PERFORATED DUODENAL ULCER REPAIR ( 7 FDA reports)
PERICARDIAL FIBROSIS ( 7 FDA reports)
PERIPHERAL ARTERY ANGIOPLASTY ( 7 FDA reports)
PERIPHERAL BLOOD STEM CELL APHERESIS ( 7 FDA reports)
PERIPHERAL NERVE DECOMPRESSION ( 7 FDA reports)
PERITONEAL INFECTION ( 7 FDA reports)
PEYRONIE'S DISEASE ( 7 FDA reports)
PH BODY FLUID ABNORMAL ( 7 FDA reports)
PLASMA PROTEIN METABOLISM DISORDER ( 7 FDA reports)
PLEURAL NEOPLASM ( 7 FDA reports)
PNEUMATOSIS CYSTOIDES INTESTINALIS ( 7 FDA reports)
PNEUMONIA ESCHERICHIA ( 7 FDA reports)
PNEUMONIA HERPES VIRAL ( 7 FDA reports)
PORIOMANIA ( 7 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 7 FDA reports)
POST PROCEDURAL CELLULITIS ( 7 FDA reports)
POST PROCEDURAL DRAINAGE ( 7 FDA reports)
POST-TRAUMATIC HEADACHE ( 7 FDA reports)
PRECANCEROUS SKIN LESION ( 7 FDA reports)
PREGNANCY TEST POSITIVE ( 7 FDA reports)
PRESBYACUSIS ( 7 FDA reports)
PROCEDURAL DIZZINESS ( 7 FDA reports)
PROLONGED EXPIRATION ( 7 FDA reports)
PROSTATIC SPECIFIC ANTIGEN DECREASED ( 7 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 7 FDA reports)
PSYCHOTIC DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 7 FDA reports)
PULMONARY ARTERIAL PRESSURE ABNORMAL ( 7 FDA reports)
PULMONARY ARTERIAL PRESSURE DECREASED ( 7 FDA reports)
PUNCTATE KERATITIS ( 7 FDA reports)
PUNCTURE SITE REACTION ( 7 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 7 FDA reports)
REGRESSIVE BEHAVIOUR ( 7 FDA reports)
RENIN INCREASED ( 7 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS TEST POSITIVE ( 7 FDA reports)
RETICULOCYTOPENIA ( 7 FDA reports)
RETINAL INFARCTION ( 7 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 7 FDA reports)
SCROTAL PAIN ( 7 FDA reports)
SINOBRONCHITIS ( 7 FDA reports)
SINUS CANCER METASTATIC ( 7 FDA reports)
SKIN DESQUAMATION ( 7 FDA reports)
SKIN MACERATION ( 7 FDA reports)
SKIN TOXICITY ( 7 FDA reports)
SMALL INTESTINE GANGRENE ( 7 FDA reports)
SOMOGYI PHENOMENON ( 7 FDA reports)
SPECIFIC GRAVITY URINE INCREASED ( 7 FDA reports)
SPERMATOCELE ( 7 FDA reports)
SPINAL CORPECTOMY ( 7 FDA reports)
SPINAL PAIN ( 7 FDA reports)
STEREOTYPY ( 7 FDA reports)
SUBDIAPHRAGMATIC ABSCESS ( 7 FDA reports)
SUSPICIOUSNESS ( 7 FDA reports)
SWEAT GLAND TUMOUR ( 7 FDA reports)
TAKAYASU'S ARTERITIS ( 7 FDA reports)
TENDON CALCIFICATION ( 7 FDA reports)
THYMUS DISORDER ( 7 FDA reports)
THYROID CANCER METASTATIC ( 7 FDA reports)
THYROIDITIS SUBACUTE ( 7 FDA reports)
TINEA VERSICOLOUR ( 7 FDA reports)
TOE OPERATION ( 7 FDA reports)
TRACHEAL STENOSIS ( 7 FDA reports)
TRICHOMONIASIS ( 7 FDA reports)
TRYPTASE INCREASED ( 7 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 7 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 7 FDA reports)
ULTRASOUND BREAST ABNORMAL ( 7 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 7 FDA reports)
UNINTENDED PREGNANCY ( 7 FDA reports)
URETHRAL STRICTURE ( 7 FDA reports)
5Q MINUS SYNDROME ( 7 FDA reports)
ABDOMINAL HERNIA REPAIR ( 7 FDA reports)
ACQUIRED CLAW TOE ( 7 FDA reports)
ACUTE DISSEMINATED ENCEPHALOMYELITIS ( 7 FDA reports)
AGE INDETERMINATE MYOCARDIAL INFARCTION ( 7 FDA reports)
AIR EMBOLISM ( 7 FDA reports)
ALCOHOLIC PANCREATITIS ( 7 FDA reports)
ALPHA 2 GLOBULIN INCREASED ( 7 FDA reports)
AMNESTIC DISORDER ( 7 FDA reports)
ANAEMIA MEGALOBLASTIC ( 7 FDA reports)
ANAL DISCOMFORT ( 7 FDA reports)
ANASTOMOTIC COMPLICATION ( 7 FDA reports)
ANTIBODY TEST ABNORMAL ( 7 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 7 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES ( 7 FDA reports)
APPLICATION SITE BLEEDING ( 7 FDA reports)
APPLICATION SITE SCAR ( 7 FDA reports)
ASPIRATION BIOPSY ( 7 FDA reports)
ASTROCYTOMA ( 7 FDA reports)
ATHERECTOMY ( 7 FDA reports)
AVULSION FRACTURE ( 7 FDA reports)
BACTERIAL PYELONEPHRITIS ( 7 FDA reports)
BASE EXCESS NEGATIVE ( 7 FDA reports)
BASILAR ARTERY OCCLUSION ( 7 FDA reports)
BENCE JONES PROTEINURIA ( 7 FDA reports)
BENIGN SALIVARY GLAND NEOPLASM ( 7 FDA reports)
BILIARY POLYP ( 7 FDA reports)
BILIARY TRACT INFECTION ( 7 FDA reports)
BLADDER DISTENSION ( 7 FDA reports)
BLOOD CREATINE ABNORMAL ( 7 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ( 7 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ABNORMAL ( 7 FDA reports)
BLOODY PERITONEAL EFFLUENT ( 7 FDA reports)
BONE INFARCTION ( 7 FDA reports)
BREATH HOLDING ( 7 FDA reports)
BRONCHOSPASM PARADOXICAL ( 7 FDA reports)
CAMPYLOBACTER INFECTION ( 7 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 7 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 7 FDA reports)
CARNITINE DECREASED ( 7 FDA reports)
CAROTID SINUS SYNDROME ( 7 FDA reports)
CHALAZION ( 7 FDA reports)
CHOLELITHOTOMY ( 7 FDA reports)
CHRONIC GASTROINTESTINAL BLEEDING ( 7 FDA reports)
CLEFT LIP ( 7 FDA reports)
COAGULATION FACTOR DEFICIENCY ( 7 FDA reports)
COAGULATION FACTOR VIII LEVEL DECREASED ( 7 FDA reports)
COLLAGEN-VASCULAR DISEASE ( 7 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 7 FDA reports)
COMPULSIONS ( 7 FDA reports)
CONFABULATION ( 7 FDA reports)
CONGENITAL AORTIC ATRESIA ( 7 FDA reports)
CONGENITAL ARTERIAL MALFORMATION ( 7 FDA reports)
CONJUNCTIVAL DISORDER ( 7 FDA reports)
CONJUNCTIVAL PALLOR ( 7 FDA reports)
CORNEAL REFLEX DECREASED ( 7 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 7 FDA reports)
CRYSTAL ARTHROPATHY ( 7 FDA reports)
CSF WHITE BLOOD CELL COUNT POSITIVE ( 7 FDA reports)
CYSTITIS RADIATION ( 7 FDA reports)
DEPENDENCE ON RESPIRATOR ( 7 FDA reports)
DEPRESSION POSTOPERATIVE ( 7 FDA reports)
DERMATOSIS ( 7 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 7 FDA reports)
DIABETIC GASTROPATHY ( 7 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 7 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 7 FDA reports)
DRUG SCREEN NEGATIVE ( 7 FDA reports)
DUODENAL NEOPLASM ( 7 FDA reports)
DUPUYTREN'S CONTRACTURE OPERATION ( 7 FDA reports)
DYSCHEZIA ( 7 FDA reports)
ECTOPIC PREGNANCY ( 7 FDA reports)
EJECTION FRACTION ( 7 FDA reports)
ENAMEL ANOMALY ( 7 FDA reports)
ENDOMETRIAL CANCER STAGE I ( 7 FDA reports)
ENDOSCOPY ABNORMAL ( 7 FDA reports)
ENTEROBACTER BACTERAEMIA ( 7 FDA reports)
ETHMOID SINUS SURGERY ( 7 FDA reports)
EXCITABILITY ( 7 FDA reports)
EXTRAMEDULLARY HAEMOPOIESIS ( 7 FDA reports)
EYE BURNS ( 7 FDA reports)
EYE OPERATION COMPLICATION ( 7 FDA reports)
EYELID BLEEDING ( 7 FDA reports)
EYELID CYST ( 7 FDA reports)
EYELID EXFOLIATION ( 7 FDA reports)
FACTITIOUS DISORDER ( 7 FDA reports)
FANCONI SYNDROME ACQUIRED ( 7 FDA reports)
FASCIOTOMY ( 7 FDA reports)
FEEDING DISORDER NEONATAL ( 7 FDA reports)
FOETAL HEART RATE ABNORMAL ( 7 FDA reports)
GAIT SPASTIC ( 7 FDA reports)
GASTRIC MUCOSA ERYTHEMA ( 7 FDA reports)
GASTRIC OUTLET OBSTRUCTION ( 7 FDA reports)
GASTROENTERITIS BACTERIAL ( 7 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 7 FDA reports)
GASTROINTESTINAL ANASTOMOTIC LEAK ( 7 FDA reports)
GENITAL CANDIDIASIS ( 7 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 7 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 7 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 7 FDA reports)
GRANULOCYTES MATURATION ARREST ( 7 FDA reports)
GROIN INFECTION ( 7 FDA reports)
HAEMORRHAGIC EROSIVE GASTRITIS ( 7 FDA reports)
HEPATIC NEOPLASM MALIGNANT RECURRENT ( 7 FDA reports)
HIP SWELLING ( 7 FDA reports)
HYDROCHOLECYSTIS ( 7 FDA reports)
HYPERALDOSTERONISM ( 7 FDA reports)
HYPERCREATININAEMIA ( 7 FDA reports)
HYPERPARATHYROIDISM TERTIARY ( 7 FDA reports)
HYPERTHERMIA MALIGNANT ( 7 FDA reports)
HYPOAESTHESIA EYE ( 7 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 7 FDA reports)
HYPOMENORRHOEA ( 7 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 7 FDA reports)
HYPOTONIC URINARY BLADDER ( 7 FDA reports)
IGA NEPHROPATHY ( 7 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 6 FDA reports)
ABNORMAL CHEST SOUND ( 6 FDA reports)
ABNORMAL WEIGHT GAIN ( 6 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 6 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 6 FDA reports)
ADHESIOLYSIS ( 6 FDA reports)
AGITATION POSTOPERATIVE ( 6 FDA reports)
AGONAL RHYTHM ( 6 FDA reports)
AGRAPHIA ( 6 FDA reports)
AIRWAY COMPLICATION OF ANAESTHESIA ( 6 FDA reports)
ALBUMIN URINE ( 6 FDA reports)
ALLERGY TO METALS ( 6 FDA reports)
ALOPECIA AREATA ( 6 FDA reports)
ANASTOMOTIC FISTULA ( 6 FDA reports)
ANGIOSARCOMA ( 6 FDA reports)
ANIMAL SCRATCH ( 6 FDA reports)
ANTI-NEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE VASCULITIS ( 6 FDA reports)
ANTIBIOTIC PROPHYLAXIS ( 6 FDA reports)
ANTICHOLINERGIC SYNDROME ( 6 FDA reports)
ANTICONVULSANT DRUG LEVEL ABNORMAL ( 6 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 6 FDA reports)
ANTINUCLEAR ANTIBODY ( 6 FDA reports)
APPLICATION SITE BURNING ( 6 FDA reports)
APPLICATION SITE DESQUAMATION ( 6 FDA reports)
APPLICATION SITE INFECTION ( 6 FDA reports)
APPLICATION SITE PUSTULES ( 6 FDA reports)
APPLICATION SITE WARMTH ( 6 FDA reports)
ARCUS LIPOIDES ( 6 FDA reports)
ARTERIAL CATHETERISATION ( 6 FDA reports)
ARTERIOVENOUS FISTULA ANEURYSM ( 6 FDA reports)
ARTERIOVENOUS FISTULA, ACQUIRED ( 6 FDA reports)
ASCITES INFECTION ( 6 FDA reports)
ASOCIAL BEHAVIOUR ( 6 FDA reports)
AV DISSOCIATION ( 6 FDA reports)
BASE EXCESS ( 6 FDA reports)
BENIGN CARDIAC NEOPLASM ( 6 FDA reports)
BENIGN HEPATIC NEOPLASM ( 6 FDA reports)
BILIRUBINURIA ( 6 FDA reports)
BIOPSY HEART ( 6 FDA reports)
BIOPSY MUSCLE ABNORMAL ( 6 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 6 FDA reports)
BLADDER DIVERTICULUM ( 6 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE II ( 6 FDA reports)
BLEPHARAL PIGMENTATION ( 6 FDA reports)
BLOOD AMYLASE DECREASED ( 6 FDA reports)
BLOOD ARSENIC INCREASED ( 6 FDA reports)
BLOOD CREATINE DECREASED ( 6 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 6 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 6 FDA reports)
BLOOD LACTIC ACID DECREASED ( 6 FDA reports)
BRAIN OPERATION ( 6 FDA reports)
BRONCHOPNEUMOPATHY ( 6 FDA reports)
BRUNNER'S GLAND HYPERPLASIA ( 6 FDA reports)
BURNING SENSATION MUCOSAL ( 6 FDA reports)
CANDIDA TEST POSITIVE ( 6 FDA reports)
CARCINOMA ( 6 FDA reports)
CARDIAC FUNCTION DISTURBANCE POSTOPERATIVE ( 6 FDA reports)
CATAPLEXY ( 6 FDA reports)
CATHETER SITE CELLULITIS ( 6 FDA reports)
CEREBROVASCULAR ACCIDENT PROPHYLAXIS ( 6 FDA reports)
CERVICITIS HUMAN PAPILLOMA VIRUS ( 6 FDA reports)
CHEMICAL BURN OF GASTROINTESTINAL TRACT ( 6 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 6 FDA reports)
CLOSED FRACTURE MANIPULATION ( 6 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 6 FDA reports)
COMPUTERISED TOMOGRAM CORONARY ARTERY ABNORMAL ( 6 FDA reports)
CONJUNCTIVITIS VIRAL ( 6 FDA reports)
COOMBS TEST POSITIVE ( 6 FDA reports)
COR PULMONALE ACUTE ( 6 FDA reports)
COUGH DECREASED ( 6 FDA reports)
CYCLOPIA ( 6 FDA reports)
CYCLOTHYMIC DISORDER ( 6 FDA reports)
CYSTITIS ESCHERICHIA ( 6 FDA reports)
CYSTOCELE REPAIR ( 6 FDA reports)
CYTOGENETIC ABNORMALITY ( 6 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 6 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 6 FDA reports)
DERMATITIS EXFOLIATIVE GENERALISED ( 6 FDA reports)
DEVICE CONNECTION ISSUE ( 6 FDA reports)
DEVICE INTOLERANCE ( 6 FDA reports)
DEVICE ISSUE ( 6 FDA reports)
DISTRACTIBILITY ( 6 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 6 FDA reports)
DISUSE SYNDROME ( 6 FDA reports)
DUODENAL SCARRING ( 6 FDA reports)
DYSHIDROSIS ( 6 FDA reports)
EAR DEFORMITY ACQUIRED ( 6 FDA reports)
EAR OPERATION ( 6 FDA reports)
EJACULATION DELAYED ( 6 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 6 FDA reports)
ENDOCARDITIS ENTEROCOCCAL ( 6 FDA reports)
ENDOCERVICAL CURETTAGE ( 6 FDA reports)
EOSINOPHILIC PNEUMONIA CHRONIC ( 6 FDA reports)
EPIDERMOID CYST EXCISION ( 6 FDA reports)
ERYTHROPENIA ( 6 FDA reports)
EXTERNAL AUDITORY CANAL ATRESIA ( 6 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 6 FDA reports)
EYE INFECTION FUNGAL ( 6 FDA reports)
EYELASH THICKENING ( 6 FDA reports)
FACTOR V LEIDEN MUTATION ( 6 FDA reports)
FACTOR XI DEFICIENCY ( 6 FDA reports)
FEMALE REPRODUCTIVE NEOPLASM ( 6 FDA reports)
FIBROSIS TENDINOUS ( 6 FDA reports)
FLAT ANTERIOR CHAMBER OF EYE ( 6 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 6 FDA reports)
FOETAL MALPRESENTATION ( 6 FDA reports)
FOREIGN BODY REACTION ( 6 FDA reports)
GALLBLADDER NECROSIS ( 6 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 6 FDA reports)
GASTROINTESTINAL STENOSIS ( 6 FDA reports)
GASTROINTESTINAL SURGERY ( 6 FDA reports)
GASTROINTESTINAL TRACT MUCOSAL PIGMENTATION ( 6 FDA reports)
GASTROSCHISIS ( 6 FDA reports)
GENETIC COUNSELLING ( 6 FDA reports)
GENITAL LESION ( 6 FDA reports)
GENITOURINARY TRACT INFECTION ( 6 FDA reports)
GLAUCOMA SURGERY ( 6 FDA reports)
GLOMERULONEPHRITIS ACUTE ( 6 FDA reports)
GLOMUS TUMOUR ( 6 FDA reports)
GRANULOCYTE COUNT INCREASED ( 6 FDA reports)
HAEMOCONCENTRATION ( 6 FDA reports)
HAEMORRHAGIC CYST ( 6 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 6 FDA reports)
HEPATIC VEIN THROMBOSIS ( 6 FDA reports)
HEPATITIS C POSITIVE ( 6 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 6 FDA reports)
HISTOLOGY ABNORMAL ( 6 FDA reports)
HISTRIONIC PERSONALITY DISORDER ( 6 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 6 FDA reports)
HYALOSIS ASTEROID ( 6 FDA reports)
HYPERADRENOCORTICISM ( 6 FDA reports)
HYPERCHLORAEMIA ( 6 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 6 FDA reports)
HYPERPLASTIC CHOLECYSTOPATHY ( 6 FDA reports)
HYPERTROPHIC OBSTRUCTIVE CARDIOMYOPATHY ( 6 FDA reports)
HYSTEROSCOPY ( 6 FDA reports)
IIIRD NERVE DISORDER ( 6 FDA reports)
IMMUNOGLOBULINS ABNORMAL ( 6 FDA reports)
IMMUNOLOGY TEST ABNORMAL ( 6 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 6 FDA reports)
UTERINE NEOPLASM ( 6 FDA reports)
VAGINAL CANCER ( 6 FDA reports)
VAGINAL CYST ( 6 FDA reports)
VASOMOTOR RHINITIS ( 6 FDA reports)
VEIN DISCOLOURATION ( 6 FDA reports)
VENOUS ANEURYSM ( 6 FDA reports)
VESSEL PERFORATION ( 6 FDA reports)
VICTIM OF CRIME ( 6 FDA reports)
VIRAL PHARYNGITIS ( 6 FDA reports)
VIROLOGIC FAILURE ( 6 FDA reports)
VITAMIN D ABNORMAL ( 6 FDA reports)
VITRITIS ( 6 FDA reports)
VOCAL CORD PARESIS ( 6 FDA reports)
VTH NERVE INJURY ( 6 FDA reports)
WHOLE BLOOD TRANSFUSION ( 6 FDA reports)
XANTHOCHROMIA ( 6 FDA reports)
IMPLANT SITE ERYTHEMA ( 6 FDA reports)
INCISIONAL HERNIA, OBSTRUCTIVE ( 6 FDA reports)
INDUCED LABOUR ( 6 FDA reports)
INFUSION SITE DISCOLOURATION ( 6 FDA reports)
INFUSION SITE INFECTION ( 6 FDA reports)
INFUSION SITE RASH ( 6 FDA reports)
INGUINAL MASS ( 6 FDA reports)
INJECTION SITE PHLEBITIS ( 6 FDA reports)
INJECTION SITE PUSTULE ( 6 FDA reports)
INTENSIVE CARE ( 6 FDA reports)
INTERMITTENT EXPLOSIVE DISORDER ( 6 FDA reports)
INTERNAL HERNIA ( 6 FDA reports)
INTESTINAL GANGRENE ( 6 FDA reports)
INTESTINAL PROLAPSE ( 6 FDA reports)
INTESTINAL STRANGULATION ( 6 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 6 FDA reports)
IRIS NEOPLASM ( 6 FDA reports)
JC VIRUS INFECTION ( 6 FDA reports)
JC VIRUS TEST POSITIVE ( 6 FDA reports)
JOINT STABILISATION ( 6 FDA reports)
KAWASAKI'S DISEASE ( 6 FDA reports)
LEGAL PROBLEM ( 6 FDA reports)
LIBIDO DISORDER ( 6 FDA reports)
LIPOHYPERTROPHY ( 6 FDA reports)
LIPOMATOSIS ( 6 FDA reports)
LIVE BIRTH ( 6 FDA reports)
LIVING IN RESIDENTIAL INSTITUTION ( 6 FDA reports)
LOWER LIMB DEFORMITY ( 6 FDA reports)
LUDWIG ANGINA ( 6 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 6 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE III ( 6 FDA reports)
LUNG TRANSPLANT ( 6 FDA reports)
LUNG TRANSPLANT REJECTION ( 6 FDA reports)
LYMPHOCYTIC LYMPHOMA ( 6 FDA reports)
MACROGLOSSIA ( 6 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 6 FDA reports)
MALIGNANT ASCITES ( 6 FDA reports)
MASTOID DISORDER ( 6 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 6 FDA reports)
MECHANICAL COMPLICATION OF IMPLANT ( 6 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 6 FDA reports)
MELAS SYNDROME ( 6 FDA reports)
MENINGITIS CHEMICAL ( 6 FDA reports)
METASTASES TO RETROPERITONEUM ( 6 FDA reports)
METASTATIC LYMPHOMA ( 6 FDA reports)
METATARSALGIA ( 6 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 6 FDA reports)
MICROCEPHALY ( 6 FDA reports)
MICROCOCCUS INFECTION ( 6 FDA reports)
MILIA ( 6 FDA reports)
MORPHOEA ( 6 FDA reports)
MUNCHAUSEN'S SYNDROME ( 6 FDA reports)
MUSCLE FLAP OPERATION ( 6 FDA reports)
MUSCLE HYPERTROPHY ( 6 FDA reports)
MYASTHENIA GRAVIS CRISIS ( 6 FDA reports)
MYCOPLASMA INFECTION ( 6 FDA reports)
MYRINGOTOMY ( 6 FDA reports)
NAIL RIDGING ( 6 FDA reports)
NARCISSISTIC PERSONALITY DISORDER ( 6 FDA reports)
NECROTISING COLITIS ( 6 FDA reports)
NEGATIVISM ( 6 FDA reports)
NEUROLOGIC NEGLECT SYNDROME ( 6 FDA reports)
NEUROMUSCULAR BLOCK PROLONGED ( 6 FDA reports)
NIPPLE SWELLING ( 6 FDA reports)
OCULAR NEOPLASM ( 6 FDA reports)
OESOPHAGEAL INFECTION ( 6 FDA reports)
OMENTECTOMY ( 6 FDA reports)
OPHTHALMOLOGICAL EXAMINATION ABNORMAL ( 6 FDA reports)
ORBITAL INFECTION ( 6 FDA reports)
PAINFUL ERECTION ( 6 FDA reports)
PANCREATIC CARCINOMA STAGE IV ( 6 FDA reports)
PANCREATIC DUCT OBSTRUCTION ( 6 FDA reports)
PANCREATIC ENLARGEMENT ( 6 FDA reports)
PANCREATIC FISTULA ( 6 FDA reports)
PARATHYROIDECTOMY ( 6 FDA reports)
PARTIAL SEIZURES WITH SECONDARY GENERALISATION ( 6 FDA reports)
PELVIC INFECTION ( 6 FDA reports)
PENILE ERYTHEMA ( 6 FDA reports)
PERICORONITIS ( 6 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED ( 6 FDA reports)
PH URINE DECREASED ( 6 FDA reports)
PHARYNGEAL MASS ( 6 FDA reports)
PHARYNGOLARYNGEAL DISCOMFORT ( 6 FDA reports)
PHOBIA ( 6 FDA reports)
PITUITARY HAEMORRHAGE ( 6 FDA reports)
PLEURISY VIRAL ( 6 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 6 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 6 FDA reports)
POST PROCEDURAL HAEMATURIA ( 6 FDA reports)
POSTINFARCTION ANGINA ( 6 FDA reports)
PREAURICULAR CYST ( 6 FDA reports)
PREMENSTRUAL SYNDROME ( 6 FDA reports)
PRIMARY HYPERALDOSTERONISM ( 6 FDA reports)
PRODUCT CONTAINER ISSUE ( 6 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 6 FDA reports)
PROSTATIC ACID PHOSPHATASE INCREASED ( 6 FDA reports)
PROSTATIC SPECIFIC ANTIGEN ABNORMAL ( 6 FDA reports)
PROSTHESIS IMPLANTATION ( 6 FDA reports)
PSEUDOPOLYPOSIS ( 6 FDA reports)
PSYCHOTIC BEHAVIOUR ( 6 FDA reports)
PULMONARY FUNCTION TEST ( 6 FDA reports)
PULMONARY HYPOPLASIA ( 6 FDA reports)
PYODERMA GANGRENOSUM ( 6 FDA reports)
RADICAL MASTECTOMY ( 6 FDA reports)
REACTION TO FOOD ADDITIVE ( 6 FDA reports)
RECTAL FISSURE ( 6 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 6 FDA reports)
REITER'S SYNDROME ( 6 FDA reports)
RENAL AMYLOIDOSIS ( 6 FDA reports)
RENAL CORTICAL NECROSIS ( 6 FDA reports)
RENAL IMPAIRMENT NEONATAL ( 6 FDA reports)
RENAL NECROSIS ( 6 FDA reports)
RESPIRATORY TRACT OEDEMA ( 6 FDA reports)
RETAINED PLACENTA OR MEMBRANES ( 6 FDA reports)
RETINOPATHY PROLIFERATIVE ( 6 FDA reports)
RHEUMATOID VASCULITIS ( 6 FDA reports)
SACRALISATION ( 6 FDA reports)
SALIVARY DUCT OBSTRUCTION ( 6 FDA reports)
SCIATIC NERVE NEUROPATHY ( 6 FDA reports)
SCLERAL HAEMORRHAGE ( 6 FDA reports)
SCROTAL HAEMATOMA ( 6 FDA reports)
SCROTAL MASS ( 6 FDA reports)
SEMEN DISCOLOURATION ( 6 FDA reports)
SENSE OF OPPRESSION ( 6 FDA reports)
SICKLE CELL TRAIT ( 6 FDA reports)
SINGLE PHOTON EMISSION COMPUTERISED TOMOGRAM ABNORMAL ( 6 FDA reports)
SINUS TARSI SYNDROME ( 6 FDA reports)
SKIN DEGENERATIVE DISORDER ( 6 FDA reports)
SLEEP PHASE RHYTHM DISTURBANCE ( 6 FDA reports)
SMALL BOWEL ANGIOEDEMA ( 6 FDA reports)
SOLAR ELASTOSIS ( 6 FDA reports)
SOLITARY KIDNEY ( 6 FDA reports)
SPINAL CORD NEOPLASM ( 6 FDA reports)
SPINAL LIGAMENT OSSIFICATION ( 6 FDA reports)
SUPERINFECTION LUNG ( 6 FDA reports)
SUTURE INSERTION ( 6 FDA reports)
SWEAT DISCOLOURATION ( 6 FDA reports)
SYPHILIS TEST ( 6 FDA reports)
TERMINAL DRIBBLING ( 6 FDA reports)
THERAPEUTIC EMBOLISATION ( 6 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE FOR UNAPPROVED INDICATION ( 6 FDA reports)
THIRST DECREASED ( 6 FDA reports)
THORACIC HAEMORRHAGE ( 6 FDA reports)
TOOTH MALFORMATION ( 6 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO ABNORMAL ( 6 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO DECREASED ( 6 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 6 FDA reports)
TRAUMATIC ARTHRITIS ( 6 FDA reports)
TROUSSEAU'S SYNDROME ( 6 FDA reports)
URETHRAL DISORDER ( 6 FDA reports)
URETHRAL OPERATION ( 6 FDA reports)
URINE CALCIUM INCREASED ( 6 FDA reports)
IMPLANT SITE EXTRAVASATION ( 5 FDA reports)
IMPLANT SITE PAIN ( 5 FDA reports)
INBORN ERROR OF METABOLISM ( 5 FDA reports)
INCISION SITE ABSCESS ( 5 FDA reports)
INCISION SITE CELLULITIS ( 5 FDA reports)
INCISION SITE ERYTHEMA ( 5 FDA reports)
INCREASED INSULIN REQUIREMENT ( 5 FDA reports)
INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS ( 5 FDA reports)
INFECTIVE SPONDYLITIS ( 5 FDA reports)
INFLAMMATION OF WOUND ( 5 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 5 FDA reports)
INJECTION SITE ANAESTHESIA ( 5 FDA reports)
INJECTION SITE ATROPHY ( 5 FDA reports)
INJECTION SITE THROMBOSIS ( 5 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 5 FDA reports)
INSULIN AUTOIMMUNE SYNDROME ( 5 FDA reports)
INTERNAL INJURY ( 5 FDA reports)
INTERRUPTION OF AORTIC ARCH ( 5 FDA reports)
INTERVERTEBRAL DISC CALCIFICATION ( 5 FDA reports)
INTESTINAL ANASTOMOSIS ( 5 FDA reports)
INTRADUCTAL PAPILLARY MUCINOUS NEOPLASM ( 5 FDA reports)
INTRAOCULAR MELANOMA ( 5 FDA reports)
ISCHAEMIC NEUROPATHY ( 5 FDA reports)
IVTH NERVE PARESIS ( 5 FDA reports)
JAUNDICE HEPATOCELLULAR ( 5 FDA reports)
LARYNGEAL STENOSIS ( 5 FDA reports)
LARYNGECTOMY ( 5 FDA reports)
LEFT ATRIAL HYPERTROPHY ( 5 FDA reports)
LEFT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 5 FDA reports)
LEFT VENTRICULAR HEAVE ( 5 FDA reports)
LIGAMENT CALCIFICATION ( 5 FDA reports)
LIPOPROTEIN (A) INCREASED ( 5 FDA reports)
LIPOSARCOMA ( 5 FDA reports)
LIQUID PRODUCT PHYSICAL ISSUE ( 5 FDA reports)
LIVER OPERATION ( 5 FDA reports)
LIVIDITY ( 5 FDA reports)
LOW TENSION GLAUCOMA ( 5 FDA reports)
LUMBAR HERNIA ( 5 FDA reports)
LUNG ADENOCARCINOMA STAGE III ( 5 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE I ( 5 FDA reports)
LYMPHORRHOEA ( 5 FDA reports)
MACULAR PSEUDOHOLE ( 5 FDA reports)
MARFAN'S SYNDROME ( 5 FDA reports)
MECONIUM IN AMNIOTIC FLUID ( 5 FDA reports)
MEDIASTINAL ABSCESS ( 5 FDA reports)
MEDIASTINAL CYST ( 5 FDA reports)
MEDIASTINOSCOPY ( 5 FDA reports)
MEDIASTINUM NEOPLASM ( 5 FDA reports)
MEDICAL DEVICE PAIN ( 5 FDA reports)
MEGAKARYOCYTES ABNORMAL ( 5 FDA reports)
MEGAKARYOCYTES DECREASED ( 5 FDA reports)
MENINGEAL NEOPLASM ( 5 FDA reports)
MENINGITIS HERPES ( 5 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 5 FDA reports)
MESENTERIC ARTERY EMBOLISM ( 5 FDA reports)
MESENTERITIS ( 5 FDA reports)
METAL POISONING ( 5 FDA reports)
METASTASES TO STOMACH ( 5 FDA reports)
METASTATIC UTERINE CANCER ( 5 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 5 FDA reports)
MICROGNATHIA ( 5 FDA reports)
MILK-ALKALI SYNDROME ( 5 FDA reports)
MINERAL DEFICIENCY ( 5 FDA reports)
MITOCHONDRIAL MYOPATHY ( 5 FDA reports)
MITRAL VALVE DISEASE MIXED ( 5 FDA reports)
MOYAMOYA DISEASE ( 5 FDA reports)
MUCORMYCOSIS ( 5 FDA reports)
MUCOSAL ATROPHY ( 5 FDA reports)
MUCOSAL MEMBRANE HYPERPLASIA ( 5 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 5 FDA reports)
MYCOBACTERIUM CHELONEI INFECTION ( 5 FDA reports)
MYCOPLASMA TEST POSITIVE ( 5 FDA reports)
MYELOID LEUKAEMIA ( 5 FDA reports)
MYOCARDIAL OEDEMA ( 5 FDA reports)
N-TERMINAL PROHORMONE BRAIN NATRIURETIC PEPTIDE ( 5 FDA reports)
NEPHRITIS ALLERGIC ( 5 FDA reports)
NITRITE URINE PRESENT ( 5 FDA reports)
NON-ALCOHOLIC STEATOHEPATITIS ( 5 FDA reports)
NON-NEUTRALISING ANTIBODIES POSITIVE ( 5 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 5 FDA reports)
NORMAL TENSION GLAUCOMA ( 5 FDA reports)
NUCLEATED RED CELLS ( 5 FDA reports)
OBSTRUCTIVE CHRONIC BRONCHITIS WITH ACUTE EXACERBATION ( 5 FDA reports)
OCULAR ISCHAEMIC SYNDROME ( 5 FDA reports)
OCULAR MYASTHENIA ( 5 FDA reports)
OESOPHAGEAL ATRESIA ( 5 FDA reports)
OESOPHAGEAL FISTULA ( 5 FDA reports)
OESOPHAGOSCOPY ABNORMAL ( 5 FDA reports)
OLIGODIPSIA ( 5 FDA reports)
ONCOLOGIC COMPLICATION ( 5 FDA reports)
ONYCHORRHEXIS ( 5 FDA reports)
OPTIC DISC DRUSEN ( 5 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 5 FDA reports)
ORAL SUBMUCOSAL FIBROSIS ( 5 FDA reports)
OROMANDIBULAR DYSTONIA ( 5 FDA reports)
OROPHARYNGEAL CANCER STAGE UNSPECIFIED ( 5 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 5 FDA reports)
OVARIAN HYPERSTIMULATION SYNDROME ( 5 FDA reports)
PAPILLOMA VIRAL INFECTION ( 5 FDA reports)
PARADOXICAL EMBOLISM ( 5 FDA reports)
PARENTERAL NUTRITION ( 5 FDA reports)
PAROPHTHALMIA ( 5 FDA reports)
PELVIC DISCOMFORT ( 5 FDA reports)
PELVIC HAEMORRHAGE ( 5 FDA reports)
PELVIC NEOPLASM ( 5 FDA reports)
PELVIC ORGAN INJURY ( 5 FDA reports)
PENIS DEVIATION ( 5 FDA reports)
PERIPROSTHETIC FRACTURE ( 5 FDA reports)
PERITONEAL ABSCESS ( 5 FDA reports)
PERITONEAL ADHESIONS ( 5 FDA reports)
PERITONSILLAR ABSCESS ( 5 FDA reports)
PERIVASCULAR DERMATITIS ( 5 FDA reports)
PHARYNGEAL INFLAMMATION ( 5 FDA reports)
PICA ( 5 FDA reports)
PITUITARY ENLARGEMENT ( 5 FDA reports)
PITYRIASIS ROSEA ( 5 FDA reports)
PLATELET AGGREGATION ( 5 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 5 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 5 FDA reports)
POLYMEDICATION ( 5 FDA reports)
POST POLIO SYNDROME ( 5 FDA reports)
POST PROCEDURAL DIARRHOEA ( 5 FDA reports)
POST PROCEDURAL PNEUMONIA ( 5 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 5 FDA reports)
POST PROCEDURAL VOMITING ( 5 FDA reports)
PROCTITIS HAEMORRHAGIC ( 5 FDA reports)
PRODUCT CONTAMINATION ( 5 FDA reports)
PRODUCT PHYSICAL ISSUE ( 5 FDA reports)
PROTEIN S DEFICIENCY ( 5 FDA reports)
PRURITUS ALLERGIC ( 5 FDA reports)
PRURITUS ANI ( 5 FDA reports)
PULMONARY ARTERIOPATHY ( 5 FDA reports)
PULMONARY ARTERY WALL HYPERTROPHY ( 5 FDA reports)
PULMONARY VALVE STENOSIS CONGENITAL ( 5 FDA reports)
PULMONARY VENOUS THROMBOSIS ( 5 FDA reports)
PULSE PRESSURE INCREASED ( 5 FDA reports)
PUNCTURE SITE INFECTION ( 5 FDA reports)
PYELONEPHRITIS CHRONIC ( 5 FDA reports)
RECTAL ADENOMA ( 5 FDA reports)
RECTAL CANCER METASTATIC ( 5 FDA reports)
RECTAL PERFORATION ( 5 FDA reports)
RECTAL SPASM ( 5 FDA reports)
RED MAN SYNDROME ( 5 FDA reports)
REFUSAL OF EXAMINATION ( 5 FDA reports)
RELAPSING FEVER ( 5 FDA reports)
RENAL ANEURYSM ( 5 FDA reports)
RENAL CYST INFECTION ( 5 FDA reports)
RENAL HYPERTENSION ( 5 FDA reports)
RENAL HYPERTROPHY ( 5 FDA reports)
RENOVASCULAR HYPERTENSION ( 5 FDA reports)
REPETITIVE STRAIN INJURY ( 5 FDA reports)
RESIDUAL URINE VOLUME ( 5 FDA reports)
RETINAL NEOVASCULARISATION ( 5 FDA reports)
RETINAL OPERATION ( 5 FDA reports)
RETINAL SCAR ( 5 FDA reports)
RETROSTERNAL INFECTION ( 5 FDA reports)
RHODOCOCCUS INFECTION ( 5 FDA reports)
RICHTER'S SYNDROME ( 5 FDA reports)
ROTAVIRUS TEST POSITIVE ( 5 FDA reports)
SCAR PAIN ( 5 FDA reports)
SCLERAL HYPERAEMIA ( 5 FDA reports)
SCLERODACTYLIA ( 5 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 5 FDA reports)
SEROSITIS ( 5 FDA reports)
SERUM SEROTONIN DECREASED ( 5 FDA reports)
SHORT-BOWEL SYNDROME ( 5 FDA reports)
SILICOSIS ( 5 FDA reports)
SINGLE UMBILICAL ARTERY ( 5 FDA reports)
SKIN TEST NEGATIVE ( 5 FDA reports)
SMALL INTESTINE CARCINOMA ( 5 FDA reports)
SOLILOQUY ( 5 FDA reports)
SOMATISATION DISORDER ( 5 FDA reports)
SPINAL X-RAY ABNORMAL ( 5 FDA reports)
SPINDLE CELL SARCOMA ( 5 FDA reports)
SPIROMETRY ABNORMAL ( 5 FDA reports)
SPLENIC HAEMATOMA ( 5 FDA reports)
SPLENIC INJURY ( 5 FDA reports)
STATUS MIGRAINOSUS ( 5 FDA reports)
STERNAL INJURY ( 5 FDA reports)
STOOLS WATERY ( 5 FDA reports)
SUBCLAVIAN ARTERY THROMBOSIS ( 5 FDA reports)
SUBDURAL HAEMATOMA EVACUATION ( 5 FDA reports)
SYSTEMIC SCLEROSIS ( 5 FDA reports)
TAENIASIS ( 5 FDA reports)
TANGENTIALITY ( 5 FDA reports)
TARSAL TUNNEL SYNDROME ( 5 FDA reports)
TENDON SHEATH INCISION ( 5 FDA reports)
THERAPEUTIC REACTION TIME DECREASED ( 5 FDA reports)
THERMOHYPERAESTHESIA ( 5 FDA reports)
THROMBOPHLEBITIS SEPTIC ( 5 FDA reports)
THYROID OPERATION ( 5 FDA reports)
TONGUE ERUPTION ( 5 FDA reports)
TONGUE SPASM ( 5 FDA reports)
TONSILLAR INFLAMMATION ( 5 FDA reports)
TRACHEAL OEDEMA ( 5 FDA reports)
TRICHIASIS ( 5 FDA reports)
TRISOMY 18 ( 5 FDA reports)
TRUNCUS ARTERIOSUS PERSISTENT ( 5 FDA reports)
TUBAL LIGATION ( 5 FDA reports)
UHTHOFF'S PHENOMENON ( 5 FDA reports)
URETHRAL CANCER ( 5 FDA reports)
URETHRAL CANCER METASTATIC ( 5 FDA reports)
URETHRAL SPASM ( 5 FDA reports)
ABSCESS OF SALIVARY GLAND ( 5 FDA reports)
ACID FAST BACILLI INFECTION ( 5 FDA reports)
ACROMEGALY ( 5 FDA reports)
ACTIVATION SYNDROME ( 5 FDA reports)
ACUTE CHEST SYNDROME ( 5 FDA reports)
ADRENOGENITAL SYNDROME ( 5 FDA reports)
ALLERGIC TRANSFUSION REACTION ( 5 FDA reports)
ALLERGY TO ARTHROPOD BITE ( 5 FDA reports)
ALOPECIA EFFLUVIUM ( 5 FDA reports)
AMBLYOPIA STRABISMIC ( 5 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 5 FDA reports)
AMPUTATION STUMP PAIN ( 5 FDA reports)
ANAL ATRESIA ( 5 FDA reports)
ANISOMETROPIA ( 5 FDA reports)
ANOGENITAL DYSPLASIA ( 5 FDA reports)
ANTI-INSULIN ANTIBODY ( 5 FDA reports)
ANTI-SS-A ANTIBODY POSITIVE ( 5 FDA reports)
AORTIC DISSECTION RUPTURE ( 5 FDA reports)
AORTIC VALVE DISEASE MIXED ( 5 FDA reports)
ARTERIAL BRUIT ( 5 FDA reports)
ARTERIAL FIBROSIS ( 5 FDA reports)
ARTERIOSCLEROTIC GANGRENE ( 5 FDA reports)
ATRIOVENTRICULAR EXTRASYSTOLES ( 5 FDA reports)
B-CELL LYMPHOMA STAGE III ( 5 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 5 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 5 FDA reports)
BACTEROIDES INFECTION ( 5 FDA reports)
BALANITIS CANDIDA ( 5 FDA reports)
BASILAR ARTERY THROMBOSIS ( 5 FDA reports)
BED REST ( 5 FDA reports)
BENIGN NEOPLASM OF SKIN ( 5 FDA reports)
BENIGN OESOPHAGEAL NEOPLASM ( 5 FDA reports)
BENIGN RENAL NEOPLASM ( 5 FDA reports)
BICUSPID AORTIC VALVE ( 5 FDA reports)
BILE DUCT STENT INSERTION ( 5 FDA reports)
BILIARY FIBROSIS ( 5 FDA reports)
BILIARY NEOPLASM ( 5 FDA reports)
BIOPSY KIDNEY ( 5 FDA reports)
BIOPSY LUNG ( 5 FDA reports)
BLADDER NECK SUSPENSION ( 5 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA RECURRENT ( 5 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE III ( 5 FDA reports)
BLAST CELL COUNT INCREASED ( 5 FDA reports)
BLINDNESS DAY ( 5 FDA reports)
BLOOD ALDOSTERONE DECREASED ( 5 FDA reports)
BLOOD ANTIDIURETIC HORMONE INCREASED ( 5 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 5 FDA reports)
BLOOD ERYTHROPOIETIN DECREASED ( 5 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 5 FDA reports)
BLOOD SODIUM ( 5 FDA reports)
BLOOD TESTOSTERONE FREE DECREASED ( 5 FDA reports)
BLOOD UREA ( 5 FDA reports)
BLUNTED AFFECT ( 5 FDA reports)
BODY HEIGHT BELOW NORMAL ( 5 FDA reports)
BOREDOM ( 5 FDA reports)
BRACHYCEPHALY ( 5 FDA reports)
BRAIN STEM THROMBOSIS ( 5 FDA reports)
BREAST CANCER MALE ( 5 FDA reports)
BREAST PROSTHESIS IMPLANTATION ( 5 FDA reports)
BRONCHIAL WALL THICKENING ( 5 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 5 FDA reports)
BRONCHOMALACIA ( 5 FDA reports)
BURN OF INTERNAL ORGANS ( 5 FDA reports)
CAMPTODACTYLY CONGENITAL ( 5 FDA reports)
CAPILLARY FRAGILITY ( 5 FDA reports)
CARDIAC ASSISTANCE DEVICE USER ( 5 FDA reports)
CARDIAC IMAGING PROCEDURE NORMAL ( 5 FDA reports)
CARDIAC MONITORING ( 5 FDA reports)
CARDIAC MYXOMA ( 5 FDA reports)
CARDIAC PACEMAKER BATTERY REPLACEMENT ( 5 FDA reports)
CARDIAC REHABILITATION THERAPY ( 5 FDA reports)
CARDITIS ( 5 FDA reports)
CAROTID ARTERIAL EMBOLUS ( 5 FDA reports)
CATHETERISATION VENOUS ( 5 FDA reports)
CENTRAL NERVOUS SYSTEM HAEMORRHAGE ( 5 FDA reports)
CENTRAL VENOUS PRESSURE DECREASED ( 5 FDA reports)
CEREBELLAR HAEMANGIOMA ( 5 FDA reports)
CEREBRAL HYGROMA ( 5 FDA reports)
CHEMICAL INJURY ( 5 FDA reports)
CHORDAE TENDINAE RUPTURE ( 5 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA STAGE 0 ( 5 FDA reports)
CHRONOTROPIC INCOMPETENCE ( 5 FDA reports)
CLINODACTYLY ( 5 FDA reports)
COLOBOMA ( 5 FDA reports)
COLON CANCER STAGE I ( 5 FDA reports)
COLON GANGRENE ( 5 FDA reports)
COLONIC ATONY ( 5 FDA reports)
COLOUR VISION TESTS ABNORMAL ( 5 FDA reports)
CONDUCTIVE DEAFNESS ( 5 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 5 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 5 FDA reports)
CORONARY BYPASS THROMBOSIS ( 5 FDA reports)
CORRECTIVE LENS USER ( 5 FDA reports)
CRANIAL NEUROPATHY ( 5 FDA reports)
CREATININE RENAL CLEARANCE ABNORMAL ( 5 FDA reports)
CROSS SENSITIVITY REACTION ( 5 FDA reports)
CRYSTAL URINE PRESENT ( 5 FDA reports)
CULTURE URINE ( 5 FDA reports)
CYANOSIS CENTRAL ( 5 FDA reports)
CYSTITIS KLEBSIELLA ( 5 FDA reports)
CYSTOSCOPY ABNORMAL ( 5 FDA reports)
CYTOMEGALOVIRUS ENTERITIS ( 5 FDA reports)
DEATH NEONATAL ( 5 FDA reports)
DECEREBRATION ( 5 FDA reports)
DELIRIUM FEBRILE ( 5 FDA reports)
DENERVATION ATROPHY ( 5 FDA reports)
DENGUE FEVER ( 5 FDA reports)
DEVICE COMPONENT ISSUE ( 5 FDA reports)
DEVICE EXPULSION ( 5 FDA reports)
DIABETIC CARDIOMYOPATHY ( 5 FDA reports)
DIABETIC ENTEROPATHY ( 5 FDA reports)
DIALYSIS DEVICE COMPLICATION ( 5 FDA reports)
DIALYSIS DISEQUILIBRIUM SYNDROME ( 5 FDA reports)
DIASTOLIC HYPERTENSION ( 5 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 5 FDA reports)
DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY ( 5 FDA reports)
DIVERTICULITIS MECKEL'S ( 5 FDA reports)
DNA ANTIBODY POSITIVE ( 5 FDA reports)
DOUBLE STRANDED DNA ANTIBODY ( 5 FDA reports)
DRUG DETOXIFICATION ( 5 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 5 FDA reports)
DRUG THERAPY ( 5 FDA reports)
EAR INJURY ( 5 FDA reports)
ELECTIVE SURGERY ( 5 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 5 FDA reports)
EMPYEMA DRAINAGE ( 5 FDA reports)
ENDOCARDITIS CANDIDA ( 5 FDA reports)
ENTEROBACTER SEPSIS ( 5 FDA reports)
ENTEROBACTER TEST POSITIVE ( 5 FDA reports)
EPIDURAL ANAESTHESIA ( 5 FDA reports)
EPIPLOIC APPENDAGITIS ( 5 FDA reports)
EPISCLERITIS ( 5 FDA reports)
EPSTEIN-BARR VIRUS ANTIGEN POSITIVE ( 5 FDA reports)
EX-TOBACCO USER ( 5 FDA reports)
EXCESSIVE EXERCISE ( 5 FDA reports)
EXCESSIVE MASTURBATION ( 5 FDA reports)
EXSANGUINATION ( 5 FDA reports)
EYE INFECTION BACTERIAL ( 5 FDA reports)
EYELID IRRITATION ( 5 FDA reports)
FACE AND MOUTH X-RAY ABNORMAL ( 5 FDA reports)
FAECAL VOMITING ( 5 FDA reports)
FEMALE GENITAL OPERATION ( 5 FDA reports)
FEMORAL HERNIA ( 5 FDA reports)
FIBRIN INCREASED ( 5 FDA reports)
FRONTOTEMPORAL DEMENTIA ( 5 FDA reports)
GASTRIC ADENOMA ( 5 FDA reports)
GASTRIC FISTULA ( 5 FDA reports)
GASTRIC LAVAGE ( 5 FDA reports)
GASTRIC VARICES HAEMORRHAGE ( 5 FDA reports)
GASTROENTERITIS CRYPTOSPORIDIAL ( 5 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 5 FDA reports)
GASTROENTERITIS SALMONELLA ( 5 FDA reports)
GASTROINTESTINAL CANCER METASTATIC ( 5 FDA reports)
GENERAL PHYSICAL CONDITION ( 5 FDA reports)
GENITAL SWELLING ( 5 FDA reports)
GESTATIONAL HYPERTENSION ( 5 FDA reports)
GINGIVITIS ULCERATIVE ( 5 FDA reports)
GLYCOPEPTIDE ANTIBIOTIC RESISTANT ENTEROCOCCAL INFECTION ( 5 FDA reports)
GRANDIOSITY ( 5 FDA reports)
GRANULOCYTES ABNORMAL ( 5 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 5 FDA reports)
HAEMODIALYSIS-INDUCED SYMPTOM ( 5 FDA reports)
HAEMODILUTION ( 5 FDA reports)
HEAD BANGING ( 5 FDA reports)
HEART VALVE CALCIFICATION ( 5 FDA reports)
HEPATIC ADENOMA ( 5 FDA reports)
HEPATIC INFECTION ( 5 FDA reports)
HEPATIC INFILTRATION EOSINOPHILIC ( 5 FDA reports)
HEPATITIS ALCOHOLIC ( 5 FDA reports)
HEPATITIS B ANTIBODY ( 5 FDA reports)
HERNIA PAIN ( 5 FDA reports)
HERNIAL EVENTRATION ( 5 FDA reports)
HETEROTAXIA ( 5 FDA reports)
HOMANS' SIGN ( 5 FDA reports)
HOUSE DUST ALLERGY ( 5 FDA reports)
HYDROMETRA ( 5 FDA reports)
HYPERDYNAMIC LEFT VENTRICLE ( 5 FDA reports)
HYPERDYNAMIC PRECORDIUM ( 5 FDA reports)
HYPERKERATOSIS PALMARIS AND PLANTARIS ( 5 FDA reports)
HYPERTENSIVE ANGIOPATHY ( 5 FDA reports)
HYPOPHONESIS ( 5 FDA reports)
ILEAL GANGRENE ( 5 FDA reports)
IMMUNODEFICIENCY COMMON VARIABLE ( 5 FDA reports)
UROGRAM ( 5 FDA reports)
VASCULAR FRAGILITY ( 5 FDA reports)
VASCULAR STENT INSERTION ( 5 FDA reports)
VENOUS PRESSURE JUGULAR ( 5 FDA reports)
VERTEBRAL ARTERY DISSECTION ( 5 FDA reports)
VESICOURETERIC REFLUX ( 5 FDA reports)
VIBRATION TEST ABNORMAL ( 5 FDA reports)
VIRAL MYOSITIS ( 5 FDA reports)
VIRUS SEROLOGY TEST POSITIVE ( 5 FDA reports)
VISCERAL PAIN ( 5 FDA reports)
VISUAL EVOKED POTENTIALS ABNORMAL ( 5 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 5 FDA reports)
VOCAL CORD INFLAMMATION ( 5 FDA reports)
VOCAL CORD POLYPECTOMY ( 5 FDA reports)
WALKING DISTANCE TEST ABNORMAL ( 5 FDA reports)
WALLENBERG SYNDROME ( 5 FDA reports)
WOUND CLOSURE ( 5 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 5 FDA reports)
ZINC DEFICIENCY ( 5 FDA reports)
URINE POTASSIUM INCREASED ( 4 FDA reports)
UROGENITAL HAEMORRHAGE ( 4 FDA reports)
URTICARIA CHRONIC ( 4 FDA reports)
URTICARIA THERMAL ( 4 FDA reports)
UTERINE RUPTURE ( 4 FDA reports)
VAGINAL FISTULA ( 4 FDA reports)
VAGINAL REMOVAL OF INTRAUTERINE FOREIGN BODY ( 4 FDA reports)
VASCULITIS GASTROINTESTINAL ( 4 FDA reports)
VASOPLEGIA SYNDROME ( 4 FDA reports)
VERTEBRAL ARTERY THROMBOSIS ( 4 FDA reports)
VIBRATORY SENSE INCREASED ( 4 FDA reports)
VIRAEMIA ( 4 FDA reports)
VISCERAL OEDEMA ( 4 FDA reports)
VISUAL ACUITY TESTS ABNORMAL ( 4 FDA reports)
VISUAL MIDLINE SHIFT SYNDROME ( 4 FDA reports)
VITILIGO ( 4 FDA reports)
VOCAL CORD NEOPLASM ( 4 FDA reports)
VOLUME BLOOD INCREASED ( 4 FDA reports)
VULVAL HAEMORRHAGE ( 4 FDA reports)
VULVAR DYSPLASIA ( 4 FDA reports)
WEIGHT ( 4 FDA reports)
WEIGHT LOSS DIET ( 4 FDA reports)
WERNICKE'S ENCEPHALOPATHY ( 4 FDA reports)
WHITE BLOOD CELLS URINE ( 4 FDA reports)
WOUND INFECTION FUNGAL ( 4 FDA reports)
XANTHELASMA ( 4 FDA reports)
IMPLANT SITE DISCHARGE ( 4 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 4 FDA reports)
INFECTED BITES ( 4 FDA reports)
INFECTIOUS PLEURAL EFFUSION ( 4 FDA reports)
INFESTATION ( 4 FDA reports)
INFLAMMATORY CARCINOMA OF THE BREAST ( 4 FDA reports)
INJECTION SITE COLDNESS ( 4 FDA reports)
INJECTION SITE EXFOLIATION ( 4 FDA reports)
INSULIN RESISTANCE SYNDROME ( 4 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 4 FDA reports)
INTESTINAL POLYP HAEMORRHAGE ( 4 FDA reports)
INTRACARDIAC MASS ( 4 FDA reports)
INTRACRANIAL TUMOUR HAEMORRHAGE ( 4 FDA reports)
INTRAPERICARDIAL THROMBOSIS ( 4 FDA reports)
INTRASPINAL ABSCESS ( 4 FDA reports)
IRIS NEOVASCULARISATION ( 4 FDA reports)
ISCHAEMIC LIMB PAIN ( 4 FDA reports)
IUCD COMPLICATION ( 4 FDA reports)
IUD MIGRATION ( 4 FDA reports)
JEJUNAL ULCER ( 4 FDA reports)
JOINT LIGAMENT RUPTURE ( 4 FDA reports)
JUVENILE ARTHRITIS ( 4 FDA reports)
KARYOTYPE ANALYSIS ABNORMAL ( 4 FDA reports)
KERATITIS BACTERIAL ( 4 FDA reports)
KERATITIS HERPETIC ( 4 FDA reports)
KERATOPATHY ( 4 FDA reports)
LACRIMAL DISORDER ( 4 FDA reports)
LARYNGEAL HAEMORRHAGE ( 4 FDA reports)
LARYNGEAL MASS ( 4 FDA reports)
LARYNGOSCOPY ABNORMAL ( 4 FDA reports)
LARYNGOTRACHEO BRONCHITIS ( 4 FDA reports)
LARYNX IRRITATION ( 4 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE DECREASED ( 4 FDA reports)
LEISHMANIASIS ( 4 FDA reports)
LENS IMPLANT ( 4 FDA reports)
LEUKAEMIA RECURRENT ( 4 FDA reports)
LOCALISED EXFOLIATION ( 4 FDA reports)
LOCALISED SKIN REACTION ( 4 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 4 FDA reports)
LOWER URINARY TRACT SYMPTOMS ( 4 FDA reports)
LUMBAR PUNCTURE ( 4 FDA reports)
LYMPH NODE TUBERCULOSIS ( 4 FDA reports)
MALIGNANT MELANOMA STAGE IV ( 4 FDA reports)
MANDIBULOFACIAL DYSOSTOSIS ( 4 FDA reports)
MERYCISM ( 4 FDA reports)
METASTASES TO BREAST ( 4 FDA reports)
METASTASES TO GALLBLADDER ( 4 FDA reports)
METASTASES TO OVARY ( 4 FDA reports)
METASTASES TO SOFT TISSUE ( 4 FDA reports)
METATARSAL EXCISION ( 4 FDA reports)
MIDDLE EAR DISORDER ( 4 FDA reports)
MILD MENTAL RETARDATION ( 4 FDA reports)
MONONUCLEOSIS SYNDROME ( 4 FDA reports)
MUCOSAL INFECTION ( 4 FDA reports)
MULTIMORBIDITY ( 4 FDA reports)
MYOCARDIAL HAEMORRHAGE ( 4 FDA reports)
MYOKYMIA ( 4 FDA reports)
MYXOEDEMA ( 4 FDA reports)
MYXOEDEMA COMA ( 4 FDA reports)
NAIL INJURY ( 4 FDA reports)
NAIL OPERATION ( 4 FDA reports)
NASAL SINUS CANCER ( 4 FDA reports)
NECROTISING RETINITIS ( 4 FDA reports)
NEEDLE ISSUE ( 4 FDA reports)
NEONATAL ASPHYXIA ( 4 FDA reports)
NEPHRITIS AUTOIMMUNE ( 4 FDA reports)
NEPHROANGIOSCLEROSIS ( 4 FDA reports)
NEPHROSTOMY TUBE PLACEMENT ( 4 FDA reports)
NERVE ROOT INJURY ( 4 FDA reports)
NEUROBORRELIOSIS ( 4 FDA reports)
NEUROGENIC SHOCK ( 4 FDA reports)
NITRITOID REACTION ( 4 FDA reports)
NONINFECTIOUS PERITONITIS ( 4 FDA reports)
OCULAR RETROBULBAR HAEMORRHAGE ( 4 FDA reports)
OPIATES POSITIVE ( 4 FDA reports)
OPTIC NERVE CUP/DISC RATIO INCREASED ( 4 FDA reports)
OPTIC NERVE INFARCTION ( 4 FDA reports)
ORAL MUCOSAL DISORDER ( 4 FDA reports)
ORAL MUCOSAL PETECHIAE ( 4 FDA reports)
OVARIAN EPITHELIAL CANCER ( 4 FDA reports)
OXYGEN SATURATION ( 4 FDA reports)
PAIN MANAGEMENT ( 4 FDA reports)
PALINDROMIC RHEUMATISM ( 4 FDA reports)
PANCREATIC INJURY ( 4 FDA reports)
PANEL-REACTIVE ANTIBODY INCREASED ( 4 FDA reports)
PAPILLARY MUSCLE DISORDER ( 4 FDA reports)
PARAESTHESIA MUCOSAL ( 4 FDA reports)
PARAGANGLION NEOPLASM ( 4 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 4 FDA reports)
PAROTID DUCT OBSTRUCTION ( 4 FDA reports)
PENILE INFECTION ( 4 FDA reports)
PENILE OPERATION ( 4 FDA reports)
PENILE SIZE REDUCED ( 4 FDA reports)
PERIANAL ERYTHEMA ( 4 FDA reports)
PERINEAL PAIN ( 4 FDA reports)
PERIORBITAL DISORDER ( 4 FDA reports)
PERIPHERAL PARALYSIS ( 4 FDA reports)
PERITONEAL HAEMATOMA ( 4 FDA reports)
PHARYNGEAL FISTULA ( 4 FDA reports)
PHARYNGEAL LESION ( 4 FDA reports)
PHOTOCOAGULATION ( 4 FDA reports)
PHOTOSENSITIVE RASH ( 4 FDA reports)
PLATELET AGGREGATION DECREASED ( 4 FDA reports)
PLATELET AGGREGATION INHIBITION ( 4 FDA reports)
PLATELET DESTRUCTION INCREASED ( 4 FDA reports)
PLEURAL MESOTHELIOMA ( 4 FDA reports)
PLEUROPERICARDITIS ( 4 FDA reports)
PLICA SYNDROME ( 4 FDA reports)
PNEUMOCEPHALUS ( 4 FDA reports)
PNEUMONIA LIPOID ( 4 FDA reports)
POLYCHONDRITIS ( 4 FDA reports)
POLYNEUROPATHY IDIOPATHIC PROGRESSIVE ( 4 FDA reports)
POLYSEROSITIS ( 4 FDA reports)
PORTAL VEIN PHLEBITIS ( 4 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 4 FDA reports)
POST PROCEDURAL CONSTIPATION ( 4 FDA reports)
POST PROCEDURAL SWELLING ( 4 FDA reports)
POSTOPERATIVE HERNIA ( 4 FDA reports)
POSTOPERATIVE RESPIRATORY DISTRESS ( 4 FDA reports)
POVERTY OF SPEECH ( 4 FDA reports)
POVERTY OF THOUGHT CONTENT ( 4 FDA reports)
PRE-EXISTING DISEASE ( 4 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 4 FDA reports)
PRODUCT COLOUR ISSUE ( 4 FDA reports)
PRODUCT COMMINGLING ( 4 FDA reports)
PRODUCT CONTAMINATION PHYSICAL ( 4 FDA reports)
PRODUCT DEPOSIT ( 4 FDA reports)
PRODUCT LABEL ISSUE ( 4 FDA reports)
PRODUCT LABEL ON WRONG PRODUCT ( 4 FDA reports)
PRODUCT SIZE ISSUE ( 4 FDA reports)
PROSTATE CANCER STAGE I ( 4 FDA reports)
PROTEIN C DECREASED ( 4 FDA reports)
PROTEIN C DEFICIENCY ( 4 FDA reports)
PSEUDARTHROSIS ( 4 FDA reports)
PSEUDOBULBAR PALSY ( 4 FDA reports)
PSEUDODIVERTICULAR DISEASE ( 4 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE DECREASED ( 4 FDA reports)
PULMONARY NECROSIS ( 4 FDA reports)
PULMONARY RADIATION INJURY ( 4 FDA reports)
PULMONARY VASCULAR RESISTANCE ABNORMALITY ( 4 FDA reports)
RAPID CORRECTION OF HYPONATRAEMIA ( 4 FDA reports)
RASH SCARLATINIFORM ( 4 FDA reports)
RECALL PHENOMENON ( 4 FDA reports)
RECTAL CANCER RECURRENT ( 4 FDA reports)
RECTAL LESION ( 4 FDA reports)
RECTOSIGMOID CANCER ( 4 FDA reports)
RECTOSIGMOID CANCER STAGE III ( 4 FDA reports)
RECURRING SKIN BOILS ( 4 FDA reports)
RED BLOOD CELL SPHEROCYTES PRESENT ( 4 FDA reports)
RED BLOOD CELL TARGET CELLS PRESENT ( 4 FDA reports)
REFRACTORY ANAEMIA WITH RINGED SIDEROBLASTS ( 4 FDA reports)
RELATIONSHIP BREAKDOWN ( 4 FDA reports)
REMOVAL OF FOREIGN BODY ( 4 FDA reports)
RENAL CELL CARCINOMA RECURRENT ( 4 FDA reports)
RENAL CYST RUPTURED ( 4 FDA reports)
RENAL EMBOLISM ( 4 FDA reports)
RENAL SURGERY ( 4 FDA reports)
REPERFUSION INJURY ( 4 FDA reports)
RESPIRATORY FATIGUE ( 4 FDA reports)
RESPIRATORY FUME INHALATION DISORDER ( 4 FDA reports)
RESTING TREMOR ( 4 FDA reports)
RETINAL CYST ( 4 FDA reports)
RETINAL MICROANEURYSMS ( 4 FDA reports)
RETINAL PIGMENTATION ( 4 FDA reports)
RETROGNATHIA ( 4 FDA reports)
RETROPLACENTAL HAEMATOMA ( 4 FDA reports)
RHINITIS PERENNIAL ( 4 FDA reports)
ROTAVIRUS INFECTION ( 4 FDA reports)
SALMONELLA SEPSIS ( 4 FDA reports)
SALPINGO-OOPHORECTOMY ( 4 FDA reports)
SCHIZOPHRENIFORM DISORDER ( 4 FDA reports)
SCINTIGRAPHY ( 4 FDA reports)
SCROTAL ERYTHEMA ( 4 FDA reports)
SCROTAL HAEMATOCOELE ( 4 FDA reports)
SCROTAL ULCER ( 4 FDA reports)
SEBACEOUS ADENOMA ( 4 FDA reports)
SEIZURE ANOXIC ( 4 FDA reports)
SELF-INDUCED VOMITING ( 4 FDA reports)
SENSITISATION ( 4 FDA reports)
SEROCONVERSION TEST POSITIVE ( 4 FDA reports)
SERRATIA TEST POSITIVE ( 4 FDA reports)
SEXUAL RELATIONSHIP CHANGE ( 4 FDA reports)
SINUSITIS BACTERIAL ( 4 FDA reports)
SKIN STRIAE ( 4 FDA reports)
SODIUM RETENTION ( 4 FDA reports)
SPIGELIAN HERNIA ( 4 FDA reports)
SPINA BIFIDA ( 4 FDA reports)
SPINAL CORD INFARCTION ( 4 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 4 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 4 FDA reports)
SUDDEN VISUAL LOSS ( 4 FDA reports)
SUPERFICIAL INJURY OF EYE ( 4 FDA reports)
SYMBOLIC DYSFUNCTION ( 4 FDA reports)
T-CELL TYPE ACUTE LEUKAEMIA ( 4 FDA reports)
T-LYMPHOCYTE COUNT INCREASED ( 4 FDA reports)
TABLET ISSUE ( 4 FDA reports)
TENDON OPERATION ( 4 FDA reports)
TETANUS ( 4 FDA reports)
THERAPY RESPONDER ( 4 FDA reports)
THORACIC CAVITY DRAINAGE ( 4 FDA reports)
THROMBOEMBOLECTOMY ( 4 FDA reports)
THYMOMA ( 4 FDA reports)
THYROGLOBULIN INCREASED ( 4 FDA reports)
THYROID HAEMORRHAGE ( 4 FDA reports)
TRACHEAL FISTULA ( 4 FDA reports)
TRACHEOSTOMY MALFUNCTION ( 4 FDA reports)
TRAUMATIC AMPUTATION ( 4 FDA reports)
TRAUMATIC LIVER INJURY ( 4 FDA reports)
TRENDELENBURG'S SYMPTOM ( 4 FDA reports)
TRIFASCICULAR BLOCK ( 4 FDA reports)
TURNER'S SYNDROME ( 4 FDA reports)
TYMPANOSCLEROSIS ( 4 FDA reports)
ULTRASOUND DOPPLER ( 4 FDA reports)
URINARY TRACT INFLAMMATION ( 4 FDA reports)
URINARY TRACT PAIN ( 4 FDA reports)
URINE ANALYSIS ( 4 FDA reports)
ABDOMINAL WALL CYST ( 4 FDA reports)
ABDOMINAL WALL MASS ( 4 FDA reports)
ABSCESS RUPTURE ( 4 FDA reports)
ACCIDENTAL POISONING ( 4 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 4 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 4 FDA reports)
ACUTE PHASE REACTION ( 4 FDA reports)
ACUTE POLYNEUROPATHY ( 4 FDA reports)
ADENOIDECTOMY ( 4 FDA reports)
ADNEXA UTERI PAIN ( 4 FDA reports)
ADRENAL SUPPRESSION ( 4 FDA reports)
ADULT T-CELL LYMPHOMA/LEUKAEMIA ( 4 FDA reports)
ALANINE AMINOTRANSFERASE ( 4 FDA reports)
ALCOHOL DETOXIFICATION ( 4 FDA reports)
ALKALOSIS HYPOKALAEMIC ( 4 FDA reports)
ALLERGIC OEDEMA ( 4 FDA reports)
ALLERGY TEST POSITIVE ( 4 FDA reports)
ALPHA-1 ANTI-TRYPSIN DEFICIENCY ( 4 FDA reports)
ALVEOLAR PROTEINOSIS ( 4 FDA reports)
AMIMIA ( 4 FDA reports)
AMNIOTIC CAVITY INFECTION ( 4 FDA reports)
ANAL CANCER ( 4 FDA reports)
ANAL SPHINCTER HYPERTONIA ( 4 FDA reports)
ANALGESIC DRUG LEVEL ABOVE THERAPEUTIC ( 4 FDA reports)
ANGIOFIBROMA ( 4 FDA reports)
ANGIOSCLEROSIS ( 4 FDA reports)
ANOSOGNOSIA ( 4 FDA reports)
ANTI-ERYTHROCYTE ANTIBODY POSITIVE ( 4 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY ( 4 FDA reports)
ANTICOAGULANT THERAPY ( 4 FDA reports)
AORTO-DUODENAL FISTULA ( 4 FDA reports)
APPENDICEAL ABSCESS ( 4 FDA reports)
APPLICATION SITE EROSION ( 4 FDA reports)
ARM AMPUTATION ( 4 FDA reports)
ARTERIAL GRAFT ( 4 FDA reports)
ARTERITIS OBLITERANS ( 4 FDA reports)
ARTHRITIS REACTIVE ( 4 FDA reports)
ASTHMA EXERCISE INDUCED ( 4 FDA reports)
ATHETOSIS ( 4 FDA reports)
ATONIC URINARY BLADDER ( 4 FDA reports)
ATOPY ( 4 FDA reports)
ATRIAL PRESSURE INCREASED ( 4 FDA reports)
B-CELL LYMPHOMA STAGE IV ( 4 FDA reports)
BABESIOSIS ( 4 FDA reports)
BARTHOLIN'S CYST REMOVAL ( 4 FDA reports)
BARTTER'S SYNDROME ( 4 FDA reports)
BENIGN COLONIC POLYP ( 4 FDA reports)
BENIGN OVARIAN TUMOUR ( 4 FDA reports)
BENIGN PANCREATIC NEOPLASM ( 4 FDA reports)
BENIGN UTERINE NEOPLASM ( 4 FDA reports)
BETA-N-ACETYL-D-GLUCOSAMINIDASE INCREASED ( 4 FDA reports)
BEZOAR ( 4 FDA reports)
BIOPSY COLON ABNORMAL ( 4 FDA reports)
BIOPSY ENDOMETRIUM ( 4 FDA reports)
BIOPSY LIVER ( 4 FDA reports)
BIOPSY LYMPH GLAND ABNORMAL ( 4 FDA reports)
BIPOLAR II DISORDER ( 4 FDA reports)
BLADDER NEOPLASM SURGERY ( 4 FDA reports)
BLADDER TRABECULATION ( 4 FDA reports)
BLIGHTED OVUM ( 4 FDA reports)
BLOOD ALDOSTERONE INCREASED ( 4 FDA reports)
BLOOD BILIRUBIN DECREASED ( 4 FDA reports)
BLOOD BRAIN BARRIER DEFECT ( 4 FDA reports)
BLOOD CORTISOL INCREASED ( 4 FDA reports)
BLOOD ETHANOL INCREASED ( 4 FDA reports)
BLOOD IMMUNOGLOBULIN A ( 4 FDA reports)
BLOOD KETONE BODY INCREASED ( 4 FDA reports)
BLOOD MAGNESIUM ( 4 FDA reports)
BLOOD PRESSURE DIFFERENCE OF EXTREMITIES ( 4 FDA reports)
BLOOD SMEAR TEST ABNORMAL ( 4 FDA reports)
BLOOD TRIGLYCERIDES ( 4 FDA reports)
BLOOD ZINC DECREASED ( 4 FDA reports)
BONE MARROW TUMOUR CELL INFILTRATION ( 4 FDA reports)
BRACHIAL PLEXOPATHY ( 4 FDA reports)
BRANCHIAL CLEFT CYST ( 4 FDA reports)
BREAST DYSPLASIA ( 4 FDA reports)
BRONCHIAL IRRITATION ( 4 FDA reports)
BURNING FEET SYNDROME ( 4 FDA reports)
BUTTERFLY RASH ( 4 FDA reports)
C-REACTIVE PROTEIN ( 4 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 4 FDA reports)
CALCIUM IONISED DECREASED ( 4 FDA reports)
CAPILLARITIS ( 4 FDA reports)
CAPILLARY FRAGILITY INCREASED ( 4 FDA reports)
CARBOHYDRATE ANTIGEN 15-3 INCREASED ( 4 FDA reports)
CARCINOID SYNDROME ( 4 FDA reports)
CARCINOID TUMOUR OF THE STOMACH ( 4 FDA reports)
CARDIAC FIBROMA ( 4 FDA reports)
CARDIAC INDEX DECREASED ( 4 FDA reports)
CARDIAC MASSAGE ( 4 FDA reports)
CARDIAC VENTRICULOGRAM LEFT ( 4 FDA reports)
CARDIOACTIVE DRUG LEVEL ( 4 FDA reports)
CARDIOSPASM ( 4 FDA reports)
CAST APPLICATION ( 4 FDA reports)
CATARACT SUBCAPSULAR ( 4 FDA reports)
CATHETER SITE INFLAMMATION ( 4 FDA reports)
CATHETER SITE RASH ( 4 FDA reports)
CENTRAL NERVOUS SYSTEM INFLAMMATION ( 4 FDA reports)
CEPHALO-PELVIC DISPROPORTION ( 4 FDA reports)
CEREBELLAR ARTERY THROMBOSIS ( 4 FDA reports)
CEREBRAL PALSY ( 4 FDA reports)
CEREBRAL PERFUSION PRESSURE DECREASED ( 4 FDA reports)
CERVICAL CONISATION ( 4 FDA reports)
CERVICAL SPINE FLATTENING ( 4 FDA reports)
CERVIX CARCINOMA STAGE II ( 4 FDA reports)
CHOLANGITIS SCLEROSING ( 4 FDA reports)
CHONDROSARCOMA ( 4 FDA reports)
CHORIORETINAL DISORDER ( 4 FDA reports)
CHRONIC HEPATIC FAILURE ( 4 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 4 FDA reports)
COAGULATION FACTOR VII LEVEL INCREASED ( 4 FDA reports)
COLD AGGLUTININS POSITIVE ( 4 FDA reports)
COMPLEMENT FACTOR ABNORMAL ( 4 FDA reports)
COMPULSIVE SEXUAL BEHAVIOUR ( 4 FDA reports)
CONGENITAL AORTIC VALVE INCOMPETENCE ( 4 FDA reports)
CONGENITAL EYE DISORDER ( 4 FDA reports)
CONGENITAL HIP DEFORMITY ( 4 FDA reports)
CONGENITAL PULMONARY VALVE DISORDER ( 4 FDA reports)
CONSTRICTED AFFECT ( 4 FDA reports)
CONTRACTED BLADDER ( 4 FDA reports)
COPPER DEFICIENCY ( 4 FDA reports)
COW'S MILK INTOLERANCE ( 4 FDA reports)
CRANIOPHARYNGIOMA ( 4 FDA reports)
CREST SYNDROME ( 4 FDA reports)
CULDOPLASTY ( 4 FDA reports)
CYTOGENETIC ANALYSIS ABNORMAL ( 4 FDA reports)
CYTOLOGY ABNORMAL ( 4 FDA reports)
CYTOMEGALOVIRUS GASTROENTERITIS ( 4 FDA reports)
DELIVERY ( 4 FDA reports)
DELUSION OF GRANDEUR ( 4 FDA reports)
DENTAL IMPRESSION PROCEDURE ( 4 FDA reports)
DEPENDENT RUBOR ( 4 FDA reports)
DERMATITIS INFECTED ( 4 FDA reports)
DEVICE ELECTRICAL FINDING ( 4 FDA reports)
DEVICE INFUSION ISSUE ( 4 FDA reports)
DIABETIC BULLOSIS ( 4 FDA reports)
DIAGNOSTIC PROCEDURE ( 4 FDA reports)
DIALYSIS DEVICE INSERTION ( 4 FDA reports)
DIAPHRAGMALGIA ( 4 FDA reports)
DRUG DIVERSION ( 4 FDA reports)
DRUG THERAPEUTIC INCOMPATIBILITY ( 4 FDA reports)
DRUG WITHDRAWAL HEADACHE ( 4 FDA reports)
DRY SOCKET ( 4 FDA reports)
DYSACUSIS ( 4 FDA reports)
DYSSOMNIA ( 4 FDA reports)
EAR INFECTION FUNGAL ( 4 FDA reports)
EAR INFECTION VIRAL ( 4 FDA reports)
EAR IRRIGATION ( 4 FDA reports)
EDUCATIONAL PROBLEM ( 4 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ( 4 FDA reports)
ELEVATED PACING THRESHOLD ( 4 FDA reports)
ENDOMETRIAL CANCER METASTATIC ( 4 FDA reports)
ENLARGED UVULA ( 4 FDA reports)
ENTEROCOLITIS BACTERIAL ( 4 FDA reports)
ENTROPION ( 4 FDA reports)
EOSINOPHIL COUNT ABNORMAL ( 4 FDA reports)
EOSINOPHIL PERCENTAGE DECREASED ( 4 FDA reports)
EOSINOPHILIC OESOPHAGITIS ( 4 FDA reports)
EPIDERMAL GROWTH FACTOR RECEPTOR DECREASED ( 4 FDA reports)
EPIDURITIS ( 4 FDA reports)
EPIGLOTTIC CARCINOMA ( 4 FDA reports)
EVANS SYNDROME ( 4 FDA reports)
EXERCISE ELECTROCARDIOGRAM ( 4 FDA reports)
EXPOSURE TO COMMUNICABLE DISEASE ( 4 FDA reports)
EXTRAVASATION BLOOD ( 4 FDA reports)
EYE DEGENERATIVE DISORDER ( 4 FDA reports)
FABRY'S DISEASE ( 4 FDA reports)
FACTOR V INHIBITION ( 4 FDA reports)
FAECAL VOLUME DECREASED ( 4 FDA reports)
FALLOPIAN TUBE DISORDER ( 4 FDA reports)
FALSE POSITIVE INVESTIGATION RESULT ( 4 FDA reports)
FAT REDISTRIBUTION ( 4 FDA reports)
FIBRINOLYSIS ( 4 FDA reports)
FINE MOTOR DELAY ( 4 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III ( 4 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III STAGE IV ( 4 FDA reports)
FOOT CRUSHING ( 4 FDA reports)
FUNGAL TEST POSITIVE ( 4 FDA reports)
FUSARIUM INFECTION ( 4 FDA reports)
FUSOBACTERIUM INFECTION ( 4 FDA reports)
GALLSTONE ILEUS ( 4 FDA reports)
GALLSTONES IN BILE DUCT REMOVAL ( 4 FDA reports)
GAS POISONING ( 4 FDA reports)
GASTRIC CANCER STAGE IV ( 4 FDA reports)
GASTRODUODENITIS HAEMORRHAGIC ( 4 FDA reports)
GASTROINTESTINAL FISTULA ( 4 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 4 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 4 FDA reports)
GASTROINTESTINAL TRACT MUCOSAL DISCOLOURATION ( 4 FDA reports)
GASTROINTESTINAL ULCER PERFORATION ( 4 FDA reports)
GASTROOESOPHAGEAL SPHINCTER INSUFFICIENCY ( 4 FDA reports)
GENE MUTATION ( 4 FDA reports)
GENERAL ANAESTHESIA ( 4 FDA reports)
GENITAL DISCOMFORT ( 4 FDA reports)
GENITAL DISORDER MALE ( 4 FDA reports)
GENITAL INFECTION FUNGAL ( 4 FDA reports)
GENITAL ULCERATION ( 4 FDA reports)
GINGIVAL DISCOLOURATION ( 4 FDA reports)
GINGIVAL OPERATION ( 4 FDA reports)
GLIOSARCOMA ( 4 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 4 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 4 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 4 FDA reports)
GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY ( 4 FDA reports)
GLYCOSYLATED HAEMOGLOBIN ( 4 FDA reports)
GRAFT HAEMORRHAGE ( 4 FDA reports)
GRANULOMA SKIN ( 4 FDA reports)
GUTTATE PSORIASIS ( 4 FDA reports)
HAEMATOCRIT ( 4 FDA reports)
HAIRY CELL LEUKAEMIA ( 4 FDA reports)
HALITOSIS ( 4 FDA reports)
HAND DERMATITIS ( 4 FDA reports)
HEAD TITUBATION ( 4 FDA reports)
HEARING AID USER ( 4 FDA reports)
HEART BLOCK CONGENITAL ( 4 FDA reports)
HEAT EXPOSURE INJURY ( 4 FDA reports)
HEMISENSORY NEGLECT ( 4 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST POSITIVE ( 4 FDA reports)
HEPATIC EMBOLISATION ( 4 FDA reports)
HEPATIC ENZYME DECREASED ( 4 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 4 FDA reports)
HEPATITIS NON-A NON-B NON-C ( 4 FDA reports)
HERPES PHARYNGITIS ( 4 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 4 FDA reports)
HERPES ZOSTER OTICUS ( 4 FDA reports)
HERPETIC STOMATITIS ( 4 FDA reports)
HUNTINGTON'S DISEASE ( 4 FDA reports)
HYDROTHORAX ( 4 FDA reports)
HYPERLIPASAEMIA ( 4 FDA reports)
HYPERTELORISM OF ORBIT ( 4 FDA reports)
HYPERTENSIVE CARDIOMEGALY ( 4 FDA reports)
ILEAL ULCER PERFORATION ( 4 FDA reports)
IMPINGEMENT SYNDROME ( 4 FDA reports)
ABORTION INCOMPLETE ( 3 FDA reports)
ABORTION MISSED ( 3 FDA reports)
ABSCESS BACTERIAL ( 3 FDA reports)
ABULIA ( 3 FDA reports)
ACCESSORY SPLEEN ( 3 FDA reports)
ACID FAST STAIN POSITIVE ( 3 FDA reports)
ACOUSTIC NEUROMA ( 3 FDA reports)
ACQUIRED CARDIAC SEPTAL DEFECT ( 3 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 3 FDA reports)
ACQUIRED VON WILLEBRAND'S DISEASE ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 3 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 3 FDA reports)
ACUTE RIGHT VENTRICULAR FAILURE ( 3 FDA reports)
ACUTE TONSILLITIS ( 3 FDA reports)
ADENOCARCINOMA OF THE CERVIX ( 3 FDA reports)
ADENOIDAL HYPERTROPHY ( 3 FDA reports)
ADENOSQUAMOUS CELL LUNG CANCER ( 3 FDA reports)
ADENOTONSILLECTOMY ( 3 FDA reports)
ADJUSTMENT DISORDER WITH ANXIETY ( 3 FDA reports)
ADMINISTRATION SITE PAIN ( 3 FDA reports)
ALCOHOL INTOLERANCE ( 3 FDA reports)
ALLERGY TO ARTHROPOD STING ( 3 FDA reports)
ALLOIMMUNISATION ( 3 FDA reports)
ALOPECIA TOTALIS ( 3 FDA reports)
AMINO ACID LEVEL INCREASED ( 3 FDA reports)
AMMONIA ABNORMAL ( 3 FDA reports)
AMNIOCENTESIS ABNORMAL ( 3 FDA reports)
ANAESTHESIA ( 3 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 3 FDA reports)
ANAL ULCER ( 3 FDA reports)
ANAL ULCER HAEMORRHAGE ( 3 FDA reports)
ANALGESIC THERAPY ( 3 FDA reports)
ANDROGENETIC ALOPECIA ( 3 FDA reports)
ANEURYSM ARTERIOVENOUS ( 3 FDA reports)
ANEURYSMECTOMY ( 3 FDA reports)
ANGIOCENTRIC LYMPHOMA ( 3 FDA reports)
ANGIOGRAM PULMONARY ( 3 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INCREASED ( 3 FDA reports)
ANORECTAL CELLULITIS ( 3 FDA reports)
ANTERIOR CHAMBER DISORDER ( 3 FDA reports)
ANTI-HBC IGG ANTIBODY POSITIVE ( 3 FDA reports)
ANTIACETYLCHOLINE RECEPTOR ANTIBODY POSITIVE ( 3 FDA reports)
ANTIBIOTIC LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
ANTIDIURETIC HORMONE ABNORMALITY ( 3 FDA reports)
ANTISOCIAL PERSONALITY DISORDER ( 3 FDA reports)
AORTIC SURGERY ( 3 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 3 FDA reports)
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA ( 3 FDA reports)
ARTERITIS CORONARY ( 3 FDA reports)
ARTHROFIBROSIS ( 3 FDA reports)
ARTICULAR CALCIFICATION ( 3 FDA reports)
ASPIRATION PLEURAL CAVITY ABNORMAL ( 3 FDA reports)
ASPIRATION TRACHEAL ( 3 FDA reports)
ATRIAL SEPTAL DEFECT REPAIR ( 3 FDA reports)
ATROPHIE BLANCHE ( 3 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 3 FDA reports)
AUDIOGRAM ABNORMAL ( 3 FDA reports)
AUTOSOMAL CHROMOSOME ANOMALY ( 3 FDA reports)
AVERSION ( 3 FDA reports)
B-CELL UNCLASSIFIABLE LYMPHOMA LOW GRADE ( 3 FDA reports)
BACILLUS TEST POSITIVE ( 3 FDA reports)
BACTERIA TISSUE SPECIMEN IDENTIFIED ( 3 FDA reports)
BACTERIAL PERICARDITIS ( 3 FDA reports)
BALLISMUS ( 3 FDA reports)
BASE EXCESS POSITIVE ( 3 FDA reports)
BASOPHIL PERCENTAGE INCREASED ( 3 FDA reports)
BENIGN GASTRIC NEOPLASM ( 3 FDA reports)
BENIGN NEOPLASM OF BLADDER ( 3 FDA reports)
BILIARY CANCER METASTATIC ( 3 FDA reports)
BILIARY SPHINCTEROTOMY ( 3 FDA reports)
BIOPSY ARTERY ( 3 FDA reports)
BIOPSY BRAIN ABNORMAL ( 3 FDA reports)
BIOPSY BRONCHUS ABNORMAL ( 3 FDA reports)
BIOPSY COLON ( 3 FDA reports)
BIOPSY OESOPHAGUS ABNORMAL ( 3 FDA reports)
BIOPSY PROSTATE ( 3 FDA reports)
BIOPSY STOMACH ABNORMAL ( 3 FDA reports)
BLADDER CANCER STAGE 0, WITH CANCER IN SITU ( 3 FDA reports)
BLADDER CANCER STAGE III ( 3 FDA reports)
BLEEDING VARICOSE VEIN ( 3 FDA reports)
BLEPHARAL PAPILLOMA ( 3 FDA reports)
BLEPHAROPLASTY ( 3 FDA reports)
BLOOD ACID PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD ALCOHOL ( 3 FDA reports)
BLOOD ANTIDIURETIC HORMONE DECREASED ( 3 FDA reports)
BLOOD BICARBONATE ABNORMAL ( 3 FDA reports)
BLOOD CHLORIDE ABNORMAL ( 3 FDA reports)
BLOOD CHOLINESTERASE INCREASED ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ABNORMAL ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MM INCREASED ( 3 FDA reports)
BLOOD HOMOCYSTEINE ( 3 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN ABNORMAL ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN G ( 3 FDA reports)
BLOOD KETONE BODY PRESENT ( 3 FDA reports)
BLOOD METHAEMOGLOBIN PRESENT ( 3 FDA reports)
BLOOD THROMBIN ABNORMAL ( 3 FDA reports)
BLOOD URIC ACID ABNORMAL ( 3 FDA reports)
BONE FISSURE ( 3 FDA reports)
BRACHYTHERAPY ( 3 FDA reports)
BRAIN NATRIURETIC PEPTIDE ( 3 FDA reports)
BRANCHIAL CYST ( 3 FDA reports)
BREAST DISCOLOURATION ( 3 FDA reports)
BREAST INDURATION ( 3 FDA reports)
BREATH SOUNDS ( 3 FDA reports)
BREATH SOUNDS ABSENT ( 3 FDA reports)
BREECH PRESENTATION ( 3 FDA reports)
BRONCHIAL OEDEMA ( 3 FDA reports)
BRONCHITIS FUNGAL ( 3 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 3 FDA reports)
BURNOUT SYNDROME ( 3 FDA reports)
CALCIFIC DEPOSITS REMOVAL ( 3 FDA reports)
CAMPYLOBACTER INTESTINAL INFECTION ( 3 FDA reports)
CAPSULE PHYSICAL ISSUE ( 3 FDA reports)
CARBOXYHAEMOGLOBIN INCREASED ( 3 FDA reports)
CARCINOID HEART DISEASE ( 3 FDA reports)
CARCINOID TUMOUR OF THE PANCREAS ( 3 FDA reports)
CARCINOMA IN SITU OF SKIN ( 3 FDA reports)
CARDIAC FAILURE HIGH OUTPUT ( 3 FDA reports)
CARDIAC IMAGING PROCEDURE ABNORMAL ( 3 FDA reports)
CARDIOPULMONARY BYPASS ( 3 FDA reports)
CARDIOTHORACIC RATIO INCREASED ( 3 FDA reports)
CAROTID ANEURYSM RUPTURE ( 3 FDA reports)
CASTLEMAN'S DISEASE ( 3 FDA reports)
CAT SCRATCH DISEASE ( 3 FDA reports)
CATABOLIC STATE ( 3 FDA reports)
CATARACT DIABETIC ( 3 FDA reports)
CATHETER SITE NECROSIS ( 3 FDA reports)
CELLULITIS GANGRENOUS ( 3 FDA reports)
CELLULITIS STREPTOCOCCAL ( 3 FDA reports)
CENTRAL PAIN SYNDROME ( 3 FDA reports)
CENTRAL-ALVEOLAR HYPOVENTILATION ( 3 FDA reports)
CEREBELLAR TUMOUR ( 3 FDA reports)
CEREBRAL AMYLOID ANGIOPATHY ( 3 FDA reports)
CEREBRAL ARTERIOVENOUS MALFORMATION HAEMORRHAGIC ( 3 FDA reports)
CERVICAL POLYP ( 3 FDA reports)
CERVIX CARCINOMA STAGE I ( 3 FDA reports)
CHEMICAL BURN OF SKIN ( 3 FDA reports)
CHEST EXPANSION DECREASED ( 3 FDA reports)
CHEST WALL ABSCESS ( 3 FDA reports)
CHOLANGITIS SUPPURATIVE ( 3 FDA reports)
CHOLEDOCHOLITHOTOMY ( 3 FDA reports)
CHONDROSIS ( 3 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 3 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA TRANSFORMATION ( 3 FDA reports)
COAGULATION FACTOR DECREASED ( 3 FDA reports)
COAGULATION FACTOR V LEVEL ABNORMAL ( 3 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 3 FDA reports)
COAGULATION FACTOR XIII LEVEL DECREASED ( 3 FDA reports)
COLECTOMY PARTIAL ( 3 FDA reports)
COLITIS VIRAL ( 3 FDA reports)
COLLATERAL CIRCULATION ( 3 FDA reports)
COLORECTAL CANCER RECURRENT ( 3 FDA reports)
COMPLEMENT FACTOR C3 INCREASED ( 3 FDA reports)
COMPLEMENT FACTOR DECREASED ( 3 FDA reports)
COMPLICATION OF PREGNANCY ( 3 FDA reports)
CONGENITAL EYE NAEVUS ( 3 FDA reports)
CONGENITAL MITRAL VALVE INCOMPETENCE ( 3 FDA reports)
CONGENITAL NOSE MALFORMATION ( 3 FDA reports)
CONGENITAL PYELOCALIECTASIS ( 3 FDA reports)
CONNECTIVE TISSUE INFLAMMATION ( 3 FDA reports)
CONUS MEDULLARIS SYNDROME ( 3 FDA reports)
CORNEAL EPITHELIUM DEFECT ( 3 FDA reports)
CORNEAL LESION ( 3 FDA reports)
CORNEAL PIGMENTATION ( 3 FDA reports)
CORNEAL STRIAE ( 3 FDA reports)
CORONARY ARTERY DILATATION ( 3 FDA reports)
CRANIOSYNOSTOSIS ( 3 FDA reports)
CREATININE RENAL CLEARANCE ( 3 FDA reports)
CREATININE URINE DECREASED ( 3 FDA reports)
CRUSH SYNDROME ( 3 FDA reports)
CRYOTHERAPY ( 3 FDA reports)
CRYPTOCOCCOSIS ( 3 FDA reports)
CSF CELL COUNT INCREASED ( 3 FDA reports)
CULTURE TISSUE SPECIMEN POSITIVE ( 3 FDA reports)
DEATH OF COMPANION ( 3 FDA reports)
DECREASED VIBRATORY SENSE ( 3 FDA reports)
DEFICIENCY ANAEMIA ( 3 FDA reports)
DEFORMITY THORAX ( 3 FDA reports)
DEHYDROEPIANDROSTERONE INCREASED ( 3 FDA reports)
DERMABRASION ( 3 FDA reports)
DERMATILLOMANIA ( 3 FDA reports)
DERMATITIS DIAPER ( 3 FDA reports)
DETOXIFICATION ( 3 FDA reports)
DEVICE ADHESION ISSUE ( 3 FDA reports)
DEVICE CAPTURING ISSUE ( 3 FDA reports)
DEVICE DIFFICULT TO USE ( 3 FDA reports)
DEVICE MIGRATION ( 3 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 3 FDA reports)
DIABETIC BLINDNESS ( 3 FDA reports)
DIABETIC END STAGE RENAL DISEASE ( 3 FDA reports)
DIASTOLIC HYPOTENSION ( 3 FDA reports)
DIGEORGE'S SYNDROME ( 3 FDA reports)
DIPHTHERIA ( 3 FDA reports)
DIRECTIONAL DOPPLER FLOW TESTS ABNORMAL ( 3 FDA reports)
DIVERTICULAR HERNIA ( 3 FDA reports)
DIVERTICULUM GASTRIC ( 3 FDA reports)
DIVORCED ( 3 FDA reports)
DRUG CHEMICAL INCOMPATIBILITY ( 3 FDA reports)
DRUG DELIVERY DEVICE IMPLANTATION ( 3 FDA reports)
DRUG THERAPY CHANGED ( 3 FDA reports)
DUANE'S SYNDROME ( 3 FDA reports)
DUCTUS ARTERIOSUS PREMATURE CLOSURE ( 3 FDA reports)
DUODENOGASTRIC REFLUX ( 3 FDA reports)
DYSPRAXIA ( 3 FDA reports)
EAR INFECTION STAPHYLOCOCCAL ( 3 FDA reports)
EASTERN COOPERATIVE ONCOLOGY GROUP PERFORMANCE STATUS WORSENED ( 3 FDA reports)
ECZEMA WEEPING ( 3 FDA reports)
ELBOW DEFORMITY ( 3 FDA reports)
ELECTROCARDIOGRAM ( 3 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL ( 3 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ELEVATION ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE BIPHASIC ( 3 FDA reports)
ENCEPHALITIC INFECTION ( 3 FDA reports)
ENCOPRESIS ( 3 FDA reports)
ENDOMETRITIS ( 3 FDA reports)
ENTEROCOLITIS VIRAL ( 3 FDA reports)
ENTEROSTOMY ( 3 FDA reports)
EOSINOPHILIC PNEUMONIA ACUTE ( 3 FDA reports)
EPENDYMOMA ( 3 FDA reports)
EPIDIDYMAL ENLARGEMENT ( 3 FDA reports)
EPISPADIAS ( 3 FDA reports)
EPITHELIOID SARCOMA ( 3 FDA reports)
EPULIS ( 3 FDA reports)
ERYTHEMA ANNULARE ( 3 FDA reports)
ERYTHEMA INDURATUM ( 3 FDA reports)
EXECUTIVE DYSFUNCTION ( 3 FDA reports)
EXTERNAL EAR CELLULITIS ( 3 FDA reports)
EXTRAVASCULAR HAEMOLYSIS ( 3 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 3 FDA reports)
EYELID PAIN ( 3 FDA reports)
EYES SUNKEN ( 3 FDA reports)
FACTOR V DEFICIENCY ( 3 FDA reports)
FACTOR VIII INHIBITION ( 3 FDA reports)
FAECAL DISIMPACTION ( 3 FDA reports)
FAILED INDUCTION OF LABOUR ( 3 FDA reports)
FALLOPIAN TUBE CANCER ( 3 FDA reports)
FAMILIAL TREMOR ( 3 FDA reports)
FEBRILE BONE MARROW APLASIA ( 3 FDA reports)
FEEDING DISORDER OF INFANCY OR EARLY CHILDHOOD ( 3 FDA reports)
FEMORAL ARTERY DISSECTION ( 3 FDA reports)
FIBRINOLYSIS INCREASED ( 3 FDA reports)
FLUID INTAKE RESTRICTION ( 3 FDA reports)
FOETAL CEREBROVASCULAR DISORDER ( 3 FDA reports)
FOETAL DISTRESS SYNDROME ( 3 FDA reports)
FOETAL MOVEMENTS DECREASED ( 3 FDA reports)
FOETOR HEPATICUS ( 3 FDA reports)
FULL BLOOD COUNT INCREASED ( 3 FDA reports)
FUNCTIONAL RESIDUAL CAPACITY DECREASED ( 3 FDA reports)
FUNGUS SPUTUM TEST POSITIVE ( 3 FDA reports)
GAIT DEVIATION ( 3 FDA reports)
GALLBLADDER FISTULA ( 3 FDA reports)
GASTRIC ATONY ( 3 FDA reports)
GASTRIC CANCER STAGE II ( 3 FDA reports)
GASTRIC ILEUS ( 3 FDA reports)
GASTRIC LAVAGE ABNORMAL ( 3 FDA reports)
GASTRIC OPERATION ( 3 FDA reports)
GASTRIC PH INCREASED ( 3 FDA reports)
GASTRITIS VIRAL ( 3 FDA reports)
GASTROENTERITIS EOSINOPHILIC ( 3 FDA reports)
GASTROINTESTINAL DISORDER POSTOPERATIVE ( 3 FDA reports)
GASTROINTESTINAL GANGRENE ( 3 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 3 FDA reports)
GENITAL DISORDER FEMALE ( 3 FDA reports)
GERM CELL CANCER ( 3 FDA reports)
GERSTMANN'S SYNDROME ( 3 FDA reports)
GIGANTISM ( 3 FDA reports)
GLOMERULONEPHRITIS CHRONIC ( 3 FDA reports)
GLOMERULONEPHROPATHY ( 3 FDA reports)
GLOSSOPHARYNGEAL NEURALGIA ( 3 FDA reports)
GRAFT LOSS ( 3 FDA reports)
HAEMATINURIA ( 3 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 3 FDA reports)
HAEMOGLOBIN S DECREASED ( 3 FDA reports)
HAEMOGLOBIN URINE PRESENT ( 3 FDA reports)
HAEMORRHAGIC ARTERIOVENOUS MALFORMATION ( 3 FDA reports)
HAEMOSTASIS ( 3 FDA reports)
HAMARTOMA ( 3 FDA reports)
HEART RATE ( 3 FDA reports)
HEAVY EXPOSURE TO ULTRAVIOLET LIGHT ( 3 FDA reports)
HEPATIC ARTERY STENOSIS ( 3 FDA reports)
HEPATIC CYST RUPTURED ( 3 FDA reports)
HEPATITIS B POSITIVE ( 3 FDA reports)
HEPATO-LENTICULAR DEGENERATION ( 3 FDA reports)
HERPES OESOPHAGITIS ( 3 FDA reports)
HIGH TURNOVER OSTEOPATHY ( 3 FDA reports)
HIP DEFORMITY ( 3 FDA reports)
HISTONE ANTIBODY POSITIVE ( 3 FDA reports)
HODGKIN'S DISEASE NODULAR SCLEROSIS STAGE UNSPECIFIED ( 3 FDA reports)
HODGKIN'S DISEASE STAGE III ( 3 FDA reports)
HOMELESS ( 3 FDA reports)
HYPERCREATINAEMIA ( 3 FDA reports)
HYPNAGOGIC HALLUCINATION ( 3 FDA reports)
HYPOALDOSTERONISM ( 3 FDA reports)
HYPOCOMPLEMENTAEMIA ( 3 FDA reports)
HYPOHIDROSIS ( 3 FDA reports)
HYPONATRAEMIC ENCEPHALOPATHY ( 3 FDA reports)
HYPOPLASTIC ANAEMIA ( 3 FDA reports)
HYPOPROTHROMBINAEMIA ( 3 FDA reports)
HYPOSIDERAEMIA ( 3 FDA reports)
HYPOSPADIAS ( 3 FDA reports)
HYPOTHALAMO-PITUITARY DISORDERS ( 3 FDA reports)
IMMEDIATE POST-INJECTION REACTION ( 3 FDA reports)
IMMUNOLOGY TEST ( 3 FDA reports)
IMPAIRED INSULIN SECRETION ( 3 FDA reports)
URINE KETONE BODY ( 3 FDA reports)
URINE OXALATE ( 3 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 3 FDA reports)
URINE SODIUM ABNORMAL ( 3 FDA reports)
UROBILIN URINE PRESENT ( 3 FDA reports)
UROGENITAL DISORDER ( 3 FDA reports)
UTERINE MASS ( 3 FDA reports)
UTEROVAGINAL PROLAPSE ( 3 FDA reports)
VACCINATION COMPLICATION ( 3 FDA reports)
VAGINAL MUCOSAL BLISTERING ( 3 FDA reports)
VANISHING BILE DUCT SYNDROME ( 3 FDA reports)
VASCULAR CAUTERISATION ( 3 FDA reports)
VASCULAR PUNCTURE SITE SEALING ( 3 FDA reports)
VEILLONELLA INFECTION ( 3 FDA reports)
VELOPHARYNGEAL INCOMPETENCE ( 3 FDA reports)
VENOUS LAKE ( 3 FDA reports)
VENOUS PRESSURE INCREASED ( 3 FDA reports)
VENOUS PRESSURE JUGULAR ABNORMAL ( 3 FDA reports)
VENOUS RECANALISATION ( 3 FDA reports)
VENOUS VALVE RUPTURED ( 3 FDA reports)
VENTRICULAR SEPTAL DEFECT ACQUIRED ( 3 FDA reports)
VERTIGO LABYRINTHINE ( 3 FDA reports)
VESTIBULITIS ( 3 FDA reports)
VIRAL SINUSITIS ( 3 FDA reports)
VIRAL SKIN INFECTION ( 3 FDA reports)
VISCERAL ARTERIAL ISCHAEMIA ( 3 FDA reports)
VITAMIN B1 DEFICIENCY ( 3 FDA reports)
VITAMIN C DECREASED ( 3 FDA reports)
VOLVULUS OF BOWEL ( 3 FDA reports)
VON HIPPEL-LINDAU DISEASE ( 3 FDA reports)
VULVAL ABSCESS ( 3 FDA reports)
VULVAL OEDEMA ( 3 FDA reports)
VULVAR EROSION ( 3 FDA reports)
VULVOVAGINAL SWELLING ( 3 FDA reports)
WARM TYPE HAEMOLYTIC ANAEMIA ( 3 FDA reports)
XERODERMA ( 3 FDA reports)
YERSINIA INFECTION ( 3 FDA reports)
INFANTILE APNOEIC ATTACK ( 3 FDA reports)
INFERIOR VENA CAVA DILATATION ( 3 FDA reports)
INFERTILITY MALE ( 3 FDA reports)
INFUSION SITE MASS ( 3 FDA reports)
INFUSION SITE URTICARIA ( 3 FDA reports)
INGROWN HAIR ( 3 FDA reports)
INJECTION SITE CYST ( 3 FDA reports)
INJECTION SITE INJURY ( 3 FDA reports)
INJECTION SITE LACERATION ( 3 FDA reports)
INJECTION SITE MOVEMENT IMPAIRMENT ( 3 FDA reports)
INJECTION SITE PALLOR ( 3 FDA reports)
INJECTION SITE STREAKING ( 3 FDA reports)
INSTILLATION SITE PAIN ( 3 FDA reports)
INSULIN RESISTANT DIABETES ( 3 FDA reports)
INSULIN-REQUIRING TYPE II DIABETES MELLITUS ( 3 FDA reports)
INTERMEDIATE UVEITIS ( 3 FDA reports)
INTESTINAL ADHESION LYSIS ( 3 FDA reports)
INTESTINAL STOMA COMPLICATION ( 3 FDA reports)
INTESTINAL ULCER PERFORATION ( 3 FDA reports)
INTRA-ABDOMINAL PRESSURE INCREASED ( 3 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE EXPELLED ( 3 FDA reports)
INTRACRANIAL INJURY ( 3 FDA reports)
INTRAOCULAR PRESSURE FLUCTUATION ( 3 FDA reports)
IODINE UPTAKE INCREASED ( 3 FDA reports)
KIDNEY RUPTURE ( 3 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 3 FDA reports)
LACRIMAL GLAND ENLARGEMENT ( 3 FDA reports)
LARGE GRANULAR LYMPHOCYTOSIS ( 3 FDA reports)
LAXATIVE ABUSE ( 3 FDA reports)
LENNOX-GASTAUT SYNDROME ( 3 FDA reports)
LICHEN SCLEROSUS ( 3 FDA reports)
LID LAG ( 3 FDA reports)
LIGAMENT LAXITY ( 3 FDA reports)
LIMB IMMOBILISATION ( 3 FDA reports)
LIP AND/OR ORAL CAVITY CANCER STAGE IV ( 3 FDA reports)
LIPIDS DECREASED ( 3 FDA reports)
LIPOEDEMA ( 3 FDA reports)
LIPOMATOUS HYPERTROPHY OF THE INTERATRIAL SEPTUM ( 3 FDA reports)
LISTERIA SEPSIS ( 3 FDA reports)
LOWER RESPIRATORY TRACT INFECTION BACTERIAL ( 3 FDA reports)
LUMBOSACRAL PLEXUS INJURY ( 3 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE I ( 3 FDA reports)
LUPUS VASCULITIS ( 3 FDA reports)
LYMPH NODE CANCER METASTATIC ( 3 FDA reports)
LYMPH NODE PALPABLE ( 3 FDA reports)
LYMPHOCYTE COUNT ( 3 FDA reports)
MACROANGIOPATHY ( 3 FDA reports)
MACROCEPHALY ( 3 FDA reports)
MACULAR CYST ( 3 FDA reports)
MALE ORGASMIC DISORDER ( 3 FDA reports)
MALE SEXUAL DYSFUNCTION ( 3 FDA reports)
MALIGNANT NEOPLASM OF SPINAL CORD ( 3 FDA reports)
MEDIAN NERVE INJURY ( 3 FDA reports)
MEDIASTINAL FIBROSIS ( 3 FDA reports)
MEDICAL OBSERVATION ( 3 FDA reports)
MELANOMA RECURRENT ( 3 FDA reports)
MENINGITIS TUBERCULOUS ( 3 FDA reports)
MENINGOCOCCAL SEPSIS ( 3 FDA reports)
MENTAL DISABILITY ( 3 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 3 FDA reports)
METAMYELOCYTE COUNT INCREASED ( 3 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 3 FDA reports)
METASTASES TO EYE ( 3 FDA reports)
METASTASES TO SALIVARY GLAND ( 3 FDA reports)
METASTASES TO SKIN ( 3 FDA reports)
METASTASES TO SMALL INTESTINE ( 3 FDA reports)
METASTATIC CARCINOMA OF THE BLADDER ( 3 FDA reports)
MICROLITHIASIS ( 3 FDA reports)
MITOCHONDRIAL TOXICITY ( 3 FDA reports)
MIXED INCONTINENCE ( 3 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 3 FDA reports)
MORAXELLA INFECTION ( 3 FDA reports)
MUCOSAL EXFOLIATION ( 3 FDA reports)
MUSCLE FIBROSIS ( 3 FDA reports)
MYELOBLAST COUNT INCREASED ( 3 FDA reports)
MYOCARDIAL STRAIN ( 3 FDA reports)
NAIL BED BLEEDING ( 3 FDA reports)
NAIL BED INFECTION ( 3 FDA reports)
NAIL PIGMENTATION ( 3 FDA reports)
NAIL TINEA ( 3 FDA reports)
NASAL MUCOSA ATROPHY ( 3 FDA reports)
NASAL SEPTUM ULCERATION ( 3 FDA reports)
NATURAL KILLER-CELL LEUKAEMIA ( 3 FDA reports)
NECK DEFORMITY ( 3 FDA reports)
NEISSERIA INFECTION ( 3 FDA reports)
NEONATAL EXCHANGE BLOOD TRANSFUSION ( 3 FDA reports)
NEPHROSTOMY ( 3 FDA reports)
NERVE DEGENERATION ( 3 FDA reports)
NEURALGIC AMYOTROPHY ( 3 FDA reports)
NODULAR VASCULITIS ( 3 FDA reports)
NORMAL DELIVERY ( 3 FDA reports)
OCULOGYRATION ( 3 FDA reports)
OCULOGYRIC CRISIS ( 3 FDA reports)
OESOPHAGEAL DILATION PROCEDURE ( 3 FDA reports)
OESOPHAGEAL DYSPLASIA ( 3 FDA reports)
OMENTUM NEOPLASM ( 3 FDA reports)
OPISTHOTONUS ( 3 FDA reports)
ORAL LICHEN PLANUS ( 3 FDA reports)
ORAL MUCOSAL ERUPTION ( 3 FDA reports)
OROPHARYNGEAL NEOPLASM ( 3 FDA reports)
OSTEOCHONDROMA ( 3 FDA reports)
OSTEOMA ( 3 FDA reports)
OXYGEN SATURATION IMMEASURABLE ( 3 FDA reports)
PACING THRESHOLD DECREASED ( 3 FDA reports)
PANCREATIC OPERATION ( 3 FDA reports)
PANIC DISORDER WITHOUT AGORAPHOBIA ( 3 FDA reports)
PAPILLITIS ( 3 FDA reports)
PARANEOPLASTIC DERMATOMYOSITIS ( 3 FDA reports)
PARAPHARYNGEAL ABSCESS ( 3 FDA reports)
PARATHYROID GLAND ENLARGEMENT ( 3 FDA reports)
PARIETAL CELL ANTIBODY POSITIVE ( 3 FDA reports)
PARVOVIRUS B19 TEST POSITIVE ( 3 FDA reports)
PASSIVE SMOKING ( 3 FDA reports)
PATIENT-DEVICE INCOMPATIBILITY ( 3 FDA reports)
PCO2 ABNORMAL ( 3 FDA reports)
PENILE ABSCESS ( 3 FDA reports)
PENILE DISCHARGE ( 3 FDA reports)
PENILE VEIN THROMBOSIS ( 3 FDA reports)
PEPTIC ULCER REACTIVATED ( 3 FDA reports)
PERICARDITIS INFECTIVE ( 3 FDA reports)
PERINEAL OPERATION ( 3 FDA reports)
PERIPHERAL ARTERY DISSECTION ( 3 FDA reports)
PERIPHERAL NERVE OPERATION ( 3 FDA reports)
PERIPHERAL REVASCULARISATION ( 3 FDA reports)
PERITONEAL NEOPLASM ( 3 FDA reports)
PH BODY FLUID DECREASED ( 3 FDA reports)
PH URINE INCREASED ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 3 FDA reports)
PHARYNGEAL EROSION ( 3 FDA reports)
PHOBIC AVOIDANCE ( 3 FDA reports)
PITUITARY INFARCTION ( 3 FDA reports)
PITUITARY TUMOUR RECURRENT ( 3 FDA reports)
PLASMA CELL DISORDER ( 3 FDA reports)
PLATELET MORPHOLOGY ABNORMAL ( 3 FDA reports)
PLATELET PRODUCTION DECREASED ( 3 FDA reports)
PLATELETCRIT DECREASED ( 3 FDA reports)
PNEUMATURIA ( 3 FDA reports)
PNEUMONIA CHLAMYDIAL ( 3 FDA reports)
POLYARTERITIS NODOSA ( 3 FDA reports)
POLYMENORRHOEA ( 3 FDA reports)
POLYOMAVIRUS-ASSOCIATED NEPHROPATHY ( 3 FDA reports)
POPLITEAL PULSE DECREASED ( 3 FDA reports)
POST PROCEDURAL SEPSIS ( 3 FDA reports)
POSTICTAL PARALYSIS ( 3 FDA reports)
POSTOPERATIVE HETEROTOPIC CALCIFICATION ( 3 FDA reports)
POSTPARTUM SEPSIS ( 3 FDA reports)
PRECANCEROUS MUCOSAL LESION ( 3 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 3 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 3 FDA reports)
PRODUCT DROPPER ISSUE ( 3 FDA reports)
PRODUCT TAMPERING ( 3 FDA reports)
PROLAPSE REPAIR ( 3 FDA reports)
PROSTATE CANCER STAGE II ( 3 FDA reports)
PROSTATIC INTRAEPITHELIAL NEOPLASIA ( 3 FDA reports)
PROSTHESIS USER ( 3 FDA reports)
PROSTRATION ( 3 FDA reports)
PROTEIN C INCREASED ( 3 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 3 FDA reports)
PSEUDOEXFOLIATION OF LENS CAPSULE ( 3 FDA reports)
PSEUDOPOLYP ( 3 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 3 FDA reports)
PSYCHIATRIC EVALUATION ABNORMAL ( 3 FDA reports)
PSYCHOMOTOR AGITATION ( 3 FDA reports)
PSYCHOSEXUAL DISORDER ( 3 FDA reports)
PULMONARY FUNCTION TEST INCREASED ( 3 FDA reports)
PULMONARY MALFORMATION ( 3 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 3 FDA reports)
Q FEVER ( 3 FDA reports)
RADIATION SICKNESS SYNDROME ( 3 FDA reports)
RADIOACTIVE IODINE THERAPY ( 3 FDA reports)
RASH FOLLICULAR ( 3 FDA reports)
REACTION TO COLOURING ( 3 FDA reports)
RECTAL NEOPLASM ( 3 FDA reports)
RED BLOOD CELL ANISOCYTES PRESENT ( 3 FDA reports)
RED BLOOD CELL MACROCYTES PRESENT ( 3 FDA reports)
RED CELL DISTRIBUTION WIDTH ABNORMAL ( 3 FDA reports)
RED CELL DISTRIBUTION WIDTH DECREASED ( 3 FDA reports)
REFRACTORY CYTOPENIA WITH MULTILINEAGE DYSPLASIA ( 3 FDA reports)
RENAL AND PANCREAS TRANSPLANT ( 3 FDA reports)
RENAL ARTERY FIBROMUSCULAR DYSPLASIA ( 3 FDA reports)
RENAL CELL CARCINOMA STAGE I ( 3 FDA reports)
RENAL LIPOMATOSIS ( 3 FDA reports)
RENAL ONCOCYTOMA ( 3 FDA reports)
RENAL SCAN ABNORMAL ( 3 FDA reports)
RENAL STONE REMOVAL ( 3 FDA reports)
RESECTION OF RECTUM ( 3 FDA reports)
RESPIRATORY MONILIASIS ( 3 FDA reports)
RESPIRATORY PARALYSIS ( 3 FDA reports)
RESPIRATORY THERAPY ( 3 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 3 FDA reports)
RETICULOCYTE PERCENTAGE INCREASED ( 3 FDA reports)
RETINAL ARTERY STENOSIS ( 3 FDA reports)
RETINOIC ACID SYNDROME ( 3 FDA reports)
RETROPERITONEAL ABSCESS ( 3 FDA reports)
RHINOVIRUS INFECTION ( 3 FDA reports)
RIGHT ATRIAL PRESSURE INCREASED ( 3 FDA reports)
SACCADIC EYE MOVEMENT ( 3 FDA reports)
SALIVARY GLAND OPERATION ( 3 FDA reports)
SCHIZOID PERSONALITY DISORDER ( 3 FDA reports)
SCHIZOPHRENIA, UNDIFFERENTIATED TYPE ( 3 FDA reports)
SCHIZOTYPAL PERSONALITY DISORDER ( 3 FDA reports)
SCLERAL OEDEMA ( 3 FDA reports)
SCLERAL PIGMENTATION ( 3 FDA reports)
SCLEROEDEMA ( 3 FDA reports)
SEBACEOUS HYPERPLASIA ( 3 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 3 FDA reports)
SEPSIS NEONATAL ( 3 FDA reports)
SEPTIC PHLEBITIS ( 3 FDA reports)
SEPTOPLASTY ( 3 FDA reports)
SHARED PSYCHOTIC DISORDER ( 3 FDA reports)
SHIGELLA TEST POSITIVE ( 3 FDA reports)
SHOULDER DEFORMITY ( 3 FDA reports)
SHUNT INFECTION ( 3 FDA reports)
SIGMOIDECTOMY ( 3 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 3 FDA reports)
SINGLE VESSEL BYPASS GRAFT ( 3 FDA reports)
SKIN GRAFT INFECTION ( 3 FDA reports)
SKIN HYPOPLASIA ( 3 FDA reports)
SOMATIC HALLUCINATION ( 3 FDA reports)
SPASMODIC DYSPHONIA ( 3 FDA reports)
SPECIFIC GRAVITY URINE DECREASED ( 3 FDA reports)
SPINAL MUSCULAR ATROPHY ( 3 FDA reports)
SPINAL VASCULAR DISORDER ( 3 FDA reports)
SPORTS INJURY ( 3 FDA reports)
STAB WOUND ( 3 FDA reports)
STAG HORN CALCULUS ( 3 FDA reports)
STENOTROPHOMONAS SEPSIS ( 3 FDA reports)
STENT-GRAFT ENDOLEAK ( 3 FDA reports)
STENT-GRAFT MALFUNCTION ( 3 FDA reports)
STICKY SKIN ( 3 FDA reports)
STOMACH MASS ( 3 FDA reports)
STRONGYLOIDIASIS ( 3 FDA reports)
SUBACUTE HEPATIC FAILURE ( 3 FDA reports)
SUBCHORIONIC HAEMORRHAGE ( 3 FDA reports)
SUBSTANCE-INDUCED PSYCHOTIC DISORDER ( 3 FDA reports)
SUCROSE INTOLERANCE ( 3 FDA reports)
SUDDEN INFANT DEATH SYNDROME ( 3 FDA reports)
SUDDEN UNEXPLAINED DEATH IN EPILEPSY ( 3 FDA reports)
SURGICAL VASCULAR SHUNT ( 3 FDA reports)
SWEAT GLAND INFECTION ( 3 FDA reports)
SYNOVIAL FLUID ANALYSIS ABNORMAL ( 3 FDA reports)
TEMPORAL LOBE EPILEPSY ( 3 FDA reports)
TESTICULAR ABSCESS ( 3 FDA reports)
TESTICULAR HAEMORRHAGE ( 3 FDA reports)
TESTICULAR OEDEMA ( 3 FDA reports)
THALASSAEMIA ( 3 FDA reports)
THANATOPHOBIA ( 3 FDA reports)
THERAPEUTIC RESPONSE PROLONGED ( 3 FDA reports)
THERAPY NAIVE ( 3 FDA reports)
THORACIC OUTLET SYNDROME ( 3 FDA reports)
THREATENED LABOUR ( 3 FDA reports)
THROMBOSED VARICOSE VEIN ( 3 FDA reports)
THYROXINE ABNORMAL ( 3 FDA reports)
TONSILLITIS STREPTOCOCCAL ( 3 FDA reports)
TOOTH RESORPTION ( 3 FDA reports)
TOXIC ANTERIOR SEGMENT SYNDROME ( 3 FDA reports)
TOXIC NEUROPATHY ( 3 FDA reports)
TRACHEAL INFLAMMATION ( 3 FDA reports)
TRACHEAL OBSTRUCTION ( 3 FDA reports)
TRANSAMINASES ABNORMAL ( 3 FDA reports)
TRANSFUSION-RELATED ACUTE LUNG INJURY ( 3 FDA reports)
TRANSPLANT ABSCESS ( 3 FDA reports)
TRAUMATIC ARTHROPATHY ( 3 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 3 FDA reports)
TRI-IODOTHYRONINE FREE DECREASED ( 3 FDA reports)
TRICUSPID VALVE REPAIR ( 3 FDA reports)
TRICUSPID VALVE STENOSIS ( 3 FDA reports)
TRIGEMINAL NERVE DISORDER ( 3 FDA reports)
TROPONIN I ( 3 FDA reports)
TROPONIN T ( 3 FDA reports)
TUBERCULOSIS OF CENTRAL NERVOUS SYSTEM ( 3 FDA reports)
TUBERCULOUS PLEURISY ( 3 FDA reports)
TYPE II HYPERLIPIDAEMIA ( 3 FDA reports)
TYPE II HYPERSENSITIVITY ( 3 FDA reports)
UBIQUINONE DECREASED ( 3 FDA reports)
ULNAR TUNNEL SYNDROME ( 3 FDA reports)
ULTRASOUND BILIARY TRACT ( 3 FDA reports)
ULTRASOUND UTERUS ABNORMAL ( 3 FDA reports)
UNEQUAL LIMB LENGTH ( 3 FDA reports)
UPPER MOTOR NEURONE LESION ( 3 FDA reports)
URETERAL CATHETERISATION ( 3 FDA reports)
URETHRAL INJURY ( 3 FDA reports)
URETHRAL INTRINSIC SPHINCTER DEFICIENCY ( 3 FDA reports)
URINARY BLADDER RUPTURE ( 3 FDA reports)
URINARY NITROGEN INCREASED ( 3 FDA reports)
URINE CALCIUM ( 3 FDA reports)
IMPLANT SITE SCAR ( 2 FDA reports)
INCLUSION BODY MYOSITIS ( 2 FDA reports)
INFECTED BUNION ( 2 FDA reports)
INFECTED INSECT BITE ( 2 FDA reports)
INFECTION PARASITIC ( 2 FDA reports)
INFECTIOUS DISEASE CARRIER ( 2 FDA reports)
INFECTIVE MYOSITIS ( 2 FDA reports)
INFERIOR VENA CAVAL OCCLUSION ( 2 FDA reports)
INFERTILITY FEMALE ( 2 FDA reports)
INFILTRATION ANAESTHESIA ( 2 FDA reports)
INFLUENZA SEROLOGY POSITIVE ( 2 FDA reports)
INFUSION SITE INFLAMMATION ( 2 FDA reports)
INFUSION SITE IRRITATION ( 2 FDA reports)
INFUSION SITE SCAR ( 2 FDA reports)
INFUSION SITE THROMBOSIS ( 2 FDA reports)
INFUSION SITE VESICLES ( 2 FDA reports)
INJECTION ( 2 FDA reports)
INJECTION SITE DESQUAMATION ( 2 FDA reports)
INJECTION SITE FIBROSIS ( 2 FDA reports)
INJECTION SITE JOINT SWELLING ( 2 FDA reports)
INJECTION SITE NERVE DAMAGE ( 2 FDA reports)
INSULINOMA ( 2 FDA reports)
INTELLIGENCE TEST ABNORMAL ( 2 FDA reports)
INTERLEUKIN LEVEL INCREASED ( 2 FDA reports)
INTERLEUKIN-2 RECEPTOR INCREASED ( 2 FDA reports)
INTERTRIGO CANDIDA ( 2 FDA reports)
INTESTINAL ANASTOMOSIS COMPLICATION ( 2 FDA reports)
INTESTINAL CYST ( 2 FDA reports)
INTESTINAL HYPOMOTILITY ( 2 FDA reports)
INTESTINAL SPASM ( 2 FDA reports)
INTOXICATION BY BREAST FEEDING ( 2 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE INSERTION ( 2 FDA reports)
INTRANASAL PARAESTHESIA ( 2 FDA reports)
IRIS HYPOPIGMENTATION ( 2 FDA reports)
IRON BINDING CAPACITY TOTAL ABNORMAL ( 2 FDA reports)
IRREGULAR SLEEP PHASE ( 2 FDA reports)
KAPOSI'S VARICELLIFORM ERUPTION ( 2 FDA reports)
KARNOFSKY SCALE WORSENED ( 2 FDA reports)
KERATITIS FUNGAL ( 2 FDA reports)
KERATOMILEUSIS ( 2 FDA reports)
KERATOSIS PILARIS ( 2 FDA reports)
KIDNEY DUPLEX ( 2 FDA reports)
KLIPPEL-FEIL SYNDROME ( 2 FDA reports)
KOEBNER PHENOMENON ( 2 FDA reports)
LABOUR INDUCTION ( 2 FDA reports)
LABYRINTHINE FISTULA ( 2 FDA reports)
LAGOPHTHALMOS ( 2 FDA reports)
LANGERHANS' CELL GRANULOMATOSIS ( 2 FDA reports)
LAPAROSCOPIC SURGERY ( 2 FDA reports)
LARYNGEAL CYST ( 2 FDA reports)
LARYNGEAL ERYTHEMA ( 2 FDA reports)
LARYNGEAL GRANULOMA ( 2 FDA reports)
LARYNGEAL INFLAMMATION ( 2 FDA reports)
LARYNGEAL ULCERATION ( 2 FDA reports)
LDL/HDL RATIO INCREASED ( 2 FDA reports)
LEGIONELLA INFECTION ( 2 FDA reports)
LEGIONELLA SEROLOGY POSITIVE ( 2 FDA reports)
LENS DISLOCATION ( 2 FDA reports)
LEPROSY ( 2 FDA reports)
LEUKAEMIA MONOCYTIC ( 2 FDA reports)
LEUKAEMIC INFILTRATION ( 2 FDA reports)
LEUKOCYTE ANTIGEN B-27 POSITIVE ( 2 FDA reports)
LEUKODYSTROPHY ( 2 FDA reports)
LEUKOENCEPHALOMYELITIS ( 2 FDA reports)
LHERMITTE'S SIGN ( 2 FDA reports)
LIGAMENT OPERATION ( 2 FDA reports)
LIGAMENT PAIN ( 2 FDA reports)
LIGHT CHAIN ANALYSIS ABNORMAL ( 2 FDA reports)
LIMB AMPUTATION ( 2 FDA reports)
LIP HAEMATOMA ( 2 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 2 FDA reports)
LIPASE ABNORMAL ( 2 FDA reports)
LIPOMA OF BREAST ( 2 FDA reports)
LIPOPROTEIN (A) ABNORMAL ( 2 FDA reports)
LIVER INDURATION ( 2 FDA reports)
LIVER SCAN ABNORMAL ( 2 FDA reports)
LIVING ALONE ( 2 FDA reports)
LOSS OF ANATOMICAL ALIGNMENT AFTER FRACTURE REDUCTION ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN ( 2 FDA reports)
LOWER MOTOR NEURONE LESION ( 2 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 2 FDA reports)
LUNG CYST BENIGN ( 2 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE II ( 2 FDA reports)
LUPUS ENCEPHALITIS ( 2 FDA reports)
LYMPHANGIOMA ( 2 FDA reports)
MACROGNATHIA ( 2 FDA reports)
MACROSOMIA ( 2 FDA reports)
MALARIA ( 2 FDA reports)
MALIGNANT HEPATOBILIARY NEOPLASM ( 2 FDA reports)
MALIGNANT MELANOMA OF SITES OTHER THAN SKIN ( 2 FDA reports)
MALIGNANT NEOPLASM OF CORNEA ( 2 FDA reports)
MALIGNANT NEOPLASM OF RENAL PELVIS ( 2 FDA reports)
MALIGNANT OMENTUM NEOPLASM ( 2 FDA reports)
MALIGNANT SPLENIC NEOPLASM ( 2 FDA reports)
MEAN ARTERIAL PRESSURE DECREASED ( 2 FDA reports)
MEAN ARTERIAL PRESSURE INCREASED ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN ( 2 FDA reports)
MEAN PLATELET VOLUME ABNORMAL ( 2 FDA reports)
MECHANICAL VENTILATION COMPLICATION ( 2 FDA reports)
MEGACOLON ACQUIRED ( 2 FDA reports)
MENINGIOMA MALIGNANT ( 2 FDA reports)
MENINGITIS COCCIDIOIDES ( 2 FDA reports)
MENINGITIS FUNGAL ( 2 FDA reports)
MENINGITIS LISTERIA ( 2 FDA reports)
MENINGITIS MENINGOCOCCAL ( 2 FDA reports)
MENINGITIS STAPHYLOCOCCAL ( 2 FDA reports)
MENSTRUATION DELAYED ( 2 FDA reports)
MESENTERIC ARTERIOSCLEROSIS ( 2 FDA reports)
MESENTERIC LYMPHADENOPATHY ( 2 FDA reports)
MESENTERIC NEOPLASM ( 2 FDA reports)
MESENTERIC PANNICULITIS ( 2 FDA reports)
METANEPHRINE URINE INCREASED ( 2 FDA reports)
METASTASES TO PELVIS ( 2 FDA reports)
METASTASES TO PLEURA ( 2 FDA reports)
METASTASES TO THYROID ( 2 FDA reports)
METASTASES TO URINARY TRACT ( 2 FDA reports)
METASTATIC OCULAR MELANOMA ( 2 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST NEGATIVE ( 2 FDA reports)
MILIARY PNEUMONIA ( 2 FDA reports)
MILLER FISHER SYNDROME ( 2 FDA reports)
MINERAL METABOLISM DISORDER ( 2 FDA reports)
MINERAL SUPPLEMENTATION ( 2 FDA reports)
MOLE EXCISION ( 2 FDA reports)
MONOCYTE COUNT ABNORMAL ( 2 FDA reports)
MORGANELLA TEST POSITIVE ( 2 FDA reports)
MORTON'S NEURALGIA ( 2 FDA reports)
MOUTH PLAQUE ( 2 FDA reports)
MUCOSAL EXCORIATION ( 2 FDA reports)
MUELLER'S MIXED TUMOUR ( 2 FDA reports)
MUIR-TORRE SYNDROME ( 2 FDA reports)
MULTIPLE CHEMICAL SENSITIVITY ( 2 FDA reports)
MUSCLE OPERATION ( 2 FDA reports)
MYCOBACTERIUM TEST POSITIVE ( 2 FDA reports)
MYCOPLASMA SEROLOGY POSITIVE ( 2 FDA reports)
MYCOTIC ANEURYSM ( 2 FDA reports)
MYOCARDIAL REPERFUSION INJURY ( 2 FDA reports)
MYOCARDITIS SEPTIC ( 2 FDA reports)
MYOGLOBIN BLOOD PRESENT ( 2 FDA reports)
MYOTONIA ( 2 FDA reports)
MYRINGITIS ( 2 FDA reports)
NASAL ABSCESS ( 2 FDA reports)
NASAL CYST ( 2 FDA reports)
NASAL DISCHARGE DISCOLOURATION ( 2 FDA reports)
NASAL FLARING ( 2 FDA reports)
NASAL NECROSIS ( 2 FDA reports)
NASAL NEOPLASM ( 2 FDA reports)
NASAL SEPTAL OPERATION ( 2 FDA reports)
NASAL TURBINATE ABNORMALITY ( 2 FDA reports)
NASOPHARYNGEAL REFLUX ( 2 FDA reports)
NEAR DROWNING ( 2 FDA reports)
NECROBIOSIS LIPOIDICA DIABETICORUM ( 2 FDA reports)
NECROSIS OF ARTERY ( 2 FDA reports)
NEMATODIASIS ( 2 FDA reports)
NEOLOGISM ( 2 FDA reports)
NEONATAL RESPIRATORY FAILURE ( 2 FDA reports)
NEOPLASM OF APPENDIX ( 2 FDA reports)
NEURECTOMY ( 2 FDA reports)
NEUROCYSTICERCOSIS ( 2 FDA reports)
NEUROLOGICAL INFECTION ( 2 FDA reports)
NEUROLYSIS ( 2 FDA reports)
NEUROMYELITIS OPTICA ( 2 FDA reports)
NEUROPATHIC ULCER ( 2 FDA reports)
NEUROSURGERY ( 2 FDA reports)
NEUTROPHIL MORPHOLOGY ABNORMAL ( 2 FDA reports)
NEUTROPHIL PELGER-HUET ANOMALY PRESENT ( 2 FDA reports)
NIEMANN-PICK DISEASE ( 2 FDA reports)
NIPPLE EXUDATE BLOODY ( 2 FDA reports)
NITRITE URINE ABSENT ( 2 FDA reports)
NITRITOID CRISIS ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE III ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BREAST ABNORMAL ( 2 FDA reports)
OCULAR CANCER METASTATIC ( 2 FDA reports)
OCULAR TOXICITY ( 2 FDA reports)
OCULOCEPHALOGYRIC REFLEX ABSENT ( 2 FDA reports)
OEDEMA NEONATAL ( 2 FDA reports)
OESOPHAGEAL ADENOCARCINOMA STAGE IV ( 2 FDA reports)
OESOPHAGECTOMY ( 2 FDA reports)
OESOPHAGOBRONCHIAL FISTULA ( 2 FDA reports)
OESOPHAGOGASTRECTOMY ( 2 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 2 FDA reports)
OESTRADIOL DECREASED ( 2 FDA reports)
OLFACTORY TEST ABNORMAL ( 2 FDA reports)
OMPHALITIS ( 2 FDA reports)
ONCOCYTOMA ( 2 FDA reports)
ONYCHOGRYPHOSIS ( 2 FDA reports)
OPTIC NERVE HYPOPLASIA ( 2 FDA reports)
ORAL ALLERGY SYNDROME ( 2 FDA reports)
ORAL DYSAESTHESIA ( 2 FDA reports)
ORGASMIC SENSATION DECREASED ( 2 FDA reports)
OROPHARYNGEAL NEOPLASM BENIGN ( 2 FDA reports)
OSTEOARTHRITIS GENERALISED ( 2 FDA reports)
OVARIAN ABSCESS ( 2 FDA reports)
OVARIAN FIBROMA ( 2 FDA reports)
OVARIAN HAEMATOMA ( 2 FDA reports)
OVERSENSING ( 2 FDA reports)
OXYGEN CONSUMPTION ( 2 FDA reports)
PACEMAKER GENERATED RHYTHM ( 2 FDA reports)
PALATAL DYSPLASIA ( 2 FDA reports)
PALLANAESTHESIA ( 2 FDA reports)
PANCREATECTOMY ( 2 FDA reports)
PANCREATIC HAEMORRHAGE ( 2 FDA reports)
PANCREATICODUODENECTOMY ( 2 FDA reports)
PARADOXICAL PRESSOR RESPONSE ( 2 FDA reports)
PARANASAL BIOPSY ABNORMAL ( 2 FDA reports)
PARANASAL CYST ( 2 FDA reports)
PARANEOPLASTIC PEMPHIGUS ( 2 FDA reports)
PARANOID PERSONALITY DISORDER ( 2 FDA reports)
PARASOMNIA ( 2 FDA reports)
PARATHYROID GLAND OPERATION ( 2 FDA reports)
PARATHYROID TUMOUR ( 2 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 2 FDA reports)
PARKINSONIAN REST TREMOR ( 2 FDA reports)
PEDAL PULSE ABSENT ( 2 FDA reports)
PELVIC PERITONEAL ADHESIONS ( 2 FDA reports)
PENILE ARTERY OCCLUSION ( 2 FDA reports)
PENOSCROTAL FUSION ( 2 FDA reports)
PERIARTICULAR DISORDER ( 2 FDA reports)
PERICARDITIS ADHESIVE ( 2 FDA reports)
PERICARDITIS MALIGNANT ( 2 FDA reports)
PERICARDITIS URAEMIC ( 2 FDA reports)
PERIDIVERTICULITIS ( 2 FDA reports)
PERINEPHRIC COLLECTION ( 2 FDA reports)
PERIODONTAL DESTRUCTION ( 2 FDA reports)
PERIPHERAL NERVE PALSY ( 2 FDA reports)
PERIPORTAL OEDEMA ( 2 FDA reports)
PERIPROSTHETIC OSTEOLYSIS ( 2 FDA reports)
PERISTALSIS VISIBLE ( 2 FDA reports)
PERITONEAL FIBROSIS ( 2 FDA reports)
PERITONEAL MEMBRANE FAILURE ( 2 FDA reports)
PERITONEAL PERFORATION ( 2 FDA reports)
PERIUMBILICAL ABSCESS ( 2 FDA reports)
PERONEAL NERVE INJURY ( 2 FDA reports)
PERSEVERATION ( 2 FDA reports)
PHAEOCHROMOCYTOMA EXCISION ( 2 FDA reports)
PHARYNGEAL OPERATION ( 2 FDA reports)
PHARYNGEAL STENOSIS ( 2 FDA reports)
PHARYNGOTONSILLITIS ( 2 FDA reports)
PHLEBITIS DEEP ( 2 FDA reports)
PHOTOSENSITIVITY ALLERGIC REACTION ( 2 FDA reports)
PHRENIC NERVE PARALYSIS ( 2 FDA reports)
PITUITARY TUMOUR REMOVAL ( 2 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 2 FDA reports)
PLASMA CELLS DECREASED ( 2 FDA reports)
PLASTIC SURGERY TO THE FACE ( 2 FDA reports)
PLEURAL FISTULA ( 2 FDA reports)
PO2 ABNORMAL ( 2 FDA reports)
POLIOMYELITIS ( 2 FDA reports)
POLYOMAVIRUS TEST POSITIVE ( 2 FDA reports)
POROKERATOSIS ( 2 FDA reports)
PORPHYRIA ACUTE ( 2 FDA reports)
PORTAL TRIADITIS ( 2 FDA reports)
PORTAL VENOUS GAS ( 2 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 2 FDA reports)
POST PROCEDURAL STROKE ( 2 FDA reports)
POST PROCEDURAL URINE LEAK ( 2 FDA reports)
POST VACCINATION SYNDROME ( 2 FDA reports)
POST-TRAUMATIC EPILEPSY ( 2 FDA reports)
POST-TRAUMATIC NECK SYNDROME ( 2 FDA reports)
POSTERIOR CAPSULE RUPTURE ( 2 FDA reports)
POSTMENOPAUSE ( 2 FDA reports)
POSTOPERATIVE CONSTIPATION ( 2 FDA reports)
POSTRESUSCITATION ENCEPHALOPATHY ( 2 FDA reports)
POSTURAL REFLEX IMPAIRMENT ( 2 FDA reports)
PRE-AURICULAR SINUS CONGENITAL ( 2 FDA reports)
PREALBUMIN DECREASED ( 2 FDA reports)
PREMATURE AGEING ( 2 FDA reports)
PRESENILE DEMENTIA ( 2 FDA reports)
PRODUCT COATING ISSUE ( 2 FDA reports)
PRODUCT OUTER PACKAGING ISSUE ( 2 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 2 FDA reports)
PRODUCT RECONSTITUTION ISSUE ( 2 FDA reports)
PROLACTINOMA ( 2 FDA reports)
PROLONGED LABOUR ( 2 FDA reports)
PROLONGED PREGNANCY ( 2 FDA reports)
PROSTATE INDURATION ( 2 FDA reports)
PROSTATE TENDERNESS ( 2 FDA reports)
PROTEIN S INCREASED ( 2 FDA reports)
PROTHROMBIN TIME ( 2 FDA reports)
PSEUDO LYMPHOMA ( 2 FDA reports)
PSYCHIATRIC EVALUATION ( 2 FDA reports)
PULMONARY ARTERY STENOSIS ( 2 FDA reports)
PULMONARY BULLA ( 2 FDA reports)
PULMONARY FISTULA ( 2 FDA reports)
PULMONARY VALVE REPLACEMENT ( 2 FDA reports)
PULMONARY VEIN OCCLUSION ( 2 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 2 FDA reports)
PUNCTURE SITE PAIN ( 2 FDA reports)
PURGING ( 2 FDA reports)
PURPURA SENILE ( 2 FDA reports)
RADIAL NERVE LESION ( 2 FDA reports)
RADIAL PULSE DECREASED ( 2 FDA reports)
RADIAL PULSE INCREASED ( 2 FDA reports)
RADIATION DYSPHAGIA ( 2 FDA reports)
RADIATION PROCTOPATHY ( 2 FDA reports)
RADIATION PROSTATITIS ( 2 FDA reports)
RADICAL HYSTERECTOMY ( 2 FDA reports)
RADICAL PROSTATECTOMY ( 2 FDA reports)
RASMUSSEN ENCEPHALITIS ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE DECREASED ( 2 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 2 FDA reports)
RENAL APLASIA ( 2 FDA reports)
RENAL CELL CARCINOMA STAGE III ( 2 FDA reports)
RENAL CELL CARCINOMA STAGE IV ( 2 FDA reports)
RENAL SALT-WASTING SYNDROME ( 2 FDA reports)
RENAL VEIN OCCLUSION ( 2 FDA reports)
RESPIRATORY PAPILLOMA ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS BRONCHIOLITIS ( 2 FDA reports)
RETINAL DYSTROPHY ( 2 FDA reports)
RETINAL MIGRAINE ( 2 FDA reports)
RETINAL NAEVUS ( 2 FDA reports)
RETINOSCHISIS ( 2 FDA reports)
RETRACTED NIPPLE ( 2 FDA reports)
RHEUMATOID FACTOR ( 2 FDA reports)
ROSAI-DORFMAN SYNDROME ( 2 FDA reports)
ROSEOLA ( 2 FDA reports)
SALMONELLA TEST POSITIVE ( 2 FDA reports)
SCAN BRAIN ( 2 FDA reports)
SCAN LYMPH NODES ( 2 FDA reports)
SCAR EXCISION ( 2 FDA reports)
SCHIZOPHRENIA, DISORGANISED TYPE ( 2 FDA reports)
SCLERODERMA RENAL CRISIS ( 2 FDA reports)
SCROTAL CANCER ( 2 FDA reports)
SCROTAL CYST ( 2 FDA reports)
SCROTAL INFECTION ( 2 FDA reports)
SCROTAL VARICOSE VEINS ( 2 FDA reports)
SEASONAL AFFECTIVE DISORDER ( 2 FDA reports)
SEBACEOUS CYST EXCISION ( 2 FDA reports)
SECONDARY HYPERTHYROIDISM ( 2 FDA reports)
SECONDARY HYPOTHYROIDISM ( 2 FDA reports)
SEIZURE LIKE PHENOMENA ( 2 FDA reports)
SENSATION OF BLOCK IN EAR ( 2 FDA reports)
SEPSIS PASTEURELLA ( 2 FDA reports)
SERUM SICKNESS-LIKE REACTION ( 2 FDA reports)
SEXUALLY INAPPROPRIATE BEHAVIOUR ( 2 FDA reports)
SHUNT STENOSIS ( 2 FDA reports)
SIGHT DISABILITY ( 2 FDA reports)
SKIN CANCER METASTATIC ( 2 FDA reports)
SMALL CELL CARCINOMA ( 2 FDA reports)
SMALL CELL LUNG CANCER EXTENSIVE STAGE ( 2 FDA reports)
SMALL INTESTINE OPERATION ( 2 FDA reports)
SMOKE SENSITIVITY ( 2 FDA reports)
SOFT TISSUE ATROPHY ( 2 FDA reports)
SOFT TISSUE NEOPLASM ( 2 FDA reports)
SPEECH REHABILITATION ( 2 FDA reports)
SPERM COUNT DECREASED ( 2 FDA reports)
SPHEROCYTIC ANAEMIA ( 2 FDA reports)
SPINAL CORD INJURY CAUDA EQUINA ( 2 FDA reports)
SPINAL CORD INJURY THORACIC ( 2 FDA reports)
SPINAL CORD ISCHAEMIA ( 2 FDA reports)
SPINAL CORD OEDEMA ( 2 FDA reports)
SPINAL FUSION ACQUIRED ( 2 FDA reports)
SPINAL ROD INSERTION ( 2 FDA reports)
SPINAL SHOCK ( 2 FDA reports)
SPINE MALFORMATION ( 2 FDA reports)
SPLENIC EMBOLISM ( 2 FDA reports)
SPLENITIS ( 2 FDA reports)
SPOUSAL ABUSE ( 2 FDA reports)
STAPHYLOCOCCAL MEDIASTINITIS ( 2 FDA reports)
STENOSIS OF VESICOURETHRAL ANASTOMOSIS ( 2 FDA reports)
STEROID THERAPY ( 2 FDA reports)
STIFF-MAN SYNDROME ( 2 FDA reports)
STREPTOCOCCAL SEROLOGY POSITIVE ( 2 FDA reports)
STRESS ECHOCARDIOGRAM ( 2 FDA reports)
STRESS ECHOCARDIOGRAM ABNORMAL ( 2 FDA reports)
STUBBORNNESS ( 2 FDA reports)
SUBCLAVIAN ARTERY OCCLUSION ( 2 FDA reports)
SUPERFICIAL SIDEROSIS OF CENTRAL NERVOUS SYSTEM ( 2 FDA reports)
SUPERIOR VENA CAVAL STENOSIS ( 2 FDA reports)
SUPPLEMENTATION THERAPY ( 2 FDA reports)
SWEAT GLAND DISORDER ( 2 FDA reports)
SWEATING FEVER ( 2 FDA reports)
SYNOVIAL FLUID WHITE BLOOD CELLS POSITIVE ( 2 FDA reports)
SYSTEMIC MYCOSIS ( 2 FDA reports)
T-CELL LYMPHOMA STAGE IV ( 2 FDA reports)
TANDEM GAIT TEST ABNORMAL ( 2 FDA reports)
TATTOO ( 2 FDA reports)
TEAR DISCOLOURATION ( 2 FDA reports)
TEETHING ( 2 FDA reports)
TENOLYSIS ( 2 FDA reports)
TESTICULAR FAILURE ( 2 FDA reports)
THORACIC OPERATION ( 2 FDA reports)
THROMBIN TIME ABNORMAL ( 2 FDA reports)
THROMBIN-ANTITHROMBIN III COMPLEX INCREASED ( 2 FDA reports)
THROMBOCYTOPENIA NEONATAL ( 2 FDA reports)
THROMBOSIS MESENTERIC VESSEL ( 2 FDA reports)
THROMBOTIC CEREBRAL INFARCTION ( 2 FDA reports)
THYROID ATROPHY ( 2 FDA reports)
THYROID FUNCTION TEST NORMAL ( 2 FDA reports)
THYROID GLAND SCAN ABNORMAL ( 2 FDA reports)
THYROXIN BINDING GLOBULIN ( 2 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 2 FDA reports)
TONGUE AMYLOIDOSIS ( 2 FDA reports)
TONGUE NECROSIS ( 2 FDA reports)
TONGUE NEOPLASM ( 2 FDA reports)
TOOTH HYPOPLASIA ( 2 FDA reports)
TOTAL LUNG CAPACITY ABNORMAL ( 2 FDA reports)
TOTAL LUNG CAPACITY INCREASED ( 2 FDA reports)
TOXIC DILATATION OF COLON ( 2 FDA reports)
TOXIC OPTIC NEUROPATHY ( 2 FDA reports)
TOXICOLOGIC TEST ( 2 FDA reports)
TRACHEAL PAIN ( 2 FDA reports)
TRACHEOBRONCHITIS VIRAL ( 2 FDA reports)
TRACHOMA ( 2 FDA reports)
TRANCE ( 2 FDA reports)
TRANSIENT ACANTHOLYTIC DERMATOSIS ( 2 FDA reports)
TRANSITIONAL CELL CANCER OF THE RENAL PELVIS AND URETER ( 2 FDA reports)
TRANSITIONAL CELL CANCER OF THE RENAL PELVIS AND URETER REGIONAL ( 2 FDA reports)
TRANSVERSE PRESENTATION ( 2 FDA reports)
TRAUMATIC ULCER ( 2 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 2 FDA reports)
TREPONEMA TEST POSITIVE ( 2 FDA reports)
TRISOMY 21 ( 2 FDA reports)
TRYPTASE ( 2 FDA reports)
TUBO-OVARIAN ABSCESS ( 2 FDA reports)
TUMOUR COMPRESSION ( 2 FDA reports)
TUMOUR MARKER TEST ( 2 FDA reports)
ULNAR NERVE PALSY ( 2 FDA reports)
UMBILICAL HERNIA PERFORATION ( 2 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 2 FDA reports)
UPPER RESPIRATORY TRACT IRRITATION ( 2 FDA reports)
URACHAL ABSCESS ( 2 FDA reports)
URATE NEPHROPATHY ( 2 FDA reports)
UREA RENAL CLEARANCE DECREASED ( 2 FDA reports)
URETERITIS ( 2 FDA reports)
URETHRAL ATROPHY ( 2 FDA reports)
URETHRITIS NONINFECTIVE ( 2 FDA reports)
URINARY BLADDER EXCISION ( 2 FDA reports)
URINARY CYSTECTOMY ( 2 FDA reports)
URINARY OCCULT BLOOD POSITIVE ( 2 FDA reports)
URINARY SEDIMENT ABNORMAL ( 2 FDA reports)
URINARY SYSTEM X-RAY ABNORMAL ( 2 FDA reports)
URINE ALBUMIN/CREATININE RATIO ABNORMAL ( 2 FDA reports)
URINE AMPHETAMINE POSITIVE ( 2 FDA reports)
URINE CHLORIDE DECREASED ( 2 FDA reports)
URINE CYTOLOGY ABNORMAL ( 2 FDA reports)
URINE ELECTROLYTES ABNORMAL ( 2 FDA reports)
ABDOMINAL AORTIC BRUIT ( 2 FDA reports)
ABDOMINAL BRUIT ( 2 FDA reports)
ABDOMINAL EXPLORATION ( 2 FDA reports)
ABDOMINOPLASTY ( 2 FDA reports)
ABORTION COMPLETE ( 2 FDA reports)
ABORTION THREATENED ( 2 FDA reports)
ABSCESS FUNGAL ( 2 FDA reports)
ACALCULIA ( 2 FDA reports)
ACID-BASE BALANCE DISORDER MIXED ( 2 FDA reports)
ACINETOBACTER TEST POSITIVE ( 2 FDA reports)
ACNE PUSTULAR ( 2 FDA reports)
ACQUIRED METHAEMOGLOBINAEMIA ( 2 FDA reports)
ACQUIRED PHIMOSIS ( 2 FDA reports)
ACROCHORDON EXCISION ( 2 FDA reports)
ACTINOMYCES TEST POSITIVE ( 2 FDA reports)
ACUTE ENDOCARDITIS ( 2 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 2 FDA reports)
ACUTE MONOCYTIC LEUKAEMIA ( 2 FDA reports)
ACUTE PULMONARY HISTOPLASMOSIS ( 2 FDA reports)
ADENOIDAL DISORDER ( 2 FDA reports)
ADENOIDITIS ( 2 FDA reports)
ADRENAL CARCINOMA ( 2 FDA reports)
ADRENALECTOMY ( 2 FDA reports)
ADRENOCORTICAL INSUFFICIENCY CHRONIC ( 2 FDA reports)
AGONAL DEATH STRUGGLE ( 2 FDA reports)
ALBUMIN GLOBULIN RATIO ( 2 FDA reports)
ALCOHOLIC ( 2 FDA reports)
ALLERGIC COLITIS ( 2 FDA reports)
ALLERGY TO PLANTS ( 2 FDA reports)
ALLERGY TO VACCINE ( 2 FDA reports)
ALOPECIA UNIVERSALIS ( 2 FDA reports)
ALPHA 1 GLOBULIN ABNORMAL ( 2 FDA reports)
ALPHA 1 GLOBULIN INCREASED ( 2 FDA reports)
ALPHA 2 GLOBULIN DECREASED ( 2 FDA reports)
ALVEOLAR SOFT PART SARCOMA METASTATIC ( 2 FDA reports)
AMERICAN TRYPANOSOMIASIS ( 2 FDA reports)
AMOEBIASIS ( 2 FDA reports)
ANAEMIA FOLATE DEFICIENCY ( 2 FDA reports)
ANAESTHETIC COMPLICATION PULMONARY ( 2 FDA reports)
ANAL EROSION ( 2 FDA reports)
ANAL FUNGAL INFECTION ( 2 FDA reports)
ANAL INFECTION ( 2 FDA reports)
ANAL INJURY ( 2 FDA reports)
ANAL NEOPLASM ( 2 FDA reports)
ANAL SPHINCTEROTOMY ( 2 FDA reports)
ANAL TINEA ( 2 FDA reports)
ANDROGENS DECREASED ( 2 FDA reports)
ANENCEPHALY ( 2 FDA reports)
ANGIOGRAM CEREBRAL ABNORMAL ( 2 FDA reports)
ANGIOTENSIN CONVERTING ENZYME DECREASED ( 2 FDA reports)
ANKLE DEFORMITY ( 2 FDA reports)
ANKLE RECONSTRUCTION ( 2 FDA reports)
ANORECTAL INFECTION ( 2 FDA reports)
ANOREXIA NERVOSA ( 2 FDA reports)
ANTASTHMATIC DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTERIOR CHAMBER FLARE ( 2 FDA reports)
ANTERIOR SPINAL ARTERY SYNDROME ( 2 FDA reports)
ANTI-CYCLIC CITRULLINATED PEPTIDE ANTIBODY POSITIVE ( 2 FDA reports)
ANTIBIOTIC THERAPY ( 2 FDA reports)
ANTIBODY TEST ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL ( 2 FDA reports)
ANTICONVULSANT TOXICITY ( 2 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTIGLIADIN ANTIBODY POSITIVE ( 2 FDA reports)
ANTITHROMBIN III INCREASED ( 2 FDA reports)
AORTIC ELONGATION ( 2 FDA reports)
AORTIC INJURY ( 2 FDA reports)
AORTIC INTRAMURAL HAEMATOMA ( 2 FDA reports)
AORTIC VALVE REPAIR ( 2 FDA reports)
AORTOGRAM ABNORMAL ( 2 FDA reports)
APHAKIA ( 2 FDA reports)
APPLICATION SITE BRUISING ( 2 FDA reports)
APPLICATION SITE INFLAMMATION ( 2 FDA reports)
APPLICATION SITE MASS ( 2 FDA reports)
APPLICATION SITE PAPULES ( 2 FDA reports)
ARTERIAL LIGATION ( 2 FDA reports)
ARTERIOGRAM ( 2 FDA reports)
ARTERIOVENOUS FISTULA SITE INFECTION ( 2 FDA reports)
ARTHROSCOPY ABNORMAL ( 2 FDA reports)
ARTICULAR DISC DISORDER ( 2 FDA reports)
ARTIFICIAL MENOPAUSE ( 2 FDA reports)
ASPERGILLOMA ( 2 FDA reports)
ASPERGILLUS TEST POSITIVE ( 2 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 2 FDA reports)
ASPIRATION BREAST ( 2 FDA reports)
ASYMPTOMATIC BACTERIURIA ( 2 FDA reports)
ATAXIA TELANGIECTASIA ( 2 FDA reports)
ATONIC SEIZURES ( 2 FDA reports)
ATRIAL CONDUCTION TIME PROLONGATION ( 2 FDA reports)
ATRIAL RUPTURE ( 2 FDA reports)
ATRIAL SEPTAL DEFECT ACQUIRED ( 2 FDA reports)
AUTOIMMUNE PANCREATITIS ( 2 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 2 FDA reports)
AUTOPSY ( 2 FDA reports)
AZOOSPERMIA ( 2 FDA reports)
B-CELL LYMPHOMA STAGE II ( 2 FDA reports)
B-CELL TYPE ACUTE LEUKAEMIA ( 2 FDA reports)
B-LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
BABINSKI REFLEX TEST ( 2 FDA reports)
BACTERIA URINE NO ORGANISM OBSERVED ( 2 FDA reports)
BACTERIAL TOXAEMIA ( 2 FDA reports)
BACTEROIDES BACTERAEMIA ( 2 FDA reports)
BACTEROIDES TEST POSITIVE ( 2 FDA reports)
BALANOPOSTHITIS ( 2 FDA reports)
BAND NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
BENIGN BILIARY NEOPLASM ( 2 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 2 FDA reports)
BENIGN NEOPLASM OF EYELID ( 2 FDA reports)
BENIGN NEOPLASM OF PROSTATE ( 2 FDA reports)
BETA 2 MICROGLOBULIN URINE INCREASED ( 2 FDA reports)
BILATERAL HYDRONEPHROSIS ( 2 FDA reports)
BILE ACID MALABSORPTION ( 2 FDA reports)
BILE OUTPUT ABNORMAL ( 2 FDA reports)
BILIARY TRACT OPERATION ( 2 FDA reports)
BILIRUBIN CONJUGATED ( 2 FDA reports)
BINGE EATING ( 2 FDA reports)
BIOPSY BREAST NORMAL ( 2 FDA reports)
BIOPSY ENDOMETRIUM ABNORMAL ( 2 FDA reports)
BIOPSY HEART ABNORMAL ( 2 FDA reports)
BIOPSY INTESTINE ABNORMAL ( 2 FDA reports)
BIOPSY SKIN ( 2 FDA reports)
BIOPSY STOMACH ( 2 FDA reports)
BLADDER ADENOCARCINOMA STAGE UNSPECIFIED ( 2 FDA reports)
BLADDER CALCULUS REMOVAL ( 2 FDA reports)
BLADDER CATHETER TEMPORARY ( 2 FDA reports)
BLADDER GRANULOMA ( 2 FDA reports)
BLADDER NECROSIS ( 2 FDA reports)
BLADDER REPAIR ( 2 FDA reports)
BLADDER SPHINCTER ATONY ( 2 FDA reports)
BLADDER STENOSIS ( 2 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE 0 ( 2 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE I ( 2 FDA reports)
BLASTOMYCOSIS ( 2 FDA reports)
BLOOD AMINO ACID LEVEL INCREASED ( 2 FDA reports)
BLOOD CAFFEINE INCREASED ( 2 FDA reports)
BLOOD CARBON MONOXIDE INCREASED ( 2 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 2 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE BB INCREASED ( 2 FDA reports)
BLOOD ELECTROLYTES INCREASED ( 2 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE ABNORMAL ( 2 FDA reports)
BLOOD GASTRIN INCREASED ( 2 FDA reports)
BLOOD GLUCOSE FALSE POSITIVE ( 2 FDA reports)
BLOOD HOMOCYSTEINE ABNORMAL ( 2 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN DECREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN G ABNORMAL ( 2 FDA reports)
BLOOD INSULIN DECREASED ( 2 FDA reports)
BLOOD KETONE BODY ( 2 FDA reports)
BLOOD LACTIC ACID ( 2 FDA reports)
BLOOD OSMOLARITY ( 2 FDA reports)
BLOOD POTASSIUM ( 2 FDA reports)
BLOOD TESTOSTERONE ABNORMAL ( 2 FDA reports)
BLOOD THROMBOPLASTIN DECREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE ( 2 FDA reports)
BODY TEMPERATURE ( 2 FDA reports)
BONE INFECTION ( 2 FDA reports)
BONE TUBERCULOSIS ( 2 FDA reports)
BORRELIA INFECTION ( 2 FDA reports)
BORRELIA TEST POSITIVE ( 2 FDA reports)
BRACHIAL PLEXUS INJURY ( 2 FDA reports)
BRACHIAL PLEXUS LESION ( 2 FDA reports)
BRADYCARDIA NEONATAL ( 2 FDA reports)
BRAIN MALFORMATION ( 2 FDA reports)
BRAIN NEOPLASM BENIGN ( 2 FDA reports)
BRAIN SCAN NORMAL ( 2 FDA reports)
BREAST ATROPHY ( 2 FDA reports)
BREAST DISORDER MALE ( 2 FDA reports)
BREAST ENGORGEMENT ( 2 FDA reports)
BREAST FIBROMA ( 2 FDA reports)
BREAST INFLAMMATION ( 2 FDA reports)
BRONCHITIS PNEUMOCOCCAL ( 2 FDA reports)
BRONCHOSCOPY ( 2 FDA reports)
BROWN-SEQUARD SYNDROME ( 2 FDA reports)
BUDD-CHIARI SYNDROME ( 2 FDA reports)
BULLOUS IMPETIGO ( 2 FDA reports)
BURSA REMOVAL ( 2 FDA reports)
BURSITIS INFECTIVE STAPHYLOCOCCAL ( 2 FDA reports)
CAMPTOCORMIA ( 2 FDA reports)
CAMPYLOBACTER TEST POSITIVE ( 2 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 2 FDA reports)
CARCINOID TUMOUR OF THE DUODENUM ( 2 FDA reports)
CARCINOID TUMOUR OF THE GASTROINTESTINAL TRACT ( 2 FDA reports)
CARDIAC COMPLICATION ASSOCIATED WITH DEVICE ( 2 FDA reports)
CARDIAC MALPOSITION ( 2 FDA reports)
CARDIAC MURMUR FUNCTIONAL ( 2 FDA reports)
CARDIAC SARCOIDOSIS ( 2 FDA reports)
CARDIAC VENTRICULOGRAM LEFT ABNORMAL ( 2 FDA reports)
CARDIOMYOPATHY ACUTE ( 2 FDA reports)
CARDIOPLEGIA ( 2 FDA reports)
CAROTID PULSE INCREASED ( 2 FDA reports)
CATHETER BACTERAEMIA ( 2 FDA reports)
CATHETERISATION CARDIAC NORMAL ( 2 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 2 FDA reports)
CD4/CD8 RATIO INCREASED ( 2 FDA reports)
CD8 LYMPHOCYTES DECREASED ( 2 FDA reports)
CENTRAL VENOUS PRESSURE ABNORMAL ( 2 FDA reports)
CEREBRAL CIRCULATORY FAILURE ( 2 FDA reports)
CEREBRAL HYPERPERFUSION SYNDROME ( 2 FDA reports)
CEREBRAL PARENCHYMAL CALCIFICATION ( 2 FDA reports)
CEREBRAL VASOCONSTRICTION ( 2 FDA reports)
CEREBROSPINAL FLUID LEAKAGE ( 2 FDA reports)
CERVICAL INCOMPETENCE ( 2 FDA reports)
CERVIX HAEMORRHAGE UTERINE ( 2 FDA reports)
CHANGE IN SUSTAINED ATTENTION ( 2 FDA reports)
CHILLBLAINS ( 2 FDA reports)
CHLORACNE ( 2 FDA reports)
CHLOROMA ( 2 FDA reports)
CHLOROPSIA ( 2 FDA reports)
CHOLURIA ( 2 FDA reports)
CHORIORETINAL ATROPHY ( 2 FDA reports)
CHORIORETINOPATHY ( 2 FDA reports)
CHOROID MELANOMA ( 2 FDA reports)
CHROMOSOMAL DELETION ( 2 FDA reports)
CHROMOSOME ABNORMALITY ( 2 FDA reports)
CHRONIC GRANULOMATOUS DISEASE ( 2 FDA reports)
CHRONIC INFANTILE NEUROLOGICAL CUTANEOUS AND ARTICULAR SYNDROME ( 2 FDA reports)
CHRONIC LEFT VENTRICULAR FAILURE ( 2 FDA reports)
CHRONIC LEUKAEMIA ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA STAGE 2 ( 2 FDA reports)
CHRONIC MYELOID LEUKAEMIA TRANSFORMATION ( 2 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 2 FDA reports)
CHRONIC RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
CLEAR CELL CARCINOMA OF THE KIDNEY ( 2 FDA reports)
CLOSTRIDIUM BACTERAEMIA ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST ( 2 FDA reports)
COAGULATION FACTOR IX LEVEL DECREASED ( 2 FDA reports)
COAGULATION FACTOR IX LEVEL INCREASED ( 2 FDA reports)
COLECTOMY TOTAL ( 2 FDA reports)
COLITIS EROSIVE ( 2 FDA reports)
COLONOSCOPY NORMAL ( 2 FDA reports)
COMMUNITY ACQUIRED INFECTION ( 2 FDA reports)
COMPLEMENT FACTOR C4 INCREASED ( 2 FDA reports)
COMPUTERISED TOMOGRAM ( 2 FDA reports)
COMPUTERISED TOMOGRAM NORMAL ( 2 FDA reports)
CONGENITAL AORTIC STENOSIS ( 2 FDA reports)
CONGENITAL DIAPHRAGMATIC HERNIA ( 2 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 2 FDA reports)
COOMBS DIRECT TEST NEGATIVE ( 2 FDA reports)
CORNEAL DEFECT ( 2 FDA reports)
CORNEAL DEGENERATION ( 2 FDA reports)
CORNEAL OPERATION ( 2 FDA reports)
CORNEAL THINNING ( 2 FDA reports)
CORYNEBACTERIUM TEST POSITIVE ( 2 FDA reports)
CRANIAL NERVE INFECTION ( 2 FDA reports)
CRANIAL NERVE PALSIES MULTIPLE ( 2 FDA reports)
CRYPTOCOCCAL CUTANEOUS INFECTION ( 2 FDA reports)
CRYSTALLURIA ( 2 FDA reports)
CSF GLUCOSE INCREASED ( 2 FDA reports)
CSF LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
CSF PRESSURE INCREASED ( 2 FDA reports)
CSF PROTEIN ( 2 FDA reports)
CUTANEOUS TUBERCULOSIS ( 2 FDA reports)
CYCLIC NEUTROPENIA ( 2 FDA reports)
CYSTIC FIBROSIS LUNG ( 2 FDA reports)
CYSTITIS BACTERIAL ( 2 FDA reports)
CYSTITIS PSEUDOMONAL ( 2 FDA reports)
CYSTOID MACULAR OEDEMA ( 2 FDA reports)
CYSTOSTOMY ( 2 FDA reports)
CYTOKINE STORM ( 2 FDA reports)
CYTOMEGALOVIRUS GASTRITIS ( 2 FDA reports)
CYTOMEGALOVIRUS OESOPHAGITIS ( 2 FDA reports)
DAWN PHENOMENON ( 2 FDA reports)
DEATH OF CHILD ( 2 FDA reports)
DEGENERATION OF UTERINE LEIOMYOMA ( 2 FDA reports)
DEHYDROEPIANDROSTERONE TEST ( 2 FDA reports)
DELAYED EFFECTS OF RADIATION ( 2 FDA reports)
DELAYED SLEEP PHASE ( 2 FDA reports)
DEPENDENCE ON ENABLING MACHINE OR DEVICE ( 2 FDA reports)
DERMATITIS HERPETIFORMIS ( 2 FDA reports)
DESMOID TUMOUR ( 2 FDA reports)
DEVICE BATTERY ISSUE ( 2 FDA reports)
DEVICE DAMAGE ( 2 FDA reports)
DEVICE INEFFECTIVE ( 2 FDA reports)
DEVICE LEAD DAMAGE ( 2 FDA reports)
DEVICE STIMULATION ISSUE ( 2 FDA reports)
DIABETIC NEUROPATHIC ULCER ( 2 FDA reports)
DIAPHRAGMATIC RUPTURE ( 2 FDA reports)
DIHYDROTESTOSTERONE INCREASED ( 2 FDA reports)
DISORDER OF GLOBE ( 2 FDA reports)
DISORDER OF ORBIT ( 2 FDA reports)
DISSOCIATIVE FUGUE ( 2 FDA reports)
DIVERTICULAR FISTULA ( 2 FDA reports)
DRUG ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE ( 2 FDA reports)
DRUG LABEL CONFUSION ( 2 FDA reports)
DRUG WITHDRAWAL MAINTENANCE THERAPY ( 2 FDA reports)
DUODENAL VARICES ( 2 FDA reports)
DUODENITIS HAEMORRHAGIC ( 2 FDA reports)
DURAL ABSCESS ( 2 FDA reports)
DYSCALCULIA ( 2 FDA reports)
EAR INFECTION BACTERIAL ( 2 FDA reports)
EAR NEOPLASM MALIGNANT ( 2 FDA reports)
ECHOGRAPHY ABNORMAL ( 2 FDA reports)
ECZEMA EYELIDS ( 2 FDA reports)
EISENMENGER'S SYNDROME ( 2 FDA reports)
ELBOW OPERATION ( 2 FDA reports)
ELDERLY ( 2 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ( 2 FDA reports)
ELECTROCARDIOGRAM DELTA WAVES ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ( 2 FDA reports)
ELECTROCUTION ( 2 FDA reports)
ELECTROPHORESIS ABNORMAL ( 2 FDA reports)
ELECTROPHORESIS PROTEIN ABNORMAL ( 2 FDA reports)
EMERGENCY CARE ( 2 FDA reports)
ENCEPHALITIS JAPANESE B ( 2 FDA reports)
ENDOCARDIAL DISEASE ( 2 FDA reports)
ENDOCARDIAL FIBROELASTOSIS ( 2 FDA reports)
ENDOLYMPHATIC HYDROPS ( 2 FDA reports)
ENDOMETRIAL ATROPHY ( 2 FDA reports)
ENDOMETRIAL NEOPLASM ( 2 FDA reports)
ENDOSCOPY SMALL INTESTINE ABNORMAL ( 2 FDA reports)
ENDOTHELIAL DYSFUNCTION ( 2 FDA reports)
ENDOTOXIC SHOCK ( 2 FDA reports)
ENTEROCLYSIS ( 2 FDA reports)
EOSINOPHILIC FASCIITIS ( 2 FDA reports)
ERYTHROPLASIA ( 2 FDA reports)
EUSTACHIAN TUBE OBSTRUCTION ( 2 FDA reports)
EXERCISE CAPACITY DECREASED ( 2 FDA reports)
EXTERNAL EAR INFLAMMATION ( 2 FDA reports)
EXTERNAL EAR PAIN ( 2 FDA reports)
EYELASH DISCOLOURATION ( 2 FDA reports)
FACTOR XIII DEFICIENCY ( 2 FDA reports)
FALLOPIAN TUBE CANCER METASTATIC ( 2 FDA reports)
FALSE NEGATIVE INVESTIGATION RESULT ( 2 FDA reports)
FAT INTOLERANCE ( 2 FDA reports)
FEAR OF WEIGHT GAIN ( 2 FDA reports)
FELTY'S SYNDROME ( 2 FDA reports)
FEMALE PATTERN BALDNESS ( 2 FDA reports)
FEMORAL NERVE INJURY ( 2 FDA reports)
FEMORAL NERVE PALSY ( 2 FDA reports)
FEMORAL PULSE DECREASED ( 2 FDA reports)
FIBRINOUS BRONCHITIS ( 2 FDA reports)
FIBROMATOSIS ( 2 FDA reports)
FIBROMUSCULAR DYSPLASIA ( 2 FDA reports)
FINGERPRINT LOSS ( 2 FDA reports)
FOETAL ARRHYTHMIA ( 2 FDA reports)
FOETAL CYSTIC HYGROMA ( 2 FDA reports)
FOETAL HEART RATE DECREASED ( 2 FDA reports)
FOETAL HYPOKINESIA ( 2 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III STAGE III ( 2 FDA reports)
FORCED EXPIRATORY VOLUME ABNORMAL ( 2 FDA reports)
FORCED EXPIRATORY VOLUME INCREASED ( 2 FDA reports)
FRACTURED ISCHIUM ( 2 FDA reports)
FREE FATTY ACIDS INCREASED ( 2 FDA reports)
FREE THYROXINE INDEX INCREASED ( 2 FDA reports)
FREEZING PHENOMENON ( 2 FDA reports)
FRUCTOSAMINE INCREASED ( 2 FDA reports)
FULL BLOOD COUNT ( 2 FDA reports)
FUNDOSCOPY ABNORMAL ( 2 FDA reports)
FUNGAL ENDOCARDITIS ( 2 FDA reports)
FUNGUS STOOL IDENTIFIED ( 2 FDA reports)
FUNGUS URINE TEST POSITIVE ( 2 FDA reports)
GALLBLADDER EMPYEMA ( 2 FDA reports)
GASTRIC BANDING ( 2 FDA reports)
GASTRIC CANCER STAGE 0 ( 2 FDA reports)
GASTRIC DYSPLASIA ( 2 FDA reports)
GASTRIC HYPOMOTILITY ( 2 FDA reports)
GASTRODUODENAL HAEMORRHAGE ( 2 FDA reports)
GASTROENTERITIS NONINFECTIOUS ( 2 FDA reports)
GASTROINTESTINAL VASCULAR MALFORMATION ( 2 FDA reports)
GENITAL ERYTHEMA ( 2 FDA reports)
GENITAL HYPOAESTHESIA ( 2 FDA reports)
GENITAL PRURITUS MALE ( 2 FDA reports)
GENITOURINARY TRACT NEOPLASM ( 2 FDA reports)
GINGIVAL HYPOPLASIA ( 2 FDA reports)
GLOSSOPTOSIS ( 2 FDA reports)
GLUCOSE URINE ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE IN LUNG ( 2 FDA reports)
GRAM STAIN POSITIVE ( 2 FDA reports)
GRANULOCYTOSIS ( 2 FDA reports)
GROWING PAINS ( 2 FDA reports)
GROWTH OF EYELASHES ( 2 FDA reports)
GROWTH RETARDATION ( 2 FDA reports)
HAEMANGIOMA CONGENITAL ( 2 FDA reports)
HAEMANGIOMA OF SKIN ( 2 FDA reports)
HAEMATURIA TRAUMATIC ( 2 FDA reports)
HAEMODYNAMIC TEST ABNORMAL ( 2 FDA reports)
HAEMOGLOBINAEMIA ( 2 FDA reports)
HAEMOPHILIA ( 2 FDA reports)
HAEMOPHILUS TEST POSITIVE ( 2 FDA reports)
HAEMOPNEUMOTHORAX ( 2 FDA reports)
HAPTOGLOBIN ( 2 FDA reports)
HEAD CIRCUMFERENCE ( 2 FDA reports)
HEAD LAG ( 2 FDA reports)
HEART VALVE STENOSIS ( 2 FDA reports)
HEAT OEDEMA ( 2 FDA reports)
HEPATECTOMY ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT NON-RESECTABLE ( 2 FDA reports)
HEPATIC RUPTURE ( 2 FDA reports)
HEPATIC VEIN DILATATION ( 2 FDA reports)
HEPATITIS A POSITIVE ( 2 FDA reports)
HEPATITIS B CORE ANTIBODY POSITIVE ( 2 FDA reports)
HEPATITIS B SURFACE ANTIBODY POSITIVE ( 2 FDA reports)
HEPATITIS C RNA INCREASED ( 2 FDA reports)
HEPATITIS C VIRUS TEST POSITIVE ( 2 FDA reports)
HEPATITIS GRANULOMATOUS ( 2 FDA reports)
HEPATITIS NON-A NON-B ( 2 FDA reports)
HEPATOBLASTOMA ( 2 FDA reports)
HEREDITARY HAEMORRHAGIC TELANGIECTASIA ( 2 FDA reports)
HERNIA GANGRENOUS ( 2 FDA reports)
HERPES DERMATITIS ( 2 FDA reports)
HERPES SIMPLEX HEPATITIS ( 2 FDA reports)
HERPES ZOSTER INFECTION NEUROLOGICAL ( 2 FDA reports)
HERPES ZOSTER MULTI-DERMATOMAL ( 2 FDA reports)
HERPETIC GINGIVOSTOMATITIS ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN ( 2 FDA reports)
HIGH RISK PREGNANCY ( 2 FDA reports)
HISTAMINE LEVEL INCREASED ( 2 FDA reports)
HISTIOCYTOSIS ( 2 FDA reports)
HISTOPLASMOSIS CUTANEOUS ( 2 FDA reports)
HODGKIN'S DISEASE MIXED CELLULARITY STAGE UNSPECIFIED ( 2 FDA reports)
HOLOPROSENCEPHALY ( 2 FDA reports)
HOMOSEXUALITY ( 2 FDA reports)
HYPERCHROMIC ANAEMIA ( 2 FDA reports)
HYPERGASTRINAEMIA ( 2 FDA reports)
HYPERGLYCAEMIC SEIZURE ( 2 FDA reports)
HYPERKINETIC HEART SYNDROME ( 2 FDA reports)
HYPERPHOSPHATASAEMIA ( 2 FDA reports)
HYPERSPLENISM ( 2 FDA reports)
HYPOKALAEMIC SYNDROME ( 2 FDA reports)
HYPONATRAEMIC SYNDROME ( 2 FDA reports)
HYPOPARATHYROIDISM SECONDARY ( 2 FDA reports)
HYPOPHARYNGEAL CANCER ( 2 FDA reports)
HYPOPHOSPHATAEMIC RICKETS ( 2 FDA reports)
HYPOPHYSITIS ( 2 FDA reports)
HYSTEROTOMY ( 2 FDA reports)
ILIAC ARTERY EMBOLISM ( 2 FDA reports)
ILLOGICAL THINKING ( 2 FDA reports)
IMMUNE COMPLEX LEVEL INCREASED ( 2 FDA reports)
IMMUNISATION ( 2 FDA reports)
IMMUNISATION REACTION ( 2 FDA reports)
URINE IRON INCREASED ( 2 FDA reports)
URINE LEUKOCYTE ESTERASE ( 2 FDA reports)
URINE POTASSIUM DECREASED ( 2 FDA reports)
URINE URIC ACID ABNORMAL ( 2 FDA reports)
UROBILIN URINE ( 2 FDA reports)
UTERINE CERVIX STENOSIS ( 2 FDA reports)
UTERINE HAEMATOMA ( 2 FDA reports)
UTERINE LEIOMYOSARCOMA ( 2 FDA reports)
UTERINE OPERATION ( 2 FDA reports)
UTERINE PERFORATION ( 2 FDA reports)
UTERINE SPASM ( 2 FDA reports)
UTERINE STENOSIS ( 2 FDA reports)
VAGINAL ABSCESS ( 2 FDA reports)
VAGINAL DYSPLASIA ( 2 FDA reports)
VAGINAL ERYTHEMA ( 2 FDA reports)
VAGINAL INFLAMMATION ( 2 FDA reports)
VAGINITIS ATROPHIC ( 2 FDA reports)
VARICELLA VIRUS TEST POSITIVE ( 2 FDA reports)
VASCULAR DISSECTION ( 2 FDA reports)
VASCULAR RESISTANCE PULMONARY INCREASED ( 2 FDA reports)
VASODILATION PROCEDURE ( 2 FDA reports)
VASOPRESSIVE THERAPY ( 2 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 2 FDA reports)
VENTILATION PERFUSION MISMATCH ( 2 FDA reports)
VENTRICULAR DYSSYNCHRONY ( 2 FDA reports)
VENTRICULAR HYPOPLASIA ( 2 FDA reports)
VENTRICULO-PERITONEAL SHUNT ( 2 FDA reports)
VERBIGERATION ( 2 FDA reports)
VERTEBRAL COLUMN MASS ( 2 FDA reports)
VESSEL PUNCTURE SITE PAIN ( 2 FDA reports)
VESTIBULAR ATAXIA ( 2 FDA reports)
VICTIM OF ABUSE ( 2 FDA reports)
VICTIM OF ELDER ABUSE ( 2 FDA reports)
VIITH NERVE INJURY ( 2 FDA reports)
VIRAL RHINITIS ( 2 FDA reports)
VIRUS URINE TEST POSITIVE ( 2 FDA reports)
VISUAL ACUITY REDUCED TRANSIENTLY ( 2 FDA reports)
VISUAL FIELD TESTS ABNORMAL ( 2 FDA reports)
VISUAL PATHWAY DISORDER ( 2 FDA reports)
VITAMIN C DEFICIENCY ( 2 FDA reports)
VITAMIN E DEFICIENCY ( 2 FDA reports)
VITAMIN K DECREASED ( 2 FDA reports)
VITH NERVE DISORDER ( 2 FDA reports)
VITREAL CELLS ( 2 FDA reports)
VOGT-KOYANAGI-HARADA SYNDROME ( 2 FDA reports)
VOLVULUS OF SMALL BOWEL ( 2 FDA reports)
VOMITING PSYCHOGENIC ( 2 FDA reports)
VON WILLEBRAND'S DISEASE ( 2 FDA reports)
VULVA CYST ( 2 FDA reports)
VULVAL CANCER STAGE 0 ( 2 FDA reports)
VULVOVAGINAL RASH ( 2 FDA reports)
WEIGHT BELOW NORMAL ( 2 FDA reports)
WEIGHT CONTROL ( 2 FDA reports)
WHITE BLOOD CELL MORPHOLOGY ABNORMAL ( 2 FDA reports)
WITHDRAWAL ARRHYTHMIA ( 2 FDA reports)
WITHDRAWAL HYPERTENSION ( 2 FDA reports)
X-RAY OF PELVIS AND HIP ABNORMAL ( 2 FDA reports)
XEROPHTHALMIA ( 2 FDA reports)
ZYGOMYCOSIS ( 2 FDA reports)
URINE ELECTROPHORESIS ABNORMAL ( 1 FDA reports)
URINE LACTIC ACID INCREASED ( 1 FDA reports)
URINE PROTEIN, QUANTITATIVE ( 1 FDA reports)
URINE PROTEIN/CREATININE RATIO ABNORMAL ( 1 FDA reports)
URINE URIC ACID INCREASED ( 1 FDA reports)
URINE VISCOSITY INCREASED ( 1 FDA reports)
URINOMA ( 1 FDA reports)
UROBILINURIA ( 1 FDA reports)
UROGENITAL FISTULA ( 1 FDA reports)
UROGRAM ABNORMAL ( 1 FDA reports)
URTICARIA LOCALISED ( 1 FDA reports)
UTERINE CERVICAL PAIN ( 1 FDA reports)
UTERINE CERVIX ATROPHY ( 1 FDA reports)
UTERINE CONTRACTIONS ABNORMAL ( 1 FDA reports)
UTERINE FIBROSIS ( 1 FDA reports)
UTERINE HYPERTONUS ( 1 FDA reports)
UTERINE INFECTION ( 1 FDA reports)
UVEITIS-GLAUCOMA-HYPHAEMA SYNDROME ( 1 FDA reports)
VACTERL SYNDROME ( 1 FDA reports)
VAGINAL ATRESIA ( 1 FDA reports)
VAGINAL CANCER STAGE III ( 1 FDA reports)
VAGINAL LACERATION ( 1 FDA reports)
VAGINAL SWELLING ( 1 FDA reports)
VAGINITIS GARDNERELLA ( 1 FDA reports)
VAGUS NERVE DISORDER ( 1 FDA reports)
VALVULOPLASTY CARDIAC ( 1 FDA reports)
VANISHING TWIN SYNDROME ( 1 FDA reports)
VARICOPHLEBITIS ( 1 FDA reports)
VASCULAR COMPLICATION ASSOCIATED WITH DEVICE ( 1 FDA reports)
VASCULAR NEOPLASM ( 1 FDA reports)
VASCULAR RESISTANCE SYSTEMIC ( 1 FDA reports)
VASCULAR TEST ABNORMAL ( 1 FDA reports)
VASOACTIVE INTESTINAL POLYPEPTIDE TEST ( 1 FDA reports)
VENA CAVA EMBOLISM ( 1 FDA reports)
VENA CAVA INJURY ( 1 FDA reports)
VENIPUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
VENIPUNCTURE SITE SWELLING ( 1 FDA reports)
VENOUS OXYGEN SATURATION DECREASED ( 1 FDA reports)
VENOUS STENT INSERTION ( 1 FDA reports)
VENOUS THROMBOSIS IN PREGNANCY ( 1 FDA reports)
VENTRICULAR HYPERKINESIA ( 1 FDA reports)
VENTRICULAR INTERNAL DIAMETER ( 1 FDA reports)
VENTRICULAR REMODELING ( 1 FDA reports)
VENTRICULAR WALL THICKENING ( 1 FDA reports)
VERTEBROBASILAR DOLICHOECTASIA ( 1 FDA reports)
VERTIGO CNS ORIGIN ( 1 FDA reports)
VERY LOW DENSITY LIPOPROTEIN ABNORMAL ( 1 FDA reports)
VESSEL PUNCTURE SITE REACTION ( 1 FDA reports)
VESSEL PUNCTURE SITE THROMBOSIS ( 1 FDA reports)
VESTIBULAR FUNCTION TEST ABNORMAL ( 1 FDA reports)
VICTIM OF HOMICIDE ( 1 FDA reports)
VIRAL LOAD ( 1 FDA reports)
VIRAL TEST NEGATIVE ( 1 FDA reports)
VIRAL TEST POSITIVE ( 1 FDA reports)
VISUAL ACUITY TESTS ( 1 FDA reports)
VISUAL TRACKING TEST ABNORMAL ( 1 FDA reports)
VITAMIN A DEFICIENCY ( 1 FDA reports)
VITAMIN D ( 1 FDA reports)
VITREOUS ADHESIONS ( 1 FDA reports)
VOCAL CORD CYST ( 1 FDA reports)
VOCAL CORD LIPOINJECTION ( 1 FDA reports)
VON WILLEBRAND'S FACTOR ACTIVITY ABNORMAL ( 1 FDA reports)
VON WILLEBRAND'S FACTOR ANTIGEN INCREASED ( 1 FDA reports)
VON WILLEBRAND'S FACTOR MULTIMERS ABNORMAL ( 1 FDA reports)
VULVA INJURY ( 1 FDA reports)
VULVAL ERYTHEMA ( 1 FDA reports)
VULVAL HAEMATOMA ( 1 FDA reports)
VULVOVAGINITIS TRICHOMONAL ( 1 FDA reports)
WART EXCISION ( 1 FDA reports)
WERNICKE-KORSAKOFF SYNDROME ( 1 FDA reports)
WHITE BLOOD CELL AGGLUTINATION PRESENT ( 1 FDA reports)
WHITE BLOOD CELL ANALYSIS INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT NORMAL ( 1 FDA reports)
WHITE BLOOD CELLS STOOL POSITIVE ( 1 FDA reports)
WITHDRAWAL BLEEDING IRREGULAR ( 1 FDA reports)
WITHDRAWAL OF LIFE SUPPORT ( 1 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 1 FDA reports)
X-RAY DENTAL ( 1 FDA reports)
X-RAY LIMB ( 1 FDA reports)
XANTHOGRANULOMA ( 1 FDA reports)
XANTHOMA ( 1 FDA reports)
YOUNG'S SYNDROME ( 1 FDA reports)
5-HYDROXYINDOLACETIC ACID INCREASED ( 1 FDA reports)
ABDOMINAL INJURY ( 1 FDA reports)
ABDOMINAL WALL NEOPLASM ( 1 FDA reports)
ABORTED PREGNANCY ( 1 FDA reports)
ABORTION OF ECTOPIC PREGNANCY ( 1 FDA reports)
ACARIASIS ( 1 FDA reports)
ACCESSORY MUSCLE ( 1 FDA reports)
ACINETOBACTER BACTERAEMIA ( 1 FDA reports)
ACNE CYSTIC ( 1 FDA reports)
ACQUIRED MACROGLOSSIA ( 1 FDA reports)
ACQUIRED PYLORIC STENOSIS ( 1 FDA reports)
ACQUIRED TRACHEO-OESOPHAGEAL FISTULA ( 1 FDA reports)
ACRODERMATITIS ENTEROPATHICA ( 1 FDA reports)
ACTH STIMULATION TEST ABNORMAL ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
ACUTE MEGAKARYOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA DIFFERENTIATION SYNDROME ( 1 FDA reports)
ACUTE VESTIBULAR SYNDROME ( 1 FDA reports)
ADENOSQUAMOUS CELL LUNG CANCER STAGE IV ( 1 FDA reports)
ADENOVIRAL CONJUNCTIVITIS ( 1 FDA reports)
ADMINISTRATION SITE REACTION ( 1 FDA reports)
ADRENAL GLAND INJURY ( 1 FDA reports)
ADRENAL HAEMATOMA ( 1 FDA reports)
ADRENOCORTICAL STEROID THERAPY ( 1 FDA reports)
ADVANCED SLEEP PHASE ( 1 FDA reports)
AEROPHAGIA ( 1 FDA reports)
AFFERENT LOOP SYNDROME ( 1 FDA reports)
AGITATION NEONATAL ( 1 FDA reports)
AIRWAY PEAK PRESSURE INCREASED ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO ABNORMAL ( 1 FDA reports)
ALCOHOL PROBLEM ( 1 FDA reports)
ALEXIA ( 1 FDA reports)
ALKALOSIS HYPOCHLORAEMIC ( 1 FDA reports)
ALKAPTONURIA ( 1 FDA reports)
ALLEN'S TEST ( 1 FDA reports)
ALLERGENIC DESENSITISATION PROCEDURE ( 1 FDA reports)
ALLERGIC RESPIRATORY SYMPTOM ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN ABNORMAL ( 1 FDA reports)
ALPHA HYDROXYBUTYRATE DEHYDROGENASE INCREASED ( 1 FDA reports)
ALPHA-1 ANTI-TRYPSIN DECREASED ( 1 FDA reports)
ALPHA-1 ANTI-TRYPSIN INCREASED ( 1 FDA reports)
ALVEOLAR OXYGEN PARTIAL PRESSURE INCREASED ( 1 FDA reports)
AMINO ACID METABOLISM DISORDER ( 1 FDA reports)
AMPHETAMINES POSITIVE ( 1 FDA reports)
AMPUTATION REVISION ( 1 FDA reports)
ANAEMIA NEONATAL ( 1 FDA reports)
ANAL CANCER STAGE III ( 1 FDA reports)
ANAL DILATION PROCEDURE ( 1 FDA reports)
ANAL INFLAMMATION ( 1 FDA reports)
ANAL SPASM ( 1 FDA reports)
ANALGESIA ( 1 FDA reports)
ANALGESIC DRUG LEVEL DECREASED ( 1 FDA reports)
ANAPLASTIC ASTROCYTOMA ( 1 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 1 FDA reports)
ANGINA BULLOSA HAEMORRHAGICA ( 1 FDA reports)
ANGIODERMATITIS ( 1 FDA reports)
ANGIOGRAM PERIPHERAL ABNORMAL ( 1 FDA reports)
ANGIOKERATOMA ( 1 FDA reports)
ANGIOSARCOMA METASTATIC ( 1 FDA reports)
ANION GAP ( 1 FDA reports)
ANISOCHROMIA ( 1 FDA reports)
ANKLE ARTHROPLASTY ( 1 FDA reports)
ANKLE BRACHIAL INDEX DECREASED ( 1 FDA reports)
ANORECTAL OPERATION ( 1 FDA reports)
ANORECTAL STENOSIS ( 1 FDA reports)
ANTERIOR CHAMBER CELL ( 1 FDA reports)
ANTERIOR CHAMBER FIBRIN ( 1 FDA reports)
ANTERIOR CHAMBER INFLAMMATION ( 1 FDA reports)
ANTEROGRADE AMNESIA ( 1 FDA reports)
ANTI FACTOR VIII ANTIBODY TEST ( 1 FDA reports)
ANTI-HBE ANTIBODY POSITIVE ( 1 FDA reports)
ANTICIPATORY ANXIETY ( 1 FDA reports)
ANTIDEPRESSANT THERAPY ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY INCREASED ( 1 FDA reports)
ANTIRETROVIRAL THERAPY ( 1 FDA reports)
ANTITHROMBIN III ( 1 FDA reports)
ANXIETY POSTOPERATIVE ( 1 FDA reports)
AORTA HYPOPLASIA ( 1 FDA reports)
APICECTOMY ( 1 FDA reports)
APOLIPOPROTEIN A-I DECREASED ( 1 FDA reports)
APOLIPOPROTEIN B ABNORMAL ( 1 FDA reports)
APOPTOSIS ( 1 FDA reports)
APPENDICEAL MUCOCOELE ( 1 FDA reports)
APPLICATION SITE ABSCESS ( 1 FDA reports)
APPLICATION SITE ATROPHY ( 1 FDA reports)
APPLICATION SITE DISCOMFORT ( 1 FDA reports)
APPLICATION SITE ECZEMA ( 1 FDA reports)
APPLICATION SITE EXCORIATION ( 1 FDA reports)
APPLICATION SITE NECROSIS ( 1 FDA reports)
APPLICATION SITE OEDEMA ( 1 FDA reports)
APPLICATION SITE PARAESTHESIA ( 1 FDA reports)
APPLICATION SITE ULCER ( 1 FDA reports)
ARRESTED LABOUR ( 1 FDA reports)
ARTERECTOMY ( 1 FDA reports)
ARTERIAL CATHETERISATION ABNORMAL ( 1 FDA reports)
ARTERIOGRAM ABNORMAL ( 1 FDA reports)
ARTERIOPATHIC DISEASE ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMATOMA ( 1 FDA reports)
ARTERIOVENOUS GRAFT SITE HAEMORRHAGE ( 1 FDA reports)
ARTERIOVENOUS GRAFT THROMBOSIS ( 1 FDA reports)
ARTIFICIAL ANUS ( 1 FDA reports)
ARTIFICIAL HEART DEVICE USER ( 1 FDA reports)
ASPERMIA ( 1 FDA reports)
ASPIRATION JOINT ABNORMAL ( 1 FDA reports)
ASPIRATION TRACHEAL ABNORMAL ( 1 FDA reports)
ATHEROSCLEROSIS OBLITERANS ( 1 FDA reports)
ATHEROSCLEROSIS PROPHYLAXIS ( 1 FDA reports)
ATROPHY OF GLOBE ( 1 FDA reports)
ATTENTION-SEEKING BEHAVIOUR ( 1 FDA reports)
ATYPICAL MYCOBACTERIAL LYMPHADENITIS ( 1 FDA reports)
AUDITORY RECRUITMENT ( 1 FDA reports)
AUTOIMMUNE APLASTIC ANAEMIA ( 1 FDA reports)
AUTOIMMUNE MYOCARDITIS ( 1 FDA reports)
AUTOIMMUNE NEUTROPENIA ( 1 FDA reports)
B PRECURSOR TYPE ACUTE LEUKAEMIA ( 1 FDA reports)
B-CELL LYMPHOMA RECURRENT ( 1 FDA reports)
B-CELL LYMPHOMA STAGE I ( 1 FDA reports)
B-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
BACTERIA BODY FLUID IDENTIFIED ( 1 FDA reports)
BACTERIA WOUND IDENTIFIED ( 1 FDA reports)
BACTERIAL FOOD POISONING ( 1 FDA reports)
BACTERIAL TRACHEITIS ( 1 FDA reports)
BACTERIAL TRANSLOCATION ( 1 FDA reports)
BALINT'S SYNDROME ( 1 FDA reports)
BARBITURATES POSITIVE ( 1 FDA reports)
BAROTITIS MEDIA ( 1 FDA reports)
BAROTRAUMA ( 1 FDA reports)
BASILAR MIGRAINE ( 1 FDA reports)
BENIGN LYMPH NODE NEOPLASM ( 1 FDA reports)
BENIGN MUSCLE NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF PINEAL GLAND ( 1 FDA reports)
BENIGN SMALL INTESTINAL NEOPLASM ( 1 FDA reports)
BENIGN SOFT TISSUE NEOPLASM ( 1 FDA reports)
BETA-2 GLYCOPROTEIN ANTIBODY POSITIVE ( 1 FDA reports)
BILE DUCT NECROSIS ( 1 FDA reports)
BILIARY DRAINAGE ( 1 FDA reports)
BILIARY FISTULA ( 1 FDA reports)
BILIOPANCREATIC BYPASS ( 1 FDA reports)
BIOPSY ABDOMINAL WALL ABNORMAL ( 1 FDA reports)
BIOPSY BRONCHUS ( 1 FDA reports)
BIOPSY CARTILAGE ABNORMAL ( 1 FDA reports)
BIOPSY CERVIX ABNORMAL ( 1 FDA reports)
BIOPSY LUNG ABNORMAL ( 1 FDA reports)
BIOPSY LYMPH GLAND NORMAL ( 1 FDA reports)
BIOPSY PANCREAS ABNORMAL ( 1 FDA reports)
BIOPSY PROSTATE ABNORMAL ( 1 FDA reports)
BIOPSY SMALL INTESTINE ( 1 FDA reports)
BIOPSY SMALL INTESTINE ABNORMAL ( 1 FDA reports)
BIOPSY TESTES ( 1 FDA reports)
BIOPSY THYROID GLAND ABNORMAL ( 1 FDA reports)
BIRTH MARK ( 1 FDA reports)
BLADDER ADENOCARCINOMA STAGE III ( 1 FDA reports)
BLADDER CANCER STAGE I, WITH CANCER IN SITU ( 1 FDA reports)
BLADDER CANCER STAGE I, WITHOUT CANCER IN SITU ( 1 FDA reports)
BLADDER CANCER STAGE IV ( 1 FDA reports)
BLADDER LESION EXCISION ( 1 FDA reports)
BLADDER PAPILLOMA ( 1 FDA reports)
BLADDER SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
BLADDER SUSPENSION ( 1 FDA reports)
BLADDER TUMOUR RESECTION ( 1 FDA reports)
BLAST CELLS PRESENT ( 1 FDA reports)
BLEEDING ANOVULATORY ( 1 FDA reports)
BLEEDING PERIPARTUM ( 1 FDA reports)
BLOOD 1,25-DIHYDROXYCHOLECALCIFEROL DECREASED ( 1 FDA reports)
BLOOD 1,25-DIHYDROXYCHOLECALCIFEROL INCREASED ( 1 FDA reports)
BLOOD 25-HYDROXYCHOLECALCIFEROL DECREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE NORMAL ( 1 FDA reports)
BLOOD ALUMINIUM ABNORMAL ( 1 FDA reports)
BLOOD ALUMINIUM INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN ( 1 FDA reports)
BLOOD CALCITONIN ABNORMAL ( 1 FDA reports)
BLOOD CALCITONIN DECREASED ( 1 FDA reports)
BLOOD CALCIUM ( 1 FDA reports)
BLOOD CANNABINOIDS ( 1 FDA reports)
BLOOD CARBON MONOXIDE DECREASED ( 1 FDA reports)
BLOOD CATECHOLAMINES INCREASED ( 1 FDA reports)
BLOOD CHOLINESTERASE ABNORMAL ( 1 FDA reports)
BLOOD CHROMIUM INCREASED ( 1 FDA reports)
BLOOD COPPER ABNORMAL ( 1 FDA reports)
BLOOD COPPER INCREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN INCREASED ( 1 FDA reports)
BLOOD CREATINE ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE NORMAL ( 1 FDA reports)
BLOOD FIBRINOGEN ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE NORMAL ( 1 FDA reports)
BLOOD GROWTH HORMONE ABNORMAL ( 1 FDA reports)
BLOOD GROWTH HORMONE INCREASED ( 1 FDA reports)
BLOOD HEAVY METAL INCREASED ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN POSITIVE ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M ( 1 FDA reports)
BLOOD INSULIN ABNORMAL ( 1 FDA reports)
BLOOD IRON ( 1 FDA reports)
BLOOD IRON ABNORMAL ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ( 1 FDA reports)
BLOOD LACTIC ACID ABNORMAL ( 1 FDA reports)
BLOOD METHANOL INCREASED ( 1 FDA reports)
BLOOD OESTROGEN INCREASED ( 1 FDA reports)
BLOOD OSMOLARITY ABNORMAL ( 1 FDA reports)
BLOOD PH ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE AMBULATORY ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INSPIRATORY DECREASED ( 1 FDA reports)
BLOOD PROLACTIN ABNORMAL ( 1 FDA reports)
BLOOD PYRUVIC ACID INCREASED ( 1 FDA reports)
BLOOD STEM CELL HARVEST FAILURE ( 1 FDA reports)
BLOOD TESTOSTERONE ( 1 FDA reports)
BLOOD THROMBIN ( 1 FDA reports)
BLOOD THROMBIN INCREASED ( 1 FDA reports)
BLOOD THROMBOPLASTIN ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO DECREASED ( 1 FDA reports)
BODY HEIGHT ( 1 FDA reports)
BODY HEIGHT ABNORMAL ( 1 FDA reports)
BONE DEFORMITY ( 1 FDA reports)
BONE MARROW GRANULOMA ( 1 FDA reports)
BONE SARCOMA ( 1 FDA reports)
BONE SCAN ( 1 FDA reports)
BORDERLINE LEPROSY ( 1 FDA reports)
BOWEL PREPARATION ( 1 FDA reports)
BOWENOID PAPULOSIS ( 1 FDA reports)
BRACHIAL PULSE ABNORMAL ( 1 FDA reports)
BRACHIAL PULSE DECREASED ( 1 FDA reports)
BRACHIOCEPHALIC VEIN STENOSIS ( 1 FDA reports)
BRAIN STEM AUDITORY EVOKED RESPONSE ABNORMAL ( 1 FDA reports)
BRAIN STEM GLIOMA ( 1 FDA reports)
BREAST CANCER STAGE IV ( 1 FDA reports)
BREAST COSMETIC SURGERY ( 1 FDA reports)
BREAST CYST EXCISION ( 1 FDA reports)
BREATH ALCOHOL TEST POSITIVE ( 1 FDA reports)
BRONCHIAL DYSPLASIA ( 1 FDA reports)
BRONCHITIS ACUTE VIRAL ( 1 FDA reports)
BRONCHITIS HAEMOPHILUS ( 1 FDA reports)
BRONCHOGRAM ABNORMAL ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ALLERGIC ( 1 FDA reports)
BUCCAL POLYP ( 1 FDA reports)
BURKHOLDERIA CEPACIA COMPLEX INFECTION ( 1 FDA reports)
BURKHOLDERIA CEPACIA INFECTION ( 1 FDA reports)
BURKHOLDERIA TEST POSITIVE ( 1 FDA reports)
BURNS FIRST DEGREE ( 1 FDA reports)
C1 ESTERASE INHIBITOR DECREASED ( 1 FDA reports)
CAFE AU LAIT SPOTS ( 1 FDA reports)
CALCIFICATION METASTATIC ( 1 FDA reports)
CALCIFICATION PANCREATIC DUCT ( 1 FDA reports)
CALCIUM IONISED ( 1 FDA reports)
CALCULUS PROSTATIC ( 1 FDA reports)
CALLUS FORMATION DELAYED ( 1 FDA reports)
CAMPBELL DE MORGAN SPOTS ( 1 FDA reports)
CANCER GENE CARRIER ( 1 FDA reports)
CANDIDA OSTEOMYELITIS ( 1 FDA reports)
CAPSULE ISSUE ( 1 FDA reports)
CARBOHYDRATE METABOLISM DISORDER ( 1 FDA reports)
CARBON DIOXIDE ABNORMAL ( 1 FDA reports)
CARCINOID TUMOUR OF THE APPENDIX ( 1 FDA reports)
CARCINOID TUMOUR OF THE CAECUM ( 1 FDA reports)
CARCINOMA EXCISION ( 1 FDA reports)
CARCINOMA IN SITU OF EYE ( 1 FDA reports)
CARCINOMA IN SITU OF TRACHEA ( 1 FDA reports)
CARDIAC ELECTROPHYSIOLOGIC STUDY ABNORMAL ( 1 FDA reports)
CARDIAC ENZYMES ( 1 FDA reports)
CARDIAC MONITORING ABNORMAL ( 1 FDA reports)
CARDIAC NEOPLASM MALIGNANT ( 1 FDA reports)
CARDIAC PACEMAKER EVALUATION ( 1 FDA reports)
CARDIAC SEPTAL DEFECT RESIDUAL SHUNT ( 1 FDA reports)
CARDIAC STRESS TEST NORMAL ( 1 FDA reports)
CARDIAC TELEMETRY ( 1 FDA reports)
CARDIAC TELEMETRY ABNORMAL ( 1 FDA reports)
CARDIAC VENTRICULOGRAM ABNORMAL ( 1 FDA reports)
CARDIOLIPIN ANTIBODY ( 1 FDA reports)
CARDIOVASCULAR FUNCTION TEST ABNORMAL ( 1 FDA reports)
CAROTID ANGIOPLASTY ( 1 FDA reports)
CAROTID PULSE ABNORMAL ( 1 FDA reports)
CATARACT CONGENITAL ( 1 FDA reports)
CATHETER SITE BRUISE ( 1 FDA reports)
CAUDAL REGRESSION SYNDROME ( 1 FDA reports)
CELL-MEDIATED CYTOTOXICITY ( 1 FDA reports)
CELLULITIS ENTEROCOCCAL ( 1 FDA reports)
CELLULITIS OF MALE EXTERNAL GENITAL ORGAN ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM NECROSIS ( 1 FDA reports)
CENTRAL PONTINE MYELINOLYSIS ( 1 FDA reports)
CEREBELLAR ARTERY OCCLUSION ( 1 FDA reports)
CEREBRAL DECOMPRESSION ( 1 FDA reports)
CEREBRAL DYSGENESIS ( 1 FDA reports)
CEREBRAL MICROHAEMORRHAGE ( 1 FDA reports)
CEREBRAL REVASCULARISATION SYNANGIOSIS ( 1 FDA reports)
CEREBROSPINAL FLUID RETENTION ( 1 FDA reports)
CEREBROVASCULAR OPERATION ( 1 FDA reports)
CEREBROVASCULAR SPASM ( 1 FDA reports)
CERULOPLASMIN INCREASED ( 1 FDA reports)
CERUMEN REMOVAL ( 1 FDA reports)
CERVICITIS CYSTIC ( 1 FDA reports)
CERVIX CANCER METASTATIC ( 1 FDA reports)
CERVIX NEOPLASM ( 1 FDA reports)
CHEILOSIS ( 1 FDA reports)
CHEMICAL PERITONITIS ( 1 FDA reports)
CHEST X-RAY NORMAL ( 1 FDA reports)
CHILD ABUSE ( 1 FDA reports)
CHOLANGIOADENOMA ( 1 FDA reports)
CHOLECYSTOSTOMY ( 1 FDA reports)
CHOLESTEATOMA ( 1 FDA reports)
CHONDRITIS ( 1 FDA reports)
CHONDRODYSTROPHY ( 1 FDA reports)
CHORIORETINAL SCAR ( 1 FDA reports)
CHOROID NEOPLASM ( 1 FDA reports)
CHOROID PLEXUS PAPILLOMA ( 1 FDA reports)
CHOROIDITIS ( 1 FDA reports)
CHROMOBLASTOMYCOSIS ( 1 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA REFRACTORY ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA STAGE 1 ( 1 FDA reports)
CHRONIC TONSILLITIS ( 1 FDA reports)
CILIARY HYPERAEMIA ( 1 FDA reports)
CIRCULATING ANTICOAGULANT POSITIVE ( 1 FDA reports)
CIRCULATORY FAILURE NEONATAL ( 1 FDA reports)
CITROBACTER TEST POSITIVE ( 1 FDA reports)
CLOACAL EXSTROPHY ( 1 FDA reports)
CLONAL EVOLUTION ( 1 FDA reports)
CLUMSY CHILD SYNDROME ( 1 FDA reports)
CNS VENTRICULITIS ( 1 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR VII LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR VIII LEVEL ABNORMAL ( 1 FDA reports)
COAGULATION FACTOR XI LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR XII LEVEL DECREASED ( 1 FDA reports)
COELIAC ARTERY OCCLUSION ( 1 FDA reports)
COITAL BLEEDING ( 1 FDA reports)
COLD EXPOSURE INJURY ( 1 FDA reports)
COLLAGEN ANTIGEN TYPE 1 ( 1 FDA reports)
COLON CANCER STAGE 0 ( 1 FDA reports)
COLONIC PERFORATION POSTOPERATIVE ( 1 FDA reports)
COLORECTAL CANCER STAGE I ( 1 FDA reports)
COLORECTAL CANCER STAGE II ( 1 FDA reports)
COLOSTOMY CLOSURE ( 1 FDA reports)
COLPORRHAPHY ( 1 FDA reports)
COMA ACIDOTIC ( 1 FDA reports)
COMPLEMENT FACTOR C4 DECREASED ( 1 FDA reports)
COMPLICATION OF DELIVERY ( 1 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 1 FDA reports)
COMPLICATION OF DEVICE REMOVAL ( 1 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED PANCREAS ( 1 FDA reports)
COMPULSIVE LIP BITING ( 1 FDA reports)
COMPUTERISED TOMOGRAM HEAD ( 1 FDA reports)
CONGENITAL AORTIC ANOMALY ( 1 FDA reports)
CONGENITAL CEREBROVASCULAR ANOMALY ( 1 FDA reports)
CONGENITAL CHOROID PLEXUS CYST ( 1 FDA reports)
CONGENITAL CORONARY ARTERY MALFORMATION ( 1 FDA reports)
CONGENITAL CYST ( 1 FDA reports)
CONGENITAL CYSTIC LUNG ( 1 FDA reports)
CONGENITAL FOOT MALFORMATION ( 1 FDA reports)
CONGENITAL GENITOURINARY ABNORMALITY ( 1 FDA reports)
CONGENITAL HAND MALFORMATION ( 1 FDA reports)
CONGENITAL HEARING DISORDER ( 1 FDA reports)
CONGENITAL HEART VALVE DISORDER ( 1 FDA reports)
CONGENITAL HYDROCEPHALUS ( 1 FDA reports)
CONGENITAL INFECTION ( 1 FDA reports)
CONGENITAL INTESTINAL MALFORMATION ( 1 FDA reports)
CONGENITAL JAW MALFORMATION ( 1 FDA reports)
CONGENITAL MEGACOLON ( 1 FDA reports)
CONGENITAL MEGAURETER ( 1 FDA reports)
CONGENITAL MITOCHONDRIAL CYTOPATHY ( 1 FDA reports)
CONGENITAL NEUROPATHY ( 1 FDA reports)
CONGENITAL NYSTAGMUS ( 1 FDA reports)
CONGENITAL ORAL MALFORMATION ( 1 FDA reports)
CONGENITAL PULMONARY ARTERY ANOMALY ( 1 FDA reports)
CONGENITAL RENAL DISORDER ( 1 FDA reports)
CONGENITAL SMALL INTESTINAL ATRESIA ( 1 FDA reports)
CONGENITAL SPINAL CORD ANOMALY ( 1 FDA reports)
CONGENITAL THROMBOCYTE DISORDER ( 1 FDA reports)
CONGENITAL TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
CONJUNCTIVAL IRRITATION ( 1 FDA reports)
CONJUNCTIVAL PRIMARY ACQUIRED MELANOSIS ( 1 FDA reports)
CONJUNCTIVAL SCAR ( 1 FDA reports)
CONTRAINDICATION TO VACCINATION ( 1 FDA reports)
CONVULSIONS LOCAL ( 1 FDA reports)
COOMBS TEST NEGATIVE ( 1 FDA reports)
COPROLALIA ( 1 FDA reports)
CORNEAL ABSCESS ( 1 FDA reports)
CORNEAL BLEEDING ( 1 FDA reports)
CORNEAL INFILTRATES ( 1 FDA reports)
CORNEAL STAINING ( 1 FDA reports)
CORNEAL THICKENING ( 1 FDA reports)
CORNEAL ULCER ( 1 FDA reports)
CORONARY NO-REFLOW PHENOMENON ( 1 FDA reports)
CORTICAL LAMINAR NECROSIS ( 1 FDA reports)
CORTISOL FREE URINE INCREASED ( 1 FDA reports)
COXSACKIE VIRAL INFECTION ( 1 FDA reports)
CRANIAL SUTURES WIDENING ( 1 FDA reports)
CRANIORACHISCHISIS ( 1 FDA reports)
CREATINE URINE INCREASED ( 1 FDA reports)
CRUSH INJURY ( 1 FDA reports)
CSF BACTERIA IDENTIFIED ( 1 FDA reports)
CSF GLUCOSE ( 1 FDA reports)
CSF IMMUNOGLOBULIN INCREASED ( 1 FDA reports)
CSF LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
CSF MONOCYTE COUNT POSITIVE ( 1 FDA reports)
CSF POLYMORPHONUCLEAR CELL COUNT INCREASED ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
CULTURE THROAT POSITIVE ( 1 FDA reports)
CUPULOLITHIASIS ( 1 FDA reports)
CYSTITIS-LIKE SYMPTOM ( 1 FDA reports)
CYSTOSARCOMA PHYLLODES ( 1 FDA reports)
CYTAPHERESIS ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 1 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 1 FDA reports)
CYTOMEGALOVIRUS TEST ( 1 FDA reports)
DACRYOCANALICULITIS ( 1 FDA reports)
DEAFNESS PERMANENT ( 1 FDA reports)
DEATH OF SPOUSE ( 1 FDA reports)
DECREASED EYE CONTACT ( 1 FDA reports)
DECREASED INSULIN REQUIREMENT ( 1 FDA reports)
DECREASED VENTRICULAR PRELOAD ( 1 FDA reports)
DEEP VEIN THROMBOSIS POSTOPERATIVE ( 1 FDA reports)
DEJA VU ( 1 FDA reports)
DELAYED DELIVERY ( 1 FDA reports)
DELUSION OF REFERENCE ( 1 FDA reports)
DENTAL FLUORIDE THERAPY ( 1 FDA reports)
DERAILMENT ( 1 FDA reports)
DESQUAMATION MOUTH ( 1 FDA reports)
DEVELOPMENTAL COORDINATION DISORDER ( 1 FDA reports)
DEVICE COLOUR ISSUE ( 1 FDA reports)
DEVICE KINK ( 1 FDA reports)
DEVICE PACING ISSUE ( 1 FDA reports)
DEXTROCARDIA ( 1 FDA reports)
DIABETES MELLITUS MALNUTRITION-RELATED ( 1 FDA reports)
DIABETIC CHEIROPATHY ( 1 FDA reports)
DIAPHRAGM MUSCLE WEAKNESS ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE I ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE IV ( 1 FDA reports)
DISEASE PRODROMAL STAGE ( 1 FDA reports)
DISSEMINATED CRYPTOCOCCOSIS ( 1 FDA reports)
DISSOCIATIVE DISORDER ( 1 FDA reports)
DISSOCIATIVE IDENTITY DISORDER ( 1 FDA reports)
DIURETIC EFFECT ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY POSITIVE ( 1 FDA reports)
DOUBLE VESSEL BYPASS GRAFT ( 1 FDA reports)
DRUG ADDICT ( 1 FDA reports)
DRUG HALF-LIFE INCREASED ( 1 FDA reports)
DRUG PHYSIOLOGIC INCOMPATIBILITY ( 1 FDA reports)
DRUG USE FOR UNKNOWN INDICATION ( 1 FDA reports)
DUBIN-JOHNSON SYNDROME ( 1 FDA reports)
DYSAESTHESIA PHARYNX ( 1 FDA reports)
DYSLOGIA ( 1 FDA reports)
DYSTROPHIA MYOTONICA ( 1 FDA reports)
EAR CANAL ERYTHEMA ( 1 FDA reports)
EAR CANAL INJURY ( 1 FDA reports)
EAR MALFORMATION ( 1 FDA reports)
EAR, NOSE AND THROAT EXAMINATION ABNORMAL ( 1 FDA reports)
EATON-LAMBERT SYNDROME ( 1 FDA reports)
EBSTEIN'S ANOMALY ( 1 FDA reports)
ECG SIGNS OF VENTRICULAR HYPERTROPHY ( 1 FDA reports)
ECHINOCOCCIASIS ( 1 FDA reports)
ECHO VIRUS INFECTION ( 1 FDA reports)
ECHOLALIA ( 1 FDA reports)
ECTHYMA ( 1 FDA reports)
ECTOPIA CORDIS ( 1 FDA reports)
ELDER ABUSE ( 1 FDA reports)
ELECTROCARDIOGRAM PACEMAKER SPIKE ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM RR INTERVAL PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE INCREASED ( 1 FDA reports)
ELLIPTOCYTOSIS ( 1 FDA reports)
ENCEPHALITIS ENTEROVIRAL ( 1 FDA reports)
ENCEPHALITIS POST VARICELLA ( 1 FDA reports)
ENCEPHALITIS TOXIC ( 1 FDA reports)
ENCEPHALOPATHY NEONATAL ( 1 FDA reports)
ENCHONDROMA ( 1 FDA reports)
ENDOCARDIAL FIBROSIS ( 1 FDA reports)
ENDOCRINE TEST ( 1 FDA reports)
ENDOMETRIAL CANCER STAGE III ( 1 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ( 1 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ABNORMAL ( 1 FDA reports)
ENDOSCOPY GASTROINTESTINAL ABNORMAL ( 1 FDA reports)
ENDOVENOUS ABLATION ( 1 FDA reports)
ENLARGED CEREBRAL PERIVASCULAR SPACES ( 1 FDA reports)
ENTERAL NUTRITION ( 1 FDA reports)
ENTEROCOLONIC FISTULA ( 1 FDA reports)
ENTEROVIRUS INFECTION ( 1 FDA reports)
ENZYME INHIBITION ( 1 FDA reports)
EOSINOPHILIC CELLULITIS ( 1 FDA reports)
EOSINOPHILIC CYSTITIS ( 1 FDA reports)
EOSINOPHILS URINE ( 1 FDA reports)
EOSINOPHILS URINE PRESENT ( 1 FDA reports)
EPIDEMIC POLYARTHRITIS ( 1 FDA reports)
EPIDIDYMAL TENDERNESS ( 1 FDA reports)
EPIDURAL INJECTION ( 1 FDA reports)
EPIDURAL LIPOMATOSIS ( 1 FDA reports)
EPIGLOTTIC CYST ( 1 FDA reports)
EPIGLOTTIS ULCER ( 1 FDA reports)
EPINEPHRINE INCREASED ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOMA ( 1 FDA reports)
ERGOT POISONING ( 1 FDA reports)
ERYTHROSIS ( 1 FDA reports)
ESCHAROTOMY ( 1 FDA reports)
EX-SMOKER ( 1 FDA reports)
EXANTHEMA SUBITUM ( 1 FDA reports)
EXCESSIVE SKIN ( 1 FDA reports)
EXPIRATORY RESERVE VOLUME DECREASED ( 1 FDA reports)
EXTRAPULMONARY TUBERCULOSIS ( 1 FDA reports)
EXTRINSIC ILIAC VEIN COMPRESSION ( 1 FDA reports)
EXTRINSIC VASCULAR COMPRESSION ( 1 FDA reports)
EXTRUSION OF DEVICE ( 1 FDA reports)
EYEBALL AVULSION ( 1 FDA reports)
EYELID INFECTION ( 1 FDA reports)
EYELID TUMOUR ( 1 FDA reports)
FACIAL DYSMORPHISM ( 1 FDA reports)
FACIAL OPERATION ( 1 FDA reports)
FACTOR II MUTATION ( 1 FDA reports)
FACTOR X DEFICIENCY ( 1 FDA reports)
FAECAL OCCULT BLOOD ( 1 FDA reports)
FAILURE TO CAPTURE ( 1 FDA reports)
FALSE NEGATIVE LABORATORY RESULT ( 1 FDA reports)
FAMILIAL PERIODIC PARALYSIS ( 1 FDA reports)
FAMILIAL RISK FACTOR ( 1 FDA reports)
FASCIECTOMY ( 1 FDA reports)
FAT ATROPHY ( 1 FDA reports)
FATTY ACID DEFICIENCY ( 1 FDA reports)
FEAR OF NEEDLES ( 1 FDA reports)
FEBRILE NONHAEMOLYTIC TRANSFUSION REACTION ( 1 FDA reports)
FEMALE GENITAL-DIGESTIVE TRACT FISTULA ( 1 FDA reports)
FEMALE ORGASMIC DISORDER ( 1 FDA reports)
FEMINISATION ACQUIRED ( 1 FDA reports)
FEMORAL PULSE ABNORMAL ( 1 FDA reports)
FIBRIN D DIMER DECREASED ( 1 FDA reports)
FIBRIN D DIMER NORMAL ( 1 FDA reports)
FIBRINOLYSIS ABNORMAL ( 1 FDA reports)
FILARIASIS ( 1 FDA reports)
FINGER CRUSHING ( 1 FDA reports)
FLAIL CHEST ( 1 FDA reports)
FLUOROSIS ( 1 FDA reports)
FOETAL CHROMOSOME ABNORMALITY ( 1 FDA reports)
FOETAL HAEMOGLOBIN ( 1 FDA reports)
FOETAL HAEMOGLOBIN INCREASED ( 1 FDA reports)
FOETAL HEART RATE INCREASED ( 1 FDA reports)
FOETAL MALFORMATION ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III STAGE I ( 1 FDA reports)
FOSTER-KENNEDY SYNDROME ( 1 FDA reports)
FRACTURE REDUCTION ( 1 FDA reports)
FRACTURE TREATMENT ( 1 FDA reports)
FREE PROSTATE-SPECIFIC ANTIGEN DECREASED ( 1 FDA reports)
FREE PROSTATE-SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
FREE PROSTATE-SPECIFIC ANTIGEN POSITIVE ( 1 FDA reports)
FRONTAL SINUS OPERATION ( 1 FDA reports)
FUCHS' SYNDROME ( 1 FDA reports)
FUMBLING ( 1 FDA reports)
FUNGAL DNA TEST POSITIVE ( 1 FDA reports)
FUNGATING WOUND ( 1 FDA reports)
FUNGUS BODY FLUID IDENTIFIED ( 1 FDA reports)
FUNGUS CULTURE POSITIVE ( 1 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
GAIT APRAXIA ( 1 FDA reports)
GALLBLADDER CANCER METASTATIC ( 1 FDA reports)
GAMMA RADIATION THERAPY TO PROSTATE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE DECREASED ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE NORMAL ( 1 FDA reports)
GANGLIONEUROMA ( 1 FDA reports)
GARDNERELLA INFECTION ( 1 FDA reports)
GASTRIC CANCER RECURRENT ( 1 FDA reports)
GASTRIC HYPERPLASIA ( 1 FDA reports)
GASTRIC ULCER SURGERY ( 1 FDA reports)
GASTRIC VOLVULUS ( 1 FDA reports)
GASTRINOMA ( 1 FDA reports)
GASTRITIS BACTERIAL ( 1 FDA reports)
GASTRITIS FUNGAL ( 1 FDA reports)
GASTROENTERITIS PROTEUS ( 1 FDA reports)
GASTROINTESTINAL AMYLOIDOSIS ( 1 FDA reports)
GASTROINTESTINAL MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL NECROSIS ( 1 FDA reports)
GASTROPARESIS POSTOPERATIVE ( 1 FDA reports)
GAUCHER'S DISEASE ( 1 FDA reports)
GENDER IDENTITY DISORDER ( 1 FDA reports)
GENERAL NUTRITION DISORDER ( 1 FDA reports)
GENERAL PHYSICAL CONDITION NORMAL ( 1 FDA reports)
GENITAL INFECTION BACTERIAL ( 1 FDA reports)
GENITAL PAIN FEMALE ( 1 FDA reports)
GENITAL TRACT INFLAMMATION ( 1 FDA reports)
GINGIVAL CANCER ( 1 FDA reports)
GINGIVAL HYPERPIGMENTATION ( 1 FDA reports)
GLABELLAR REFLEX ABNORMAL ( 1 FDA reports)
GLASGOW COMA SCALE ( 1 FDA reports)
GLAUCOMATOUS OPTIC DISC ATROPHY ( 1 FDA reports)
GLOMERULAR FILTRATION RATE ( 1 FDA reports)
GLOTTIS CARCINOMA ( 1 FDA reports)
GLUCAGONOMA ( 1 FDA reports)
GLUTAMATE DEHYDROGENASE INCREASED ( 1 FDA reports)
GLYCOGEN STORAGE DISEASE TYPE V ( 1 FDA reports)
GONORRHOEA ( 1 FDA reports)
GROWTH HORMONE DEFICIENCY ( 1 FDA reports)
GYNAECOLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
HAEMANGIOMA OF SPLEEN ( 1 FDA reports)
HAEMATOTYMPANUM ( 1 FDA reports)
HAEMODIALYSIS COMPLICATION ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ENZYME SPECIFIC ( 1 FDA reports)
HAEMOLYTIC TRANSFUSION REACTION ( 1 FDA reports)
HAEMORRHAGE SUBEPIDERMAL ( 1 FDA reports)
HAEMORRHAGIC HEPATIC CYST ( 1 FDA reports)
HAND AMPUTATION ( 1 FDA reports)
HANGNAIL ( 1 FDA reports)
HEART ALTERNATION ( 1 FDA reports)
HEART-LUNG TRANSPLANT REJECTION ( 1 FDA reports)
HELMINTHIC INFECTION ( 1 FDA reports)
HEPATIC ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
HEPATIC ARTERY ANEURYSM ( 1 FDA reports)
HEPATIC CANCER STAGE I ( 1 FDA reports)
HEPATIC CYST INFECTION ( 1 FDA reports)
HEPATIC INFECTION BACTERIAL ( 1 FDA reports)
HEPATIC VEIN OCCLUSION ( 1 FDA reports)
HEPATITIS A VIRUS TEST ( 1 FDA reports)
HEPATITIS B E ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS B VIRUS ( 1 FDA reports)
HEPATITIS C ANTIBODY ( 1 FDA reports)
HEPATITIS C RNA ( 1 FDA reports)
HEPATITIS C VIRUS ( 1 FDA reports)
HEPATITIS INFECTIOUS ( 1 FDA reports)
HEPATOBILIARY INFECTION ( 1 FDA reports)
HEPATOBILIARY NEOPLASM ( 1 FDA reports)
HEPATOCELLULAR FOAMY CELL SYNDROME ( 1 FDA reports)
HEREDITARY CEREBRAL DEGENERATION ( 1 FDA reports)
HEREDITARY SPHEROCYTOSIS ( 1 FDA reports)
HERPES OPHTHALMIC ( 1 FDA reports)
HERPES SEPSIS ( 1 FDA reports)
HERPES SIMPLEX SEROLOGY NEGATIVE ( 1 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 1 FDA reports)
HIGH RISK SEXUAL BEHAVIOUR ( 1 FDA reports)
HIPPOCAMPAL SCLEROSIS ( 1 FDA reports)
HISTAMINE LEVEL DECREASED ( 1 FDA reports)
HIV TEST POSITIVE ( 1 FDA reports)
HODGKIN'S DISEASE RECURRENT ( 1 FDA reports)
HOMANS' SIGN POSITIVE ( 1 FDA reports)
HTLV-1 TEST POSITIVE ( 1 FDA reports)
HTLV-2 TEST POSITIVE ( 1 FDA reports)
HUMAN ANAPLASMOSIS ( 1 FDA reports)
HUMAN BITE ( 1 FDA reports)
HUMAN CHORIONIC GONADOTROPIN INCREASED ( 1 FDA reports)
HUMAN HERPESVIRUS 8 INFECTION ( 1 FDA reports)
HUNGRY BONE SYNDROME ( 1 FDA reports)
HY'S LAW CASE ( 1 FDA reports)
HYDRAEMIA ( 1 FDA reports)
HYDROPHOBIA ( 1 FDA reports)
HYDROPS FOETALIS ( 1 FDA reports)
HYPERAMMONAEMIC ENCEPHALOPATHY ( 1 FDA reports)
HYPERCALCAEMIC NEPHROPATHY ( 1 FDA reports)
HYPERCAPNIC ENCEPHALOPATHY ( 1 FDA reports)
HYPERCATABOLISM ( 1 FDA reports)
HYPERCORTICOIDISM ( 1 FDA reports)
HYPERGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
HYPERINSULINISM ( 1 FDA reports)
HYPERMOBILITY SYNDROME ( 1 FDA reports)
HYPERSOMNIA RELATED TO ANOTHER MENTAL CONDITION ( 1 FDA reports)
HYPERTENSION NEONATAL ( 1 FDA reports)
HYPERTROPHIC ANAL PAPILLA ( 1 FDA reports)
HYPERTROPHIC OSTEOARTHROPATHY ( 1 FDA reports)
HYPERTROPHIC SCAR ( 1 FDA reports)
HYPERTROPHY OF TONGUE PAPILLAE ( 1 FDA reports)
HYPERURICOSURIA ( 1 FDA reports)
HYPERVITAMINOSIS ( 1 FDA reports)
HYPERVITAMINOSIS D ( 1 FDA reports)
HYPOAESTHESIA TEETH ( 1 FDA reports)
HYPOFIBRINOGENAEMIA ( 1 FDA reports)
HYPOGLOBULINAEMIA ( 1 FDA reports)
HYPOGLOSSAL NERVE PARESIS ( 1 FDA reports)
HYPOPHARYNGEAL NEOPLASM ( 1 FDA reports)
HYPORESPONSIVE TO STIMULI ( 1 FDA reports)
HYPOSTHENURIA ( 1 FDA reports)
HYPOTHERMIA NEONATAL ( 1 FDA reports)
HYPOTHROMBINAEMIA ( 1 FDA reports)
HYPOTHYROIDIC GOITRE ( 1 FDA reports)
HYPOTONIC-HYPORESPONSIVE EPISODE ( 1 FDA reports)
HYSTEROCELE ( 1 FDA reports)
HYSTEROSALPINGO-OOPHORECTOMY ( 1 FDA reports)
ICHTHYOSIS ACQUIRED ( 1 FDA reports)
IDEAS OF REFERENCE ( 1 FDA reports)
IDIOPATHIC CAPILLARITIS ( 1 FDA reports)
IIIRD NERVE PARESIS ( 1 FDA reports)
ILEAL FISTULA ( 1 FDA reports)
ILEOCOLOSTOMY ( 1 FDA reports)
ILEOSTOMY CLOSURE ( 1 FDA reports)
ILEUS SPASTIC ( 1 FDA reports)
ILLITERACY ( 1 FDA reports)
IMMOBILISATION PROLONGED ( 1 FDA reports)
IMMUNE TOLERANCE INDUCTION ( 1 FDA reports)
IMMUNOGLOBULINS ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG THERAPY ( 1 FDA reports)
IMMUNOTACTOID GLOMERULONEPHRITIS ( 1 FDA reports)
IMPACTED FRACTURE ( 1 FDA reports)
IMPAIRED REASONING ( 1 FDA reports)
IMPLANT EXPULSION ( 1 FDA reports)
IMPLANT SITE ABSCESS ( 1 FDA reports)
IMPLANT SITE CELLULITIS ( 1 FDA reports)
IMPLANT SITE INDURATION ( 1 FDA reports)
IMPLANT SITE SWELLING ( 1 FDA reports)
IMPLANT SITE THROMBOSIS ( 1 FDA reports)
IMPLANT SITE WARMTH ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR REMOVAL ( 1 FDA reports)
IN VITRO FERTILISATION ( 1 FDA reports)
INAPPROPRIATE DEVICE SIGNAL DETECTION ( 1 FDA reports)
INCREASED VISCOSITY OF NASAL SECRETION ( 1 FDA reports)
INDWELLING CATHETER MANAGEMENT ( 1 FDA reports)
INFANTILE SPASMS ( 1 FDA reports)
INFECTED EPIDERMAL CYST ( 1 FDA reports)
INFECTION MASKED ( 1 FDA reports)
INFECTION PROTOZOAL ( 1 FDA reports)
INFECTIVE TENOSYNOVITIS ( 1 FDA reports)
INFLUENZA IMMUNISATION ( 1 FDA reports)
INFLUENZA SEROLOGY ( 1 FDA reports)
INFUSION SITE BRUISING ( 1 FDA reports)
INFUSION SITE BURNING ( 1 FDA reports)
INFUSION SITE CELLULITIS ( 1 FDA reports)
INFUSION SITE DERMATITIS ( 1 FDA reports)
INFUSION SITE INDURATION ( 1 FDA reports)
INFUSION SITE PHLEBITIS ( 1 FDA reports)
INJECTED LIMB MOBILITY DECREASED ( 1 FDA reports)
INJECTION SITE ABSCESS STERILE ( 1 FDA reports)
INJECTION SITE DERMATITIS ( 1 FDA reports)
INJECTION SITE HYPERSENSITIVITY ( 1 FDA reports)
INJECTION SITE HYPERTROPHY ( 1 FDA reports)
INJECTION SITE JOINT PAIN ( 1 FDA reports)
INJECTION SITE JOINT REDNESS ( 1 FDA reports)
INJECTION SITE MACULE ( 1 FDA reports)
INJECTION SITE PARAESTHESIA ( 1 FDA reports)
INSTILLATION SITE IRRITATION ( 1 FDA reports)
INSTILLATION SITE REACTION ( 1 FDA reports)
INTERCEPTED DRUG PRESCRIBING ERROR ( 1 FDA reports)
INTERCOSTAL RETRACTION ( 1 FDA reports)
INTERSTITIAL GRANULOMATOUS DERMATITIS ( 1 FDA reports)
INTESTINAL ANGINA ( 1 FDA reports)
INTESTINAL FISTULA REPAIR ( 1 FDA reports)
INTESTINAL HYPERMOTILITY ( 1 FDA reports)
INTESTINAL POLYPECTOMY ( 1 FDA reports)
INTRA-ABDOMINAL HAEMANGIOMA ( 1 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 1 FDA reports)
INTRANASAL NUMBNESS ( 1 FDA reports)
INTRATHECAL PUMP INSERTION ( 1 FDA reports)
IODINE UPTAKE DECREASED ( 1 FDA reports)
IRIDECTOMY ( 1 FDA reports)
IRIDOTOMY ( 1 FDA reports)
IRIS HAEMORRHAGE ( 1 FDA reports)
IRIS INJURY ( 1 FDA reports)
IRIS OPERATION ( 1 FDA reports)
IRON BINDING CAPACITY UNSATURATED DECREASED ( 1 FDA reports)
JAW CYST ( 1 FDA reports)
JEJUNAL GANGRENE ( 1 FDA reports)
JEJUNAL PERFORATION ( 1 FDA reports)
JEJUNAL STENOSIS ( 1 FDA reports)
JEJUNAL ULCER PERFORATION ( 1 FDA reports)
JEJUNITIS ( 1 FDA reports)
JEJUNOSTOMY ( 1 FDA reports)
JEJUNOSTOMY REFASHIONING ( 1 FDA reports)
JOINT ADHESION ( 1 FDA reports)
JOINT DEPOSIT ( 1 FDA reports)
JOINT FLUID DRAINAGE ( 1 FDA reports)
JOINT RESURFACING SURGERY ( 1 FDA reports)
JOINT TUBERCULOSIS ( 1 FDA reports)
KERATOCONUS ( 1 FDA reports)
KERATOPLASTY ( 1 FDA reports)
KERATOSIS FOLLICULAR ( 1 FDA reports)
KIDNEY PERFORATION ( 1 FDA reports)
KORSAKOFF'S PSYCHOSIS ALCOHOLIC ( 1 FDA reports)
LABELLED DRUG-DISEASE INTERACTION MEDICATION ERROR ( 1 FDA reports)
LABOUR COMPLICATION ( 1 FDA reports)
LACRIMAL DUCT PROCEDURE ( 1 FDA reports)
LACTATION DISORDER ( 1 FDA reports)
LARGE CELL CARCINOMA OF THE RESPIRATORY TRACT STAGE UNSPECIFIED ( 1 FDA reports)
LARGE FOR DATES BABY ( 1 FDA reports)
LARGE INTESTINAL STRICTURE ( 1 FDA reports)
LARYNGEAL DYSPNOEA ( 1 FDA reports)
LARYNGEAL HAEMATOMA ( 1 FDA reports)
LARYNGEAL OBSTRUCTION ( 1 FDA reports)
LARYNGITIS VIRAL ( 1 FDA reports)
LARYNGOMALACIA ( 1 FDA reports)
LARYNGOPHARYNGITIS ( 1 FDA reports)
LASEGUE'S TEST NEGATIVE ( 1 FDA reports)
LATENT SYPHILIS ( 1 FDA reports)
LATENT TUBERCULOSIS ( 1 FDA reports)
LATERAL MEDULLARY SYNDROME ( 1 FDA reports)
LDL/HDL RATIO DECREASED ( 1 FDA reports)
LENTICULAR PIGMENTATION ( 1 FDA reports)
LEUKAEMIA GRANULOCYTIC ( 1 FDA reports)
LEUKAEMIC INFILTRATION BRAIN ( 1 FDA reports)
LEUKAEMIC INFILTRATION EXTRAMEDULLARY ( 1 FDA reports)
LEUKAEMOID REACTION ( 1 FDA reports)
LEUKOCYTE VACUOLISATION ( 1 FDA reports)
LEUKOSTASIS ( 1 FDA reports)
LEUKOTRIENE INCREASED ( 1 FDA reports)
LIMB MALFORMATION ( 1 FDA reports)
LIMB PROSTHESIS USER ( 1 FDA reports)
LIMB SALVAGE THERAPY ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER STAGE III ( 1 FDA reports)
LIP LESION EXCISION ( 1 FDA reports)
LIP NEOPLASM ( 1 FDA reports)
LIP PRURITUS ( 1 FDA reports)
LIP SLOUGHING ( 1 FDA reports)
LIPAEMIA RETINALIS ( 1 FDA reports)
LIPECTOMY ( 1 FDA reports)
LIPIDOSIS ( 1 FDA reports)
LIVER FUNCTION TEST NORMAL ( 1 FDA reports)
LIVER SARCOIDOSIS ( 1 FDA reports)
LIVER TENDERNESS ( 1 FDA reports)
LOCAL ANAESTHESIA ( 1 FDA reports)
LOCAL REACTION ( 1 FDA reports)
LORDOSIS POST SURGICAL ( 1 FDA reports)
LOW INCOME ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
LUMBAR PUNCTURE HEADACHE ( 1 FDA reports)
LUMBAR VERTEBRA INJURY ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE I ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE II ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA METASTATIC ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE 0 ( 1 FDA reports)
LUNG WEDGE RESECTION ( 1 FDA reports)
LUPUS MYOCARDITIS ( 1 FDA reports)
LUPUS PNEUMONITIS ( 1 FDA reports)
LUPUS VULGARIS ( 1 FDA reports)
LYMPHADENITIS BACTERIAL ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE ABNORMAL ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST NEGATIVE ( 1 FDA reports)
LYMPHOCYTIC DERMATITIS ( 1 FDA reports)
LYMPHOCYTIC HYPOPHYSITIS ( 1 FDA reports)
LYMPHOHISTIOCYTOSIS ( 1 FDA reports)
LYMPHOMA CUTIS ( 1 FDA reports)
LYMPHOMA TRANSFORMATION ( 1 FDA reports)
MACROAMYLASAEMIA ( 1 FDA reports)
MALE GENITAL TRACT OPERATION ( 1 FDA reports)
MALE PATTERN BALDNESS ( 1 FDA reports)
MALIGNANT MEDIASTINAL NEOPLASM ( 1 FDA reports)
MALIGNANT MELANOMA STAGE I ( 1 FDA reports)
MALIGNANT MESENTERIC NEOPLASM ( 1 FDA reports)
MALIGNANT MYOPIA ( 1 FDA reports)
MALIGNANT NEOPLASM OF AMPULLA OF VATER ( 1 FDA reports)
MALIGNANT NEOPLASM OF EYE ( 1 FDA reports)
MALIGNANT NEOPLASM OF EYELID ( 1 FDA reports)
MALIGNANT NEOPLASM OF ISLETS OF LANGERHANS ( 1 FDA reports)
MALIGNANT NEOPLASM OF ORBIT ( 1 FDA reports)
MALIGNANT NERVOUS SYSTEM NEOPLASM ( 1 FDA reports)
MALIGNANT OVARIAN CYST ( 1 FDA reports)
MALIGNANT PALATE NEOPLASM ( 1 FDA reports)
MALIGNANT SOFT TISSUE NEOPLASM ( 1 FDA reports)
MANTLE CELL LYMPHOMA STAGE IV ( 1 FDA reports)
MAST CELL DEGRANULATION TEST ( 1 FDA reports)
MATERNAL DISTRESS DURING LABOUR ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION ( 1 FDA reports)
MECONIUM PLUG SYNDROME ( 1 FDA reports)
MEDIAL TIBIAL STRESS SYNDROME ( 1 FDA reports)
MEDIASTINAL OPERATION ( 1 FDA reports)
MEDICAL DEVICE ENTRAPMENT ( 1 FDA reports)
MEDICAL DEVICE SITE REACTION ( 1 FDA reports)
MEDICATION TAMPERING ( 1 FDA reports)
MEDULLARY THYROID CANCER ( 1 FDA reports)
MEIBOMIAN GLAND DYSFUNCTION ( 1 FDA reports)
MEIGE'S SYNDROME ( 1 FDA reports)
MELANODERMIA ( 1 FDA reports)
MENDELSON'S SYNDROME ( 1 FDA reports)
MENINGITIS NEONATAL ( 1 FDA reports)
MENINGITIS STREPTOCOCCAL ( 1 FDA reports)
MENINGOCELE ( 1 FDA reports)
MENINGORADICULITIS ( 1 FDA reports)
MENINGORRHAGIA ( 1 FDA reports)
MENOPAUSAL DEPRESSION ( 1 FDA reports)
MENTAL RETARDATION SEVERITY UNSPECIFIED ( 1 FDA reports)
METASTASES TO PERIPHERAL VASCULAR SYSTEM ( 1 FDA reports)
METASTASES TO THE RESPIRATORY SYSTEM ( 1 FDA reports)
MICROPHTHALMOS ( 1 FDA reports)
MICROSCOPIC POLYANGIITIS ( 1 FDA reports)
MITOCHONDRIAL ENCEPHALOMYOPATHY ( 1 FDA reports)
MITOCHONDRIAL ENZYME DEFICIENCY ( 1 FDA reports)
MITOCHONDRIAL NEUROGASTROINTESTINAL ENCEPHALOPATHY ( 1 FDA reports)
MODERATE MENTAL RETARDATION ( 1 FDA reports)
MOROSE ( 1 FDA reports)
MOTOR DEVELOPMENTAL DELAY ( 1 FDA reports)
MUCOPOLYSACCHARIDOSIS II ( 1 FDA reports)
MUCOSA VESICLE ( 1 FDA reports)
MUCOSAL PIGMENTATION ( 1 FDA reports)
MULTIFOCAL MOTOR NEUROPATHY ( 1 FDA reports)
MULTIPLE ENDOCRINE ADENOMATOSIS TYPE I ( 1 FDA reports)
MULTIPLE ENDOCRINE ADENOMATOSIS TYPE II ( 1 FDA reports)
MULTIPLE GATED ACQUISITION SCAN ABNORMAL ( 1 FDA reports)
MULTIPLE LENTIGINES SYNDROME ( 1 FDA reports)
MURPHY'S SIGN POSITIVE ( 1 FDA reports)
MYALGIA INTERCOSTAL ( 1 FDA reports)
MYCETOMA MYCOTIC ( 1 FDA reports)
MYCOBACTERIA TEST ( 1 FDA reports)
MYCOBACTERIUM ABSCESSUS INFECTION ( 1 FDA reports)
MYCOBACTERIUM FORTUITUM INFECTION ( 1 FDA reports)
MYCOTIC ALLERGY ( 1 FDA reports)
MYELOCYTE COUNT DECREASED ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME UNCLASSIFIABLE ( 1 FDA reports)
MYOCARDIAC ABSCESS ( 1 FDA reports)
MYOCARDIAL BRIDGING ( 1 FDA reports)
MYOCARDIAL DEPRESSION ( 1 FDA reports)
MYOFASCITIS ( 1 FDA reports)
MYOGLOBIN BLOOD DECREASED ( 1 FDA reports)
MYOSITIS OSSIFICANS ( 1 FDA reports)
MYRINGOPLASTY ( 1 FDA reports)
N-TERMINAL PROHORMONE BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
NAIL DISCOMFORT ( 1 FDA reports)
NAIL PSORIASIS ( 1 FDA reports)
NARROW ANTERIOR CHAMBER ANGLE ( 1 FDA reports)
NASAL MUCOSAL DISCOLOURATION ( 1 FDA reports)
NASAL MUCOSAL HYPERTROPHY ( 1 FDA reports)
NASAL POLYPECTOMY ( 1 FDA reports)
NASOPHARYNGEAL CANCER ( 1 FDA reports)
NATURAL KILLER-CELL LYMPHOBLASTIC LYMPHOMA ( 1 FDA reports)
NECROBIOSIS ( 1 FDA reports)
NEEDLE TRACK MARKS ( 1 FDA reports)
NEGATIVE CARDIAC INOTROPIC EFFECT ( 1 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 1 FDA reports)
NEONATAL ANURIA ( 1 FDA reports)
NEONATAL APNOEIC ATTACK ( 1 FDA reports)
NEOPLASM GROWTH ACCELERATED ( 1 FDA reports)
NERVE GRAFT ( 1 FDA reports)
NEURAL TUBE DEFECT ( 1 FDA reports)
NEUROLOGICAL EYELID DISORDER ( 1 FDA reports)
NEUROLYSIS SURGICAL ( 1 FDA reports)
NEUROPSYCHOLOGICAL TEST ABNORMAL ( 1 FDA reports)
NEUROSYPHILIS ( 1 FDA reports)
NEUROTRANSMITTER LEVEL ALTERED ( 1 FDA reports)
NEUTROPENIA NEONATAL ( 1 FDA reports)
NITRITE URINE ( 1 FDA reports)
NON-CONSUMMATION ( 1 FDA reports)
NON-HIGH-DENSITY LIPOPROTEIN CHOLESTEROL DECREASED ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER RECURRENT ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE III ( 1 FDA reports)
NOREPINEPHRINE INCREASED ( 1 FDA reports)
NOROVIRUS TEST POSITIVE ( 1 FDA reports)
NOSE DEFORMITY ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABDOMINAL ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABDOMINAL ABNORMAL ( 1 FDA reports)
NUMB CHIN SYNDROME ( 1 FDA reports)
OCCUPATIONAL EXPOSURE TO DUST ( 1 FDA reports)
OCCUPATIONAL PHYSICAL PROBLEM ( 1 FDA reports)
OCULAR DYSMETRIA ( 1 FDA reports)
ODDI'S SPHINCTER CONSTRICTION ( 1 FDA reports)
ODONTOGENIC CYST ( 1 FDA reports)
OEDEMA DUE TO HEPATIC DISEASE ( 1 FDA reports)
OEDEMA DUE TO RENAL DISEASE ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA METASTATIC ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA STAGE III ( 1 FDA reports)
OESOPHAGEAL STENT INSERTION ( 1 FDA reports)
OESOPHAGEAL ULCER PERFORATION ( 1 FDA reports)
OESOPHAGOENTEROSTOMY ( 1 FDA reports)
OESTRADIOL INCREASED ( 1 FDA reports)
OESTRIOL DECREASED ( 1 FDA reports)
OESTROGENIC EFFECT ( 1 FDA reports)
ONYCHOPHAGIA ( 1 FDA reports)
OPTIC DISC VASCULAR DISORDER ( 1 FDA reports)
OPTICOKINETIC NYSTAGMUS TESTS ABNORMAL ( 1 FDA reports)
ORAL ADMINISTRATION COMPLICATION ( 1 FDA reports)
ORBITAL IMPLANT INSERTION ( 1 FDA reports)
ORF ( 1 FDA reports)
ORGAN TRANSPLANT ( 1 FDA reports)
OROPHARYNGITIS FUNGAL ( 1 FDA reports)
ORTHOSTATIC TREMOR ( 1 FDA reports)
OSLER'S NODES ( 1 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 1 FDA reports)
OSTEOCALCIN DECREASED ( 1 FDA reports)
OSTEOMYELITIS FUNGAL ( 1 FDA reports)
OSTEOSIS ( 1 FDA reports)
OTITIS MEDIA FUNGAL ( 1 FDA reports)
OTORHINOLARYNGOLOGICAL SURGERY ( 1 FDA reports)
OVARIAN EPITHELIAL CANCER STAGE IV ( 1 FDA reports)
OVARIAN GERM CELL EMBRYONAL CARCINOMA STAGE III ( 1 FDA reports)
OVARIAN HYPERFUNCTION ( 1 FDA reports)
OVARIAN TORSION ( 1 FDA reports)
OVULATION DISORDER ( 1 FDA reports)
OXYGEN SATURATION INCREASED ( 1 FDA reports)
PACEMAKER GENERATED ARRHYTHMIA ( 1 FDA reports)
PACHYMENINGITIS ( 1 FDA reports)
PAGET'S DISEASE OF THE VULVA ( 1 FDA reports)
PALLIATIVE CARE ( 1 FDA reports)
PALPATORY FINDING ABNORMAL ( 1 FDA reports)
PANCREATIC NEUROENDOCRINE TUMOUR ( 1 FDA reports)
PANCREATIC PHLEGMON ( 1 FDA reports)
PANCREATIC SPHINCTEROTOMY ( 1 FDA reports)
PANCREATOBILIARY SPHINCTEROTOMY ( 1 FDA reports)
PANNICULITIS LOBULAR ( 1 FDA reports)
PAO2/FIO2 RATIO DECREASED ( 1 FDA reports)
PARAESTHESIA OF GENITAL FEMALE ( 1 FDA reports)
PARAESTHESIA OF GENITAL MALE ( 1 FDA reports)
PARASPINAL ABSCESS ( 1 FDA reports)
PARATHYROID TUMOUR MALIGNANT ( 1 FDA reports)
PARESIS ANAL SPHINCTER ( 1 FDA reports)
PAROXYSMAL PERCEPTUAL ALTERATION ( 1 FDA reports)
PATELLA REPLACEMENT ( 1 FDA reports)
PATENT DUCTUS ARTERIOSUS REPAIR ( 1 FDA reports)
PEAK EXPIRATORY FLOW RATE ABNORMAL ( 1 FDA reports)
PELIOSIS HEPATIS ( 1 FDA reports)
PELVIC FLOOR REPAIR ( 1 FDA reports)
PELVIC PROLAPSE ( 1 FDA reports)
PELVIC SEPSIS ( 1 FDA reports)
PENILE CURVATURE ( 1 FDA reports)
PENILE NECROSIS ( 1 FDA reports)
PENILE NEOPLASM ( 1 FDA reports)
PENILE WART ( 1 FDA reports)
PERFORMANCE FEAR ( 1 FDA reports)
PERFUME SENSITIVITY ( 1 FDA reports)
PERICARDIAL CALCIFICATION ( 1 FDA reports)
PERICARDIAL EXCISION ( 1 FDA reports)
PERICARDIAL NEOPLASM ( 1 FDA reports)
PERICARDITIS RHEUMATIC ( 1 FDA reports)
PERICARDITIS TUBERCULOUS ( 1 FDA reports)
PERIHEPATIC DISCOMFORT ( 1 FDA reports)
PERINEAL CYST ( 1 FDA reports)
PERINEPHRIC ABSCESS ( 1 FDA reports)
PERINEPHRIC EFFUSION ( 1 FDA reports)
PERIORBITAL ABSCESS ( 1 FDA reports)
PERIOSTITIS ( 1 FDA reports)
PERIPANCREATIC FLUID COLLECTION ( 1 FDA reports)
PERIPHERAL NERVE TRANSPOSITION ( 1 FDA reports)
PERITONEAL CANDIDIASIS ( 1 FDA reports)
PERITONEAL EFFLUENT ABNORMAL ( 1 FDA reports)
PERITONEAL FLUID ANALYSIS ABNORMAL ( 1 FDA reports)
PERITONEAL HERNIA ( 1 FDA reports)
PERITONEAL LESION ( 1 FDA reports)
PERITONEAL TUBERCULOSIS ( 1 FDA reports)
PERITONITIS SCLEROSING ( 1 FDA reports)
PERSONALITY CHANGE DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
PHAGOPHOBIA ( 1 FDA reports)
PHARMACOPHOBIA ( 1 FDA reports)
PHARYNGEAL CANCER STAGE UNSPECIFIED ( 1 FDA reports)
PHARYNGEAL CANDIDIASIS ( 1 FDA reports)
PHARYNGEAL CYST ( 1 FDA reports)
PHARYNGEAL HAEMATOMA ( 1 FDA reports)
PHARYNGEAL POLYP ( 1 FDA reports)
PHARYNGITIS BACTERIAL ( 1 FDA reports)
PHENYLKETONURIA ( 1 FDA reports)
PHLEBECTOMY ( 1 FDA reports)
PHOTOKERATITIS ( 1 FDA reports)
PHYLLODES TUMOUR ( 1 FDA reports)
PHYTOTHERAPY ( 1 FDA reports)
PIERRE ROBIN SYNDROME ( 1 FDA reports)
PIGMENT NEPHROPATHY ( 1 FDA reports)
PIGMENTATION LIP ( 1 FDA reports)
PILONIDAL CYST CONGENITAL ( 1 FDA reports)
PINEAL NEOPLASM ( 1 FDA reports)
PITUITARY CYST ( 1 FDA reports)
PLACENTA ACCRETA ( 1 FDA reports)
PLACENTAL CHORIOANGIOMA ( 1 FDA reports)
PLAGUE ( 1 FDA reports)
PLANTAR ERYTHEMA ( 1 FDA reports)
PLASMA CELLS PRESENT ( 1 FDA reports)
PLASMA VISCOSITY DECREASED ( 1 FDA reports)
PLATELET ADHESIVENESS DECREASED ( 1 FDA reports)
PLATELET COUNT ( 1 FDA reports)
PLATELET COUNT NORMAL ( 1 FDA reports)
PLATELET MATURATION ARREST ( 1 FDA reports)
PLEURAL INFECTION ( 1 FDA reports)
PLEURAL RUB ( 1 FDA reports)
PNEUMOBILIA ( 1 FDA reports)
PNEUMOCOCCAL BACTERAEMIA ( 1 FDA reports)
PNEUMOCYSTIS CARINII INFECTION ( 1 FDA reports)
PNEUMOCYSTIS TEST POSITIVE ( 1 FDA reports)
PNEUMONECTOMY ( 1 FDA reports)
PNEUMONIA ASPERGILLUS ( 1 FDA reports)
PNEUMOTHORAX SPONTANEOUS TENSION ( 1 FDA reports)
POLYDIPSIA PSYCHOGENIC ( 1 FDA reports)
POLYGLANDULAR DISORDER ( 1 FDA reports)
POLYMENORRHAGIA ( 1 FDA reports)
POLYNEUROPATHY TOXIC ( 1 FDA reports)
POLYOMAVIRUS INTERSTITIAL NEPHRITIS ( 1 FDA reports)
POPLITEAL PULSE ABNORMAL ( 1 FDA reports)
PORPHYRIA ( 1 FDA reports)
PORPHYRINS URINE INCREASED ( 1 FDA reports)
PORTAL SHUNT ( 1 FDA reports)
PORTAL VEIN OCCLUSION ( 1 FDA reports)
PORTAL VEIN STENOSIS ( 1 FDA reports)
POSITIVE CARDIAC INOTROPIC EFFECT ( 1 FDA reports)
POSITIVE END-EXPIRATORY PRESSURE ( 1 FDA reports)
POST PROCEDURAL DIZZINESS ( 1 FDA reports)
POST PROCEDURAL HYPOTHYROIDISM ( 1 FDA reports)
POST STREPTOCOCCAL GLOMERULONEPHRITIS ( 1 FDA reports)
POST-THORACOTOMY PAIN SYNDROME ( 1 FDA reports)
POSTICTAL HEADACHE ( 1 FDA reports)
POSTMATURE BABY ( 1 FDA reports)
POSTPARTUM VENOUS THROMBOSIS ( 1 FDA reports)
PREDISPOSITION TO DISEASE ( 1 FDA reports)
PREGNANCY OF PARTNER ( 1 FDA reports)
PREGNANCY TEST FALSE POSITIVE ( 1 FDA reports)
PREHYPERTENSION ( 1 FDA reports)
PREMATURE MENOPAUSE ( 1 FDA reports)
PRENATAL SCREENING TEST ABNORMAL ( 1 FDA reports)
PREPYLORIC STENOSIS ( 1 FDA reports)
PRERENAL FAILURE ( 1 FDA reports)
PRIMARY ADRENAL INSUFFICIENCY ( 1 FDA reports)
PRIMARY CEREBELLAR DEGENERATION ( 1 FDA reports)
PRIMARY HYPOTHYROIDISM ( 1 FDA reports)
PRIMARY IMMUNODEFICIENCY SYNDROME ( 1 FDA reports)
PROCTOCOLECTOMY ( 1 FDA reports)
PRODUCT CLOSURE ISSUE ( 1 FDA reports)
PRODUCT LOT NUMBER ISSUE ( 1 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 1 FDA reports)
PRODUCT SHAPE ISSUE ( 1 FDA reports)
PRODUCT USED FOR UNKNOWN INDICATION ( 1 FDA reports)
PROLYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
PROMISCUITY ( 1 FDA reports)
PROMOTION OF WOUND HEALING ( 1 FDA reports)
PROPHYLAXIS ( 1 FDA reports)
PROPIONIBACTERIUM INFECTION ( 1 FDA reports)
PROSTATE CANCER STAGE III ( 1 FDA reports)
PROSTATE EXAMINATION ( 1 FDA reports)
PROSTATIC ATROPHY ( 1 FDA reports)
PROSTATIC DYSPLASIA ( 1 FDA reports)
PROSTATIC MASS ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN ( 1 FDA reports)
PROSTATITIS ESCHERICHIA COLI ( 1 FDA reports)
PROTEIN TOTAL ( 1 FDA reports)
PROTHROMBIN TIME RATIO ABNORMAL ( 1 FDA reports)
PSEUDO-BARTTER SYNDROME ( 1 FDA reports)
PSEUDOALDOSTERONISM ( 1 FDA reports)
PSEUDOCHOLINESTERASE DEFICIENCY ( 1 FDA reports)
PSEUDOEPITHELIOMATOUS HYPERPLASIA ( 1 FDA reports)
PSEUDOHYPERKALAEMIA ( 1 FDA reports)
PSEUDOMYXOMA PERITONEI ( 1 FDA reports)
PSYCHOGENIC ERECTILE DYSFUNCTION ( 1 FDA reports)
PSYCHOGENIC PAIN DISORDER ( 1 FDA reports)
PSYCHOSOCIAL SUPPORT ( 1 FDA reports)
PSYCHOTHERAPY ( 1 FDA reports)
PTOSIS REPAIR ( 1 FDA reports)
PUBIC PAIN ( 1 FDA reports)
PULMONARY ARTERY ATRESIA ( 1 FDA reports)
PULMONARY COCCIDIOIDES ( 1 FDA reports)
PULMONARY FUNCTION CHALLENGE TEST ABNORMAL ( 1 FDA reports)
PULMONARY HAEMATOMA ( 1 FDA reports)
PULMONARY HILAR ENLARGEMENT ( 1 FDA reports)
PULMONARY MICROEMBOLI ( 1 FDA reports)
PULMONARY PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PULMONARY RENAL SYNDROME ( 1 FDA reports)
PULMONARY SEQUESTRATION ( 1 FDA reports)
PULMONARY VALVE DISEASE ( 1 FDA reports)
PULMONARY VALVE SCLEROSIS ( 1 FDA reports)
PULMONARY VEIN STENOSIS ( 1 FDA reports)
PUNCTURE SITE ABSCESS ( 1 FDA reports)
PUNCTURE SITE DISCHARGE ( 1 FDA reports)
PUPILLARY DEFORMITY ( 1 FDA reports)
PURULENT PERICARDITIS ( 1 FDA reports)
PYELONEPHRITIS FUNGAL ( 1 FDA reports)
PYOMYOSITIS ( 1 FDA reports)
PYOPNEUMOTHORAX ( 1 FDA reports)
PYROGLUTAMATE INCREASED ( 1 FDA reports)
PYRUVATE KINASE INCREASED ( 1 FDA reports)
RADIAL NERVE INJURY ( 1 FDA reports)
RADIAL TUNNEL SYNDROME ( 1 FDA reports)
RADIATION EXPOSURE ( 1 FDA reports)
RADIATION FIBROSIS ( 1 FDA reports)
RADIATION FIBROSIS - LUNG ( 1 FDA reports)
RADIATION NECROSIS ( 1 FDA reports)
RADIATION RETINOPATHY ( 1 FDA reports)
RADIOFREQUENCY ABLATION ( 1 FDA reports)
RADIOISOTOPE SCAN ( 1 FDA reports)
RADIOTHERAPY TO BONE ( 1 FDA reports)
RADIOTHERAPY TO THROAT ( 1 FDA reports)
RADIOULNAR SYNOSTOSIS ( 1 FDA reports)
RASH MACULOVESICULAR ( 1 FDA reports)
REACTION TO MEDICAL AGENT PRESERVATIVES ( 1 FDA reports)
REACTION TO PRESERVATIVES ( 1 FDA reports)
REBOUND HYPERTENSION ( 1 FDA reports)
RECTAL CANCER STAGE III ( 1 FDA reports)
RECTAL EXAMINATION ABNORMAL ( 1 FDA reports)
RECTAL POLYPECTOMY ( 1 FDA reports)
RECTAL PROLAPSE REPAIR ( 1 FDA reports)
RECTAL STENOSIS ( 1 FDA reports)
RED BLOOD CELL HYPOCHROMIC MORPHOLOGY PRESENT ( 1 FDA reports)
RED BLOOD CELL MICROCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELL POIKILOCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELLS SEMEN ( 1 FDA reports)
REDUCED DEXTERITY ( 1 FDA reports)
REFLUX NEPHROPATHY ( 1 FDA reports)
REMOVAL OF FOREIGN BODY FROM OESOPHAGUS ( 1 FDA reports)
RENAL ARTERY DISSECTION ( 1 FDA reports)
RENAL CANCER RECURRENT ( 1 FDA reports)
RENAL CANCER STAGE IV ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE II ( 1 FDA reports)
RENAL DYSPLASIA ( 1 FDA reports)
RENAL FUSION ANOMALY ( 1 FDA reports)
RENAL GRAFT LOSS ( 1 FDA reports)
RENAL HYPOPLASIA ( 1 FDA reports)
RENIN DECREASED ( 1 FDA reports)
REPRODUCTIVE TRACT DISORDER ( 1 FDA reports)
RETICULOCYTE COUNT ABNORMAL ( 1 FDA reports)
RETINAL ARTERY SPASM ( 1 FDA reports)
RETINAL DEPIGMENTATION ( 1 FDA reports)
RETINAL LASER COAGULATION ( 1 FDA reports)
RETINAL NEOPLASM ( 1 FDA reports)
RETINITIS PIGMENTOSA ( 1 FDA reports)
RETINOPATHY HAEMORRHAGIC ( 1 FDA reports)
RETINOPATHY OF PREMATURITY ( 1 FDA reports)
RETROPERITONEAL CANCER ( 1 FDA reports)
RETROPERITONEAL MASS ( 1 FDA reports)
RETROPERITONEAL NEOPLASM METASTATIC ( 1 FDA reports)
RETROPHARYNGEAL ABSCESS ( 1 FDA reports)
RHABDOMYOSARCOMA ( 1 FDA reports)
RHESUS ANTIBODIES POSITIVE ( 1 FDA reports)
RHEUMATOID FACTOR DECREASED ( 1 FDA reports)
RHEUMATOID NODULE REMOVAL ( 1 FDA reports)
RIB EXCISION ( 1 FDA reports)
RIFT VALLEY FEVER ( 1 FDA reports)
RIGHT AORTIC ARCH ( 1 FDA reports)
RIGHT ATRIAL HYPERTROPHY ( 1 FDA reports)
RIGHT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 1 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE DECREASED ( 1 FDA reports)
ROCKY MOUNTAIN SPOTTED FEVER ( 1 FDA reports)
RUBELLA ANTIBODY POSITIVE ( 1 FDA reports)
RUBIVIRUS TEST POSITIVE ( 1 FDA reports)
RUPTURED ECTOPIC PREGNANCY ( 1 FDA reports)
RUSSELL'S VIPER VENOM TIME ABNORMAL ( 1 FDA reports)
SALIVA DISCOLOURATION ( 1 FDA reports)
SALIVARY GLAND RESECTION ( 1 FDA reports)
SALMONELLA BACTERAEMIA ( 1 FDA reports)
SARCOMA METASTATIC ( 1 FDA reports)
SCAN GALLIUM ABNORMAL ( 1 FDA reports)
SCEDOSPORIUM INFECTION ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER BIPOLAR TYPE ( 1 FDA reports)
SCLERAL CYST ( 1 FDA reports)
SCLEREMA ( 1 FDA reports)
SCLEROTHERAPY ( 1 FDA reports)
SCROTAL OPERATION ( 1 FDA reports)
SCRUB TYPHUS ( 1 FDA reports)
SEBACEOUS GLAND INFECTION ( 1 FDA reports)
SECONDARY AMYLOIDOSIS ( 1 FDA reports)
SECONDARY PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
SECONDARY SYPHILIS ( 1 FDA reports)
SEMEN ABNORMAL ( 1 FDA reports)
SEMEN ANALYSIS ABNORMAL ( 1 FDA reports)
SEMEN VISCOSITY ABNORMAL ( 1 FDA reports)
SEMEN VOLUME ABNORMAL ( 1 FDA reports)
SEMEN VOLUME INCREASED ( 1 FDA reports)
SEMINOMA ( 1 FDA reports)
SENSORY GANGLIONITIS ( 1 FDA reports)
SENSORY INTEGRATIVE DYSFUNCTION ( 1 FDA reports)
SEROLOGY ABNORMAL ( 1 FDA reports)
SERUM FERRITIN NORMAL ( 1 FDA reports)
SEVERED DIGIT REIMPLANTATION ( 1 FDA reports)
SEXUAL ACTIVITY INCREASED ( 1 FDA reports)
SHIFT TO THE RIGHT ( 1 FDA reports)
SHOPLIFTING ( 1 FDA reports)
SHUNT ANEURYSM ( 1 FDA reports)
SICK RELATIVE ( 1 FDA reports)
SIGMOIDOSCOPY ( 1 FDA reports)
SIGMOIDOSCOPY ABNORMAL ( 1 FDA reports)
SIGNET-RING CELL CARCINOMA ( 1 FDA reports)
SKELETAL MUSCLE ENZYMES ( 1 FDA reports)
SKELETON DYSPLASIA ( 1 FDA reports)
SKIN GRAFT REJECTION ( 1 FDA reports)
SKIN IMPLANT ( 1 FDA reports)
SKIN SQUAMOUS CELL CARCINOMA SURGERY ( 1 FDA reports)
SLEEP PARALYSIS ( 1 FDA reports)
SLEEP STUDY ABNORMAL ( 1 FDA reports)
SLOW SPEECH ( 1 FDA reports)
SMALL CELL LUNG CANCER LIMITED STAGE ( 1 FDA reports)
SMALL INTESTINAL ANASTOMOSIS ( 1 FDA reports)
SMEAR VAGINAL ABNORMAL ( 1 FDA reports)
SMOOTH MUSCLE CELL NEOPLASM ( 1 FDA reports)
SNAKE BITE ( 1 FDA reports)
SOCIAL FEAR ( 1 FDA reports)
SPERMATOZOA ABNORMAL ( 1 FDA reports)
SPINAL ANAESTHESIA ( 1 FDA reports)
SPINAL ARTERY THROMBOSIS ( 1 FDA reports)
SPINAL CORD HERNIATION ( 1 FDA reports)
SPINAL CORD INFECTION ( 1 FDA reports)
SPINAL CORD OPERATION ( 1 FDA reports)
SPINAL CORD PARALYSIS ( 1 FDA reports)
SPINAL INFECTION VIRAL ( 1 FDA reports)
SPINAL SUPPORT ( 1 FDA reports)
SPINOCEREBELLAR ATAXIA ( 1 FDA reports)
SPLEEN PALPABLE ( 1 FDA reports)
SPLENIC INFECTION BACTERIAL ( 1 FDA reports)
SPLENIC NECROSIS ( 1 FDA reports)
SPLENIC VEIN OCCLUSION ( 1 FDA reports)
SPLENORENAL SHUNT ( 1 FDA reports)
SPUTUM CULTURE ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF THE CERVIX ( 1 FDA reports)
STAPHYLOCOCCAL PHARYNGITIS ( 1 FDA reports)
STENOTROPHOMONAS TEST POSITIVE ( 1 FDA reports)
STENT MALAPPOSITION ( 1 FDA reports)
STENT REMOVAL ( 1 FDA reports)
STERNAL WIRING ( 1 FDA reports)
STEROID WITHDRAWAL SYNDROME ( 1 FDA reports)
STITCH ABSCESS ( 1 FDA reports)
STOMATITIS HAEMORRHAGIC ( 1 FDA reports)
STOMATOCYTES PRESENT ( 1 FDA reports)
STOOL PH DECREASED ( 1 FDA reports)
STREPTOCOCCAL ABSCESS ( 1 FDA reports)
STREPTOCOCCAL URINARY TRACT INFECTION ( 1 FDA reports)
STRUCK BY LIGHTNING ( 1 FDA reports)
SUBCORNEAL PUSTULAR DERMATOSIS ( 1 FDA reports)
SUBDURAL EFFUSION ( 1 FDA reports)
SUBDURAL EMPYEMA ( 1 FDA reports)
SUBMAXILLARY GLAND ENLARGEMENT ( 1 FDA reports)
SUPERFICIAL SPREADING MELANOMA STAGE UNSPECIFIED ( 1 FDA reports)
SUPERFICIAL VEIN PROMINENCE ( 1 FDA reports)
SUPRAVALVULAR AORTIC STENOSIS ( 1 FDA reports)
SURFACTANT PROTEIN INCREASED ( 1 FDA reports)
SWAN GANZ CATHETER PLACEMENT ( 1 FDA reports)
SYMBLEPHARON ( 1 FDA reports)
SYMPATHECTOMY ( 1 FDA reports)
SYNDACTYLY ( 1 FDA reports)
SYNOSTOSIS ( 1 FDA reports)
SYNOVIAL FLUID ANALYSIS ( 1 FDA reports)
SYPHILIS TEST POSITIVE ( 1 FDA reports)
SYSTEMIC LEAKAGE ( 1 FDA reports)
SYSTEMIC MASTOCYTOSIS ( 1 FDA reports)
TACHYPHYLAXIS ( 1 FDA reports)
TACITURNITY ( 1 FDA reports)
TANDEM GAIT TEST ( 1 FDA reports)
TEMPERATURE DIFFERENCE OF EXTREMITIES ( 1 FDA reports)
TENDON NECROSIS ( 1 FDA reports)
TENDON NEOPLASM ( 1 FDA reports)
TERATOMA ( 1 FDA reports)
TESTICULAR APPENDAGE TORSION ( 1 FDA reports)
TESTICULAR CYST ( 1 FDA reports)
TESTICULAR NEOPLASM ( 1 FDA reports)
TESTICULAR TORSION ( 1 FDA reports)
TETRALOGY OF FALLOT REPAIR ( 1 FDA reports)
THEFT ( 1 FDA reports)
THERAPEUTIC HYPOTHERMIA ( 1 FDA reports)
THERMOHYPOAESTHESIA ( 1 FDA reports)
THERMOMETRY ABNORMAL ( 1 FDA reports)
THORACIC CAVITY DRAINAGE TEST ABNORMAL ( 1 FDA reports)
THREAT OF REDUNDANCY ( 1 FDA reports)
THROMBASTHENIA ( 1 FDA reports)
THROMBOANGIITIS OBLITERANS ( 1 FDA reports)
THYMIC CANCER METASTATIC ( 1 FDA reports)
THYROGLOSSAL CYST ( 1 FDA reports)
THYROID CANCER STAGE IV ( 1 FDA reports)
TINEA CAPITIS ( 1 FDA reports)
TONGUE CARCINOMA STAGE III ( 1 FDA reports)
TONGUE CYST ( 1 FDA reports)
TONGUE NEOPLASM BENIGN ( 1 FDA reports)
TONGUE OPERATION ( 1 FDA reports)
TONGUE PIGMENTATION ( 1 FDA reports)
TONSILLAR CYST ( 1 FDA reports)
TOXIC SHOCK SYNDROME STAPHYLOCOCCAL ( 1 FDA reports)
TOXICOLOGIC TEST NORMAL ( 1 FDA reports)
TOXOCARIASIS ( 1 FDA reports)
TOXOPLASMA SEROLOGY POSITIVE ( 1 FDA reports)
TRABECULECTOMY ( 1 FDA reports)
TRACHEAL INJURY ( 1 FDA reports)
TRANSFERRIN DECREASED ( 1 FDA reports)
TRANSFUSION RELATED COMPLICATION ( 1 FDA reports)
TRANSIENT PSYCHOSIS ( 1 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 1 FDA reports)
TRANSMYOCARDIAL REVASCULARISATION ( 1 FDA reports)
TRANSURETHRAL BLADDER RESECTION ( 1 FDA reports)
TRAUMATIC ANURIA ( 1 FDA reports)
TRAUMATIC SHOCK ( 1 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 1 FDA reports)
TRI-IODOTHYRONINE UPTAKE ABNORMAL ( 1 FDA reports)
TRI-IODOTHYRONINE UPTAKE INCREASED ( 1 FDA reports)
TRICHOSPORON INFECTION ( 1 FDA reports)
TRICUSPID VALVE CALCIFICATION ( 1 FDA reports)
TRICUSPID VALVE REPLACEMENT ( 1 FDA reports)
TRICUSPID VALVE SCLEROSIS ( 1 FDA reports)
TRISOMY 14 ( 1 FDA reports)
TRISOMY 22 ( 1 FDA reports)
TROPICAL ULCER ( 1 FDA reports)
TUBERCULOSIS BLADDER ( 1 FDA reports)
TUBERCULOSIS GASTROINTESTINAL ( 1 FDA reports)
TUBERCULOSIS LIVER ( 1 FDA reports)
TUBERCULOSIS SKIN TEST POSITIVE ( 1 FDA reports)
TUMOUR ASSOCIATED FEVER ( 1 FDA reports)
TUMOUR EMBOLISM ( 1 FDA reports)
TUMOUR PAIN ( 1 FDA reports)
TUMOUR RUPTURE ( 1 FDA reports)
TYMPANIC MEMBRANE ATROPHIC ( 1 FDA reports)
TYMPANIC MEMBRANE HYPERAEMIA ( 1 FDA reports)
TYMPANOMETRY ABNORMAL ( 1 FDA reports)
TYPE IIA HYPERLIPIDAEMIA ( 1 FDA reports)
TYPHUS RICKETTSIA TEST POSITIVE ( 1 FDA reports)
ULNAR NEURITIS ( 1 FDA reports)
ULTRASONIC ANGIOGRAM ABNORMAL ( 1 FDA reports)
ULTRASOUND ABDOMEN ( 1 FDA reports)
ULTRASOUND LIVER ( 1 FDA reports)
ULTRASOUND THYROID ABNORMAL ( 1 FDA reports)
UMBILICAL CORD AROUND NECK ( 1 FDA reports)
UMBILICAL MALFORMATION ( 1 FDA reports)
UNEQUAL LEG LENGTH ACQUIRED ( 1 FDA reports)
UNEVALUABLE INVESTIGATION ( 1 FDA reports)
UNWANTED AWARENESS DURING ANAESTHESIA ( 1 FDA reports)
UP AND DOWN PHENOMENON ( 1 FDA reports)
UPPER AERODIGESTIVE TRACT INFECTION ( 1 FDA reports)
UPPER LIMB DEFORMITY ( 1 FDA reports)
UPPER RESPIRATORY FUNGAL INFECTION ( 1 FDA reports)
URACHAL ABNORMALITY ( 1 FDA reports)
URAEMIC PRURITUS ( 1 FDA reports)
UREA URINE INCREASED ( 1 FDA reports)
URETERAL NEOPLASM ( 1 FDA reports)
URETERAL STENT REMOVAL ( 1 FDA reports)
URETERIC CANCER LOCAL ( 1 FDA reports)
URETERIC DIVERSION OPERATION ( 1 FDA reports)
URETERIC OPERATION ( 1 FDA reports)
URETERIC REPAIR ( 1 FDA reports)
URETEROSCOPY ( 1 FDA reports)
URETHRAL ABSCESS ( 1 FDA reports)
URETHRAL DISCHARGE ( 1 FDA reports)
URETHRAL MEATOTOMY ( 1 FDA reports)
URETHRAL NEOPLASM ( 1 FDA reports)
URINARY BLADDER ABSCESS ( 1 FDA reports)
URINARY BLADDER ATROPHY ( 1 FDA reports)
URINARY CALCULUS REMOVAL ( 1 FDA reports)
URINARY CASTS PRESENT ( 1 FDA reports)
URINARY RETENTION POSTOPERATIVE ( 1 FDA reports)
URINARY TRACT NEOPLASM ( 1 FDA reports)
URINE ALCOHOL TEST POSITIVE ( 1 FDA reports)
URINE ARSENIC ( 1 FDA reports)

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