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

NAUSEA ( 5903 FDA reports)
DYSPNOEA ( 5617 FDA reports)
PAIN ( 5394 FDA reports)
DIZZINESS ( 4887 FDA reports)
FATIGUE ( 4570 FDA reports)
DIARRHOEA ( 4076 FDA reports)
ASTHENIA ( 3935 FDA reports)
ANXIETY ( 3794 FDA reports)
DRUG INEFFECTIVE ( 3733 FDA reports)
VOMITING ( 3657 FDA reports)
HEADACHE ( 3370 FDA reports)
HYPERTENSION ( 3360 FDA reports)
HYPOTENSION ( 3197 FDA reports)
FALL ( 3143 FDA reports)
MYOCARDIAL INFARCTION ( 3078 FDA reports)
CHEST PAIN ( 3074 FDA reports)
OEDEMA PERIPHERAL ( 2911 FDA reports)
RENAL FAILURE ACUTE ( 2893 FDA reports)
ANAEMIA ( 2814 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2723 FDA reports)
WEIGHT DECREASED ( 2712 FDA reports)
BLOOD GLUCOSE INCREASED ( 2663 FDA reports)
DEPRESSION ( 2635 FDA reports)
PAIN IN EXTREMITY ( 2547 FDA reports)
ARTHRALGIA ( 2533 FDA reports)
FLUSHING ( 2500 FDA reports)
BACK PAIN ( 2497 FDA reports)
COUGH ( 2479 FDA reports)
PNEUMONIA ( 2478 FDA reports)
DEHYDRATION ( 2455 FDA reports)
RENAL FAILURE ( 2416 FDA reports)
PRURITUS ( 2206 FDA reports)
INJURY ( 2187 FDA reports)
ABDOMINAL PAIN ( 2174 FDA reports)
INSOMNIA ( 2166 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2031 FDA reports)
ATRIAL FIBRILLATION ( 2029 FDA reports)
MALAISE ( 2003 FDA reports)
PYREXIA ( 1926 FDA reports)
RASH ( 1913 FDA reports)
BLOOD PRESSURE INCREASED ( 1807 FDA reports)
CONSTIPATION ( 1776 FDA reports)
CONFUSIONAL STATE ( 1680 FDA reports)
DEATH ( 1665 FDA reports)
PARAESTHESIA ( 1659 FDA reports)
ANGIOEDEMA ( 1651 FDA reports)
CORONARY ARTERY DISEASE ( 1625 FDA reports)
WEIGHT INCREASED ( 1594 FDA reports)
MYALGIA ( 1563 FDA reports)
URINARY TRACT INFECTION ( 1545 FDA reports)
DECREASED APPETITE ( 1519 FDA reports)
HYPOAESTHESIA ( 1519 FDA reports)
SYNCOPE ( 1518 FDA reports)
FEELING ABNORMAL ( 1494 FDA reports)
ABDOMINAL PAIN UPPER ( 1491 FDA reports)
MUSCLE SPASMS ( 1488 FDA reports)
LOSS OF CONSCIOUSNESS ( 1476 FDA reports)
DIABETES MELLITUS ( 1469 FDA reports)
GAIT DISTURBANCE ( 1435 FDA reports)
ERYTHEMA ( 1420 FDA reports)
EMOTIONAL DISTRESS ( 1373 FDA reports)
VISION BLURRED ( 1332 FDA reports)
HYPERHIDROSIS ( 1319 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1301 FDA reports)
DRUG INTERACTION ( 1296 FDA reports)
PLEURAL EFFUSION ( 1293 FDA reports)
SOMNOLENCE ( 1291 FDA reports)
DYSPHAGIA ( 1263 FDA reports)
TREMOR ( 1218 FDA reports)
MUSCULAR WEAKNESS ( 1208 FDA reports)
HYPERKALAEMIA ( 1186 FDA reports)
CONDITION AGGRAVATED ( 1183 FDA reports)
BLOOD CREATININE INCREASED ( 1170 FDA reports)
HAEMOGLOBIN DECREASED ( 1160 FDA reports)
PALPITATIONS ( 1103 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1097 FDA reports)
OSTEONECROSIS OF JAW ( 1084 FDA reports)
DEEP VEIN THROMBOSIS ( 1077 FDA reports)
OSTEOARTHRITIS ( 1074 FDA reports)
PANCREATITIS ( 1057 FDA reports)
CARDIAC DISORDER ( 1057 FDA reports)
ANHEDONIA ( 1036 FDA reports)
SEPSIS ( 1025 FDA reports)
CARDIAC ARREST ( 1019 FDA reports)
RESPIRATORY FAILURE ( 1004 FDA reports)
NEUROPATHY PERIPHERAL ( 998 FDA reports)
CONVULSION ( 984 FDA reports)
UNEVALUABLE EVENT ( 973 FDA reports)
RENAL IMPAIRMENT ( 957 FDA reports)
CHEST DISCOMFORT ( 954 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 952 FDA reports)
THROMBOCYTOPENIA ( 931 FDA reports)
HEART RATE INCREASED ( 922 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 917 FDA reports)
TYPE 2 DIABETES MELLITUS ( 915 FDA reports)
PULMONARY EMBOLISM ( 912 FDA reports)
BRADYCARDIA ( 911 FDA reports)
CONTUSION ( 911 FDA reports)
DYSPEPSIA ( 907 FDA reports)
BRONCHITIS ( 900 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 900 FDA reports)
FEELING HOT ( 892 FDA reports)
BLOOD PRESSURE DECREASED ( 879 FDA reports)
STRESS ( 870 FDA reports)
CELLULITIS ( 869 FDA reports)
HYPERSENSITIVITY ( 861 FDA reports)
ATELECTASIS ( 856 FDA reports)
CHOLELITHIASIS ( 856 FDA reports)
INFECTION ( 848 FDA reports)
HYPERLIPIDAEMIA ( 829 FDA reports)
MENTAL STATUS CHANGES ( 827 FDA reports)
MITRAL VALVE INCOMPETENCE ( 824 FDA reports)
RENAL FAILURE CHRONIC ( 818 FDA reports)
FEAR ( 809 FDA reports)
CHILLS ( 806 FDA reports)
URTICARIA ( 797 FDA reports)
ABDOMINAL DISCOMFORT ( 796 FDA reports)
HYPOGLYCAEMIA ( 792 FDA reports)
HAEMORRHAGE ( 785 FDA reports)
TACHYCARDIA ( 782 FDA reports)
ECONOMIC PROBLEM ( 779 FDA reports)
CARDIOMEGALY ( 777 FDA reports)
OSTEOMYELITIS ( 761 FDA reports)
RECTAL HAEMORRHAGE ( 752 FDA reports)
JOINT SWELLING ( 751 FDA reports)
BALANCE DISORDER ( 748 FDA reports)
SWELLING ( 745 FDA reports)
SWELLING FACE ( 742 FDA reports)
MUSCULOSKELETAL PAIN ( 742 FDA reports)
HYPONATRAEMIA ( 738 FDA reports)
HYPOKALAEMIA ( 736 FDA reports)
MEMORY IMPAIRMENT ( 733 FDA reports)
OEDEMA ( 729 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 722 FDA reports)
AMNESIA ( 714 FDA reports)
ABDOMINAL DISTENSION ( 706 FDA reports)
MULTI-ORGAN FAILURE ( 693 FDA reports)
BONE DISORDER ( 692 FDA reports)
COMPLETED SUICIDE ( 692 FDA reports)
SINUSITIS ( 691 FDA reports)
DRUG DOSE OMISSION ( 687 FDA reports)
OVERDOSE ( 685 FDA reports)
BLOOD GLUCOSE DECREASED ( 680 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 665 FDA reports)
DRUG HYPERSENSITIVITY ( 663 FDA reports)
PLATELET COUNT DECREASED ( 653 FDA reports)
ASTHMA ( 651 FDA reports)
HYPERGLYCAEMIA ( 644 FDA reports)
BURNING SENSATION ( 643 FDA reports)
SWOLLEN TONGUE ( 640 FDA reports)
ARTHRITIS ( 639 FDA reports)
RHABDOMYOLYSIS ( 637 FDA reports)
AGITATION ( 636 FDA reports)
CARDIAC FAILURE ( 625 FDA reports)
SPINAL OSTEOARTHRITIS ( 625 FDA reports)
LETHARGY ( 624 FDA reports)
DRY MOUTH ( 616 FDA reports)
CATARACT ( 610 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 608 FDA reports)
PRODUCT QUALITY ISSUE ( 607 FDA reports)
SUICIDAL IDEATION ( 600 FDA reports)
RENAL INJURY ( 598 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 593 FDA reports)
ARRHYTHMIA ( 591 FDA reports)
INCORRECT DOSE ADMINISTERED ( 589 FDA reports)
CARDIOMYOPATHY ( 586 FDA reports)
INJECTION SITE PAIN ( 585 FDA reports)
PULMONARY OEDEMA ( 584 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 575 FDA reports)
WHEEZING ( 572 FDA reports)
HYPOXIA ( 572 FDA reports)
VISUAL IMPAIRMENT ( 571 FDA reports)
NECK PAIN ( 570 FDA reports)
ANGINA PECTORIS ( 568 FDA reports)
ALOPECIA ( 567 FDA reports)
HAEMORRHOIDS ( 566 FDA reports)
GASTRITIS ( 564 FDA reports)
DYSGEUSIA ( 563 FDA reports)
HAEMATOCHEZIA ( 562 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 561 FDA reports)
EPISTAXIS ( 561 FDA reports)
BLOOD UREA INCREASED ( 560 FDA reports)
IMPAIRED HEALING ( 560 FDA reports)
PAIN IN JAW ( 558 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 549 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 541 FDA reports)
THROMBOSIS ( 540 FDA reports)
ABASIA ( 537 FDA reports)
OROPHARYNGEAL PAIN ( 534 FDA reports)
ARTERIOSCLEROSIS ( 529 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 528 FDA reports)
URINARY INCONTINENCE ( 525 FDA reports)
OSTEOPOROSIS ( 520 FDA reports)
HIATUS HERNIA ( 517 FDA reports)
NERVOUSNESS ( 516 FDA reports)
PANCREATITIS ACUTE ( 515 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 513 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 513 FDA reports)
DYSPNOEA EXERTIONAL ( 506 FDA reports)
INFLUENZA LIKE ILLNESS ( 506 FDA reports)
BONE PAIN ( 505 FDA reports)
MULTIPLE INJURIES ( 505 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 502 FDA reports)
OSTEONECROSIS ( 500 FDA reports)
ARTHROPATHY ( 493 FDA reports)
PULMONARY HYPERTENSION ( 491 FDA reports)
PANCYTOPENIA ( 489 FDA reports)
OFF LABEL USE ( 484 FDA reports)
TREATMENT NONCOMPLIANCE ( 484 FDA reports)
MOBILITY DECREASED ( 484 FDA reports)
NEUTROPENIA ( 481 FDA reports)
NASOPHARYNGITIS ( 479 FDA reports)
DYSPHONIA ( 479 FDA reports)
DYSURIA ( 479 FDA reports)
HEART RATE DECREASED ( 479 FDA reports)
HAEMATOCRIT DECREASED ( 476 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 472 FDA reports)
POLLAKIURIA ( 471 FDA reports)
DIVERTICULUM ( 465 FDA reports)
SLEEP APNOEA SYNDROME ( 461 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 461 FDA reports)
VISUAL ACUITY REDUCED ( 460 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 460 FDA reports)
UNRESPONSIVE TO STIMULI ( 459 FDA reports)
HOT FLUSH ( 459 FDA reports)
DISORIENTATION ( 454 FDA reports)
OBESITY ( 453 FDA reports)
CORONARY ARTERY OCCLUSION ( 450 FDA reports)
FLATULENCE ( 450 FDA reports)
RESPIRATORY DISTRESS ( 449 FDA reports)
NEPHROLITHIASIS ( 445 FDA reports)
HALLUCINATION ( 445 FDA reports)
TOOTH EXTRACTION ( 444 FDA reports)
VERTIGO ( 442 FDA reports)
SPEECH DISORDER ( 440 FDA reports)
DRUG EFFECT DECREASED ( 439 FDA reports)
HAEMATURIA ( 439 FDA reports)
ANGIONEUROTIC OEDEMA ( 436 FDA reports)
ANOREXIA ( 436 FDA reports)
DYSARTHRIA ( 435 FDA reports)
NEOPLASM MALIGNANT ( 432 FDA reports)
BLOOD POTASSIUM DECREASED ( 430 FDA reports)
LIP SWELLING ( 426 FDA reports)
ERECTILE DYSFUNCTION ( 422 FDA reports)
MENTAL DISORDER ( 413 FDA reports)
MYOCARDIAL ISCHAEMIA ( 411 FDA reports)
HEPATIC ENZYME INCREASED ( 410 FDA reports)
OSTEOPENIA ( 410 FDA reports)
SKIN DISCOLOURATION ( 410 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 409 FDA reports)
CARDIO-RESPIRATORY ARREST ( 409 FDA reports)
RASH PRURITIC ( 406 FDA reports)
STAPHYLOCOCCAL INFECTION ( 404 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 404 FDA reports)
ROAD TRAFFIC ACCIDENT ( 403 FDA reports)
SCAR ( 401 FDA reports)
HEPATIC STEATOSIS ( 401 FDA reports)
HEART RATE IRREGULAR ( 398 FDA reports)
BLOOD POTASSIUM INCREASED ( 397 FDA reports)
RENAL CYST ( 396 FDA reports)
RENAL DISORDER ( 394 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 392 FDA reports)
EJECTION FRACTION DECREASED ( 392 FDA reports)
HERPES ZOSTER ( 392 FDA reports)
CYSTITIS ( 391 FDA reports)
METABOLIC ACIDOSIS ( 390 FDA reports)
PRESYNCOPE ( 389 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 388 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 388 FDA reports)
SLEEP DISORDER ( 386 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 386 FDA reports)
BLOOD SODIUM DECREASED ( 386 FDA reports)
VENTRICULAR TACHYCARDIA ( 384 FDA reports)
SKIN ULCER ( 382 FDA reports)
DEFORMITY ( 377 FDA reports)
EXOSTOSIS ( 375 FDA reports)
HYPOPHAGIA ( 374 FDA reports)
MIGRAINE ( 374 FDA reports)
ABNORMAL DREAMS ( 373 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 373 FDA reports)
SKIN BURNING SENSATION ( 369 FDA reports)
METASTASES TO BONE ( 365 FDA reports)
ROTATOR CUFF SYNDROME ( 363 FDA reports)
ANAPHYLACTIC REACTION ( 358 FDA reports)
DIABETIC NEUROPATHY ( 358 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 357 FDA reports)
DIVERTICULITIS ( 357 FDA reports)
FLUID RETENTION ( 357 FDA reports)
HYPOVOLAEMIA ( 357 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 357 FDA reports)
AGGRESSION ( 356 FDA reports)
ILL-DEFINED DISORDER ( 356 FDA reports)
IRRITABILITY ( 352 FDA reports)
LUNG NEOPLASM ( 352 FDA reports)
SURGERY ( 352 FDA reports)
GALLBLADDER DISORDER ( 350 FDA reports)
SINUS TACHYCARDIA ( 347 FDA reports)
INJECTION SITE ERYTHEMA ( 346 FDA reports)
LEUKOCYTOSIS ( 345 FDA reports)
GOUT ( 344 FDA reports)
CARDIAC MURMUR ( 343 FDA reports)
DENTAL CARIES ( 343 FDA reports)
LYMPHADENOPATHY ( 342 FDA reports)
RESPIRATORY ARREST ( 342 FDA reports)
DECREASED INTEREST ( 341 FDA reports)
HYPOTHYROIDISM ( 341 FDA reports)
SKIN EXFOLIATION ( 339 FDA reports)
BLISTER ( 338 FDA reports)
HAEMATEMESIS ( 337 FDA reports)
RIB FRACTURE ( 337 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 336 FDA reports)
MULTIPLE MYELOMA ( 335 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 333 FDA reports)
TINNITUS ( 330 FDA reports)
RHEUMATOID ARTHRITIS ( 329 FDA reports)
MEDICATION ERROR ( 326 FDA reports)
ASCITES ( 325 FDA reports)
RHINORRHOEA ( 325 FDA reports)
PSORIASIS ( 322 FDA reports)
DISTURBANCE IN ATTENTION ( 320 FDA reports)
GASTROINTESTINAL DISORDER ( 319 FDA reports)
EXPOSED BONE IN JAW ( 318 FDA reports)
HAEMOPTYSIS ( 316 FDA reports)
NASAL CONGESTION ( 315 FDA reports)
ORTHOSTATIC HYPOTENSION ( 314 FDA reports)
SUICIDE ATTEMPT ( 314 FDA reports)
BONE LESION ( 314 FDA reports)
COLONIC POLYP ( 314 FDA reports)
HEAD INJURY ( 314 FDA reports)
PHARYNGEAL OEDEMA ( 313 FDA reports)
HYPERCHOLESTEROLAEMIA ( 312 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 312 FDA reports)
FEMUR FRACTURE ( 310 FDA reports)
PERICARDIAL EFFUSION ( 310 FDA reports)
PANIC ATTACK ( 309 FDA reports)
URINARY RETENTION ( 306 FDA reports)
DRY SKIN ( 305 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 299 FDA reports)
PRODUCTIVE COUGH ( 298 FDA reports)
DISEASE PROGRESSION ( 293 FDA reports)
LUNG INFILTRATION ( 293 FDA reports)
CHOLECYSTITIS ( 291 FDA reports)
OXYGEN SATURATION DECREASED ( 291 FDA reports)
INFLUENZA ( 290 FDA reports)
SEPTIC SHOCK ( 289 FDA reports)
SINUS BRADYCARDIA ( 288 FDA reports)
STOMATITIS ( 288 FDA reports)
ABNORMAL BEHAVIOUR ( 288 FDA reports)
ANGINA UNSTABLE ( 287 FDA reports)
HIP FRACTURE ( 287 FDA reports)
RASH GENERALISED ( 287 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 287 FDA reports)
FAECES DISCOLOURED ( 286 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 285 FDA reports)
DRUG TOXICITY ( 284 FDA reports)
FEBRILE NEUTROPENIA ( 283 FDA reports)
VENTRICULAR FIBRILLATION ( 283 FDA reports)
COMA ( 280 FDA reports)
FLUID OVERLOAD ( 280 FDA reports)
BLINDNESS ( 275 FDA reports)
BURSITIS ( 275 FDA reports)
EMOTIONAL DISORDER ( 275 FDA reports)
TOOTHACHE ( 275 FDA reports)
EMPHYSEMA ( 274 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 273 FDA reports)
BREAST CANCER ( 272 FDA reports)
DYSKINESIA ( 272 FDA reports)
LEUKOPENIA ( 270 FDA reports)
TOOTH DISORDER ( 270 FDA reports)
ATRIAL FLUTTER ( 269 FDA reports)
MUSCLE TWITCHING ( 268 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 267 FDA reports)
GASTRIC ULCER ( 266 FDA reports)
SKIN DISORDER ( 266 FDA reports)
SKIN INDURATION ( 266 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 264 FDA reports)
HAEMODIALYSIS ( 263 FDA reports)
INTENTIONAL DRUG MISUSE ( 263 FDA reports)
COMPRESSION FRACTURE ( 262 FDA reports)
BLOOD BILIRUBIN INCREASED ( 259 FDA reports)
COAGULOPATHY ( 259 FDA reports)
INFLAMMATION ( 258 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 257 FDA reports)
PRURITUS GENERALISED ( 256 FDA reports)
SKIN HYPERTROPHY ( 255 FDA reports)
DISABILITY ( 255 FDA reports)
LACTIC ACIDOSIS ( 254 FDA reports)
DEMENTIA ( 253 FDA reports)
FIBROMYALGIA ( 253 FDA reports)
TOOTH LOSS ( 252 FDA reports)
NIGHTMARE ( 251 FDA reports)
RASH ERYTHEMATOUS ( 249 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 249 FDA reports)
NEURALGIA ( 248 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 248 FDA reports)
COLITIS ( 248 FDA reports)
DYSLIPIDAEMIA ( 248 FDA reports)
DIABETIC KETOACIDOSIS ( 246 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 246 FDA reports)
ORAL PAIN ( 246 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 245 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 242 FDA reports)
ANGER ( 240 FDA reports)
CARDIOVASCULAR DISORDER ( 240 FDA reports)
HYPERSOMNIA ( 239 FDA reports)
APHASIA ( 238 FDA reports)
DISCOMFORT ( 238 FDA reports)
GLAUCOMA ( 238 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 238 FDA reports)
RASH MACULAR ( 238 FDA reports)
THROAT IRRITATION ( 237 FDA reports)
DRY EYE ( 237 FDA reports)
MOUTH ULCERATION ( 237 FDA reports)
CHOLECYSTITIS CHRONIC ( 235 FDA reports)
EYE PAIN ( 234 FDA reports)
HEPATIC FAILURE ( 234 FDA reports)
HYPOMAGNESAEMIA ( 234 FDA reports)
JOINT STIFFNESS ( 234 FDA reports)
PULMONARY FIBROSIS ( 233 FDA reports)
PALLOR ( 232 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 232 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 231 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 231 FDA reports)
DYSSTASIA ( 231 FDA reports)
SKIN TIGHTNESS ( 230 FDA reports)
TOOTH ABSCESS ( 230 FDA reports)
PRIMARY SEQUESTRUM ( 229 FDA reports)
RESTLESSNESS ( 229 FDA reports)
SKIN LESION ( 229 FDA reports)
SPINAL COLUMN STENOSIS ( 229 FDA reports)
HAEMATOMA ( 229 FDA reports)
JOINT INJURY ( 229 FDA reports)
CAROTID ARTERY STENOSIS ( 226 FDA reports)
DEPRESSED MOOD ( 226 FDA reports)
LUNG DISORDER ( 226 FDA reports)
GASTRIC DISORDER ( 224 FDA reports)
ADVERSE EVENT ( 223 FDA reports)
PROTHROMBIN TIME PROLONGED ( 223 FDA reports)
PULMONARY CONGESTION ( 222 FDA reports)
DELIRIUM ( 222 FDA reports)
GASTROENTERITIS ( 221 FDA reports)
MIDDLE INSOMNIA ( 221 FDA reports)
RENAL TUBULAR NECROSIS ( 220 FDA reports)
TENDONITIS ( 220 FDA reports)
OESOPHAGITIS ( 218 FDA reports)
PROTEINURIA ( 218 FDA reports)
SPINAL COMPRESSION FRACTURE ( 218 FDA reports)
CEREBRAL ATROPHY ( 218 FDA reports)
INJECTION SITE HAEMATOMA ( 218 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 217 FDA reports)
CEREBRAL HAEMORRHAGE ( 216 FDA reports)
POST PROCEDURAL COMPLICATION ( 216 FDA reports)
EYE SWELLING ( 215 FDA reports)
AORTIC VALVE INCOMPETENCE ( 214 FDA reports)
DIALYSIS ( 214 FDA reports)
RETCHING ( 214 FDA reports)
ACUTE CORONARY SYNDROME ( 213 FDA reports)
CARDIOGENIC SHOCK ( 213 FDA reports)
CARPAL TUNNEL SYNDROME ( 213 FDA reports)
DIPLOPIA ( 213 FDA reports)
ADVERSE DRUG REACTION ( 212 FDA reports)
METASTASES TO LUNG ( 212 FDA reports)
NIGHT SWEATS ( 212 FDA reports)
RESTLESS LEGS SYNDROME ( 212 FDA reports)
AZOTAEMIA ( 211 FDA reports)
MOVEMENT DISORDER ( 211 FDA reports)
CEREBRAL INFARCTION ( 210 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 209 FDA reports)
MELAENA ( 209 FDA reports)
NOCTURIA ( 209 FDA reports)
SHOCK ( 208 FDA reports)
ERUCTATION ( 208 FDA reports)
MALNUTRITION ( 208 FDA reports)
COGNITIVE DISORDER ( 207 FDA reports)
DRUG ADMINISTRATION ERROR ( 206 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 206 FDA reports)
ENCEPHALOPATHY ( 206 FDA reports)
PHYSICAL DISABILITY ( 205 FDA reports)
PROSTATE CANCER ( 204 FDA reports)
VIRAL INFECTION ( 204 FDA reports)
MUCOSAL INFLAMMATION ( 204 FDA reports)
ABSCESS ( 203 FDA reports)
ACUTE RESPIRATORY FAILURE ( 203 FDA reports)
HEMIPARESIS ( 203 FDA reports)
CRYING ( 202 FDA reports)
INJECTION SITE HAEMORRHAGE ( 200 FDA reports)
FOOT FRACTURE ( 199 FDA reports)
GASTRITIS EROSIVE ( 199 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 198 FDA reports)
DRUG INTOLERANCE ( 198 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 198 FDA reports)
BASAL CELL CARCINOMA ( 197 FDA reports)
EYE DISORDER ( 197 FDA reports)
BLOOD URINE PRESENT ( 196 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 194 FDA reports)
SCIATICA ( 194 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 193 FDA reports)
IMPAIRED WORK ABILITY ( 193 FDA reports)
HYPERCALCAEMIA ( 192 FDA reports)
LIMB INJURY ( 192 FDA reports)
SINUS DISORDER ( 190 FDA reports)
LIVER DISORDER ( 189 FDA reports)
LOOSE TOOTH ( 188 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 188 FDA reports)
ULCER ( 188 FDA reports)
PATHOLOGICAL FRACTURE ( 186 FDA reports)
SCOLIOSIS ( 186 FDA reports)
EAR PAIN ( 185 FDA reports)
CHOLECYSTECTOMY ( 183 FDA reports)
LEFT ATRIAL DILATATION ( 183 FDA reports)
PARANOIA ( 183 FDA reports)
ORTHOPNOEA ( 182 FDA reports)
BONE DENSITY DECREASED ( 181 FDA reports)
HYPOCALCAEMIA ( 181 FDA reports)
CORONARY ARTERY STENOSIS ( 180 FDA reports)
DEAFNESS ( 180 FDA reports)
LACERATION ( 180 FDA reports)
ABDOMINAL PAIN LOWER ( 179 FDA reports)
THROAT TIGHTNESS ( 179 FDA reports)
WITHDRAWAL SYNDROME ( 179 FDA reports)
PNEUMONIA ASPIRATION ( 178 FDA reports)
FAECAL INCONTINENCE ( 178 FDA reports)
TARDIVE DYSKINESIA ( 177 FDA reports)
ORAL DISORDER ( 176 FDA reports)
AORTIC ANEURYSM ( 176 FDA reports)
BLOOD CALCIUM DECREASED ( 176 FDA reports)
BIPOLAR DISORDER ( 175 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 174 FDA reports)
JAUNDICE ( 174 FDA reports)
LUNG NEOPLASM MALIGNANT ( 174 FDA reports)
FLANK PAIN ( 172 FDA reports)
LOCAL SWELLING ( 172 FDA reports)
MUSCLE STRAIN ( 172 FDA reports)
COLD SWEAT ( 171 FDA reports)
FEELING COLD ( 171 FDA reports)
HALLUCINATION, VISUAL ( 171 FDA reports)
INTERSTITIAL LUNG DISEASE ( 171 FDA reports)
VISUAL DISTURBANCE ( 171 FDA reports)
ANKLE FRACTURE ( 170 FDA reports)
MENTAL IMPAIRMENT ( 170 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 169 FDA reports)
FEELING JITTERY ( 169 FDA reports)
SPLENOMEGALY ( 169 FDA reports)
THINKING ABNORMAL ( 168 FDA reports)
EATING DISORDER ( 168 FDA reports)
GINGIVAL BLEEDING ( 168 FDA reports)
JAW DISORDER ( 168 FDA reports)
MOOD SWINGS ( 168 FDA reports)
GINGIVITIS ( 166 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 165 FDA reports)
DIABETIC RETINOPATHY ( 165 FDA reports)
HYPOKINESIA ( 165 FDA reports)
NERVOUS SYSTEM DISORDER ( 165 FDA reports)
PERIODONTITIS ( 165 FDA reports)
APLASIA PURE RED CELL ( 164 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 164 FDA reports)
ECCHYMOSIS ( 164 FDA reports)
CEREBRAL ISCHAEMIA ( 163 FDA reports)
COLON CANCER ( 163 FDA reports)
DIVERTICULUM INTESTINAL ( 163 FDA reports)
KNEE ARTHROPLASTY ( 162 FDA reports)
LOBAR PNEUMONIA ( 161 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 161 FDA reports)
ATAXIA ( 160 FDA reports)
BLOOD ALBUMIN DECREASED ( 160 FDA reports)
CANDIDIASIS ( 159 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 159 FDA reports)
CARDIAC VALVE DISEASE ( 158 FDA reports)
DIASTOLIC DYSFUNCTION ( 158 FDA reports)
MASTICATION DISORDER ( 158 FDA reports)
CORONARY ARTERY BYPASS ( 157 FDA reports)
IRON DEFICIENCY ANAEMIA ( 157 FDA reports)
LEFT VENTRICULAR FAILURE ( 157 FDA reports)
OCULAR HYPERAEMIA ( 157 FDA reports)
ORAL INTAKE REDUCED ( 156 FDA reports)
RASH PAPULAR ( 156 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 156 FDA reports)
CHROMATURIA ( 155 FDA reports)
CYANOSIS ( 155 FDA reports)
INFUSION RELATED REACTION ( 155 FDA reports)
INTENTIONAL OVERDOSE ( 155 FDA reports)
KYPHOSIS ( 154 FDA reports)
PSYCHOTIC DISORDER ( 154 FDA reports)
UPPER LIMB FRACTURE ( 153 FDA reports)
CHOKING ( 153 FDA reports)
COLITIS ISCHAEMIC ( 152 FDA reports)
ILEUS ( 152 FDA reports)
METASTASES TO LIVER ( 152 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 152 FDA reports)
STEVENS-JOHNSON SYNDROME ( 152 FDA reports)
TENDERNESS ( 152 FDA reports)
TYPE 1 DIABETES MELLITUS ( 152 FDA reports)
HYPOACUSIS ( 151 FDA reports)
FIBROSIS ( 150 FDA reports)
INTERMITTENT CLAUDICATION ( 150 FDA reports)
POOR QUALITY SLEEP ( 150 FDA reports)
THYROID DISORDER ( 150 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 149 FDA reports)
FAILURE TO THRIVE ( 149 FDA reports)
DECUBITUS ULCER ( 148 FDA reports)
HYPOAESTHESIA ORAL ( 148 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 147 FDA reports)
URINE OUTPUT DECREASED ( 146 FDA reports)
EYE IRRITATION ( 146 FDA reports)
GRAND MAL CONVULSION ( 146 FDA reports)
HEPATITIS ( 146 FDA reports)
AGEUSIA ( 145 FDA reports)
CYST ( 145 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 145 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 145 FDA reports)
FUNGAL INFECTION ( 144 FDA reports)
BODY TEMPERATURE INCREASED ( 143 FDA reports)
DEVICE MALFUNCTION ( 143 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 143 FDA reports)
MASS ( 143 FDA reports)
PERIODONTAL DISEASE ( 143 FDA reports)
RHINITIS ALLERGIC ( 143 FDA reports)
VARICOSE VEIN ( 143 FDA reports)
SYNOVIAL CYST ( 142 FDA reports)
TOOTH FRACTURE ( 142 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 142 FDA reports)
ISCHAEMIA ( 142 FDA reports)
GLOSSODYNIA ( 141 FDA reports)
IRRITABLE BOWEL SYNDROME ( 141 FDA reports)
SINUS CONGESTION ( 141 FDA reports)
SUBDURAL HAEMATOMA ( 141 FDA reports)
PHARYNGITIS ( 140 FDA reports)
RESPIRATORY DISORDER ( 140 FDA reports)
CIRCULATORY COLLAPSE ( 140 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 139 FDA reports)
ELECTROLYTE IMBALANCE ( 139 FDA reports)
HOSPITALISATION ( 139 FDA reports)
LABORATORY TEST ABNORMAL ( 139 FDA reports)
MUSCLE TIGHTNESS ( 139 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 139 FDA reports)
SKIN LACERATION ( 139 FDA reports)
TROPONIN INCREASED ( 138 FDA reports)
BACK DISORDER ( 138 FDA reports)
BLINDNESS UNILATERAL ( 138 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 138 FDA reports)
JOINT EFFUSION ( 138 FDA reports)
CATARACT OPERATION ( 137 FDA reports)
DILATATION VENTRICULAR ( 137 FDA reports)
JAW FRACTURE ( 137 FDA reports)
INJECTION SITE PRURITUS ( 136 FDA reports)
NO THERAPEUTIC RESPONSE ( 136 FDA reports)
PULSE ABSENT ( 136 FDA reports)
RIGHT VENTRICULAR FAILURE ( 136 FDA reports)
WOUND INFECTION ( 136 FDA reports)
ESSENTIAL HYPERTENSION ( 135 FDA reports)
EXCORIATION ( 135 FDA reports)
MUSCLE ATROPHY ( 135 FDA reports)
COORDINATION ABNORMAL ( 134 FDA reports)
OEDEMA MOUTH ( 134 FDA reports)
RESPIRATORY RATE INCREASED ( 133 FDA reports)
SEDATION ( 133 FDA reports)
HYDRONEPHROSIS ( 133 FDA reports)
DRUG DEPENDENCE ( 132 FDA reports)
ECZEMA ( 132 FDA reports)
FACE OEDEMA ( 132 FDA reports)
LACRIMATION INCREASED ( 132 FDA reports)
METASTASES TO SPINE ( 132 FDA reports)
NEOPLASM PROGRESSION ( 132 FDA reports)
OSTEOLYSIS ( 132 FDA reports)
STENT PLACEMENT ( 132 FDA reports)
VISUAL FIELD DEFECT ( 132 FDA reports)
SKIN HYPERPIGMENTATION ( 131 FDA reports)
ACCIDENTAL EXPOSURE ( 131 FDA reports)
DERMATITIS ( 131 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 131 FDA reports)
AORTIC STENOSIS ( 130 FDA reports)
CLOSTRIDIAL INFECTION ( 130 FDA reports)
CROHN'S DISEASE ( 130 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 130 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 130 FDA reports)
STOMACH DISCOMFORT ( 129 FDA reports)
VENTRICULAR HYPOKINESIA ( 129 FDA reports)
VITAMIN D DEFICIENCY ( 129 FDA reports)
ATRIOVENTRICULAR BLOCK ( 129 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 129 FDA reports)
HEPATOMEGALY ( 129 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 129 FDA reports)
LIPASE INCREASED ( 129 FDA reports)
HYPOPNOEA ( 128 FDA reports)
KIDNEY INFECTION ( 128 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 127 FDA reports)
DILATATION ATRIAL ( 127 FDA reports)
LUMBAR SPINAL STENOSIS ( 127 FDA reports)
MULTIPLE SCLEROSIS ( 127 FDA reports)
ORAL CANDIDIASIS ( 127 FDA reports)
PURULENT DISCHARGE ( 127 FDA reports)
THYROID NEOPLASM ( 127 FDA reports)
VITREOUS FLOATERS ( 127 FDA reports)
MYOSITIS ( 126 FDA reports)
NO ADVERSE EVENT ( 126 FDA reports)
PNEUMOTHORAX ( 126 FDA reports)
TACHYPNOEA ( 126 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 126 FDA reports)
HEART INJURY ( 126 FDA reports)
FACIAL PAIN ( 125 FDA reports)
GASTROENTERITIS VIRAL ( 125 FDA reports)
HERNIA ( 125 FDA reports)
INTESTINAL ISCHAEMIA ( 125 FDA reports)
INTESTINAL OBSTRUCTION ( 125 FDA reports)
MACULAR DEGENERATION ( 125 FDA reports)
MAJOR DEPRESSION ( 125 FDA reports)
NEUTROPHIL COUNT INCREASED ( 125 FDA reports)
VENTRICULAR HYPERTROPHY ( 124 FDA reports)
GROIN PAIN ( 124 FDA reports)
HEPATIC CIRRHOSIS ( 124 FDA reports)
MENISCUS LESION ( 124 FDA reports)
GINGIVAL DISORDER ( 123 FDA reports)
GOITRE ( 123 FDA reports)
INCREASED APPETITE ( 123 FDA reports)
INJECTION SITE SWELLING ( 123 FDA reports)
OSTEITIS ( 123 FDA reports)
SICK SINUS SYNDROME ( 123 FDA reports)
SPINAL FRACTURE ( 123 FDA reports)
ONYCHOMYCOSIS ( 122 FDA reports)
RADICULOPATHY ( 122 FDA reports)
FRACTURE ( 122 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 121 FDA reports)
LOCALISED INFECTION ( 121 FDA reports)
MOOD ALTERED ( 121 FDA reports)
PERIPHERAL COLDNESS ( 121 FDA reports)
PULMONARY MASS ( 121 FDA reports)
PERITONITIS ( 120 FDA reports)
SENSORY DISTURBANCE ( 120 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 120 FDA reports)
THIRST ( 120 FDA reports)
GINGIVAL PAIN ( 120 FDA reports)
JOINT DISLOCATION ( 120 FDA reports)
LUNG INFECTION ( 120 FDA reports)
DUODENAL ULCER ( 119 FDA reports)
BACTERIAL INFECTION ( 118 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 118 FDA reports)
DEBRIDEMENT ( 117 FDA reports)
NEUTROPHIL COUNT DECREASED ( 117 FDA reports)
RESPIRATORY TRACT CONGESTION ( 117 FDA reports)
SENSATION OF HEAVINESS ( 117 FDA reports)
TENDON RUPTURE ( 117 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 116 FDA reports)
VAGINAL HAEMORRHAGE ( 116 FDA reports)
ACCIDENTAL OVERDOSE ( 116 FDA reports)
BONE LOSS ( 116 FDA reports)
BONE MARROW FAILURE ( 116 FDA reports)
BLADDER CANCER ( 115 FDA reports)
DIABETIC NEPHROPATHY ( 115 FDA reports)
GENERALISED OEDEMA ( 115 FDA reports)
PAIN OF SKIN ( 115 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 115 FDA reports)
TORSADE DE POINTES ( 115 FDA reports)
WOUND ( 115 FDA reports)
BRONCHOSPASM ( 114 FDA reports)
DISEASE RECURRENCE ( 114 FDA reports)
INJECTION SITE REACTION ( 114 FDA reports)
LIMB DISCOMFORT ( 114 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 113 FDA reports)
PARAESTHESIA ORAL ( 113 FDA reports)
PEPTIC ULCER ( 113 FDA reports)
SUDDEN DEATH ( 113 FDA reports)
TENDON DISORDER ( 113 FDA reports)
OLIGURIA ( 112 FDA reports)
RENAL PAIN ( 112 FDA reports)
TOOTH INFECTION ( 112 FDA reports)
UROSEPSIS ( 112 FDA reports)
WOUND DEHISCENCE ( 112 FDA reports)
ACIDOSIS ( 112 FDA reports)
ANAL FISSURE ( 112 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 112 FDA reports)
CHRONIC SINUSITIS ( 112 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 112 FDA reports)
EXTRASYSTOLES ( 112 FDA reports)
HEPATIC LESION ( 112 FDA reports)
JOINT CONTRACTURE ( 112 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 111 FDA reports)
FAMILY STRESS ( 111 FDA reports)
HEARING IMPAIRED ( 111 FDA reports)
RASH MACULO-PAPULAR ( 111 FDA reports)
SQUAMOUS CELL CARCINOMA ( 111 FDA reports)
PETECHIAE ( 110 FDA reports)
QUALITY OF LIFE DECREASED ( 110 FDA reports)
IMPAIRED DRIVING ABILITY ( 110 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 109 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 109 FDA reports)
EAR INFECTION ( 109 FDA reports)
PLATELET COUNT INCREASED ( 109 FDA reports)
REFRACTORY ANAEMIA ( 109 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 108 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 108 FDA reports)
BACK INJURY ( 108 FDA reports)
CHOLECYSTITIS ACUTE ( 108 FDA reports)
EYE HAEMORRHAGE ( 108 FDA reports)
LIFE EXPECTANCY SHORTENED ( 108 FDA reports)
MICTURITION URGENCY ( 108 FDA reports)
BACTERAEMIA ( 107 FDA reports)
BODY HEIGHT DECREASED ( 107 FDA reports)
OPEN WOUND ( 107 FDA reports)
NON-CARDIAC CHEST PAIN ( 106 FDA reports)
PNEUMONITIS ( 106 FDA reports)
POLYURIA ( 106 FDA reports)
FISTULA ( 106 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 105 FDA reports)
BONE SWELLING ( 105 FDA reports)
HYPERTENSIVE HEART DISEASE ( 105 FDA reports)
INCONTINENCE ( 105 FDA reports)
ISCHAEMIC STROKE ( 105 FDA reports)
NEPHROPATHY ( 105 FDA reports)
PYELONEPHRITIS ( 105 FDA reports)
NEUTRALISING ANTIBODIES POSITIVE ( 104 FDA reports)
PARKINSON'S DISEASE ( 104 FDA reports)
PELVIC PAIN ( 104 FDA reports)
ACTINOMYCOSIS ( 104 FDA reports)
BLOOD PRESSURE ABNORMAL ( 104 FDA reports)
CARDIAC PACEMAKER INSERTION ( 104 FDA reports)
ABDOMINAL TENDERNESS ( 103 FDA reports)
BLOOD CALCIUM INCREASED ( 103 FDA reports)
DIZZINESS POSTURAL ( 103 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 103 FDA reports)
ODYNOPHAGIA ( 103 FDA reports)
SKIN FIBROSIS ( 103 FDA reports)
PARALYSIS ( 102 FDA reports)
INTRACARDIAC THROMBUS ( 102 FDA reports)
MALIGNANT MELANOMA ( 102 FDA reports)
DRUG PRESCRIBING ERROR ( 101 FDA reports)
HALLUCINATION, AUDITORY ( 101 FDA reports)
HEPATIC CYST ( 101 FDA reports)
INCREASED TENDENCY TO BRUISE ( 101 FDA reports)
MANIA ( 101 FDA reports)
OSTEOSCLEROSIS ( 101 FDA reports)
PHOTOPHOBIA ( 101 FDA reports)
PLASMACYTOMA ( 101 FDA reports)
SENSORY LOSS ( 101 FDA reports)
VENTRICULAR DYSFUNCTION ( 101 FDA reports)
NERVE INJURY ( 100 FDA reports)
VAGINAL ABSCESS ( 100 FDA reports)
WALKING AID USER ( 100 FDA reports)
MYOPATHY ( 99 FDA reports)
PROCTALGIA ( 99 FDA reports)
RALES ( 99 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 99 FDA reports)
DERMAL CYST ( 99 FDA reports)
DIABETIC COMPLICATION ( 99 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 99 FDA reports)
SPINAL DISORDER ( 98 FDA reports)
VASCULITIS ( 98 FDA reports)
WRIST FRACTURE ( 98 FDA reports)
APHAGIA ( 97 FDA reports)
APNOEA ( 97 FDA reports)
DRUG LEVEL INCREASED ( 96 FDA reports)
DUODENITIS ( 96 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 96 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 95 FDA reports)
PLEURAL FIBROSIS ( 95 FDA reports)
PROCEDURAL COMPLICATION ( 95 FDA reports)
BLADDER DISORDER ( 95 FDA reports)
BLOOD CREATINE INCREASED ( 95 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 95 FDA reports)
HIP ARTHROPLASTY ( 95 FDA reports)
HYPERKERATOSIS ( 95 FDA reports)
MUSCLE DISORDER ( 95 FDA reports)
ABDOMINAL HERNIA ( 94 FDA reports)
ANEURYSM ( 94 FDA reports)
BREAST CANCER FEMALE ( 94 FDA reports)
BREAST PAIN ( 94 FDA reports)
CATHETERISATION CARDIAC ( 94 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 94 FDA reports)
SNORING ( 94 FDA reports)
BONE DEBRIDEMENT ( 93 FDA reports)
BLOOD CHLORIDE DECREASED ( 92 FDA reports)
DIFFICULTY IN WALKING ( 92 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 92 FDA reports)
HYPOTHERMIA ( 92 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 92 FDA reports)
INGROWING NAIL ( 92 FDA reports)
MULTIPLE DRUG OVERDOSE ( 92 FDA reports)
RETINAL HAEMORRHAGE ( 92 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 92 FDA reports)
UTERINE LEIOMYOMA ( 92 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 91 FDA reports)
LARYNGEAL OEDEMA ( 91 FDA reports)
MEDICATION RESIDUE ( 91 FDA reports)
MITRAL VALVE PROLAPSE ( 91 FDA reports)
SKIN PLAQUE ( 90 FDA reports)
SPONDYLOLISTHESIS ( 90 FDA reports)
ORAL INFECTION ( 89 FDA reports)
THERAPY NON-RESPONDER ( 89 FDA reports)
ANOSMIA ( 89 FDA reports)
BREATH SOUNDS ABNORMAL ( 89 FDA reports)
GYNAECOMASTIA ( 89 FDA reports)
HYPERPARATHYROIDISM ( 89 FDA reports)
INITIAL INSOMNIA ( 89 FDA reports)
LYMPHOEDEMA ( 89 FDA reports)
ABSCESS JAW ( 88 FDA reports)
ANAPHYLACTIC SHOCK ( 88 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 88 FDA reports)
EXERCISE TOLERANCE DECREASED ( 88 FDA reports)
HEPATOTOXICITY ( 88 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 88 FDA reports)
LIVER INJURY ( 88 FDA reports)
OCCULT BLOOD POSITIVE ( 88 FDA reports)
ORGAN FAILURE ( 88 FDA reports)
SNEEZING ( 87 FDA reports)
BLOOD COUNT ABNORMAL ( 87 FDA reports)
DRUG DISPENSING ERROR ( 87 FDA reports)
DEVICE RELATED INFECTION ( 86 FDA reports)
POISONING ( 86 FDA reports)
PROCEDURAL PAIN ( 86 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 86 FDA reports)
PERIORBITAL OEDEMA ( 85 FDA reports)
ACUTE PRERENAL FAILURE ( 85 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 85 FDA reports)
HYPERBILIRUBINAEMIA ( 85 FDA reports)
INJECTION SITE IRRITATION ( 85 FDA reports)
BARRETT'S OESOPHAGUS ( 84 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 84 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 84 FDA reports)
HYPERTENSIVE CRISIS ( 84 FDA reports)
HYPOAESTHESIA FACIAL ( 84 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 84 FDA reports)
SINUS HEADACHE ( 84 FDA reports)
VENOUS INSUFFICIENCY ( 84 FDA reports)
PROSTATOMEGALY ( 83 FDA reports)
SEXUAL DYSFUNCTION ( 83 FDA reports)
SKIN CANCER ( 83 FDA reports)
ASPIRATION ( 83 FDA reports)
INGUINAL HERNIA ( 83 FDA reports)
DIABETIC COMA ( 82 FDA reports)
NODULE ( 82 FDA reports)
ORAL DISCOMFORT ( 82 FDA reports)
TRISMUS ( 82 FDA reports)
ORAL HERPES ( 81 FDA reports)
PHOTOSENSITIVITY REACTION ( 81 FDA reports)
BEDRIDDEN ( 81 FDA reports)
BLOOD MAGNESIUM DECREASED ( 81 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 81 FDA reports)
BREAST MASS ( 80 FDA reports)
CERVICAL SPINAL STENOSIS ( 80 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 80 FDA reports)
GANGRENE ( 80 FDA reports)
HEART VALVE INCOMPETENCE ( 80 FDA reports)
LACUNAR INFARCTION ( 80 FDA reports)
LYMPHOMA ( 80 FDA reports)
RESPIRATORY TRACT INFECTION ( 80 FDA reports)
OESOPHAGEAL DISORDER ( 79 FDA reports)
SINUS ARRHYTHMIA ( 79 FDA reports)
OESOPHAGEAL STENOSIS ( 78 FDA reports)
STRIDOR ( 78 FDA reports)
BLINDNESS TRANSIENT ( 78 FDA reports)
BONE FRAGMENTATION ( 78 FDA reports)
COMA SCALE ABNORMAL ( 78 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 78 FDA reports)
ENTEROCOCCAL INFECTION ( 78 FDA reports)
FAECALOMA ( 78 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 78 FDA reports)
LUNG CONSOLIDATION ( 78 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 78 FDA reports)
ACUTE SINUSITIS ( 77 FDA reports)
COLITIS ULCERATIVE ( 77 FDA reports)
GENERALISED ERYTHEMA ( 77 FDA reports)
LARGE INTESTINE PERFORATION ( 77 FDA reports)
PANCREATITIS CHRONIC ( 77 FDA reports)
SERUM FERRITIN INCREASED ( 76 FDA reports)
UMBILICAL HERNIA ( 76 FDA reports)
BRAIN OEDEMA ( 76 FDA reports)
DECREASED ACTIVITY ( 76 FDA reports)
DENTAL OPERATION ( 76 FDA reports)
DERMATITIS CONTACT ( 76 FDA reports)
EYE PRURITUS ( 76 FDA reports)
GASTRIC HAEMORRHAGE ( 76 FDA reports)
HYPERTHYROIDISM ( 76 FDA reports)
ENDODONTIC PROCEDURE ( 75 FDA reports)
INJECTION SITE BRUISING ( 75 FDA reports)
PLEURITIC PAIN ( 75 FDA reports)
RENAL ARTERY STENOSIS ( 75 FDA reports)
TONGUE DISORDER ( 75 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 74 FDA reports)
RHONCHI ( 74 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 74 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 74 FDA reports)
FORMICATION ( 74 FDA reports)
HAEMORRHAGIC STROKE ( 74 FDA reports)
INTESTINAL PERFORATION ( 74 FDA reports)
MARROW HYPERPLASIA ( 74 FDA reports)
ACUTE HEPATIC FAILURE ( 73 FDA reports)
ANURIA ( 73 FDA reports)
AORTIC CALCIFICATION ( 73 FDA reports)
CREPITATIONS ( 73 FDA reports)
GRANULOCYTOPENIA ( 73 FDA reports)
HEPATITIS C ( 73 FDA reports)
LOWER LIMB FRACTURE ( 73 FDA reports)
OESOPHAGEAL ULCER ( 73 FDA reports)
POLYP ( 73 FDA reports)
PROTEIN URINE PRESENT ( 73 FDA reports)
STRESS URINARY INCONTINENCE ( 73 FDA reports)
TOBACCO USER ( 73 FDA reports)
WEIGHT FLUCTUATION ( 73 FDA reports)
PERIPHERAL ISCHAEMIA ( 72 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 72 FDA reports)
SPINAL CORD COMPRESSION ( 72 FDA reports)
DELUSION ( 72 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 72 FDA reports)
HAEMOLYTIC ANAEMIA ( 72 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 72 FDA reports)
CARDIAC FLUTTER ( 71 FDA reports)
CAROTID BRUIT ( 71 FDA reports)
DENTAL FISTULA ( 71 FDA reports)
DRUG ABUSE ( 71 FDA reports)
DRY THROAT ( 71 FDA reports)
EAR DISCOMFORT ( 71 FDA reports)
EXPIRED DRUG ADMINISTERED ( 71 FDA reports)
FACIAL BONES FRACTURE ( 71 FDA reports)
FOOT DEFORMITY ( 71 FDA reports)
METASTATIC NEOPLASM ( 71 FDA reports)
PSEUDOMONAS INFECTION ( 71 FDA reports)
SEBORRHOEIC KERATOSIS ( 70 FDA reports)
WRONG DRUG ADMINISTERED ( 70 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 70 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 70 FDA reports)
DYSTONIA ( 70 FDA reports)
INJECTION SITE NODULE ( 70 FDA reports)
LIGAMENT SPRAIN ( 70 FDA reports)
MECHANICAL VENTILATION ( 70 FDA reports)
MOTOR DYSFUNCTION ( 70 FDA reports)
MYELODYSPLASTIC SYNDROME ( 70 FDA reports)
ACNE ( 69 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 69 FDA reports)
ANGIOPATHY ( 69 FDA reports)
DROOLING ( 69 FDA reports)
FACET JOINT SYNDROME ( 69 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 69 FDA reports)
HYPERPLASIA ( 69 FDA reports)
HYPOPHOSPHATAEMIA ( 69 FDA reports)
MENORRHAGIA ( 69 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 69 FDA reports)
PANCREATITIS NECROTISING ( 69 FDA reports)
PELVIC FRACTURE ( 69 FDA reports)
VASCULAR CALCIFICATION ( 69 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 69 FDA reports)
SEQUESTRECTOMY ( 68 FDA reports)
STREPTOCOCCAL INFECTION ( 68 FDA reports)
ULCER HAEMORRHAGE ( 68 FDA reports)
BLOOD URIC ACID INCREASED ( 68 FDA reports)
DEVICE FAILURE ( 68 FDA reports)
EMBOLIC STROKE ( 68 FDA reports)
JOINT SPRAIN ( 68 FDA reports)
APHONIA ( 67 FDA reports)
ENTERITIS ( 67 FDA reports)
GINGIVAL SWELLING ( 67 FDA reports)
HOMICIDAL IDEATION ( 67 FDA reports)
HUMERUS FRACTURE ( 67 FDA reports)
LIBIDO DECREASED ( 67 FDA reports)
PERSONALITY CHANGE ( 67 FDA reports)
SENSATION OF FOREIGN BODY ( 67 FDA reports)
RESORPTION BONE INCREASED ( 66 FDA reports)
STRESS FRACTURE ( 66 FDA reports)
THROMBOPHLEBITIS ( 66 FDA reports)
ACTINIC KERATOSIS ( 66 FDA reports)
CHEST X-RAY ABNORMAL ( 66 FDA reports)
JAW OPERATION ( 66 FDA reports)
MOUTH HAEMORRHAGE ( 66 FDA reports)
BLOOD CULTURE POSITIVE ( 65 FDA reports)
BLOOD DISORDER ( 65 FDA reports)
BLOOD IRON DECREASED ( 65 FDA reports)
BONE NEOPLASM MALIGNANT ( 65 FDA reports)
CAROTID ARTERY DISEASE ( 65 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 65 FDA reports)
EROSIVE OESOPHAGITIS ( 65 FDA reports)
HAEMORRHAGIC ANAEMIA ( 65 FDA reports)
NERVE COMPRESSION ( 65 FDA reports)
OTITIS MEDIA ( 65 FDA reports)
OVARIAN CYST ( 65 FDA reports)
VIITH NERVE PARALYSIS ( 65 FDA reports)
NASAL SEPTUM DEVIATION ( 64 FDA reports)
POLYNEUROPATHY ( 64 FDA reports)
RAYNAUD'S PHENOMENON ( 64 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 64 FDA reports)
SOCIAL PROBLEM ( 64 FDA reports)
THERMAL BURN ( 64 FDA reports)
APPLICATION SITE ERYTHEMA ( 64 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 64 FDA reports)
DRUG SCREEN POSITIVE ( 64 FDA reports)
HAEMANGIOMA ( 64 FDA reports)
HUNGER ( 64 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 64 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 64 FDA reports)
INJECTION SITE RASH ( 64 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 64 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 64 FDA reports)
MEDICAL DEVICE COMPLICATION ( 64 FDA reports)
METASTASES TO LYMPH NODES ( 64 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 63 FDA reports)
APATHY ( 63 FDA reports)
BLOOD AMYLASE INCREASED ( 63 FDA reports)
BRONCHOPNEUMONIA ( 63 FDA reports)
CAROTID ARTERY OCCLUSION ( 63 FDA reports)
CONCUSSION ( 63 FDA reports)
DEAFNESS NEUROSENSORY ( 63 FDA reports)
DRUG ERUPTION ( 63 FDA reports)
FURUNCLE ( 63 FDA reports)
GINGIVAL INFECTION ( 63 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 63 FDA reports)
REFLUX OESOPHAGITIS ( 63 FDA reports)
RHINITIS ( 63 FDA reports)
NECROSIS ( 62 FDA reports)
OESOPHAGEAL PAIN ( 62 FDA reports)
OSTEORADIONECROSIS ( 62 FDA reports)
SKIN NECROSIS ( 62 FDA reports)
STEM CELL TRANSPLANT ( 62 FDA reports)
TRANSAMINASES INCREASED ( 62 FDA reports)
WHEELCHAIR USER ( 62 FDA reports)
ANGIOPLASTY ( 62 FDA reports)
EYELID OEDEMA ( 62 FDA reports)
GASTROINTESTINAL PAIN ( 62 FDA reports)
HAEMODYNAMIC INSTABILITY ( 62 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 62 FDA reports)
HYPERAESTHESIA ( 62 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 62 FDA reports)
HYPERVENTILATION ( 62 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 62 FDA reports)
HYSTERECTOMY ( 62 FDA reports)
LOCALISED OEDEMA ( 62 FDA reports)
MENINGIOMA ( 62 FDA reports)
HYDROCEPHALUS ( 61 FDA reports)
INADEQUATE ANALGESIA ( 61 FDA reports)
NEPHROPATHY TOXIC ( 61 FDA reports)
PIGMENTATION DISORDER ( 61 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 61 FDA reports)
OTITIS EXTERNA ( 60 FDA reports)
PANCREATIC CARCINOMA ( 60 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 60 FDA reports)
ACUTE PULMONARY OEDEMA ( 60 FDA reports)
ANOXIC ENCEPHALOPATHY ( 60 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 60 FDA reports)
EOSINOPHILIA ( 60 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 60 FDA reports)
MACROCYTOSIS ( 60 FDA reports)
MELANOCYTIC NAEVUS ( 60 FDA reports)
MITRAL VALVE CALCIFICATION ( 60 FDA reports)
APPLICATION SITE PRURITUS ( 59 FDA reports)
BLOOD TEST ABNORMAL ( 59 FDA reports)
BODY TEMPERATURE DECREASED ( 59 FDA reports)
CONDUCTION DISORDER ( 59 FDA reports)
ESCHERICHIA INFECTION ( 59 FDA reports)
FACIAL PALSY ( 59 FDA reports)
HAND FRACTURE ( 59 FDA reports)
HYPERURICAEMIA ( 59 FDA reports)
MONOCLONAL GAMMOPATHY ( 59 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 59 FDA reports)
PANIC REACTION ( 59 FDA reports)
SCAB ( 59 FDA reports)
SKIN INFECTION ( 59 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 59 FDA reports)
MYOCLONUS ( 58 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 58 FDA reports)
SCHIZOPHRENIA ( 58 FDA reports)
APHTHOUS STOMATITIS ( 58 FDA reports)
BLEPHARITIS ( 58 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 58 FDA reports)
HYPOALBUMINAEMIA ( 58 FDA reports)
INCOHERENT ( 58 FDA reports)
ANORECTAL DISCOMFORT ( 57 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 57 FDA reports)
COSTOCHONDRITIS ( 57 FDA reports)
FLUID INTAKE REDUCED ( 57 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 57 FDA reports)
INJECTION SITE EXTRAVASATION ( 57 FDA reports)
LABILE BLOOD PRESSURE ( 57 FDA reports)
RETINOPATHY ( 57 FDA reports)
SKIN WARM ( 57 FDA reports)
SLUGGISHNESS ( 57 FDA reports)
VITREOUS HAEMORRHAGE ( 57 FDA reports)
PROSTATE CANCER METASTATIC ( 56 FDA reports)
SALIVARY HYPERSECRETION ( 56 FDA reports)
SUBCUTANEOUS ABSCESS ( 56 FDA reports)
VITREOUS DETACHMENT ( 56 FDA reports)
BREAST CANCER METASTATIC ( 56 FDA reports)
BRONCHITIS CHRONIC ( 56 FDA reports)
COLON ADENOMA ( 56 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 56 FDA reports)
EXTREMITY CONTRACTURE ( 56 FDA reports)
FULL BLOOD COUNT DECREASED ( 56 FDA reports)
GINGIVAL RECESSION ( 56 FDA reports)
INTRACRANIAL ANEURYSM ( 56 FDA reports)
BONE OPERATION ( 55 FDA reports)
CARDIAC OPERATION ( 55 FDA reports)
HYPERNATRAEMIA ( 55 FDA reports)
NEPHRITIS INTERSTITIAL ( 55 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 55 FDA reports)
SOFT TISSUE DISORDER ( 55 FDA reports)
VASCULAR PSEUDOANEURYSM ( 55 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 54 FDA reports)
PERITONITIS BACTERIAL ( 54 FDA reports)
SECRETION DISCHARGE ( 54 FDA reports)
SEROTONIN SYNDROME ( 54 FDA reports)
ALCOHOL USE ( 54 FDA reports)
BRUXISM ( 54 FDA reports)
BUNDLE BRANCH BLOCK ( 54 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 54 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 54 FDA reports)
ABNORMAL FAECES ( 53 FDA reports)
ADRENAL INSUFFICIENCY ( 53 FDA reports)
BREATH ODOUR ( 53 FDA reports)
CARDIAC TAMPONADE ( 53 FDA reports)
CONJUNCTIVITIS ( 53 FDA reports)
EDENTULOUS ( 53 FDA reports)
EPILEPSY ( 53 FDA reports)
HEMIPLEGIA ( 53 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 53 FDA reports)
KETOACIDOSIS ( 53 FDA reports)
OROPHARYNGEAL BLISTERING ( 53 FDA reports)
PRODUCT ADHESION ISSUE ( 53 FDA reports)
PSYCHIATRIC SYMPTOM ( 53 FDA reports)
SEASONAL ALLERGY ( 53 FDA reports)
TIBIA FRACTURE ( 53 FDA reports)
VASCULAR OCCLUSION ( 53 FDA reports)
NEPHROSCLEROSIS ( 52 FDA reports)
OCULAR ICTERUS ( 52 FDA reports)
OVERWEIGHT ( 52 FDA reports)
PARKINSONISM ( 52 FDA reports)
SKIN SWELLING ( 52 FDA reports)
URINARY TRACT DISORDER ( 52 FDA reports)
VITAMIN B12 DEFICIENCY ( 52 FDA reports)
WOUND SECRETION ( 52 FDA reports)
APPARENT DEATH ( 52 FDA reports)
CACHEXIA ( 52 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 52 FDA reports)
EARLY SATIETY ( 52 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 52 FDA reports)
ENDOTRACHEAL INTUBATION ( 52 FDA reports)
FEELING DRUNK ( 52 FDA reports)
LUMBAR RADICULOPATHY ( 52 FDA reports)
METABOLIC SYNDROME ( 52 FDA reports)
GRANULOMA ( 51 FDA reports)
HAEMOLYSIS ( 51 FDA reports)
HEPATOCELLULAR DAMAGE ( 51 FDA reports)
LEG AMPUTATION ( 51 FDA reports)
LISTLESS ( 51 FDA reports)
PERONEAL NERVE PALSY ( 51 FDA reports)
SCREAMING ( 51 FDA reports)
PHOTOPSIA ( 50 FDA reports)
PLANTAR FASCIITIS ( 50 FDA reports)
RADIOTHERAPY ( 50 FDA reports)
RENAL CELL CARCINOMA ( 50 FDA reports)
VITAMIN D DECREASED ( 50 FDA reports)
APPENDICITIS ( 50 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 50 FDA reports)
CALCULUS URETERIC ( 50 FDA reports)
COLLAPSE OF LUNG ( 50 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 50 FDA reports)
AREFLEXIA ( 49 FDA reports)
BILIARY DYSKINESIA ( 49 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 49 FDA reports)
FEMORAL ARTERY OCCLUSION ( 49 FDA reports)
FRUSTRATION ( 49 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 49 FDA reports)
MUSCLE CONTRACTURE ( 49 FDA reports)
OVARIAN CANCER ( 49 FDA reports)
PROSTATITIS ( 49 FDA reports)
RENAL TUBULAR ACIDOSIS ( 49 FDA reports)
SKIN ATROPHY ( 49 FDA reports)
TEARFULNESS ( 49 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 49 FDA reports)
TONGUE INJURY ( 49 FDA reports)
NICOTINE DEPENDENCE ( 48 FDA reports)
OPEN REDUCTION OF FRACTURE ( 48 FDA reports)
ORAL CAVITY FISTULA ( 48 FDA reports)
PITTING OEDEMA ( 48 FDA reports)
SOMNAMBULISM ( 48 FDA reports)
VASODILATATION ( 48 FDA reports)
ABSCESS DRAINAGE ( 48 FDA reports)
BILE DUCT OBSTRUCTION ( 48 FDA reports)
DEVICE OCCLUSION ( 48 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 48 FDA reports)
ILEUS PARALYTIC ( 48 FDA reports)
LARYNGITIS ( 48 FDA reports)
ACCIDENT ( 47 FDA reports)
ANAEMIA POSTOPERATIVE ( 47 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 47 FDA reports)
CULTURE URINE POSITIVE ( 47 FDA reports)
CYSTOCELE ( 47 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 47 FDA reports)
FIBRIN D DIMER INCREASED ( 47 FDA reports)
HAEMORRHAGIC DIATHESIS ( 47 FDA reports)
HAIR GROWTH ABNORMAL ( 47 FDA reports)
HYPOVENTILATION ( 47 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 47 FDA reports)
LOW TURNOVER OSTEOPATHY ( 47 FDA reports)
NEUROGENIC BLADDER ( 47 FDA reports)
OCULAR HYPERTENSION ( 47 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 47 FDA reports)
PROTEIN TOTAL DECREASED ( 47 FDA reports)
TEMPERATURE INTOLERANCE ( 47 FDA reports)
TENDON INJURY ( 47 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 47 FDA reports)
VENTRICULAR ARRHYTHMIA ( 47 FDA reports)
POLYMYALGIA RHEUMATICA ( 46 FDA reports)
RASH PUSTULAR ( 46 FDA reports)
RENAL CANCER ( 46 FDA reports)
RETINAL DETACHMENT ( 46 FDA reports)
UTERINE HAEMORRHAGE ( 46 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 46 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 46 FDA reports)
CEREBROVASCULAR DISORDER ( 46 FDA reports)
CORONARY ARTERY THROMBOSIS ( 46 FDA reports)
EUPHORIC MOOD ( 46 FDA reports)
FEAR OF DEATH ( 46 FDA reports)
HERPES SIMPLEX ( 46 FDA reports)
MUSCLE RIGIDITY ( 46 FDA reports)
MUSCULOSKELETAL DISORDER ( 46 FDA reports)
ARTERIAL STENOSIS ( 45 FDA reports)
ARTHROPOD BITE ( 45 FDA reports)
BILE DUCT STONE ( 45 FDA reports)
BRONCHIECTASIS ( 45 FDA reports)
DERMATITIS EXFOLIATIVE ( 45 FDA reports)
FRACTURED SACRUM ( 45 FDA reports)
HICCUPS ( 45 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 45 FDA reports)
LEUKOENCEPHALOPATHY ( 45 FDA reports)
LUNG HYPERINFLATION ( 45 FDA reports)
MENSTRUATION IRREGULAR ( 45 FDA reports)
METABOLIC ENCEPHALOPATHY ( 45 FDA reports)
PSORIATIC ARTHROPATHY ( 45 FDA reports)
UNDERDOSE ( 45 FDA reports)
OESOPHAGITIS ULCERATIVE ( 44 FDA reports)
ONYCHOCLASIS ( 44 FDA reports)
PAROSMIA ( 44 FDA reports)
PLEURISY ( 44 FDA reports)
SEROMA ( 44 FDA reports)
TINEA PEDIS ( 44 FDA reports)
ABSCESS ORAL ( 44 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 44 FDA reports)
BRAIN DEATH ( 44 FDA reports)
CARDIAC ENZYMES INCREASED ( 44 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 44 FDA reports)
FIBULA FRACTURE ( 44 FDA reports)
FISTULA DISCHARGE ( 44 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 44 FDA reports)
HELICOBACTER INFECTION ( 44 FDA reports)
INJECTION SITE URTICARIA ( 44 FDA reports)
IRON DEFICIENCY ( 44 FDA reports)
KLEBSIELLA INFECTION ( 44 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 44 FDA reports)
LYMPHADENITIS ( 44 FDA reports)
MITRAL VALVE DISEASE ( 44 FDA reports)
ABDOMINAL ABSCESS ( 43 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 43 FDA reports)
CHOLESTASIS ( 43 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 43 FDA reports)
ENDOCARDITIS ( 43 FDA reports)
FACE INJURY ( 43 FDA reports)
HEAD DISCOMFORT ( 43 FDA reports)
INJECTION SITE MASS ( 43 FDA reports)
LARYNGOSPASM ( 43 FDA reports)
LIVEDO RETICULARIS ( 43 FDA reports)
MACULAR OEDEMA ( 43 FDA reports)
MULTIPLE ALLERGIES ( 43 FDA reports)
SPUTUM DISCOLOURED ( 43 FDA reports)
THYROID CANCER ( 43 FDA reports)
TRIGEMINAL NEURALGIA ( 43 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 42 FDA reports)
OSTEITIS DEFORMANS ( 42 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 42 FDA reports)
POLYDIPSIA ( 42 FDA reports)
PUBIS FRACTURE ( 42 FDA reports)
QRS AXIS ABNORMAL ( 42 FDA reports)
RESPIRATORY ACIDOSIS ( 42 FDA reports)
SKIN HAEMORRHAGE ( 42 FDA reports)
SPONDYLITIS ( 42 FDA reports)
SYNOVITIS ( 42 FDA reports)
TUBERCULOSIS ( 42 FDA reports)
AKATHISIA ( 42 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 42 FDA reports)
AORTIC VALVE SCLEROSIS ( 42 FDA reports)
ARTERIOSPASM CORONARY ( 42 FDA reports)
ASPIRATION PLEURAL CAVITY ( 42 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 42 FDA reports)
DEAFNESS UNILATERAL ( 42 FDA reports)
EJECTION FRACTION ABNORMAL ( 42 FDA reports)
EMBOLISM ( 42 FDA reports)
EYE INFECTION ( 42 FDA reports)
GINGIVAL ULCERATION ( 42 FDA reports)
HEPATIC CONGESTION ( 42 FDA reports)
IRITIS ( 42 FDA reports)
LIPOMA ( 42 FDA reports)
MASTECTOMY ( 42 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 41 FDA reports)
BRAIN INJURY ( 41 FDA reports)
CHEILITIS ( 41 FDA reports)
DIABETIC FOOT ( 41 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 41 FDA reports)
EYELID PTOSIS ( 41 FDA reports)
HYPERPHOSPHATAEMIA ( 41 FDA reports)
JAUNDICE CHOLESTATIC ( 41 FDA reports)
NEPHROGENIC ANAEMIA ( 41 FDA reports)
PARAPLEGIA ( 41 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 41 FDA reports)
PREGNANCY ( 41 FDA reports)
PULMONARY THROMBOSIS ( 41 FDA reports)
PURULENCE ( 41 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 41 FDA reports)
SKIN REACTION ( 41 FDA reports)
UTERINE CANCER ( 41 FDA reports)
WOUND DRAINAGE ( 41 FDA reports)
NEPHROTIC SYNDROME ( 40 FDA reports)
PERIARTHRITIS ( 40 FDA reports)
PLASMACYTOSIS ( 40 FDA reports)
PURPURA ( 40 FDA reports)
RESUSCITATION ( 40 FDA reports)
SUDDEN CARDIAC DEATH ( 40 FDA reports)
TEMPORAL ARTERITIS ( 40 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 40 FDA reports)
ADNEXA UTERI MASS ( 40 FDA reports)
ADRENAL DISORDER ( 40 FDA reports)
ALVEOLAR OSTEITIS ( 40 FDA reports)
AORTIC VALVE CALCIFICATION ( 40 FDA reports)
APPLICATION SITE IRRITATION ( 40 FDA reports)
APPLICATION SITE RASH ( 40 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 40 FDA reports)
BLOOD UREA DECREASED ( 40 FDA reports)
BURNS SECOND DEGREE ( 40 FDA reports)
CARDIAC ANEURYSM ( 40 FDA reports)
CERUMEN IMPACTION ( 40 FDA reports)
CHOKING SENSATION ( 40 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 40 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 40 FDA reports)
HYPERTONIC BLADDER ( 40 FDA reports)
MALIGNANT HYPERTENSION ( 40 FDA reports)
ABSCESS LIMB ( 39 FDA reports)
ADENOCARCINOMA ( 39 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 39 FDA reports)
CARDIAC OUTPUT DECREASED ( 39 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 39 FDA reports)
CARDIOTOXICITY ( 39 FDA reports)
DRUG EFFECT INCREASED ( 39 FDA reports)
EPICONDYLITIS ( 39 FDA reports)
GOUTY ARTHRITIS ( 39 FDA reports)
INTRAOCULAR LENS IMPLANT ( 39 FDA reports)
MUSCLE FATIGUE ( 39 FDA reports)
NEOPLASM ( 39 FDA reports)
NEUROLOGICAL SYMPTOM ( 39 FDA reports)
PEAU D'ORANGE ( 39 FDA reports)
PERFORMANCE STATUS DECREASED ( 39 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 39 FDA reports)
PULMONARY HAEMORRHAGE ( 39 FDA reports)
RADIUS FRACTURE ( 39 FDA reports)
RENAL ATROPHY ( 39 FDA reports)
RESPIRATORY DEPRESSION ( 39 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 39 FDA reports)
VASCULAR GRAFT ( 39 FDA reports)
WEIGHT BEARING DIFFICULTY ( 39 FDA reports)
NAIL DISORDER ( 38 FDA reports)
NASAL DISCOMFORT ( 38 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 38 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 38 FDA reports)
PRESBYOPIA ( 38 FDA reports)
SELF-MEDICATION ( 38 FDA reports)
THYROID CYST ( 38 FDA reports)
TOE OPERATION ( 38 FDA reports)
URINE FLOW DECREASED ( 38 FDA reports)
ABORTION SPONTANEOUS ( 38 FDA reports)
ANXIETY DISORDER ( 38 FDA reports)
ARTHRITIS BACTERIAL ( 38 FDA reports)
AUTONOMIC NEUROPATHY ( 38 FDA reports)
BREAST HYPERPLASIA ( 38 FDA reports)
CARBON DIOXIDE DECREASED ( 38 FDA reports)
CARDIAC FAILURE ACUTE ( 38 FDA reports)
DYSAESTHESIA ( 38 FDA reports)
EAR DISORDER ( 38 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 38 FDA reports)
EYE MOVEMENT DISORDER ( 38 FDA reports)
FEAR OF EATING ( 38 FDA reports)
GALLBLADDER OPERATION ( 38 FDA reports)
HEART RATE ABNORMAL ( 38 FDA reports)
HEPATIC ENCEPHALOPATHY ( 38 FDA reports)
HILAR LYMPHADENOPATHY ( 38 FDA reports)
ISCHAEMIC HEPATITIS ( 38 FDA reports)
JOINT LOCK ( 38 FDA reports)
JUGULAR VEIN DISTENSION ( 38 FDA reports)
JUGULAR VEIN THROMBOSIS ( 38 FDA reports)
LABYRINTHITIS ( 38 FDA reports)
MENINGITIS ( 38 FDA reports)
ADENOMA BENIGN ( 37 FDA reports)
ASTHENOPIA ( 37 FDA reports)
ATRIAL TACHYCARDIA ( 37 FDA reports)
BILIARY DILATATION ( 37 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 37 FDA reports)
FEMORAL NECK FRACTURE ( 37 FDA reports)
METAPLASIA ( 37 FDA reports)
NECK INJURY ( 37 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 37 FDA reports)
PARONYCHIA ( 37 FDA reports)
POSTURE ABNORMAL ( 37 FDA reports)
PRESCRIBED OVERDOSE ( 37 FDA reports)
TACHYARRHYTHMIA ( 37 FDA reports)
TONGUE OEDEMA ( 37 FDA reports)
VERTEBROPLASTY ( 37 FDA reports)
NEUROPATHY ( 36 FDA reports)
NODAL RHYTHM ( 36 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 36 FDA reports)
PANCREATIC DISORDER ( 36 FDA reports)
PAPILLOEDEMA ( 36 FDA reports)
PHLEBITIS ( 36 FDA reports)
POLYARTHRITIS ( 36 FDA reports)
RENAL MASS ( 36 FDA reports)
SKIN IRRITATION ( 36 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 36 FDA reports)
URINE ANALYSIS ABNORMAL ( 36 FDA reports)
AFFECTIVE DISORDER ( 36 FDA reports)
ALCOHOL ABUSE ( 36 FDA reports)
ANAL HAEMORRHAGE ( 36 FDA reports)
ARTERIAL DISORDER ( 36 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 36 FDA reports)
CLAVICLE FRACTURE ( 36 FDA reports)
DYSPHEMIA ( 36 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 36 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 36 FDA reports)
FOREIGN BODY ( 36 FDA reports)
GASTROINTESTINAL ULCER ( 36 FDA reports)
HYDROCELE ( 36 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 36 FDA reports)
METASTASIS ( 36 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 35 FDA reports)
AMMONIA INCREASED ( 35 FDA reports)
AORTIC VALVE STENOSIS ( 35 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 35 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 35 FDA reports)
BLOOD PH DECREASED ( 35 FDA reports)
CALCINOSIS ( 35 FDA reports)
CAPILLARY LEAK SYNDROME ( 35 FDA reports)
COR PULMONALE ( 35 FDA reports)
DIABETIC EYE DISEASE ( 35 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 35 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 35 FDA reports)
IMMUNE SYSTEM DISORDER ( 35 FDA reports)
JOINT CREPITATION ( 35 FDA reports)
LOSS OF EMPLOYMENT ( 35 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 35 FDA reports)
METABOLIC DISORDER ( 35 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 35 FDA reports)
PANCREATIC PSEUDOCYST ( 35 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 35 FDA reports)
ROSACEA ( 35 FDA reports)
SCRATCH ( 35 FDA reports)
SCROTAL SWELLING ( 35 FDA reports)
SEBORRHOEIC DERMATITIS ( 35 FDA reports)
THROMBOSIS IN DEVICE ( 35 FDA reports)
URINARY HESITATION ( 35 FDA reports)
VERTIGO POSITIONAL ( 35 FDA reports)
OBSTRUCTION GASTRIC ( 34 FDA reports)
SENSITIVITY OF TEETH ( 34 FDA reports)
TONGUE BITING ( 34 FDA reports)
TUMOUR LYSIS SYNDROME ( 34 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 34 FDA reports)
VULVOVAGINAL DRYNESS ( 34 FDA reports)
ABDOMINAL ADHESIONS ( 34 FDA reports)
APPENDICITIS PERFORATED ( 34 FDA reports)
ATRIAL SEPTAL DEFECT ( 34 FDA reports)
BIPOLAR I DISORDER ( 34 FDA reports)
BLOOD BLISTER ( 34 FDA reports)
BLOOD CHLORIDE INCREASED ( 34 FDA reports)
BREAST CALCIFICATIONS ( 34 FDA reports)
CEREBELLAR INFARCTION ( 34 FDA reports)
CORONARY ANGIOPLASTY ( 34 FDA reports)
FRACTURE NONUNION ( 34 FDA reports)
HEPATITIS B ( 34 FDA reports)
HOSTILITY ( 34 FDA reports)
INJECTION SITE WARMTH ( 34 FDA reports)
LIPIDS INCREASED ( 34 FDA reports)
AORTIC DILATATION ( 33 FDA reports)
AORTIC VALVE REPLACEMENT ( 33 FDA reports)
ASPHYXIA ( 33 FDA reports)
AXILLARY PAIN ( 33 FDA reports)
BLOOD BICARBONATE DECREASED ( 33 FDA reports)
BLOOD BICARBONATE INCREASED ( 33 FDA reports)
BONE CYST ( 33 FDA reports)
CATHETER PLACEMENT ( 33 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 33 FDA reports)
CHOLANGITIS ( 33 FDA reports)
DENTURE WEARER ( 33 FDA reports)
DRUG ABUSER ( 33 FDA reports)
ENCEPHALITIS ( 33 FDA reports)
HERNIA REPAIR ( 33 FDA reports)
MUSCLE CRAMP ( 33 FDA reports)
MUSCLE SPASTICITY ( 33 FDA reports)
NEUTROPENIC SEPSIS ( 33 FDA reports)
OESOPHAGEAL SPASM ( 33 FDA reports)
OPTIC NEURITIS ( 33 FDA reports)
ROTATOR CUFF REPAIR ( 33 FDA reports)
SELF-INJURIOUS IDEATION ( 33 FDA reports)
SHOCK HAEMORRHAGIC ( 33 FDA reports)
SKELETAL INJURY ( 33 FDA reports)
SMALL BOWEL ANGIOEDEMA ( 33 FDA reports)
SPINAL FUSION SURGERY ( 33 FDA reports)
SUBDURAL HAEMORRHAGE ( 33 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 33 FDA reports)
NEPHROCALCINOSIS ( 32 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 32 FDA reports)
OSTEOMYELITIS CHRONIC ( 32 FDA reports)
PANIC DISORDER ( 32 FDA reports)
PARTIAL SEIZURES ( 32 FDA reports)
PEMPHIGOID ( 32 FDA reports)
SHOULDER PAIN ( 32 FDA reports)
TENSION ( 32 FDA reports)
TOBACCO ABUSE ( 32 FDA reports)
TOE AMPUTATION ( 32 FDA reports)
URINARY TRACT OBSTRUCTION ( 32 FDA reports)
ADHESION ( 32 FDA reports)
BONE MARROW TRANSPLANT ( 32 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 32 FDA reports)
CHONDROPATHY ( 32 FDA reports)
COELIAC DISEASE ( 32 FDA reports)
COMMUNICATION DISORDER ( 32 FDA reports)
EYE DISCHARGE ( 32 FDA reports)
HEART TRANSPLANT ( 32 FDA reports)
HYPOTONIA ( 32 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 32 FDA reports)
METRORRHAGIA ( 32 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 31 FDA reports)
ALCOHOLISM ( 31 FDA reports)
BENCE JONES PROTEINURIA ( 31 FDA reports)
BLADDER SPASM ( 31 FDA reports)
BONE MARROW DISORDER ( 31 FDA reports)
CALCULUS URINARY ( 31 FDA reports)
CARDIAC FAILURE CHRONIC ( 31 FDA reports)
CHONDROMALACIA ( 31 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 31 FDA reports)
DEPENDENCE ( 31 FDA reports)
DRUG LEVEL DECREASED ( 31 FDA reports)
EFFUSION ( 31 FDA reports)
GASTRIC POLYPS ( 31 FDA reports)
GLOSSITIS ( 31 FDA reports)
HIGH FREQUENCY ABLATION ( 31 FDA reports)
ILIAC ARTERY STENOSIS ( 31 FDA reports)
LYMPHOPENIA ( 31 FDA reports)
MASTOIDITIS ( 31 FDA reports)
MONOPLEGIA ( 31 FDA reports)
MYELITIS TRANSVERSE ( 31 FDA reports)
NON-SMALL CELL LUNG CANCER ( 31 FDA reports)
NYSTAGMUS ( 31 FDA reports)
OBSTRUCTION ( 31 FDA reports)
PROTEIN TOTAL INCREASED ( 31 FDA reports)
RENAL TRANSPLANT ( 31 FDA reports)
SKIN FISSURES ( 31 FDA reports)
SUBMANDIBULAR MASS ( 31 FDA reports)
SYNCOPE VASOVAGAL ( 31 FDA reports)
TELANGIECTASIA ( 31 FDA reports)
THROMBOCYTOSIS ( 31 FDA reports)
TOOTH IMPACTED ( 31 FDA reports)
TRAUMATIC BRAIN INJURY ( 31 FDA reports)
TROPONIN I INCREASED ( 31 FDA reports)
URINE ODOUR ABNORMAL ( 31 FDA reports)
UTERINE DISORDER ( 31 FDA reports)
NASAL DRYNESS ( 30 FDA reports)
NECK MASS ( 30 FDA reports)
PERIORBITAL HAEMATOMA ( 30 FDA reports)
PROSTATIC DISORDER ( 30 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 30 FDA reports)
RASH VESICULAR ( 30 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 30 FDA reports)
RETINAL VEIN OCCLUSION ( 30 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 30 FDA reports)
VAGINAL DISCHARGE ( 30 FDA reports)
VASCULAR INJURY ( 30 FDA reports)
ADRENAL MASS ( 30 FDA reports)
ADVERSE REACTION ( 30 FDA reports)
APPLICATION SITE PAIN ( 30 FDA reports)
BACTERIAL TEST POSITIVE ( 30 FDA reports)
BLADDER PROLAPSE ( 30 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 30 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 30 FDA reports)
BRAIN NEOPLASM ( 30 FDA reports)
BREAST TENDERNESS ( 30 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 30 FDA reports)
CARDIOPULMONARY FAILURE ( 30 FDA reports)
CEREBRAL THROMBOSIS ( 30 FDA reports)
CHOLECYSTITIS INFECTIVE ( 30 FDA reports)
CYSTITIS HAEMORRHAGIC ( 30 FDA reports)
DIABETIC GASTROPARESIS ( 30 FDA reports)
ENERGY INCREASED ( 30 FDA reports)
EYE INJURY ( 30 FDA reports)
FOOT OPERATION ( 30 FDA reports)
GASTROINTESTINAL INFECTION ( 30 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 30 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 30 FDA reports)
LIP BLISTER ( 30 FDA reports)
MUSCLE INJURY ( 30 FDA reports)
MYDRIASIS ( 30 FDA reports)
AORTIC VALVE DISEASE ( 29 FDA reports)
ARTERIOVENOUS MALFORMATION ( 29 FDA reports)
BACTERIAL SEPSIS ( 29 FDA reports)
BK VIRUS INFECTION ( 29 FDA reports)
CARDIOVERSION ( 29 FDA reports)
CERVICOBRACHIAL SYNDROME ( 29 FDA reports)
CLAUSTROPHOBIA ( 29 FDA reports)
CUBITAL TUNNEL SYNDROME ( 29 FDA reports)
DEMYELINATION ( 29 FDA reports)
DEVICE BREAKAGE ( 29 FDA reports)
DISSOCIATION ( 29 FDA reports)
GALLBLADDER POLYP ( 29 FDA reports)
HAIR COLOUR CHANGES ( 29 FDA reports)
HEPATIC NECROSIS ( 29 FDA reports)
HEPATIC NEOPLASM ( 29 FDA reports)
HYPERCAPNIA ( 29 FDA reports)
HYPERCOAGULATION ( 29 FDA reports)
IMMUNOSUPPRESSION ( 29 FDA reports)
IMPAIRED SELF-CARE ( 29 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 29 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 29 FDA reports)
LIGAMENT RUPTURE ( 29 FDA reports)
MICTURITION DISORDER ( 29 FDA reports)
MIGRAINE WITH AURA ( 29 FDA reports)
PAINFUL RESPIRATION ( 29 FDA reports)
PATHOLOGICAL GAMBLING ( 29 FDA reports)
PERICARDITIS ( 29 FDA reports)
PNEUMONIA BACTERIAL ( 29 FDA reports)
POST PROCEDURAL INFECTION ( 29 FDA reports)
PUPIL FIXED ( 29 FDA reports)
RIGHT ATRIAL DILATATION ( 29 FDA reports)
SCLERODERMA ( 29 FDA reports)
SUICIDAL BEHAVIOUR ( 29 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 29 FDA reports)
TOXIC ENCEPHALOPATHY ( 29 FDA reports)
TREATMENT FAILURE ( 29 FDA reports)
TUBERCULIN TEST POSITIVE ( 29 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 29 FDA reports)
URINE COLOUR ABNORMAL ( 29 FDA reports)
VAGINAL INFECTION ( 29 FDA reports)
VOCAL CORD DISORDER ( 29 FDA reports)
OROANTRAL FISTULA ( 28 FDA reports)
PANCREATIC CYST ( 28 FDA reports)
POLYCYSTIC OVARIES ( 28 FDA reports)
POOR DENTAL CONDITION ( 28 FDA reports)
SPINAL COLUMN INJURY ( 28 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 28 FDA reports)
VARICES OESOPHAGEAL ( 28 FDA reports)
ASPERGILLOSIS ( 28 FDA reports)
BLOOD LACTIC ACID INCREASED ( 28 FDA reports)
CATHETER RELATED INFECTION ( 28 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 28 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 28 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 28 FDA reports)
DYSPAREUNIA ( 28 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 28 FDA reports)
EOSINOPHIL COUNT INCREASED ( 28 FDA reports)
ESCHERICHIA TEST POSITIVE ( 28 FDA reports)
EXOPHTHALMOS ( 28 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 28 FDA reports)
HAEMATOCRIT INCREASED ( 28 FDA reports)
HEPATITIS ACUTE ( 28 FDA reports)
HEPATORENAL SYNDROME ( 28 FDA reports)
HERPES VIRUS INFECTION ( 28 FDA reports)
HYPERPHAGIA ( 28 FDA reports)
INDURATION ( 28 FDA reports)
MENIERE'S DISEASE ( 28 FDA reports)
MIOSIS ( 28 FDA reports)
ABDOMINAL RIGIDITY ( 27 FDA reports)
AUTOIMMUNE HEPATITIS ( 27 FDA reports)
BENIGN BREAST NEOPLASM ( 27 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 27 FDA reports)
BLOODY DISCHARGE ( 27 FDA reports)
BRADYPHRENIA ( 27 FDA reports)
CARDIAC HYPERTROPHY ( 27 FDA reports)
CATHETER SEPSIS ( 27 FDA reports)
DIABETIC FOOT INFECTION ( 27 FDA reports)
DYSPNOEA EXACERBATED ( 27 FDA reports)
ENCEPHALOMALACIA ( 27 FDA reports)
HEPATITIS CHOLESTATIC ( 27 FDA reports)
HIP SURGERY ( 27 FDA reports)
MULTIPLE FRACTURES ( 27 FDA reports)
MYOPIA ( 27 FDA reports)
NERVE BLOCK ( 27 FDA reports)
NERVE ROOT COMPRESSION ( 27 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 27 FDA reports)
OSTEOMYELITIS ACUTE ( 27 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 27 FDA reports)
PNEUMONIA KLEBSIELLA ( 27 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 27 FDA reports)
POOR PERIPHERAL CIRCULATION ( 27 FDA reports)
POOR PERSONAL HYGIENE ( 27 FDA reports)
PREMATURE BABY ( 27 FDA reports)
RENAL INFARCT ( 27 FDA reports)
RESPIRATION ABNORMAL ( 27 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 27 FDA reports)
SARCOIDOSIS ( 27 FDA reports)
SPLENIC GRANULOMA ( 27 FDA reports)
STATUS EPILEPTICUS ( 27 FDA reports)
TESTICULAR PAIN ( 27 FDA reports)
MYOGLOBINURIA ( 26 FDA reports)
OBSTRUCTIVE UROPATHY ( 26 FDA reports)
OPERATIVE HAEMORRHAGE ( 26 FDA reports)
PARAPROTEINAEMIA ( 26 FDA reports)
PARTNER STRESS ( 26 FDA reports)
PCO2 DECREASED ( 26 FDA reports)
PROCTITIS ( 26 FDA reports)
RENAL HAEMORRHAGE ( 26 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 26 FDA reports)
SPONDYLOLYSIS ( 26 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 26 FDA reports)
TRIGGER FINGER ( 26 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 26 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 26 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 26 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 26 FDA reports)
WOUND COMPLICATION ( 26 FDA reports)
ACROCHORDON ( 26 FDA reports)
CALCIPHYLAXIS ( 26 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 26 FDA reports)
CORNEAL OEDEMA ( 26 FDA reports)
FACIAL PARESIS ( 26 FDA reports)
HEPATOCELLULAR INJURY ( 26 FDA reports)
HYPOPERFUSION ( 26 FDA reports)
IMMOBILE ( 26 FDA reports)
INCORRECT STORAGE OF DRUG ( 26 FDA reports)
ABNORMAL SENSATION IN EYE ( 25 FDA reports)
ANAL PRURITUS ( 25 FDA reports)
BILIARY COLIC ( 25 FDA reports)
BILIARY TRACT DISORDER ( 25 FDA reports)
CATHETER RELATED COMPLICATION ( 25 FDA reports)
CONVERSION DISORDER ( 25 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 25 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 25 FDA reports)
ENURESIS ( 25 FDA reports)
HEARING DISABILITY ( 25 FDA reports)
HYPOGONADISM ( 25 FDA reports)
HYPOREFLEXIA ( 25 FDA reports)
INJECTION SITE DISCOLOURATION ( 25 FDA reports)
LOSS OF LIBIDO ( 25 FDA reports)
LUPUS-LIKE SYNDROME ( 25 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 25 FDA reports)
MEAN CELL VOLUME INCREASED ( 25 FDA reports)
MUSCLE SWELLING ( 25 FDA reports)
MYELOPATHY ( 25 FDA reports)
NASAL POLYPS ( 25 FDA reports)
NEUROPATHIC ARTHROPATHY ( 25 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 25 FDA reports)
OESOPHAGEAL CARCINOMA ( 25 FDA reports)
PERSONALITY DISORDER ( 25 FDA reports)
POLYCYTHAEMIA ( 25 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 25 FDA reports)
RECURRENT CANCER ( 25 FDA reports)
RETINAL TEAR ( 25 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 25 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 25 FDA reports)
STENT OCCLUSION ( 25 FDA reports)
TENOSYNOVITIS ( 25 FDA reports)
URINE ABNORMALITY ( 25 FDA reports)
URINE OUTPUT INCREASED ( 25 FDA reports)
UTERINE POLYP ( 25 FDA reports)
VEIN DISORDER ( 25 FDA reports)
NEUROTOXICITY ( 24 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 24 FDA reports)
OLFACTORY NERVE DISORDER ( 24 FDA reports)
OLIGOHYDRAMNIOS ( 24 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 24 FDA reports)
PRODUCT TASTE ABNORMAL ( 24 FDA reports)
RECTAL POLYP ( 24 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 24 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 24 FDA reports)
SKIN GRAFT ( 24 FDA reports)
SKIN INJURY ( 24 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 24 FDA reports)
THORACOTOMY ( 24 FDA reports)
TOOTH EROSION ( 24 FDA reports)
URINE KETONE BODY PRESENT ( 24 FDA reports)
UTERINE PROLAPSE ( 24 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 24 FDA reports)
YELLOW SKIN ( 24 FDA reports)
AORTIC DISORDER ( 24 FDA reports)
APPENDIX DISORDER ( 24 FDA reports)
ATROPHIC VULVOVAGINITIS ( 24 FDA reports)
BLOOD URINE ( 24 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 24 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 24 FDA reports)
CHEST WALL PAIN ( 24 FDA reports)
COAGULATION TIME PROLONGED ( 24 FDA reports)
CUSHINGOID ( 24 FDA reports)
DEMENTIA WITH LEWY BODIES ( 24 FDA reports)
DERMATITIS BULLOUS ( 24 FDA reports)
DERMATOPHYTOSIS ( 24 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 24 FDA reports)
ENTEROBACTER INFECTION ( 24 FDA reports)
ERYTHEMA MULTIFORME ( 24 FDA reports)
EXFOLIATIVE RASH ( 24 FDA reports)
FUNGAL SKIN INFECTION ( 24 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 24 FDA reports)
HEPATIC MASS ( 24 FDA reports)
HYPERCHLORHYDRIA ( 24 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 24 FDA reports)
HYPOGLYCAEMIC COMA ( 24 FDA reports)
INCISION SITE HAEMORRHAGE ( 24 FDA reports)
INJECTION SITE INDURATION ( 24 FDA reports)
INJECTION SITE INFECTION ( 24 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 24 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 24 FDA reports)
KNEE OPERATION ( 24 FDA reports)
LIP PAIN ( 24 FDA reports)
MUCOSAL DRYNESS ( 24 FDA reports)
MULTI-ORGAN DISORDER ( 24 FDA reports)
ACCELERATED HYPERTENSION ( 23 FDA reports)
ADJUSTMENT DISORDER ( 23 FDA reports)
AGRANULOCYTOSIS ( 23 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 23 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 23 FDA reports)
ATROPHY ( 23 FDA reports)
BONE EROSION ( 23 FDA reports)
BREAKTHROUGH PAIN ( 23 FDA reports)
BREAST CANCER RECURRENT ( 23 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 23 FDA reports)
CHANGE OF BOWEL HABIT ( 23 FDA reports)
DERMATITIS ALLERGIC ( 23 FDA reports)
ENDOMETRIAL CANCER ( 23 FDA reports)
EPIGASTRIC DISCOMFORT ( 23 FDA reports)
FOLLICULITIS ( 23 FDA reports)
GASTRITIS HAEMORRHAGIC ( 23 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 23 FDA reports)
HAEMARTHROSIS ( 23 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 23 FDA reports)
HYPOVITAMINOSIS ( 23 FDA reports)
IMPAIRED FASTING GLUCOSE ( 23 FDA reports)
INFECTED SKIN ULCER ( 23 FDA reports)
INFERTILITY ( 23 FDA reports)
LOOSE BODY IN JOINT ( 23 FDA reports)
LUNG CANCER METASTATIC ( 23 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 23 FDA reports)
MALABSORPTION ( 23 FDA reports)
MALLORY-WEISS SYNDROME ( 23 FDA reports)
MICROANGIOPATHY ( 23 FDA reports)
MUCOSAL ULCERATION ( 23 FDA reports)
ORAL SURGERY ( 23 FDA reports)
PREMATURE LABOUR ( 23 FDA reports)
PULPITIS DENTAL ( 23 FDA reports)
PYODERMA GANGRENOSUM ( 23 FDA reports)
REGURGITATION ( 23 FDA reports)
SPUTUM CULTURE POSITIVE ( 23 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 23 FDA reports)
STARING ( 23 FDA reports)
THYROXINE FREE DECREASED ( 23 FDA reports)
TONGUE ULCERATION ( 23 FDA reports)
TOURETTE'S DISORDER ( 23 FDA reports)
TRACHEAL DEVIATION ( 23 FDA reports)
TRANSFUSION ( 23 FDA reports)
TUMOUR MARKER INCREASED ( 23 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 23 FDA reports)
UVEITIS ( 23 FDA reports)
WOUND HAEMORRHAGE ( 23 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 22 FDA reports)
OTITIS MEDIA ACUTE ( 22 FDA reports)
PCO2 INCREASED ( 22 FDA reports)
PETIT MAL EPILEPSY ( 22 FDA reports)
PHARYNGEAL ERYTHEMA ( 22 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 22 FDA reports)
RECTAL PROLAPSE ( 22 FDA reports)
RESPIRATORY RATE DECREASED ( 22 FDA reports)
RETINAL DISORDER ( 22 FDA reports)
RETINAL OEDEMA ( 22 FDA reports)
SENSATION OF PRESSURE ( 22 FDA reports)
SPINAL DECOMPRESSION ( 22 FDA reports)
TRACHEOBRONCHITIS ( 22 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 22 FDA reports)
VESTIBULAR DISORDER ( 22 FDA reports)
XEROSIS ( 22 FDA reports)
AFFECT LABILITY ( 22 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 22 FDA reports)
ALVEOLOPLASTY ( 22 FDA reports)
ANAL FISTULA ( 22 FDA reports)
ANAPHYLACTOID REACTION ( 22 FDA reports)
ANION GAP INCREASED ( 22 FDA reports)
ARTERIAL THROMBOSIS ( 22 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 22 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 22 FDA reports)
BLEPHAROSPASM ( 22 FDA reports)
BONE GRAFT ( 22 FDA reports)
BREAST CELLULITIS ( 22 FDA reports)
BREAST CYST ( 22 FDA reports)
BREAST DISORDER ( 22 FDA reports)
BREAST ENLARGEMENT ( 22 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 22 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 22 FDA reports)
CORNEAL DYSTROPHY ( 22 FDA reports)
DRUG TOLERANCE ( 22 FDA reports)
DYSGRAPHIA ( 22 FDA reports)
EAR HAEMORRHAGE ( 22 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 22 FDA reports)
EPIDIDYMITIS ( 22 FDA reports)
FOOD INTOLERANCE ( 22 FDA reports)
FOOD POISONING ( 22 FDA reports)
FOREIGN BODY TRAUMA ( 22 FDA reports)
GASTROINTESTINAL NECROSIS ( 22 FDA reports)
GLYCOSURIA ( 22 FDA reports)
HAEMORRHAGE URINARY TRACT ( 22 FDA reports)
HALLUCINATIONS, MIXED ( 22 FDA reports)
HISTOPLASMOSIS ( 22 FDA reports)
INJECTION SITE PAPULE ( 22 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 22 FDA reports)
KERATITIS ( 22 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 22 FDA reports)
LIP DRY ( 22 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 22 FDA reports)
MELANOSIS COLI ( 22 FDA reports)
METASTASES TO MENINGES ( 22 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 22 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 22 FDA reports)
ALCOHOL POISONING ( 21 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 21 FDA reports)
ANORECTAL DISORDER ( 21 FDA reports)
APLASTIC ANAEMIA ( 21 FDA reports)
APPLICATION SITE REACTION ( 21 FDA reports)
APPLICATION SITE VESICLES ( 21 FDA reports)
ARTHRITIS INFECTIVE ( 21 FDA reports)
AXILLARY MASS ( 21 FDA reports)
BLADDER DIVERTICULUM ( 21 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 21 FDA reports)
BONE ABSCESS ( 21 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 21 FDA reports)
BRONCHITIS ACUTE ( 21 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 21 FDA reports)
CEREBELLAR ATROPHY ( 21 FDA reports)
CERVICAL MYELOPATHY ( 21 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 21 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 21 FDA reports)
ENTEROCUTANEOUS FISTULA ( 21 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 21 FDA reports)
FAECES HARD ( 21 FDA reports)
FEELING OF DESPAIR ( 21 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 21 FDA reports)
FOOD CRAVING ( 21 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 21 FDA reports)
FUNGAEMIA ( 21 FDA reports)
GASTROINTESTINAL PERFORATION ( 21 FDA reports)
HAEMOGLOBIN INCREASED ( 21 FDA reports)
HEPATOJUGULAR REFLUX ( 21 FDA reports)
INFARCTION ( 21 FDA reports)
INJECTION SITE BURNING ( 21 FDA reports)
INTENTIONAL SELF-INJURY ( 21 FDA reports)
INTESTINAL DILATATION ( 21 FDA reports)
MENINGITIS VIRAL ( 21 FDA reports)
METASTASES TO THE MEDIASTINUM ( 21 FDA reports)
MYASTHENIA GRAVIS ( 21 FDA reports)
NARCOLEPSY ( 21 FDA reports)
OPTIC NERVE DISORDER ( 21 FDA reports)
OROPHARYNGEAL SWELLING ( 21 FDA reports)
PAROTITIS ( 21 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 21 FDA reports)
PROTEIN URINE ( 21 FDA reports)
PROTHROMBIN TIME SHORTENED ( 21 FDA reports)
RADICULITIS ( 21 FDA reports)
RECTAL ULCER ( 21 FDA reports)
RECTOCELE ( 21 FDA reports)
SKIN WRINKLING ( 21 FDA reports)
SKULL MALFORMATION ( 21 FDA reports)
VASCULAR GRAFT OCCLUSION ( 21 FDA reports)
OPTIC NEUROPATHY ( 20 FDA reports)
PARAPARESIS ( 20 FDA reports)
PENIS DISORDER ( 20 FDA reports)
PERIPHERAL EMBOLISM ( 20 FDA reports)
POST PROCEDURAL HAEMATOMA ( 20 FDA reports)
PROCEDURAL HYPOTENSION ( 20 FDA reports)
PRODUCT ODOUR ABNORMAL ( 20 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 20 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 20 FDA reports)
SACROILIITIS ( 20 FDA reports)
SEPSIS SYNDROME ( 20 FDA reports)
SKIN MASS ( 20 FDA reports)
SKIN NEOPLASM EXCISION ( 20 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 20 FDA reports)
SPINAL LAMINECTOMY ( 20 FDA reports)
TACHYPHRENIA ( 20 FDA reports)
TERATOMA BENIGN ( 20 FDA reports)
THROAT CANCER ( 20 FDA reports)
TONGUE DISCOLOURATION ( 20 FDA reports)
TRANSPLANT REJECTION ( 20 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 20 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 20 FDA reports)
VOMITING PROJECTILE ( 20 FDA reports)
VULVOVAGINAL PRURITUS ( 20 FDA reports)
X-RAY ABNORMAL ( 20 FDA reports)
ABDOMINAL HAEMATOMA ( 20 FDA reports)
ABDOMINAL INFECTION ( 20 FDA reports)
ABDOMINAL MASS ( 20 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 20 FDA reports)
AGORAPHOBIA ( 20 FDA reports)
AMENORRHOEA ( 20 FDA reports)
ANAESTHETIC COMPLICATION ( 20 FDA reports)
BIOPSY ( 20 FDA reports)
BLOOD UREA ABNORMAL ( 20 FDA reports)
BONE NEOPLASM ( 20 FDA reports)
BREAST CANCER IN SITU ( 20 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 20 FDA reports)
CARTILAGE INJURY ( 20 FDA reports)
CATARACT NUCLEAR ( 20 FDA reports)
CHONDROCALCINOSIS ( 20 FDA reports)
CULTURE WOUND POSITIVE ( 20 FDA reports)
CYST REMOVAL ( 20 FDA reports)
DEVICE DISLOCATION ( 20 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 20 FDA reports)
EJACULATION FAILURE ( 20 FDA reports)
EYE OPERATION ( 20 FDA reports)
FEELINGS OF WORTHLESSNESS ( 20 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 20 FDA reports)
GENERALISED ANXIETY DISORDER ( 20 FDA reports)
GINGIVAL EROSION ( 20 FDA reports)
H1N1 INFLUENZA ( 20 FDA reports)
HAIR TEXTURE ABNORMAL ( 20 FDA reports)
HANGOVER ( 20 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 20 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 20 FDA reports)
HYPOVOLAEMIC SHOCK ( 20 FDA reports)
INCISIONAL HERNIA ( 20 FDA reports)
IRIS DISORDER ( 20 FDA reports)
LARGE INTESTINAL ULCER ( 20 FDA reports)
LOSS OF CONTROL OF LEGS ( 20 FDA reports)
LYMPHOCYTOSIS ( 20 FDA reports)
MENOPAUSAL SYMPTOMS ( 20 FDA reports)
MITRAL VALVE STENOSIS ( 20 FDA reports)
B-CELL LYMPHOMA ( 19 FDA reports)
BILE DUCT CANCER ( 19 FDA reports)
BLADDER DYSFUNCTION ( 19 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 19 FDA reports)
BREAST INFECTION ( 19 FDA reports)
CARDIAC FIBRILLATION ( 19 FDA reports)
CEREBELLAR HAEMORRHAGE ( 19 FDA reports)
CERVICAL DYSPLASIA ( 19 FDA reports)
CHAPPED LIPS ( 19 FDA reports)
CORONARY ARTERY DISSECTION ( 19 FDA reports)
DERMOID CYST ( 19 FDA reports)
DUODENAL ULCER PERFORATION ( 19 FDA reports)
DUPUYTREN'S CONTRACTURE ( 19 FDA reports)
EMBOLISM ARTERIAL ( 19 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 19 FDA reports)
EOSINOPHILIC OESOPHAGITIS ( 19 FDA reports)
ERYSIPELAS ( 19 FDA reports)
EXTRAVASATION ( 19 FDA reports)
EYE OEDEMA ( 19 FDA reports)
FLAT AFFECT ( 19 FDA reports)
FOOD ALLERGY ( 19 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 19 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 19 FDA reports)
GRIP STRENGTH DECREASED ( 19 FDA reports)
GUILLAIN-BARRE SYNDROME ( 19 FDA reports)
HODGKIN'S DISEASE ( 19 FDA reports)
HYPERTENSIVE EMERGENCY ( 19 FDA reports)
IMMUNODEFICIENCY ( 19 FDA reports)
INHALATION THERAPY ( 19 FDA reports)
INTERTRIGO ( 19 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 19 FDA reports)
LOGORRHOEA ( 19 FDA reports)
MONOCYTE COUNT INCREASED ( 19 FDA reports)
MUCOUS MEMBRANE DISORDER ( 19 FDA reports)
NEPHRITIS ( 19 FDA reports)
NIPPLE PAIN ( 19 FDA reports)
NOCTURNAL DYSPNOEA ( 19 FDA reports)
NONSPECIFIC REACTION ( 19 FDA reports)
PAINFUL DEFAECATION ( 19 FDA reports)
PANCREATITIS RELAPSING ( 19 FDA reports)
PAPULE ( 19 FDA reports)
PERIRECTAL ABSCESS ( 19 FDA reports)
PHARYNGEAL DISORDER ( 19 FDA reports)
POLYTRAUMATISM ( 19 FDA reports)
POSTOPERATIVE INFECTION ( 19 FDA reports)
POTENTIATING DRUG INTERACTION ( 19 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 19 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 19 FDA reports)
PYELOCALIECTASIS ( 19 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 19 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 19 FDA reports)
RETROPERITONEAL HAEMATOMA ( 19 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 19 FDA reports)
STAPHYLOMA ( 19 FDA reports)
STASIS DERMATITIS ( 19 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 19 FDA reports)
TONSILLAR DISORDER ( 19 FDA reports)
TOOTH INJURY ( 19 FDA reports)
TUMOUR HAEMORRHAGE ( 19 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 19 FDA reports)
WHITE BLOOD CELL DISORDER ( 19 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 18 FDA reports)
ORAL TORUS ( 18 FDA reports)
PANCREATIC MASS ( 18 FDA reports)
PANNICULITIS ( 18 FDA reports)
PNEUMONIA FUNGAL ( 18 FDA reports)
POLYP COLORECTAL ( 18 FDA reports)
PORTAL HYPERTENSION ( 18 FDA reports)
POST LAMINECTOMY SYNDROME ( 18 FDA reports)
PRIAPISM ( 18 FDA reports)
PROSTHESIS USER ( 18 FDA reports)
PULMONARY GRANULOMA ( 18 FDA reports)
PULMONARY TOXICITY ( 18 FDA reports)
PULSE ABNORMAL ( 18 FDA reports)
PUSTULAR PSORIASIS ( 18 FDA reports)
RECTAL FISSURE ( 18 FDA reports)
RENAL COLIC ( 18 FDA reports)
SINUS ARREST ( 18 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 18 FDA reports)
SPLENIC CALCIFICATION ( 18 FDA reports)
STUPOR ( 18 FDA reports)
TESTICULAR SWELLING ( 18 FDA reports)
THERAPY CESSATION ( 18 FDA reports)
TOXIC SHOCK SYNDROME ( 18 FDA reports)
URETERIC OBSTRUCTION ( 18 FDA reports)
VERBAL ABUSE ( 18 FDA reports)
VOCAL CORD PARALYSIS ( 18 FDA reports)
ACETABULUM FRACTURE ( 18 FDA reports)
ADRENAL NEOPLASM ( 18 FDA reports)
AMAUROSIS FUGAX ( 18 FDA reports)
AMYLOIDOSIS ( 18 FDA reports)
APPENDICECTOMY ( 18 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 18 FDA reports)
BLADDER MASS ( 18 FDA reports)
BLOOD CREATININE DECREASED ( 18 FDA reports)
BONE DEFORMITY ( 18 FDA reports)
BRAIN HERNIATION ( 18 FDA reports)
CALCULUS BLADDER ( 18 FDA reports)
CARBON DIOXIDE INCREASED ( 18 FDA reports)
CHOLESTEROSIS ( 18 FDA reports)
CLOSTRIDIUM COLITIS ( 18 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 18 FDA reports)
CULTURE POSITIVE ( 18 FDA reports)
CYTOLYTIC HEPATITIS ( 18 FDA reports)
DEFAECATION URGENCY ( 18 FDA reports)
DERMATITIS ACNEIFORM ( 18 FDA reports)
DEVICE LEAKAGE ( 18 FDA reports)
FAT NECROSIS ( 18 FDA reports)
FRACTURE DISPLACEMENT ( 18 FDA reports)
GASTROENTERITIS RADIATION ( 18 FDA reports)
GINGIVAL HYPERPLASIA ( 18 FDA reports)
GINGIVAL OEDEMA ( 18 FDA reports)
HAEMANGIOMA OF LIVER ( 18 FDA reports)
HEPATIC CALCIFICATION ( 18 FDA reports)
HEPATIC FIBROSIS ( 18 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 18 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 18 FDA reports)
INTESTINAL HAEMORRHAGE ( 18 FDA reports)
INTESTINAL ULCER ( 18 FDA reports)
LIMB ASYMMETRY ( 18 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 18 FDA reports)
MEGACOLON ( 18 FDA reports)
MENOPAUSE ( 18 FDA reports)
METASTASES TO PERITONEUM ( 18 FDA reports)
MUSCLE HAEMORRHAGE ( 18 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 17 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 17 FDA reports)
ASPIRATION JOINT ( 17 FDA reports)
BACTERIAL DISEASE CARRIER ( 17 FDA reports)
BIOPSY BREAST ( 17 FDA reports)
BLOOD SODIUM INCREASED ( 17 FDA reports)
BRADYARRHYTHMIA ( 17 FDA reports)
BREAST ABSCESS ( 17 FDA reports)
BREAST FIBROSIS ( 17 FDA reports)
CENTRAL OBESITY ( 17 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 17 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 17 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 17 FDA reports)
CLUMSINESS ( 17 FDA reports)
COLOSTOMY ( 17 FDA reports)
COMPARTMENT SYNDROME ( 17 FDA reports)
COMPLEX PARTIAL SEIZURES ( 17 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 17 FDA reports)
CORONARY ARTERY SURGERY ( 17 FDA reports)
CYSTITIS NONINFECTIVE ( 17 FDA reports)
DIABETIC ULCER ( 17 FDA reports)
DIAPHRAGMATIC HERNIA ( 17 FDA reports)
DROP ATTACKS ( 17 FDA reports)
DYSPHORIA ( 17 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 17 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 17 FDA reports)
ERECTION INCREASED ( 17 FDA reports)
EROSIVE DUODENITIS ( 17 FDA reports)
ERYTHEMA OF EYELID ( 17 FDA reports)
ESCHERICHIA SEPSIS ( 17 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 17 FDA reports)
GASTRINOMA ( 17 FDA reports)
GLARE ( 17 FDA reports)
HAEMOTHORAX ( 17 FDA reports)
HEAT RASH ( 17 FDA reports)
HELICOBACTER GASTRITIS ( 17 FDA reports)
HEMIANOPIA ( 17 FDA reports)
HIDRADENITIS ( 17 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 17 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 17 FDA reports)
LEUKAEMIA ( 17 FDA reports)
LICHEN PLANUS ( 17 FDA reports)
LIP HAEMORRHAGE ( 17 FDA reports)
MONOCYTOSIS ( 17 FDA reports)
NASAL OEDEMA ( 17 FDA reports)
NODAL ARRHYTHMIA ( 17 FDA reports)
OEDEMA GENITAL ( 17 FDA reports)
ORAL FUNGAL INFECTION ( 17 FDA reports)
ORCHITIS ( 17 FDA reports)
ORTHOSIS USER ( 17 FDA reports)
PHAEOCHROMOCYTOMA ( 17 FDA reports)
PROTRUSION TONGUE ( 17 FDA reports)
PSYCHOLOGICAL TRAUMA ( 17 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 17 FDA reports)
READING DISORDER ( 17 FDA reports)
REFLUX GASTRITIS ( 17 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 17 FDA reports)
RETINAL ARTERY OCCLUSION ( 17 FDA reports)
SERUM SICKNESS ( 17 FDA reports)
SKIN ODOUR ABNORMAL ( 17 FDA reports)
SKIN PAPILLOMA ( 17 FDA reports)
TONGUE BLISTERING ( 17 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 17 FDA reports)
VASCULAR DEMENTIA ( 17 FDA reports)
VENOUS OCCLUSION ( 17 FDA reports)
VENOUS THROMBOSIS LIMB ( 17 FDA reports)
VENTRICULAR DYSKINESIA ( 17 FDA reports)
NEOPLASM PROSTATE ( 16 FDA reports)
OCULAR VASCULAR DISORDER ( 16 FDA reports)
PARATHYROID TUMOUR BENIGN ( 16 FDA reports)
PATELLA FRACTURE ( 16 FDA reports)
PEMPHIGUS ( 16 FDA reports)
PERITONEAL DIALYSIS ( 16 FDA reports)
PHYSICAL ASSAULT ( 16 FDA reports)
PLATELET COUNT ABNORMAL ( 16 FDA reports)
PNEUMOPERICARDIUM ( 16 FDA reports)
PO2 DECREASED ( 16 FDA reports)
PROSTATE INFECTION ( 16 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 16 FDA reports)
PULMONARY INFARCTION ( 16 FDA reports)
RADICULAR PAIN ( 16 FDA reports)
RASH MORBILLIFORM ( 16 FDA reports)
RENAL OSTEODYSTROPHY ( 16 FDA reports)
RENAL TUBULAR DISORDER ( 16 FDA reports)
SJOGREN'S SYNDROME ( 16 FDA reports)
SKIN OEDEMA ( 16 FDA reports)
SLEEP TERROR ( 16 FDA reports)
SPLENIC INFARCTION ( 16 FDA reports)
TERMINAL INSOMNIA ( 16 FDA reports)
TRICUSPID VALVE DISEASE ( 16 FDA reports)
ULNAR NEURITIS ( 16 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 16 FDA reports)
VAGINITIS BACTERIAL ( 16 FDA reports)
VENA CAVA THROMBOSIS ( 16 FDA reports)
ABSCESS NECK ( 16 FDA reports)
ADENOMYOSIS ( 16 FDA reports)
ALBUMIN URINE PRESENT ( 16 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 16 FDA reports)
APPETITE DISORDER ( 16 FDA reports)
BACTERIA URINE IDENTIFIED ( 16 FDA reports)
BASEDOW'S DISEASE ( 16 FDA reports)
BIOPSY BONE ( 16 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 16 FDA reports)
BUNION ( 16 FDA reports)
CALCIUM DEFICIENCY ( 16 FDA reports)
CARDIAC DEATH ( 16 FDA reports)
CARTILAGE ATROPHY ( 16 FDA reports)
CATHETER SITE HAEMORRHAGE ( 16 FDA reports)
CAUDA EQUINA SYNDROME ( 16 FDA reports)
CERVICITIS ( 16 FDA reports)
CHRONIC FATIGUE SYNDROME ( 16 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 16 FDA reports)
COLECTOMY ( 16 FDA reports)
COLONOSCOPY ( 16 FDA reports)
COMMINUTED FRACTURE ( 16 FDA reports)
DENTAL CARE ( 16 FDA reports)
DRUG RESISTANCE ( 16 FDA reports)
ERB'S PALSY ( 16 FDA reports)
EXCESSIVE EYE BLINKING ( 16 FDA reports)
EYELID FUNCTION DISORDER ( 16 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 16 FDA reports)
FEELING GUILTY ( 16 FDA reports)
FOAMING AT MOUTH ( 16 FDA reports)
HAEMATOSPERMIA ( 16 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 16 FDA reports)
HEPATIC INFARCTION ( 16 FDA reports)
HEPATITIS TOXIC ( 16 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 16 FDA reports)
IMPATIENCE ( 16 FDA reports)
IMPULSIVE BEHAVIOUR ( 16 FDA reports)
INCISIONAL DRAINAGE ( 16 FDA reports)
INJECTION SITE INFLAMMATION ( 16 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 16 FDA reports)
LERICHE SYNDROME ( 16 FDA reports)
LICHENOID KERATOSIS ( 16 FDA reports)
LIP OEDEMA ( 16 FDA reports)
LONG QT SYNDROME ( 16 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 16 FDA reports)
ABDOMINAL NEOPLASM ( 15 FDA reports)
ASPIRATION BREAST ( 15 FDA reports)
BLADDER NEOPLASM ( 15 FDA reports)
BLADDER PAIN ( 15 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 15 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 15 FDA reports)
BLOOD CREATININE ABNORMAL ( 15 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 15 FDA reports)
BONE MARROW OEDEMA ( 15 FDA reports)
BONE METABOLISM DISORDER ( 15 FDA reports)
BRAIN STEM INFARCTION ( 15 FDA reports)
BREAST DISORDER FEMALE ( 15 FDA reports)
BRONCHITIS VIRAL ( 15 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 15 FDA reports)
CATHETER SITE INFECTION ( 15 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 15 FDA reports)
CEREBRAL DISORDER ( 15 FDA reports)
CERVIX HAEMORRHAGE UTERINE ( 15 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 15 FDA reports)
CONJUNCTIVOCHALASIS ( 15 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 15 FDA reports)
CONTRAST MEDIA REACTION ( 15 FDA reports)
COR PULMONALE CHRONIC ( 15 FDA reports)
DEVICE INEFFECTIVE ( 15 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 15 FDA reports)
EPIGLOTTITIS ( 15 FDA reports)
EXTRASKELETAL OSSIFICATION ( 15 FDA reports)
EYE INFLAMMATION ( 15 FDA reports)
FINGER DEFORMITY ( 15 FDA reports)
FRACTURE DELAYED UNION ( 15 FDA reports)
FUNGAL SEPSIS ( 15 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 15 FDA reports)
GALLBLADDER INJURY ( 15 FDA reports)
GESTATIONAL DIABETES ( 15 FDA reports)
HAEMOGLOBIN ABNORMAL ( 15 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 15 FDA reports)
HALO VISION ( 15 FDA reports)
HEART SOUNDS ABNORMAL ( 15 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 15 FDA reports)
HYDROPNEUMOTHORAX ( 15 FDA reports)
HYPERKINESIA ( 15 FDA reports)
HYPERREFLEXIA ( 15 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 15 FDA reports)
ILEITIS ( 15 FDA reports)
ILIAC ARTERY THROMBOSIS ( 15 FDA reports)
INAPPROPRIATE AFFECT ( 15 FDA reports)
INCISION SITE PAIN ( 15 FDA reports)
INJECTION SITE DISCOMFORT ( 15 FDA reports)
INJECTION SITE VESICLES ( 15 FDA reports)
INTESTINAL INFARCTION ( 15 FDA reports)
JAW CYST ( 15 FDA reports)
KIDNEY FIBROSIS ( 15 FDA reports)
LIGAMENT INJURY ( 15 FDA reports)
MEDIASTINITIS ( 15 FDA reports)
METASTASES TO BONE MARROW ( 15 FDA reports)
MICROCYTIC ANAEMIA ( 15 FDA reports)
MORTON'S NEUROMA ( 15 FDA reports)
MUSCLE RUPTURE ( 15 FDA reports)
NOSOCOMIAL INFECTION ( 15 FDA reports)
ORTHOSTATIC INTOLERANCE ( 15 FDA reports)
PERICARDIAL HAEMORRHAGE ( 15 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 15 FDA reports)
PORTAL VEIN THROMBOSIS ( 15 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 15 FDA reports)
PROTEUS INFECTION ( 15 FDA reports)
PUPILS UNEQUAL ( 15 FDA reports)
SERRATIA INFECTION ( 15 FDA reports)
SPINAL OPERATION ( 15 FDA reports)
SPLENIC CYST ( 15 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 15 FDA reports)
SUNBURN ( 15 FDA reports)
TENDON PAIN ( 15 FDA reports)
TENSION HEADACHE ( 15 FDA reports)
TERMINAL STATE ( 15 FDA reports)
THERAPEUTIC PROCEDURE ( 15 FDA reports)
THYROIDECTOMY ( 15 FDA reports)
TOOTH DEPOSIT ( 15 FDA reports)
URGE INCONTINENCE ( 15 FDA reports)
VENOUS THROMBOSIS ( 15 FDA reports)
WEIGHT LOSS POOR ( 15 FDA reports)
WOUND DEBRIDEMENT ( 15 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 15 FDA reports)
NAIL DISCOLOURATION ( 14 FDA reports)
NARCOTIC INTOXICATION ( 14 FDA reports)
NEPHRECTOMY ( 14 FDA reports)
NEURITIS ( 14 FDA reports)
NEUROFIBROMA ( 14 FDA reports)
OEDEMA MUCOSAL ( 14 FDA reports)
OESOPHAGEAL FOOD IMPACTION ( 14 FDA reports)
OPTIC ATROPHY ( 14 FDA reports)
ORAL MUCOSAL BLISTERING ( 14 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 14 FDA reports)
ORAL MUCOSAL HYPERTROPHY ( 14 FDA reports)
PALATAL OEDEMA ( 14 FDA reports)
PELVIC ABSCESS ( 14 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 14 FDA reports)
PERITONEAL ADHESIONS ( 14 FDA reports)
PHARYNGEAL ULCERATION ( 14 FDA reports)
PLATELET DISORDER ( 14 FDA reports)
PO2 INCREASED ( 14 FDA reports)
POSTICTAL STATE ( 14 FDA reports)
PULMONARY RADIATION INJURY ( 14 FDA reports)
PYELONEPHRITIS ACUTE ( 14 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 14 FDA reports)
RENAL ARTERIOSCLEROSIS ( 14 FDA reports)
RESPIRATORY TRACT IRRITATION ( 14 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 14 FDA reports)
SCROTAL CYST ( 14 FDA reports)
SELF ESTEEM DECREASED ( 14 FDA reports)
SKIN CHAPPED ( 14 FDA reports)
SOFT TISSUE MASS ( 14 FDA reports)
SPINAL CORPECTOMY ( 14 FDA reports)
SUBCUTANEOUS NODULE ( 14 FDA reports)
SUPERINFECTION ( 14 FDA reports)
THALAMIC INFARCTION ( 14 FDA reports)
THROAT LESION ( 14 FDA reports)
THROMBOCYTHAEMIA ( 14 FDA reports)
TONGUE DRY ( 14 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 14 FDA reports)
TRANSFUSION REACTION ( 14 FDA reports)
TRANSPLANT FAILURE ( 14 FDA reports)
VULVOVAGINAL PAIN ( 14 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 14 FDA reports)
ACUTE ABDOMEN ( 14 FDA reports)
ANORGASMIA ( 14 FDA reports)
APRAXIA ( 14 FDA reports)
BEHCET'S SYNDROME ( 14 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 14 FDA reports)
BIOPSY BREAST ABNORMAL ( 14 FDA reports)
BIOPSY LIVER ( 14 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 14 FDA reports)
BONE MARROW TOXICITY ( 14 FDA reports)
BRAIN MASS ( 14 FDA reports)
BREAST LUMP REMOVAL ( 14 FDA reports)
BREAST SWELLING ( 14 FDA reports)
CARDIAC ABLATION ( 14 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 14 FDA reports)
CEREBELLAR SYNDROME ( 14 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 14 FDA reports)
CLUSTER HEADACHE ( 14 FDA reports)
COLITIS MICROSCOPIC ( 14 FDA reports)
DENTAL NECROSIS ( 14 FDA reports)
DENTAL PLAQUE ( 14 FDA reports)
DIVERTICULAR PERFORATION ( 14 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 14 FDA reports)
DYSPHASIA ( 14 FDA reports)
DYSTHYMIC DISORDER ( 14 FDA reports)
ECTROPION ( 14 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 14 FDA reports)
ENDOCARDITIS BACTERIAL ( 14 FDA reports)
ENDOMETRIOSIS ( 14 FDA reports)
ESCHERICHIA BACTERAEMIA ( 14 FDA reports)
EXTREMITY NECROSIS ( 14 FDA reports)
FOOT AMPUTATION ( 14 FDA reports)
GASTRIC INFECTION ( 14 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 14 FDA reports)
GLOMERULONEPHRITIS ( 14 FDA reports)
GLUCOSE URINE PRESENT ( 14 FDA reports)
GRAFT VERSUS HOST DISEASE ( 14 FDA reports)
HEARING AID USER ( 14 FDA reports)
HEPATIC ENZYME ABNORMAL ( 14 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 14 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 14 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 14 FDA reports)
HYPOMANIA ( 14 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 14 FDA reports)
JUDGEMENT IMPAIRED ( 14 FDA reports)
LIBIDO INCREASED ( 14 FDA reports)
LYME DISEASE ( 14 FDA reports)
MACULOPATHY ( 14 FDA reports)
MADAROSIS ( 14 FDA reports)
MEDIASTINAL DISORDER ( 14 FDA reports)
METASTASES TO ABDOMINAL WALL ( 14 FDA reports)
METASTASES TO ADRENALS ( 14 FDA reports)
MICTURITION FREQUENCY DECREASED ( 14 FDA reports)
MITRAL VALVE REPLACEMENT ( 14 FDA reports)
MUCOSAL HAEMORRHAGE ( 14 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 13 FDA reports)
ADDISON'S DISEASE ( 13 FDA reports)
ANIMAL BITE ( 13 FDA reports)
ANIMAL SCRATCH ( 13 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 13 FDA reports)
ASBESTOSIS ( 13 FDA reports)
ATHEROSCLEROSIS ( 13 FDA reports)
ATRIAL THROMBOSIS ( 13 FDA reports)
AUTOIMMUNE DISORDER ( 13 FDA reports)
BACTERIURIA ( 13 FDA reports)
BILIARY SEPSIS ( 13 FDA reports)
BIOPSY LYMPH GLAND ABNORMAL ( 13 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 13 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 13 FDA reports)
CAECUM OPERATION ( 13 FDA reports)
CATHETER SITE PAIN ( 13 FDA reports)
CHOROIDAL DETACHMENT ( 13 FDA reports)
CIRRHOSIS ALCOHOLIC ( 13 FDA reports)
COLON CANCER METASTATIC ( 13 FDA reports)
CYANOPSIA ( 13 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 13 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 13 FDA reports)
EAR CONGESTION ( 13 FDA reports)
EJACULATION DISORDER ( 13 FDA reports)
ENTEROCOCCAL SEPSIS ( 13 FDA reports)
FAECES PALE ( 13 FDA reports)
FRACTURED COCCYX ( 13 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 13 FDA reports)
GINGIVAL DISCOLOURATION ( 13 FDA reports)
GINGIVAL ERYTHEMA ( 13 FDA reports)
GLIOSIS ( 13 FDA reports)
GLOBAL AMNESIA ( 13 FDA reports)
HYPERTHERMIA ( 13 FDA reports)
IATROGENIC INJURY ( 13 FDA reports)
INFECTED CYST ( 13 FDA reports)
INFUSION SITE REACTION ( 13 FDA reports)
INJECTION SITE CELLULITIS ( 13 FDA reports)
INJECTION SITE OEDEMA ( 13 FDA reports)
INTESTINAL POLYP ( 13 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 13 FDA reports)
JOINT INSTABILITY ( 13 FDA reports)
LABORATORY TEST INTERFERENCE ( 13 FDA reports)
LAZINESS ( 13 FDA reports)
LINEAR IGA DISEASE ( 13 FDA reports)
LIPIDS ABNORMAL ( 13 FDA reports)
MALIGNANT MELANOMA IN SITU ( 13 FDA reports)
MANDIBULAR PROSTHESIS USER ( 13 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 13 FDA reports)
MENOMETRORRHAGIA ( 13 FDA reports)
MENSTRUAL DISORDER ( 13 FDA reports)
METASTASES TO CHEST WALL ( 13 FDA reports)
MYELOMA RECURRENCE ( 13 FDA reports)
MYOCARDITIS ( 13 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 13 FDA reports)
NEUROMUSCULAR BLOCKADE ( 13 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 13 FDA reports)
ONYCHALGIA ( 13 FDA reports)
ORAL NEOPLASM ( 13 FDA reports)
PANCREATIC NECROSIS ( 13 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 13 FDA reports)
PERFORATED ULCER ( 13 FDA reports)
PNEUMONIA VIRAL ( 13 FDA reports)
POLYARTERITIS NODOSA ( 13 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 13 FDA reports)
PROSTATECTOMY ( 13 FDA reports)
RADIATION INJURY ( 13 FDA reports)
RADIATION OESOPHAGITIS ( 13 FDA reports)
RADIATION SKIN INJURY ( 13 FDA reports)
RECTAL DISCHARGE ( 13 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 13 FDA reports)
RETINAL ISCHAEMIA ( 13 FDA reports)
RETINITIS ( 13 FDA reports)
SCOTOMA ( 13 FDA reports)
SHOULDER OPERATION ( 13 FDA reports)
SPLENIC LESION ( 13 FDA reports)
SPUTUM PURULENT ( 13 FDA reports)
STRABISMUS ( 13 FDA reports)
SUBSTANCE ABUSE ( 13 FDA reports)
SUDDEN ONSET OF SLEEP ( 13 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 13 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 13 FDA reports)
TRACHEOSTOMY ( 13 FDA reports)
TRAUMATIC LUNG INJURY ( 13 FDA reports)
TROPONIN T INCREASED ( 13 FDA reports)
VASCULAR RUPTURE ( 13 FDA reports)
VASCULITIC RASH ( 13 FDA reports)
VENOUS STASIS ( 13 FDA reports)
VITAMIN B12 DECREASED ( 13 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 13 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 13 FDA reports)
X-RAY ( 13 FDA reports)
MYODESOPSIA ( 12 FDA reports)
MYOSCLEROSIS ( 12 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 12 FDA reports)
OESTRADIOL DECREASED ( 12 FDA reports)
ONYCHOMADESIS ( 12 FDA reports)
PANCREATIC NEOPLASM ( 12 FDA reports)
PERITONEAL HAEMORRHAGE ( 12 FDA reports)
PSEUDOLYMPHOMA ( 12 FDA reports)
RECTAL ABSCESS ( 12 FDA reports)
RECTAL PROLAPSE REPAIR ( 12 FDA reports)
RENAL ISCHAEMIA ( 12 FDA reports)
RENAL TUBULAR ATROPHY ( 12 FDA reports)
RETINAL INJURY ( 12 FDA reports)
RHEUMATIC HEART DISEASE ( 12 FDA reports)
SECONDARY SEQUESTRUM ( 12 FDA reports)
SKULL FRACTURE ( 12 FDA reports)
SLEEP WALKING ( 12 FDA reports)
SOFT TISSUE INFLAMMATION ( 12 FDA reports)
STEAL SYNDROME ( 12 FDA reports)
SURGICAL PROCEDURE REPEATED ( 12 FDA reports)
UNEMPLOYMENT ( 12 FDA reports)
URETHRAL PAIN ( 12 FDA reports)
VASCULAR BYPASS GRAFT ( 12 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 12 FDA reports)
VASCULAR INSUFFICIENCY ( 12 FDA reports)
VIRAL LOAD INCREASED ( 12 FDA reports)
VOCAL CORD THICKENING ( 12 FDA reports)
VOLVULUS ( 12 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 12 FDA reports)
WOUND NECROSIS ( 12 FDA reports)
ACCIDENT AT WORK ( 12 FDA reports)
ACCIDENTAL DEATH ( 12 FDA reports)
ACCIDENTAL NEEDLE STICK ( 12 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 12 FDA reports)
ALCOHOLIC LIVER DISEASE ( 12 FDA reports)
AMBLYOPIA ( 12 FDA reports)
ANAL STENOSIS ( 12 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 12 FDA reports)
AORTIC THROMBOSIS ( 12 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 12 FDA reports)
AURA ( 12 FDA reports)
AUTOIMMUNE THYROIDITIS ( 12 FDA reports)
BIOPSY ENDOMETRIUM ( 12 FDA reports)
BLADDER OBSTRUCTION ( 12 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 12 FDA reports)
BLOOD MAGNESIUM INCREASED ( 12 FDA reports)
BREAST CANCER STAGE I ( 12 FDA reports)
BREAST HAEMATOMA ( 12 FDA reports)
CARDIAC ASTHMA ( 12 FDA reports)
CARDIORENAL SYNDROME ( 12 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 12 FDA reports)
CHEMOTHERAPY ( 12 FDA reports)
CHOREA ( 12 FDA reports)
COLORECTAL CANCER ( 12 FDA reports)
COMPRESSION STOCKINGS APPLICATION ( 12 FDA reports)
CORONARY ARTERY RESTENOSIS ( 12 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 12 FDA reports)
DEAFNESS BILATERAL ( 12 FDA reports)
ENCEPHALITIS HERPES ( 12 FDA reports)
ENDOCRINE DISORDER ( 12 FDA reports)
ERYTHRODERMIC PSORIASIS ( 12 FDA reports)
EXTRADURAL HAEMATOMA ( 12 FDA reports)
EYE ROLLING ( 12 FDA reports)
EYELID DISORDER ( 12 FDA reports)
FEEDING TUBE COMPLICATION ( 12 FDA reports)
FISTULA REPAIR ( 12 FDA reports)
GAMMOPATHY ( 12 FDA reports)
GENITAL HERPES ( 12 FDA reports)
GRAVITATIONAL OEDEMA ( 12 FDA reports)
HAEMOCHROMATOSIS ( 12 FDA reports)
HAEMOPHILUS INFECTION ( 12 FDA reports)
HAIR DISORDER ( 12 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 12 FDA reports)
HAND DEFORMITY ( 12 FDA reports)
HEAD BANGING ( 12 FDA reports)
HEPATIC CANCER METASTATIC ( 12 FDA reports)
HEPATIC PAIN ( 12 FDA reports)
HORMONE LEVEL ABNORMAL ( 12 FDA reports)
HYPERACUSIS ( 12 FDA reports)
HYPERALBUMINAEMIA ( 12 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 12 FDA reports)
HYPEROSMOLAR STATE ( 12 FDA reports)
HYPOCOAGULABLE STATE ( 12 FDA reports)
HYPOTONY OF EYE ( 12 FDA reports)
IMPULSE-CONTROL DISORDER ( 12 FDA reports)
INCISION SITE COMPLICATION ( 12 FDA reports)
INFUSION SITE SWELLING ( 12 FDA reports)
INJECTION SITE ABSCESS ( 12 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 12 FDA reports)
KIDNEY ENLARGEMENT ( 12 FDA reports)
LACTOSE INTOLERANCE ( 12 FDA reports)
LAPAROTOMY ( 12 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 12 FDA reports)
LIGHT CHAIN DISEASE ( 12 FDA reports)
LIP DISORDER ( 12 FDA reports)
LOWER URINARY TRACT SYMPTOMS ( 12 FDA reports)
MACULAR HOLE ( 12 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 12 FDA reports)
MENINGITIS ASEPTIC ( 12 FDA reports)
MENINGITIS HERPES ( 12 FDA reports)
MERALGIA PARAESTHETICA ( 12 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 12 FDA reports)
MICROALBUMINURIA ( 12 FDA reports)
MOANING ( 12 FDA reports)
ABSCESS INTESTINAL ( 11 FDA reports)
ADENOCARCINOMA PANCREAS ( 11 FDA reports)
ADRENAL ADENOMA ( 11 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 11 FDA reports)
ANAL ABSCESS ( 11 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 11 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 11 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 11 FDA reports)
AORTIC DISSECTION ( 11 FDA reports)
BENIGN TUMOUR EXCISION ( 11 FDA reports)
BICYTOPENIA ( 11 FDA reports)
BLEEDING TIME PROLONGED ( 11 FDA reports)
BLOOD OSMOLARITY DECREASED ( 11 FDA reports)
BLOOD PH INCREASED ( 11 FDA reports)
BONE MARROW DEPRESSION ( 11 FDA reports)
BOWEL SOUNDS ABNORMAL ( 11 FDA reports)
BRAIN ABSCESS ( 11 FDA reports)
BRAIN HYPOXIA ( 11 FDA reports)
BRONCHIAL SECRETION RETENTION ( 11 FDA reports)
BULLOUS LUNG DISEASE ( 11 FDA reports)
BURN OESOPHAGEAL ( 11 FDA reports)
CALCIUM METABOLISM DISORDER ( 11 FDA reports)
CARBUNCLE ( 11 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 11 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 11 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 11 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 11 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 11 FDA reports)
CONJUNCTIVAL ABRASION ( 11 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 11 FDA reports)
DEPERSONALISATION ( 11 FDA reports)
DIPLEGIA ( 11 FDA reports)
DISEASE COMPLICATION ( 11 FDA reports)
DIZZINESS EXERTIONAL ( 11 FDA reports)
DRUG LEVEL FLUCTUATING ( 11 FDA reports)
FANCONI SYNDROME ( 11 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 11 FDA reports)
FLOPPY IRIS SYNDROME ( 11 FDA reports)
GENERAL SYMPTOM ( 11 FDA reports)
GRIMACING ( 11 FDA reports)
GUN SHOT WOUND ( 11 FDA reports)
HEPATOSPLENOMEGALY ( 11 FDA reports)
HYDROURETER ( 11 FDA reports)
HYPERAMMONAEMIA ( 11 FDA reports)
HYPERPROLACTINAEMIA ( 11 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 11 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 11 FDA reports)
ILIAC ARTERY OCCLUSION ( 11 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 11 FDA reports)
IMPRISONMENT ( 11 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 11 FDA reports)
INSULIN RESISTANCE ( 11 FDA reports)
INTENTIONAL MISUSE ( 11 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 11 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE EXPELLED ( 11 FDA reports)
INTRAOCULAR MELANOMA ( 11 FDA reports)
KELOID SCAR ( 11 FDA reports)
LARYNGEAL CYST ( 11 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 11 FDA reports)
LYMPHADENECTOMY ( 11 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 11 FDA reports)
MARITAL PROBLEM ( 11 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 11 FDA reports)
MENISCAL DEGENERATION ( 11 FDA reports)
METABOLIC ALKALOSIS ( 11 FDA reports)
METAMORPHOPSIA ( 11 FDA reports)
METASTASES TO HEART ( 11 FDA reports)
METASTASES TO LARGE INTESTINE ( 11 FDA reports)
MONARTHRITIS ( 11 FDA reports)
MONONEURITIS ( 11 FDA reports)
MORBID THOUGHTS ( 11 FDA reports)
MOTION SICKNESS ( 11 FDA reports)
NASAL DISORDER ( 11 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 11 FDA reports)
NEUROMA ( 11 FDA reports)
NODAL OSTEOARTHRITIS ( 11 FDA reports)
OESOPHAGEAL DILATATION ( 11 FDA reports)
OMENTUM NEOPLASM ( 11 FDA reports)
OPEN ANGLE GLAUCOMA ( 11 FDA reports)
ORAL PRURITUS ( 11 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 11 FDA reports)
PARAKERATOSIS ( 11 FDA reports)
PAROTIDECTOMY ( 11 FDA reports)
PENILE PAIN ( 11 FDA reports)
PERIPHERAL NERVE OPERATION ( 11 FDA reports)
PERNICIOUS ANAEMIA ( 11 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 11 FDA reports)
PLEURAL DISORDER ( 11 FDA reports)
PNEUMATOSIS ( 11 FDA reports)
POST PROCEDURAL DISCHARGE ( 11 FDA reports)
POSTOPERATIVE ADHESION ( 11 FDA reports)
POSTOPERATIVE ILEUS ( 11 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 11 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 11 FDA reports)
PULMONARY HILUM MASS ( 11 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 11 FDA reports)
RADICAL MASTECTOMY ( 11 FDA reports)
RENAL ARTERY OCCLUSION ( 11 FDA reports)
RETINAL VASCULAR OCCLUSION ( 11 FDA reports)
RHYTHM IDIOVENTRICULAR ( 11 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 11 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 11 FDA reports)
SPINAL CORD DISORDER ( 11 FDA reports)
SPINAL DEFORMITY ( 11 FDA reports)
STERNAL FRACTURE ( 11 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 11 FDA reports)
TETANY ( 11 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 11 FDA reports)
TINEA CRURIS ( 11 FDA reports)
ULCERATIVE KERATITIS ( 11 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 11 FDA reports)
URETHRAL STENOSIS ( 11 FDA reports)
UTERINE ENLARGEMENT ( 11 FDA reports)
VENOUS STENOSIS ( 11 FDA reports)
XANTHOGRANULOMA ( 11 FDA reports)
YAWNING ( 11 FDA reports)
NEUROMYOPATHY ( 10 FDA reports)
NIGHT BLINDNESS ( 10 FDA reports)
NO ADVERSE EFFECT ( 10 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 10 FDA reports)
OPTIC NERVE INJURY ( 10 FDA reports)
PARATHYROID DISORDER ( 10 FDA reports)
PERINEAL PAIN ( 10 FDA reports)
PERIPHERAL NERVE INJURY ( 10 FDA reports)
PEYRONIE'S DISEASE ( 10 FDA reports)
PHIMOSIS ( 10 FDA reports)
POISONING DELIBERATE ( 10 FDA reports)
POST HERPETIC NEURALGIA ( 10 FDA reports)
POST PROCEDURAL PAIN ( 10 FDA reports)
POSTPARTUM DISORDER ( 10 FDA reports)
PROCEDURAL SITE REACTION ( 10 FDA reports)
RADICULAR CYST ( 10 FDA reports)
RENAL ANEURYSM ( 10 FDA reports)
RENAL NEOPLASM ( 10 FDA reports)
SARCOMA ( 10 FDA reports)
SCAPULA FRACTURE ( 10 FDA reports)
SCROTAL IRRITATION ( 10 FDA reports)
SEMEN VOLUME DECREASED ( 10 FDA reports)
SHOULDER ARTHROPLASTY ( 10 FDA reports)
SINUS OPERATION ( 10 FDA reports)
SKIN NODULE ( 10 FDA reports)
SLEEP TALKING ( 10 FDA reports)
SOFT TISSUE NECROSIS ( 10 FDA reports)
SPINAL CLAUDICATION ( 10 FDA reports)
SPLENIC RUPTURE ( 10 FDA reports)
SPLENIC VEIN THROMBOSIS ( 10 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 10 FDA reports)
STRESS CARDIOMYOPATHY ( 10 FDA reports)
STRESS SYMPTOMS ( 10 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 10 FDA reports)
THYROIDITIS ( 10 FDA reports)
TONGUE COATED ( 10 FDA reports)
TOOTH DISCOLOURATION ( 10 FDA reports)
TOOTH REPAIR ( 10 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 10 FDA reports)
VASOSPASM ( 10 FDA reports)
VITAMIN D ABNORMAL ( 10 FDA reports)
WEANING FAILURE ( 10 FDA reports)
WOUND TREATMENT ( 10 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 10 FDA reports)
ACCOMMODATION DISORDER ( 10 FDA reports)
ADMINISTRATION SITE INFECTION ( 10 FDA reports)
ALVEOLITIS ( 10 FDA reports)
AMYLASE INCREASED ( 10 FDA reports)
ANISOCYTOSIS ( 10 FDA reports)
APNOEIC ATTACK ( 10 FDA reports)
APPLICATION SITE URTICARIA ( 10 FDA reports)
ARTERIAL BYPASS OPERATION ( 10 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 10 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 10 FDA reports)
ASTIGMATISM ( 10 FDA reports)
AURICULAR SWELLING ( 10 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 10 FDA reports)
BENCE JONES PROTEIN URINE PRESENT ( 10 FDA reports)
BIOPSY BONE ABNORMAL ( 10 FDA reports)
BITE ( 10 FDA reports)
BLADDER OPERATION ( 10 FDA reports)
BLOOD CALCIUM ABNORMAL ( 10 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ABNORMAL ( 10 FDA reports)
BLOOD SODIUM ABNORMAL ( 10 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 10 FDA reports)
BRAIN SCAN ABNORMAL ( 10 FDA reports)
BURNS THIRD DEGREE ( 10 FDA reports)
CAROTID ARTERY ANEURYSM ( 10 FDA reports)
CENTRAL LINE INFECTION ( 10 FDA reports)
CHOLESTATIC LIVER INJURY ( 10 FDA reports)
CHROMATOPSIA ( 10 FDA reports)
COLON CANCER STAGE III ( 10 FDA reports)
COLON OPERATION ( 10 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 10 FDA reports)
CSF PROTEIN INCREASED ( 10 FDA reports)
DENTAL PROSTHESIS USER ( 10 FDA reports)
DENTOFACIAL FUNCTIONAL DISORDER ( 10 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 10 FDA reports)
DISSEMINATED TUBERCULOSIS ( 10 FDA reports)
DRUG TOLERANCE INCREASED ( 10 FDA reports)
DYSMENORRHOEA ( 10 FDA reports)
EAR PRURITUS ( 10 FDA reports)
ENZYME ABNORMALITY ( 10 FDA reports)
EXTRADURAL ABSCESS ( 10 FDA reports)
FASCIITIS ( 10 FDA reports)
GALLBLADDER ENLARGEMENT ( 10 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 10 FDA reports)
GASTRECTOMY ( 10 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 10 FDA reports)
GASTROINTESTINAL BACTERIAL INFECTION ( 10 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 10 FDA reports)
GENITAL HAEMORRHAGE ( 10 FDA reports)
GENITAL RASH ( 10 FDA reports)
GLIOBLASTOMA MULTIFORME ( 10 FDA reports)
GRAM STAIN POSITIVE ( 10 FDA reports)
GROIN ABSCESS ( 10 FDA reports)
HAEMANGIOMA OF SPLEEN ( 10 FDA reports)
HAEMATOMA INFECTION ( 10 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 10 FDA reports)
HEART VALVE REPLACEMENT ( 10 FDA reports)
HEPATIC ISCHAEMIA ( 10 FDA reports)
HERPES ZOSTER OTICUS ( 10 FDA reports)
HOARSENESS ( 10 FDA reports)
HYPERAEMIA ( 10 FDA reports)
HYPERMAGNESAEMIA ( 10 FDA reports)
HYPERTROPHY OF TONGUE PAPILLAE ( 10 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 10 FDA reports)
IMPLANT SITE THROMBOSIS ( 10 FDA reports)
INFUSION SITE ERYTHEMA ( 10 FDA reports)
INFUSION SITE PAIN ( 10 FDA reports)
INNER EAR DISORDER ( 10 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 10 FDA reports)
INTRAVENOUS CATHETER MANAGEMENT ( 10 FDA reports)
LARYNGOTRACHEAL OEDEMA ( 10 FDA reports)
LIMB OPERATION ( 10 FDA reports)
LIVER TRANSPLANT ( 10 FDA reports)
LUMBAR SPINE FLATTENING ( 10 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 10 FDA reports)
MENINGEAL NEOPLASM ( 10 FDA reports)
MYELOFIBROSIS ( 10 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 9 FDA reports)
ABDOMINAL OPERATION ( 9 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 9 FDA reports)
AKINESIA ( 9 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 9 FDA reports)
ALBUMIN GLOBULIN RATIO INCREASED ( 9 FDA reports)
ALLERGIC SINUSITIS ( 9 FDA reports)
ANKYLOSING SPONDYLITIS ( 9 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 9 FDA reports)
APTYALISM ( 9 FDA reports)
ASEPTIC NECROSIS BONE ( 9 FDA reports)
ASTERIXIS ( 9 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 9 FDA reports)
BACTERIA URINE ( 9 FDA reports)
BENIGN GASTRIC NEOPLASM ( 9 FDA reports)
BLADDER DISCOMFORT ( 9 FDA reports)
BLADDER NECK SCLEROSIS ( 9 FDA reports)
BLADDER TRABECULATION ( 9 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 9 FDA reports)
BRAIN CANCER METASTATIC ( 9 FDA reports)
BUTTOCK PAIN ( 9 FDA reports)
CANDIDA SEPSIS ( 9 FDA reports)
CANDIDURIA ( 9 FDA reports)
CARDIAC VALVE VEGETATION ( 9 FDA reports)
CAROTID ARTERY STENT INSERTION ( 9 FDA reports)
CAUSTIC INJURY ( 9 FDA reports)
CEREBELLAR ISCHAEMIA ( 9 FDA reports)
CERVIX CARCINOMA ( 9 FDA reports)
CERVIX DISORDER ( 9 FDA reports)
CHEMICAL INJURY ( 9 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 9 FDA reports)
COCCIDIOIDOMYCOSIS ( 9 FDA reports)
COLITIS COLLAGENOUS ( 9 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 9 FDA reports)
COMPUTERISED TOMOGRAM CORONARY ARTERY ABNORMAL ( 9 FDA reports)
CONGENITAL TRACHEOMALACIA ( 9 FDA reports)
CUSHING'S SYNDROME ( 9 FDA reports)
CYSTITIS RADIATION ( 9 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 9 FDA reports)
DELIRIUM TREMENS ( 9 FDA reports)
DENTAL IMPRESSION PROCEDURE ( 9 FDA reports)
DEVICE MISUSE ( 9 FDA reports)
DEVICE RELATED SEPSIS ( 9 FDA reports)
DEXTROCARDIA ( 9 FDA reports)
DIET REFUSAL ( 9 FDA reports)
DYSMORPHISM ( 9 FDA reports)
DYSPLASIA ( 9 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 9 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 9 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 9 FDA reports)
ENDOMETRIAL DISORDER ( 9 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 9 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 9 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 9 FDA reports)
EPIDIDYMAL CYST ( 9 FDA reports)
EYE BURNS ( 9 FDA reports)
EYELIDS PRURITUS ( 9 FDA reports)
FEAR OF DISEASE ( 9 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 9 FDA reports)
FOOD AVERSION ( 9 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 9 FDA reports)
GASTRIC BYPASS ( 9 FDA reports)
GASTRIC PERFORATION ( 9 FDA reports)
GASTROINTESTINAL OEDEMA ( 9 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 9 FDA reports)
GLOMERULOSCLEROSIS ( 9 FDA reports)
HAEMOGLOBINURIA ( 9 FDA reports)
HAEMORRHOID OPERATION ( 9 FDA reports)
HELICOBACTER TEST POSITIVE ( 9 FDA reports)
HYPERCORTICOIDISM ( 9 FDA reports)
HYPERMETABOLISM ( 9 FDA reports)
HYPERMETROPIA ( 9 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 9 FDA reports)
HYPERTONIA ( 9 FDA reports)
HYPERVOLAEMIA ( 9 FDA reports)
HYPOMETABOLISM ( 9 FDA reports)
INCORRECT PRODUCT STORAGE ( 9 FDA reports)
INCREASED BRONCHIAL SECRETION ( 9 FDA reports)
INFUSION SITE HAEMATOMA ( 9 FDA reports)
INFUSION SITE HAEMORRHAGE ( 9 FDA reports)
INJECTION SITE DISCHARGE ( 9 FDA reports)
INJECTION SITE NECROSIS ( 9 FDA reports)
INTERMITTENT EXPLOSIVE DISORDER ( 9 FDA reports)
INTESTINAL RESECTION ( 9 FDA reports)
INTRACRANIAL HYPOTENSION ( 9 FDA reports)
KERATOACANTHOMA ( 9 FDA reports)
LEUKOPLAKIA ( 9 FDA reports)
LICHENIFICATION ( 9 FDA reports)
LIMB CRUSHING INJURY ( 9 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 9 FDA reports)
MAMMOGRAM ABNORMAL ( 9 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 9 FDA reports)
MENINGITIS CHEMICAL ( 9 FDA reports)
METATARSALGIA ( 9 FDA reports)
METATARSUS PRIMUS VARUS ( 9 FDA reports)
MICROCEPHALY ( 9 FDA reports)
MIXED HYPERLIPIDAEMIA ( 9 FDA reports)
MONOPARESIS ( 9 FDA reports)
MYCOSIS FUNGOIDES ( 9 FDA reports)
NAIL HYPERTROPHY ( 9 FDA reports)
NEEDLE ISSUE ( 9 FDA reports)
NEGATIVE THOUGHTS ( 9 FDA reports)
NEOPLASM RECURRENCE ( 9 FDA reports)
NEOPLASM SKIN ( 9 FDA reports)
NEUTROPHIL COUNT ( 9 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 9 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 9 FDA reports)
OPHTHALMOPLEGIA ( 9 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 9 FDA reports)
OSTEOPETROSIS ( 9 FDA reports)
OVARIAN NEOPLASM ( 9 FDA reports)
PAINFUL ERECTION ( 9 FDA reports)
PANCREATIC ATROPHY ( 9 FDA reports)
PARESIS ( 9 FDA reports)
PATHOGEN RESISTANCE ( 9 FDA reports)
PELVIC ADHESIONS ( 9 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 9 FDA reports)
PHARYNGEAL INFLAMMATION ( 9 FDA reports)
PLEURAL CALCIFICATION ( 9 FDA reports)
PNEUMATOSIS INTESTINALIS ( 9 FDA reports)
PNEUMONIA LEGIONELLA ( 9 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 9 FDA reports)
POOR VENOUS ACCESS ( 9 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 9 FDA reports)
POST PROCEDURAL DRAINAGE ( 9 FDA reports)
POSTNASAL DRIP ( 9 FDA reports)
PRESSURE OF SPEECH ( 9 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 9 FDA reports)
PROSTATE CANCER RECURRENT ( 9 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 9 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 9 FDA reports)
PULMONARY VASCULAR DISORDER ( 9 FDA reports)
PURPURA SENILE ( 9 FDA reports)
QUADRUPLE VESSEL BYPASS GRAFT ( 9 FDA reports)
RECTAL CANCER ( 9 FDA reports)
RECTAL TENESMUS ( 9 FDA reports)
RED BLOOD CELL ABNORMALITY ( 9 FDA reports)
RENAL CYST HAEMORRHAGE ( 9 FDA reports)
RESIDUAL URINE ( 9 FDA reports)
RETINAL EXUDATES ( 9 FDA reports)
SALPINGITIS ( 9 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 9 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 9 FDA reports)
SENSATION OF BLOOD FLOW ( 9 FDA reports)
SERRATIA BACTERAEMIA ( 9 FDA reports)
SKIN TEST POSITIVE ( 9 FDA reports)
SOFT TISSUE INFECTION ( 9 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 9 FDA reports)
SUPRAPUBIC PAIN ( 9 FDA reports)
SYNOVIAL DISORDER ( 9 FDA reports)
THYROID MASS ( 9 FDA reports)
TRACHEITIS ( 9 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 9 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 9 FDA reports)
ULNA FRACTURE ( 9 FDA reports)
URACHAL ABNORMALITY ( 9 FDA reports)
VARICOCELE ( 9 FDA reports)
VASCULAR ANOMALY ( 9 FDA reports)
VASCULAR CAUTERISATION ( 9 FDA reports)
VASCULAR GRAFT COMPLICATION ( 9 FDA reports)
VASCULAR RESISTANCE SYSTEMIC DECREASED ( 9 FDA reports)
VASCULAR STENOSIS ( 9 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 9 FDA reports)
VENA CAVA FILTER INSERTION ( 9 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 9 FDA reports)
VITAMIN B12 INCREASED ( 9 FDA reports)
WALKING DISABILITY ( 9 FDA reports)
XANTHOPSIA ( 9 FDA reports)
MYXOEDEMA COMA ( 8 FDA reports)
NAIL DYSTROPHY ( 8 FDA reports)
NASAL SEPTUM DISORDER ( 8 FDA reports)
NASAL ULCER ( 8 FDA reports)
NEURODERMATITIS ( 8 FDA reports)
NEUTROPHILIA ( 8 FDA reports)
NOCARDIOSIS ( 8 FDA reports)
NON-NEUTRALISING ANTIBODIES POSITIVE ( 8 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 8 FDA reports)
OPTIC NERVE INFARCTION ( 8 FDA reports)
ORCHIDECTOMY ( 8 FDA reports)
PAIN EXACERBATED ( 8 FDA reports)
PALMAR ERYTHEMA ( 8 FDA reports)
PANCREATIC CALCIFICATION ( 8 FDA reports)
PANCREATIC ENZYMES INCREASED ( 8 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 8 FDA reports)
PEDAL PULSE DECREASED ( 8 FDA reports)
PELVIC MASS ( 8 FDA reports)
PERINEURIAL CYST ( 8 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 8 FDA reports)
PHLEBITIS SUPERFICIAL ( 8 FDA reports)
PITUITARY TUMOUR ( 8 FDA reports)
PLATELET AGGREGATION INCREASED ( 8 FDA reports)
PNEUMOCEPHALUS ( 8 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 8 FDA reports)
PNEUMOMEDIASTINUM ( 8 FDA reports)
PNEUMOPERITONEUM ( 8 FDA reports)
POST CONCUSSION SYNDROME ( 8 FDA reports)
POST THROMBOTIC SYNDROME ( 8 FDA reports)
POSTOPERATIVE FEVER ( 8 FDA reports)
PRODUCT COLOUR ISSUE ( 8 FDA reports)
PRODUCT CONTAMINATION ( 8 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 8 FDA reports)
PRODUCT PACKAGING ISSUE ( 8 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 8 FDA reports)
PRURITUS GENITAL ( 8 FDA reports)
PSEUDOEPITHELIOMATOUS HYPERPLASIA ( 8 FDA reports)
PULSE PRESSURE DECREASED ( 8 FDA reports)
RECTAL FISTULA REPAIR ( 8 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE DECREASED ( 8 FDA reports)
RENAL STONE REMOVAL ( 8 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 8 FDA reports)
RESPIRATORY TRACT MALFORMATION ( 8 FDA reports)
RETINAL SCAR ( 8 FDA reports)
SALIVA ALTERED ( 8 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 8 FDA reports)
SCLERAL DISORDER ( 8 FDA reports)
SIALOADENITIS ( 8 FDA reports)
SINUS POLYP ( 8 FDA reports)
SKIN CANDIDA ( 8 FDA reports)
SOMATOFORM DISORDER ( 8 FDA reports)
SPLEEN DISORDER ( 8 FDA reports)
SPLENECTOMY ( 8 FDA reports)
SPONDYLOARTHROPATHY ( 8 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 8 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 8 FDA reports)
SUDDEN HEARING LOSS ( 8 FDA reports)
SUFFOCATION FEELING ( 8 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 8 FDA reports)
SURGICAL FAILURE ( 8 FDA reports)
T-CELL LYMPHOMA ( 8 FDA reports)
TARSAL TUNNEL SYNDROME ( 8 FDA reports)
TEETH BRITTLE ( 8 FDA reports)
THERAPY REGIMEN CHANGED ( 8 FDA reports)
THROMBOTIC STROKE ( 8 FDA reports)
TIC ( 8 FDA reports)
TINEA INFECTION ( 8 FDA reports)
TONGUE HAEMORRHAGE ( 8 FDA reports)
TORTICOLLIS ( 8 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 8 FDA reports)
TRIGONITIS ( 8 FDA reports)
TUNNEL VISION ( 8 FDA reports)
UPPER EXTREMITY MASS ( 8 FDA reports)
URETERIC STENOSIS ( 8 FDA reports)
URINE BILIRUBIN INCREASED ( 8 FDA reports)
VASOMOTOR RHINITIS ( 8 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 8 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 8 FDA reports)
VITAMIN D INCREASED ( 8 FDA reports)
VITAMIN SUPPLEMENTATION ( 8 FDA reports)
VITRECTOMY ( 8 FDA reports)
VULVOVAGINITIS ( 8 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 8 FDA reports)
WEIGHT ABNORMAL ( 8 FDA reports)
ABDOMINAL SYMPTOM ( 8 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 8 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 8 FDA reports)
ACUTE LEUKAEMIA ( 8 FDA reports)
ALVEOLITIS ALLERGIC ( 8 FDA reports)
ANAEMIA MACROCYTIC ( 8 FDA reports)
ANAL SKIN TAGS ( 8 FDA reports)
ANGIOGRAM ABNORMAL ( 8 FDA reports)
ANION GAP DECREASED ( 8 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 8 FDA reports)
ANTIDIURETIC HORMONE ABNORMALITY ( 8 FDA reports)
ARTERIAL RUPTURE ( 8 FDA reports)
ARTERIAL STENT INSERTION ( 8 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 8 FDA reports)
ARTERIOVENOUS SHUNT OPERATION ( 8 FDA reports)
BASAL GANGLIA INFARCTION ( 8 FDA reports)
BASOPHIL COUNT INCREASED ( 8 FDA reports)
BENIGN BONE NEOPLASM ( 8 FDA reports)
BILE DUCT STENOSIS ( 8 FDA reports)
BLADDER CATHETERISATION ( 8 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 8 FDA reports)
BLOOD CORTISOL ABNORMAL ( 8 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 8 FDA reports)
BLOOD PRESSURE ( 8 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 8 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 8 FDA reports)
BONE SCAN ABNORMAL ( 8 FDA reports)
BRADYKINESIA ( 8 FDA reports)
BRAIN DAMAGE ( 8 FDA reports)
BRAIN STEM STROKE ( 8 FDA reports)
BREAST OPERATION ( 8 FDA reports)
CAESAREAN SECTION ( 8 FDA reports)
CARBON DIOXIDE ABNORMAL ( 8 FDA reports)
CARDIAC PSEUDOANEURYSM ( 8 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 8 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 8 FDA reports)
CEREBRAL CALCIFICATION ( 8 FDA reports)
CEREBRAL MICROANGIOPATHY ( 8 FDA reports)
CHOLANGITIS SCLEROSING ( 8 FDA reports)
CHOREOATHETOSIS ( 8 FDA reports)
COLLAGEN-VASCULAR DISEASE ( 8 FDA reports)
COLOUR BLINDNESS ( 8 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 8 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 8 FDA reports)
COMPULSIVE SHOPPING ( 8 FDA reports)
DEPRESSIVE SYMPTOM ( 8 FDA reports)
DIABETIC VASCULAR DISORDER ( 8 FDA reports)
DISLOCATION OF VERTEBRA ( 8 FDA reports)
DISSOCIATIVE DISORDER ( 8 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 8 FDA reports)
DRUG EFFECT DELAYED ( 8 FDA reports)
DRUG SCREEN NEGATIVE ( 8 FDA reports)
DUODENAL POLYP ( 8 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 8 FDA reports)
EOSINOPHIL COUNT DECREASED ( 8 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 8 FDA reports)
ESCHAR ( 8 FDA reports)
ESSENTIAL TREMOR ( 8 FDA reports)
EXPOSURE TO TOXIC AGENT ( 8 FDA reports)
EYEBALL RUPTURE ( 8 FDA reports)
FIBROMA ( 8 FDA reports)
GASTRIC CANCER RECURRENT ( 8 FDA reports)
GASTRIC VARICES ( 8 FDA reports)
GASTROINTESTINAL EROSION ( 8 FDA reports)
GASTROINTESTINAL INJURY ( 8 FDA reports)
GASTROINTESTINAL TOXICITY ( 8 FDA reports)
GIANT CELL EPULIS ( 8 FDA reports)
GLOBULINS DECREASED ( 8 FDA reports)
GRAFT DYSFUNCTION ( 8 FDA reports)
GRAFT THROMBOSIS ( 8 FDA reports)
GRANULOMA ANNULARE ( 8 FDA reports)
GRIEF REACTION ( 8 FDA reports)
HAEMOBILIA ( 8 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 8 FDA reports)
HEART DISEASE CONGENITAL ( 8 FDA reports)
HEMISENSORY NEGLECT ( 8 FDA reports)
HEPATIC VEIN THROMBOSIS ( 8 FDA reports)
HEPATITIS VIRAL ( 8 FDA reports)
HIGH DENSITY LIPOPROTEIN ABNORMAL ( 8 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 8 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 8 FDA reports)
HYPOTENSIVE TRANSFUSION REACTION ( 8 FDA reports)
HYPOTRICHOSIS ( 8 FDA reports)
INFECTED DERMAL CYST ( 8 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 8 FDA reports)
INJECTION SITE ANAESTHESIA ( 8 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 8 FDA reports)
INTENTION TREMOR ( 8 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 8 FDA reports)
INTESTINAL MASS ( 8 FDA reports)
INTESTINAL STENOSIS ( 8 FDA reports)
LABILE HYPERTENSION ( 8 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 8 FDA reports)
LARYNGEAL STENOSIS ( 8 FDA reports)
LIPOSARCOMA ( 8 FDA reports)
LIQUID PRODUCT PHYSICAL ISSUE ( 8 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 8 FDA reports)
LUNG ABSCESS ( 8 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 8 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 8 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 8 FDA reports)
MENINGOENCEPHALITIS BACTERIAL ( 8 FDA reports)
METHAEMOGLOBINAEMIA ( 8 FDA reports)
MITRAL VALVE SCLEROSIS ( 8 FDA reports)
MUCOUS STOOLS ( 8 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 8 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 8 FDA reports)
ABDOMEN CRUSHING ( 7 FDA reports)
ABSCESS RUPTURE ( 7 FDA reports)
ACARODERMATITIS ( 7 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 7 FDA reports)
ACUTE PHOSPHATE NEPHROPATHY ( 7 FDA reports)
ADRENOMEGALY ( 7 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 7 FDA reports)
ANDROGEN DEFICIENCY ( 7 FDA reports)
ANEURYSM RUPTURED ( 7 FDA reports)
ANTISOCIAL BEHAVIOUR ( 7 FDA reports)
APPLICATION SITE BURN ( 7 FDA reports)
APPLICATION SITE DERMATITIS ( 7 FDA reports)
ARM AMPUTATION ( 7 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 7 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 7 FDA reports)
BLADDER DILATATION ( 7 FDA reports)
BLOOD PARATHYROID HORMONE ABNORMAL ( 7 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 7 FDA reports)
BLOOD VISCOSITY INCREASED ( 7 FDA reports)
BLUE TOE SYNDROME ( 7 FDA reports)
BOVINE TUBERCULOSIS ( 7 FDA reports)
BREAST NECROSIS ( 7 FDA reports)
BREAST OEDEMA ( 7 FDA reports)
BRONCHOPLEURAL FISTULA ( 7 FDA reports)
BURNS FIRST DEGREE ( 7 FDA reports)
CAECITIS ( 7 FDA reports)
CALCULUS URETHRAL ( 7 FDA reports)
CARDIAC ASSISTANCE DEVICE USER ( 7 FDA reports)
CARDIAC DISCOMFORT ( 7 FDA reports)
CATARACT CORTICAL ( 7 FDA reports)
CATATONIA ( 7 FDA reports)
CATHETER SITE ERYTHEMA ( 7 FDA reports)
CHEST TUBE INSERTION ( 7 FDA reports)
COLON NEOPLASM ( 7 FDA reports)
COLONIC FISTULA ( 7 FDA reports)
COLONIC STENOSIS ( 7 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 7 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 7 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 7 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 7 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 7 FDA reports)
CULTURE STOOL POSITIVE ( 7 FDA reports)
CUTANEOUS VASCULITIS ( 7 FDA reports)
DARK CIRCLES UNDER EYES ( 7 FDA reports)
DEATH OF RELATIVE ( 7 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 7 FDA reports)
DEVICE INTERACTION ( 7 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 7 FDA reports)
DISBACTERIOSIS ( 7 FDA reports)
DRUG TOLERANCE DECREASED ( 7 FDA reports)
DRY GANGRENE ( 7 FDA reports)
DUODENAL OBSTRUCTION ( 7 FDA reports)
DUPUYTREN'S CONTRACTURE OPERATION ( 7 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 7 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 7 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 7 FDA reports)
EMPTY SELLA SYNDROME ( 7 FDA reports)
ENTEROBACTER SEPSIS ( 7 FDA reports)
ENTHESOPATHY ( 7 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 7 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 7 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 7 FDA reports)
EYELID IRRITATION ( 7 FDA reports)
FAT EMBOLISM ( 7 FDA reports)
FEAR OF FALLING ( 7 FDA reports)
FEEDING DISORDER ( 7 FDA reports)
FOOD INTERACTION ( 7 FDA reports)
GALLBLADDER PAIN ( 7 FDA reports)
GALLOP RHYTHM PRESENT ( 7 FDA reports)
GASTRIC CANCER ( 7 FDA reports)
GASTRIC OPERATION ( 7 FDA reports)
GASTRODUODENAL ULCER ( 7 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 7 FDA reports)
GASTROINTESTINAL NEOPLASM ( 7 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 7 FDA reports)
GROWTH RETARDATION ( 7 FDA reports)
HAEMOPHILUS TEST POSITIVE ( 7 FDA reports)
HEART TRANSPLANT REJECTION ( 7 FDA reports)
HEPATITIS FULMINANT ( 7 FDA reports)
HERPES ZOSTER DISSEMINATED ( 7 FDA reports)
HIP SWELLING ( 7 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 7 FDA reports)
HYPERTRICHOSIS ( 7 FDA reports)
HYPOGEUSIA ( 7 FDA reports)
HYPOPROTEINAEMIA ( 7 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 7 FDA reports)
INCISION SITE HAEMATOMA ( 7 FDA reports)
INFECTED SEBACEOUS CYST ( 7 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 7 FDA reports)
INHIBITORY DRUG INTERACTION ( 7 FDA reports)
INJECTION SITE STINGING ( 7 FDA reports)
INTUBATION COMPLICATION ( 7 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 7 FDA reports)
JOINT STABILISATION ( 7 FDA reports)
KNEE DEFORMITY ( 7 FDA reports)
LABIA ENLARGED ( 7 FDA reports)
LEUKOPLAKIA ORAL ( 7 FDA reports)
LIMB DEFORMITY ( 7 FDA reports)
LIP EXFOLIATION ( 7 FDA reports)
LIPOHYPERTROPHY ( 7 FDA reports)
LIPOPROTEIN (A) INCREASED ( 7 FDA reports)
LOOSE STOOLS ( 7 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 7 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 7 FDA reports)
MEDIASTINAL MASS ( 7 FDA reports)
MEDICAL DEVICE REMOVAL ( 7 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 7 FDA reports)
METASTASES TO SMALL INTESTINE ( 7 FDA reports)
METASTATIC PAIN ( 7 FDA reports)
MITRAL VALVE REPAIR ( 7 FDA reports)
MOUTH INJURY ( 7 FDA reports)
MUSCLE FIBROSIS ( 7 FDA reports)
MYOGLOBIN URINE PRESENT ( 7 FDA reports)
ORAL DISCHARGE ( 7 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 7 FDA reports)
OTORRHOEA ( 7 FDA reports)
OXYGEN SATURATION ABNORMAL ( 7 FDA reports)
PANCREAS LIPOMATOSIS ( 7 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 7 FDA reports)
PANCREATIC INSUFFICIENCY ( 7 FDA reports)
PARKINSONIAN GAIT ( 7 FDA reports)
PARVOVIRUS B19 SEROLOGY POSITIVE ( 7 FDA reports)
PELVIC HAEMATOMA ( 7 FDA reports)
PENILE ABSCESS ( 7 FDA reports)
PENILE HAEMORRHAGE ( 7 FDA reports)
PENILE OEDEMA ( 7 FDA reports)
PERICARDIAL DISEASE ( 7 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 7 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 7 FDA reports)
PERTUSSIS ( 7 FDA reports)
PHANTOM PAIN ( 7 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 7 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 7 FDA reports)
PHYSIOTHERAPY ( 7 FDA reports)
PNEUMONIA MYCOPLASMAL ( 7 FDA reports)
POST PROCEDURAL DISCOMFORT ( 7 FDA reports)
POST PROCEDURAL MYOCARDIAL INFARCTION ( 7 FDA reports)
POST-THORACOTOMY PAIN SYNDROME ( 7 FDA reports)
PRECANCEROUS CELLS PRESENT ( 7 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 7 FDA reports)
PRIMARY HYPERALDOSTERONISM ( 7 FDA reports)
PROCEDURAL DIZZINESS ( 7 FDA reports)
PROTEIN S DEFICIENCY ( 7 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 7 FDA reports)
PSYCHOTIC BEHAVIOUR ( 7 FDA reports)
PYURIA ( 7 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 7 FDA reports)
RENAL CORTICAL NECROSIS ( 7 FDA reports)
RENAL VEIN THROMBOSIS ( 7 FDA reports)
RESPIRATORY ALKALOSIS ( 7 FDA reports)
RETINAL DEGENERATION ( 7 FDA reports)
REVERSIBLE AIRWAYS OBSTRUCTION ( 7 FDA reports)
RHEUMATOID FACTOR INCREASED ( 7 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 7 FDA reports)
SCROTAL OEDEMA ( 7 FDA reports)
SEPTIC EMBOLUS ( 7 FDA reports)
SERUM FERRITIN DECREASED ( 7 FDA reports)
SHOCK HYPOGLYCAEMIC ( 7 FDA reports)
SIGMOIDECTOMY ( 7 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 7 FDA reports)
SLEEP ATTACKS ( 7 FDA reports)
SMOKER ( 7 FDA reports)
SOMATIC DELUSION ( 7 FDA reports)
STEATORRHOEA ( 7 FDA reports)
SUBILEUS ( 7 FDA reports)
SUSPICIOUSNESS ( 7 FDA reports)
TESTICULAR ATROPHY ( 7 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 7 FDA reports)
THORACIC OPERATION ( 7 FDA reports)
TONGUE PARALYSIS ( 7 FDA reports)
TONSILLAR HYPERTROPHY ( 7 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO DECREASED ( 7 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 7 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 7 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 7 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 7 FDA reports)
URETHRAL STRICTURE ( 7 FDA reports)
URINE SODIUM INCREASED ( 7 FDA reports)
UTERINE FIBROSIS ( 7 FDA reports)
VAGINAL EROSION ( 7 FDA reports)
VAGOTOMY ( 7 FDA reports)
VITAMIN B1 INCREASED ( 7 FDA reports)
VITILIGO ( 7 FDA reports)
WOUND CLOSURE ( 7 FDA reports)
MYOCARDIAL RUPTURE ( 6 FDA reports)
MYOPATHY TOXIC ( 6 FDA reports)
NEUROENDOCRINE CARCINOMA ( 6 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 6 FDA reports)
NEUTROPENIC COLITIS ( 6 FDA reports)
NIPPLE EXUDATE BLOODY ( 6 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 6 FDA reports)
OCCIPITAL NEURALGIA ( 6 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 6 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 6 FDA reports)
OESOPHAGEAL OEDEMA ( 6 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 6 FDA reports)
OPISTHOTONUS ( 6 FDA reports)
ORAL SOFT TISSUE DISORDER ( 6 FDA reports)
OVARIAN ATROPHY ( 6 FDA reports)
OVARIAN CANCER METASTATIC ( 6 FDA reports)
OVARIAN MASS ( 6 FDA reports)
OXYGEN SUPPLEMENTATION ( 6 FDA reports)
PACEMAKER COMPLICATION ( 6 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 6 FDA reports)
PALATAL DISORDER ( 6 FDA reports)
PANCREAS INFECTION ( 6 FDA reports)
PANCREATIC INJURY ( 6 FDA reports)
PAROTID GLAND ENLARGEMENT ( 6 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 6 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 6 FDA reports)
PERITONEAL DISORDER ( 6 FDA reports)
PHLEBOSCLEROSIS ( 6 FDA reports)
PICKWICKIAN SYNDROME ( 6 FDA reports)
PINGUECULA ( 6 FDA reports)
PLATELET COUNT ( 6 FDA reports)
POLYCYTHAEMIA VERA ( 6 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 6 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 6 FDA reports)
POST POLIO SYNDROME ( 6 FDA reports)
PROCEDURAL HYPERTENSION ( 6 FDA reports)
PRODUCT CONTAMINATION PHYSICAL ( 6 FDA reports)
PRODUCT COUNTERFEIT ( 6 FDA reports)
PROLONGED EXPIRATION ( 6 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 6 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 6 FDA reports)
PSEUDOMONAL SEPSIS ( 6 FDA reports)
PULMONARY CALCIFICATION ( 6 FDA reports)
PULMONARY MYCOSIS ( 6 FDA reports)
PULMONARY VALVE STENOSIS ( 6 FDA reports)
RADICULITIS LUMBOSACRAL ( 6 FDA reports)
RASH SCALY ( 6 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 6 FDA reports)
REDUCED BLADDER CAPACITY ( 6 FDA reports)
RENAL ARTERY ATHEROSCLEROSIS ( 6 FDA reports)
RENAL ARTERY STENT PLACEMENT ( 6 FDA reports)
RENAL CANCER METASTATIC ( 6 FDA reports)
RENAL IMPAIRMENT NEONATAL ( 6 FDA reports)
RENAL VESSEL DISORDER ( 6 FDA reports)
RETINOPATHY HYPERTENSIVE ( 6 FDA reports)
SALMONELLA SEPSIS ( 6 FDA reports)
SCINTILLATING SCOTOMA ( 6 FDA reports)
SCLERAL HAEMORRHAGE ( 6 FDA reports)
SELF MUTILATION ( 6 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 6 FDA reports)
SHIFT TO THE LEFT ( 6 FDA reports)
SIMPLE PARTIAL SEIZURES ( 6 FDA reports)
SKIN TOXICITY ( 6 FDA reports)
SKIN TURGOR DECREASED ( 6 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 6 FDA reports)
SMALL INTESTINAL STENOSIS ( 6 FDA reports)
SOFT TISSUE INJURY ( 6 FDA reports)
SPINAL HAEMANGIOMA ( 6 FDA reports)
SPONTANEOUS PENILE ERECTION ( 6 FDA reports)
STEROID THERAPY ( 6 FDA reports)
STREPTOCOCCAL SEPSIS ( 6 FDA reports)
STRESS AT WORK ( 6 FDA reports)
STRESS ULCER ( 6 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 6 FDA reports)
SUPRANUCLEAR PALSY ( 6 FDA reports)
SYSTEMIC CANDIDA ( 6 FDA reports)
SYSTOLIC HYPERTENSION ( 6 FDA reports)
TACHYCARDIA PAROXYSMAL ( 6 FDA reports)
TAENIASIS ( 6 FDA reports)
TEMPERATURE REGULATION DISORDER ( 6 FDA reports)
TESTICULAR DISORDER ( 6 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE FOR UNAPPROVED INDICATION ( 6 FDA reports)
THROMBOCYTOPENIC PURPURA ( 6 FDA reports)
THROMBOPHLEBITIS SEPTIC ( 6 FDA reports)
THROMBOSIS PROPHYLAXIS ( 6 FDA reports)
THYROID ADENOMA ( 6 FDA reports)
TONSIL CANCER ( 6 FDA reports)
TOXIC SKIN ERUPTION ( 6 FDA reports)
TOXOPLASMA SEROLOGY POSITIVE ( 6 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 6 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 6 FDA reports)
TROPONIN ( 6 FDA reports)
TUMOUR FLARE ( 6 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 6 FDA reports)
UNDERWEIGHT ( 6 FDA reports)
URETHRAL PROLAPSE ( 6 FDA reports)
URINARY BLADDER POLYP ( 6 FDA reports)
URTICARIA GENERALISED ( 6 FDA reports)
UTERINE DILATION AND CURETTAGE ( 6 FDA reports)
VAGINAL ODOUR ( 6 FDA reports)
VARICOSE ULCERATION ( 6 FDA reports)
VASCULAR OPERATION ( 6 FDA reports)
VASOCONSTRICTION ( 6 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 6 FDA reports)
VIRAL MYOCARDITIS ( 6 FDA reports)
VIRAL PERICARDITIS ( 6 FDA reports)
VOCAL CORD PARESIS ( 6 FDA reports)
VULVAR DYSPLASIA ( 6 FDA reports)
WEIGHT LOSS DIET ( 6 FDA reports)
WHITE CLOT SYNDROME ( 6 FDA reports)
ACCIDENT AT HOME ( 6 FDA reports)
ACUTE DISSEMINATED ENCEPHALOMYELITIS ( 6 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 6 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 6 FDA reports)
AIRWAY COMPLICATION OF ANAESTHESIA ( 6 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 6 FDA reports)
ALBUMINURIA ( 6 FDA reports)
ALCOHOL INTERACTION ( 6 FDA reports)
ALLERGY TO METALS ( 6 FDA reports)
ANASTOMOTIC COMPLICATION ( 6 FDA reports)
ANKLE OPERATION ( 6 FDA reports)
ANOXIA ( 6 FDA reports)
ANTI FACTOR IX ANTIBODY POSITIVE ( 6 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 6 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 6 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 6 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 6 FDA reports)
AORTIC ATHEROSCLEROSIS ( 6 FDA reports)
AORTIC OCCLUSION ( 6 FDA reports)
APPLICATION SITE HAEMATOMA ( 6 FDA reports)
ARTERIAL STENOSIS LIMB ( 6 FDA reports)
ARTERIOVENOUS GRAFT SITE INFECTION ( 6 FDA reports)
ARTHRODESIS ( 6 FDA reports)
ARTHROPOD STING ( 6 FDA reports)
ARTIFICIAL MENOPAUSE ( 6 FDA reports)
ASPLENIA ( 6 FDA reports)
ATRIAL NATRIURETIC PEPTIDE INCREASED ( 6 FDA reports)
BACTERIA STOOL IDENTIFIED ( 6 FDA reports)
BELLIGERENCE ( 6 FDA reports)
BENIGN COLONIC NEOPLASM ( 6 FDA reports)
BENIGN NEOPLASM ( 6 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 6 FDA reports)
BILIARY CIRRHOSIS ( 6 FDA reports)
BINGE EATING ( 6 FDA reports)
BIOPSY KIDNEY ( 6 FDA reports)
BIOPSY SKIN ABNORMAL ( 6 FDA reports)
BLADDER NECK OBSTRUCTION ( 6 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 6 FDA reports)
BLOOD AMYLASE DECREASED ( 6 FDA reports)
BLOOD CHOLESTEROL ( 6 FDA reports)
BLOOD OSMOLARITY INCREASED ( 6 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 6 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 6 FDA reports)
BONE DENSITY ABNORMAL ( 6 FDA reports)
BRAIN CONTUSION ( 6 FDA reports)
BREAST CANCER STAGE II ( 6 FDA reports)
BREAST NEOPLASM ( 6 FDA reports)
BRONCHIAL CARCINOMA ( 6 FDA reports)
BURSA DISORDER ( 6 FDA reports)
BUTTERFLY RASH ( 6 FDA reports)
CARCINOID SYNDROME ( 6 FDA reports)
CARDIAC INFECTION ( 6 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 6 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 6 FDA reports)
CATHETER REMOVAL ( 6 FDA reports)
CATHETER SITE DISCHARGE ( 6 FDA reports)
CATHETER SITE HAEMATOMA ( 6 FDA reports)
CEREBRAL ARTERIOVENOUS MALFORMATION HAEMORRHAGIC ( 6 FDA reports)
CEREBRAL HAEMATOMA ( 6 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 6 FDA reports)
CLONUS ( 6 FDA reports)
COGNITIVE DETERIORATION ( 6 FDA reports)
COGWHEEL RIGIDITY ( 6 FDA reports)
COLONIC OBSTRUCTION ( 6 FDA reports)
COMPULSIONS ( 6 FDA reports)
CONGENITAL ANOMALY ( 6 FDA reports)
CONJUNCTIVAL SCAR ( 6 FDA reports)
CORONARY ARTERY EMBOLISM ( 6 FDA reports)
CRANIOTOMY ( 6 FDA reports)
CUTANEOUS CONTOUR DEFORMITY ( 6 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 6 FDA reports)
DENTAL TREATMENT ( 6 FDA reports)
DETOXIFICATION ( 6 FDA reports)
DIALYSIS DEVICE COMPLICATION ( 6 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 6 FDA reports)
DRUG EFFECT PROLONGED ( 6 FDA reports)
DRUG THERAPY ( 6 FDA reports)
EJECTION FRACTION ( 6 FDA reports)
ELECTROCARDIOGRAM PQ INTERVAL PROLONGED ( 6 FDA reports)
EMPYEMA ( 6 FDA reports)
ENDARTERECTOMY ( 6 FDA reports)
ENDOPHTHALMITIS ( 6 FDA reports)
ENDOSALPINGIOSIS ( 6 FDA reports)
ENDOSCOPY ( 6 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 6 FDA reports)
ENTEROCOLITIS ( 6 FDA reports)
EOSINOPHILIC PNEUMONIA ( 6 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 6 FDA reports)
EYES SUNKEN ( 6 FDA reports)
FACIAL WASTING ( 6 FDA reports)
FEEDING DISORDER OF INFANCY OR EARLY CHILDHOOD ( 6 FDA reports)
GALLBLADDER OBSTRUCTION ( 6 FDA reports)
GASTRIC ULCER HELICOBACTER ( 6 FDA reports)
GASTRIC ULCER PERFORATION ( 6 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 6 FDA reports)
GLOBULINS INCREASED ( 6 FDA reports)
GLYCOGEN STORAGE DISEASE TYPE V ( 6 FDA reports)
GOUTY TOPHUS ( 6 FDA reports)
GRAFT COMPLICATION ( 6 FDA reports)
GRAFT INFECTION ( 6 FDA reports)
HAEMATOCRIT ABNORMAL ( 6 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 6 FDA reports)
HAEMOPHILUS BACTERAEMIA ( 6 FDA reports)
HAEMORRHAGIC DISORDER ( 6 FDA reports)
HAEMORRHAGIC EROSIVE GASTRITIS ( 6 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 6 FDA reports)
HEAD AND NECK CANCER ( 6 FDA reports)
HEAD TITUBATION ( 6 FDA reports)
HEAT EXHAUSTION ( 6 FDA reports)
HEAT STROKE ( 6 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 6 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 6 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 6 FDA reports)
HYPERPLASTIC CHOLECYSTOPATHY ( 6 FDA reports)
HYPERSEXUALITY ( 6 FDA reports)
HYPERTHERMIA MALIGNANT ( 6 FDA reports)
HYPOCHLORAEMIA ( 6 FDA reports)
HYPOCHOLESTEROLAEMIA ( 6 FDA reports)
HYPOCHROMIC ANAEMIA ( 6 FDA reports)
HYPOSMIA ( 6 FDA reports)
IMPETIGO ( 6 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 6 FDA reports)
INFECTIOUS PERITONITIS ( 6 FDA reports)
INFUSION SITE EXTRAVASATION ( 6 FDA reports)
INJECTION SITE SCAR ( 6 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 6 FDA reports)
LARYNGEAL CANCER ( 6 FDA reports)
LARYNGEAL DISORDER ( 6 FDA reports)
LEIOMYOSARCOMA ( 6 FDA reports)
LIP DISCOLOURATION ( 6 FDA reports)
LIPID METABOLISM DISORDER ( 6 FDA reports)
LIVER ABSCESS ( 6 FDA reports)
LOWER EXTREMITY MASS ( 6 FDA reports)
LUNG ADENOCARCINOMA ( 6 FDA reports)
LYMPH NODE PAIN ( 6 FDA reports)
LYMPHANGITIS ( 6 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 6 FDA reports)
MALE SEXUAL DYSFUNCTION ( 6 FDA reports)
MALIGNANT MESENTERIC NEOPLASM ( 6 FDA reports)
MASS EXCISION ( 6 FDA reports)
MEAN CELL VOLUME DECREASED ( 6 FDA reports)
MEDIASTINAL HAEMATOMA ( 6 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 6 FDA reports)
MEGAKARYOCYTES ABNORMAL ( 6 FDA reports)
MIDDLE EAR EFFUSION ( 6 FDA reports)
MODIFIED RADICAL MASTECTOMY ( 6 FDA reports)
MUCOSAL EROSION ( 6 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 6 FDA reports)
MUSCLE MASS ( 6 FDA reports)
MYELITIS ( 6 FDA reports)
MYOCARDIAL FIBROSIS ( 6 FDA reports)
ABDOMINAL WALL CYST ( 5 FDA reports)
ACHLORHYDRIA ( 5 FDA reports)
ACTINOMYCES TEST POSITIVE ( 5 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 5 FDA reports)
ACUTE LUNG INJURY ( 5 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 5 FDA reports)
ADENOVIRUS INFECTION ( 5 FDA reports)
ADHESIOLYSIS ( 5 FDA reports)
ALCOHOLIC PANCREATITIS ( 5 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 5 FDA reports)
AMOEBIC DYSENTERY ( 5 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 5 FDA reports)
ANAL CANCER ( 5 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 5 FDA reports)
AORTIC ANEURYSM REPAIR ( 5 FDA reports)
AORTIC ANEURYSM RUPTURE ( 5 FDA reports)
AORTIC ELONGATION ( 5 FDA reports)
AORTIC EMBOLUS ( 5 FDA reports)
APPLICATION SITE DISCOLOURATION ( 5 FDA reports)
APPLICATION SITE EROSION ( 5 FDA reports)
ARTERIAL CATHETERISATION ( 5 FDA reports)
ARTERIAL HAEMORRHAGE ( 5 FDA reports)
ARTERIAL INJURY ( 5 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 5 FDA reports)
ARTERIOVENOUS FISTULA OCCLUSION ( 5 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 5 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 5 FDA reports)
BALANOPOSTHITIS ( 5 FDA reports)
BENIGN HEPATIC NEOPLASM ( 5 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 5 FDA reports)
BILIARY POLYP ( 5 FDA reports)
BIOPSY LIVER ABNORMAL ( 5 FDA reports)
BIOPSY SKIN ( 5 FDA reports)
BLADDER CANCER RECURRENT ( 5 FDA reports)
BLADDER CANCER STAGE III ( 5 FDA reports)
BLAST CELL COUNT INCREASED ( 5 FDA reports)
BLOOD ALBUMIN INCREASED ( 5 FDA reports)
BLOOD GLUCOSE ( 5 FDA reports)
BLOOD IRON INCREASED ( 5 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 5 FDA reports)
BLOOD PROLACTIN INCREASED ( 5 FDA reports)
BONE FISTULA ( 5 FDA reports)
BONE TRIMMING ( 5 FDA reports)
BRACHIAL PLEXOPATHY ( 5 FDA reports)
BRAIN STEM HAEMORRHAGE ( 5 FDA reports)
BREAST MICROCALCIFICATION ( 5 FDA reports)
BREAST RECONSTRUCTION ( 5 FDA reports)
BREATH ALCOHOL TEST POSITIVE ( 5 FDA reports)
BRONCHIAL INFECTION ( 5 FDA reports)
BRONCHIOLITIS ( 5 FDA reports)
CARBON MONOXIDE POISONING ( 5 FDA reports)
CARDITIS ( 5 FDA reports)
CATHETER SITE RELATED REACTION ( 5 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 5 FDA reports)
CEREBRAL HYPOPERFUSION ( 5 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 5 FDA reports)
CHEST INJURY ( 5 FDA reports)
CHONDROSARCOMA ( 5 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 5 FDA reports)
CLUBBING ( 5 FDA reports)
COLON POLYPECTOMY ( 5 FDA reports)
COMPLEMENT FACTOR C4 DECREASED ( 5 FDA reports)
CONDUCTIVE DEAFNESS ( 5 FDA reports)
CONJUNCTIVAL OEDEMA ( 5 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 5 FDA reports)
CONNECTIVE TISSUE DISORDER ( 5 FDA reports)
CORNEAL DISORDER ( 5 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 5 FDA reports)
CORONARY ARTERY REOCCLUSION ( 5 FDA reports)
CROUP INFECTIOUS ( 5 FDA reports)
CSF TEST ABNORMAL ( 5 FDA reports)
CYANOSIS CENTRAL ( 5 FDA reports)
CYSTITIS INTERSTITIAL ( 5 FDA reports)
DECEREBRATION ( 5 FDA reports)
DELAYED SLEEP PHASE ( 5 FDA reports)
DENTAL IMPLANTATION ( 5 FDA reports)
DERMATITIS INFECTED ( 5 FDA reports)
DEVICE EXPULSION ( 5 FDA reports)
DIABETES INSIPIDUS ( 5 FDA reports)
DIAPHRAGMATIC DISORDER ( 5 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 5 FDA reports)
DRUG CLEARANCE DECREASED ( 5 FDA reports)
DRUG DETOXIFICATION ( 5 FDA reports)
DRUG INTERACTION POTENTIATION ( 5 FDA reports)
DRUG THERAPY CHANGED ( 5 FDA reports)
DRUG WITHDRAWAL HEADACHE ( 5 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 5 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 5 FDA reports)
EAR OPERATION ( 5 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 5 FDA reports)
ENDOTHELIAL DYSFUNCTION ( 5 FDA reports)
EOSINOPHILIC CELLULITIS ( 5 FDA reports)
EPIGLOTTIC OEDEMA ( 5 FDA reports)
ERYTHEMA NODOSUM ( 5 FDA reports)
EXCESSIVE MASTURBATION ( 5 FDA reports)
EYE LASER SURGERY ( 5 FDA reports)
EYE OPERATION COMPLICATION ( 5 FDA reports)
EYELID PAIN ( 5 FDA reports)
FACTOR VIII INHIBITION ( 5 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 5 FDA reports)
FANCONI SYNDROME ACQUIRED ( 5 FDA reports)
FEELING OF RELAXATION ( 5 FDA reports)
FEMALE STERILISATION ( 5 FDA reports)
FIBROADENOMA OF BREAST ( 5 FDA reports)
FIBROUS HISTIOCYTOMA ( 5 FDA reports)
FOETAL GROWTH RETARDATION ( 5 FDA reports)
FRACTURE MALUNION ( 5 FDA reports)
FUNGAL OESOPHAGITIS ( 5 FDA reports)
FUNGAL TEST POSITIVE ( 5 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 5 FDA reports)
GASTRIC DILATATION ( 5 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 5 FDA reports)
GASTRIC PH DECREASED ( 5 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 5 FDA reports)
GENITAL BURNING SENSATION ( 5 FDA reports)
GENITAL DISCHARGE ( 5 FDA reports)
GILBERT'S SYNDROME ( 5 FDA reports)
GLIOMA ( 5 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 5 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 5 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 5 FDA reports)
HEART VALVE OPERATION ( 5 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 5 FDA reports)
HEPATIC ADENOMA ( 5 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 5 FDA reports)
HEPATITIS B CORE ANTIGEN POSITIVE ( 5 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 5 FDA reports)
HEPATORENAL FAILURE ( 5 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 5 FDA reports)
HORDEOLUM ( 5 FDA reports)
HORNER'S SYNDROME ( 5 FDA reports)
HYPERCALCIURIA ( 5 FDA reports)
HYPERCHLORAEMIA ( 5 FDA reports)
HYPERLACTACIDAEMIA ( 5 FDA reports)
HYPEROXALURIA ( 5 FDA reports)
HYPERPROTEINAEMIA ( 5 FDA reports)
HYPERPYREXIA ( 5 FDA reports)
HYPERTENSIVE ANGIOPATHY ( 5 FDA reports)
HYPERVITAMINOSIS ( 5 FDA reports)
HYPOPHYSITIS ( 5 FDA reports)
HYPOPITUITARISM ( 5 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 5 FDA reports)
IMPLANT SITE HAEMATOMA ( 5 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 5 FDA reports)
IMPLANT SITE INDURATION ( 5 FDA reports)
IMPLANT SITE INFECTION ( 5 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 5 FDA reports)
INCISION SITE INFECTION ( 5 FDA reports)
INGUINAL HERNIA STRANGULATED ( 5 FDA reports)
INJECTION SITE DRYNESS ( 5 FDA reports)
INJECTION SITE MACULE ( 5 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 5 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 5 FDA reports)
INTRASPINAL ABSCESS ( 5 FDA reports)
IRIDOCELE ( 5 FDA reports)
IRON OVERLOAD ( 5 FDA reports)
JC VIRUS INFECTION ( 5 FDA reports)
JOINT ARTHROPLASTY ( 5 FDA reports)
KERATITIS HERPETIC ( 5 FDA reports)
LATEX ALLERGY ( 5 FDA reports)
LIGAMENT DISORDER ( 5 FDA reports)
LIP EROSION ( 5 FDA reports)
LIPASE ABNORMAL ( 5 FDA reports)
LISTERIA SEPSIS ( 5 FDA reports)
LIVER TENDERNESS ( 5 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 5 FDA reports)
LYMPH NODE CANCER METASTATIC ( 5 FDA reports)
LYMPHOCYTIC INFILTRATION ( 5 FDA reports)
MACULE ( 5 FDA reports)
MALIGNANT TUMOUR EXCISION ( 5 FDA reports)
MAMMOPLASTY ( 5 FDA reports)
MASTOCYTOSIS ( 5 FDA reports)
MEAN PLATELET VOLUME INCREASED ( 5 FDA reports)
MEDICAL DIET ( 5 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 5 FDA reports)
METASTASES TO KIDNEY ( 5 FDA reports)
METASTASES TO MOUTH ( 5 FDA reports)
METASTASES TO PANCREAS ( 5 FDA reports)
METASTATIC CARCINOMA OF THE BLADDER ( 5 FDA reports)
MICROCYTOSIS ( 5 FDA reports)
MILK-ALKALI SYNDROME ( 5 FDA reports)
MUSCLE ABSCESS ( 5 FDA reports)
MYOGLOBIN URINE ( 5 FDA reports)
NAIL INFECTION ( 5 FDA reports)
NASAL SEPTUM PERFORATION ( 5 FDA reports)
NASOPHARYNGEAL DISORDER ( 5 FDA reports)
NECROBIOSIS LIPOIDICA DIABETICORUM ( 5 FDA reports)
NECROSIS ISCHAEMIC ( 5 FDA reports)
NECROTISING FASCIITIS ( 5 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 5 FDA reports)
NEUROMUSCULAR BLOCK PROLONGED ( 5 FDA reports)
NEUROSIS ( 5 FDA reports)
NEUROSURGERY ( 5 FDA reports)
NIPPLE SWELLING ( 5 FDA reports)
NO ADVERSE DRUG EFFECT ( 5 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 5 FDA reports)
OBESITY SURGERY ( 5 FDA reports)
OBSESSIVE THOUGHTS ( 5 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 5 FDA reports)
ONYCHOLYSIS ( 5 FDA reports)
ONYCHOPHAGIA ( 5 FDA reports)
OPTIC DISC DRUSEN ( 5 FDA reports)
OPTIC DISC HAEMORRHAGE ( 5 FDA reports)
ORAL FIBROMA ( 5 FDA reports)
ORGANISING PNEUMONIA ( 5 FDA reports)
OSTEOMALACIA ( 5 FDA reports)
OSTEOPOROTIC FRACTURE ( 5 FDA reports)
OVARIAN ADHESION ( 5 FDA reports)
PANCREATIC ENLARGEMENT ( 5 FDA reports)
PARACENTESIS ( 5 FDA reports)
PARADOXICAL EMBOLISM ( 5 FDA reports)
PENILE SWELLING ( 5 FDA reports)
PERIHEPATIC ABSCESS ( 5 FDA reports)
PERIPHERAL NERVE LESION ( 5 FDA reports)
PHOBIA ( 5 FDA reports)
PLANTAR ERYTHEMA ( 5 FDA reports)
PNEUMONIA HAEMOPHILUS ( 5 FDA reports)
POLYMYOSITIS ( 5 FDA reports)
POLYPECTOMY ( 5 FDA reports)
POLYSUBSTANCE ABUSE ( 5 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 5 FDA reports)
POST PROCEDURAL BILE LEAK ( 5 FDA reports)
POST PROCEDURAL NAUSEA ( 5 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 5 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 5 FDA reports)
PSEUDOCYST ( 5 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 5 FDA reports)
RADIATION NEUROPATHY ( 5 FDA reports)
RADICAL PROSTATECTOMY ( 5 FDA reports)
REACTION TO COLOURING ( 5 FDA reports)
RECALL PHENOMENON ( 5 FDA reports)
RECTAL PERFORATION ( 5 FDA reports)
REFLEXES ABNORMAL ( 5 FDA reports)
RELAPSING FEVER ( 5 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 5 FDA reports)
REPETITIVE SPEECH ( 5 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS TEST POSITIVE ( 5 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 5 FDA reports)
RESPIRATORY TRACT OEDEMA ( 5 FDA reports)
RETICULOCYTE COUNT INCREASED ( 5 FDA reports)
RETINAL VASCULAR DISORDER ( 5 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 5 FDA reports)
RETROPERITONEAL NEOPLASM ( 5 FDA reports)
RHEUMATOID NODULE ( 5 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 5 FDA reports)
ROTAVIRUS TEST POSITIVE ( 5 FDA reports)
SALMONELLA BACTERAEMIA ( 5 FDA reports)
SCAN ABNORMAL ( 5 FDA reports)
SCIATIC NERVE INJURY ( 5 FDA reports)
SINOATRIAL BLOCK ( 5 FDA reports)
SINUS TARSI SYNDROME ( 5 FDA reports)
SITUS INVERSUS ( 5 FDA reports)
SKIN BACTERIAL INFECTION ( 5 FDA reports)
SKIN DEPIGMENTATION ( 5 FDA reports)
SKIN DESQUAMATION ( 5 FDA reports)
SKIN DISCOMFORT ( 5 FDA reports)
SKIN EROSION ( 5 FDA reports)
SMALL INTESTINAL PERFORATION ( 5 FDA reports)
SOMATISATION DISORDER ( 5 FDA reports)
SPERMATOCELE ( 5 FDA reports)
SPLINTER HAEMORRHAGES ( 5 FDA reports)
SPONDYLITIC MYELOPATHY ( 5 FDA reports)
STATUS ASTHMATICUS ( 5 FDA reports)
STENT MALFUNCTION ( 5 FDA reports)
STOMATITIS NECROTISING ( 5 FDA reports)
STOOL ANALYSIS ABNORMAL ( 5 FDA reports)
STROKE IN EVOLUTION ( 5 FDA reports)
SUPRAVENTRICULAR TACHYARRHYTHMIA ( 5 FDA reports)
SUTURE RELATED COMPLICATION ( 5 FDA reports)
SYMBLEPHARON ( 5 FDA reports)
THALAMUS HAEMORRHAGE ( 5 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 5 FDA reports)
THORACIC OUTLET SYNDROME ( 5 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 5 FDA reports)
TONIC CLONIC MOVEMENTS ( 5 FDA reports)
TONSILLECTOMY ( 5 FDA reports)
TRACHEAL OEDEMA ( 5 FDA reports)
TRAUMATIC FRACTURE ( 5 FDA reports)
TRAUMATIC HAEMATOMA ( 5 FDA reports)
TRENDELENBURG'S SYMPTOM ( 5 FDA reports)
TRICHORRHEXIS ( 5 FDA reports)
TUMOUR EMBOLISM ( 5 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 5 FDA reports)
ULNAR NERVE PALSY ( 5 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 5 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 5 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 5 FDA reports)
URETERIC DILATATION ( 5 FDA reports)
URINARY SEDIMENT PRESENT ( 5 FDA reports)
URINE OXALATE INCREASED ( 5 FDA reports)
UTERINE MALPOSITION ( 5 FDA reports)
UTEROVAGINAL PROLAPSE ( 5 FDA reports)
VASCULAR STENT INSERTION ( 5 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 5 FDA reports)
VIRAL CARDIOMYOPATHY ( 5 FDA reports)
VISUAL BRIGHTNESS ( 5 FDA reports)
VITAL CAPACITY DECREASED ( 5 FDA reports)
VITAMIN C DECREASED ( 5 FDA reports)
WEGENER'S GRANULOMATOSIS ( 5 FDA reports)
WHITE BLOOD CELLS URINE ( 5 FDA reports)
WOUND ABSCESS ( 5 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 5 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 4 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 4 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 4 FDA reports)
NITRITE URINE PRESENT ( 4 FDA reports)
NODULE ON EXTREMITY ( 4 FDA reports)
NUCHAL RIGIDITY ( 4 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 4 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 4 FDA reports)
OESOPHAGEAL ACHALASIA ( 4 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 4 FDA reports)
OESOPHAGEAL DISCOMFORT ( 4 FDA reports)
OLIGOMENORRHOEA ( 4 FDA reports)
OMENTECTOMY ( 4 FDA reports)
OPEN FRACTURE ( 4 FDA reports)
ORBITAL OEDEMA ( 4 FDA reports)
OVARIAN DISORDER ( 4 FDA reports)
PANIC DISORDER WITHOUT AGORAPHOBIA ( 4 FDA reports)
PARALYSIS FLACCID ( 4 FDA reports)
PARAPSORIASIS ( 4 FDA reports)
PAROPHTHALMIA ( 4 FDA reports)
PARVOVIRUS B19 TEST POSITIVE ( 4 FDA reports)
PEDAL PULSE ABNORMAL ( 4 FDA reports)
PELVIC NEOPLASM ( 4 FDA reports)
PENILE INFECTION ( 4 FDA reports)
PENILE NECROSIS ( 4 FDA reports)
PENILE ULCERATION ( 4 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 4 FDA reports)
PERICARDIAL RUB ( 4 FDA reports)
PERICARDITIS CONSTRICTIVE ( 4 FDA reports)
PHLEBOLITH ( 4 FDA reports)
PLEURAL ADHESION ( 4 FDA reports)
PNEUMATOSIS CYSTOIDES INTESTINALIS ( 4 FDA reports)
PNEUMOCOCCAL INFECTION ( 4 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 4 FDA reports)
PNEUMONIA NECROTISING ( 4 FDA reports)
POLYSEROSITIS ( 4 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 4 FDA reports)
POST PROCEDURAL CELLULITIS ( 4 FDA reports)
POST PROCEDURAL DIARRHOEA ( 4 FDA reports)
POST PROCEDURAL PNEUMONIA ( 4 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 4 FDA reports)
POST-TRAUMATIC NECK SYNDROME ( 4 FDA reports)
POSTMENOPAUSE ( 4 FDA reports)
POSTOPERATIVE HETEROTOPIC CALCIFICATION ( 4 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 4 FDA reports)
POSTURING ( 4 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 4 FDA reports)
PROCEDURAL NAUSEA ( 4 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 4 FDA reports)
PRODUCT SIZE ISSUE ( 4 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 4 FDA reports)
PROSTATIC OPERATION ( 4 FDA reports)
PROSTATIC SPECIFIC ANTIGEN ABNORMAL ( 4 FDA reports)
PROTEIN C DEFICIENCY ( 4 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 4 FDA reports)
PULMONARY CAVITATION ( 4 FDA reports)
PULMONARY TUBERCULOSIS ( 4 FDA reports)
REBOUND EFFECT ( 4 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 4 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 4 FDA reports)
RED CELL DISTRIBUTION WIDTH DECREASED ( 4 FDA reports)
RED MAN SYNDROME ( 4 FDA reports)
RENAL HAEMATOMA ( 4 FDA reports)
RENAL HYPERTENSION ( 4 FDA reports)
RETICULOCYTE COUNT DECREASED ( 4 FDA reports)
RETINAL INFARCTION ( 4 FDA reports)
RETINAL VEIN THROMBOSIS ( 4 FDA reports)
RHINALGIA ( 4 FDA reports)
SALIVARY GLAND DISORDER ( 4 FDA reports)
SALMONELLOSIS ( 4 FDA reports)
SCAN ABDOMEN ABNORMAL ( 4 FDA reports)
SCLERITIS ( 4 FDA reports)
SCROTAL ABSCESS ( 4 FDA reports)
SCROTAL DISORDER ( 4 FDA reports)
SECONDARY HYPERTENSION ( 4 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 4 FDA reports)
SENILE DEMENTIA ( 4 FDA reports)
SERRATIA SEPSIS ( 4 FDA reports)
SKIN GRAFT FAILURE ( 4 FDA reports)
SKIN LESION EXCISION ( 4 FDA reports)
SLEEP-RELATED EATING DISORDER ( 4 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 4 FDA reports)
SOLAR ELASTOSIS ( 4 FDA reports)
SOLILOQUY ( 4 FDA reports)
SPECIFIC GRAVITY URINE INCREASED ( 4 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 4 FDA reports)
SPINAL CORD INFARCTION ( 4 FDA reports)
SPINAL CORD INJURY CERVICAL ( 4 FDA reports)
SPINAL CORD OPERATION ( 4 FDA reports)
SPINAL PAIN ( 4 FDA reports)
SPUTUM ABNORMAL ( 4 FDA reports)
SPUTUM INCREASED ( 4 FDA reports)
SPUTUM RETENTION ( 4 FDA reports)
STENOTROPHOMONAS INFECTION ( 4 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 4 FDA reports)
STRESS INCONTINENCE ( 4 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 4 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 4 FDA reports)
TANGENTIALITY ( 4 FDA reports)
TESTIS CANCER ( 4 FDA reports)
THYROID CANCER METASTATIC ( 4 FDA reports)
THYROXINE INCREASED ( 4 FDA reports)
TOLOSA-HUNT SYNDROME ( 4 FDA reports)
TONGUE ERUPTION ( 4 FDA reports)
TONGUE GEOGRAPHIC ( 4 FDA reports)
TONGUE PRURITUS ( 4 FDA reports)
TONIC CONVULSION ( 4 FDA reports)
TONSILLAR INFLAMMATION ( 4 FDA reports)
TONSILLITIS ( 4 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO INCREASED ( 4 FDA reports)
TOXIC SHOCK SYNDROME STAPHYLOCOCCAL ( 4 FDA reports)
TRACHEAL STENOSIS ( 4 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 4 FDA reports)
TRAUMATIC HAEMORRHAGE ( 4 FDA reports)
TRAUMATIC LIVER INJURY ( 4 FDA reports)
TYPE I HYPERSENSITIVITY ( 4 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 4 FDA reports)
UMBILICAL HERNIA REPAIR ( 4 FDA reports)
URETHRAL DISORDER ( 4 FDA reports)
URINARY CASTS ( 4 FDA reports)
URINE KETONE BODY ( 4 FDA reports)
URINE POTASSIUM INCREASED ( 4 FDA reports)
UVULITIS ( 4 FDA reports)
VAGINAL CANDIDIASIS ( 4 FDA reports)
VARICOSE VEIN RUPTURED ( 4 FDA reports)
VASCULAR ENCEPHALOPATHY ( 4 FDA reports)
VASCULITIS CEREBRAL ( 4 FDA reports)
VASCULITIS NECROTISING ( 4 FDA reports)
VENTRICULAR FAILURE ( 4 FDA reports)
VENTRICULAR FLUTTER ( 4 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 4 FDA reports)
VIRAL HAEMORRHAGIC CYSTITIS ( 4 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 4 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 4 FDA reports)
VITH NERVE PARALYSIS ( 4 FDA reports)
VOCAL CORD INFLAMMATION ( 4 FDA reports)
VULVAL ULCERATION ( 4 FDA reports)
VULVOVAGINAL DISCOMFORT ( 4 FDA reports)
XANTHOMA ( 4 FDA reports)
ABSCESS SOFT TISSUE ( 4 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 4 FDA reports)
ACUTE POLYNEUROPATHY ( 4 FDA reports)
ACUTE PSYCHOSIS ( 4 FDA reports)
ADJUSTMENT DISORDER WITH ANXIETY ( 4 FDA reports)
ADRENAL HAEMORRHAGE ( 4 FDA reports)
ALLERGIC COUGH ( 4 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 4 FDA reports)
AMPUTATION ( 4 FDA reports)
ANAEMIA MEGALOBLASTIC ( 4 FDA reports)
ANAL DISCOMFORT ( 4 FDA reports)
ANAL SPHINCTER ATONY ( 4 FDA reports)
ANGIOMYOLIPOMA ( 4 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST ( 4 FDA reports)
ANTIBODY TEST POSITIVE ( 4 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 4 FDA reports)
AORTIC VALVE DISEASE MIXED ( 4 FDA reports)
APALLIC SYNDROME ( 4 FDA reports)
APPARENT LIFE THREATENING EVENT ( 4 FDA reports)
APPLICATION SITE BURNING ( 4 FDA reports)
APPLICATION SITE INFECTION ( 4 FDA reports)
APPLICATION SITE SCAB ( 4 FDA reports)
APPLICATION SITE SWELLING ( 4 FDA reports)
ARACHNOID CYST ( 4 FDA reports)
ARTERIOVENOUS GRAFT SITE ABSCESS ( 4 FDA reports)
ARTERITIS CORONARY ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 4 FDA reports)
ATRIAL HYPERTROPHY ( 4 FDA reports)
ATRIAL PRESSURE INCREASED ( 4 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 4 FDA reports)
AXONAL NEUROPATHY ( 4 FDA reports)
BALANITIS ( 4 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 4 FDA reports)
BILIARY TRACT INFECTION ( 4 FDA reports)
BIOPSY ENDOMETRIUM ABNORMAL ( 4 FDA reports)
BLADDER INJURY ( 4 FDA reports)
BLOOD ALCOHOL INCREASED ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 4 FDA reports)
BLOOD BICARBONATE ABNORMAL ( 4 FDA reports)
BLOOD COPPER DECREASED ( 4 FDA reports)
BLOOD CREATINE ABNORMAL ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 4 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 4 FDA reports)
BLOOD FOLATE DECREASED ( 4 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 4 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 4 FDA reports)
BLOOD INSULIN INCREASED ( 4 FDA reports)
BLOOD KETONE BODY ( 4 FDA reports)
BLOOD KETONE BODY PRESENT ( 4 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 4 FDA reports)
BLUNTED AFFECT ( 4 FDA reports)
BOWEN'S DISEASE ( 4 FDA reports)
BRAIN MIDLINE SHIFT ( 4 FDA reports)
BRAIN NATRIURETIC PEPTIDE ABNORMAL ( 4 FDA reports)
BREAST DISCOMFORT ( 4 FDA reports)
BREAST PROSTHESIS USER ( 4 FDA reports)
BREATH SOUNDS DECREASED ( 4 FDA reports)
BRONCHIAL DISORDER ( 4 FDA reports)
BURNING MOUTH SYNDROME ( 4 FDA reports)
CAPILLARY DISORDER ( 4 FDA reports)
CARDIAC SEPTAL DEFECT ( 4 FDA reports)
CAROTID ARTERY ATHEROMA ( 4 FDA reports)
CAROTID ENDARTERECTOMY ( 4 FDA reports)
CATAPLEXY ( 4 FDA reports)
CENTRAL NERVOUS SYSTEM FUNCTION TEST ABNORMAL ( 4 FDA reports)
CEREBRAL VASOCONSTRICTION ( 4 FDA reports)
CERVICAL CORD COMPRESSION ( 4 FDA reports)
CHORIORETINOPATHY ( 4 FDA reports)
CHRONIC GASTROINTESTINAL BLEEDING ( 4 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 4 FDA reports)
CHRONIC HEPATIC FAILURE ( 4 FDA reports)
CHRONIC HEPATITIS ( 4 FDA reports)
CITROBACTER INFECTION ( 4 FDA reports)
CNS VENTRICULITIS ( 4 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 4 FDA reports)
COAGULATION FACTOR X LEVEL INCREASED ( 4 FDA reports)
COAGULATION TIME ABNORMAL ( 4 FDA reports)
COAGULATION TIME SHORTENED ( 4 FDA reports)
COLD AGGLUTININS ( 4 FDA reports)
COLON CANCER STAGE IV ( 4 FDA reports)
COMA HEPATIC ( 4 FDA reports)
COMPLEMENT FACTOR C3 DECREASED ( 4 FDA reports)
COMPLEMENT FACTOR DECREASED ( 4 FDA reports)
COMPLICATIONS OF TRANSPLANTED HEART ( 4 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 4 FDA reports)
CONJUNCTIVAL PALLOR ( 4 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 4 FDA reports)
CORNEAL SCAR ( 4 FDA reports)
CORONARY OSTIAL STENOSIS ( 4 FDA reports)
CORRECTIVE LENS USER ( 4 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 4 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 4 FDA reports)
DAYDREAMING ( 4 FDA reports)
DEAFNESS TRANSITORY ( 4 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 4 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 4 FDA reports)
DEPRESSION SUICIDAL ( 4 FDA reports)
DERMATITIS ATOPIC ( 4 FDA reports)
DERMATITIS PSORIASIFORM ( 4 FDA reports)
DIABETIC BLINDNESS ( 4 FDA reports)
DIABETIC ENTEROPATHY ( 4 FDA reports)
DISINHIBITION ( 4 FDA reports)
DRESSLER'S SYNDROME ( 4 FDA reports)
DRUG DIVERSION ( 4 FDA reports)
DRUG NAME CONFUSION ( 4 FDA reports)
DUODENAL FISTULA ( 4 FDA reports)
DYSHIDROSIS ( 4 FDA reports)
DYSSOMNIA ( 4 FDA reports)
ELECTRIC SHOCK ( 4 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 4 FDA reports)
ELECTROCARDIOGRAM T WAVE BIPHASIC ( 4 FDA reports)
ELECTROLYTE DEPLETION ( 4 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 4 FDA reports)
EMBOLISM VENOUS ( 4 FDA reports)
ENCEPHALITIC INFECTION ( 4 FDA reports)
ENDOMETRIAL CANCER STAGE III ( 4 FDA reports)
ENTERITIS INFECTIOUS ( 4 FDA reports)
EPIDERMOID CYST EXCISION ( 4 FDA reports)
EPIDERMOLYSIS ( 4 FDA reports)
EPISCLERITIS ( 4 FDA reports)
ERYTHEMA ANNULARE ( 4 FDA reports)
EXANTHEM ( 4 FDA reports)
EXSANGUINATION ( 4 FDA reports)
EXTERNAL AUDITORY CANAL ATRESIA ( 4 FDA reports)
EXTERNAL EAR PAIN ( 4 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 4 FDA reports)
EXTUBATION ( 4 FDA reports)
FABRY'S DISEASE ( 4 FDA reports)
FACTOR XI DEFICIENCY ( 4 FDA reports)
FEMORAL NERVE INJURY ( 4 FDA reports)
FIBRINOLYSIS ( 4 FDA reports)
FINGER AMPUTATION ( 4 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 4 FDA reports)
FOETAL DISORDER ( 4 FDA reports)
FUNGUS STOOL IDENTIFIED ( 4 FDA reports)
GAMBLING ( 4 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 4 FDA reports)
GASTROINTESTINAL AMYLOIDOSIS ( 4 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 4 FDA reports)
GENERALISED NON-CONVULSIVE EPILEPSY ( 4 FDA reports)
GINGIVAL ABSCESS ( 4 FDA reports)
GLIOBLASTOMA ( 4 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 4 FDA reports)
GLYCOSYLATED HAEMOGLOBIN DECREASED ( 4 FDA reports)
GRANULOCYTE COUNT DECREASED ( 4 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 4 FDA reports)
HAEMOGLOBIN ( 4 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 4 FDA reports)
HAPTOGLOBIN INCREASED ( 4 FDA reports)
HEART VALVE CALCIFICATION ( 4 FDA reports)
HEPATIC CANCER STAGE IV ( 4 FDA reports)
HEPATITIS ALCOHOLIC ( 4 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 4 FDA reports)
HERNIA HIATUS REPAIR ( 4 FDA reports)
HERNIA OBSTRUCTIVE ( 4 FDA reports)
HETEROTAXIA ( 4 FDA reports)
HISTAMINE LEVEL INCREASED ( 4 FDA reports)
HISTIOCYTIC NECROTISING LYMPHADENITIS ( 4 FDA reports)
HIV INFECTION ( 4 FDA reports)
HOMELESS ( 4 FDA reports)
HOSPICE CARE ( 4 FDA reports)
HYPERSPLENISM ( 4 FDA reports)
HYPERTRANSAMINASAEMIA ( 4 FDA reports)
HYPERVISCOSITY SYNDROME ( 4 FDA reports)
HYPHAEMA ( 4 FDA reports)
HYPOAESTHESIA EYE ( 4 FDA reports)
HYPOCHROMASIA ( 4 FDA reports)
HYPOCOMPLEMENTAEMIA ( 4 FDA reports)
HYPOPARATHYROIDISM ( 4 FDA reports)
HYPOSPADIAS ( 4 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 4 FDA reports)
ILEAL STENOSIS ( 4 FDA reports)
ILIAC VEIN OCCLUSION ( 4 FDA reports)
ILLUSION ( 4 FDA reports)
IMPLANT SITE REACTION ( 4 FDA reports)
INADEQUATE DIET ( 4 FDA reports)
INCISION SITE ERYTHEMA ( 4 FDA reports)
INCISION SITE OEDEMA ( 4 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 4 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 4 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 4 FDA reports)
INFUSION SITE INFLAMMATION ( 4 FDA reports)
INGROWN HAIR ( 4 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 4 FDA reports)
INJECTION SITE INJURY ( 4 FDA reports)
INTERCAPILLARY GLOMERULOSCLEROSIS ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 4 FDA reports)
INTERSTITIAL GRANULOMATOUS DERMATITIS ( 4 FDA reports)
INTERVERTEBRAL DISC INJURY ( 4 FDA reports)
INTERVERTEBRAL DISCITIS ( 4 FDA reports)
INTESTINAL MUCOSAL ATROPHY ( 4 FDA reports)
INTRA-UTERINE DEATH ( 4 FDA reports)
INTRAPERICARDIAL THROMBOSIS ( 4 FDA reports)
INVESTIGATION ABNORMAL ( 4 FDA reports)
IRIDOCYCLITIS ( 4 FDA reports)
ISCHAEMIC NEPHROPATHY ( 4 FDA reports)
ISCHAEMIC NEUROPATHY ( 4 FDA reports)
ISCHAEMIC ULCER ( 4 FDA reports)
IUCD COMPLICATION ( 4 FDA reports)
JAW LESION EXCISION ( 4 FDA reports)
JEJUNAL PERFORATION ( 4 FDA reports)
JOB DISSATISFACTION ( 4 FDA reports)
JOINT DISLOCATION REDUCTION ( 4 FDA reports)
JOINT SURGERY ( 4 FDA reports)
JOINT WARMTH ( 4 FDA reports)
KAPOSI'S SARCOMA ( 4 FDA reports)
KIDNEY SMALL ( 4 FDA reports)
LARGE GRANULAR LYMPHOCYTOSIS ( 4 FDA reports)
LARGE INTESTINAL STRICTURE ( 4 FDA reports)
LEFT ATRIAL HYPERTROPHY ( 4 FDA reports)
LEIOMYOMA ( 4 FDA reports)
LENS DISORDER ( 4 FDA reports)
LENTIGO ( 4 FDA reports)
LIP INJURY ( 4 FDA reports)
LIPODYSTROPHY ACQUIRED ( 4 FDA reports)
LIPOEDEMA ( 4 FDA reports)
LIVER OPERATION ( 4 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 4 FDA reports)
LORDOSIS ( 4 FDA reports)
LOSS OF PROPRIOCEPTION ( 4 FDA reports)
LOWER LIMB DEFORMITY ( 4 FDA reports)
LUNG CREPITATION ( 4 FDA reports)
LUNG OPERATION ( 4 FDA reports)
LUNG TRANSPLANT REJECTION ( 4 FDA reports)
LUPUS NEPHRITIS ( 4 FDA reports)
LYMPH NODE CALCIFICATION ( 4 FDA reports)
LYMPHATIC OBSTRUCTION ( 4 FDA reports)
LYMPHOCYTE COUNT ( 4 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 4 FDA reports)
MALIGNANT ASCITES ( 4 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 4 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 4 FDA reports)
MENINGOCOCCAL INFECTION ( 4 FDA reports)
MENISCUS OPERATION ( 4 FDA reports)
MENISCUS REMOVAL ( 4 FDA reports)
MENSTRUATION DELAYED ( 4 FDA reports)
MESENTERIC ARTERY STENOSIS ( 4 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 4 FDA reports)
METASTASES TO PLEURA ( 4 FDA reports)
METASTATIC CARCINOID TUMOUR ( 4 FDA reports)
MICROGNATHIA ( 4 FDA reports)
MICROTIA ( 4 FDA reports)
MICROVASCULAR ANGINA ( 4 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 4 FDA reports)
MORPHOEA ( 4 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 4 FDA reports)
ABDOMINAL REBOUND TENDERNESS ( 3 FDA reports)
ABDOMINAL WALL DISORDER ( 3 FDA reports)
ABNORMAL WEIGHT GAIN ( 3 FDA reports)
ABORTION INDUCED ( 3 FDA reports)
ABORTION MISSED ( 3 FDA reports)
ACCELERATED IDIOVENTRICULAR RHYTHM ( 3 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 3 FDA reports)
ACINETOBACTER TEST POSITIVE ( 3 FDA reports)
ACNE PUSTULAR ( 3 FDA reports)
ACQUIRED MACROGLOSSIA ( 3 FDA reports)
ACQUIRED PHIMOSIS ( 3 FDA reports)
ACROMEGALY ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 3 FDA reports)
ADENOIDECTOMY ( 3 FDA reports)
ADENOTONSILLECTOMY ( 3 FDA reports)
ADJUSTMENT DISORDER WITH MIXED ANXIETY AND DEPRESSED MOOD ( 3 FDA reports)
ADRENAL CYST ( 3 FDA reports)
AIDS RELATED COMPLICATION ( 3 FDA reports)
ALCOHOLIC ( 3 FDA reports)
ALDOLASE INCREASED ( 3 FDA reports)
ALLERGIC OEDEMA ( 3 FDA reports)
ALLERGY TO ARTHROPOD STING ( 3 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 3 FDA reports)
AMPHETAMINES POSITIVE ( 3 FDA reports)
ANEURYSMECTOMY ( 3 FDA reports)
ANGIOTENSIN CONVERTING ENZYME DECREASED ( 3 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INHIBITOR FOETOPATHY ( 3 FDA reports)
ANTICHOLINERGIC SYNDROME ( 3 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 3 FDA reports)
ANTISOCIAL PERSONALITY DISORDER ( 3 FDA reports)
ANTITHROMBIN III DECREASED ( 3 FDA reports)
APOPTOSIS ( 3 FDA reports)
APPLICATION SITE DRYNESS ( 3 FDA reports)
ARACHNOIDITIS ( 3 FDA reports)
ARTERIAL SPASM ( 3 FDA reports)
ARTERIOVENOUS FISTULA ( 3 FDA reports)
ARTHRITIS REACTIVE ( 3 FDA reports)
ARTHROSCOPY ( 3 FDA reports)
ASPIRATION BIOPSY ( 3 FDA reports)
ATRIAL CONDUCTION TIME PROLONGATION ( 3 FDA reports)
ATROPHIE BLANCHE ( 3 FDA reports)
AVULSION FRACTURE ( 3 FDA reports)
BECKWITH-WIEDEMANN SYNDROME ( 3 FDA reports)
BENIGN OVARIAN TUMOUR ( 3 FDA reports)
BENIGN RENAL NEOPLASM ( 3 FDA reports)
BICUSPID AORTIC VALVE ( 3 FDA reports)
BIOPSY BONE MARROW ( 3 FDA reports)
BIOPSY HEART ( 3 FDA reports)
BIOPSY LUNG ( 3 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 3 FDA reports)
BLADDER NECK SUSPENSION ( 3 FDA reports)
BLADDER PERFORATION ( 3 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 3 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 3 FDA reports)
BLOOD COPPER INCREASED ( 3 FDA reports)
BLOOD CREATININE ( 3 FDA reports)
BLOOD HIV RNA DECREASED ( 3 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 3 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 3 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 3 FDA reports)
BODY TEMPERATURE ( 3 FDA reports)
BODY TINEA ( 3 FDA reports)
BONE INFECTION ( 3 FDA reports)
BORDERLINE GLAUCOMA ( 3 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 3 FDA reports)
BOREDOM ( 3 FDA reports)
BRACHIOCEPHALIC VEIN STENOSIS ( 3 FDA reports)
BRAIN STEM SYNDROME ( 3 FDA reports)
BREAST CANCER MALE ( 3 FDA reports)
BREAST CANCER STAGE III ( 3 FDA reports)
BREATH SOUNDS ( 3 FDA reports)
BRONCHIAL HYPERACTIVITY ( 3 FDA reports)
BRONCHIAL OEDEMA ( 3 FDA reports)
BRONCHITIS BACTERIAL ( 3 FDA reports)
BRONCHOSCOPY ABNORMAL ( 3 FDA reports)
BRUNNER'S GLAND HYPERPLASIA ( 3 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 3 FDA reports)
CALCIUM IONISED DECREASED ( 3 FDA reports)
CALCIUM IONISED INCREASED ( 3 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 3 FDA reports)
CARCINOID TUMOUR ( 3 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 3 FDA reports)
CARDIAC MONITORING ( 3 FDA reports)
CARDIAC PACEMAKER REVISION ( 3 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 3 FDA reports)
CARDIOVASCULAR FUNCTION TEST ABNORMAL ( 3 FDA reports)
CAROTID ARTERY DISSECTION ( 3 FDA reports)
CAROTID ARTERY INSUFFICIENCY ( 3 FDA reports)
CATHETER BACTERAEMIA ( 3 FDA reports)
CATHETER THROMBOSIS ( 3 FDA reports)
CATHETERISATION VENOUS ( 3 FDA reports)
CD8 LYMPHOCYTES DECREASED ( 3 FDA reports)
CEREBELLAR TUMOUR ( 3 FDA reports)
CEREBRAL ARTERY STENOSIS ( 3 FDA reports)
CEREBRAL HYGROMA ( 3 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 3 FDA reports)
CERULOPLASMIN INCREASED ( 3 FDA reports)
CERVICAL POLYP ( 3 FDA reports)
CHEMICAL BURN OF GASTROINTESTINAL TRACT ( 3 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 3 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA TRANSFORMATION ( 3 FDA reports)
CHYLOTHORAX ( 3 FDA reports)
CIRCUMORAL OEDEMA ( 3 FDA reports)
CLEFT PALATE ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 3 FDA reports)
COAGULATION TEST ABNORMAL ( 3 FDA reports)
COITAL BLEEDING ( 3 FDA reports)
COLONIC ATONY ( 3 FDA reports)
COLONOSCOPY ABNORMAL ( 3 FDA reports)
COLOUR VISION TESTS ABNORMAL ( 3 FDA reports)
CONFUSION POSTOPERATIVE ( 3 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 3 FDA reports)
CONSTRICTED AFFECT ( 3 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 3 FDA reports)
CONTRAST MEDIA ALLERGY ( 3 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 3 FDA reports)
CORNEAL EPITHELIUM DEFECT ( 3 FDA reports)
CRACKLES LUNG ( 3 FDA reports)
CREATININE URINE INCREASED ( 3 FDA reports)
CYSTITIS ESCHERICHIA ( 3 FDA reports)
CYTOLOGY ABNORMAL ( 3 FDA reports)
CYTOMEGALOVIRUS OESOPHAGITIS ( 3 FDA reports)
DACRYOCYSTORHINOSTOMY ( 3 FDA reports)
DEEP VEIN THROMBOSIS POSTOPERATIVE ( 3 FDA reports)
DENTAL DISCOMFORT ( 3 FDA reports)
DEPENDENCE ON RESPIRATOR ( 3 FDA reports)
DEREALISATION ( 3 FDA reports)
DEVELOPMENTAL DELAY ( 3 FDA reports)
DEVICE ISSUE ( 3 FDA reports)
DIABETIC MICROANGIOPATHY ( 3 FDA reports)
DIABETIC MONONEUROPATHY ( 3 FDA reports)
DIALYSIS DISEQUILIBRIUM SYNDROME ( 3 FDA reports)
DIARRHOEA INFECTIOUS ( 3 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 3 FDA reports)
DISSOCIATIVE IDENTITY DISORDER ( 3 FDA reports)
DISTRACTIBILITY ( 3 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 3 FDA reports)
DRUG LEVEL CHANGED ( 3 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 3 FDA reports)
DUODENITIS HAEMORRHAGIC ( 3 FDA reports)
DYSKINESIA OESOPHAGEAL ( 3 FDA reports)
DYSLEXIA ( 3 FDA reports)
DYSPNOEA AT REST ( 3 FDA reports)
EATING DISORDER SYMPTOM ( 3 FDA reports)
ECG SIGNS OF VENTRICULAR HYPERTROPHY ( 3 FDA reports)
EJACULATION DELAYED ( 3 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 3 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 3 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 3 FDA reports)
ELEVATED MOOD ( 3 FDA reports)
EMPHYSEMATOUS CYSTITIS ( 3 FDA reports)
ENAMEL ANOMALY ( 3 FDA reports)
ENDOMETRIAL CANCER STAGE I ( 3 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 3 FDA reports)
ENLARGED UVULA ( 3 FDA reports)
EOSINOPHILIC FASCIITIS ( 3 FDA reports)
EOSINOPHILIC MYOCARDITIS ( 3 FDA reports)
EOSINOPHILIC PNEUMONIA CHRONIC ( 3 FDA reports)
EPIDERMAL NECROSIS ( 3 FDA reports)
EPIDURAL ANAESTHESIA ( 3 FDA reports)
EPIPLOIC APPENDAGITIS ( 3 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 3 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 3 FDA reports)
EXERCISE LACK OF ( 3 FDA reports)
EXTRAVASATION BLOOD ( 3 FDA reports)
EYE ALLERGY ( 3 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 3 FDA reports)
EYELID MARGIN CRUSTING ( 3 FDA reports)
FACIAL ASYMMETRY ( 3 FDA reports)
FACIAL LESION EXCISION ( 3 FDA reports)
FACIAL NERVE DISORDER ( 3 FDA reports)
FAECAL VOLUME INCREASED ( 3 FDA reports)
FAILURE OF IMPLANT ( 3 FDA reports)
FAT TISSUE INCREASED ( 3 FDA reports)
FATTY LIVER ALCOHOLIC ( 3 FDA reports)
FEEDING DISORDER NEONATAL ( 3 FDA reports)
FEELING HOT AND COLD ( 3 FDA reports)
FIBROMUSCULAR DYSPLASIA ( 3 FDA reports)
FIBROSIS TENDINOUS ( 3 FDA reports)
FILARIASIS ( 3 FDA reports)
FLASHBACK ( 3 FDA reports)
FOREARM FRACTURE ( 3 FDA reports)
FOREIGN BODY IN EYE ( 3 FDA reports)
FREEZING PHENOMENON ( 3 FDA reports)
FUNGAL PARONYCHIA ( 3 FDA reports)
FUNGAL PERITONITIS ( 3 FDA reports)
FUNGATING WOUND ( 3 FDA reports)
GALLBLADDER CANCER ( 3 FDA reports)
GAMMA RADIATION THERAPY ( 3 FDA reports)
GASTRIC BANDING ( 3 FDA reports)
GASTRIC ILEUS ( 3 FDA reports)
GASTRIC MUCOSAL LESION ( 3 FDA reports)
GASTRIC NEOPLASM ( 3 FDA reports)
GASTROENTERITIS BACTERIAL ( 3 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 3 FDA reports)
GASTROINTESTINAL CARCINOMA ( 3 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 3 FDA reports)
GASTROINTESTINAL MALFORMATION ( 3 FDA reports)
GASTROINTESTINAL STENOSIS ( 3 FDA reports)
GASTROINTESTINAL SURGERY ( 3 FDA reports)
GASTROOESOPHAGEAL CANCER ( 3 FDA reports)
GAZE PALSY ( 3 FDA reports)
GENITAL DISORDER MALE ( 3 FDA reports)
GIARDIASIS ( 3 FDA reports)
GIGANTISM ( 3 FDA reports)
GINGIVAL ATROPHY ( 3 FDA reports)
GINGIVAL INJURY ( 3 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 3 FDA reports)
GLUCOSE TOLERANCE TEST ABNORMAL ( 3 FDA reports)
GRANDIOSITY ( 3 FDA reports)
GRANULOCYTE COUNT INCREASED ( 3 FDA reports)
GROWING PAINS ( 3 FDA reports)
GRUNTING ( 3 FDA reports)
HAEMATINURIA ( 3 FDA reports)
HAEMODIALYSIS-INDUCED SYMPTOM ( 3 FDA reports)
HAIRY CELL LEUKAEMIA ( 3 FDA reports)
HALLUCINATION, TACTILE ( 3 FDA reports)
HAPTOGLOBIN DECREASED ( 3 FDA reports)
HEART VALVE INSUFFICIENCY ( 3 FDA reports)
HEMIANOPIA HOMONYMOUS ( 3 FDA reports)
HEMICEPHALALGIA ( 3 FDA reports)
HEPATIC HAEMORRHAGE ( 3 FDA reports)
HEPATIC NEOPLASM MALIGNANT NON-RESECTABLE ( 3 FDA reports)
HEPATIC TRAUMA ( 3 FDA reports)
HEPATITIS B ANTIBODY ( 3 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 3 FDA reports)
HERPES PHARYNGITIS ( 3 FDA reports)
HODGKIN'S DISEASE MIXED CELLULARITY STAGE UNSPECIFIED ( 3 FDA reports)
HOMICIDE ( 3 FDA reports)
HUNTINGTON'S DISEASE ( 3 FDA reports)
HYPERAMMONAEMIC ENCEPHALOPATHY ( 3 FDA reports)
HYPERAMYLASAEMIA ( 3 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 3 FDA reports)
HYPERTROPHY ( 3 FDA reports)
HYPNOPOMPIC HALLUCINATION ( 3 FDA reports)
HYPOALDOSTERONISM ( 3 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 3 FDA reports)
HYPOPROTHROMBINAEMIA ( 3 FDA reports)
HYPORESPONSIVE TO STIMULI ( 3 FDA reports)
IGA NEPHROPATHY ( 3 FDA reports)
ILEAL ULCER ( 3 FDA reports)
IMMUNOLOGY TEST ABNORMAL ( 3 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 3 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 3 FDA reports)
INFLAMMATORY MARKER INCREASED ( 3 FDA reports)
INFUSION SITE OEDEMA ( 3 FDA reports)
INGUINAL HERNIA REPAIR ( 3 FDA reports)
INJECTION SITE ATROPHY ( 3 FDA reports)
INJECTION SITE PUSTULE ( 3 FDA reports)
INJECTION SITE ULCER ( 3 FDA reports)
INJURY ASPHYXIATION ( 3 FDA reports)
INTESTINAL FISTULA ( 3 FDA reports)
INTESTINAL OPERATION ( 3 FDA reports)
INTRACRANIAL HAEMATOMA ( 3 FDA reports)
INTRADUCTAL PAPILLOMA OF BREAST ( 3 FDA reports)
INTRAOCULAR PRESSURE DECREASED ( 3 FDA reports)
INVESTIGATION ( 3 FDA reports)
IODINE UPTAKE INCREASED ( 3 FDA reports)
IRON BINDING CAPACITY TOTAL INCREASED ( 3 FDA reports)
JOINT ADHESION ( 3 FDA reports)
KETONURIA ( 3 FDA reports)
KETOSIS ( 3 FDA reports)
KLEBSIELLA BACTERAEMIA ( 3 FDA reports)
KLEBSIELLA SEPSIS ( 3 FDA reports)
LACRIMAL DUCT PROCEDURE ( 3 FDA reports)
LACTOBACILLUS INFECTION ( 3 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 3 FDA reports)
LENS DISCOLOURATION ( 3 FDA reports)
LENTICULAR OPACITIES ( 3 FDA reports)
LEUKOSTASIS ( 3 FDA reports)
LICHEN SCLEROSUS ( 3 FDA reports)
LIFE SUPPORT ( 3 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 3 FDA reports)
LIPOMA EXCISION ( 3 FDA reports)
LITHOTRIPSY ( 3 FDA reports)
LOCALISED OSTEOARTHRITIS ( 3 FDA reports)
LOSS OF VISUAL CONTRAST SENSITIVITY ( 3 FDA reports)
LOW DENSITY LIPOPROTEIN ABNORMAL ( 3 FDA reports)
LUNG CYST BENIGN ( 3 FDA reports)
LUNG WEDGE RESECTION ( 3 FDA reports)
LYMPH GLAND INFECTION ( 3 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 3 FDA reports)
MAGNESIUM DEFICIENCY ( 3 FDA reports)
MAMMARY DUCT ECTASIA ( 3 FDA reports)
MASKED FACIES ( 3 FDA reports)
MASTITIS ( 3 FDA reports)
MASTOID DISORDER ( 3 FDA reports)
MASTOID EFFUSION ( 3 FDA reports)
MAXILLOFACIAL OPERATION ( 3 FDA reports)
MEAN ARTERIAL PRESSURE DECREASED ( 3 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 3 FDA reports)
MENTAL DISABILITY ( 3 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 3 FDA reports)
METASTASES TO OVARY ( 3 FDA reports)
METASTASES TO SPLEEN ( 3 FDA reports)
MIDDLE EAR DISORDER ( 3 FDA reports)
MILK ALLERGY ( 3 FDA reports)
MINERAL DEFICIENCY ( 3 FDA reports)
MINERAL METABOLISM DISORDER ( 3 FDA reports)
MOLE EXCISION ( 3 FDA reports)
MONOCYTE COUNT DECREASED ( 3 FDA reports)
MONONEUROPATHY MULTIPLEX ( 3 FDA reports)
MONONUCLEOSIS HETEROPHILE TEST POSITIVE ( 3 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 3 FDA reports)
MORGANELLA INFECTION ( 3 FDA reports)
MORNING GLORY SYNDROME ( 3 FDA reports)
MUCOSAL DISCOLOURATION ( 3 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 3 FDA reports)
MUSCLE NECROSIS ( 3 FDA reports)
MUTISM ( 3 FDA reports)
MYASTHENIA GRAVIS CRISIS ( 3 FDA reports)
MYELOCYTE COUNT INCREASED ( 3 FDA reports)
MYOCARDIAL CALCIFICATION ( 3 FDA reports)
MYOPATHY STEROID ( 3 FDA reports)
MYRINGITIS ( 3 FDA reports)
NAIL AVULSION ( 3 FDA reports)
NAIL DISCOMFORT ( 3 FDA reports)
NAIL GROWTH ABNORMAL ( 3 FDA reports)
NARCISSISTIC PERSONALITY DISORDER ( 3 FDA reports)
NASAL CAVITY CANCER ( 3 FDA reports)
NASAL MUCOSAL DISORDER ( 3 FDA reports)
NASAL TURBINATE ABNORMALITY ( 3 FDA reports)
NASOPHARYNGEAL CANCER ( 3 FDA reports)
NEGATIVISM ( 3 FDA reports)
NEPHROANGIOSCLEROSIS ( 3 FDA reports)
NICOTINIC ACID DEFICIENCY ( 3 FDA reports)
NIKOLSKY'S SIGN ( 3 FDA reports)
NIPPLE INFECTION ( 3 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 3 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 3 FDA reports)
NUCLEATED RED CELLS ( 3 FDA reports)
OCULAR DISCOMFORT ( 3 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 3 FDA reports)
OESOPHAGEAL INJURY ( 3 FDA reports)
OESOPHAGEAL IRRITATION ( 3 FDA reports)
OESOPHAGEAL NEOPLASM ( 3 FDA reports)
OESOPHAGOSCOPY ABNORMAL ( 3 FDA reports)
ONYCHOGRYPHOSIS ( 3 FDA reports)
OPTIC NERVE CUPPING ( 3 FDA reports)
ORAL MUCOSA EROSION ( 3 FDA reports)
ORBITAL PSEUDOTUMOUR ( 3 FDA reports)
OROPHARYNGEAL SPASM ( 3 FDA reports)
OSTECTOMY ( 3 FDA reports)
OSTEOGENESIS IMPERFECTA ( 3 FDA reports)
OVARIAN ENLARGEMENT ( 3 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 3 FDA reports)
OXYGEN SATURATION INCREASED ( 3 FDA reports)
PALLIATIVE CARE ( 3 FDA reports)
PANCREATECTOMY ( 3 FDA reports)
PANCREATIC HAEMORRHAGE ( 3 FDA reports)
PANCREATIC PHLEGMON ( 3 FDA reports)
PARADOXICAL DRUG REACTION ( 3 FDA reports)
PARANEOPLASTIC SYNDROME ( 3 FDA reports)
PATIENT ISOLATION ( 3 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 3 FDA reports)
PENILE VASCULAR DISORDER ( 3 FDA reports)
PENIS CARCINOMA ( 3 FDA reports)
PEPTIC ULCER PERFORATION ( 3 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 3 FDA reports)
PERIRENAL HAEMATOMA ( 3 FDA reports)
PERITONEAL ABSCESS ( 3 FDA reports)
PERITONEAL CARCINOMA ( 3 FDA reports)
PERIVASCULAR DERMATITIS ( 3 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 3 FDA reports)
PHOBIA OF DRIVING ( 3 FDA reports)
PILOERECTION ( 3 FDA reports)
PITUITARY TUMOUR BENIGN ( 3 FDA reports)
PLACENTA PRAEVIA ( 3 FDA reports)
PLEURAL HAEMORRHAGE ( 3 FDA reports)
PNEUMOBILIA ( 3 FDA reports)
PNEUMOCOCCAL SEPSIS ( 3 FDA reports)
PNEUMONITIS CHEMICAL ( 3 FDA reports)
POLIOMYELITIS ( 3 FDA reports)
POLYMYALGIA ( 3 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 3 FDA reports)
PORTAL TRIADITIS ( 3 FDA reports)
PORTAL VENOUS GAS ( 3 FDA reports)
POST PROCEDURAL HAEMATURIA ( 3 FDA reports)
POST-TRAUMATIC PAIN ( 3 FDA reports)
POST-TRAUMATIC SYNDROME ( 3 FDA reports)
POSTICTAL PARALYSIS ( 3 FDA reports)
POSTOPERATIVE RESPIRATORY DISTRESS ( 3 FDA reports)
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME ( 3 FDA reports)
PRE-ECLAMPSIA ( 3 FDA reports)
PRE-EXISTING DISEASE ( 3 FDA reports)
PREGNANCY AFTER POST COITAL CONTRACEPTION ( 3 FDA reports)
PROCEDURAL HAEMORRHAGE ( 3 FDA reports)
PROCTOCOLECTOMY ( 3 FDA reports)
PRODUCT LABEL ISSUE ( 3 FDA reports)
PROSTATE CANCER STAGE I ( 3 FDA reports)
PROSTATIC ABSCESS ( 3 FDA reports)
PROSTATIC SPECIFIC ANTIGEN DECREASED ( 3 FDA reports)
PROSTATISM ( 3 FDA reports)
PROTEIN TOTAL ABNORMAL ( 3 FDA reports)
PRURIGO ( 3 FDA reports)
PSYCHOSOMATIC DISEASE ( 3 FDA reports)
PULMONARY EOSINOPHILIA ( 3 FDA reports)
PUNCTATE KERATITIS ( 3 FDA reports)
PUPILLARY DISORDER ( 3 FDA reports)
PYOGENIC GRANULOMA ( 3 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 3 FDA reports)
QUADRIPARESIS ( 3 FDA reports)
RED BLOOD CELLS SEMEN POSITIVE ( 3 FDA reports)
RED BLOOD CELLS URINE ( 3 FDA reports)
REFLUX LARYNGITIS ( 3 FDA reports)
RENAL APLASIA ( 3 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 3 FDA reports)
RESIDUAL URINE VOLUME ( 3 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 3 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 3 FDA reports)
RETINAL ANEURYSM ( 3 FDA reports)
RETINAL ARTERY THROMBOSIS ( 3 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 3 FDA reports)
RETROGRADE EJACULATION ( 3 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 3 FDA reports)
RHINITIS SEASONAL ( 3 FDA reports)
RIB DEFORMITY ( 3 FDA reports)
SCLERAL DISCOLOURATION ( 3 FDA reports)
SCROTAL INFECTION ( 3 FDA reports)
SCROTAL MASS ( 3 FDA reports)
SCROTAL PAIN ( 3 FDA reports)
SEASONAL AFFECTIVE DISORDER ( 3 FDA reports)
SEBACEOUS CARCINOMA ( 3 FDA reports)
SECONDARY HYPOTHYROIDISM ( 3 FDA reports)
SECONDARY PROGRESSIVE MULTIPLE SCLEROSIS ( 3 FDA reports)
SEROSITIS ( 3 FDA reports)
SILICOSIS ( 3 FDA reports)
SKIN HYPOPIGMENTATION ( 3 FDA reports)
SMALL INTESTINAL ULCER HAEMORRHAGE ( 3 FDA reports)
SMEAR CERVIX ABNORMAL ( 3 FDA reports)
SPIDER NAEVUS ( 3 FDA reports)
SPIDER VEIN ( 3 FDA reports)
SPINAL CORD INJURY ( 3 FDA reports)
SPLENIC ARTERY ANEURYSM ( 3 FDA reports)
STAB WOUND ( 3 FDA reports)
STAPHYLOCOCCAL MEDIASTINITIS ( 3 FDA reports)
STARVATION ( 3 FDA reports)
STENT REMOVAL ( 3 FDA reports)
STERNOTOMY ( 3 FDA reports)
STOMACH MASS ( 3 FDA reports)
SUNCT SYNDROME ( 3 FDA reports)
SUTURE RUPTURE ( 3 FDA reports)
SWEAT GLAND INFECTION ( 3 FDA reports)
SYMBOLIC DYSFUNCTION ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 3 FDA reports)
SYSTOLIC DYSFUNCTION ( 3 FDA reports)
TABLET ISSUE ( 3 FDA reports)
TABLET PHYSICAL ISSUE ( 3 FDA reports)
TANDEM GAIT TEST ABNORMAL ( 3 FDA reports)
TEMPERATURE DIFFERENCE OF EXTREMITIES ( 3 FDA reports)
THERAPEUTIC REACTION TIME DECREASED ( 3 FDA reports)
THOUGHT BLOCKING ( 3 FDA reports)
THROMBECTOMY ( 3 FDA reports)
TONGUE HAEMATOMA ( 3 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 3 FDA reports)
TRICHOMONIASIS ( 3 FDA reports)
TRICUSPID VALVE REPAIR ( 3 FDA reports)
TUBERCULOSIS SKIN TEST POSITIVE ( 3 FDA reports)
TUMOUR NECROSIS ( 3 FDA reports)
TYMPANIC MEMBRANE HYPERAEMIA ( 3 FDA reports)
UHTHOFF'S PHENOMENON ( 3 FDA reports)
ULTRASOUND LIVER ( 3 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 3 FDA reports)
UNEQUAL LIMB LENGTH ( 3 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 3 FDA reports)
URETERAL DISORDER ( 3 FDA reports)
URETERAL STENT INSERTION ( 3 FDA reports)
URETHRAL MEATUS STENOSIS ( 3 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 3 FDA reports)
URINE ALCOHOL TEST POSITIVE ( 3 FDA reports)
URINE AMPHETAMINE POSITIVE ( 3 FDA reports)
URINE OXALATE ( 3 FDA reports)
UTERINE ATROPHY ( 3 FDA reports)
VAGINAL DISORDER ( 3 FDA reports)
VAGINAL LESION ( 3 FDA reports)
VAGINITIS ( 3 FDA reports)
VAGUS NERVE DISORDER ( 3 FDA reports)
VARICELLA ( 3 FDA reports)
VENOUS INJURY ( 3 FDA reports)
VENTILATION PERFUSION MISMATCH ( 3 FDA reports)
VERTEBRAL INJURY ( 3 FDA reports)
VESTIBULAR NEURONITIS ( 3 FDA reports)
VICTIM OF CRIME ( 3 FDA reports)
VIRAL PHARYNGITIS ( 3 FDA reports)
VIROLOGIC FAILURE ( 3 FDA reports)
VULVAL CANCER ( 3 FDA reports)
VULVAL LEUKOPLAKIA ( 3 FDA reports)
WATER INTOXICATION ( 3 FDA reports)
WEIGHT ( 3 FDA reports)
WHITE BLOOD CELL COUNT ( 3 FDA reports)
WRIST SURGERY ( 3 FDA reports)
X-RAY LIMB ABNORMAL ( 3 FDA reports)
MYOCARDIAL REPERFUSION INJURY ( 2 FDA reports)
MYOCLONIC EPILEPSY ( 2 FDA reports)
MYOTONIA ( 2 FDA reports)
NAIL BED BLEEDING ( 2 FDA reports)
NASAL ABSCESS ( 2 FDA reports)
NASAL NECROSIS ( 2 FDA reports)
NASAL SINUS DRAINAGE ( 2 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 2 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 2 FDA reports)
NEMATODIASIS ( 2 FDA reports)
NEPHRITIC SYNDROME ( 2 FDA reports)
NEPHROSTOMY TUBE PLACEMENT ( 2 FDA reports)
NERVE ROOT LESION ( 2 FDA reports)
NEUTROPHIL PELGER-HUET ANOMALY PRESENT ( 2 FDA reports)
NICOTINAMIDE DECREASED ( 2 FDA reports)
NON-ALCOHOLIC STEATOHEPATITIS ( 2 FDA reports)
NON-OBSTRUCTIVE CARDIOMYOPATHY ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE II ( 2 FDA reports)
OCCULT BLOOD ( 2 FDA reports)
OCULAR MYASTHENIA ( 2 FDA reports)
OEDEMA DUE TO HEPATIC DISEASE ( 2 FDA reports)
OEDEMATOUS PANCREATITIS ( 2 FDA reports)
OESOPHAGEAL INFECTION ( 2 FDA reports)
OESOPHAGEAL RUPTURE ( 2 FDA reports)
OESOPHAGITIS CHEMICAL ( 2 FDA reports)
OLIGODENDROGLIOMA ( 2 FDA reports)
ONCOLOGIC COMPLICATION ( 2 FDA reports)
OOPHORECTOMY ( 2 FDA reports)
OPIATES POSITIVE ( 2 FDA reports)
OPTIC NERVE SHEATH HAEMORRHAGE ( 2 FDA reports)
ORAL DYSAESTHESIA ( 2 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 2 FDA reports)
ORAL MUCOSAL ERUPTION ( 2 FDA reports)
ORAL NEOPLASM BENIGN ( 2 FDA reports)
ORCHITIS NONINFECTIVE ( 2 FDA reports)
ORGASM ABNORMAL ( 2 FDA reports)
OROPHARYNGEAL NEOPLASM BENIGN ( 2 FDA reports)
OROPHARYNGEAL PLAQUE ( 2 FDA reports)
ORTHOSTATIC HYPERTENSION ( 2 FDA reports)
OSCILLOPSIA ( 2 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 2 FDA reports)
OTOTOXICITY ( 2 FDA reports)
OVERGROWTH BACTERIAL ( 2 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 2 FDA reports)
PALPABLE PURPURA ( 2 FDA reports)
PANCREATIC DUCT DILATATION ( 2 FDA reports)
PANCREATIC LEAK ( 2 FDA reports)
PANCREATITIS BACTERIAL ( 2 FDA reports)
PANCREATOLITHIASIS ( 2 FDA reports)
PAPILLARY THYROID CANCER ( 2 FDA reports)
PAPILLOMA ( 2 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 2 FDA reports)
PARAMNESIA ( 2 FDA reports)
PARANASAL BIOPSY ABNORMAL ( 2 FDA reports)
PARANASAL CYST ( 2 FDA reports)
PARANOID PERSONALITY DISORDER ( 2 FDA reports)
PARASPINAL ABSCESS ( 2 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 2 FDA reports)
PAROTID ABSCESS ( 2 FDA reports)
PAROTID GLAND INFLAMMATION ( 2 FDA reports)
PARTIAL SEIZURES WITH SECONDARY GENERALISATION ( 2 FDA reports)
PASSIVE SMOKING ( 2 FDA reports)
PCO2 ABNORMAL ( 2 FDA reports)
PELVIC DISCOMFORT ( 2 FDA reports)
PELVIC FLUID COLLECTION ( 2 FDA reports)
PELVIC PERITONEAL ADHESIONS ( 2 FDA reports)
PELVIC PROLAPSE ( 2 FDA reports)
PELVIC VENOUS THROMBOSIS ( 2 FDA reports)
PEPTOSTREPTOCOCCUS INFECTION ( 2 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 2 FDA reports)
PERICARDIAL EXCISION ( 2 FDA reports)
PERIDIVERTICULAR ABSCESS ( 2 FDA reports)
PERINEAL CYST ( 2 FDA reports)
PERINEPHRIC EFFUSION ( 2 FDA reports)
PERIODONTAL INFECTION ( 2 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 2 FDA reports)
PERITONEAL CLOUDY EFFLUENT ( 2 FDA reports)
PERITONEAL EFFLUENT ABNORMAL ( 2 FDA reports)
PERITONEAL EFFUSION ( 2 FDA reports)
PERITONEAL FIBROSIS ( 2 FDA reports)
PERITONITIS SCLEROSING ( 2 FDA reports)
PERITONSILLAR ABSCESS ( 2 FDA reports)
PERSEVERATION ( 2 FDA reports)
PHAEOCHROMOCYTOMA CRISIS ( 2 FDA reports)
PHARYNGEAL MASS ( 2 FDA reports)
PHARYNGOLARYNGEAL DISCOMFORT ( 2 FDA reports)
PHARYNX DISCOMFORT ( 2 FDA reports)
PHLEBITIS DEEP ( 2 FDA reports)
PHONOPHOBIA ( 2 FDA reports)
PHOSPHORUS METABOLISM DISORDER ( 2 FDA reports)
PHYSICAL PRODUCT LABEL ISSUE ( 2 FDA reports)
PILONIDAL CYST ( 2 FDA reports)
PITUITARY HAEMORRHAGE ( 2 FDA reports)
PITUITARY TUMOUR RECURRENT ( 2 FDA reports)
PITUITARY TUMOUR REMOVAL ( 2 FDA reports)
PITYRIASIS ROSEA ( 2 FDA reports)
PLASMA CELLS INCREASED ( 2 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 2 FDA reports)
PLATELET TRANSFUSION ( 2 FDA reports)
PLEURODESIS ( 2 FDA reports)
PLICATED TONGUE ( 2 FDA reports)
PNEUMATURIA ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 2 FDA reports)
PNEUMONECTOMY ( 2 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 2 FDA reports)
PNEUMONIA ESCHERICHIA ( 2 FDA reports)
POIKILOCYTOSIS ( 2 FDA reports)
POLYCHONDRITIS ( 2 FDA reports)
PORCELAIN GALLBLADDER ( 2 FDA reports)
POST PROCEDURAL OEDEMA ( 2 FDA reports)
POST PROCEDURAL VOMITING ( 2 FDA reports)
POST-TRAUMATIC HEADACHE ( 2 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 2 FDA reports)
POSTOPERATIVE ABSCESS ( 2 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 2 FDA reports)
PREMATURE DELIVERY ( 2 FDA reports)
PREMENSTRUAL SYNDROME ( 2 FDA reports)
PRESBYOESOPHAGUS ( 2 FDA reports)
PRIMARY HYPOTHYROIDISM ( 2 FDA reports)
PRINZMETAL ANGINA ( 2 FDA reports)
PRODUCT DEPOSIT ( 2 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 2 FDA reports)
PROSTATIC HAEMORRHAGE ( 2 FDA reports)
PROSTATIC OBSTRUCTION ( 2 FDA reports)
PROSTATIC PAIN ( 2 FDA reports)
PROTEIN S DECREASED ( 2 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 2 FDA reports)
PSEUDOENDOPHTHALMITIS ( 2 FDA reports)
PSEUDOPHAKIA ( 2 FDA reports)
PSYCHIATRIC EVALUATION ABNORMAL ( 2 FDA reports)
PSYCHOGENIC PAIN DISORDER ( 2 FDA reports)
PSYCHOMOTOR AGITATION ( 2 FDA reports)
PSYCHOMOTOR RETARDATION ( 2 FDA reports)
PSYCHOTIC DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
PULMONARY AIR LEAKAGE ( 2 FDA reports)
PULMONARY ARTERIAL PRESSURE ABNORMAL ( 2 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 2 FDA reports)
PULMONARY BULLA ( 2 FDA reports)
PULMONARY HYPOPLASIA ( 2 FDA reports)
PULMONARY VENOUS THROMBOSIS ( 2 FDA reports)
PULSE PRESSURE INCREASED ( 2 FDA reports)
PYELONEPHRITIS CHRONIC ( 2 FDA reports)
QUADRIPLEGIA ( 2 FDA reports)
RADIAL NERVE PALSY ( 2 FDA reports)
RADIAL PULSE ABNORMAL ( 2 FDA reports)
RASH FOLLICULAR ( 2 FDA reports)
REACTION TO AZO-DYES ( 2 FDA reports)
REACTION TO PRESERVATIVES ( 2 FDA reports)
RECTAL ADENOMA ( 2 FDA reports)
RECTAL CANCER METASTATIC ( 2 FDA reports)
RECURRING SKIN BOILS ( 2 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
RED BLOOD CELL MORPHOLOGY ABNORMAL ( 2 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 2 FDA reports)
RED CELL DISTRIBUTION WIDTH ABNORMAL ( 2 FDA reports)
REFRACTORY ANAEMIA WITH RINGED SIDEROBLASTS ( 2 FDA reports)
REGURGITATION OF FOOD ( 2 FDA reports)
RENAL ARTERY DISSECTION ( 2 FDA reports)
RENAL ARTERY FIBROMUSCULAR DYSPLASIA ( 2 FDA reports)
RENAL ARTERY THROMBOSIS ( 2 FDA reports)
RENAL CELL CARCINOMA STAGE IV ( 2 FDA reports)
RENAL NECROSIS ( 2 FDA reports)
RENAL TUMOUR EXCISION ( 2 FDA reports)
RENAL VEIN OCCLUSION ( 2 FDA reports)
RENIN INCREASED ( 2 FDA reports)
REPRODUCTIVE TRACT DISORDER ( 2 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
RETINAL ARTERY EMBOLISM ( 2 FDA reports)
RETINITIS PIGMENTOSA ( 2 FDA reports)
RETROGRADE AMNESIA ( 2 FDA reports)
RETROPERITONEAL FIBROSIS ( 2 FDA reports)
RHEUMATOID FACTOR ( 2 FDA reports)
RHEUMATOID LUNG ( 2 FDA reports)
ROTAVIRUS INFECTION ( 2 FDA reports)
SACRAL PAIN ( 2 FDA reports)
SALIVA DISCOLOURATION ( 2 FDA reports)
SALIVARY GLAND MASS ( 2 FDA reports)
SALIVARY GLAND NEOPLASM ( 2 FDA reports)
SALPINGECTOMY ( 2 FDA reports)
SCAN ADRENAL GLAND ABNORMAL ( 2 FDA reports)
SCAN LYMPH NODES ( 2 FDA reports)
SCAN MYOCARDIAL PERFUSION ( 2 FDA reports)
SCAPHOCEPHALY ( 2 FDA reports)
SCHIZOPHRENIA, DISORGANISED TYPE ( 2 FDA reports)
SCHIZOPHRENIA, UNDIFFERENTIATED TYPE ( 2 FDA reports)
SCHIZOPHRENIFORM DISORDER ( 2 FDA reports)
SCLERAL PIGMENTATION ( 2 FDA reports)
SCROTAL HAEMATOCOELE ( 2 FDA reports)
SEBACEOUS ADENOMA ( 2 FDA reports)
SEBORRHOEA ( 2 FDA reports)
SENSORY GANGLIONITIS ( 2 FDA reports)
SEPTOPLASTY ( 2 FDA reports)
SERUM SEROTONIN INCREASED ( 2 FDA reports)
SHOPLIFTING ( 2 FDA reports)
SINGLE VESSEL BYPASS GRAFT ( 2 FDA reports)
SINUS ANTROSTOMY ( 2 FDA reports)
SINUSITIS BACTERIAL ( 2 FDA reports)
SINUSITIS FUNGAL ( 2 FDA reports)
SKIN BLEEDING ( 2 FDA reports)
SKIN DYSTROPHY ( 2 FDA reports)
SKIN FRAGILITY ( 2 FDA reports)
SKULL X-RAY ABNORMAL ( 2 FDA reports)
SLOW RESPONSE TO STIMULI ( 2 FDA reports)
SMALL CELL CARCINOMA ( 2 FDA reports)
SMALL INTESTINE CARCINOMA METASTATIC ( 2 FDA reports)
SODIUM RETENTION ( 2 FDA reports)
SOFT TISSUE ATROPHY ( 2 FDA reports)
SPERM COUNT DECREASED ( 2 FDA reports)
SPERM COUNT ZERO ( 2 FDA reports)
SPINAL CORD HAEMORRHAGE ( 2 FDA reports)
SPINAL CORD OEDEMA ( 2 FDA reports)
SPINAL SHOCK ( 2 FDA reports)
SPINAL X-RAY ABNORMAL ( 2 FDA reports)
SPIROMETRY ABNORMAL ( 2 FDA reports)
SPLEEN CONGESTION ( 2 FDA reports)
SPLENIC ABSCESS ( 2 FDA reports)
SPLENIC VEIN OCCLUSION ( 2 FDA reports)
STENT EMBOLISATION ( 2 FDA reports)
STEREOTYPY ( 2 FDA reports)
STERNAL INJURY ( 2 FDA reports)
STILLBIRTH ( 2 FDA reports)
STITCH ABSCESS ( 2 FDA reports)
STOMACH SCAN ABNORMAL ( 2 FDA reports)
SUBACUTE ENDOCARDITIS ( 2 FDA reports)
SUBCLAVIAN ARTERY THROMBOSIS ( 2 FDA reports)
SUDDEN VISUAL LOSS ( 2 FDA reports)
SWEAT GLAND DISORDER ( 2 FDA reports)
SYSTEMIC SCLEROSIS ( 2 FDA reports)
TENOSYNOVITIS STENOSANS ( 2 FDA reports)
TESTICULAR FAILURE ( 2 FDA reports)
TESTICULAR MASS ( 2 FDA reports)
TESTICULAR NEOPLASM ( 2 FDA reports)
THALASSAEMIA ( 2 FDA reports)
THEFT ( 2 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 2 FDA reports)
THERAPEUTIC RESPONSE PROLONGED ( 2 FDA reports)
THERMOHYPERAESTHESIA ( 2 FDA reports)
THIRST DECREASED ( 2 FDA reports)
THROMBIN TIME ABNORMAL ( 2 FDA reports)
THYMIC CANCER METASTATIC ( 2 FDA reports)
THYMOMA ( 2 FDA reports)
THYROTOXIC CRISIS ( 2 FDA reports)
THYROXINE DECREASED ( 2 FDA reports)
THYROXINE FREE INCREASED ( 2 FDA reports)
TINEA VERSICOLOUR ( 2 FDA reports)
TINEL'S SIGN ( 2 FDA reports)
TONGUE BLACK HAIRY ( 2 FDA reports)
TONGUE PIGMENTATION ( 2 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO ( 2 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO ABNORMAL ( 2 FDA reports)
TOXIC NEUROPATHY ( 2 FDA reports)
TOXIC OPTIC NEUROPATHY ( 2 FDA reports)
TRACHEOSTOMY MALFUNCTION ( 2 FDA reports)
TRANCE ( 2 FDA reports)
TRANSAMINASES ABNORMAL ( 2 FDA reports)
TRANSFERRIN SATURATION INCREASED ( 2 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 2 FDA reports)
TRICHIASIS ( 2 FDA reports)
TRICHOTILLOMANIA ( 2 FDA reports)
TROUSSEAU'S SYNDROME ( 2 FDA reports)
TRYPTASE ( 2 FDA reports)
TUMOUR ASSOCIATED FEVER ( 2 FDA reports)
TUMOUR COMPRESSION ( 2 FDA reports)
TYMPANOSCLEROSIS ( 2 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 2 FDA reports)
UMBILICAL HERNIA PERFORATION ( 2 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 2 FDA reports)
URAEMIC ENCEPHALOPATHY ( 2 FDA reports)
URETERAL NEOPLASM ( 2 FDA reports)
URETERIC CANCER ( 2 FDA reports)
URETHRAL CARUNCLE ( 2 FDA reports)
URETHRAL POLYP ( 2 FDA reports)
URETHRAL VALVES ( 2 FDA reports)
URINARY TRACT PAIN ( 2 FDA reports)
URINE OSMOLARITY INCREASED ( 2 FDA reports)
URINE OUTPUT ( 2 FDA reports)
UROBILIN URINE PRESENT ( 2 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 2 FDA reports)
UTERINE CYST ( 2 FDA reports)
VACCINATION FAILURE ( 2 FDA reports)
VAGINAL BURNING SENSATION ( 2 FDA reports)
VAGINAL CANCER ( 2 FDA reports)
VAGINAL MYCOSIS ( 2 FDA reports)
VAGINAL PROLAPSE ( 2 FDA reports)
VAGINAL ULCERATION ( 2 FDA reports)
VASCULAR PUNCTURE SITE SEALING ( 2 FDA reports)
VASOPLEGIA SYNDROME ( 2 FDA reports)
VENOUS HAEMORRHAGE ( 2 FDA reports)
VENTRICULAR INTERNAL DIAMETER ABNORMAL ( 2 FDA reports)
VERBIGERATION ( 2 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 2 FDA reports)
VESSEL PUNCTURE SITE HAEMORRHAGE ( 2 FDA reports)
VESSEL PUNCTURE SITE REACTION ( 2 FDA reports)
VESTIBULITIS ( 2 FDA reports)
VIBRATION TEST ABNORMAL ( 2 FDA reports)
VICTIM OF ABUSE ( 2 FDA reports)
VIITH NERVE INJURY ( 2 FDA reports)
VIRAL LABYRINTHITIS ( 2 FDA reports)
VIRAL RASH ( 2 FDA reports)
VIRUS STOOL TEST POSITIVE ( 2 FDA reports)
VISCERAL CONGESTION ( 2 FDA reports)
VISUAL ACUITY TESTS ABNORMAL ( 2 FDA reports)
VISUAL PATHWAY DISORDER ( 2 FDA reports)
VOCAL CORD POLYPECTOMY ( 2 FDA reports)
VULVAL ABSCESS ( 2 FDA reports)
VULVAL DISORDER ( 2 FDA reports)
VULVOVAGINAL SWELLING ( 2 FDA reports)
WART EXCISION ( 2 FDA reports)
WEIGHT CONTROL ( 2 FDA reports)
WEIGHT DECREASE NEONATAL ( 2 FDA reports)
WHIPLASH INJURY ( 2 FDA reports)
WITHDRAWAL HYPERTENSION ( 2 FDA reports)
WITHDRAWAL OF LIFE SUPPORT ( 2 FDA reports)
WOUND DECOMPOSITION ( 2 FDA reports)
ABDOMINAL AORTIC BRUIT ( 2 FDA reports)
ABDOMINAL BRUIT ( 2 FDA reports)
ABDOMINAL HERNIA OBSTRUCTIVE ( 2 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 2 FDA reports)
ABNORMAL CLOTTING FACTOR ( 2 FDA reports)
ACANTHOSIS ( 2 FDA reports)
ACID FAST BACILLI INFECTION ( 2 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 2 FDA reports)
ACUTE PHASE REACTION ( 2 FDA reports)
ACUTE STRESS DISORDER ( 2 FDA reports)
ADAMS-STOKES SYNDROME ( 2 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 2 FDA reports)
ADNEXA UTERI CYST ( 2 FDA reports)
ADNEXA UTERI PAIN ( 2 FDA reports)
ADRENAL CARCINOMA ( 2 FDA reports)
ADRENALITIS ( 2 FDA reports)
AGITATION POSTOPERATIVE ( 2 FDA reports)
AGRAPHIA ( 2 FDA reports)
ALBUMIN URINE ( 2 FDA reports)
ALCOHOL INTOLERANCE ( 2 FDA reports)
ALKALOSIS ( 2 FDA reports)
ALLERGY TEST POSITIVE ( 2 FDA reports)
ALLERGY TO CHEMICALS ( 2 FDA reports)
ALVEOLITIS FIBROSING ( 2 FDA reports)
AMBLYOPIA STRABISMIC ( 2 FDA reports)
AMNESTIC DISORDER ( 2 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 2 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 2 FDA reports)
ANAL POLYP ( 2 FDA reports)
ANAL SPHINCTER HYPERTONIA ( 2 FDA reports)
ANASTOMOTIC LEAK ( 2 FDA reports)
ANASTOMOTIC ULCER ( 2 FDA reports)
ANGIODYSPLASIA ( 2 FDA reports)
ANGIOFIBROMA ( 2 FDA reports)
ANHIDROSIS ( 2 FDA reports)
ANOMALY OF EXTERNAL EAR CONGENITAL ( 2 FDA reports)
ANTERIOR CHAMBER INFLAMMATION ( 2 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 2 FDA reports)
ANTI-SS-A ANTIBODY POSITIVE ( 2 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 2 FDA reports)
ANTICOAGULANT THERAPY ( 2 FDA reports)
ANTICONVULSANT TOXICITY ( 2 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 2 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY INCREASED ( 2 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ( 2 FDA reports)
AORTITIS ( 2 FDA reports)
AORTOGRAM ABNORMAL ( 2 FDA reports)
APLASIA ( 2 FDA reports)
APPENDICEAL ABSCESS ( 2 FDA reports)
APPLICATION SITE BLEEDING ( 2 FDA reports)
APPLICATION SITE DISCHARGE ( 2 FDA reports)
APPLICATION SITE OEDEMA ( 2 FDA reports)
APPLICATION SITE PERSPIRATION ( 2 FDA reports)
APPLICATION SITE PUSTULES ( 2 FDA reports)
APPLICATION SITE SCAR ( 2 FDA reports)
APPLICATION SITE ULCER ( 2 FDA reports)
ARCUS LIPOIDES ( 2 FDA reports)
ARTERIAL INSUFFICIENCY ( 2 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 2 FDA reports)
ARTERIOGRAM CORONARY ( 2 FDA reports)
ARTERIOPATHIC DISEASE ( 2 FDA reports)
ASPERGILLOMA ( 2 FDA reports)
ASPIRATION BRONCHIAL ( 2 FDA reports)
ASPIRATION PLEURAL CAVITY ABNORMAL ( 2 FDA reports)
ASTHMATIC CRISIS ( 2 FDA reports)
ASYMPTOMATIC BACTERIURIA ( 2 FDA reports)
ATELECTASIS NEONATAL ( 2 FDA reports)
ATOPY ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 2 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 2 FDA reports)
BACILLUS INFECTION ( 2 FDA reports)
BACTERIAL TEST ( 2 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
BASAL GANGLIA STROKE ( 2 FDA reports)
BENIGN LUNG NEOPLASM ( 2 FDA reports)
BENIGN NEOPLASM OF PROSTATE ( 2 FDA reports)
BENIGN NEOPLASM OF SKIN ( 2 FDA reports)
BENIGN OESOPHAGEAL NEOPLASM ( 2 FDA reports)
BENIGN VAGINAL NEOPLASM ( 2 FDA reports)
BETA-2 GLYCOPROTEIN ANTIBODY POSITIVE ( 2 FDA reports)
BIFASCICULAR BLOCK ( 2 FDA reports)
BILIARY NEOPLASM ( 2 FDA reports)
BILIARY TRACT OPERATION ( 2 FDA reports)
BILOMA ( 2 FDA reports)
BIOPSY ARTERY ( 2 FDA reports)
BIOPSY INTESTINE ABNORMAL ( 2 FDA reports)
BIOPSY PROSTATE ABNORMAL ( 2 FDA reports)
BLADDER CANCER STAGE I, WITHOUT CANCER IN SITU ( 2 FDA reports)
BLADDER CANDIDIASIS ( 2 FDA reports)
BLADDER DISTENSION ( 2 FDA reports)
BLADDER DYSPLASIA ( 2 FDA reports)
BLADDER NECROSIS ( 2 FDA reports)
BLADDER NEOPLASM SURGERY ( 2 FDA reports)
BLADDER PAPILLOMA ( 2 FDA reports)
BLEEDING VARICOSE VEIN ( 2 FDA reports)
BLEPHAROPLASTY ( 2 FDA reports)
BLINDNESS CORTICAL ( 2 FDA reports)
BLISTER INFECTED ( 2 FDA reports)
BLOOD ALDOSTERONE DECREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 2 FDA reports)
BLOOD ALUMINIUM INCREASED ( 2 FDA reports)
BLOOD ANTIDIURETIC HORMONE DECREASED ( 2 FDA reports)
BLOOD BILIRUBIN DECREASED ( 2 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 2 FDA reports)
BLOOD CORTISOL DECREASED ( 2 FDA reports)
BLOOD CREATINE DECREASED ( 2 FDA reports)
BLOOD GROWTH HORMONE INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 2 FDA reports)
BLOOD IRON ( 2 FDA reports)
BLOOD IRON ABNORMAL ( 2 FDA reports)
BLOOD KETONE BODY INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 2 FDA reports)
BLOOD LACTIC ACID DECREASED ( 2 FDA reports)
BLOOD OESTROGEN INCREASED ( 2 FDA reports)
BLOOD PH ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE AMBULATORY ABNORMAL ( 2 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 2 FDA reports)
BLOOD PROLACTIN ABNORMAL ( 2 FDA reports)
BLOOD TESTOSTERONE ABNORMAL ( 2 FDA reports)
BLOOD TESTOSTERONE FREE DECREASED ( 2 FDA reports)
BODY HEIGHT INCREASED ( 2 FDA reports)
BONE CALLUS EXCESSIVE ( 2 FDA reports)
BONE MARROW PLASMACYTE COUNT INCREASED ( 2 FDA reports)
BOTULISM ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE ( 2 FDA reports)
BRAIN NEOPLASM BENIGN ( 2 FDA reports)
BREAST COSMETIC SURGERY ( 2 FDA reports)
BREAST INDURATION ( 2 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 2 FDA reports)
BREECH PRESENTATION ( 2 FDA reports)
BRONCHIAL IRRITATION ( 2 FDA reports)
BRONCHIAL OBSTRUCTION ( 2 FDA reports)
BRONCHITIS MORAXELLA ( 2 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 2 FDA reports)
BUDD-CHIARI SYNDROME ( 2 FDA reports)
BUNION OPERATION ( 2 FDA reports)
BURSITIS INFECTIVE STAPHYLOCOCCAL ( 2 FDA reports)
CAFE AU LAIT SPOTS ( 2 FDA reports)
CALCIFIC DEPOSITS REMOVAL ( 2 FDA reports)
CALCIUM IONISED ABNORMAL ( 2 FDA reports)
CAMPYLOBACTER GASTROENTERITIS ( 2 FDA reports)
CAMPYLOBACTER INTESTINAL INFECTION ( 2 FDA reports)
CAMPYLOBACTER TEST POSITIVE ( 2 FDA reports)
CANCER PAIN ( 2 FDA reports)
CANDIDA PNEUMONIA ( 2 FDA reports)
CAPILLARY FRAGILITY ( 2 FDA reports)
CAPSULE PHYSICAL ISSUE ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 27.29 INCREASED ( 2 FDA reports)
CARCINOID TUMOUR OF THE STOMACH ( 2 FDA reports)
CARDIAC CIRRHOSIS ( 2 FDA reports)
CARDIAC ELECTROPHYSIOLOGIC STUDY ABNORMAL ( 2 FDA reports)
CARDIAC ENZYMES ( 2 FDA reports)
CARDIAC RESYNCHRONISATION THERAPY ( 2 FDA reports)
CARDIAC STRESS TEST ( 2 FDA reports)
CARDIAC VALVE ABSCESS ( 2 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL ( 2 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 2 FDA reports)
CARDIOPLEGIA ( 2 FDA reports)
CARDIOPULMONARY BYPASS ( 2 FDA reports)
CARNITINE DEFICIENCY ( 2 FDA reports)
CATARACT SUBCAPSULAR ( 2 FDA reports)
CATHETER SITE OEDEMA ( 2 FDA reports)
CATHETER SITE SWELLING ( 2 FDA reports)
CELLS IN URINE ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 2 FDA reports)
CEREBELLAR ATAXIA ( 2 FDA reports)
CEREBRAL ARTERITIS ( 2 FDA reports)
CEREBRAL CIRCULATORY FAILURE ( 2 FDA reports)
CEREBRAL REVASCULARISATION SYNANGIOSIS ( 2 FDA reports)
CEREBROVASCULAR STENOSIS ( 2 FDA reports)
CERVICAL SPINE FLATTENING ( 2 FDA reports)
CHALAZION ( 2 FDA reports)
CHEMICAL POISONING ( 2 FDA reports)
CHEST WALL ABSCESS ( 2 FDA reports)
CHEYNE-STOKES RESPIRATION ( 2 FDA reports)
CHLORACNE ( 2 FDA reports)
CHOLELITHOTOMY ( 2 FDA reports)
CHORIORETINITIS ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA STAGE 2 ( 2 FDA reports)
CLONIC CONVULSION ( 2 FDA reports)
COAGULATION FACTOR DECREASED ( 2 FDA reports)
COELIAC ARTERY STENOSIS ( 2 FDA reports)
COLD TYPE HAEMOLYTIC ANAEMIA ( 2 FDA reports)
COLECTOMY TOTAL ( 2 FDA reports)
COLLATERAL CIRCULATION ( 2 FDA reports)
COLON CANCER RECURRENT ( 2 FDA reports)
COLON DYSPLASIA ( 2 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 2 FDA reports)
COMPLICATION OF DEVICE REMOVAL ( 2 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 2 FDA reports)
CONGENITAL HYDRONEPHROSIS ( 2 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 2 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 2 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 2 FDA reports)
COOMBS TEST POSITIVE ( 2 FDA reports)
CORNEAL ABRASION ( 2 FDA reports)
CORNEAL DECOMPENSATION ( 2 FDA reports)
CORNEAL OPACITY ( 2 FDA reports)
CORNEAL PERFORATION ( 2 FDA reports)
CORNEAL REFLEX DECREASED ( 2 FDA reports)
CORNEAL TRANSPLANT ( 2 FDA reports)
CORONARY REVASCULARISATION ( 2 FDA reports)
CORYNEBACTERIUM INFECTION ( 2 FDA reports)
CRANIOCEREBRAL INJURY ( 2 FDA reports)
CREST SYNDROME ( 2 FDA reports)
CRITICAL ILLNESS POLYNEUROPATHY ( 2 FDA reports)
CRUSH INJURY ( 2 FDA reports)
CRYSTAL ARTHROPATHY ( 2 FDA reports)
CRYSTAL URINE ( 2 FDA reports)
CRYSTAL URINE PRESENT ( 2 FDA reports)
CUTANEOUS SARCOIDOSIS ( 2 FDA reports)
CUTIS LAXA ( 2 FDA reports)
CYCLOTHYMIC DISORDER ( 2 FDA reports)
CYSTITIS KLEBSIELLA ( 2 FDA reports)
CYSTOSTOMY ( 2 FDA reports)
CYTOMEGALOVIRUS SYNDROME ( 2 FDA reports)
CYTOMEGALOVIRUS TEST ( 2 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 2 FDA reports)
DANDRUFF ( 2 FDA reports)
DECREASED VIBRATORY SENSE ( 2 FDA reports)
DEFICIENCY ANAEMIA ( 2 FDA reports)
DEFORMITY THORAX ( 2 FDA reports)
DEGENERATION OF UTERINE LEIOMYOMA ( 2 FDA reports)
DELAYED FONTANELLE CLOSURE ( 2 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 2 FDA reports)
DELUSIONAL PERCEPTION ( 2 FDA reports)
DEPENDENT RUBOR ( 2 FDA reports)
DERMATITIS HERPETIFORMIS ( 2 FDA reports)
DETACHMENT OF MACULAR RETINAL PIGMENT EPITHELIUM ( 2 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 2 FDA reports)
DEVICE COMPONENT ISSUE ( 2 FDA reports)
DEVICE ELECTRICAL FINDING ( 2 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 2 FDA reports)
DIABETIC GASTROPATHY ( 2 FDA reports)
DIABETIC HYPERGLYCAEMIC COMA ( 2 FDA reports)
DIABETIC NEUROPATHIC ULCER ( 2 FDA reports)
DIABETIC RETINAL OEDEMA ( 2 FDA reports)
DIAGNOSTIC PROCEDURE ( 2 FDA reports)
DIAPHRAGM MUSCLE WEAKNESS ( 2 FDA reports)
DIASTOLIC HYPERTENSION ( 2 FDA reports)
DISABLED RELATIVE ( 2 FDA reports)
DIVORCED ( 2 FDA reports)
DREAMY STATE ( 2 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 2 FDA reports)
DRUG INTERACTION INHIBITION ( 2 FDA reports)
DRUG USE FOR UNKNOWN INDICATION ( 2 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 2 FDA reports)
DYSCALCULIA ( 2 FDA reports)
DYSENTERY ( 2 FDA reports)
EARLY MORNING AWAKENING ( 2 FDA reports)
ECLAMPSIA ( 2 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM R ON T PHENOMENON ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE INCREASED ( 2 FDA reports)
ELECTROCUTION ( 2 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 2 FDA reports)
ENDOMETRITIS ( 2 FDA reports)
ENDOSCOPY ABNORMAL ( 2 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 2 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 2 FDA reports)
ENTERAL NUTRITION ( 2 FDA reports)
ENTEROBACTER BACTERAEMIA ( 2 FDA reports)
ENTEROBACTER TEST POSITIVE ( 2 FDA reports)
ENTROPION ( 2 FDA reports)
ENZYME LEVEL INCREASED ( 2 FDA reports)
EOSINOPHILS URINE PRESENT ( 2 FDA reports)
EPIDERMAL NAEVUS ( 2 FDA reports)
EPIGLOTTIC CARCINOMA ( 2 FDA reports)
EPIGLOTTIC CYST ( 2 FDA reports)
ETHMOID SINUS SURGERY ( 2 FDA reports)
EX-SMOKER ( 2 FDA reports)
EX-TOBACCO USER ( 2 FDA reports)
EXCESSIVE SKIN ( 2 FDA reports)
EXCITABILITY ( 2 FDA reports)
EXERCISE TEST ABNORMAL ( 2 FDA reports)
EXPOSURE TO COMMUNICABLE DISEASE ( 2 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 2 FDA reports)
EYE EXCISION ( 2 FDA reports)
EYE INFECTION BACTERIAL ( 2 FDA reports)
EYE INFECTION VIRAL ( 2 FDA reports)
EYE REDNESS ( 2 FDA reports)
FAECAL VOLUME DECREASED ( 2 FDA reports)
FAECAL VOMITING ( 2 FDA reports)
FAILURE TO ANASTOMOSE ( 2 FDA reports)
FASCIOTOMY ( 2 FDA reports)
FEBRILE CONVULSION ( 2 FDA reports)
FEMALE PATTERN BALDNESS ( 2 FDA reports)
FIBRIN D DIMER ( 2 FDA reports)
FIBRINOLYSIS INCREASED ( 2 FDA reports)
FLIGHT OF IDEAS ( 2 FDA reports)
FLUID IMBALANCE ( 2 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 2 FDA reports)
FOETAL GROWTH RESTRICTION ( 2 FDA reports)
FOETOR HEPATICUS ( 2 FDA reports)
FOLATE DEFICIENCY ( 2 FDA reports)
FONTANELLE DEPRESSED ( 2 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 2 FDA reports)
FOREIGN BODY REACTION ( 2 FDA reports)
FULL BLOOD COUNT INCREASED ( 2 FDA reports)
FUNGAL RASH ( 2 FDA reports)
FUNGUS CULTURE POSITIVE ( 2 FDA reports)
FUSARIUM INFECTION ( 2 FDA reports)
GALLBLADDER OEDEMA ( 2 FDA reports)
GALLBLADDER PERFORATION ( 2 FDA reports)
GALLSTONE ILEUS ( 2 FDA reports)
GASTRIC HYPOMOTILITY ( 2 FDA reports)
GASTRIC MUCOSA ERYTHEMA ( 2 FDA reports)
GASTRIC VARICES HAEMORRHAGE ( 2 FDA reports)
GASTRITIS VIRAL ( 2 FDA reports)
GASTRODUODENITIS ( 2 FDA reports)
GASTRODUODENITIS HAEMORRHAGIC ( 2 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 2 FDA reports)
GASTROENTERITIS NORWALK VIRUS ( 2 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA HAEMORRHAGIC ( 2 FDA reports)
GASTROINTESTINAL CANCER METASTATIC ( 2 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 2 FDA reports)
GASTROINTESTINAL FISTULA ( 2 FDA reports)
GENE MUTATION ( 2 FDA reports)
GENITAL CYST ( 2 FDA reports)
GENITAL DISCOMFORT ( 2 FDA reports)
GENITAL HYPOAESTHESIA ( 2 FDA reports)
GENITAL INFECTION FUNGAL ( 2 FDA reports)
GENITAL PRURITUS FEMALE ( 2 FDA reports)
GENITAL PRURITUS MALE ( 2 FDA reports)
GENITAL TRACT INFLAMMATION ( 2 FDA reports)
GENITAL ULCERATION ( 2 FDA reports)
GESTATIONAL HYPERTENSION ( 2 FDA reports)
GINGIVAL BLISTER ( 2 FDA reports)
GINGIVAL HYPERPIGMENTATION ( 2 FDA reports)
GLOMERULONEPHRITIS ACUTE ( 2 FDA reports)
GLOSSOPHARYNGEAL NEURALGIA ( 2 FDA reports)
GLOSSOPTOSIS ( 2 FDA reports)
GLYCOGEN STORAGE DISEASE TYPE II ( 2 FDA reports)
GLYCOPEPTIDE ANTIBIOTIC RESISTANT ENTEROCOCCAL INFECTION ( 2 FDA reports)
GRANULOMA SKIN ( 2 FDA reports)
GROIN INFECTION ( 2 FDA reports)
GROWTH OF EYELASHES ( 2 FDA reports)
GUTTATE PSORIASIS ( 2 FDA reports)
HAEMATURIA TRAUMATIC ( 2 FDA reports)
HAEMOPHILUS SEPSIS ( 2 FDA reports)
HAEMORRHAGIC URTICARIA ( 2 FDA reports)
HAEMOSIDEROSIS ( 2 FDA reports)
HEART BLOCK CONGENITAL ( 2 FDA reports)
HEART VALVE STENOSIS ( 2 FDA reports)
HEAVY EXPOSURE TO ULTRAVIOLET LIGHT ( 2 FDA reports)
HEPATIC ENZYME DECREASED ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT RECURRENT ( 2 FDA reports)
HEPATIC SIDEROSIS ( 2 FDA reports)
HEPATITIS A ( 2 FDA reports)
HEPATITIS B VIRUS TEST ( 2 FDA reports)
HERPES OESOPHAGITIS ( 2 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 2 FDA reports)
HIRSUTISM ( 2 FDA reports)
HIV TEST FALSE POSITIVE ( 2 FDA reports)
HUNGRY BONE SYNDROME ( 2 FDA reports)
HYALOSIS ASTEROID ( 2 FDA reports)
HYPERDYNAMIC LEFT VENTRICLE ( 2 FDA reports)
HYPERINSULINAEMIA ( 2 FDA reports)
HYPERPARATHYROIDISM TERTIARY ( 2 FDA reports)
HYPERTONIA NEONATAL ( 2 FDA reports)
HYPERTROPHIC OSTEOARTHROPATHY ( 2 FDA reports)
HYPOAESTHESIA TEETH ( 2 FDA reports)
HYPOLIPIDAEMIA ( 2 FDA reports)
HYPOMENORRHOEA ( 2 FDA reports)
IIIRD NERVE PARESIS ( 2 FDA reports)
ILEOSTOMY ( 2 FDA reports)
ILIAC ARTERY EMBOLISM ( 2 FDA reports)
ILLOGICAL THINKING ( 2 FDA reports)
IN-STENT ARTERIAL RESTENOSIS ( 2 FDA reports)
INCISION SITE ABSCESS ( 2 FDA reports)
INCISION SITE HYPOAESTHESIA ( 2 FDA reports)
INCISIONAL HERNIA REPAIR ( 2 FDA reports)
INDIFFERENCE ( 2 FDA reports)
INDUCED LABOUR ( 2 FDA reports)
INDWELLING CATHETER MANAGEMENT ( 2 FDA reports)
INFECTION PARASITIC ( 2 FDA reports)
INFERIOR VENA CAVA DILATATION ( 2 FDA reports)
INFERTILITY FEMALE ( 2 FDA reports)
INFUSION SITE INFECTION ( 2 FDA reports)
INFUSION SITE RASH ( 2 FDA reports)
INFUSION SITE SCAR ( 2 FDA reports)
INFUSION SITE URTICARIA ( 2 FDA reports)
INJECTION ( 2 FDA reports)
INJECTION SITE DESQUAMATION ( 2 FDA reports)
INJECTION SITE PALLOR ( 2 FDA reports)
INJECTION SITE SCAB ( 2 FDA reports)
INSULIN RESISTANCE SYNDROME ( 2 FDA reports)
INSULIN-LIKE GROWTH FACTOR INCREASED ( 2 FDA reports)
INTENSIVE CARE ( 2 FDA reports)
INTESTINAL ANASTOMOTIC LEAK ( 2 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE INSERTION ( 2 FDA reports)
INTUBATION ( 2 FDA reports)
IRON METABOLISM DISORDER ( 2 FDA reports)
IUD MIGRATION ( 2 FDA reports)
JEJUNAL STENOSIS ( 2 FDA reports)
JOINT ABSCESS ( 2 FDA reports)
JOINT ANKYLOSIS ( 2 FDA reports)
JOINT HYPEREXTENSION ( 2 FDA reports)
JOINT LAXITY ( 2 FDA reports)
KERATOPATHY ( 2 FDA reports)
KERATORHEXIS ( 2 FDA reports)
KLEBSIELLA TEST POSITIVE ( 2 FDA reports)
KLIPPEL-FEIL SYNDROME ( 2 FDA reports)
KUSSMAUL RESPIRATION ( 2 FDA reports)
LACRIMATION DECREASED ( 2 FDA reports)
LARYNGEAL CANCER STAGE IV ( 2 FDA reports)
LARYNGECTOMY ( 2 FDA reports)
LARYNGOSCOPY ABNORMAL ( 2 FDA reports)
LEARNING DISORDER ( 2 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE DECREASED ( 2 FDA reports)
LEUKAEMIA PLASMACYTIC ( 2 FDA reports)
LEUKAEMIA RECURRENT ( 2 FDA reports)
LEUKAEMIC INFILTRATION ( 2 FDA reports)
LEUKOCYTURIA ( 2 FDA reports)
LIBIDO DISORDER ( 2 FDA reports)
LIPOMATOSIS ( 2 FDA reports)
LOCAL REACTION ( 2 FDA reports)
LOCALISED EXFOLIATION ( 2 FDA reports)
LUDWIG ANGINA ( 2 FDA reports)
LUMBARISATION ( 2 FDA reports)
LUNG INJURY ( 2 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 2 FDA reports)
LYMPHOCELE ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 2 FDA reports)
MACROANGIOPATHY ( 2 FDA reports)
MACROGLOSSIA ( 2 FDA reports)
MACULAR CYST ( 2 FDA reports)
MACULAR SCAR ( 2 FDA reports)
MALE ORGASMIC DISORDER ( 2 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 2 FDA reports)
MALIGNANT URINARY TRACT NEOPLASM ( 2 FDA reports)
MALOCCLUSION ( 2 FDA reports)
MAMMOGRAM ( 2 FDA reports)
MANTLE CELL LYMPHOMA ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN ( 2 FDA reports)
MECHANICAL COMPLICATION OF IMPLANT ( 2 FDA reports)
MENINGISM ( 2 FDA reports)
MENINGITIS BACTERIAL ( 2 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 2 FDA reports)
MESENTERIC OCCLUSION ( 2 FDA reports)
MESOTHELIOMA ( 2 FDA reports)
MESOTHELIOMA MALIGNANT ( 2 FDA reports)
METAL POISONING ( 2 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 2 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 2 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 2 FDA reports)
MIXED INCONTINENCE ( 2 FDA reports)
MONONEUROPATHY ( 2 FDA reports)
MOUTH CYST ( 2 FDA reports)
MOUTH PLAQUE ( 2 FDA reports)
MUCOPOLYSACCHARIDOSIS II ( 2 FDA reports)
MUCOSA VESICLE ( 2 FDA reports)
MUCOSAL ATROPHY ( 2 FDA reports)
MULTIFOCAL MOTOR NEUROPATHY ( 2 FDA reports)
MULTIMORBIDITY ( 2 FDA reports)
MUSCLE OPERATION ( 2 FDA reports)
MUSCLE REATTACHMENT ( 2 FDA reports)
MYCOBACTERIUM TEST POSITIVE ( 2 FDA reports)
ABDOMINAL CAVITY DRAINAGE ( 1 FDA reports)
ABDOMINAL INJURY ( 1 FDA reports)
ABDOMINAL PANNICULECTOMY ( 1 FDA reports)
ABDOMINAL WALL HAEMORRHAGE ( 1 FDA reports)
ABNORMAL WITHDRAWAL BLEEDING ( 1 FDA reports)
ABORTION INCOMPLETE ( 1 FDA reports)
ABSCESS BACTERIAL ( 1 FDA reports)
ABSTAINS FROM ALCOHOL ( 1 FDA reports)
ACALCULIA ( 1 FDA reports)
ACCESSORY MUSCLE ( 1 FDA reports)
ACCIDENTAL POISONING ( 1 FDA reports)
ACID FAST STAIN POSITIVE ( 1 FDA reports)
ACID-BASE BALANCE DISORDER MIXED ( 1 FDA reports)
ACINETOBACTER BACTERAEMIA ( 1 FDA reports)
ACINETOBACTER INFECTION ( 1 FDA reports)
ACOUSTIC STIMULATION TESTS ABNORMAL ( 1 FDA reports)
ACQUIRED CARDIAC SEPTAL DEFECT ( 1 FDA reports)
ACQUIRED HAEMOPHILIA ( 1 FDA reports)
ACQUIRED METHAEMOGLOBINAEMIA ( 1 FDA reports)
ACQUIRED PYLORIC STENOSIS ( 1 FDA reports)
ACTINOMYCOTIC SKIN INFECTION ( 1 FDA reports)
ACUTE CHEST SYNDROME ( 1 FDA reports)
ACUTE ENDOCARDITIS ( 1 FDA reports)
ACUTE MONOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 1 FDA reports)
ADMINISTRATION SITE PAIN ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY CHRONIC ( 1 FDA reports)
ADVANCED SLEEP PHASE ( 1 FDA reports)
AEROPHAGIA ( 1 FDA reports)
AGE INDETERMINATE MYOCARDIAL INFARCTION ( 1 FDA reports)
AGITATED DEPRESSION ( 1 FDA reports)
AGNOSIA ( 1 FDA reports)
AGONAL RHYTHM ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ( 1 FDA reports)
ALBUMIN URINE ABSENT ( 1 FDA reports)
ALCOHOL DETOXIFICATION ( 1 FDA reports)
ALCOHOLIC PSYCHOSIS ( 1 FDA reports)
ALLERGIC COLITIS ( 1 FDA reports)
ALLERGY TO VENOM ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN ABNORMAL ( 1 FDA reports)
ALPHA-1 ANTI-TRYPSIN DEFICIENCY ( 1 FDA reports)
AMIMIA ( 1 FDA reports)
AMINO ACID LEVEL INCREASED ( 1 FDA reports)
AMMONIA ABNORMAL ( 1 FDA reports)
AMYOTROPHY ( 1 FDA reports)
ANAESTHETIC COMPLICATION PULMONARY ( 1 FDA reports)
ANAL CANCER STAGE II ( 1 FDA reports)
ANAL SPASM ( 1 FDA reports)
ANAL ULCER ( 1 FDA reports)
ANALGESIA ( 1 FDA reports)
ANALGESIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANALGESIC EFFECT ( 1 FDA reports)
ANALGESIC THERAPY ( 1 FDA reports)
ANAPHYLACTIC TRANSFUSION REACTION ( 1 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 1 FDA reports)
ANASTOMOTIC STENOSIS ( 1 FDA reports)
ANASTOMOTIC ULCER HAEMORRHAGE ( 1 FDA reports)
ANDROGENETIC ALOPECIA ( 1 FDA reports)
ANEURYSM REPAIR ( 1 FDA reports)
ANGIOGRAM PERIPHERAL ABNORMAL ( 1 FDA reports)
ANGIOLIPOMA ( 1 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INCREASED ( 1 FDA reports)
ANISOMETROPIA ( 1 FDA reports)
ANKLE BRACHIAL INDEX DECREASED ( 1 FDA reports)
ANORECTAL CELLULITIS ( 1 FDA reports)
ANORECTAL OPERATION ( 1 FDA reports)
ANOSOGNOSIA ( 1 FDA reports)
ANTERIOR CHAMBER CELL ( 1 FDA reports)
ANTERIOR SPINAL ARTERY SYNDROME ( 1 FDA reports)
ANTI-CYCLIC CITRULLINATED PEPTIDE ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-ERYTHROCYTE ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY ( 1 FDA reports)
ANTI-HBC IGG ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 1 FDA reports)
ANTIACETYLCHOLINE RECEPTOR ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBODY TEST ABNORMAL ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABNORMAL ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY ( 1 FDA reports)
ANTITHROMBIN III INCREASED ( 1 FDA reports)
AORTIC BYPASS ( 1 FDA reports)
AORTIC RUPTURE ( 1 FDA reports)
AORTIC SURGERY ( 1 FDA reports)
APHAKIA ( 1 FDA reports)
APOLIPOPROTEIN A-I DECREASED ( 1 FDA reports)
APPLICATION SITE BRUISING ( 1 FDA reports)
APPLICATION SITE CELLULITIS ( 1 FDA reports)
APPLICATION SITE DISCOMFORT ( 1 FDA reports)
APPLICATION SITE EXCORIATION ( 1 FDA reports)
APPLICATION SITE EXFOLIATION ( 1 FDA reports)
APPLICATION SITE INFLAMMATION ( 1 FDA reports)
APPLICATION SITE PAPULES ( 1 FDA reports)
APPLICATION SITE PARAESTHESIA ( 1 FDA reports)
APPLICATION SITE WARMTH ( 1 FDA reports)
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA ( 1 FDA reports)
ARTERIAL FIBROSIS ( 1 FDA reports)
ARTERIAL REPAIR ( 1 FDA reports)
ARTERIOGRAM ABNORMAL ( 1 FDA reports)
ARTERIOSCLEROTIC GANGRENE ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE INFECTION ( 1 FDA reports)
ARTERIOVENOUS GRAFT ANEURYSM ( 1 FDA reports)
ARTERIOVENOUS GRAFT SITE HAEMORRHAGE ( 1 FDA reports)
ARTERIOVENOUS GRAFT THROMBOSIS ( 1 FDA reports)
ARTERY DISSECTION ( 1 FDA reports)
ARTHROFIBROSIS ( 1 FDA reports)
ARTHROSCOPIC SURGERY ( 1 FDA reports)
ARTICULAR CALCIFICATION ( 1 FDA reports)
ARTIFICIAL URINARY SPHINCTER IMPLANT ( 1 FDA reports)
ASOCIAL BEHAVIOUR ( 1 FDA reports)
ASPIRATION BONE MARROW ( 1 FDA reports)
ASPIRATION TRACHEAL ( 1 FDA reports)
ASTHMA EXERCISE INDUCED ( 1 FDA reports)
ASTHMA PROPHYLAXIS ( 1 FDA reports)
ATROPHY OF GLOBE ( 1 FDA reports)
ATYPICAL FIBROXANTHOMA ( 1 FDA reports)
AUDIOGRAM ABNORMAL ( 1 FDA reports)
AUTISM SPECTRUM DISORDER ( 1 FDA reports)
AUTOIMMUNE MYOCARDITIS ( 1 FDA reports)
AV DISSOCIATION ( 1 FDA reports)
AVERSION ( 1 FDA reports)
B-CELL TYPE ACUTE LEUKAEMIA ( 1 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 1 FDA reports)
BACTERIAL CULTURE POSITIVE ( 1 FDA reports)
BACTEROIDES BACTERAEMIA ( 1 FDA reports)
BACTEROIDES TEST POSITIVE ( 1 FDA reports)
BALANITIS CANDIDA ( 1 FDA reports)
BARIUM SWALLOW ABNORMAL ( 1 FDA reports)
BASE EXCESS ( 1 FDA reports)
BASILAR ARTERY STENOSIS ( 1 FDA reports)
BASOPHIL COUNT DECREASED ( 1 FDA reports)
BASOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
BASOPHILIA ( 1 FDA reports)
BED REST ( 1 FDA reports)
BENCE JONES PROTEIN URINE ( 1 FDA reports)
BENIGN FAMILIAL HAEMATURIA ( 1 FDA reports)
BENIGN LYMPH NODE NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF BLADDER ( 1 FDA reports)
BENIGN NEOPLASM OF EYELID ( 1 FDA reports)
BENIGN SALIVARY GLAND NEOPLASM ( 1 FDA reports)
BENIGN SMALL INTESTINAL NEOPLASM ( 1 FDA reports)
BENIGN SOFT TISSUE NEOPLASM ( 1 FDA reports)
BEREAVEMENT ( 1 FDA reports)
BEREAVEMENT REACTION ( 1 FDA reports)
BEZOAR ( 1 FDA reports)
BILATERAL HYDRONEPHROSIS ( 1 FDA reports)
BILIARY CYST ( 1 FDA reports)
BILIRUBIN URINE ( 1 FDA reports)
BILIRUBINURIA ( 1 FDA reports)
BIOPSY BRAIN NORMAL ( 1 FDA reports)
BIOPSY CARTILAGE ABNORMAL ( 1 FDA reports)
BIOPSY HEART ABNORMAL ( 1 FDA reports)
BIOPSY LYMPH GLAND ( 1 FDA reports)
BIOPSY MUCOSA ABNORMAL ( 1 FDA reports)
BIOPSY OESOPHAGUS ABNORMAL ( 1 FDA reports)
BIOPSY PHARYNX ( 1 FDA reports)
BIOPSY THYROID GLAND ( 1 FDA reports)
BIPOLAR II DISORDER ( 1 FDA reports)
BISEXUALITY ( 1 FDA reports)
BLADDER ADENOCARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
BLADDER CANCER STAGE 0, WITH CANCER IN SITU ( 1 FDA reports)
BLADDER CANCER STAGE II ( 1 FDA reports)
BLADDER CYST ( 1 FDA reports)
BLADDER HYPERTROPHY ( 1 FDA reports)
BLADDER STENOSIS ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA RECURRENT ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE I ( 1 FDA reports)
BLAST CELL PROLIFERATION ( 1 FDA reports)
BLASTOMYCOSIS ( 1 FDA reports)
BLEEDING TIME ABNORMAL ( 1 FDA reports)
BLEPHAROPACHYNSIS ( 1 FDA reports)
BLOOD 1,25-DIHYDROXYCHOLECALCIFEROL DECREASED ( 1 FDA reports)
BLOOD ALDOSTERONE ABNORMAL ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE NORMAL ( 1 FDA reports)
BLOOD AMYLASE NORMAL ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE INCREASED ( 1 FDA reports)
BLOOD ARSENIC INCREASED ( 1 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN ( 1 FDA reports)
BLOOD CANNABINOIDS INCREASED ( 1 FDA reports)
BLOOD CARBON MONOXIDE DECREASED ( 1 FDA reports)
BLOOD CATECHOLAMINES ABNORMAL ( 1 FDA reports)
BLOOD CHLORIDE ABNORMAL ( 1 FDA reports)
BLOOD CHROMIUM INCREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN INCREASED ( 1 FDA reports)
BLOOD CORTISOL INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ABNORMAL ( 1 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 1 FDA reports)
BLOOD FOLATE INCREASED ( 1 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE NORMAL ( 1 FDA reports)
BLOOD HEAVY METAL INCREASED ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN POSITIVE ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 1 FDA reports)
BLOOD INSULIN DECREASED ( 1 FDA reports)
BLOOD LUTEINISING HORMONE ABNORMAL ( 1 FDA reports)
BLOOD LUTEINISING HORMONE DECREASED ( 1 FDA reports)
BLOOD PRESSURE NORMAL ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC ABNORMAL ( 1 FDA reports)
BLOOD TEST ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BLOOD ZINC DECREASED ( 1 FDA reports)
BODY FAT DISORDER ( 1 FDA reports)
BODY MASS INDEX DECREASED ( 1 FDA reports)
BODY MASS INDEX INCREASED ( 1 FDA reports)
BONE ATROPHY ( 1 FDA reports)
BONE DENSITY INCREASED ( 1 FDA reports)
BONE FORMATION DECREASED ( 1 FDA reports)
BONE FORMATION INCREASED ( 1 FDA reports)
BONE INFARCTION ( 1 FDA reports)
BONE MARROW GRANULOMA ( 1 FDA reports)
BONE MARROW TUMOUR CELL INFILTRATION ( 1 FDA reports)
BONE TUBERCULOSIS ( 1 FDA reports)
BRACHIAL PLEXUS INJURY ( 1 FDA reports)
BRAIN COMPRESSION ( 1 FDA reports)
BRAIN OPERATION ( 1 FDA reports)
BRAIN SCAN NORMAL ( 1 FDA reports)
BRAIN STEM ISCHAEMIA ( 1 FDA reports)
BREAST CANCER STAGE IV ( 1 FDA reports)
BREAST CYST EXCISION ( 1 FDA reports)
BREAST DISCHARGE ( 1 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ( 1 FDA reports)
BRONCHOGENIC CYST ( 1 FDA reports)
BRONCHOPNEUMOPATHY ( 1 FDA reports)
BRONCHOPULMONARY DISEASE ( 1 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 1 FDA reports)
BRONCHOSPASM PARADOXICAL ( 1 FDA reports)
BRONCHOSTENOSIS ( 1 FDA reports)
BRUGADA SYNDROME ( 1 FDA reports)
BULBAR PALSY ( 1 FDA reports)
BULLOUS IMPETIGO ( 1 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 1 FDA reports)
BURNING SENSATION MUCOSAL ( 1 FDA reports)
BURSITIS INFECTIVE ( 1 FDA reports)
C-REACTIVE PROTEIN ( 1 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 1 FDA reports)
C1 ESTERASE INHIBITOR DECREASED ( 1 FDA reports)
CANDIDA TEST POSITIVE ( 1 FDA reports)
CAPSULE ISSUE ( 1 FDA reports)
CARCINOID TUMOUR OF THE DUODENUM ( 1 FDA reports)
CARCINOID TUMOUR OF THE GASTROINTESTINAL TRACT ( 1 FDA reports)
CARCINOID TUMOUR OF THE PROSTATE ( 1 FDA reports)
CARCINOMA ( 1 FDA reports)
CARDIAC ANEURYSM REPAIR ( 1 FDA reports)
CARDIAC FAILURE HIGH OUTPUT ( 1 FDA reports)
CARDIAC FUNCTION DISTURBANCE POSTOPERATIVE ( 1 FDA reports)
CARDIAC MASSAGE ( 1 FDA reports)
CARDIAC PACEMAKER BATTERY REPLACEMENT ( 1 FDA reports)
CARDIAC VENTRICULOGRAM LEFT ( 1 FDA reports)
CARDIAC VENTRICULOGRAM LEFT ABNORMAL ( 1 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 1 FDA reports)
CARDIOMYOPATHY ALCOHOLIC ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CAST APPLICATION ( 1 FDA reports)
CASTLEMAN'S DISEASE ( 1 FDA reports)
CAT SCRATCH DISEASE ( 1 FDA reports)
CATARACT OPERATION COMPLICATION ( 1 FDA reports)
CATARACT TRAUMATIC ( 1 FDA reports)
CATECHOLAMINES URINE INCREASED ( 1 FDA reports)
CATHETER SITE CELLULITIS ( 1 FDA reports)
CD4 LYMPHOCYTES ABNORMAL ( 1 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
CELLULITIS OF MALE EXTERNAL GENITAL ORGAN ( 1 FDA reports)
CENTRAL AUDITORY PROCESSING DISORDER ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFLAMMATION ( 1 FDA reports)
CENTRAL VENOUS PRESSURE ABNORMAL ( 1 FDA reports)
CENTRAL VENOUS PRESSURE DECREASED ( 1 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 1 FDA reports)
CEREBELLAR HAEMATOMA ( 1 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 1 FDA reports)
CEREBRAL CYST ( 1 FDA reports)
CEREBRAL SARCOIDOSIS ( 1 FDA reports)
CEREBROSCLEROSIS ( 1 FDA reports)
CEREBROVASCULAR OPERATION ( 1 FDA reports)
CEREBROVASCULAR SPASM ( 1 FDA reports)
CERVICAL CYST ( 1 FDA reports)
CERVICAL INCOMPETENCE ( 1 FDA reports)
CERVIX CARCINOMA RECURRENT ( 1 FDA reports)
CHANGE IN SUSTAINED ATTENTION ( 1 FDA reports)
CHEMICAL BURNS OF EYE ( 1 FDA reports)
CHEMICAL PERITONITIS ( 1 FDA reports)
CHEST EXPANSION DECREASED ( 1 FDA reports)
CHILD ABUSE ( 1 FDA reports)
CHILLBLAINS ( 1 FDA reports)
CHOLANGIOGRAM ( 1 FDA reports)
CHOLANGITIS SUPPURATIVE ( 1 FDA reports)
CHOLEDOCHOLITHOTOMY ( 1 FDA reports)
CHOLELITHIASIS OBSTRUCTIVE ( 1 FDA reports)
CHOLINERGIC SYNDROME ( 1 FDA reports)
CHORDAE TENDINAE RUPTURE ( 1 FDA reports)
CHOROID MELANOMA ( 1 FDA reports)
CHOROIDAL COLOBOMA ( 1 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 1 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 1 FDA reports)
CHRYSIASIS ( 1 FDA reports)
CITRIC ACID URINE DECREASED ( 1 FDA reports)
COAGULATION FACTOR DEFICIENCY ( 1 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR XI LEVEL DECREASED ( 1 FDA reports)
COCCYDYNIA ( 1 FDA reports)
COCHLEA IMPLANT ( 1 FDA reports)
COELIAC ARTERY OCCLUSION ( 1 FDA reports)
COLECTOMY PARTIAL ( 1 FDA reports)
COLONIC HAEMATOMA ( 1 FDA reports)
COLONIC HAEMORRHAGE ( 1 FDA reports)
COLORECTAL CANCER STAGE II ( 1 FDA reports)
COLOSTOMY INFECTION ( 1 FDA reports)
COMMUNITY ACQUIRED INFECTION ( 1 FDA reports)
COMPLEMENT FACTOR ABNORMAL ( 1 FDA reports)
COMPLEMENT FACTOR C3 INCREASED ( 1 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
COMPULSIVE SEXUAL BEHAVIOUR ( 1 FDA reports)
COMPUTERISED TOMOGRAM ( 1 FDA reports)
CONGENITAL AORTIC ANOMALY ( 1 FDA reports)
CONGENITAL ATRIAL SEPTAL DEFECT ( 1 FDA reports)
CONGENITAL BLADDER ANOMALY ( 1 FDA reports)
CONGENITAL CORNEAL ANOMALY ( 1 FDA reports)
CONGENITAL CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
CONGENITAL EYELID MALFORMATION ( 1 FDA reports)
CONGENITAL NEUROPATHY ( 1 FDA reports)
CONGENITAL NOSE MALFORMATION ( 1 FDA reports)
CONGENITAL NYSTAGMUS ( 1 FDA reports)
CONGENITAL OPTIC NERVE ANOMALY ( 1 FDA reports)
CONGENITAL RENAL DISORDER ( 1 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 1 FDA reports)
CONJUNCTIVITIS VIRAL ( 1 FDA reports)
COPROLALIA ( 1 FDA reports)
CORNEAL DEPOSITS ( 1 FDA reports)
CORNEAL EROSION ( 1 FDA reports)
CORNEAL GRAFT REJECTION ( 1 FDA reports)
CORNEAL LIGHT REFLEX TEST ABNORMAL ( 1 FDA reports)
CORNEAL STAPHYLOMA ( 1 FDA reports)
CORNEAL THINNING ( 1 FDA reports)
CORONARY ARTERY ANEURYSM ( 1 FDA reports)
CORONARY ARTERY DILATATION ( 1 FDA reports)
CORONARY ARTERY PERFORATION ( 1 FDA reports)
CORTICAL LAMINAR NECROSIS ( 1 FDA reports)
COUGH DECREASED ( 1 FDA reports)
COUNTERFEIT DRUG ADMINISTERED ( 1 FDA reports)
CRANIAL NERVE DISORDER ( 1 FDA reports)
CRANIAL NERVE PALSIES MULTIPLE ( 1 FDA reports)
CRANIAL NERVE PARALYSIS ( 1 FDA reports)
CRANIAL NEUROPATHY ( 1 FDA reports)
CRANIAL SUTURES WIDENING ( 1 FDA reports)
CREATININE RENAL CLEARANCE ABNORMAL ( 1 FDA reports)
CRYOGLOBULINAEMIA ( 1 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 1 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 1 FDA reports)
CSF BACTERIA IDENTIFIED ( 1 FDA reports)
CSF SHUNT OPERATION ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
CULTURE THROAT POSITIVE ( 1 FDA reports)
CULTURE TISSUE SPECIMEN POSITIVE ( 1 FDA reports)
CYCLIC VOMITING SYNDROME ( 1 FDA reports)
CYSTIC FIBROSIS PANCREATIC ( 1 FDA reports)
CYSTITIS BACTERIAL ( 1 FDA reports)
CYSTITIS GLANDULARIS ( 1 FDA reports)
CYSTITIS PSEUDOMONAL ( 1 FDA reports)
CYSTOSARCOMA PHYLLODES ( 1 FDA reports)
CYTOGENETIC ANALYSIS ABNORMAL ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 1 FDA reports)
DAWN PHENOMENON ( 1 FDA reports)
DEAFNESS PERMANENT ( 1 FDA reports)
DEATH NEONATAL ( 1 FDA reports)
DEATH OF COMPANION ( 1 FDA reports)
DEATH OF SIBLING ( 1 FDA reports)
DECREASED EYE CONTACT ( 1 FDA reports)
DELAYED EFFECTS OF RADIATION ( 1 FDA reports)
DELIRIUM FEBRILE ( 1 FDA reports)
DELUSION OF GRANDEUR ( 1 FDA reports)
DENERVATION ATROPHY ( 1 FDA reports)
DENGUE FEVER ( 1 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 1 FDA reports)
DEPOSIT EYE ( 1 FDA reports)
DERMABRASION ( 1 FDA reports)
DERMATILLOMANIA ( 1 FDA reports)
DERMATITIS EXFOLIATIVE GENERALISED ( 1 FDA reports)
DERMATOSIS ( 1 FDA reports)
DESQUAMATION MOUTH ( 1 FDA reports)
DEVICE CAPTURING ISSUE ( 1 FDA reports)
DEVICE DAMAGE ( 1 FDA reports)
DEVICE DIFFICULT TO USE ( 1 FDA reports)
DEVICE INTOLERANCE ( 1 FDA reports)
DEVICE PACING ISSUE ( 1 FDA reports)
DEVICE PHYSICAL PROPERTY ISSUE ( 1 FDA reports)
DEVICE THERAPY ( 1 FDA reports)
DIABETIC CARDIOMYOPATHY ( 1 FDA reports)
DIABETIC GANGRENE ( 1 FDA reports)
DIET NONCOMPLIANCE ( 1 FDA reports)
DIEULAFOY'S VASCULAR MALFORMATION ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE I ( 1 FDA reports)
DIRECTIONAL DOPPLER FLOW TESTS ABNORMAL ( 1 FDA reports)
DIURETIC EFFECT ( 1 FDA reports)
DIURETIC THERAPY ( 1 FDA reports)
DIVERTICULAR FISTULA ( 1 FDA reports)
DIVERTICULUM GASTRIC ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY POSITIVE ( 1 FDA reports)
DROWNING ( 1 FDA reports)
DRUG CHEMICAL INCOMPATIBILITY ( 1 FDA reports)
DRUG CLEARANCE INCREASED ( 1 FDA reports)
DRUG DELIVERY DEVICE IMPLANTATION ( 1 FDA reports)
DRUG LABEL CONFUSION ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
DRY SOCKET ( 1 FDA reports)
DUODENAL PERFORATION ( 1 FDA reports)
DUODENAL STENOSIS ( 1 FDA reports)
DUODENAL ULCER, OBSTRUCTIVE ( 1 FDA reports)
DUODENAL VARICES ( 1 FDA reports)
DYSCHEZIA ( 1 FDA reports)
EAR CANAL ABRASION ( 1 FDA reports)
EAR INFECTION FUNGAL ( 1 FDA reports)
EAR INFECTION VIRAL ( 1 FDA reports)
EAR NEOPLASM MALIGNANT ( 1 FDA reports)
ECHINOCOCCIASIS ( 1 FDA reports)
ECHO VIRUS INFECTION ( 1 FDA reports)
ECTHYMA ( 1 FDA reports)
ECTOPIC PREGNANCY ( 1 FDA reports)
ECZEMA NUMMULAR ( 1 FDA reports)
ECZEMA VESICULAR ( 1 FDA reports)
ECZEMA WEEPING ( 1 FDA reports)
EISENMENGER'S SYNDROME ( 1 FDA reports)
ELBOW DEFORMITY ( 1 FDA reports)
ELECTROCARDIOGRAM ( 1 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ( 1 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ELEVATION ( 1 FDA reports)
ELECTROOCULOGRAM ABNORMAL ( 1 FDA reports)
ELEVATED PACING THRESHOLD ( 1 FDA reports)
EMPHYSEMATOUS BULLA ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENDOCARDIAL DISEASE ( 1 FDA reports)
ENDOCARDITIS CANDIDA ( 1 FDA reports)
ENDOLYMPHATIC HYDROPS ( 1 FDA reports)
ENDOMETRIAL CANCER RECURRENT ( 1 FDA reports)
ENDOSCOPY GASTROINTESTINAL ABNORMAL ( 1 FDA reports)
ENDOTOXIC SHOCK ( 1 FDA reports)
ENTEROBACTER PNEUMONIA ( 1 FDA reports)
ENTEROCELE ( 1 FDA reports)
ENTEROCOLITIS BACTERIAL ( 1 FDA reports)
ENTEROSTOMY ( 1 FDA reports)
ENTEROVESICAL FISTULA ( 1 FDA reports)
ENZYME INHIBITION ( 1 FDA reports)
EOSINOPHIL COUNT ABNORMAL ( 1 FDA reports)
EOSINOPHIL PERCENTAGE DECREASED ( 1 FDA reports)
EOSINOPHILS URINE ( 1 FDA reports)
EPHELIDES ( 1 FDA reports)
EPIDERMAL GROWTH FACTOR RECEPTOR DECREASED ( 1 FDA reports)
EPIDURAL INJECTION ( 1 FDA reports)
EPIGLOTTIS ULCER ( 1 FDA reports)
EPILEPTIC AURA ( 1 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 1 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 1 FDA reports)
ERYTHEMA TOXICUM NEONATORUM ( 1 FDA reports)
EUTHYROID SICK SYNDROME ( 1 FDA reports)
EVAN'S SYNDROME ( 1 FDA reports)
EXCESSIVE EXERCISE ( 1 FDA reports)
EXCESSIVE SEXUAL FANTASIES ( 1 FDA reports)
EXECUTIVE DYSFUNCTION ( 1 FDA reports)
EXERCISE ELECTROCARDIOGRAM ( 1 FDA reports)
EXPLORATIVE LAPAROTOMY ( 1 FDA reports)
EXPOSURE TO CHEMICAL POLLUTION ( 1 FDA reports)
EXPOSURE VIA FATHER ( 1 FDA reports)
EXTERNAL EAR DISORDER ( 1 FDA reports)
EXTERNAL EAR INFLAMMATION ( 1 FDA reports)
EXTRAMEDULLARY HAEMOPOIESIS ( 1 FDA reports)
EXTRAOCULAR MUSCLE DISORDER ( 1 FDA reports)
EXTRINSIC VASCULAR COMPRESSION ( 1 FDA reports)
EXTRUSION OF DEVICE ( 1 FDA reports)
EYE ABSCESS ( 1 FDA reports)
EYE COMPLICATION ASSOCIATED WITH DEVICE ( 1 FDA reports)
EYELID EXFOLIATION ( 1 FDA reports)
EYELID INFECTION ( 1 FDA reports)
EYELID RETRACTION ( 1 FDA reports)
FACIAL NEURALGIA ( 1 FDA reports)
FACIAL OPERATION ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
FACTITIOUS DISORDER ( 1 FDA reports)
FACTOR V DEFICIENCY ( 1 FDA reports)
FACTOR V LEIDEN MUTATION ( 1 FDA reports)
FACTOR VIII DEFICIENCY ( 1 FDA reports)
FALLOPIAN TUBE CYST ( 1 FDA reports)
FALLOPIAN TUBE DISORDER ( 1 FDA reports)
FALLOT'S TETRALOGY ( 1 FDA reports)
FALSE NEGATIVE INVESTIGATION RESULT ( 1 FDA reports)
FALSE NEGATIVE LABORATORY RESULT ( 1 FDA reports)
FAT REDISTRIBUTION ( 1 FDA reports)
FEAR OF CROWDED PLACES ( 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)
FEMORAL ARTERY ANEURYSM ( 1 FDA reports)
FEMORAL ARTERY EMBOLISM ( 1 FDA reports)
FEMORAL BRUIT ( 1 FDA reports)
FEMORAL PULSE DECREASED ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 1 FDA reports)
FIBRIN INCREASED ( 1 FDA reports)
FIBRINOLYSIS ABNORMAL ( 1 FDA reports)
FLAIL CHEST ( 1 FDA reports)
FLUID INTAKE RESTRICTION ( 1 FDA reports)
FOETAL DEATH ( 1 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III STAGE IV ( 1 FDA reports)
FORAMINOTOMY ( 1 FDA reports)
FORCED EXPIRATORY VOLUME ABNORMAL ( 1 FDA reports)
FORCED EXPIRATORY VOLUME INCREASED ( 1 FDA reports)
FRACTION OF INSPIRED OXYGEN ( 1 FDA reports)
FRONTAL SINUS OPERATION ( 1 FDA reports)
FULL BLOOD COUNT ( 1 FDA reports)
FUNGUS SPUTUM TEST POSITIVE ( 1 FDA reports)
FUNGUS URINE TEST POSITIVE ( 1 FDA reports)
FUSOBACTERIUM INFECTION ( 1 FDA reports)
GAIT SPASTIC ( 1 FDA reports)
GALACTORRHOEA ( 1 FDA reports)
GALLBLADDER ABSCESS ( 1 FDA reports)
GALLBLADDER CANCER METASTATIC ( 1 FDA reports)
GALLBLADDER EMPYEMA ( 1 FDA reports)
GANGLION ( 1 FDA reports)
GARDNERELLA INFECTION ( 1 FDA reports)
GASTRIC CANCER STAGE IV ( 1 FDA reports)
GASTRIC CANCER STAGE IV WITH METASTASES ( 1 FDA reports)
GASTRIC CYST ( 1 FDA reports)
GASTRIC FISTULA ( 1 FDA reports)
GASTRIC VOLVULUS ( 1 FDA reports)
GASTRITIS ATROPHIC ( 1 FDA reports)
GASTROENTERITIS ADENOVIRUS ( 1 FDA reports)
GASTROENTERITIS EOSINOPHILIC ( 1 FDA reports)
GASTROENTERITIS HELICOBACTER ( 1 FDA reports)
GASTROENTERITIS PROTEUS ( 1 FDA reports)
GASTROINTESTINAL DISORDER POSTOPERATIVE ( 1 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 1 FDA reports)
GASTROINTESTINAL MUCOCOELE ( 1 FDA reports)
GASTROINTESTINAL TELANGIECTASIA ( 1 FDA reports)
GASTROINTESTINAL TRACT MUCOSAL DISCOLOURATION ( 1 FDA reports)
GASTROOESOPHAGEAL SPHINCTER INSUFFICIENCY ( 1 FDA reports)
GASTROSTOMY TUBE INSERTION ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ( 1 FDA reports)
GENITAL ABSCESS ( 1 FDA reports)
GENITAL CANDIDIASIS ( 1 FDA reports)
GENITAL LESION ( 1 FDA reports)
GENITAL SWELLING ( 1 FDA reports)
GENITOURINARY TRACT INFECTION ( 1 FDA reports)
GENOTYPE DRUG RESISTANCE TEST POSITIVE ( 1 FDA reports)
GINGIVAL CANCER ( 1 FDA reports)
GINGIVAL HYPERTROPHY ( 1 FDA reports)
GINGIVAL OPERATION ( 1 FDA reports)
GINGIVAL PRURITUS ( 1 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 1 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 1 FDA reports)
GLUCOSE URINE ( 1 FDA reports)
GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN ( 1 FDA reports)
GRAFT HAEMORRHAGE ( 1 FDA reports)
GRANULOCYTES ABNORMAL ( 1 FDA reports)
HAEMATOMA EVACUATION ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HAEMOCONCENTRATION ( 1 FDA reports)
HAEMODIALYSIS COMPLICATION ( 1 FDA reports)
HAEMODILUTION ( 1 FDA reports)
HAEMORRHAGIC INFARCTION ( 1 FDA reports)
HALITOSIS ( 1 FDA reports)
HAND AMPUTATION ( 1 FDA reports)
HANGNAIL ( 1 FDA reports)
HEAD DEFORMITY ( 1 FDA reports)
HEAD LAG ( 1 FDA reports)
HELLP SYNDROME ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST POSITIVE ( 1 FDA reports)
HEPATIC ANGIOSARCOMA ( 1 FDA reports)
HEPATIC ARTERY OCCLUSION ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC CANDIDIASIS ( 1 FDA reports)
HEPATIC HAEMATOMA ( 1 FDA reports)
HEPATIC SEQUESTRATION ( 1 FDA reports)
HEPATIC VEIN DILATATION ( 1 FDA reports)
HEPATITIS A VIRUS TEST ( 1 FDA reports)
HEPATITIS B ANTIBODY ABNORMAL ( 1 FDA reports)
HEPATITIS B CORE ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS B POSITIVE ( 1 FDA reports)
HEPATITIS B SURFACE ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS B VIRUS ( 1 FDA reports)
HEPATITIS C RNA ( 1 FDA reports)
HEPATITIS C RNA POSITIVE ( 1 FDA reports)
HEPATITIS C VIRUS ( 1 FDA reports)
HEPATITIS GRANULOMATOUS ( 1 FDA reports)
HEREDITARY ANGIOEDEMA ( 1 FDA reports)
HERNIA PAIN ( 1 FDA reports)
HERPES OPHTHALMIC ( 1 FDA reports)
HERPES SEPSIS ( 1 FDA reports)
HERPES ZOSTER MULTI-DERMATOMAL ( 1 FDA reports)
HIP DYSPLASIA ( 1 FDA reports)
HISTAMINE LEVEL DECREASED ( 1 FDA reports)
HISTOLOGY ABNORMAL ( 1 FDA reports)
HISTRIONIC PERSONALITY DISORDER ( 1 FDA reports)
HOLMES-ADIE PUPIL ( 1 FDA reports)
HOMOCYSTINAEMIA ( 1 FDA reports)
HOUSE DUST ALLERGY ( 1 FDA reports)
HUMAN ANTICHIMERIC ANTIBODY POSITIVE ( 1 FDA reports)
HUMAN BITE ( 1 FDA reports)
HUMAN EHRLICHIOSIS ( 1 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 1 FDA reports)
HY'S LAW CASE ( 1 FDA reports)
HYDROCHOLECYSTIS ( 1 FDA reports)
HYDROMETRA ( 1 FDA reports)
HYPERADRENALISM ( 1 FDA reports)
HYPERALDOSTERONISM ( 1 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 1 FDA reports)
HYPERCREATININAEMIA ( 1 FDA reports)
HYPERGLOBULINAEMIA ( 1 FDA reports)
HYPERKALIURIA ( 1 FDA reports)
HYPERKERATOSIS PALMARIS AND PLANTARIS ( 1 FDA reports)
HYPERMOBILITY SYNDROME ( 1 FDA reports)
HYPERTROPHIC SCAR ( 1 FDA reports)
HYPERVIGILANCE ( 1 FDA reports)
HYPOCHONDRIASIS ( 1 FDA reports)
HYPOGLOSSAL NERVE DISORDER ( 1 FDA reports)
HYPOGONADISM MALE ( 1 FDA reports)
HYPOHIDROSIS ( 1 FDA reports)
HYPOPHONESIS ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDERS ( 1 FDA reports)
HYPOTONIC URINARY BLADDER ( 1 FDA reports)
HYSTEROSALPINGO-OOPHORECTOMY ( 1 FDA reports)
ICHTHYOSIS ACQUIRED ( 1 FDA reports)
IDEAS OF REFERENCE ( 1 FDA reports)
IDIOPATHIC URTICARIA ( 1 FDA reports)
IIIRD NERVE PARALYSIS ( 1 FDA reports)
ILIUM FRACTURE ( 1 FDA reports)
ILLITERACY ( 1 FDA reports)
IMMOBILIZATION PROLONGED ( 1 FDA reports)
IMMUNOGLOBULINS DECREASED ( 1 FDA reports)
IMMUNOGLOBULINS INCREASED ( 1 FDA reports)
IMPLANT SITE DISCHARGE ( 1 FDA reports)
IMPLANT SITE EFFUSION ( 1 FDA reports)
IMPLANT SITE INFLAMMATION ( 1 FDA reports)
IMPLANT SITE IRRITATION ( 1 FDA reports)
IMPLANT SITE PAIN ( 1 FDA reports)
IMPLANT SITE SWELLING ( 1 FDA reports)
INBORN ERROR OF METABOLISM ( 1 FDA reports)
INCISION SITE CELLULITIS ( 1 FDA reports)
INFECTED BITES ( 1 FDA reports)
INFECTED LYMPHOCELE ( 1 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
INFECTIVE TENOSYNOVITIS ( 1 FDA reports)
INFERIORITY COMPLEX ( 1 FDA reports)
INFLUENZA A VIRUS TEST POSITIVE ( 1 FDA reports)
INFUSION SITE ABSCESS ( 1 FDA reports)
INFUSION SITE BRUISING ( 1 FDA reports)
INFUSION SITE PRURITUS ( 1 FDA reports)
INHIBITING ANTIBODIES ( 1 FDA reports)
INJECTION SITE ABSCESS STERILE ( 1 FDA reports)
INJECTION SITE CYST ( 1 FDA reports)
INJECTION SITE EXFOLIATION ( 1 FDA reports)
INJECTION SITE HYPERTROPHY ( 1 FDA reports)
INJECTION SITE JOINT WARMTH ( 1 FDA reports)
INJECTION SITE PARAESTHESIA ( 1 FDA reports)
INJECTION SITE THROMBOSIS ( 1 FDA reports)
INSOMNIA RELATED TO ANOTHER MENTAL CONDITION ( 1 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 1 FDA reports)
INSTILLATION SITE ABNORMAL SENSATION ( 1 FDA reports)
INSULIN C-PEPTIDE INCREASED ( 1 FDA reports)
INTERNAL INJURY ( 1 FDA reports)
INTESTINAL ADHESION LYSIS ( 1 FDA reports)
INTESTINAL ANGINA ( 1 FDA reports)
INTESTINAL GANGRENE ( 1 FDA reports)
INTESTINAL HYPOMOTILITY ( 1 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 1 FDA reports)
INTRA-ABDOMINAL PRESSURE INCREASED ( 1 FDA reports)
INTRA-AORTIC BALLOON PLACEMENT ( 1 FDA reports)
INTRA-CEREBRAL ANEURYSM OPERATION ( 1 FDA reports)
INTRACRANIAL INJURY ( 1 FDA reports)
INTRACRANIAL TUMOUR HAEMORRHAGE ( 1 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 1 FDA reports)
IODINE ALLERGY ( 1 FDA reports)
IRIS HAEMORRHAGE ( 1 FDA reports)
IRON BINDING CAPACITY UNSATURATED DECREASED ( 1 FDA reports)
ISCHAEMIC LIMB PAIN ( 1 FDA reports)
JAUNDICE HEPATOCELLULAR ( 1 FDA reports)
JEJUNOSTOMY REFASHIONING ( 1 FDA reports)
JOINT DESTRUCTION ( 1 FDA reports)
JOINT RESURFACING SURGERY ( 1 FDA reports)
JUVENILE ARTHRITIS ( 1 FDA reports)
KERATOPLASTY ( 1 FDA reports)
KIDNEY RUPTURE ( 1 FDA reports)
KORSAKOFF'S PSYCHOSIS ALCOHOLIC ( 1 FDA reports)
KYPHOSCOLIOSIS ( 1 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 1 FDA reports)
LANGERHANS' CELL GRANULOMATOSIS ( 1 FDA reports)
LARGE CELL LUNG CANCER STAGE III ( 1 FDA reports)
LARGE CELL LUNG CANCER STAGE IV ( 1 FDA reports)
LARGE INTESTINE CARCINOMA ( 1 FDA reports)
LARYNGEAL MASS ( 1 FDA reports)
LARYNGEAL OBSTRUCTION ( 1 FDA reports)
LARYNGEAL OPERATION ( 1 FDA reports)
LARYNGEAL ULCERATION ( 1 FDA reports)
LARYNGOMALACIA ( 1 FDA reports)
LARYNX IRRITATION ( 1 FDA reports)
LASER THERAPY ( 1 FDA reports)
LDL/HDL RATIO DECREASED ( 1 FDA reports)
LEG CRUSHING ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LEGIONELLA INFECTION ( 1 FDA reports)
LEGIONELLA SEROLOGY POSITIVE ( 1 FDA reports)
LEGIONELLA TEST POSITIVE ( 1 FDA reports)
LEIOMYOSARCOMA METASTATIC ( 1 FDA reports)
LENS DISLOCATION ( 1 FDA reports)
LEPTOSPIROSIS ( 1 FDA reports)
LESION EXCISION ( 1 FDA reports)
LEUCINE AMINOPEPTIDASE DECREASED ( 1 FDA reports)
LEUKAEMOID REACTION ( 1 FDA reports)
LEUKOARAIOSIS ( 1 FDA reports)
LID LAG ( 1 FDA reports)
LIGHT CHAIN ANALYSIS ABNORMAL ( 1 FDA reports)
LIMB IMMOBILISATION ( 1 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER STAGE IV ( 1 FDA reports)
LIP INFECTION ( 1 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
LIPASE NORMAL ( 1 FDA reports)
LIPOATROPHY ( 1 FDA reports)
LIPOGRANULOMA ( 1 FDA reports)
LIVE BIRTH ( 1 FDA reports)
LIVER FUNCTION TEST ( 1 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 1 FDA reports)
LIVER SCAN ABNORMAL ( 1 FDA reports)
LIVER TRANSPLANT REJECTION ( 1 FDA reports)
LIVING IN RESIDENTIAL INSTITUTION ( 1 FDA reports)
LOCKED-IN SYNDROME ( 1 FDA reports)
LOEFFLER'S SYNDROME ( 1 FDA reports)
LOOSE ASSOCIATIONS ( 1 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 1 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 1 FDA reports)
LUNG NEOPLASM SURGERY ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE IV ( 1 FDA reports)
LYMPH NODE PALPABLE ( 1 FDA reports)
LYMPHANGIECTASIA ( 1 FDA reports)
LYMPHATIC DISORDER ( 1 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
LYMPHOMATOID PAPULOSIS ( 1 FDA reports)
LYMPHORRHOEA ( 1 FDA reports)
MACULAR ISCHAEMIA ( 1 FDA reports)
MACULAR PIGMENTATION ( 1 FDA reports)
MALABSORPTION FROM INJECTION SITE ( 1 FDA reports)
MALIGNANT MELANOMA OF SITES OTHER THAN SKIN ( 1 FDA reports)
MALIGNANT MYOPIA ( 1 FDA reports)
MALIGNANT NEOPLASM OF ISLETS OF LANGERHANS ( 1 FDA reports)
MALIGNANT PALATE NEOPLASM ( 1 FDA reports)
MALIGNANT SPLENIC NEOPLASM ( 1 FDA reports)
MANTLE CELL LYMPHOMA RECURRENT ( 1 FDA reports)
MARASMUS ( 1 FDA reports)
MASTOPTOSIS ( 1 FDA reports)
MEASLES ( 1 FDA reports)
MEDIAL TIBIAL STRESS SYNDROME ( 1 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 1 FDA reports)
MEDIASTINAL INFECTION ( 1 FDA reports)
MEDIASTINAL OPERATION ( 1 FDA reports)
MEDICAL DEVICE SITE REACTION ( 1 FDA reports)
MEGAKARYOCYTES INCREASED ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENINGIOMA BENIGN ( 1 FDA reports)
MENINGITIS LISTERIA ( 1 FDA reports)
MENINGITIS TUBERCULOUS ( 1 FDA reports)
MENSTRUAL DISCOMFORT ( 1 FDA reports)
MENTAL STATUS CHANGES POSTOPERATIVE ( 1 FDA reports)
MERYCISM ( 1 FDA reports)
MESENTERIC HAEMORRHAGE ( 1 FDA reports)
MESENTERIC LYMPHADENOPATHY ( 1 FDA reports)
MESENTERITIS ( 1 FDA reports)
METANEPHRINE URINE INCREASED ( 1 FDA reports)
METAPNEUMOVIRUS INFECTION ( 1 FDA reports)
METASTASES TO BLADDER ( 1 FDA reports)
METASTASES TO GASTROINTESTINAL TRACT ( 1 FDA reports)
METASTASES TO PELVIS ( 1 FDA reports)
METASTASES TO PROSTATE ( 1 FDA reports)
METASTASES TO SKIN ( 1 FDA reports)
METASTASES TO STOMACH ( 1 FDA reports)
METASTASES TO THYROID ( 1 FDA reports)
METASTASES TO TRACHEA ( 1 FDA reports)
METASTATIC GASTRIC CANCER ( 1 FDA reports)
METASTATIC LYMPHOMA ( 1 FDA reports)
METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY ( 1 FDA reports)
MICROCOCCUS INFECTION ( 1 FDA reports)
MICROLITHIASIS ( 1 FDA reports)
MICROSCOPIC POLYANGIITIS ( 1 FDA reports)
MILIA ( 1 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 1 FDA reports)
MITRAL VALVE DISEASE MIXED ( 1 FDA reports)
MITRAL VALVOTOMY ( 1 FDA reports)
MIXED DEAFNESS ( 1 FDA reports)
MIXED LIVER INJURY ( 1 FDA reports)
MIXED OLIGO-ASTROCYTOMA ( 1 FDA reports)
MOUTH BREATHING ( 1 FDA reports)
MOYAMOYA DISEASE ( 1 FDA reports)
MUCKLE-WELLS SYNDROME ( 1 FDA reports)
MUCOCUTANEOUS CANDIDIASIS ( 1 FDA reports)
MUCORMYCOSIS ( 1 FDA reports)
MUCOSAL EXFOLIATION ( 1 FDA reports)
MUMPS ( 1 FDA reports)
MUSCLE ENZYME INCREASED ( 1 FDA reports)
MUSCULAR DYSTROPHY ( 1 FDA reports)
MYCETOMA MYCOTIC ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
MYCOBACTERIUM FORTUITUM INFECTION ( 1 FDA reports)
MYCOBACTERIUM KANSASII INFECTION ( 1 FDA reports)
MYCOBACTERIUM MARINUM INFECTION ( 1 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 1 FDA reports)
MYELOMALACIA ( 1 FDA reports)
MYOCARDIAL OEDEMA ( 1 FDA reports)
MYOCARDIAL STRAIN ( 1 FDA reports)
MYOGLOBIN BLOOD ( 1 FDA reports)
MYOGLOBIN BLOOD PRESENT ( 1 FDA reports)
MYOSITIS OSSIFICANS ( 1 FDA reports)
MYXOEDEMA ( 1 FDA reports)
NAIL BED INFECTION FUNGAL ( 1 FDA reports)
NAIL OPERATION ( 1 FDA reports)
NAIL PITTING ( 1 FDA reports)
NAIL TINEA ( 1 FDA reports)
NASAL INFLAMMATION ( 1 FDA reports)
NASAL OBSTRUCTION ( 1 FDA reports)
NASAL OPERATION ( 1 FDA reports)
NASAL SEPTUM ULCERATION ( 1 FDA reports)
NASOPHARYNGEAL CANCER RECURRENT ( 1 FDA reports)
NECK DEFORMITY ( 1 FDA reports)
NECK SURGERY ( 1 FDA reports)
NECROBIOSIS ( 1 FDA reports)
NECROTISING COLITIS ( 1 FDA reports)
NECROTISING FASCIITIS STREPTOCOCCAL ( 1 FDA reports)
NECROTISING RETINITIS ( 1 FDA reports)
NEONATAL RESPIRATORY FAILURE ( 1 FDA reports)
NEONATAL TACHYPNOEA ( 1 FDA reports)
NEOPLASM OF APPENDIX ( 1 FDA reports)
NEOPLASM OF THYMUS ( 1 FDA reports)
NEPHRITIS ALLERGIC ( 1 FDA reports)
NEPHROPTOSIS ( 1 FDA reports)
NEPHROSTOMY ( 1 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 1 FDA reports)
NERVE ROOT INJURY ( 1 FDA reports)
NEURALGIC AMYOTROPHY ( 1 FDA reports)
NEURODEGENERATIVE DISORDER ( 1 FDA reports)
NEUROENDOCRINE TUMOUR ( 1 FDA reports)
NEUROGENIC BOWEL ( 1 FDA reports)
NEUROGENIC SHOCK ( 1 FDA reports)
NEUROGLYCOPENIA ( 1 FDA reports)
NEUROPATHIC PAIN ( 1 FDA reports)
NEUROTROPHIC KERATOPATHY ( 1 FDA reports)
NEUTROPENIC INFECTION ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NIEMANN-PICK DISEASE ( 1 FDA reports)
NIGHT CRAMPS ( 1 FDA reports)
NIPPLE DISORDER ( 1 FDA reports)
NITRITE URINE ABSENT ( 1 FDA reports)
NO ADVERSE REACTION ( 1 FDA reports)
NOCARDIA SEPSIS ( 1 FDA reports)
NOCTURNAL FEAR ( 1 FDA reports)
NODULAR REGENERATIVE HYPERPLASIA ( 1 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE III ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER RECURRENT ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE I ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 1 FDA reports)
NOREPINEPHRINE INCREASED ( 1 FDA reports)
NORMAL NEWBORN ( 1 FDA reports)
OBSTRUCTIVE CHRONIC BRONCHITIS WITH ACUTE EXACERBATION ( 1 FDA reports)
OCCUPATIONAL EXPOSURE TO DUST ( 1 FDA reports)
OCCUPATIONAL EXPOSURE TO TOXIC AGENT ( 1 FDA reports)
OCULAR DYSMETRIA ( 1 FDA reports)
OCULAR TOXICITY ( 1 FDA reports)
OCULOCEPHALOGYRIC REFLEX ABSENT ( 1 FDA reports)
ODDI'S SPHINCTER CONSTRICTION ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA STAGE IV ( 1 FDA reports)
OESOPHAGEAL DILATION PROCEDURE ( 1 FDA reports)
OESOPHAGEAL MASS ( 1 FDA reports)
OESOPHAGEAL MUCOSA ERYTHEMA ( 1 FDA reports)
OESOPHAGEAL PERFORATION ( 1 FDA reports)
OESOPHAGEAL POLYP ( 1 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL ULCER PERFORATION ( 1 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 1 FDA reports)
OESTROGEN DEFICIENCY ( 1 FDA reports)
OLIGODIPSIA ( 1 FDA reports)
OMPHALITIS ( 1 FDA reports)
OPHTHALMOLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
OPTIC DISC DISORDER ( 1 FDA reports)
OPTIC DISCS BLURRED ( 1 FDA reports)
ORAL ALLERGY SYNDROME ( 1 FDA reports)
ORAL HAIRY LEUKOPLAKIA ( 1 FDA reports)
ORAL MUCOSAL DISORDER ( 1 FDA reports)
ORAL PUSTULE ( 1 FDA reports)
ORBITAL GRANULOMA ( 1 FDA reports)
OROMANDIBULAR DYSTONIA ( 1 FDA reports)
OROPHARYNGEAL CANCER RECURRENT ( 1 FDA reports)
OROPHARYNGEAL NEOPLASM ( 1 FDA reports)
OROPHARYNGITIS FUNGAL ( 1 FDA reports)
ORTHOSTATIC TREMOR ( 1 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 1 FDA reports)
OSTEOMYELITIS BACTERIAL ( 1 FDA reports)
OSTEOTOMY ( 1 FDA reports)
OTOSCLEROSIS ( 1 FDA reports)
OVARIAN ABSCESS ( 1 FDA reports)
OVARIAN CANCER RECURRENT ( 1 FDA reports)
OVARIAN CANCER STAGE III ( 1 FDA reports)
OVARIAN CYST RUPTURED ( 1 FDA reports)
OVARIAN CYST TORSION ( 1 FDA reports)
OVARIAN FIBROMA ( 1 FDA reports)
OVARIAN FIBROSIS ( 1 FDA reports)
OVARIAN TORSION ( 1 FDA reports)
OXYGEN CONSUMPTION ( 1 FDA reports)
OXYGEN SATURATION IMMEASURABLE ( 1 FDA reports)
PACEMAKER GENERATED RHYTHM ( 1 FDA reports)
PAGET'S DISEASE OF THE VULVA ( 1 FDA reports)
PALLANAESTHESIA ( 1 FDA reports)
PANCREATIC ABSCESS ( 1 FDA reports)
PANCREATIC FISTULA ( 1 FDA reports)
PANCREATIC NEUROENDOCRINE TUMOUR ( 1 FDA reports)
PANCREATIC OPERATION ( 1 FDA reports)
PANCREATIC SPHINCTEROTOMY ( 1 FDA reports)
PANCREATOGENOUS DIABETES ( 1 FDA reports)
PANOPHTHALMITIS ( 1 FDA reports)
PAPILLARY MUSCLE DISORDER ( 1 FDA reports)
PAPILLOMA VIRAL INFECTION ( 1 FDA reports)
PARAESTHESIA OF GENITAL MALE ( 1 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 1 FDA reports)
PARASOMNIA ( 1 FDA reports)
PARATHYROID GLAND OPERATION ( 1 FDA reports)
PARATHYROID HAEMORRHAGE ( 1 FDA reports)
PARATHYROID HORMONE-RELATED PROTEIN ABNORMAL ( 1 FDA reports)
PARATHYROID HORMONE-RELATED PROTEIN INCREASED ( 1 FDA reports)
PARATHYROID TUMOUR ( 1 FDA reports)
PARENTERAL NUTRITION ( 1 FDA reports)
PARESIS CRANIAL NERVE ( 1 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 1 FDA reports)
PASTEURELLA INFECTION ( 1 FDA reports)
PATIENT-DEVICE INCOMPATIBILITY ( 1 FDA reports)
PECTUS EXCAVATUM ( 1 FDA reports)
PEDAL PULSE ABSENT ( 1 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 1 FDA reports)
PELVIC FLOOR DYSSYNERGIA ( 1 FDA reports)
PELVIC FLOOR MUSCLE WEAKNESS ( 1 FDA reports)
PELVIC INFECTION ( 1 FDA reports)
PELVIC ORGAN INJURY ( 1 FDA reports)
PENETRATING ABDOMINAL TRAUMA ( 1 FDA reports)
PENILE BLISTER ( 1 FDA reports)
PENILE ERYTHEMA ( 1 FDA reports)
PENILE OPERATION ( 1 FDA reports)
PENILE PROSTHESIS INSERTION ( 1 FDA reports)
PENILE SIZE REDUCED ( 1 FDA reports)
PERFUME SENSITIVITY ( 1 FDA reports)
PERIANAL ABSCESS ( 1 FDA reports)
PERICARDIAL FIBROSIS ( 1 FDA reports)
PERICARDITIS RHEUMATIC ( 1 FDA reports)
PERICARDITIS URAEMIC ( 1 FDA reports)
PERINEAL ABSCESS ( 1 FDA reports)
PERINEAL LACERATION ( 1 FDA reports)
PERINEPHRIC COLLECTION ( 1 FDA reports)
PERIORBITAL DISORDER ( 1 FDA reports)
PERIPANCREATIC FLUID COLLECTION ( 1 FDA reports)
PERIPHERAL BLOOD STEM CELL APHERESIS ( 1 FDA reports)
PERIPHERAL NERVE DESTRUCTION ( 1 FDA reports)
PERIPHERAL PARALYSIS ( 1 FDA reports)
PERIPHERAL PULSE DECREASED ( 1 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED ( 1 FDA reports)
PERIPROCTITIS ( 1 FDA reports)
PERIPROSTHETIC FRACTURE ( 1 FDA reports)
PERITONEAL CARCINOMA METASTATIC ( 1 FDA reports)
PERITONEAL NECROSIS ( 1 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 1 FDA reports)
PERONEAL MUSCULAR ATROPHY ( 1 FDA reports)
PERONEAL NERVE INJURY ( 1 FDA reports)
PERONEAL NERVE PALSY POSTOPERATIVE ( 1 FDA reports)
PERSONALITY CHANGE DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 1 FDA reports)
PHARYNGEAL ABSCESS ( 1 FDA reports)
PHARYNGEAL CANCER STAGE UNSPECIFIED ( 1 FDA reports)
PHARYNGEAL LESION ( 1 FDA reports)
PHARYNGEAL POUCH ( 1 FDA reports)
PHOTOCOAGULATION ( 1 FDA reports)
PHOTODERMATOSIS ( 1 FDA reports)
PHOTOSENSITIVE RASH ( 1 FDA reports)
PHOTOSENSITIVITY ALLERGIC REACTION ( 1 FDA reports)
PIGMENTATION BUCCAL ( 1 FDA reports)
PIGMENTED NAEVUS ( 1 FDA reports)
PILONIDAL CYST CONGENITAL ( 1 FDA reports)
PIRIFORMIS SYNDROME ( 1 FDA reports)
PITUITARY CYST ( 1 FDA reports)
PITUITARY INFARCTION ( 1 FDA reports)
PLASMA CELL DISORDER ( 1 FDA reports)
PLASMA CELLS DECREASED ( 1 FDA reports)
PLASMA PROTEIN METABOLISM DISORDER ( 1 FDA reports)
PLASMA VISCOSITY DECREASED ( 1 FDA reports)
PLASMAPHERESIS ( 1 FDA reports)
PLASTIC SURGERY ( 1 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 1 FDA reports)
PLATELET FACTOR 4 ( 1 FDA reports)
PLATELET PRODUCTION DECREASED ( 1 FDA reports)
PLATYPNOEA ( 1 FDA reports)
PLEURAL INFECTION ( 1 FDA reports)
PLEURAL MESOTHELIOMA ( 1 FDA reports)
PLEUROPERICARDITIS ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PNEUMONIA HERPES VIRAL ( 1 FDA reports)
PNEUMONIA INFLUENZAL ( 1 FDA reports)
PO2 ABNORMAL ( 1 FDA reports)
POLYCHROMASIA ( 1 FDA reports)
POLYGLANDULAR DISORDER ( 1 FDA reports)
POLYMEDICATION ( 1 FDA reports)
POPLITEAL PULSE DECREASED ( 1 FDA reports)
POPLITEAL STENOSIS ( 1 FDA reports)
PORPHYRIA ( 1 FDA reports)
PORPHYRIA NON-ACUTE ( 1 FDA reports)
POST PROCEDURAL STROKE ( 1 FDA reports)
POST PROCEDURAL SWELLING ( 1 FDA reports)
POST STREPTOCOCCAL GLOMERULONEPHRITIS ( 1 FDA reports)
POST-TRAUMATIC AMNESTIC DISORDER ( 1 FDA reports)
POSTICTAL HEADACHE ( 1 FDA reports)
POSTOPERATIVE CARE ( 1 FDA reports)
POSTOPERATIVE HERNIA ( 1 FDA reports)
POSTOPERATIVE THROMBOSIS ( 1 FDA reports)
POVERTY OF SPEECH ( 1 FDA reports)
POVERTY OF THOUGHT CONTENT ( 1 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 1 FDA reports)
PREALBUMIN DECREASED ( 1 FDA reports)
PRECANCEROUS MUCOSAL LESION ( 1 FDA reports)
PREGNANCY OF PARTNER ( 1 FDA reports)
PREHYPERTENSION ( 1 FDA reports)
PREMATURE EJACULATION ( 1 FDA reports)
PREMATURE MENOPAUSE ( 1 FDA reports)
PRERENAL FAILURE ( 1 FDA reports)
PRESBYACUSIS ( 1 FDA reports)
PRODUCT CLOSURE ISSUE ( 1 FDA reports)
PRODUCT COMMINGLING ( 1 FDA reports)
PRODUCT COMPOUNDING QUALITY ISSUE ( 1 FDA reports)
PRODUCT CONTAINER SEAL ISSUE ( 1 FDA reports)
PRODUCT EXPIRATION DATE ISSUE ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PRODUCT LABEL ON WRONG PRODUCT ( 1 FDA reports)
PRODUCT PHYSICAL ISSUE ( 1 FDA reports)
PRODUCT RECONSTITUTION ISSUE ( 1 FDA reports)
PRODUCT SHAPE ISSUE ( 1 FDA reports)
PROLACTINOMA ( 1 FDA reports)
PROSTATE CANCER STAGE II ( 1 FDA reports)
PROSTATE TENDERNESS ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN ( 1 FDA reports)
PROTEIN C INCREASED ( 1 FDA reports)
PROTEIN S INCREASED ( 1 FDA reports)
PROTEUS TEST POSITIVE ( 1 FDA reports)
PRURITUS ANI ( 1 FDA reports)
PSEUDO LYMPHOMA ( 1 FDA reports)
PSEUDOBULBAR PALSY ( 1 FDA reports)
PSEUDODEMENTIA ( 1 FDA reports)
PSEUDOEXFOLIATION OF LENS CAPSULE ( 1 FDA reports)
PSEUDOHYPERKALAEMIA ( 1 FDA reports)
PSEUDOMENINGOCELE ( 1 FDA reports)
PSEUDOPORPHYRIA ( 1 FDA reports)
PSOAS ABSCESS ( 1 FDA reports)
PUBIC PAIN ( 1 FDA reports)
PUBIC RAMI FRACTURE ( 1 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE DECREASED ( 1 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 1 FDA reports)
PULMONARY HILAR ENLARGEMENT ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PULMONARY VALVE REPLACEMENT ( 1 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 1 FDA reports)
PULSE PRESSURE ABNORMAL ( 1 FDA reports)
PULSE VOLUME DECREASED ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
PYELECTASIA ( 1 FDA reports)
PYLORIC STENOSIS ( 1 FDA reports)
PYODERMA ( 1 FDA reports)
PYOMYOSITIS ( 1 FDA reports)
PYROGLUTAMATE INCREASED ( 1 FDA reports)
RADIAL PULSE ( 1 FDA reports)
RADIAL PULSE DECREASED ( 1 FDA reports)
RADIATION ASSOCIATED PAIN ( 1 FDA reports)
RADIATION PNEUMONITIS ( 1 FDA reports)
RADIATION RETINOPATHY ( 1 FDA reports)
RADICAL HYSTERECTOMY ( 1 FDA reports)
RASH MACULOVESICULAR ( 1 FDA reports)
RASH PAPULOSQUAMOUS ( 1 FDA reports)
RATHKE'S CLEFT CYST ( 1 FDA reports)
REACTION TO FOOD ADDITIVE ( 1 FDA reports)
REBOUND PSORIASIS ( 1 FDA reports)
RECTAL CRAMPS ( 1 FDA reports)
RECTOSIGMOID CANCER ( 1 FDA reports)
RED BLOOD CELL HYPOCHROMIC MORPHOLOGY PRESENT ( 1 FDA reports)
RED BLOOD CELLS SEMEN ( 1 FDA reports)
RED CELL FRAGMENTATION SYNDROME ( 1 FDA reports)
REFLEX TEST ABNORMAL ( 1 FDA reports)
REFRACTION DISORDER ( 1 FDA reports)
REHABILITATION THERAPY ( 1 FDA reports)
REITER'S SYNDROME ( 1 FDA reports)
RELATIONSHIP BREAKDOWN ( 1 FDA reports)
REMOVAL OF FOREIGN BODY ( 1 FDA reports)
RENAL ABSCESS ( 1 FDA reports)
RENAL AND PANCREAS TRANSPLANT ( 1 FDA reports)
RENAL ARTERITIS ( 1 FDA reports)
RENAL DYSPLASIA ( 1 FDA reports)
RENAL FAILURE NEONATAL ( 1 FDA reports)
RENAL LIPOMATOSIS ( 1 FDA reports)
RENAL LYMPHOCELE ( 1 FDA reports)
RENAL PAPILLARY NECROSIS ( 1 FDA reports)
RENAL SCAN ABNORMAL ( 1 FDA reports)
RENAL VASCULITIS ( 1 FDA reports)
RENOVASCULAR HYPERTENSION ( 1 FDA reports)
REOCCLUSION ( 1 FDA reports)
REPETITIVE STRAIN INJURY ( 1 FDA reports)
RESPIRATORY DEPTH INCREASED ( 1 FDA reports)
RESPIRATORY FREMITUS ( 1 FDA reports)
RESPIRATORY FUME INHALATION DISORDER ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS BRONCHIOLITIS ( 1 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
RESTING TREMOR ( 1 FDA reports)
RETAINED PLACENTA OR MEMBRANES ( 1 FDA reports)
RETICULOCYTE COUNT ABNORMAL ( 1 FDA reports)
RETINAL ANOMALY CONGENITAL ( 1 FDA reports)
RETINAL DEPIGMENTATION ( 1 FDA reports)
RETINAL MIGRAINE ( 1 FDA reports)
RETINAL NEOVASCULARISATION ( 1 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 1 FDA reports)
RETINAL PIGMENTATION ( 1 FDA reports)
RETINAL VASCULITIS ( 1 FDA reports)
RETROGNATHIA ( 1 FDA reports)
RETROPERITONEAL EFFUSION ( 1 FDA reports)
RETROPHARYNGEAL ABSCESS ( 1 FDA reports)
RHESUS ANTIBODIES POSITIVE ( 1 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 1 FDA reports)
RHINITIS PERENNIAL ( 1 FDA reports)
RIB EXCISION ( 1 FDA reports)
RIFT VALLEY FEVER ( 1 FDA reports)
RIGHT ATRIAL PRESSURE INCREASED ( 1 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE DECREASED ( 1 FDA reports)
ROCKY MOUNTAIN SPOTTED FEVER ( 1 FDA reports)
ROSAI-DORFMAN SYNDROME ( 1 FDA reports)
RUSSELL'S VIPER VENOM TIME ABNORMAL ( 1 FDA reports)
SALIVARY GLAND CALCULUS ( 1 FDA reports)
SALIVARY GLAND CANCER ( 1 FDA reports)
SALIVARY GLAND PAIN ( 1 FDA reports)
SCAN ( 1 FDA reports)
SCAN GALLIUM ABNORMAL ( 1 FDA reports)
SCAR EXCISION ( 1 FDA reports)
SCAR PAIN ( 1 FDA reports)
SCHISTOSOMA TEST POSITIVE ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER BIPOLAR TYPE ( 1 FDA reports)
SCIATIC NERVE NEUROPATHY ( 1 FDA reports)
SCLERODACTYLIA ( 1 FDA reports)
SCLEROEDEMA ( 1 FDA reports)
SCROTAL ERYTHEMA ( 1 FDA reports)
SCROTAL VARICOSE VEINS ( 1 FDA reports)
SEBACEOUS CYST EXCISION ( 1 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 1 FDA reports)
SECONDARY HYPERTHYROIDISM ( 1 FDA reports)
SELF-INDUCED VOMITING ( 1 FDA reports)
SEMEN ANALYSIS ABNORMAL ( 1 FDA reports)
SEMEN DISCOLOURATION ( 1 FDA reports)
SENILE OSTEOPOROSIS ( 1 FDA reports)
SENSATION OF BLOCK IN EAR ( 1 FDA reports)
SENSE OF OPPRESSION ( 1 FDA reports)
SEROLOGY ABNORMAL ( 1 FDA reports)
SERRATIA TEST POSITIVE ( 1 FDA reports)
SERUM SICKNESS-LIKE REACTION ( 1 FDA reports)
SEXUAL ABUSE ( 1 FDA reports)
SEXUAL ASSAULT VICTIM ( 1 FDA reports)
SEXUAL RELATIONSHIP CHANGE ( 1 FDA reports)
SHARED PSYCHOTIC DISORDER ( 1 FDA reports)
SHORT-BOWEL SYNDROME ( 1 FDA reports)
SHUNT MALFUNCTION ( 1 FDA reports)
SICCA SYNDROME ( 1 FDA reports)
SIGMOIDOSCOPY ( 1 FDA reports)
SIGMOIDOSCOPY ABNORMAL ( 1 FDA reports)
SINGLE PHOTON EMISSION COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
SINOBRONCHITIS ( 1 FDA reports)
SINUS PAIN ( 1 FDA reports)
SINUS RHYTHM ( 1 FDA reports)
SINUSITIS ASPERGILLUS ( 1 FDA reports)
SKELETAL MUSCLE ENZYMES ( 1 FDA reports)
SKIN CANCER METASTATIC ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN MACERATION ( 1 FDA reports)
SKIN NEOPLASM BLEEDING ( 1 FDA reports)
SKIN ULCER HAEMORRHAGE ( 1 FDA reports)
SKULL FRACTURED BASE ( 1 FDA reports)
SLEEP PHASE RHYTHM DISTURBANCE ( 1 FDA reports)
SLOW SPEECH ( 1 FDA reports)
SMALL FOR DATES BABY ( 1 FDA reports)
SMALL INTESTINAL RESECTION ( 1 FDA reports)
SMALL INTESTINE CARCINOMA ( 1 FDA reports)
SMALL INTESTINE CARCINOMA RECURRENT ( 1 FDA reports)
SMOKING CESSATION THERAPY ( 1 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 1 FDA reports)
SOCIAL PHOBIA ( 1 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 1 FDA reports)
SOFT TISSUE NEOPLASM ( 1 FDA reports)
SOMOGYI PHENOMENON ( 1 FDA reports)
SPASTIC PARALYSIS ( 1 FDA reports)
SPECIFIC GRAVITY URINE DECREASED ( 1 FDA reports)
SPERM CONCENTRATION DECREASED ( 1 FDA reports)
SPERMATOZOA ABNORMAL ( 1 FDA reports)
SPERMATOZOA PROGRESSIVE MOTILITY DECREASED ( 1 FDA reports)
SPINA BIFIDA ( 1 FDA reports)
SPINAL CORD HERNIATION ( 1 FDA reports)
SPINAL CORD INJURY LUMBAR ( 1 FDA reports)
SPINAL CORD ISCHAEMIA ( 1 FDA reports)
SPINAL CORD PARALYSIS ( 1 FDA reports)
SPINAL EPIDURAL HAEMORRHAGE ( 1 FDA reports)
SPINAL HAEMATOMA ( 1 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 1 FDA reports)
SPLENIC HAEMORRHAGE ( 1 FDA reports)
SPLENIC NECROSIS ( 1 FDA reports)
SPONDYLOSIS ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF THE CERVIX ( 1 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 1 FDA reports)
STENOTROPHOMONAS SEPSIS ( 1 FDA reports)
STENOTROPHOMONAS TEST POSITIVE ( 1 FDA reports)
STICKY SKIN ( 1 FDA reports)
STOMA SITE ABSCESS ( 1 FDA reports)
STOOLS WATERY ( 1 FDA reports)
STRABISMUS CONGENITAL ( 1 FDA reports)
STRAWBERRY TONGUE ( 1 FDA reports)
STRONGYLOIDIASIS ( 1 FDA reports)
SUBCLAVIAN STEAL SYNDROME ( 1 FDA reports)
SUBCORNEAL PUSTULAR DERMATOSIS ( 1 FDA reports)
SUBMAXILLARY GLAND ENLARGEMENT ( 1 FDA reports)
SUBSTANCE ABUSER ( 1 FDA reports)
SUBSTANCE-INDUCED PSYCHOTIC DISORDER ( 1 FDA reports)
SULPHAEMOGLOBINAEMIA ( 1 FDA reports)
SUPERFICIAL INJURY OF EYE ( 1 FDA reports)
SUPERFICIAL SPREADING MELANOMA STAGE III ( 1 FDA reports)
SUPERINFECTION BACTERIAL ( 1 FDA reports)
SUPERIOR VENA CAVAL STENOSIS ( 1 FDA reports)
SUPRAVALVULAR AORTIC STENOSIS ( 1 FDA reports)
SUTURE INSERTION ( 1 FDA reports)
SUTURE REMOVAL ( 1 FDA reports)
SWEAT DISCOLOURATION ( 1 FDA reports)
SWEATING FEVER ( 1 FDA reports)
SYNOVECTOMY ( 1 FDA reports)
SYNOVIAL RUPTURE ( 1 FDA reports)
SYRINGOMYELIA ( 1 FDA reports)
TACITURNITY ( 1 FDA reports)
TANDEM GAIT TEST ( 1 FDA reports)
TATTOO ( 1 FDA reports)
TEAR DISCOLOURATION ( 1 FDA reports)
TENDON CALCIFICATION ( 1 FDA reports)
TENDON TRANSFER ( 1 FDA reports)
TENODESIS ( 1 FDA reports)
TESTICULAR ABSCESS ( 1 FDA reports)
TESTICULAR APPENDAGE TORSION ( 1 FDA reports)
TESTICULAR OEDEMA ( 1 FDA reports)
TESTICULAR RETRACTION ( 1 FDA reports)
TESTICULAR TORSION ( 1 FDA reports)
THALASSAEMIA BETA ( 1 FDA reports)
THALASSAEMIA TRAIT ( 1 FDA reports)
THERAPEUTIC HYPOTHERMIA ( 1 FDA reports)
THORACIC CAVITY DRAINAGE ( 1 FDA reports)
THROMBIN TIME PROLONGED ( 1 FDA reports)
THROMBIN-ANTITHROMBIN III COMPLEX INCREASED ( 1 FDA reports)
THROMBOANGIITIS OBLITERANS ( 1 FDA reports)
THROMBOEMBOLECTOMY ( 1 FDA reports)
THROMBOLYSIS ( 1 FDA reports)
THYROID FUNCTION TEST NORMAL ( 1 FDA reports)
THYROXINE ABNORMAL ( 1 FDA reports)
TICK-BORNE FEVER ( 1 FDA reports)
TILT TABLE TEST ( 1 FDA reports)
TISSUE ANOXIA ( 1 FDA reports)
TOE DEFORMITY ( 1 FDA reports)
TONGUE NEOPLASM ( 1 FDA reports)
TONGUE SPASM ( 1 FDA reports)
TORULOPSIS INFECTION ( 1 FDA reports)
TOTAL LUNG CAPACITY INCREASED ( 1 FDA reports)
TOXIC ANTERIOR SEGMENT SYNDROME ( 1 FDA reports)
TOXICOLOGIC TEST ( 1 FDA reports)
TOXICOLOGIC TEST NORMAL ( 1 FDA reports)
TRABECULECTOMY ( 1 FDA reports)
TRACHEAL HAEMORRHAGE ( 1 FDA reports)
TRACHEAL PAIN ( 1 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 1 FDA reports)
TRACHEOMALACIA ( 1 FDA reports)
TRACHOMA ( 1 FDA reports)
TRANSAMINASES ( 1 FDA reports)
TRANSITIONAL CELL CANCER OF THE RENAL PELVIS AND URETER ( 1 FDA reports)
TRANSVESTISM ( 1 FDA reports)
TRAUMATIC ARTHRITIS ( 1 FDA reports)
TRAUMATIC INTRACRANIAL HAEMORRHAGE ( 1 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 1 FDA reports)
TRICUSPID VALVE PROLAPSE ( 1 FDA reports)
TRICUSPID VALVE STENOSIS ( 1 FDA reports)
TRIGEMINAL NERVE DISORDER ( 1 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 1 FDA reports)
TRUNCUS COELIACUS THROMBOSIS ( 1 FDA reports)
TUBERCULOSIS TEST POSITIVE ( 1 FDA reports)
TUMOUR EXCISION ( 1 FDA reports)
TUMOUR INVASION ( 1 FDA reports)
TUMOUR THROMBOSIS ( 1 FDA reports)
TURNER'S SYNDROME ( 1 FDA reports)
TYMPANIC MEMBRANE ATROPHIC ( 1 FDA reports)
TYMPANIC MEMBRANE SCARRING ( 1 FDA reports)
TYPHOID FEVER ( 1 FDA reports)
ULTRASOUND BREAST ABNORMAL ( 1 FDA reports)
UMBILICAL HAEMORRHAGE ( 1 FDA reports)
UPPER MOTOR NEURONE LESION ( 1 FDA reports)
UPPER RESPIRATORY FUNGAL INFECTION ( 1 FDA reports)
UPPER RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
URATE NEPHROPATHY ( 1 FDA reports)
URETERIC CANCER METASTATIC ( 1 FDA reports)
URETERIC OPERATION ( 1 FDA reports)
URETHRAL ABSCESS ( 1 FDA reports)
URETHRAL CANCER ( 1 FDA reports)
URETHRAL CANCER METASTATIC ( 1 FDA reports)
URETHRAL FISTULA ( 1 FDA reports)
URETHRAL OBSTRUCTION ( 1 FDA reports)
URETHRAL PAPILLOMA ( 1 FDA reports)
URETHRITIS ( 1 FDA reports)
URINARY CASTS PRESENT ( 1 FDA reports)
URINARY CYSTECTOMY ( 1 FDA reports)
URINARY SYSTEM X-RAY ABNORMAL ( 1 FDA reports)
URINARY TRACT NEOPLASM ( 1 FDA reports)
URINARY TRACT OPERATION ( 1 FDA reports)
URINE CHLORIDE INCREASED ( 1 FDA reports)
URINE COPPER DECREASED ( 1 FDA reports)
URINE LACTIC ACID ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE ( 1 FDA reports)
URINE OXALATE DECREASED ( 1 FDA reports)
URINE PROTEIN/CREATININE RATIO ABNORMAL ( 1 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 1 FDA reports)
UROBILIN URINE ( 1 FDA reports)
UROBILINOGEN URINE ( 1 FDA reports)
UROGENITAL DISORDER ( 1 FDA reports)
UROGENITAL FISTULA ( 1 FDA reports)
URTICARIA LOCALISED ( 1 FDA reports)
URTICARIA PAPULAR ( 1 FDA reports)
URTICARIA PHYSICAL ( 1 FDA reports)
UTERINE CERVIX STENOSIS ( 1 FDA reports)
UTERINE LEIOMYOSARCOMA ( 1 FDA reports)
UTERINE MASS ( 1 FDA reports)
UTERINE OPERATION ( 1 FDA reports)
UTERINE STENOSIS ( 1 FDA reports)
VAGINAL CANCER STAGE III ( 1 FDA reports)
VAGINAL INFLAMMATION ( 1 FDA reports)
VAGINAL SWELLING ( 1 FDA reports)
VASCULAR ACCESS COMPLICATION ( 1 FDA reports)
VASCULAR BYPASS DYSFUNCTION ( 1 FDA reports)
VASCULAR COMPRESSION ( 1 FDA reports)
VASCULAR RESISTANCE SYSTEMIC INCREASED ( 1 FDA reports)
VEIN PAIN ( 1 FDA reports)
VELOPHARYNGEAL INCOMPETENCE ( 1 FDA reports)
VENA CAVA INJURY ( 1 FDA reports)
VENIPUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
VENOOCCLUSIVE DISEASE ( 1 FDA reports)
VENOUS PRESSURE JUGULAR ABNORMAL ( 1 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 1 FDA reports)
VENTRICLE RUPTURE ( 1 FDA reports)
VENTRICULAR ASYSTOLE ( 1 FDA reports)
VENTRICULAR TACHYARRHYTHMIA ( 1 FDA reports)
VENTRICULAR WALL THICKENING ( 1 FDA reports)
VERTEBRAL COLUMN MASS ( 1 FDA reports)
VERTEBRAL WEDGING ( 1 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
VESICAL FISTULA ( 1 FDA reports)
VESSEL PERFORATION ( 1 FDA reports)
VICTIM OF ELDER ABUSE ( 1 FDA reports)
VIRAEMIA ( 1 FDA reports)
VIRAL DIARRHOEA ( 1 FDA reports)
VIRAL MYOSITIS ( 1 FDA reports)
VIRAL OESOPHAGITIS ( 1 FDA reports)
VIRAL SINUSITIS ( 1 FDA reports)
VIRUS CULTURE POSITIVE ( 1 FDA reports)
VIRUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
VISUAL ACUITY TESTS NORMAL ( 1 FDA reports)
VISUAL EVOKED POTENTIALS ABNORMAL ( 1 FDA reports)
VITAMIN A DECREASED ( 1 FDA reports)
VITRITIS ( 1 FDA reports)
VOCAL CORD NEOPLASM ( 1 FDA reports)
VOCAL CORD POLYP ( 1 FDA reports)
VOLVULUS OF BOWEL ( 1 FDA reports)
VOLVULUS OF SMALL BOWEL ( 1 FDA reports)
VOMITING IN PREGNANCY ( 1 FDA reports)
VOMITING PSYCHOGENIC ( 1 FDA reports)
VULVAL OEDEMA ( 1 FDA reports)
VULVAR EROSION ( 1 FDA reports)
VULVITIS ( 1 FDA reports)
VULVOVAGINITIS GONOCOCCAL ( 1 FDA reports)
WALLENBERG SYNDROME ( 1 FDA reports)
WANDERING PACEMAKER ( 1 FDA reports)
WEIGHT GAIN POOR ( 1 FDA reports)
WHITE BLOOD CELL ANALYSIS INCREASED ( 1 FDA reports)
WHITE BLOOD CELL MORPHOLOGY ABNORMAL ( 1 FDA reports)
WHOLE BLOOD TRANSFUSION ( 1 FDA reports)
WINGED SCAPULA ( 1 FDA reports)
WOUND INFECTION BACTERIAL ( 1 FDA reports)
XANTHELASMA ( 1 FDA reports)
YOUNG'S SYNDROME ( 1 FDA reports)