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

DRUG DOSE OMISSION ( 9816 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 7433 FDA reports)
NAUSEA ( 6749 FDA reports)
PAIN ( 6253 FDA reports)
DRUG INEFFECTIVE ( 6006 FDA reports)
MALAISE ( 5247 FDA reports)
VOMITING ( 5140 FDA reports)
DYSPNOEA ( 5083 FDA reports)
DIARRHOEA ( 4468 FDA reports)
DYSPEPSIA ( 4341 FDA reports)
HEADACHE ( 4118 FDA reports)
CHEST PAIN ( 3886 FDA reports)
FATIGUE ( 3818 FDA reports)
ANXIETY ( 3763 FDA reports)
DIZZINESS ( 3724 FDA reports)
FALL ( 3646 FDA reports)
ABDOMINAL PAIN UPPER ( 3560 FDA reports)
ASTHENIA ( 3221 FDA reports)
DEPRESSION ( 3185 FDA reports)
WEIGHT DECREASED ( 3052 FDA reports)
OSTEOPOROSIS ( 3000 FDA reports)
ABDOMINAL PAIN ( 2997 FDA reports)
ARTHRALGIA ( 2885 FDA reports)
BACK PAIN ( 2874 FDA reports)
PNEUMONIA ( 2845 FDA reports)
PAIN IN EXTREMITY ( 2821 FDA reports)
HYPERTENSION ( 2772 FDA reports)
INSOMNIA ( 2729 FDA reports)
ANAEMIA ( 2653 FDA reports)
PYREXIA ( 2584 FDA reports)
OEDEMA PERIPHERAL ( 2488 FDA reports)
MYOCARDIAL INFARCTION ( 2353 FDA reports)
COUGH ( 2277 FDA reports)
ABDOMINAL DISCOMFORT ( 2191 FDA reports)
CONSTIPATION ( 2114 FDA reports)
OFF LABEL USE ( 2010 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2008 FDA reports)
DYSPHAGIA ( 1897 FDA reports)
FEELING ABNORMAL ( 1786 FDA reports)
DEHYDRATION ( 1763 FDA reports)
RASH ( 1731 FDA reports)
INTENTIONAL DRUG MISUSE ( 1668 FDA reports)
DIABETES MELLITUS ( 1635 FDA reports)
INJURY ( 1625 FDA reports)
PRURITUS ( 1591 FDA reports)
WEIGHT INCREASED ( 1577 FDA reports)
MUSCLE SPASMS ( 1569 FDA reports)
HYPOTENSION ( 1567 FDA reports)
OSTEOARTHRITIS ( 1547 FDA reports)
HYPOAESTHESIA ( 1491 FDA reports)
URINARY TRACT INFECTION ( 1473 FDA reports)
PARAESTHESIA ( 1440 FDA reports)
RENAL FAILURE ACUTE ( 1438 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1429 FDA reports)
CONFUSIONAL STATE ( 1426 FDA reports)
BRONCHITIS ( 1422 FDA reports)
MYALGIA ( 1415 FDA reports)
DEATH ( 1414 FDA reports)
DECREASED APPETITE ( 1414 FDA reports)
RENAL FAILURE ( 1405 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1398 FDA reports)
GAIT DISTURBANCE ( 1392 FDA reports)
TREMOR ( 1370 FDA reports)
MULTIPLE FRACTURES ( 1367 FDA reports)
HIATUS HERNIA ( 1348 FDA reports)
ARTHRITIS ( 1347 FDA reports)
SOMNOLENCE ( 1316 FDA reports)
DRUG INTERACTION ( 1305 FDA reports)
BLOOD GLUCOSE INCREASED ( 1280 FDA reports)
ABDOMINAL DISTENSION ( 1275 FDA reports)
ATRIAL FIBRILLATION ( 1271 FDA reports)
GASTRIC DISORDER ( 1254 FDA reports)
SINUSITIS ( 1248 FDA reports)
EMOTIONAL DISTRESS ( 1234 FDA reports)
CONDITION AGGRAVATED ( 1230 FDA reports)
BONE DISORDER ( 1225 FDA reports)
ASTHMA ( 1221 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1174 FDA reports)
CHEST DISCOMFORT ( 1171 FDA reports)
CARDIAC DISORDER ( 1167 FDA reports)
HYPERHIDROSIS ( 1161 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1124 FDA reports)
GASTRITIS ( 1124 FDA reports)
PLEURAL EFFUSION ( 1113 FDA reports)
BLOOD PRESSURE INCREASED ( 1112 FDA reports)
CONVULSION ( 1096 FDA reports)
THROMBOCYTOPENIA ( 1091 FDA reports)
VISION BLURRED ( 1088 FDA reports)
PALPITATIONS ( 1080 FDA reports)
OSTEONECROSIS OF JAW ( 1078 FDA reports)
DRY MOUTH ( 1065 FDA reports)
LOSS OF CONSCIOUSNESS ( 1065 FDA reports)
MUSCULAR WEAKNESS ( 1051 FDA reports)
CORONARY ARTERY DISEASE ( 1027 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1002 FDA reports)
DEEP VEIN THROMBOSIS ( 995 FDA reports)
THROAT IRRITATION ( 992 FDA reports)
MEMORY IMPAIRMENT ( 986 FDA reports)
CHOLELITHIASIS ( 983 FDA reports)
CHILLS ( 980 FDA reports)
FLATULENCE ( 974 FDA reports)
NEOPLASM MALIGNANT ( 971 FDA reports)
DYSGEUSIA ( 970 FDA reports)
SEPSIS ( 957 FDA reports)
PULMONARY EMBOLISM ( 956 FDA reports)
INFECTION ( 945 FDA reports)
ERYTHEMA ( 942 FDA reports)
HAEMOGLOBIN DECREASED ( 942 FDA reports)
SYNCOPE ( 942 FDA reports)
NEUROPATHY PERIPHERAL ( 941 FDA reports)
APHAGIA ( 940 FDA reports)
NECK PAIN ( 930 FDA reports)
ADVERSE EVENT ( 914 FDA reports)
NASOPHARYNGITIS ( 908 FDA reports)
DYSPHONIA ( 900 FDA reports)
MUSCULOSKELETAL PAIN ( 878 FDA reports)
OROPHARYNGEAL PAIN ( 862 FDA reports)
OSTEOMYELITIS ( 855 FDA reports)
AMNESIA ( 853 FDA reports)
BONE PAIN ( 852 FDA reports)
FLUSHING ( 848 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 842 FDA reports)
SPINAL OSTEOARTHRITIS ( 837 FDA reports)
CONTUSION ( 834 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 826 FDA reports)
CATARACT ( 821 FDA reports)
OSTEOPENIA ( 804 FDA reports)
ROAD TRAFFIC ACCIDENT ( 800 FDA reports)
SWELLING ( 795 FDA reports)
RESPIRATORY FAILURE ( 789 FDA reports)
MIGRAINE ( 786 FDA reports)
HYPERSENSITIVITY ( 784 FDA reports)
HEART RATE INCREASED ( 777 FDA reports)
HYPOKALAEMIA ( 773 FDA reports)
OSTEONECROSIS ( 769 FDA reports)
BURNING SENSATION ( 767 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 759 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 754 FDA reports)
BALANCE DISORDER ( 741 FDA reports)
FOOT FRACTURE ( 725 FDA reports)
PANCREATITIS ( 721 FDA reports)
CELLULITIS ( 713 FDA reports)
NERVOUSNESS ( 706 FDA reports)
PAIN IN JAW ( 703 FDA reports)
TOOTH EXTRACTION ( 703 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 703 FDA reports)
TACHYCARDIA ( 693 FDA reports)
ULCER ( 686 FDA reports)
ANHEDONIA ( 685 FDA reports)
GALLBLADDER DISORDER ( 685 FDA reports)
HYPONATRAEMIA ( 685 FDA reports)
NEUTROPENIA ( 652 FDA reports)
JOINT SWELLING ( 651 FDA reports)
HYPERLIPIDAEMIA ( 650 FDA reports)
HAEMORRHAGE ( 649 FDA reports)
URTICARIA ( 646 FDA reports)
ERUCTATION ( 645 FDA reports)
IMPAIRED HEALING ( 638 FDA reports)
THROMBOSIS ( 636 FDA reports)
STRESS ( 634 FDA reports)
ATELECTASIS ( 631 FDA reports)
HAEMORRHOIDS ( 626 FDA reports)
DRUG EFFECT DECREASED ( 625 FDA reports)
VISUAL IMPAIRMENT ( 622 FDA reports)
CARDIAC ARREST ( 621 FDA reports)
ARTHROPATHY ( 618 FDA reports)
ALOPECIA ( 617 FDA reports)
CHOLECYSTITIS CHRONIC ( 614 FDA reports)
OVERDOSE ( 601 FDA reports)
PANCYTOPENIA ( 597 FDA reports)
DENTAL CARIES ( 597 FDA reports)
ILL-DEFINED DISORDER ( 596 FDA reports)
GASTRIC ULCER ( 594 FDA reports)
RECTAL HAEMORRHAGE ( 592 FDA reports)
INFLUENZA ( 587 FDA reports)
DRUG HYPERSENSITIVITY ( 585 FDA reports)
MENTAL STATUS CHANGES ( 577 FDA reports)
AGITATION ( 574 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 574 FDA reports)
VERTIGO ( 568 FDA reports)
DIVERTICULUM ( 563 FDA reports)
TYPE 2 DIABETES MELLITUS ( 561 FDA reports)
ANGINA PECTORIS ( 558 FDA reports)
ANKLE FRACTURE ( 555 FDA reports)
BARRETT'S OESOPHAGUS ( 554 FDA reports)
BLOOD CREATININE INCREASED ( 553 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 549 FDA reports)
LUNG DISORDER ( 545 FDA reports)
CARDIOMEGALY ( 537 FDA reports)
MITRAL VALVE INCOMPETENCE ( 536 FDA reports)
NEPHROLITHIASIS ( 536 FDA reports)
SUICIDAL IDEATION ( 536 FDA reports)
OEDEMA ( 533 FDA reports)
RIB FRACTURE ( 529 FDA reports)
SPEECH DISORDER ( 529 FDA reports)
SLEEP APNOEA SYNDROME ( 528 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 525 FDA reports)
UPPER LIMB FRACTURE ( 524 FDA reports)
LYMPHADENOPATHY ( 519 FDA reports)
RENAL FAILURE CHRONIC ( 518 FDA reports)
STAPHYLOCOCCAL INFECTION ( 516 FDA reports)
METASTASES TO BONE ( 514 FDA reports)
GASTROINTESTINAL DISORDER ( 508 FDA reports)
EPISTAXIS ( 505 FDA reports)
BONE DENSITY DECREASED ( 504 FDA reports)
LETHARGY ( 497 FDA reports)
OESOPHAGITIS ( 497 FDA reports)
DISCOMFORT ( 494 FDA reports)
HAEMATOCHEZIA ( 494 FDA reports)
FIBROMYALGIA ( 493 FDA reports)
SURGERY ( 493 FDA reports)
ABASIA ( 491 FDA reports)
HYPOTHYROIDISM ( 486 FDA reports)
PLATELET COUNT DECREASED ( 485 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 484 FDA reports)
MENTAL DISORDER ( 484 FDA reports)
POLLAKIURIA ( 480 FDA reports)
BREAST CANCER ( 479 FDA reports)
HALLUCINATION ( 476 FDA reports)
DEFORMITY ( 473 FDA reports)
STOMATITIS ( 469 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 469 FDA reports)
CARDIAC FAILURE ( 467 FDA reports)
DYSURIA ( 465 FDA reports)
LOWER LIMB FRACTURE ( 465 FDA reports)
ECONOMIC PROBLEM ( 464 FDA reports)
REGURGITATION ( 464 FDA reports)
VITAMIN D DEFICIENCY ( 463 FDA reports)
SWELLING FACE ( 462 FDA reports)
HAEMATEMESIS ( 461 FDA reports)
CHOKING ( 459 FDA reports)
DYSPNOEA EXERTIONAL ( 459 FDA reports)
INJECTION SITE PAIN ( 456 FDA reports)
TOOTHACHE ( 456 FDA reports)
WHEEZING ( 454 FDA reports)
HEPATIC ENZYME INCREASED ( 453 FDA reports)
NASAL CONGESTION ( 452 FDA reports)
BRADYCARDIA ( 450 FDA reports)
INFLUENZA LIKE ILLNESS ( 447 FDA reports)
ARRHYTHMIA ( 443 FDA reports)
ANOREXIA ( 442 FDA reports)
DISORIENTATION ( 439 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 439 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 437 FDA reports)
LEUKOPENIA ( 436 FDA reports)
ROTATOR CUFF SYNDROME ( 434 FDA reports)
IRRITABLE BOWEL SYNDROME ( 432 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 430 FDA reports)
INFLAMMATION ( 429 FDA reports)
HERPES ZOSTER ( 428 FDA reports)
HYPERGLYCAEMIA ( 428 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 427 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 427 FDA reports)
FEMUR FRACTURE ( 423 FDA reports)
PANIC ATTACK ( 423 FDA reports)
HOT FLUSH ( 422 FDA reports)
EXOSTOSIS ( 419 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 418 FDA reports)
BLOOD PRESSURE DECREASED ( 414 FDA reports)
BLOOD GLUCOSE DECREASED ( 412 FDA reports)
HEPATIC STEATOSIS ( 411 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 411 FDA reports)
TINNITUS ( 409 FDA reports)
TOOTH DISORDER ( 409 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 407 FDA reports)
HERNIA ( 406 FDA reports)
RHEUMATOID ARTHRITIS ( 405 FDA reports)
SLEEP DISORDER ( 405 FDA reports)
PULMONARY OEDEMA ( 404 FDA reports)
BLINDNESS ( 404 FDA reports)
FAECES DISCOLOURED ( 404 FDA reports)
DIVERTICULITIS ( 401 FDA reports)
SEPTIC SHOCK ( 399 FDA reports)
SPINAL FRACTURE ( 397 FDA reports)
HAEMATURIA ( 395 FDA reports)
PRODUCT QUALITY ISSUE ( 391 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 390 FDA reports)
HIP FRACTURE ( 387 FDA reports)
HYPOXIA ( 384 FDA reports)
MOUTH ULCERATION ( 383 FDA reports)
BURSITIS ( 380 FDA reports)
CANDIDIASIS ( 376 FDA reports)
LUNG NEOPLASM ( 373 FDA reports)
SCAR ( 371 FDA reports)
PULMONARY HYPERTENSION ( 370 FDA reports)
FEELING HOT ( 370 FDA reports)
RENAL IMPAIRMENT ( 369 FDA reports)
OESOPHAGEAL DISORDER ( 368 FDA reports)
RENAL DISORDER ( 367 FDA reports)
WRONG DRUG ADMINISTERED ( 365 FDA reports)
DISTURBANCE IN ATTENTION ( 365 FDA reports)
GLAUCOMA ( 365 FDA reports)
BLOOD POTASSIUM DECREASED ( 364 FDA reports)
IRRITABILITY ( 364 FDA reports)
MULTIPLE MYELOMA ( 363 FDA reports)
COMA ( 362 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 361 FDA reports)
DISABILITY ( 361 FDA reports)
JAUNDICE ( 360 FDA reports)
COLITIS ( 359 FDA reports)
HEART RATE IRREGULAR ( 358 FDA reports)
VISUAL ACUITY REDUCED ( 358 FDA reports)
URINARY INCONTINENCE ( 357 FDA reports)
EAR PAIN ( 354 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 354 FDA reports)
RENAL CYST ( 352 FDA reports)
HYPERCHOLESTEROLAEMIA ( 351 FDA reports)
HYPERKALAEMIA ( 350 FDA reports)
JOINT INJURY ( 348 FDA reports)
DISEASE PROGRESSION ( 347 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 346 FDA reports)
EATING DISORDER ( 346 FDA reports)
HAEMATOMA ( 344 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 343 FDA reports)
EMPHYSEMA ( 341 FDA reports)
MULTI-ORGAN FAILURE ( 341 FDA reports)
DYSARTHRIA ( 340 FDA reports)
TOOTH ABSCESS ( 340 FDA reports)
FLUID RETENTION ( 337 FDA reports)
UNEVALUABLE EVENT ( 336 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 336 FDA reports)
TOOTH FRACTURE ( 334 FDA reports)
ABNORMAL DREAMS ( 333 FDA reports)
CHOLECYSTITIS ( 331 FDA reports)
HAEMATOCRIT DECREASED ( 331 FDA reports)
CROHN'S DISEASE ( 330 FDA reports)
SINUS DISORDER ( 330 FDA reports)
RHABDOMYOLYSIS ( 329 FDA reports)
DRY EYE ( 328 FDA reports)
HYPOGLYCAEMIA ( 325 FDA reports)
RHINORRHOEA ( 325 FDA reports)
FEBRILE NEUTROPENIA ( 321 FDA reports)
BACK INJURY ( 318 FDA reports)
CYSTITIS ( 318 FDA reports)
HAEMOPTYSIS ( 318 FDA reports)
TOOTH LOSS ( 318 FDA reports)
BACK DISORDER ( 316 FDA reports)
COLONIC POLYP ( 316 FDA reports)
CYTOLYTIC HEPATITIS ( 316 FDA reports)
MOBILITY DECREASED ( 316 FDA reports)
ASCITES ( 314 FDA reports)
HEAD INJURY ( 313 FDA reports)
INTERSTITIAL LUNG DISEASE ( 313 FDA reports)
RESPIRATORY DISTRESS ( 309 FDA reports)
PERICARDIAL EFFUSION ( 307 FDA reports)
TREATMENT NONCOMPLIANCE ( 307 FDA reports)
HYPOPHAGIA ( 303 FDA reports)
ERECTILE DYSFUNCTION ( 302 FDA reports)
LIVER DISORDER ( 302 FDA reports)
NIGHT SWEATS ( 302 FDA reports)
RESTLESS LEGS SYNDROME ( 301 FDA reports)
OBESITY ( 299 FDA reports)
ARTERIOSCLEROSIS ( 299 FDA reports)
LIMB INJURY ( 299 FDA reports)
PRIMARY SEQUESTRUM ( 298 FDA reports)
VIRAL INFECTION ( 297 FDA reports)
ADVERSE DRUG REACTION ( 297 FDA reports)
EYE PAIN ( 297 FDA reports)
DEAFNESS ( 296 FDA reports)
DRUG PRESCRIBING ERROR ( 296 FDA reports)
OXYGEN SATURATION DECREASED ( 296 FDA reports)
WRIST FRACTURE ( 296 FDA reports)
CARPAL TUNNEL SYNDROME ( 295 FDA reports)
PRODUCTIVE COUGH ( 294 FDA reports)
PANCREATITIS ACUTE ( 292 FDA reports)
BLOOD BILIRUBIN INCREASED ( 292 FDA reports)
FEAR ( 289 FDA reports)
DYSKINESIA ( 288 FDA reports)
CARDIOMYOPATHY ( 287 FDA reports)
CORONARY ARTERY OCCLUSION ( 287 FDA reports)
LARYNGITIS ( 287 FDA reports)
LUNG INFILTRATION ( 287 FDA reports)
SPINAL COMPRESSION FRACTURE ( 285 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 284 FDA reports)
FRACTURE ( 284 FDA reports)
BLISTER ( 283 FDA reports)
CHOLESTASIS ( 282 FDA reports)
DECREASED INTEREST ( 282 FDA reports)
BILIARY DYSKINESIA ( 281 FDA reports)
GASTROENTERITIS ( 281 FDA reports)
GLOSSODYNIA ( 281 FDA reports)
RETCHING ( 281 FDA reports)
SPINAL COLUMN STENOSIS ( 280 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 279 FDA reports)
LUNG NEOPLASM MALIGNANT ( 279 FDA reports)
MUCOSAL INFLAMMATION ( 278 FDA reports)
JOINT DISLOCATION ( 276 FDA reports)
MEDICATION ERROR ( 276 FDA reports)
RHINITIS ALLERGIC ( 276 FDA reports)
OESOPHAGEAL PAIN ( 275 FDA reports)
EMOTIONAL DISORDER ( 274 FDA reports)
SKIN EXFOLIATION ( 273 FDA reports)
URINARY RETENTION ( 273 FDA reports)
SUICIDE ATTEMPT ( 271 FDA reports)
HEPATITIS ( 271 FDA reports)
DRUG INTOLERANCE ( 270 FDA reports)
MELAENA ( 270 FDA reports)
MULTIPLE INJURIES ( 270 FDA reports)
MULTIPLE SCLEROSIS ( 270 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 268 FDA reports)
AGGRESSION ( 266 FDA reports)
BONE LESION ( 266 FDA reports)
INTESTINAL OBSTRUCTION ( 266 FDA reports)
CHOLECYSTECTOMY ( 265 FDA reports)
CARDIO-RESPIRATORY ARREST ( 262 FDA reports)
MENISCUS LESION ( 262 FDA reports)
NEURALGIA ( 262 FDA reports)
TOOTH INFECTION ( 262 FDA reports)
SCOLIOSIS ( 261 FDA reports)
DIPLOPIA ( 261 FDA reports)
ABSCESS ( 259 FDA reports)
FUNGAL INFECTION ( 259 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 259 FDA reports)
METABOLIC ACIDOSIS ( 259 FDA reports)
RASH PRURITIC ( 259 FDA reports)
SINUS TACHYCARDIA ( 258 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 258 FDA reports)
ULCER HAEMORRHAGE ( 258 FDA reports)
DRY SKIN ( 258 FDA reports)
INJECTION SITE ERYTHEMA ( 257 FDA reports)
ABNORMAL BEHAVIOUR ( 255 FDA reports)
AGRANULOCYTOSIS ( 255 FDA reports)
BLOOD SODIUM DECREASED ( 254 FDA reports)
ABDOMINAL PAIN LOWER ( 253 FDA reports)
METASTASES TO LIVER ( 252 FDA reports)
CRYING ( 251 FDA reports)
INJECTION SITE HAEMORRHAGE ( 250 FDA reports)
THROAT TIGHTNESS ( 250 FDA reports)
LEUKOCYTOSIS ( 247 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 246 FDA reports)
EYE DISORDER ( 246 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 246 FDA reports)
BONE DEBRIDEMENT ( 245 FDA reports)
EROSIVE OESOPHAGITIS ( 245 FDA reports)
POOR QUALITY SLEEP ( 245 FDA reports)
RESTLESSNESS ( 245 FDA reports)
ORAL PAIN ( 244 FDA reports)
PNEUMONIA ASPIRATION ( 244 FDA reports)
RASH ERYTHEMATOUS ( 244 FDA reports)
ANGER ( 244 FDA reports)
ENCEPHALOPATHY ( 244 FDA reports)
LOOSE TOOTH ( 244 FDA reports)
HAND FRACTURE ( 243 FDA reports)
FLANK PAIN ( 242 FDA reports)
ORAL DISCOMFORT ( 241 FDA reports)
PHARYNGEAL OEDEMA ( 241 FDA reports)
GASTRIC POLYPS ( 240 FDA reports)
GINGIVAL PAIN ( 240 FDA reports)
LIMB DISCOMFORT ( 240 FDA reports)
PATHOLOGICAL FRACTURE ( 239 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 239 FDA reports)
SWOLLEN TONGUE ( 238 FDA reports)
RASH MACULO-PAPULAR ( 237 FDA reports)
SKIN ULCER ( 237 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 236 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 235 FDA reports)
HEPATIC FAILURE ( 235 FDA reports)
STOMACH DISCOMFORT ( 235 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 234 FDA reports)
APHASIA ( 234 FDA reports)
HYPERCHLORHYDRIA ( 234 FDA reports)
BLOOD UREA INCREASED ( 233 FDA reports)
PURULENT DISCHARGE ( 232 FDA reports)
RESPIRATORY DISORDER ( 232 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 231 FDA reports)
CALCIUM DEFICIENCY ( 229 FDA reports)
DIVERTICULUM INTESTINAL ( 229 FDA reports)
POST PROCEDURAL COMPLICATION ( 229 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 228 FDA reports)
HYPOACUSIS ( 228 FDA reports)
BLOOD CALCIUM DECREASED ( 227 FDA reports)
ANAPHYLACTIC REACTION ( 226 FDA reports)
CYST ( 226 FDA reports)
DEMENTIA ( 225 FDA reports)
COGNITIVE DISORDER ( 224 FDA reports)
NERVOUS SYSTEM DISORDER ( 224 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 223 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 223 FDA reports)
COMPRESSION FRACTURE ( 221 FDA reports)
DRUG DEPENDENCE ( 221 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 221 FDA reports)
SKIN LESION ( 221 FDA reports)
DELIRIUM ( 220 FDA reports)
HEARING IMPAIRED ( 219 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 218 FDA reports)
GASTRIC HAEMORRHAGE ( 218 FDA reports)
IRON DEFICIENCY ANAEMIA ( 218 FDA reports)
PULMONARY FIBROSIS ( 218 FDA reports)
UNRESPONSIVE TO STIMULI ( 218 FDA reports)
RASH GENERALISED ( 217 FDA reports)
CARDIAC MURMUR ( 216 FDA reports)
CEREBRAL ATROPHY ( 216 FDA reports)
LUMBAR SPINAL STENOSIS ( 215 FDA reports)
OSTEOLYSIS ( 215 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 214 FDA reports)
DIABETIC NEUROPATHY ( 214 FDA reports)
BIPOLAR DISORDER ( 213 FDA reports)
APHONIA ( 212 FDA reports)
MYOCARDIAL ISCHAEMIA ( 212 FDA reports)
POLYP ( 212 FDA reports)
TENDONITIS ( 212 FDA reports)
PROSTATE CANCER ( 211 FDA reports)
DEPRESSED MOOD ( 211 FDA reports)
ECZEMA ( 211 FDA reports)
HOSPITALISATION ( 211 FDA reports)
JAW DISORDER ( 210 FDA reports)
ENDODONTIC PROCEDURE ( 209 FDA reports)
PRURITUS GENERALISED ( 207 FDA reports)
DEBRIDEMENT ( 206 FDA reports)
INJECTION SITE HAEMATOMA ( 206 FDA reports)
ANGINA UNSTABLE ( 205 FDA reports)
MALNUTRITION ( 205 FDA reports)
BASAL CELL CARCINOMA ( 204 FDA reports)
HEART RATE DECREASED ( 204 FDA reports)
EJECTION FRACTION DECREASED ( 203 FDA reports)
ORAL CANDIDIASIS ( 203 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 203 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 202 FDA reports)
EXPOSED BONE IN JAW ( 201 FDA reports)
ILEUS ( 201 FDA reports)
EOSINOPHILIA ( 199 FDA reports)
FEELING JITTERY ( 198 FDA reports)
VENTRICULAR TACHYCARDIA ( 198 FDA reports)
OESOPHAGEAL ULCER ( 197 FDA reports)
TARDIVE DYSKINESIA ( 197 FDA reports)
KNEE ARTHROPLASTY ( 197 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 196 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 196 FDA reports)
HYPERCALCAEMIA ( 196 FDA reports)
MASTICATION DISORDER ( 196 FDA reports)
SKIN DISCOLOURATION ( 196 FDA reports)
SKIN DISORDER ( 196 FDA reports)
UTERINE LEIOMYOMA ( 195 FDA reports)
CEREBRAL HAEMORRHAGE ( 195 FDA reports)
EYE SWELLING ( 195 FDA reports)
MACULAR DEGENERATION ( 195 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 194 FDA reports)
PNEUMOTHORAX ( 194 FDA reports)
PEPTIC ULCER ( 193 FDA reports)
CHROMATURIA ( 193 FDA reports)
GENERALISED OEDEMA ( 193 FDA reports)
GINGIVAL BLEEDING ( 191 FDA reports)
SENSATION OF FOREIGN BODY ( 191 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 190 FDA reports)
MUSCLE TWITCHING ( 190 FDA reports)
CAROTID ARTERY STENOSIS ( 189 FDA reports)
DRUG TOXICITY ( 188 FDA reports)
PERIODONTITIS ( 187 FDA reports)
RASH MACULAR ( 187 FDA reports)
HEPATIC CYST ( 186 FDA reports)
HYPOAESTHESIA ORAL ( 186 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 185 FDA reports)
NIGHTMARE ( 185 FDA reports)
ORTHOSTATIC HYPOTENSION ( 184 FDA reports)
RADICULOPATHY ( 183 FDA reports)
SCIATICA ( 183 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 183 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 183 FDA reports)
GOUT ( 183 FDA reports)
MENTAL IMPAIRMENT ( 183 FDA reports)
CARDIOVASCULAR DISORDER ( 181 FDA reports)
GASTRITIS EROSIVE ( 181 FDA reports)
MIDDLE INSOMNIA ( 181 FDA reports)
ACCIDENT ( 180 FDA reports)
HEPATIC LESION ( 179 FDA reports)
HYPERSOMNIA ( 179 FDA reports)
HYPOKINESIA ( 179 FDA reports)
LIGAMENT SPRAIN ( 179 FDA reports)
MUSCLE STRAIN ( 179 FDA reports)
THYROID DISORDER ( 179 FDA reports)
STEVENS-JOHNSON SYNDROME ( 178 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 178 FDA reports)
BLOOD POTASSIUM INCREASED ( 178 FDA reports)
BONE LOSS ( 178 FDA reports)
DENTAL OPERATION ( 178 FDA reports)
FISTULA ( 178 FDA reports)
AGEUSIA ( 177 FDA reports)
COLITIS ULCERATIVE ( 177 FDA reports)
HAEMODIALYSIS ( 177 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 176 FDA reports)
SINUS BRADYCARDIA ( 175 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 175 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 174 FDA reports)
HEPATIC CIRRHOSIS ( 174 FDA reports)
HYPOMAGNESAEMIA ( 174 FDA reports)
PARANOIA ( 174 FDA reports)
SPINAL DISORDER ( 173 FDA reports)
EAR INFECTION ( 173 FDA reports)
HYPOCALCAEMIA ( 173 FDA reports)
INFUSION RELATED REACTION ( 173 FDA reports)
MOOD SWINGS ( 173 FDA reports)
DRUG ADMINISTRATION ERROR ( 172 FDA reports)
IMPAIRED WORK ABILITY ( 172 FDA reports)
PARKINSON'S DISEASE ( 172 FDA reports)
THINKING ABNORMAL ( 172 FDA reports)
FACE OEDEMA ( 171 FDA reports)
PRESYNCOPE ( 170 FDA reports)
PSYCHOTIC DISORDER ( 170 FDA reports)
COLITIS ISCHAEMIC ( 169 FDA reports)
DISEASE RECURRENCE ( 169 FDA reports)
ASPIRATION ( 168 FDA reports)
COORDINATION ABNORMAL ( 168 FDA reports)
DYSSTASIA ( 168 FDA reports)
GINGIVITIS ( 168 FDA reports)
GRAND MAL CONVULSION ( 168 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 168 FDA reports)
FLUID OVERLOAD ( 167 FDA reports)
PULMONARY CONGESTION ( 167 FDA reports)
PSORIASIS ( 166 FDA reports)
GASTROENTERITIS VIRAL ( 166 FDA reports)
JOINT STIFFNESS ( 166 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 166 FDA reports)
HYDRONEPHROSIS ( 165 FDA reports)
MOVEMENT DISORDER ( 164 FDA reports)
RHINITIS ( 164 FDA reports)
SKIN CANCER ( 164 FDA reports)
JOINT EFFUSION ( 163 FDA reports)
OESOPHAGEAL SPASM ( 162 FDA reports)
TIBIA FRACTURE ( 162 FDA reports)
PELVIC FRACTURE ( 161 FDA reports)
LUNG INFECTION ( 161 FDA reports)
MULTIPLE ALLERGIES ( 161 FDA reports)
COAGULOPATHY ( 160 FDA reports)
DYSLIPIDAEMIA ( 160 FDA reports)
SKIN BURNING SENSATION ( 160 FDA reports)
WITHDRAWAL SYNDROME ( 160 FDA reports)
VAGINAL HAEMORRHAGE ( 158 FDA reports)
HIP ARTHROPLASTY ( 158 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 156 FDA reports)
LOCALISED INFECTION ( 156 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 156 FDA reports)
PERIODONTAL DISEASE ( 156 FDA reports)
PHARYNGITIS ( 156 FDA reports)
RESPIRATORY ARREST ( 155 FDA reports)
EXCORIATION ( 155 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 155 FDA reports)
HEPATOMEGALY ( 155 FDA reports)
MITRAL VALVE PROLAPSE ( 155 FDA reports)
AORTIC VALVE INCOMPETENCE ( 154 FDA reports)
DERMATITIS ( 154 FDA reports)
GOITRE ( 154 FDA reports)
JAW OPERATION ( 154 FDA reports)
MASS ( 154 FDA reports)
PROCEDURAL PAIN ( 154 FDA reports)
STRESS FRACTURE ( 154 FDA reports)
TENDERNESS ( 154 FDA reports)
COLON CANCER ( 153 FDA reports)
FOOT DEFORMITY ( 153 FDA reports)
LUMBAR RADICULOPATHY ( 153 FDA reports)
CEREBRAL INFARCTION ( 152 FDA reports)
HYPOVOLAEMIA ( 152 FDA reports)
METASTATIC NEOPLASM ( 152 FDA reports)
ORAL DISORDER ( 152 FDA reports)
PELVIC PAIN ( 151 FDA reports)
DIALYSIS ( 151 FDA reports)
EYE IRRITATION ( 151 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 151 FDA reports)
GINGIVAL SWELLING ( 151 FDA reports)
METASTASES TO SPINE ( 150 FDA reports)
OSTEITIS ( 150 FDA reports)
PHYSICAL DISABILITY ( 150 FDA reports)
TOXIC SKIN ERUPTION ( 150 FDA reports)
NEOPLASM PROGRESSION ( 149 FDA reports)
TYPE 1 DIABETES MELLITUS ( 148 FDA reports)
ATRIAL FLUTTER ( 148 FDA reports)
BACTERIAL INFECTION ( 148 FDA reports)
CYANOSIS ( 148 FDA reports)
FEELING COLD ( 148 FDA reports)
BLADDER DISORDER ( 147 FDA reports)
CERVICAL SPINAL STENOSIS ( 147 FDA reports)
DECUBITUS ULCER ( 147 FDA reports)
MAJOR DEPRESSION ( 147 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 147 FDA reports)
OESOPHAGEAL CARCINOMA ( 146 FDA reports)
OVARIAN CYST ( 146 FDA reports)
SPONDYLOLISTHESIS ( 146 FDA reports)
BODY HEIGHT DECREASED ( 146 FDA reports)
BONE MARROW FAILURE ( 146 FDA reports)
KYPHOSIS ( 146 FDA reports)
LYMPHOMA ( 146 FDA reports)
ANGIOEDEMA ( 145 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 145 FDA reports)
CHRONIC SINUSITIS ( 145 FDA reports)
FAECAL INCONTINENCE ( 145 FDA reports)
GROIN PAIN ( 145 FDA reports)
HALLUCINATION, VISUAL ( 145 FDA reports)
HEMIPARESIS ( 144 FDA reports)
TRANSAMINASES INCREASED ( 144 FDA reports)
KIDNEY INFECTION ( 143 FDA reports)
METASTASES TO LUNG ( 143 FDA reports)
ACUTE SINUSITIS ( 142 FDA reports)
BREAST MASS ( 142 FDA reports)
LIP SWELLING ( 142 FDA reports)
SEDATION ( 142 FDA reports)
STENT PLACEMENT ( 142 FDA reports)
WALKING AID USER ( 142 FDA reports)
OESOPHAGEAL STENOSIS ( 141 FDA reports)
SINUS CONGESTION ( 141 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 141 FDA reports)
MICTURITION URGENCY ( 141 FDA reports)
MUSCULOSKELETAL DISORDER ( 141 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 140 FDA reports)
PALLOR ( 140 FDA reports)
PARAESTHESIA ORAL ( 139 FDA reports)
ACCIDENTAL OVERDOSE ( 139 FDA reports)
LOBAR PNEUMONIA ( 139 FDA reports)
ACCIDENT AT WORK ( 138 FDA reports)
BREAST PAIN ( 137 FDA reports)
CEREBRAL ISCHAEMIA ( 137 FDA reports)
HEPATITIS C ( 137 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 137 FDA reports)
ELECTROLYTE IMBALANCE ( 136 FDA reports)
HYPERKERATOSIS ( 136 FDA reports)
OCULAR HYPERAEMIA ( 136 FDA reports)
SHOCK ( 136 FDA reports)
PERONEAL NERVE PALSY ( 135 FDA reports)
PROTHROMBIN TIME PROLONGED ( 135 FDA reports)
SPLENOMEGALY ( 135 FDA reports)
COLD SWEAT ( 135 FDA reports)
CIRCULATORY COLLAPSE ( 134 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 134 FDA reports)
NERVE COMPRESSION ( 133 FDA reports)
BLINDNESS UNILATERAL ( 133 FDA reports)
DUODENAL ULCER ( 133 FDA reports)
ESCHERICHIA INFECTION ( 133 FDA reports)
VASCULITIS ( 132 FDA reports)
THIRST ( 131 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 131 FDA reports)
HAEMANGIOMA ( 131 FDA reports)
HELICOBACTER INFECTION ( 131 FDA reports)
JOINT SPRAIN ( 131 FDA reports)
BRONCHOSPASM ( 130 FDA reports)
GINGIVAL DISORDER ( 130 FDA reports)
ACUTE RESPIRATORY FAILURE ( 129 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 129 FDA reports)
BRONCHOPNEUMONIA ( 129 FDA reports)
LIPASE INCREASED ( 129 FDA reports)
ORAL CAVITY FISTULA ( 129 FDA reports)
TENDON RUPTURE ( 128 FDA reports)
DEVICE RELATED INFECTION ( 128 FDA reports)
LACRIMATION INCREASED ( 128 FDA reports)
IMPAIRED DRIVING ABILITY ( 127 FDA reports)
NON-CARDIAC CHEST PAIN ( 127 FDA reports)
QUALITY OF LIFE DECREASED ( 127 FDA reports)
PROTEINURIA ( 126 FDA reports)
REFLUX OESOPHAGITIS ( 126 FDA reports)
BLOOD ALBUMIN DECREASED ( 126 FDA reports)
DERMAL CYST ( 126 FDA reports)
LYMPHOEDEMA ( 126 FDA reports)
CARDIAC VALVE DISEASE ( 125 FDA reports)
COELIAC DISEASE ( 125 FDA reports)
MUSCLE TIGHTNESS ( 125 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 124 FDA reports)
CONJUNCTIVITIS ( 124 FDA reports)
DIFFICULTY IN WALKING ( 124 FDA reports)
GALLBLADDER INJURY ( 124 FDA reports)
GASTROINTESTINAL PAIN ( 124 FDA reports)
JAW FRACTURE ( 124 FDA reports)
NERVE INJURY ( 124 FDA reports)
PNEUMONITIS ( 123 FDA reports)
PURPURA ( 123 FDA reports)
VITAMIN B12 DEFICIENCY ( 123 FDA reports)
HALLUCINATION, AUDITORY ( 123 FDA reports)
ABDOMINAL HERNIA ( 122 FDA reports)
BLOOD CALCIUM INCREASED ( 122 FDA reports)
BLOOD URINE PRESENT ( 122 FDA reports)
PHOTOPHOBIA ( 122 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 121 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 121 FDA reports)
DEVICE FAILURE ( 121 FDA reports)
ECCHYMOSIS ( 121 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 120 FDA reports)
HEPATOCELLULAR INJURY ( 120 FDA reports)
MUSCLE ATROPHY ( 120 FDA reports)
OSTEOSCLEROSIS ( 120 FDA reports)
POLYURIA ( 120 FDA reports)
SEQUESTRECTOMY ( 120 FDA reports)
NOCTURIA ( 119 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 119 FDA reports)
WOUND ( 119 FDA reports)
CORONARY ARTERY STENOSIS ( 119 FDA reports)
EPILEPSY ( 119 FDA reports)
BONE FRAGMENTATION ( 118 FDA reports)
CORONARY ARTERY BYPASS ( 118 FDA reports)
LEFT ATRIAL DILATATION ( 118 FDA reports)
LOCAL SWELLING ( 118 FDA reports)
ORAL INFECTION ( 118 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 118 FDA reports)
SUBDURAL HAEMATOMA ( 118 FDA reports)
THYROID NEOPLASM ( 118 FDA reports)
ODYNOPHAGIA ( 117 FDA reports)
POLYNEUROPATHY ( 117 FDA reports)
RESPIRATORY TRACT INFECTION ( 117 FDA reports)
VENTRICULAR FIBRILLATION ( 117 FDA reports)
AORTIC ANEURYSM ( 117 FDA reports)
BLOOD MAGNESIUM DECREASED ( 117 FDA reports)
CARDIAC OPERATION ( 116 FDA reports)
GINGIVAL INFECTION ( 116 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 116 FDA reports)
INCREASED APPETITE ( 116 FDA reports)
ISCHAEMIC STROKE ( 116 FDA reports)
PANCREATIC CARCINOMA ( 116 FDA reports)
PETECHIAE ( 114 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 114 FDA reports)
CLOSTRIDIAL INFECTION ( 114 FDA reports)
BODY TEMPERATURE INCREASED ( 113 FDA reports)
DRY THROAT ( 113 FDA reports)
ESSENTIAL HYPERTENSION ( 113 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 113 FDA reports)
VENTRICULAR HYPERTROPHY ( 113 FDA reports)
PHLEBITIS ( 112 FDA reports)
TONGUE DISORDER ( 112 FDA reports)
BEDRIDDEN ( 112 FDA reports)
BREAST CANCER FEMALE ( 112 FDA reports)
CARDIAC PACEMAKER INSERTION ( 112 FDA reports)
FIBROSIS ( 112 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 112 FDA reports)
HEMIPLEGIA ( 112 FDA reports)
MANIA ( 112 FDA reports)
MYOCLONUS ( 112 FDA reports)
ACUTE CORONARY SYNDROME ( 111 FDA reports)
BACTERAEMIA ( 111 FDA reports)
DIABETIC KETOACIDOSIS ( 111 FDA reports)
PLEURITIC PAIN ( 111 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 111 FDA reports)
NODULE ( 110 FDA reports)
PARALYSIS ( 110 FDA reports)
RADIOTHERAPY ( 110 FDA reports)
SENSORY DISTURBANCE ( 110 FDA reports)
ACTINOMYCOSIS ( 110 FDA reports)
BRAIN NEOPLASM ( 110 FDA reports)
DUODENITIS ( 110 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 110 FDA reports)
ATAXIA ( 109 FDA reports)
CATARACT OPERATION ( 109 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 109 FDA reports)
HEPATITIS CHOLESTATIC ( 109 FDA reports)
ABDOMINAL TENDERNESS ( 108 FDA reports)
BONE EROSION ( 108 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 108 FDA reports)
DENTURE WEARER ( 107 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 107 FDA reports)
INJECTION SITE REACTION ( 107 FDA reports)
MOUTH HAEMORRHAGE ( 107 FDA reports)
MYOSITIS ( 107 FDA reports)
PLATELET COUNT INCREASED ( 107 FDA reports)
BREATH ODOUR ( 106 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 106 FDA reports)
HEPATIC ENCEPHALOPATHY ( 106 FDA reports)
ABSCESS JAW ( 105 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 105 FDA reports)
HYPOALBUMINAEMIA ( 105 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 105 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 105 FDA reports)
SEBORRHOEIC KERATOSIS ( 105 FDA reports)
SKIN INDURATION ( 105 FDA reports)
VISUAL DISTURBANCE ( 105 FDA reports)
SKIN LACERATION ( 104 FDA reports)
ACNE ( 104 FDA reports)
HUMERUS FRACTURE ( 104 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 104 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 103 FDA reports)
AZOTAEMIA ( 103 FDA reports)
INTENTIONAL OVERDOSE ( 103 FDA reports)
LYMPHOPENIA ( 103 FDA reports)
NEUTROPHIL COUNT DECREASED ( 103 FDA reports)
PANCREATITIS CHRONIC ( 103 FDA reports)
RASH PAPULAR ( 103 FDA reports)
NO THERAPEUTIC RESPONSE ( 102 FDA reports)
CONCUSSION ( 102 FDA reports)
DERMATITIS CONTACT ( 102 FDA reports)
HICCUPS ( 102 FDA reports)
EAR DISCOMFORT ( 101 FDA reports)
MOOD ALTERED ( 101 FDA reports)
MYELODYSPLASTIC SYNDROME ( 101 FDA reports)
ANGIOPATHY ( 100 FDA reports)
BLEPHARITIS ( 100 FDA reports)
BONE FORMATION DECREASED ( 100 FDA reports)
DEVICE MALFUNCTION ( 100 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 100 FDA reports)
TONGUE DISCOLOURATION ( 100 FDA reports)
NECK INJURY ( 99 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 99 FDA reports)
PROCTALGIA ( 99 FDA reports)
PYELONEPHRITIS ( 99 FDA reports)
RENAL INJURY ( 99 FDA reports)
THROAT CANCER ( 99 FDA reports)
ANURIA ( 99 FDA reports)
AORTIC STENOSIS ( 99 FDA reports)
BLOOD PRESSURE ABNORMAL ( 99 FDA reports)
EXPIRED DRUG ADMINISTERED ( 98 FDA reports)
LACTIC ACIDOSIS ( 98 FDA reports)
SENSORY LOSS ( 98 FDA reports)
TONGUE ULCERATION ( 98 FDA reports)
CHOLECYSTITIS ACUTE ( 97 FDA reports)
ENTEROCOCCAL INFECTION ( 97 FDA reports)
GALLBLADDER OPERATION ( 97 FDA reports)
GRANULOMA ( 97 FDA reports)
LACERATION ( 97 FDA reports)
NASAL SEPTUM DEVIATION ( 97 FDA reports)
ANAPHYLACTIC SHOCK ( 96 FDA reports)
FIBULA FRACTURE ( 96 FDA reports)
ORAL SURGERY ( 96 FDA reports)
RESPIRATORY TRACT CONGESTION ( 96 FDA reports)
PHOTOSENSITIVITY REACTION ( 95 FDA reports)
RENAL TUBULAR NECROSIS ( 95 FDA reports)
SYNOVIAL CYST ( 95 FDA reports)
THYROID CANCER ( 95 FDA reports)
ACTINIC KERATOSIS ( 95 FDA reports)
ANEURYSM ( 95 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 95 FDA reports)
INCONTINENCE ( 95 FDA reports)
DILATATION VENTRICULAR ( 94 FDA reports)
KNEE OPERATION ( 94 FDA reports)
OSTEORADIONECROSIS ( 94 FDA reports)
UROSEPSIS ( 94 FDA reports)
PERIPHERAL ISCHAEMIA ( 93 FDA reports)
PLEURISY ( 93 FDA reports)
PSEUDOMONAS INFECTION ( 93 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 93 FDA reports)
BLADDER CANCER ( 93 FDA reports)
CATHETERISATION CARDIAC ( 93 FDA reports)
CHOKING SENSATION ( 93 FDA reports)
EYELID OEDEMA ( 93 FDA reports)
HERPES SIMPLEX ( 93 FDA reports)
LIBIDO DECREASED ( 93 FDA reports)
LIVER INJURY ( 93 FDA reports)
FACIAL PAIN ( 92 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 92 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 92 FDA reports)
RENAL PAIN ( 92 FDA reports)
SPONDYLITIS ( 92 FDA reports)
BREAST CANCER METASTATIC ( 91 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 91 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 91 FDA reports)
FAILURE TO THRIVE ( 90 FDA reports)
PERSONALITY CHANGE ( 90 FDA reports)
SINUS HEADACHE ( 90 FDA reports)
STEM CELL TRANSPLANT ( 90 FDA reports)
SCAB ( 89 FDA reports)
APPARENT DEATH ( 89 FDA reports)
DENTAL FISTULA ( 89 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 89 FDA reports)
INJECTION SITE PRURITUS ( 89 FDA reports)
METASTASES TO LYMPH NODES ( 89 FDA reports)
ACUTE PULMONARY OEDEMA ( 88 FDA reports)
ALVEOLOPLASTY ( 88 FDA reports)
MYOPATHY ( 88 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 88 FDA reports)
THROMBOCYTOSIS ( 88 FDA reports)
NEOPLASM ( 87 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 87 FDA reports)
ACIDOSIS ( 87 FDA reports)
COMPLETED SUICIDE ( 87 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 87 FDA reports)
DRUG ABUSE ( 86 FDA reports)
EYE PRURITUS ( 86 FDA reports)
GASTRIC CANCER ( 86 FDA reports)
HYPERTHYROIDISM ( 86 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 86 FDA reports)
SJOGREN'S SYNDROME ( 86 FDA reports)
SPINAL CORD COMPRESSION ( 86 FDA reports)
VITREOUS FLOATERS ( 86 FDA reports)
ONYCHOMYCOSIS ( 85 FDA reports)
SKIN HYPERPIGMENTATION ( 85 FDA reports)
LIFE EXPECTANCY SHORTENED ( 85 FDA reports)
APLASTIC ANAEMIA ( 84 FDA reports)
EPIGASTRIC DISCOMFORT ( 84 FDA reports)
EXTRASYSTOLES ( 84 FDA reports)
HYPERBILIRUBINAEMIA ( 84 FDA reports)
HYPOAESTHESIA FACIAL ( 84 FDA reports)
PROCEDURAL COMPLICATION ( 84 FDA reports)
VITAMIN D DECREASED ( 84 FDA reports)
ROSACEA ( 83 FDA reports)
COSTOCHONDRITIS ( 83 FDA reports)
MUSCLE DISORDER ( 83 FDA reports)
BLOOD IRON DECREASED ( 82 FDA reports)
DIASTOLIC DYSFUNCTION ( 82 FDA reports)
MALIGNANT MELANOMA ( 82 FDA reports)
OTITIS MEDIA ( 82 FDA reports)
PERICARDITIS ( 82 FDA reports)
VIITH NERVE PARALYSIS ( 82 FDA reports)
PANIC DISORDER ( 81 FDA reports)
PLASMACYTOSIS ( 81 FDA reports)
RALES ( 81 FDA reports)
SUDDEN DEATH ( 81 FDA reports)
DILATATION ATRIAL ( 81 FDA reports)
EYE HAEMORRHAGE ( 81 FDA reports)
HEART VALVE INCOMPETENCE ( 81 FDA reports)
HYSTERECTOMY ( 81 FDA reports)
MEDICAL DEVICE COMPLICATION ( 81 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 80 FDA reports)
ADRENAL INSUFFICIENCY ( 80 FDA reports)
AREFLEXIA ( 80 FDA reports)
BRAIN OEDEMA ( 80 FDA reports)
CARDIAC FLUTTER ( 80 FDA reports)
LOW TURNOVER OSTEOPATHY ( 80 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 80 FDA reports)
PERITONITIS ( 80 FDA reports)
PLANTAR FASCIITIS ( 80 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 80 FDA reports)
SCLERODERMA ( 80 FDA reports)
SKIN HYPERTROPHY ( 80 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 80 FDA reports)
VENOUS THROMBOSIS ( 80 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 80 FDA reports)
NEURITIS ( 79 FDA reports)
ORAL INTAKE REDUCED ( 79 FDA reports)
SEROTONIN SYNDROME ( 79 FDA reports)
SKIN TIGHTNESS ( 79 FDA reports)
SQUAMOUS CELL CARCINOMA ( 79 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 79 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 79 FDA reports)
MELANOCYTIC NAEVUS ( 79 FDA reports)
MUSCLE CRAMP ( 79 FDA reports)
APATHY ( 78 FDA reports)
APPENDICITIS ( 78 FDA reports)
DELUSION ( 78 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 78 FDA reports)
GYNAECOMASTIA ( 78 FDA reports)
IMMUNE SYSTEM DISORDER ( 78 FDA reports)
INITIAL INSOMNIA ( 78 FDA reports)
INTESTINAL PERFORATION ( 78 FDA reports)
ISCHAEMIA ( 78 FDA reports)
RESORPTION BONE INCREASED ( 78 FDA reports)
VOCAL CORD DISORDER ( 78 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 77 FDA reports)
CHOLANGITIS ( 77 FDA reports)
HYPERVENTILATION ( 77 FDA reports)
INCREASED TENDENCY TO BRUISE ( 77 FDA reports)
LIGAMENT RUPTURE ( 77 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 76 FDA reports)
CLUSTER HEADACHE ( 76 FDA reports)
DIZZINESS POSTURAL ( 76 FDA reports)
DYSPHEMIA ( 76 FDA reports)
INTERMITTENT CLAUDICATION ( 76 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 76 FDA reports)
SEASONAL ALLERGY ( 76 FDA reports)
TEMPERATURE INTOLERANCE ( 76 FDA reports)
URINE OUTPUT DECREASED ( 76 FDA reports)
PATHOLOGICAL GAMBLING ( 75 FDA reports)
SPUTUM DISCOLOURED ( 75 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 75 FDA reports)
APNOEA ( 75 FDA reports)
BLOOD DISORDER ( 75 FDA reports)
BONE NEOPLASM MALIGNANT ( 75 FDA reports)
BRONCHITIS CHRONIC ( 75 FDA reports)
DERMATITIS EXFOLIATIVE ( 75 FDA reports)
FOOD INTOLERANCE ( 75 FDA reports)
GINGIVAL ULCERATION ( 75 FDA reports)
HAEMORRHAGIC ANAEMIA ( 75 FDA reports)
HYDROCEPHALUS ( 75 FDA reports)
INGROWING NAIL ( 75 FDA reports)
INTESTINAL HAEMORRHAGE ( 75 FDA reports)
LABORATORY TEST ABNORMAL ( 75 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 75 FDA reports)
DRUG DISPENSING ERROR ( 74 FDA reports)
DRUG LEVEL INCREASED ( 74 FDA reports)
HYPERTHERMIA ( 74 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 74 FDA reports)
MASTECTOMY ( 74 FDA reports)
NECROSIS ( 74 FDA reports)
NO ADVERSE EVENT ( 74 FDA reports)
PERIPHERAL COLDNESS ( 74 FDA reports)
SNEEZING ( 74 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 74 FDA reports)
WOUND INFECTION ( 74 FDA reports)
NEUROPATHY ( 73 FDA reports)
ORAL HERPES ( 73 FDA reports)
PULMONARY MASS ( 73 FDA reports)
SARCOIDOSIS ( 73 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 73 FDA reports)
GASTROINTESTINAL ULCER ( 73 FDA reports)
GINGIVAL RECESSION ( 73 FDA reports)
MEDICATION RESIDUE ( 73 FDA reports)
LIMB CRUSHING INJURY ( 72 FDA reports)
MOTOR DYSFUNCTION ( 72 FDA reports)
OCCULT BLOOD POSITIVE ( 72 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 72 FDA reports)
OSTEOPOROTIC FRACTURE ( 71 FDA reports)
TRISMUS ( 71 FDA reports)
APLASIA PURE RED CELL ( 71 FDA reports)
ASTIGMATISM ( 71 FDA reports)
BRAIN INJURY ( 71 FDA reports)
FRACTURE NONUNION ( 71 FDA reports)
HAEMODYNAMIC INSTABILITY ( 71 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 71 FDA reports)
LEUKAEMIA ( 71 FDA reports)
ABDOMINAL ADHESIONS ( 70 FDA reports)
BRONCHIECTASIS ( 70 FDA reports)
CAROTID ARTERY DISEASE ( 70 FDA reports)
CAROTID ARTERY OCCLUSION ( 70 FDA reports)
DEVICE OCCLUSION ( 70 FDA reports)
DIABETIC RETINOPATHY ( 70 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 70 FDA reports)
IMMUNODEFICIENCY ( 70 FDA reports)
INADEQUATE ANALGESIA ( 70 FDA reports)
INCOHERENT ( 70 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 70 FDA reports)
OLIGURIA ( 70 FDA reports)
OPTIC NEURITIS ( 70 FDA reports)
OROPHARYNGEAL BLISTERING ( 70 FDA reports)
PANCREATIC DISORDER ( 70 FDA reports)
PLEURAL FIBROSIS ( 70 FDA reports)
SERUM FERRITIN INCREASED ( 70 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 70 FDA reports)
WOUND DEHISCENCE ( 70 FDA reports)
PRODUCT TASTE ABNORMAL ( 69 FDA reports)
RADIUS FRACTURE ( 69 FDA reports)
SENSITIVITY OF TEETH ( 69 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 69 FDA reports)
TACHYPNOEA ( 69 FDA reports)
ANOSMIA ( 69 FDA reports)
BILE DUCT STENOSIS ( 69 FDA reports)
CERVICOBRACHIAL SYNDROME ( 69 FDA reports)
CHANGE OF BOWEL HABIT ( 69 FDA reports)
FACIAL PALSY ( 69 FDA reports)
FEELING DRUNK ( 69 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 69 FDA reports)
INJECTION SITE SWELLING ( 69 FDA reports)
MUSCLE INJURY ( 69 FDA reports)
ARTHROPOD BITE ( 68 FDA reports)
CHEST X-RAY ABNORMAL ( 68 FDA reports)
DERMATITIS BULLOUS ( 68 FDA reports)
DRUG SCREEN POSITIVE ( 68 FDA reports)
DYSTONIA ( 68 FDA reports)
EYELID PTOSIS ( 68 FDA reports)
HAEMOLYTIC ANAEMIA ( 68 FDA reports)
HYPERTENSIVE CRISIS ( 68 FDA reports)
MENORRHAGIA ( 68 FDA reports)
POSTNASAL DRIP ( 68 FDA reports)
SALIVARY HYPERSECRETION ( 68 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 68 FDA reports)
OPEN WOUND ( 67 FDA reports)
PROTEIN URINE PRESENT ( 67 FDA reports)
SPINAL FUSION SURGERY ( 67 FDA reports)
SYNOVITIS ( 67 FDA reports)
APHTHOUS STOMATITIS ( 67 FDA reports)
BILIARY COLIC ( 67 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 67 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 67 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 67 FDA reports)
ABNORMAL SENSATION IN EYE ( 66 FDA reports)
CALCULUS URETERIC ( 66 FDA reports)
HEPATOCELLULAR DAMAGE ( 66 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 66 FDA reports)
SLUGGISHNESS ( 66 FDA reports)
THROMBOPHLEBITIS ( 66 FDA reports)
RESPIRATORY RATE INCREASED ( 65 FDA reports)
RIGHT VENTRICULAR FAILURE ( 65 FDA reports)
VENOUS INSUFFICIENCY ( 65 FDA reports)
VISUAL FIELD DEFECT ( 65 FDA reports)
ANAEMIA POSTOPERATIVE ( 65 FDA reports)
CARDIOGENIC SHOCK ( 65 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 65 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 65 FDA reports)
MENOPAUSE ( 65 FDA reports)
NAIL DISORDER ( 65 FDA reports)
NASAL DISCOMFORT ( 65 FDA reports)
CARTILAGE INJURY ( 64 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 64 FDA reports)
GRIEF REACTION ( 64 FDA reports)
ILEITIS ( 64 FDA reports)
RAYNAUD'S PHENOMENON ( 64 FDA reports)
SKELETAL INJURY ( 64 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 63 FDA reports)
SEROMA ( 63 FDA reports)
FORMICATION ( 63 FDA reports)
GASTRIC INFECTION ( 63 FDA reports)
HYPERAESTHESIA ( 63 FDA reports)
KYPHOSCOLIOSIS ( 63 FDA reports)
LACUNAR INFARCTION ( 63 FDA reports)
ABSCESS DRAINAGE ( 62 FDA reports)
BILE DUCT STONE ( 62 FDA reports)
BRADYPHRENIA ( 62 FDA reports)
CACHEXIA ( 62 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 62 FDA reports)
DRUG ERUPTION ( 62 FDA reports)
FRACTURED SACRUM ( 62 FDA reports)
INJECTION SITE BRUISING ( 62 FDA reports)
PAIN OF SKIN ( 62 FDA reports)
PULMONARY THROMBOSIS ( 62 FDA reports)
PULSE ABSENT ( 62 FDA reports)
SICK SINUS SYNDROME ( 62 FDA reports)
OEDEMA MOUTH ( 61 FDA reports)
RECTAL POLYP ( 61 FDA reports)
TROPONIN INCREASED ( 61 FDA reports)
UMBILICAL HERNIA ( 61 FDA reports)
ADRENAL MASS ( 61 FDA reports)
AMENORRHOEA ( 61 FDA reports)
APPLICATION SITE PRURITUS ( 61 FDA reports)
ASPIRATION PLEURAL CAVITY ( 61 FDA reports)
AUTOIMMUNE HEPATITIS ( 61 FDA reports)
BONE OPERATION ( 61 FDA reports)
DYSAESTHESIA ( 61 FDA reports)
GENERALISED ERYTHEMA ( 61 FDA reports)
GLOSSITIS ( 61 FDA reports)
HILAR LYMPHADENOPATHY ( 61 FDA reports)
INGUINAL HERNIA ( 61 FDA reports)
ANXIETY DISORDER ( 60 FDA reports)
BRUXISM ( 60 FDA reports)
HAEMOLYSIS ( 60 FDA reports)
HEPATOTOXICITY ( 60 FDA reports)
MUSCLE HAEMORRHAGE ( 60 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 59 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 59 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 59 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 59 FDA reports)
CHEILITIS ( 59 FDA reports)
DEAFNESS NEUROSENSORY ( 59 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 59 FDA reports)
LARYNGEAL OEDEMA ( 59 FDA reports)
ORTHOPNOEA ( 59 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 59 FDA reports)
PERIARTHRITIS ( 59 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 59 FDA reports)
STATUS EPILEPTICUS ( 59 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 58 FDA reports)
OSTEOMYELITIS CHRONIC ( 58 FDA reports)
PURULENCE ( 58 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 58 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 58 FDA reports)
ATRIOVENTRICULAR BLOCK ( 58 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 58 FDA reports)
DERMATITIS ALLERGIC ( 58 FDA reports)
FAECALOMA ( 58 FDA reports)
HEPATIC NECROSIS ( 58 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 58 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 58 FDA reports)
ANGIONEUROTIC OEDEMA ( 57 FDA reports)
DIABETIC COMPLICATION ( 57 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 57 FDA reports)
HUNGER ( 57 FDA reports)
HYPERPARATHYROIDISM ( 57 FDA reports)
JAUNDICE CHOLESTATIC ( 57 FDA reports)
NASAL DISORDER ( 57 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 57 FDA reports)
PSYCHIATRIC SYMPTOM ( 57 FDA reports)
TOBACCO USER ( 57 FDA reports)
PAROSMIA ( 56 FDA reports)
RENAL ATROPHY ( 56 FDA reports)
SKIN PAPILLOMA ( 56 FDA reports)
SOMNAMBULISM ( 56 FDA reports)
TONGUE OEDEMA ( 56 FDA reports)
TORSADE DE POINTES ( 56 FDA reports)
URINE ODOUR ABNORMAL ( 56 FDA reports)
UTERINE CANCER ( 56 FDA reports)
WHEELCHAIR USER ( 56 FDA reports)
WOUND DRAINAGE ( 56 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 56 FDA reports)
CYSTOCELE ( 56 FDA reports)
ESCHERICHIA SEPSIS ( 56 FDA reports)
EYE INFECTION ( 56 FDA reports)
FACE INJURY ( 56 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 56 FDA reports)
HYPOPHOSPHATAEMIA ( 56 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 56 FDA reports)
INTRACRANIAL ANEURYSM ( 56 FDA reports)
LOCALISED OEDEMA ( 56 FDA reports)
AMMONIA INCREASED ( 55 FDA reports)
APPLICATION SITE ERYTHEMA ( 55 FDA reports)
BLOOD AMYLASE INCREASED ( 55 FDA reports)
BLOOD CHLORIDE DECREASED ( 55 FDA reports)
DEAFNESS UNILATERAL ( 55 FDA reports)
DECREASED ACTIVITY ( 55 FDA reports)
ENTERITIS ( 55 FDA reports)
EPICONDYLITIS ( 55 FDA reports)
LUNG CONSOLIDATION ( 55 FDA reports)
PLASMACYTOMA ( 55 FDA reports)
POOR DENTAL CONDITION ( 55 FDA reports)
VARICOSE VEIN ( 55 FDA reports)
VITREOUS DETACHMENT ( 55 FDA reports)
OESOPHAGEAL DILATATION ( 54 FDA reports)
POLYDIPSIA ( 54 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 54 FDA reports)
SENSATION OF HEAVINESS ( 54 FDA reports)
THERMAL BURN ( 54 FDA reports)
TOOTH IMPACTED ( 54 FDA reports)
TOOTH INJURY ( 54 FDA reports)
ULNA FRACTURE ( 54 FDA reports)
VARICES OESOPHAGEAL ( 54 FDA reports)
WEIGHT FLUCTUATION ( 54 FDA reports)
ACUTE HEPATIC FAILURE ( 54 FDA reports)
BLADDER SPASM ( 54 FDA reports)
BREAST CYST ( 54 FDA reports)
BREAST TENDERNESS ( 54 FDA reports)
DRUG ABUSER ( 54 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 54 FDA reports)
FEBRILE BONE MARROW APLASIA ( 54 FDA reports)
HYPOTHERMIA ( 54 FDA reports)
ABORTION SPONTANEOUS ( 53 FDA reports)
BIPOLAR I DISORDER ( 53 FDA reports)
BREATH SOUNDS ABNORMAL ( 53 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 53 FDA reports)
ENDOSCOPY ( 53 FDA reports)
INCISIONAL HERNIA ( 53 FDA reports)
MYELOMA RECURRENCE ( 53 FDA reports)
OCULAR ICTERUS ( 53 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 53 FDA reports)
TUBERCULOSIS ( 53 FDA reports)
VENOUS THROMBOSIS LIMB ( 53 FDA reports)
VENTRICULAR HYPOKINESIA ( 53 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 52 FDA reports)
ORGAN FAILURE ( 52 FDA reports)
POSTURE ABNORMAL ( 52 FDA reports)
PRODUCT ADHESION ISSUE ( 52 FDA reports)
RHONCHI ( 52 FDA reports)
SELF-MEDICATION ( 52 FDA reports)
SKIN FIBROSIS ( 52 FDA reports)
SOFT TISSUE DISORDER ( 52 FDA reports)
ANORECTAL DISCOMFORT ( 52 FDA reports)
DRUG TOLERANCE ( 52 FDA reports)
GASTRIC BYPASS ( 52 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 52 FDA reports)
HODGKIN'S DISEASE ( 52 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 52 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 52 FDA reports)
LARGE INTESTINE PERFORATION ( 52 FDA reports)
MENSTRUATION IRREGULAR ( 52 FDA reports)
MYDRIASIS ( 52 FDA reports)
AKATHISIA ( 51 FDA reports)
AORTIC CALCIFICATION ( 51 FDA reports)
BODY TEMPERATURE DECREASED ( 51 FDA reports)
EAR DISORDER ( 51 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 51 FDA reports)
NICOTINE DEPENDENCE ( 51 FDA reports)
OESOPHAGEAL FOOD IMPACTION ( 51 FDA reports)
SHOCK HAEMORRHAGIC ( 51 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 51 FDA reports)
STRESS URINARY INCONTINENCE ( 51 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 51 FDA reports)
TONGUE INJURY ( 51 FDA reports)
PARONYCHIA ( 50 FDA reports)
CATHETER RELATED INFECTION ( 50 FDA reports)
CERUMEN IMPACTION ( 50 FDA reports)
COLON ADENOMA ( 50 FDA reports)
DIABETIC GASTROPARESIS ( 50 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 50 FDA reports)
EYE DISCHARGE ( 50 FDA reports)
FACET JOINT SYNDROME ( 50 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 50 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 50 FDA reports)
HELICOBACTER GASTRITIS ( 50 FDA reports)
HEPATIC MASS ( 50 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 50 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 50 FDA reports)
IRON DEFICIENCY ( 50 FDA reports)
METAPLASIA ( 50 FDA reports)
ADNEXA UTERI MASS ( 49 FDA reports)
BLOOD CULTURE POSITIVE ( 49 FDA reports)
BUNDLE BRANCH BLOCK ( 49 FDA reports)
COLLAPSE OF LUNG ( 49 FDA reports)
ENDOCARDITIS ( 49 FDA reports)
FURUNCLE ( 49 FDA reports)
HEPATIC FIBROSIS ( 49 FDA reports)
HYPERTENSIVE HEART DISEASE ( 49 FDA reports)
KERATITIS ( 49 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 49 FDA reports)
METRORRHAGIA ( 49 FDA reports)
NEPHRITIS INTERSTITIAL ( 49 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 49 FDA reports)
PATELLA FRACTURE ( 49 FDA reports)
PROSTATOMEGALY ( 49 FDA reports)
RENAL CANCER ( 49 FDA reports)
SKIN PLAQUE ( 49 FDA reports)
TELANGIECTASIA ( 49 FDA reports)
TENDON DISORDER ( 49 FDA reports)
TOOTH DEPOSIT ( 49 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 48 FDA reports)
POLYMYALGIA RHEUMATICA ( 48 FDA reports)
POOR PERSONAL HYGIENE ( 48 FDA reports)
ROTATOR CUFF REPAIR ( 48 FDA reports)
SCREAMING ( 48 FDA reports)
STUPOR ( 48 FDA reports)
AFFECTIVE DISORDER ( 48 FDA reports)
BURN OESOPHAGEAL ( 48 FDA reports)
CATHETER PLACEMENT ( 48 FDA reports)
CHONDROMALACIA ( 48 FDA reports)
EARLY SATIETY ( 48 FDA reports)
ENDOMETRIOSIS ( 48 FDA reports)
ENERGY INCREASED ( 48 FDA reports)
GASTROINTESTINAL INFECTION ( 48 FDA reports)
HYPERTONIC BLADDER ( 48 FDA reports)
LIPOMA ( 48 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 48 FDA reports)
MALOCCLUSION ( 48 FDA reports)
MONOPLEGIA ( 48 FDA reports)
MULTIPLE DRUG OVERDOSE ( 48 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 47 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 47 FDA reports)
ALVEOLITIS ( 47 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 47 FDA reports)
BLOOD TEST ABNORMAL ( 47 FDA reports)
CARDIOPULMONARY FAILURE ( 47 FDA reports)
CHOLESTEROSIS ( 47 FDA reports)
CLOSTRIDIUM COLITIS ( 47 FDA reports)
FOOD POISONING ( 47 FDA reports)
GALLBLADDER POLYP ( 47 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 47 FDA reports)
INJECTION SITE RASH ( 47 FDA reports)
MITRAL VALVE CALCIFICATION ( 47 FDA reports)
MONONEUROPATHY ( 47 FDA reports)
NEUTROPHIL COUNT INCREASED ( 47 FDA reports)
PANIC REACTION ( 47 FDA reports)
PERITONITIS BACTERIAL ( 47 FDA reports)
PRECANCEROUS CELLS PRESENT ( 47 FDA reports)
SKIN INFECTION ( 47 FDA reports)
VASCULAR CALCIFICATION ( 47 FDA reports)
NECK MASS ( 46 FDA reports)
PHOTOPSIA ( 46 FDA reports)
PREGNANCY ( 46 FDA reports)
PROTEIN TOTAL DECREASED ( 46 FDA reports)
PSORIATIC ARTHROPATHY ( 46 FDA reports)
RASH PUSTULAR ( 46 FDA reports)
SCIATIC NERVE INJURY ( 46 FDA reports)
SHOULDER ARTHROPLASTY ( 46 FDA reports)
THERAPY NON-RESPONDER ( 46 FDA reports)
TOOTH EROSION ( 46 FDA reports)
TRIGEMINAL NEURALGIA ( 46 FDA reports)
UTERINE DISORDER ( 46 FDA reports)
WALKING DISABILITY ( 46 FDA reports)
ACUTE PRERENAL FAILURE ( 46 FDA reports)
APPLICATION SITE RASH ( 46 FDA reports)
BLOOD COUNT ABNORMAL ( 46 FDA reports)
BONE NEOPLASM ( 46 FDA reports)
CARDIAC TAMPONADE ( 46 FDA reports)
FULL BLOOD COUNT DECREASED ( 46 FDA reports)
GANGRENE ( 46 FDA reports)
GASTRIC PERFORATION ( 46 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 46 FDA reports)
INJECTION SITE IRRITATION ( 46 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 46 FDA reports)
MORTON'S NEUROMA ( 46 FDA reports)
ABNORMAL FAECES ( 45 FDA reports)
ADENOCARCINOMA ( 45 FDA reports)
APTYALISM ( 45 FDA reports)
ASPERGILLOSIS ( 45 FDA reports)
BREAST RECONSTRUCTION ( 45 FDA reports)
DENTAL DISCOMFORT ( 45 FDA reports)
EMBOLISM ( 45 FDA reports)
GASTRIC PH DECREASED ( 45 FDA reports)
HEPATITIS ACUTE ( 45 FDA reports)
JOINT CONTRACTURE ( 45 FDA reports)
PAROTITIS ( 45 FDA reports)
RETINAL DETACHMENT ( 45 FDA reports)
SHOULDER OPERATION ( 45 FDA reports)
SKIN NECROSIS ( 45 FDA reports)
TERMINAL STATE ( 45 FDA reports)
TOBACCO ABUSE ( 45 FDA reports)
TOXIC ENCEPHALOPATHY ( 45 FDA reports)
UNDERDOSE ( 45 FDA reports)
VENTRICULAR DYSFUNCTION ( 45 FDA reports)
TENOSYNOVITIS STENOSANS ( 44 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 44 FDA reports)
BONE SWELLING ( 44 FDA reports)
BRONCHIOLITIS ( 44 FDA reports)
CEREBROVASCULAR DISORDER ( 44 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 44 FDA reports)
DRUG EFFECT INCREASED ( 44 FDA reports)
DYSGRAPHIA ( 44 FDA reports)
FAMILY STRESS ( 44 FDA reports)
HEPATIC PAIN ( 44 FDA reports)
JOINT INSTABILITY ( 44 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 43 FDA reports)
DENTAL CARE ( 43 FDA reports)
DROOLING ( 43 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 43 FDA reports)
EYELID DISORDER ( 43 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 43 FDA reports)
FOOD ALLERGY ( 43 FDA reports)
HYPOVENTILATION ( 43 FDA reports)
INTESTINAL ISCHAEMIA ( 43 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 43 FDA reports)
PHARYNGEAL DISORDER ( 43 FDA reports)
PIGMENTATION DISORDER ( 43 FDA reports)
PNEUMONIA BACTERIAL ( 43 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 43 FDA reports)
PYODERMA GANGRENOSUM ( 43 FDA reports)
RECTAL CANCER ( 43 FDA reports)
RENAL TUBULAR ACIDOSIS ( 43 FDA reports)
SPONDYLOLYSIS ( 43 FDA reports)
VERTEBROPLASTY ( 43 FDA reports)
WOUND SECRETION ( 43 FDA reports)
PAPILLOMA ( 42 FDA reports)
PARAPLEGIA ( 42 FDA reports)
POLYPECTOMY ( 42 FDA reports)
PRESCRIBED OVERDOSE ( 42 FDA reports)
TENDON INJURY ( 42 FDA reports)
ANGIOPLASTY ( 42 FDA reports)
ATRIAL SEPTAL DEFECT ( 42 FDA reports)
BLINDNESS TRANSIENT ( 42 FDA reports)
CERVICAL DYSPLASIA ( 42 FDA reports)
CHOLECYSTITIS INFECTIVE ( 42 FDA reports)
CLAVICLE FRACTURE ( 42 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 42 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 42 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 42 FDA reports)
DYSPAREUNIA ( 42 FDA reports)
EXCESSIVE EYE BLINKING ( 42 FDA reports)
HEAD DISCOMFORT ( 42 FDA reports)
INCISIONAL DRAINAGE ( 42 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 42 FDA reports)
LABYRINTHITIS ( 42 FDA reports)
ABSCESS ORAL ( 41 FDA reports)
ARTHRITIS BACTERIAL ( 41 FDA reports)
DIAPHRAGMATIC DISORDER ( 41 FDA reports)
FEELINGS OF WORTHLESSNESS ( 41 FDA reports)
HEPATITIS TOXIC ( 41 FDA reports)
HYPERPLASIA ( 41 FDA reports)
HYPERTONIA ( 41 FDA reports)
MITRAL VALVE DISEASE ( 41 FDA reports)
NEPHROPATHY ( 41 FDA reports)
OTITIS EXTERNA ( 41 FDA reports)
OVARIAN CANCER ( 41 FDA reports)
POOR PERIPHERAL CIRCULATION ( 41 FDA reports)
PROSTATITIS ( 41 FDA reports)
PULMONARY GRANULOMA ( 41 FDA reports)
RENAL MASS ( 41 FDA reports)
TACHYPHRENIA ( 41 FDA reports)
TRANSFUSION ( 41 FDA reports)
VOCAL CORD PARALYSIS ( 41 FDA reports)
POST PROCEDURAL INFECTION ( 40 FDA reports)
SINUS POLYP ( 40 FDA reports)
TACHYARRHYTHMIA ( 40 FDA reports)
THERAPY REGIMEN CHANGED ( 40 FDA reports)
VAGINAL DISCHARGE ( 40 FDA reports)
ABDOMINAL RIGIDITY ( 40 FDA reports)
AUTOIMMUNE DISORDER ( 40 FDA reports)
CARDIAC ENZYMES INCREASED ( 40 FDA reports)
EMBOLIC STROKE ( 40 FDA reports)
HEART INJURY ( 40 FDA reports)
HERPES VIRUS INFECTION ( 40 FDA reports)
INJECTION SITE NODULE ( 40 FDA reports)
LARYNGOSPASM ( 40 FDA reports)
LUPUS-LIKE SYNDROME ( 40 FDA reports)
METABOLIC SYNDROME ( 40 FDA reports)
MONOCYTE COUNT INCREASED ( 40 FDA reports)
ANIMAL BITE ( 39 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 39 FDA reports)
COR PULMONALE ( 39 FDA reports)
FOOT OPERATION ( 39 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 39 FDA reports)
GRAFT VERSUS HOST DISEASE ( 39 FDA reports)
HERNIA REPAIR ( 39 FDA reports)
HOSTILITY ( 39 FDA reports)
HYPERCAPNIA ( 39 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 39 FDA reports)
KLEBSIELLA INFECTION ( 39 FDA reports)
METASTASIS ( 39 FDA reports)
MUSCLE RUPTURE ( 39 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 39 FDA reports)
POLYARTHRITIS ( 39 FDA reports)
PORTAL HYPERTENSION ( 39 FDA reports)
PORTAL VEIN THROMBOSIS ( 39 FDA reports)
RIGHT ATRIAL DILATATION ( 39 FDA reports)
SINUS OPERATION ( 39 FDA reports)
SKIN REACTION ( 39 FDA reports)
SPONDYLOARTHROPATHY ( 39 FDA reports)
THERAPY CESSATION ( 39 FDA reports)
VASCULAR GRAFT ( 39 FDA reports)
VASCULAR OCCLUSION ( 39 FDA reports)
PARKINSONISM ( 38 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 38 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 38 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 38 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 38 FDA reports)
STREPTOCOCCAL INFECTION ( 38 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 38 FDA reports)
THYROIDECTOMY ( 38 FDA reports)
AXILLARY PAIN ( 38 FDA reports)
BREAKTHROUGH PAIN ( 38 FDA reports)
CALCINOSIS ( 38 FDA reports)
DIABETIC NEPHROPATHY ( 38 FDA reports)
ENDOTRACHEAL INTUBATION ( 38 FDA reports)
FEMORAL NECK FRACTURE ( 38 FDA reports)
FISTULA DISCHARGE ( 38 FDA reports)
GASTRODUODENITIS ( 38 FDA reports)
GENITAL HERPES ( 38 FDA reports)
LIMB OPERATION ( 38 FDA reports)
MALABSORPTION ( 38 FDA reports)
MENINGITIS ( 38 FDA reports)
APPENDICECTOMY ( 37 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 37 FDA reports)
BRONCHIAL SECRETION RETENTION ( 37 FDA reports)
CORONARY ARTERY THROMBOSIS ( 37 FDA reports)
CULTURE URINE POSITIVE ( 37 FDA reports)
EUPHORIC MOOD ( 37 FDA reports)
FEAR OF DEATH ( 37 FDA reports)
GASTROOESOPHAGEAL SPHINCTER INSUFFICIENCY ( 37 FDA reports)
HAEMORRHAGIC STROKE ( 37 FDA reports)
HISTOPLASMOSIS ( 37 FDA reports)
HYPERMETROPIA ( 37 FDA reports)
HYPOVITAMINOSIS ( 37 FDA reports)
LEFT VENTRICULAR FAILURE ( 37 FDA reports)
METASTATIC PAIN ( 37 FDA reports)
MYASTHENIA GRAVIS ( 37 FDA reports)
NEUTROPENIC SEPSIS ( 37 FDA reports)
OPEN REDUCTION OF FRACTURE ( 37 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 37 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 37 FDA reports)
RENAL TRANSPLANT ( 37 FDA reports)
RETINAL HAEMORRHAGE ( 37 FDA reports)
SPLENIC INFARCTION ( 37 FDA reports)
SPLENIC LESION ( 37 FDA reports)
TENSION ( 37 FDA reports)
TENSION HEADACHE ( 37 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 37 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 37 FDA reports)
TONGUE BITING ( 37 FDA reports)
TONGUE COATED ( 37 FDA reports)
VAGINAL INFECTION ( 37 FDA reports)
VEIN DISORDER ( 37 FDA reports)
PERFORMANCE STATUS DECREASED ( 36 FDA reports)
PERIORBITAL OEDEMA ( 36 FDA reports)
PROSTATE CANCER METASTATIC ( 36 FDA reports)
PROTEIN TOTAL INCREASED ( 36 FDA reports)
PULMONARY HAEMORRHAGE ( 36 FDA reports)
SCHIZOPHRENIA ( 36 FDA reports)
SINUS ARRHYTHMIA ( 36 FDA reports)
SNORING ( 36 FDA reports)
TRIGGER FINGER ( 36 FDA reports)
ARTERIAL DISORDER ( 36 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 36 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 36 FDA reports)
BACTERIAL TEST POSITIVE ( 36 FDA reports)
BREAST DISCHARGE ( 36 FDA reports)
CERVICAL CORD COMPRESSION ( 36 FDA reports)
ERYTHEMA OF EYELID ( 36 FDA reports)
EXOPHTHALMOS ( 36 FDA reports)
FOLLICULITIS ( 36 FDA reports)
HEART RATE ABNORMAL ( 36 FDA reports)
IMMOBILE ( 36 FDA reports)
IMPAIRED SELF-CARE ( 36 FDA reports)
INJECTION SITE WARMTH ( 36 FDA reports)
LIP DRY ( 36 FDA reports)
MENIERE'S DISEASE ( 36 FDA reports)
MITRAL VALVE STENOSIS ( 36 FDA reports)
BILIARY DILATATION ( 35 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 35 FDA reports)
CHEST WALL PAIN ( 35 FDA reports)
DEMYELINATION ( 35 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 35 FDA reports)
EATING DISORDER SYMPTOM ( 35 FDA reports)
EROSIVE DUODENITIS ( 35 FDA reports)
FACIAL NEURALGIA ( 35 FDA reports)
FOREIGN BODY TRAUMA ( 35 FDA reports)
GALLBLADDER PAIN ( 35 FDA reports)
GENITAL RASH ( 35 FDA reports)
HYPOTONIA ( 35 FDA reports)
INFARCTION ( 35 FDA reports)
INTERVERTEBRAL DISC INJURY ( 35 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 35 FDA reports)
LACTOSE INTOLERANCE ( 35 FDA reports)
LICHENOID KERATOSIS ( 35 FDA reports)
LUNG HYPERINFLATION ( 35 FDA reports)
NASAL DRYNESS ( 35 FDA reports)
OSTEITIS DEFORMANS ( 35 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 35 FDA reports)
PERSONALITY DISORDER ( 35 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 35 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 35 FDA reports)
TOE AMPUTATION ( 35 FDA reports)
URINE ANALYSIS ABNORMAL ( 35 FDA reports)
VERTIGO POSITIONAL ( 35 FDA reports)
VITAMIN B12 DECREASED ( 35 FDA reports)
WEGENER'S GRANULOMATOSIS ( 35 FDA reports)
PREMATURE BABY ( 34 FDA reports)
PULPITIS DENTAL ( 34 FDA reports)
RECTOCELE ( 34 FDA reports)
SHOULDER PAIN ( 34 FDA reports)
STOMATITIS NECROTISING ( 34 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 34 FDA reports)
UTERINE POLYP ( 34 FDA reports)
VULVOVAGINAL DRYNESS ( 34 FDA reports)
ACCIDENTAL EXPOSURE ( 34 FDA reports)
BLADDER PROLAPSE ( 34 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 34 FDA reports)
BUNION ( 34 FDA reports)
CATHETER RELATED COMPLICATION ( 34 FDA reports)
CHEMOTHERAPY ( 34 FDA reports)
CHRONIC FATIGUE SYNDROME ( 34 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 34 FDA reports)
CREPITATIONS ( 34 FDA reports)
DEPENDENCE ( 34 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 34 FDA reports)
ERYTHEMA MULTIFORME ( 34 FDA reports)
HEPATIC NEOPLASM ( 34 FDA reports)
HYPERCOAGULATION ( 34 FDA reports)
HYPERPHAGIA ( 34 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 34 FDA reports)
LARGE INTESTINAL ULCER ( 34 FDA reports)
LIGAMENT DISORDER ( 34 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 34 FDA reports)
MENINGIOMA ( 34 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 34 FDA reports)
MUSCLE SPASTICITY ( 34 FDA reports)
ANAEMIA MACROCYTIC ( 33 FDA reports)
ANOXIC ENCEPHALOPATHY ( 33 FDA reports)
BILE DUCT OBSTRUCTION ( 33 FDA reports)
DIABETIC COMA ( 33 FDA reports)
EJECTION FRACTION ABNORMAL ( 33 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 33 FDA reports)
FRUSTRATION ( 33 FDA reports)
HEPATIC ENZYME ABNORMAL ( 33 FDA reports)
INDURATION ( 33 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 33 FDA reports)
INTESTINAL POLYP ( 33 FDA reports)
MARROW HYPERPLASIA ( 33 FDA reports)
MIOSIS ( 33 FDA reports)
NASAL POLYPS ( 33 FDA reports)
NEUROGENIC BLADDER ( 33 FDA reports)
ONYCHOCLASIS ( 33 FDA reports)
ORAL TORUS ( 33 FDA reports)
PAINFUL RESPIRATION ( 33 FDA reports)
PANCREATIC NEOPLASM ( 33 FDA reports)
PAPILLOEDEMA ( 33 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 33 FDA reports)
REFLUX GASTRITIS ( 33 FDA reports)
STREPTOCOCCAL SEPSIS ( 33 FDA reports)
TENOSYNOVITIS ( 33 FDA reports)
TOOTH REPAIR ( 33 FDA reports)
URINE COLOUR ABNORMAL ( 33 FDA reports)
UVEITIS ( 33 FDA reports)
WEIGHT BEARING DIFFICULTY ( 33 FDA reports)
OESOPHAGEAL DISCOMFORT ( 32 FDA reports)
OOPHORECTOMY ( 32 FDA reports)
OVERWEIGHT ( 32 FDA reports)
PAROTID GLAND ENLARGEMENT ( 32 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 32 FDA reports)
PHARYNGEAL ERYTHEMA ( 32 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 32 FDA reports)
RESPIRATORY DEPRESSION ( 32 FDA reports)
SECRETION DISCHARGE ( 32 FDA reports)
SKIN GRAFT ( 32 FDA reports)
SUPERINFECTION ( 32 FDA reports)
VARICELLA ( 32 FDA reports)
ALCOHOL USE ( 32 FDA reports)
ALCOHOLISM ( 32 FDA reports)
ANAL FISTULA ( 32 FDA reports)
BONE MARROW TRANSPLANT ( 32 FDA reports)
BOWEN'S DISEASE ( 32 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 32 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 32 FDA reports)
CONDUCTION DISORDER ( 32 FDA reports)
DEFAECATION URGENCY ( 32 FDA reports)
DISSOCIATION ( 32 FDA reports)
ERYSIPELAS ( 32 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 32 FDA reports)
EXTREMITY CONTRACTURE ( 32 FDA reports)
FISTULA REPAIR ( 32 FDA reports)
GASTRIC OPERATION ( 32 FDA reports)
HAND DEFORMITY ( 32 FDA reports)
HYPOREFLEXIA ( 32 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 32 FDA reports)
LUNG CANCER METASTATIC ( 32 FDA reports)
MACROCYTOSIS ( 32 FDA reports)
METABOLIC ENCEPHALOPATHY ( 32 FDA reports)
METASTASES TO ADRENALS ( 32 FDA reports)
NASAL ULCER ( 32 FDA reports)
AORTIC DILATATION ( 31 FDA reports)
APPLICATION SITE IRRITATION ( 31 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 31 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 31 FDA reports)
BREAST ENLARGEMENT ( 31 FDA reports)
CAESAREAN SECTION ( 31 FDA reports)
CARBON DIOXIDE INCREASED ( 31 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 31 FDA reports)
CEREBRAL HAEMATOMA ( 31 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 31 FDA reports)
COMMUNICATION DISORDER ( 31 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 31 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 31 FDA reports)
EMPYEMA ( 31 FDA reports)
ENCEPHALOMALACIA ( 31 FDA reports)
ERYTHEMA NODOSUM ( 31 FDA reports)
EXERCISE TOLERANCE DECREASED ( 31 FDA reports)
FRACTURE DELAYED UNION ( 31 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 31 FDA reports)
GENERALISED ANXIETY DISORDER ( 31 FDA reports)
GUILLAIN-BARRE SYNDROME ( 31 FDA reports)
GUN SHOT WOUND ( 31 FDA reports)
HAIR TEXTURE ABNORMAL ( 31 FDA reports)
HYPERNATRAEMIA ( 31 FDA reports)
HYPOCOAGULABLE STATE ( 31 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 31 FDA reports)
LYME DISEASE ( 31 FDA reports)
MECHANICAL VENTILATION ( 31 FDA reports)
OBSTRUCTION GASTRIC ( 31 FDA reports)
OTORRHOEA ( 31 FDA reports)
PITTING OEDEMA ( 31 FDA reports)
RECTAL FISSURE ( 31 FDA reports)
RETINAL DISORDER ( 31 FDA reports)
SENSATION OF PRESSURE ( 31 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 31 FDA reports)
URINARY HESITATION ( 31 FDA reports)
NEUROLOGICAL SYMPTOM ( 30 FDA reports)
ORAL FUNGAL INFECTION ( 30 FDA reports)
OSTEOMALACIA ( 30 FDA reports)
OTITIS MEDIA ACUTE ( 30 FDA reports)
PANCREATITIS RELAPSING ( 30 FDA reports)
POST LAMINECTOMY SYNDROME ( 30 FDA reports)
RENAL CELL CARCINOMA ( 30 FDA reports)
SEXUAL DYSFUNCTION ( 30 FDA reports)
TARSAL TUNNEL SYNDROME ( 30 FDA reports)
THROMBOSIS IN DEVICE ( 30 FDA reports)
TINEA PEDIS ( 30 FDA reports)
TRACHEOBRONCHITIS ( 30 FDA reports)
TRICUSPID VALVE DISEASE ( 30 FDA reports)
UTERINE ENLARGEMENT ( 30 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 30 FDA reports)
ADRENAL DISORDER ( 30 FDA reports)
ALCOHOL POISONING ( 30 FDA reports)
ATHEROSCLEROSIS ( 30 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 30 FDA reports)
BLADDER PAIN ( 30 FDA reports)
BONE SCAN ABNORMAL ( 30 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 30 FDA reports)
CELL DEATH ( 30 FDA reports)
CHOLESTATIC LIVER INJURY ( 30 FDA reports)
COLONOSCOPY ( 30 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 30 FDA reports)
DRUG EFFECT DELAYED ( 30 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 30 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 30 FDA reports)
FOREIGN BODY ( 30 FDA reports)
HAEMANGIOMA OF LIVER ( 30 FDA reports)
HEPATORENAL SYNDROME ( 30 FDA reports)
HOMICIDAL IDEATION ( 30 FDA reports)
HORMONE LEVEL ABNORMAL ( 30 FDA reports)
HYPOVOLAEMIC SHOCK ( 30 FDA reports)
INNER EAR DISORDER ( 30 FDA reports)
INTRA-UTERINE DEATH ( 30 FDA reports)
LEG AMPUTATION ( 30 FDA reports)
LISTLESS ( 30 FDA reports)
LYMPHADENECTOMY ( 30 FDA reports)
MICROCYTIC ANAEMIA ( 30 FDA reports)
MUSCLE RIGIDITY ( 30 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 30 FDA reports)
ANAPHYLACTOID REACTION ( 29 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 29 FDA reports)
ATROPHY ( 29 FDA reports)
BIOPSY BREAST ABNORMAL ( 29 FDA reports)
BLADDER CANCER RECURRENT ( 29 FDA reports)
BONE MARROW DEPRESSION ( 29 FDA reports)
BREAST CANCER RECURRENT ( 29 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 29 FDA reports)
EYE MOVEMENT DISORDER ( 29 FDA reports)
FACIAL BONES FRACTURE ( 29 FDA reports)
FLUID INTAKE REDUCED ( 29 FDA reports)
INAPPROPRIATE AFFECT ( 29 FDA reports)
INJECTION SITE DISCOLOURATION ( 29 FDA reports)
INTESTINAL INFARCTION ( 29 FDA reports)
LIP PAIN ( 29 FDA reports)
LOSS OF EMPLOYMENT ( 29 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 29 FDA reports)
MENINGITIS ASEPTIC ( 29 FDA reports)
MICROANGIOPATHY ( 29 FDA reports)
NEPHROSCLEROSIS ( 29 FDA reports)
OEDEMA MUCOSAL ( 29 FDA reports)
OESOPHAGEAL OPERATION ( 29 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 29 FDA reports)
PANCREATIC CYST ( 29 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 29 FDA reports)
PROSTATIC DISORDER ( 29 FDA reports)
PYELOCALIECTASIS ( 29 FDA reports)
RECTAL ABSCESS ( 29 FDA reports)
RENAL TUBULAR DISORDER ( 29 FDA reports)
SOCIAL PROBLEM ( 29 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 29 FDA reports)
SPINAL LAMINECTOMY ( 29 FDA reports)
SPINAL OPERATION ( 29 FDA reports)
SPUTUM CULTURE POSITIVE ( 29 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 29 FDA reports)
SUNBURN ( 29 FDA reports)
TEARFULNESS ( 29 FDA reports)
TEMPORAL ARTERITIS ( 29 FDA reports)
UTERINE HAEMORRHAGE ( 29 FDA reports)
VASCULAR PURPURA ( 29 FDA reports)
NEPHROTIC SYNDROME ( 28 FDA reports)
NEUROMA ( 28 FDA reports)
NOCTURNAL DYSPNOEA ( 28 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 28 FDA reports)
OESOPHAGEAL PERFORATION ( 28 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 28 FDA reports)
PERIRECTAL ABSCESS ( 28 FDA reports)
REFLUX LARYNGITIS ( 28 FDA reports)
SKIN HAEMORRHAGE ( 28 FDA reports)
SLEEP TALKING ( 28 FDA reports)
SPINAL DEFORMITY ( 28 FDA reports)
STATUS ASTHMATICUS ( 28 FDA reports)
SUBCUTANEOUS NODULE ( 28 FDA reports)
VENA CAVA THROMBOSIS ( 28 FDA reports)
VOMITING PROJECTILE ( 28 FDA reports)
AFFECT LABILITY ( 28 FDA reports)
ANKLE OPERATION ( 28 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 28 FDA reports)
AORTIC VALVE SCLEROSIS ( 28 FDA reports)
APLASIA ( 28 FDA reports)
BLADDER NEOPLASM ( 28 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 28 FDA reports)
BLOODY DISCHARGE ( 28 FDA reports)
BONE TRIMMING ( 28 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 28 FDA reports)
CEREBRAL DISORDER ( 28 FDA reports)
COLECTOMY ( 28 FDA reports)
COLOSTOMY ( 28 FDA reports)
CUBITAL TUNNEL SYNDROME ( 28 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 28 FDA reports)
DIVERTICULAR PERFORATION ( 28 FDA reports)
DYSMENORRHOEA ( 28 FDA reports)
ENCEPHALITIS ( 28 FDA reports)
ENDOMETRIAL CANCER ( 28 FDA reports)
EYE OPERATION ( 28 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 28 FDA reports)
HEPATOSPLENOMEGALY ( 28 FDA reports)
LYMPHOCYTOSIS ( 28 FDA reports)
MELANOSIS COLI ( 28 FDA reports)
ADDISON'S DISEASE ( 27 FDA reports)
BIOPSY ( 27 FDA reports)
BLADDER CATHETERISATION ( 27 FDA reports)
BLOOD CREATINE INCREASED ( 27 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 27 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 27 FDA reports)
DIAPHRAGMATIC HERNIA ( 27 FDA reports)
DROP ATTACKS ( 27 FDA reports)
GALACTORRHOEA ( 27 FDA reports)
HANGOVER ( 27 FDA reports)
HIP SURGERY ( 27 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 27 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 27 FDA reports)
INTRAOCULAR LENS IMPLANT ( 27 FDA reports)
LICHEN PLANUS ( 27 FDA reports)
LYMPHADENITIS ( 27 FDA reports)
METASTASES TO MENINGES ( 27 FDA reports)
MIXED LIVER INJURY ( 27 FDA reports)
MUCOUS STOOLS ( 27 FDA reports)
PARTIAL SEIZURES ( 27 FDA reports)
PHARYNGEAL EROSION ( 27 FDA reports)
PROCEDURAL HYPOTENSION ( 27 FDA reports)
SKIN NEOPLASM EXCISION ( 27 FDA reports)
SKIN NODULE ( 27 FDA reports)
SOFT TISSUE INFLAMMATION ( 27 FDA reports)
SUBCUTANEOUS ABSCESS ( 27 FDA reports)
VENOUS OCCLUSION ( 27 FDA reports)
OPTIC NERVE CUPPING ( 26 FDA reports)
ORAL DISCHARGE ( 26 FDA reports)
OSTEOCHONDROSIS ( 26 FDA reports)
PANCREATIC ENZYMES INCREASED ( 26 FDA reports)
PARAPARESIS ( 26 FDA reports)
PROTHROMBIN TIME SHORTENED ( 26 FDA reports)
RECURRENT CANCER ( 26 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 26 FDA reports)
SCOTOMA ( 26 FDA reports)
SEBORRHOEIC DERMATITIS ( 26 FDA reports)
SINUS RHYTHM ( 26 FDA reports)
SKIN WARM ( 26 FDA reports)
SUBDURAL HAEMORRHAGE ( 26 FDA reports)
THROMBOCYTHAEMIA ( 26 FDA reports)
TONGUE DRY ( 26 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 26 FDA reports)
URINE ABNORMALITY ( 26 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 26 FDA reports)
ACETABULUM FRACTURE ( 26 FDA reports)
ANAL FISSURE ( 26 FDA reports)
BILIARY TRACT DISORDER ( 26 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 26 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 26 FDA reports)
BLOOD URIC ACID INCREASED ( 26 FDA reports)
BREAST CALCIFICATIONS ( 26 FDA reports)
CARDIAC ANEURYSM ( 26 FDA reports)
CARDIAC FAILURE ACUTE ( 26 FDA reports)
CATARACT NUCLEAR ( 26 FDA reports)
CERVICAL MYELOPATHY ( 26 FDA reports)
CHAPPED LIPS ( 26 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 26 FDA reports)
CYSTITIS INTERSTITIAL ( 26 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 26 FDA reports)
DEVICE BREAKAGE ( 26 FDA reports)
DYSTHYMIC DISORDER ( 26 FDA reports)
EOSINOPHIL COUNT INCREASED ( 26 FDA reports)
EYE LASER SURGERY ( 26 FDA reports)
GASTRECTOMY ( 26 FDA reports)
GLOMERULONEPHRITIS ( 26 FDA reports)
HAEMORRHAGIC DIATHESIS ( 26 FDA reports)
HAIR COLOUR CHANGES ( 26 FDA reports)
HYPERACUSIS ( 26 FDA reports)
LIP ULCERATION ( 26 FDA reports)
LIVER ABSCESS ( 26 FDA reports)
MACULAR OEDEMA ( 26 FDA reports)
MECHANICAL URTICARIA ( 26 FDA reports)
MUSCLE CONTRACTURE ( 26 FDA reports)
NARCOLEPSY ( 26 FDA reports)
ABDOMINAL ABSCESS ( 25 FDA reports)
ANISOCYTOSIS ( 25 FDA reports)
ANORECTAL DISORDER ( 25 FDA reports)
AORTIC VALVE DISEASE ( 25 FDA reports)
APPENDIX DISORDER ( 25 FDA reports)
APPLICATION SITE REACTION ( 25 FDA reports)
BLADDER SPHINCTER ATONY ( 25 FDA reports)
BONE FORMATION INCREASED ( 25 FDA reports)
BREAST SWELLING ( 25 FDA reports)
CAROTID BRUIT ( 25 FDA reports)
CHRONIC HEPATITIS ( 25 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 25 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 25 FDA reports)
EYE NAEVUS ( 25 FDA reports)
EYE OEDEMA ( 25 FDA reports)
GRIMACING ( 25 FDA reports)
LIVER TRANSPLANT REJECTION ( 25 FDA reports)
METABOLIC DISORDER ( 25 FDA reports)
NERVE ROOT COMPRESSION ( 25 FDA reports)
NON-SMALL CELL LUNG CANCER ( 25 FDA reports)
NYSTAGMUS ( 25 FDA reports)
ORAL MUCOSAL BLISTERING ( 25 FDA reports)
PARATHYROID TUMOUR BENIGN ( 25 FDA reports)
PSEUDOMONAL SEPSIS ( 25 FDA reports)
PUPILS UNEQUAL ( 25 FDA reports)
RENAL COLIC ( 25 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 25 FDA reports)
SKIN IRRITATION ( 25 FDA reports)
SKIN ODOUR ABNORMAL ( 25 FDA reports)
TEETH BRITTLE ( 25 FDA reports)
TESTICULAR PAIN ( 25 FDA reports)
THYROIDITIS ( 25 FDA reports)
TUMOUR MARKER INCREASED ( 25 FDA reports)
VESICAL FISTULA ( 25 FDA reports)
OBSTRUCTION ( 24 FDA reports)
OESOPHAGEAL RUPTURE ( 24 FDA reports)
OROANTRAL FISTULA ( 24 FDA reports)
OVARIAN MASS ( 24 FDA reports)
PELVIC DEFORMITY ( 24 FDA reports)
PERNICIOUS ANAEMIA ( 24 FDA reports)
PLASTIC SURGERY TO THE FACE ( 24 FDA reports)
RESPIRATORY RATE DECREASED ( 24 FDA reports)
RETINAL VEIN OCCLUSION ( 24 FDA reports)
SEPSIS SYNDROME ( 24 FDA reports)
SIALOADENITIS ( 24 FDA reports)
TRAUMATIC HAEMATOMA ( 24 FDA reports)
ABDOMINAL MASS ( 24 FDA reports)
APPENDICITIS PERFORATED ( 24 FDA reports)
ARTERIAL STENOSIS ( 24 FDA reports)
ATROPHIC VULVOVAGINITIS ( 24 FDA reports)
AUTOIMMUNE INNER EAR DISEASE ( 24 FDA reports)
BASEDOW'S DISEASE ( 24 FDA reports)
BLEPHAROSPASM ( 24 FDA reports)
BLOOD PROLACTIN INCREASED ( 24 FDA reports)
BREAST DISORDER ( 24 FDA reports)
CATHETER REMOVAL ( 24 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 24 FDA reports)
CHONDROPATHY ( 24 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 24 FDA reports)
CONNECTIVE TISSUE DISORDER ( 24 FDA reports)
CSF PROTEIN INCREASED ( 24 FDA reports)
DEVICE DISLOCATION ( 24 FDA reports)
DYSKINESIA OESOPHAGEAL ( 24 FDA reports)
EAR PRURITUS ( 24 FDA reports)
ECZEMA ASTEATOTIC ( 24 FDA reports)
FAECES PALE ( 24 FDA reports)
FEELING OF DESPAIR ( 24 FDA reports)
GALLBLADDER ENLARGEMENT ( 24 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 24 FDA reports)
GASTROINTESTINAL NECROSIS ( 24 FDA reports)
INFUSION SITE ERYTHEMA ( 24 FDA reports)
INTRACARDIAC THROMBUS ( 24 FDA reports)
MALIGNANT TUMOUR EXCISION ( 24 FDA reports)
ACUTE ABDOMEN ( 23 FDA reports)
ACUTE PSYCHOSIS ( 23 FDA reports)
ADHESION ( 23 FDA reports)
ADRENAL NEOPLASM ( 23 FDA reports)
ALKALOSIS ( 23 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 23 FDA reports)
ANGIOMYOLIPOMA ( 23 FDA reports)
APPETITE DISORDER ( 23 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 23 FDA reports)
BLOOD BLISTER ( 23 FDA reports)
BLOOD CHLORIDE INCREASED ( 23 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 23 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 23 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 23 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 23 FDA reports)
FIBROUS HISTIOCYTOMA ( 23 FDA reports)
FLAT AFFECT ( 23 FDA reports)
FOAMING AT MOUTH ( 23 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 23 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 23 FDA reports)
HEPATIC CONGESTION ( 23 FDA reports)
HYPERURICAEMIA ( 23 FDA reports)
IATROGENIC INJURY ( 23 FDA reports)
ICHTHYOSIS ( 23 FDA reports)
ILEUS PARALYTIC ( 23 FDA reports)
ILIAC ARTERY STENOSIS ( 23 FDA reports)
ILIAC ARTERY THROMBOSIS ( 23 FDA reports)
INCORRECT STORAGE OF DRUG ( 23 FDA reports)
INJECTION SITE URTICARIA ( 23 FDA reports)
INTESTINAL STENOSIS ( 23 FDA reports)
ISCHAEMIC HEPATITIS ( 23 FDA reports)
JUGULAR VEIN THROMBOSIS ( 23 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 23 FDA reports)
LIVER TRANSPLANT ( 23 FDA reports)
MICTURITION DISORDER ( 23 FDA reports)
OESOPHAGITIS ULCERATIVE ( 23 FDA reports)
OPEN FRACTURE ( 23 FDA reports)
ORAL MUCOSA ATROPHY ( 23 FDA reports)
PAINFUL DEFAECATION ( 23 FDA reports)
PERFORATED ULCER ( 23 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 23 FDA reports)
POTENTIATING DRUG INTERACTION ( 23 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 23 FDA reports)
REBOUND EFFECT ( 23 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 23 FDA reports)
RENAL ARTERY STENOSIS ( 23 FDA reports)
RESPIRATORY ACIDOSIS ( 23 FDA reports)
RETINOPATHY ( 23 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 23 FDA reports)
SUBILEUS ( 23 FDA reports)
SYNCOPE VASOVAGAL ( 23 FDA reports)
THROAT LESION ( 23 FDA reports)
TONSILLITIS ( 23 FDA reports)
TOOTH DISCOLOURATION ( 23 FDA reports)
URETERIC OBSTRUCTION ( 23 FDA reports)
URGE INCONTINENCE ( 23 FDA reports)
VULVOVAGINAL PRURITUS ( 23 FDA reports)
YAWNING ( 23 FDA reports)
NEURODERMATITIS ( 22 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 22 FDA reports)
PERIORBITAL HAEMATOMA ( 22 FDA reports)
PITUITARY TUMOUR ( 22 FDA reports)
PNEUMOPERITONEUM ( 22 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 22 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 22 FDA reports)
PYELONEPHRITIS ACUTE ( 22 FDA reports)
RADIATION INJURY ( 22 FDA reports)
RADIATION SKIN INJURY ( 22 FDA reports)
RESPIRATION ABNORMAL ( 22 FDA reports)
RETROPERITONEAL HAEMATOMA ( 22 FDA reports)
SCRATCH ( 22 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 22 FDA reports)
SKIN CANDIDA ( 22 FDA reports)
SKIN SWELLING ( 22 FDA reports)
SPINAL DECOMPRESSION ( 22 FDA reports)
SPINAL HAEMANGIOMA ( 22 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 22 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 22 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 22 FDA reports)
URINARY TRACT DISORDER ( 22 FDA reports)
VASCULAR DEMENTIA ( 22 FDA reports)
AORTIC VALVE CALCIFICATION ( 22 FDA reports)
ARTERIOSPASM CORONARY ( 22 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 22 FDA reports)
BREAST CANCER STAGE IV ( 22 FDA reports)
BRONCHITIS ACUTE ( 22 FDA reports)
BULLOUS LUNG DISEASE ( 22 FDA reports)
CIRRHOSIS ALCOHOLIC ( 22 FDA reports)
COLON POLYPECTOMY ( 22 FDA reports)
FEEDING TUBE COMPLICATION ( 22 FDA reports)
GASTRIC NEOPLASM ( 22 FDA reports)
HALLUCINATIONS, MIXED ( 22 FDA reports)
HYPERREFLEXIA ( 22 FDA reports)
HYPOCHLORAEMIA ( 22 FDA reports)
IMMUNOSUPPRESSION ( 22 FDA reports)
INJECTION SITE MASS ( 22 FDA reports)
INTESTINAL DILATATION ( 22 FDA reports)
LEUKOENCEPHALOPATHY ( 22 FDA reports)
LOGORRHOEA ( 22 FDA reports)
LUNG ADENOCARCINOMA ( 22 FDA reports)
LYMPH NODE PAIN ( 22 FDA reports)
MAMMOGRAM ABNORMAL ( 22 FDA reports)
METASTASES TO PERITONEUM ( 22 FDA reports)
ANAL SPHINCTER ATONY ( 21 FDA reports)
BENIGN COLONIC NEOPLASM ( 21 FDA reports)
BIOPSY BONE MARROW ( 21 FDA reports)
BLOOD IRON INCREASED ( 21 FDA reports)
BLOOD SODIUM INCREASED ( 21 FDA reports)
BREAST LUMP REMOVAL ( 21 FDA reports)
CARDIAC FAILURE CHRONIC ( 21 FDA reports)
CARDIOTOXICITY ( 21 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 21 FDA reports)
CERVIX CARCINOMA ( 21 FDA reports)
CHRONIC HEPATIC FAILURE ( 21 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 21 FDA reports)
COLON OPERATION ( 21 FDA reports)
CRANIOTOMY ( 21 FDA reports)
EFFUSION ( 21 FDA reports)
ENTEROBACTER INFECTION ( 21 FDA reports)
FACIAL PARESIS ( 21 FDA reports)
FAECES HARD ( 21 FDA reports)
FIBRIN D DIMER INCREASED ( 21 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 21 FDA reports)
HAEMARTHROSIS ( 21 FDA reports)
HAEMOTHORAX ( 21 FDA reports)
HYDROCELE ( 21 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 21 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 21 FDA reports)
INJECTION SITE EXTRAVASATION ( 21 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 21 FDA reports)
JOINT CREPITATION ( 21 FDA reports)
LIGAMENT INJURY ( 21 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 21 FDA reports)
LIP OEDEMA ( 21 FDA reports)
LOSS OF LIBIDO ( 21 FDA reports)
MALIGNANT HYPERTENSION ( 21 FDA reports)
MALLORY-WEISS SYNDROME ( 21 FDA reports)
NEPHRITIS ( 21 FDA reports)
OCCULT BLOOD ( 21 FDA reports)
OESOPHAGEAL ACHALASIA ( 21 FDA reports)
OESOPHAGEAL INJURY ( 21 FDA reports)
ORTHODONTIC APPLIANCE USER ( 21 FDA reports)
PANCREATITIS NECROTISING ( 21 FDA reports)
PCO2 DECREASED ( 21 FDA reports)
PLASTIC SURGERY ( 21 FDA reports)
POLYTRAUMATISM ( 21 FDA reports)
POOR VENOUS ACCESS ( 21 FDA reports)
PROTRUSION TONGUE ( 21 FDA reports)
PRURIGO ( 21 FDA reports)
PSYCHOLOGICAL TRAUMA ( 21 FDA reports)
PSYCHOMOTOR RETARDATION ( 21 FDA reports)
PULMONARY INFARCTION ( 21 FDA reports)
RASH VESICULAR ( 21 FDA reports)
RESUSCITATION ( 21 FDA reports)
RHEUMATOID FACTOR INCREASED ( 21 FDA reports)
RHINALGIA ( 21 FDA reports)
SICCA SYNDROME ( 21 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 21 FDA reports)
SKIN ATROPHY ( 21 FDA reports)
SKIN FISSURES ( 21 FDA reports)
THROMBOCYTOPENIC PURPURA ( 21 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 21 FDA reports)
TRANSPLANT REJECTION ( 21 FDA reports)
TRAUMATIC LUNG INJURY ( 21 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 21 FDA reports)
X-RAY ABNORMAL ( 21 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 20 FDA reports)
PARANASAL SINUS BENIGN NEOPLASM ( 20 FDA reports)
PARESIS ( 20 FDA reports)
PEMPHIGOID ( 20 FDA reports)
POSTOPERATIVE ADHESION ( 20 FDA reports)
PULMONARY ARTERY DILATATION ( 20 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 20 FDA reports)
SACROILIITIS ( 20 FDA reports)
SCAN BONE MARROW ABNORMAL ( 20 FDA reports)
SELF-INJURIOUS IDEATION ( 20 FDA reports)
SLEEP WALKING ( 20 FDA reports)
SPINAL CORD DISORDER ( 20 FDA reports)
SPLENIC ARTERY ANEURYSM ( 20 FDA reports)
STENT OCCLUSION ( 20 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 20 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 20 FDA reports)
UTERINE DILATION AND CURETTAGE ( 20 FDA reports)
VASCULAR STENOSIS ( 20 FDA reports)
VENTRICULAR ARRHYTHMIA ( 20 FDA reports)
WOUND DEBRIDEMENT ( 20 FDA reports)
ADENOMA BENIGN ( 20 FDA reports)
AMYLOIDOSIS ( 20 FDA reports)
ANAL ABSCESS ( 20 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 20 FDA reports)
APPLICATION SITE PAIN ( 20 FDA reports)
ASTHENOPIA ( 20 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 20 FDA reports)
BONE FISTULA ( 20 FDA reports)
BONE MARROW DISORDER ( 20 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 20 FDA reports)
CARDIAC ASSISTANCE DEVICE USER ( 20 FDA reports)
CATHETER SITE INFECTION ( 20 FDA reports)
CLAUSTROPHOBIA ( 20 FDA reports)
CLUMSINESS ( 20 FDA reports)
CONVERSION DISORDER ( 20 FDA reports)
COUNTERFEIT DRUG ADMINISTERED ( 20 FDA reports)
CUSHINGOID ( 20 FDA reports)
DERMATITIS ACNEIFORM ( 20 FDA reports)
DERMATITIS ATOPIC ( 20 FDA reports)
DEVICE LEAKAGE ( 20 FDA reports)
DYSPNOEA EXACERBATED ( 20 FDA reports)
EAR CONGESTION ( 20 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 20 FDA reports)
ENTEROCOLITIS ( 20 FDA reports)
FOREARM FRACTURE ( 20 FDA reports)
GASTROINTESTINAL INJURY ( 20 FDA reports)
GLARE ( 20 FDA reports)
GRANULOCYTOPENIA ( 20 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 20 FDA reports)
HEART DISEASE CONGENITAL ( 20 FDA reports)
HERNIA HIATUS REPAIR ( 20 FDA reports)
HYPERKINESIA ( 20 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 20 FDA reports)
JOINT ARTHROPLASTY ( 20 FDA reports)
MACULOPATHY ( 20 FDA reports)
METASTASES TO SPLEEN ( 20 FDA reports)
METASTASES TO STOMACH ( 20 FDA reports)
MUCOUS MEMBRANE DISORDER ( 20 FDA reports)
MYOPIA ( 20 FDA reports)
ABORTION INDUCED ( 19 FDA reports)
ACROCHORDON ( 19 FDA reports)
ADJUSTMENT DISORDER ( 19 FDA reports)
ANGIOFIBROMA ( 19 FDA reports)
AORTIC THROMBOSIS ( 19 FDA reports)
APPLICATION SITE VESICLES ( 19 FDA reports)
ARTERIAL THROMBOSIS ( 19 FDA reports)
BLOOD MAGNESIUM INCREASED ( 19 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 19 FDA reports)
BONE GRAFT ( 19 FDA reports)
BREAST CANCER IN SITU ( 19 FDA reports)
BRONCHIAL OBSTRUCTION ( 19 FDA reports)
BURNS THIRD DEGREE ( 19 FDA reports)
CALCULUS URINARY ( 19 FDA reports)
CARCINOID TUMOUR ( 19 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 19 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 19 FDA reports)
CEREBRAL THROMBOSIS ( 19 FDA reports)
CHOLANGITIS SCLEROSING ( 19 FDA reports)
CRANIOCEREBRAL INJURY ( 19 FDA reports)
DARK CIRCLES UNDER EYES ( 19 FDA reports)
DIABETIC EYE DISEASE ( 19 FDA reports)
DIET REFUSAL ( 19 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 19 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 19 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 19 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 19 FDA reports)
EXTRAVASATION ( 19 FDA reports)
EYE ROLLING ( 19 FDA reports)
FAT TISSUE INCREASED ( 19 FDA reports)
FEELING HOT AND COLD ( 19 FDA reports)
FEMORAL ARTERY OCCLUSION ( 19 FDA reports)
FINGER DEFORMITY ( 19 FDA reports)
FOOD CRAVING ( 19 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 19 FDA reports)
HAEMOGLOBIN ABNORMAL ( 19 FDA reports)
HAEMOPHILUS INFECTION ( 19 FDA reports)
HAEMORRHAGE URINARY TRACT ( 19 FDA reports)
HEPATITIS FULMINANT ( 19 FDA reports)
HIDRADENITIS ( 19 FDA reports)
INTENTIONAL SELF-INJURY ( 19 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 19 FDA reports)
INTERTRIGO ( 19 FDA reports)
INTESTINAL ULCER ( 19 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 19 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 19 FDA reports)
KETOACIDOSIS ( 19 FDA reports)
LUNG ABSCESS ( 19 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 19 FDA reports)
MAGNESIUM DEFICIENCY ( 19 FDA reports)
MASTOIDITIS ( 19 FDA reports)
MIDDLE EAR EFFUSION ( 19 FDA reports)
MONOCYTOSIS ( 19 FDA reports)
MYCOSIS FUNGOIDES ( 19 FDA reports)
OESOPHAGEAL MUCOSAL HYPERPLASIA ( 19 FDA reports)
OESOPHAGEAL OEDEMA ( 19 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 19 FDA reports)
OPTIC NEUROPATHY ( 19 FDA reports)
OROPHARYNGEAL PLAQUE ( 19 FDA reports)
OROPHARYNGEAL SWELLING ( 19 FDA reports)
OSTEOGENESIS IMPERFECTA ( 19 FDA reports)
PEAU D'ORANGE ( 19 FDA reports)
PENILE PAIN ( 19 FDA reports)
PHARYNGEAL ULCERATION ( 19 FDA reports)
PULMONARY RADIATION INJURY ( 19 FDA reports)
RADICULITIS LUMBOSACRAL ( 19 FDA reports)
RETINAL TEAR ( 19 FDA reports)
SERUM SICKNESS ( 19 FDA reports)
SKULL FRACTURE ( 19 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 19 FDA reports)
SPINAL COLUMN INJURY ( 19 FDA reports)
STARING ( 19 FDA reports)
STRESS SYMPTOMS ( 19 FDA reports)
SUDDEN CARDIAC DEATH ( 19 FDA reports)
SUFFOCATION FEELING ( 19 FDA reports)
SUPRAPUBIC PAIN ( 19 FDA reports)
TRACHEITIS ( 19 FDA reports)
TREATMENT FAILURE ( 19 FDA reports)
VAGINAL DISORDER ( 19 FDA reports)
VASODILATATION ( 19 FDA reports)
WOUND COMPLICATION ( 19 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 19 FDA reports)
NEPHROCALCINOSIS ( 18 FDA reports)
NEUROENDOCRINE CARCINOMA ( 18 FDA reports)
NIKOLSKY'S SIGN ( 18 FDA reports)
NOSOCOMIAL INFECTION ( 18 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 18 FDA reports)
PANCREAS INFECTION ( 18 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 18 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 18 FDA reports)
PULMONARY TOXICITY ( 18 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 18 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 18 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 18 FDA reports)
SPINAL FUSION ACQUIRED ( 18 FDA reports)
SUICIDAL BEHAVIOUR ( 18 FDA reports)
TIC ( 18 FDA reports)
TRAUMATIC BRAIN INJURY ( 18 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 18 FDA reports)
VASCULAR GRAFT OCCLUSION ( 18 FDA reports)
VASCULAR INSUFFICIENCY ( 18 FDA reports)
VESTIBULAR DISORDER ( 18 FDA reports)
VITH NERVE PARALYSIS ( 18 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 18 FDA reports)
WEIGHT LOSS POOR ( 18 FDA reports)
ACUTE STRESS DISORDER ( 18 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 18 FDA reports)
BLADDER OBSTRUCTION ( 18 FDA reports)
BLOOD CHOLESTEROL ( 18 FDA reports)
BLOOD UREA DECREASED ( 18 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 18 FDA reports)
CARDIAC DISCOMFORT ( 18 FDA reports)
CHEST INJURY ( 18 FDA reports)
CHOREA ( 18 FDA reports)
COLONIC STENOSIS ( 18 FDA reports)
COR PULMONALE CHRONIC ( 18 FDA reports)
CORNEAL DYSTROPHY ( 18 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 18 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 18 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 18 FDA reports)
ESCHERICHIA BACTERAEMIA ( 18 FDA reports)
EYE INJURY ( 18 FDA reports)
FAT NECROSIS ( 18 FDA reports)
FOOD AVERSION ( 18 FDA reports)
FRACTURED COCCYX ( 18 FDA reports)
FUNGAL OESOPHAGITIS ( 18 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 18 FDA reports)
GLYCOSURIA ( 18 FDA reports)
HAIR DISORDER ( 18 FDA reports)
HYPOGONADISM ( 18 FDA reports)
INCREASED BRONCHIAL SECRETION ( 18 FDA reports)
INTESTINAL RESECTION ( 18 FDA reports)
KERATOSIS PILARIS ( 18 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 18 FDA reports)
LIPIDS INCREASED ( 18 FDA reports)
METASTASES TO SKIN ( 18 FDA reports)
MICROCYTOSIS ( 18 FDA reports)
MULTI-ORGAN DISORDER ( 18 FDA reports)
MUTISM ( 18 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 17 FDA reports)
ALCOHOL ABUSE ( 17 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 17 FDA reports)
ANAESTHETIC COMPLICATION ( 17 FDA reports)
ANDROGENS ABNORMAL ( 17 FDA reports)
ARTERIAL STENT INSERTION ( 17 FDA reports)
ARTHRITIS INFECTIVE ( 17 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 17 FDA reports)
BLOOD CREATININE DECREASED ( 17 FDA reports)
BLOOD GASTRIN INCREASED ( 17 FDA reports)
BLOOD PH DECREASED ( 17 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 17 FDA reports)
BONE CYST ( 17 FDA reports)
BRADYPNOEA ( 17 FDA reports)
BRAIN HERNIATION ( 17 FDA reports)
BREAST CANCER STAGE I ( 17 FDA reports)
CARDIAC VALVE SCLEROSIS ( 17 FDA reports)
COAGULATION TIME PROLONGED ( 17 FDA reports)
CYST RUPTURE ( 17 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 17 FDA reports)
DIABETES INSIPIDUS ( 17 FDA reports)
DIABETIC ULCER ( 17 FDA reports)
DRUG NAME CONFUSION ( 17 FDA reports)
DYSPLASIA ( 17 FDA reports)
ENTERITIS INFECTIOUS ( 17 FDA reports)
EYELID FUNCTION DISORDER ( 17 FDA reports)
FALLOT'S TETRALOGY ( 17 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 17 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 17 FDA reports)
GASTROINTESTINAL OEDEMA ( 17 FDA reports)
GRIP STRENGTH DECREASED ( 17 FDA reports)
HEARING AID USER ( 17 FDA reports)
HEAT STROKE ( 17 FDA reports)
HYDROPNEUMOTHORAX ( 17 FDA reports)
HYPERLACTACIDAEMIA ( 17 FDA reports)
LABILE BLOOD PRESSURE ( 17 FDA reports)
LIMB DEFORMITY ( 17 FDA reports)
LIP BLISTER ( 17 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 17 FDA reports)
LOWER EXTREMITY MASS ( 17 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 17 FDA reports)
MASS EXCISION ( 17 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 17 FDA reports)
MAXILLOFACIAL OPERATION ( 17 FDA reports)
MEIBOMIANITIS ( 17 FDA reports)
MENINGEAL DISORDER ( 17 FDA reports)
MENOPAUSAL SYMPTOMS ( 17 FDA reports)
MENSTRUAL DISORDER ( 17 FDA reports)
METASTASES TO KIDNEY ( 17 FDA reports)
METASTASES TO NECK ( 17 FDA reports)
METASTASES TO PLEURA ( 17 FDA reports)
MUSCLE FATIGUE ( 17 FDA reports)
NAIL DISCOLOURATION ( 17 FDA reports)
NEPHRECTOMY ( 17 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 17 FDA reports)
NODULE ON EXTREMITY ( 17 FDA reports)
PERIODONTAL INFECTION ( 17 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 17 FDA reports)
PO2 DECREASED ( 17 FDA reports)
PREMATURE LABOUR ( 17 FDA reports)
PRODUCT ODOUR ABNORMAL ( 17 FDA reports)
QRS AXIS ABNORMAL ( 17 FDA reports)
QUADRIPARESIS ( 17 FDA reports)
RASH MORBILLIFORM ( 17 FDA reports)
RED BLOOD CELL ABNORMALITY ( 17 FDA reports)
RHINITIS SEASONAL ( 17 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 17 FDA reports)
SOMATISATION DISORDER ( 17 FDA reports)
SPINAL CORD OEDEMA ( 17 FDA reports)
SPLEEN DISORDER ( 17 FDA reports)
STASIS DERMATITIS ( 17 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 17 FDA reports)
TINEA CRURIS ( 17 FDA reports)
TONGUE BLISTERING ( 17 FDA reports)
TONSILLAR DISORDER ( 17 FDA reports)
TRANSPLANT FAILURE ( 17 FDA reports)
ULNAR NEURITIS ( 17 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 17 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 17 FDA reports)
VASOCONSTRICTION ( 17 FDA reports)
VENTRICULO-PERITONEAL SHUNT ( 17 FDA reports)
VITAMIN B1 DEFICIENCY ( 17 FDA reports)
NEGATIVE THOUGHTS ( 16 FDA reports)
NEOPLASM SKIN ( 16 FDA reports)
NEPHROPATHY TOXIC ( 16 FDA reports)
ONYCHOMADESIS ( 16 FDA reports)
ORAL FIBROMA ( 16 FDA reports)
ORAL PUSTULE ( 16 FDA reports)
PALATAL DISORDER ( 16 FDA reports)
PELVIC ABSCESS ( 16 FDA reports)
PRESBYOPIA ( 16 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 16 FDA reports)
PROLAPSE REPAIR ( 16 FDA reports)
PUBIS FRACTURE ( 16 FDA reports)
RENAL CANCER METASTATIC ( 16 FDA reports)
RETINAL ARTERY OCCLUSION ( 16 FDA reports)
SALIVARY GLAND DISORDER ( 16 FDA reports)
SKIN CHAPPED ( 16 FDA reports)
SKIN INJURY ( 16 FDA reports)
SOFT TISSUE INJURY ( 16 FDA reports)
STILLBIRTH ( 16 FDA reports)
TENDON PAIN ( 16 FDA reports)
THYMUS DISORDER ( 16 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 16 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 16 FDA reports)
URINE FLOW DECREASED ( 16 FDA reports)
VENTRICULAR SEPTAL DEFECT REPAIR ( 16 FDA reports)
YELLOW SKIN ( 16 FDA reports)
ADENOMYOSIS ( 16 FDA reports)
ADVERSE REACTION ( 16 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 16 FDA reports)
AMYLASE INCREASED ( 16 FDA reports)
AORTIC VALVE REPLACEMENT ( 16 FDA reports)
AORTIC VALVE STENOSIS ( 16 FDA reports)
ASPHYXIA ( 16 FDA reports)
ASPIRATION BRONCHIAL ( 16 FDA reports)
ATRIAL TACHYCARDIA ( 16 FDA reports)
BACTERIAL SEPSIS ( 16 FDA reports)
BENIGN BREAST NEOPLASM ( 16 FDA reports)
BENIGN OVARIAN TUMOUR ( 16 FDA reports)
BIOPSY BONE ABNORMAL ( 16 FDA reports)
BLOOD PRESSURE ( 16 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 16 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 16 FDA reports)
BRADYARRHYTHMIA ( 16 FDA reports)
BRADYKINESIA ( 16 FDA reports)
BREAST OPERATION ( 16 FDA reports)
CARDIAC FIBRILLATION ( 16 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 16 FDA reports)
CARDIOVERSION ( 16 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 16 FDA reports)
CARTILAGE ATROPHY ( 16 FDA reports)
CEREBELLAR ATROPHY ( 16 FDA reports)
CEREBELLAR INFARCTION ( 16 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 16 FDA reports)
CERVICITIS ( 16 FDA reports)
CHEST TUBE INSERTION ( 16 FDA reports)
CHEST WALL OPERATION ( 16 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 16 FDA reports)
CONJUNCTIVOCHALASIS ( 16 FDA reports)
DENTAL TREATMENT ( 16 FDA reports)
DERMOID CYST ( 16 FDA reports)
DIABETIC FOOT ( 16 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 16 FDA reports)
EDENTULOUS ( 16 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 16 FDA reports)
ENURESIS ( 16 FDA reports)
EXPOSURE TO TOXIC AGENT ( 16 FDA reports)
FIBROMA ( 16 FDA reports)
FUNGAL SKIN INFECTION ( 16 FDA reports)
GAMMOPATHY ( 16 FDA reports)
GASTRIC DILATATION ( 16 FDA reports)
GASTRIC MUCOSAL LESION ( 16 FDA reports)
GASTRITIS HAEMORRHAGIC ( 16 FDA reports)
GASTROINTESTINAL CARCINOMA ( 16 FDA reports)
GLIOSIS ( 16 FDA reports)
HYPOPROTEINAEMIA ( 16 FDA reports)
INFECTIOUS PERITONITIS ( 16 FDA reports)
INTESTINAL GANGRENE ( 16 FDA reports)
JOINT SURGERY ( 16 FDA reports)
LENTIGO ( 16 FDA reports)
LUDWIG ANGINA ( 16 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 16 FDA reports)
MEDIASTINAL MASS ( 16 FDA reports)
METABOLIC ALKALOSIS ( 16 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 16 FDA reports)
MIGRAINE WITH AURA ( 16 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 16 FDA reports)
ALVEOLITIS ALLERGIC ( 15 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 15 FDA reports)
ANAL HAEMORRHAGE ( 15 FDA reports)
ANDROGEN DEFICIENCY ( 15 FDA reports)
AORTIC DISORDER ( 15 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 15 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 15 FDA reports)
BLADDER DISCOMFORT ( 15 FDA reports)
BRAIN DEATH ( 15 FDA reports)
CANCER IN REMISSION ( 15 FDA reports)
CATHETER SITE ERYTHEMA ( 15 FDA reports)
CEREBELLAR SYNDROME ( 15 FDA reports)
CITROBACTER INFECTION ( 15 FDA reports)
COLITIS COLLAGENOUS ( 15 FDA reports)
COLITIS MICROSCOPIC ( 15 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 15 FDA reports)
CORONARY ANGIOPLASTY ( 15 FDA reports)
CORONARY ARTERY RESTENOSIS ( 15 FDA reports)
CRYOGLOBULINAEMIA ( 15 FDA reports)
DENTAL IMPLANTATION ( 15 FDA reports)
DENTAL PULP DISORDER ( 15 FDA reports)
DRUG RESISTANCE ( 15 FDA reports)
EJACULATION FAILURE ( 15 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 15 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 15 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 15 FDA reports)
ENTHESOPATHY ( 15 FDA reports)
EXFOLIATIVE RASH ( 15 FDA reports)
EXTREMITY NECROSIS ( 15 FDA reports)
FRACTURE DISPLACEMENT ( 15 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 15 FDA reports)
GINGIVAL ERYTHEMA ( 15 FDA reports)
GINGIVAL GRAFT ( 15 FDA reports)
HELICOBACTER TEST POSITIVE ( 15 FDA reports)
HEPATIC VEIN THROMBOSIS ( 15 FDA reports)
HIGH FREQUENCY ABLATION ( 15 FDA reports)
HOARSENESS ( 15 FDA reports)
HYPERMETABOLISM ( 15 FDA reports)
HYPOCHROMASIA ( 15 FDA reports)
HYPOCHROMIC ANAEMIA ( 15 FDA reports)
INCISION SITE PAIN ( 15 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 15 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 15 FDA reports)
INJECTION SITE PAPULE ( 15 FDA reports)
IRREGULAR SLEEP PHASE ( 15 FDA reports)
JOINT LOCK ( 15 FDA reports)
LEARNING DISORDER ( 15 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 15 FDA reports)
LOOSE STOOLS ( 15 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 15 FDA reports)
METAMORPHOPSIA ( 15 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 15 FDA reports)
MONOPARESIS ( 15 FDA reports)
MYELOPATHY ( 15 FDA reports)
MYOFASCITIS ( 15 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 15 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ( 15 FDA reports)
OCULAR NEOPLASM ( 15 FDA reports)
ORAL NEOPLASM ( 15 FDA reports)
PANCREATIC ATROPHY ( 15 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 15 FDA reports)
PERITONEAL EFFUSION ( 15 FDA reports)
PLEURAL DISORDER ( 15 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 15 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 15 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 15 FDA reports)
POSTOPERATIVE ABSCESS ( 15 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 15 FDA reports)
PULMONARY VASCULAR DISORDER ( 15 FDA reports)
PUSTULAR PSORIASIS ( 15 FDA reports)
RADICULITIS ( 15 FDA reports)
RENAL ABSCESS ( 15 FDA reports)
RENAL NEOPLASM ( 15 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 15 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 15 FDA reports)
SPIDER VEIN ( 15 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 15 FDA reports)
SYNOVIAL RUPTURE ( 15 FDA reports)
THERAPEUTIC PROCEDURE ( 15 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 15 FDA reports)
TONSIL CANCER ( 15 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 15 FDA reports)
URINE OUTPUT INCREASED ( 15 FDA reports)
VENTRICULAR DYSKINESIA ( 15 FDA reports)
VOCAL CORD POLYP ( 15 FDA reports)
VOLVULUS ( 15 FDA reports)
VULVOVAGINITIS ( 15 FDA reports)
WOUND HAEMORRHAGE ( 15 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 14 FDA reports)
NEUTROPENIC COLITIS ( 14 FDA reports)
NODAL RHYTHM ( 14 FDA reports)
OPERATIVE HAEMORRHAGE ( 14 FDA reports)
OPTIC ATROPHY ( 14 FDA reports)
OVARIAN CANCER STAGE I ( 14 FDA reports)
OVERGROWTH BACTERIAL ( 14 FDA reports)
OXYGEN SUPPLEMENTATION ( 14 FDA reports)
PANCREATIC DUCT STENOSIS ( 14 FDA reports)
PARTNER STRESS ( 14 FDA reports)
PATHOGEN RESISTANCE ( 14 FDA reports)
PECTUS EXCAVATUM ( 14 FDA reports)
PERICARDITIS CONSTRICTIVE ( 14 FDA reports)
PERIPHERAL EMBOLISM ( 14 FDA reports)
PETIT MAL EPILEPSY ( 14 FDA reports)
PHARYNGEAL INFLAMMATION ( 14 FDA reports)
PHARYNGEAL MASS ( 14 FDA reports)
PLEURODESIS ( 14 FDA reports)
PNEUMONIA FUNGAL ( 14 FDA reports)
POLYCYSTIC OVARIES ( 14 FDA reports)
POLYP COLORECTAL ( 14 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 14 FDA reports)
PROTEIN S DEFICIENCY ( 14 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 14 FDA reports)
READING DISORDER ( 14 FDA reports)
RENAL STONE REMOVAL ( 14 FDA reports)
RESPIRATORY THERAPY ( 14 FDA reports)
SENILE DEMENTIA ( 14 FDA reports)
SERUM FERRITIN DECREASED ( 14 FDA reports)
STEATORRHOEA ( 14 FDA reports)
STRABISMUS ( 14 FDA reports)
T-CELL LYMPHOMA ( 14 FDA reports)
TRACHEAL INJURY ( 14 FDA reports)
TRACHEOSTOMY ( 14 FDA reports)
VASCULAR INJURY ( 14 FDA reports)
VASCULAR PSEUDOANEURYSM ( 14 FDA reports)
VASCULITIS CEREBRAL ( 14 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 14 FDA reports)
ABSCESS LIMB ( 14 FDA reports)
ACCIDENTAL NEEDLE STICK ( 14 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 14 FDA reports)
ANAL CANCER ( 14 FDA reports)
APRAXIA ( 14 FDA reports)
ASTEATOSIS ( 14 FDA reports)
AUTOIMMUNE THYROIDITIS ( 14 FDA reports)
B-CELL LYMPHOMA ( 14 FDA reports)
BALANITIS ( 14 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 14 FDA reports)
BICYTOPENIA ( 14 FDA reports)
BIOPSY CHEST WALL ABNORMAL ( 14 FDA reports)
BLOOD BICARBONATE DECREASED ( 14 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 14 FDA reports)
BRAIN SCAN ABNORMAL ( 14 FDA reports)
BREAST CELLULITIS ( 14 FDA reports)
CANDIDA SEPSIS ( 14 FDA reports)
CARDIAC DEATH ( 14 FDA reports)
CARDIAC SEPTAL DEFECT ( 14 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 14 FDA reports)
COMPLEX PARTIAL SEIZURES ( 14 FDA reports)
CORNEAL ABRASION ( 14 FDA reports)
CYTARABINE SYNDROME ( 14 FDA reports)
DENTAL PLAQUE ( 14 FDA reports)
DIURETIC THERAPY ( 14 FDA reports)
DYSPHORIA ( 14 FDA reports)
DYSPNOEA AT REST ( 14 FDA reports)
ESCHAR ( 14 FDA reports)
FAECAL VOMITING ( 14 FDA reports)
FEAR OF DISEASE ( 14 FDA reports)
GASTROINTESTINAL EROSION ( 14 FDA reports)
GASTROINTESTINAL PERFORATION ( 14 FDA reports)
GENERAL SYMPTOM ( 14 FDA reports)
GROIN ABSCESS ( 14 FDA reports)
HAEMOCHROMATOSIS ( 14 FDA reports)
HAIR GROWTH ABNORMAL ( 14 FDA reports)
HEAD AND NECK CANCER ( 14 FDA reports)
HERNIA PAIN ( 14 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 14 FDA reports)
HYPERSEXUALITY ( 14 FDA reports)
HYPERTROPHY ( 14 FDA reports)
HYPOMANIA ( 14 FDA reports)
ILIAC ARTERY OCCLUSION ( 14 FDA reports)
IMPAIRED FASTING GLUCOSE ( 14 FDA reports)
INCISION SITE COMPLICATION ( 14 FDA reports)
INTESTINAL MASS ( 14 FDA reports)
INTRACRANIAL HYPOTENSION ( 14 FDA reports)
JUGULAR VEIN DISTENSION ( 14 FDA reports)
LERICHE SYNDROME ( 14 FDA reports)
LIGAMENT OPERATION ( 14 FDA reports)
LOOSE BODY IN JOINT ( 14 FDA reports)
LOSS OF CONTROL OF LEGS ( 14 FDA reports)
LYMPHOCYTIC INFILTRATION ( 14 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 14 FDA reports)
MITRAL VALVE REPAIR ( 14 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 14 FDA reports)
MUCOEPIDERMOID CARCINOMA ( 14 FDA reports)
MUCOSAL EROSION ( 14 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 14 FDA reports)
ACANTHOSIS ( 13 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 13 FDA reports)
ADNEXA UTERI CYST ( 13 FDA reports)
AMBLYOPIA ( 13 FDA reports)
ANAL PRURITUS ( 13 FDA reports)
ANASTOMOTIC STENOSIS ( 13 FDA reports)
ANGIOCENTRIC LYMPHOMA ( 13 FDA reports)
ANKYLOSING SPONDYLITIS ( 13 FDA reports)
ANTIBODY TEST POSITIVE ( 13 FDA reports)
APALLIC SYNDROME ( 13 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 13 FDA reports)
ASBESTOSIS ( 13 FDA reports)
ASEPTIC NECROSIS BONE ( 13 FDA reports)
AXILLARY MASS ( 13 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 13 FDA reports)
BLEEDING TIME PROLONGED ( 13 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 13 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 13 FDA reports)
BONE CANCER METASTATIC ( 13 FDA reports)
BRAIN OPERATION ( 13 FDA reports)
BRONCHIAL DISORDER ( 13 FDA reports)
CARBON DIOXIDE DECREASED ( 13 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 13 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 13 FDA reports)
CATATONIA ( 13 FDA reports)
CENTRAL LINE INFECTION ( 13 FDA reports)
CHOLESTEATOMA ( 13 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 13 FDA reports)
CHORIORETINOPATHY ( 13 FDA reports)
COMMINUTED FRACTURE ( 13 FDA reports)
DISEASE COMPLICATION ( 13 FDA reports)
DRUG LEVEL DECREASED ( 13 FDA reports)
DRUG TOLERANCE INCREASED ( 13 FDA reports)
EAR HAEMORRHAGE ( 13 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 13 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 13 FDA reports)
GASTROENTERITIS RADIATION ( 13 FDA reports)
GASTROSTOMY TUBE INSERTION ( 13 FDA reports)
GLIOBLASTOMA ( 13 FDA reports)
HAPTOGLOBIN DECREASED ( 13 FDA reports)
HEAT EXHAUSTION ( 13 FDA reports)
HEMIANOPIA ( 13 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 13 FDA reports)
HYPERAMMONAEMIA ( 13 FDA reports)
HYPERPROTEINAEMIA ( 13 FDA reports)
HYPOGEUSIA ( 13 FDA reports)
INCISION SITE INFECTION ( 13 FDA reports)
INFUSION SITE EXTRAVASATION ( 13 FDA reports)
INGUINAL HERNIA REPAIR ( 13 FDA reports)
INJECTION SITE INDURATION ( 13 FDA reports)
INJECTION SITE NECROSIS ( 13 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 13 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 13 FDA reports)
INTENTIONAL MISUSE ( 13 FDA reports)
INTESTINAL OPERATION ( 13 FDA reports)
IRITIS ( 13 FDA reports)
JAW LESION EXCISION ( 13 FDA reports)
KIDNEY FIBROSIS ( 13 FDA reports)
LARYNGEAL CANCER ( 13 FDA reports)
LEUKOCYTURIA ( 13 FDA reports)
LIVEDO RETICULARIS ( 13 FDA reports)
LYMPH GLAND INFECTION ( 13 FDA reports)
MAMMOPLASTY ( 13 FDA reports)
MEDIASTINAL DISORDER ( 13 FDA reports)
METASTASES TO PANCREAS ( 13 FDA reports)
METATARSALGIA ( 13 FDA reports)
NASAL SINUS CANCER ( 13 FDA reports)
NEURODEGENERATIVE DISORDER ( 13 FDA reports)
NIPPLE PAIN ( 13 FDA reports)
OESOPHAGEAL DILATION PROCEDURE ( 13 FDA reports)
OESOPHAGEAL NEOPLASM ( 13 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 13 FDA reports)
ORTHOSIS USER ( 13 FDA reports)
OVARIAN CANCER METASTATIC ( 13 FDA reports)
OXYGEN SATURATION ABNORMAL ( 13 FDA reports)
PANCREATIC INSUFFICIENCY ( 13 FDA reports)
PELVIC DISCOMFORT ( 13 FDA reports)
PENIS DISORDER ( 13 FDA reports)
PERIPHERAL NERVE INJURY ( 13 FDA reports)
PILONIDAL CYST ( 13 FDA reports)
PLATELET COUNT ABNORMAL ( 13 FDA reports)
PNEUMONIA KLEBSIELLA ( 13 FDA reports)
PNEUMONIA NECROTISING ( 13 FDA reports)
POISONING ( 13 FDA reports)
POLYCYTHAEMIA ( 13 FDA reports)
POST PROCEDURAL FISTULA ( 13 FDA reports)
PRECANCEROUS MUCOSAL LESION ( 13 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 13 FDA reports)
RADICULAR PAIN ( 13 FDA reports)
RADICULAR SYNDROME ( 13 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 13 FDA reports)
RETINAL DEGENERATION ( 13 FDA reports)
SALIVARY GLAND MASS ( 13 FDA reports)
SALMONELLOSIS ( 13 FDA reports)
SEMEN VOLUME DECREASED ( 13 FDA reports)
SKIN EROSION ( 13 FDA reports)
SKULL MALFORMATION ( 13 FDA reports)
SPLENECTOMY ( 13 FDA reports)
TOE DEFORMITY ( 13 FDA reports)
TORTICOLLIS ( 13 FDA reports)
TOXIC NEUROPATHY ( 13 FDA reports)
TROPONIN I INCREASED ( 13 FDA reports)
TUMOUR HAEMORRHAGE ( 13 FDA reports)
TUMOUR LYSIS SYNDROME ( 13 FDA reports)
UTERINE PROLAPSE ( 13 FDA reports)
VASCULAR RUPTURE ( 13 FDA reports)
VENOUS STENOSIS ( 13 FDA reports)
VOCAL CORD INFLAMMATION ( 13 FDA reports)
VOCAL CORD THICKENING ( 13 FDA reports)
WISDOM TEETH REMOVAL ( 13 FDA reports)
NODAL OSTEOARTHRITIS ( 12 FDA reports)
ORAL SOFT TISSUE DISORDER ( 12 FDA reports)
ORCHITIS ( 12 FDA reports)
ORGANISING PNEUMONIA ( 12 FDA reports)
ORTHOPEDIC PROCEDURE ( 12 FDA reports)
OSTEOSYNTHESIS ( 12 FDA reports)
PAROTIDECTOMY ( 12 FDA reports)
PCO2 INCREASED ( 12 FDA reports)
PERIODONTAL OPERATION ( 12 FDA reports)
PHYSICAL ASSAULT ( 12 FDA reports)
PIRIFORMIS SYNDROME ( 12 FDA reports)
PRODUCT COUNTERFEIT ( 12 FDA reports)
PSEUDOMONAS BRONCHITIS ( 12 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 12 FDA reports)
RECTAL ULCER ( 12 FDA reports)
RETINAL ISCHAEMIA ( 12 FDA reports)
RHINOPLASTY ( 12 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 12 FDA reports)
SALIVA ALTERED ( 12 FDA reports)
SALPINGO-OOPHORECTOMY ( 12 FDA reports)
SELF ESTEEM DECREASED ( 12 FDA reports)
SKIN HYPOPIGMENTATION ( 12 FDA reports)
SKIN ULCER HAEMORRHAGE ( 12 FDA reports)
SMEAR CERVIX ABNORMAL ( 12 FDA reports)
SMOKER ( 12 FDA reports)
SPINAL CORD INJURY ( 12 FDA reports)
STERNAL FRACTURE ( 12 FDA reports)
TERATOMA ( 12 FDA reports)
THYMOMA ( 12 FDA reports)
THYROID OPERATION ( 12 FDA reports)
TUNNEL VISION ( 12 FDA reports)
ULCERATIVE KERATITIS ( 12 FDA reports)
URINARY TRACT PAIN ( 12 FDA reports)
URINE KETONE BODY PRESENT ( 12 FDA reports)
URTICARIA GENERALISED ( 12 FDA reports)
VAGINITIS BACTERIAL ( 12 FDA reports)
VOCAL CORD NEOPLASM ( 12 FDA reports)
ABDOMINAL INFECTION ( 12 FDA reports)
ABDOMINAL OPERATION ( 12 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 12 FDA reports)
ABSCESS NECK ( 12 FDA reports)
ACCOMMODATION DISORDER ( 12 FDA reports)
ALVEOLAR OSTEITIS ( 12 FDA reports)
ANORGASMIA ( 12 FDA reports)
ARTERIAL BYPASS OPERATION ( 12 FDA reports)
ARTHROSCOPY ( 12 FDA reports)
BACTERIAL DISEASE CARRIER ( 12 FDA reports)
BENIGN TUMOUR EXCISION ( 12 FDA reports)
BILE DUCT CANCER ( 12 FDA reports)
BLOOD CALCIUM ABNORMAL ( 12 FDA reports)
BLOOD PH INCREASED ( 12 FDA reports)
BONE MARROW OEDEMA ( 12 FDA reports)
BRACHIAL PLEXOPATHY ( 12 FDA reports)
BREAST DISCOMFORT ( 12 FDA reports)
BREAST FIBROSIS ( 12 FDA reports)
BREAST HAEMATOMA ( 12 FDA reports)
CAPILLARY LEAK SYNDROME ( 12 FDA reports)
CARDIAC OUTPUT DECREASED ( 12 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 12 FDA reports)
CONGO-CRIMEAN HAEMORRHAGIC FEVER ( 12 FDA reports)
DEAFNESS BILATERAL ( 12 FDA reports)
DENTAL CLEANING ( 12 FDA reports)
DEPRESSIVE SYMPTOM ( 12 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 12 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 12 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 12 FDA reports)
DUODENAL ULCER PERFORATION ( 12 FDA reports)
DYSPHASIA ( 12 FDA reports)
ENZYME ABNORMALITY ( 12 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 12 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 12 FDA reports)
FEEDING DISORDER ( 12 FDA reports)
FOLATE DEFICIENCY ( 12 FDA reports)
GASTRIC XANTHOMA ( 12 FDA reports)
GASTRINOMA ( 12 FDA reports)
GINGIVAL ATROPHY ( 12 FDA reports)
GROWTH RETARDATION ( 12 FDA reports)
HAEMOGLOBIN INCREASED ( 12 FDA reports)
HALO VISION ( 12 FDA reports)
HEPATIC TRAUMA ( 12 FDA reports)
HEPATITIS B ( 12 FDA reports)
HEREDITARY ANGIOEDEMA ( 12 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 12 FDA reports)
HYPERAEMIA ( 12 FDA reports)
IMMUNOGLOBULINS DECREASED ( 12 FDA reports)
INFUSION SITE PAIN ( 12 FDA reports)
INJECTION SITE INFLAMMATION ( 12 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 12 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 12 FDA reports)
JAUNDICE NEONATAL ( 12 FDA reports)
JOINT ANKYLOSIS ( 12 FDA reports)
KERATOMILEUSIS ( 12 FDA reports)
LARYNX IRRITATION ( 12 FDA reports)
LUNG TRANSPLANT REJECTION ( 12 FDA reports)
MEDICAL DEVICE REMOVAL ( 12 FDA reports)
METASTASES TO THE MEDIASTINUM ( 12 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 12 FDA reports)
MYOCARDITIS ( 12 FDA reports)
ABDOMINAL INJURY ( 11 FDA reports)
ABDOMINAL NEOPLASM ( 11 FDA reports)
ABDOMINAL WALL DISORDER ( 11 FDA reports)
ABORTION ( 11 FDA reports)
ACCELERATED HYPERTENSION ( 11 FDA reports)
ACTINOMYCES TEST POSITIVE ( 11 FDA reports)
ACUTE LEUKAEMIA ( 11 FDA reports)
ADRENAL SUPPRESSION ( 11 FDA reports)
AMAUROSIS FUGAX ( 11 FDA reports)
ANAEMIA MEGALOBLASTIC ( 11 FDA reports)
ANAL DISCOMFORT ( 11 FDA reports)
ANAL INFLAMMATION ( 11 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 11 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 11 FDA reports)
AORTIC ATHEROSCLEROSIS ( 11 FDA reports)
ARTERIAL RUPTURE ( 11 FDA reports)
ARTERIOVENOUS MALFORMATION ( 11 FDA reports)
ARTERITIS ( 11 FDA reports)
BACTERIA URINE IDENTIFIED ( 11 FDA reports)
BENIGN GASTRIC NEOPLASM ( 11 FDA reports)
BLADDER DILATATION ( 11 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 11 FDA reports)
BLOOD OSMOLARITY DECREASED ( 11 FDA reports)
BONE DENSITY ABNORMAL ( 11 FDA reports)
BRAIN DAMAGE ( 11 FDA reports)
BRAIN STEM STROKE ( 11 FDA reports)
BREAST HYPERPLASIA ( 11 FDA reports)
CATHETER SITE HAEMORRHAGE ( 11 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 11 FDA reports)
CEREBRAL CALCIFICATION ( 11 FDA reports)
CHEMICAL POISONING ( 11 FDA reports)
CHONDROCALCINOSIS ( 11 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 11 FDA reports)
COLON CANCER METASTATIC ( 11 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 11 FDA reports)
CROUP INFECTIOUS ( 11 FDA reports)
CUSHING'S SYNDROME ( 11 FDA reports)
DENTAL IMPRESSION PROCEDURE ( 11 FDA reports)
DISSEMINATED TUBERCULOSIS ( 11 FDA reports)
DUODENOGASTRIC REFLUX ( 11 FDA reports)
DYSHIDROSIS ( 11 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 11 FDA reports)
EOSINOPHILIC PNEUMONIA ( 11 FDA reports)
EXOMPHALOS ( 11 FDA reports)
FAILURE OF IMPLANT ( 11 FDA reports)
FEELING GUILTY ( 11 FDA reports)
FEMALE STERILISATION ( 11 FDA reports)
FULGURATION ( 11 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 11 FDA reports)
GIANT CELL TUMOUR OF TENDON SHEATH ( 11 FDA reports)
GOUTY ARTHRITIS ( 11 FDA reports)
GRANULOCYTES MATURATION ARREST ( 11 FDA reports)
HEART VALVE REPLACEMENT ( 11 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 11 FDA reports)
HORNER'S SYNDROME ( 11 FDA reports)
HYDROURETER ( 11 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 11 FDA reports)
HYPOTONIA NEONATAL ( 11 FDA reports)
HYPOTRICHOSIS ( 11 FDA reports)
INFECTED SKIN ULCER ( 11 FDA reports)
INFECTIVE TENOSYNOVITIS ( 11 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 11 FDA reports)
JUDGEMENT IMPAIRED ( 11 FDA reports)
LARYNGEAL INFLAMMATION ( 11 FDA reports)
LESION EXCISION ( 11 FDA reports)
LEUKOPLAKIA ( 11 FDA reports)
LIGHT CHAIN ANALYSIS ( 11 FDA reports)
LIP DISORDER ( 11 FDA reports)
LIPID METABOLISM DISORDER ( 11 FDA reports)
LISTERIOSIS ( 11 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 11 FDA reports)
LUNG TRANSPLANT ( 11 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 11 FDA reports)
MICTURITION FREQUENCY DECREASED ( 11 FDA reports)
NASAL ODOUR ( 11 FDA reports)
NECROTISING FASCIITIS ( 11 FDA reports)
NEGATIVISM ( 11 FDA reports)
NEUROTOXICITY ( 11 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 11 FDA reports)
OESOPHAGEAL INFECTION ( 11 FDA reports)
ORAL MUCOSA EROSION ( 11 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 11 FDA reports)
ORAL PRURITUS ( 11 FDA reports)
PANNICULITIS ( 11 FDA reports)
PAPILLOMA VIRAL INFECTION ( 11 FDA reports)
PORTAL VEIN OCCLUSION ( 11 FDA reports)
POST HERPETIC NEURALGIA ( 11 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 11 FDA reports)
POST PROCEDURAL CELLULITIS ( 11 FDA reports)
POST PROCEDURAL PAIN ( 11 FDA reports)
POSTOPERATIVE FEVER ( 11 FDA reports)
POSTOPERATIVE INFECTION ( 11 FDA reports)
PROTEIN TOTAL ABNORMAL ( 11 FDA reports)
PROTEIN URINE ABSENT ( 11 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 11 FDA reports)
PULMONARY MYCOSIS ( 11 FDA reports)
PULMONARY TUBERCULOSIS ( 11 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 11 FDA reports)
RECTAL PROLAPSE ( 11 FDA reports)
RENAL INFARCT ( 11 FDA reports)
SEBORRHOEA ( 11 FDA reports)
SKIN OPERATION ( 11 FDA reports)
SLOW SPEECH ( 11 FDA reports)
SOPOR ( 11 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 11 FDA reports)
SUTURE RUPTURE ( 11 FDA reports)
THORACOSTOMY ( 11 FDA reports)
THORACOTOMY ( 11 FDA reports)
TINEL'S SIGN ( 11 FDA reports)
TONIC CLONIC MOVEMENTS ( 11 FDA reports)
TRANSFUSION REACTION ( 11 FDA reports)
URETHRAL OBSTRUCTION ( 11 FDA reports)
URINE CALCIUM INCREASED ( 11 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 11 FDA reports)
UTERINE MASS ( 11 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 11 FDA reports)
VERTEBRAL WEDGING ( 11 FDA reports)
VITREOUS HAEMORRHAGE ( 11 FDA reports)
VULVOVAGINAL DISCOMFORT ( 11 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 11 FDA reports)
NEEDLE ISSUE ( 10 FDA reports)
NEPHROGENIC ANAEMIA ( 10 FDA reports)
NEUROPATHIC ARTHROPATHY ( 10 FDA reports)
NO ADVERSE EFFECT ( 10 FDA reports)
NONSPECIFIC REACTION ( 10 FDA reports)
OBSTRUCTIVE UROPATHY ( 10 FDA reports)
OESOPHAGEAL MASS ( 10 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 10 FDA reports)
PANCREATIC PSEUDOCYST ( 10 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 10 FDA reports)
PENILE OEDEMA ( 10 FDA reports)
PERSECUTORY DELUSION ( 10 FDA reports)
PHOTODERMATOSIS ( 10 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 10 FDA reports)
PLEURECTOMY ( 10 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 10 FDA reports)
POLYCHROMASIA ( 10 FDA reports)
POLYMYOSITIS ( 10 FDA reports)
POST PROCEDURAL HAEMATOMA ( 10 FDA reports)
POSTICTAL STATE ( 10 FDA reports)
PROCEDURAL VOMITING ( 10 FDA reports)
PROCTITIS ( 10 FDA reports)
PULSE PRESSURE DECREASED ( 10 FDA reports)
PUNCTATE KERATITIS ( 10 FDA reports)
RADIATION OESOPHAGITIS ( 10 FDA reports)
RADICULITIS CERVICAL ( 10 FDA reports)
RECTAL NEOPLASM ( 10 FDA reports)
RIB DEFORMITY ( 10 FDA reports)
SERRATIA BACTERAEMIA ( 10 FDA reports)
SEVERE ACUTE RESPIRATORY SYNDROME ( 10 FDA reports)
SINUS ARREST ( 10 FDA reports)
SKIN TOXICITY ( 10 FDA reports)
SKULL FRACTURED BASE ( 10 FDA reports)
SPINAL CLAUDICATION ( 10 FDA reports)
SPLINTER ( 10 FDA reports)
STERNOTOMY ( 10 FDA reports)
STRIDOR ( 10 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 10 FDA reports)
SUBDURAL HAEMATOMA EVACUATION ( 10 FDA reports)
SUBSTANCE ABUSE ( 10 FDA reports)
SURGICAL PROCEDURE REPEATED ( 10 FDA reports)
SYSTEMIC CANDIDA ( 10 FDA reports)
THORACIC OUTLET SYNDROME ( 10 FDA reports)
TROPONIN T INCREASED ( 10 FDA reports)
TUMOUR EXCISION ( 10 FDA reports)
URETERAL NEOPLASM ( 10 FDA reports)
UTERINE PROLAPSE REPAIR ( 10 FDA reports)
UTEROVAGINAL PROLAPSE ( 10 FDA reports)
VAGINAL BURNING SENSATION ( 10 FDA reports)
VAGINAL NEOPLASM ( 10 FDA reports)
VEIN PAIN ( 10 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 10 FDA reports)
WRIST SURGERY ( 10 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 10 FDA reports)
ACNE CYSTIC ( 10 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 10 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 10 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 10 FDA reports)
ADMINISTRATION SITE INFECTION ( 10 FDA reports)
AGORAPHOBIA ( 10 FDA reports)
ANOGENITAL WARTS ( 10 FDA reports)
APPLICATION SITE BURN ( 10 FDA reports)
APPLICATION SITE INFECTION ( 10 FDA reports)
APPLICATION SITE URTICARIA ( 10 FDA reports)
ARACHNOIDITIS ( 10 FDA reports)
BACTERIAL DIARRHOEA ( 10 FDA reports)
BASAL GANGLIA INFARCTION ( 10 FDA reports)
BENIGN BONE NEOPLASM ( 10 FDA reports)
BIOPSY LYMPH GLAND ( 10 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 10 FDA reports)
BLOOD LACTIC ACID INCREASED ( 10 FDA reports)
BONE DECALCIFICATION ( 10 FDA reports)
BONE SARCOMA ( 10 FDA reports)
BRAIN CANCER METASTATIC ( 10 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 10 FDA reports)
CARBON MONOXIDE POISONING ( 10 FDA reports)
CARDIAC HYPERTROPHY ( 10 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 10 FDA reports)
CEREBELLAR ISCHAEMIA ( 10 FDA reports)
COLON CANCER STAGE I ( 10 FDA reports)
COLON NEOPLASM ( 10 FDA reports)
COLONIC OBSTRUCTION ( 10 FDA reports)
COLONOSCOPY ABNORMAL ( 10 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 10 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 10 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 10 FDA reports)
CORONARY ARTERY SURGERY ( 10 FDA reports)
CULTURE POSITIVE ( 10 FDA reports)
CYST ASPIRATION ( 10 FDA reports)
DEVICE RELATED SEPSIS ( 10 FDA reports)
DIABETIC GASTROPATHY ( 10 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 10 FDA reports)
DISSOCIATIVE IDENTITY DISORDER ( 10 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 10 FDA reports)
DRUG TOLERANCE DECREASED ( 10 FDA reports)
DUODENAL POLYP ( 10 FDA reports)
DYSLEXIA ( 10 FDA reports)
DYSPLASTIC NAEVUS ( 10 FDA reports)
EAR OPERATION ( 10 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 10 FDA reports)
EPHELIDES ( 10 FDA reports)
EXPOSURE TO COMMUNICABLE DISEASE ( 10 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 10 FDA reports)
EXTRADURAL HAEMATOMA ( 10 FDA reports)
EYE INFLAMMATION ( 10 FDA reports)
FANCONI SYNDROME ( 10 FDA reports)
GASTRIC CANCER RECURRENT ( 10 FDA reports)
GASTRIC MUCOSA ERYTHEMA ( 10 FDA reports)
GASTROINTESTINAL BACTERIAL INFECTION ( 10 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 10 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 10 FDA reports)
GASTROSTOMY ( 10 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 10 FDA reports)
HEPATIC ARTERY STENOSIS ( 10 FDA reports)
HEPATOSPLENIC T-CELL LYMPHOMA ( 10 FDA reports)
HYPERPHOSPHATAEMIA ( 10 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 10 FDA reports)
HYPERTRANSAMINASAEMIA ( 10 FDA reports)
HYPOGLYCAEMIC COMA ( 10 FDA reports)
IMPATIENCE ( 10 FDA reports)
IMPULSE-CONTROL DISORDER ( 10 FDA reports)
IMPULSIVE BEHAVIOUR ( 10 FDA reports)
INJECTION SITE BURNING ( 10 FDA reports)
INJECTION SITE CELLULITIS ( 10 FDA reports)
INJECTION SITE INFECTION ( 10 FDA reports)
INJECTION SITE OEDEMA ( 10 FDA reports)
IRIDOCYCLITIS ( 10 FDA reports)
KNEE DEFORMITY ( 10 FDA reports)
LABORATORY TEST INTERFERENCE ( 10 FDA reports)
LIMB ASYMMETRY ( 10 FDA reports)
LIP INJURY ( 10 FDA reports)
MALIGNANT MELANOMA IN SITU ( 10 FDA reports)
MASKED FACIES ( 10 FDA reports)
MASTITIS ( 10 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 10 FDA reports)
MEAN CELL VOLUME INCREASED ( 10 FDA reports)
MOUTH INJURY ( 10 FDA reports)
MUSCLE ENZYME INCREASED ( 10 FDA reports)
MYOCLONIC EPILEPSY ( 10 FDA reports)
MYOMECTOMY ( 10 FDA reports)
ALLODYNIA ( 9 FDA reports)
AMINO ACID LEVEL ABNORMAL ( 9 FDA reports)
ANAL FISSURE EXCISION ( 9 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 9 FDA reports)
ANOPLASTY ( 9 FDA reports)
AUTONOMIC NEUROPATHY ( 9 FDA reports)
AXONAL NEUROPATHY ( 9 FDA reports)
BACTERIA STOOL IDENTIFIED ( 9 FDA reports)
BENCE JONES PROTEIN URINE PRESENT ( 9 FDA reports)
BIOPSY COLON ABNORMAL ( 9 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 9 FDA reports)
BLOOD GASES ABNORMAL ( 9 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 9 FDA reports)
BLOOD URINE ( 9 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 9 FDA reports)
BOVINE TUBERCULOSIS ( 9 FDA reports)
BRAIN MASS ( 9 FDA reports)
BREAST CANCER STAGE II ( 9 FDA reports)
BREAST PROSTHESIS REMOVAL ( 9 FDA reports)
BRONCHIAL INFECTION ( 9 FDA reports)
CAECITIS ( 9 FDA reports)
CARCINOMA ( 9 FDA reports)
CARDIAC ABLATION ( 9 FDA reports)
CARDIAC STRESS TEST ( 9 FDA reports)
CATARACT OPERATION COMPLICATION ( 9 FDA reports)
CATHETER SEPSIS ( 9 FDA reports)
CATHETERISATION VENOUS ( 9 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 9 FDA reports)
CEREBRAL CYST ( 9 FDA reports)
CEREBRAL HYPOPERFUSION ( 9 FDA reports)
CERVICAL POLYP ( 9 FDA reports)
CHORIORETINAL DISORDER ( 9 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 9 FDA reports)
COCCYDYNIA ( 9 FDA reports)
COLON CANCER STAGE IV ( 9 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 9 FDA reports)
CONGENITAL TRACHEOMALACIA ( 9 FDA reports)
CONJUNCTIVITIS VIRAL ( 9 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 9 FDA reports)
CREST SYNDROME ( 9 FDA reports)
CULTURE WOUND POSITIVE ( 9 FDA reports)
CUTANEOUS VASCULITIS ( 9 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 9 FDA reports)
DELUSIONAL PERCEPTION ( 9 FDA reports)
DERMATOMYOSITIS ( 9 FDA reports)
DEVELOPMENTAL DELAY ( 9 FDA reports)
DEXTROCARDIA ( 9 FDA reports)
DISTRACTIBILITY ( 9 FDA reports)
DRUG CLEARANCE DECREASED ( 9 FDA reports)
DRUG SCREEN NEGATIVE ( 9 FDA reports)
ENDOCARDIAL FIBROSIS ( 9 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 9 FDA reports)
ESCHERICHIA TEST POSITIVE ( 9 FDA reports)
ETHMOID SINUS SURGERY ( 9 FDA reports)
EYELASH DISCOLOURATION ( 9 FDA reports)
GALLBLADDER CANCER ( 9 FDA reports)
GALLBLADDER PERFORATION ( 9 FDA reports)
GASTRIC ULCER HELICOBACTER ( 9 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 9 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 9 FDA reports)
GASTROINTESTINAL NEOPLASM ( 9 FDA reports)
GASTROINTESTINAL SURGERY ( 9 FDA reports)
GASTROINTESTINAL TOXICITY ( 9 FDA reports)
GASTROOESOPHAGITIS ( 9 FDA reports)
GINGIVAL OPERATION ( 9 FDA reports)
GRAFT COMPLICATION ( 9 FDA reports)
GRAFT THROMBOSIS ( 9 FDA reports)
HAEMORRHAGIC DISORDER ( 9 FDA reports)
HEAD TITUBATION ( 9 FDA reports)
HEPATIC SIDEROSIS ( 9 FDA reports)
HOMOCYSTINAEMIA ( 9 FDA reports)
HYPERPATHIA ( 9 FDA reports)
HYPERPYREXIA ( 9 FDA reports)
HYPERSPLENISM ( 9 FDA reports)
HYPERTROPHY BREAST ( 9 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 9 FDA reports)
HYPOPNOEA ( 9 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 9 FDA reports)
INFUSION SITE RASH ( 9 FDA reports)
INJECTION SITE ABSCESS ( 9 FDA reports)
INJECTION SITE DISCOMFORT ( 9 FDA reports)
INJURY ASPHYXIATION ( 9 FDA reports)
INTUSSUSCEPTION ( 9 FDA reports)
IRON METABOLISM DISORDER ( 9 FDA reports)
IRON OVERLOAD ( 9 FDA reports)
JOINT ADHESION ( 9 FDA reports)
KLEBSIELLA SEPSIS ( 9 FDA reports)
LIBIDO INCREASED ( 9 FDA reports)
LIP EROSION ( 9 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 9 FDA reports)
LUNG ADENOCARCINOMA STAGE III ( 9 FDA reports)
LUNG OPERATION ( 9 FDA reports)
MASTOID DISORDER ( 9 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 9 FDA reports)
MENISCAL DEGENERATION ( 9 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 9 FDA reports)
METASTASES TO THYROID ( 9 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 9 FDA reports)
MYELOID MATURATION ARREST ( 9 FDA reports)
NAIL OPERATION ( 9 FDA reports)
NEONATAL TACHYPNOEA ( 9 FDA reports)
NEPHRITIC SYNDROME ( 9 FDA reports)
NEPHRITIS ALLERGIC ( 9 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 9 FDA reports)
NOSE DEFORMITY ( 9 FDA reports)
OCULAR HYPERTENSION ( 9 FDA reports)
OEDEMA GENITAL ( 9 FDA reports)
OESOPHAGEAL IRRITATION ( 9 FDA reports)
OPHTHALMOPLEGIA ( 9 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 9 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 9 FDA reports)
OSTECTOMY ( 9 FDA reports)
OVARIAN ATROPHY ( 9 FDA reports)
PARANASAL SINUS DISCOMFORT ( 9 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 9 FDA reports)
PENILE INFECTION ( 9 FDA reports)
PERIANAL ABSCESS ( 9 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED ( 9 FDA reports)
PERITONEAL DIALYSIS ( 9 FDA reports)
PERITONEAL HAEMORRHAGE ( 9 FDA reports)
PEYRONIE'S DISEASE ( 9 FDA reports)
PILOERECTION ( 9 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 9 FDA reports)
PNEUMOCOCCAL SEPSIS ( 9 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 9 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 9 FDA reports)
POST-TRAUMATIC NECK SYNDROME ( 9 FDA reports)
PRESBYACUSIS ( 9 FDA reports)
PROTEIN URINE ( 9 FDA reports)
PSYCHOTIC BEHAVIOUR ( 9 FDA reports)
PULMONARY HILUM MASS ( 9 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 9 FDA reports)
PYLORIC STENOSIS ( 9 FDA reports)
RECALL PHENOMENON ( 9 FDA reports)
RENAL HAEMORRHAGE ( 9 FDA reports)
REPETITIVE STRAIN INJURY ( 9 FDA reports)
RESPIRATORY ALKALOSIS ( 9 FDA reports)
ROULEAUX FORMATION ( 9 FDA reports)
SALIVARY GLAND CANCER ( 9 FDA reports)
SALIVARY GLAND PAIN ( 9 FDA reports)
SCROTAL CYST ( 9 FDA reports)
SENSATION OF BLOOD FLOW ( 9 FDA reports)
SMALL INTESTINAL ULCER HAEMORRHAGE ( 9 FDA reports)
SPLENIC RUPTURE ( 9 FDA reports)
SPONDYLOPATHY TRAUMATIC ( 9 FDA reports)
SPUTUM INCREASED ( 9 FDA reports)
STRESS CARDIOMYOPATHY ( 9 FDA reports)
SUDDEN HEARING LOSS ( 9 FDA reports)
TACHYCARDIA PAROXYSMAL ( 9 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 9 FDA reports)
THORACIC CAVITY DRAINAGE ( 9 FDA reports)
THROMBOTIC STROKE ( 9 FDA reports)
THYROID MASS ( 9 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 9 FDA reports)
URINARY BLADDER POLYP ( 9 FDA reports)
VASCULAR STENT INSERTION ( 9 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 9 FDA reports)
VICTIM OF CRIME ( 9 FDA reports)
VULVAL CANCER ( 9 FDA reports)
WITHDRAWAL OF LIFE SUPPORT ( 9 FDA reports)
WOUND DECOMPOSITION ( 9 FDA reports)
NERVE ROOT LESION ( 8 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 8 FDA reports)
NITRITE URINE PRESENT ( 8 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 8 FDA reports)
OCCIPITAL NEURALGIA ( 8 FDA reports)
OESOPHAGEAL POLYP ( 8 FDA reports)
OROPHARYNGEAL SPASM ( 8 FDA reports)
PANCREATIC CALCIFICATION ( 8 FDA reports)
PARATHYROID DISORDER ( 8 FDA reports)
PERICARDIAL HAEMORRHAGE ( 8 FDA reports)
PERTUSSIS ( 8 FDA reports)
PHARYNGEAL OPERATION ( 8 FDA reports)
PHOTOPHERESIS ( 8 FDA reports)
PNEUMONIA HAEMOPHILUS ( 8 FDA reports)
POST PROCEDURAL BILE LEAK ( 8 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 8 FDA reports)
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME ( 8 FDA reports)
POUCHITIS ( 8 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 8 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 8 FDA reports)
PSYCHOTIC DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 8 FDA reports)
PULSE ABNORMAL ( 8 FDA reports)
PUPIL FIXED ( 8 FDA reports)
RADICULITIS BRACHIAL ( 8 FDA reports)
RECTAL FISTULA REPAIR ( 8 FDA reports)
RECTAL TENESMUS ( 8 FDA reports)
RESIDUAL URINE ( 8 FDA reports)
RESPIRATORY TRACT MALFORMATION ( 8 FDA reports)
RETICULOCYTE COUNT DECREASED ( 8 FDA reports)
RETINAL SCAR ( 8 FDA reports)
SARCOMA ( 8 FDA reports)
SEGMENTED HYALINISING VASCULITIS ( 8 FDA reports)
SINOBRONCHITIS ( 8 FDA reports)
SINUS ANTROSTOMY ( 8 FDA reports)
SKIN FRAGILITY ( 8 FDA reports)
SKIN MASS ( 8 FDA reports)
SPINAL PAIN ( 8 FDA reports)
SPONDYLITIC MYELOPATHY ( 8 FDA reports)
SUBDIAPHRAGMATIC ABSCESS ( 8 FDA reports)
SUDDEN ONSET OF SLEEP ( 8 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 8 FDA reports)
TERMINAL INSOMNIA ( 8 FDA reports)
TOE OPERATION ( 8 FDA reports)
TOOTH DECALCIFICATION ( 8 FDA reports)
TOXIC OPTIC NEUROPATHY ( 8 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 8 FDA reports)
TRACHEAL DEVIATION ( 8 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 8 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 8 FDA reports)
TUMOUR FLARE ( 8 FDA reports)
TUMOUR INVASION ( 8 FDA reports)
URETERAL STENT INSERTION ( 8 FDA reports)
URETHRAL HAEMORRHAGE ( 8 FDA reports)
URETHRAL STENOSIS ( 8 FDA reports)
VAGINAL FISTULA ( 8 FDA reports)
VAGINAL MYCOSIS ( 8 FDA reports)
VASCULAR OPERATION ( 8 FDA reports)
VENA CAVA INJURY ( 8 FDA reports)
VENOOCCLUSIVE DISEASE ( 8 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 8 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 8 FDA reports)
VENOUS STASIS ( 8 FDA reports)
VIRAL LOAD INCREASED ( 8 FDA reports)
VIRAL PHARYNGITIS ( 8 FDA reports)
VITAL CAPACITY DECREASED ( 8 FDA reports)
VITAMIN B12 INCREASED ( 8 FDA reports)
VITILIGO ( 8 FDA reports)
VOCAL CORD CYST ( 8 FDA reports)
VOCAL CORD PARESIS ( 8 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 8 FDA reports)
WEST NILE VIRAL INFECTION ( 8 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 8 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 8 FDA reports)
AKINESIA ( 8 FDA reports)
ALLERGIC SINUSITIS ( 8 FDA reports)
AMPUTATION ( 8 FDA reports)
ANASTOMOTIC COMPLICATION ( 8 FDA reports)
ANGIODYSPLASIA ( 8 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 8 FDA reports)
AORTIC ANEURYSM RUPTURE ( 8 FDA reports)
ARTHROPOD STING ( 8 FDA reports)
AUTISM ( 8 FDA reports)
BED REST ( 8 FDA reports)
BEZOAR ( 8 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 8 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 8 FDA reports)
BIOPSY BREAST ( 8 FDA reports)
BIOPSY LYMPH GLAND ABNORMAL ( 8 FDA reports)
BLADDER PERFORATION ( 8 FDA reports)
BLINDNESS CORTICAL ( 8 FDA reports)
BLOOD BICARBONATE INCREASED ( 8 FDA reports)
BLOOD GLUCOSE ( 8 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 8 FDA reports)
BONE MARROW TOXICITY ( 8 FDA reports)
BONE RESORPTION TEST ABNORMAL ( 8 FDA reports)
BOWEL SOUNDS ABNORMAL ( 8 FDA reports)
BRAIN STEM HAEMORRHAGE ( 8 FDA reports)
BREAST ABSCESS ( 8 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 8 FDA reports)
CALCIUM METABOLISM DISORDER ( 8 FDA reports)
CALCULUS URETHRAL ( 8 FDA reports)
CATARACT CORTICAL ( 8 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 8 FDA reports)
CELLULITIS ORBITAL ( 8 FDA reports)
CELLULITIS STREPTOCOCCAL ( 8 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 8 FDA reports)
COARCTATION OF THE AORTA ( 8 FDA reports)
COGWHEEL RIGIDITY ( 8 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 8 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 8 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 8 FDA reports)
CRANIOSYNOSTOSIS ( 8 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 8 FDA reports)
DERMATITIS PSORIASIFORM ( 8 FDA reports)
DIPLEGIA ( 8 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 8 FDA reports)
DRESSLER'S SYNDROME ( 8 FDA reports)
DRY GANGRENE ( 8 FDA reports)
DUODENAL OBSTRUCTION ( 8 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 8 FDA reports)
EAR DEFORMITY ACQUIRED ( 8 FDA reports)
ECZEMA INFECTED ( 8 FDA reports)
EJACULATION DISORDER ( 8 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 8 FDA reports)
EMBOLISM ARTERIAL ( 8 FDA reports)
ENANTHEMA ( 8 FDA reports)
ENCEPHALITIS VIRAL ( 8 FDA reports)
ENDOCARDITIS BACTERIAL ( 8 FDA reports)
ENTEROCOCCAL SEPSIS ( 8 FDA reports)
EOSINOPHILIC FASCIITIS ( 8 FDA reports)
EPIDERMAL NAEVUS ( 8 FDA reports)
EXANTHEM ( 8 FDA reports)
EYE ALLERGY ( 8 FDA reports)
EYELID PAIN ( 8 FDA reports)
EYELIDS PRURITUS ( 8 FDA reports)
FLASHBACK ( 8 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 8 FDA reports)
FUNGAL SEPSIS ( 8 FDA reports)
GASTROENTERITIS SALMONELLA ( 8 FDA reports)
GESTATIONAL DIABETES ( 8 FDA reports)
GINGIVAL DISCOLOURATION ( 8 FDA reports)
GLIOBLASTOMA MULTIFORME ( 8 FDA reports)
GRANULOMA ANNULARE ( 8 FDA reports)
H1N1 INFLUENZA ( 8 FDA reports)
HAEMATOMA INFECTION ( 8 FDA reports)
HEART SOUNDS ABNORMAL ( 8 FDA reports)
HEART TRANSPLANT ( 8 FDA reports)
HEPATIC INFARCTION ( 8 FDA reports)
HEPATIC NEOPLASM MALIGNANT RECURRENT ( 8 FDA reports)
HEPATOJUGULAR REFLUX ( 8 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 8 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 8 FDA reports)
ILEECTOMY ( 8 FDA reports)
IMPETIGO ( 8 FDA reports)
INFERTILITY MALE ( 8 FDA reports)
INFUSION SITE SWELLING ( 8 FDA reports)
INHIBITORY DRUG INTERACTION ( 8 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 8 FDA reports)
ITCHING SCAR ( 8 FDA reports)
JAW CYST ( 8 FDA reports)
KELOID SCAR ( 8 FDA reports)
KLEBSIELLA TEST POSITIVE ( 8 FDA reports)
LARYNGEAL NEOPLASM ( 8 FDA reports)
LARYNGECTOMY ( 8 FDA reports)
LIMB PROSTHESIS USER ( 8 FDA reports)
LUNG LOBECTOMY ( 8 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 8 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 8 FDA reports)
MENINGITIS CHEMICAL ( 8 FDA reports)
MENTAL DISABILITY ( 8 FDA reports)
METAL POISONING ( 8 FDA reports)
METASTASES TO EYE ( 8 FDA reports)
METASTASES TO MOUTH ( 8 FDA reports)
MONOCLONAL GAMMOPATHY ( 8 FDA reports)
MONONEURITIS ( 8 FDA reports)
MOTION SICKNESS ( 8 FDA reports)
MUCOSAL DRYNESS ( 8 FDA reports)
MUSCLE ABSCESS ( 8 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 7 FDA reports)
ABSCESS INTESTINAL ( 7 FDA reports)
ACCIDENT AT HOME ( 7 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 7 FDA reports)
ACUTE PHASE REACTION ( 7 FDA reports)
ADENOCARCINOMA PANCREAS ( 7 FDA reports)
ADENOIDAL DISORDER ( 7 FDA reports)
ADENOVIRUS INFECTION ( 7 FDA reports)
ADRENAL ADENOMA ( 7 FDA reports)
ALOPECIA AREATA ( 7 FDA reports)
ANAL SKIN TAGS ( 7 FDA reports)
ANAL ULCER ( 7 FDA reports)
ANASTOMOTIC LEAK ( 7 FDA reports)
ANOSOGNOSIA ( 7 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 7 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 7 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 7 FDA reports)
AORTIC DISSECTION ( 7 FDA reports)
APPLICATION SITE DERMATITIS ( 7 FDA reports)
APPLICATION SITE DISCOLOURATION ( 7 FDA reports)
APPLICATION SITE EXFOLIATION ( 7 FDA reports)
ARACHNOID CYST ( 7 FDA reports)
ARTERIOVENOUS FISTULA OCCLUSION ( 7 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 7 FDA reports)
ASPIRATION JOINT ( 7 FDA reports)
ATRIAL THROMBOSIS ( 7 FDA reports)
AUTOIMMUNE PANCREATITIS ( 7 FDA reports)
BEHCET'S SYNDROME ( 7 FDA reports)
BELLIGERENCE ( 7 FDA reports)
BENIGN CARDIAC NEOPLASM ( 7 FDA reports)
BENIGN NEOPLASM OF SKIN ( 7 FDA reports)
BICUSPID AORTIC VALVE ( 7 FDA reports)
BIOPSY LIVER ABNORMAL ( 7 FDA reports)
BLADDER DISTENSION ( 7 FDA reports)
BLADDER INJURY ( 7 FDA reports)
BLADDER NEOPLASM SURGERY ( 7 FDA reports)
BLOOD ALBUMIN INCREASED ( 7 FDA reports)
BLOOD ALCOHOL INCREASED ( 7 FDA reports)
BLOOD CREATININE ABNORMAL ( 7 FDA reports)
BLOOD SODIUM ABNORMAL ( 7 FDA reports)
BLOOD THYROID STIMULATING HORMONE ( 7 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 7 FDA reports)
BONE METABOLISM DISORDER ( 7 FDA reports)
BRAIN CONTUSION ( 7 FDA reports)
BRAIN MIDLINE SHIFT ( 7 FDA reports)
BRONCHITIS BACTERIAL ( 7 FDA reports)
BRONCHOPNEUMOPATHY ( 7 FDA reports)
CALCULUS BLADDER ( 7 FDA reports)
CANDIDURIA ( 7 FDA reports)
CARCINOID SYNDROME ( 7 FDA reports)
CARDIAC VALVE VEGETATION ( 7 FDA reports)
CAROTID ARTERY ANEURYSM ( 7 FDA reports)
CATARACT CONGENITAL ( 7 FDA reports)
CEREBRAL ARTERY STENOSIS ( 7 FDA reports)
CERVICAL CYST ( 7 FDA reports)
CHLOASMA ( 7 FDA reports)
COLORECTAL CANCER ( 7 FDA reports)
COLOUR BLINDNESS ( 7 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 7 FDA reports)
CONGENITAL AORTIC STENOSIS ( 7 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 7 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 7 FDA reports)
CYSTITIS NONINFECTIVE ( 7 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 7 FDA reports)
DEATH OF RELATIVE ( 7 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 7 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 7 FDA reports)
DEVICE MISUSE ( 7 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 7 FDA reports)
DRUG DIVERSION ( 7 FDA reports)
DRUG-INDUCED LIVER INJURY ( 7 FDA reports)
EAR NEOPLASM ( 7 FDA reports)
ENTEROBACTER BACTERAEMIA ( 7 FDA reports)
ENTEROVESICAL FISTULA ( 7 FDA reports)
EPIDERMAL NECROSIS ( 7 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 7 FDA reports)
EXTRADURAL ABSCESS ( 7 FDA reports)
FASCIITIS ( 7 FDA reports)
FATTY LIVER ALCOHOLIC ( 7 FDA reports)
GAMBLING ( 7 FDA reports)
GASTRIC POLYPECTOMY ( 7 FDA reports)
GASTRIC VARICES ( 7 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 7 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 7 FDA reports)
GRAFT LOSS ( 7 FDA reports)
GUTTATE PSORIASIS ( 7 FDA reports)
HEPATIC ADENOMA ( 7 FDA reports)
HEPATIC CANCER METASTATIC ( 7 FDA reports)
HEPATIC CANCER STAGE IV ( 7 FDA reports)
HEPATIC INFECTION BACTERIAL ( 7 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 7 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 7 FDA reports)
HIV INFECTION ( 7 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 7 FDA reports)
HYPOCALCIURIA ( 7 FDA reports)
HYPOPARATHYROIDISM ( 7 FDA reports)
HYPOSPADIAS ( 7 FDA reports)
ILLUSION ( 7 FDA reports)
INCORRECT PRODUCT STORAGE ( 7 FDA reports)
INFLAMMATORY MARKER INCREASED ( 7 FDA reports)
INFUSION SITE HAEMORRHAGE ( 7 FDA reports)
INFUSION SITE PRURITUS ( 7 FDA reports)
INJECTION SITE ANAESTHESIA ( 7 FDA reports)
INJECTION SITE VESICLES ( 7 FDA reports)
INSULIN RESISTANCE ( 7 FDA reports)
INTERCEPTED MEDICATION ERROR ( 7 FDA reports)
INTESTINAL FISTULA ( 7 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 7 FDA reports)
JOB DISSATISFACTION ( 7 FDA reports)
JOINT DISLOCATION POSTOPERATIVE ( 7 FDA reports)
LEUKAEMIA RECURRENT ( 7 FDA reports)
LIFE SUPPORT ( 7 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 7 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 7 FDA reports)
LUNG INJURY ( 7 FDA reports)
MALIGNANT NEOPLASM OF SPINAL CORD ( 7 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 7 FDA reports)
MEGACOLON ( 7 FDA reports)
MENINGORRHAGIA ( 7 FDA reports)
MESENTERIC ARTERY STENOSIS ( 7 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 7 FDA reports)
METASTASES TO BONE MARROW ( 7 FDA reports)
METASTASES TO PELVIS ( 7 FDA reports)
METASTATIC CARCINOID TUMOUR ( 7 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 7 FDA reports)
MITRAL VALVE REPLACEMENT ( 7 FDA reports)
MOANING ( 7 FDA reports)
MONARTHRITIS ( 7 FDA reports)
MUSCLE SWELLING ( 7 FDA reports)
MYELOFIBROSIS ( 7 FDA reports)
MYOCARDIAL FIBROSIS ( 7 FDA reports)
NASAL OEDEMA ( 7 FDA reports)
NASOPHARYNGEAL DISORDER ( 7 FDA reports)
NEOPLASM RECURRENCE ( 7 FDA reports)
NEUTROPHILIA ( 7 FDA reports)
NOCARDIOSIS ( 7 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 7 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 7 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 7 FDA reports)
OESTRADIOL DECREASED ( 7 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 7 FDA reports)
OS TRIGONUM SYNDROME ( 7 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 7 FDA reports)
OTITIS MEDIA CHRONIC ( 7 FDA reports)
OVARIAN DISORDER ( 7 FDA reports)
PAIN MANAGEMENT ( 7 FDA reports)
PALATAL OEDEMA ( 7 FDA reports)
PALMAR ERYTHEMA ( 7 FDA reports)
PANCREATIC MASS ( 7 FDA reports)
PARADOXICAL DRUG REACTION ( 7 FDA reports)
PARANEOPLASTIC SYNDROME ( 7 FDA reports)
PENILE SIZE REDUCED ( 7 FDA reports)
PERIARTICULAR DISORDER ( 7 FDA reports)
PERIORBITAL CELLULITIS ( 7 FDA reports)
PERITONEAL DISORDER ( 7 FDA reports)
PERITONEAL HAEMATOMA ( 7 FDA reports)
PLASMAPHERESIS ( 7 FDA reports)
PLATELET DISORDER ( 7 FDA reports)
PLEUROTHOTONUS ( 7 FDA reports)
PNEUMONECTOMY ( 7 FDA reports)
PNEUMONIA VIRAL ( 7 FDA reports)
POLYSUBSTANCE ABUSE ( 7 FDA reports)
PORPHYRIA NON-ACUTE ( 7 FDA reports)
POST CONCUSSION SYNDROME ( 7 FDA reports)
POST PROCEDURAL DIARRHOEA ( 7 FDA reports)
POST PROCEDURAL DISCOMFORT ( 7 FDA reports)
POST PROCEDURAL NAUSEA ( 7 FDA reports)
POSTOPERATIVE ILEUS ( 7 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 7 FDA reports)
PRECEREBRAL ARTERY OCCLUSION ( 7 FDA reports)
PRINZMETAL ANGINA ( 7 FDA reports)
PROCEDURAL SITE REACTION ( 7 FDA reports)
PROSTATIC OPERATION ( 7 FDA reports)
PROSTATISM ( 7 FDA reports)
PTERYGIUM ( 7 FDA reports)
PUPILLARY DISORDER ( 7 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 7 FDA reports)
RECTAL DISCHARGE ( 7 FDA reports)
REGURGITATION OF FOOD ( 7 FDA reports)
REHABILITATION THERAPY ( 7 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 7 FDA reports)
RETINAL INJURY ( 7 FDA reports)
SALIVARY DUCT OBSTRUCTION ( 7 FDA reports)
SCAPULA FRACTURE ( 7 FDA reports)
SCROTAL SWELLING ( 7 FDA reports)
SEROSITIS ( 7 FDA reports)
SIGMOIDITIS ( 7 FDA reports)
SKIN CYST EXCISION ( 7 FDA reports)
SKIN OEDEMA ( 7 FDA reports)
SKIN TEST NEGATIVE ( 7 FDA reports)
SMALL INTESTINAL RESECTION ( 7 FDA reports)
SOMATOFORM DISORDER ( 7 FDA reports)
SPLENIC INJURY ( 7 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 7 FDA reports)
SUPERINFECTION LUNG ( 7 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 7 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 7 FDA reports)
TINEA INFECTION ( 7 FDA reports)
TONGUE BLACK HAIRY ( 7 FDA reports)
TONIC CONVULSION ( 7 FDA reports)
TONSILLECTOMY ( 7 FDA reports)
TRANSPLANT ( 7 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 7 FDA reports)
TUMOUR PAIN ( 7 FDA reports)
UNINTENDED PREGNANCY ( 7 FDA reports)
URINE OUTPUT ( 7 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 7 FDA reports)
VARICOSE ULCERATION ( 7 FDA reports)
VARICOSE VEIN RUPTURED ( 7 FDA reports)
VASOPLEGIA SYNDROME ( 7 FDA reports)
VENOUS INJURY ( 7 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 7 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 7 FDA reports)
VITAMIN D ABNORMAL ( 7 FDA reports)
VOLVULUS OF BOWEL ( 7 FDA reports)
VULVAL ABSCESS ( 7 FDA reports)
VULVAL ULCERATION ( 7 FDA reports)
VULVOVAGINAL PAIN ( 7 FDA reports)
NECK EXPLORATION ( 6 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 6 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 6 FDA reports)
NEUROPATHIC PAIN ( 6 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 6 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 6 FDA reports)
OBSESSIVE THOUGHTS ( 6 FDA reports)
OESOPHAGEAL ATRESIA ( 6 FDA reports)
ORAL SUBMUCOSAL FIBROSIS ( 6 FDA reports)
OROPHARYNGEAL CANCER STAGE UNSPECIFIED ( 6 FDA reports)
ORTHOSTATIC HYPERTENSION ( 6 FDA reports)
OVARIAN NEOPLASM ( 6 FDA reports)
PAIN EXACERBATED ( 6 FDA reports)
PANCREATOBILIARY SPHINCTEROTOMY ( 6 FDA reports)
PAPULE ( 6 FDA reports)
PARALYSIS FLACCID ( 6 FDA reports)
PARANOID PERSONALITY DISORDER ( 6 FDA reports)
PARAPROTEINAEMIA ( 6 FDA reports)
PARATHYROID TUMOUR ( 6 FDA reports)
PEDAL PULSE DECREASED ( 6 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 6 FDA reports)
PERIHEPATIC ABSCESS ( 6 FDA reports)
PERIPHERAL NERVE LESION ( 6 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 6 FDA reports)
PHARYNGEAL POLYP ( 6 FDA reports)
PHIMOSIS ( 6 FDA reports)
PHOBIA ( 6 FDA reports)
PHYSIOTHERAPY ( 6 FDA reports)
PLACENTAL DISORDER ( 6 FDA reports)
PNEUMOCEPHALUS ( 6 FDA reports)
PNEUMONIA LEGIONELLA ( 6 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 6 FDA reports)
PO2 INCREASED ( 6 FDA reports)
POSITIVE ROMBERGISM ( 6 FDA reports)
POST PROCEDURAL CONSTIPATION ( 6 FDA reports)
POSTMENOPAUSE ( 6 FDA reports)
PRE-ECLAMPSIA ( 6 FDA reports)
PREAURICULAR CYST ( 6 FDA reports)
PRESSURE OF SPEECH ( 6 FDA reports)
PRIAPISM ( 6 FDA reports)
PROCTOCOLITIS ( 6 FDA reports)
PROGRESSIVE MASSIVE FIBROSIS ( 6 FDA reports)
PROSTATE INFECTION ( 6 FDA reports)
PROTEUS INFECTION ( 6 FDA reports)
PSEUDOCYST ( 6 FDA reports)
PSYCHOSOMATIC DISEASE ( 6 FDA reports)
PULMONARY AIR LEAKAGE ( 6 FDA reports)
PYOGENIC GRANULOMA ( 6 FDA reports)
PYURIA ( 6 FDA reports)
RADIATION PNEUMONITIS ( 6 FDA reports)
RECTAL PERFORATION ( 6 FDA reports)
RENAL ARTERIOSCLEROSIS ( 6 FDA reports)
RENAL ARTERY THROMBOSIS ( 6 FDA reports)
RENAL CANCER STAGE IV ( 6 FDA reports)
RENAL EMBOLISM ( 6 FDA reports)
RENAL VESSEL DISORDER ( 6 FDA reports)
RESPIRATORY TRACT IRRITATION ( 6 FDA reports)
RETICULOCYTE COUNT INCREASED ( 6 FDA reports)
RETINAL EXUDATES ( 6 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 6 FDA reports)
RETROGRADE EJACULATION ( 6 FDA reports)
RETROPERITONEAL ABSCESS ( 6 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 6 FDA reports)
RHINOVIRUS INFECTION ( 6 FDA reports)
SALIVARY GLAND NEOPLASM ( 6 FDA reports)
SCAN ABDOMEN ABNORMAL ( 6 FDA reports)
SCARLET FEVER ( 6 FDA reports)
SCLERITIS ( 6 FDA reports)
SCROTAL INFECTION ( 6 FDA reports)
SEPTIC EMBOLUS ( 6 FDA reports)
SHOCK HYPOGLYCAEMIC ( 6 FDA reports)
SPINAL CORPECTOMY ( 6 FDA reports)
SPLENIC VEIN THROMBOSIS ( 6 FDA reports)
SPONDYLOSIS ( 6 FDA reports)
STEROID THERAPY ( 6 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 6 FDA reports)
SUBMANDIBULAR MASS ( 6 FDA reports)
SUPERFICIAL INJURY OF EYE ( 6 FDA reports)
SUTURE INSERTION ( 6 FDA reports)
SWEAT GLAND DISORDER ( 6 FDA reports)
SYSTEMIC SCLEROSIS ( 6 FDA reports)
SYSTOLIC DYSFUNCTION ( 6 FDA reports)
TETANY ( 6 FDA reports)
THYROID CYST ( 6 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 6 FDA reports)
TONGUE HAEMORRHAGE ( 6 FDA reports)
TRANSFERRIN INCREASED ( 6 FDA reports)
TRAUMATIC RENAL INJURY ( 6 FDA reports)
TRICHORRHEXIS ( 6 FDA reports)
TRIGEMINAL NERVE DISORDER ( 6 FDA reports)
ULTRASOUND BREAST ABNORMAL ( 6 FDA reports)
UNDERWEIGHT ( 6 FDA reports)
UNEMPLOYMENT ( 6 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 6 FDA reports)
URETHRITIS ( 6 FDA reports)
URINE BILIRUBIN INCREASED ( 6 FDA reports)
UTERINE MALPOSITION ( 6 FDA reports)
UTERINE RUPTURE ( 6 FDA reports)
VAGOTOMY ( 6 FDA reports)
VASCULITIS NECROTISING ( 6 FDA reports)
VASOSPASM ( 6 FDA reports)
VERTEBRAL INJURY ( 6 FDA reports)
VESTIBULAR NEURONITIS ( 6 FDA reports)
VIRAL LABYRINTHITIS ( 6 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 6 FDA reports)
WOUND TREATMENT ( 6 FDA reports)
XEROSIS ( 6 FDA reports)
ABDOMINAL BRUIT ( 6 FDA reports)
ABDOMINAL HERNIA REPAIR ( 6 FDA reports)
ABNORMAL WEIGHT GAIN ( 6 FDA reports)
ADRENAL HAEMORRHAGE ( 6 FDA reports)
ALDOLASE INCREASED ( 6 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 6 FDA reports)
ALLERGY TO CHEMICALS ( 6 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 6 FDA reports)
AMINO ACID LEVEL INCREASED ( 6 FDA reports)
ANAL ATRESIA ( 6 FDA reports)
ANGIOGRAM ( 6 FDA reports)
APPLICATION SITE DISCHARGE ( 6 FDA reports)
ARTERIAL HAEMORRHAGE ( 6 FDA reports)
ARTERIAL INSUFFICIENCY ( 6 FDA reports)
ASCITES INFECTION ( 6 FDA reports)
ASPIRATION BREAST ( 6 FDA reports)
ASPLENIA ( 6 FDA reports)
ASTERIXIS ( 6 FDA reports)
AVERSION ( 6 FDA reports)
BABESIOSIS ( 6 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 6 FDA reports)
BACTERIURIA ( 6 FDA reports)
BACTEROIDES INFECTION ( 6 FDA reports)
BENIGN NEOPLASM ( 6 FDA reports)
BENIGN PANCREATIC NEOPLASM ( 6 FDA reports)
BILE DUCT STENT INSERTION ( 6 FDA reports)
BILIARY CIRRHOSIS ( 6 FDA reports)
BINGE EATING ( 6 FDA reports)
BIOPSY ENDOMETRIUM ( 6 FDA reports)
BK VIRUS INFECTION ( 6 FDA reports)
BLASTOMYCOSIS ( 6 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 6 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 6 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 6 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 6 FDA reports)
BRADYCARDIA NEONATAL ( 6 FDA reports)
BREAST DISORDER FEMALE ( 6 FDA reports)
BREAST INJURY ( 6 FDA reports)
BREAST OEDEMA ( 6 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 6 FDA reports)
CARDIAC PERFORATION ( 6 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 6 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 6 FDA reports)
CAROTID ARTERY ATHEROMA ( 6 FDA reports)
CAROTID ENDARTERECTOMY ( 6 FDA reports)
CATHETER SITE PAIN ( 6 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 6 FDA reports)
CENTRAL NERVOUS SYSTEM INFLAMMATION ( 6 FDA reports)
CEREBELLAR HAEMATOMA ( 6 FDA reports)
CEREBRAL MICROANGIOPATHY ( 6 FDA reports)
CEREBRAL PERFUSION PRESSURE DECREASED ( 6 FDA reports)
CERVICAL NEURITIS ( 6 FDA reports)
CERVICAL SPINE FLATTENING ( 6 FDA reports)
CERVIX DISORDER ( 6 FDA reports)
CHALAZION ( 6 FDA reports)
CHEST CRUSHING ( 6 FDA reports)
CHONDROSARCOMA ( 6 FDA reports)
CHROMATOPSIA ( 6 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 6 FDA reports)
COAGULATION TEST ABNORMAL ( 6 FDA reports)
COLON CANCER STAGE II ( 6 FDA reports)
COMPULSIONS ( 6 FDA reports)
COMPULSIVE SHOPPING ( 6 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 6 FDA reports)
CONTRAST MEDIA REACTION ( 6 FDA reports)
CORNEAL DEPOSITS ( 6 FDA reports)
CORNEAL DISORDER ( 6 FDA reports)
COW'S MILK INTOLERANCE ( 6 FDA reports)
CYTOKINE RELEASE SYNDROME ( 6 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 6 FDA reports)
DERMO-HYPODERMITIS ( 6 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 6 FDA reports)
DREAMY STATE ( 6 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 6 FDA reports)
DRUG LEVEL FLUCTUATING ( 6 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 6 FDA reports)
ELECTRIC SHOCK ( 6 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 6 FDA reports)
ENAMEL ANOMALY ( 6 FDA reports)
ENDOMETRIAL ATROPHY ( 6 FDA reports)
ENTEROCUTANEOUS FISTULA ( 6 FDA reports)
ENTEROVIRUS INFECTION ( 6 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 6 FDA reports)
EPISCLERITIS ( 6 FDA reports)
ERYTHROPENIA ( 6 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 6 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 6 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 6 FDA reports)
FEMORAL HERNIA ( 6 FDA reports)
FEMORAL NERVE INJURY ( 6 FDA reports)
FIBRINOLYSIS ( 6 FDA reports)
FOOD INTERACTION ( 6 FDA reports)
FULL BLOOD COUNT INCREASED ( 6 FDA reports)
GASTRIC BANDING ( 6 FDA reports)
GASTRIC CYST ( 6 FDA reports)
GASTRIC PH INCREASED ( 6 FDA reports)
GASTROENTERITIS SHIGELLA ( 6 FDA reports)
GASTROINTESTINAL TRACT MUCOSAL DISCOLOURATION ( 6 FDA reports)
GINGIVAL EROSION ( 6 FDA reports)
GINGIVAL HYPERPLASIA ( 6 FDA reports)
GRAVITATIONAL OEDEMA ( 6 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 6 FDA reports)
HAEMOPHILUS BACTERAEMIA ( 6 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 6 FDA reports)
HEART VALVE CALCIFICATION ( 6 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 6 FDA reports)
HEPATIC HAEMORRHAGE ( 6 FDA reports)
HEPATITIS E ( 6 FDA reports)
HIV TEST POSITIVE ( 6 FDA reports)
HOUSE DUST ALLERGY ( 6 FDA reports)
HYDROCHOLECYSTIS ( 6 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 6 FDA reports)
HYPERPROLACTINAEMIA ( 6 FDA reports)
HYPERTENSIVE EMERGENCY ( 6 FDA reports)
HYPERTHERMIA MALIGNANT ( 6 FDA reports)
HYPOGONADISM MALE ( 6 FDA reports)
IIIRD NERVE PARALYSIS ( 6 FDA reports)
ILIOTIBIAL BAND SYNDROME ( 6 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 6 FDA reports)
INFECTED SEBACEOUS CYST ( 6 FDA reports)
INFERTILITY ( 6 FDA reports)
INJECTION SITE STINGING ( 6 FDA reports)
INJECTION SITE THROMBOSIS ( 6 FDA reports)
INSULIN-LIKE GROWTH FACTOR INCREASED ( 6 FDA reports)
INTERNAL HERNIA ( 6 FDA reports)
INTERNAL INJURY ( 6 FDA reports)
INTERVERTEBRAL DISCITIS ( 6 FDA reports)
IRIS DISORDER ( 6 FDA reports)
JOINT DISLOCATION REDUCTION ( 6 FDA reports)
KERATITIS HERPETIC ( 6 FDA reports)
KLEBSIELLA BACTERAEMIA ( 6 FDA reports)
LABILE HYPERTENSION ( 6 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 6 FDA reports)
LATERAL PATELLAR COMPRESSION SYNDROME ( 6 FDA reports)
LIP HAEMORRHAGE ( 6 FDA reports)
LIPODYSTROPHY ACQUIRED ( 6 FDA reports)
LOCALISED OSTEOARTHRITIS ( 6 FDA reports)
LONG QT SYNDROME ( 6 FDA reports)
LOW BIRTH WEIGHT BABY ( 6 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 6 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE I ( 6 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 6 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 6 FDA reports)
MALIGNANT MELANOMA STAGE IV ( 6 FDA reports)
MANTLE CELL LYMPHOMA ( 6 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 6 FDA reports)
MEDICAL DIET ( 6 FDA reports)
MENISCUS OPERATION ( 6 FDA reports)
MENOMETRORRHAGIA ( 6 FDA reports)
METASTASES TO SOFT TISSUE ( 6 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 6 FDA reports)
METATARSUS PRIMUS VARUS ( 6 FDA reports)
MIGRAINE WITHOUT AURA ( 6 FDA reports)
MORBID THOUGHTS ( 6 FDA reports)
MUCOSAL ULCERATION ( 6 FDA reports)
MURPHY'S SIGN POSITIVE ( 6 FDA reports)
MUSCLE NECROSIS ( 6 FDA reports)
MUSCULAR DYSTROPHY ( 6 FDA reports)
NAIL HYPERTROPHY ( 6 FDA reports)
NAIL INFECTION ( 6 FDA reports)
NAIL TINEA ( 6 FDA reports)
NASAL VESTIBULITIS ( 6 FDA reports)
ABDOMINAL SYMPTOM ( 5 FDA reports)
ABDOMINAL WALL ABSCESS ( 5 FDA reports)
ABDOMINOPLASTY ( 5 FDA reports)
ABSCESS SOFT TISSUE ( 5 FDA reports)
ACHLORHYDRIA ( 5 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 5 FDA reports)
ADRENAL CARCINOMA ( 5 FDA reports)
AEROPHAGIA ( 5 FDA reports)
AGITATION POSTOPERATIVE ( 5 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 5 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 5 FDA reports)
ALCOHOL INTERACTION ( 5 FDA reports)
ALLERGIC COUGH ( 5 FDA reports)
AMYOTROPHY ( 5 FDA reports)
ANAL EROSION ( 5 FDA reports)
ANAL POLYP ( 5 FDA reports)
ANGIOGRAM ABNORMAL ( 5 FDA reports)
ANION GAP DECREASED ( 5 FDA reports)
ANOXIA ( 5 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 5 FDA reports)
APPARENT LIFE THREATENING EVENT ( 5 FDA reports)
APPLICATION SITE ULCER ( 5 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 5 FDA reports)
ARTERIAL SPASM ( 5 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 5 FDA reports)
ARTERIOVENOUS GRAFT SITE INFECTION ( 5 FDA reports)
ARTHRODESIS ( 5 FDA reports)
ARTIFICIAL MENOPAUSE ( 5 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 5 FDA reports)
ASPIRATION BONE MARROW ( 5 FDA reports)
ASTHMATIC CRISIS ( 5 FDA reports)
ATHERECTOMY ( 5 FDA reports)
ATRIAL PRESSURE INCREASED ( 5 FDA reports)
AURA ( 5 FDA reports)
AXILLARY VEIN THROMBOSIS ( 5 FDA reports)
BENIGN LUNG NEOPLASM ( 5 FDA reports)
BIOPSY LUNG ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 5 FDA reports)
BLOOD BILIRUBIN DECREASED ( 5 FDA reports)
BLOOD CORTISOL DECREASED ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 5 FDA reports)
BLOOD FOLATE INCREASED ( 5 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 5 FDA reports)
BLOOD OESTROGEN DECREASED ( 5 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 5 FDA reports)
BLOOD VISCOSITY INCREASED ( 5 FDA reports)
BLOODY PERITONEAL EFFLUENT ( 5 FDA reports)
BODY MASS INDEX DECREASED ( 5 FDA reports)
BONE LESION EXCISION ( 5 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 5 FDA reports)
BRAIN COMPRESSION ( 5 FDA reports)
BRAIN HYPOXIA ( 5 FDA reports)
BRAIN STEM INFARCTION ( 5 FDA reports)
BRAIN STEM SYNDROME ( 5 FDA reports)
BRAIN TUMOUR OPERATION ( 5 FDA reports)
BREAST PROSTHESIS IMPLANTATION ( 5 FDA reports)
BREATH ALCOHOL TEST POSITIVE ( 5 FDA reports)
BURNING MOUTH SYNDROME ( 5 FDA reports)
BUTTERFLY RASH ( 5 FDA reports)
CARBON MONOXIDE DIFFUSING CAPACITY DECREASED ( 5 FDA reports)
CARCINOID TUMOUR OF THE STOMACH ( 5 FDA reports)
CARDIAC INFECTION ( 5 FDA reports)
CAROTID ARTERY STENT INSERTION ( 5 FDA reports)
CAROTID BODY TUMOUR ( 5 FDA reports)
CAUDA EQUINA SYNDROME ( 5 FDA reports)
CELLULITIS GANGRENOUS ( 5 FDA reports)
CENTRAL OBESITY ( 5 FDA reports)
CHEMICAL INJURY ( 5 FDA reports)
CHRONIC TONSILLITIS ( 5 FDA reports)
CLONUS ( 5 FDA reports)
COELIAC ARTERY STENOSIS ( 5 FDA reports)
COLON CANCER RECURRENT ( 5 FDA reports)
COMPARTMENT SYNDROME ( 5 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 5 FDA reports)
CONGENITAL AORTIC ATRESIA ( 5 FDA reports)
CONJUNCTIVAL OEDEMA ( 5 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 5 FDA reports)
COOMBS TEST POSITIVE ( 5 FDA reports)
CORONARY ARTERY REOCCLUSION ( 5 FDA reports)
CULTURE STOOL POSITIVE ( 5 FDA reports)
CYANOPSIA ( 5 FDA reports)
CYST REMOVAL ( 5 FDA reports)
CYSTITIS HAEMORRHAGIC ( 5 FDA reports)
DELIRIUM TREMENS ( 5 FDA reports)
DENTAL NECROSIS ( 5 FDA reports)
DEPRESSION SUICIDAL ( 5 FDA reports)
DERMATOPHYTOSIS ( 5 FDA reports)
DEVICE EXPULSION ( 5 FDA reports)
DISSOCIATIVE DISORDER ( 5 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 5 FDA reports)
DRUG EFFECT PROLONGED ( 5 FDA reports)
DRUG INTERACTION POTENTIATION ( 5 FDA reports)
DRUG LEVEL ( 5 FDA reports)
DRUG LEVEL CHANGED ( 5 FDA reports)
DRUG WITHDRAWAL HEADACHE ( 5 FDA reports)
DUANE'S SYNDROME ( 5 FDA reports)
DUODENAL STENOSIS ( 5 FDA reports)
ECTOPIC PREGNANCY ( 5 FDA reports)
ELECTROCUTION ( 5 FDA reports)
ELECTROLYTE DEPLETION ( 5 FDA reports)
ELEVATED MOOD ( 5 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 5 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 5 FDA reports)
EOSINOPHIL COUNT DECREASED ( 5 FDA reports)
ERYTHEMA MIGRANS ( 5 FDA reports)
ESSENTIAL TREMOR ( 5 FDA reports)
EUSTACHIAN TUBE DISORDER ( 5 FDA reports)
EYE BURNS ( 5 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 5 FDA reports)
FAECAL VOLUME DECREASED ( 5 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 5 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 5 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 5 FDA reports)
FOETAL DEATH ( 5 FDA reports)
FORAMINOTOMY ( 5 FDA reports)
FOREIGN BODY ASPIRATION ( 5 FDA reports)
GALLBLADDER ABSCESS ( 5 FDA reports)
GALLBLADDER OBSTRUCTION ( 5 FDA reports)
GASTRITIS ATROPHIC ( 5 FDA reports)
GASTROENTERITIS BACTERIAL ( 5 FDA reports)
GENITAL ABSCESS ( 5 FDA reports)
GENITAL EROSION ( 5 FDA reports)
GENITAL PAIN FEMALE ( 5 FDA reports)
GLOBULINS INCREASED ( 5 FDA reports)
GLUCOSE URINE PRESENT ( 5 FDA reports)
HAEMORRHOID OPERATION ( 5 FDA reports)
HAEMOSIDEROSIS ( 5 FDA reports)
HEAT RASH ( 5 FDA reports)
HEPATIC ARTERY OCCLUSION ( 5 FDA reports)
HEPATIC HAEMATOMA ( 5 FDA reports)
HEPATIC INFECTION ( 5 FDA reports)
HEPATIC RUPTURE ( 5 FDA reports)
HEPATITIS A ( 5 FDA reports)
HEPATITIS ALCOHOLIC ( 5 FDA reports)
HEPATITIS B DNA INCREASED ( 5 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 5 FDA reports)
HERPES OPHTHALMIC ( 5 FDA reports)
HISTONE ANTIBODY POSITIVE ( 5 FDA reports)
HOMICIDE ( 5 FDA reports)
HORDEOLUM ( 5 FDA reports)
HYPERCREATININAEMIA ( 5 FDA reports)
HYPERPARATHYROIDISM PRIMARY ( 5 FDA reports)
HYPERTRICHOSIS ( 5 FDA reports)
HYPOCOMPLEMENTAEMIA ( 5 FDA reports)
HYPONATRAEMIC ENCEPHALOPATHY ( 5 FDA reports)
HYPOPERFUSION ( 5 FDA reports)
HYPOPITUITARISM ( 5 FDA reports)
HYPOPLASTIC RIGHT HEART SYNDROME ( 5 FDA reports)
HYPOPROTHROMBINAEMIA ( 5 FDA reports)
HYPOSMIA ( 5 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 5 FDA reports)
ILEOSTOMY ( 5 FDA reports)
IMMUNOGLOBULINS INCREASED ( 5 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 5 FDA reports)
IMPLANT SITE INFECTION ( 5 FDA reports)
IMPLANT SITE REACTION ( 5 FDA reports)
INADEQUATE DIET ( 5 FDA reports)
INCISION SITE HAEMATOMA ( 5 FDA reports)
INFUSION SITE HAEMATOMA ( 5 FDA reports)
INFUSION SITE INFECTION ( 5 FDA reports)
INFUSION SITE REACTION ( 5 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 5 FDA reports)
INJURY CORNEAL ( 5 FDA reports)
INSULIN-REQUIRING TYPE II DIABETES MELLITUS ( 5 FDA reports)
INTENTION TREMOR ( 5 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 5 FDA reports)
INTRACRANIAL HAEMATOMA ( 5 FDA reports)
INTRINSIC FACTOR ANTIBODY NEGATIVE ( 5 FDA reports)
IODINE ALLERGY ( 5 FDA reports)
JEJUNOSTOMY ( 5 FDA reports)
JOINT WARMTH ( 5 FDA reports)
KIDNEY ENLARGEMENT ( 5 FDA reports)
LACTOBACILLUS INFECTION ( 5 FDA reports)
LAPAROTOMY ( 5 FDA reports)
LARGE GRANULAR LYMPHOCYTOSIS ( 5 FDA reports)
LENTICULAR OPACITIES ( 5 FDA reports)
LEUKOPLAKIA ORAL ( 5 FDA reports)
LIGAMENT LAXITY ( 5 FDA reports)
LIPOMATOUS HYPERTROPHY OF THE INTERATRIAL SEPTUM ( 5 FDA reports)
LIVING IN RESIDENTIAL INSTITUTION ( 5 FDA reports)
LUMBAR SPINE FLATTENING ( 5 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 5 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 5 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 5 FDA reports)
MADAROSIS ( 5 FDA reports)
MARITAL PROBLEM ( 5 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 5 FDA reports)
MEDICAL DEVICE CHANGE ( 5 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 5 FDA reports)
MESENTERITIS ( 5 FDA reports)
METASTASES TO MUSCLE ( 5 FDA reports)
METASTASES TO NASAL SINUSES ( 5 FDA reports)
METASTATIC LYMPHOMA ( 5 FDA reports)
MILIA ( 5 FDA reports)
MILK ALLERGY ( 5 FDA reports)
MONONUCLEOSIS SYNDROME ( 5 FDA reports)
MUCKLE-WELLS SYNDROME ( 5 FDA reports)
MUCOSAL DISCOLOURATION ( 5 FDA reports)
MUMPS ( 5 FDA reports)
MUSCLE MASS ( 5 FDA reports)
MYCOTIC ALLERGY ( 5 FDA reports)
MYOPERICARDITIS ( 5 FDA reports)
NAIL BED INFECTION ( 5 FDA reports)
NASAL CAVITY CANCER ( 5 FDA reports)
NASAL MUCOSAL DISORDER ( 5 FDA reports)
NASAL OPERATION ( 5 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 5 FDA reports)
NEOPLASM PROSTATE ( 5 FDA reports)
NEUROMYOPATHY ( 5 FDA reports)
NEUROSIS ( 5 FDA reports)
OBESITY SURGERY ( 5 FDA reports)
OCULAR DISCOMFORT ( 5 FDA reports)
OEDEMATOUS PANCREATITIS ( 5 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 5 FDA reports)
OESOPHAGEAL DYSPLASIA ( 5 FDA reports)
OESTROGEN DEFICIENCY ( 5 FDA reports)
ONYCHALGIA ( 5 FDA reports)
OPPORTUNISTIC INFECTION ( 5 FDA reports)
ORAL LICHEN PLANUS ( 5 FDA reports)
ORGASM ABNORMAL ( 5 FDA reports)
OROPHARYNGITIS FUNGAL ( 5 FDA reports)
OTITIS EXTERNA FUNGAL ( 5 FDA reports)
OTOTOXICITY ( 5 FDA reports)
OVARIAN ADHESION ( 5 FDA reports)
PALPABLE PURPURA ( 5 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 5 FDA reports)
PARAKERATOSIS ( 5 FDA reports)
PAROTID DUCT OBSTRUCTION ( 5 FDA reports)
PELVIC ADHESIONS ( 5 FDA reports)
PELVIC FLOOR MUSCLE WEAKNESS ( 5 FDA reports)
PELVIC MASS ( 5 FDA reports)
PELVIC VENOUS THROMBOSIS ( 5 FDA reports)
PEMPHIGUS ( 5 FDA reports)
PERICARDIAL DISEASE ( 5 FDA reports)
PERICARDIAL DRAINAGE ( 5 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 5 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 5 FDA reports)
PERIPHERAL NERVE OPERATION ( 5 FDA reports)
PHONOPHOBIA ( 5 FDA reports)
PHOSPHENES ( 5 FDA reports)
PITUITARY CYST ( 5 FDA reports)
PLATELET AGGREGATION INCREASED ( 5 FDA reports)
PLEURAL MESOTHELIOMA ( 5 FDA reports)
PNEUMATOSIS INTESTINALIS ( 5 FDA reports)
PNEUMOCONIOSIS ( 5 FDA reports)
POLYSEROSITIS ( 5 FDA reports)
POSTOPERATIVE RESPIRATORY DISTRESS ( 5 FDA reports)
POSTPARTUM HAEMORRHAGE ( 5 FDA reports)
PREMATURE DELIVERY ( 5 FDA reports)
PROCEDURAL DIZZINESS ( 5 FDA reports)
PROCEDURAL NAUSEA ( 5 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 5 FDA reports)
PROSTHESIS IMPLANTATION ( 5 FDA reports)
PROTEIN S DECREASED ( 5 FDA reports)
PUBIC PAIN ( 5 FDA reports)
PULMONARY CALCIFICATION ( 5 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 5 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 5 FDA reports)
RED MAN SYNDROME ( 5 FDA reports)
REFRACTORY ANAEMIA ( 5 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 5 FDA reports)
REPETITIVE SPEECH ( 5 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 5 FDA reports)
RUBELLA ( 5 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 5 FDA reports)
SCAR EXCISION ( 5 FDA reports)
SENSE OF OPPRESSION ( 5 FDA reports)
SERRATIA INFECTION ( 5 FDA reports)
SHUNT MALFUNCTION ( 5 FDA reports)
SIGMOIDOSCOPY ABNORMAL ( 5 FDA reports)
SINOATRIAL BLOCK ( 5 FDA reports)
SITUS INVERSUS ( 5 FDA reports)
SKIN STRIAE ( 5 FDA reports)
SKIN WRINKLING ( 5 FDA reports)
SLEEP PHASE RHYTHM DISTURBANCE ( 5 FDA reports)
SMALL FOR DATES BABY ( 5 FDA reports)
SMALL INTESTINAL PERFORATION ( 5 FDA reports)
SMALL INTESTINE CARCINOMA ( 5 FDA reports)
SMALL INTESTINE ULCER ( 5 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 5 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 5 FDA reports)
SPLENIC CYST ( 5 FDA reports)
SPOUSAL ABUSE ( 5 FDA reports)
STRESS INCONTINENCE ( 5 FDA reports)
SURGICAL FAILURE ( 5 FDA reports)
SUTURE RELATED COMPLICATION ( 5 FDA reports)
TEMPOROMANDIBULAR JOINT SURGERY ( 5 FDA reports)
TENDINOUS CONTRACTURE ( 5 FDA reports)
TESTICULAR SWELLING ( 5 FDA reports)
TESTIS CANCER ( 5 FDA reports)
THALAMIC INFARCTION ( 5 FDA reports)
THEFT ( 5 FDA reports)
THROMBECTOMY ( 5 FDA reports)
TONGUE NEOPLASM ( 5 FDA reports)
TONGUE PARALYSIS ( 5 FDA reports)
TONSILLAR HYPERTROPHY ( 5 FDA reports)
TRACHEAL OEDEMA ( 5 FDA reports)
TRANSFERRIN SATURATION INCREASED ( 5 FDA reports)
TRICUSPID VALVE SCLEROSIS ( 5 FDA reports)
TUBERCULIN TEST POSITIVE ( 5 FDA reports)
TUMOUR ASSOCIATED FEVER ( 5 FDA reports)
TUMOUR NECROSIS ( 5 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 5 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 5 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 5 FDA reports)
URETHRAL DISORDER ( 5 FDA reports)
URETHRAL SPASM ( 5 FDA reports)
URINE SODIUM DECREASED ( 5 FDA reports)
VACCINATION COMPLICATION ( 5 FDA reports)
VACTERL SYNDROME ( 5 FDA reports)
VAGINAL CELLULITIS ( 5 FDA reports)
VAGUS NERVE DISORDER ( 5 FDA reports)
VESTIBULOPLASTY ( 5 FDA reports)
VIITH NERVE INJURY ( 5 FDA reports)
VIRAL TEST POSITIVE ( 5 FDA reports)
WHIPLASH INJURY ( 5 FDA reports)
X-RAY ( 5 FDA reports)
NECK DEFORMITY ( 4 FDA reports)
NECROTISING GRANULOMATOUS LYMPHADENITIS ( 4 FDA reports)
NECROTISING ULCERATIVE PERIODONTITIS ( 4 FDA reports)
NERVE GRAFT ( 4 FDA reports)
NEUROMYELITIS OPTICA ( 4 FDA reports)
NIGHT CRAMPS ( 4 FDA reports)
NON-OBSTRUCTIVE CARDIOMYOPATHY ( 4 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIA ( 4 FDA reports)
OCULAR RETROBULBAR HAEMORRHAGE ( 4 FDA reports)
OCULAR VASCULAR DISORDER ( 4 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 4 FDA reports)
OESOPHAGOSCOPY ( 4 FDA reports)
OLIGOMENORRHOEA ( 4 FDA reports)
OPTIC DISC DISORDER ( 4 FDA reports)
OPTIC NERVE DISORDER ( 4 FDA reports)
ORAL DYSAESTHESIA ( 4 FDA reports)
ORAL MUCOSAL ERUPTION ( 4 FDA reports)
ORBITAL CYST ( 4 FDA reports)
ORTHOSTATIC INTOLERANCE ( 4 FDA reports)
OSTEOARTHROPATHY ( 4 FDA reports)
OSTEODYSTROPHY ( 4 FDA reports)
OSTEOMA ( 4 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 4 FDA reports)
PACHYMENINGITIS ( 4 FDA reports)
PANCREATIC DUCT DILATATION ( 4 FDA reports)
PANCREATIC OPERATION ( 4 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 4 FDA reports)
PARACENTESIS ( 4 FDA reports)
PARACENTESIS ABDOMEN ( 4 FDA reports)
PARVOVIRUS B19 SEROLOGY POSITIVE ( 4 FDA reports)
PCO2 ABNORMAL ( 4 FDA reports)
PELVIC FLUID COLLECTION ( 4 FDA reports)
PELVIC HAEMATOMA ( 4 FDA reports)
PELVIC PROLAPSE ( 4 FDA reports)
PEPTIC ULCER PERFORATION ( 4 FDA reports)
PERICARDIAL EXCISION ( 4 FDA reports)
PERIHEPATIC DISCOMFORT ( 4 FDA reports)
PERIPHERAL REVASCULARISATION ( 4 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 4 FDA reports)
PERITONEAL INFECTION ( 4 FDA reports)
PERITONEAL TUBERCULOSIS ( 4 FDA reports)
PHAGOPHOBIA ( 4 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 4 FDA reports)
PLATELET COUNT ( 4 FDA reports)
PLICA SYNDROME ( 4 FDA reports)
PNEUMONIA CHLAMYDIAL ( 4 FDA reports)
PNEUMONIA ESCHERICHIA ( 4 FDA reports)
PNEUMONITIS CHEMICAL ( 4 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 4 FDA reports)
POST PROCEDURAL HAEMATURIA ( 4 FDA reports)
POST PROCEDURAL PNEUMONIA ( 4 FDA reports)
POSTPARTUM DEPRESSION ( 4 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 4 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 4 FDA reports)
PREMENSTRUAL SYNDROME ( 4 FDA reports)
PRODUCT PACKAGING ISSUE ( 4 FDA reports)
PROSTATITIS ESCHERICHIA COLI ( 4 FDA reports)
PROSTHESIS USER ( 4 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 4 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 4 FDA reports)
PRURITUS GENITAL ( 4 FDA reports)
PSEUDOEPITHELIOMATOUS HYPERPLASIA ( 4 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 4 FDA reports)
PUBIC RAMI FRACTURE ( 4 FDA reports)
PULMONARY VALVE STENOSIS ( 4 FDA reports)
PYODERMA ( 4 FDA reports)
QUADRIPLEGIA ( 4 FDA reports)
RADIAL NERVE PALSY ( 4 FDA reports)
RADIATION MUCOSITIS ( 4 FDA reports)
RADICAL HYSTERECTOMY ( 4 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 4 FDA reports)
REFLEXES ABNORMAL ( 4 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 4 FDA reports)
RENAL ISCHAEMIA ( 4 FDA reports)
RESECTION OF RECTUM ( 4 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 4 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 4 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 4 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 4 FDA reports)
RETINAL DYSTROPHY ( 4 FDA reports)
RETINAL OEDEMA ( 4 FDA reports)
RETINAL OPERATION ( 4 FDA reports)
RETINAL VASCULAR OCCLUSION ( 4 FDA reports)
RETROPERITONEAL FIBROSIS ( 4 FDA reports)
RETROVIRAL INFECTION ( 4 FDA reports)
RHEUMATOID NODULE ( 4 FDA reports)
ROUTINE HEALTH MAINTENANCE ( 4 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 4 FDA reports)
SELF-INDUCED VOMITING ( 4 FDA reports)
SEMEN ABNORMAL ( 4 FDA reports)
SERUM SEROTONIN INCREASED ( 4 FDA reports)
SHORT-BOWEL SYNDROME ( 4 FDA reports)
SKIN DESQUAMATION ( 4 FDA reports)
SKIN TEST POSITIVE ( 4 FDA reports)
SKIN TURGOR DECREASED ( 4 FDA reports)
SLEEP TERROR ( 4 FDA reports)
SMALL INTESTINAL STENOSIS ( 4 FDA reports)
SODIUM RETENTION ( 4 FDA reports)
SOFT TISSUE ATROPHY ( 4 FDA reports)
SOFT TISSUE INFECTION ( 4 FDA reports)
SOFT TISSUE NECROSIS ( 4 FDA reports)
SPASMODIC DYSPHONIA ( 4 FDA reports)
SPERM COUNT ABNORMAL ( 4 FDA reports)
SPHINGOMONAS PAUCIMOBILIS INFECTION ( 4 FDA reports)
SPINAL CORD NEOPLASM ( 4 FDA reports)
SPUTUM PURULENT ( 4 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 4 FDA reports)
STENOTROPHOMONAS INFECTION ( 4 FDA reports)
STEREOTYPY ( 4 FDA reports)
STIFF-MAN SYNDROME ( 4 FDA reports)
STITCH ABSCESS ( 4 FDA reports)
STOMACH MASS ( 4 FDA reports)
STOOL ANALYSIS ABNORMAL ( 4 FDA reports)
SYMPHYSIOLYSIS ( 4 FDA reports)
SYRINGOMYELIA ( 4 FDA reports)
TABLET PHYSICAL ISSUE ( 4 FDA reports)
TACHYCARDIA FOETAL ( 4 FDA reports)
TENDON OPERATION ( 4 FDA reports)
THYMUS ENLARGEMENT ( 4 FDA reports)
THYROTOXIC CRISIS ( 4 FDA reports)
TOURETTE'S DISORDER ( 4 FDA reports)
TRACHEAL DISORDER ( 4 FDA reports)
TRANSFERRIN DECREASED ( 4 FDA reports)
TRANSPLANT ABSCESS ( 4 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 4 FDA reports)
TYPE I HYPERSENSITIVITY ( 4 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 4 FDA reports)
UMBILICAL HERNIA REPAIR ( 4 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 4 FDA reports)
UPPER EXTREMITY MASS ( 4 FDA reports)
URETHRAL CARUNCLE ( 4 FDA reports)
URETHRAL STENT INSERTION ( 4 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 4 FDA reports)
URINE ARSENIC INCREASED ( 4 FDA reports)
URTICARIA PAPULAR ( 4 FDA reports)
UTERINE ATONY ( 4 FDA reports)
UTERINE PAIN ( 4 FDA reports)
UVULAR SPASM ( 4 FDA reports)
VAGINAL PAIN ( 4 FDA reports)
VAGINAL SWELLING ( 4 FDA reports)
VASCULAR RESISTANCE SYSTEMIC DECREASED ( 4 FDA reports)
VEIN DISCOLOURATION ( 4 FDA reports)
VENOGRAM ( 4 FDA reports)
VENOUS PRESSURE INCREASED ( 4 FDA reports)
VENTRICULAR FAILURE ( 4 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 4 FDA reports)
VERTEBRAL COLUMN MASS ( 4 FDA reports)
VIRAL PERICARDITIS ( 4 FDA reports)
VITAMIN K DECREASED ( 4 FDA reports)
VULVOVAGINAL HUMAN PAPILLOMA VIRUS INFECTION ( 4 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 4 FDA reports)
WEIGHT ( 4 FDA reports)
WEIGHT ABNORMAL ( 4 FDA reports)
WEIGHT GAIN POOR ( 4 FDA reports)
WOUND INFECTION BACTERIAL ( 4 FDA reports)
X-RAY LIMB ABNORMAL ( 4 FDA reports)
ABDOMINAL SEPSIS ( 4 FDA reports)
ABDOMINAL WALL HAEMORRHAGE ( 4 FDA reports)
ABDOMINAL WALL MASS ( 4 FDA reports)
ACARODERMATITIS ( 4 FDA reports)
ACINETOBACTER INFECTION ( 4 FDA reports)
ACROMEGALY ( 4 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 4 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 4 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 4 FDA reports)
ADENOTONSILLECTOMY ( 4 FDA reports)
ALBUMINURIA ( 4 FDA reports)
AMAUROSIS ( 4 FDA reports)
AMNESTIC DISORDER ( 4 FDA reports)
AMPHETAMINES POSITIVE ( 4 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 4 FDA reports)
ANHIDROSIS ( 4 FDA reports)
ANION GAP INCREASED ( 4 FDA reports)
ANKLE DEFORMITY ( 4 FDA reports)
ANTIBIOTIC LEVEL ABOVE THERAPEUTIC ( 4 FDA reports)
ANTIBIOTIC THERAPY ( 4 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 4 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 4 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 4 FDA reports)
ANTISOCIAL BEHAVIOUR ( 4 FDA reports)
AORTIC OCCLUSION ( 4 FDA reports)
ARTERIAL CATHETERISATION ( 4 FDA reports)
ARTERIAL REPAIR ( 4 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 4 FDA reports)
ARTERIOVENOUS GRAFT THROMBOSIS ( 4 FDA reports)
ARTERY DISSECTION ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 4 FDA reports)
ASTROCYTOMA ( 4 FDA reports)
ATONIC URINARY BLADDER ( 4 FDA reports)
ATRIAL NATRIURETIC PEPTIDE INCREASED ( 4 FDA reports)
BARTHOLIN'S ABSCESS ( 4 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 4 FDA reports)
BENIGN RENAL NEOPLASM ( 4 FDA reports)
BENIGN SALIVARY GLAND NEOPLASM ( 4 FDA reports)
BIFASCICULAR BLOCK ( 4 FDA reports)
BILE DUCT NECROSIS ( 4 FDA reports)
BILIARY NEOPLASM ( 4 FDA reports)
BIOPSY SKIN ( 4 FDA reports)
BIPOLAR II DISORDER ( 4 FDA reports)
BLADDER DYSFUNCTION ( 4 FDA reports)
BLADDER IRRITATION ( 4 FDA reports)
BLADDER NECK SUSPENSION ( 4 FDA reports)
BLIGHTED OVUM ( 4 FDA reports)
BLOOD ALDOSTERONE DECREASED ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 4 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 4 FDA reports)
BLOOD GROWTH HORMONE INCREASED ( 4 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 4 FDA reports)
BODY MASS INDEX INCREASED ( 4 FDA reports)
BODY TINEA ( 4 FDA reports)
BRAIN ABSCESS ( 4 FDA reports)
BREAST CANCER STAGE III ( 4 FDA reports)
BREATH SOUNDS DECREASED ( 4 FDA reports)
BRONCHIAL CARCINOMA ( 4 FDA reports)
BRONCHOSCOPY ABNORMAL ( 4 FDA reports)
BURNING SENSATION MUCOSAL ( 4 FDA reports)
BURNS SECOND DEGREE ( 4 FDA reports)
CALCIPHYLAXIS ( 4 FDA reports)
CAMPYLOBACTER INFECTION ( 4 FDA reports)
CARBON DIOXIDE ABNORMAL ( 4 FDA reports)
CARBUNCLE ( 4 FDA reports)
CARCINOMA IN SITU ( 4 FDA reports)
CARDIAC FIBROMA ( 4 FDA reports)
CARDIAC INDEX DECREASED ( 4 FDA reports)
CARDIAC MYXOMA ( 4 FDA reports)
CAROTID ARTERY THROMBOSIS ( 4 FDA reports)
CASTLEMAN'S DISEASE ( 4 FDA reports)
CATAPLEXY ( 4 FDA reports)
CATHETER SITE RELATED REACTION ( 4 FDA reports)
CATHETER THROMBOSIS ( 4 FDA reports)
CD4/CD8 RATIO DECREASED ( 4 FDA reports)
CENTRAL NERVOUS SYSTEM NEOPLASM ( 4 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 4 FDA reports)
CEREBRAL ASPERGILLOSIS ( 4 FDA reports)
CERVICAL ROOT PAIN ( 4 FDA reports)
CHEMICAL BURN OF SKIN ( 4 FDA reports)
CHEST WALL MASS ( 4 FDA reports)
CHOLELITHOTOMY ( 4 FDA reports)
CHOROIDITIS ( 4 FDA reports)
CHRONIC GASTROINTESTINAL BLEEDING ( 4 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 4 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 4 FDA reports)
CIRCUMORAL OEDEMA ( 4 FDA reports)
COAGULATION FACTOR DECREASED ( 4 FDA reports)
COLON CANCER STAGE III ( 4 FDA reports)
COLON INJURY ( 4 FDA reports)
COMA HEPATIC ( 4 FDA reports)
COMA SCALE ABNORMAL ( 4 FDA reports)
COMPUTERISED TOMOGRAM CORONARY ARTERY ABNORMAL ( 4 FDA reports)
CONFUSION POSTOPERATIVE ( 4 FDA reports)
CONGENITAL HAND MALFORMATION ( 4 FDA reports)
CONGENITAL TRICUSPID VALVE INCOMPETENCE ( 4 FDA reports)
CONJUNCTIVAL PRIMARY ACQUIRED MELANOSIS ( 4 FDA reports)
COPPER DEFICIENCY ( 4 FDA reports)
CORNEAL OEDEMA ( 4 FDA reports)
CORNEAL SCAR ( 4 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 4 FDA reports)
CRANIAL NERVE PARALYSIS ( 4 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 4 FDA reports)
CRITICAL ILLNESS POLYNEUROPATHY ( 4 FDA reports)
CSF TEST ABNORMAL ( 4 FDA reports)
CUTANEOUS SARCOIDOSIS ( 4 FDA reports)
CYSTITIS GLANDULARIS ( 4 FDA reports)
DEAFNESS TRANSITORY ( 4 FDA reports)
DECREASED VIBRATORY SENSE ( 4 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 4 FDA reports)
DEMENTIA WITH LEWY BODIES ( 4 FDA reports)
DENGUE FEVER ( 4 FDA reports)
DEREALISATION ( 4 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 4 FDA reports)
DIABETIC GANGRENE ( 4 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE III ( 4 FDA reports)
DISINHIBITION ( 4 FDA reports)
DNA ANTIBODY POSITIVE ( 4 FDA reports)
DOUGLAS' ABSCESS ( 4 FDA reports)
EAR INFECTION VIRAL ( 4 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 4 FDA reports)
ENCEPHALITIS TOXIC ( 4 FDA reports)
ENDARTERECTOMY ( 4 FDA reports)
ENDOMETRIAL CANCER STAGE II ( 4 FDA reports)
ENDOMETRIAL CANCER STAGE III ( 4 FDA reports)
ENDOMETRIAL NEOPLASM ( 4 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ( 4 FDA reports)
ENTEROBACTER PNEUMONIA ( 4 FDA reports)
EOSINOPHILIC PNEUMONIA CHRONIC ( 4 FDA reports)
EPIDIDYMITIS ( 4 FDA reports)
ERYTHEMA INFECTIOSUM ( 4 FDA reports)
ERYTHROSIS ( 4 FDA reports)
EXTERNAL EAR PAIN ( 4 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 4 FDA reports)
EYE PROSTHESIS INSERTION ( 4 FDA reports)
FACTOR V LEIDEN MUTATION ( 4 FDA reports)
FALSE NEGATIVE INVESTIGATION RESULT ( 4 FDA reports)
FAT INTOLERANCE ( 4 FDA reports)
FEAR OF FALLING ( 4 FDA reports)
FEMALE GENITAL OPERATION ( 4 FDA reports)
FIBROUS DYSPLASIA OF BONE ( 4 FDA reports)
FINGER AMPUTATION ( 4 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 4 FDA reports)
FOETAL GROWTH RETARDATION ( 4 FDA reports)
FOOT AMPUTATION ( 4 FDA reports)
FRACTURE MALUNION ( 4 FDA reports)
FUNGAEMIA ( 4 FDA reports)
GALLOP RHYTHM PRESENT ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ( 4 FDA reports)
GANGLION ( 4 FDA reports)
GASTRIC HYPOMOTILITY ( 4 FDA reports)
GASTRIC STENOSIS ( 4 FDA reports)
GASTRITIS BACTERIAL ( 4 FDA reports)
GASTRITIS VIRAL ( 4 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 4 FDA reports)
GASTROINTESTINAL CARCINOMA IN SITU ( 4 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 4 FDA reports)
GASTROINTESTINAL STENOSIS ( 4 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 4 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 4 FDA reports)
GAZE PALSY ( 4 FDA reports)
GENERAL ANAESTHESIA ( 4 FDA reports)
GENITAL DISORDER FEMALE ( 4 FDA reports)
GENITAL PAIN ( 4 FDA reports)
GENITAL PRURITUS FEMALE ( 4 FDA reports)
GIANT CELL EPULIS ( 4 FDA reports)
GLIOMA ( 4 FDA reports)
GLOBAL AMNESIA ( 4 FDA reports)
GLOBULIN ABNORMAL ( 4 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 4 FDA reports)
GRANULOCYTE COUNT INCREASED ( 4 FDA reports)
GRUNTING ( 4 FDA reports)
HAEMOCONCENTRATION ( 4 FDA reports)
HAEMOPHILUS TEST POSITIVE ( 4 FDA reports)
HAEMORRHAGIC EROSIVE GASTRITIS ( 4 FDA reports)
HAEMORRHAGIC INFARCTION ( 4 FDA reports)
HEART TRANSPLANT REJECTION ( 4 FDA reports)
HEART VALVE INSUFFICIENCY ( 4 FDA reports)
HEMIANOPIA HOMONYMOUS ( 4 FDA reports)
HEPATECTOMY ( 4 FDA reports)
HEPATIC ISCHAEMIA ( 4 FDA reports)
HEPATOSPLENIC CANDIDIASIS ( 4 FDA reports)
HERNIA OBSTRUCTIVE ( 4 FDA reports)
HERPES DERMATITIS ( 4 FDA reports)
HERPES ZOSTER DISSEMINATED ( 4 FDA reports)
HETEROTAXIA ( 4 FDA reports)
HOSPICE CARE ( 4 FDA reports)
HYPERCHROMIC ANAEMIA ( 4 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 4 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 4 FDA reports)
HYPERMOBILITY SYNDROME ( 4 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 4 FDA reports)
HYPOCHOLESTEROLAEMIA ( 4 FDA reports)
HYPOFIBRINOGENAEMIA ( 4 FDA reports)
HYPOPHARYNGEAL CANCER ( 4 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 4 FDA reports)
ILIAC ARTERY EMBOLISM ( 4 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 4 FDA reports)
INFANTILE SPITTING UP ( 4 FDA reports)
INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS ( 4 FDA reports)
INFESTATION ( 4 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 4 FDA reports)
INTESTINAL PROLAPSE ( 4 FDA reports)
INTUBATION ( 4 FDA reports)
INVESTIGATION ( 4 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 4 FDA reports)
ISCHAEMIC ULCER ( 4 FDA reports)
JAUNDICE HEPATOCELLULAR ( 4 FDA reports)
JOINT ABSCESS ( 4 FDA reports)
JOINT DESTRUCTION ( 4 FDA reports)
JUVENILE ARTHRITIS ( 4 FDA reports)
KIDNEY SMALL ( 4 FDA reports)
LABELLED DRUG-FOOD INTERACTION MEDICATION ERROR ( 4 FDA reports)
LACRIMAL DISORDER ( 4 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 4 FDA reports)
LARYNGEAL DISORDER ( 4 FDA reports)
LARYNGEAL INJURY ( 4 FDA reports)
LARYNGEAL ULCERATION ( 4 FDA reports)
LARYNGOCELE ( 4 FDA reports)
LATEX ALLERGY ( 4 FDA reports)
LEARNING DISABILITY ( 4 FDA reports)
LEIOMYOSARCOMA ( 4 FDA reports)
LENS DISORDER ( 4 FDA reports)
LICHENIFICATION ( 4 FDA reports)
LIVER CARCINOMA RUPTURED ( 4 FDA reports)
LIVER SCAN ABNORMAL ( 4 FDA reports)
LOCKED-IN SYNDROME ( 4 FDA reports)
LOW DENSITY LIPOPROTEIN ABNORMAL ( 4 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 4 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 4 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE II ( 4 FDA reports)
MACULAR HOLE ( 4 FDA reports)
MALIGNANT NEOPLASM OF EYE ( 4 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 4 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 4 FDA reports)
MEDIASTINITIS ( 4 FDA reports)
MEIGE'S SYNDROME ( 4 FDA reports)
MENINGITIS LISTERIA ( 4 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 4 FDA reports)
MENINGITIS VIRAL ( 4 FDA reports)
METASTASES TO GASTROINTESTINAL TRACT ( 4 FDA reports)
METASTASES TO RETROPERITONEUM ( 4 FDA reports)
METASTATIC GASTRIC CANCER ( 4 FDA reports)
MIDDLE EAR DISORDER ( 4 FDA reports)
MUSCLE FLAP OPERATION ( 4 FDA reports)
MYCOBACTERIAL INFECTION ( 4 FDA reports)
MYCOBACTERIUM CHELONEI INFECTION ( 4 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 4 FDA reports)
MYELOID LEUKAEMIA ( 4 FDA reports)
MYOSCLEROSIS ( 4 FDA reports)
NAIL INJURY ( 4 FDA reports)
ABDOMINAL EXPLORATION ( 3 FDA reports)
ABDOMINAL HAEMATOMA ( 3 FDA reports)
ABDOMINAL WALL INFECTION ( 3 FDA reports)
ACANTHOLYSIS ( 3 FDA reports)
ACID BASE BALANCE ABNORMAL ( 3 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 3 FDA reports)
ACUTE LUNG INJURY ( 3 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 3 FDA reports)
ADRENAL GLAND INJURY ( 3 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 3 FDA reports)
ALLERGY TO ANIMAL ( 3 FDA reports)
ANAL STENOSIS ( 3 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 3 FDA reports)
ANALGESIC INTERVENTION SUPPORTIVE THERAPY ( 3 FDA reports)
ANAPHYLACTOID SHOCK ( 3 FDA reports)
ANDROGENETIC ALOPECIA ( 3 FDA reports)
ANKLE ARTHROPLASTY ( 3 FDA reports)
ANKYLOGLOSSIA CONGENITAL ( 3 FDA reports)
ANOTIA ( 3 FDA reports)
ANTEROGRADE AMNESIA ( 3 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 3 FDA reports)
ANTIBODY TEST ABNORMAL ( 3 FDA reports)
ANTICHOLINERGIC SYNDROME ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL ABNORMAL ( 3 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 3 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 3 FDA reports)
AORTIC BYPASS ( 3 FDA reports)
AORTIC VALVE DISEASE MIXED ( 3 FDA reports)
APGAR SCORE LOW ( 3 FDA reports)
APNOEIC ATTACK ( 3 FDA reports)
APPENDICEAL ABSCESS ( 3 FDA reports)
ARTERIAL INJURY ( 3 FDA reports)
ARTERIAL STENOSIS LIMB ( 3 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 3 FDA reports)
ARTHROSCOPIC SURGERY ( 3 FDA reports)
ASYMPTOMATIC BACTERIURIA ( 3 FDA reports)
AURICULAR SWELLING ( 3 FDA reports)
AVULSION FRACTURE ( 3 FDA reports)
BACILLUS INFECTION ( 3 FDA reports)
BALANITIS CANDIDA ( 3 FDA reports)
BAND SENSATION ( 3 FDA reports)
BARTHOLIN'S CYST ( 3 FDA reports)
BASOPHIL COUNT DECREASED ( 3 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 3 FDA reports)
BENIGN UTERINE NEOPLASM ( 3 FDA reports)
BILE OUTPUT INCREASED ( 3 FDA reports)
BINOCULAR EYE MOVEMENT DISORDER ( 3 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 3 FDA reports)
BIOPSY LIVER ( 3 FDA reports)
BIOPSY OESOPHAGUS ABNORMAL ( 3 FDA reports)
BIOPSY STOMACH ( 3 FDA reports)
BLADDER CANCER STAGE III ( 3 FDA reports)
BLADDER OPERATION ( 3 FDA reports)
BLADDER STENOSIS ( 3 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 3 FDA reports)
BLEEDING VARICOSE VEIN ( 3 FDA reports)
BLEPHAROPLASTY ( 3 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 3 FDA reports)
BLOOD CHLORIDE ABNORMAL ( 3 FDA reports)
BLOOD CREATINE ABNORMAL ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 3 FDA reports)
BLOOD CREATININE ( 3 FDA reports)
BLOOD ELECTROLYTES INCREASED ( 3 FDA reports)
BLOOD FOLATE DECREASED ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 3 FDA reports)
BLOOD IRON ABNORMAL ( 3 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 3 FDA reports)
BLOOD OSMOLARITY INCREASED ( 3 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 3 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 3 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 3 FDA reports)
BLOOD TRIGLYCERIDES ( 3 FDA reports)
BLUNTED AFFECT ( 3 FDA reports)
BODY DYSMORPHIC DISORDER ( 3 FDA reports)
BONE ABSCESS ( 3 FDA reports)
BONE DENSITY INCREASED ( 3 FDA reports)
BONE INFARCTION ( 3 FDA reports)
BONE MARROW NECROSIS ( 3 FDA reports)
BONE MARROW TUMOUR CELL INFILTRATION ( 3 FDA reports)
BRACHIOCEPHALIC VEIN STENOSIS ( 3 FDA reports)
BREAST ATROPHY ( 3 FDA reports)
BREAST CANCER MALE ( 3 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 3 FDA reports)
BRONCHITIS CHEMICAL ( 3 FDA reports)
BRONCHITIS VIRAL ( 3 FDA reports)
BUDD-CHIARI SYNDROME ( 3 FDA reports)
BURNOUT SYNDROME ( 3 FDA reports)
CANCER PAIN ( 3 FDA reports)
CANDIDA TEST POSITIVE ( 3 FDA reports)
CAPSULE ISSUE ( 3 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 3 FDA reports)
CARDIOSPASM ( 3 FDA reports)
CAROTID ARTERY DISSECTION ( 3 FDA reports)
CAROTID ARTERY INSUFFICIENCY ( 3 FDA reports)
CATHETER SITE HAEMATOMA ( 3 FDA reports)
CD8 LYMPHOCYTES INCREASED ( 3 FDA reports)
CEPHALHAEMATOMA ( 3 FDA reports)
CEREBELLAR ARTERY THROMBOSIS ( 3 FDA reports)
CEREBELLAR ATAXIA ( 3 FDA reports)
CEREBELLAR HAEMORRHAGE ( 3 FDA reports)
CEREBRAL PALSY ( 3 FDA reports)
CEREBROVASCULAR ARTERIOVENOUS MALFORMATION ( 3 FDA reports)
CERVICAL STRICTURE ( 3 FDA reports)
CERVIX INFLAMMATION ( 3 FDA reports)
CHEMICAL PERITONITIS ( 3 FDA reports)
CHOLANGITIS ACUTE ( 3 FDA reports)
CHOLANGITIS SUPPURATIVE ( 3 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 3 FDA reports)
CLEAR CELL CARCINOMA OF THE KIDNEY ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 3 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 3 FDA reports)
COCCIDIOIDOMYCOSIS ( 3 FDA reports)
COLLAGEN-VASCULAR DISEASE ( 3 FDA reports)
COLOBOMA ( 3 FDA reports)
COLONIC FISTULA ( 3 FDA reports)
COMPLEMENT FACTOR ABNORMAL ( 3 FDA reports)
COMPLICATION OF DEVICE REMOVAL ( 3 FDA reports)
COMPLICATIONS OF TRANSPLANTED LUNG ( 3 FDA reports)
CONDUCTIVE DEAFNESS ( 3 FDA reports)
CONGENITAL HYPOTHYROIDISM ( 3 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 3 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 3 FDA reports)
CORNEAL DECOMPENSATION ( 3 FDA reports)
CORONARY ARTERY EMBOLISM ( 3 FDA reports)
CORRECTIVE LENS USER ( 3 FDA reports)
CRANIAL NEUROPATHY ( 3 FDA reports)
CREATININE RENAL CLEARANCE ( 3 FDA reports)
CRUSH INJURY ( 3 FDA reports)
CRYPTOCOCCOSIS ( 3 FDA reports)
CRYSTAL URINE ( 3 FDA reports)
CRYSTALLURIA ( 3 FDA reports)
CSF PRESSURE INCREASED ( 3 FDA reports)
CYANOSIS NEONATAL ( 3 FDA reports)
CYST DRAINAGE ( 3 FDA reports)
CYSTITIS ESCHERICHIA ( 3 FDA reports)
CYTOGENETIC ABNORMALITY ( 3 FDA reports)
DANDRUFF ( 3 FDA reports)
DAYDREAMING ( 3 FDA reports)
DENTAL DISORDER PROPHYLAXIS ( 3 FDA reports)
DEPENDENCE ON RESPIRATOR ( 3 FDA reports)
DEPERSONALISATION ( 3 FDA reports)
DEPRESSION POSTOPERATIVE ( 3 FDA reports)
DERMATITIS EXFOLIATIVE GENERALISED ( 3 FDA reports)
DERMATOSIS ( 3 FDA reports)
DETOXIFICATION ( 3 FDA reports)
DEVELOPMENTAL COORDINATION DISORDER ( 3 FDA reports)
DEVICE ISSUE ( 3 FDA reports)
DIABETIC BLINDNESS ( 3 FDA reports)
DIASTOLIC HYPERTENSION ( 3 FDA reports)
DIHYDROTESTOSTERONE DECREASED ( 3 FDA reports)
DISLOCATION OF VERTEBRA ( 3 FDA reports)
DIURETIC EFFECT ( 3 FDA reports)
DIVERTICULAR FISTULA ( 3 FDA reports)
DOLICHOCOLON ( 3 FDA reports)
DRUG INTERACTION INHIBITION ( 3 FDA reports)
DRUG THERAPY CHANGED ( 3 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 3 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 3 FDA reports)
DUODENAL FISTULA ( 3 FDA reports)
DUODENAL PERFORATION ( 3 FDA reports)
DUPUYTREN'S CONTRACTURE ( 3 FDA reports)
EARLY MORNING AWAKENING ( 3 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
ECZEMA NUMMULAR ( 3 FDA reports)
EJECTION FRACTION ( 3 FDA reports)
ELBOW OPERATION ( 3 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 3 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 3 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 3 FDA reports)
EMPTY SELLA SYNDROME ( 3 FDA reports)
ENCEPHALITIS HERPES ( 3 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 3 FDA reports)
ENDOPHTHALMITIS ( 3 FDA reports)
ENDOSCOPY ABNORMAL ( 3 FDA reports)
ENTERAL NUTRITION ( 3 FDA reports)
EOSINOPHILIC PNEUMONIA ACUTE ( 3 FDA reports)
EPIDERMOLYSIS ( 3 FDA reports)
EPIDERMOLYSIS BULLOSA ( 3 FDA reports)
EPIDURITIS ( 3 FDA reports)
EPIGLOTTITIS ( 3 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 3 FDA reports)
ERYTHRODERMIC PSORIASIS ( 3 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 3 FDA reports)
EXECUTIVE DYSFUNCTION ( 3 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 3 FDA reports)
EXERCISE LACK OF ( 3 FDA reports)
EXPOSURE VIA FATHER ( 3 FDA reports)
EYELID MARGIN CRUSTING ( 3 FDA reports)
FACE AND MOUTH X-RAY ABNORMAL ( 3 FDA reports)
FACIAL SPASM ( 3 FDA reports)
FACIAL WASTING ( 3 FDA reports)
FACTOR V DEFICIENCY ( 3 FDA reports)
FAECAL VOLUME INCREASED ( 3 FDA reports)
FAILURE TO ANASTOMOSE ( 3 FDA reports)
FALSE POSITIVE INVESTIGATION RESULT ( 3 FDA reports)
FASCIECTOMY ( 3 FDA reports)
FAT EMBOLISM ( 3 FDA reports)
FEBRILE CONVULSION ( 3 FDA reports)
FEEDING DISORDER NEONATAL ( 3 FDA reports)
FEELING OF RELAXATION ( 3 FDA reports)
FIBROMUSCULAR DYSPLASIA ( 3 FDA reports)
FLAIL CHEST ( 3 FDA reports)
FLIGHT OF IDEAS ( 3 FDA reports)
FLUID IMBALANCE ( 3 FDA reports)
FLUID INTAKE RESTRICTION ( 3 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III ( 3 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 3 FDA reports)
FUNGAL RASH ( 3 FDA reports)
FUNGUS CULTURE POSITIVE ( 3 FDA reports)
GASTRIC HYPERTONIA ( 3 FDA reports)
GASTRIC ULCER PERFORATION ( 3 FDA reports)
GASTRIC ULCER SURGERY ( 3 FDA reports)
GASTRODUODENAL ULCER ( 3 FDA reports)
GASTROENTERITIS ADENOVIRUS ( 3 FDA reports)
GASTROINTESTINAL ANASTOMOTIC LEAK ( 3 FDA reports)
GASTROINTESTINAL MUCOSAL EXFOLIATION ( 3 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 3 FDA reports)
GENERAL NUTRITION DISORDER ( 3 FDA reports)
GENITAL BURNING SENSATION ( 3 FDA reports)
GENITAL DISCOMFORT ( 3 FDA reports)
GENITAL HAEMORRHAGE ( 3 FDA reports)
GENITAL SWELLING ( 3 FDA reports)
GINGIVAL BLISTER ( 3 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 3 FDA reports)
GLOMERULONEPHROPATHY ( 3 FDA reports)
GRAFT INFECTION ( 3 FDA reports)
GRANULOCYTE COUNT DECREASED ( 3 FDA reports)
GRANULOMA SKIN ( 3 FDA reports)
HAEMOGLOBINURIA ( 3 FDA reports)
HAEMORRHAGIC ASCITES ( 3 FDA reports)
HALLUCINATION, OLFACTORY ( 3 FDA reports)
HAND AMPUTATION ( 3 FDA reports)
HEARING DISABILITY ( 3 FDA reports)
HEART AND LUNG TRANSPLANT ( 3 FDA reports)
HEART VALVE STENOSIS ( 3 FDA reports)
HEMICEPHALALGIA ( 3 FDA reports)
HEPATIC ATROPHY ( 3 FDA reports)
HEPATIC CALCIFICATION ( 3 FDA reports)
HEPATIC ENZYME DECREASED ( 3 FDA reports)
HEPATITIS C VIRUS TEST POSITIVE ( 3 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 3 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 3 FDA reports)
HIP DEFORMITY ( 3 FDA reports)
HIRSUTISM ( 3 FDA reports)
HYPERADRENALISM ( 3 FDA reports)
HYPERAMMONAEMIC ENCEPHALOPATHY ( 3 FDA reports)
HYPERGLYCAEMIC SEIZURE ( 3 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 3 FDA reports)
HYPERINSULINAEMIA ( 3 FDA reports)
HYPERTROPHIC OSTEOARTHROPATHY ( 3 FDA reports)
HYPERVIGILANCE ( 3 FDA reports)
HYPERVOLAEMIA ( 3 FDA reports)
ILEAL PERFORATION ( 3 FDA reports)
ILEAL STENOSIS ( 3 FDA reports)
IMMEDIATE POST-INJECTION REACTION ( 3 FDA reports)
IMPRISONMENT ( 3 FDA reports)
INABILITY TO CRAWL ( 3 FDA reports)
INCISION SITE ABSCESS ( 3 FDA reports)
INCISION SITE HAEMORRHAGE ( 3 FDA reports)
INDUCED LABOUR ( 3 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 3 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 3 FDA reports)
INFERTILITY FEMALE ( 3 FDA reports)
INFLAMMATORY PAIN ( 3 FDA reports)
INFUSION SITE IRRITATION ( 3 FDA reports)
INFUSION SITE URTICARIA ( 3 FDA reports)
INJECTION SITE DISCHARGE ( 3 FDA reports)
INJECTION SITE JOINT REDNESS ( 3 FDA reports)
INJECTION SITE PHLEBITIS ( 3 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 3 FDA reports)
INSULIN RESISTANCE SYNDROME ( 3 FDA reports)
INTERNAL FIXATION OF SPINE ( 3 FDA reports)
INTESTINAL ADENOCARCINOMA ( 3 FDA reports)
INTESTINAL STOMA COMPLICATION ( 3 FDA reports)
INTRACRANIAL TUMOUR HAEMORRHAGE ( 3 FDA reports)
INTRADUCTAL PAPILLOMA OF BREAST ( 3 FDA reports)
INVESTIGATION ABNORMAL ( 3 FDA reports)
IVTH NERVE PARALYSIS ( 3 FDA reports)
KETOSIS ( 3 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 3 FDA reports)
LABORATORY TEST ( 3 FDA reports)
LACRIMATION DECREASED ( 3 FDA reports)
LANGERHANS' CELL GRANULOMATOSIS ( 3 FDA reports)
LAPAROSCOPY ( 3 FDA reports)
LARYNGOTRACHEITIS ( 3 FDA reports)
LAXATIVE ABUSE ( 3 FDA reports)
LDL/HDL RATIO ( 3 FDA reports)
LEGAL PROBLEM ( 3 FDA reports)
LEIOMYOMA ( 3 FDA reports)
LENTICULAR PIGMENTATION ( 3 FDA reports)
LICHEN SCLEROSUS ( 3 FDA reports)
LIMB IMMOBILISATION ( 3 FDA reports)
LIPOMATOSIS ( 3 FDA reports)
LISTERIA SEPSIS ( 3 FDA reports)
LITHOTRIPSY ( 3 FDA reports)
LIVER OPERATION ( 3 FDA reports)
LIVER TENDERNESS ( 3 FDA reports)
LOCAL REACTION ( 3 FDA reports)
LORDOSIS ( 3 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 3 FDA reports)
LYMPHATIC OBSTRUCTION ( 3 FDA reports)
LYMPHOCYTE COUNT ( 3 FDA reports)
LYMPHORRHOEA ( 3 FDA reports)
MACULAR FIBROSIS ( 3 FDA reports)
MACULAR SCAR ( 3 FDA reports)
MACULE ( 3 FDA reports)
MALARIA ( 3 FDA reports)
MALIGNANT ASCITES ( 3 FDA reports)
MATERNAL EXPOSURE BEFORE PREGNANCY ( 3 FDA reports)
MEAN CELL VOLUME DECREASED ( 3 FDA reports)
MEDIAL TIBIAL STRESS SYNDROME ( 3 FDA reports)
MELANODERMIA ( 3 FDA reports)
MENINGITIS BACTERIAL ( 3 FDA reports)
MENINGOENCEPHALITIS HERPETIC ( 3 FDA reports)
MENISCUS REMOVAL ( 3 FDA reports)
MENOPAUSAL DISORDER ( 3 FDA reports)
MENSTRUATION DELAYED ( 3 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 3 FDA reports)
MESENTERIC LYMPHADENOPATHY ( 3 FDA reports)
METASTASES TO THORAX ( 3 FDA reports)
METHAEMOGLOBINAEMIA ( 3 FDA reports)
MINERAL SUPPLEMENTATION ( 3 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 3 FDA reports)
MITRAL VALVE SCLEROSIS ( 3 FDA reports)
MIXED HEPATOCELLULAR-CHOLESTATIC INJURY ( 3 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 3 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 3 FDA reports)
MORPHOEA ( 3 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 3 FDA reports)
MYCETOMA MYCOTIC ( 3 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX IMMUNE RESTORATION DISEASE ( 3 FDA reports)
MYCOPLASMA INFECTION ( 3 FDA reports)
MYOCARDIAL STRAIN ( 3 FDA reports)
MYODESOPSIA ( 3 FDA reports)
MYOPATHY TOXIC ( 3 FDA reports)
NAIL AVULSION ( 3 FDA reports)
NARCOTIC INTOXICATION ( 3 FDA reports)
NASAL INFLAMMATION ( 3 FDA reports)
NECROTISING COLITIS ( 3 FDA reports)
NEONATAL DISORDER ( 3 FDA reports)
NEUROENDOCRINE TUMOUR ( 3 FDA reports)
NIGHT BLINDNESS ( 3 FDA reports)
NIPPLE EXUDATE BLOODY ( 3 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 3 FDA reports)
NORMAL NEWBORN ( 3 FDA reports)
OCULAR MYASTHENIA ( 3 FDA reports)
OLIGODIPSIA ( 3 FDA reports)
ONYCHOGRYPHOSIS ( 3 FDA reports)
OPHTHALMOLOGICAL EXAMINATION ABNORMAL ( 3 FDA reports)
OPTIC NERVE INJURY ( 3 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 3 FDA reports)
OROMANDIBULAR DYSTONIA ( 3 FDA reports)
OSTEOCHONDROMA ( 3 FDA reports)
OVARIAN ADENOMA ( 3 FDA reports)
OVARIAN CANCER RECURRENT ( 3 FDA reports)
OVARIAN EPITHELIAL CANCER ( 3 FDA reports)
OVARIAN GERM CELL TERATOMA BENIGN ( 3 FDA reports)
PALATAL DYSPLASIA ( 3 FDA reports)
PANCREATIC INJURY ( 3 FDA reports)
PARASITIC INFECTION INTESTINAL ( 3 FDA reports)
PARASOMNIA ( 3 FDA reports)
PARATHYROID GLAND OPERATION ( 3 FDA reports)
PASSIVE SMOKING ( 3 FDA reports)
PELVIC INFECTION ( 3 FDA reports)
PENILE DISCHARGE ( 3 FDA reports)
PENILE HAEMORRHAGE ( 3 FDA reports)
PENILE SWELLING ( 3 FDA reports)
PEPTIC ULCER REACTIVATED ( 3 FDA reports)
PERINEAL ABSCESS ( 3 FDA reports)
PERIORBITAL DISORDER ( 3 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 3 FDA reports)
PERIPHLEBITIS ( 3 FDA reports)
PERIRENAL HAEMATOMA ( 3 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 3 FDA reports)
PERONEAL NERVE INJURY ( 3 FDA reports)
PH BODY FLUID ABNORMAL ( 3 FDA reports)
PHARYNGOLARYNGEAL DISCOMFORT ( 3 FDA reports)
PHRENIC NERVE PARALYSIS ( 3 FDA reports)
PICKWICKIAN SYNDROME ( 3 FDA reports)
PITUITARY TUMOUR BENIGN ( 3 FDA reports)
PITYRIASIS ROSEA ( 3 FDA reports)
PLATELET DESTRUCTION INCREASED ( 3 FDA reports)
PLATELET TRANSFUSION ( 3 FDA reports)
PLEOCYTOSIS ( 3 FDA reports)
PLEURAL INFECTION ( 3 FDA reports)
PLEUROPERICARDITIS ( 3 FDA reports)
PNEUMATOSIS ( 3 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 3 FDA reports)
PNEUMOMEDIASTINUM ( 3 FDA reports)
PNEUMONIA ADENOVIRAL ( 3 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 3 FDA reports)
PNEUMONIA MYCOPLASMAL ( 3 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 3 FDA reports)
POIKILOCYTOSIS ( 3 FDA reports)
POLYMENORRHOEA ( 3 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 3 FDA reports)
PORCELAIN GALLBLADDER ( 3 FDA reports)
PORPHYRIA ( 3 FDA reports)
POST POLIO SYNDROME ( 3 FDA reports)
POST-TRAUMATIC PAIN ( 3 FDA reports)
POSTURING ( 3 FDA reports)
PREALBUMIN DECREASED ( 3 FDA reports)
PREMATURE AGEING ( 3 FDA reports)
PROCEDURAL HEADACHE ( 3 FDA reports)
PRODUCT BLISTER PACKAGING ISSUE ( 3 FDA reports)
PRODUCT CONTAMINATION ( 3 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 3 FDA reports)
PRODUCT LABEL ON WRONG PRODUCT ( 3 FDA reports)
PRODUCT OUTER PACKAGING ISSUE ( 3 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 3 FDA reports)
PRODUCT TAMPERING ( 3 FDA reports)
PROLACTINOMA ( 3 FDA reports)
PROLONGED LABOUR ( 3 FDA reports)
PROTEIN C DEFICIENCY ( 3 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 3 FDA reports)
PRURITUS ALLERGIC ( 3 FDA reports)
PSEUDOANGINA ( 3 FDA reports)
PSEUDOFOLLICULITIS BARBAE ( 3 FDA reports)
PULMONARY SEQUESTRATION ( 3 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 3 FDA reports)
PURPURA SENILE ( 3 FDA reports)
RADICAL NECK DISSECTION ( 3 FDA reports)
RECTAL SPASM ( 3 FDA reports)
RED BLOOD CELLS URINE ( 3 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 3 FDA reports)
RELAPSING FEVER ( 3 FDA reports)
RENAL ARTERY OCCLUSION ( 3 FDA reports)
RENAL ARTERY STENT PLACEMENT ( 3 FDA reports)
RENAL CYST HAEMORRHAGE ( 3 FDA reports)
RENAL LIPOMATOSIS ( 3 FDA reports)
RENAL SURGERY ( 3 FDA reports)
RENAL TUBULAR ATROPHY ( 3 FDA reports)
REPRODUCTIVE TRACT DISORDER ( 3 FDA reports)
RESPIRATORY FATIGUE ( 3 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 3 FDA reports)
RETINAL ANEURYSM ( 3 FDA reports)
RETINOPEXY ( 3 FDA reports)
RETROGRADE AMNESIA ( 3 FDA reports)
RHEUMATOID VASCULITIS ( 3 FDA reports)
RIGHT ATRIAL PRESSURE INCREASED ( 3 FDA reports)
SCLERAL DISCOLOURATION ( 3 FDA reports)
SCROTAL OEDEMA ( 3 FDA reports)
SCROTAL PAIN ( 3 FDA reports)
SECONDARY HYPERTENSION ( 3 FDA reports)
SENSORIMOTOR DISORDER ( 3 FDA reports)
SEPTIC ENCEPHALOPATHY ( 3 FDA reports)
SHUNT INFECTION ( 3 FDA reports)
SICKLE CELL ANAEMIA ( 3 FDA reports)
SIMPLE PARTIAL SEIZURES ( 3 FDA reports)
SINUSITIS BACTERIAL ( 3 FDA reports)
SKIN BACTERIAL INFECTION ( 3 FDA reports)
SKIN DEPIGMENTATION ( 3 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, HYPERSOMNIA TYPE ( 3 FDA reports)
SLOW RESPONSE TO STIMULI ( 3 FDA reports)
SMALL INTESTINE OPERATION ( 3 FDA reports)
SMALLPOX ( 3 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 3 FDA reports)
SPERMATOZOA ABNORMAL ( 3 FDA reports)
SPIDER NAEVUS ( 3 FDA reports)
SPLENIC ABSCESS ( 3 FDA reports)
SPUTUM RETENTION ( 3 FDA reports)
STAG HORN CALCULUS ( 3 FDA reports)
STARVATION ( 3 FDA reports)
STENT MALFUNCTION ( 3 FDA reports)
STENT-GRAFT MALFUNCTION ( 3 FDA reports)
STREPTOCOCCAL ABSCESS ( 3 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 3 FDA reports)
STRESS POLYCYTHAEMIA ( 3 FDA reports)
STRESS ULCER ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 3 FDA reports)
TACHYPHYLAXIS ( 3 FDA reports)
TANDEM GAIT TEST ABNORMAL ( 3 FDA reports)
TEMPERATURE REGULATION DISORDER ( 3 FDA reports)
TENDON CALCIFICATION ( 3 FDA reports)
TESTICULAR DISORDER ( 3 FDA reports)
THERAPEUTIC REACTION TIME DECREASED ( 3 FDA reports)
THERMOHYPERAESTHESIA ( 3 FDA reports)
THERMOHYPOAESTHESIA ( 3 FDA reports)
THOUGHT BLOCKING ( 3 FDA reports)
THROMBIN TIME PROLONGED ( 3 FDA reports)
THYROXINE INCREASED ( 3 FDA reports)
TINEA VERSICOLOUR ( 3 FDA reports)
TONGUE ERUPTION ( 3 FDA reports)
TONGUE EXFOLIATION ( 3 FDA reports)
TOXIC SHOCK SYNDROME ( 3 FDA reports)
TRACHEAL STENOSIS ( 3 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 3 FDA reports)
TUBO-OVARIAN ABSCESS ( 3 FDA reports)
TYPE II HYPERLIPIDAEMIA ( 3 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 3 FDA reports)
UNEQUAL LIMB LENGTH ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFECTION BACTERIAL ( 3 FDA reports)
UPPER RESPIRATORY TRACT IRRITATION ( 3 FDA reports)
URAEMIC ENCEPHALOPATHY ( 3 FDA reports)
URETERAL DISORDER ( 3 FDA reports)
URETERIC CANCER ( 3 FDA reports)
URETERIC STENOSIS ( 3 FDA reports)
URINARY RETENTION POSTOPERATIVE ( 3 FDA reports)
URINARY TRACT OBSTRUCTION ( 3 FDA reports)
UTERINE CYST ( 3 FDA reports)
UTERINE PERFORATION ( 3 FDA reports)
VAGINAL CANCER ( 3 FDA reports)
VAGINAL CYST ( 3 FDA reports)
VAGINAL ERYTHEMA ( 3 FDA reports)
VAGINAL LESION ( 3 FDA reports)
VAGINAL PROLAPSE ( 3 FDA reports)
VARICELLA VIRUS TEST POSITIVE ( 3 FDA reports)
VENA CAVA FILTER INSERTION ( 3 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 3 FDA reports)
VENTRICULOPERITONEAL SHUNT MALFUNCTION ( 3 FDA reports)
VERBAL ABUSE ( 3 FDA reports)
VIIITH NERVE LESION ( 3 FDA reports)
VISUAL ACUITY REDUCED TRANSIENTLY ( 3 FDA reports)
VISUAL ACUITY TESTS ABNORMAL ( 3 FDA reports)
VISUAL BRIGHTNESS ( 3 FDA reports)
VITAMIN C DEFICIENCY ( 3 FDA reports)
VOMITING PSYCHOGENIC ( 3 FDA reports)
WARM TYPE HAEMOLYTIC ANAEMIA ( 3 FDA reports)
WHITE BLOOD CELL COUNT ( 3 FDA reports)
WHITE BLOOD CELLS URINE ( 3 FDA reports)
WHITE CLOT SYNDROME ( 3 FDA reports)
WITHDRAWAL BLEEDING IRREGULAR ( 3 FDA reports)
WOUND CLOSURE ( 3 FDA reports)
XEROPHTHALMIA ( 3 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 2 FDA reports)
NERVE DEGENERATION ( 2 FDA reports)
NEURALGIC AMYOTROPHY ( 2 FDA reports)
NEUROFIBROMA ( 2 FDA reports)
NEUROLOGICAL EYELID DISORDER ( 2 FDA reports)
NEUTROPENIC INFECTION ( 2 FDA reports)
NO ADVERSE DRUG EFFECT ( 2 FDA reports)
NON-ALCOHOLIC STEATOHEPATITIS ( 2 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE III ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE IV ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER RECURRENT ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE III ( 2 FDA reports)
NONINFECTIOUS PERITONITIS ( 2 FDA reports)
NUCHAL RIGIDITY ( 2 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 2 FDA reports)
OCCUPATIONAL PHYSICAL PROBLEM ( 2 FDA reports)
OESOPHAGEAL STENT INSERTION ( 2 FDA reports)
OESOPHAGECTOMY ( 2 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 2 FDA reports)
OESOPHAGOBRONCHIAL FISTULA ( 2 FDA reports)
OESOPHAGOGASTRECTOMY ( 2 FDA reports)
OLIGOHYDRAMNIOS ( 2 FDA reports)
OPEN ANGLE GLAUCOMA ( 2 FDA reports)
OPTIC NERVE NEOPLASM ( 2 FDA reports)
ORAL MUCOSAL DISORDER ( 2 FDA reports)
ORGASMIC SENSATION DECREASED ( 2 FDA reports)
OROPHARYNGEAL SURGERY ( 2 FDA reports)
OSCILLOPSIA ( 2 FDA reports)
OSTEOPETROSIS ( 2 FDA reports)
OSTEOTOMY ( 2 FDA reports)
OVARIAN CANCER STAGE III ( 2 FDA reports)
OVARIAN CYST RUPTURED ( 2 FDA reports)
OVARIAN OPERATION ( 2 FDA reports)
OVERLAP SYNDROME ( 2 FDA reports)
OVULATION PAIN ( 2 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 2 FDA reports)
PACEMAKER GENERATED RHYTHM ( 2 FDA reports)
PAINFUL ERECTION ( 2 FDA reports)
PALLIATIVE CARE ( 2 FDA reports)
PANCREAS LIPOMATOSIS ( 2 FDA reports)
PANCREATECTOMY ( 2 FDA reports)
PANCREATIC DUCT OBSTRUCTION ( 2 FDA reports)
PANCREATIC ENLARGEMENT ( 2 FDA reports)
PANCREATIC NECROSIS ( 2 FDA reports)
PANCREATITIS BACTERIAL ( 2 FDA reports)
PANCREATOLITHIASIS ( 2 FDA reports)
PAPILLARY THYROID CANCER ( 2 FDA reports)
PAPILLITIS ( 2 FDA reports)
PARANASAL CYST ( 2 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 2 FDA reports)
PARESIS CRANIAL NERVE ( 2 FDA reports)
PAROTID ABSCESS ( 2 FDA reports)
PARVOVIRUS INFECTION ( 2 FDA reports)
PEDAL PULSE ABNORMAL ( 2 FDA reports)
PELVIC FLOOR DYSSYNERGIA ( 2 FDA reports)
PELVIC HAEMORRHAGE ( 2 FDA reports)
PENILE PROSTHESIS INSERTION ( 2 FDA reports)
PENILE ULCERATION ( 2 FDA reports)
PENIS DEVIATION ( 2 FDA reports)
PEPTOSTREPTOCOCCUS INFECTION ( 2 FDA reports)
PERFUME SENSITIVITY ( 2 FDA reports)
PERICARDIAL CYST ( 2 FDA reports)
PERINEPHRIC COLLECTION ( 2 FDA reports)
PERIPANCREATIC FLUID COLLECTION ( 2 FDA reports)
PERIPHERAL PULSE DECREASED ( 2 FDA reports)
PERITONEAL ABSCESS ( 2 FDA reports)
PERITONEAL CARCINOMA ( 2 FDA reports)
PERITONEAL NEOPLASM ( 2 FDA reports)
PERIVASCULAR DERMATITIS ( 2 FDA reports)
PERSONALITY CHANGE DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
PHANTOM PAIN ( 2 FDA reports)
PHARYNGEAL LEUKOPLAKIA ( 2 FDA reports)
PHARYNX DISCOMFORT ( 2 FDA reports)
PHLEBECTOMY ( 2 FDA reports)
PHLEBOLITH ( 2 FDA reports)
PITUITARY TUMOUR RECURRENT ( 2 FDA reports)
PITYRIASIS RUBRA PILARIS ( 2 FDA reports)
PLASMA PROTEIN METABOLISM DISORDER ( 2 FDA reports)
PLATELET ADHESIVENESS DECREASED ( 2 FDA reports)
PLATELET AGGREGATION ( 2 FDA reports)
PLEURA CARCINOMA ( 2 FDA reports)
PLEURAL CALCIFICATION ( 2 FDA reports)
PLEURAL HAEMORRHAGE ( 2 FDA reports)
PNEUMATURIA ( 2 FDA reports)
PNEUMOBILIA ( 2 FDA reports)
PNEUMONIA SALMONELLA ( 2 FDA reports)
PNEUMONITIS CRYPTOCOCCAL ( 2 FDA reports)
POLYCHROMIC RED BLOOD CELLS PRESENT ( 2 FDA reports)
POLYMYALGIA ( 2 FDA reports)
PORTAL TRIADITIS ( 2 FDA reports)
PORTAL VEIN PHLEBITIS ( 2 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 2 FDA reports)
POST PROCEDURAL DISCHARGE ( 2 FDA reports)
POST PROCEDURAL MYOCARDIAL INFARCTION ( 2 FDA reports)
POSTINFARCTION ANGINA ( 2 FDA reports)
POSTOPERATIVE THORACIC PROCEDURE COMPLICATION ( 2 FDA reports)
PRE-EXISTING DISEASE ( 2 FDA reports)
PRECANCEROUS SKIN LESION ( 2 FDA reports)
PREGNANCY TEST URINE POSITIVE ( 2 FDA reports)
PREMATURE MENOPAUSE ( 2 FDA reports)
PRESBYOESOPHAGUS ( 2 FDA reports)
PRESCRIPTION FORM TAMPERING ( 2 FDA reports)
PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
PROCEDURAL HYPERTENSION ( 2 FDA reports)
PRODUCT LABEL ISSUE ( 2 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 2 FDA reports)
PRODUCT USED FOR UNKNOWN INDICATION ( 2 FDA reports)
PROLONGED EXPIRATION ( 2 FDA reports)
PROSTATE CANCER RECURRENT ( 2 FDA reports)
PROSTATE TENDERNESS ( 2 FDA reports)
PROSTATECTOMY ( 2 FDA reports)
PROSTATIC PAIN ( 2 FDA reports)
PROTEUS TEST POSITIVE ( 2 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 2 FDA reports)
PSEUDOBULBAR PALSY ( 2 FDA reports)
PSEUDODEMENTIA ( 2 FDA reports)
PSEUDODIVERTICULAR DISEASE ( 2 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 2 FDA reports)
PSEUDOPORPHYRIA ( 2 FDA reports)
PSYCHOGENIC PAIN DISORDER ( 2 FDA reports)
PULMONARY NECROSIS ( 2 FDA reports)
PULMONARY SARCOIDOSIS ( 2 FDA reports)
PULMONARY SEPSIS ( 2 FDA reports)
PULMONARY VASCULAR RESISTANCE ABNORMALITY ( 2 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 2 FDA reports)
PURGING ( 2 FDA reports)
PURPURA NON-THROMBOCYTOPENIC ( 2 FDA reports)
RADIAL NERVE INJURY ( 2 FDA reports)
RASH SCARLATINIFORM ( 2 FDA reports)
REACTION TO COLOURING ( 2 FDA reports)
RECURRING SKIN BOILS ( 2 FDA reports)
RED BLOOD CELL TARGET CELLS PRESENT ( 2 FDA reports)
REFLEX SYMPATHETIC DYSTROPHY ( 2 FDA reports)
REFRACTION DISORDER ( 2 FDA reports)
REFUSAL OF EXAMINATION ( 2 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 2 FDA reports)
RENAL CELL CARCINOMA RECURRENT ( 2 FDA reports)
RENAL CELL CARCINOMA STAGE II ( 2 FDA reports)
RENAL CELL CARCINOMA STAGE IV ( 2 FDA reports)
RENAL FAILURE NEONATAL ( 2 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 2 FDA reports)
RENAL NECROSIS ( 2 FDA reports)
RENAL OSTEODYSTROPHY ( 2 FDA reports)
RESIDUAL URINE VOLUME ( 2 FDA reports)
RESPIRATORY FUME INHALATION DISORDER ( 2 FDA reports)
RESPIRATORY PARALYSIS ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS TEST POSITIVE ( 2 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 2 FDA reports)
RETINAL ARTERY EMBOLISM ( 2 FDA reports)
RETINAL ARTERY STENOSIS ( 2 FDA reports)
RETINAL INFARCTION ( 2 FDA reports)
RETINAL PIGMENTATION ( 2 FDA reports)
RETINAL VEIN THROMBOSIS ( 2 FDA reports)
RETINOIC ACID SYNDROME ( 2 FDA reports)
RETINOPATHY HYPERTENSIVE ( 2 FDA reports)
RETROGRADE PORTAL VEIN FLOW ( 2 FDA reports)
RETROPERITONEAL NEOPLASM ( 2 FDA reports)
REVERSIBLE AIRWAYS OBSTRUCTION ( 2 FDA reports)
RICKETS ( 2 FDA reports)
RUPTURED ECTOPIC PREGNANCY ( 2 FDA reports)
SALIVA DISCOLOURATION ( 2 FDA reports)
SALPINGITIS ( 2 FDA reports)
SCAN LYMPH NODES ( 2 FDA reports)
SCHAMBERG'S DISEASE ( 2 FDA reports)
SCHIZOAFFECTIVE DISORDER BIPOLAR TYPE ( 2 FDA reports)
SCHIZOID PERSONALITY DISORDER ( 2 FDA reports)
SCIATIC NERVE NEUROPATHY ( 2 FDA reports)
SCLERAL DISORDER ( 2 FDA reports)
SCLEROEDEMA ( 2 FDA reports)
SCROTAL DISORDER ( 2 FDA reports)
SECONDARY HYPERTHYROIDISM ( 2 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 2 FDA reports)
SECONDARY PROGRESSIVE MULTIPLE SCLEROSIS ( 2 FDA reports)
SEPTIC ARTHRITIS STREPTOCOCCAL ( 2 FDA reports)
SERRATIA TEST POSITIVE ( 2 FDA reports)
SEXUAL RELATIONSHIP CHANGE ( 2 FDA reports)
SHOULDER DEFORMITY ( 2 FDA reports)
SHUNT OCCLUSION ( 2 FDA reports)
SIGHT DISABILITY ( 2 FDA reports)
SIGMOIDECTOMY ( 2 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 2 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 2 FDA reports)
SINUS PAIN ( 2 FDA reports)
SINUSITIS FUNGAL ( 2 FDA reports)
SKIN DISCOMFORT ( 2 FDA reports)
SKIN GRAFT FAILURE ( 2 FDA reports)
SKIN INFLAMMATION ( 2 FDA reports)
SLEEP ATTACKS ( 2 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 2 FDA reports)
SOCIAL PHOBIA ( 2 FDA reports)
SPEECH REHABILITATION ( 2 FDA reports)
SPINAL CORD HERNIATION ( 2 FDA reports)
SPINAL CORD ISCHAEMIA ( 2 FDA reports)
SPINAL MENINGEAL CYST ( 2 FDA reports)
SPLEEN CONGESTION ( 2 FDA reports)
SPLEEN PALPABLE ( 2 FDA reports)
SPLENIC NECROSIS ( 2 FDA reports)
SPLINTER HAEMORRHAGES ( 2 FDA reports)
SPUTUM ABNORMAL ( 2 FDA reports)
STAB WOUND ( 2 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 2 FDA reports)
STRESS AT WORK ( 2 FDA reports)
SUBACUTE ENDOCARDITIS ( 2 FDA reports)
SUBCLAVIAN ARTERY THROMBOSIS ( 2 FDA reports)
SUBDURAL HYGROMA ( 2 FDA reports)
SUBSTANCE-INDUCED PSYCHOTIC DISORDER ( 2 FDA reports)
SUPERIOR VENA CAVAL STENOSIS ( 2 FDA reports)
SWAN GANZ CATHETER PLACEMENT ( 2 FDA reports)
SWEAT DISCOLOURATION ( 2 FDA reports)
SWEAT GLAND INFECTION ( 2 FDA reports)
SYNOVIAL FLUID RED BLOOD CELLS POSITIVE ( 2 FDA reports)
SYNOVIAL FLUID WHITE BLOOD CELLS POSITIVE ( 2 FDA reports)
SYSTEMIC MYCOSIS ( 2 FDA reports)
SYSTOLIC HYPERTENSION ( 2 FDA reports)
T-CELL TYPE ACUTE LEUKAEMIA ( 2 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
TEETHING ( 2 FDA reports)
TEMPORAL LOBE EPILEPSY ( 2 FDA reports)
TESTICULAR FAILURE ( 2 FDA reports)
TESTIS DISCOMFORT ( 2 FDA reports)
THANATOPHOBIA ( 2 FDA reports)
THREATENED LABOUR ( 2 FDA reports)
THROMBOANGIITIS OBLITERANS ( 2 FDA reports)
THROMBOEMBOLECTOMY ( 2 FDA reports)
THROMBOLYSIS ( 2 FDA reports)
THROMBOSIS MESENTERIC VESSEL ( 2 FDA reports)
THYROID ADENOMA ( 2 FDA reports)
THYROID GLAND CANCER ( 2 FDA reports)
THYROXINE FREE DECREASED ( 2 FDA reports)
TONGUE CARCINOMA STAGE IV ( 2 FDA reports)
TOOTH MALFORMATION ( 2 FDA reports)
TOXIC NODULAR GOITRE ( 2 FDA reports)
TOXOPLASMA SEROLOGY POSITIVE ( 2 FDA reports)
TOXOPLASMOSIS ( 2 FDA reports)
TRANSAMINASES ABNORMAL ( 2 FDA reports)
TRANSFUSION RELATED COMPLICATION ( 2 FDA reports)
TRANSFUSION-RELATED CIRCULATORY OVERLOAD ( 2 FDA reports)
TRANSIENT TACHYPNOEA OF THE NEWBORN ( 2 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 2 FDA reports)
TRAUMATIC ARTHRITIS ( 2 FDA reports)
TRAUMATIC LIVER INJURY ( 2 FDA reports)
TRAUMATIC ULCER ( 2 FDA reports)
TRICHOMONIASIS ( 2 FDA reports)
TRICHOPHYTIC GRANULOMA ( 2 FDA reports)
TRYPTASE INCREASED ( 2 FDA reports)
TUBERCULOSIS SKIN TEST POSITIVE ( 2 FDA reports)
TUBERCULOUS PLEURISY ( 2 FDA reports)
TUMOUR PERFORATION ( 2 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 2 FDA reports)
TYPE IV HYPERLIPIDAEMIA ( 2 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 2 FDA reports)
UHTHOFF'S PHENOMENON ( 2 FDA reports)
ULTRASOUND SCAN ( 2 FDA reports)
UMBILICAL HERNIA PERFORATION ( 2 FDA reports)
UPPER MOTOR NEURONE LESION ( 2 FDA reports)
UPPER RESPIRATORY FUNGAL INFECTION ( 2 FDA reports)
URETERIC ANASTOMOSIS COMPLICATION ( 2 FDA reports)
URETERIC DIVERSION OPERATION ( 2 FDA reports)
URETHRAL DILATATION ( 2 FDA reports)
URETHRAL INJURY ( 2 FDA reports)
URINARY BLADDER RUPTURE ( 2 FDA reports)
URINARY CASTS ( 2 FDA reports)
URINE SODIUM INCREASED ( 2 FDA reports)
UTERINE FIBROSIS ( 2 FDA reports)
VACUUM EXTRACTOR DELIVERY ( 2 FDA reports)
VAGINAL INFLAMMATION ( 2 FDA reports)
VAGINAL LACERATION ( 2 FDA reports)
VAGINAL ODOUR ( 2 FDA reports)
VAGINAL ULCERATION ( 2 FDA reports)
VAGINITIS ( 2 FDA reports)
VASCULAR ENCEPHALOPATHY ( 2 FDA reports)
VASCULAR GRAFT COMPLICATION ( 2 FDA reports)
VASCULAR SKIN DISORDER ( 2 FDA reports)
VASOMOTOR RHINITIS ( 2 FDA reports)
VEILLONELLA INFECTION ( 2 FDA reports)
VENOUS ANEURYSM ( 2 FDA reports)
VENOUS OPERATION ( 2 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 2 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 2 FDA reports)
VESSEL PUNCTURE SITE HAEMORRHAGE ( 2 FDA reports)
VESTIBULITIS ( 2 FDA reports)
VIRAEMIA ( 2 FDA reports)
VIRAL DIARRHOEA ( 2 FDA reports)
VIRAL RASH ( 2 FDA reports)
VISUAL EVOKED POTENTIALS ABNORMAL ( 2 FDA reports)
VITAMIN E DEFICIENCY ( 2 FDA reports)
VITAMIN K DEFICIENCY ( 2 FDA reports)
VITH NERVE DISORDER ( 2 FDA reports)
VITRECTOMY ( 2 FDA reports)
VITRITIS ( 2 FDA reports)
VON HIPPEL-LINDAU DISEASE ( 2 FDA reports)
VULVECTOMY ( 2 FDA reports)
WEANING FAILURE ( 2 FDA reports)
WHITE BLOOD CELL DISORDER ( 2 FDA reports)
WHOLE BLOOD TRANSFUSION ( 2 FDA reports)
WOUND EVISCERATION ( 2 FDA reports)
WOUND NECROSIS ( 2 FDA reports)
WOUND SEPSIS ( 2 FDA reports)
WRIST DEFORMITY ( 2 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 2 FDA reports)
XANTHOPSIA ( 2 FDA reports)
ZINC DEFICIENCY ( 2 FDA reports)
5-HYDROXYINDOLACETIC ACID IN URINE INCREASED ( 2 FDA reports)
ABDOMINAL HERNIA OBSTRUCTIVE ( 2 FDA reports)
ABORTION THREATENED ( 2 FDA reports)
ABSCESS BACTERIAL ( 2 FDA reports)
ABSCESS RUPTURE ( 2 FDA reports)
ACQUIRED HAEMOPHILIA ( 2 FDA reports)
ACTH STIMULATION TEST ABNORMAL ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 2 FDA reports)
ACUTE PHOSPHATE NEPHROPATHY ( 2 FDA reports)
ACUTE PULMONARY HISTOPLASMOSIS ( 2 FDA reports)
ACUTE TONSILLITIS ( 2 FDA reports)
ADENOCARCINOMA OF THE CERVIX ( 2 FDA reports)
ADIPOSIS DOLOROSA ( 2 FDA reports)
ADNEXA UTERI PAIN ( 2 FDA reports)
AEROMONA INFECTION ( 2 FDA reports)
AIR EMBOLISM ( 2 FDA reports)
ALCOHOLIC ( 2 FDA reports)
ALCOHOLIC LIVER DISEASE ( 2 FDA reports)
ALCOHOLIC PANCREATITIS ( 2 FDA reports)
ALLERGY TO VACCINE ( 2 FDA reports)
ALPHA 2 GLOBULIN INCREASED ( 2 FDA reports)
ANAEMIA FOLATE DEFICIENCY ( 2 FDA reports)
ANAESTHESIA ( 2 FDA reports)
ANAPLASTIC ASTROCYTOMA ( 2 FDA reports)
ANASTOMOTIC ULCER HAEMORRHAGE ( 2 FDA reports)
ANEURYSM REPAIR ( 2 FDA reports)
ANGIOIMMUNOBLASTIC T-CELL LYMPHOMA ( 2 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INCREASED ( 2 FDA reports)
ANIMAL SCRATCH ( 2 FDA reports)
ANOMALOUS PULMONARY VENOUS CONNECTION ( 2 FDA reports)
ANORECTAL INFECTION ( 2 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 2 FDA reports)
ANTERIOR CHAMBER DISORDER ( 2 FDA reports)
ANTERIOR CHAMBER INFLAMMATION ( 2 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 2 FDA reports)
ANTI-SS-A ANTIBODY POSITIVE ( 2 FDA reports)
ANTITHROMBIN III INCREASED ( 2 FDA reports)
APICAL GRANULOMA ( 2 FDA reports)
APPLICATION SITE ANAESTHESIA ( 2 FDA reports)
APPLICATION SITE BLEEDING ( 2 FDA reports)
APPLICATION SITE DRYNESS ( 2 FDA reports)
APPLICATION SITE HAEMATOMA ( 2 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 2 FDA reports)
APPLICATION SITE OEDEMA ( 2 FDA reports)
APPLICATION SITE SCAB ( 2 FDA reports)
APPLICATION SITE SCAR ( 2 FDA reports)
ARTERECTOMY ( 2 FDA reports)
ARTERIAL RESTENOSIS ( 2 FDA reports)
ARTERIOVENOUS GRAFT SITE ABSCESS ( 2 FDA reports)
ATHETOSIS ( 2 FDA reports)
ATRIAL HYPERTROPHY ( 2 FDA reports)
ATTENTION-SEEKING BEHAVIOUR ( 2 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 2 FDA reports)
AURICULAR PERICHONDRITIS ( 2 FDA reports)
AZYGOS LOBE ( 2 FDA reports)
B-CELL LYMPHOMA STAGE I ( 2 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA STAGE IV ( 2 FDA reports)
BACK CRUSHING ( 2 FDA reports)
BACTERIAL CULTURE POSITIVE ( 2 FDA reports)
BANDAEMIA ( 2 FDA reports)
BASILAR ARTERY OCCLUSION ( 2 FDA reports)
BASOPHIL COUNT INCREASED ( 2 FDA reports)
BENIGN NEOPLASM OF BLADDER ( 2 FDA reports)
BENIGN SPLEEN TUMOUR ( 2 FDA reports)
BETA-2 GLYCOPROTEIN ANTIBODY POSITIVE ( 2 FDA reports)
BILE OUTPUT ABNORMAL ( 2 FDA reports)
BILIARY ANASTOMOSIS COMPLICATION ( 2 FDA reports)
BILIARY FIBROSIS ( 2 FDA reports)
BILIRUBIN CONJUGATED ( 2 FDA reports)
BIOPSY KIDNEY ( 2 FDA reports)
BIOPSY STOMACH ABNORMAL ( 2 FDA reports)
BITE ( 2 FDA reports)
BLADDER NECK OBSTRUCTION ( 2 FDA reports)
BLEPHARAL PIGMENTATION ( 2 FDA reports)
BLISTER INFECTED ( 2 FDA reports)
BLOOD ACID PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD BICARBONATE ABNORMAL ( 2 FDA reports)
BLOOD CALCIUM ( 2 FDA reports)
BLOOD CATECHOLAMINES INCREASED ( 2 FDA reports)
BLOOD CORTISOL INCREASED ( 2 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 2 FDA reports)
BLOOD KETONE BODY PRESENT ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 2 FDA reports)
BLOOD MAGNESIUM ( 2 FDA reports)
BLOOD OESTROGEN INCREASED ( 2 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 2 FDA reports)
BLOOD SODIUM ( 2 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO DECREASED ( 2 FDA reports)
BLUE TOE SYNDROME ( 2 FDA reports)
BONE CALLUS EXCESSIVE ( 2 FDA reports)
BONE MARROW BASOPHILIC LEUKOCYTE COUNT INCREASED ( 2 FDA reports)
BORRELIA TEST POSITIVE ( 2 FDA reports)
BRACHIAL PLEXUS INJURY ( 2 FDA reports)
BRAIN STEM ISCHAEMIA ( 2 FDA reports)
BREAST COSMETIC SURGERY ( 2 FDA reports)
BREAST ENGORGEMENT ( 2 FDA reports)
BREAST HAEMORRHAGE ( 2 FDA reports)
BREAST INFECTION ( 2 FDA reports)
BREAST NEOPLASM ( 2 FDA reports)
BRIEF PSYCHOTIC DISORDER WITH MARKED STRESSORS ( 2 FDA reports)
BRONCHIAL HYPERACTIVITY ( 2 FDA reports)
BRONCHIAL INJURY ( 2 FDA reports)
BRONCHIAL IRRITATION ( 2 FDA reports)
BRONCHIAL NEOPLASM ( 2 FDA reports)
BRONCHOALVEOLAR LAVAGE ( 2 FDA reports)
BRONCHOSCOPY ( 2 FDA reports)
BRONCHOSCOPY NORMAL ( 2 FDA reports)
BRONCHOSTENOSIS ( 2 FDA reports)
BRUGADA SYNDROME ( 2 FDA reports)
BUNION OPERATION ( 2 FDA reports)
BURKITT'S LYMPHOMA ( 2 FDA reports)
BURN OF INTERNAL ORGANS ( 2 FDA reports)
BURNING FEET SYNDROME ( 2 FDA reports)
BURSA DISORDER ( 2 FDA reports)
C-REACTIVE PROTEIN ( 2 FDA reports)
CALCIUM IONISED DECREASED ( 2 FDA reports)
CARBOHYDRATE METABOLISM DISORDER ( 2 FDA reports)
CARCINOID TUMOUR OF THE GASTROINTESTINAL TRACT ( 2 FDA reports)
CARDIAC ASTHMA ( 2 FDA reports)
CARDIAC FAILURE HIGH OUTPUT ( 2 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 2 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 2 FDA reports)
CARDIOMYOPATHY ALCOHOLIC ( 2 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 2 FDA reports)
CATARACT DIABETIC ( 2 FDA reports)
CATHETER SITE DISCHARGE ( 2 FDA reports)
CATHETER SITE SWELLING ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 2 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 2 FDA reports)
CEREBRAL FUNGAL INFECTION ( 2 FDA reports)
CEREBRAL MALARIA ( 2 FDA reports)
CEREBROSPINAL FISTULA ( 2 FDA reports)
CEREBROSPINAL FLUID DRAINAGE ( 2 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 2 FDA reports)
CERVIX CANCER METASTATIC ( 2 FDA reports)
CHEST EXPANSION DECREASED ( 2 FDA reports)
CHEST WALL CYST ( 2 FDA reports)
CHEYNE-STOKES RESPIRATION ( 2 FDA reports)
CHOLANGIOLITIS ( 2 FDA reports)
CHOLELITHIASIS OBSTRUCTIVE ( 2 FDA reports)
CHORIORETINITIS ( 2 FDA reports)
CHOROIDAL HAEMORRHAGE ( 2 FDA reports)
CLEFT LIP ( 2 FDA reports)
CLEFT PALATE ( 2 FDA reports)
CLONIC CONVULSION ( 2 FDA reports)
CLOSED FRACTURE MANIPULATION ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST ( 2 FDA reports)
CLUBBING ( 2 FDA reports)
CNS VENTRICULITIS ( 2 FDA reports)
COGAN'S SYNDROME ( 2 FDA reports)
COITAL BLEEDING ( 2 FDA reports)
COLECTOMY PARTIAL ( 2 FDA reports)
COLONIC ATONY ( 2 FDA reports)
COLONIC HAEMORRHAGE ( 2 FDA reports)
COLORECTOSTOMY ( 2 FDA reports)
COMPLICATED MIGRAINE ( 2 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 2 FDA reports)
COMPUTERISED TOMOGRAM ( 2 FDA reports)
CONGENITAL ANOMALY ( 2 FDA reports)
CONGENITAL EYE NAEVUS ( 2 FDA reports)
CONGENITAL PYLORIC STENOSIS ( 2 FDA reports)
CONGENITAL RENAL DISORDER ( 2 FDA reports)
CONJUNCTIVAL CYST ( 2 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 2 FDA reports)
CONSTRICTED AFFECT ( 2 FDA reports)
CONTRACTED BLADDER ( 2 FDA reports)
CONTRALATERAL BREAST CANCER ( 2 FDA reports)
CONTRAST MEDIA ALLERGY ( 2 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 2 FDA reports)
COPPER METABOLISM DISORDER ( 2 FDA reports)
CORNEAL INFECTION ( 2 FDA reports)
CORNEAL OPACITY ( 2 FDA reports)
CORNEAL REFLEX DECREASED ( 2 FDA reports)
CORONARY ARTERY PERFORATION ( 2 FDA reports)
CORONARY OSTIAL STENOSIS ( 2 FDA reports)
CORONARY REVASCULARISATION ( 2 FDA reports)
CORYNEBACTERIUM INFECTION ( 2 FDA reports)
CRANIAL NERVE OPERATION ( 2 FDA reports)
CREUTZFELDT-JAKOB DISEASE ( 2 FDA reports)
CROSS SENSITIVITY REACTION ( 2 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 2 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 2 FDA reports)
CRYSTAL URINE PRESENT ( 2 FDA reports)
CSF SHUNT OPERATION ( 2 FDA reports)
CUTIS LAXA ( 2 FDA reports)
CYCLOTHYMIC DISORDER ( 2 FDA reports)
CYSTIC FIBROSIS ( 2 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 2 FDA reports)
DACRYOCYSTITIS ( 2 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 2 FDA reports)
DEAFNESS TRAUMATIC ( 2 FDA reports)
DEATH OF PARENT ( 2 FDA reports)
DECEREBRATION ( 2 FDA reports)
DECREASED INSULIN REQUIREMENT ( 2 FDA reports)
DEGENERATION OF UTERINE FIBROID ( 2 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 2 FDA reports)
DELAYED SLEEP PHASE ( 2 FDA reports)
DENERVATION ATROPHY ( 2 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 2 FDA reports)
DERMATITIS HERPETIFORMIS ( 2 FDA reports)
DERMATITIS INFECTED ( 2 FDA reports)
DESMOID TUMOUR ( 2 FDA reports)
DEVICE MIGRATION ( 2 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 2 FDA reports)
DIABETIC CARDIOMYOPATHY ( 2 FDA reports)
DIABETIC ENTEROPATHY ( 2 FDA reports)
DIABETIC FOOT INFECTION ( 2 FDA reports)
DIABETIC VASCULAR DISORDER ( 2 FDA reports)
DIAGNOSTIC PROCEDURE ( 2 FDA reports)
DIAPHRAGMALGIA ( 2 FDA reports)
DIET NONCOMPLIANCE ( 2 FDA reports)
DIGITAL ULCER ( 2 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 2 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 2 FDA reports)
DIVERTICULECTOMY ( 2 FDA reports)
DIVERTICULUM DUODENAL ( 2 FDA reports)
DIZZINESS EXERTIONAL ( 2 FDA reports)
DOUBLE STRANDED DNA ANTIBODY ( 2 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 2 FDA reports)
DUBIN-JOHNSON SYNDROME ( 2 FDA reports)
DUODENAL NEOPLASM ( 2 FDA reports)
DUODENITIS HAEMORRHAGIC ( 2 FDA reports)
DYSGLOBULINAEMIA ( 2 FDA reports)
DYSPRAXIA ( 2 FDA reports)
EAR INFECTION FUNGAL ( 2 FDA reports)
EAR INJURY ( 2 FDA reports)
EAR TUBE INSERTION ( 2 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 2 FDA reports)
EMERGENCY CARE ( 2 FDA reports)
ENCEPHALITIS CYTOMEGALOVIRUS ( 2 FDA reports)
ENDOMETRIAL CANCER RECURRENT ( 2 FDA reports)
ENDOMETRIAL CANCER STAGE I ( 2 FDA reports)
ENDOSCOPY GASTROINTESTINAL ( 2 FDA reports)
EOSINOPHILIC COLITIS ( 2 FDA reports)
EOSINOPHILIC OESOPHAGITIS ( 2 FDA reports)
EPIDIDYMAL CYST ( 2 FDA reports)
EPIDURAL ANAESTHESIA ( 2 FDA reports)
EPIGLOTTIC OEDEMA ( 2 FDA reports)
EPSTEIN-BARR VIRUS ANTIGEN POSITIVE ( 2 FDA reports)
ERECTION INCREASED ( 2 FDA reports)
EUSTACHIAN TUBE OBSTRUCTION ( 2 FDA reports)
EXAGGERATED STARTLE RESPONSE ( 2 FDA reports)
EXERCISE TEST ABNORMAL ( 2 FDA reports)
EXPOSURE TO MOULD ( 2 FDA reports)
EXSANGUINATION ( 2 FDA reports)
EYE DEGENERATIVE DISORDER ( 2 FDA reports)
EYE INFECTION TOXOPLASMAL ( 2 FDA reports)
EYE OPERATION COMPLICATION ( 2 FDA reports)
EYE REDNESS ( 2 FDA reports)
EYELASH THICKENING ( 2 FDA reports)
EYELID CYST ( 2 FDA reports)
EYELID TUMOUR ( 2 FDA reports)
FACE CRUSHING ( 2 FDA reports)
FACIAL ASYMMETRY ( 2 FDA reports)
FALLOPIAN TUBE CYST ( 2 FDA reports)
FALLOPIAN TUBE DISORDER ( 2 FDA reports)
FEAR OF EATING ( 2 FDA reports)
FEBRILE NONHAEMOLYTIC TRANSFUSION REACTION ( 2 FDA reports)
FIBRINOLYSIS INCREASED ( 2 FDA reports)
FIBROADENOMA OF BREAST ( 2 FDA reports)
FLAT ANTERIOR CHAMBER OF EYE ( 2 FDA reports)
FLAVOBACTERIUM INFECTION ( 2 FDA reports)
FLUCTUANCE ( 2 FDA reports)
FOETAL HEART RATE ABNORMAL ( 2 FDA reports)
FRACTURE TREATMENT ( 2 FDA reports)
FRONTAL SINUS OPERATION ( 2 FDA reports)
FUMBLING ( 2 FDA reports)
FUNGAL TEST POSITIVE ( 2 FDA reports)
GAIT SPASTIC ( 2 FDA reports)
GALLBLADDER FISTULA ( 2 FDA reports)
GASTRIC ADENOMA ( 2 FDA reports)
GASTRIC CANCER STAGE IV ( 2 FDA reports)
GASTRO-JEJUNOSTOMY ( 2 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 2 FDA reports)
GASTROENTERITIS EOSINOPHILIC ( 2 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 2 FDA reports)
GASTROINTESTINAL DISORDER POSTOPERATIVE ( 2 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL TRACT MUCOSAL PIGMENTATION ( 2 FDA reports)
GASTROINTESTINAL ULCER PERFORATION ( 2 FDA reports)
GASTROOESOPHAGEAL CANCER ( 2 FDA reports)
GASTROSTOMY FAILURE ( 2 FDA reports)
GENITAL INFECTION FUNGAL ( 2 FDA reports)
GENITAL NEOPLASM MALIGNANT FEMALE ( 2 FDA reports)
GENITAL TRACT INFLAMMATION ( 2 FDA reports)
GEOTRICHUM INFECTION ( 2 FDA reports)
GESTATIONAL HYPERTENSION ( 2 FDA reports)
GINGIVAL ABSCESS ( 2 FDA reports)
GINGIVAL OEDEMA ( 2 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 2 FDA reports)
GLAUCOMA SURGERY ( 2 FDA reports)
GLOBULINS DECREASED ( 2 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 2 FDA reports)
GLOMERULOSCLEROSIS ( 2 FDA reports)
GLOMUS TUMOUR ( 2 FDA reports)
GLOSSOPHARYNGEAL NEURALGIA ( 2 FDA reports)
GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY ( 2 FDA reports)
GOUTY TOPHUS ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE IN INTESTINE ( 2 FDA reports)
GRANULOCYTOSIS ( 2 FDA reports)
GROWTH OF EYELASHES ( 2 FDA reports)
HAEMATOCRIT ABNORMAL ( 2 FDA reports)
HAEMATOCRIT INCREASED ( 2 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 2 FDA reports)
HAEMATOMA EVACUATION ( 2 FDA reports)
HAEMATOPOIETIC NEOPLASM ( 2 FDA reports)
HAEMATOTOXICITY ( 2 FDA reports)
HAEMOPHILIA ( 2 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 2 FDA reports)
HAPTOGLOBIN ( 2 FDA reports)
HEART BLOCK CONGENITAL ( 2 FDA reports)
HEMIANOPIA HETERONYMOUS ( 2 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 2 FDA reports)
HEPATITIS B POSITIVE ( 2 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 2 FDA reports)
HEREDITARY HAEMORRHAGIC TELANGIECTASIA ( 2 FDA reports)
HERPES OESOPHAGITIS ( 2 FDA reports)
HETEROPHORIA ( 2 FDA reports)
HIGH RISK PREGNANCY ( 2 FDA reports)
HIGH TURNOVER OSTEOPATHY ( 2 FDA reports)
HIV WASTING SYNDROME ( 2 FDA reports)
HLA MARKER STUDY POSITIVE ( 2 FDA reports)
HOFFMANN'S SIGN ( 2 FDA reports)
HUMAN BITE ( 2 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 2 FDA reports)
HUNTINGTON'S DISEASE ( 2 FDA reports)
HYPERBILIRUBINAEMIA NEONATAL ( 2 FDA reports)
HYPERCALCIURIA ( 2 FDA reports)
HYPERCAPNIC ENCEPHALOPATHY ( 2 FDA reports)
HYPEREMESIS GRAVIDARUM ( 2 FDA reports)
HYPERLIPASAEMIA ( 2 FDA reports)
HYPEROSMOLAR STATE ( 2 FDA reports)
HYPERVISCOSITY SYNDROME ( 2 FDA reports)
HYPHAEMA ( 2 FDA reports)
HYPOAESTHESIA EYE ( 2 FDA reports)
HYPOALDOSTERONISM ( 2 FDA reports)
HYPOCAPNIA ( 2 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 2 FDA reports)
HYPOHIDROSIS ( 2 FDA reports)
HYPOMETABOLISM ( 2 FDA reports)
ILIAC VEIN OCCLUSION ( 2 FDA reports)
IMMUNISATION REACTION ( 2 FDA reports)
IMPINGEMENT SYNDROME ( 2 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 2 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 2 FDA reports)
IN-STENT ARTERIAL RESTENOSIS ( 2 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 2 FDA reports)
INCISION SITE ERYTHEMA ( 2 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 2 FDA reports)
INDIFFERENCE ( 2 FDA reports)
INFECTED BUNION ( 2 FDA reports)
INFECTED DERMAL CYST ( 2 FDA reports)
INFECTED INSECT BITE ( 2 FDA reports)
INFECTION PARASITIC ( 2 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 2 FDA reports)
INFLAMMATION LOCALISED ( 2 FDA reports)
INFLAMMATORY CARCINOMA OF THE BREAST ( 2 FDA reports)
INFLUENZA VIRUS TEST POSITIVE ( 2 FDA reports)
INFUSION SITE BRUISING ( 2 FDA reports)
INFUSION SITE INDURATION ( 2 FDA reports)
INFUSION SITE OEDEMA ( 2 FDA reports)
INFUSION SITE PHLEBITIS ( 2 FDA reports)
INFUSION SITE ULCER ( 2 FDA reports)
INJECTION SITE CYST ( 2 FDA reports)
INJECTION SITE DERMATITIS ( 2 FDA reports)
INJECTION SITE HYPERSENSITIVITY ( 2 FDA reports)
INJECTION SITE INJURY ( 2 FDA reports)
INJECTION SITE MACULE ( 2 FDA reports)
INJECTION SITE PALLOR ( 2 FDA reports)
INJECTION SITE PARAESTHESIA ( 2 FDA reports)
INJECTION SITE SCAR ( 2 FDA reports)
INJECTION SITE STREAKING ( 2 FDA reports)
INSULIN RESISTANT DIABETES ( 2 FDA reports)
INSULINOMA ( 2 FDA reports)
INTENSIVE CARE ( 2 FDA reports)
INTERCAPILLARY GLOMERULOSCLEROSIS ( 2 FDA reports)
INTERMEDIATE DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
INTERMITTENT EXPLOSIVE DISORDER ( 2 FDA reports)
INTESTINAL ANASTOMOSIS ( 2 FDA reports)
INTESTINAL MUCOSAL ATROPHY ( 2 FDA reports)
INTRA-AORTIC BALLOON PLACEMENT ( 2 FDA reports)
INTRADUCTAL PAPILLARY MUCINOUS NEOPLASM ( 2 FDA reports)
INTRAOCULAR MELANOMA ( 2 FDA reports)
INTRAOCULAR PRESSURE DECREASED ( 2 FDA reports)
IRIS CYST ( 2 FDA reports)
IUCD COMPLICATION ( 2 FDA reports)
JEJUNAL ULCER ( 2 FDA reports)
JOINT INJECTION ( 2 FDA reports)
KERATOACANTHOMA ( 2 FDA reports)
LACRIMAL ATROPHY ( 2 FDA reports)
LARYNGEAL DYSPNOEA ( 2 FDA reports)
LARYNGEAL ERYTHEMA ( 2 FDA reports)
LARYNGEAL MASS ( 2 FDA reports)
LARYNGEAL OPERATION ( 2 FDA reports)
LARYNGOSCOPY ABNORMAL ( 2 FDA reports)
LARYNGOTRACHEO BRONCHITIS ( 2 FDA reports)
LHERMITTE'S SIGN ( 2 FDA reports)
LIGAMENT PAIN ( 2 FDA reports)
LIGHT CHAIN DISEASE ( 2 FDA reports)
LIMB REDUCTION DEFECT ( 2 FDA reports)
LIP DISCOLOURATION ( 2 FDA reports)
LIP SLOUGHING ( 2 FDA reports)
LIPIDS ABNORMAL ( 2 FDA reports)
LIPOATROPHY ( 2 FDA reports)
LIPOHYPERTROPHY ( 2 FDA reports)
LIVIDITY ( 2 FDA reports)
LOSS OF DREAMING ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
LOWER URINARY TRACT SYMPTOMS ( 2 FDA reports)
LUMBAR HERNIA ( 2 FDA reports)
LUMBARISATION ( 2 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE III ( 2 FDA reports)
LUNG CREPITATION ( 2 FDA reports)
LUNG WEDGE RESECTION ( 2 FDA reports)
LUPUS ENCEPHALITIS ( 2 FDA reports)
LUPUS ENTERITIS ( 2 FDA reports)
LUPUS NEPHRITIS ( 2 FDA reports)
LYMPH NODE CANCER METASTATIC ( 2 FDA reports)
LYMPH NODE TUBERCULOSIS ( 2 FDA reports)
LYMPHANGITIS ( 2 FDA reports)
LYMPHATIC DISORDER ( 2 FDA reports)
LYMPHOCELE ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
LYMPHOCYTIC LYMPHOMA ( 2 FDA reports)
LYMPHOHISTIOCYTOSIS ( 2 FDA reports)
MACULAR REFLEX ABNORMAL ( 2 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 2 FDA reports)
MALE PATTERN BALDNESS ( 2 FDA reports)
MALE SEXUAL DYSFUNCTION ( 2 FDA reports)
MALIGNANT DYSPHAGIA ( 2 FDA reports)
MALIGNANT MELANOMA STAGE II ( 2 FDA reports)
MARASMUS ( 2 FDA reports)
MARFAN'S SYNDROME ( 2 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 2 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 2 FDA reports)
MECONIUM ABNORMAL ( 2 FDA reports)
MEDICAL DEVICE PAIN ( 2 FDA reports)
MEDICAL INDUCTION OF COMA ( 2 FDA reports)
MELANOSIS ( 2 FDA reports)
MENINGEAL NEOPLASM ( 2 FDA reports)
MENINGITIS MENINGOCOCCAL ( 2 FDA reports)
MENINGOCOCCAL SEPSIS ( 2 FDA reports)
MERYCISM ( 2 FDA reports)
METASTASES TO BLADDER ( 2 FDA reports)
METASTASES TO HEART ( 2 FDA reports)
METASTASES TO OVARY ( 2 FDA reports)
METASTATIC BRONCHIAL CARCINOMA ( 2 FDA reports)
MICROLITHIASIS ( 2 FDA reports)
MITOCHONDRIAL ENCEPHALOMYOPATHY ( 2 FDA reports)
MIXED HYPERLIPIDAEMIA ( 2 FDA reports)
MONOCYTE COUNT DECREASED ( 2 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
MOUTH CYST ( 2 FDA reports)
MOUTH PLAQUE ( 2 FDA reports)
MUCOSA VESICLE ( 2 FDA reports)
MUCOSAL HAEMORRHAGE ( 2 FDA reports)
MUELLER'S MIXED TUMOUR ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 2 FDA reports)
MUSCLE HYPERTROPHY ( 2 FDA reports)
MYCOBACTERIUM CHELONAE INFECTION ( 2 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 2 FDA reports)
MYCOTIC ANEURYSM ( 2 FDA reports)
MYCOTOXICOSIS ( 2 FDA reports)
MYELITIS ( 2 FDA reports)
MYELITIS TRANSVERSE ( 2 FDA reports)
MYOCARDIAL CALCIFICATION ( 2 FDA reports)
MYOCARDIAL RUPTURE ( 2 FDA reports)
MYOGLOBINURIA ( 2 FDA reports)
MYOTONIA ( 2 FDA reports)
NAIL BED BLEEDING ( 2 FDA reports)
NASAL DISCHARGE DISCOLOURATION ( 2 FDA reports)
NASAL OBSTRUCTION ( 2 FDA reports)
NASAL SEPTUM DISORDER ( 2 FDA reports)
5'NUCLEOTIDASE INCREASED ( 1 FDA reports)
ABDOMINAL CAVITY DRAINAGE ( 1 FDA reports)
ABDOMINAL WALL OPERATION ( 1 FDA reports)
ABNORMAL CHEST SOUND ( 1 FDA reports)
ABNORMAL LABOUR ( 1 FDA reports)
ABSCESS FUNGAL ( 1 FDA reports)
ABSCESS OF EXTERNAL AUDITORY MEATUS ( 1 FDA reports)
ABSCESS OF SALIVARY GLAND ( 1 FDA reports)
ACCESSORY LIVER LOBE ( 1 FDA reports)
ACCIDENTAL POISONING ( 1 FDA reports)
ACOUSTIC NEUROMA ( 1 FDA reports)
ACQUIRED CARDIAC SEPTAL DEFECT ( 1 FDA reports)
ACQUIRED HAEMOPHILIA WITH ANTI FVIII, XI, OR XIII ( 1 FDA reports)
ACQUIRED MACROGLOSSIA ( 1 FDA reports)
ACRAL LENTIGINOUS MELANOMA STAGE UNSPECIFIED ( 1 FDA reports)
ACROCHORDON EXCISION ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 1 FDA reports)
ACUTE CHEST SYNDROME ( 1 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE POST ASTHMATIC AMYOTROPHY ( 1 FDA reports)
ACUTE VESTIBULAR SYNDROME ( 1 FDA reports)
ADAMS-STOKES SYNDROME ( 1 FDA reports)
ADENOIDAL HYPERTROPHY ( 1 FDA reports)
ADENOIDECTOMY ( 1 FDA reports)
ADENOSQUAMOUS CELL LUNG CANCER STAGE IV ( 1 FDA reports)
ADENOVIRAL HEPATITIS ( 1 FDA reports)
ADHESIOLYSIS ( 1 FDA reports)
ADMINISTRATION SITE PAIN ( 1 FDA reports)
ADMINISTRATION SITE REACTION ( 1 FDA reports)
ADRENAL CORTICAL INSUFFICIENCY ( 1 FDA reports)
ADRENALECTOMY ( 1 FDA reports)
ADVERSE EVENT FOLLOWING IMMUNISATION ( 1 FDA reports)
AGITATED DEPRESSION ( 1 FDA reports)
AGNOSIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO ABNORMAL ( 1 FDA reports)
ALCOHOL INTOLERANCE ( 1 FDA reports)
ALCOHOLIC PSYCHOSIS ( 1 FDA reports)
ALLERGIC COLITIS ( 1 FDA reports)
ALLERGIC RESPIRATORY DISEASE ( 1 FDA reports)
ALLERGY TO ARTHROPOD STING ( 1 FDA reports)
ALLERGY TO PLANTS ( 1 FDA reports)
ALLOGENIC BONE MARROW TRANSPLANTATION THERAPY ( 1 FDA reports)
ALOPECIA EFFLUVIUM ( 1 FDA reports)
ALPHA 2 GLOBULIN DECREASED ( 1 FDA reports)
ALTERNARIA INFECTION ( 1 FDA reports)
AMIMIA ( 1 FDA reports)
AMMONIA ABNORMAL ( 1 FDA reports)
AMMONIA DECREASED ( 1 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 1 FDA reports)
AMNIOTIC FLUID VOLUME INCREASED ( 1 FDA reports)
AMOEBIASIS ( 1 FDA reports)
AMPUTATION STUMP PAIN ( 1 FDA reports)
ANAEMIA OF PREGNANCY ( 1 FDA reports)
ANAESTHETIC COMPLICATION CARDIAC ( 1 FDA reports)
ANAL CANCER STAGE 0 ( 1 FDA reports)
ANAL CANDIDIASIS ( 1 FDA reports)
ANAL SPASM ( 1 FDA reports)
ANAL TINEA ( 1 FDA reports)
ANALGESIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANAPHYLACTIC TRANSFUSION REACTION ( 1 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 1 FDA reports)
ANASTOMOTIC ULCER ( 1 FDA reports)
ANDROGEN INSENSITIVITY SYNDROME ( 1 FDA reports)
ANDROGENS DECREASED ( 1 FDA reports)
ANEURYSM RUPTURED ( 1 FDA reports)
ANGIODERMATITIS ( 1 FDA reports)
ANGIOGRAM PERIPHERAL ( 1 FDA reports)
ANGIOLIPOMA ( 1 FDA reports)
ANGIOSARCOMA ( 1 FDA reports)
ANISOCHROMIA ( 1 FDA reports)
ANTERIOR SPINAL ARTERY SYNDROME ( 1 FDA reports)
ANTI-PLATELET ANTIBODY ( 1 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTIGLIADIN ANTIBODY POSITIVE ( 1 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTISOCIAL PERSONALITY DISORDER ( 1 FDA reports)
ANTITHROMBIN III DECREASED ( 1 FDA reports)
AORTIC ANEURYSM REPAIR ( 1 FDA reports)
AORTIC BIFURCATION GRAFT ( 1 FDA reports)
AORTIC INJURY ( 1 FDA reports)
AORTIC RUPTURE ( 1 FDA reports)
AORTIC VALVE PROLAPSE ( 1 FDA reports)
AORTITIS ( 1 FDA reports)
APPLICATION SITE BRUISING ( 1 FDA reports)
APPLICATION SITE CELLULITIS ( 1 FDA reports)
APPLICATION SITE EXCORIATION ( 1 FDA reports)
APPLICATION SITE INDURATION ( 1 FDA reports)
APPLICATION SITE MASS ( 1 FDA reports)
APPLICATION SITE PARAESTHESIA ( 1 FDA reports)
APPLICATION SITE SWELLING ( 1 FDA reports)
ARACHNOPHOBIA ( 1 FDA reports)
ARCUS LIPOIDES ( 1 FDA reports)
ARRHYTHMIA NEONATAL ( 1 FDA reports)
ARTERIAL FIBROSIS ( 1 FDA reports)
ARTERIAL GRAFT ( 1 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 1 FDA reports)
ARTERIOGRAM CAROTID ABNORMAL ( 1 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 1 FDA reports)
ARTERIOPATHIC DISEASE ( 1 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 1 FDA reports)
ARTERIOVENOUS FISTULA ANEURYSM ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE INFECTION ( 1 FDA reports)
ARTERIOVENOUS SHUNT OPERATION ( 1 FDA reports)
ARTICULAR DISC DISORDER ( 1 FDA reports)
ASOCIAL BEHAVIOUR ( 1 FDA reports)
ASPERGILLUS TEST POSITIVE ( 1 FDA reports)
ASPERMIA ( 1 FDA reports)
ASPIRATION BIOPSY ( 1 FDA reports)
ASPIRATION TRACHEAL ( 1 FDA reports)
ASTHMA EXERCISE INDUCED ( 1 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 1 FDA reports)
ATRIOVENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
AURICULAR HAEMATOMA ( 1 FDA reports)
AUTOANTIBODY POSITIVE ( 1 FDA reports)
AUTOMATIC BLADDER ( 1 FDA reports)
AZOOSPERMIA ( 1 FDA reports)
BACILLUS TEST POSITIVE ( 1 FDA reports)
BACTERIA BODY FLUID IDENTIFIED ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BACTERIAL PYELONEPHRITIS ( 1 FDA reports)
BACTERIAL TEST ( 1 FDA reports)
BACTERIAL TRACHEITIS ( 1 FDA reports)
BAND NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
BARIUM ENEMA ( 1 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 1 FDA reports)
BASE EXCESS NEGATIVE ( 1 FDA reports)
BASILAR ARTERY THROMBOSIS ( 1 FDA reports)
BASOPHIL COUNT ABNORMAL ( 1 FDA reports)
BEHAVIOURAL AND PSYCHIATRIC SYMPTOMS OF DEMENTIA ( 1 FDA reports)
BENIGN HEPATIC NEOPLASM ( 1 FDA reports)
BENIGN LYMPH NODE NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF EYE ( 1 FDA reports)
BENIGN NEOPLASM OF EYELID ( 1 FDA reports)
BENIGN NEOPLASM OF PINEAL GLAND ( 1 FDA reports)
BENIGN NEOPLASM OF PROSTATE ( 1 FDA reports)
BEREAVEMENT ( 1 FDA reports)
BEREAVEMENT REACTION ( 1 FDA reports)
BETA GLOBULIN INCREASED ( 1 FDA reports)
BILE DUCT CANCER STAGE III ( 1 FDA reports)
BILE DUCT PRESSURE ( 1 FDA reports)
BILIARY ANASTOMOSIS ( 1 FDA reports)
BILIARY ISCHAEMIA ( 1 FDA reports)
BILIARY SEPSIS ( 1 FDA reports)
BILIARY TRACT INFECTION ( 1 FDA reports)
BILIRUBIN URINE ( 1 FDA reports)
BIOPSY BRAIN ABNORMAL ( 1 FDA reports)
BIOPSY HEART ( 1 FDA reports)
BIOPSY MUCOSA ABNORMAL ( 1 FDA reports)
BIOPSY PANCREAS ABNORMAL ( 1 FDA reports)
BIOPSY PLEURA ABNORMAL ( 1 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BIOPSY VAGINA ( 1 FDA reports)
BIOPSY VAGINA ABNORMAL ( 1 FDA reports)
BIRT-HOGG-DUBE SYNDROME ( 1 FDA reports)
BIRTH MARK ( 1 FDA reports)
BLADDER ADENOCARCINOMA STAGE III ( 1 FDA reports)
BLADDER DIVERTICULUM ( 1 FDA reports)
BLADDER HYPERTROPHY ( 1 FDA reports)
BLADDER IRRIGATION ( 1 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 1 FDA reports)
BLADDER TAMPONADE ( 1 FDA reports)
BLAST CELL COUNT INCREASED ( 1 FDA reports)
BLAST CELL CRISIS ( 1 FDA reports)
BLASTOCYSTIS INFECTION ( 1 FDA reports)
BLEEDING TIME ABNORMAL ( 1 FDA reports)
BLOOD 1,25-DIHYDROXYCHOLECALCIFEROL DECREASED ( 1 FDA reports)
BLOOD 25-HYDROXYCHOLECALCIFEROL DECREASED ( 1 FDA reports)
BLOOD ALBUMIN ( 1 FDA reports)
BLOOD ALDOSTERONE ABNORMAL ( 1 FDA reports)
BLOOD AMYLASE DECREASED ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE DECREASED ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE INCREASED ( 1 FDA reports)
BLOOD CALCITONIN ( 1 FDA reports)
BLOOD CALCITONIN INCREASED ( 1 FDA reports)
BLOOD CANNABINOIDS ( 1 FDA reports)
BLOOD CARBON MONOXIDE ( 1 FDA reports)
BLOOD CATECHOLAMINES DECREASED ( 1 FDA reports)
BLOOD CHOLINESTERASE ABNORMAL ( 1 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 1 FDA reports)
BLOOD COPPER INCREASED ( 1 FDA reports)
BLOOD CORTICOSTERONE ABNORMAL ( 1 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 1 FDA reports)
BLOOD CORTISOL ABNORMAL ( 1 FDA reports)
BLOOD CREATINE DECREASED ( 1 FDA reports)
BLOOD ERYTHROPOIETIN DECREASED ( 1 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD HOMOCYSTEINE ABNORMAL ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN POSITIVE ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 1 FDA reports)
BLOOD IRON ( 1 FDA reports)
BLOOD LUTEINISING HORMONE DECREASED ( 1 FDA reports)
BLOOD METHAEMOGLOBIN PRESENT ( 1 FDA reports)
BLOOD PARATHYROID HORMONE ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC ABNORMAL ( 1 FDA reports)
BLOOD PROLACTIN ( 1 FDA reports)
BLOOD PROLACTIN ABNORMAL ( 1 FDA reports)
BLOOD PROLACTIN DECREASED ( 1 FDA reports)
BLOOD PYRUVIC ACID INCREASED ( 1 FDA reports)
BLOOD TESTOSTERONE ( 1 FDA reports)
BLOOD TESTOSTERONE ABNORMAL ( 1 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 1 FDA reports)
BLOOD URIC ACID ABNORMAL ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BONE FISSURE ( 1 FDA reports)
BONE MARROW ISCHAEMIA ( 1 FDA reports)
BONE TUBERCULOSIS ( 1 FDA reports)
BORDERLINE GLAUCOMA ( 1 FDA reports)
BOREDOM ( 1 FDA reports)
BOTULISM ( 1 FDA reports)
BRACHYTHERAPY TO PROSTATE ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE ABNORMAL ( 1 FDA reports)
BRAIN STEM THROMBOSIS ( 1 FDA reports)
BREAST DISCOLOURATION ( 1 FDA reports)
BREAST INFLAMMATION ( 1 FDA reports)
BREAST NECROSIS ( 1 FDA reports)
BREAST NEOPLASM MALE ( 1 FDA reports)
BREAST PROSTHESIS USER ( 1 FDA reports)
BREAST SARCOMA ( 1 FDA reports)
BREATH ALCOHOL TEST ( 1 FDA reports)
BREATH HOLDING ( 1 FDA reports)
BREATH SOUNDS ABSENT ( 1 FDA reports)
BREECH PRESENTATION ( 1 FDA reports)
BRONCHIAL HAEMORRHAGE ( 1 FDA reports)
BRONCHIAL OEDEMA ( 1 FDA reports)
BRONCHIAL WALL THICKENING ( 1 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 1 FDA reports)
BRUNNER'S GLAND HYPERPLASIA ( 1 FDA reports)
BULBAR PALSY ( 1 FDA reports)
BULIMIA NERVOSA ( 1 FDA reports)
BURGLARY VICTIM ( 1 FDA reports)
BURKHOLDERIA CEPACIA COMPLEX INFECTION ( 1 FDA reports)
BURNS FIRST DEGREE ( 1 FDA reports)
BURNS FOURTH DEGREE ( 1 FDA reports)
BURSA INJURY ( 1 FDA reports)
BUTTOCK PAIN ( 1 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 1 FDA reports)
CALCIFICATION OF MUSCLE ( 1 FDA reports)
CALCIUM IONISED INCREASED ( 1 FDA reports)
CAMPYLOBACTER INTESTINAL INFECTION ( 1 FDA reports)
CANCER GENE CARRIER ( 1 FDA reports)
CANDIDA OSTEOMYELITIS ( 1 FDA reports)
CANDIDA PNEUMONIA ( 1 FDA reports)
CAPILLARY DISORDER ( 1 FDA reports)
CAPILLARY FRAGILITY ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 27.29 INCREASED ( 1 FDA reports)
CARCINOID TUMOUR OF THE CAECUM ( 1 FDA reports)
CARCINOID TUMOUR OF THE PROSTATE ( 1 FDA reports)
CARCINOID TUMOUR OF THE SMALL BOWEL ( 1 FDA reports)
CARCINOID TUMOUR PULMONARY ( 1 FDA reports)
CARDIAC AMYLOIDOSIS ( 1 FDA reports)
CARDIAC COMPLICATION ASSOCIATED WITH DEVICE ( 1 FDA reports)
CARDIAC MONITORING ( 1 FDA reports)
CARDIAC MURMUR FUNCTIONAL ( 1 FDA reports)
CARDIAC NEOPLASM MALIGNANT ( 1 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 1 FDA reports)
CARDIAC PSEUDOANEURYSM ( 1 FDA reports)
CARDIAC STRESS TEST NORMAL ( 1 FDA reports)
CARDIAC VALVE PROSTHESIS USER ( 1 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ( 1 FDA reports)
CARDIORENAL SYNDROME ( 1 FDA reports)
CARDIOVASCULAR EVALUATION ( 1 FDA reports)
CARDITIS ( 1 FDA reports)
CATABOLIC STATE ( 1 FDA reports)
CATARACT SUBCAPSULAR ( 1 FDA reports)
CATHETER CULTURE POSITIVE ( 1 FDA reports)
CATHETER SITE INFLAMMATION ( 1 FDA reports)
CATHETER SITE PRURITUS ( 1 FDA reports)
CAUSTIC INJURY ( 1 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 1 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM STIMULATION ( 1 FDA reports)
CEPHALO-PELVIC DISPROPORTION ( 1 FDA reports)
CEREBRAL ARTERIOVENOUS MALFORMATION HAEMORRHAGIC ( 1 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 1 FDA reports)
CEREBRAL HAEMORRHAGE TRAUMATIC ( 1 FDA reports)
CEREBRAL PARENCHYMAL CALCIFICATION ( 1 FDA reports)
CEREBROSCLEROSIS ( 1 FDA reports)
CEREBROVASCULAR STENOSIS ( 1 FDA reports)
CERVICAL CONISATION ( 1 FDA reports)
CERVICAL SPASM ( 1 FDA reports)
CERVICAL VERTEBRA INJURY ( 1 FDA reports)
CERVICITIS HUMAN PAPILLOMA VIRUS ( 1 FDA reports)
CERVIX CARCINOMA RECURRENT ( 1 FDA reports)
CERVIX CARCINOMA STAGE 0 ( 1 FDA reports)
CERVIX CERCLAGE PROCEDURE ( 1 FDA reports)
CERVIX DYSTOCIA ( 1 FDA reports)
CERVIX OPERATION ( 1 FDA reports)
CHEILOSIS ( 1 FDA reports)
CHEMICAL BURN OF GASTROINTESTINAL TRACT ( 1 FDA reports)
CHEMICAL BURNS OF EYE ( 1 FDA reports)
CHEMICAL EYE INJURY ( 1 FDA reports)
CHEST X-RAY NORMAL ( 1 FDA reports)
CHOLECYSTOSTOMY ( 1 FDA reports)
CHOLEDOCHAL CYST ( 1 FDA reports)
CHOLEDOCHOLITHOTOMY ( 1 FDA reports)
CHOLINERGIC SYNDROME ( 1 FDA reports)
CHONDROMATOSIS ( 1 FDA reports)
CHORDOMA ( 1 FDA reports)
CHORIOAMNIONITIS ( 1 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 1 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
CHRONOTROPIC INCOMPETENCE ( 1 FDA reports)
CIRCUMCISION ( 1 FDA reports)
CITROBACTER SEPSIS ( 1 FDA reports)
CLITORAL ENGORGEMENT ( 1 FDA reports)
CLOT RETRACTION TIME SHORTENED ( 1 FDA reports)
COAGULATION FACTOR DEFICIENCY ( 1 FDA reports)
COAGULATION FACTOR VII LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR X LEVEL DECREASED ( 1 FDA reports)
COAGULATION TIME ABNORMAL ( 1 FDA reports)
COAGULATION TIME SHORTENED ( 1 FDA reports)
COCHLEA IMPLANT ( 1 FDA reports)
COLITIS PSEUDOMEMBRANOUS ( 1 FDA reports)
COLLAGEN DISORDER ( 1 FDA reports)
COLON DYSPLASIA ( 1 FDA reports)
COLON GANGRENE ( 1 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 1 FDA reports)
COLORECTAL CANCER STAGE I ( 1 FDA reports)
COLORECTAL CANCER STAGE II ( 1 FDA reports)
COLORECTAL CANCER STAGE III ( 1 FDA reports)
COLORECTAL CANCER STAGE IV ( 1 FDA reports)
COLOSTOMY CLOSURE ( 1 FDA reports)
COLOUR VISION TESTS ABNORMAL ( 1 FDA reports)
COLPORRHAPHY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED HEART ( 1 FDA reports)
COMPULSIVE SEXUAL BEHAVIOUR ( 1 FDA reports)
COMPUTERISED TOMOGRAM HEAD ( 1 FDA reports)
CONDYLOMA ACUMINATUM ( 1 FDA reports)
CONGENITAL CEREBROVASCULAR ANOMALY ( 1 FDA reports)
CONGENITAL CORONARY ARTERY MALFORMATION ( 1 FDA reports)
CONNECTIVE TISSUE INFLAMMATION ( 1 FDA reports)
CONTACT LENS INTOLERANCE ( 1 FDA reports)
CONVULSIONS LOCAL ( 1 FDA reports)
COR PULMONALE ACUTE ( 1 FDA reports)
CORNEAL BLEEDING ( 1 FDA reports)
CORNEAL ENDOTHELIITIS ( 1 FDA reports)
CORNEAL NEOVASCULARISATION ( 1 FDA reports)
CORONARY ARTERY ANEURYSM ( 1 FDA reports)
CORONARY ARTERY DISSECTION ( 1 FDA reports)
CORONARY BYPASS THROMBOSIS ( 1 FDA reports)
COUGH DECREASED ( 1 FDA reports)
COXSACKIE VIRAL INFECTION ( 1 FDA reports)
CRACKLES LUNG ( 1 FDA reports)
CRANIAL NERVE DISORDER ( 1 FDA reports)
CREATINE URINE INCREASED ( 1 FDA reports)
CREATININE RENAL CLEARANCE ABNORMAL ( 1 FDA reports)
CRUSH SYNDROME ( 1 FDA reports)
CRYPTOSPORIDIOSIS INFECTION ( 1 FDA reports)
CRYSTAL ARTHROPATHY ( 1 FDA reports)
CSF GLUCOSE ABNORMAL ( 1 FDA reports)
CSF PROTEIN ABNORMAL ( 1 FDA reports)
CSF VOLUME INCREASED ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
CULTURE TISSUE SPECIMEN POSITIVE ( 1 FDA reports)
CULTURE URINE ( 1 FDA reports)
CYCLIC VOMITING SYNDROME ( 1 FDA reports)
CYSTIC FIBROSIS PANCREATIC ( 1 FDA reports)
CYSTITIS KLEBSIELLA ( 1 FDA reports)
CYSTITIS PSEUDOMONAL ( 1 FDA reports)
CYSTOPEXY ( 1 FDA reports)
CYSTOSCOPY ABNORMAL ( 1 FDA reports)
CYTOGENETIC ANALYSIS ABNORMAL ( 1 FDA reports)
CYTOMEGALOVIRUS TEST ( 1 FDA reports)
CYTOTOXIC OEDEMA ( 1 FDA reports)
DEATH NEONATAL ( 1 FDA reports)
DEATH OF COMPANION ( 1 FDA reports)
DEATH OF SPOUSE ( 1 FDA reports)
DEEP BRAIN STIMULATION ( 1 FDA reports)
DELINQUENCY ( 1 FDA reports)
DELIVERY ( 1 FDA reports)
DENTAL PROSTHESIS USER ( 1 FDA reports)
DEPOSIT EYE ( 1 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 1 FDA reports)
DEVICE COMPONENT ISSUE ( 1 FDA reports)
DEVICE DIFFICULT TO USE ( 1 FDA reports)
DEVICE ELECTRICAL FINDING ( 1 FDA reports)
DEVICE LEAD DAMAGE ( 1 FDA reports)
DEVICE PACING ISSUE ( 1 FDA reports)
DEVICE PHYSICAL PROPERTY ISSUE ( 1 FDA reports)
DEVICE STIMULATION ISSUE ( 1 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 1 FDA reports)
DIABETIC AMYOTROPHY ( 1 FDA reports)
DIABETIC CHEIROPATHY ( 1 FDA reports)
DIABETIC MICROANGIOPATHY ( 1 FDA reports)
DIABETIC RETINAL OEDEMA ( 1 FDA reports)
DIALYSIS DEVICE COMPLICATION ( 1 FDA reports)
DIALYSIS DEVICE INSERTION ( 1 FDA reports)
DIAPHRAGM MUSCLE WEAKNESS ( 1 FDA reports)
DIAPHRAGMATIC OPERATION ( 1 FDA reports)
DIAPHRAGMATIC RUPTURE ( 1 FDA reports)
DIARRHOEA INFECTIOUS ( 1 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA RECURRENT ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE IV ( 1 FDA reports)
DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY ( 1 FDA reports)
DIPHTHERIA IMMUNISATION ( 1 FDA reports)
DISACCHARIDE METABOLISM DISORDER ( 1 FDA reports)
DISBACTERIOSIS ( 1 FDA reports)
DISEASE PRODROMAL STAGE ( 1 FDA reports)
DISSEMINATED CRYPTOCOCCOSIS ( 1 FDA reports)
DISSOCIATIVE FUGUE ( 1 FDA reports)
DIVERTICULUM GASTRIC ( 1 FDA reports)
DIVORCED ( 1 FDA reports)
DROWNING ( 1 FDA reports)
DRUG ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE ( 1 FDA reports)
DRUG DELIVERY DEVICE IMPLANTATION ( 1 FDA reports)
DRUG DETOXIFICATION ( 1 FDA reports)
DRUG HALF-LIFE INCREASED ( 1 FDA reports)
DRUG THERAPEUTIC INCOMPATIBILITY ( 1 FDA reports)
DRUG THERAPY ( 1 FDA reports)
DRY SOCKET ( 1 FDA reports)
DURAL TEAR ( 1 FDA reports)
DYSACUSIS ( 1 FDA reports)
DYSCHEZIA ( 1 FDA reports)
DYSENTERY ( 1 FDA reports)
EAR CANAL ERYTHEMA ( 1 FDA reports)
EBSTEIN'S ANOMALY ( 1 FDA reports)
ECHOCARDIOGRAM ( 1 FDA reports)
ECHOLALIA ( 1 FDA reports)
ECTHYMA ( 1 FDA reports)
ECTROPION ( 1 FDA reports)
EJACULATION DELAYED ( 1 FDA reports)
ELECTIVE PROCEDURE ( 1 FDA reports)
ELECTIVE SURGERY ( 1 FDA reports)
ELECTROCARDIOGRAM ( 1 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM DELTA WAVES ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ELEVATION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE BIPHASIC ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
ELECTROCAUTERISATION ( 1 FDA reports)
ELECTRONEUROGRAPHY ( 1 FDA reports)
ELECTROPHORESIS ABNORMAL ( 1 FDA reports)
ELECTROPHORESIS PROTEIN ABNORMAL ( 1 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 1 FDA reports)
EMBOLISM VENOUS ( 1 FDA reports)
EMOTIONAL DISORDER OF CHILDHOOD ( 1 FDA reports)
EMPHYSEMATOUS CYSTITIS ( 1 FDA reports)
ENCEPHALITIS BRAIN STEM ( 1 FDA reports)
ENDOCARDITIS CANDIDA ( 1 FDA reports)
ENDOCRINE DISORDER ( 1 FDA reports)
ENDOLYMPHATIC HYDROPS ( 1 FDA reports)
ENDOMETRIAL CANCER METASTATIC ( 1 FDA reports)
ENDOSCOPY GASTROINTESTINAL ABNORMAL ( 1 FDA reports)
ENDOSCOPY SMALL INTESTINE ABNORMAL ( 1 FDA reports)
ENEMA ADMINISTRATION ( 1 FDA reports)
ENLARGED CLITORIS ( 1 FDA reports)
ENTEROBACTER SEPSIS ( 1 FDA reports)
ENTEROBACTER TEST POSITIVE ( 1 FDA reports)
ENTEROCELE ( 1 FDA reports)
ENTEROCOLITIS BACTERIAL ( 1 FDA reports)
ENTEROCOLONIC FISTULA ( 1 FDA reports)
ENTEROSTOMY ( 1 FDA reports)
ENZYME LEVEL INCREASED ( 1 FDA reports)
EOSINOPHIL COUNT ABNORMAL ( 1 FDA reports)
EOSINOPHILIC CYSTITIS ( 1 FDA reports)
EPIDURAL LIPOMATOSIS ( 1 FDA reports)
EPIGLOTTIC CARCINOMA ( 1 FDA reports)
EPIPHYSEAL FRACTURE ( 1 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOMA ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
ERGOT POISONING ( 1 FDA reports)
ERYTHEMA INDURATUM ( 1 FDA reports)
ERYTHEMA MARGINATUM ( 1 FDA reports)
ERYTHROBLASTOSIS ( 1 FDA reports)
EX-TOBACCO USER ( 1 FDA reports)
EXCESSIVE EXERCISE ( 1 FDA reports)
EXCESSIVE OCULAR CONVERGENCE ( 1 FDA reports)
EXCITABILITY ( 1 FDA reports)
EXPLORATIVE LAPAROTOMY ( 1 FDA reports)
EXPOSURE TO CHEMICAL POLLUTION ( 1 FDA reports)
EXTERNAL EAR CELLULITIS ( 1 FDA reports)
EXTERNAL EAR DISORDER ( 1 FDA reports)
EXTRACORPOREAL MEMBRANE OXYGENATION ( 1 FDA reports)
EXTRAMEDULLARY HAEMOPOIESIS ( 1 FDA reports)
EXTRAOCULAR MUSCLE DISORDER ( 1 FDA reports)
EYE INFECTION INTRAOCULAR ( 1 FDA reports)
EYE PATCH APPLICATION ( 1 FDA reports)
EYELID BLEEDING ( 1 FDA reports)
EYELID EXFOLIATION ( 1 FDA reports)
FABRY'S DISEASE ( 1 FDA reports)
FACE LIFT ( 1 FDA reports)
FACIAL DYSMORPHISM ( 1 FDA reports)
FACIAL NERVE DISORDER ( 1 FDA reports)
FACIAL OPERATION ( 1 FDA reports)
FACTITIOUS DISORDER ( 1 FDA reports)
FAECAL DISIMPACTION ( 1 FDA reports)
FAECALITH ( 1 FDA reports)
FALLOPIAN TUBE PERFORATION ( 1 FDA reports)
FAMILIAL COLD AUTOINFLAMMATORY SYNDROME ( 1 FDA reports)
FAMILIAL TREMOR ( 1 FDA reports)
FANCONI SYNDROME ACQUIRED ( 1 FDA reports)
FASCIOTOMY ( 1 FDA reports)
FEAR OF NEEDLES ( 1 FDA reports)
FELTY'S SYNDROME ( 1 FDA reports)
FEMALE GENITAL-DIGESTIVE TRACT FISTULA ( 1 FDA reports)
FEMALE REPRODUCTIVE NEOPLASM ( 1 FDA reports)
FEMORAL ARTERY ANEURYSM ( 1 FDA reports)
FIBRIN D DIMER ( 1 FDA reports)
FINGER REPAIR OPERATION ( 1 FDA reports)
FIXED ERUPTION ( 1 FDA reports)
FLATBACK SYNDROME ( 1 FDA reports)
FOETAL GROWTH RESTRICTION ( 1 FDA reports)
FOETAL HEART RATE DECELERATION ( 1 FDA reports)
FOETAL HEART RATE DECREASED ( 1 FDA reports)
FOETAL THERAPEUTIC PROCEDURE ( 1 FDA reports)
FOETOR HEPATICUS ( 1 FDA reports)
FORCED EXPIRATORY VOLUME INCREASED ( 1 FDA reports)
FORCEPS DELIVERY ( 1 FDA reports)
FOREIGN BODY IN EYE ( 1 FDA reports)
FOREIGN BODY REACTION ( 1 FDA reports)
FRACTURED ISCHIUM ( 1 FDA reports)
FREE THYROXINE INDEX DECREASED ( 1 FDA reports)
FUCHS' SYNDROME ( 1 FDA reports)
FUNDOPLICATION ( 1 FDA reports)
FUNGAL PERITONITIS ( 1 FDA reports)
FUNGUS SPUTUM TEST POSITIVE ( 1 FDA reports)
FUNGUS STOOL IDENTIFIED ( 1 FDA reports)
FUNGUS URINE TEST POSITIVE ( 1 FDA reports)
GALLBLADDER OEDEMA ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 1 FDA reports)
GAS POISONING ( 1 FDA reports)
GASTRECTOMY TOTAL ( 1 FDA reports)
GASTRIC ATONY ( 1 FDA reports)
GASTRIC CANCER STAGE III ( 1 FDA reports)
GASTRIC DYSPLASIA ( 1 FDA reports)
GASTRIC HYPERPLASIA ( 1 FDA reports)
GASTRIC ILEUS ( 1 FDA reports)
GASTRIC STAPLING ( 1 FDA reports)
GASTRIC VARICES HAEMORRHAGE ( 1 FDA reports)
GASTRO-INTESTINAL FISTULA ( 1 FDA reports)
GASTROENTERITIS CRYPTOSPORIDIAL ( 1 FDA reports)
GASTROENTERITIS PARACOLON BACILLUS ( 1 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 1 FDA reports)
GASTROENTERITIS STAPHYLOCOCCAL ( 1 FDA reports)
GASTROINTESTINAL AMYLOIDOSIS ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA HAEMORRHAGIC ( 1 FDA reports)
GASTROINTESTINAL ANTHRAX ( 1 FDA reports)
GASTROINTESTINAL CANCER METASTATIC ( 1 FDA reports)
GASTROINTESTINAL ENDOSCOPIC THERAPY ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL NECROSIS ( 1 FDA reports)
GENE MUTATION ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ( 1 FDA reports)
GENERAL PHYSICAL CONDITION NORMAL ( 1 FDA reports)
GENITAL DISCHARGE ( 1 FDA reports)
GENITAL DISORDER MALE ( 1 FDA reports)
GENITOURINARY TRACT INFECTION ( 1 FDA reports)
GINGIVAL CANCER ( 1 FDA reports)
GINGIVAL HYPERTROPHY ( 1 FDA reports)
GINGIVAL INJURY ( 1 FDA reports)
GINGIVAL PRURITUS ( 1 FDA reports)
GINGIVITIS ULCERATIVE ( 1 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 1 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 1 FDA reports)
GLOMERULONEPHRITIS CHRONIC ( 1 FDA reports)
GLOSSECTOMY ( 1 FDA reports)
GLOSSOPHARYNGEAL NERVE DISORDER ( 1 FDA reports)
GLUCOSE TOLERANCE TEST ABNORMAL ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN ( 1 FDA reports)
GONORRHOEA ( 1 FDA reports)
GRAFT DYSFUNCTION ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
GRANULOMATOUS PNEUMONITIS ( 1 FDA reports)
GREY SYNDROME NEONATAL ( 1 FDA reports)
GROWTH HORMONE DEFICIENCY ( 1 FDA reports)
GYNAECOLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
HAEMATOCRIT NORMAL ( 1 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 1 FDA reports)
HAEMOBILIA ( 1 FDA reports)
HAEMODIALYSIS COMPLICATION ( 1 FDA reports)
HAEMORRHAGIC CYST ( 1 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 1 FDA reports)
HALLUCINATION, TACTILE ( 1 FDA reports)
HEART RATE ( 1 FDA reports)
HEART SOUNDS ( 1 FDA reports)
HEART VALVE OPERATION ( 1 FDA reports)
HEAT EXPOSURE INJURY ( 1 FDA reports)
HEAT ILLNESS ( 1 FDA reports)
HEAT THERAPY ( 1 FDA reports)
HELLP SYNDROME ( 1 FDA reports)
HELMINTHIC INFECTION ( 1 FDA reports)
HEMIPLEGIA TRANSIENT ( 1 FDA reports)
HEPATIC ARTERY EMBOLISM ( 1 FDA reports)
HEPATIC CANDIDIASIS ( 1 FDA reports)
HEPATIC INFILTRATION EOSINOPHILIC ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT RESECTABLE ( 1 FDA reports)
HEPATIC VEIN DILATATION ( 1 FDA reports)
HEPATIC VEIN OCCLUSION ( 1 FDA reports)
HEPATIC VEIN STENOSIS ( 1 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS A IMMUNISATION ( 1 FDA reports)
HEPATITIS A VIRUS TEST ( 1 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS C POSITIVE ( 1 FDA reports)
HEPATITIS C RNA POSITIVE ( 1 FDA reports)
HEPATITIS D ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HEPATO-LENTICULAR DEGENERATION ( 1 FDA reports)
HEPATOBILIARY DISEASE ( 1 FDA reports)
HEPATOBILIARY SCAN ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HERNIAL EVENTRATION ( 1 FDA reports)
HERPES ZOSTER OTICUS ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN ABNORMAL ( 1 FDA reports)
HIGH RISK SEXUAL BEHAVIOUR ( 1 FDA reports)
HIP DISARTICULATION ( 1 FDA reports)
HIP DYSPLASIA ( 1 FDA reports)
HISTAMINE LEVEL INCREASED ( 1 FDA reports)
HISTRIONIC PERSONALITY DISORDER ( 1 FDA reports)
HODGKIN'S DISEASE STAGE II ( 1 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 1 FDA reports)
HOLMES-ADIE PUPIL ( 1 FDA reports)
HOLOPROSENCEPHALY ( 1 FDA reports)
HUMAN HERPES VIRUS 8 TEST POSITIVE ( 1 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 1 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 1 FDA reports)
HUNTINGTON'S CHOREA ( 1 FDA reports)
HYDROTHORAX ( 1 FDA reports)
HYGROMA COLLI ( 1 FDA reports)
HYPERADRENOCORTICISM ( 1 FDA reports)
HYPERALDOSTERONISM ( 1 FDA reports)
HYPERCATABOLISM ( 1 FDA reports)
HYPERCHLORAEMIA ( 1 FDA reports)
HYPERCREATINAEMIA ( 1 FDA reports)
HYPERDYNAMIC LEFT VENTRICLE ( 1 FDA reports)
HYPERGASTRINAEMIA ( 1 FDA reports)
HYPERKERATOSIS PALMARIS AND PLANTARIS ( 1 FDA reports)
HYPERPHOSPHATURIA ( 1 FDA reports)
HYPERPLASTIC CHOLECYSTOPATHY ( 1 FDA reports)
HYPERTROPHY OF TONGUE PAPILLAE ( 1 FDA reports)
HYPERVITAMINOSIS A ( 1 FDA reports)
HYPOCHONDRIASIS ( 1 FDA reports)
HYPOGLYCAEMIC ENCEPHALOPATHY ( 1 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 1 FDA reports)
HYPOMENORRHOEA ( 1 FDA reports)
HYPOPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPOPHONESIS ( 1 FDA reports)
HYPOPHOSPHATAEMIC RICKETS ( 1 FDA reports)
HYPOPLASTIC ANAEMIA ( 1 FDA reports)
HYPOPYON ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDERS ( 1 FDA reports)
IGA NEPHROPATHY ( 1 FDA reports)
IIIRD NERVE DISORDER ( 1 FDA reports)
IIIRD NERVE PARESIS ( 1 FDA reports)
ILEAL FISTULA ( 1 FDA reports)
ILEAL ULCER ( 1 FDA reports)
ILEOSTOMY CLOSURE ( 1 FDA reports)
ILIUM FRACTURE ( 1 FDA reports)
ILLOGICAL THINKING ( 1 FDA reports)
IMMOBILISATION PROLONGED ( 1 FDA reports)
IMMUNE TOLERANCE INDUCTION ( 1 FDA reports)
IMMUNODEFICIENCY COMMON VARIABLE ( 1 FDA reports)
IMMUNOLOGY TEST ABNORMAL ( 1 FDA reports)
IMPERFORATE OESOPHAGUS ( 1 FDA reports)
IMPETIGO HERPETIFORMIS ( 1 FDA reports)
IMPLANT SITE EFFUSION ( 1 FDA reports)
IMPLANT SITE FIBROSIS ( 1 FDA reports)
IMPLANT SITE PAIN ( 1 FDA reports)
IMPLANT SITE THROMBOSIS ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 1 FDA reports)
INCISION SITE OEDEMA ( 1 FDA reports)
INDUCED ABORTION FAILED ( 1 FDA reports)
INFANTILE SPASMS ( 1 FDA reports)
INFECTED BITES ( 1 FDA reports)
INFECTED CYST ( 1 FDA reports)
INFECTIVE MYOSITIS ( 1 FDA reports)
INFERIOR VENA CAVA DILATATION ( 1 FDA reports)
INFERIORITY COMPLEX ( 1 FDA reports)
INFLAMMATION OF WOUND ( 1 FDA reports)
INFLAMMATORY PSEUDOTUMOUR ( 1 FDA reports)
INFLUENZA IMMUNISATION ( 1 FDA reports)
INFUSION ( 1 FDA reports)
INFUSION SITE ABSCESS ( 1 FDA reports)
INFUSION SITE DISCOLOURATION ( 1 FDA reports)
INFUSION SITE NECROSIS ( 1 FDA reports)
INFUSION SITE SCAR ( 1 FDA reports)
INFUSION SITE THROMBOSIS ( 1 FDA reports)
INGUINAL HERNIA STRANGULATED ( 1 FDA reports)
INHALATION THERAPY ( 1 FDA reports)
INJECTION ( 1 FDA reports)
INJECTION SITE COLDNESS ( 1 FDA reports)
INJECTION SITE DESQUAMATION ( 1 FDA reports)
INJECTION SITE JOINT PAIN ( 1 FDA reports)
INJECTION SITE LACERATION ( 1 FDA reports)
INJECTION SITE RECALL REACTION ( 1 FDA reports)
INJECTION SITE SCAB ( 1 FDA reports)
INJECTION SITE ULCER ( 1 FDA reports)
INSOMNIA RELATED TO ANOTHER MENTAL CONDITION ( 1 FDA reports)
INSTILLATION SITE IRRITATION ( 1 FDA reports)
INTERCOSTAL NEURALGIA ( 1 FDA reports)
INTESTINAL ADHESION LYSIS ( 1 FDA reports)
INTESTINAL ANGINA ( 1 FDA reports)
INTESTINAL HYPERMOTILITY ( 1 FDA reports)
INTESTINAL HYPOMOTILITY ( 1 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 1 FDA reports)
INTESTINAL POLYP HAEMORRHAGE ( 1 FDA reports)
INTESTINAL POLYPECTOMY ( 1 FDA reports)
INTESTINAL SPASM ( 1 FDA reports)
INTESTINAL ULCER PERFORATION ( 1 FDA reports)
INTRA-ABDOMINAL PRESSURE INCREASED ( 1 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE EXPELLED ( 1 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 1 FDA reports)
INTUBATION COMPLICATION ( 1 FDA reports)
IRIDECTOMY ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL INCREASED ( 1 FDA reports)
ISCHAEMIC NEPHROPATHY ( 1 FDA reports)
IVTH NERVE PARESIS ( 1 FDA reports)
JC VIRUS INFECTION ( 1 FDA reports)
JEJUNITIS ( 1 FDA reports)
JEJUNOSTOMY REFASHIONING ( 1 FDA reports)
JOINT DEPOSIT ( 1 FDA reports)
JOINT FLUID DRAINAGE ( 1 FDA reports)
JOINT HYPEREXTENSION ( 1 FDA reports)
JOINT LIGAMENT RUPTURE ( 1 FDA reports)
JOINT TUBERCULOSIS ( 1 FDA reports)
JUVENILE MYOCLONIC EPILEPSY ( 1 FDA reports)
KAOLIN CEPHALIN CLOTTING TIME PROLONGED ( 1 FDA reports)
KAPOSI'S SARCOMA ( 1 FDA reports)
KERATITIS BACTERIAL ( 1 FDA reports)
KERATITIS INTERSTITIAL ( 1 FDA reports)
KERATOCONUS ( 1 FDA reports)
KERATORHEXIS ( 1 FDA reports)
KETONURIA ( 1 FDA reports)
LABOUR INDUCTION ( 1 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 1 FDA reports)
LACRIMAL DUCT PROCEDURE ( 1 FDA reports)
LAPAROSCOPIC SURGERY ( 1 FDA reports)
LAPAROSCOPY ABNORMAL ( 1 FDA reports)
LARGE INTESTINAL STRICTURE ( 1 FDA reports)
LARGE INTESTINE ANASTOMOSIS ( 1 FDA reports)
LARGE INTESTINE CARCINOMA ( 1 FDA reports)
LARYNGEAL OBSTRUCTION ( 1 FDA reports)
LARYNGEAL PAIN ( 1 FDA reports)
LARYNGEAL POLYP ( 1 FDA reports)
LARYNGEAL PROSTHESIS USER ( 1 FDA reports)
LARYNGITIS VIRAL ( 1 FDA reports)
LARYNGOMALACIA ( 1 FDA reports)
LASER THERAPY ( 1 FDA reports)
LAZINESS ( 1 FDA reports)
LDL/HDL RATIO DECREASED ( 1 FDA reports)
LDL/HDL RATIO INCREASED ( 1 FDA reports)
LEFT ATRIAL HYPERTROPHY ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE DECREASED ( 1 FDA reports)
LEGIONELLA INFECTION ( 1 FDA reports)
LEGIONELLA TEST POSITIVE ( 1 FDA reports)
LEUKAEMIA CUTIS ( 1 FDA reports)
LEUKAEMIC INFILTRATION ( 1 FDA reports)
LEUKAEMIC INFILTRATION BRAIN ( 1 FDA reports)
LEUKAEMIC INFILTRATION PULMONARY ( 1 FDA reports)
LEUKOENCEPHALOMYELITIS ( 1 FDA reports)
LICE INFESTATION ( 1 FDA reports)
LIGAMENT CALCIFICATION ( 1 FDA reports)
LINEAR IGA DISEASE ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER RECURRENT ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER STAGE III ( 1 FDA reports)
LIP EXFOLIATION ( 1 FDA reports)
LIP INFECTION ( 1 FDA reports)
LIP PRURITUS ( 1 FDA reports)
LIPASE ( 1 FDA reports)
LIPOGRANULOMA ( 1 FDA reports)
LIPOMA EXCISION ( 1 FDA reports)
LIPOPROTEIN (A) INCREASED ( 1 FDA reports)
LIPOSARCOMA ( 1 FDA reports)
LIPOSUCTION ( 1 FDA reports)
LIQUID PRODUCT PHYSICAL ISSUE ( 1 FDA reports)
LIVER FUNCTION TEST ( 1 FDA reports)
LIVER FUNCTION TEST NORMAL ( 1 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 1 FDA reports)
LIVER SARCOIDOSIS ( 1 FDA reports)
LOOSE ASSOCIATIONS ( 1 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE I ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE 0 ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE I ( 1 FDA reports)
LUNG CYST ( 1 FDA reports)
LYMPHANGIOLEIOMYOMATOSIS ( 1 FDA reports)
LYMPHOCYTE TRANSFORMATION TEST POSITIVE ( 1 FDA reports)
LYMPHOSTASIS ( 1 FDA reports)
LYSINURIC PROTEIN INTOLERANCE ( 1 FDA reports)
MACROANGIOPATHY ( 1 FDA reports)
MACULAR ISCHAEMIA ( 1 FDA reports)
MALIGNANT GLIOMA ( 1 FDA reports)
MALIGNANT MEDIASTINAL NEOPLASM ( 1 FDA reports)
MALIGNANT MELANOMA STAGE I ( 1 FDA reports)
MALIGNANT MYOPIA ( 1 FDA reports)
MALIGNANT NEOPLASM OF AMPULLA OF VATER ( 1 FDA reports)
MALIGNANT NEOPLASM OF PLEURA ( 1 FDA reports)
MALIGNANT PALATE NEOPLASM ( 1 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 1 FDA reports)
MALIGNANT SPLENIC NEOPLASM ( 1 FDA reports)
MAMMOGRAM ( 1 FDA reports)
MASTOCYTOSIS ( 1 FDA reports)
MASTOPTOSIS ( 1 FDA reports)
MAXILLARY ANTRUM OPERATIONS ( 1 FDA reports)
MECHANICAL COMPLICATION OF IMPLANT ( 1 FDA reports)
MEDIASTINAL SHIFT ( 1 FDA reports)
MEDIASTINOSCOPY ( 1 FDA reports)
MEDICAL DEVICE SITE REACTION ( 1 FDA reports)
MEDICAL OBSERVATION ABNORMAL ( 1 FDA reports)
MEDICATION TAMPERING ( 1 FDA reports)
MEDULLARY THYROID CANCER ( 1 FDA reports)
MEGAKARYOCYTES DECREASED ( 1 FDA reports)
MELANOMA RECURRENT ( 1 FDA reports)
MENINGIOMA BENIGN ( 1 FDA reports)
MENINGISM ( 1 FDA reports)
MENINGITIS ENTEROCOCCAL ( 1 FDA reports)
MENTAL RETARDATION ( 1 FDA reports)
MERALGIA PARAESTHETICA ( 1 FDA reports)
MESANGIOPROLIFERATIVE GLOMERULONEPHRITIS ( 1 FDA reports)
MESENTERIC OCCLUSION ( 1 FDA reports)
MESOTHELIOMA ( 1 FDA reports)
MESOTHELIOMA MALIGNANT ( 1 FDA reports)
METABOLIC FUNCTION TEST ABNORMAL ( 1 FDA reports)
METAPNEUMOVIRUS INFECTION ( 1 FDA reports)
METASTASES TO CHEST WALL ( 1 FDA reports)
METASTASES TO OESOPHAGUS ( 1 FDA reports)
METASTASES TO PROSTATE ( 1 FDA reports)
METASTASES TO THE RESPIRATORY SYSTEM ( 1 FDA reports)
METASTATIC CARCINOMA OF THE BLADDER ( 1 FDA reports)
METATARSAL EXCISION ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST NEGATIVE ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 1 FDA reports)
MICROCOCCUS INFECTION ( 1 FDA reports)
MILIARY PNEUMONIA ( 1 FDA reports)
MITOCHONDRIAL CYTOPATHY ( 1 FDA reports)
MITOCHONDRIAL MYOPATHY ( 1 FDA reports)
MONONUCLEOSIS HETEROPHILE TEST POSITIVE ( 1 FDA reports)
MORAXELLA INFECTION ( 1 FDA reports)
MORGANELLA INFECTION ( 1 FDA reports)
MOTOR NEURONE DISEASE ( 1 FDA reports)
MUCOCUTANEOUS CANDIDIASIS ( 1 FDA reports)
MUCOPOLYSACCHARIDOSIS II ( 1 FDA reports)
MUCORMYCOSIS ( 1 FDA reports)
MUCOSAL EXFOLIATION ( 1 FDA reports)
MULTIFOCAL MOTOR NEUROPATHY ( 1 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 1 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 1 FDA reports)
MURDER ( 1 FDA reports)
MYASTHENIC SYNDROME ( 1 FDA reports)
MYELOCYTOSIS ( 1 FDA reports)
MYOCARDIAL REPERFUSION INJURY ( 1 FDA reports)
MYOCARDITIS SEPTIC ( 1 FDA reports)
MYOGLOBIN URINE PRESENT ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
NAIL BED INFLAMMATION ( 1 FDA reports)
NAIL DISCOMFORT ( 1 FDA reports)
NAIL GROWTH ABNORMAL ( 1 FDA reports)
NAIL PITTING ( 1 FDA reports)
NARROW ANTERIOR CHAMBER ANGLE ( 1 FDA reports)
NASAL CYST ( 1 FDA reports)
NASAL MUCOSAL DISCOLOURATION ( 1 FDA reports)
NASAL SEPTAL OPERATION ( 1 FDA reports)
NASOPHARYNGEAL CANCER ( 1 FDA reports)
NASOPHARYNGEAL REFLUX ( 1 FDA reports)
NASOPHARYNGEAL SURGERY ( 1 FDA reports)
NEAR DROWNING ( 1 FDA reports)
NECK SURGERY ( 1 FDA reports)
NECROBIOSIS ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NECROTISING FASCIITIS STAPHYLOCOCCAL ( 1 FDA reports)
NEONATAL ASPIRATION ( 1 FDA reports)
NEOPLASM OF THYMUS ( 1 FDA reports)
NEPHROANGIOSCLEROSIS ( 1 FDA reports)
NEPHROBLASTOMA ( 1 FDA reports)
NEPHROSTOMY ( 1 FDA reports)
NERVE ROOT INJURY ( 1 FDA reports)
NERVE STIMULATION TEST ( 1 FDA reports)
NEURECTOMY ( 1 FDA reports)
NEURILEMMOMA ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 1 FDA reports)
NEUROGENIC BOWEL ( 1 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 1 FDA reports)
NIPPLE SWELLING ( 1 FDA reports)
NITRITE URINE ABSENT ( 1 FDA reports)
NO ADVERSE DRUG REACTION ( 1 FDA reports)
NO ADVERSE REACTION ( 1 FDA reports)
NOCARDIA SEPSIS ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE I ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 1 FDA reports)
NORMAL DELIVERY ( 1 FDA reports)
NOSOPHOBIA ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABDOMINAL ABNORMAL ( 1 FDA reports)
NUCLEATED RED CELLS ( 1 FDA reports)
NUTRITIONAL SUPPORT ( 1 FDA reports)
OBSESSIVE RUMINATION ( 1 FDA reports)
OBSTRUCTIVE CHRONIC BRONCHITIS WITH ACUTE EXACERBATION ( 1 FDA reports)
OCULAR ISCHAEMIC SYNDROME ( 1 FDA reports)
OCULAR SARCOIDOSIS ( 1 FDA reports)
OEDEMA DUE TO RENAL DISEASE ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA METASTATIC ( 1 FDA reports)
OESOPHAGEAL CARCINOMA RECURRENT ( 1 FDA reports)
OESOPHAGEAL FISTULA ( 1 FDA reports)
OESOPHAGEAL MUCOSA ERYTHEMA ( 1 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
OESOPHAGITIS CHEMICAL ( 1 FDA reports)
OESOPHAGOSCOPY ABNORMAL ( 1 FDA reports)
OESTRADIOL INCREASED ( 1 FDA reports)
OMENTECTOMY ( 1 FDA reports)
ONCOLOGIC COMPLICATION ( 1 FDA reports)
OPIATES POSITIVE ( 1 FDA reports)
OPISTHOTONUS ( 1 FDA reports)
OPSOCLONUS MYOCLONUS ( 1 FDA reports)
OPTIC NERVE HYPOPLASIA ( 1 FDA reports)
ORAL PAPILLOMA ( 1 FDA reports)
ORBITAL PSEUDOTUMOUR ( 1 FDA reports)
ORCHIDECTOMY ( 1 FDA reports)
OROPHARYNGEAL CANCER STAGE III ( 1 FDA reports)
OSTEOMYELITIS ACUTE ( 1 FDA reports)
OSTEOMYELITIS BACTERIAL ( 1 FDA reports)
OSTEOSIS ( 1 FDA reports)
OVARIAN FIBROMA ( 1 FDA reports)
OVARIAN TORSION ( 1 FDA reports)
OVERWORK ( 1 FDA reports)
OXYGEN CONSUMPTION ( 1 FDA reports)
OXYGEN SATURATION ( 1 FDA reports)
OXYGEN SATURATION INCREASED ( 1 FDA reports)
PACEMAKER COMPLICATION ( 1 FDA reports)
PANCREAS TRANSPLANT ( 1 FDA reports)
PANCREATIC CARCINOMA NON-RESECTABLE ( 1 FDA reports)
PANCREATIC ENZYME ABNORMALITY ( 1 FDA reports)
PANCREATIC FISTULA ( 1 FDA reports)
PANCREATIC NEUROENDOCRINE TUMOUR ( 1 FDA reports)
PANCREATICODUODENECTOMY ( 1 FDA reports)
PANNICULITIS LOBULAR ( 1 FDA reports)
PAPILLA OF VATER STENOSIS ( 1 FDA reports)
PARAESTHESIA OF GENITAL MALE ( 1 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 1 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 1 FDA reports)
PARANEOPLASTIC PEMPHIGUS ( 1 FDA reports)
PARAPSORIASIS ( 1 FDA reports)
PARENT-CHILD PROBLEM ( 1 FDA reports)
PARENTERAL NUTRITION ( 1 FDA reports)
PARKINSONIAN CRISIS ( 1 FDA reports)
PARKINSONIAN REST TREMOR ( 1 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 1 FDA reports)
PATIENT ISOLATION ( 1 FDA reports)
PATIENT-DEVICE INCOMPATIBILITY ( 1 FDA reports)
PEAK EXPIRATORY FLOW RATE ABNORMAL ( 1 FDA reports)
PEAK EXPIRATORY FLOW RATE INCREASED ( 1 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 1 FDA reports)
PELVIC CONGESTION ( 1 FDA reports)
PELVIC NEOPLASM ( 1 FDA reports)
PENICILLIOSIS ( 1 FDA reports)
PENILE BLISTER ( 1 FDA reports)
PENIS CARCINOMA ( 1 FDA reports)
PENIS CARCINOMA METASTATIC ( 1 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 1 FDA reports)
PERENNIAL ALLERGY ( 1 FDA reports)
PERFORATION BILE DUCT ( 1 FDA reports)
PERICARDITIS LUPUS ( 1 FDA reports)
PERICARDITIS URAEMIC ( 1 FDA reports)
PERINEAL CYST ( 1 FDA reports)
PERINEAL INDURATION ( 1 FDA reports)
PERINEAL PAIN ( 1 FDA reports)
PERINEAL ULCERATION ( 1 FDA reports)
PERIPHERAL ARTERY ANGIOPLASTY ( 1 FDA reports)
PERIPHERAL PARALYSIS ( 1 FDA reports)
PERIPORTAL SINUS DILATATION ( 1 FDA reports)
PERITONEAL FLUID ANALYSIS ABNORMAL ( 1 FDA reports)
PERITONEAL LESION ( 1 FDA reports)
PERITONITIS SCLEROSING ( 1 FDA reports)
PERITONSILLAR ABSCESS ( 1 FDA reports)
PERONEAL MUSCULAR ATROPHY ( 1 FDA reports)
PERSEVERATION ( 1 FDA reports)
PERTUSSIS IMMUNISATION ( 1 FDA reports)
PHAEOCHROMOCYTOMA ( 1 FDA reports)
PHARYNGEAL ABSCESS ( 1 FDA reports)
PHARYNGEAL EXUDATE ( 1 FDA reports)
PHARYNGEAL LESION ( 1 FDA reports)
PHARYNGEAL STENOSIS ( 1 FDA reports)
PHARYNGITIS BACTERIAL ( 1 FDA reports)
PHLEBITIS SUPERFICIAL ( 1 FDA reports)
PHLEBOSCLEROSIS ( 1 FDA reports)
PHLEBOTOMY ( 1 FDA reports)
PHOTOSENSITIVITY ALLERGIC REACTION ( 1 FDA reports)
PICA ( 1 FDA reports)
PIGMENT NEPHROPATHY ( 1 FDA reports)
PIGMENTATION BUCCAL ( 1 FDA reports)
PINEAL GLAND CYST ( 1 FDA reports)
PITUITARY HAEMORRHAGE ( 1 FDA reports)
PITUITARY TUMOUR REMOVAL ( 1 FDA reports)
PLACENTA PRAEVIA ( 1 FDA reports)
PLANTAR ERYTHEMA ( 1 FDA reports)
PLASMODIUM FALCIPARUM INFECTION ( 1 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 1 FDA reports)
PLATELET TOXICITY ( 1 FDA reports)
PLEURAL DECORTICATION ( 1 FDA reports)
PLEURAL MESOTHELIOMA MALIGNANT ( 1 FDA reports)
PLEURAL NEOPLASM ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 1 FDA reports)
PNEUMOVIRUS TEST POSITIVE ( 1 FDA reports)
PODAGRA ( 1 FDA reports)
POISONING DELIBERATE ( 1 FDA reports)
POLIOMYELITIS ( 1 FDA reports)
POLYARTERITIS NODOSA ( 1 FDA reports)
POLYCHONDRITIS ( 1 FDA reports)
POLYCYTHAEMIA VERA ( 1 FDA reports)
POLYGLANDULAR DISORDER ( 1 FDA reports)
POLYOMAVIRUS TEST POSITIVE ( 1 FDA reports)
POOR SUCKING REFLEX ( 1 FDA reports)
POOR WEIGHT GAIN NEONATAL ( 1 FDA reports)
POPLITEAL PULSE DECREASED ( 1 FDA reports)
PORPHYROMONAS INFECTION ( 1 FDA reports)
PORTAL VEIN STENOSIS ( 1 FDA reports)
PORTOPULMONARY HYPERTENSION ( 1 FDA reports)
POST PROCEDURAL DRAINAGE ( 1 FDA reports)
POST PROCEDURAL HYPOTHYROIDISM ( 1 FDA reports)
POST PROCEDURAL OEDEMA ( 1 FDA reports)
POST PROCEDURAL SEPSIS ( 1 FDA reports)
POST PROCEDURAL SWELLING ( 1 FDA reports)
POST PROCEDURAL VOMITING ( 1 FDA reports)
POST TRANSPLANT DISTAL LIMB SYNDROME ( 1 FDA reports)
POST-TRAUMATIC HEADACHE ( 1 FDA reports)
POST-TUSSIVE VOMITING ( 1 FDA reports)
POSTICTAL PARALYSIS ( 1 FDA reports)
POSTMATURE BABY ( 1 FDA reports)
POSTOPERATIVE HERNIA ( 1 FDA reports)
POSTRENAL FAILURE ( 1 FDA reports)
PRECURSOR B-LYMPHOBLASTIC LYMPHOMA STAGE IV ( 1 FDA reports)
PREGNANCY WITH CONTRACEPTIVE PATCH ( 1 FDA reports)
PREMATURE EJACULATION ( 1 FDA reports)
PRERENAL FAILURE ( 1 FDA reports)
PRIMARY ADRENAL INSUFFICIENCY ( 1 FDA reports)
PRIMARY PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
PROCALCITONIN INCREASED ( 1 FDA reports)
PROCTITIS HAEMORRHAGIC ( 1 FDA reports)
PROCTITIS HERPES ( 1 FDA reports)
PRODUCT CLOSURE ISSUE ( 1 FDA reports)
PRODUCT DROPPER ISSUE ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PROGESTERONE DECREASED ( 1 FDA reports)
PROGESTERONE INCREASED ( 1 FDA reports)
PROSTATE CANCER STAGE 0 ( 1 FDA reports)
PROSTATE CANCER STAGE IV ( 1 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 1 FDA reports)
PROSTATIC HAEMORRHAGE ( 1 FDA reports)
PROSTATIC OBSTRUCTION ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN ABNORMAL ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN DECREASED ( 1 FDA reports)
PROTEIN S INCREASED ( 1 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 1 FDA reports)
PSEUDARTHROSIS ( 1 FDA reports)
PSEUDOLYMPHOMA ( 1 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 1 FDA reports)
PSEUDOMYXOMA PERITONEI ( 1 FDA reports)
PSEUDOPHAKIA ( 1 FDA reports)
PSEUDOPOLYP ( 1 FDA reports)
PSOAS ABSCESS ( 1 FDA reports)
PSYCHIATRIC EVALUATION ( 1 FDA reports)
PSYCHIATRIC EVALUATION ABNORMAL ( 1 FDA reports)
PSYCHOMOTOR AGITATION ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE ( 1 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 1 FDA reports)
PULMONARY ARTERIOPATHY ( 1 FDA reports)
PULMONARY ARTERY ANEURYSM ( 1 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 1 FDA reports)
PULMONARY EOSINOPHILIA ( 1 FDA reports)
PULMONARY HILAR ENLARGEMENT ( 1 FDA reports)
PULMONARY MALFORMATION ( 1 FDA reports)
PULMONARY MICROEMBOLI ( 1 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 1 FDA reports)
PULSE PRESSURE INCREASED ( 1 FDA reports)
PUNCTURE SITE PAIN ( 1 FDA reports)
PYLOROSPASM ( 1 FDA reports)
PYLORUS DILATATION ( 1 FDA reports)
PYONEPHROSIS ( 1 FDA reports)
PYROMANIA ( 1 FDA reports)
Q FEVER ( 1 FDA reports)
QUADRUPLE VESSEL BYPASS GRAFT ( 1 FDA reports)
RADIAL PULSE DECREASED ( 1 FDA reports)
RADIATION FIBROSIS ( 1 FDA reports)
RADIATION INTERACTION ( 1 FDA reports)
RADIATION THYROIDITIS ( 1 FDA reports)
RADIOTHERAPY TO BRAIN ( 1 FDA reports)
RADIOTHERAPY TO BREAST ( 1 FDA reports)
RADIOTHERAPY TO THROAT ( 1 FDA reports)
RASH SCALY ( 1 FDA reports)
RASMUSSEN ENCEPHALITIS ( 1 FDA reports)
REACTION TO AZO-DYES ( 1 FDA reports)
REACTION TO PRESERVATIVES ( 1 FDA reports)
RECTAL CANCER RECURRENT ( 1 FDA reports)
RECTAL LESION ( 1 FDA reports)
RECTAL TUBE INSERTION ( 1 FDA reports)
RECTOCELE REPAIR ( 1 FDA reports)
RED BLOOD CELL MORPHOLOGY ABNORMAL ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE DECREASED ( 1 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH DECREASED ( 1 FDA reports)
REGRESSIVE BEHAVIOUR ( 1 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 1 FDA reports)
REMOVAL OF FOREIGN BODY FROM NOSE ( 1 FDA reports)
REMOVAL OF INTERNAL FIXATION ( 1 FDA reports)
RENAL ANEURYSM ( 1 FDA reports)
RENAL ARTERY FIBROMUSCULAR DYSPLASIA ( 1 FDA reports)
RENAL CYST INFECTION ( 1 FDA reports)
RENAL FUSION ANOMALY ( 1 FDA reports)
RENAL HYPERTENSION ( 1 FDA reports)
RENAL VEIN OCCLUSION ( 1 FDA reports)
RENAL VEIN THROMBOSIS ( 1 FDA reports)
REOCCLUSION ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS BRONCHIOLITIS ( 1 FDA reports)
RESPIRATORY TRACT NEOPLASM ( 1 FDA reports)
RESPIRATORY TRACT OEDEMA ( 1 FDA reports)
RESPIRATORY TRACT ULCERATION ( 1 FDA reports)
RETICULIN INCREASED ( 1 FDA reports)
RETICULOCYTE COUNT ABNORMAL ( 1 FDA reports)
RETICULOCYTOSIS ( 1 FDA reports)
RETINAL ARTERY THROMBOSIS ( 1 FDA reports)
RETINAL DEPIGMENTATION ( 1 FDA reports)
RETINAL DEPOSITS ( 1 FDA reports)
RETINAL NEOPLASM ( 1 FDA reports)
RETINAL TOXICITY ( 1 FDA reports)
RETINAL VASCULAR DISORDER ( 1 FDA reports)
RETINITIS ( 1 FDA reports)
RETINOGRAM ABNORMAL ( 1 FDA reports)
RETROPERITONEAL NEOPLASM METASTATIC ( 1 FDA reports)
REVISION OF INTERNAL FIXATION ( 1 FDA reports)
RHEUMATIC FEVER ( 1 FDA reports)
RHEUMATIC HEART DISEASE ( 1 FDA reports)
RHEUMATOID FACTOR ( 1 FDA reports)
RHEUMATOID LUNG ( 1 FDA reports)
RHINITIS PERENNIAL ( 1 FDA reports)
RHINOSPORIDIOSIS ( 1 FDA reports)
RHYTHM IDIOVENTRICULAR ( 1 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE DECREASED ( 1 FDA reports)
ROCKY MOUNTAIN SPOTTED FEVER ( 1 FDA reports)
ROTAVIRUS TEST POSITIVE ( 1 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 1 FDA reports)
RUPTURED DIVERTICULUM OF COLON ( 1 FDA reports)
RUSSELL'S VIPER VENOM TIME ABNORMAL ( 1 FDA reports)
SALIVA ANALYSIS ABNORMAL ( 1 FDA reports)
SALIVARY DUCT STENOSIS ( 1 FDA reports)
SALIVARY GLAND ATROPHY ( 1 FDA reports)
SALIVARY GLAND CALCULUS ( 1 FDA reports)
SALMONELLA BACTERAEMIA ( 1 FDA reports)
SALPINGO-OOPHORECTOMY UNILATERAL ( 1 FDA reports)
SANDIFER'S SYNDROME ( 1 FDA reports)
SARCOMA UTERUS ( 1 FDA reports)
SCAN ABNORMAL ( 1 FDA reports)
SCEDOSPORIUM INFECTION ( 1 FDA reports)
SCINTILLATING SCOTOMA ( 1 FDA reports)
SCLERAL CYST ( 1 FDA reports)
SCLERAL HAEMORRHAGE ( 1 FDA reports)
SCLERODERMA RENAL CRISIS ( 1 FDA reports)
SCLEROTHERAPY ( 1 FDA reports)
SCROTAL ERYTHEMA ( 1 FDA reports)
SCROTAL IRRITATION ( 1 FDA reports)
SEBACEOUS CYST EXCISION ( 1 FDA reports)
SEIZURE LIKE PHENOMENA ( 1 FDA reports)
SEMEN ANALYSIS ABNORMAL ( 1 FDA reports)
SEMEN VISCOSITY INCREASED ( 1 FDA reports)
SEMINOMA ( 1 FDA reports)
SENILE OSTEOPOROSIS ( 1 FDA reports)
SENSATION OF BLOCK IN EAR ( 1 FDA reports)
SEPSIS NEONATAL ( 1 FDA reports)
SEPTAL PANNICULITIS ( 1 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 1 FDA reports)
SERUM SICKNESS-LIKE REACTION ( 1 FDA reports)
SEXUAL ACTIVITY INCREASED ( 1 FDA reports)
SEXUAL INHIBITION ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SHUNT THROMBOSIS ( 1 FDA reports)
SICK RELATIVE ( 1 FDA reports)
SICKLE CELL TRAIT ( 1 FDA reports)
SIGMOIDOSCOPY ( 1 FDA reports)
SIGNET-RING CELL CARCINOMA ( 1 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 1 FDA reports)
SINUSITIS ASPERGILLUS ( 1 FDA reports)
SKELETAL MUSCLE ENZYMES ( 1 FDA reports)
SKIN CANCER METASTATIC ( 1 FDA reports)
SKULL X-RAY ABNORMAL ( 1 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, PARASOMNIA TYPE ( 1 FDA reports)
SLEEP STUDY ABNORMAL ( 1 FDA reports)
SMALL BOWEL ANGIOEDEMA ( 1 FDA reports)
SMALL INTESTINE CARCINOMA METASTATIC ( 1 FDA reports)
SNAKE BITE ( 1 FDA reports)
SOCIAL FEAR ( 1 FDA reports)
SOFT TISSUE MASS ( 1 FDA reports)
SOFT TISSUE NEOPLASM ( 1 FDA reports)
SOLAR ELASTOSIS ( 1 FDA reports)
SOMATIC DELUSION ( 1 FDA reports)
SOMNOLENCE NEONATAL ( 1 FDA reports)
SPASTIC PARAPLEGIA ( 1 FDA reports)
SPERM CONCENTRATION ZERO ( 1 FDA reports)
SPERM COUNT DECREASED ( 1 FDA reports)
SPERMATORRHOEA ( 1 FDA reports)
SPINA BIFIDA ( 1 FDA reports)
SPINAL CORD DRAINAGE ( 1 FDA reports)
SPINAL MYELOGRAM ( 1 FDA reports)
SPINAL MYELOGRAM ABNORMAL ( 1 FDA reports)
SPINAL ROD INSERTION ( 1 FDA reports)
SPIROMETRY ABNORMAL ( 1 FDA reports)
SPLENIC CANDIDIASIS ( 1 FDA reports)
SPLENIC EMBOLISM ( 1 FDA reports)
SPLENIC HAEMATOMA ( 1 FDA reports)
SPLENIC HAEMORRHAGE ( 1 FDA reports)
SPLENIC VARICES ( 1 FDA reports)
SPONTANEOUS HAEMATOMA ( 1 FDA reports)
SPONTANEOUS PENILE ERECTION ( 1 FDA reports)
SPORTS INJURY ( 1 FDA reports)
STAPHYLOCOCCAL PHARYNGITIS ( 1 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 1 FDA reports)
STASIS SYNDROME ( 1 FDA reports)
STATUS MIGRAINOSUS ( 1 FDA reports)
STENT REMOVAL ( 1 FDA reports)
STENT-GRAFT ENDOLEAK ( 1 FDA reports)
STERNAL INJURY ( 1 FDA reports)
STOMACH GRANULOMA ( 1 FDA reports)
STOMACH LESION EXCISION ( 1 FDA reports)
STOMATOCOCCAL INFECTION ( 1 FDA reports)
STOMATOCOCCUS TEST POSITIVE ( 1 FDA reports)
STRANGULATED HERNIA REPAIR ( 1 FDA reports)
STRANGURY ( 1 FDA reports)
STREPTOCOCCAL URINARY TRACT INFECTION ( 1 FDA reports)
STROKE IN EVOLUTION ( 1 FDA reports)
STRONGYLOIDIASIS ( 1 FDA reports)
SUBSTANCE USE ( 1 FDA reports)
SUDDEN VISUAL LOSS ( 1 FDA reports)
SUPERINFECTION BACTERIAL ( 1 FDA reports)
SUPPLEMENTATION THERAPY ( 1 FDA reports)
SUTURE REMOVAL ( 1 FDA reports)
SWEATING FEVER ( 1 FDA reports)
SYMPATHETIC POSTERIOR CERVICAL SYNDROME ( 1 FDA reports)
SYNDACTYLY ( 1 FDA reports)
SYRINGE ISSUE ( 1 FDA reports)
TATTOO ( 1 FDA reports)
TESTICULAR INJURY ( 1 FDA reports)
TESTICULAR NEOPLASM ( 1 FDA reports)
TETANUS IMMUNISATION ( 1 FDA reports)
THALAMUS HAEMORRHAGE ( 1 FDA reports)
THERAPEUTIC AGENT URINE NEGATIVE ( 1 FDA reports)
THERAPEUTIC AGENT URINE POSITIVE ( 1 FDA reports)
THERAPEUTIC RESPONSE PROLONGED ( 1 FDA reports)
THIRST DECREASED ( 1 FDA reports)
THORACIC HAEMORRHAGE ( 1 FDA reports)
THROMBOPHLEBITIS MIGRANS ( 1 FDA reports)
THROMBOSED VARICOSE VEIN ( 1 FDA reports)
THYROGLOSSAL CYST ( 1 FDA reports)
THYROID CANCER STAGE II ( 1 FDA reports)
THYROIDITIS SUBACUTE ( 1 FDA reports)
THYROXINE ABNORMAL ( 1 FDA reports)
THYROXINE DECREASED ( 1 FDA reports)
THYROXINE FREE INCREASED ( 1 FDA reports)
TINEA CAPITIS ( 1 FDA reports)
TOBACCO POISONING ( 1 FDA reports)
TONGUE CARCINOMA STAGE III ( 1 FDA reports)
TONGUE DESQUAMATION ( 1 FDA reports)
TONGUE DYSPLASIA ( 1 FDA reports)
TONGUE NEOPLASM BENIGN ( 1 FDA reports)
TONGUE SPASM ( 1 FDA reports)
TOOTH HYPOPLASIA ( 1 FDA reports)
TOOTH RESORPTION ( 1 FDA reports)
TORULOPSIS INFECTION ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO INCREASED ( 1 FDA reports)
TOTAL LUNG CAPACITY INCREASED ( 1 FDA reports)
TOXIC SHOCK SYNDROME STREPTOCOCCAL ( 1 FDA reports)
TRACHEAL INFLAMMATION ( 1 FDA reports)
TRACHEAL OBSTRUCTION ( 1 FDA reports)
TRACHEAL PAIN ( 1 FDA reports)
TRACHEAL ULCER ( 1 FDA reports)
TRACHEOSTOMY MALFUNCTION ( 1 FDA reports)
TRACHOMA ( 1 FDA reports)
TRANCE ( 1 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 1 FDA reports)
TRANSIENT PSYCHOSIS ( 1 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
TRAUMATIC FRACTURE ( 1 FDA reports)
TRAUMATIC HAEMORRHAGE ( 1 FDA reports)
TRI-IODOTHYRONINE ABNORMAL ( 1 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 1 FDA reports)
TRI-IODOTHYRONINE FREE DECREASED ( 1 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 1 FDA reports)
TRI-IODOTHYRONINE UPTAKE DECREASED ( 1 FDA reports)
TRICHIASIS ( 1 FDA reports)
TRISOMY 21 ( 1 FDA reports)
TRISOMY 8 ( 1 FDA reports)
TRYPTASE ( 1 FDA reports)
TUBERCULOSIS BLADDER ( 1 FDA reports)
TUBERCULOSIS GASTROINTESTINAL ( 1 FDA reports)
TUMOUR LOCAL INVASION ( 1 FDA reports)
TUMOUR ULCERATION ( 1 FDA reports)
TWIN PREGNANCY ( 1 FDA reports)
TYMPANIC MEMBRANE ATROPHIC ( 1 FDA reports)
TYPE II HYPERSENSITIVITY ( 1 FDA reports)
TYRAMINE REACTION ( 1 FDA reports)
ULNAR NERVE INJURY ( 1 FDA reports)
ULTRASOUND ABDOMEN ( 1 FDA reports)
ULTRASOUND KIDNEY ( 1 FDA reports)
UMBILICAL CORD AROUND NECK ( 1 FDA reports)
UMBILICAL ERYTHEMA ( 1 FDA reports)
UMBILICAL HAEMORRHAGE ( 1 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 1 FDA reports)
UPPER AIRWAY NECROSIS ( 1 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 1 FDA reports)
URETERIC CANCER METASTATIC ( 1 FDA reports)
URETERIC DILATATION ( 1 FDA reports)
URETHRAL DISCHARGE ( 1 FDA reports)
URETHRAL PAIN ( 1 FDA reports)
URETHRAL POLYP ( 1 FDA reports)
URINARY SEDIMENT PRESENT ( 1 FDA reports)
URINE ALCOHOL TEST POSITIVE ( 1 FDA reports)
URINE AMPHETAMINE POSITIVE ( 1 FDA reports)
URINE COPPER INCREASED ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE ( 1 FDA reports)
URINE OSMOLARITY INCREASED ( 1 FDA reports)
URINE POTASSIUM DECREASED ( 1 FDA reports)
URINE VISCOSITY INCREASED ( 1 FDA reports)
UROBILIN URINE ( 1 FDA reports)
UROBILIN URINE PRESENT ( 1 FDA reports)
UROBILINOGEN URINE INCREASED ( 1 FDA reports)
UROGENITAL HAEMORRHAGE ( 1 FDA reports)
UROGRAM ABNORMAL ( 1 FDA reports)
UROSTOMY ( 1 FDA reports)
UROSTOMY COMPLICATION ( 1 FDA reports)
URTICARIA AQUAGENIC ( 1 FDA reports)
URTICARIA CHOLINERGIC ( 1 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 1 FDA reports)
UTERINE CONTRACTIONS ABNORMAL ( 1 FDA reports)
UTERINE CONTRACTIONS DURING PREGNANCY ( 1 FDA reports)
UTERINE NEOPLASM ( 1 FDA reports)
UTERINE SPASM ( 1 FDA reports)
VAGAL NERVE STIMULATOR IMPLANTATION ( 1 FDA reports)
VAGINAL CANCER RECURRENT ( 1 FDA reports)
VAGINAL CYST EXCISION ( 1 FDA reports)
VAGINAL DYSPLASIA ( 1 FDA reports)
VAGINAL MUCOSAL BLISTERING ( 1 FDA reports)
VAGINAL REMOVAL OF INTRAUTERINE FOREIGN BODY ( 1 FDA reports)
VAGINOPLASTY ( 1 FDA reports)
VARICOCELE ( 1 FDA reports)
VARICOSE VEIN OPERATION ( 1 FDA reports)
VASCULAR ACCESS COMPLICATION ( 1 FDA reports)
VASCULAR ANOMALY ( 1 FDA reports)
VASCULAR BYPASS GRAFT ( 1 FDA reports)
VASCULAR DISSECTION ( 1 FDA reports)
VASCULAR FRAGILITY ( 1 FDA reports)
VASCULAR HEADACHE ( 1 FDA reports)
VASCULAR NEOPLASM ( 1 FDA reports)
VASCULAR PSEUDOANEURYSM RUPTURED ( 1 FDA reports)
VASCULITIC RASH ( 1 FDA reports)
VEIN WALL HYPERTROPHY ( 1 FDA reports)
VENOUS STENT INSERTION ( 1 FDA reports)
VENOUS VALVE RUPTURED ( 1 FDA reports)
VENTILATION PERFUSION MISMATCH ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT ACQUIRED ( 1 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 1 FDA reports)
VERTEBROBASILAR DOLICHOECTASIA ( 1 FDA reports)
VESSEL PERFORATION ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 1 FDA reports)
VESSEL PUNCTURE SITE REACTION ( 1 FDA reports)
VICTIM OF ELDER ABUSE ( 1 FDA reports)
VICTIM OF HOMICIDE ( 1 FDA reports)
VIRAL CARDIOMYOPATHY ( 1 FDA reports)
VIRAL LOAD DECREASED ( 1 FDA reports)
VIRAL MYOSITIS ( 1 FDA reports)
VIRAL SINUSITIS ( 1 FDA reports)
VIRAL TRACHEITIS ( 1 FDA reports)
VIROLOGIC FAILURE ( 1 FDA reports)
VIRUS CULTURE POSITIVE ( 1 FDA reports)
VISCERAL CONGESTION ( 1 FDA reports)
VISUAL FIELD TESTS ABNORMAL ( 1 FDA reports)
VITAMIN B1 DECREASED ( 1 FDA reports)
VITAMIN B12 ABNORMAL ( 1 FDA reports)
VITAMIN B6 DECREASED ( 1 FDA reports)
VITAMIN B6 DEFICIENCY ( 1 FDA reports)
VITAMIN D INCREASED ( 1 FDA reports)
VITREOUS DEGENERATION ( 1 FDA reports)
VITREOUS DISORDER ( 1 FDA reports)
VOCAL CORD ATROPHY ( 1 FDA reports)
VOCAL CORDECTOMY ( 1 FDA reports)
VOLUME BLOOD DECREASED ( 1 FDA reports)
VOLUME BLOOD INCREASED ( 1 FDA reports)
VOMITING IN PREGNANCY ( 1 FDA reports)
VULVA CYST ( 1 FDA reports)
VULVA INJURY ( 1 FDA reports)
VULVAL DISORDER ( 1 FDA reports)
VULVAL LEUKOPLAKIA ( 1 FDA reports)
VULVAL OEDEMA ( 1 FDA reports)
VULVITIS ( 1 FDA reports)
VULVOVAGINAL ERYTHEMA ( 1 FDA reports)
VULVOVAGINITIS GONOCOCCAL ( 1 FDA reports)
WALKING DISTANCE TEST ABNORMAL ( 1 FDA reports)
WALLENBERG SYNDROME ( 1 FDA reports)
WANDERING PACEMAKER ( 1 FDA reports)
WART EXCISION ( 1 FDA reports)
WATER POLLUTION ( 1 FDA reports)
WEST NILE VIRUS TEST POSITIVE ( 1 FDA reports)
WHITE BLOOD CELL ANALYSIS DECREASED ( 1 FDA reports)
WINGED SCAPULA ( 1 FDA reports)
X-RAY OF PELVIS AND HIP ABNORMAL ( 1 FDA reports)
X-RAY WITH CONTRAST UPPER GASTROINTESTINAL TRACT ( 1 FDA reports)
YELLOW NAIL SYNDROME ( 1 FDA reports)
ZYGOMYCOSIS ( 1 FDA reports)