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

NAUSEA ( 4108 FDA reports)
PAIN ( 4104 FDA reports)
ANXIETY ( 3266 FDA reports)
DYSPNOEA ( 3203 FDA reports)
DRUG INEFFECTIVE ( 3101 FDA reports)
FATIGUE ( 2960 FDA reports)
DIARRHOEA ( 2644 FDA reports)
VOMITING ( 2604 FDA reports)
DEPRESSION ( 2563 FDA reports)
ASTHENIA ( 2494 FDA reports)
HEADACHE ( 2483 FDA reports)
CHEST PAIN ( 2383 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2377 FDA reports)
DIZZINESS ( 2373 FDA reports)
BACK PAIN ( 2285 FDA reports)
FALL ( 2210 FDA reports)
ARTHRALGIA ( 2179 FDA reports)
ANAEMIA ( 2040 FDA reports)
PAIN IN EXTREMITY ( 1989 FDA reports)
HYPERTENSION ( 1955 FDA reports)
WEIGHT DECREASED ( 1866 FDA reports)
ABDOMINAL PAIN ( 1819 FDA reports)
OEDEMA PERIPHERAL ( 1772 FDA reports)
INSOMNIA ( 1748 FDA reports)
INJURY ( 1701 FDA reports)
PNEUMONIA ( 1691 FDA reports)
PYREXIA ( 1664 FDA reports)
MYOCARDIAL INFARCTION ( 1582 FDA reports)
ABDOMINAL PAIN UPPER ( 1519 FDA reports)
CONSTIPATION ( 1441 FDA reports)
MALAISE ( 1426 FDA reports)
DEHYDRATION ( 1374 FDA reports)
COUGH ( 1369 FDA reports)
DYSPEPSIA ( 1314 FDA reports)
URINARY TRACT INFECTION ( 1313 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1275 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1271 FDA reports)
HYPOTENSION ( 1266 FDA reports)
OSTEOARTHRITIS ( 1234 FDA reports)
OSTEONECROSIS OF JAW ( 1204 FDA reports)
BONE DISORDER ( 1130 FDA reports)
HYPOAESTHESIA ( 1098 FDA reports)
GAIT DISTURBANCE ( 1077 FDA reports)
WEIGHT INCREASED ( 1071 FDA reports)
BRONCHITIS ( 1070 FDA reports)
MUSCLE SPASMS ( 1065 FDA reports)
DYSPHAGIA ( 1060 FDA reports)
RENAL FAILURE ( 1056 FDA reports)
CORONARY ARTERY DISEASE ( 1035 FDA reports)
DECREASED APPETITE ( 1029 FDA reports)
EMOTIONAL DISTRESS ( 997 FDA reports)
DRUG DOSE OMISSION ( 996 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 990 FDA reports)
PRURITUS ( 981 FDA reports)
DEEP VEIN THROMBOSIS ( 971 FDA reports)
ATRIAL FIBRILLATION ( 955 FDA reports)
SINUSITIS ( 955 FDA reports)
NEUROPATHY PERIPHERAL ( 952 FDA reports)
RASH ( 951 FDA reports)
FEELING ABNORMAL ( 941 FDA reports)
CHOLELITHIASIS ( 935 FDA reports)
MYALGIA ( 914 FDA reports)
PARAESTHESIA ( 912 FDA reports)
OSTEOMYELITIS ( 900 FDA reports)
CONFUSIONAL STATE ( 885 FDA reports)
BLOOD GLUCOSE INCREASED ( 871 FDA reports)
PAIN IN JAW ( 859 FDA reports)
HIATUS HERNIA ( 855 FDA reports)
DEATH ( 854 FDA reports)
DIABETES MELLITUS ( 840 FDA reports)
SPINAL OSTEOARTHRITIS ( 831 FDA reports)
RENAL FAILURE ACUTE ( 820 FDA reports)
TREMOR ( 818 FDA reports)
CELLULITIS ( 812 FDA reports)
ARTHRITIS ( 811 FDA reports)
PLEURAL EFFUSION ( 793 FDA reports)
OSTEOPOROSIS ( 792 FDA reports)
CHEST DISCOMFORT ( 777 FDA reports)
OSTEOPENIA ( 776 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 775 FDA reports)
PALPITATIONS ( 763 FDA reports)
BLOOD PRESSURE INCREASED ( 754 FDA reports)
PULMONARY EMBOLISM ( 749 FDA reports)
SOMNOLENCE ( 740 FDA reports)
SYNCOPE ( 738 FDA reports)
ERYTHEMA ( 728 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 728 FDA reports)
CHILLS ( 715 FDA reports)
HAEMOGLOBIN DECREASED ( 711 FDA reports)
NECK PAIN ( 706 FDA reports)
ANHEDONIA ( 702 FDA reports)
OSTEONECROSIS ( 702 FDA reports)
IMPAIRED HEALING ( 700 FDA reports)
VISION BLURRED ( 695 FDA reports)
ABDOMINAL DISCOMFORT ( 691 FDA reports)
THROMBOCYTOPENIA ( 689 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 688 FDA reports)
ASTHMA ( 687 FDA reports)
GASTRITIS ( 687 FDA reports)
MUSCULOSKELETAL PAIN ( 683 FDA reports)
CONTUSION ( 681 FDA reports)
MUSCULAR WEAKNESS ( 678 FDA reports)
HYPERHIDROSIS ( 669 FDA reports)
INFECTION ( 668 FDA reports)
CONDITION AGGRAVATED ( 666 FDA reports)
HYPERLIPIDAEMIA ( 659 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 654 FDA reports)
ATELECTASIS ( 641 FDA reports)
SEPSIS ( 634 FDA reports)
MITRAL VALVE INCOMPETENCE ( 628 FDA reports)
ABDOMINAL DISTENSION ( 625 FDA reports)
CATARACT ( 624 FDA reports)
TOOTH EXTRACTION ( 622 FDA reports)
FLUSHING ( 621 FDA reports)
CONVULSION ( 620 FDA reports)
LOSS OF CONSCIOUSNESS ( 610 FDA reports)
BONE PAIN ( 609 FDA reports)
SWELLING ( 598 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 582 FDA reports)
ARTHROPATHY ( 579 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 573 FDA reports)
DIVERTICULUM ( 568 FDA reports)
HAEMORRHOIDS ( 561 FDA reports)
HYPOKALAEMIA ( 558 FDA reports)
DRY MOUTH ( 557 FDA reports)
STRESS ( 555 FDA reports)
MEMORY IMPAIRMENT ( 549 FDA reports)
CHOLECYSTITIS CHRONIC ( 544 FDA reports)
CARDIOMEGALY ( 540 FDA reports)
AMNESIA ( 528 FDA reports)
DENTAL CARIES ( 525 FDA reports)
HEART RATE INCREASED ( 515 FDA reports)
BALANCE DISORDER ( 504 FDA reports)
PANCYTOPENIA ( 503 FDA reports)
CARDIAC DISORDER ( 497 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 497 FDA reports)
ANGINA PECTORIS ( 488 FDA reports)
TYPE 2 DIABETES MELLITUS ( 487 FDA reports)
PANCREATITIS ( 485 FDA reports)
ROTATOR CUFF SYNDROME ( 479 FDA reports)
HYPERSENSITIVITY ( 477 FDA reports)
RENAL FAILURE CHRONIC ( 476 FDA reports)
BLOOD CREATININE INCREASED ( 471 FDA reports)
RESPIRATORY FAILURE ( 470 FDA reports)
TACHYCARDIA ( 468 FDA reports)
RECTAL HAEMORRHAGE ( 462 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 462 FDA reports)
FEMUR FRACTURE ( 444 FDA reports)
FLATULENCE ( 442 FDA reports)
ALOPECIA ( 436 FDA reports)
TOOTH DISORDER ( 436 FDA reports)
WHEEZING ( 435 FDA reports)
SUICIDAL IDEATION ( 432 FDA reports)
JOINT SWELLING ( 430 FDA reports)
MENTAL STATUS CHANGES ( 429 FDA reports)
GALLBLADDER DISORDER ( 425 FDA reports)
HERPES ZOSTER ( 425 FDA reports)
DYSGEUSIA ( 424 FDA reports)
NEOPLASM MALIGNANT ( 423 FDA reports)
RIB FRACTURE ( 422 FDA reports)
DYSPNOEA EXERTIONAL ( 418 FDA reports)
DRUG HYPERSENSITIVITY ( 417 FDA reports)
MIGRAINE ( 414 FDA reports)
ARTERIOSCLEROSIS ( 411 FDA reports)
NERVOUSNESS ( 411 FDA reports)
DYSPHONIA ( 408 FDA reports)
METASTASES TO BONE ( 402 FDA reports)
OEDEMA ( 401 FDA reports)
CARDIAC ARREST ( 400 FDA reports)
DEFORMITY ( 398 FDA reports)
DYSURIA ( 397 FDA reports)
ECONOMIC PROBLEM ( 397 FDA reports)
HAEMATOCHEZIA ( 390 FDA reports)
RENAL CYST ( 389 FDA reports)
SLEEP APNOEA SYNDROME ( 388 FDA reports)
THROMBOSIS ( 386 FDA reports)
POLLAKIURIA ( 383 FDA reports)
VISUAL IMPAIRMENT ( 376 FDA reports)
HYPERGLYCAEMIA ( 375 FDA reports)
BURNING SENSATION ( 371 FDA reports)
TOOTH ABSCESS ( 371 FDA reports)
NEPHROLITHIASIS ( 370 FDA reports)
LYMPHADENOPATHY ( 369 FDA reports)
OFF LABEL USE ( 369 FDA reports)
COLONIC POLYP ( 368 FDA reports)
HYPONATRAEMIA ( 368 FDA reports)
EXOSTOSIS ( 367 FDA reports)
INFLUENZA LIKE ILLNESS ( 367 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 366 FDA reports)
OROPHARYNGEAL PAIN ( 364 FDA reports)
ROAD TRAFFIC ACCIDENT ( 363 FDA reports)
HYPOTHYROIDISM ( 362 FDA reports)
OESOPHAGITIS ( 360 FDA reports)
DECREASED INTEREST ( 358 FDA reports)
HAEMORRHAGE ( 357 FDA reports)
VERTIGO ( 356 FDA reports)
LETHARGY ( 355 FDA reports)
ORAL PAIN ( 355 FDA reports)
HYPERCHOLESTEROLAEMIA ( 353 FDA reports)
HYPOXIA ( 353 FDA reports)
LUNG NEOPLASM ( 353 FDA reports)
EPISTAXIS ( 352 FDA reports)
INJECTION SITE PAIN ( 351 FDA reports)
PLATELET COUNT DECREASED ( 351 FDA reports)
TOOTHACHE ( 348 FDA reports)
URTICARIA ( 348 FDA reports)
HOT FLUSH ( 347 FDA reports)
SWELLING FACE ( 346 FDA reports)
URINARY INCONTINENCE ( 345 FDA reports)
SLEEP DISORDER ( 336 FDA reports)
ADVERSE EVENT ( 332 FDA reports)
HAEMATURIA ( 329 FDA reports)
HEPATIC STEATOSIS ( 329 FDA reports)
DRUG INTERACTION ( 328 FDA reports)
ARRHYTHMIA ( 325 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 324 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 324 FDA reports)
HAEMATOCRIT DECREASED ( 322 FDA reports)
NEUTROPENIA ( 322 FDA reports)
NASOPHARYNGITIS ( 318 FDA reports)
EAR PAIN ( 317 FDA reports)
AGITATION ( 316 FDA reports)
DYSARTHRIA ( 314 FDA reports)
STOMATITIS ( 312 FDA reports)
PANIC ATTACK ( 311 FDA reports)
INFLUENZA ( 308 FDA reports)
STAPHYLOCOCCAL INFECTION ( 308 FDA reports)
SINUS TACHYCARDIA ( 307 FDA reports)
MULTIPLE MYELOMA ( 306 FDA reports)
BURSITIS ( 305 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 304 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 302 FDA reports)
SINUS DISORDER ( 302 FDA reports)
UNEVALUABLE EVENT ( 300 FDA reports)
FIBROMYALGIA ( 300 FDA reports)
IRRITABILITY ( 300 FDA reports)
OVERDOSE ( 298 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 297 FDA reports)
LUMBAR SPINAL STENOSIS ( 296 FDA reports)
RHEUMATOID ARTHRITIS ( 294 FDA reports)
TOOTH FRACTURE ( 292 FDA reports)
BLOOD PRESSURE DECREASED ( 291 FDA reports)
BRADYCARDIA ( 291 FDA reports)
HYPOPHAGIA ( 291 FDA reports)
NASAL CONGESTION ( 291 FDA reports)
DRUG DEPENDENCE ( 290 FDA reports)
VIRAL INFECTION ( 290 FDA reports)
PULMONARY OEDEMA ( 288 FDA reports)
SPEECH DISORDER ( 288 FDA reports)
BONE LESION ( 288 FDA reports)
HIP FRACTURE ( 288 FDA reports)
CARDIOMYOPATHY ( 282 FDA reports)
SURGERY ( 282 FDA reports)
DRUG EFFECT DECREASED ( 281 FDA reports)
HALLUCINATION ( 281 FDA reports)
FEAR ( 280 FDA reports)
LUNG DISORDER ( 280 FDA reports)
SPINAL COMPRESSION FRACTURE ( 280 FDA reports)
GASTRIC DISORDER ( 279 FDA reports)
ANOREXIA ( 278 FDA reports)
GINGIVAL BLEEDING ( 278 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 277 FDA reports)
CARPAL TUNNEL SYNDROME ( 276 FDA reports)
COMPRESSION FRACTURE ( 276 FDA reports)
DISTURBANCE IN ATTENTION ( 276 FDA reports)
PRIMARY SEQUESTRUM ( 276 FDA reports)
SCOLIOSIS ( 275 FDA reports)
NOCTURIA ( 275 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 274 FDA reports)
TOOTH LOSS ( 273 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 272 FDA reports)
MENTAL DISORDER ( 271 FDA reports)
URINARY RETENTION ( 271 FDA reports)
HEART RATE IRREGULAR ( 270 FDA reports)
MOUTH ULCERATION ( 270 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 269 FDA reports)
PULMONARY HYPERTENSION ( 269 FDA reports)
SCAR ( 268 FDA reports)
TINNITUS ( 268 FDA reports)
GASTROINTESTINAL DISORDER ( 266 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 266 FDA reports)
BLOOD GLUCOSE DECREASED ( 265 FDA reports)
BONE DENSITY DECREASED ( 264 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 261 FDA reports)
IRRITABLE BOWEL SYNDROME ( 261 FDA reports)
DISCOMFORT ( 257 FDA reports)
ANGINA UNSTABLE ( 254 FDA reports)
FEBRILE NEUTROPENIA ( 254 FDA reports)
INFLAMMATION ( 254 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 250 FDA reports)
DISEASE PROGRESSION ( 250 FDA reports)
EMPHYSEMA ( 250 FDA reports)
LEUKOPENIA ( 250 FDA reports)
TENDONITIS ( 250 FDA reports)
ILL-DEFINED DISORDER ( 249 FDA reports)
BLOOD UREA INCREASED ( 248 FDA reports)
FOOT FRACTURE ( 248 FDA reports)
TENDERNESS ( 248 FDA reports)
FLANK PAIN ( 246 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 245 FDA reports)
LUNG INFILTRATION ( 244 FDA reports)
RHINITIS ALLERGIC ( 244 FDA reports)
FISTULA ( 243 FDA reports)
COLITIS ( 242 FDA reports)
HAEMOPTYSIS ( 241 FDA reports)
RENAL IMPAIRMENT ( 240 FDA reports)
TREATMENT NONCOMPLIANCE ( 239 FDA reports)
CROHN'S DISEASE ( 239 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 238 FDA reports)
CHOLECYSTECTOMY ( 238 FDA reports)
DISABILITY ( 238 FDA reports)
HYPERKALAEMIA ( 238 FDA reports)
ABNORMAL DREAMS ( 237 FDA reports)
GASTRIC ULCER ( 237 FDA reports)
CARDIAC MURMUR ( 236 FDA reports)
ABNORMAL BEHAVIOUR ( 235 FDA reports)
BLOOD POTASSIUM DECREASED ( 234 FDA reports)
FUNGAL INFECTION ( 234 FDA reports)
INCORRECT DOSE ADMINISTERED ( 232 FDA reports)
LEUKOCYTOSIS ( 232 FDA reports)
MYOCARDIAL ISCHAEMIA ( 232 FDA reports)
RENAL DISORDER ( 231 FDA reports)
GINGIVITIS ( 229 FDA reports)
LOOSE TOOTH ( 228 FDA reports)
CHOLECYSTITIS ( 227 FDA reports)
ABSCESS ( 226 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 226 FDA reports)
PRODUCT QUALITY ISSUE ( 225 FDA reports)
PRODUCTIVE COUGH ( 225 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 225 FDA reports)
DISORIENTATION ( 225 FDA reports)
MULTIPLE INJURIES ( 224 FDA reports)
RASH PRURITIC ( 224 FDA reports)
ERECTILE DYSFUNCTION ( 223 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 223 FDA reports)
DIVERTICULITIS ( 222 FDA reports)
ABASIA ( 221 FDA reports)
MASS ( 221 FDA reports)
THROAT IRRITATION ( 221 FDA reports)
DRY SKIN ( 220 FDA reports)
INTENTIONAL DRUG MISUSE ( 220 FDA reports)
METASTASES TO LIVER ( 220 FDA reports)
OBESITY ( 220 FDA reports)
CEREBRAL ATROPHY ( 219 FDA reports)
SPINAL COLUMN STENOSIS ( 219 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 219 FDA reports)
INJECTION SITE ERYTHEMA ( 218 FDA reports)
KYPHOSIS ( 217 FDA reports)
FEELING HOT ( 216 FDA reports)
CANDIDIASIS ( 213 FDA reports)
EJECTION FRACTION DECREASED ( 213 FDA reports)
PERIODONTAL DISEASE ( 212 FDA reports)
IRON DEFICIENCY ANAEMIA ( 211 FDA reports)
SPONDYLOLISTHESIS ( 211 FDA reports)
RESPIRATORY DISTRESS ( 210 FDA reports)
CYSTITIS ( 210 FDA reports)
DYSKINESIA ( 210 FDA reports)
HYPOGLYCAEMIA ( 210 FDA reports)
BASAL CELL CARCINOMA ( 208 FDA reports)
MALNUTRITION ( 208 FDA reports)
BARRETT'S OESOPHAGUS ( 205 FDA reports)
MOBILITY DECREASED ( 205 FDA reports)
RHINORRHOEA ( 205 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 204 FDA reports)
ADVERSE DRUG REACTION ( 204 FDA reports)
HYDRONEPHROSIS ( 204 FDA reports)
MEDICATION ERROR ( 203 FDA reports)
EMOTIONAL DISORDER ( 200 FDA reports)
GASTROENTERITIS ( 199 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 199 FDA reports)
RESTLESS LEGS SYNDROME ( 198 FDA reports)
ULCER ( 198 FDA reports)
ENDODONTIC PROCEDURE ( 198 FDA reports)
HAEMATOMA ( 198 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 198 FDA reports)
CARDIAC FAILURE ( 197 FDA reports)
DRUG INTOLERANCE ( 197 FDA reports)
HYPERCALCAEMIA ( 197 FDA reports)
PERIODONTITIS ( 197 FDA reports)
VISUAL ACUITY REDUCED ( 197 FDA reports)
CAROTID ARTERY STENOSIS ( 195 FDA reports)
LEFT ATRIAL DILATATION ( 195 FDA reports)
ORAL DISORDER ( 195 FDA reports)
AGGRESSION ( 194 FDA reports)
MASTICATION DISORDER ( 194 FDA reports)
HAEMATEMESIS ( 193 FDA reports)
TOOTH INFECTION ( 193 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 192 FDA reports)
HEPATIC ENZYME INCREASED ( 192 FDA reports)
FLUID RETENTION ( 191 FDA reports)
ORTHOSTATIC HYPOTENSION ( 191 FDA reports)
BONE DEBRIDEMENT ( 189 FDA reports)
EATING DISORDER ( 189 FDA reports)
JAW DISORDER ( 189 FDA reports)
SINUS BRADYCARDIA ( 189 FDA reports)
UNRESPONSIVE TO STIMULI ( 189 FDA reports)
AORTIC VALVE INCOMPETENCE ( 188 FDA reports)
DYSLIPIDAEMIA ( 188 FDA reports)
ORAL INFECTION ( 188 FDA reports)
ANGER ( 187 FDA reports)
NIGHT SWEATS ( 187 FDA reports)
PRESYNCOPE ( 187 FDA reports)
ASCITES ( 186 FDA reports)
PULMONARY CONGESTION ( 185 FDA reports)
SKIN ULCER ( 185 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 184 FDA reports)
FAECES DISCOLOURED ( 184 FDA reports)
PERICARDIAL EFFUSION ( 184 FDA reports)
JOINT INJURY ( 183 FDA reports)
CARDIO-RESPIRATORY ARREST ( 182 FDA reports)
CORONARY ARTERY OCCLUSION ( 182 FDA reports)
DIVERTICULUM INTESTINAL ( 182 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 182 FDA reports)
LIVER DISORDER ( 182 FDA reports)
OSTEOLYSIS ( 182 FDA reports)
MULTI-ORGAN FAILURE ( 181 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 180 FDA reports)
PEPTIC ULCER ( 179 FDA reports)
SPINAL FRACTURE ( 179 FDA reports)
VENTRICULAR HYPERTROPHY ( 178 FDA reports)
CHRONIC SINUSITIS ( 178 FDA reports)
GINGIVAL PAIN ( 178 FDA reports)
INTERSTITIAL LUNG DISEASE ( 178 FDA reports)
NEURALGIA ( 178 FDA reports)
BREAST CANCER ( 177 FDA reports)
DEBRIDEMENT ( 175 FDA reports)
PHYSICAL DISABILITY ( 175 FDA reports)
GOUT ( 174 FDA reports)
CHOLECYSTITIS ACUTE ( 173 FDA reports)
GLAUCOMA ( 173 FDA reports)
PATHOLOGICAL FRACTURE ( 172 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 172 FDA reports)
PURULENT DISCHARGE ( 171 FDA reports)
SKIN DISCOLOURATION ( 171 FDA reports)
DIPLOPIA ( 171 FDA reports)
DRY EYE ( 171 FDA reports)
CARDIOVASCULAR DISORDER ( 170 FDA reports)
CEREBRAL INFARCTION ( 170 FDA reports)
ABDOMINAL PAIN LOWER ( 169 FDA reports)
DIABETIC NEUROPATHY ( 169 FDA reports)
SKIN DISORDER ( 169 FDA reports)
RASH ERYTHEMATOUS ( 168 FDA reports)
ERUCTATION ( 168 FDA reports)
BLISTER ( 167 FDA reports)
BLINDNESS ( 165 FDA reports)
DEAFNESS ( 165 FDA reports)
FEELING COLD ( 165 FDA reports)
MENISCUS LESION ( 165 FDA reports)
RADICULOPATHY ( 165 FDA reports)
EXPOSED BONE IN JAW ( 164 FDA reports)
HEPATIC CYST ( 164 FDA reports)
LYMPHOEDEMA ( 164 FDA reports)
ACTINOMYCOSIS ( 163 FDA reports)
ORAL CANDIDIASIS ( 162 FDA reports)
GINGIVAL DISORDER ( 161 FDA reports)
LIMB INJURY ( 161 FDA reports)
RHABDOMYOLYSIS ( 161 FDA reports)
SCIATICA ( 160 FDA reports)
SINUS CONGESTION ( 160 FDA reports)
BACTERIAL INFECTION ( 160 FDA reports)
BLOOD CALCIUM DECREASED ( 160 FDA reports)
HEPATOMEGALY ( 160 FDA reports)
INTESTINAL OBSTRUCTION ( 160 FDA reports)
MUSCLE TWITCHING ( 160 FDA reports)
BILIARY DYSKINESIA ( 158 FDA reports)
BLOOD BILIRUBIN INCREASED ( 158 FDA reports)
COLITIS ULCERATIVE ( 158 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 158 FDA reports)
METASTASES TO SPINE ( 157 FDA reports)
OSTEOSCLEROSIS ( 157 FDA reports)
PANCREATITIS ACUTE ( 157 FDA reports)
HEAD INJURY ( 156 FDA reports)
APHAGIA ( 155 FDA reports)
SKIN LESION ( 155 FDA reports)
SUICIDE ATTEMPT ( 155 FDA reports)
EYE PAIN ( 154 FDA reports)
HYPOMAGNESAEMIA ( 154 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 154 FDA reports)
LIFE EXPECTANCY SHORTENED ( 153 FDA reports)
PELVIC FRACTURE ( 153 FDA reports)
VENTRICULAR TACHYCARDIA ( 153 FDA reports)
PULMONARY FIBROSIS ( 152 FDA reports)
DEMENTIA ( 152 FDA reports)
MENTAL IMPAIRMENT ( 152 FDA reports)
BACK DISORDER ( 151 FDA reports)
FOOT DEFORMITY ( 151 FDA reports)
LUMBAR RADICULOPATHY ( 149 FDA reports)
HEMIPARESIS ( 148 FDA reports)
HEPATITIS ( 148 FDA reports)
SYNOVIAL CYST ( 148 FDA reports)
HEART RATE DECREASED ( 147 FDA reports)
DELIRIUM ( 146 FDA reports)
COGNITIVE DISORDER ( 145 FDA reports)
HYPOCALCAEMIA ( 145 FDA reports)
MUCOSAL INFLAMMATION ( 145 FDA reports)
MUSCLE TIGHTNESS ( 145 FDA reports)
INJECTION SITE HAEMATOMA ( 144 FDA reports)
MOOD ALTERED ( 144 FDA reports)
TARDIVE DYSKINESIA ( 144 FDA reports)
PROTHROMBIN TIME PROLONGED ( 143 FDA reports)
SPLENOMEGALY ( 143 FDA reports)
ANKLE FRACTURE ( 143 FDA reports)
ATRIAL FLUTTER ( 143 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 142 FDA reports)
OSTEITIS ( 142 FDA reports)
LOW TURNOVER OSTEOPATHY ( 141 FDA reports)
ORAL DISCOMFORT ( 141 FDA reports)
RENAL INJURY ( 141 FDA reports)
CORONARY ARTERY STENOSIS ( 140 FDA reports)
DEPRESSED MOOD ( 140 FDA reports)
LIMB DISCOMFORT ( 140 FDA reports)
PHARYNGITIS ( 140 FDA reports)
FIBROSIS ( 139 FDA reports)
BLOOD SODIUM DECREASED ( 138 FDA reports)
CYST ( 138 FDA reports)
DERMATITIS ( 138 FDA reports)
PHARYNGEAL OEDEMA ( 138 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 138 FDA reports)
UPPER LIMB FRACTURE ( 138 FDA reports)
STRESS FRACTURE ( 137 FDA reports)
HYPOAESTHESIA ORAL ( 137 FDA reports)
INJECTION SITE HAEMORRHAGE ( 137 FDA reports)
ORAL SURGERY ( 137 FDA reports)
FEELING JITTERY ( 136 FDA reports)
HYPERSOMNIA ( 136 FDA reports)
PSORIASIS ( 136 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 135 FDA reports)
GINGIVAL SWELLING ( 135 FDA reports)
METABOLIC ACIDOSIS ( 135 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 133 FDA reports)
GENERALISED OEDEMA ( 132 FDA reports)
JOINT STIFFNESS ( 132 FDA reports)
AORTIC ANEURYSM ( 131 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 131 FDA reports)
CERVICAL SPINAL STENOSIS ( 131 FDA reports)
COORDINATION ABNORMAL ( 131 FDA reports)
CRYING ( 131 FDA reports)
FAECAL INCONTINENCE ( 131 FDA reports)
MOOD SWINGS ( 131 FDA reports)
SKIN EXFOLIATION ( 131 FDA reports)
SWOLLEN TONGUE ( 131 FDA reports)
WITHDRAWAL SYNDROME ( 131 FDA reports)
CEREBRAL ISCHAEMIA ( 130 FDA reports)
DRUG TOXICITY ( 130 FDA reports)
EXCORIATION ( 130 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 130 FDA reports)
GASTRIC POLYPS ( 129 FDA reports)
LACERATION ( 129 FDA reports)
PNEUMONITIS ( 129 FDA reports)
SEBORRHOEIC KERATOSIS ( 129 FDA reports)
VASCULITIS ( 129 FDA reports)
WOUND DEHISCENCE ( 129 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 128 FDA reports)
JAW OPERATION ( 128 FDA reports)
OXYGEN SATURATION DECREASED ( 128 FDA reports)
BIPOLAR DISORDER ( 127 FDA reports)
BONE LOSS ( 127 FDA reports)
HYPOVOLAEMIA ( 127 FDA reports)
SEPTIC SHOCK ( 127 FDA reports)
THROAT TIGHTNESS ( 127 FDA reports)
ONYCHOMYCOSIS ( 126 FDA reports)
ILEUS ( 125 FDA reports)
NERVOUS SYSTEM DISORDER ( 124 FDA reports)
DEVICE RELATED INFECTION ( 123 FDA reports)
PARANOIA ( 123 FDA reports)
SKIN BURNING SENSATION ( 123 FDA reports)
SOFT TISSUE DISORDER ( 123 FDA reports)
COAGULOPATHY ( 122 FDA reports)
EYE DISORDER ( 122 FDA reports)
HYPERKERATOSIS ( 122 FDA reports)
ATAXIA ( 121 FDA reports)
RETCHING ( 121 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 121 FDA reports)
VITAMIN D DEFICIENCY ( 121 FDA reports)
STOMACH DISCOMFORT ( 120 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 120 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 120 FDA reports)
DENTAL FISTULA ( 120 FDA reports)
HEPATIC LESION ( 120 FDA reports)
JOINT DISLOCATION ( 120 FDA reports)
JOINT EFFUSION ( 120 FDA reports)
JOINT SPRAIN ( 120 FDA reports)
MOVEMENT DISORDER ( 120 FDA reports)
OSTEORADIONECROSIS ( 120 FDA reports)
PELVIC PAIN ( 120 FDA reports)
ACTINIC KERATOSIS ( 119 FDA reports)
CERUMEN IMPACTION ( 119 FDA reports)
ECCHYMOSIS ( 119 FDA reports)
GINGIVAL ULCERATION ( 119 FDA reports)
MICTURITION URGENCY ( 119 FDA reports)
NODULE ( 119 FDA reports)
NON-CARDIAC CHEST PAIN ( 119 FDA reports)
CAROTID ARTERY DISEASE ( 118 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 118 FDA reports)
SPINAL DISORDER ( 118 FDA reports)
RASH GENERALISED ( 117 FDA reports)
VISUAL DISTURBANCE ( 117 FDA reports)
GLOSSODYNIA ( 117 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 117 FDA reports)
NEOPLASM PROGRESSION ( 117 FDA reports)
FAILURE TO THRIVE ( 116 FDA reports)
OESOPHAGEAL DISORDER ( 116 FDA reports)
PROTEINURIA ( 116 FDA reports)
RHINITIS ( 116 FDA reports)
POST PROCEDURAL COMPLICATION ( 115 FDA reports)
AORTIC STENOSIS ( 115 FDA reports)
CHOKING ( 115 FDA reports)
GROIN PAIN ( 115 FDA reports)
LUNG NEOPLASM MALIGNANT ( 115 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 115 FDA reports)
FLUID OVERLOAD ( 114 FDA reports)
GINGIVAL INFECTION ( 114 FDA reports)
MULTIPLE SCLEROSIS ( 114 FDA reports)
ACUTE RESPIRATORY FAILURE ( 113 FDA reports)
AZOTAEMIA ( 113 FDA reports)
HERNIA ( 113 FDA reports)
INTERMITTENT CLAUDICATION ( 113 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 113 FDA reports)
UTERINE LEIOMYOMA ( 113 FDA reports)
CHROMATURIA ( 112 FDA reports)
FRACTURED SACRUM ( 112 FDA reports)
IMPAIRED WORK ABILITY ( 112 FDA reports)
MELAENA ( 112 FDA reports)
APHASIA ( 111 FDA reports)
JAW FRACTURE ( 111 FDA reports)
SENSITIVITY OF TEETH ( 111 FDA reports)
VAGINAL HAEMORRHAGE ( 111 FDA reports)
PNEUMONIA ASPIRATION ( 110 FDA reports)
HALLUCINATION, AUDITORY ( 110 FDA reports)
INCREASED APPETITE ( 110 FDA reports)
MYELODYSPLASTIC SYNDROME ( 110 FDA reports)
HEPATIC FAILURE ( 109 FDA reports)
PALLOR ( 109 FDA reports)
ABSCESS JAW ( 108 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 108 FDA reports)
CATARACT OPERATION ( 108 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 108 FDA reports)
JAUNDICE ( 108 FDA reports)
SEQUESTRECTOMY ( 108 FDA reports)
UROSEPSIS ( 108 FDA reports)
PRURITUS GENERALISED ( 107 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 107 FDA reports)
ASPIRATION ( 107 FDA reports)
GOITRE ( 107 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 106 FDA reports)
RESTLESSNESS ( 106 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 105 FDA reports)
ENCEPHALOPATHY ( 104 FDA reports)
BACK INJURY ( 103 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 103 FDA reports)
METASTATIC NEOPLASM ( 103 FDA reports)
NASAL SEPTUM DEVIATION ( 103 FDA reports)
WALKING AID USER ( 103 FDA reports)
PROCTALGIA ( 102 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 102 FDA reports)
ACUTE SINUSITIS ( 102 FDA reports)
BLOOD ALBUMIN DECREASED ( 102 FDA reports)
BLOOD URINE PRESENT ( 102 FDA reports)
DENTURE WEARER ( 102 FDA reports)
ELECTROLYTE IMBALANCE ( 102 FDA reports)
GASTROENTERITIS VIRAL ( 102 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 102 FDA reports)
LOBAR PNEUMONIA ( 102 FDA reports)
MUSCLE STRAIN ( 102 FDA reports)
ODYNOPHAGIA ( 102 FDA reports)
OEDEMA MOUTH ( 102 FDA reports)
BREATH ODOUR ( 101 FDA reports)
COMA ( 101 FDA reports)
DIASTOLIC DYSFUNCTION ( 101 FDA reports)
FACIAL PAIN ( 101 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 101 FDA reports)
THIRST ( 101 FDA reports)
VENTRICULAR FIBRILLATION ( 101 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 101 FDA reports)
RASH MACULAR ( 100 FDA reports)
TENSION ( 100 FDA reports)
FRACTURE NONUNION ( 100 FDA reports)
MIDDLE INSOMNIA ( 100 FDA reports)
BLINDNESS UNILATERAL ( 99 FDA reports)
DENTAL OPERATION ( 99 FDA reports)
DIABETIC KETOACIDOSIS ( 99 FDA reports)
LYMPHOMA ( 99 FDA reports)
MOUTH HAEMORRHAGE ( 99 FDA reports)
OVARIAN CYST ( 99 FDA reports)
PSYCHOTIC DISORDER ( 99 FDA reports)
TOBACCO USER ( 99 FDA reports)
ANAPHYLACTIC REACTION ( 98 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 98 FDA reports)
COSTOCHONDRITIS ( 98 FDA reports)
EROSIVE OESOPHAGITIS ( 98 FDA reports)
FACET JOINT SYNDROME ( 98 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 97 FDA reports)
LARYNGITIS ( 97 FDA reports)
MAJOR DEPRESSION ( 97 FDA reports)
PYELONEPHRITIS ( 97 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 97 FDA reports)
PLANTAR FASCIITIS ( 96 FDA reports)
RESPIRATORY DISORDER ( 96 FDA reports)
DECUBITUS ULCER ( 96 FDA reports)
INJECTION SITE REACTION ( 96 FDA reports)
LOWER LIMB FRACTURE ( 96 FDA reports)
OESOPHAGEAL PAIN ( 96 FDA reports)
CONJUNCTIVITIS ( 95 FDA reports)
NIGHTMARE ( 95 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 95 FDA reports)
BONE OPERATION ( 94 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 94 FDA reports)
DUODENITIS ( 94 FDA reports)
HERPES SIMPLEX ( 94 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 94 FDA reports)
PLATELET COUNT INCREASED ( 94 FDA reports)
SQUAMOUS CELL CARCINOMA ( 94 FDA reports)
TOOTH IMPACTED ( 94 FDA reports)
WRIST FRACTURE ( 94 FDA reports)
TENDON RUPTURE ( 93 FDA reports)
THYROID NEOPLASM ( 93 FDA reports)
VENTRICULAR HYPOKINESIA ( 93 FDA reports)
ABORTION SPONTANEOUS ( 93 FDA reports)
HYPOACUSIS ( 93 FDA reports)
LABORATORY TEST ABNORMAL ( 93 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 92 FDA reports)
TENDON INJURY ( 92 FDA reports)
QUALITY OF LIFE DECREASED ( 91 FDA reports)
RALES ( 91 FDA reports)
SENSORY LOSS ( 91 FDA reports)
BODY TEMPERATURE INCREASED ( 91 FDA reports)
COLD SWEAT ( 91 FDA reports)
HEARING IMPAIRED ( 91 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 91 FDA reports)
NEUTROPHIL COUNT DECREASED ( 91 FDA reports)
PHLEBITIS ( 91 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 90 FDA reports)
ESCHERICHIA INFECTION ( 90 FDA reports)
FRUSTRATION ( 90 FDA reports)
HAEMANGIOMA ( 90 FDA reports)
HUMERUS FRACTURE ( 90 FDA reports)
METASTASES TO LYMPH NODES ( 90 FDA reports)
POLYNEUROPATHY ( 90 FDA reports)
POOR QUALITY SLEEP ( 90 FDA reports)
REGURGITATION ( 90 FDA reports)
SOMNAMBULISM ( 90 FDA reports)
SKIN LACERATION ( 89 FDA reports)
VENOUS INSUFFICIENCY ( 89 FDA reports)
BLOOD POTASSIUM INCREASED ( 89 FDA reports)
BONE FRAGMENTATION ( 89 FDA reports)
DILATATION ATRIAL ( 89 FDA reports)
EPICONDYLITIS ( 88 FDA reports)
INJECTION SITE PRURITUS ( 88 FDA reports)
LIBIDO DECREASED ( 88 FDA reports)
LIPOMA ( 88 FDA reports)
THYROID DISORDER ( 88 FDA reports)
POLYP ( 87 FDA reports)
ADRENAL INSUFFICIENCY ( 87 FDA reports)
LIGAMENT SPRAIN ( 87 FDA reports)
MENOPAUSE ( 87 FDA reports)
MYOPATHY ( 87 FDA reports)
OPEN WOUND ( 87 FDA reports)
ANGIOEDEMA ( 86 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 86 FDA reports)
GALLBLADDER INJURY ( 86 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 86 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 86 FDA reports)
ORAL HERPES ( 86 FDA reports)
SKIN INDURATION ( 86 FDA reports)
BREAST CANCER METASTATIC ( 85 FDA reports)
DRUG ADMINISTRATION ERROR ( 85 FDA reports)
HYPERTONIC BLADDER ( 85 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 85 FDA reports)
AGEUSIA ( 84 FDA reports)
BREAST MASS ( 84 FDA reports)
CAROTID BRUIT ( 84 FDA reports)
INFUSION RELATED REACTION ( 84 FDA reports)
SENSATION OF FOREIGN BODY ( 84 FDA reports)
SKIN TIGHTNESS ( 84 FDA reports)
SHOCK ( 83 FDA reports)
SPINAL CORD COMPRESSION ( 83 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 83 FDA reports)
ACUTE CORONARY SYNDROME ( 83 FDA reports)
HYPOPHOSPHATAEMIA ( 83 FDA reports)
MENORRHAGIA ( 83 FDA reports)
ACNE ( 82 FDA reports)
BREAST PAIN ( 82 FDA reports)
EYELID PTOSIS ( 82 FDA reports)
INCREASED TENDENCY TO BRUISE ( 82 FDA reports)
ISCHAEMIA ( 82 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 82 FDA reports)
METASTASES TO LUNG ( 82 FDA reports)
MUSCLE CRAMP ( 82 FDA reports)
OESOPHAGEAL STENOSIS ( 82 FDA reports)
PLEURAL FIBROSIS ( 82 FDA reports)
THINKING ABNORMAL ( 81 FDA reports)
WRONG DRUG ADMINISTERED ( 81 FDA reports)
CEREBRAL HAEMORRHAGE ( 81 FDA reports)
GYNAECOMASTIA ( 81 FDA reports)
PARALYSIS ( 81 FDA reports)
ABDOMINAL HERNIA ( 80 FDA reports)
CYSTOCELE ( 80 FDA reports)
DUODENAL ULCER ( 80 FDA reports)
GINGIVAL RECESSION ( 80 FDA reports)
LOCALISED INFECTION ( 80 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 80 FDA reports)
MACULAR DEGENERATION ( 80 FDA reports)
MUSCLE ATROPHY ( 80 FDA reports)
PARKINSON'S DISEASE ( 80 FDA reports)
PATHOLOGICAL GAMBLING ( 80 FDA reports)
RECTAL POLYP ( 80 FDA reports)
SKIN HYPERTROPHY ( 80 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 80 FDA reports)
SUBCUTANEOUS ABSCESS ( 80 FDA reports)
PROSTATE CANCER ( 79 FDA reports)
DEAFNESS NEUROSENSORY ( 79 FDA reports)
INCONTINENCE ( 79 FDA reports)
ANEURYSM ( 78 FDA reports)
BRUXISM ( 78 FDA reports)
DIFFICULTY IN WALKING ( 78 FDA reports)
DISEASE RECURRENCE ( 78 FDA reports)
FRACTURE ( 78 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 78 FDA reports)
OESOPHAGEAL ULCER ( 78 FDA reports)
PHOTOPHOBIA ( 78 FDA reports)
PNEUMOTHORAX ( 78 FDA reports)
RESPIRATORY ARREST ( 78 FDA reports)
SICK SINUS SYNDROME ( 77 FDA reports)
SPUTUM DISCOLOURED ( 77 FDA reports)
TYPE 1 DIABETES MELLITUS ( 77 FDA reports)
BACTERAEMIA ( 77 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 77 FDA reports)
DILATATION VENTRICULAR ( 77 FDA reports)
EAR INFECTION ( 77 FDA reports)
FIBULA FRACTURE ( 77 FDA reports)
HOSPITALISATION ( 77 FDA reports)
INJECTION SITE SWELLING ( 77 FDA reports)
OTITIS MEDIA ( 77 FDA reports)
PAROSMIA ( 77 FDA reports)
PETECHIAE ( 77 FDA reports)
EYE IRRITATION ( 76 FDA reports)
GASTRITIS EROSIVE ( 76 FDA reports)
ORTHOPNOEA ( 76 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 76 FDA reports)
WOUND ( 76 FDA reports)
POLYDIPSIA ( 75 FDA reports)
SEASONAL ALLERGY ( 75 FDA reports)
BREATH SOUNDS ABNORMAL ( 75 FDA reports)
CARDIAC VALVE DISEASE ( 75 FDA reports)
CAROTID ARTERY OCCLUSION ( 75 FDA reports)
DYSSTASIA ( 75 FDA reports)
HIP ARTHROPLASTY ( 75 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 75 FDA reports)
HYPOKINESIA ( 75 FDA reports)
INGUINAL HERNIA ( 75 FDA reports)
LUNG HYPERINFLATION ( 75 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 75 FDA reports)
MYOSITIS ( 75 FDA reports)
DEVICE FAILURE ( 74 FDA reports)
LACRIMATION INCREASED ( 74 FDA reports)
SINUS HEADACHE ( 74 FDA reports)
SLEEP TALKING ( 74 FDA reports)
STEM CELL TRANSPLANT ( 74 FDA reports)
STRESS URINARY INCONTINENCE ( 74 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 73 FDA reports)
RESPIRATORY TRACT INFECTION ( 73 FDA reports)
VENTRICULAR DYSFUNCTION ( 73 FDA reports)
CHONDROMALACIA ( 73 FDA reports)
DRY THROAT ( 73 FDA reports)
ENTERITIS ( 73 FDA reports)
HEPATIC CIRRHOSIS ( 73 FDA reports)
INADEQUATE ANALGESIA ( 73 FDA reports)
BLADDER DISORDER ( 72 FDA reports)
ESSENTIAL HYPERTENSION ( 72 FDA reports)
FURUNCLE ( 72 FDA reports)
GASTRIC HAEMORRHAGE ( 72 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 72 FDA reports)
SHOULDER PAIN ( 72 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 72 FDA reports)
RADIOTHERAPY ( 71 FDA reports)
URINARY HESITATION ( 71 FDA reports)
VASCULAR CALCIFICATION ( 71 FDA reports)
VERTEBROPLASTY ( 71 FDA reports)
VITREOUS DETACHMENT ( 71 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 71 FDA reports)
DRUG TOLERANCE ( 71 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 71 FDA reports)
BONE SWELLING ( 70 FDA reports)
EYE HAEMORRHAGE ( 70 FDA reports)
IMMUNOSUPPRESSION ( 70 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 70 FDA reports)
OCULAR HYPERAEMIA ( 70 FDA reports)
OESOPHAGEAL SPASM ( 70 FDA reports)
PERIPHERAL COLDNESS ( 70 FDA reports)
SEDATION ( 70 FDA reports)
TENDON DISORDER ( 70 FDA reports)
TONGUE INJURY ( 70 FDA reports)
PLEURITIC PAIN ( 69 FDA reports)
POLYURIA ( 69 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 69 FDA reports)
UMBILICAL HERNIA ( 69 FDA reports)
VENOUS THROMBOSIS ( 69 FDA reports)
BILIARY COLIC ( 69 FDA reports)
CARDIAC PACEMAKER INSERTION ( 69 FDA reports)
ISCHAEMIC STROKE ( 69 FDA reports)
KNEE ARTHROPLASTY ( 69 FDA reports)
MENSTRUAL DISORDER ( 69 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 69 FDA reports)
ANGIOPATHY ( 68 FDA reports)
BREAST CANCER FEMALE ( 68 FDA reports)
BRONCHIECTASIS ( 68 FDA reports)
BRONCHOSPASM ( 68 FDA reports)
CIRCULATORY COLLAPSE ( 68 FDA reports)
DECREASED ACTIVITY ( 68 FDA reports)
DERMATITIS CONTACT ( 68 FDA reports)
MANIA ( 68 FDA reports)
PARAESTHESIA ORAL ( 68 FDA reports)
PULPITIS DENTAL ( 68 FDA reports)
SUBDURAL HAEMATOMA ( 68 FDA reports)
TRIGGER FINGER ( 68 FDA reports)
VITAMIN B12 DEFICIENCY ( 68 FDA reports)
PLASMACYTOMA ( 67 FDA reports)
POST HERPETIC NEURALGIA ( 67 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 67 FDA reports)
CLOSTRIDIAL INFECTION ( 67 FDA reports)
COLITIS ISCHAEMIC ( 67 FDA reports)
EXERCISE TOLERANCE DECREASED ( 67 FDA reports)
EYE SWELLING ( 67 FDA reports)
HELICOBACTER INFECTION ( 67 FDA reports)
INTENTIONAL OVERDOSE ( 67 FDA reports)
APHONIA ( 66 FDA reports)
CALCULUS URETERIC ( 66 FDA reports)
DIABETIC RETINOPATHY ( 66 FDA reports)
ECZEMA ( 66 FDA reports)
FACIAL PALSY ( 66 FDA reports)
GRAND MAL CONVULSION ( 66 FDA reports)
HEPATITIS C ( 66 FDA reports)
MITRAL VALVE PROLAPSE ( 66 FDA reports)
NERVE INJURY ( 66 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 66 FDA reports)
PROSTATITIS ( 66 FDA reports)
VARICOSE VEIN ( 66 FDA reports)
ROSACEA ( 65 FDA reports)
SENSORY DISTURBANCE ( 65 FDA reports)
SKIN HYPERPIGMENTATION ( 65 FDA reports)
BONE SCAN ABNORMAL ( 65 FDA reports)
BRONCHOPNEUMONIA ( 65 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 65 FDA reports)
CORONARY ARTERY BYPASS ( 65 FDA reports)
FISTULA DISCHARGE ( 65 FDA reports)
HAEMORRHAGIC ANAEMIA ( 65 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 65 FDA reports)
HYPOALBUMINAEMIA ( 65 FDA reports)
LACUNAR INFARCTION ( 65 FDA reports)
MUSCULOSKELETAL DISORDER ( 65 FDA reports)
ORAL CAVITY FISTULA ( 65 FDA reports)
AORTIC CALCIFICATION ( 64 FDA reports)
CONCUSSION ( 64 FDA reports)
GRANULOMA ( 64 FDA reports)
HAEMODIALYSIS ( 64 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 64 FDA reports)
REFLUX OESOPHAGITIS ( 64 FDA reports)
URINE OUTPUT DECREASED ( 64 FDA reports)
WHEELCHAIR USER ( 64 FDA reports)
POOR DENTAL CONDITION ( 63 FDA reports)
RENAL TUBULAR NECROSIS ( 63 FDA reports)
THROMBOCYTOSIS ( 63 FDA reports)
BLOOD CALCIUM INCREASED ( 63 FDA reports)
CYANOSIS ( 63 FDA reports)
OCCULT BLOOD POSITIVE ( 63 FDA reports)
AFFECTIVE DISORDER ( 62 FDA reports)
APNOEA ( 62 FDA reports)
ATHEROSCLEROSIS ( 62 FDA reports)
CERVICOBRACHIAL SYNDROME ( 62 FDA reports)
DERMAL CYST ( 62 FDA reports)
ENTEROCOCCAL INFECTION ( 62 FDA reports)
INCISIONAL DRAINAGE ( 62 FDA reports)
INGROWING NAIL ( 62 FDA reports)
MELANOCYTIC NAEVUS ( 62 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 62 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 62 FDA reports)
RASH PAPULAR ( 62 FDA reports)
VULVOVAGINAL DRYNESS ( 62 FDA reports)
PULMONARY MASS ( 61 FDA reports)
TONGUE DISORDER ( 61 FDA reports)
WOUND DRAINAGE ( 61 FDA reports)
ARTHROPOD BITE ( 61 FDA reports)
ATRIAL TACHYCARDIA ( 61 FDA reports)
DEVICE MALFUNCTION ( 61 FDA reports)
DIALYSIS ( 61 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 61 FDA reports)
LOCAL SWELLING ( 61 FDA reports)
MITRAL VALVE CALCIFICATION ( 61 FDA reports)
NO ADVERSE EVENT ( 61 FDA reports)
BLOOD MAGNESIUM DECREASED ( 60 FDA reports)
BONE MARROW FAILURE ( 60 FDA reports)
EYE PRURITUS ( 60 FDA reports)
LIP SWELLING ( 60 FDA reports)
LUNG INFECTION ( 60 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 60 FDA reports)
OTITIS EXTERNA ( 60 FDA reports)
STEVENS-JOHNSON SYNDROME ( 60 FDA reports)
VITAMIN D DECREASED ( 60 FDA reports)
PULMONARY GRANULOMA ( 59 FDA reports)
ABDOMINAL TENDERNESS ( 59 FDA reports)
BLINDNESS TRANSIENT ( 59 FDA reports)
BODY HEIGHT DECREASED ( 59 FDA reports)
BONE EROSION ( 59 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 59 FDA reports)
DRUG ABUSER ( 59 FDA reports)
EUPHORIC MOOD ( 59 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 59 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 59 FDA reports)
LIPASE INCREASED ( 59 FDA reports)
NEURITIS ( 59 FDA reports)
PANCREATITIS CHRONIC ( 59 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 58 FDA reports)
ANXIETY DISORDER ( 58 FDA reports)
BED REST ( 58 FDA reports)
CHEST X-RAY ABNORMAL ( 58 FDA reports)
ENURESIS ( 58 FDA reports)
HYPERCHLORHYDRIA ( 58 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 58 FDA reports)
INTESTINAL PERFORATION ( 58 FDA reports)
LABYRINTHITIS ( 58 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 58 FDA reports)
MEDICAL DEVICE COMPLICATION ( 58 FDA reports)
METABOLIC ENCEPHALOPATHY ( 58 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 58 FDA reports)
SYNOVITIS ( 58 FDA reports)
TONGUE DISCOLOURATION ( 58 FDA reports)
PROSTATOMEGALY ( 57 FDA reports)
RESPIRATORY RATE INCREASED ( 57 FDA reports)
TENOSYNOVITIS ( 57 FDA reports)
TIBIA FRACTURE ( 57 FDA reports)
VAGINAL INFECTION ( 57 FDA reports)
ACIDOSIS ( 57 FDA reports)
COLON CANCER ( 57 FDA reports)
HICCUPS ( 57 FDA reports)
INTRAOCULAR LENS IMPLANT ( 57 FDA reports)
KIDNEY INFECTION ( 57 FDA reports)
MULTIPLE ALLERGIES ( 57 FDA reports)
NERVE COMPRESSION ( 57 FDA reports)
NO THERAPEUTIC RESPONSE ( 57 FDA reports)
DIZZINESS POSTURAL ( 56 FDA reports)
EXTRASYSTOLES ( 56 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 56 FDA reports)
HYPERPARATHYROIDISM ( 56 FDA reports)
NECROSIS ( 56 FDA reports)
NEUTROPHIL COUNT INCREASED ( 56 FDA reports)
AORTIC VALVE SCLEROSIS ( 55 FDA reports)
ATROPHIC VULVOVAGINITIS ( 55 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 55 FDA reports)
BUNION ( 55 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 55 FDA reports)
PERITONITIS ( 55 FDA reports)
PROCEDURAL PAIN ( 55 FDA reports)
PURULENCE ( 55 FDA reports)
RENAL MASS ( 55 FDA reports)
RHONCHI ( 55 FDA reports)
SCLERODERMA ( 55 FDA reports)
SPONDYLOLYSIS ( 55 FDA reports)
SKIN PAPILLOMA ( 54 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 54 FDA reports)
UTERINE POLYP ( 54 FDA reports)
VISUAL FIELD DEFECT ( 54 FDA reports)
VITREOUS FLOATERS ( 54 FDA reports)
APHTHOUS STOMATITIS ( 54 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 54 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 54 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 54 FDA reports)
GASTROINTESTINAL PAIN ( 54 FDA reports)
GINGIVAL EROSION ( 54 FDA reports)
HALLUCINATION, VISUAL ( 54 FDA reports)
HAND FRACTURE ( 54 FDA reports)
HEART INJURY ( 54 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 54 FDA reports)
MOTOR DYSFUNCTION ( 54 FDA reports)
MUSCLE INJURY ( 54 FDA reports)
OLIGURIA ( 54 FDA reports)
AFFECT LABILITY ( 53 FDA reports)
BREAST TENDERNESS ( 53 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 53 FDA reports)
EAR DISORDER ( 53 FDA reports)
FACIAL BONES FRACTURE ( 53 FDA reports)
IMPAIRED DRIVING ABILITY ( 53 FDA reports)
MALABSORPTION ( 53 FDA reports)
NEUROGENIC BLADDER ( 53 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 53 FDA reports)
PERICARDITIS ( 53 FDA reports)
PRESBYOPIA ( 53 FDA reports)
PSEUDOMONAS INFECTION ( 53 FDA reports)
RENAL PAIN ( 53 FDA reports)
SCAB ( 53 FDA reports)
PLASMACYTOSIS ( 52 FDA reports)
SKIN CANCER ( 52 FDA reports)
ULCER HAEMORRHAGE ( 52 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 52 FDA reports)
BEDRIDDEN ( 52 FDA reports)
BILE DUCT STONE ( 52 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 52 FDA reports)
CARDIOGENIC SHOCK ( 52 FDA reports)
CEREBROVASCULAR DISORDER ( 52 FDA reports)
CORONARY ARTERY RESTENOSIS ( 52 FDA reports)
DRUG ABUSE ( 52 FDA reports)
DYSPHEMIA ( 52 FDA reports)
EDENTULOUS ( 52 FDA reports)
GENERALISED ANXIETY DISORDER ( 52 FDA reports)
HAEMANGIOMA OF LIVER ( 52 FDA reports)
HYPOAESTHESIA FACIAL ( 52 FDA reports)
ADVERSE REACTION ( 51 FDA reports)
ANAEMIA POSTOPERATIVE ( 51 FDA reports)
ANOSMIA ( 51 FDA reports)
APPENDICITIS ( 51 FDA reports)
CATHETER PLACEMENT ( 51 FDA reports)
CATHETERISATION CARDIAC ( 51 FDA reports)
EYE INFECTION ( 51 FDA reports)
HOMICIDAL IDEATION ( 51 FDA reports)
JOINT CONTRACTURE ( 51 FDA reports)
NEOPLASM ( 51 FDA reports)
SJOGREN'S SYNDROME ( 51 FDA reports)
SKIN IRRITATION ( 51 FDA reports)
TRISMUS ( 51 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 51 FDA reports)
URINE ODOUR ABNORMAL ( 51 FDA reports)
WOUND INFECTION ( 51 FDA reports)
RECTOCELE ( 50 FDA reports)
SINUS OPERATION ( 50 FDA reports)
SNORING ( 50 FDA reports)
STENT PLACEMENT ( 50 FDA reports)
TACHYPNOEA ( 50 FDA reports)
ADNEXA UTERI MASS ( 50 FDA reports)
BLEPHARITIS ( 50 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 50 FDA reports)
HEMIPLEGIA ( 50 FDA reports)
HERNIA REPAIR ( 50 FDA reports)
MUSCLE DISORDER ( 50 FDA reports)
NAIL DISORDER ( 50 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 50 FDA reports)
ORGAN FAILURE ( 50 FDA reports)
APATHY ( 49 FDA reports)
APLASIA PURE RED CELL ( 49 FDA reports)
ATRIAL SEPTAL DEFECT ( 49 FDA reports)
CERVICAL DYSPLASIA ( 49 FDA reports)
DYSTONIA ( 49 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 49 FDA reports)
EMPYEMA ( 49 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 49 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 49 FDA reports)
PHOTOSENSITIVITY REACTION ( 49 FDA reports)
SNEEZING ( 49 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 49 FDA reports)
THERAPY NON-RESPONDER ( 49 FDA reports)
POSTNASAL DRIP ( 48 FDA reports)
SEXUAL DYSFUNCTION ( 48 FDA reports)
SOFT TISSUE INFECTION ( 48 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 48 FDA reports)
VERTIGO POSITIONAL ( 48 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 48 FDA reports)
BACTERIAL TEST POSITIVE ( 48 FDA reports)
BLOOD IRON DECREASED ( 48 FDA reports)
DYSTHYMIC DISORDER ( 48 FDA reports)
FACE INJURY ( 48 FDA reports)
FAT NECROSIS ( 48 FDA reports)
HUNGER ( 48 FDA reports)
METASTASIS ( 48 FDA reports)
OCULAR HYPERTENSION ( 48 FDA reports)
OCULAR ICTERUS ( 48 FDA reports)
ABDOMINAL ADHESIONS ( 47 FDA reports)
ACCIDENTAL OVERDOSE ( 47 FDA reports)
BLOOD PRESSURE ABNORMAL ( 47 FDA reports)
BRONCHITIS CHRONIC ( 47 FDA reports)
FAMILY STRESS ( 47 FDA reports)
HEPATIC ENCEPHALOPATHY ( 47 FDA reports)
PERONEAL NERVE PALSY ( 47 FDA reports)
RESPIRATORY TRACT CONGESTION ( 47 FDA reports)
SINUS POLYP ( 47 FDA reports)
TONGUE ULCERATION ( 47 FDA reports)
TRANSAMINASES INCREASED ( 47 FDA reports)
URINARY TRACT DISORDER ( 47 FDA reports)
PLEURISY ( 46 FDA reports)
POLYMYALGIA RHEUMATICA ( 46 FDA reports)
STREPTOCOCCAL SEPSIS ( 46 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 46 FDA reports)
ATRIOVENTRICULAR BLOCK ( 46 FDA reports)
BLOOD CHLORIDE DECREASED ( 46 FDA reports)
BLOOD CULTURE POSITIVE ( 46 FDA reports)
COMPLETED SUICIDE ( 46 FDA reports)
DEPENDENCE ( 46 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 46 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 46 FDA reports)
GINGIVAL OEDEMA ( 46 FDA reports)
INCOHERENT ( 46 FDA reports)
LIPIDS INCREASED ( 46 FDA reports)
BLADDER OBSTRUCTION ( 45 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 45 FDA reports)
DRUG PRESCRIBING ERROR ( 45 FDA reports)
HEPATIC NEOPLASM ( 45 FDA reports)
LUNG CONSOLIDATION ( 45 FDA reports)
LYMPHOPENIA ( 45 FDA reports)
PERFORMANCE STATUS DECREASED ( 45 FDA reports)
RADIUS FRACTURE ( 45 FDA reports)
RASH MACULO-PAPULAR ( 45 FDA reports)
RAYNAUD'S PHENOMENON ( 45 FDA reports)
SENSATION OF HEAVINESS ( 45 FDA reports)
SOCIAL PROBLEM ( 45 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 45 FDA reports)
PURPURA ( 44 FDA reports)
TOOTH INJURY ( 44 FDA reports)
VAGINAL DISCHARGE ( 44 FDA reports)
BRAIN OEDEMA ( 44 FDA reports)
DYSAESTHESIA ( 44 FDA reports)
EAR DISCOMFORT ( 44 FDA reports)
HYPERTHYROIDISM ( 44 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 44 FDA reports)
MAMMOGRAM ABNORMAL ( 44 FDA reports)
MARROW HYPERPLASIA ( 44 FDA reports)
NEPHROPATHY ( 44 FDA reports)
OESOPHAGITIS ULCERATIVE ( 44 FDA reports)
ABSCESS DRAINAGE ( 43 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 43 FDA reports)
APPENDICECTOMY ( 43 FDA reports)
CLAVICLE FRACTURE ( 43 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 43 FDA reports)
EMBOLISM ( 43 FDA reports)
ENDOTRACHEAL INTUBATION ( 43 FDA reports)
GLOSSITIS ( 43 FDA reports)
KLEBSIELLA INFECTION ( 43 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 43 FDA reports)
TINEA PEDIS ( 43 FDA reports)
THROMBOPHLEBITIS ( 42 FDA reports)
ADHESION ( 42 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 42 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 42 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 42 FDA reports)
DRUG ERUPTION ( 42 FDA reports)
EXPIRED DRUG ADMINISTERED ( 42 FDA reports)
HORMONE LEVEL ABNORMAL ( 42 FDA reports)
LICE INFESTATION ( 42 FDA reports)
MAXILLOFACIAL OPERATION ( 42 FDA reports)
ANAPHYLACTIC SHOCK ( 41 FDA reports)
ASPIRATION PLEURAL CAVITY ( 41 FDA reports)
BONE GRAFT ( 41 FDA reports)
COLON ADENOMA ( 41 FDA reports)
DIABETIC NEPHROPATHY ( 41 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 41 FDA reports)
EPIGASTRIC DISCOMFORT ( 41 FDA reports)
FLAT AFFECT ( 41 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 41 FDA reports)
GRIEF REACTION ( 41 FDA reports)
HEPATIC MASS ( 41 FDA reports)
JOINT CREPITATION ( 41 FDA reports)
NECK MASS ( 41 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 41 FDA reports)
PREGNANCY ( 41 FDA reports)
PULSE ABSENT ( 41 FDA reports)
SUBCUTANEOUS NODULE ( 41 FDA reports)
TOOTH DEPOSIT ( 41 FDA reports)
TRAUMATIC BRAIN INJURY ( 41 FDA reports)
PROTEIN TOTAL DECREASED ( 40 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 40 FDA reports)
TRANSFUSION ( 40 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 40 FDA reports)
ABDOMINAL MASS ( 40 FDA reports)
ABSCESS ORAL ( 40 FDA reports)
ACUTE PRERENAL FAILURE ( 40 FDA reports)
APLASTIC ANAEMIA ( 40 FDA reports)
BREAST DISORDER ( 40 FDA reports)
COLLAPSE OF LUNG ( 40 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 40 FDA reports)
LIP DRY ( 40 FDA reports)
MALIGNANT MELANOMA ( 40 FDA reports)
ARTERIAL STENOSIS ( 39 FDA reports)
AUTOIMMUNE HEPATITIS ( 39 FDA reports)
CATHETER RELATED COMPLICATION ( 39 FDA reports)
EYE DISCHARGE ( 39 FDA reports)
FOLLICULITIS ( 39 FDA reports)
HEPATOTOXICITY ( 39 FDA reports)
LARYNGEAL OEDEMA ( 39 FDA reports)
NEOPLASM SKIN ( 39 FDA reports)
NEUROPATHY ( 39 FDA reports)
PERIODONTAL OPERATION ( 39 FDA reports)
POOR PERSONAL HYGIENE ( 39 FDA reports)
THORACOTOMY ( 39 FDA reports)
VOCAL CORD PARALYSIS ( 39 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 38 FDA reports)
PULMONARY THROMBOSIS ( 38 FDA reports)
TOBACCO ABUSE ( 38 FDA reports)
WEIGHT FLUCTUATION ( 38 FDA reports)
ABDOMINAL ABSCESS ( 38 FDA reports)
ABSCESS LIMB ( 38 FDA reports)
ABSCESS NECK ( 38 FDA reports)
APTYALISM ( 38 FDA reports)
BIPOLAR I DISORDER ( 38 FDA reports)
BREAST CANCER IN SITU ( 38 FDA reports)
BREAST CANCER RECURRENT ( 38 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 38 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 38 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 38 FDA reports)
ESSENTIAL TREMOR ( 38 FDA reports)
FACE OEDEMA ( 38 FDA reports)
GANGRENE ( 38 FDA reports)
KERATITIS ( 38 FDA reports)
LYMPHADENITIS ( 38 FDA reports)
MACROCYTOSIS ( 38 FDA reports)
NERVE ROOT LESION ( 38 FDA reports)
OSTEITIS DEFORMANS ( 38 FDA reports)
OTITIS MEDIA ACUTE ( 38 FDA reports)
PAIN OF SKIN ( 38 FDA reports)
PANCREATIC CARCINOMA ( 38 FDA reports)
ANAEMIA MACROCYTIC ( 37 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 37 FDA reports)
CHEILITIS ( 37 FDA reports)
CHOLECYSTITIS INFECTIVE ( 37 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 37 FDA reports)
EYELID OEDEMA ( 37 FDA reports)
HEART VALVE INCOMPETENCE ( 37 FDA reports)
HEPATIC NECROSIS ( 37 FDA reports)
HYDROCELE ( 37 FDA reports)
LEUKOENCEPHALOPATHY ( 37 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 37 FDA reports)
MICROCYTIC ANAEMIA ( 37 FDA reports)
NASAL POLYPS ( 37 FDA reports)
ORAL INTAKE REDUCED ( 37 FDA reports)
OVERWEIGHT ( 37 FDA reports)
PARONYCHIA ( 37 FDA reports)
POLYARTHRITIS ( 37 FDA reports)
SARCOIDOSIS ( 37 FDA reports)
STREPTOCOCCAL INFECTION ( 37 FDA reports)
TONSILLAR DISORDER ( 37 FDA reports)
VIITH NERVE PARALYSIS ( 37 FDA reports)
PSORIATIC ARTHROPATHY ( 36 FDA reports)
RIGHT VENTRICULAR FAILURE ( 36 FDA reports)
SCAPULA FRACTURE ( 36 FDA reports)
BILIARY DILATATION ( 36 FDA reports)
BONE NEOPLASM MALIGNANT ( 36 FDA reports)
BRAIN NEOPLASM ( 36 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 36 FDA reports)
DERMATITIS ALLERGIC ( 36 FDA reports)
DRUG SCREEN POSITIVE ( 36 FDA reports)
ENDOCARDITIS ( 36 FDA reports)
FOOD INTOLERANCE ( 36 FDA reports)
GINGIVAL HYPERPLASIA ( 36 FDA reports)
HEPATOSPLENOMEGALY ( 36 FDA reports)
HYPERAESTHESIA ( 36 FDA reports)
HYPERCOAGULATION ( 36 FDA reports)
HYPERMETROPIA ( 36 FDA reports)
INCISIONAL HERNIA ( 36 FDA reports)
LARGE INTESTINAL ULCER ( 36 FDA reports)
METABOLIC SYNDROME ( 36 FDA reports)
MULTIPLE FRACTURES ( 36 FDA reports)
MYELOMA RECURRENCE ( 36 FDA reports)
NECK INJURY ( 36 FDA reports)
OESOPHAGEAL CARCINOMA ( 36 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 36 FDA reports)
PARKINSONISM ( 36 FDA reports)
PERIPHERAL EMBOLISM ( 36 FDA reports)
ACCIDENT ( 35 FDA reports)
BREAST CALCIFICATIONS ( 35 FDA reports)
ENCEPHALOMALACIA ( 35 FDA reports)
EXERCISE LACK OF ( 35 FDA reports)
GINGIVAL ERYTHEMA ( 35 FDA reports)
HAEMOLYTIC ANAEMIA ( 35 FDA reports)
HYPERPLASIA ( 35 FDA reports)
IRON DEFICIENCY ( 35 FDA reports)
JUGULAR VEIN THROMBOSIS ( 35 FDA reports)
KNEE OPERATION ( 35 FDA reports)
MALOCCLUSION ( 35 FDA reports)
SKIN FIBROSIS ( 35 FDA reports)
SUDDEN CARDIAC DEATH ( 35 FDA reports)
TACHYARRHYTHMIA ( 35 FDA reports)
POST LAMINECTOMY SYNDROME ( 34 FDA reports)
TELANGIECTASIA ( 34 FDA reports)
TEMPERATURE INTOLERANCE ( 34 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 34 FDA reports)
VOCAL CORD DISORDER ( 34 FDA reports)
AUTOIMMUNE DISORDER ( 34 FDA reports)
BLADDER CANCER ( 34 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 34 FDA reports)
BODY TEMPERATURE DECREASED ( 34 FDA reports)
BONE MARROW TRANSPLANT ( 34 FDA reports)
BONE TRIMMING ( 34 FDA reports)
BRONCHITIS ACUTE ( 34 FDA reports)
CORONARY ARTERY THROMBOSIS ( 34 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 34 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 34 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 34 FDA reports)
GASTRITIS HAEMORRHAGIC ( 34 FDA reports)
HEPATITIS B ( 34 FDA reports)
HYPOVENTILATION ( 34 FDA reports)
INJECTION SITE MASS ( 34 FDA reports)
INTESTINAL POLYP ( 34 FDA reports)
INTRACARDIAC THROMBUS ( 34 FDA reports)
LIVER INJURY ( 34 FDA reports)
MASTECTOMY ( 34 FDA reports)
METASTASES TO THORAX ( 34 FDA reports)
METRORRHAGIA ( 34 FDA reports)
NASAL DISCOMFORT ( 34 FDA reports)
OPEN REDUCTION OF FRACTURE ( 34 FDA reports)
PANCREATIC CYST ( 34 FDA reports)
PERIODONTAL INFECTION ( 34 FDA reports)
ANAL FISTULA ( 33 FDA reports)
ARTERIOSPASM CORONARY ( 33 FDA reports)
BACTERIAL SEPSIS ( 33 FDA reports)
CACHEXIA ( 33 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 33 FDA reports)
CREPITATIONS ( 33 FDA reports)
CULTURE URINE POSITIVE ( 33 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 33 FDA reports)
EOSINOPHIL COUNT INCREASED ( 33 FDA reports)
GENITAL HERPES ( 33 FDA reports)
HYPERTENSIVE HEART DISEASE ( 33 FDA reports)
HYSTERECTOMY ( 33 FDA reports)
METAPLASIA ( 33 FDA reports)
MICTURITION DISORDER ( 33 FDA reports)
NEURODERMATITIS ( 33 FDA reports)
NICOTINE DEPENDENCE ( 33 FDA reports)
NYSTAGMUS ( 33 FDA reports)
OSTEOCHONDROSIS ( 33 FDA reports)
PANCREATIC MASS ( 33 FDA reports)
PARAPLEGIA ( 33 FDA reports)
PORTAL VEIN THROMBOSIS ( 33 FDA reports)
RADICULITIS ( 33 FDA reports)
RADICULITIS CERVICAL ( 33 FDA reports)
SCHIZOPHRENIA ( 33 FDA reports)
SEPSIS SYNDROME ( 33 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 33 FDA reports)
THYROID CANCER ( 33 FDA reports)
TOOTH EROSION ( 33 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 33 FDA reports)
WOUND COMPLICATION ( 33 FDA reports)
PROSTATE CANCER METASTATIC ( 32 FDA reports)
RESORPTION BONE INCREASED ( 32 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 32 FDA reports)
SKIN INJURY ( 32 FDA reports)
SPINAL FUSION SURGERY ( 32 FDA reports)
STRESS INCONTINENCE ( 32 FDA reports)
URINARY TRACT OBSTRUCTION ( 32 FDA reports)
AORTIC DISORDER ( 32 FDA reports)
ARTHRITIS BACTERIAL ( 32 FDA reports)
BREAKTHROUGH PAIN ( 32 FDA reports)
BREAST CYST ( 32 FDA reports)
CALCINOSIS ( 32 FDA reports)
CARDIAC OPERATION ( 32 FDA reports)
CATARACT NUCLEAR ( 32 FDA reports)
FEAR OF DEATH ( 32 FDA reports)
INJECTION SITE WARMTH ( 32 FDA reports)
MYOCLONUS ( 32 FDA reports)
OROPHARYNGEAL PLAQUE ( 32 FDA reports)
PAPILLOMA ( 32 FDA reports)
ANORECTAL DISCOMFORT ( 31 FDA reports)
BILE DUCT OBSTRUCTION ( 31 FDA reports)
BIOPSY ( 31 FDA reports)
BLADDER CATHETERISATION ( 31 FDA reports)
BLOOD COUNT ABNORMAL ( 31 FDA reports)
CALCIUM DEFICIENCY ( 31 FDA reports)
DENTAL PLAQUE ( 31 FDA reports)
FAECALOMA ( 31 FDA reports)
GALLBLADDER OPERATION ( 31 FDA reports)
INITIAL INSOMNIA ( 31 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 31 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 31 FDA reports)
MENSTRUATION IRREGULAR ( 31 FDA reports)
MONOCYTE COUNT INCREASED ( 31 FDA reports)
MYOPIA ( 31 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 31 FDA reports)
PANIC DISORDER ( 31 FDA reports)
PERIPHERAL ISCHAEMIA ( 31 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 31 FDA reports)
REFLUX GASTRITIS ( 31 FDA reports)
SERUM FERRITIN INCREASED ( 31 FDA reports)
SHOULDER OPERATION ( 31 FDA reports)
SPINAL CORD DISORDER ( 31 FDA reports)
URINE FLOW DECREASED ( 31 FDA reports)
UTERINE CANCER ( 31 FDA reports)
UTERINE DISORDER ( 31 FDA reports)
VENOUS OCCLUSION ( 31 FDA reports)
WOUND SECRETION ( 31 FDA reports)
PROCEDURAL COMPLICATION ( 30 FDA reports)
PYELOCALIECTASIS ( 30 FDA reports)
RENAL CELL CARCINOMA ( 30 FDA reports)
SPONDYLOSIS ( 30 FDA reports)
TRANSPLANT REJECTION ( 30 FDA reports)
TROPONIN INCREASED ( 30 FDA reports)
UTERINE ENLARGEMENT ( 30 FDA reports)
WEGENER'S GRANULOMATOSIS ( 30 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 30 FDA reports)
CHANGE OF BOWEL HABIT ( 30 FDA reports)
DENTAL CARE ( 30 FDA reports)
EFFUSION ( 30 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 30 FDA reports)
EMBOLIC STROKE ( 30 FDA reports)
FORMICATION ( 30 FDA reports)
GRAVITATIONAL OEDEMA ( 30 FDA reports)
INTESTINAL ISCHAEMIA ( 30 FDA reports)
NASAL DISORDER ( 30 FDA reports)
PANCREATIC DISORDER ( 30 FDA reports)
PAROTITIS ( 30 FDA reports)
ADRENAL MASS ( 29 FDA reports)
ANAL FISSURE ( 29 FDA reports)
ANIMAL BITE ( 29 FDA reports)
APPLICATION SITE PRURITUS ( 29 FDA reports)
BLOOD DISORDER ( 29 FDA reports)
BONE CYST ( 29 FDA reports)
CAESAREAN SECTION ( 29 FDA reports)
CATHETER RELATED INFECTION ( 29 FDA reports)
DENTAL DISCOMFORT ( 29 FDA reports)
DIABETIC COMPLICATION ( 29 FDA reports)
DRUG DISPENSING ERROR ( 29 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 29 FDA reports)
EAR CONGESTION ( 29 FDA reports)
EYE LASER SURGERY ( 29 FDA reports)
FEMORAL NECK FRACTURE ( 29 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 29 FDA reports)
HAIR TEXTURE ABNORMAL ( 29 FDA reports)
HEPATOCELLULAR DAMAGE ( 29 FDA reports)
HYPERVENTILATION ( 29 FDA reports)
INJECTION SITE RASH ( 29 FDA reports)
INTESTINAL RESECTION ( 29 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 29 FDA reports)
LUDWIG ANGINA ( 29 FDA reports)
MENOPAUSAL SYMPTOMS ( 29 FDA reports)
MUCOSAL DRYNESS ( 29 FDA reports)
NEUROLOGICAL SYMPTOM ( 29 FDA reports)
PAPILLOEDEMA ( 29 FDA reports)
PERSONALITY CHANGE ( 29 FDA reports)
PITTING OEDEMA ( 29 FDA reports)
PNEUMONIA BACTERIAL ( 29 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 29 FDA reports)
PSYCHIATRIC SYMPTOM ( 29 FDA reports)
RENAL ARTERY STENOSIS ( 29 FDA reports)
RENAL ATROPHY ( 29 FDA reports)
SKELETAL INJURY ( 29 FDA reports)
X-RAY ABNORMAL ( 29 FDA reports)
PLATELET DISORDER ( 28 FDA reports)
POLYP COLORECTAL ( 28 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 28 FDA reports)
RASH MORBILLIFORM ( 28 FDA reports)
SINUS ARRHYTHMIA ( 28 FDA reports)
SKIN FISSURES ( 28 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 28 FDA reports)
STASIS DERMATITIS ( 28 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 28 FDA reports)
SUNBURN ( 28 FDA reports)
TENSION HEADACHE ( 28 FDA reports)
THERMAL BURN ( 28 FDA reports)
TUBERCULOSIS ( 28 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 28 FDA reports)
ASTIGMATISM ( 28 FDA reports)
BACTERIAL DISEASE CARRIER ( 28 FDA reports)
BILE DUCT STENOSIS ( 28 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 28 FDA reports)
CANCER PAIN ( 28 FDA reports)
DEAFNESS UNILATERAL ( 28 FDA reports)
DEMYELINATION ( 28 FDA reports)
DEVICE BREAKAGE ( 28 FDA reports)
DEVICE OCCLUSION ( 28 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 28 FDA reports)
EAR HAEMORRHAGE ( 28 FDA reports)
FACIAL NEURALGIA ( 28 FDA reports)
FOOT OPERATION ( 28 FDA reports)
GASTRODUODENITIS ( 28 FDA reports)
GLARE ( 28 FDA reports)
HEART RATE ABNORMAL ( 28 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 28 FDA reports)
INJECTION SITE BRUISING ( 28 FDA reports)
INJECTION SITE IRRITATION ( 28 FDA reports)
LARGE INTESTINE PERFORATION ( 28 FDA reports)
MYASTHENIA GRAVIS ( 28 FDA reports)
PERIARTHRITIS ( 28 FDA reports)
AKATHISIA ( 27 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 27 FDA reports)
ALVEOLOPLASTY ( 27 FDA reports)
APPLICATION SITE ERYTHEMA ( 27 FDA reports)
BLADDER SPASM ( 27 FDA reports)
CARDIAC FLUTTER ( 27 FDA reports)
CEREBELLAR INFARCTION ( 27 FDA reports)
CHOLESTASIS ( 27 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 27 FDA reports)
GINGIVAL OPERATION ( 27 FDA reports)
GLOBULINS INCREASED ( 27 FDA reports)
GLOMERULONEPHRITIS ( 27 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 27 FDA reports)
NEUROMA ( 27 FDA reports)
PERIRECTAL ABSCESS ( 27 FDA reports)
PERITONITIS BACTERIAL ( 27 FDA reports)
POLYTRAUMATISM ( 27 FDA reports)
POSTOPERATIVE INFECTION ( 27 FDA reports)
PUBIS FRACTURE ( 27 FDA reports)
SHOCK HAEMORRHAGIC ( 27 FDA reports)
STRESS SYMPTOMS ( 27 FDA reports)
TEARFULNESS ( 27 FDA reports)
TOOTH REPAIR ( 27 FDA reports)
PULMONARY VASCULAR DISORDER ( 26 FDA reports)
SIALOADENITIS ( 26 FDA reports)
SKIN FRAGILITY ( 26 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 26 FDA reports)
TIC ( 26 FDA reports)
VENA CAVA FILTER INSERTION ( 26 FDA reports)
ADJUSTMENT DISORDER ( 26 FDA reports)
ADRENAL DISORDER ( 26 FDA reports)
APPARENT DEATH ( 26 FDA reports)
BLOOD CREATINE INCREASED ( 26 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 26 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 26 FDA reports)
BONE MARROW OEDEMA ( 26 FDA reports)
BRAIN INJURY ( 26 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 26 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 26 FDA reports)
COLON POLYPECTOMY ( 26 FDA reports)
CORNEAL ABRASION ( 26 FDA reports)
CORONARY ANGIOPLASTY ( 26 FDA reports)
DELUSION ( 26 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 26 FDA reports)
DERMATITIS EXFOLIATIVE ( 26 FDA reports)
DIABETIC COMA ( 26 FDA reports)
ENCEPHALITIS ( 26 FDA reports)
EPIDIDYMITIS ( 26 FDA reports)
FEELINGS OF WORTHLESSNESS ( 26 FDA reports)
HYDROCEPHALUS ( 26 FDA reports)
INTESTINAL STENOSIS ( 26 FDA reports)
LUPUS-LIKE SYNDROME ( 26 FDA reports)
MEDICAL DEVICE REMOVAL ( 26 FDA reports)
MUCOSAL HAEMORRHAGE ( 26 FDA reports)
MUCOSAL ULCERATION ( 26 FDA reports)
MUSCLE RIGIDITY ( 26 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 26 FDA reports)
PARAPROTEINAEMIA ( 26 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 26 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 25 FDA reports)
AORTIC VALVE STENOSIS ( 25 FDA reports)
B-CELL LYMPHOMA ( 25 FDA reports)
BLOOD CHLORIDE INCREASED ( 25 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 25 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 25 FDA reports)
CHOLESTEROSIS ( 25 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 25 FDA reports)
COMMUNICATION DISORDER ( 25 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 25 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 25 FDA reports)
EATING DISORDER SYMPTOM ( 25 FDA reports)
FEELING DRUNK ( 25 FDA reports)
FUNGAL SKIN INFECTION ( 25 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 25 FDA reports)
HAEMORRHAGIC STROKE ( 25 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 25 FDA reports)
INTERVERTEBRAL DISC INJURY ( 25 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 25 FDA reports)
LIGAMENT RUPTURE ( 25 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 25 FDA reports)
LIP ULCERATION ( 25 FDA reports)
MECHANICAL VENTILATION ( 25 FDA reports)
MITRAL VALVE DISEASE ( 25 FDA reports)
MORTON'S NEUROMA ( 25 FDA reports)
ORAL FUNGAL INFECTION ( 25 FDA reports)
OSTEOMYELITIS CHRONIC ( 25 FDA reports)
PALATAL DISORDER ( 25 FDA reports)
POLYSUBSTANCE ABUSE ( 25 FDA reports)
PULMONARY INFARCTION ( 25 FDA reports)
RETINAL TEAR ( 25 FDA reports)
RETINOPATHY ( 25 FDA reports)
RHINALGIA ( 25 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 25 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 25 FDA reports)
VAGINITIS BACTERIAL ( 25 FDA reports)
VARICES OESOPHAGEAL ( 25 FDA reports)
PROCTITIS ( 24 FDA reports)
PRODUCT ADHESION ISSUE ( 24 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 24 FDA reports)
PULMONARY HAEMORRHAGE ( 24 FDA reports)
RADICULAR PAIN ( 24 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 24 FDA reports)
REFLUX LARYNGITIS ( 24 FDA reports)
RETINAL DETACHMENT ( 24 FDA reports)
SELF-MEDICATION ( 24 FDA reports)
SEROMA ( 24 FDA reports)
SKIN ATROPHY ( 24 FDA reports)
SKIN INFECTION ( 24 FDA reports)
SKIN NECROSIS ( 24 FDA reports)
SPLENIC LESION ( 24 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 24 FDA reports)
SUDDEN DEATH ( 24 FDA reports)
THROAT CANCER ( 24 FDA reports)
ULNA FRACTURE ( 24 FDA reports)
VENOUS THROMBOSIS LIMB ( 24 FDA reports)
ABNORMAL SENSATION IN EYE ( 24 FDA reports)
ADENOMA BENIGN ( 24 FDA reports)
ADRENAL NEOPLASM ( 24 FDA reports)
AMMONIA INCREASED ( 24 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 24 FDA reports)
ARTERIAL DISORDER ( 24 FDA reports)
ASPIRATION JOINT ( 24 FDA reports)
BILIARY TRACT DISORDER ( 24 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 24 FDA reports)
BRONCHIAL SECRETION RETENTION ( 24 FDA reports)
CARDIAC ENZYMES INCREASED ( 24 FDA reports)
CARTILAGE ATROPHY ( 24 FDA reports)
CHRONIC FATIGUE SYNDROME ( 24 FDA reports)
COMMINUTED FRACTURE ( 24 FDA reports)
CONDUCTION DISORDER ( 24 FDA reports)
CONNECTIVE TISSUE DISORDER ( 24 FDA reports)
CUBITAL TUNNEL SYNDROME ( 24 FDA reports)
DIABETIC GASTROPARESIS ( 24 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 24 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 24 FDA reports)
DYSMENORRHOEA ( 24 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 24 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 24 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 24 FDA reports)
FRACTURE DELAYED UNION ( 24 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 24 FDA reports)
INNER EAR DISORDER ( 24 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 24 FDA reports)
LABILE HYPERTENSION ( 24 FDA reports)
LEG AMPUTATION ( 24 FDA reports)
LIVEDO RETICULARIS ( 24 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 24 FDA reports)
MEDICATION RESIDUE ( 24 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 24 FDA reports)
OVARIAN CANCER ( 24 FDA reports)
PAIN EXACERBATED ( 24 FDA reports)
PELVIC PROLAPSE ( 24 FDA reports)
ANGIONEUROTIC OEDEMA ( 23 FDA reports)
ANOXIC ENCEPHALOPATHY ( 23 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 23 FDA reports)
BENIGN BREAST NEOPLASM ( 23 FDA reports)
BIOPSY BONE ABNORMAL ( 23 FDA reports)
BLADDER NEOPLASM ( 23 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 23 FDA reports)
COELIAC DISEASE ( 23 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 23 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ( 23 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 23 FDA reports)
EYE INJURY ( 23 FDA reports)
GASTROINTESTINAL INFECTION ( 23 FDA reports)
GUILLAIN-BARRE SYNDROME ( 23 FDA reports)
HAEMODYNAMIC INSTABILITY ( 23 FDA reports)
HEPATIC FIBROSIS ( 23 FDA reports)
HYPERNATRAEMIA ( 23 FDA reports)
HYPERPHAGIA ( 23 FDA reports)
HYPERTENSIVE CRISIS ( 23 FDA reports)
ILIAC ARTERY STENOSIS ( 23 FDA reports)
IMPULSIVE BEHAVIOUR ( 23 FDA reports)
INDURATION ( 23 FDA reports)
INFARCTION ( 23 FDA reports)
INJECTION SITE URTICARIA ( 23 FDA reports)
LACTIC ACIDOSIS ( 23 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 23 FDA reports)
MENIERE'S DISEASE ( 23 FDA reports)
MONOCLONAL GAMMOPATHY ( 23 FDA reports)
MYCOSIS FUNGOIDES ( 23 FDA reports)
NEPHRITIS INTERSTITIAL ( 23 FDA reports)
NON-SMALL CELL LUNG CANCER ( 23 FDA reports)
PANIC REACTION ( 23 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 23 FDA reports)
PERSONALITY DISORDER ( 23 FDA reports)
POLYPECTOMY ( 23 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 23 FDA reports)
PREMATURE BABY ( 23 FDA reports)
PRESBYOESOPHAGUS ( 23 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 23 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 23 FDA reports)
PULMONARY TOXICITY ( 23 FDA reports)
SALIVARY HYPERSECRETION ( 23 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 23 FDA reports)
SPONDYLITIS ( 23 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 23 FDA reports)
VEIN DISORDER ( 23 FDA reports)
VENOOCCLUSIVE DISEASE ( 23 FDA reports)
PHOTOPSIA ( 22 FDA reports)
PYURIA ( 22 FDA reports)
RADIATION INJURY ( 22 FDA reports)
RADICULAR SYNDROME ( 22 FDA reports)
RENAL CANCER ( 22 FDA reports)
SACROILIITIS ( 22 FDA reports)
SEBORRHOEIC DERMATITIS ( 22 FDA reports)
SYNCOPE VASOVAGAL ( 22 FDA reports)
TESTICULAR PAIN ( 22 FDA reports)
TOOTH DISCOLOURATION ( 22 FDA reports)
TREATMENT FAILURE ( 22 FDA reports)
UNDERDOSE ( 22 FDA reports)
URETERIC OBSTRUCTION ( 22 FDA reports)
VERBAL ABUSE ( 22 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 22 FDA reports)
ABNORMAL FAECES ( 22 FDA reports)
ACCIDENT AT WORK ( 22 FDA reports)
ADENOCARCINOMA ( 22 FDA reports)
ANORECTAL DISORDER ( 22 FDA reports)
AORTIC DILATATION ( 22 FDA reports)
APPETITE DISORDER ( 22 FDA reports)
BLOOD AMYLASE INCREASED ( 22 FDA reports)
BLOOD TEST ABNORMAL ( 22 FDA reports)
BREAST INFECTION ( 22 FDA reports)
BULLOUS LUNG DISEASE ( 22 FDA reports)
CHOKING SENSATION ( 22 FDA reports)
COLONOSCOPY ABNORMAL ( 22 FDA reports)
COR PULMONALE CHRONIC ( 22 FDA reports)
DIVERTICULAR PERFORATION ( 22 FDA reports)
EARLY SATIETY ( 22 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 22 FDA reports)
EOSINOPHIL COUNT DECREASED ( 22 FDA reports)
FACIAL PARESIS ( 22 FDA reports)
FOREIGN BODY IN EYE ( 22 FDA reports)
GASTROINTESTINAL NECROSIS ( 22 FDA reports)
GENERALISED ERYTHEMA ( 22 FDA reports)
HAEMOLYSIS ( 22 FDA reports)
HEAD DISCOMFORT ( 22 FDA reports)
HYDROPNEUMOTHORAX ( 22 FDA reports)
HYPERBILIRUBINAEMIA ( 22 FDA reports)
ILEITIS ( 22 FDA reports)
INFECTIVE TENOSYNOVITIS ( 22 FDA reports)
INJECTION SITE PAPULE ( 22 FDA reports)
LIGAMENT INJURY ( 22 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 22 FDA reports)
LUNG ADENOCARCINOMA ( 22 FDA reports)
MALIGNANT HYPERTENSION ( 22 FDA reports)
MIXED HYPERLIPIDAEMIA ( 22 FDA reports)
MONOCYTE COUNT DECREASED ( 22 FDA reports)
MYELITIS TRANSVERSE ( 22 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 22 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 22 FDA reports)
PARATHYROID DISORDER ( 22 FDA reports)
AGRANULOCYTOSIS ( 21 FDA reports)
ALVEOLAR OSTEITIS ( 21 FDA reports)
ARTHRITIS INFECTIVE ( 21 FDA reports)
BENIGN COLONIC NEOPLASM ( 21 FDA reports)
BENIGN NEOPLASM ( 21 FDA reports)
BLOOD CREATININE DECREASED ( 21 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 21 FDA reports)
BUNDLE BRANCH BLOCK ( 21 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 21 FDA reports)
CEREBELLAR SYNDROME ( 21 FDA reports)
CHEST WALL PAIN ( 21 FDA reports)
DEVICE RELATED SEPSIS ( 21 FDA reports)
DIABETIC FOOT ( 21 FDA reports)
EPISCLERITIS ( 21 FDA reports)
FELTY'S SYNDROME ( 21 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 21 FDA reports)
FLIGHT OF IDEAS ( 21 FDA reports)
GRANULOCYTOPENIA ( 21 FDA reports)
HAEMATOCRIT INCREASED ( 21 FDA reports)
HELICOBACTER GASTRITIS ( 21 FDA reports)
HIDRADENITIS ( 21 FDA reports)
HYPERPHOSPHATAEMIA ( 21 FDA reports)
HYPERURICAEMIA ( 21 FDA reports)
ILEUS PARALYTIC ( 21 FDA reports)
IMMUNE SYSTEM DISORDER ( 21 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 21 FDA reports)
JUGULAR VEIN DISTENSION ( 21 FDA reports)
LOOSE STOOLS ( 21 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 21 FDA reports)
MULTIPLE DRUG OVERDOSE ( 21 FDA reports)
MUSCLE SPASTICITY ( 21 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 21 FDA reports)
NEUTROPENIC SEPSIS ( 21 FDA reports)
OESOPHAGEAL ACHALASIA ( 21 FDA reports)
PANCREATITIS RELAPSING ( 21 FDA reports)
PERIORBITAL OEDEMA ( 21 FDA reports)
PERITONEAL DISORDER ( 21 FDA reports)
PHARYNGEAL ERYTHEMA ( 21 FDA reports)
POOR PERIPHERAL CIRCULATION ( 21 FDA reports)
RETINAL DISORDER ( 21 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 21 FDA reports)
SPINAL DEFORMITY ( 21 FDA reports)
SPONDYLOARTHROPATHY ( 21 FDA reports)
TESTICULAR SWELLING ( 21 FDA reports)
THYROID CYST ( 21 FDA reports)
THYROID MASS ( 21 FDA reports)
TONSIL CANCER ( 21 FDA reports)
TOXIC ENCEPHALOPATHY ( 21 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 21 FDA reports)
URGE INCONTINENCE ( 21 FDA reports)
PNEUMONIA VIRAL ( 20 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 20 FDA reports)
PROTEIN URINE PRESENT ( 20 FDA reports)
RENAL ISCHAEMIA ( 20 FDA reports)
RHINITIS SEASONAL ( 20 FDA reports)
SCAN BONE MARROW ABNORMAL ( 20 FDA reports)
SELF-INJURIOUS IDEATION ( 20 FDA reports)
SERUM SICKNESS ( 20 FDA reports)
SKIN REACTION ( 20 FDA reports)
SKIN WARM ( 20 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 20 FDA reports)
SPINAL LAMINECTOMY ( 20 FDA reports)
TENOSYNOVITIS STENOSANS ( 20 FDA reports)
TOE DEFORMITY ( 20 FDA reports)
TUMOUR LYSIS SYNDROME ( 20 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 20 FDA reports)
URINE ABNORMALITY ( 20 FDA reports)
VESTIBULAR DISORDER ( 20 FDA reports)
VIRAL PHARYNGITIS ( 20 FDA reports)
ADNEXA UTERI CYST ( 20 FDA reports)
ADRENAL ADENOMA ( 20 FDA reports)
AMENORRHOEA ( 20 FDA reports)
ANOGENITAL WARTS ( 20 FDA reports)
APICECTOMY ( 20 FDA reports)
APPENDICITIS PERFORATED ( 20 FDA reports)
BRAIN SCAN ABNORMAL ( 20 FDA reports)
CAECITIS ( 20 FDA reports)
CARBON DIOXIDE DECREASED ( 20 FDA reports)
CARDIAC VALVE ABSCESS ( 20 FDA reports)
CHEST INJURY ( 20 FDA reports)
DENTAL IMPLANTATION ( 20 FDA reports)
DROOLING ( 20 FDA reports)
EJECTION FRACTION ABNORMAL ( 20 FDA reports)
FAECES HARD ( 20 FDA reports)
GALLBLADDER PAIN ( 20 FDA reports)
GASTROINTESTINAL ULCER ( 20 FDA reports)
GINGIVAL ABSCESS ( 20 FDA reports)
GINGIVAL ATROPHY ( 20 FDA reports)
HILAR LYMPHADENOPATHY ( 20 FDA reports)
HYDROURETER ( 20 FDA reports)
INJECTION SITE INDURATION ( 20 FDA reports)
INTENTION TREMOR ( 20 FDA reports)
IRITIS ( 20 FDA reports)
JAW LESION EXCISION ( 20 FDA reports)
JOINT INSTABILITY ( 20 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 20 FDA reports)
METABOLIC DISORDER ( 20 FDA reports)
MIGRAINE WITH AURA ( 20 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 20 FDA reports)
OSTEOSYNTHESIS ( 20 FDA reports)
PATELLA FRACTURE ( 20 FDA reports)
PEAU D'ORANGE ( 20 FDA reports)
ACUTE PULMONARY OEDEMA ( 19 FDA reports)
BLOOD BICARBONATE DECREASED ( 19 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 19 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 19 FDA reports)
BRONCHOPLEURAL FISTULA ( 19 FDA reports)
CARDIAC FAILURE CHRONIC ( 19 FDA reports)
CERVICAL CORD COMPRESSION ( 19 FDA reports)
COLOSTOMY ( 19 FDA reports)
CYST ASPIRATION ( 19 FDA reports)
DIABETIC EYE DISEASE ( 19 FDA reports)
DYSPHORIA ( 19 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 19 FDA reports)
ENERGY INCREASED ( 19 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 19 FDA reports)
FIBROUS HISTIOCYTOMA ( 19 FDA reports)
FULL BLOOD COUNT DECREASED ( 19 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 19 FDA reports)
GRAFT VERSUS HOST DISEASE ( 19 FDA reports)
HYPERMETABOLISM ( 19 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 19 FDA reports)
KERATITIS HERPETIC ( 19 FDA reports)
KYPHOSCOLIOSIS ( 19 FDA reports)
LICHENOID KERATOSIS ( 19 FDA reports)
LIMB DEFORMITY ( 19 FDA reports)
LIVER ABSCESS ( 19 FDA reports)
LOSS OF EMPLOYMENT ( 19 FDA reports)
LUNG CANCER METASTATIC ( 19 FDA reports)
MAMMOPLASTY ( 19 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 19 FDA reports)
METATARSALGIA ( 19 FDA reports)
MICROCYTOSIS ( 19 FDA reports)
MITRAL VALVE SCLEROSIS ( 19 FDA reports)
MOANING ( 19 FDA reports)
NARCOLEPSY ( 19 FDA reports)
NASAL ULCER ( 19 FDA reports)
NERVE ROOT COMPRESSION ( 19 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 19 FDA reports)
ONYCHALGIA ( 19 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 19 FDA reports)
PERIODONTAL DESTRUCTION ( 19 FDA reports)
PERIORBITAL HAEMATOMA ( 19 FDA reports)
POSTOPERATIVE ILEUS ( 19 FDA reports)
PRESCRIBED OVERDOSE ( 19 FDA reports)
PROSTATIC DISORDER ( 19 FDA reports)
PUPILLARY DISORDER ( 19 FDA reports)
RETINAL HAEMORRHAGE ( 19 FDA reports)
SPINAL FUSION ACQUIRED ( 19 FDA reports)
SUPERINFECTION ( 19 FDA reports)
THORACIC OUTLET SYNDROME ( 19 FDA reports)
TUBERCULIN TEST POSITIVE ( 19 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 19 FDA reports)
VASCULAR ANOMALY ( 19 FDA reports)
VASCULAR OCCLUSION ( 19 FDA reports)
VITREOUS HAEMORRHAGE ( 19 FDA reports)
WHIPLASH INJURY ( 19 FDA reports)
PNEUMONIA FUNGAL ( 18 FDA reports)
PORTAL HYPERTENSION ( 18 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 18 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 18 FDA reports)
SENSATION OF PRESSURE ( 18 FDA reports)
SEROTONIN SYNDROME ( 18 FDA reports)
SICCA SYNDROME ( 18 FDA reports)
STENT OCCLUSION ( 18 FDA reports)
STRABISMUS ( 18 FDA reports)
TERMINAL STATE ( 18 FDA reports)
THROMBOSIS IN DEVICE ( 18 FDA reports)
TRACHEITIS ( 18 FDA reports)
UTERINE HAEMORRHAGE ( 18 FDA reports)
VASCULAR PSEUDOANEURYSM ( 18 FDA reports)
VASOCONSTRICTION ( 18 FDA reports)
VENA CAVA THROMBOSIS ( 18 FDA reports)
VULVITIS ( 18 FDA reports)
VULVOVAGINAL PAIN ( 18 FDA reports)
ALCOHOL USE ( 18 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 18 FDA reports)
APPLICATION SITE IRRITATION ( 18 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 18 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 18 FDA reports)
BREAST LUMP REMOVAL ( 18 FDA reports)
CARDIOPULMONARY FAILURE ( 18 FDA reports)
CATHETER REMOVAL ( 18 FDA reports)
CATHETER SITE INFECTION ( 18 FDA reports)
CEREBRAL ARTERY STENOSIS ( 18 FDA reports)
CEREBRAL DISORDER ( 18 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 18 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 18 FDA reports)
COLECTOMY ( 18 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 18 FDA reports)
CONTRAST MEDIA REACTION ( 18 FDA reports)
DIABETIC ULCER ( 18 FDA reports)
DUODENAL STENOSIS ( 18 FDA reports)
DYSPNOEA EXACERBATED ( 18 FDA reports)
DYSTROPHIC CALCIFICATION ( 18 FDA reports)
ENDOSCOPY ( 18 FDA reports)
ENTHESOPATHY ( 18 FDA reports)
EXTREMITY NECROSIS ( 18 FDA reports)
EYE MOVEMENT DISORDER ( 18 FDA reports)
EYE OPERATION ( 18 FDA reports)
GASTROSTOMY TUBE INSERTION ( 18 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 18 FDA reports)
HOARSENESS ( 18 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 18 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 18 FDA reports)
INJECTION SITE DISCOLOURATION ( 18 FDA reports)
INJECTION SITE NODULE ( 18 FDA reports)
JAUNDICE CHOLESTATIC ( 18 FDA reports)
LEUKODYSTROPHY ( 18 FDA reports)
MALIGNANT MELANOMA IN SITU ( 18 FDA reports)
MASTOIDITIS ( 18 FDA reports)
MONONEURITIS ( 18 FDA reports)
MOUTH INJURY ( 18 FDA reports)
NASAL DRYNESS ( 18 FDA reports)
NEOPLASM RECURRENCE ( 18 FDA reports)
NIGHT CRAMPS ( 18 FDA reports)
PARESIS ( 18 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 17 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 17 FDA reports)
ANISOCYTOSIS ( 17 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 17 FDA reports)
APPENDIX DISORDER ( 17 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 17 FDA reports)
ATRIAL THROMBOSIS ( 17 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 17 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 17 FDA reports)
BURN OESOPHAGEAL ( 17 FDA reports)
CARDIAC VALVE SCLEROSIS ( 17 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 17 FDA reports)
COLONOSCOPY ( 17 FDA reports)
EYE INFLAMMATION ( 17 FDA reports)
FIBRIN D DIMER INCREASED ( 17 FDA reports)
FOREIGN BODY ( 17 FDA reports)
FRACTURED ISCHIUM ( 17 FDA reports)
GASTRIC CANCER ( 17 FDA reports)
GRIMACING ( 17 FDA reports)
HAND DEFORMITY ( 17 FDA reports)
HEARING AID USER ( 17 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 17 FDA reports)
HYPERREFLEXIA ( 17 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 17 FDA reports)
HYPOTONIA ( 17 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 17 FDA reports)
IMMUNOGLOBULINS DECREASED ( 17 FDA reports)
JAUNDICE NEONATAL ( 17 FDA reports)
JOINT ARTHROPLASTY ( 17 FDA reports)
KERATOACANTHOMA ( 17 FDA reports)
LACTOSE INTOLERANCE ( 17 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 17 FDA reports)
LARYNGITIS VIRAL ( 17 FDA reports)
LARYNGOSPASM ( 17 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 17 FDA reports)
MASTITIS ( 17 FDA reports)
MEAN CELL VOLUME INCREASED ( 17 FDA reports)
MENINGITIS ( 17 FDA reports)
METASTASES TO MENINGES ( 17 FDA reports)
MITRAL VALVE DISEASE MIXED ( 17 FDA reports)
NEPHROSCLEROSIS ( 17 FDA reports)
NEPHROTIC SYNDROME ( 17 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 17 FDA reports)
OVARIAN CANCER METASTATIC ( 17 FDA reports)
PHLEBOLITH ( 17 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 17 FDA reports)
PSYCHOLOGICAL TRAUMA ( 17 FDA reports)
PUPIL FIXED ( 17 FDA reports)
RECURRENT CANCER ( 17 FDA reports)
RETINAL INFARCTION ( 17 FDA reports)
SINUS POLYP DEGENERATION ( 17 FDA reports)
SKIN OEDEMA ( 17 FDA reports)
SLUGGISHNESS ( 17 FDA reports)
SMOKER ( 17 FDA reports)
SUBDURAL HAEMORRHAGE ( 17 FDA reports)
SUICIDAL BEHAVIOUR ( 17 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 17 FDA reports)
TRACHEOBRONCHITIS ( 17 FDA reports)
TROPONIN I INCREASED ( 17 FDA reports)
UVEITIS ( 17 FDA reports)
VASCULAR OPERATION ( 17 FDA reports)
VIRAL LABYRINTHITIS ( 17 FDA reports)
WEIGHT BEARING DIFFICULTY ( 17 FDA reports)
YELLOW SKIN ( 17 FDA reports)
PROSTHESIS USER ( 16 FDA reports)
PULMONARY RADIATION INJURY ( 16 FDA reports)
QRS AXIS ABNORMAL ( 16 FDA reports)
RENAL COLIC ( 16 FDA reports)
SALPINGITIS ( 16 FDA reports)
SECRETION DISCHARGE ( 16 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 16 FDA reports)
SKIN NEOPLASM EXCISION ( 16 FDA reports)
TONGUE OEDEMA ( 16 FDA reports)
TRAUMATIC ARTHRITIS ( 16 FDA reports)
TRIGEMINAL NEURALGIA ( 16 FDA reports)
URINE ANALYSIS ABNORMAL ( 16 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 16 FDA reports)
AMBLYOPIA ( 16 FDA reports)
ANAL SPHINCTER ATONY ( 16 FDA reports)
ANURIA ( 16 FDA reports)
APPLICATION SITE RASH ( 16 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 16 FDA reports)
BLADDER PAIN ( 16 FDA reports)
BURNS SECOND DEGREE ( 16 FDA reports)
CARCINOID SYNDROME ( 16 FDA reports)
CARDIAC ANEURYSM ( 16 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 16 FDA reports)
CERVICAL MYELOPATHY ( 16 FDA reports)
CHEST TUBE INSERTION ( 16 FDA reports)
CHOLANGITIS SCLEROSING ( 16 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 16 FDA reports)
COR PULMONALE ( 16 FDA reports)
CYSTITIS NONINFECTIVE ( 16 FDA reports)
DENTAL PULP DISORDER ( 16 FDA reports)
DEVELOPMENTAL DELAY ( 16 FDA reports)
DROP ATTACKS ( 16 FDA reports)
DYSGRAPHIA ( 16 FDA reports)
ECZEMA INFECTED ( 16 FDA reports)
EMBOLISM ARTERIAL ( 16 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 16 FDA reports)
EXCESSIVE EYE BLINKING ( 16 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 16 FDA reports)
HEART DISEASE CONGENITAL ( 16 FDA reports)
HEPATITIS ACUTE ( 16 FDA reports)
HERNIA HIATUS REPAIR ( 16 FDA reports)
HIP SURGERY ( 16 FDA reports)
IMMUNODEFICIENCY ( 16 FDA reports)
INJECTION SITE EXTRAVASATION ( 16 FDA reports)
INTENTIONAL SELF-INJURY ( 16 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 16 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 16 FDA reports)
LEUKAEMIA ( 16 FDA reports)
LEUKOPLAKIA ORAL ( 16 FDA reports)
LIMB OPERATION ( 16 FDA reports)
LIP DISCOLOURATION ( 16 FDA reports)
LIP PAIN ( 16 FDA reports)
LISTLESS ( 16 FDA reports)
LOCALISED OEDEMA ( 16 FDA reports)
LYMPH NODE PALPABLE ( 16 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 16 FDA reports)
MEGACOLON ( 16 FDA reports)
MENINGITIS ASEPTIC ( 16 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 16 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 16 FDA reports)
MONOPLEGIA ( 16 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 16 FDA reports)
OPTIC NERVE DISORDER ( 16 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 16 FDA reports)
ORTHOSIS USER ( 16 FDA reports)
OSTEOMA ( 16 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 16 FDA reports)
PERICARDIAL DISEASE ( 16 FDA reports)
ABDOMINAL NEOPLASM ( 15 FDA reports)
ADENOMYOSIS ( 15 FDA reports)
ALCOHOL ABUSE ( 15 FDA reports)
ALVEOLITIS ( 15 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 15 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 15 FDA reports)
BASEDOW'S DISEASE ( 15 FDA reports)
BENIGN BONE NEOPLASM ( 15 FDA reports)
BENIGN OVARIAN TUMOUR ( 15 FDA reports)
BIOPSY BONE MARROW ( 15 FDA reports)
BLADDER CANCER RECURRENT ( 15 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 15 FDA reports)
BLOOD SODIUM INCREASED ( 15 FDA reports)
BLOOD URINE ( 15 FDA reports)
BRADYPHRENIA ( 15 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 15 FDA reports)
BREAST SWELLING ( 15 FDA reports)
CATHETER SITE HAEMORRHAGE ( 15 FDA reports)
CERVIX CARCINOMA ( 15 FDA reports)
CHAPPED LIPS ( 15 FDA reports)
CHONDROPATHY ( 15 FDA reports)
CLAUSTROPHOBIA ( 15 FDA reports)
CLUSTER HEADACHE ( 15 FDA reports)
COLITIS MICROSCOPIC ( 15 FDA reports)
COMPLEX PARTIAL SEIZURES ( 15 FDA reports)
CONVERSION DISORDER ( 15 FDA reports)
DERMATITIS BULLOUS ( 15 FDA reports)
DEVICE DISLOCATION ( 15 FDA reports)
DISSOCIATION ( 15 FDA reports)
DRUG LEVEL INCREASED ( 15 FDA reports)
DUODENAL POLYP ( 15 FDA reports)
DUODENAL ULCER PERFORATION ( 15 FDA reports)
ENDOMETRIOSIS ( 15 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 15 FDA reports)
EPILEPSY ( 15 FDA reports)
EYELID DISORDER ( 15 FDA reports)
FOREIGN BODY TRAUMA ( 15 FDA reports)
FRACTURE DISPLACEMENT ( 15 FDA reports)
GAMMOPATHY ( 15 FDA reports)
GASTRIC BYPASS ( 15 FDA reports)
GASTROINTESTINAL TOXICITY ( 15 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 15 FDA reports)
GROIN ABSCESS ( 15 FDA reports)
HAEMOGLOBIN INCREASED ( 15 FDA reports)
HAEMORRHOID OPERATION ( 15 FDA reports)
HALLUCINATIONS, MIXED ( 15 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 15 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 15 FDA reports)
IATROGENIC INJURY ( 15 FDA reports)
INJURY CORNEAL ( 15 FDA reports)
LOCALISED OSTEOARTHRITIS ( 15 FDA reports)
LOSS OF LIBIDO ( 15 FDA reports)
METASTASES TO ADRENALS ( 15 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 15 FDA reports)
MUSCLE FATIGUE ( 15 FDA reports)
OBSTRUCTION ( 15 FDA reports)
OBSTRUCTION GASTRIC ( 15 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 15 FDA reports)
OVARIAN DISORDER ( 15 FDA reports)
PANCREATIC INSUFFICIENCY ( 15 FDA reports)
PHOTOPHERESIS ( 15 FDA reports)
PIGMENTATION DISORDER ( 15 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 15 FDA reports)
POST PROCEDURAL HAEMATOMA ( 15 FDA reports)
PRIMARY HYPOGONADISM ( 15 FDA reports)
PROSTATIC OBSTRUCTION ( 15 FDA reports)
PULMONARY AIR LEAKAGE ( 15 FDA reports)
PULMONARY HILUM MASS ( 15 FDA reports)
RADIATION OESOPHAGITIS ( 15 FDA reports)
RASH VESICULAR ( 15 FDA reports)
RETINAL MELANOMA ( 15 FDA reports)
SCLERODACTYLIA ( 15 FDA reports)
SCRATCH ( 15 FDA reports)
SENILE DEMENTIA ( 15 FDA reports)
SPONDYLITIC MYELOPATHY ( 15 FDA reports)
STEATORRHOEA ( 15 FDA reports)
SWEAT GLAND INFECTION ( 15 FDA reports)
TACHYPHRENIA ( 15 FDA reports)
THYROID ADENOMA ( 15 FDA reports)
THYROIDITIS ( 15 FDA reports)
TONGUE DRY ( 15 FDA reports)
UTERINE PROLAPSE ( 15 FDA reports)
VASCULAR INSUFFICIENCY ( 15 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 15 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 15 FDA reports)
VITAMIN B12 DECREASED ( 15 FDA reports)
VOLVULUS ( 15 FDA reports)
VOMITING PROJECTILE ( 15 FDA reports)
PNEUMONIA ESCHERICHIA ( 14 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 14 FDA reports)
PROTEIN URINE ( 14 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 14 FDA reports)
RENAL TUBULAR ACIDOSIS ( 14 FDA reports)
RESPIRATORY DEPRESSION ( 14 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 14 FDA reports)
RIGHT ATRIAL DILATATION ( 14 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 14 FDA reports)
SELF ESTEEM DECREASED ( 14 FDA reports)
SKIN HAEMORRHAGE ( 14 FDA reports)
SKIN NODULE ( 14 FDA reports)
SKIN ODOUR ABNORMAL ( 14 FDA reports)
SPINAL HAEMANGIOMA ( 14 FDA reports)
SPLENIC CYST ( 14 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 14 FDA reports)
TENDON PAIN ( 14 FDA reports)
THERAPY REGIMEN CHANGED ( 14 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 14 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 14 FDA reports)
URETHRAL OBSTRUCTION ( 14 FDA reports)
URINE COLOUR ABNORMAL ( 14 FDA reports)
VAGINAL BURNING SENSATION ( 14 FDA reports)
VENTRICLE RUPTURE ( 14 FDA reports)
VITH NERVE PARALYSIS ( 14 FDA reports)
VULVOVAGINITIS ( 14 FDA reports)
ACUTE LEUKAEMIA ( 14 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 14 FDA reports)
ALCOHOLIC LIVER DISEASE ( 14 FDA reports)
ALLERGIC SINUSITIS ( 14 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 14 FDA reports)
ANGIODYSPLASIA ( 14 FDA reports)
AORTIC ATHEROSCLEROSIS ( 14 FDA reports)
AORTIC VALVE REPLACEMENT ( 14 FDA reports)
ARTERIOVENOUS MALFORMATION ( 14 FDA reports)
ASPERGILLOSIS ( 14 FDA reports)
AXILLARY MASS ( 14 FDA reports)
AXONAL NEUROPATHY ( 14 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 14 FDA reports)
BIOPSY CHEST WALL ABNORMAL ( 14 FDA reports)
BIOPSY TONGUE ABNORMAL ( 14 FDA reports)
BLADDER MASS ( 14 FDA reports)
BLOOD CORTISOL ABNORMAL ( 14 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 14 FDA reports)
BLOOD MAGNESIUM INCREASED ( 14 FDA reports)
BLOOD PH DECREASED ( 14 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 14 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 14 FDA reports)
BONE FISTULA ( 14 FDA reports)
BREAST CANCER STAGE II ( 14 FDA reports)
BREAST FIBROSIS ( 14 FDA reports)
BULIMIA NERVOSA ( 14 FDA reports)
BURNING MOUTH SYNDROME ( 14 FDA reports)
CARBUNCLE ( 14 FDA reports)
CARCINOID TUMOUR OF THE SMALL BOWEL ( 14 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 14 FDA reports)
CHEMOTHERAPY ( 14 FDA reports)
CLOSTRIDIUM COLITIS ( 14 FDA reports)
COELIAC ARTERY COMPRESSION SYNDROME ( 14 FDA reports)
CULTURE WOUND POSITIVE ( 14 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 14 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 14 FDA reports)
DENTAL PROSTHESIS USER ( 14 FDA reports)
DIAPHRAGMATIC HERNIA ( 14 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 14 FDA reports)
DRUG TOLERANCE DECREASED ( 14 FDA reports)
EAR PRURITUS ( 14 FDA reports)
EMBOLISM VENOUS ( 14 FDA reports)
ENCEPHALITIS HERPES ( 14 FDA reports)
FEELING GUILTY ( 14 FDA reports)
FORAMEN MAGNUM STENOSIS ( 14 FDA reports)
GASTRIC INFECTION ( 14 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 14 FDA reports)
GLOMERULOSCLEROSIS ( 14 FDA reports)
GRIP STRENGTH DECREASED ( 14 FDA reports)
HEPATIC CONGESTION ( 14 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 14 FDA reports)
HYPOPROTEINAEMIA ( 14 FDA reports)
IMPETIGO ( 14 FDA reports)
INFECTED SEBACEOUS CYST ( 14 FDA reports)
INJECTION SITE DISCOMFORT ( 14 FDA reports)
INTRADUCTAL PAPILLOMA OF BREAST ( 14 FDA reports)
LOOSE BODY IN JOINT ( 14 FDA reports)
LUNG OPERATION ( 14 FDA reports)
LYMPHADENECTOMY ( 14 FDA reports)
MENINGIOMA ( 14 FDA reports)
METASTASES TO EYE ( 14 FDA reports)
MONONUCLEOSIS SYNDROME ( 14 FDA reports)
MUSCLE HAEMORRHAGE ( 14 FDA reports)
NAIL DISCOLOURATION ( 14 FDA reports)
NEPHROGENIC ANAEMIA ( 14 FDA reports)
NODULE ON EXTREMITY ( 14 FDA reports)
OCCULT BLOOD ( 14 FDA reports)
OPHTHALMOPLEGIA ( 14 FDA reports)
ORCHITIS ( 14 FDA reports)
OSTEOGENESIS IMPERFECTA ( 14 FDA reports)
OSTEOTOMY ( 14 FDA reports)
PAPILLARY THYROID CANCER ( 14 FDA reports)
PCO2 DECREASED ( 14 FDA reports)
PELVIC ABSCESS ( 14 FDA reports)
ABSCESS INTESTINAL ( 13 FDA reports)
ALVEOLITIS ALLERGIC ( 13 FDA reports)
ANTIBODY TEST POSITIVE ( 13 FDA reports)
APICAL GRANULOMA ( 13 FDA reports)
AREFLEXIA ( 13 FDA reports)
ATROPHY ( 13 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 13 FDA reports)
BLADDER DIVERTICULUM ( 13 FDA reports)
BLADDER PROLAPSE ( 13 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 13 FDA reports)
BLOOD ERYTHROPOIETIN DECREASED ( 13 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 13 FDA reports)
BLOOD PROLACTIN INCREASED ( 13 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 13 FDA reports)
BRAIN DAMAGE ( 13 FDA reports)
BREAST ENLARGEMENT ( 13 FDA reports)
BREAST NEOPLASM ( 13 FDA reports)
BRONCHIOLITIS ( 13 FDA reports)
CALCULUS URINARY ( 13 FDA reports)
CARCINOID TUMOUR ( 13 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 13 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 13 FDA reports)
CERVIX DISORDER ( 13 FDA reports)
CERVIX HAEMORRHAGE UTERINE ( 13 FDA reports)
CHOLANGITIS ( 13 FDA reports)
COLONIC STENOSIS ( 13 FDA reports)
CORNEAL DYSTROPHY ( 13 FDA reports)
CUTIS LAXA ( 13 FDA reports)
DERMOID CYST ( 13 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 13 FDA reports)
DISLOCATION OF VERTEBRA ( 13 FDA reports)
DRUG LEVEL DECREASED ( 13 FDA reports)
EPIDURAL LIPOMATOSIS ( 13 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 13 FDA reports)
EXFOLIATIVE RASH ( 13 FDA reports)
EYE OEDEMA ( 13 FDA reports)
FAECES PALE ( 13 FDA reports)
FEELING OF DESPAIR ( 13 FDA reports)
FINGER DEFORMITY ( 13 FDA reports)
FRACTURED COCCYX ( 13 FDA reports)
GASTRITIS ATROPHIC ( 13 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 13 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 13 FDA reports)
HAEMORRHAGIC DIATHESIS ( 13 FDA reports)
HEMIANOPIA HOMONYMOUS ( 13 FDA reports)
HORDEOLUM ( 13 FDA reports)
HYPOREFLEXIA ( 13 FDA reports)
INJECTION SITE INFECTION ( 13 FDA reports)
INTERCOSTAL NEURALGIA ( 13 FDA reports)
LYMPHOCYTIC INFILTRATION ( 13 FDA reports)
LYMPHOCYTOSIS ( 13 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 13 FDA reports)
METASTASES TO BONE MARROW ( 13 FDA reports)
METASTASES TO THE MEDIASTINUM ( 13 FDA reports)
METASTATIC CARCINOID TUMOUR ( 13 FDA reports)
NASAL TURBINATE ABNORMALITY ( 13 FDA reports)
NECROTISING FASCIITIS ( 13 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 13 FDA reports)
OESOPHAGEAL POLYP ( 13 FDA reports)
ORAL NEOPLASM ( 13 FDA reports)
PATHOGEN RESISTANCE ( 13 FDA reports)
PERITONEAL DIALYSIS ( 13 FDA reports)
PLATELET COUNT ABNORMAL ( 13 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 13 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 13 FDA reports)
POST THROMBOTIC SYNDROME ( 13 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 13 FDA reports)
POSTURE ABNORMAL ( 13 FDA reports)
POTENTIATING DRUG INTERACTION ( 13 FDA reports)
PROCEDURAL VOMITING ( 13 FDA reports)
PUPILS UNEQUAL ( 13 FDA reports)
RESPIRATORY THERAPY ( 13 FDA reports)
RESUSCITATION ( 13 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 13 FDA reports)
SCLEROMALACIA ( 13 FDA reports)
SCREAMING ( 13 FDA reports)
SECONDARY SEQUESTRUM ( 13 FDA reports)
SINUS ANTROSTOMY ( 13 FDA reports)
SPLENIC INFARCTION ( 13 FDA reports)
STAG HORN CALCULUS ( 13 FDA reports)
TEETH BRITTLE ( 13 FDA reports)
TOE AMPUTATION ( 13 FDA reports)
TONSILLITIS ( 13 FDA reports)
TOOTH DEVELOPMENT DISORDER ( 13 FDA reports)
UMBILICAL CORD VASCULAR DISORDER ( 13 FDA reports)
VULVOVAGINAL PRURITUS ( 13 FDA reports)
PHLEBITIS SUPERFICIAL ( 12 FDA reports)
POLYCHROMASIA ( 12 FDA reports)
POST PROCEDURAL INFECTION ( 12 FDA reports)
POSTERIOR CAPSULOTOMY ( 12 FDA reports)
POSTOPERATIVE FEVER ( 12 FDA reports)
PRECANCEROUS CELLS PRESENT ( 12 FDA reports)
RADICAL MASTECTOMY ( 12 FDA reports)
RECTAL ABSCESS ( 12 FDA reports)
RENAL STONE REMOVAL ( 12 FDA reports)
RESPIRATION ABNORMAL ( 12 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 12 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 12 FDA reports)
RETICULOCYTE COUNT ABNORMAL ( 12 FDA reports)
RETINAL VEIN OCCLUSION ( 12 FDA reports)
ROTATOR CUFF REPAIR ( 12 FDA reports)
SHOULDER DEFORMITY ( 12 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 12 FDA reports)
SOFT TISSUE INFLAMMATION ( 12 FDA reports)
SPIDER VEIN ( 12 FDA reports)
SPINAL OPERATION ( 12 FDA reports)
STARING ( 12 FDA reports)
STERNAL FRACTURE ( 12 FDA reports)
SUBMANDIBULAR MASS ( 12 FDA reports)
SUBSTANCE ABUSE ( 12 FDA reports)
TARSAL TUNNEL SYNDROME ( 12 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 12 FDA reports)
TORSADE DE POINTES ( 12 FDA reports)
ULCERATIVE KERATITIS ( 12 FDA reports)
URETERAL STENT INSERTION ( 12 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 12 FDA reports)
VAGINAL PROLAPSE ( 12 FDA reports)
VASCULAR CAUTERISATION ( 12 FDA reports)
VASCULAR DEMENTIA ( 12 FDA reports)
VERTEBRAL COLUMN MASS ( 12 FDA reports)
VULVOVAGINAL DISCOMFORT ( 12 FDA reports)
WOUND DEBRIDEMENT ( 12 FDA reports)
ABDOMINAL RIGIDITY ( 12 FDA reports)
ACCIDENTAL EXPOSURE ( 12 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 12 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 12 FDA reports)
ANGIOMYOLIPOMA ( 12 FDA reports)
ANGIOPLASTY ( 12 FDA reports)
ANKYLOSING SPONDYLITIS ( 12 FDA reports)
AORTIC VALVE CALCIFICATION ( 12 FDA reports)
APPLICATION SITE BURN ( 12 FDA reports)
BENIGN NEOPLASM OF SKIN ( 12 FDA reports)
BENIGN TUMOUR EXCISION ( 12 FDA reports)
BILE DUCT CANCER ( 12 FDA reports)
BIOPSY BONE ( 12 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 12 FDA reports)
BLOOD BLISTER ( 12 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 12 FDA reports)
BLOOD CREATININE ABNORMAL ( 12 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 12 FDA reports)
BREAST HYPERPLASIA ( 12 FDA reports)
CALCIUM METABOLISM DISORDER ( 12 FDA reports)
CARDIAC ASTHMA ( 12 FDA reports)
CARDIORENAL SYNDROME ( 12 FDA reports)
CATARACT CORTICAL ( 12 FDA reports)
CEREBROSCLEROSIS ( 12 FDA reports)
CHOLESTEATOMA ( 12 FDA reports)
COGWHEEL RIGIDITY ( 12 FDA reports)
COMPRESSION STOCKINGS APPLICATION ( 12 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 12 FDA reports)
CONGO-CRIMEAN HAEMORRHAGIC FEVER ( 12 FDA reports)
DERMATITIS ATOPIC ( 12 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 12 FDA reports)
ENTEROCOLITIS ( 12 FDA reports)
ENZYME ABNORMALITY ( 12 FDA reports)
EOSINOPHILIA ( 12 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 12 FDA reports)
FACTOR V LEIDEN MUTATION ( 12 FDA reports)
FAT TISSUE INCREASED ( 12 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 12 FDA reports)
FEMORAL ARTERY OCCLUSION ( 12 FDA reports)
FISTULA REPAIR ( 12 FDA reports)
FLUID INTAKE REDUCED ( 12 FDA reports)
FOOD CRAVING ( 12 FDA reports)
FOOD POISONING ( 12 FDA reports)
FUNGAL OESOPHAGITIS ( 12 FDA reports)
GASTRECTOMY ( 12 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 12 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 12 FDA reports)
HAIR COLOUR CHANGES ( 12 FDA reports)
HEART TRANSPLANT REJECTION ( 12 FDA reports)
HEPATIC CALCIFICATION ( 12 FDA reports)
HISTOPLASMOSIS ( 12 FDA reports)
HYPERACUSIS ( 12 FDA reports)
HYPERTROPHY ( 12 FDA reports)
HYPOPERFUSION ( 12 FDA reports)
HYPOTHERMIA ( 12 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 12 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 12 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 12 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 12 FDA reports)
INTRACRANIAL ANEURYSM ( 12 FDA reports)
MASS EXCISION ( 12 FDA reports)
METASTASES TO LARGE INTESTINE ( 12 FDA reports)
METASTASES TO SPLEEN ( 12 FDA reports)
MITRAL VALVE REPAIR ( 12 FDA reports)
MYELOPATHY ( 12 FDA reports)
NASAL MUCOSAL DISORDER ( 12 FDA reports)
NASAL SEPTAL OPERATION ( 12 FDA reports)
NONSPECIFIC REACTION ( 12 FDA reports)
OPTIC ATROPHY ( 12 FDA reports)
ORAL SOFT TISSUE DISORDER ( 12 FDA reports)
OXYGEN SUPPLEMENTATION ( 12 FDA reports)
PAROTIDECTOMY ( 12 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 12 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 11 FDA reports)
ACETABULUM FRACTURE ( 11 FDA reports)
ACUTE PSYCHOSIS ( 11 FDA reports)
ADRENAL SUPPRESSION ( 11 FDA reports)
ANION GAP DECREASED ( 11 FDA reports)
AORTIC VALVE DISEASE ( 11 FDA reports)
APPLICATION SITE REACTION ( 11 FDA reports)
APPLICATION SITE VESICLES ( 11 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 11 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 11 FDA reports)
ASBESTOSIS ( 11 FDA reports)
AUTONOMIC NEUROPATHY ( 11 FDA reports)
BIOPSY MUSCLE ( 11 FDA reports)
BIOPSY PERIPHERAL NERVE ( 11 FDA reports)
BLADDER DISCOMFORT ( 11 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 11 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 11 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 11 FDA reports)
BONE CANCER METASTATIC ( 11 FDA reports)
BONE FORMATION INCREASED ( 11 FDA reports)
BONE METABOLISM DISORDER ( 11 FDA reports)
BRADYKINESIA ( 11 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 11 FDA reports)
CARDIAC ABLATION ( 11 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 11 FDA reports)
CARTILAGE INJURY ( 11 FDA reports)
CATHETER SITE RELATED REACTION ( 11 FDA reports)
CAUDA EQUINA SYNDROME ( 11 FDA reports)
CEREBRAL THROMBOSIS ( 11 FDA reports)
CHRONIC HEPATITIS ( 11 FDA reports)
CLUMSINESS ( 11 FDA reports)
COLLAGEN-VASCULAR DISEASE ( 11 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 11 FDA reports)
COMPULSIVE SHOPPING ( 11 FDA reports)
CONGENITAL ANOMALY ( 11 FDA reports)
CONJUNCTIVAL ABRASION ( 11 FDA reports)
CRANIOTOMY ( 11 FDA reports)
CULTURE POSITIVE ( 11 FDA reports)
DENTAL TREATMENT ( 11 FDA reports)
EBSTEIN'S ANOMALY ( 11 FDA reports)
EYELID FUNCTION DISORDER ( 11 FDA reports)
FOOD AVERSION ( 11 FDA reports)
FUNGAL RASH ( 11 FDA reports)
GALLBLADDER POLYP ( 11 FDA reports)
GASTRIC PH DECREASED ( 11 FDA reports)
GASTROINTESTINAL CARCINOMA ( 11 FDA reports)
HAIR DISORDER ( 11 FDA reports)
HELICOBACTER TEST POSITIVE ( 11 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 11 FDA reports)
HYPERSEXUALITY ( 11 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 11 FDA reports)
IMMOBILE ( 11 FDA reports)
INGUINAL HERNIA REPAIR ( 11 FDA reports)
INTESTINAL HAEMORRHAGE ( 11 FDA reports)
ISCHAEMIC HEPATITIS ( 11 FDA reports)
KETOACIDOSIS ( 11 FDA reports)
LASER THERAPY ( 11 FDA reports)
LIMB CRUSHING INJURY ( 11 FDA reports)
LIPOMA EXCISION ( 11 FDA reports)
LOGORRHOEA ( 11 FDA reports)
MALLORY-WEISS SYNDROME ( 11 FDA reports)
MANTLE CELL LYMPHOMA ( 11 FDA reports)
MENINGITIS VIRAL ( 11 FDA reports)
MITRAL VALVE STENOSIS ( 11 FDA reports)
MONOPARESIS ( 11 FDA reports)
MYDRIASIS ( 11 FDA reports)
NASAL OBSTRUCTION ( 11 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 11 FDA reports)
NEONATAL ASPIRATION ( 11 FDA reports)
NEPHRITIC SYNDROME ( 11 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 11 FDA reports)
NERVE BLOCK ( 11 FDA reports)
NEUROPATHIC ARTHROPATHY ( 11 FDA reports)
NEUROSENSORY HYPOACUSIS ( 11 FDA reports)
NOCTURNAL DYSPNOEA ( 11 FDA reports)
NODAL ARRHYTHMIA ( 11 FDA reports)
OESOPHAGEAL RUPTURE ( 11 FDA reports)
ONYCHOMADESIS ( 11 FDA reports)
OSTEOSARCOMA METASTATIC ( 11 FDA reports)
PANCREATIC ATROPHY ( 11 FDA reports)
PAPILLOMA VIRAL INFECTION ( 11 FDA reports)
PARAPARESIS ( 11 FDA reports)
PHARYNGEAL DISORDER ( 11 FDA reports)
POIKILOCYTOSIS ( 11 FDA reports)
PRESUMED OCULAR HISTOPLASMOSIS SYNDROME ( 11 FDA reports)
PROTEIN TOTAL INCREASED ( 11 FDA reports)
PSEUDODEMENTIA ( 11 FDA reports)
PSEUDOMONAL SEPSIS ( 11 FDA reports)
RASH PUSTULAR ( 11 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 11 FDA reports)
RELAPSING FEVER ( 11 FDA reports)
RENAL NEOPLASM ( 11 FDA reports)
RESPIRATORY MUSCLE WEAKNESS ( 11 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 11 FDA reports)
SALIVARY GLAND MASS ( 11 FDA reports)
SKIN LESION EXCISION ( 11 FDA reports)
STATUS EPILEPTICUS ( 11 FDA reports)
SUBGALEAL HAEMATOMA ( 11 FDA reports)
T-CELL LYMPHOMA ( 11 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 11 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 11 FDA reports)
URETHRAL CARUNCLE ( 11 FDA reports)
URETHRAL DISORDER ( 11 FDA reports)
URETHRITIS ( 11 FDA reports)
VASCULAR GRAFT ( 11 FDA reports)
VASOSPASM ( 11 FDA reports)
VENTRICULAR ARRHYTHMIA ( 11 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 11 FDA reports)
PHLEBOSCLEROSIS ( 10 FDA reports)
PNEUMONIA KLEBSIELLA ( 10 FDA reports)
PORTAL VEIN OCCLUSION ( 10 FDA reports)
PTERYGIUM ( 10 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 10 FDA reports)
PYELONEPHRITIS ACUTE ( 10 FDA reports)
RENAL LIPOMATOSIS ( 10 FDA reports)
RETINOPATHY HYPERTENSIVE ( 10 FDA reports)
SCAN MYOCARDIAL PERFUSION ( 10 FDA reports)
SEBORRHOEA ( 10 FDA reports)
SINUSITIS FUNGAL ( 10 FDA reports)
SKIN CHAPPED ( 10 FDA reports)
SKIN PLAQUE ( 10 FDA reports)
SPASMODIC DYSPHONIA ( 10 FDA reports)
SPINAL CLAUDICATION ( 10 FDA reports)
SPINAL COLUMN INJURY ( 10 FDA reports)
SPINAL CORPECTOMY ( 10 FDA reports)
SPUTUM CULTURE POSITIVE ( 10 FDA reports)
TACHYCARDIA PAROXYSMAL ( 10 FDA reports)
THORACIC OPERATION ( 10 FDA reports)
TONGUE BLACK HAIRY ( 10 FDA reports)
TRANSFUSION REACTION ( 10 FDA reports)
TRIGONITIS ( 10 FDA reports)
TUMOUR MARKER INCREASED ( 10 FDA reports)
UTERINE MALPOSITION ( 10 FDA reports)
VOCAL CORD POLYP ( 10 FDA reports)
ACCIDENTAL NEEDLE STICK ( 10 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 10 FDA reports)
ACTINOMYCES TEST POSITIVE ( 10 FDA reports)
ACUTE HEPATIC FAILURE ( 10 FDA reports)
ADMINISTRATION SITE INFECTION ( 10 FDA reports)
ALCOHOLISM ( 10 FDA reports)
ALLERGY TO ARTHROPOD STING ( 10 FDA reports)
ALLODYNIA ( 10 FDA reports)
ANAL CANDIDIASIS ( 10 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 10 FDA reports)
ANTISOCIAL BEHAVIOUR ( 10 FDA reports)
BACTERIAL DIARRHOEA ( 10 FDA reports)
BENIGN GASTRIC NEOPLASM ( 10 FDA reports)
BETA GLOBULIN INCREASED ( 10 FDA reports)
BILIARY CIRRHOSIS ( 10 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 10 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 10 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 10 FDA reports)
BLOOD URIC ACID INCREASED ( 10 FDA reports)
BRAIN STEM INFARCTION ( 10 FDA reports)
BREAST DISCHARGE ( 10 FDA reports)
BREAST OEDEMA ( 10 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 10 FDA reports)
CALCULUS BLADDER ( 10 FDA reports)
COARCTATION OF THE AORTA ( 10 FDA reports)
COITAL BLEEDING ( 10 FDA reports)
CYSTITIS INTERSTITIAL ( 10 FDA reports)
DERMATITIS ACNEIFORM ( 10 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 10 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 10 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 10 FDA reports)
ERYTHEMA NODOSUM ( 10 FDA reports)
EYELID OPERATION ( 10 FDA reports)
FIBROADENOMA OF BREAST ( 10 FDA reports)
FIBROUS DYSPLASIA OF JAW ( 10 FDA reports)
FOLATE DEFICIENCY ( 10 FDA reports)
FUNGAEMIA ( 10 FDA reports)
GALACTORRHOEA ( 10 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 10 FDA reports)
GOUTY ARTHRITIS ( 10 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 10 FDA reports)
HAEMARTHROSIS ( 10 FDA reports)
HAEMOGLOBIN ABNORMAL ( 10 FDA reports)
HEART SOUNDS ABNORMAL ( 10 FDA reports)
HEPATITIS A ( 10 FDA reports)
HEPATITIS TOXIC ( 10 FDA reports)
HYPERPLASTIC CHOLECYSTOPATHY ( 10 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 10 FDA reports)
INCORRECT STORAGE OF DRUG ( 10 FDA reports)
INFECTED DERMAL CYST ( 10 FDA reports)
INJECTION SITE OEDEMA ( 10 FDA reports)
INTESTINAL ULCER ( 10 FDA reports)
LEARNING DISORDER ( 10 FDA reports)
LICHEN PLANUS ( 10 FDA reports)
LICHEN SCLEROSUS ( 10 FDA reports)
LIP DISORDER ( 10 FDA reports)
LIVER TRANSPLANT REJECTION ( 10 FDA reports)
LUMBAR SPINE FLATTENING ( 10 FDA reports)
LYMPHANGITIS ( 10 FDA reports)
MACULOPATHY ( 10 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 10 FDA reports)
MENINGITIS CHEMICAL ( 10 FDA reports)
METASTASES TO THYROID ( 10 FDA reports)
MICTURITION FREQUENCY DECREASED ( 10 FDA reports)
MUCOUS STOOLS ( 10 FDA reports)
MUSCLE RUPTURE ( 10 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 10 FDA reports)
NASAL CYST ( 10 FDA reports)
NASAL OEDEMA ( 10 FDA reports)
NEUROENDOCRINE TUMOUR ( 10 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 10 FDA reports)
NEUTRALISING ANTIBODIES POSITIVE ( 10 FDA reports)
PAROTID GLAND ENLARGEMENT ( 10 FDA reports)
PARTIAL SEIZURES ( 10 FDA reports)
PELVIC DISCOMFORT ( 10 FDA reports)
PETIT MAL EPILEPSY ( 10 FDA reports)
PHIMOSIS ( 10 FDA reports)
ABDOMINAL WALL ABSCESS ( 9 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 9 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 9 FDA reports)
AKINESIA ( 9 FDA reports)
ALCOHOL POISONING ( 9 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 9 FDA reports)
ANAPHYLACTOID REACTION ( 9 FDA reports)
ANIMAL SCRATCH ( 9 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST ( 9 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 9 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 9 FDA reports)
ARTERIAL HAEMORRHAGE ( 9 FDA reports)
ARTERIOGRAM CORONARY ( 9 FDA reports)
ASTHENOPIA ( 9 FDA reports)
BIOPSY MUCOSA ABNORMAL ( 9 FDA reports)
BLEPHAROSPASM ( 9 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 9 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 9 FDA reports)
BODY TINEA ( 9 FDA reports)
BONE DENSITY ABNORMAL ( 9 FDA reports)
BRAIN MASS ( 9 FDA reports)
BRONCHIAL DISORDER ( 9 FDA reports)
BRONCHITIS VIRAL ( 9 FDA reports)
CARDIAC SEPTAL DEFECT ( 9 FDA reports)
CARTILAGE NEOPLASM ( 9 FDA reports)
CATATONIA ( 9 FDA reports)
CATHETER SEPSIS ( 9 FDA reports)
CENTRAL LINE INFECTION ( 9 FDA reports)
CENTRAL OBESITY ( 9 FDA reports)
CHRONIC HEPATIC FAILURE ( 9 FDA reports)
COLLAGEN DISORDER ( 9 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 9 FDA reports)
CONJUNCTIVITIS VIRAL ( 9 FDA reports)
DEAFNESS BILATERAL ( 9 FDA reports)
DEFAECATION URGENCY ( 9 FDA reports)
DENTAL IMPRESSION PROCEDURE ( 9 FDA reports)
DEPRESSIVE SYMPTOM ( 9 FDA reports)
DUODENAL OBSTRUCTION ( 9 FDA reports)
DYSPLASIA ( 9 FDA reports)
ENCHONDROMA ( 9 FDA reports)
ENTEROCUTANEOUS FISTULA ( 9 FDA reports)
EPIDIDYMAL CYST ( 9 FDA reports)
ERYTHEMA OF EYELID ( 9 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 9 FDA reports)
ESCHERICHIA SEPSIS ( 9 FDA reports)
EXOPHTHALMOS ( 9 FDA reports)
FACET JOINT BLOCK ( 9 FDA reports)
FEEDING TUBE COMPLICATION ( 9 FDA reports)
FIBROMA ( 9 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 9 FDA reports)
GASTRIC PERFORATION ( 9 FDA reports)
GENERAL SYMPTOM ( 9 FDA reports)
GLYCOSURIA ( 9 FDA reports)
HAEMATOSPERMIA ( 9 FDA reports)
HERPES VIRUS INFECTION ( 9 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 9 FDA reports)
HUMAN CHORIONIC GONADOTROPIN INCREASED ( 9 FDA reports)
HYPERCAPNIA ( 9 FDA reports)
HYPERMAGNESAEMIA ( 9 FDA reports)
HYPERPATHIA ( 9 FDA reports)
HYPOCHROMASIA ( 9 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 9 FDA reports)
ILEAL STENOSIS ( 9 FDA reports)
IMPAIRED SELF-CARE ( 9 FDA reports)
INADEQUATE DIET ( 9 FDA reports)
INCISION SITE ABSCESS ( 9 FDA reports)
INCISION SITE COMPLICATION ( 9 FDA reports)
INCISION SITE PAIN ( 9 FDA reports)
INJECTION SITE ABSCESS ( 9 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 9 FDA reports)
JOINT SURGERY ( 9 FDA reports)
LATEX ALLERGY ( 9 FDA reports)
LAZINESS ( 9 FDA reports)
LEUKAEMIA PLASMACYTIC ( 9 FDA reports)
LIP BLISTER ( 9 FDA reports)
LORDOSIS ( 9 FDA reports)
LOWER EXTREMITY MASS ( 9 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 9 FDA reports)
LUNG ABSCESS ( 9 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 9 FDA reports)
MALIGNANT ASCITES ( 9 FDA reports)
MAMMOGRAM ( 9 FDA reports)
MARBURG DISEASE ( 9 FDA reports)
MENISCUS REMOVAL ( 9 FDA reports)
MILK ALLERGY ( 9 FDA reports)
MUSCLE CONTRACTURE ( 9 FDA reports)
NEPHRECTOMY ( 9 FDA reports)
NERVE ROOT INJURY CERVICAL ( 9 FDA reports)
NON-NEUTRALISING ANTIBODIES POSITIVE ( 9 FDA reports)
OCULAR VASCULAR DISORDER ( 9 FDA reports)
OESOPHAGEAL DISCOMFORT ( 9 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 9 FDA reports)
ONYCHOCLASIS ( 9 FDA reports)
PANCREATIC PSEUDOCYST ( 9 FDA reports)
PARTNER STRESS ( 9 FDA reports)
PELVIC ADHESIONS ( 9 FDA reports)
PERICARDIAL HAEMORRHAGE ( 9 FDA reports)
PERIPHERAL NERVE INJURY ( 9 FDA reports)
PHYSICAL ASSAULT ( 9 FDA reports)
POISONING ( 9 FDA reports)
POST-TRAUMATIC NECK SYNDROME ( 9 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 9 FDA reports)
PROCEDURAL NAUSEA ( 9 FDA reports)
PSEUDARTHROSIS ( 9 FDA reports)
PSEUDOCYST ( 9 FDA reports)
RADIOTHERAPY TO BRAIN ( 9 FDA reports)
RENAL TRANSPLANT ( 9 FDA reports)
RETINAL ARTERY OCCLUSION ( 9 FDA reports)
RHINITIS PERENNIAL ( 9 FDA reports)
ROULEAUX FORMATION ( 9 FDA reports)
SCOTOMA ( 9 FDA reports)
SCROTAL CYST ( 9 FDA reports)
SCROTAL IRRITATION ( 9 FDA reports)
SEXUALLY TRANSMITTED DISEASE ( 9 FDA reports)
SKIN EROSION ( 9 FDA reports)
SKIN OPERATION ( 9 FDA reports)
SMEAR CERVIX ABNORMAL ( 9 FDA reports)
SOCIAL PHOBIA ( 9 FDA reports)
SOMATISATION DISORDER ( 9 FDA reports)
SPINAL CORD INJURY THORACIC ( 9 FDA reports)
SPINAL PAIN ( 9 FDA reports)
SPLENECTOMY ( 9 FDA reports)
SUFFOCATION FEELING ( 9 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 9 FDA reports)
SURGICAL PROCEDURE REPEATED ( 9 FDA reports)
TEMPORAL ARTERITIS ( 9 FDA reports)
TERMINAL DRIBBLING ( 9 FDA reports)
TESTICULAR FAILURE ( 9 FDA reports)
THERAPY CESSATION ( 9 FDA reports)
THROMBOCYTHAEMIA ( 9 FDA reports)
TINEA CRURIS ( 9 FDA reports)
TONGUE COATED ( 9 FDA reports)
TOURETTE'S DISORDER ( 9 FDA reports)
TRACHEOSTOMY ( 9 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 9 FDA reports)
TRICUSPID VALVE DISEASE ( 9 FDA reports)
TUMOUR EMBOLISM ( 9 FDA reports)
URETERIC STENOSIS ( 9 FDA reports)
URETHRAL STENOSIS ( 9 FDA reports)
URTICARIA GENERALISED ( 9 FDA reports)
VAGINAL ULCERATION ( 9 FDA reports)
VARICOCELE ( 9 FDA reports)
WALKING DISABILITY ( 9 FDA reports)
PHOTODERMATOSIS ( 8 FDA reports)
PIGMENTED NAEVUS ( 8 FDA reports)
PNEUMATOSIS INTESTINALIS ( 8 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 8 FDA reports)
POSTOPERATIVE ADHESION ( 8 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 8 FDA reports)
PRIAPISM ( 8 FDA reports)
PROCEDURAL HYPERTENSION ( 8 FDA reports)
PROCEDURAL HYPOTENSION ( 8 FDA reports)
PRODUCT LABEL ISSUE ( 8 FDA reports)
PULMONARY CALCIFICATION ( 8 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 8 FDA reports)
QUADRIPARESIS ( 8 FDA reports)
RECTAL CANCER ( 8 FDA reports)
RECTAL FISTULA REPAIR ( 8 FDA reports)
RHEUMATOID NODULE ( 8 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 8 FDA reports)
SCROTAL OEDEMA ( 8 FDA reports)
SMALL INTESTINE ULCER ( 8 FDA reports)
SPINAL X-RAY ABNORMAL ( 8 FDA reports)
SPLENIC ARTERY ANEURYSM ( 8 FDA reports)
SPLENIC VEIN THROMBOSIS ( 8 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 8 FDA reports)
STATUS ASTHMATICUS ( 8 FDA reports)
STERNAL INJURY ( 8 FDA reports)
STUPOR ( 8 FDA reports)
TABLET PHYSICAL ISSUE ( 8 FDA reports)
TENDON SHEATH INCISION ( 8 FDA reports)
TINEA INFECTION ( 8 FDA reports)
TONGUE BITING ( 8 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 8 FDA reports)
URINE KETONE BODY PRESENT ( 8 FDA reports)
URINE OUTPUT INCREASED ( 8 FDA reports)
VASCULAR GRAFT OCCLUSION ( 8 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 8 FDA reports)
VOCAL CORD PARESIS ( 8 FDA reports)
VOCAL CORD THICKENING ( 8 FDA reports)
XEROSIS ( 8 FDA reports)
YAWNING ( 8 FDA reports)
ABDOMINAL OPERATION ( 8 FDA reports)
ABORTION INDUCED ( 8 FDA reports)
ACQUIRED PORPHYRIA ( 8 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 8 FDA reports)
ADRENOMEGALY ( 8 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 8 FDA reports)
APRAXIA ( 8 FDA reports)
ARTHROSCOPIC SURGERY ( 8 FDA reports)
ASEPTIC NECROSIS BONE ( 8 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 8 FDA reports)
BACILLUS INFECTION ( 8 FDA reports)
BLADDER DYSFUNCTION ( 8 FDA reports)
BLINDNESS CORTICAL ( 8 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 8 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 8 FDA reports)
BLOOD PRESSURE SYSTOLIC ABNORMAL ( 8 FDA reports)
BRAIN DEATH ( 8 FDA reports)
BUTTOCK PAIN ( 8 FDA reports)
CARDIAC TAMPONADE ( 8 FDA reports)
CARDIAC VALVE VEGETATION ( 8 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 8 FDA reports)
CARDIOVERSION ( 8 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 8 FDA reports)
CAUSTIC INJURY ( 8 FDA reports)
CERVICITIS ( 8 FDA reports)
CHOREA ( 8 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 8 FDA reports)
CLOSED HEAD INJURY ( 8 FDA reports)
COCCYDYNIA ( 8 FDA reports)
COLON NEOPLASM ( 8 FDA reports)
CUSHINGOID ( 8 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 8 FDA reports)
DEPERSONALISATION ( 8 FDA reports)
DEPRESSION SUICIDAL ( 8 FDA reports)
DISBACTERIOSIS ( 8 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 8 FDA reports)
DYSPAREUNIA ( 8 FDA reports)
DYSPHASIA ( 8 FDA reports)
ENCEPHALITIS POST MEASLES ( 8 FDA reports)
ENTEROBACTER INFECTION ( 8 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 8 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 8 FDA reports)
EROSIVE DUODENITIS ( 8 FDA reports)
ESCHERICHIA BACTERAEMIA ( 8 FDA reports)
EXTRAVASATION ( 8 FDA reports)
EYELID CYST ( 8 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 8 FDA reports)
FOOD ALLERGY ( 8 FDA reports)
FUSOBACTERIUM INFECTION ( 8 FDA reports)
GANGLION ( 8 FDA reports)
GASTRIC CANCER RECURRENT ( 8 FDA reports)
GASTRIC OPERATION ( 8 FDA reports)
GASTROINTESTINAL OEDEMA ( 8 FDA reports)
GASTROSTOMY ( 8 FDA reports)
GENITAL SWELLING ( 8 FDA reports)
HAEMORRHAGE URINARY TRACT ( 8 FDA reports)
HAIR GROWTH ABNORMAL ( 8 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 8 FDA reports)
HEPATOSPLENIC T-CELL LYMPHOMA ( 8 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 8 FDA reports)
HIGH FREQUENCY ABLATION ( 8 FDA reports)
HOSTILITY ( 8 FDA reports)
HYPERCHLORAEMIA ( 8 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 8 FDA reports)
HYPERVIGILANCE ( 8 FDA reports)
HYPOPARATHYROIDISM ( 8 FDA reports)
INCISION SITE INFECTION ( 8 FDA reports)
INFUSION SITE PAIN ( 8 FDA reports)
INJECTION SITE CELLULITIS ( 8 FDA reports)
INJECTION SITE VESICLES ( 8 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 8 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 8 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 8 FDA reports)
IRON METABOLISM DISORDER ( 8 FDA reports)
IRON OVERLOAD ( 8 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 8 FDA reports)
JOINT PROSTHESIS USER ( 8 FDA reports)
LEFT VENTRICULAR FAILURE ( 8 FDA reports)
LHERMITTE'S SIGN ( 8 FDA reports)
LIPIDS ABNORMAL ( 8 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 8 FDA reports)
MACULAR OEDEMA ( 8 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 8 FDA reports)
MEDIASTINAL SHIFT ( 8 FDA reports)
METASTASES TO OVARY ( 8 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 8 FDA reports)
MONARTHRITIS ( 8 FDA reports)
MYELITIS ( 8 FDA reports)
NAIL BED TENDERNESS ( 8 FDA reports)
NODAL OSTEOARTHRITIS ( 8 FDA reports)
ODONTOGENIC CYST ( 8 FDA reports)
OESOPHAGEAL OPERATION ( 8 FDA reports)
OESTROGEN DEFICIENCY ( 8 FDA reports)
ONYCHOLYSIS ( 8 FDA reports)
OOPHORECTOMY ( 8 FDA reports)
OPPORTUNISTIC INFECTION ( 8 FDA reports)
OPTIC NEURITIS ( 8 FDA reports)
ORAL FIBROMA ( 8 FDA reports)
ORAL PRURITUS ( 8 FDA reports)
ORBITAL OEDEMA ( 8 FDA reports)
OROPHARYNGEAL SWELLING ( 8 FDA reports)
OSTEOMALACIA ( 8 FDA reports)
OSTEOSARCOMA LOCALISED ( 8 FDA reports)
OTORRHOEA ( 8 FDA reports)
OVARIAN ABSCESS ( 8 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 8 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 8 FDA reports)
PANCREATIC DUCT DILATATION ( 8 FDA reports)
PANCREATIC NEUROENDOCRINE TUMOUR METASTATIC ( 8 FDA reports)
PENILE OEDEMA ( 8 FDA reports)
PENIS DISORDER ( 8 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 8 FDA reports)
PERFORATED ULCER ( 8 FDA reports)
PERONEAL MUSCULAR ATROPHY ( 8 FDA reports)
PHARYNGEAL EROSION ( 8 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 7 FDA reports)
AEROPHAGIA ( 7 FDA reports)
AGORAPHOBIA ( 7 FDA reports)
AMYLASE INCREASED ( 7 FDA reports)
ANAESTHETIC COMPLICATION ( 7 FDA reports)
ANDROGEN DEFICIENCY ( 7 FDA reports)
AORTIC ANEURYSM RUPTURE ( 7 FDA reports)
AORTIC BYPASS ( 7 FDA reports)
APPLICATION SITE PAIN ( 7 FDA reports)
ARTERIAL INSUFFICIENCY ( 7 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 7 FDA reports)
AURA ( 7 FDA reports)
BASAL GANGLIA INFARCTION ( 7 FDA reports)
BASAL GANGLION DEGENERATION ( 7 FDA reports)
BIOPSY BREAST ABNORMAL ( 7 FDA reports)
BIOPSY LIVER ABNORMAL ( 7 FDA reports)
BLADDER HYPERTROPHY ( 7 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 7 FDA reports)
BLOOD PH INCREASED ( 7 FDA reports)
BLOOD UREA DECREASED ( 7 FDA reports)
BONE INFARCTION ( 7 FDA reports)
BONE MARROW DEPRESSION ( 7 FDA reports)
BOWEL SOUNDS ABNORMAL ( 7 FDA reports)
BRAIN HERNIATION ( 7 FDA reports)
BREAST DISCOMFORT ( 7 FDA reports)
BRONCHIAL HYPERACTIVITY ( 7 FDA reports)
BUNION OPERATION ( 7 FDA reports)
CALCIFICATION METASTATIC ( 7 FDA reports)
CALCULUS URETHRAL ( 7 FDA reports)
CARBOHYDRATE METABOLISM DISORDER ( 7 FDA reports)
CARDIAC FAILURE ACUTE ( 7 FDA reports)
CARDIAC HYPERTROPHY ( 7 FDA reports)
CARDIAC MURMUR FUNCTIONAL ( 7 FDA reports)
CARDIAC OUTPUT DECREASED ( 7 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 7 FDA reports)
CAROTID ARTERY ANEURYSM ( 7 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 7 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 7 FDA reports)
CEREBRAL PALSY ( 7 FDA reports)
CHOLANGITIS CHRONIC ( 7 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 7 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 7 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 7 FDA reports)
CORNEAL OPACITY ( 7 FDA reports)
CRANIOCEREBRAL INJURY ( 7 FDA reports)
CUSHING'S SYNDROME ( 7 FDA reports)
CYTOGENETIC ABNORMALITY ( 7 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 7 FDA reports)
DENTAL CLEANING ( 7 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 7 FDA reports)
DUPUYTREN'S CONTRACTURE ( 7 FDA reports)
DYSPNOEA AT REST ( 7 FDA reports)
EARLY MORNING AWAKENING ( 7 FDA reports)
ELECTROLYTE DEPLETION ( 7 FDA reports)
ENCEPHALITIS VIRAL ( 7 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 7 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 7 FDA reports)
ENTEROVESICAL FISTULA ( 7 FDA reports)
EPIDERMAL NAEVUS ( 7 FDA reports)
EPIDERMAL NECROSIS ( 7 FDA reports)
ERYTHEMA MULTIFORME ( 7 FDA reports)
ESCHERICHIA TEST POSITIVE ( 7 FDA reports)
ETHMOID SINUS SURGERY ( 7 FDA reports)
FAILURE OF IMPLANT ( 7 FDA reports)
FEEDING DISORDER ( 7 FDA reports)
FEMALE STERILISATION ( 7 FDA reports)
FINGER AMPUTATION ( 7 FDA reports)
FOREARM FRACTURE ( 7 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 7 FDA reports)
GASTRIC ULCER PERFORATION ( 7 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 7 FDA reports)
GASTROINTESTINAL INJURY ( 7 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 7 FDA reports)
GENITAL HAEMORRHAGE ( 7 FDA reports)
GINGIVAL HYPERTROPHY ( 7 FDA reports)
GLIOBLASTOMA MULTIFORME ( 7 FDA reports)
GUN SHOT WOUND ( 7 FDA reports)
H1N1 INFLUENZA ( 7 FDA reports)
HAEMOTHORAX ( 7 FDA reports)
HEPATIC ENZYME ABNORMAL ( 7 FDA reports)
HEPATIC PAIN ( 7 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 7 FDA reports)
HERPES OESOPHAGITIS ( 7 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 7 FDA reports)
HODGKIN'S DISEASE ( 7 FDA reports)
HYPERTONIA ( 7 FDA reports)
HYPOCHLORAEMIA ( 7 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 7 FDA reports)
HYPOGONADISM MALE ( 7 FDA reports)
HYPOTRICHOSIS ( 7 FDA reports)
HYPOVITAMINOSIS ( 7 FDA reports)
ILEOSTOMY ( 7 FDA reports)
IMPRISONMENT ( 7 FDA reports)
IMPULSE-CONTROL DISORDER ( 7 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 7 FDA reports)
INFUSION SITE ERYTHEMA ( 7 FDA reports)
INFUSION SITE PRURITUS ( 7 FDA reports)
INFUSION SITE SWELLING ( 7 FDA reports)
INJECTION SITE SCAR ( 7 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 7 FDA reports)
INTERVERTEBRAL DISCITIS ( 7 FDA reports)
IUCD COMPLICATION ( 7 FDA reports)
JOINT DISLOCATION POSTOPERATIVE ( 7 FDA reports)
JOINT LOCK ( 7 FDA reports)
KIDNEY MALROTATION ( 7 FDA reports)
KLEBSIELLA SEPSIS ( 7 FDA reports)
KNEE DEFORMITY ( 7 FDA reports)
LACRIMAL DUCT PROCEDURE ( 7 FDA reports)
LARYNGEAL REPAIR ( 7 FDA reports)
LARYNX IRRITATION ( 7 FDA reports)
LEUKOPLAKIA ( 7 FDA reports)
LIPID METABOLISM DISORDER ( 7 FDA reports)
LIPOATROPHY ( 7 FDA reports)
LYME DISEASE ( 7 FDA reports)
LYMPH NODE PAIN ( 7 FDA reports)
MALIGNANT MESENTERIC NEOPLASM ( 7 FDA reports)
MALIGNANT TUMOUR EXCISION ( 7 FDA reports)
MENINGITIS HERPES ( 7 FDA reports)
METABOLIC ALKALOSIS ( 7 FDA reports)
MIDDLE EAR EFFUSION ( 7 FDA reports)
MONOCYTOSIS ( 7 FDA reports)
MUCOUS MEMBRANE DISORDER ( 7 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 7 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 7 FDA reports)
MUSCLE SWELLING ( 7 FDA reports)
NAIL DYSTROPHY ( 7 FDA reports)
NAIL INFECTION ( 7 FDA reports)
NEPHROPATHY TOXIC ( 7 FDA reports)
NEURODEGENERATIVE DISORDER ( 7 FDA reports)
NEUROTOXICITY ( 7 FDA reports)
NEUTROPHILIA ( 7 FDA reports)
NIGHT BLINDNESS ( 7 FDA reports)
NODAL RHYTHM ( 7 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 7 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 7 FDA reports)
OESOPHAGEAL DILATATION ( 7 FDA reports)
OESOPHAGEAL FOOD IMPACTION ( 7 FDA reports)
OOPHORECTOMY BILATERAL ( 7 FDA reports)
OPEN ANGLE GLAUCOMA ( 7 FDA reports)
OPERATIVE HAEMORRHAGE ( 7 FDA reports)
OPTIC NEUROPATHY ( 7 FDA reports)
OSTEOPETROSIS ( 7 FDA reports)
PAINFUL RESPIRATION ( 7 FDA reports)
PALATAL OEDEMA ( 7 FDA reports)
PANCREATIC NEOPLASM ( 7 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 7 FDA reports)
PELVIC HAEMATOMA ( 7 FDA reports)
PELVIC MASS ( 7 FDA reports)
PEPTOSTREPTOCOCCUS INFECTION ( 7 FDA reports)
PERIVASCULAR DERMATITIS ( 7 FDA reports)
PH BODY FLUID ABNORMAL ( 7 FDA reports)
PHAEOCHROMOCYTOMA ( 7 FDA reports)
PHYSIOTHERAPY ( 7 FDA reports)
PLASMAPHERESIS ( 7 FDA reports)
PLEURAL ADHESION ( 7 FDA reports)
PNEUMONITIS CHEMICAL ( 7 FDA reports)
PO2 DECREASED ( 7 FDA reports)
POST PROCEDURAL OEDEMA ( 7 FDA reports)
POST PROCEDURAL PAIN ( 7 FDA reports)
POSTICTAL STATE ( 7 FDA reports)
POSTMENOPAUSE ( 7 FDA reports)
PRECEREBRAL ARTERY OCCLUSION ( 7 FDA reports)
PROCEDURAL HAEMORRHAGE ( 7 FDA reports)
PROSTATECTOMY ( 7 FDA reports)
PROSTATISM ( 7 FDA reports)
PSEUDOHYPERKALAEMIA ( 7 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 7 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 7 FDA reports)
PULSE PRESSURE DECREASED ( 7 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 7 FDA reports)
PYOGENIC GRANULOMA ( 7 FDA reports)
RADICULITIS LUMBOSACRAL ( 7 FDA reports)
RECTAL PROLAPSE ( 7 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 7 FDA reports)
RHEUMATIC HEART DISEASE ( 7 FDA reports)
SCAN ABNORMAL ( 7 FDA reports)
SCLERAL DISCOLOURATION ( 7 FDA reports)
SERUM FERRITIN DECREASED ( 7 FDA reports)
SKIN DEPIGMENTATION ( 7 FDA reports)
SKULL FRACTURE ( 7 FDA reports)
SLEEP WALKING ( 7 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 7 FDA reports)
SMALL INTESTINAL STENOSIS ( 7 FDA reports)
SOFT TISSUE NECROSIS ( 7 FDA reports)
SOMATOFORM DISORDER ( 7 FDA reports)
SPINAL DECOMPRESSION ( 7 FDA reports)
SPLEEN DISORDER ( 7 FDA reports)
SWEAT DISCOLOURATION ( 7 FDA reports)
TANDEM GAIT TEST ABNORMAL ( 7 FDA reports)
THROAT LESION ( 7 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 7 FDA reports)
THYROIDECTOMY ( 7 FDA reports)
TOE OPERATION ( 7 FDA reports)
TOXOPLASMOSIS ( 7 FDA reports)
TRACHEAL STENOSIS ( 7 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 7 FDA reports)
URAEMIC ENCEPHALOPATHY ( 7 FDA reports)
VAGINAL LEUKOPLAKIA ( 7 FDA reports)
VAGINAL ODOUR ( 7 FDA reports)
VAGINAL SWELLING ( 7 FDA reports)
VAGINITIS ATROPHIC ( 7 FDA reports)
VARICELLA ( 7 FDA reports)
VENOUS INJURY ( 7 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 7 FDA reports)
VERTEBRAL WEDGING ( 7 FDA reports)
VITAMIN B12 INCREASED ( 7 FDA reports)
VITREOUS DEGENERATION ( 7 FDA reports)
PINGUECULA ( 6 FDA reports)
PIRIFORMIS SYNDROME ( 6 FDA reports)
PNEUMONIA ASPERGILLUS ( 6 FDA reports)
POLYCYSTIC OVARIES ( 6 FDA reports)
POLYCYTHAEMIA ( 6 FDA reports)
POST PROCEDURAL CELLULITIS ( 6 FDA reports)
POST PROCEDURAL PNEUMONIA ( 6 FDA reports)
POST-TRAUMATIC EPILEPSY ( 6 FDA reports)
PREMATURE LABOUR ( 6 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 6 FDA reports)
PULMONARY CAVITATION ( 6 FDA reports)
PULSE ABNORMAL ( 6 FDA reports)
RADIATION ASSOCIATED PAIN ( 6 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 6 FDA reports)
READING DISORDER ( 6 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 6 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 6 FDA reports)
RENAL OSTEODYSTROPHY ( 6 FDA reports)
RESPIRATORY RATE DECREASED ( 6 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 6 FDA reports)
SARCOMA ( 6 FDA reports)
SEBACEOUS GLAND DISORDER ( 6 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 6 FDA reports)
SEPTIC EMBOLUS ( 6 FDA reports)
SINOBRONCHITIS ( 6 FDA reports)
SKIN GRAFT ( 6 FDA reports)
SKIN MASS ( 6 FDA reports)
SKIN TOXICITY ( 6 FDA reports)
SKIN WRINKLING ( 6 FDA reports)
SMALL INTESTINAL RESECTION ( 6 FDA reports)
SPINDLE CELL SARCOMA ( 6 FDA reports)
SPLEEN CONGESTION ( 6 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 6 FDA reports)
STILL'S DISEASE ADULT ONSET ( 6 FDA reports)
STRIDOR ( 6 FDA reports)
SUBRETINAL FIBROSIS ( 6 FDA reports)
TEMPERATURE REGULATION DISORDER ( 6 FDA reports)
TESTICULAR ATROPHY ( 6 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 6 FDA reports)
THYROGLOBULIN INCREASED ( 6 FDA reports)
TONGUE GEOGRAPHIC ( 6 FDA reports)
TORTICOLLIS ( 6 FDA reports)
TOXOPLASMA SEROLOGY POSITIVE ( 6 FDA reports)
TRANSFERRIN DECREASED ( 6 FDA reports)
TRAUMATIC RENAL INJURY ( 6 FDA reports)
UMBILICAL HERNIA REPAIR ( 6 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 6 FDA reports)
URINE LEUKOCYTE ESTERASE ( 6 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 6 FDA reports)
UTERINE DILATION AND CURETTAGE ( 6 FDA reports)
UTEROVAGINAL PROLAPSE ( 6 FDA reports)
VAGINAL CANDIDIASIS ( 6 FDA reports)
VAGINAL LESION ( 6 FDA reports)
VAGOTOMY ( 6 FDA reports)
VENTRICULAR DYSKINESIA ( 6 FDA reports)
WEIGHT LOSS POOR ( 6 FDA reports)
WEST NILE VIRAL INFECTION ( 6 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 6 FDA reports)
ACCELERATED HYPERTENSION ( 6 FDA reports)
ACCIDENTAL DEATH ( 6 FDA reports)
ADENOIDAL DISORDER ( 6 FDA reports)
ADHESIOLYSIS ( 6 FDA reports)
ALCOHOLIC PANCREATITIS ( 6 FDA reports)
ALOPECIA AREATA ( 6 FDA reports)
AMYLOIDOSIS ( 6 FDA reports)
AMYOTROPHY ( 6 FDA reports)
ANOXIA ( 6 FDA reports)
ANTICOAGULANT THERAPY ( 6 FDA reports)
ARTHROPOD STING ( 6 FDA reports)
ASPHYXIA ( 6 FDA reports)
AURICULAR SWELLING ( 6 FDA reports)
BACTERIA STOOL IDENTIFIED ( 6 FDA reports)
BACTERIA TISSUE SPECIMEN IDENTIFIED ( 6 FDA reports)
BENCE JONES PROTEIN URINE PRESENT ( 6 FDA reports)
BENIGN RENAL NEOPLASM ( 6 FDA reports)
BILIARY CYST ( 6 FDA reports)
BILIARY NEOPLASM ( 6 FDA reports)
BLADDER IRRITATION ( 6 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 6 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 6 FDA reports)
BLOOD IRON INCREASED ( 6 FDA reports)
BLOOD OESTROGEN INCREASED ( 6 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 6 FDA reports)
BONE ATROPHY ( 6 FDA reports)
BRACHIAL PLEXOPATHY ( 6 FDA reports)
BRONCHIAL IRRITATION ( 6 FDA reports)
BURNOUT SYNDROME ( 6 FDA reports)
CANDIDURIA ( 6 FDA reports)
CARDIAC STRESS TEST ( 6 FDA reports)
CARDIAC VENTRICULOGRAM LEFT ( 6 FDA reports)
CAROTID ARTERY ATHEROMA ( 6 FDA reports)
CELLULITIS STREPTOCOCCAL ( 6 FDA reports)
CEREBRAL PERFUSION PRESSURE DECREASED ( 6 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 6 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA RECURRENT ( 6 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 6 FDA reports)
COLONIC OBSTRUCTION ( 6 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 6 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 6 FDA reports)
CRYOGLOBULINAEMIA ( 6 FDA reports)
CRYOTHERAPY ( 6 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 6 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 6 FDA reports)
DACRYOCYSTORHINOSTOMY ( 6 FDA reports)
DARK CIRCLES UNDER EYES ( 6 FDA reports)
DEVICE EXPULSION ( 6 FDA reports)
DIAPHRAGMATIC DISORDER ( 6 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 6 FDA reports)
DISORDER OF ORBIT ( 6 FDA reports)
DIVERTICULAR FISTULA ( 6 FDA reports)
DYSENTERY ( 6 FDA reports)
EAR DEFORMITY ACQUIRED ( 6 FDA reports)
ECHOCARDIOGRAM ( 6 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 6 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 6 FDA reports)
ENDOMETRIAL CANCER ( 6 FDA reports)
EPIDERMOID CYST EXCISION ( 6 FDA reports)
EXPOSURE TO CHEMICAL POLLUTION ( 6 FDA reports)
FASCIITIS ( 6 FDA reports)
FAT INTOLERANCE ( 6 FDA reports)
FIBROMUSCULAR DYSPLASIA ( 6 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 6 FDA reports)
FOOD INTERACTION ( 6 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 6 FDA reports)
GAIT DEVIATION ( 6 FDA reports)
GALLBLADDER ENLARGEMENT ( 6 FDA reports)
GASTRIC MUCOSAL LESION ( 6 FDA reports)
GASTRIC NEOPLASM ( 6 FDA reports)
GASTROENTERITIS RADIATION ( 6 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 6 FDA reports)
HAEMATOCRIT ABNORMAL ( 6 FDA reports)
HAEMOGLOBINURIA ( 6 FDA reports)
HAEMOPHILUS BACTERAEMIA ( 6 FDA reports)
HAEMORRHAGIC EROSIVE GASTRITIS ( 6 FDA reports)
HANGOVER ( 6 FDA reports)
HEAT EXHAUSTION ( 6 FDA reports)
HEMIANOPIA ( 6 FDA reports)
HEPATIC CANCER METASTATIC ( 6 FDA reports)
HEPATIC VEIN THROMBOSIS ( 6 FDA reports)
HEPATITIS CHOLESTATIC ( 6 FDA reports)
HOSPICE CARE ( 6 FDA reports)
HOUSE DUST ALLERGY ( 6 FDA reports)
HYPERAEMIA ( 6 FDA reports)
HYPERPARATHYROIDISM PRIMARY ( 6 FDA reports)
HYPOMANIA ( 6 FDA reports)
HYPOVOLAEMIC SHOCK ( 6 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 6 FDA reports)
ILIAC ARTERY THROMBOSIS ( 6 FDA reports)
ILIOTIBIAL BAND SYNDROME ( 6 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 6 FDA reports)
INCREASED BRONCHIAL SECRETION ( 6 FDA reports)
INFECTED SKIN ULCER ( 6 FDA reports)
INFECTIOUS DISEASE CARRIER ( 6 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 6 FDA reports)
KIDNEY FIBROSIS ( 6 FDA reports)
LARYNGEAL DISORDER ( 6 FDA reports)
LEIOMYOMA ( 6 FDA reports)
LEUKOERYTHROBLASTIC ANAEMIA ( 6 FDA reports)
LIQUID PRODUCT PHYSICAL ISSUE ( 6 FDA reports)
LIVER TRANSPLANT ( 6 FDA reports)
LUNG TRANSPLANT ( 6 FDA reports)
MACULAR SCAR ( 6 FDA reports)
MASKED FACIES ( 6 FDA reports)
MEDICAL DEVICE PAIN ( 6 FDA reports)
MEDICAL DIET ( 6 FDA reports)
MELANOSIS COLI ( 6 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 6 FDA reports)
METAMORPHOPSIA ( 6 FDA reports)
METASTASES TO BLADDER ( 6 FDA reports)
METASTASES TO PLEURA ( 6 FDA reports)
MICROANGIOPATHY ( 6 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 6 FDA reports)
MIXED INCONTINENCE ( 6 FDA reports)
MOTION SICKNESS ( 6 FDA reports)
MURDER ( 6 FDA reports)
MURPHY'S SIGN POSITIVE ( 6 FDA reports)
MUSCLE FLAP OPERATION ( 6 FDA reports)
MYCOBACTERIAL INFECTION ( 6 FDA reports)
MYELOFIBROSIS ( 6 FDA reports)
NASAL SEPTUM DISORDER ( 6 FDA reports)
NASAL SEPTUM PERFORATION ( 6 FDA reports)
NECROSIS ISCHAEMIC ( 6 FDA reports)
NEGATIVE THOUGHTS ( 6 FDA reports)
NEPHROCALCINOSIS ( 6 FDA reports)
NEUROPATHIC PAIN ( 6 FDA reports)
NUCHAL RIGIDITY ( 6 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 6 FDA reports)
OESOPHAGEAL INFECTION ( 6 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 6 FDA reports)
ORAL MUCOSAL BLISTERING ( 6 FDA reports)
ORAL SUBMUCOSAL FIBROSIS ( 6 FDA reports)
ORAL TORUS ( 6 FDA reports)
OROANTRAL FISTULA ( 6 FDA reports)
OROPHARYNGEAL BLISTERING ( 6 FDA reports)
OVARIAN MASS ( 6 FDA reports)
PANCREATITIS NECROTISING ( 6 FDA reports)
PANCREATOBILIARY SPHINCTEROTOMY ( 6 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 6 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 6 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 6 FDA reports)
PEMPHIGOID ( 6 FDA reports)
PERINEAL PAIN ( 6 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 6 FDA reports)
PERNICIOUS ANAEMIA ( 6 FDA reports)
PHARYNGEAL ULCERATION ( 6 FDA reports)
ABDOMINAL HERNIA REPAIR ( 5 FDA reports)
ACARODERMATITIS ( 5 FDA reports)
ACOUSTIC NEUROMA ( 5 FDA reports)
ACROCHORDON ( 5 FDA reports)
ADDISON'S DISEASE ( 5 FDA reports)
ADENOVIRUS INFECTION ( 5 FDA reports)
ADRENAL CYST ( 5 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 5 FDA reports)
AMAUROSIS FUGAX ( 5 FDA reports)
AMINO ACID LEVEL INCREASED ( 5 FDA reports)
ANAL ULCER ( 5 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 5 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 5 FDA reports)
AORTIC ANEURYSM REPAIR ( 5 FDA reports)
APPLICATION SITE DERMATITIS ( 5 FDA reports)
ARACHNOID CYST ( 5 FDA reports)
ARTERIAL BYPASS OPERATION ( 5 FDA reports)
ARTERIAL STENOSIS LIMB ( 5 FDA reports)
ARTERIAL THROMBOSIS ( 5 FDA reports)
ARTERIOVENOUS GRAFT SITE INFECTION ( 5 FDA reports)
ARTERITIS ( 5 FDA reports)
ARTHRODESIS ( 5 FDA reports)
ARTHROSCOPY ( 5 FDA reports)
ASTROCYTOMA ( 5 FDA reports)
ATONIC URINARY BLADDER ( 5 FDA reports)
AVULSION FRACTURE ( 5 FDA reports)
AXILLARY PAIN ( 5 FDA reports)
BACTERIURIA ( 5 FDA reports)
BEREAVEMENT REACTION ( 5 FDA reports)
BILOMA ( 5 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 5 FDA reports)
BLAST CELL COUNT INCREASED ( 5 FDA reports)
BLISTER INFECTED ( 5 FDA reports)
BLOOD ALBUMIN INCREASED ( 5 FDA reports)
BLOOD ALCOHOL INCREASED ( 5 FDA reports)
BLOOD CORTISOL DECREASED ( 5 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 5 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 5 FDA reports)
BLOOD SODIUM ABNORMAL ( 5 FDA reports)
BODY FAT DISORDER ( 5 FDA reports)
BONE NEOPLASM ( 5 FDA reports)
BRADYARRHYTHMIA ( 5 FDA reports)
BRAIN COMPRESSION ( 5 FDA reports)
BRAIN HYPOXIA ( 5 FDA reports)
BREAST CANCER STAGE I ( 5 FDA reports)
BREAST CELLULITIS ( 5 FDA reports)
BREAST ENGORGEMENT ( 5 FDA reports)
BREAST MICROCALCIFICATION ( 5 FDA reports)
BREAST NECROSIS ( 5 FDA reports)
BURNS FIRST DEGREE ( 5 FDA reports)
CARDIAC DEATH ( 5 FDA reports)
CARDIAC IMAGING PROCEDURE NORMAL ( 5 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 5 FDA reports)
CARDIOSPASM ( 5 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 5 FDA reports)
CATHETER SITE ERYTHEMA ( 5 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 5 FDA reports)
CEREBELLAR ARTERY THROMBOSIS ( 5 FDA reports)
CEREBELLAR ATROPHY ( 5 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 5 FDA reports)
CEREBRAL HAEMATOMA ( 5 FDA reports)
CHEMICAL POISONING ( 5 FDA reports)
CHILD ABUSE ( 5 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 5 FDA reports)
COELIAC ARTERY STENOSIS ( 5 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 5 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 5 FDA reports)
CORNEAL DEPOSITS ( 5 FDA reports)
CORONARY OSTIAL STENOSIS ( 5 FDA reports)
CYSTITIS HAEMORRHAGIC ( 5 FDA reports)
DEATH OF RELATIVE ( 5 FDA reports)
DENERVATION ATROPHY ( 5 FDA reports)
DERMATITIS HERPETIFORMIS ( 5 FDA reports)
DEVICE INEFFECTIVE ( 5 FDA reports)
DEVICE LEAKAGE ( 5 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 5 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 5 FDA reports)
DYSHIDROSIS ( 5 FDA reports)
ECZEMA NUMMULAR ( 5 FDA reports)
EJACULATION FAILURE ( 5 FDA reports)
ELBOW OPERATION ( 5 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 5 FDA reports)
EMPYEMA DRAINAGE ( 5 FDA reports)
ENDOLYMPHATIC HYDROPS ( 5 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 5 FDA reports)
ENDOPHTHALMITIS ( 5 FDA reports)
ESCHAR ( 5 FDA reports)
EXPOSURE TO TOXIC AGENT ( 5 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 5 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 5 FDA reports)
EXTRAVASATION BLOOD ( 5 FDA reports)
EXTREMITY CONTRACTURE ( 5 FDA reports)
FACIAL SPASM ( 5 FDA reports)
FACTOR V DEFICIENCY ( 5 FDA reports)
FEELING HOT AND COLD ( 5 FDA reports)
FLATBACK SYNDROME ( 5 FDA reports)
FOREIGN BODY REACTION ( 5 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 5 FDA reports)
GASTRIC DILATATION ( 5 FDA reports)
GASTRIC VARICES HAEMORRHAGE ( 5 FDA reports)
GASTROENTERITIS BACTERIAL ( 5 FDA reports)
GASTROENTERITIS HELICOBACTER ( 5 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 5 FDA reports)
GASTROINTESTINAL PERFORATION ( 5 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 5 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 5 FDA reports)
GASTROOESOPHAGEAL SPHINCTER INSUFFICIENCY ( 5 FDA reports)
GILBERT'S SYNDROME ( 5 FDA reports)
GLIOSIS ( 5 FDA reports)
GLOBULINS DECREASED ( 5 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 5 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 5 FDA reports)
HEAD AND NECK CANCER ( 5 FDA reports)
HEAD TITUBATION ( 5 FDA reports)
HEPATITIS VIRAL ( 5 FDA reports)
HEPATOJUGULAR REFLUX ( 5 FDA reports)
HEREDITARY ANGIOEDEMA ( 5 FDA reports)
HIV INFECTION ( 5 FDA reports)
HOMANS' SIGN ( 5 FDA reports)
HOMOCYSTINAEMIA ( 5 FDA reports)
HYPERALBUMINAEMIA ( 5 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 5 FDA reports)
HYPOTHYROIDIC GOITRE ( 5 FDA reports)
IIIRD NERVE DISORDER ( 5 FDA reports)
IMPACTED FRACTURE ( 5 FDA reports)
IMPLANT SITE INFECTION ( 5 FDA reports)
INCISION SITE ERYTHEMA ( 5 FDA reports)
INCISION SITE HAEMORRHAGE ( 5 FDA reports)
INFANTILE SPITTING UP ( 5 FDA reports)
INFERTILITY ( 5 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 5 FDA reports)
INFUSION SITE EXTRAVASATION ( 5 FDA reports)
INGUINAL HERNIA STRANGULATED ( 5 FDA reports)
INHIBITORY DRUG INTERACTION ( 5 FDA reports)
INJECTION SITE ATROPHY ( 5 FDA reports)
INJECTION SITE STINGING ( 5 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 5 FDA reports)
INTERTRIGO ( 5 FDA reports)
INTESTINAL DILATATION ( 5 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 5 FDA reports)
INTRA-UTERINE DEATH ( 5 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 5 FDA reports)
JOINT HYPEREXTENSION ( 5 FDA reports)
JOINT INJECTION ( 5 FDA reports)
JUDGEMENT IMPAIRED ( 5 FDA reports)
KAPOSI'S SARCOMA ( 5 FDA reports)
LABILE BLOOD PRESSURE ( 5 FDA reports)
LENTIGO ( 5 FDA reports)
LENTIGO MALIGNA STAGE UNSPECIFIED ( 5 FDA reports)
LEUKAEMOID REACTION ( 5 FDA reports)
LIBIDO INCREASED ( 5 FDA reports)
LIP INJURY ( 5 FDA reports)
LIPOMATOSIS ( 5 FDA reports)
LOSS OF CONTROL OF LEGS ( 5 FDA reports)
LUNG LOBECTOMY ( 5 FDA reports)
LYMPHOCELE ( 5 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 5 FDA reports)
MASTOCYTOSIS ( 5 FDA reports)
MASTOID DISORDER ( 5 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 5 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 5 FDA reports)
MEDIASTINAL DISORDER ( 5 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 5 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 5 FDA reports)
MENOMETRORRHAGIA ( 5 FDA reports)
METAPNEUMOVIRUS INFECTION ( 5 FDA reports)
METASTASES TO PERITONEUM ( 5 FDA reports)
MICROALBUMINURIA ( 5 FDA reports)
MILIA ( 5 FDA reports)
MOLLUSCUM CONTAGIOSUM ( 5 FDA reports)
MONONEUROPATHY MULTIPLEX ( 5 FDA reports)
MORBID THOUGHTS ( 5 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 5 FDA reports)
MUCOSAL EROSION ( 5 FDA reports)
MULTI-ORGAN DISORDER ( 5 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 5 FDA reports)
MYELOID LEUKAEMIA ( 5 FDA reports)
MYOPERICARDITIS ( 5 FDA reports)
NECK DEFORMITY ( 5 FDA reports)
NEPHRITIS ( 5 FDA reports)
NERVE ROOT INJURY LUMBAR ( 5 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 5 FDA reports)
NIPPLE PAIN ( 5 FDA reports)
NITRITE URINE PRESENT ( 5 FDA reports)
NOSOCOMIAL INFECTION ( 5 FDA reports)
OBSESSIVE THOUGHTS ( 5 FDA reports)
OBSTRUCTIVE UROPATHY ( 5 FDA reports)
OESOPHAGEAL PERFORATION ( 5 FDA reports)
OESOPHAGOSCOPY ABNORMAL ( 5 FDA reports)
ONCOLOGIC COMPLICATION ( 5 FDA reports)
OPEN FRACTURE ( 5 FDA reports)
OPTIC NERVE INJURY ( 5 FDA reports)
OSTEOPOROTIC FRACTURE ( 5 FDA reports)
OVARIAN EPITHELIAL CANCER ( 5 FDA reports)
PANCREAS INFECTION ( 5 FDA reports)
PANCREAS TRANSPLANT ( 5 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 5 FDA reports)
PARANASAL CYST ( 5 FDA reports)
PARANOID PERSONALITY DISORDER ( 5 FDA reports)
PAROXYSMAL ARRHYTHMIA ( 5 FDA reports)
PCO2 INCREASED ( 5 FDA reports)
PENILE SIZE REDUCED ( 5 FDA reports)
PENILE SWELLING ( 5 FDA reports)
PERINEURIAL CYST ( 5 FDA reports)
PERITONEAL LESION ( 5 FDA reports)
PHOTOREFRACTIVE KERATECTOMY ( 5 FDA reports)
POLYMENORRHOEA ( 5 FDA reports)
POLYMYOSITIS ( 5 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 5 FDA reports)
POST PROCEDURAL BILE LEAK ( 5 FDA reports)
PRINZMETAL ANGINA ( 5 FDA reports)
PROCEDURAL SITE REACTION ( 5 FDA reports)
PRODUCT TASTE ABNORMAL ( 5 FDA reports)
PROSTATE CANCER RECURRENT ( 5 FDA reports)
PROTEUS INFECTION ( 5 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 5 FDA reports)
PROTHROMBIN TIME SHORTENED ( 5 FDA reports)
PROTRUSION TONGUE ( 5 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 5 FDA reports)
PULMONARY MYCOSIS ( 5 FDA reports)
PULMONARY VALVE STENOSIS ( 5 FDA reports)
PYLORIC STENOSIS ( 5 FDA reports)
PYODERMA GANGRENOSUM ( 5 FDA reports)
RADIATION SKIN INJURY ( 5 FDA reports)
REBOUND EFFECT ( 5 FDA reports)
RECTAL ULCER ( 5 FDA reports)
REFRACTORY ANAEMIA ( 5 FDA reports)
RESIDUAL URINE ( 5 FDA reports)
RESPIRATORY TRACT IRRITATION ( 5 FDA reports)
RETICULOCYTE COUNT DECREASED ( 5 FDA reports)
RETINAL DEGENERATION ( 5 FDA reports)
RETROPERITONEAL HAEMATOMA ( 5 FDA reports)
RHEUMATOID FACTOR INCREASED ( 5 FDA reports)
RHINOVIRUS INFECTION ( 5 FDA reports)
SCROTAL SWELLING ( 5 FDA reports)
SHIFT TO THE LEFT ( 5 FDA reports)
SHUNT MALFUNCTION ( 5 FDA reports)
SINUSITIS BACTERIAL ( 5 FDA reports)
STAPHYLOCOCCAL PHARYNGITIS ( 5 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 5 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 5 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 5 FDA reports)
SUPRAPUBIC PAIN ( 5 FDA reports)
SYRINGOMYELIA ( 5 FDA reports)
SYSTEMIC CANDIDA ( 5 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 5 FDA reports)
TAENIASIS ( 5 FDA reports)
TETANY ( 5 FDA reports)
THROMBOEMBOLIC STROKE ( 5 FDA reports)
THROMBOTIC STROKE ( 5 FDA reports)
TONGUE BLISTERING ( 5 FDA reports)
TONGUE PARALYSIS ( 5 FDA reports)
TOOTH ANKYLOSIS ( 5 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 5 FDA reports)
TRANSPLANT ( 5 FDA reports)
TRICUSPID VALVE SCLEROSIS ( 5 FDA reports)
TUBERCULOSIS SKIN TEST POSITIVE ( 5 FDA reports)
TUMOUR EXCISION ( 5 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 5 FDA reports)
URETERIC DILATATION ( 5 FDA reports)
URETHRAL STRICTURE ( 5 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 5 FDA reports)
VAGINAL CYST ( 5 FDA reports)
VAGINAL DISORDER ( 5 FDA reports)
VAGINAL MYCOSIS ( 5 FDA reports)
VAGUS NERVE DISORDER ( 5 FDA reports)
VASCULAR INJURY ( 5 FDA reports)
VASODILATATION ( 5 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 5 FDA reports)
VENOUS STASIS ( 5 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 5 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 5 FDA reports)
VESICAL FISTULA ( 5 FDA reports)
VON WILLEBRAND'S FACTOR MULTIMERS ABNORMAL ( 5 FDA reports)
VULVA CYST ( 5 FDA reports)
VULVAL ABSCESS ( 5 FDA reports)
VULVAL LEUKOPLAKIA ( 5 FDA reports)
WEANING FAILURE ( 5 FDA reports)
WEIGHT ABNORMAL ( 5 FDA reports)
WOUND HAEMORRHAGE ( 5 FDA reports)
XERODERMA ( 5 FDA reports)
PHOBIA ( 4 FDA reports)
PHONOPHOBIA ( 4 FDA reports)
PILOERECTION ( 4 FDA reports)
PILONIDAL CYST ( 4 FDA reports)
PITUITARY TUMOUR ( 4 FDA reports)
PITYRIASIS ROSEA ( 4 FDA reports)
PNEUMATOSIS ( 4 FDA reports)
PNEUMOCOCCAL SEPSIS ( 4 FDA reports)
PNEUMOMEDIASTINUM ( 4 FDA reports)
PNEUMONIA LEGIONELLA ( 4 FDA reports)
PNEUMOPERITONEUM ( 4 FDA reports)
POLYCHONDRITIS ( 4 FDA reports)
POOR VENOUS ACCESS ( 4 FDA reports)
POST PROCEDURAL DIARRHOEA ( 4 FDA reports)
POST PROCEDURAL DRAINAGE ( 4 FDA reports)
POST PROCEDURAL SEPSIS ( 4 FDA reports)
POST PROCEDURAL SWELLING ( 4 FDA reports)
POST STREPTOCOCCAL GLOMERULONEPHRITIS ( 4 FDA reports)
POST-TRAUMATIC PAIN ( 4 FDA reports)
POSTOPERATIVE RESPIRATORY DISTRESS ( 4 FDA reports)
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME ( 4 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 4 FDA reports)
PREMATURE MENOPAUSE ( 4 FDA reports)
PRESSURE OF SPEECH ( 4 FDA reports)
PRODUCT FORMULATION ISSUE ( 4 FDA reports)
PRODUCT ODOUR ABNORMAL ( 4 FDA reports)
PSYCHOTIC DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 4 FDA reports)
RADIAL NERVE PALSY ( 4 FDA reports)
RADIATION MUCOSITIS ( 4 FDA reports)
RADIATION PNEUMONITIS ( 4 FDA reports)
RECTAL ADENOMA ( 4 FDA reports)
RECTAL CANCER METASTATIC ( 4 FDA reports)
RECTAL DISCHARGE ( 4 FDA reports)
RECTAL PROLAPSE REPAIR ( 4 FDA reports)
RECURRING SKIN BOILS ( 4 FDA reports)
REGURGITATION OF FOOD ( 4 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS TEST POSITIVE ( 4 FDA reports)
RETINAL NEOPLASM ( 4 FDA reports)
SALMONELLA BACTERAEMIA ( 4 FDA reports)
SENSATION OF BLOOD FLOW ( 4 FDA reports)
SERUM SEROTONIN DECREASED ( 4 FDA reports)
SHORT-BOWEL SYNDROME ( 4 FDA reports)
SHOULDER ARTHROPLASTY ( 4 FDA reports)
SOFT TISSUE INJURY ( 4 FDA reports)
SOFT TISSUE NEOPLASM ( 4 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 4 FDA reports)
SPLENIC NEOPLASM MALIGNANCY UNSPECIFIED ( 4 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 4 FDA reports)
STEREOTYPY ( 4 FDA reports)
STEROID WITHDRAWAL SYNDROME ( 4 FDA reports)
STICKY PLATELET SYNDROME ( 4 FDA reports)
STRESS ULCER ( 4 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 4 FDA reports)
SUTURE RUPTURE ( 4 FDA reports)
SWEAT GLAND DISORDER ( 4 FDA reports)
T-CELL TYPE ACUTE LEUKAEMIA ( 4 FDA reports)
TALIPES ( 4 FDA reports)
TERMINAL INSOMNIA ( 4 FDA reports)
THALAMIC INFARCTION ( 4 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO DECREASED ( 4 FDA reports)
TOXIC NEUROPATHY ( 4 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 4 FDA reports)
TRAUMATIC LUNG INJURY ( 4 FDA reports)
TRICHOMONIASIS ( 4 FDA reports)
TUMOUR HAEMORRHAGE ( 4 FDA reports)
TUMOUR INVASION ( 4 FDA reports)
TUMOUR PAIN ( 4 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 4 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 4 FDA reports)
UMBILICAL CORD ABNORMALITY ( 4 FDA reports)
URETERAL DISORDER ( 4 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 4 FDA reports)
VACCINATION COMPLICATION ( 4 FDA reports)
VAGINAL CONTRACEPTIVE DEVICE EXPELLED ( 4 FDA reports)
VAGINITIS ( 4 FDA reports)
VARICELLA VIRUS TEST POSITIVE ( 4 FDA reports)
VASCULAR RUPTURE ( 4 FDA reports)
VENA CAVA INJURY ( 4 FDA reports)
VITILIGO ( 4 FDA reports)
VULVOVAGINAL ERYTHEMA ( 4 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 4 FDA reports)
WERNICKE'S ENCEPHALOPATHY ( 4 FDA reports)
WHITE BLOOD CELL DISORDER ( 4 FDA reports)
WOUND ABSCESS ( 4 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 4 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 4 FDA reports)
ABSCESS SOFT TISSUE ( 4 FDA reports)
ACCOMMODATION DISORDER ( 4 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 4 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 4 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 4 FDA reports)
ALLERGY TO ANIMAL ( 4 FDA reports)
ANAL HAEMORRHAGE ( 4 FDA reports)
ANGIOGRAM ABNORMAL ( 4 FDA reports)
ANKYLOGLOSSIA CONGENITAL ( 4 FDA reports)
ANTHRAX ( 4 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 4 FDA reports)
AORTIC BRUIT ( 4 FDA reports)
AORTIC EMBOLUS ( 4 FDA reports)
APHERESIS ( 4 FDA reports)
APPLICATION SITE SCAR ( 4 FDA reports)
APPLICATION SITE SWELLING ( 4 FDA reports)
ARTERIAL STENT INSERTION ( 4 FDA reports)
BACTERIA URINE IDENTIFIED ( 4 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 4 FDA reports)
BARTHOLIN'S CYST REMOVAL ( 4 FDA reports)
BENCE JONES PROTEINURIA ( 4 FDA reports)
BENIGN COLONIC POLYP ( 4 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 4 FDA reports)
BICUSPID AORTIC VALVE ( 4 FDA reports)
BILE DUCT STENT INSERTION ( 4 FDA reports)
BLADDER DILATATION ( 4 FDA reports)
BLADDER OPERATION ( 4 FDA reports)
BLADDER PERFORATION ( 4 FDA reports)
BLIGHTED OVUM ( 4 FDA reports)
BLOOD CORTISOL INCREASED ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 4 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 4 FDA reports)
BLOOD FOLATE DECREASED ( 4 FDA reports)
BLOOD IRON ABNORMAL ( 4 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 4 FDA reports)
BLOOD SMEAR TEST ABNORMAL ( 4 FDA reports)
BLOOD UREA ABNORMAL ( 4 FDA reports)
BLOODY DISCHARGE ( 4 FDA reports)
BONE CALLUS EXCESSIVE ( 4 FDA reports)
BONE DENSITY INCREASED ( 4 FDA reports)
BREAST RECONSTRUCTION ( 4 FDA reports)
BRONCHIAL OBSTRUCTION ( 4 FDA reports)
BURSA DISORDER ( 4 FDA reports)
BUTTERFLY RASH ( 4 FDA reports)
CALCIPHYLAXIS ( 4 FDA reports)
CAPILLARY DISORDER ( 4 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 4 FDA reports)
CARDIAC FAILURE HIGH OUTPUT ( 4 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 4 FDA reports)
CATHETER SITE PAIN ( 4 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 4 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 4 FDA reports)
CENTRAL NERVOUS SYSTEM NECROSIS ( 4 FDA reports)
CEREBRAL CYST ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT PROPHYLAXIS ( 4 FDA reports)
CHEST WALL CYST ( 4 FDA reports)
CHONDROPLASTY ( 4 FDA reports)
CHORIORETINOPATHY ( 4 FDA reports)
CHROMATOPSIA ( 4 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 4 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 4 FDA reports)
CHYLOTHORAX ( 4 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 4 FDA reports)
CLEFT PALATE ( 4 FDA reports)
COLON CANCER METASTATIC ( 4 FDA reports)
COLONIC FISTULA ( 4 FDA reports)
COLOUR BLINDNESS ( 4 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 4 FDA reports)
CONJUNCTIVAL PRIMARY ACQUIRED MELANOSIS ( 4 FDA reports)
CONNECTIVE TISSUE INFLAMMATION ( 4 FDA reports)
CORONARY ARTERY EMBOLISM ( 4 FDA reports)
CORONARY ARTERY SURGERY ( 4 FDA reports)
CORRECTIVE LENS USER ( 4 FDA reports)
COW'S MILK INTOLERANCE ( 4 FDA reports)
CRANIAL NEUROPATHY ( 4 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 4 FDA reports)
CREST SYNDROME ( 4 FDA reports)
CYANOPSIA ( 4 FDA reports)
CYSTITIS RADIATION ( 4 FDA reports)
DAYDREAMING ( 4 FDA reports)
DELUSIONAL PERCEPTION ( 4 FDA reports)
DEPRESSION POSTOPERATIVE ( 4 FDA reports)
DIABETES INSIPIDUS ( 4 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 4 FDA reports)
DIABETIC FOOT INFECTION ( 4 FDA reports)
DIABETIC VASCULAR DISORDER ( 4 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA RECURRENT ( 4 FDA reports)
DISEASE COMPLICATION ( 4 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 4 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 4 FDA reports)
DIZZINESS EXERTIONAL ( 4 FDA reports)
DRUG EFFECT PROLONGED ( 4 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 4 FDA reports)
DRUG LEVEL CHANGED ( 4 FDA reports)
DRUG LEVEL FLUCTUATING ( 4 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 4 FDA reports)
DRUG RESISTANCE ( 4 FDA reports)
DRUG TOLERANCE INCREASED ( 4 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 4 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 4 FDA reports)
DRY GANGRENE ( 4 FDA reports)
EJACULATION DISORDER ( 4 FDA reports)
ELECTRIC SHOCK ( 4 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 4 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 4 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 4 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 4 FDA reports)
ENDOCRINE DISORDER ( 4 FDA reports)
ENDOMETRIAL DISORDER ( 4 FDA reports)
ENDOSCOPY GASTROINTESTINAL ABNORMAL ( 4 FDA reports)
EXTRADURAL ABSCESS ( 4 FDA reports)
EYE PROSTHESIS INSERTION ( 4 FDA reports)
EYE ROLLING ( 4 FDA reports)
FACIAL NERVE DISORDER ( 4 FDA reports)
FACIAL WASTING ( 4 FDA reports)
FEAR OF FALLING ( 4 FDA reports)
FLASHBACK ( 4 FDA reports)
FOAMING AT MOUTH ( 4 FDA reports)
FUNGUS SPUTUM TEST POSITIVE ( 4 FDA reports)
GALLOP RHYTHM PRESENT ( 4 FDA reports)
GASTRIC CYST ( 4 FDA reports)
GASTROINTESTINAL EROSION ( 4 FDA reports)
GASTROOESOPHAGITIS ( 4 FDA reports)
GAZE PALSY ( 4 FDA reports)
GLIOMA ( 4 FDA reports)
HAEMATOTOXICITY ( 4 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 4 FDA reports)
HALLUCINATION, TACTILE ( 4 FDA reports)
HEART BLOCK CONGENITAL ( 4 FDA reports)
HEART TRANSPLANT ( 4 FDA reports)
HEART VALVE REPLACEMENT ( 4 FDA reports)
HEPATIC ARTERY STENOSIS ( 4 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 4 FDA reports)
HEPATIC INFARCTION ( 4 FDA reports)
HEPATIC INFECTION ( 4 FDA reports)
HEPATIC TRAUMA ( 4 FDA reports)
HEPATOCELLULAR INJURY ( 4 FDA reports)
HEPATORENAL FAILURE ( 4 FDA reports)
HEPATORENAL SYNDROME ( 4 FDA reports)
HERPES ZOSTER DISSEMINATED ( 4 FDA reports)
HIGH RISK PREGNANCY ( 4 FDA reports)
HYPERCORTICOIDISM ( 4 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 4 FDA reports)
HYPERPROTEINAEMIA ( 4 FDA reports)
HYPERTRANSAMINASAEMIA ( 4 FDA reports)
HYPOPNOEA ( 4 FDA reports)
IDIOPATHIC URTICARIA ( 4 FDA reports)
IMPLANT SITE DISCHARGE ( 4 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 4 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 4 FDA reports)
INCORRECT PRODUCT STORAGE ( 4 FDA reports)
INFANTILE APNOEIC ATTACK ( 4 FDA reports)
INFECTIOUS PERITONITIS ( 4 FDA reports)
INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS ( 4 FDA reports)
INFUSION SITE OEDEMA ( 4 FDA reports)
INFUSION SITE REACTION ( 4 FDA reports)
INHALATION THERAPY ( 4 FDA reports)
INJECTION SITE NERVE DAMAGE ( 4 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 4 FDA reports)
INSULIN RESISTANCE ( 4 FDA reports)
INSULIN RESISTANT DIABETES ( 4 FDA reports)
INTENTIONAL MISUSE ( 4 FDA reports)
INTESTINAL INFARCTION ( 4 FDA reports)
INTUBATION ( 4 FDA reports)
JOINT DESTRUCTION ( 4 FDA reports)
JUVENILE ARTHRITIS ( 4 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 4 FDA reports)
LACRIMATION DECREASED ( 4 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 4 FDA reports)
LEUKAEMIA RECURRENT ( 4 FDA reports)
LEUKOARAIOSIS ( 4 FDA reports)
LIGAMENT DISORDER ( 4 FDA reports)
LIP EXFOLIATION ( 4 FDA reports)
LUNG INJURY ( 4 FDA reports)
LYMPH NODES SCAN ABNORMAL ( 4 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 4 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 4 FDA reports)
MACULAR HOLE ( 4 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 4 FDA reports)
MARITAL PROBLEM ( 4 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 4 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 4 FDA reports)
METASTASES TO HEART ( 4 FDA reports)
METASTASES TO SOFT TISSUE ( 4 FDA reports)
METASTATIC PAIN ( 4 FDA reports)
MIDDLE EAR DISORDER ( 4 FDA reports)
MIGRAINE WITHOUT AURA ( 4 FDA reports)
MOLE EXCISION ( 4 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 4 FDA reports)
MUCOSAL DISCOLOURATION ( 4 FDA reports)
MYELOMALACIA ( 4 FDA reports)
MYOCARDITIS ( 4 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 4 FDA reports)
NAIL GROWTH ABNORMAL ( 4 FDA reports)
NAIL HYPERTROPHY ( 4 FDA reports)
NARCOTIC INTOXICATION ( 4 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 4 FDA reports)
NEUROGENIC BOWEL ( 4 FDA reports)
NEUTROPENIC INFECTION ( 4 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 4 FDA reports)
NOCARDIOSIS ( 4 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 4 FDA reports)
NOREPINEPHRINE INCREASED ( 4 FDA reports)
NORMAL NEWBORN ( 4 FDA reports)
OCCIPITAL NEURALGIA ( 4 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 4 FDA reports)
OESOPHAGEAL DILATION PROCEDURE ( 4 FDA reports)
OESOPHAGEAL IRRITATION ( 4 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 4 FDA reports)
OLIGOMENORRHOEA ( 4 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 4 FDA reports)
ORAL PAPILLOMA ( 4 FDA reports)
ORTHOSTATIC INTOLERANCE ( 4 FDA reports)
OSTEOMYELITIS ACUTE ( 4 FDA reports)
PACEMAKER COMPLICATION ( 4 FDA reports)
PAINFUL DEFAECATION ( 4 FDA reports)
PANCREAS LIPOMATOSIS ( 4 FDA reports)
PARACENTESIS ABDOMEN ( 4 FDA reports)
PARATHYROIDECTOMY ( 4 FDA reports)
PEPTIC ULCER PERFORATION ( 4 FDA reports)
PERIANAL ABSCESS ( 4 FDA reports)
PERICARDIAL DRAINAGE ( 4 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 4 FDA reports)
PERONEAL NERVE INJURY ( 4 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 4 FDA reports)
5Q MINUS SYNDROME ( 3 FDA reports)
ABDOMINAL INFECTION ( 3 FDA reports)
ABDOMINAL INJURY ( 3 FDA reports)
ABDOMINAL SEPSIS ( 3 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 3 FDA reports)
ABDOMINAL WALL NEOPLASM ( 3 FDA reports)
ACCIDENT AT HOME ( 3 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 3 FDA reports)
ACTINIC ELASTOSIS ( 3 FDA reports)
ACUTE ABDOMEN ( 3 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 3 FDA reports)
ADENOCARCINOMA PANCREAS ( 3 FDA reports)
ADNEXA UTERI PAIN ( 3 FDA reports)
AGE INDETERMINATE MYOCARDIAL INFARCTION ( 3 FDA reports)
AGONAL RHYTHM ( 3 FDA reports)
AIR EMBOLISM ( 3 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 3 FDA reports)
ALLERGIC PHARYNGITIS ( 3 FDA reports)
ALOPECIA EFFLUVIUM ( 3 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 3 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 3 FDA reports)
ANAL ABSCESS ( 3 FDA reports)
ANAL CANCER ( 3 FDA reports)
ANAL DISCOMFORT ( 3 FDA reports)
ANAL PRURITUS ( 3 FDA reports)
ANAL SPHINCTEROTOMY ( 3 FDA reports)
ANASTOMOTIC COMPLICATION ( 3 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 3 FDA reports)
ANION GAP INCREASED ( 3 FDA reports)
ANOMALOUS PULMONARY VENOUS CONNECTION ( 3 FDA reports)
ANTI-ERYTHROCYTE ANTIBODY POSITIVE ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
AORTIC DISSECTION ( 3 FDA reports)
AORTIC THROMBOSIS ( 3 FDA reports)
APOPTOSIS ( 3 FDA reports)
APPLICATION SITE BLEEDING ( 3 FDA reports)
APPLICATION SITE ULCER ( 3 FDA reports)
APPLICATION SITE URTICARIA ( 3 FDA reports)
ARACHNOIDITIS ( 3 FDA reports)
ARTERIAL BRUIT ( 3 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 3 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 3 FDA reports)
ASTERIXIS ( 3 FDA reports)
AUTISM ( 3 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 3 FDA reports)
BACTERIA URINE ( 3 FDA reports)
BACTERIAL TEST ( 3 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 3 FDA reports)
BENIGN LUNG NEOPLASM ( 3 FDA reports)
BENIGN NEOPLASM OF SPINAL CORD ( 3 FDA reports)
BIFASCICULAR BLOCK ( 3 FDA reports)
BILE OUTPUT ABNORMAL ( 3 FDA reports)
BILIARY FIBROSIS ( 3 FDA reports)
BIOPSY BREAST ( 3 FDA reports)
BIPOLAR II DISORDER ( 3 FDA reports)
BLADDER DISTENSION ( 3 FDA reports)
BLADDER NEOPLASM SURGERY ( 3 FDA reports)
BLADDER REPAIR ( 3 FDA reports)
BLEEDING TIME PROLONGED ( 3 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 3 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 3 FDA reports)
BLOOD CALCIUM ABNORMAL ( 3 FDA reports)
BLOOD CREATINE ABNORMAL ( 3 FDA reports)
BLOOD GASTRIN INCREASED ( 3 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 3 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 3 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 3 FDA reports)
BONE LESION EXCISION ( 3 FDA reports)
BONE MARROW DISORDER ( 3 FDA reports)
BONE MARROW TOXICITY ( 3 FDA reports)
BONE SARCOMA ( 3 FDA reports)
BORDERLINE GLAUCOMA ( 3 FDA reports)
BRAIN ABSCESS ( 3 FDA reports)
BRAIN OPERATION ( 3 FDA reports)
BREAST OPERATION ( 3 FDA reports)
BREAST PROSTHESIS USER ( 3 FDA reports)
BRONCHIAL WALL THICKENING ( 3 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 3 FDA reports)
BURNS THIRD DEGREE ( 3 FDA reports)
CAPILLARY LEAK SYNDROME ( 3 FDA reports)
CARDIAC FUNCTION DISTURBANCE POSTOPERATIVE ( 3 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 3 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 3 FDA reports)
CAROTID ARTERY THROMBOSIS ( 3 FDA reports)
CATHETER SITE CELLULITIS ( 3 FDA reports)
CEREBELLAR ATAXIA ( 3 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 3 FDA reports)
CEREBRAL CALCIFICATION ( 3 FDA reports)
CEREBRAL MICROANGIOPATHY ( 3 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 3 FDA reports)
CERVICAL NEURITIS ( 3 FDA reports)
CERVICAL POLYP ( 3 FDA reports)
CHOLESTATIC LIVER INJURY ( 3 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 3 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 3 FDA reports)
CLONIC CONVULSION ( 3 FDA reports)
CLONUS ( 3 FDA reports)
COAGULATION TIME PROLONGED ( 3 FDA reports)
COCCIDIOIDOMYCOSIS ( 3 FDA reports)
COLON GANGRENE ( 3 FDA reports)
COLONIC HAEMORRHAGE ( 3 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 3 FDA reports)
CORNEAL DISORDER ( 3 FDA reports)
CORNEAL REFLEX DECREASED ( 3 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 3 FDA reports)
CORONARY ARTERY REOCCLUSION ( 3 FDA reports)
CYSTIC FIBROSIS ( 3 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 3 FDA reports)
DEAFNESS TRANSITORY ( 3 FDA reports)
DENTAL NECROSIS ( 3 FDA reports)
DEVICE ADHESION ISSUE ( 3 FDA reports)
DEVICE MISUSE ( 3 FDA reports)
DIARRHOEA INFECTIOUS ( 3 FDA reports)
DIET REFUSAL ( 3 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 3 FDA reports)
DIVORCED ( 3 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 3 FDA reports)
DRUG DELIVERY DEVICE IMPLANTATION ( 3 FDA reports)
DRUG EFFECT DELAYED ( 3 FDA reports)
DRUG EFFECT INCREASED ( 3 FDA reports)
DUCTUS ARTERIOSUS STENOSIS FOETAL ( 3 FDA reports)
DUODENAL PERFORATION ( 3 FDA reports)
DYSMORPHISM ( 3 FDA reports)
EMPTY SELLA SYNDROME ( 3 FDA reports)
ENDOCARDITIS CANDIDA ( 3 FDA reports)
ENDOMETRIAL ATROPHY ( 3 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 3 FDA reports)
ENTEROCOCCAL SEPSIS ( 3 FDA reports)
EOSINOPHILIC PNEUMONIA ( 3 FDA reports)
ERYSIPELAS ( 3 FDA reports)
ERYTHEMA INFECTIOSUM ( 3 FDA reports)
EUSTACHIAN TUBE DISORDER ( 3 FDA reports)
EUSTACHIAN TUBE OBSTRUCTION ( 3 FDA reports)
EX-TOBACCO USER ( 3 FDA reports)
EYE INFECTION FUNGAL ( 3 FDA reports)
EYE NAEVUS ( 3 FDA reports)
EYE OPERATION COMPLICATION ( 3 FDA reports)
EYE REDNESS ( 3 FDA reports)
EYELIDS PRURITUS ( 3 FDA reports)
EYES SUNKEN ( 3 FDA reports)
FATTY LIVER ALCOHOLIC ( 3 FDA reports)
FEAR OF DISEASE ( 3 FDA reports)
FEEDING DISORDER NEONATAL ( 3 FDA reports)
FEELING OF RELAXATION ( 3 FDA reports)
FOETAL CARDIAC DISORDER ( 3 FDA reports)
FOOT AMPUTATION ( 3 FDA reports)
FUNGAL PARONYCHIA ( 3 FDA reports)
GAMBLING ( 3 FDA reports)
GASTRIC HYPOMOTILITY ( 3 FDA reports)
GASTRIC MUCOSA ERYTHEMA ( 3 FDA reports)
GASTRIC ULCER HELICOBACTER ( 3 FDA reports)
GASTROENTERITIS EOSINOPHILIC ( 3 FDA reports)
GASTROENTERITIS SALMONELLA ( 3 FDA reports)
GASTROINTESTINAL FISTULA ( 3 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 3 FDA reports)
GASTROINTESTINAL TRACT MUCOSAL DISCOLOURATION ( 3 FDA reports)
GENITAL BURNING SENSATION ( 3 FDA reports)
GENITAL RASH ( 3 FDA reports)
GLIOBLASTOMA ( 3 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 3 FDA reports)
GREENSTICK FRACTURE ( 3 FDA reports)
HAEMOCHROMATOSIS ( 3 FDA reports)
HAEMORRHAGE SUBEPIDERMAL ( 3 FDA reports)
HAEMOSIDEROSIS ( 3 FDA reports)
HEPATIC HAEMORRHAGE ( 3 FDA reports)
HEPATOBILIARY DISEASE ( 3 FDA reports)
HERNIA PAIN ( 3 FDA reports)
HETEROPHORIA ( 3 FDA reports)
HYALOSIS ASTEROID ( 3 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 3 FDA reports)
HYPERGLOBULINAEMIA ( 3 FDA reports)
HYPERINSULINAEMIA ( 3 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 3 FDA reports)
HYPERTENSIVE EMERGENCY ( 3 FDA reports)
HYPERTHERMIA ( 3 FDA reports)
HYPOCHONDRIASIS ( 3 FDA reports)
HYPOGEUSIA ( 3 FDA reports)
HYPOGLYCAEMIC COMA ( 3 FDA reports)
HYPOGONADISM ( 3 FDA reports)
HYPOLIPIDAEMIA ( 3 FDA reports)
HYPOSMIA ( 3 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 3 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 3 FDA reports)
IMPAIRED FASTING GLUCOSE ( 3 FDA reports)
IMPLANT SITE REACTION ( 3 FDA reports)
INAPPROPRIATE AFFECT ( 3 FDA reports)
INCISION SITE BLISTER ( 3 FDA reports)
INDIFFERENCE ( 3 FDA reports)
INJECTION SITE ANAESTHESIA ( 3 FDA reports)
INJECTION SITE BURNING ( 3 FDA reports)
INJECTION SITE DERMATITIS ( 3 FDA reports)
INJECTION SITE DISCHARGE ( 3 FDA reports)
INJECTION SITE INFLAMMATION ( 3 FDA reports)
INJECTION SITE PUSTULE ( 3 FDA reports)
INJECTION SITE ULCER ( 3 FDA reports)
INTERNAL HERNIA ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 3 FDA reports)
INTERTRIGO CANDIDA ( 3 FDA reports)
INTRACRANIAL HYPOTENSION ( 3 FDA reports)
INTRACRANIAL TUMOUR HAEMORRHAGE ( 3 FDA reports)
IRIDOCYCLITIS ( 3 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 3 FDA reports)
ISCHAEMIC ULCER ( 3 FDA reports)
JAW CYST ( 3 FDA reports)
JEJUNAL STENOSIS ( 3 FDA reports)
KELOID SCAR ( 3 FDA reports)
KIDNEY ENLARGEMENT ( 3 FDA reports)
KLEBSIELLA TEST POSITIVE ( 3 FDA reports)
LABORATORY TEST INTERFERENCE ( 3 FDA reports)
LARGE INTESTINE FIBROMA ( 3 FDA reports)
LARYNGECTOMY ( 3 FDA reports)
LEGAL PROBLEM ( 3 FDA reports)
LIP NEOPLASM ( 3 FDA reports)
LIPOHYPERTROPHY ( 3 FDA reports)
LIPOPROTEIN (A) INCREASED ( 3 FDA reports)
LIPOSARCOMA ( 3 FDA reports)
LIVER SCAN ABNORMAL ( 3 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 3 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 3 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 3 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 3 FDA reports)
MEDIASTINAL MASS ( 3 FDA reports)
MENINGISM ( 3 FDA reports)
MENISCUS OPERATION ( 3 FDA reports)
MENSTRUATION DELAYED ( 3 FDA reports)
METASTASES TO STOMACH ( 3 FDA reports)
MITRAL VALVE REPLACEMENT ( 3 FDA reports)
MONOCYTE COUNT ABNORMAL ( 3 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 3 FDA reports)
MUCOEPIDERMOID CARCINOMA ( 3 FDA reports)
MULTIPLE LENTIGINES SYNDROME ( 3 FDA reports)
MUSCLE MASS ( 3 FDA reports)
MYCOBACTERIUM TEST POSITIVE ( 3 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 3 FDA reports)
MYCOPLASMA INFECTION ( 3 FDA reports)
MYCOPLASMA SEROLOGY POSITIVE ( 3 FDA reports)
MYOCLONIC EPILEPSY ( 3 FDA reports)
MYODESOPSIA ( 3 FDA reports)
NASAL POLYPECTOMY ( 3 FDA reports)
NEEDLE ISSUE ( 3 FDA reports)
NEOPLASM PROSTATE ( 3 FDA reports)
NEURILEMMOMA ( 3 FDA reports)
OBTURATOR HERNIA ( 3 FDA reports)
OEDEMA MUCOSAL ( 3 FDA reports)
OESOPHAGEAL INJURY ( 3 FDA reports)
OESOPHAGEAL OEDEMA ( 3 FDA reports)
ORGANISING PNEUMONIA ( 3 FDA reports)
ORTHOPEDIC PROCEDURE ( 3 FDA reports)
OVARIAN CANCER RECURRENT ( 3 FDA reports)
OVERGROWTH BACTERIAL ( 3 FDA reports)
OVERLAP SYNDROME ( 3 FDA reports)
PALMAR ERYTHEMA ( 3 FDA reports)
PANCREATIC ENZYMES INCREASED ( 3 FDA reports)
PANCREATOLITHIASIS ( 3 FDA reports)
PANIC DISORDER WITHOUT AGORAPHOBIA ( 3 FDA reports)
PANNICULITIS ( 3 FDA reports)
PAPULE ( 3 FDA reports)
PARANEOPLASTIC SYNDROME ( 3 FDA reports)
PARAPSORIASIS ( 3 FDA reports)
PARATHYROID TUMOUR BENIGN ( 3 FDA reports)
PAROTID DUCT OBSTRUCTION ( 3 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 3 FDA reports)
PEDAL PULSE DECREASED ( 3 FDA reports)
PENILE HAEMORRHAGE ( 3 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 3 FDA reports)
PERICARDITIS TUBERCULOUS ( 3 FDA reports)
PERINEAL OPERATION ( 3 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 3 FDA reports)
PLACENTAL INFARCTION ( 3 FDA reports)
PLASMA PROTEIN METABOLISM DISORDER ( 3 FDA reports)
PLATELET ADHESIVENESS INCREASED ( 3 FDA reports)
PLATELET AGGREGATION INCREASED ( 3 FDA reports)
PLATELET PRODUCTION DECREASED ( 3 FDA reports)
PNEUMOBILIA ( 3 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 3 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 3 FDA reports)
PNEUMONIA HAEMOPHILUS ( 3 FDA reports)
PNEUMONIA NECROTISING ( 3 FDA reports)
PNEUMONIA PARAINFLUENZAE VIRAL ( 3 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 3 FDA reports)
PO2 INCREASED ( 3 FDA reports)
POLIOMYELITIS ( 3 FDA reports)
POLYCYSTIC LIVER DISEASE ( 3 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 3 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 3 FDA reports)
POSITIONAL PLAGIOCEPHALY ( 3 FDA reports)
POST POLIO SYNDROME ( 3 FDA reports)
POST PROCEDURAL DISCOMFORT ( 3 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 3 FDA reports)
POSTOPERATIVE THORACIC PROCEDURE COMPLICATION ( 3 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 3 FDA reports)
PREMATURE DELIVERY ( 3 FDA reports)
PREMENSTRUAL SYNDROME ( 3 FDA reports)
PRODUCT LOT NUMBER ISSUE ( 3 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 3 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 3 FDA reports)
PROSTHESIS IMPLANTATION ( 3 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 3 FDA reports)
PULMONARY ARTERY DILATATION ( 3 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 3 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 3 FDA reports)
PUSTULAR PSORIASIS ( 3 FDA reports)
RADIATION NEUROPATHY ( 3 FDA reports)
RATHKE'S CLEFT CYST ( 3 FDA reports)
RECTAL FISSURE ( 3 FDA reports)
RED BLOOD CELL SPHEROCYTES PRESENT ( 3 FDA reports)
REFRACTION DISORDER ( 3 FDA reports)
REFUSAL OF EXAMINATION ( 3 FDA reports)
REMOVAL OF FOREIGN BODY ( 3 FDA reports)
RENAL ARTERIOSCLEROSIS ( 3 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 3 FDA reports)
RENAL CELL CARCINOMA STAGE IV ( 3 FDA reports)
RENAL HAEMATOMA ( 3 FDA reports)
RENAL VASCULITIS ( 3 FDA reports)
RETINAL INJURY ( 3 FDA reports)
RETINAL SCAR ( 3 FDA reports)
RETINAL VASCULAR DISORDER ( 3 FDA reports)
RETROPERITONEAL FIBROSIS ( 3 FDA reports)
RHEUMATIC FEVER ( 3 FDA reports)
RHEUMATOID LUNG ( 3 FDA reports)
RHEUMATOID VASCULITIS ( 3 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 3 FDA reports)
SALMONELLOSIS ( 3 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 3 FDA reports)
SCINTILLATING SCOTOMA ( 3 FDA reports)
SCLERODERMA RENAL CRISIS ( 3 FDA reports)
SEBACEOUS ADENOMA ( 3 FDA reports)
SEBACEOUS HYPERPLASIA ( 3 FDA reports)
SEROSITIS ( 3 FDA reports)
SHONE COMPLEX ( 3 FDA reports)
SICKLE CELL ANAEMIA ( 3 FDA reports)
SIMPLE PARTIAL SEIZURES ( 3 FDA reports)
SINUS ARREST ( 3 FDA reports)
SKIN CANDIDA ( 3 FDA reports)
SKIN DISCOMFORT ( 3 FDA reports)
SKIN HYPOPIGMENTATION ( 3 FDA reports)
SLEEP-RELATED EATING DISORDER ( 3 FDA reports)
SPASTIC DIPLEGIA ( 3 FDA reports)
SPECIFIC GRAVITY URINE INCREASED ( 3 FDA reports)
SPEECH REHABILITATION ( 3 FDA reports)
SPIDER NAEVUS ( 3 FDA reports)
SPLENIC HAEMORRHAGE ( 3 FDA reports)
SPUTUM INCREASED ( 3 FDA reports)
SPUTUM PURULENT ( 3 FDA reports)
SPUTUM RETENTION ( 3 FDA reports)
STRESS AT WORK ( 3 FDA reports)
STRESS CARDIOMYOPATHY ( 3 FDA reports)
SURGICAL FAILURE ( 3 FDA reports)
SYMBOLIC DYSFUNCTION ( 3 FDA reports)
SYRINGE ISSUE ( 3 FDA reports)
TENDON GRAFT ( 3 FDA reports)
TERATOMA ( 3 FDA reports)
TESTIS DISCOMFORT ( 3 FDA reports)
THALAMUS HAEMORRHAGE ( 3 FDA reports)
THERAPEUTIC PROCEDURE ( 3 FDA reports)
THYROID GLAND SCAN ABNORMAL ( 3 FDA reports)
TINEA VERSICOLOUR ( 3 FDA reports)
TONSILLECTOMY ( 3 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 3 FDA reports)
TRANSPLANT FAILURE ( 3 FDA reports)
TRAUMATIC ARTHROPATHY ( 3 FDA reports)
TRICHORRHEXIS ( 3 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 3 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 3 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 3 FDA reports)
UNEMPLOYMENT ( 3 FDA reports)
UNINTENDED PREGNANCY ( 3 FDA reports)
URATE NEPHROPATHY ( 3 FDA reports)
URINARY SEDIMENT PRESENT ( 3 FDA reports)
UTERINE ATROPHY ( 3 FDA reports)
UTERINE SPASM ( 3 FDA reports)
VAGINAL ERYTHEMA ( 3 FDA reports)
VAGINAL FISTULA ( 3 FDA reports)
VAGINAL REMOVAL OF INTRAUTERINE FOREIGN BODY ( 3 FDA reports)
VASCULAR BYPASS GRAFT ( 3 FDA reports)
VASCULITIS CEREBRAL ( 3 FDA reports)
VEIN PAIN ( 3 FDA reports)
VIRAL LOAD INCREASED ( 3 FDA reports)
VISCERAL CONGESTION ( 3 FDA reports)
VOCAL CORD INFLAMMATION ( 3 FDA reports)
VOCAL CORD NEOPLASM ( 3 FDA reports)
VULVAL DISORDER ( 3 FDA reports)
VULVAL OEDEMA ( 3 FDA reports)
VULVAR EROSION ( 3 FDA reports)
WISDOM TEETH REMOVAL ( 3 FDA reports)
WOUND INFECTION FUNGAL ( 3 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 3 FDA reports)
XANTHOCHROMIA ( 3 FDA reports)
ZYGOMYCOSIS ( 3 FDA reports)
PHOBIA OF DRIVING ( 2 FDA reports)
PHOTOSENSITIVE RASH ( 2 FDA reports)
PHYSICAL BREAST EXAMINATION ABNORMAL ( 2 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 2 FDA reports)
PICKWICKIAN SYNDROME ( 2 FDA reports)
PLASMA CELLS INCREASED ( 2 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 2 FDA reports)
PLATELET TRANSFUSION ( 2 FDA reports)
PLEOCYTOSIS ( 2 FDA reports)
PLEURAL DISORDER ( 2 FDA reports)
PLEURAL HAEMORRHAGE ( 2 FDA reports)
PLEURODESIS ( 2 FDA reports)
PNEUMOCONIOSIS ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 2 FDA reports)
POROKERATOSIS ( 2 FDA reports)
POST PROCEDURAL NAUSEA ( 2 FDA reports)
POSTICTAL PARALYSIS ( 2 FDA reports)
POSTOPERATIVE HERNIA ( 2 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 2 FDA reports)
POUCHITIS ( 2 FDA reports)
PRE-ECLAMPSIA ( 2 FDA reports)
PREALBUMIN DECREASED ( 2 FDA reports)
PRECANCEROUS MUCOSAL LESION ( 2 FDA reports)
PREGNANCY WITH CONTRACEPTIVE PATCH ( 2 FDA reports)
PREGNANCY WITH IMPLANT CONTRACEPTIVE ( 2 FDA reports)
PRIMARY EFFUSION LYMPHOMA ( 2 FDA reports)
PRODUCT DEPOSIT ( 2 FDA reports)
PRODUCT DROPPER ISSUE ( 2 FDA reports)
PRODUCT TAMPERING ( 2 FDA reports)
PROSTATE TENDERNESS ( 2 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 2 FDA reports)
PRURITUS GENITAL ( 2 FDA reports)
PSYCHOMOTOR SEIZURES ( 2 FDA reports)
PSYCHOSOMATIC DISEASE ( 2 FDA reports)
PSYCHOTHERAPY ( 2 FDA reports)
PSYCHOTIC BEHAVIOUR ( 2 FDA reports)
PULMONARY ARTERY ATRESIA ( 2 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 2 FDA reports)
PYODERMA ( 2 FDA reports)
RADIAL PULSE ABNORMAL ( 2 FDA reports)
RADIATION FIBROSIS ( 2 FDA reports)
RADICULITIS BRACHIAL ( 2 FDA reports)
REACTION TO FOOD ADDITIVE ( 2 FDA reports)
RECALL PHENOMENON ( 2 FDA reports)
RECTAL LESION ( 2 FDA reports)
RECTAL PERFORATION ( 2 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
RED BLOOD CELLS URINE ( 2 FDA reports)
RED MAN SYNDROME ( 2 FDA reports)
REFLEXES ABNORMAL ( 2 FDA reports)
REMOVAL OF TRANSPLANTED ORGAN ( 2 FDA reports)
RENAL CANCER METASTATIC ( 2 FDA reports)
REPRODUCTIVE TRACT DISORDER ( 2 FDA reports)
RESPIRATORY ACIDOSIS ( 2 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 2 FDA reports)
RESPIRATORY FUME INHALATION DISORDER ( 2 FDA reports)
RESPIRATORY MONILIASIS ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS BRONCHIOLITIS ( 2 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 2 FDA reports)
RESTING TREMOR ( 2 FDA reports)
RETICULOCYTE COUNT INCREASED ( 2 FDA reports)
RETINAL ARTERY STENOSIS ( 2 FDA reports)
RETINAL COLOBOMA ( 2 FDA reports)
RETINITIS PIGMENTOSA ( 2 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 2 FDA reports)
ROSAI-DORFMAN SYNDROME ( 2 FDA reports)
SALIVARY GLAND CYST ( 2 FDA reports)
SALIVARY GLAND DISORDER ( 2 FDA reports)
SCAN BRAIN ( 2 FDA reports)
SCLERAL HYPERAEMIA ( 2 FDA reports)
SCROTAL ABSCESS ( 2 FDA reports)
SCROTAL HAEMATOCOELE ( 2 FDA reports)
SCROTAL PAIN ( 2 FDA reports)
SEBACEOUS CYST EXCISION ( 2 FDA reports)
SELF-INDUCED VOMITING ( 2 FDA reports)
SEMEN VOLUME DECREASED ( 2 FDA reports)
SENSORY INTEGRATIVE DYSFUNCTION ( 2 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 2 FDA reports)
SHOULDER DYSTOCIA ( 2 FDA reports)
SKIN BACTERIAL INFECTION ( 2 FDA reports)
SKIN DESQUAMATION ( 2 FDA reports)
SKIN TURGOR DECREASED ( 2 FDA reports)
SMALL INTESTINAL PERFORATION ( 2 FDA reports)
SMALL INTESTINE CARCINOMA ( 2 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 2 FDA reports)
SPINA BIFIDA ( 2 FDA reports)
SPINAL LIGAMENT OSSIFICATION ( 2 FDA reports)
SPLENIC ABSCESS ( 2 FDA reports)
SPLENIC RUPTURE ( 2 FDA reports)
SPLINT APPLICATION ( 2 FDA reports)
SPONTANEOUS HAEMATOMA ( 2 FDA reports)
SPONTANEOUS PENILE ERECTION ( 2 FDA reports)
SPUTUM ABNORMAL ( 2 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 2 FDA reports)
STENOTROPHOMONAS INFECTION ( 2 FDA reports)
STENOTROPHOMONAS SEPSIS ( 2 FDA reports)
SUBCLAVIAN ARTERY THROMBOSIS ( 2 FDA reports)
SUBDURAL HAEMATOMA EVACUATION ( 2 FDA reports)
SUTURE RELATED COMPLICATION ( 2 FDA reports)
SYNDACTYLY ( 2 FDA reports)
SYNOVIAL RUPTURE ( 2 FDA reports)
SYSTOLIC DYSFUNCTION ( 2 FDA reports)
SYSTOLIC HYPERTENSION ( 2 FDA reports)
TABLET ISSUE ( 2 FDA reports)
TENDINOUS CONTRACTURE ( 2 FDA reports)
TENDON CALCIFICATION ( 2 FDA reports)
TENDON OPERATION ( 2 FDA reports)
TESTIS CANCER ( 2 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 2 FDA reports)
THERAPEUTIC RESPONSE PROLONGED ( 2 FDA reports)
THROMBECTOMY ( 2 FDA reports)
TONGUE CARCINOMA STAGE IV ( 2 FDA reports)
TONGUE EXFOLIATION ( 2 FDA reports)
TONGUE HAEMORRHAGE ( 2 FDA reports)
TONGUE NEOPLASM ( 2 FDA reports)
TONIC CLONIC MOVEMENTS ( 2 FDA reports)
TONSILLAR HYPERTROPHY ( 2 FDA reports)
TOOTH RESORPTION ( 2 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO ( 2 FDA reports)
TRACHEOBRONCHITIS VIRAL ( 2 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 2 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 2 FDA reports)
TRAUMATIC HAEMORRHAGE ( 2 FDA reports)
TUBAL LIGATION ( 2 FDA reports)
TUMOUR MARKER TEST ( 2 FDA reports)
TUMOUR NECROSIS ( 2 FDA reports)
TUNNEL VISION ( 2 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 2 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 2 FDA reports)
UMBILICAL CORD AROUND NECK ( 2 FDA reports)
UNDERWEIGHT ( 2 FDA reports)
UNEQUAL LIMB LENGTH ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
URETERAL NEOPLASM ( 2 FDA reports)
URETHRAL ATROPHY ( 2 FDA reports)
URETHRAL HAEMORRHAGE ( 2 FDA reports)
URETHRAL INJURY ( 2 FDA reports)
URETHRAL PAIN ( 2 FDA reports)
URETHRAL SPASM ( 2 FDA reports)
URINARY TRACT INFLAMMATION ( 2 FDA reports)
URINE BILIRUBIN INCREASED ( 2 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 2 FDA reports)
VAGINAL EROSION ( 2 FDA reports)
VAGINAL PAIN ( 2 FDA reports)
VAGINITIS GARDNERELLA ( 2 FDA reports)
VARICOSE VEIN OPERATION ( 2 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 2 FDA reports)
VASCULAR RESISTANCE PULMONARY INCREASED ( 2 FDA reports)
VASCULITIC RASH ( 2 FDA reports)
VASODILATION PROCEDURE ( 2 FDA reports)
VEIN DISCOLOURATION ( 2 FDA reports)
VENOUS HAEMORRHAGE ( 2 FDA reports)
VENOUS OPERATION ( 2 FDA reports)
VENOUS PRESSURE INCREASED ( 2 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 2 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 2 FDA reports)
VENTRICULAR DYSSYNCHRONY ( 2 FDA reports)
VENTRICULAR FAILURE ( 2 FDA reports)
VIBRATORY SENSE INCREASED ( 2 FDA reports)
VITREAL CELLS ( 2 FDA reports)
VITRECTOMY ( 2 FDA reports)
VOCAL CORD CYST ( 2 FDA reports)
VOLUME BLOOD DECREASED ( 2 FDA reports)
VOLVULUS OF BOWEL ( 2 FDA reports)
VOMITING IN PREGNANCY ( 2 FDA reports)
VULVAL CANCER ( 2 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 2 FDA reports)
WEIGHT ( 2 FDA reports)
WHOLE BLOOD TRANSFUSION ( 2 FDA reports)
WOUND INFECTION BACTERIAL ( 2 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 2 FDA reports)
WRIST SURGERY ( 2 FDA reports)
XANTHOPSIA ( 2 FDA reports)
ABDOMEN CRUSHING ( 2 FDA reports)
ABDOMINAL HERNIA OBSTRUCTIVE ( 2 FDA reports)
ABNORMAL WEIGHT GAIN ( 2 FDA reports)
ABNORMAL WITHDRAWAL BLEEDING ( 2 FDA reports)
ABORTION ( 2 FDA reports)
ABORTION COMPLETE ( 2 FDA reports)
ABORTION EARLY ( 2 FDA reports)
ACINETOBACTER INFECTION ( 2 FDA reports)
ACQUIRED CARDIAC SEPTAL DEFECT ( 2 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 2 FDA reports)
ACUTE ENDOCARDITIS ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 2 FDA reports)
ACUTE PHASE REACTION ( 2 FDA reports)
ADAMS-STOKES SYNDROME ( 2 FDA reports)
ADENOIDECTOMY ( 2 FDA reports)
ADRENALITIS ( 2 FDA reports)
AGITATED DEPRESSION ( 2 FDA reports)
AGITATION POSTOPERATIVE ( 2 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
ALBUMIN URINE PRESENT ( 2 FDA reports)
ALBUMINURIA ( 2 FDA reports)
ALLERGY TO METALS ( 2 FDA reports)
ALOPECIA SCARRING ( 2 FDA reports)
ALPHA-1 ANTI-TRYPSIN DEFICIENCY ( 2 FDA reports)
AMPUTATION ( 2 FDA reports)
ANAEMIA MEGALOBLASTIC ( 2 FDA reports)
ANAL SKIN TAGS ( 2 FDA reports)
ANAL SPASM ( 2 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 2 FDA reports)
ANASTOMOTIC LEAK ( 2 FDA reports)
ANASTOMOTIC STENOSIS ( 2 FDA reports)
ANASTOMOTIC ULCER ( 2 FDA reports)
ANDROGENETIC ALOPECIA ( 2 FDA reports)
ANGIOFIBROMA ( 2 FDA reports)
ANGIOGRAM ( 2 FDA reports)
ANGIOSARCOMA ( 2 FDA reports)
ANKLE OPERATION ( 2 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTICONVULSANT TOXICITY ( 2 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 2 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES ( 2 FDA reports)
AORTIC OCCLUSION ( 2 FDA reports)
AORTITIS ( 2 FDA reports)
APGAR SCORE LOW ( 2 FDA reports)
APPLICATION SITE BURNING ( 2 FDA reports)
APPLICATION SITE DESQUAMATION ( 2 FDA reports)
APPLICATION SITE DISCOLOURATION ( 2 FDA reports)
APPLICATION SITE HAEMATOMA ( 2 FDA reports)
APPLICATION SITE WARMTH ( 2 FDA reports)
ARRESTED LABOUR ( 2 FDA reports)
ARTERIAL REPAIR ( 2 FDA reports)
ARTERIAL RESTENOSIS ( 2 FDA reports)
ARTERIAL RUPTURE ( 2 FDA reports)
ARTERIOGRAM CAROTID ABNORMAL ( 2 FDA reports)
ARTERIOVENOUS FISTULA ( 2 FDA reports)
ARTERIOVENOUS FISTULA ANEURYSM ( 2 FDA reports)
ARTERIOVENOUS FISTULA OCCLUSION ( 2 FDA reports)
ARTERIOVENOUS FISTULA SITE INFECTION ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
ASPIRATION PLEURAL CAVITY ABNORMAL ( 2 FDA reports)
ASTHMA EXERCISE INDUCED ( 2 FDA reports)
ATAXIA TELANGIECTASIA ( 2 FDA reports)
ATOPY ( 2 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 2 FDA reports)
AUTOIMMUNE NEUTROPENIA ( 2 FDA reports)
AUTOIMMUNE THYROIDITIS ( 2 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 2 FDA reports)
AVERSION ( 2 FDA reports)
B-CELL LYMPHOMA STAGE I ( 2 FDA reports)
B-CELL UNCLASSIFIABLE LYMPHOMA LOW GRADE ( 2 FDA reports)
BACTERIAL CULTURE POSITIVE ( 2 FDA reports)
BACTEROIDES BACTERAEMIA ( 2 FDA reports)
BASAL GANGLIA STROKE ( 2 FDA reports)
BASOPHIL COUNT INCREASED ( 2 FDA reports)
BENIGN OESOPHAGEAL NEOPLASM ( 2 FDA reports)
BICYTOPENIA ( 2 FDA reports)
BILE OUTPUT INCREASED ( 2 FDA reports)
BILIARY TRACT INFECTION ( 2 FDA reports)
BILIARY TRACT OPERATION ( 2 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 2 FDA reports)
BIOPSY KIDNEY ( 2 FDA reports)
BIOPSY LIP ( 2 FDA reports)
BITE ( 2 FDA reports)
BLADDER NECK OBSTRUCTION ( 2 FDA reports)
BLAST CELLS PRESENT ( 2 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 2 FDA reports)
BLASTOMYCOSIS ( 2 FDA reports)
BLEEDING TIME ABNORMAL ( 2 FDA reports)
BLOOD BICARBONATE ( 2 FDA reports)
BLOOD BICARBONATE INCREASED ( 2 FDA reports)
BLOOD BILIRUBIN DECREASED ( 2 FDA reports)
BLOOD COPPER DECREASED ( 2 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 2 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 2 FDA reports)
BLOOD GLUCAGON INCREASED ( 2 FDA reports)
BLOOD LUTEINISING HORMONE DECREASED ( 2 FDA reports)
BLOOD OESTROGEN DECREASED ( 2 FDA reports)
BLUE TOE SYNDROME ( 2 FDA reports)
BLUNTED AFFECT ( 2 FDA reports)
BODY MASS INDEX INCREASED ( 2 FDA reports)
BONE INFECTION ( 2 FDA reports)
BRACHIAL PLEXUS INJURY ( 2 FDA reports)
BRAIN CANCER METASTATIC ( 2 FDA reports)
BRAIN MIDLINE SHIFT ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE DECREASED ( 2 FDA reports)
BRANCHIAL CYST ( 2 FDA reports)
BREAST CANCER STAGE IV ( 2 FDA reports)
BREAST DISORDER FEMALE ( 2 FDA reports)
BRONCHIAL FISTULA ( 2 FDA reports)
BRONCHITIS BACTERIAL ( 2 FDA reports)
BRONCHOSPASM PARADOXICAL ( 2 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 2 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 2 FDA reports)
CARBON DIOXIDE INCREASED ( 2 FDA reports)
CARBON MONOXIDE DIFFUSING CAPACITY DECREASED ( 2 FDA reports)
CARBOXYHAEMOGLOBIN INCREASED ( 2 FDA reports)
CARCINOID TUMOUR OF THE STOMACH ( 2 FDA reports)
CARCINOID TUMOUR PULMONARY ( 2 FDA reports)
CARDIAC AMYLOIDOSIS ( 2 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 2 FDA reports)
CARDIAC INFECTION ( 2 FDA reports)
CARDIAC REHABILITATION THERAPY ( 2 FDA reports)
CAROTIDYNIA ( 2 FDA reports)
CATABOLIC STATE ( 2 FDA reports)
CATARACT OPERATION COMPLICATION ( 2 FDA reports)
CATHETER SITE SWELLING ( 2 FDA reports)
CENTRAL PAIN SYNDROME ( 2 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 2 FDA reports)
CEREBRAL ASPERGILLOSIS ( 2 FDA reports)
CEREBRAL HYPOPERFUSION ( 2 FDA reports)
CHARGE SYNDROME ( 2 FDA reports)
CHEMICAL INJURY ( 2 FDA reports)
CHEYNE-STOKES RESPIRATION ( 2 FDA reports)
CHLAMYDIAL INFECTION ( 2 FDA reports)
CHONDROCALCINOSIS ( 2 FDA reports)
CHONDROSARCOMA ( 2 FDA reports)
CHOROIDAL COLOBOMA ( 2 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 2 FDA reports)
CITROBACTER INFECTION ( 2 FDA reports)
CLEFT UVULA ( 2 FDA reports)
COLECTOMY PARTIAL ( 2 FDA reports)
COLECTOMY TOTAL ( 2 FDA reports)
COLON CANCER RECURRENT ( 2 FDA reports)
COLON CANCER STAGE IV ( 2 FDA reports)
COLON INJURY ( 2 FDA reports)
COLON OPERATION ( 2 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 2 FDA reports)
COLPOCELE ( 2 FDA reports)
COMPARTMENT SYNDROME ( 2 FDA reports)
COMPLEMENT FACTOR C4 DECREASED ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED LUNG ( 2 FDA reports)
CONDUCTIVE DEAFNESS ( 2 FDA reports)
CONFUSION POSTOPERATIVE ( 2 FDA reports)
CONGENITAL ANAEMIA ( 2 FDA reports)
CONGENITAL AORTIC VALVE STENOSIS ( 2 FDA reports)
CONGENITAL CORONARY ARTERY MALFORMATION ( 2 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 2 FDA reports)
CONGENITAL HEART VALVE DISORDER ( 2 FDA reports)
CONGENITAL HYPOTHYROIDISM ( 2 FDA reports)
CONGENITAL MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
CONGENITAL MITRAL VALVE STENOSIS ( 2 FDA reports)
CONGENITAL RENAL DISORDER ( 2 FDA reports)
CONJUNCTIVAL OEDEMA ( 2 FDA reports)
COOMBS TEST POSITIVE ( 2 FDA reports)
CORNEAL EPITHELIUM DEFECT ( 2 FDA reports)
CORNEAL INFECTION ( 2 FDA reports)
CORNEAL OEDEMA ( 2 FDA reports)
CORNEAL SCAR ( 2 FDA reports)
CORONARY ARTERY DISSECTION ( 2 FDA reports)
CORONARY REVASCULARISATION ( 2 FDA reports)
CORYNEBACTERIUM INFECTION ( 2 FDA reports)
CRANIAL NERVE DISORDER ( 2 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 2 FDA reports)
CSF CULTURE POSITIVE ( 2 FDA reports)
CSF WHITE BLOOD CELL COUNT POSITIVE ( 2 FDA reports)
CULTURE STOOL POSITIVE ( 2 FDA reports)
CYANOSIS NEONATAL ( 2 FDA reports)
CYSTITIS GLANDULARIS ( 2 FDA reports)
CYTOLOGY ABNORMAL ( 2 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 2 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 2 FDA reports)
DAWN PHENOMENON ( 2 FDA reports)
DEPENDENCE ON RESPIRATOR ( 2 FDA reports)
DEREALISATION ( 2 FDA reports)
DERMATITIS PSORIASIFORM ( 2 FDA reports)
DEVICE ELECTRICAL FINDING ( 2 FDA reports)
DIABETIC GASTROPATHY ( 2 FDA reports)
DISINHIBITION ( 2 FDA reports)
DISSOCIATIVE DISORDER ( 2 FDA reports)
DOUBLE STRANDED DNA ANTIBODY ( 2 FDA reports)
DRUG DETOXIFICATION ( 2 FDA reports)
DRUG NAME CONFUSION ( 2 FDA reports)
DRUG SCREEN NEGATIVE ( 2 FDA reports)
DUODENAL NEOPLASM ( 2 FDA reports)
DYSKINESIA OESOPHAGEAL ( 2 FDA reports)
DYSLEXIA ( 2 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ELEVATION ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 2 FDA reports)
ENDOMETRIAL CANCER STAGE I ( 2 FDA reports)
ENDOMETRITIS ( 2 FDA reports)
ENLARGED UVULA ( 2 FDA reports)
ENTERAL NUTRITION ( 2 FDA reports)
ENTEROBACTER BACTERAEMIA ( 2 FDA reports)
ENTEROSTOMY ( 2 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 2 FDA reports)
EPENDYMOMA ( 2 FDA reports)
EPHELIDES ( 2 FDA reports)
EPIDIDYMAL ENLARGEMENT ( 2 FDA reports)
EPIGLOTTITIS ( 2 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 2 FDA reports)
EPULIS ( 2 FDA reports)
ERECTION INCREASED ( 2 FDA reports)
EVANS SYNDROME ( 2 FDA reports)
EXPLORATIVE LAPAROTOMY ( 2 FDA reports)
EXPOSURE TO COMMUNICABLE DISEASE ( 2 FDA reports)
EXSANGUINATION ( 2 FDA reports)
EXTERNAL EAR PAIN ( 2 FDA reports)
EXTRADURAL HAEMATOMA ( 2 FDA reports)
EYE INFECTION VIRAL ( 2 FDA reports)
EYELASH DISCOLOURATION ( 2 FDA reports)
EYELID MARGIN CRUSTING ( 2 FDA reports)
EYELID PTOSIS CONGENITAL ( 2 FDA reports)
FACTOR II MUTATION ( 2 FDA reports)
FAILED INDUCTION OF LABOUR ( 2 FDA reports)
FAMILIAL COLD AUTOINFLAMMATORY SYNDROME ( 2 FDA reports)
FIBRIN D DIMER ( 2 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 2 FDA reports)
FIBROMATOSIS ( 2 FDA reports)
FINE MOTOR DELAY ( 2 FDA reports)
FLAT ANTERIOR CHAMBER OF EYE ( 2 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 2 FDA reports)
FOETAL ARRHYTHMIA ( 2 FDA reports)
FOETAL GROWTH RETARDATION ( 2 FDA reports)
FUNGAL CYSTITIS ( 2 FDA reports)
GAIT SPASTIC ( 2 FDA reports)
GALLBLADDER CANCER ( 2 FDA reports)
GALLBLADDER NECROSIS ( 2 FDA reports)
GALLBLADDER OEDEMA ( 2 FDA reports)
GALLBLADDER PERFORATION ( 2 FDA reports)
GASTRIC VARICES ( 2 FDA reports)
GASTRITIS BACTERIAL ( 2 FDA reports)
GASTROINTESTINAL BACTERIAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL MUCOSAL NECROSIS ( 2 FDA reports)
GASTROINTESTINAL NEOPLASM ( 2 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 2 FDA reports)
GASTROINTESTINAL STENOSIS ( 2 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 2 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 2 FDA reports)
GENITAL ABSCESS ( 2 FDA reports)
GENITAL DISORDER FEMALE ( 2 FDA reports)
GENITAL NEOPLASM MALIGNANT FEMALE ( 2 FDA reports)
GESTATIONAL DIABETES ( 2 FDA reports)
GINGIVAL INJURY ( 2 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 2 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 2 FDA reports)
GLUCOSE URINE PRESENT ( 2 FDA reports)
GRAFT THROMBOSIS ( 2 FDA reports)
GRANULOCYTE COUNT DECREASED ( 2 FDA reports)
GRANULOMA SKIN ( 2 FDA reports)
GROWTH OF EYELASHES ( 2 FDA reports)
GUTTATE PSORIASIS ( 2 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 2 FDA reports)
HAEMOPHILUS INFECTION ( 2 FDA reports)
HAEMORRHAGIC DISORDER ( 2 FDA reports)
HALLUCINATION, OLFACTORY ( 2 FDA reports)
HEART RATE ( 2 FDA reports)
HEART VALVE INSUFFICIENCY ( 2 FDA reports)
HEAT RASH ( 2 FDA reports)
HEAT STROKE ( 2 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 2 FDA reports)
HEMISENSORY NEGLECT ( 2 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 2 FDA reports)
HEPATECTOMY ( 2 FDA reports)
HEPATITIS ALCOHOLIC ( 2 FDA reports)
HEPATITIS B CORE ANTIGEN POSITIVE ( 2 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 2 FDA reports)
HEPATITIS C VIRUS TEST ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HERPES ZOSTER OTICUS ( 2 FDA reports)
HIRSUTISM ( 2 FDA reports)
HOFFMANN'S SIGN ( 2 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 2 FDA reports)
HUNTINGTON'S DISEASE ( 2 FDA reports)
HYDROTHORAX ( 2 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 2 FDA reports)
HYPERCALCIURIA ( 2 FDA reports)
HYPEREMESIS GRAVIDARUM ( 2 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 2 FDA reports)
HYPERKINESIA ( 2 FDA reports)
HYPEROSMOLAR STATE ( 2 FDA reports)
HYPERPARATHYROIDISM TERTIARY ( 2 FDA reports)
HYPERSPLENISM ( 2 FDA reports)
HYPERTENSIVE CARDIOMEGALY ( 2 FDA reports)
HYPOAESTHESIA EYE ( 2 FDA reports)
HYPOCOAGULABLE STATE ( 2 FDA reports)
HYPOHIDROSIS ( 2 FDA reports)
HYPOMENORRHOEA ( 2 FDA reports)
HYPOPLASTIC RIGHT HEART SYNDROME ( 2 FDA reports)
HYPOPYON ( 2 FDA reports)
HYPOTONIC URINARY BLADDER ( 2 FDA reports)
HYSTEROSCOPY ( 2 FDA reports)
ILEAL ULCER ( 2 FDA reports)
ILIAC ARTERY OCCLUSION ( 2 FDA reports)
IMMUNODEFICIENCY COMMON VARIABLE ( 2 FDA reports)
IMPATIENCE ( 2 FDA reports)
IMPLANT EXPULSION ( 2 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 2 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 2 FDA reports)
INCISION SITE CELLULITIS ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 2 FDA reports)
INFECTED BITES ( 2 FDA reports)
INFECTED BUNION ( 2 FDA reports)
INFECTED CYST ( 2 FDA reports)
INFECTION PARASITIC ( 2 FDA reports)
INFLAMMATION OF LACRIMAL PASSAGE ( 2 FDA reports)
INFLAMMATION OF WOUND ( 2 FDA reports)
INFLAMMATORY MARKER INCREASED ( 2 FDA reports)
INFLUENZA SEROLOGY POSITIVE ( 2 FDA reports)
INFUSION SITE HAEMORRHAGE ( 2 FDA reports)
INJECTION SITE PARAESTHESIA ( 2 FDA reports)
INJECTION SITE PHLEBITIS ( 2 FDA reports)
INTESTINAL ADHESION LYSIS ( 2 FDA reports)
INTESTINAL MASS ( 2 FDA reports)
INTESTINAL STOMA COMPLICATION ( 2 FDA reports)
INTRACRANIAL HAEMATOMA ( 2 FDA reports)
INTRAOSSEOUS ANGIOMA ( 2 FDA reports)
IRIS COLOBOMA ( 2 FDA reports)
IRIS CYST ( 2 FDA reports)
IRREGULAR SLEEP PHASE ( 2 FDA reports)
KAWASAKI'S DISEASE ( 2 FDA reports)
LANGERHANS' CELL GRANULOMATOSIS ( 2 FDA reports)
LAPAROSCOPIC SURGERY ( 2 FDA reports)
LARYNGEAL CYST ( 2 FDA reports)
LARYNGEAL MASS ( 2 FDA reports)
LARYNGEAL NEOPLASM ( 2 FDA reports)
LARYNGEAL ULCERATION ( 2 FDA reports)
LATENT TUBERCULOSIS ( 2 FDA reports)
LATERAL MEDULLARY SYNDROME ( 2 FDA reports)
LATERAL PATELLAR COMPRESSION SYNDROME ( 2 FDA reports)
LEVATOR SYNDROME ( 2 FDA reports)
LIFE SUPPORT ( 2 FDA reports)
LIMB ASYMMETRY ( 2 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 2 FDA reports)
LIP HAEMORRHAGE ( 2 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 2 FDA reports)
LIPOGRANULOMA ( 2 FDA reports)
LIPOPROTEIN (A) ABNORMAL ( 2 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 2 FDA reports)
LIVER SARCOIDOSIS ( 2 FDA reports)
LONG QT SYNDROME ( 2 FDA reports)
LOWER LIMB DEFORMITY ( 2 FDA reports)
LOWER URINARY TRACT SYMPTOMS ( 2 FDA reports)
LUMBAR HERNIA ( 2 FDA reports)
LUNG ADENOCARCINOMA STAGE III ( 2 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 2 FDA reports)
LUNG INFILTRATION MALIGNANT ( 2 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 2 FDA reports)
LUNG TRANSPLANT REJECTION ( 2 FDA reports)
LYMPH NODE CALCIFICATION ( 2 FDA reports)
LYMPHATIC OBSTRUCTION ( 2 FDA reports)
LYMPHOCYTIC HYPOPHYSITIS ( 2 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 2 FDA reports)
MACROPHAGES INCREASED ( 2 FDA reports)
MACULAR REFLEX ABNORMAL ( 2 FDA reports)
MALARIA ( 2 FDA reports)
MALFORMATION VENOUS ( 2 FDA reports)
MALIGNANT NEOPLASM OF AMPULLA OF VATER ( 2 FDA reports)
MANDIBULECTOMY ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 2 FDA reports)
MEAN CELL VOLUME DECREASED ( 2 FDA reports)
MECHANICAL COMPLICATION OF IMPLANT ( 2 FDA reports)
MEIBOMIANITIS ( 2 FDA reports)
MELANOCYTIC HYPERPLASIA ( 2 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 2 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
MERALGIA PARAESTHETICA ( 2 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 2 FDA reports)
MESENTERIC OCCLUSION ( 2 FDA reports)
MESOTHELIOMA ( 2 FDA reports)
MESOTHELIOMA MALIGNANT ( 2 FDA reports)
METASTASES TO BREAST ( 2 FDA reports)
METASTASES TO PELVIS ( 2 FDA reports)
METASTASES TO SMALL INTESTINE ( 2 FDA reports)
METASTATIC GASTRIC CANCER ( 2 FDA reports)
METASTATIC UTERINE CANCER ( 2 FDA reports)
METHAEMOGLOBINAEMIA ( 2 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 2 FDA reports)
MICROCEPHALY ( 2 FDA reports)
MIOSIS ( 2 FDA reports)
MIXED RECEPTIVE-EXPRESSIVE LANGUAGE DISORDER ( 2 FDA reports)
MOUTH CYST ( 2 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 2 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 2 FDA reports)
MUSCLE ABSCESS ( 2 FDA reports)
MYCOTIC ALLERGY ( 2 FDA reports)
MYOCARDIAC ABSCESS ( 2 FDA reports)
MYOFASCITIS ( 2 FDA reports)
MYOPATHY STEROID ( 2 FDA reports)
N-TELOPEPTIDE URINE INCREASED ( 2 FDA reports)
NAIL TINEA ( 2 FDA reports)
NASAL SINUS CANCER ( 2 FDA reports)
NASOPHARYNGEAL DISORDER ( 2 FDA reports)
NECROTISING COLITIS ( 2 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 2 FDA reports)
NEISSERIA INFECTION ( 2 FDA reports)
NEOPLASM OF THYMUS ( 2 FDA reports)
NEPHRITIS ALLERGIC ( 2 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 2 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 2 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 2 FDA reports)
NEUROMYOPATHY ( 2 FDA reports)
NIPPLE EXUDATE BLOODY ( 2 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 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 IV ( 2 FDA reports)
OBESITY SURGERY ( 2 FDA reports)
OCULAR DISCOMFORT ( 2 FDA reports)
OEDEMA GENITAL ( 2 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 2 FDA reports)
OLIGODIPSIA ( 2 FDA reports)
OPISTHOTONUS ( 2 FDA reports)
OPTIC DISC DISORDER ( 2 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 2 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 2 FDA reports)
OSTEOMYELITIS FUNGAL ( 2 FDA reports)
OVARIAN CYST RUPTURED ( 2 FDA reports)
OVARIAN NEOPLASM ( 2 FDA reports)
OXYGEN SATURATION ABNORMAL ( 2 FDA reports)
PAIN MANAGEMENT ( 2 FDA reports)
PALLIATIVE CARE ( 2 FDA reports)
PANCREAS TRANSPLANT REJECTION ( 2 FDA reports)
PANCREATIC ENLARGEMENT ( 2 FDA reports)
PANCREATIC INJURY ( 2 FDA reports)
PARADOXICAL DRUG REACTION ( 2 FDA reports)
PAROPHTHALMIA ( 2 FDA reports)
PELVIC VENOUS THROMBOSIS ( 2 FDA reports)
PENILE PAIN ( 2 FDA reports)
PENILE ULCERATION ( 2 FDA reports)
PENILE VEIN THROMBOSIS ( 2 FDA reports)
PERFORATION BILE DUCT ( 2 FDA reports)
PERIARTICULAR DISORDER ( 2 FDA reports)
PERICORONITIS ( 2 FDA reports)
PERIDIVERTICULITIS ( 2 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 2 FDA reports)
PERIPHERAL NERVE LESION ( 2 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 2 FDA reports)
PERITONEAL ABSCESS ( 2 FDA reports)
PERITONEAL ADHESIONS ( 2 FDA reports)
PERITONEAL CLOUDY EFFLUENT ( 2 FDA reports)
PERITONEAL EFFUSION ( 2 FDA reports)
PERITONEAL HAEMORRHAGE ( 2 FDA reports)
PEYRONIE'S DISEASE ( 2 FDA reports)
PHARYNGEAL INFLAMMATION ( 2 FDA reports)
PHARYNGEAL MASS ( 2 FDA reports)
PHARYNGITIS BACTERIAL ( 2 FDA reports)
5-HYDROXYINDOLACETIC ACID INCREASED ( 1 FDA reports)
ABDOMINAL BRUIT ( 1 FDA reports)
ABDOMINAL CAVITY DRAINAGE ( 1 FDA reports)
ABDOMINAL PANNICULECTOMY ( 1 FDA reports)
ABDOMINAL REBOUND TENDERNESS ( 1 FDA reports)
ABDOMINAL SYMPTOM ( 1 FDA reports)
ABDOMINAL WALL DISORDER ( 1 FDA reports)
ABDOMINAL WALL HAEMORRHAGE ( 1 FDA reports)
ABDOMINAL WALL INFECTION ( 1 FDA reports)
ABDOMINAL X-RAY ( 1 FDA reports)
ABSCESS BACTERIAL ( 1 FDA reports)
ABSCESS MANAGEMENT ( 1 FDA reports)
ACANTHOSIS ( 1 FDA reports)
ACCESSORY MUSCLE ( 1 FDA reports)
ACCIDENTAL POISONING ( 1 FDA reports)
ACETONAEMIA ( 1 FDA reports)
ACHLORHYDRIA ( 1 FDA reports)
ACID BASE BALANCE ABNORMAL ( 1 FDA reports)
ACID FAST STAIN POSITIVE ( 1 FDA reports)
ACINETOBACTER BACTERAEMIA ( 1 FDA reports)
ACNE CYSTIC ( 1 FDA reports)
ACNE PUSTULAR ( 1 FDA reports)
ACQUIRED MACROGLOSSIA ( 1 FDA reports)
ACQUIRED PHIMOSIS ( 1 FDA reports)
ACROMEGALY ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ACUTE CHEST SYNDROME ( 1 FDA reports)
ACUTE DISSEMINATED ENCEPHALOMYELITIS ( 1 FDA reports)
ACUTE PHOSPHATE NEPHROPATHY ( 1 FDA reports)
ACUTE RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
ADENOIDITIS ( 1 FDA reports)
ADJUSTMENT DISORDER WITH MIXED ANXIETY AND DEPRESSED MOOD ( 1 FDA reports)
ADJUSTMENT DISORDER WITH MIXED DISTURBANCE OF EMOTION AND CONDUCT ( 1 FDA reports)
ADRENOCORTICAL CARCINOMA ( 1 FDA reports)
ADULT T-CELL LYMPHOMA/LEUKAEMIA ( 1 FDA reports)
AGNOSIA ( 1 FDA reports)
AIRWAY COMPLICATION OF ANAESTHESIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ( 1 FDA reports)
ALCOHOL INTOLERANCE ( 1 FDA reports)
ALDOLASE INCREASED ( 1 FDA reports)
ALKALOSIS HYPOKALAEMIC ( 1 FDA reports)
ALLERGY TO ARTHROPOD BITE ( 1 FDA reports)
ALLERGY TO CHEMICALS ( 1 FDA reports)
ALLERGY TO PLANTS ( 1 FDA reports)
ALLOIMMUNISATION ( 1 FDA reports)
ALPHA 1 GLOBULIN INCREASED ( 1 FDA reports)
ALPHA 2 GLOBULIN INCREASED ( 1 FDA reports)
AMNESTIC DISORDER ( 1 FDA reports)
AMPHETAMINES POSITIVE ( 1 FDA reports)
ANAL ATRESIA ( 1 FDA reports)
ANAL CANCER STAGE 0 ( 1 FDA reports)
ANAL INFLAMMATION ( 1 FDA reports)
ANAL SPHINCTER HYPERTONIA ( 1 FDA reports)
ANAPLASTIC ASTROCYTOMA ( 1 FDA reports)
ANASTOMOTIC ULCER HAEMORRHAGE ( 1 FDA reports)
ANEURYSMECTOMY ( 1 FDA reports)
ANGIOGRAM PULMONARY ( 1 FDA reports)
ANION GAP ( 1 FDA reports)
ANISOMETROPIA ( 1 FDA reports)
ANKLE BRACHIAL INDEX DECREASED ( 1 FDA reports)
ANORECTAL INFECTION BACTERIAL ( 1 FDA reports)
ANORECTAL OPERATION ( 1 FDA reports)
ANORGASMIA ( 1 FDA reports)
ANOSOGNOSIA ( 1 FDA reports)
ANTI-CYCLIC CITRULLINATED PEPTIDE ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY ( 1 FDA reports)
ANTI-HBC IGG ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-SS-A ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBODY TEST NEGATIVE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABNORMAL ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIGLIADIN ANTIBODY POSITIVE ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTITHROMBIN III DEFICIENCY ( 1 FDA reports)
ANXIETY DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
APACHE II SCORE ( 1 FDA reports)
APALLIC SYNDROME ( 1 FDA reports)
APLASIA ( 1 FDA reports)
APPLICATION SITE CELLULITIS ( 1 FDA reports)
APPLICATION SITE DISCOMFORT ( 1 FDA reports)
APPLICATION SITE EROSION ( 1 FDA reports)
APPLICATION SITE EXFOLIATION ( 1 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 1 FDA reports)
APPLICATION SITE INFECTION ( 1 FDA reports)
APPLICATION SITE MASS ( 1 FDA reports)
APPLICATION SITE PAPULES ( 1 FDA reports)
APPLICATION SITE SCAB ( 1 FDA reports)
ARCUS LIPOIDES ( 1 FDA reports)
ARTERIOGRAM ( 1 FDA reports)
ARTERIOGRAM ABNORMAL ( 1 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 1 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 1 FDA reports)
ARTERY DISSECTION ( 1 FDA reports)
ARTHRITIS REACTIVE ( 1 FDA reports)
ARTHROFIBROSIS ( 1 FDA reports)
ARTICULAR CALCIFICATION ( 1 FDA reports)
ARTIFICIAL MENOPAUSE ( 1 FDA reports)
ASPERGER'S DISORDER ( 1 FDA reports)
ASPIRATION BONE MARROW ( 1 FDA reports)
ASTHMA LATE ONSET ( 1 FDA reports)
ASTHMA PROPHYLAXIS ( 1 FDA reports)
ASTHMATIC CRISIS ( 1 FDA reports)
ATRIAL HYPERTROPHY ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ACQUIRED ( 1 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 1 FDA reports)
AURICULAR PERICHONDRITIS ( 1 FDA reports)
AUTOANTIBODY TEST ( 1 FDA reports)
AUTOIMMUNE PANCREATITIS ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
AV DISSOCIATION ( 1 FDA reports)
AXILLARY VEIN THROMBOSIS ( 1 FDA reports)
B PRECURSOR TYPE ACUTE LEUKAEMIA ( 1 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 1 FDA reports)
BACILLUS TEST POSITIVE ( 1 FDA reports)
BACTERIAL PYELONEPHRITIS ( 1 FDA reports)
BACTEROIDES INFECTION ( 1 FDA reports)
BALANITIS CANDIDA ( 1 FDA reports)
BALANTIDIASIS ( 1 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
BARTHOLIN'S CYST ( 1 FDA reports)
BASE EXCESS DECREASED ( 1 FDA reports)
BASILAR ARTERY OCCLUSION ( 1 FDA reports)
BASILAR ARTERY STENOSIS ( 1 FDA reports)
BASOPHILIA ( 1 FDA reports)
BEHCET'S SYNDROME ( 1 FDA reports)
BENIGN EAR NEOPLASM ( 1 FDA reports)
BENIGN GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
BENIGN HEPATIC NEOPLASM ( 1 FDA reports)
BENIGN LARYNGEAL NEOPLASM ( 1 FDA reports)
BENIGN MESOTHELIOMA ( 1 FDA reports)
BENIGN NEOPLASM OF PROSTATE ( 1 FDA reports)
BENIGN PANCREATIC NEOPLASM ( 1 FDA reports)
BENIGN SALIVARY GLAND NEOPLASM ( 1 FDA reports)
BEZOAR ( 1 FDA reports)
BILATERAL HYDRONEPHROSIS ( 1 FDA reports)
BILE DUCT CANCER STAGE III ( 1 FDA reports)
BILE OUTPUT ( 1 FDA reports)
BILIARY ADENOMA ( 1 FDA reports)
BILIARY SEPSIS ( 1 FDA reports)
BILIRUBIN URINE ( 1 FDA reports)
BINGE EATING ( 1 FDA reports)
BIOPSY BREAST NORMAL ( 1 FDA reports)
BIOPSY COLON ABNORMAL ( 1 FDA reports)
BIOPSY GINGIVAL ( 1 FDA reports)
BIOPSY OESOPHAGUS ABNORMAL ( 1 FDA reports)
BIOPSY PLEURA ABNORMAL ( 1 FDA reports)
BIOPSY PROSTATE ABNORMAL ( 1 FDA reports)
BIOPSY SKIN ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BIOPSY STOMACH ABNORMAL ( 1 FDA reports)
BLADDER CANCER STAGE IV ( 1 FDA reports)
BLEEDING VARICOSE VEIN ( 1 FDA reports)
BLOOD ACID PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 1 FDA reports)
BLOOD ALDOSTERONE DECREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 1 FDA reports)
BLOOD AMYLASE ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE INCREASED ( 1 FDA reports)
BLOOD CAFFEINE INCREASED ( 1 FDA reports)
BLOOD CALCITONIN INCREASED ( 1 FDA reports)
BLOOD CALCIUM ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ( 1 FDA reports)
BLOOD ETHANOL INCREASED ( 1 FDA reports)
BLOOD FOLATE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN POSITIVE ( 1 FDA reports)
BLOOD INSULIN INCREASED ( 1 FDA reports)
BLOOD KETONE BODY ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD LUTEINISING HORMONE ABNORMAL ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD OSMOLARITY INCREASED ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ABNORMAL ( 1 FDA reports)
BLOOD PYRUVIC ACID DECREASED ( 1 FDA reports)
BLOOD TESTOSTERONE ABNORMAL ( 1 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE ( 1 FDA reports)
BLOOD TRIGLYCERIDES ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO DECREASED ( 1 FDA reports)
BLOOD URIC ACID ABNORMAL ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BLOOD ZINC DECREASED ( 1 FDA reports)
BODY MASS INDEX DECREASED ( 1 FDA reports)
BODY TEMPERATURE ( 1 FDA reports)
BONE DECALCIFICATION ( 1 FDA reports)
BONE FORMATION DECREASED ( 1 FDA reports)
BONE MARROW GRANULOMA ( 1 FDA reports)
BONE SCAN ( 1 FDA reports)
BOREDOM ( 1 FDA reports)
BOWEN'S DISEASE ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE ABNORMAL ( 1 FDA reports)
BRAIN NEOPLASM BENIGN ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BRAIN STEM ISCHAEMIA ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BRAIN STEM THROMBOSIS ( 1 FDA reports)
BREAST ABSCESS ( 1 FDA reports)
BREAST ATROPHY ( 1 FDA reports)
BREAST CANCER STAGE III ( 1 FDA reports)
BREAST COSMETIC SURGERY ( 1 FDA reports)
BREAST CYST EXCISION ( 1 FDA reports)
BREAST INDURATION ( 1 FDA reports)
BREAST INFLAMMATION ( 1 FDA reports)
BREATH ALCOHOL TEST POSITIVE ( 1 FDA reports)
BREATH SOUNDS DECREASED ( 1 FDA reports)
BREECH PRESENTATION ( 1 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 1 FDA reports)
BRONCHOPULMONARY DISEASE ( 1 FDA reports)
BRUCELLOSIS ( 1 FDA reports)
BRUNNER'S GLAND HYPERPLASIA ( 1 FDA reports)
BUCCAL POLYP ( 1 FDA reports)
BUDD-CHIARI SYNDROME ( 1 FDA reports)
BURGLARY VICTIM ( 1 FDA reports)
BURN DRESSING ( 1 FDA reports)
BURNING SENSATION MUCOSAL ( 1 FDA reports)
BURSA REMOVAL ( 1 FDA reports)
C-REACTIVE PROTEIN ( 1 FDA reports)
CAFE AU LAIT SPOTS ( 1 FDA reports)
CAFFEINE CONSUMPTION ( 1 FDA reports)
CAMPYLOBACTER INTESTINAL INFECTION ( 1 FDA reports)
CANDIDA PNEUMONIA ( 1 FDA reports)
CANDIDA TEST POSITIVE ( 1 FDA reports)
CAPILLARY FRAGILITY ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 15-3 INCREASED ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 27.29 INCREASED ( 1 FDA reports)
CARBON DIOXIDE ABNORMAL ( 1 FDA reports)
CARBON MONOXIDE POISONING ( 1 FDA reports)
CARCINOID TUMOUR OF THE PROSTATE ( 1 FDA reports)
CARDIAC ASSISTANCE DEVICE USER ( 1 FDA reports)
CARDIAC DISCOMFORT ( 1 FDA reports)
CARDIAC FIBRILLATION ( 1 FDA reports)
CARDIAC MONITORING ( 1 FDA reports)
CARDIAC PACEMAKER BATTERY REPLACEMENT ( 1 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 1 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CAROTID ARTERY INSUFFICIENCY ( 1 FDA reports)
CAROTID ENDARTERECTOMY ( 1 FDA reports)
CAROTID PULSE DECREASED ( 1 FDA reports)
CATARACT SUBCAPSULAR ( 1 FDA reports)
CATHETER SITE HAEMATOMA ( 1 FDA reports)
CATHETER SITE INFLAMMATION ( 1 FDA reports)
CATHETER THROMBOSIS ( 1 FDA reports)
CD4 LYMPHOCYTES ( 1 FDA reports)
CD4/CD8 RATIO INCREASED ( 1 FDA reports)
CELLULITIS ORBITAL ( 1 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM MASS ( 1 FDA reports)
CEREBELLAR HAEMATOMA ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBRAL ARTERIOVENOUS MALFORMATION HAEMORRHAGIC ( 1 FDA reports)
CEREBRAL HYGROMA ( 1 FDA reports)
CEREBROVASCULAR SPASM ( 1 FDA reports)
CEREBROVASCULAR STENOSIS ( 1 FDA reports)
CERVICAL CYST ( 1 FDA reports)
CERVIX CARCINOMA STAGE IV ( 1 FDA reports)
CHEILOSIS ( 1 FDA reports)
CHEMICAL BURN OF SKIN ( 1 FDA reports)
CHEMOTHERAPY EXTRAVASATION MANAGEMENT ( 1 FDA reports)
CHEST EXPANSION DECREASED ( 1 FDA reports)
CHOLANGIOLITIS ( 1 FDA reports)
CHOLELITHIASIS OBSTRUCTIVE ( 1 FDA reports)
CHONDROSIS ( 1 FDA reports)
CHORDAE TENDINAE RUPTURE ( 1 FDA reports)
CHORIOAMNIONITIS ( 1 FDA reports)
CHOROID NEOPLASM ( 1 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA REFRACTORY ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA STAGE 0 ( 1 FDA reports)
CHRONOTROPIC INCOMPETENCE ( 1 FDA reports)
CHRYSIASIS ( 1 FDA reports)
CINCHONISM ( 1 FDA reports)
CIRCULATING ANTICOAGULANT POSITIVE ( 1 FDA reports)
CLEFT LIP ( 1 FDA reports)
CLINICALLY ISOLATED SYNDROME ( 1 FDA reports)
CLOSTRIDIUM BACTERAEMIA ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 1 FDA reports)
COAGULATION TEST ABNORMAL ( 1 FDA reports)
COAGULATION TIME ABNORMAL ( 1 FDA reports)
COLD-STIMULUS HEADACHE ( 1 FDA reports)
COLITIS COLLAGENOUS ( 1 FDA reports)
COLLATERAL CIRCULATION ( 1 FDA reports)
COLON CANCER STAGE I ( 1 FDA reports)
COLON CANCER STAGE II ( 1 FDA reports)
COLON CANCER STAGE III ( 1 FDA reports)
COLORECTAL CANCER STAGE II ( 1 FDA reports)
COLOSTOMY CLOSURE ( 1 FDA reports)
COLOSTOMY INFECTION ( 1 FDA reports)
COLOUR VISION TESTS ABNORMAL ( 1 FDA reports)
COLPORRHAPHY ( 1 FDA reports)
COMA SCALE ABNORMAL ( 1 FDA reports)
COMPLEMENT FACTOR C3 DECREASED ( 1 FDA reports)
COMPLICATED FRACTURE ( 1 FDA reports)
COMPLICATED MIGRAINE ( 1 FDA reports)
COMPLICATION OF DEVICE REMOVAL ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED HEART ( 1 FDA reports)
CONFUSIONAL AROUSAL ( 1 FDA reports)
CONGENITAL ARTERIAL MALFORMATION ( 1 FDA reports)
CONGENITAL BRONCHOMALACIA ( 1 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 1 FDA reports)
CONGENITAL TRACHEOMALACIA ( 1 FDA reports)
CONJUNCTIVAL DISORDER ( 1 FDA reports)
CONJUNCTIVAL PALLOR ( 1 FDA reports)
CONSTRICTED AFFECT ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 1 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 1 FDA reports)
COPROLALIA ( 1 FDA reports)
CORD BLOOD TRANSPLANT THERAPY ( 1 FDA reports)
CORNEAL EROSION ( 1 FDA reports)
CORNEAL TRANSPLANT ( 1 FDA reports)
CORONARY BYPASS THROMBOSIS ( 1 FDA reports)
COUGH DECREASED ( 1 FDA reports)
CRACKLES LUNG ( 1 FDA reports)
CRANIOPLASTY ( 1 FDA reports)
CRANIOSYNOSTOSIS ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
CREATINE URINE INCREASED ( 1 FDA reports)
CREATININE URINE INCREASED ( 1 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 1 FDA reports)
CRYPTOSPORIDIOSIS INFECTION ( 1 FDA reports)
CSF GLUCOSE INCREASED ( 1 FDA reports)
CSF PRESSURE INCREASED ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
CSF VOLUME INCREASED ( 1 FDA reports)
CULTURE URINE ( 1 FDA reports)
CUTANEOUS AMYLOIDOSIS ( 1 FDA reports)
CUTANEOUS SARCOIDOSIS ( 1 FDA reports)
CYCLIC VOMITING SYNDROME ( 1 FDA reports)
CYST DRAINAGE ( 1 FDA reports)
CYSTOCELE REPAIR ( 1 FDA reports)
CYSTOSCOPY ( 1 FDA reports)
CYSTOURETHROCELE ( 1 FDA reports)
CYTOGENETIC ANALYSIS ABNORMAL ( 1 FDA reports)
CYTOKINE RELEASE SYNDROME ( 1 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 1 FDA reports)
CYTOMEGALOVIRUS TEST ( 1 FDA reports)
DEATH OF PARENT ( 1 FDA reports)
DEEP VEIN THROMBOSIS POSTOPERATIVE ( 1 FDA reports)
DEHYDROEPIANDROSTERONE INCREASED ( 1 FDA reports)
DEJA VU ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 1 FDA reports)
DENTAL FLUORIDE THERAPY ( 1 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 1 FDA reports)
DEPENDENT RUBOR ( 1 FDA reports)
DERMATILLOMANIA ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DERMATOPHYTOSIS ( 1 FDA reports)
DEVELOPMENTAL COORDINATION DISORDER ( 1 FDA reports)
DEVICE DIFFICULT TO USE ( 1 FDA reports)
DEVICE EXTRUSION ( 1 FDA reports)
DEVICE INTERACTION ( 1 FDA reports)
DEVICE PACING ISSUE ( 1 FDA reports)
DEVICE STIMULATION ISSUE ( 1 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 1 FDA reports)
DIABETIC BLINDNESS ( 1 FDA reports)
DIABETIC MICROANGIOPATHY ( 1 FDA reports)
DIABETIC NEUROPATHIC ULCER ( 1 FDA reports)
DIABETIC RETINAL OEDEMA ( 1 FDA reports)
DIAGNOSTIC PROCEDURE ( 1 FDA reports)
DIALYSIS DEVICE COMPLICATION ( 1 FDA reports)
DIASTOLIC HYPOTENSION ( 1 FDA reports)
DIEULAFOY'S VASCULAR MALFORMATION ( 1 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 1 FDA reports)
DIPLEGIA ( 1 FDA reports)
DIRECTIONAL DOPPLER FLOW TESTS ABNORMAL ( 1 FDA reports)
DISSEMINATED TUBERCULOSIS ( 1 FDA reports)
DISTAL ILEAL OBSTRUCTION SYNDROME ( 1 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DNA ANTIBODY POSITIVE ( 1 FDA reports)
DREAMY STATE ( 1 FDA reports)
DRESSLER'S SYNDROME ( 1 FDA reports)
DRUG CLEARANCE DECREASED ( 1 FDA reports)
DRUG LABEL CONFUSION ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 1 FDA reports)
DRUG THERAPY ( 1 FDA reports)
DRUG WITHDRAWAL MAINTENANCE THERAPY ( 1 FDA reports)
DRY SOCKET ( 1 FDA reports)
DUODENOGASTRIC REFLUX ( 1 FDA reports)
DYSAESTHESIA PHARYNX ( 1 FDA reports)
EAR INFECTION FUNGAL ( 1 FDA reports)
EAR INJURY ( 1 FDA reports)
EAR OPERATION ( 1 FDA reports)
EAR TUBE INSERTION ( 1 FDA reports)
ECTROPION ( 1 FDA reports)
EDUCATIONAL PROBLEM ( 1 FDA reports)
EISENMENGER'S SYNDROME ( 1 FDA reports)
EJECTION FRACTION ( 1 FDA reports)
ELDER ABUSE ( 1 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 1 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE INCREASED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
ELECTROCAUTERISATION ( 1 FDA reports)
ELECTROCONVULSIVE THERAPY ( 1 FDA reports)
ELEVATED PACING THRESHOLD ( 1 FDA reports)
ENAMEL ANOMALY ( 1 FDA reports)
ENDARTERECTOMY ( 1 FDA reports)
ENDOMETRIAL NEOPLASM ( 1 FDA reports)
ENDOSCOPY ABNORMAL ( 1 FDA reports)
ENDOSCOPY GASTROINTESTINAL ( 1 FDA reports)
ENGRAFTMENT SYNDROME ( 1 FDA reports)
ENTERITIS INFECTIOUS ( 1 FDA reports)
ENTEROBACTER SEPSIS ( 1 FDA reports)
ENTEROCOLITIS BACTERIAL ( 1 FDA reports)
ENTEROCOLITIS VIRAL ( 1 FDA reports)
ENZYME LEVEL DECREASED ( 1 FDA reports)
EOSINOPHILIC OESOPHAGITIS ( 1 FDA reports)
EOSINOPHILS URINE PRESENT ( 1 FDA reports)
EPIDURAL ANAESTHESIA ( 1 FDA reports)
EPIPHYSIOLYSIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
EXCESSIVE MASTURBATION ( 1 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EXPOSURE TO CONTAMINATED AIR ( 1 FDA reports)
EXPOSURE TO EXTREME TEMPERATURE ( 1 FDA reports)
EXPOSURE VIA FATHER ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EXTERNAL EAR INFLAMMATION ( 1 FDA reports)
EXTERNAL EAR LESION EXCISION ( 1 FDA reports)
EXTRAMEDULLARY HAEMOPOIESIS ( 1 FDA reports)
EXTRAOCULAR MUSCLE DISORDER ( 1 FDA reports)
EYE BURNS ( 1 FDA reports)
EYELID IRRITATION ( 1 FDA reports)
EYELID PAIN ( 1 FDA reports)
EYELID VASCULAR DISORDER ( 1 FDA reports)
FACIAL ASYMMETRY ( 1 FDA reports)
FACIAL DYSMORPHISM ( 1 FDA reports)
FAECAL VOLUME DECREASED ( 1 FDA reports)
FALLOT'S TETRALOGY ( 1 FDA reports)
FALSE NEGATIVE INVESTIGATION RESULT ( 1 FDA reports)
FALSE POSITIVE INVESTIGATION RESULT ( 1 FDA reports)
FAMILIAL TREMOR ( 1 FDA reports)
FASCIOTOMY ( 1 FDA reports)
FEMORAL ARTERY ANEURYSM ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS ( 1 FDA reports)
FILARIASIS ( 1 FDA reports)
FLAT CHEST ( 1 FDA reports)
FLOPPY IRIS SYNDROME ( 1 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 1 FDA reports)
FOETAL DISORDER ( 1 FDA reports)
FOETAL HEART RATE DECELERATION ( 1 FDA reports)
FOETAL HYPOKINESIA ( 1 FDA reports)
FOETAL MALFORMATION ( 1 FDA reports)
FOETOR HEPATICUS ( 1 FDA reports)
FORAMINOTOMY ( 1 FDA reports)
FRACTURE MALUNION ( 1 FDA reports)
FREE PROSTATE-SPECIFIC ANTIGEN DECREASED ( 1 FDA reports)
FREE THYROXINE INDEX DECREASED ( 1 FDA reports)
FREEZING PHENOMENON ( 1 FDA reports)
FRONTOTEMPORAL DEMENTIA ( 1 FDA reports)
FUNGAL PERITONITIS ( 1 FDA reports)
FUNGAL SEPSIS ( 1 FDA reports)
FUNGATING WOUND ( 1 FDA reports)
FUNGUS STOOL IDENTIFIED ( 1 FDA reports)
FUSARIUM INFECTION ( 1 FDA reports)
GANGLIONEUROMA ( 1 FDA reports)
GASTRIC POLYPECTOMY ( 1 FDA reports)
GASTRIC STENOSIS ( 1 FDA reports)
GASTRIC ULCER SURGERY ( 1 FDA reports)
GASTRODUODENAL ULCER ( 1 FDA reports)
GASTROENTERITIS CRYPTOSPORIDIAL ( 1 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 1 FDA reports)
GASTROENTERITIS NONINFECTIOUS ( 1 FDA reports)
GASTROENTERITIS NOROVIRUS ( 1 FDA reports)
GASTROINTESTINAL DISORDER POSTOPERATIVE ( 1 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 1 FDA reports)
GASTROINTESTINAL SURGERY ( 1 FDA reports)
GASTROOESOPHAGEAL CANCER ( 1 FDA reports)
GENERAL NUTRITION DISORDER ( 1 FDA reports)
GENITAL CANDIDIASIS ( 1 FDA reports)
GENITAL INJURY ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GENITAL PRURITUS FEMALE ( 1 FDA reports)
GINGIVAL BLISTER ( 1 FDA reports)
GINGIVAL DISCOLOURATION ( 1 FDA reports)
GLAUCOMATOUS OPTIC DISC ATROPHY ( 1 FDA reports)
GLOBAL AMNESIA ( 1 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 1 FDA reports)
GLOMERULONEPHROPATHY ( 1 FDA reports)
GLOMUS TUMOUR ( 1 FDA reports)
GLOSSECTOMY ( 1 FDA reports)
GLOSSOPHARYNGEAL NERVE DISORDER ( 1 FDA reports)
GLUCOSE TOLERANCE INCREASED ( 1 FDA reports)
GLUCOSE TOLERANCE TEST ABNORMAL ( 1 FDA reports)
GLYCOGEN STORAGE DISEASE TYPE VIII ( 1 FDA reports)
GLYCOPEPTIDE ANTIBIOTIC RESISTANT ENTEROCOCCAL INFECTION ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN DECREASED ( 1 FDA reports)
GONORRHOEA ( 1 FDA reports)
GOUTY TOPHUS ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRAFT INFECTION ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
GRAM STAIN POSITIVE ( 1 FDA reports)
GRANULOMA ANNULARE ( 1 FDA reports)
GROWING PAINS ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
HAEMANGIOMA OF SKIN ( 1 FDA reports)
HAEMANGIOMA OF SPLEEN ( 1 FDA reports)
HAEMATOCRIT ( 1 FDA reports)
HAEMATOPOIETIC NEOPLASM ( 1 FDA reports)
HAEMOBILIA ( 1 FDA reports)
HAEMODIALYSIS COMPLICATION ( 1 FDA reports)
HAEMODIALYSIS-INDUCED SYMPTOM ( 1 FDA reports)
HAEMODYNAMIC TEST ABNORMAL ( 1 FDA reports)
HAEMOLYTIC TRANSFUSION REACTION ( 1 FDA reports)
HAEMORRHAGIC ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
HAEMORRHAGIC CYST ( 1 FDA reports)
HAIRY CELL LEUKAEMIA ( 1 FDA reports)
HALO VISION ( 1 FDA reports)
HAPTOGLOBIN INCREASED ( 1 FDA reports)
HEAD AND NECK CANCER STAGE III ( 1 FDA reports)
HEARING DISABILITY ( 1 FDA reports)
HEART ALTERNATION ( 1 FDA reports)
HEART SOUNDS ( 1 FDA reports)
HEART VALVE CALCIFICATION ( 1 FDA reports)
HEART VALVE STENOSIS ( 1 FDA reports)
HEAT THERAPY ( 1 FDA reports)
HEMIANOPIA HETERONYMOUS ( 1 FDA reports)
HEMICEPHALALGIA ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 1 FDA reports)
HEPATIC ANGIOSARCOMA ( 1 FDA reports)
HEPATIC HAEMATOMA ( 1 FDA reports)
HEPATIC ISCHAEMIA ( 1 FDA reports)
HEPATIC VEIN DILATATION ( 1 FDA reports)
HEPATITIS A POSITIVE ( 1 FDA reports)
HEPATITIS C VIRUS ( 1 FDA reports)
HEPATOBILIARY SCAN ( 1 FDA reports)
HEREDITARY HAEMORRHAGIC TELANGIECTASIA ( 1 FDA reports)
HERNIA OBSTRUCTIVE ( 1 FDA reports)
HERPES OPHTHALMIC ( 1 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 1 FDA reports)
HERPES ZOSTER MULTI-DERMATOMAL ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN ABNORMAL ( 1 FDA reports)
HIP SWELLING ( 1 FDA reports)
HISTONE ANTIBODY POSITIVE ( 1 FDA reports)
HODGKIN'S DISEASE MIXED CELLULARITY STAGE IV ( 1 FDA reports)
HOMICIDE ( 1 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 1 FDA reports)
HUMAN SEMINAL PLASMA HYPERSENSITIVITY ( 1 FDA reports)
HYDROCHOLECYSTIS ( 1 FDA reports)
HYDROMETRA ( 1 FDA reports)
HYPERADRENALISM ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERCATABOLISM ( 1 FDA reports)
HYPERKINETIC HEART SYNDROME ( 1 FDA reports)
HYPEROXALURIA ( 1 FDA reports)
HYPERPROLACTINAEMIA ( 1 FDA reports)
HYPERPYREXIA ( 1 FDA reports)
HYPERSPLENISM ACQUIRED ( 1 FDA reports)
HYPERTRICHOSIS ( 1 FDA reports)
HYPERTROPHIC SCAR ( 1 FDA reports)
HYPERTROPHY BREAST ( 1 FDA reports)
HYPERTROPHY OF TONGUE PAPILLAE ( 1 FDA reports)
HYPERVOLAEMIA ( 1 FDA reports)
HYPOALDOSTERONISM ( 1 FDA reports)
HYPOMETABOLISM ( 1 FDA reports)
HYPOPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPOPHONESIS ( 1 FDA reports)
HYPOPHYSITIS ( 1 FDA reports)
HYPOPITUITARISM ( 1 FDA reports)
HYPOSPADIAS ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDERS ( 1 FDA reports)
HYPOTHYROIDISM POSTOPERATIVE ( 1 FDA reports)
IDIOPATHIC CAPILLARITIS ( 1 FDA reports)
IGA NEPHROPATHY ( 1 FDA reports)
IIIRD NERVE PARALYSIS ( 1 FDA reports)
ILEAL PERFORATION ( 1 FDA reports)
ILIAC VEIN THROMBOSIS ( 1 FDA reports)
IMMEDIATE POST-INJECTION REACTION ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 1 FDA reports)
IMPERFORATE OESOPHAGUS ( 1 FDA reports)
IMPLANT SITE CELLULITIS ( 1 FDA reports)
IMPLANT SITE EFFUSION ( 1 FDA reports)
IMPLANT SITE PAIN ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR REMOVAL ( 1 FDA reports)
INCISION SITE HAEMATOMA ( 1 FDA reports)
INCISIONAL HERNIA REPAIR ( 1 FDA reports)
INFANTILE SPASMS ( 1 FDA reports)
INFECTED INSECT BITE ( 1 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
INFERIOR VENA CAVA DILATATION ( 1 FDA reports)
INFERTILITY FEMALE ( 1 FDA reports)
INFLUENZA A VIRUS TEST POSITIVE ( 1 FDA reports)
INFUSION ( 1 FDA reports)
INFUSION SITE IRRITATION ( 1 FDA reports)
INFUSION SITE PHLEBITIS ( 1 FDA reports)
INFUSION SITE RASH ( 1 FDA reports)
INJECTION RELATED REACTION ( 1 FDA reports)
INJECTION SITE COLDNESS ( 1 FDA reports)
INJECTION SITE CYST ( 1 FDA reports)
INJECTION SITE EXFOLIATION ( 1 FDA reports)
INJECTION SITE HYPERSENSITIVITY ( 1 FDA reports)
INJECTION SITE HYPERTROPHY ( 1 FDA reports)
INJECTION SITE JOINT REDNESS ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INJECTION SITE RECALL REACTION ( 1 FDA reports)
INJECTION SITE STREAKING ( 1 FDA reports)
INJECTION SITE THROMBOSIS ( 1 FDA reports)
INJURY ASPHYXIATION ( 1 FDA reports)
INSOMNIA RELATED TO ANOTHER MENTAL CONDITION ( 1 FDA reports)
INSTILLATION SITE ERYTHEMA ( 1 FDA reports)
INSULIN RESISTANCE SYNDROME ( 1 FDA reports)
INSULIN-REQUIRING TYPE II DIABETES MELLITUS ( 1 FDA reports)
INTERCEPTED MEDICATION ERROR ( 1 FDA reports)
INTERMITTENT EXPLOSIVE DISORDER ( 1 FDA reports)
INTERVERTEBRAL DISC CALCIFICATION ( 1 FDA reports)
INTESTINAL ANASTOMOSIS COMPLICATION ( 1 FDA reports)
INTESTINAL FISTULA REPAIR ( 1 FDA reports)
INTESTINAL GASTRIC METAPLASIA ( 1 FDA reports)
INTESTINAL HAEMATOMA ( 1 FDA reports)
INTESTINAL HYPOMOTILITY ( 1 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 1 FDA reports)
INTESTINAL SPASM ( 1 FDA reports)
INTESTINAL STRANGULATION ( 1 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE EXPELLED ( 1 FDA reports)
INTRACARDIAC MASS ( 1 FDA reports)
INTUBATION COMPLICATION ( 1 FDA reports)
INVESTIGATION ( 1 FDA reports)
IODINE ALLERGY ( 1 FDA reports)
IRIS DISORDER ( 1 FDA reports)
ISCHAEMIC NEPHROPATHY ( 1 FDA reports)
JEJUNITIS ( 1 FDA reports)
JOINT WARMTH ( 1 FDA reports)
KERATITIS BACTERIAL ( 1 FDA reports)
KERATOMILEUSIS ( 1 FDA reports)
KETOSIS ( 1 FDA reports)
KLEBSIELLA BACTERAEMIA ( 1 FDA reports)
KYPHOSIS CONGENITAL ( 1 FDA reports)
LACRIMAL ATROPHY ( 1 FDA reports)
LACRIMAL DISORDER ( 1 FDA reports)
LACTATION DISORDER ( 1 FDA reports)
LACTOBACILLUS INFECTION ( 1 FDA reports)
LAPAROTOMY ( 1 FDA reports)
LARGE CELL CARCINOMA OF THE RESPIRATORY TRACT STAGE UNSPECIFIED ( 1 FDA reports)
LARGE INTESTINAL STRICTURE ( 1 FDA reports)
LARYNGEAL INJURY ( 1 FDA reports)
LARYNGEAL POLYP ( 1 FDA reports)
LARYNGEAL STENOSIS ( 1 FDA reports)
LAXATIVE ABUSE ( 1 FDA reports)
LEFT ATRIAL HYPERTROPHY ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE DECREASED ( 1 FDA reports)
LENS DISORDER ( 1 FDA reports)
LENS EXTRACTION ( 1 FDA reports)
LESION EXCISION ( 1 FDA reports)
LEUKOCYTE ANTIGEN B-27 POSITIVE ( 1 FDA reports)
LIGHT CHAIN DISEASE ( 1 FDA reports)
LIMB PROSTHESIS USER ( 1 FDA reports)
LINEAR IGA DISEASE ( 1 FDA reports)
LIPASE ( 1 FDA reports)
LIPASE ABNORMAL ( 1 FDA reports)
LIPASE DECREASED ( 1 FDA reports)
LIPIDOSIS ( 1 FDA reports)
LIPODYSTROPHY ACQUIRED ( 1 FDA reports)
LIPOSUCTION ( 1 FDA reports)
LISTERIOSIS ( 1 FDA reports)
LIVE BIRTH ( 1 FDA reports)
LIVER FUNCTION TEST ( 1 FDA reports)
LIVING IN RESIDENTIAL INSTITUTION ( 1 FDA reports)
LOCALISED EXFOLIATION ( 1 FDA reports)
LOCALISED SKIN REACTION ( 1 FDA reports)
LOCKED-IN SYNDROME ( 1 FDA reports)
LOEFFLER'S SYNDROME ( 1 FDA reports)
LOOSE ASSOCIATIONS ( 1 FDA reports)
LOSS OF DREAMING ( 1 FDA reports)
LOSS OF PROPRIOCEPTION ( 1 FDA reports)
LOW BIRTH WEIGHT BABY ( 1 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE I ( 1 FDA reports)
LUNG CYST ( 1 FDA reports)
LUNG HERNIA ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE III ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE IV ( 1 FDA reports)
LUNG WEDGE RESECTION ( 1 FDA reports)
LUPUS NEPHRITIS ( 1 FDA reports)
LYMPHATIC DISORDER ( 1 FDA reports)
LYMPHOCYTE COUNT ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE ABNORMAL ( 1 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
LYMPHOHISTIOCYTOSIS ( 1 FDA reports)
MACROGNATHIA ( 1 FDA reports)
MACULAR ISCHAEMIA ( 1 FDA reports)
MAGNESIUM DEFICIENCY ( 1 FDA reports)
MALIGNANT FIBROUS HISTIOCYTOMA ( 1 FDA reports)
MALIGNANT NEOPLASM OF SPINAL CORD ( 1 FDA reports)
MALIGNANT TRANSFORMATION ( 1 FDA reports)
MANTLE CELL LYMPHOMA REFRACTORY ( 1 FDA reports)
MASTOIDECTOMY ( 1 FDA reports)
MASTOPTOSIS ( 1 FDA reports)
MATERNAL EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
MATERNAL EXPOSURE DURING DELIVERY ( 1 FDA reports)
MAY-THURNER SYNDROME ( 1 FDA reports)
MEASLES ( 1 FDA reports)
MEDICAL DEVICE CHANGE ( 1 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 1 FDA reports)
MEDICAL INDUCTION OF COMA ( 1 FDA reports)
MEGACOLON ACQUIRED ( 1 FDA reports)
MEIGE'S SYNDROME ( 1 FDA reports)
MELANODERMIA ( 1 FDA reports)
MELANOMA RECURRENT ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENINGITIS LISTERIA ( 1 FDA reports)
MENINGITIS STAPHYLOCOCCAL ( 1 FDA reports)
MENINGOCELE ( 1 FDA reports)
MENINGOENCEPHALITIS BACTERIAL ( 1 FDA reports)
MENTAL DISABILITY ( 1 FDA reports)
MENTAL RETARDATION ( 1 FDA reports)
MESENTERIC PANNICULITIS ( 1 FDA reports)
METAMYELOCYTE COUNT INCREASED ( 1 FDA reports)
METANEPHRINE URINE INCREASED ( 1 FDA reports)
METASTASES TO PANCREAS ( 1 FDA reports)
METASTASES TO PERIPHERAL VASCULAR SYSTEM ( 1 FDA reports)
METASTATIC CARCINOMA OF THE BLADDER ( 1 FDA reports)
METATARSAL EXCISION ( 1 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 1 FDA reports)
MICROCOCCUS INFECTION ( 1 FDA reports)
MICROGNATHIA ( 1 FDA reports)
MICROGRAPHIA ( 1 FDA reports)
MICROVASCULAR ANGINA ( 1 FDA reports)
MIDDLE EAR PROSTHESIS INSERTION ( 1 FDA reports)
MILD MENTAL RETARDATION ( 1 FDA reports)
MINERAL DEFICIENCY ( 1 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 1 FDA reports)
MITOCHONDRIAL TOXICITY ( 1 FDA reports)
MIXED DEAFNESS ( 1 FDA reports)
MONONEUROPATHY ( 1 FDA reports)
MUCOCUTANEOUS CANDIDIASIS ( 1 FDA reports)
MUCOSA VESICLE ( 1 FDA reports)
MUCOSAL ATROPHY ( 1 FDA reports)
MUCOSAL EXFOLIATION ( 1 FDA reports)
MULTIFOCAL MICRONODULAR PNEUMOCYTE HYPERPLASIA ( 1 FDA reports)
MULTIPLE CHEMICAL SENSITIVITY ( 1 FDA reports)
MUMPS ( 1 FDA reports)
MUNCHAUSEN'S SYNDROME ( 1 FDA reports)
MUSCLE ENZYME INCREASED ( 1 FDA reports)
MUSCLE NECROSIS ( 1 FDA reports)
MUTISM ( 1 FDA reports)
MYCOBACTERIUM ABSCESSUS INFECTION ( 1 FDA reports)
MYCOBACTERIUM CHELONAE INFECTION ( 1 FDA reports)
MYCOBACTERIUM CHELONEI INFECTION ( 1 FDA reports)
MYELOCYTE COUNT INCREASED ( 1 FDA reports)
MYELOCYTE PRESENT ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 1 FDA reports)
MYOCARDIAL CALCIFICATION ( 1 FDA reports)
MYOCARDIAL FIBROSIS ( 1 FDA reports)
MYOCARDIAL RUPTURE ( 1 FDA reports)
MYOFASCIAL SPASM ( 1 FDA reports)
MYOGLOBINURIA ( 1 FDA reports)
MYOSITIS OSSIFICANS ( 1 FDA reports)
N-TELOPEPTIDE URINE DECREASED ( 1 FDA reports)
NAIL AVULSION ( 1 FDA reports)
NAIL OPERATION ( 1 FDA reports)
NARROW ANTERIOR CHAMBER ANGLE ( 1 FDA reports)
NASAL ABSCESS ( 1 FDA reports)
NASAL CAVITY CANCER ( 1 FDA reports)
NASAL INFLAMMATION ( 1 FDA reports)
NASAL MUCOSAL DISCOLOURATION ( 1 FDA reports)
NASAL VESTIBULITIS ( 1 FDA reports)
NECK EXPLORATION ( 1 FDA reports)
NEOPLASM OF APPENDIX ( 1 FDA reports)
NEPHROSTOMY ( 1 FDA reports)
NERVE DEGENERATION ( 1 FDA reports)
NEURECTOMY ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 1 FDA reports)
NEUROFIBROMA ( 1 FDA reports)
NEUROMYELITIS OPTICA ( 1 FDA reports)
NEUROTRANSMITTER LEVEL ALTERED ( 1 FDA reports)
NEUTROPENIC COLITIS ( 1 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 1 FDA reports)
NIPPLE DISORDER ( 1 FDA reports)
NON-ALCOHOLIC STEATOHEPATITIS ( 1 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE III ( 1 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 1 FDA reports)
NOSE DEFORMITY ( 1 FDA reports)
NUCLEATED RED CELLS ( 1 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 1 FDA reports)
OCULAR MYASTHENIA ( 1 FDA reports)
OCULAR NEOPLASM ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA STAGE IV ( 1 FDA reports)
OESOPHAGEAL DYSPLASIA ( 1 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 1 FDA reports)
OESOPHAGEAL PAPILLOMA ( 1 FDA reports)
OESOPHAGEAL ULCER PERFORATION ( 1 FDA reports)
OESOPHAGOENTEROSTOMY ( 1 FDA reports)
OESOPHAGOSCOPY ( 1 FDA reports)
OESTROGENIC EFFECT ( 1 FDA reports)
OLFACTORY NERVE DISORDER ( 1 FDA reports)
ONCOCYTOMA ( 1 FDA reports)
ONYCHORRHEXIS ( 1 FDA reports)
OPIATES POSITIVE ( 1 FDA reports)
OPTIC NERVE CUPPING ( 1 FDA reports)
OPTIC NERVE INFARCTION ( 1 FDA reports)
OPTIC NERVE OPERATION ( 1 FDA reports)
ORAL ADMINISTRATION COMPLICATION ( 1 FDA reports)
ORAL DISCHARGE ( 1 FDA reports)
ORAL DYSAESTHESIA ( 1 FDA reports)
ORAL MUCOSA EROSION ( 1 FDA reports)
OROPHARYNGEAL SPASM ( 1 FDA reports)
OROPHARYNGEAL SURGERY ( 1 FDA reports)
OROPHARYNGITIS FUNGAL ( 1 FDA reports)
ORTHODONTIC APPLIANCE COMPLICATION ( 1 FDA reports)
OSSICLE DISORDER ( 1 FDA reports)
OSTECTOMY ( 1 FDA reports)
OSTEOCHONDRITIS ( 1 FDA reports)
OSTEOMYELITIS BACTERIAL ( 1 FDA reports)
OTITIS MEDIA CHRONIC ( 1 FDA reports)
OTOTOXICITY ( 1 FDA reports)
OVARIAN ADENOMA ( 1 FDA reports)
OVARIAN ATROPHY ( 1 FDA reports)
OVARIAN CYSTECTOMY ( 1 FDA reports)
OVARIAN ENLARGEMENT ( 1 FDA reports)
OVULATION DISORDER ( 1 FDA reports)
OVULATION PAIN ( 1 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 1 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 1 FDA reports)
OXYGEN SATURATION ( 1 FDA reports)
PACEMAKER GENERATED RHYTHM ( 1 FDA reports)
PANCREATIC ABSCESS ( 1 FDA reports)
PANCREATIC FISTULA ( 1 FDA reports)
PANCREATIC HAEMORRHAGE ( 1 FDA reports)
PANCREATIC OPERATION ( 1 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 1 FDA reports)
PAPILLITIS ( 1 FDA reports)
PARACENTESIS ( 1 FDA reports)
PARAKERATOSIS ( 1 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 1 FDA reports)
PARASITE STOOL TEST POSITIVE ( 1 FDA reports)
PARASOMNIA ( 1 FDA reports)
PARATHYROID GLAND ENLARGEMENT ( 1 FDA reports)
PARATHYROID TUMOUR ( 1 FDA reports)
PARENTERAL NUTRITION ( 1 FDA reports)
PARKINSONIAN GAIT ( 1 FDA reports)
PARVOVIRUS INFECTION ( 1 FDA reports)
PATIENT ISOLATION ( 1 FDA reports)
PATIENT-DEVICE INCOMPATIBILITY ( 1 FDA reports)
PECTUS EXCAVATUM ( 1 FDA reports)
PELVIC DEFORMITY ( 1 FDA reports)
PELVIC HAEMORRHAGE ( 1 FDA reports)
PELVIC INFECTION ( 1 FDA reports)
PELVIC ORGAN INJURY ( 1 FDA reports)
PEMPHIGUS ( 1 FDA reports)
PERICARDITIS ADHESIVE ( 1 FDA reports)
PERIDIVERTICULAR ABSCESS ( 1 FDA reports)
PERINEAL ABSCESS ( 1 FDA reports)
PERINEAL ULCERATION ( 1 FDA reports)
PERINEPHRIC COLLECTION ( 1 FDA reports)
PERIPHERAL PULSE DECREASED ( 1 FDA reports)
PERIPORTAL SINUS DILATATION ( 1 FDA reports)
PERIPROSTHETIC FRACTURE ( 1 FDA reports)
PERIPROSTHETIC OSTEOLYSIS ( 1 FDA reports)
PERISTALSIS VISIBLE ( 1 FDA reports)
PERITONEAL CARCINOMA ( 1 FDA reports)
PERITONEAL EFFLUENT ABNORMAL ( 1 FDA reports)
PERITONEAL FLUID ANALYSIS ABNORMAL ( 1 FDA reports)
PERITONEAL INFECTION ( 1 FDA reports)
PERITONSILLAR ABSCESS ( 1 FDA reports)
PERSECUTORY DELUSION ( 1 FDA reports)
PERTUSSIS ( 1 FDA reports)
PH BODY FLUID DECREASED ( 1 FDA reports)
PHARYNGEAL LESION ( 1 FDA reports)
PHARYNGEAL LEUKOPLAKIA ( 1 FDA reports)
PHARYNGEAL NECROSIS ( 1 FDA reports)
PHARYNGOLARYNGEAL DISCOMFORT ( 1 FDA reports)
PHARYNX DISCOMFORT ( 1 FDA reports)
PHLEBOTHROMBOSIS ( 1 FDA reports)
PHOTOSENSITIVITY ALLERGIC REACTION ( 1 FDA reports)
PIGMENT DISPERSION SYNDROME ( 1 FDA reports)
PIGMENT NEPHROPATHY ( 1 FDA reports)
PITUITARY TUMOUR BENIGN ( 1 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 1 FDA reports)
PITYRIASIS RUBRA PILARIS ( 1 FDA reports)
PLACENTAL DISORDER ( 1 FDA reports)
PLASMABLASTIC LYMPHOMA ( 1 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 1 FDA reports)
PLATELET MORPHOLOGY ABNORMAL ( 1 FDA reports)
PLEURISY VIRAL ( 1 FDA reports)
PLEUROPERICARDITIS ( 1 FDA reports)
PLICA SYNDROME ( 1 FDA reports)
PNEUMATURIA ( 1 FDA reports)
PNEUMOCEPHALUS ( 1 FDA reports)
PNEUMONIA CHLAMYDIAL ( 1 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 1 FDA reports)
PNEUMONIA HERPES VIRAL ( 1 FDA reports)
PNEUMONITIS CRYPTOCOCCAL ( 1 FDA reports)
PNEUMOTHORAX SPONTANEOUS TENSION ( 1 FDA reports)
POISONING DELIBERATE ( 1 FDA reports)
POLYARTERITIS NODOSA ( 1 FDA reports)
POLYCYTHAEMIA VERA ( 1 FDA reports)
POLYGLANDULAR DISORDER ( 1 FDA reports)
POLYHYDRAMNIOS ( 1 FDA reports)
POLYMEDICATION ( 1 FDA reports)
POLYMYALGIA ( 1 FDA reports)
POLYNEUROPATHY IDIOPATHIC PROGRESSIVE ( 1 FDA reports)
POPLITEAL PULSE DECREASED ( 1 FDA reports)
PORPHYRIA ( 1 FDA reports)
PORTAL SHUNT ( 1 FDA reports)
PORTAL TRIADITIS ( 1 FDA reports)
PORTOPULMONARY HYPERTENSION ( 1 FDA reports)
POSITIVE END-EXPIRATORY PRESSURE ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 1 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 1 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 1 FDA reports)
POST PROCEDURAL DISCHARGE ( 1 FDA reports)
POST PROCEDURAL MYOCARDIAL INFARCTION ( 1 FDA reports)
POST PROCEDURAL URINE LEAK ( 1 FDA reports)
POST PROCEDURAL VOMITING ( 1 FDA reports)
POST-TRAUMATIC HEADACHE ( 1 FDA reports)
POSTINFARCTION ANGINA ( 1 FDA reports)
POSTOPERATIVE ABSCESS ( 1 FDA reports)
POSTURAL REFLEX IMPAIRMENT ( 1 FDA reports)
POSTURING ( 1 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 1 FDA reports)
PREGNANCY AFTER POST COITAL CONTRACEPTION ( 1 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 1 FDA reports)
PREGNANCY OF PARTNER ( 1 FDA reports)
PREHYPERTENSION ( 1 FDA reports)
PREMATURE AGEING ( 1 FDA reports)
PREMATURE EJACULATION ( 1 FDA reports)
PRESBYACUSIS ( 1 FDA reports)
PRESCRIPTION FORM TAMPERING ( 1 FDA reports)
PRODUCT BLISTER PACKAGING ISSUE ( 1 FDA reports)
PRODUCT COATING ISSUE ( 1 FDA reports)
PRODUCT COLOUR ISSUE ( 1 FDA reports)
PRODUCT CONTAINER ISSUE ( 1 FDA reports)
PRODUCT CONTAINER SEAL ISSUE ( 1 FDA reports)
PRODUCT CONTAMINATION ( 1 FDA reports)
PRODUCT COUNTERFEIT ( 1 FDA reports)
PRODUCT GEL FORMATION ( 1 FDA reports)
PRODUCT OUTER PACKAGING ISSUE ( 1 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 1 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 1 FDA reports)
PROGRESSIVE RELAPSING MULTIPLE SCLEROSIS ( 1 FDA reports)
PROLONGED EXPIRATION ( 1 FDA reports)
PROSTATE CANCER STAGE II ( 1 FDA reports)
PROSTATE INFECTION ( 1 FDA reports)
PROSTATIC CALCIFICATION ( 1 FDA reports)
PROSTATIC HAEMORRHAGE ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN ABNORMAL ( 1 FDA reports)
PROTEIN C DEFICIENCY ( 1 FDA reports)
PROTEUS TEST POSITIVE ( 1 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PRURITUS ANI ( 1 FDA reports)
PSEUDOEXFOLIATION OF LENS CAPSULE ( 1 FDA reports)
PSEUDOLYMPHOMA ( 1 FDA reports)
PSEUDOMENINGOCELE ( 1 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 1 FDA reports)
PSEUDOMYXOMA PERITONEI ( 1 FDA reports)
PSYCHIATRIC EVALUATION ABNORMAL ( 1 FDA reports)
PSYCHOGENIC PAIN DISORDER ( 1 FDA reports)
PSYCHOPATHIC PERSONALITY ( 1 FDA reports)
PUBIC PAIN ( 1 FDA reports)
PULMONARY AMYLOIDOSIS ( 1 FDA reports)
PULMONARY FISTULA ( 1 FDA reports)
PULMONARY FUNCTION TEST INCREASED ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PULMONARY RENAL SYNDROME ( 1 FDA reports)
PULMONARY SARCOIDOSIS ( 1 FDA reports)
PULMONARY VALVE STENOSIS CONGENITAL ( 1 FDA reports)
PULMONARY VASCULAR RESISTANCE ABNORMALITY ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
PYELONEPHRITIS CHRONIC ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RADIAL NERVE INJURY ( 1 FDA reports)
RADIATION FIBROSIS - LUNG ( 1 FDA reports)
RADICAL NECK DISSECTION ( 1 FDA reports)
RADIOISOTOPE SCAN ( 1 FDA reports)
RASH FOLLICULAR ( 1 FDA reports)
REACTION TO COLOURING ( 1 FDA reports)
REACTIVE AIRWAYS DYSFUNCTION SYNDROME ( 1 FDA reports)
RECTAL STENOSIS ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
RECTOSIGMOID CANCER ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RED BLOOD CELL MORPHOLOGY ABNORMAL ( 1 FDA reports)
RED BLOOD CELL NUCLEATED MORPHOLOGY PRESENT ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELLS SEMEN ( 1 FDA reports)
REFLEX SYMPATHETIC DYSTROPHY ( 1 FDA reports)
REMOVAL OF FOREIGN BODY FROM THROAT ( 1 FDA reports)
RENAL ARTERY FIBROMUSCULAR DYSPLASIA ( 1 FDA reports)
RENAL ARTERY STENT PLACEMENT ( 1 FDA reports)
RENAL CANCER STAGE IV ( 1 FDA reports)
RENAL CORTICAL NECROSIS ( 1 FDA reports)
RENAL CYST HAEMORRHAGE ( 1 FDA reports)
RENAL EMBOLISM ( 1 FDA reports)
RENAL INFARCT ( 1 FDA reports)
RENAL NECROSIS ( 1 FDA reports)
RENAL TUBULAR ATROPHY ( 1 FDA reports)
RENAL VENOUS CONGESTION ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
RENIN DECREASED ( 1 FDA reports)
RENOVASCULAR HYPERTENSION ( 1 FDA reports)
REPETITIVE SPEECH ( 1 FDA reports)
RESPIRATORY TRACT NEOPLASM ( 1 FDA reports)
RESPIRATORY TRACT OEDEMA ( 1 FDA reports)
RESPIROVIRUS TEST POSITIVE ( 1 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 1 FDA reports)
RETICULOCYTOSIS ( 1 FDA reports)
RETINAL ANEURYSM ( 1 FDA reports)
RETINAL DEPIGMENTATION ( 1 FDA reports)
RETINAL DEPOSITS ( 1 FDA reports)
RETINAL EXUDATES ( 1 FDA reports)
RETINAL ISCHAEMIA ( 1 FDA reports)
RETINAL MICROANEURYSMS ( 1 FDA reports)
RETINAL OEDEMA ( 1 FDA reports)
RETINAL PIGMENTATION ( 1 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 1 FDA reports)
RETINITIS ( 1 FDA reports)
RETROGRADE EJACULATION ( 1 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
RHEUMATOID FACTOR ( 1 FDA reports)
RHYTHM IDIOVENTRICULAR ( 1 FDA reports)
RIB EXCISION ( 1 FDA reports)
RUBELLA ANTIBODY POSITIVE ( 1 FDA reports)
RUPTURED ECTOPIC PREGNANCY ( 1 FDA reports)
SACRAL PAIN ( 1 FDA reports)
SALIVA ALTERED ( 1 FDA reports)
SALIVA DISCOLOURATION ( 1 FDA reports)
SALIVARY GLAND ATROPHY ( 1 FDA reports)
SALIVARY GLAND NEOPLASM ( 1 FDA reports)
SALIVARY GLAND PAIN ( 1 FDA reports)
SALMONELLA SEPSIS ( 1 FDA reports)
SALPINGO-OOPHORECTOMY ( 1 FDA reports)
SARCOMA METASTATIC ( 1 FDA reports)
SCAN ABDOMEN ABNORMAL ( 1 FDA reports)
SCAR PAIN ( 1 FDA reports)
SCARLET FEVER ( 1 FDA reports)
SCHAMBERG'S DISEASE ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER BIPOLAR TYPE ( 1 FDA reports)
SCHOOL REFUSAL ( 1 FDA reports)
SCIATIC NERVE INJURY ( 1 FDA reports)
SCLERAL HAEMORRHAGE ( 1 FDA reports)
SCLERITIS ( 1 FDA reports)
SCLEROEDEMA ( 1 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 1 FDA reports)
SECONDARY HYPERTENSION ( 1 FDA reports)
SEIZURE LIKE PHENOMENA ( 1 FDA reports)
SEMINOMA ( 1 FDA reports)
SENSATION OF BLOCK IN EAR ( 1 FDA reports)
SERUM FERRITIN ABNORMAL ( 1 FDA reports)
SERUM SICKNESS-LIKE REACTION ( 1 FDA reports)
SHARED PSYCHOTIC DISORDER ( 1 FDA reports)
SHOCK HYPOGLYCAEMIC ( 1 FDA reports)
SHOPLIFTING ( 1 FDA reports)
SHUNT THROMBOSIS ( 1 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SKIN ULCER HAEMORRHAGE ( 1 FDA reports)
SKULL FRACTURED BASE ( 1 FDA reports)
SLEEP TERROR ( 1 FDA reports)
SLOW RESPONSE TO STIMULI ( 1 FDA reports)
SMEAR VAGINAL ABNORMAL ( 1 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 1 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 1 FDA reports)
SPINAL CORD INFARCTION ( 1 FDA reports)
SPINAL CORD INJURY ( 1 FDA reports)
SPINAL CORD OPERATION ( 1 FDA reports)
SPINAL MUSCULAR ATROPHY ( 1 FDA reports)
SPINAL MYELOGRAM ABNORMAL ( 1 FDA reports)
SPIROMETRY ABNORMAL ( 1 FDA reports)
SPLENIC INJURY ( 1 FDA reports)
SPLENIC VARICES ( 1 FDA reports)
SPLENORENAL SHUNT ( 1 FDA reports)
SPLINTER ( 1 FDA reports)
SPONDYLOLISTHESIS ACQUIRED ( 1 FDA reports)
STARVATION ( 1 FDA reports)
STATUS MIGRAINOSUS ( 1 FDA reports)
STEAL SYNDROME ( 1 FDA reports)
STENOTROPHOMONAS TEST POSITIVE ( 1 FDA reports)
STENT MALFUNCTION ( 1 FDA reports)
STENT REMOVAL ( 1 FDA reports)
STERNOTOMY ( 1 FDA reports)
STEROID THERAPY ( 1 FDA reports)
STOMACH MASS ( 1 FDA reports)
STOMATITIS NECROTISING ( 1 FDA reports)
STOOLS WATERY ( 1 FDA reports)
STRABISMUS CONGENITAL ( 1 FDA reports)
STREPTOBACILLUS INFECTION ( 1 FDA reports)
SUBCLAVIAN ARTERY OCCLUSION ( 1 FDA reports)
SUBCLAVIAN STEAL SYNDROME ( 1 FDA reports)
SUBCORNEAL PUSTULAR DERMATOSIS ( 1 FDA reports)
SUBDURAL EMPYEMA ( 1 FDA reports)
SUBDURAL HYGROMA ( 1 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 1 FDA reports)
SUBMAXILLARY GLAND ENLARGEMENT ( 1 FDA reports)
SUDDEN HEARING LOSS ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
SUDDEN VISUAL LOSS ( 1 FDA reports)
SUPPRESSED LACTATION ( 1 FDA reports)
SUTURE REMOVAL ( 1 FDA reports)
SWAN GANZ CATHETER PLACEMENT ( 1 FDA reports)
SYMPATHETIC POSTERIOR CERVICAL SYNDROME ( 1 FDA reports)
SYNOVIAL DISORDER ( 1 FDA reports)
SYSTEMIC SCLEROSIS ( 1 FDA reports)
TARSAL TUNNEL DECOMPRESSION ( 1 FDA reports)
TEMPORAL LOBE EPILEPSY ( 1 FDA reports)
TESTICULAR ABSCESS ( 1 FDA reports)
TESTICULAR DISORDER ( 1 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 1 FDA reports)
THERAPY NAIVE ( 1 FDA reports)
THIRST DECREASED ( 1 FDA reports)
THOUGHT BLOCKING ( 1 FDA reports)
THROMBOEMBOLECTOMY ( 1 FDA reports)
THROMBOENDARTERECTOMY ( 1 FDA reports)
THYMOMA MALIGNANT ( 1 FDA reports)
THYMUS DISORDER ( 1 FDA reports)
THYROID CANCER METASTATIC ( 1 FDA reports)
THYROXINE DECREASED ( 1 FDA reports)
THYROXINE FREE INCREASED ( 1 FDA reports)
THYROXINE INCREASED ( 1 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 1 FDA reports)
TONGUE PRURITUS ( 1 FDA reports)
TONGUE SPASM ( 1 FDA reports)
TOOTH MALFORMATION ( 1 FDA reports)
TOTAL HYSTERECTOMY ( 1 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 1 FDA reports)
TOXIC NODULAR GOITRE ( 1 FDA reports)
TRACHEAL DISORDER ( 1 FDA reports)
TRACHEAL HAEMORRHAGE ( 1 FDA reports)
TRACHEAL PAIN ( 1 FDA reports)
TRANCE ( 1 FDA reports)
TRI-IODOTHYRONINE FREE INCREASED ( 1 FDA reports)
TRICHIASIS ( 1 FDA reports)
TRICUSPID VALVE REPAIR ( 1 FDA reports)
TRISOMY 13 ( 1 FDA reports)
TRISOMY 14 ( 1 FDA reports)
TROPONIN I ( 1 FDA reports)
TRUNCUS COELIACUS THROMBOSIS ( 1 FDA reports)
TUBERCULOSIS LIVER ( 1 FDA reports)
TUBERCULOSIS TEST POSITIVE ( 1 FDA reports)
TUMOUR ASSOCIATED FEVER ( 1 FDA reports)
TUMOUR ULCERATION ( 1 FDA reports)
TYMPANIC MEMBRANE HYPERAEMIA ( 1 FDA reports)
TYMPANOPLASTY ( 1 FDA reports)
TYPE I HYPERSENSITIVITY ( 1 FDA reports)
TYPHUS RICKETTSIA TEST POSITIVE ( 1 FDA reports)
ULNAR NERVE INJURY ( 1 FDA reports)
ULNAR NEURITIS ( 1 FDA reports)
ULTRASOUND BILIARY TRACT ( 1 FDA reports)
ULTRASOUND BREAST ABNORMAL ( 1 FDA reports)
ULTRASOUND FOETAL ( 1 FDA reports)
ULTRASOUND PELVIS ABNORMAL ( 1 FDA reports)
ULTRASOUND UTERUS ABNORMAL ( 1 FDA reports)
UMBILICAL MALFORMATION ( 1 FDA reports)
UNDERSENSING ( 1 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 1 FDA reports)
UPPER MOTOR NEURONE LESION ( 1 FDA reports)
UPPER RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
UREA URINE INCREASED ( 1 FDA reports)
URETERIC INJURY ( 1 FDA reports)
URINARY CASTS ( 1 FDA reports)
URINARY NITROGEN INCREASED ( 1 FDA reports)
URINARY TRACT PAIN ( 1 FDA reports)
URINE CALCIUM INCREASED ( 1 FDA reports)
URINE CANNABINOIDS INCREASED ( 1 FDA reports)
URINE COPPER DECREASED ( 1 FDA reports)
URINE OSMOLARITY INCREASED ( 1 FDA reports)
URINE URIC ACID INCREASED ( 1 FDA reports)
UROBILIN URINE ( 1 FDA reports)
UROBILIN URINE PRESENT ( 1 FDA reports)
UROBILINOGEN URINE INCREASED ( 1 FDA reports)
UROGENITAL DISORDER ( 1 FDA reports)
UTERINE CERVIX STENOSIS ( 1 FDA reports)
UTERINE CONTRACTIONS ABNORMAL ( 1 FDA reports)
UTERINE CYST ( 1 FDA reports)
UTERINE LEIOMYOSARCOMA ( 1 FDA reports)
UTERINE MASS ( 1 FDA reports)
UTERINE OPERATION ( 1 FDA reports)
UTERINE PAIN ( 1 FDA reports)
UTERINE PROLAPSE REPAIR ( 1 FDA reports)
UVEITIS-GLAUCOMA-HYPHAEMA SYNDROME ( 1 FDA reports)
UVULITIS ( 1 FDA reports)
VAGINAL CANCER ( 1 FDA reports)
VAGINAL CYST EXCISION ( 1 FDA reports)
VAGINAL INFLAMMATION ( 1 FDA reports)
VAGINAL MUCOSAL BLISTERING ( 1 FDA reports)
VAGINISMUS ( 1 FDA reports)
VARICELLA ZOSTER VIRUS SEROLOGY POSITIVE ( 1 FDA reports)
VARICOSE ULCERATION ( 1 FDA reports)
VARICOSE VEIN RUPTURED ( 1 FDA reports)
VASCULAR ENCEPHALOPATHY ( 1 FDA reports)
VASCULAR HEADACHE ( 1 FDA reports)
VASCULAR NEOPLASM ( 1 FDA reports)
VASCULAR PROCEDURE COMPLICATION ( 1 FDA reports)
VASCULAR PURPURA ( 1 FDA reports)
VASCULITIS NECROTISING ( 1 FDA reports)
VASOMOTOR RHINITIS ( 1 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 1 FDA reports)
VENTILATION PERFUSION MISMATCH ( 1 FDA reports)
VENTRICULAR INTERNAL DIAMETER ABNORMAL ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT ACQUIRED ( 1 FDA reports)
VERTIGO LABYRINTHINE ( 1 FDA reports)
VESSEL PUNCTURE SITE PRURITUS ( 1 FDA reports)
VESSEL PUNCTURE SITE REACTION ( 1 FDA reports)
VICTIM OF CRIME ( 1 FDA reports)
VICTIM OF ELDER ABUSE ( 1 FDA reports)
VIITH NERVE INJURY ( 1 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 1 FDA reports)
VIRAL CARDIOMYOPATHY ( 1 FDA reports)
VIRAL MYOCARDITIS ( 1 FDA reports)
VIRUS CULTURE POSITIVE ( 1 FDA reports)
VISUAL ACUITY TESTS ABNORMAL ( 1 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 1 FDA reports)
VITAMIN D ABNORMAL ( 1 FDA reports)
VITAMIN E INCREASED ( 1 FDA reports)
VITREOUS DISORDER ( 1 FDA reports)
VITREOUS PROLAPSE ( 1 FDA reports)
VOCAL CORD ATROPHY ( 1 FDA reports)
VOLUME BLOOD INCREASED ( 1 FDA reports)
VOLVULUS OF SMALL BOWEL ( 1 FDA reports)
VULVAL CANCER STAGE I ( 1 FDA reports)
VULVAL ULCERATION ( 1 FDA reports)
VULVAR DYSPLASIA ( 1 FDA reports)
VULVOVAGINAL ULCERATION ( 1 FDA reports)
WALKING DISTANCE TEST ABNORMAL ( 1 FDA reports)
WANDERING PACEMAKER ( 1 FDA reports)
WEIGHT GAIN POOR ( 1 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 1 FDA reports)
WOUND CLOSURE ( 1 FDA reports)
WOUND DECOMPOSITION ( 1 FDA reports)
WOUND NECROSIS ( 1 FDA reports)
WOUND TREATMENT ( 1 FDA reports)
X-RAY DENTAL ( 1 FDA reports)
X-RAY LIMB ABNORMAL ( 1 FDA reports)
XANTHOMA ( 1 FDA reports)
YERSINIA INFECTION ( 1 FDA reports)