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

NAUSEA ( 3177 FDA reports)
DYSPNOEA ( 3039 FDA reports)
PAIN ( 2881 FDA reports)
FATIGUE ( 2755 FDA reports)
DIZZINESS ( 2659 FDA reports)
MYOCARDIAL INFARCTION ( 2452 FDA reports)
ANXIETY ( 2361 FDA reports)
DIARRHOEA ( 2214 FDA reports)
HYPERTENSION ( 2194 FDA reports)
HEADACHE ( 2180 FDA reports)
CHEST PAIN ( 2142 FDA reports)
ASTHENIA ( 2126 FDA reports)
DRUG INEFFECTIVE ( 1920 FDA reports)
VOMITING ( 1669 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1637 FDA reports)
FALL ( 1619 FDA reports)
OEDEMA PERIPHERAL ( 1601 FDA reports)
BACK PAIN ( 1585 FDA reports)
PAIN IN EXTREMITY ( 1571 FDA reports)
DEPRESSION ( 1565 FDA reports)
ANAEMIA ( 1481 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1459 FDA reports)
WEIGHT DECREASED ( 1442 FDA reports)
ATRIAL FIBRILLATION ( 1400 FDA reports)
MALAISE ( 1368 FDA reports)
INJURY ( 1354 FDA reports)
ARTHRALGIA ( 1314 FDA reports)
HYPOTENSION ( 1310 FDA reports)
RENAL FAILURE ( 1309 FDA reports)
BLOOD PRESSURE INCREASED ( 1280 FDA reports)
PNEUMONIA ( 1268 FDA reports)
INSOMNIA ( 1259 FDA reports)
CORONARY ARTERY DISEASE ( 1251 FDA reports)
COUGH ( 1138 FDA reports)
ABDOMINAL PAIN ( 1101 FDA reports)
BLOOD GLUCOSE INCREASED ( 1097 FDA reports)
PYREXIA ( 1093 FDA reports)
CONSTIPATION ( 1071 FDA reports)
WEIGHT INCREASED ( 1069 FDA reports)
PALPITATIONS ( 1027 FDA reports)
DEHYDRATION ( 1000 FDA reports)
CARDIAC DISORDER ( 953 FDA reports)
HYPOAESTHESIA ( 951 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 929 FDA reports)
URINARY TRACT INFECTION ( 895 FDA reports)
PRURITUS ( 889 FDA reports)
RASH ( 877 FDA reports)
MYALGIA ( 873 FDA reports)
ABDOMINAL PAIN UPPER ( 845 FDA reports)
FEELING ABNORMAL ( 844 FDA reports)
PARAESTHESIA ( 843 FDA reports)
DIABETES MELLITUS ( 812 FDA reports)
CONFUSIONAL STATE ( 803 FDA reports)
EMOTIONAL DISTRESS ( 796 FDA reports)
HEART RATE INCREASED ( 793 FDA reports)
DEATH ( 787 FDA reports)
MUSCLE SPASMS ( 780 FDA reports)
VISION BLURRED ( 770 FDA reports)
GAIT DISTURBANCE ( 755 FDA reports)
SOMNOLENCE ( 748 FDA reports)
RENAL FAILURE ACUTE ( 746 FDA reports)
HYPERHIDROSIS ( 714 FDA reports)
TREMOR ( 710 FDA reports)
DRUG DOSE OMISSION ( 705 FDA reports)
SYNCOPE ( 701 FDA reports)
DECREASED APPETITE ( 687 FDA reports)
BRONCHITIS ( 678 FDA reports)
UNEVALUABLE EVENT ( 666 FDA reports)
STRESS ( 662 FDA reports)
OSTEOARTHRITIS ( 655 FDA reports)
MEMORY IMPAIRMENT ( 646 FDA reports)
PLEURAL EFFUSION ( 644 FDA reports)
DYSPHAGIA ( 642 FDA reports)
FLUSHING ( 626 FDA reports)
DYSPEPSIA ( 622 FDA reports)
ANHEDONIA ( 620 FDA reports)
MUSCULAR WEAKNESS ( 608 FDA reports)
LOSS OF CONSCIOUSNESS ( 600 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 597 FDA reports)
CHEST DISCOMFORT ( 591 FDA reports)
ARTHRITIS ( 585 FDA reports)
CONVULSION ( 582 FDA reports)
FEAR ( 572 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 567 FDA reports)
AMNESIA ( 566 FDA reports)
SINUSITIS ( 564 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 563 FDA reports)
ALOPECIA ( 528 FDA reports)
OSTEONECROSIS OF JAW ( 527 FDA reports)
HAEMOGLOBIN DECREASED ( 522 FDA reports)
ANGINA PECTORIS ( 516 FDA reports)
MITRAL VALVE INCOMPETENCE ( 503 FDA reports)
BONE DISORDER ( 501 FDA reports)
ERYTHEMA ( 498 FDA reports)
CONTUSION ( 491 FDA reports)
RENAL IMPAIRMENT ( 491 FDA reports)
CONDITION AGGRAVATED ( 487 FDA reports)
NEUROPATHY PERIPHERAL ( 485 FDA reports)
DEEP VEIN THROMBOSIS ( 470 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 468 FDA reports)
ABDOMINAL DISCOMFORT ( 467 FDA reports)
ECONOMIC PROBLEM ( 466 FDA reports)
HYPERSENSITIVITY ( 466 FDA reports)
NERVOUSNESS ( 464 FDA reports)
BLOOD CREATININE INCREASED ( 457 FDA reports)
SEPSIS ( 457 FDA reports)
TACHYCARDIA ( 451 FDA reports)
PULMONARY EMBOLISM ( 449 FDA reports)
CATARACT ( 446 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 440 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 438 FDA reports)
THROMBOCYTOPENIA ( 431 FDA reports)
ABDOMINAL DISTENSION ( 428 FDA reports)
CHILLS ( 427 FDA reports)
DRY MOUTH ( 427 FDA reports)
SPINAL OSTEOARTHRITIS ( 426 FDA reports)
ARTHROPATHY ( 423 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 422 FDA reports)
BLOOD PRESSURE DECREASED ( 420 FDA reports)
HYPERLIPIDAEMIA ( 417 FDA reports)
ILL-DEFINED DISORDER ( 414 FDA reports)
PAIN IN JAW ( 412 FDA reports)
HEART RATE IRREGULAR ( 411 FDA reports)
HYPOKALAEMIA ( 409 FDA reports)
DYSGEUSIA ( 408 FDA reports)
RESPIRATORY FAILURE ( 406 FDA reports)
VISUAL IMPAIRMENT ( 406 FDA reports)
THROMBOSIS ( 401 FDA reports)
BRADYCARDIA ( 400 FDA reports)
JOINT SWELLING ( 399 FDA reports)
SWELLING ( 390 FDA reports)
ARRHYTHMIA ( 389 FDA reports)
CHOLELITHIASIS ( 388 FDA reports)
MEDICATION ERROR ( 386 FDA reports)
ASTHMA ( 384 FDA reports)
CELLULITIS ( 382 FDA reports)
MUSCULOSKELETAL PAIN ( 379 FDA reports)
NECK PAIN ( 379 FDA reports)
RENAL INJURY ( 377 FDA reports)
ADVERSE EVENT ( 376 FDA reports)
CORONARY ARTERY OCCLUSION ( 375 FDA reports)
OSTEOMYELITIS ( 373 FDA reports)
OSTEOPOROSIS ( 373 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 370 FDA reports)
DRUG INTERACTION ( 367 FDA reports)
CARDIOMEGALY ( 363 FDA reports)
BLOOD GLUCOSE DECREASED ( 360 FDA reports)
RECTAL HAEMORRHAGE ( 359 FDA reports)
RENAL FAILURE CHRONIC ( 359 FDA reports)
HALLUCINATION ( 352 FDA reports)
SLEEP APNOEA SYNDROME ( 350 FDA reports)
HEART RATE DECREASED ( 349 FDA reports)
CARDIAC ARREST ( 345 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 345 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 344 FDA reports)
ATELECTASIS ( 343 FDA reports)
BALANCE DISORDER ( 341 FDA reports)
MYOCARDIAL ISCHAEMIA ( 338 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 338 FDA reports)
LETHARGY ( 336 FDA reports)
MENTAL STATUS CHANGES ( 334 FDA reports)
INFECTION ( 332 FDA reports)
GASTRITIS ( 331 FDA reports)
MULTI-ORGAN FAILURE ( 331 FDA reports)
INFLUENZA LIKE ILLNESS ( 330 FDA reports)
NASOPHARYNGITIS ( 330 FDA reports)
OSTEONECROSIS ( 330 FDA reports)
OEDEMA ( 326 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 325 FDA reports)
VERTIGO ( 324 FDA reports)
CARDIOMYOPATHY ( 323 FDA reports)
DYSPNOEA EXERTIONAL ( 323 FDA reports)
DRUG HYPERSENSITIVITY ( 322 FDA reports)
URTICARIA ( 320 FDA reports)
OFF LABEL USE ( 319 FDA reports)
ABNORMAL DREAMS ( 318 FDA reports)
BLOOD UREA INCREASED ( 314 FDA reports)
MULTIPLE INJURIES ( 313 FDA reports)
SLEEP DISORDER ( 312 FDA reports)
ROAD TRAFFIC ACCIDENT ( 311 FDA reports)
HAEMORRHAGE ( 311 FDA reports)
ARTERIOSCLEROSIS ( 310 FDA reports)
ABASIA ( 304 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 303 FDA reports)
TINNITUS ( 303 FDA reports)
VISUAL ACUITY REDUCED ( 300 FDA reports)
PULMONARY HYPERTENSION ( 298 FDA reports)
WHEEZING ( 297 FDA reports)
TYPE 2 DIABETES MELLITUS ( 295 FDA reports)
OSTEOPENIA ( 295 FDA reports)
TOOTH EXTRACTION ( 294 FDA reports)
IRRITABILITY ( 292 FDA reports)
BURNING SENSATION ( 291 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 287 FDA reports)
DYSURIA ( 286 FDA reports)
DYSPHONIA ( 284 FDA reports)
EPISTAXIS ( 284 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 283 FDA reports)
HAEMORRHOIDS ( 282 FDA reports)
POLLAKIURIA ( 278 FDA reports)
PLATELET COUNT DECREASED ( 276 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 274 FDA reports)
AGITATION ( 273 FDA reports)
HYPERGLYCAEMIA ( 273 FDA reports)
BONE PAIN ( 270 FDA reports)
PANIC ATTACK ( 270 FDA reports)
PULMONARY OEDEMA ( 270 FDA reports)
NEOPLASM MALIGNANT ( 269 FDA reports)
FLATULENCE ( 268 FDA reports)
INCORRECT DOSE ADMINISTERED ( 265 FDA reports)
PANCREATITIS ( 264 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 264 FDA reports)
MENTAL DISORDER ( 263 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 261 FDA reports)
MIGRAINE ( 261 FDA reports)
VIRAL INFECTION ( 261 FDA reports)
FIBROMYALGIA ( 260 FDA reports)
DIVERTICULUM ( 257 FDA reports)
HOT FLUSH ( 257 FDA reports)
HIATUS HERNIA ( 253 FDA reports)
IMPAIRED HEALING ( 253 FDA reports)
ANGINA UNSTABLE ( 251 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 250 FDA reports)
OROPHARYNGEAL PAIN ( 250 FDA reports)
DISTURBANCE IN ATTENTION ( 249 FDA reports)
LYMPHADENOPATHY ( 249 FDA reports)
DYSARTHRIA ( 247 FDA reports)
HYPONATRAEMIA ( 247 FDA reports)
RENAL DISORDER ( 246 FDA reports)
DENTAL CARIES ( 245 FDA reports)
NEPHROLITHIASIS ( 244 FDA reports)
RENAL CYST ( 241 FDA reports)
BLOOD POTASSIUM DECREASED ( 237 FDA reports)
FLUID RETENTION ( 236 FDA reports)
PANCYTOPENIA ( 236 FDA reports)
ANOREXIA ( 233 FDA reports)
SPEECH DISORDER ( 232 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 231 FDA reports)
HYPERCHOLESTEROLAEMIA ( 230 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 230 FDA reports)
FEELING HOT ( 229 FDA reports)
CARDIAC MURMUR ( 227 FDA reports)
HAEMATOCRIT DECREASED ( 227 FDA reports)
HAEMATOCHEZIA ( 226 FDA reports)
HERPES ZOSTER ( 224 FDA reports)
NASAL CONGESTION ( 224 FDA reports)
EJECTION FRACTION DECREASED ( 223 FDA reports)
SURGERY ( 222 FDA reports)
ERECTILE DYSFUNCTION ( 221 FDA reports)
BREAST CANCER ( 219 FDA reports)
CARDIAC FAILURE ( 219 FDA reports)
MOBILITY DECREASED ( 219 FDA reports)
GOUT ( 217 FDA reports)
HYPOGLYCAEMIA ( 217 FDA reports)
RIB FRACTURE ( 216 FDA reports)
SWELLING FACE ( 216 FDA reports)
LUNG NEOPLASM ( 214 FDA reports)
HYPOTHYROIDISM ( 213 FDA reports)
HAEMATURIA ( 212 FDA reports)
HEPATIC STEATOSIS ( 210 FDA reports)
HYPERSOMNIA ( 208 FDA reports)
DRUG EFFECT DECREASED ( 207 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 206 FDA reports)
OVERDOSE ( 206 FDA reports)
DECREASED INTEREST ( 205 FDA reports)
VENTRICULAR TACHYCARDIA ( 205 FDA reports)
DRY SKIN ( 203 FDA reports)
EMOTIONAL DISORDER ( 203 FDA reports)
INJECTION SITE PAIN ( 203 FDA reports)
EXOSTOSIS ( 202 FDA reports)
RHABDOMYOLYSIS ( 202 FDA reports)
TOOTHACHE ( 200 FDA reports)
COLONIC POLYP ( 200 FDA reports)
INFLUENZA ( 198 FDA reports)
STAPHYLOCOCCAL INFECTION ( 196 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 196 FDA reports)
SUICIDAL IDEATION ( 194 FDA reports)
OBESITY ( 194 FDA reports)
AORTIC VALVE INCOMPETENCE ( 193 FDA reports)
ABNORMAL BEHAVIOUR ( 192 FDA reports)
MULTIPLE MYELOMA ( 192 FDA reports)
TREATMENT NONCOMPLIANCE ( 191 FDA reports)
SKIN DISCOLOURATION ( 190 FDA reports)
FEELING COLD ( 190 FDA reports)
HAEMATOMA ( 190 FDA reports)
HYPERKALAEMIA ( 189 FDA reports)
SINUS TACHYCARDIA ( 188 FDA reports)
URINARY INCONTINENCE ( 188 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 187 FDA reports)
BLINDNESS ( 187 FDA reports)
EYE PAIN ( 187 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 186 FDA reports)
RESPIRATORY DISTRESS ( 186 FDA reports)
SKIN DISORDER ( 185 FDA reports)
HYPOXIA ( 185 FDA reports)
CARDIOVASCULAR DISORDER ( 184 FDA reports)
DEFORMITY ( 183 FDA reports)
WITHDRAWAL SYNDROME ( 183 FDA reports)
URINARY RETENTION ( 180 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 178 FDA reports)
MENTAL IMPAIRMENT ( 178 FDA reports)
CARDIO-RESPIRATORY ARREST ( 177 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 177 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 175 FDA reports)
DISEASE PROGRESSION ( 175 FDA reports)
NEUTROPENIA ( 175 FDA reports)
UNRESPONSIVE TO STIMULI ( 175 FDA reports)
HAEMOPTYSIS ( 174 FDA reports)
ANGER ( 173 FDA reports)
HEAD INJURY ( 173 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 173 FDA reports)
VENTRICULAR HYPERTROPHY ( 171 FDA reports)
PRESYNCOPE ( 170 FDA reports)
LUNG DISORDER ( 169 FDA reports)
SINUS BRADYCARDIA ( 169 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 169 FDA reports)
SKIN ULCER ( 168 FDA reports)
GASTRIC ULCER ( 168 FDA reports)
HEPATIC ENZYME INCREASED ( 168 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 167 FDA reports)
HIP FRACTURE ( 167 FDA reports)
PROTHROMBIN TIME PROLONGED ( 167 FDA reports)
ROTATOR CUFF SYNDROME ( 167 FDA reports)
PURULENT DISCHARGE ( 166 FDA reports)
DIVERTICULITIS ( 165 FDA reports)
DRUG INTOLERANCE ( 164 FDA reports)
MOOD ALTERED ( 162 FDA reports)
PRODUCT QUALITY ISSUE ( 162 FDA reports)
STOMATITIS ( 162 FDA reports)
TOOTH DISORDER ( 162 FDA reports)
SPINAL COMPRESSION FRACTURE ( 161 FDA reports)
BURSITIS ( 161 FDA reports)
DIPLOPIA ( 159 FDA reports)
GALLBLADDER DISORDER ( 159 FDA reports)
HALLUCINATION, AUDITORY ( 159 FDA reports)
INCREASED APPETITE ( 159 FDA reports)
TOOTH LOSS ( 158 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 157 FDA reports)
DEAFNESS ( 156 FDA reports)
INTENTIONAL DRUG MISUSE ( 156 FDA reports)
SPINAL COLUMN STENOSIS ( 155 FDA reports)
CORONARY ARTERY STENOSIS ( 154 FDA reports)
JOINT INJURY ( 154 FDA reports)
LUNG INFILTRATION ( 153 FDA reports)
STENT PLACEMENT ( 153 FDA reports)
FLUID OVERLOAD ( 152 FDA reports)
NOCTURIA ( 152 FDA reports)
BLOOD SODIUM DECREASED ( 151 FDA reports)
PULMONARY CONGESTION ( 151 FDA reports)
TENSION ( 151 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 151 FDA reports)
DRY EYE ( 150 FDA reports)
HYPOPHAGIA ( 150 FDA reports)
METASTASES TO BONE ( 150 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 149 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 149 FDA reports)
SINUS DISORDER ( 147 FDA reports)
RHINITIS ALLERGIC ( 146 FDA reports)
SKIN EXFOLIATION ( 146 FDA reports)
CAROTID ARTERY STENOSIS ( 146 FDA reports)
OESOPHAGITIS ( 146 FDA reports)
DISORIENTATION ( 145 FDA reports)
GLAUCOMA ( 145 FDA reports)
NIGHTMARE ( 145 FDA reports)
RASH MACULAR ( 145 FDA reports)
ULCER ( 145 FDA reports)
CYSTITIS ( 144 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 144 FDA reports)
DEMENTIA ( 143 FDA reports)
RHINORRHOEA ( 143 FDA reports)
SCAR ( 143 FDA reports)
HYPOACUSIS ( 142 FDA reports)
HYPOVOLAEMIA ( 142 FDA reports)
EAR PAIN ( 141 FDA reports)
GASTRIC DISORDER ( 141 FDA reports)
GINGIVAL PAIN ( 141 FDA reports)
INFLAMMATION ( 141 FDA reports)
INJECTION SITE ERYTHEMA ( 141 FDA reports)
LOOSE TOOTH ( 141 FDA reports)
SKIN INDURATION ( 141 FDA reports)
BACK DISORDER ( 140 FDA reports)
NIGHT SWEATS ( 140 FDA reports)
PERIPHERAL COLDNESS ( 140 FDA reports)
RHEUMATOID ARTHRITIS ( 139 FDA reports)
COAGULOPATHY ( 138 FDA reports)
PERICARDIAL EFFUSION ( 138 FDA reports)
EMPHYSEMA ( 137 FDA reports)
FEBRILE NEUTROPENIA ( 137 FDA reports)
SOMNAMBULISM ( 137 FDA reports)
SLEEP TALKING ( 135 FDA reports)
FLANK PAIN ( 135 FDA reports)
MUSCLE TIGHTNESS ( 135 FDA reports)
PROSTATE CANCER ( 135 FDA reports)
ADVERSE DRUG REACTION ( 134 FDA reports)
COMA ( 134 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 134 FDA reports)
ORAL PAIN ( 134 FDA reports)
VISUAL DISTURBANCE ( 134 FDA reports)
BLOOD BILIRUBIN INCREASED ( 133 FDA reports)
BONE LESION ( 133 FDA reports)
CYST ( 133 FDA reports)
LEFT ATRIAL DILATATION ( 133 FDA reports)
ORTHOSTATIC HYPOTENSION ( 133 FDA reports)
ABSCESS ( 132 FDA reports)
ACUTE CORONARY SYNDROME ( 132 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 132 FDA reports)
FACIAL PAIN ( 132 FDA reports)
GASTROINTESTINAL DISORDER ( 132 FDA reports)
MENORRHAGIA ( 132 FDA reports)
DEPRESSED MOOD ( 131 FDA reports)
LIMB INJURY ( 131 FDA reports)
MELAENA ( 131 FDA reports)
PHYSICAL DISABILITY ( 130 FDA reports)
AGGRESSION ( 129 FDA reports)
BLOOD POTASSIUM INCREASED ( 129 FDA reports)
DIABETIC NEUROPATHY ( 129 FDA reports)
FAECES DISCOLOURED ( 129 FDA reports)
FEMUR FRACTURE ( 129 FDA reports)
PRIMARY SEQUESTRUM ( 129 FDA reports)
SKIN LESION ( 129 FDA reports)
TOOTH FRACTURE ( 129 FDA reports)
MENOPAUSE ( 128 FDA reports)
COMPRESSION FRACTURE ( 127 FDA reports)
DYSLIPIDAEMIA ( 127 FDA reports)
FEELING JITTERY ( 127 FDA reports)
PANCREATITIS ACUTE ( 126 FDA reports)
CEREBRAL INFARCTION ( 125 FDA reports)
DISCOMFORT ( 125 FDA reports)
BONE DENSITY DECREASED ( 124 FDA reports)
SKIN HYPERTROPHY ( 124 FDA reports)
VENTRICULAR FIBRILLATION ( 124 FDA reports)
RESTLESS LEGS SYNDROME ( 123 FDA reports)
AORTIC ANEURYSM ( 123 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 123 FDA reports)
BLOOD CALCIUM DECREASED ( 123 FDA reports)
DYSKINESIA ( 123 FDA reports)
HEPATIC FAILURE ( 123 FDA reports)
IRRITABLE BOWEL SYNDROME ( 123 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 123 FDA reports)
ABORTION SPONTANEOUS ( 122 FDA reports)
ASCITES ( 122 FDA reports)
DISABILITY ( 122 FDA reports)
LARYNGITIS ( 122 FDA reports)
ATRIAL FLUTTER ( 121 FDA reports)
GASTROENTERITIS ( 121 FDA reports)
POLYDIPSIA ( 121 FDA reports)
RASH PRURITIC ( 121 FDA reports)
SKIN TIGHTNESS ( 121 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 121 FDA reports)
TOOTH INFECTION ( 120 FDA reports)
AORTIC STENOSIS ( 120 FDA reports)
APHASIA ( 119 FDA reports)
BED REST ( 119 FDA reports)
ENCEPHALOPATHY ( 119 FDA reports)
FRUSTRATION ( 119 FDA reports)
RESTLESSNESS ( 119 FDA reports)
TENDONITIS ( 118 FDA reports)
GENERALISED OEDEMA ( 118 FDA reports)
MACULAR DEGENERATION ( 118 FDA reports)
MENSTRUAL DISORDER ( 118 FDA reports)
MUSCLE TWITCHING ( 118 FDA reports)
OXYGEN SATURATION DECREASED ( 117 FDA reports)
THROAT IRRITATION ( 117 FDA reports)
SCOLIOSIS ( 116 FDA reports)
STOMACH DISCOMFORT ( 116 FDA reports)
CARPAL TUNNEL SYNDROME ( 116 FDA reports)
JOINT STIFFNESS ( 116 FDA reports)
ENURESIS ( 115 FDA reports)
ISCHAEMIA ( 115 FDA reports)
TOBACCO USER ( 115 FDA reports)
TOOTH ABSCESS ( 115 FDA reports)
AZOTAEMIA ( 114 FDA reports)
BLISTER ( 114 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 114 FDA reports)
OCULAR HYPERAEMIA ( 114 FDA reports)
RASH ERYTHEMATOUS ( 114 FDA reports)
CHOLECYSTITIS ( 113 FDA reports)
EYE SWELLING ( 113 FDA reports)
MITRAL VALVE PROLAPSE ( 113 FDA reports)
BLINDNESS UNILATERAL ( 112 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 112 FDA reports)
HEARING IMPAIRED ( 112 FDA reports)
COLD SWEAT ( 111 FDA reports)
DRUG DISPENSING ERROR ( 111 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 110 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 110 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 110 FDA reports)
INTERMITTENT CLAUDICATION ( 110 FDA reports)
HAEMATEMESIS ( 109 FDA reports)
HEPATITIS ( 109 FDA reports)
MALNUTRITION ( 109 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 108 FDA reports)
COGNITIVE DISORDER ( 108 FDA reports)
EYE HAEMORRHAGE ( 108 FDA reports)
POST PROCEDURAL COMPLICATION ( 108 FDA reports)
SKIN BURNING SENSATION ( 108 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 107 FDA reports)
PRODUCTIVE COUGH ( 107 FDA reports)
DRY THROAT ( 106 FDA reports)
PSORIASIS ( 106 FDA reports)
CANDIDIASIS ( 105 FDA reports)
DYSSTASIA ( 105 FDA reports)
GINGIVAL BLEEDING ( 105 FDA reports)
GLOSSODYNIA ( 105 FDA reports)
INJECTION SITE HAEMORRHAGE ( 105 FDA reports)
LEUKOCYTOSIS ( 105 FDA reports)
SWOLLEN TONGUE ( 105 FDA reports)
DIFFICULTY IN WALKING ( 104 FDA reports)
HERNIA ( 104 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 104 FDA reports)
NODULE ( 104 FDA reports)
BACK INJURY ( 103 FDA reports)
CARDIAC FLUTTER ( 103 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 103 FDA reports)
LUMBAR SPINAL STENOSIS ( 103 FDA reports)
MOVEMENT DISORDER ( 103 FDA reports)
PAROSMIA ( 103 FDA reports)
CARDIAC PACEMAKER INSERTION ( 102 FDA reports)
CARDIAC VALVE DISEASE ( 102 FDA reports)
CHOLECYSTECTOMY ( 102 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 102 FDA reports)
FIBROSIS ( 102 FDA reports)
RETCHING ( 102 FDA reports)
SICK SINUS SYNDROME ( 102 FDA reports)
SEPTIC SHOCK ( 101 FDA reports)
DILATATION ATRIAL ( 101 FDA reports)
ESSENTIAL HYPERTENSION ( 101 FDA reports)
COLITIS ( 100 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 100 FDA reports)
ENDODONTIC PROCEDURE ( 100 FDA reports)
ERUCTATION ( 100 FDA reports)
LEUKOPENIA ( 100 FDA reports)
MASTICATION DISORDER ( 100 FDA reports)
MULTIPLE SCLEROSIS ( 100 FDA reports)
NEURALGIA ( 100 FDA reports)
PHARYNGEAL OEDEMA ( 100 FDA reports)
PNEUMONIA ASPIRATION ( 100 FDA reports)
VITREOUS FLOATERS ( 100 FDA reports)
ECCHYMOSIS ( 99 FDA reports)
HYPERCALCAEMIA ( 99 FDA reports)
MENISCUS LESION ( 99 FDA reports)
NERVOUS SYSTEM DISORDER ( 99 FDA reports)
PALLOR ( 99 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 99 FDA reports)
BLOOD PRESSURE ABNORMAL ( 98 FDA reports)
FOOT FRACTURE ( 98 FDA reports)
JOINT EFFUSION ( 98 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 98 FDA reports)
MUSCLE STRAIN ( 98 FDA reports)
JAW DISORDER ( 97 FDA reports)
KNEE ARTHROPLASTY ( 97 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 97 FDA reports)
CAROTID ARTERY DISEASE ( 96 FDA reports)
MOUTH ULCERATION ( 96 FDA reports)
PULMONARY FIBROSIS ( 96 FDA reports)
DERMATITIS ( 95 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 95 FDA reports)
IMPAIRED WORK ABILITY ( 95 FDA reports)
MUCOSAL INFLAMMATION ( 95 FDA reports)
ABDOMINAL PAIN LOWER ( 94 FDA reports)
BONE DEBRIDEMENT ( 94 FDA reports)
CRYING ( 94 FDA reports)
DIASTOLIC DYSFUNCTION ( 94 FDA reports)
GRAND MAL CONVULSION ( 94 FDA reports)
PEPTIC ULCER ( 94 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 94 FDA reports)
EYE IRRITATION ( 93 FDA reports)
GROIN PAIN ( 93 FDA reports)
SKIN CANCER ( 93 FDA reports)
ANAPHYLACTIC REACTION ( 92 FDA reports)
DRUG TOXICITY ( 92 FDA reports)
CHROMATURIA ( 91 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 91 FDA reports)
IRON DEFICIENCY ANAEMIA ( 91 FDA reports)
PARKINSON'S DISEASE ( 91 FDA reports)
PERIODONTITIS ( 91 FDA reports)
WOUND DEHISCENCE ( 91 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 90 FDA reports)
FUNGAL INFECTION ( 90 FDA reports)
HALLUCINATION, VISUAL ( 90 FDA reports)
METASTASES TO LUNG ( 90 FDA reports)
ORTHOPNOEA ( 90 FDA reports)
CATARACT OPERATION ( 89 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 89 FDA reports)
EXCORIATION ( 89 FDA reports)
EXTRASYSTOLES ( 89 FDA reports)
LUNG NEOPLASM MALIGNANT ( 89 FDA reports)
SCIATICA ( 89 FDA reports)
ACTINOMYCOSIS ( 88 FDA reports)
BLOOD CALCIUM INCREASED ( 88 FDA reports)
CARDIOGENIC SHOCK ( 88 FDA reports)
ADVERSE REACTION ( 87 FDA reports)
HEMIPARESIS ( 87 FDA reports)
HEPATOMEGALY ( 87 FDA reports)
METASTASES TO LIVER ( 87 FDA reports)
SINUS CONGESTION ( 87 FDA reports)
UPPER LIMB FRACTURE ( 86 FDA reports)
COLON CANCER ( 86 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 86 FDA reports)
EYE DISORDER ( 86 FDA reports)
GINGIVITIS ( 86 FDA reports)
MIDDLE INSOMNIA ( 86 FDA reports)
BASAL CELL CARCINOMA ( 85 FDA reports)
CORONARY ARTERY BYPASS ( 85 FDA reports)
JOINT CONTRACTURE ( 85 FDA reports)
RASH GENERALISED ( 85 FDA reports)
ACUTE RESPIRATORY FAILURE ( 84 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 84 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 84 FDA reports)
MASS ( 84 FDA reports)
PLEURITIC PAIN ( 84 FDA reports)
SPONDYLOLISTHESIS ( 84 FDA reports)
THROAT TIGHTNESS ( 84 FDA reports)
RESPIRATORY ARREST ( 83 FDA reports)
CEREBRAL ATROPHY ( 83 FDA reports)
CHRONIC SINUSITIS ( 83 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 83 FDA reports)
FISTULA ( 83 FDA reports)
GINGIVAL INFECTION ( 83 FDA reports)
GYNAECOMASTIA ( 83 FDA reports)
HEART INJURY ( 83 FDA reports)
HYPOMAGNESAEMIA ( 83 FDA reports)
HYPOPHOSPHATAEMIA ( 83 FDA reports)
LACUNAR INFARCTION ( 83 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 82 FDA reports)
HIP ARTHROPLASTY ( 82 FDA reports)
PRURITUS GENERALISED ( 82 FDA reports)
BLOOD URINE PRESENT ( 81 FDA reports)
LACRIMATION INCREASED ( 81 FDA reports)
SPINAL FRACTURE ( 81 FDA reports)
UTERINE LEIOMYOMA ( 81 FDA reports)
THYROID NEOPLASM ( 80 FDA reports)
ATRIAL TACHYCARDIA ( 80 FDA reports)
CERUMEN IMPACTION ( 80 FDA reports)
CYANOSIS ( 80 FDA reports)
EUPHORIC MOOD ( 80 FDA reports)
HYPOAESTHESIA ORAL ( 80 FDA reports)
INTERSTITIAL LUNG DISEASE ( 80 FDA reports)
PERIODONTAL DISEASE ( 80 FDA reports)
LABORATORY TEST ABNORMAL ( 79 FDA reports)
LIVER DISORDER ( 79 FDA reports)
SKIN FIBROSIS ( 79 FDA reports)
UROSEPSIS ( 79 FDA reports)
CARDIAC OPERATION ( 78 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 78 FDA reports)
CEREBRAL HAEMORRHAGE ( 78 FDA reports)
DEVICE RELATED INFECTION ( 78 FDA reports)
DIALYSIS ( 78 FDA reports)
GINGIVAL RECESSION ( 78 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 78 FDA reports)
HORMONE LEVEL ABNORMAL ( 78 FDA reports)
LIMB DISCOMFORT ( 78 FDA reports)
PHARYNGITIS ( 78 FDA reports)
BARRETT'S OESOPHAGUS ( 77 FDA reports)
BODY TEMPERATURE INCREASED ( 77 FDA reports)
CEREBRAL ISCHAEMIA ( 77 FDA reports)
LYMPHOEDEMA ( 77 FDA reports)
PNEUMONITIS ( 77 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 77 FDA reports)
ATRIOVENTRICULAR BLOCK ( 76 FDA reports)
BREAST PAIN ( 76 FDA reports)
DRUG ADMINISTRATION ERROR ( 76 FDA reports)
EATING DISORDER ( 76 FDA reports)
GASTROENTERITIS VIRAL ( 76 FDA reports)
JOINT DISLOCATION ( 76 FDA reports)
WRONG DRUG ADMINISTERED ( 76 FDA reports)
THYROID DISORDER ( 75 FDA reports)
BACTERAEMIA ( 75 FDA reports)
CAROTID BRUIT ( 75 FDA reports)
HAEMODIALYSIS ( 75 FDA reports)
RADICULOPATHY ( 75 FDA reports)
DECUBITUS ULCER ( 74 FDA reports)
FAECAL INCONTINENCE ( 74 FDA reports)
INTESTINAL OBSTRUCTION ( 74 FDA reports)
LICE INFESTATION ( 74 FDA reports)
STEM CELL TRANSPLANT ( 74 FDA reports)
LIP SWELLING ( 73 FDA reports)
PATHOLOGICAL FRACTURE ( 73 FDA reports)
BLOOD ALBUMIN DECREASED ( 72 FDA reports)
BREAST CANCER FEMALE ( 72 FDA reports)
VITAMIN D DEFICIENCY ( 72 FDA reports)
ANKLE FRACTURE ( 71 FDA reports)
BACTERIAL INFECTION ( 71 FDA reports)
CHOLECYSTITIS CHRONIC ( 71 FDA reports)
COORDINATION ABNORMAL ( 71 FDA reports)
DRUG DEPENDENCE ( 71 FDA reports)
EXPOSED BONE IN JAW ( 71 FDA reports)
HYPERKERATOSIS ( 71 FDA reports)
INCREASED TENDENCY TO BRUISE ( 71 FDA reports)
JAW OPERATION ( 71 FDA reports)
KIDNEY INFECTION ( 71 FDA reports)
LOWER LIMB FRACTURE ( 71 FDA reports)
PHOTOPHOBIA ( 71 FDA reports)
ANGIOPATHY ( 70 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 70 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 70 FDA reports)
HYPERTENSIVE HEART DISEASE ( 70 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 70 FDA reports)
KYPHOSIS ( 70 FDA reports)
RESPIRATORY DISORDER ( 70 FDA reports)
RHINITIS ( 70 FDA reports)
SEDATION ( 70 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 69 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 69 FDA reports)
BLADDER CANCER ( 69 FDA reports)
DELIRIUM ( 69 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 69 FDA reports)
METABOLIC ACIDOSIS ( 69 FDA reports)
ORAL SURGERY ( 69 FDA reports)
ANEURYSM ( 68 FDA reports)
ANGIOEDEMA ( 68 FDA reports)
EAR INFECTION ( 68 FDA reports)
ORAL CANDIDIASIS ( 68 FDA reports)
SQUAMOUS CELL CARCINOMA ( 68 FDA reports)
SUBDURAL HAEMATOMA ( 68 FDA reports)
VENTRICULAR HYPOKINESIA ( 67 FDA reports)
CAROTID ARTERY OCCLUSION ( 67 FDA reports)
DIVERTICULUM INTESTINAL ( 67 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 67 FDA reports)
HEPATITIS C ( 67 FDA reports)
HYSTERECTOMY ( 67 FDA reports)
LOCAL SWELLING ( 67 FDA reports)
PHOTOPSIA ( 67 FDA reports)
POLYP ( 67 FDA reports)
PROTEINURIA ( 67 FDA reports)
APHONIA ( 66 FDA reports)
HYPERTHYROIDISM ( 66 FDA reports)
ORAL CAVITY FISTULA ( 66 FDA reports)
RESPIRATORY RATE INCREASED ( 66 FDA reports)
SEASONAL ALLERGY ( 65 FDA reports)
SPLENOMEGALY ( 65 FDA reports)
TARDIVE DYSKINESIA ( 65 FDA reports)
BLADDER DISORDER ( 65 FDA reports)
DEBRIDEMENT ( 65 FDA reports)
MYELODYSPLASTIC SYNDROME ( 65 FDA reports)
ABDOMINAL HERNIA ( 64 FDA reports)
ATAXIA ( 64 FDA reports)
CATHETERISATION CARDIAC ( 64 FDA reports)
HEPATIC CYST ( 64 FDA reports)
HYDRONEPHROSIS ( 64 FDA reports)
METASTASES TO SPINE ( 64 FDA reports)
PARAESTHESIA ORAL ( 64 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 64 FDA reports)
RALES ( 64 FDA reports)
SPINAL DISORDER ( 64 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 63 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 63 FDA reports)
THIRST ( 63 FDA reports)
VASCULAR PSEUDOANEURYSM ( 63 FDA reports)
ECZEMA ( 63 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 63 FDA reports)
ELECTROLYTE IMBALANCE ( 63 FDA reports)
GINGIVAL DISORDER ( 63 FDA reports)
GINGIVAL ULCERATION ( 63 FDA reports)
HAND FRACTURE ( 63 FDA reports)
HOSPITALISATION ( 63 FDA reports)
IMPAIRED DRIVING ABILITY ( 63 FDA reports)
JAUNDICE ( 63 FDA reports)
LYMPHOMA ( 63 FDA reports)
MITRAL VALVE DISEASE ( 63 FDA reports)
NERVE INJURY ( 63 FDA reports)
OSTEOLYSIS ( 63 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 63 FDA reports)
AGEUSIA ( 62 FDA reports)
ILEUS ( 62 FDA reports)
JAW FRACTURE ( 62 FDA reports)
LIFE EXPECTANCY SHORTENED ( 62 FDA reports)
LOCALISED INFECTION ( 62 FDA reports)
POOR QUALITY SLEEP ( 62 FDA reports)
RASH PAPULAR ( 62 FDA reports)
TENDERNESS ( 62 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 61 FDA reports)
TYPE 1 DIABETES MELLITUS ( 61 FDA reports)
BONE FRAGMENTATION ( 61 FDA reports)
DENTAL FISTULA ( 61 FDA reports)
FAILURE TO THRIVE ( 61 FDA reports)
HEPATIC CIRRHOSIS ( 61 FDA reports)
INCONTINENCE ( 61 FDA reports)
MOOD SWINGS ( 61 FDA reports)
APHAGIA ( 60 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 60 FDA reports)
INTRACRANIAL ANEURYSM ( 60 FDA reports)
MANIA ( 60 FDA reports)
ACTINIC KERATOSIS ( 59 FDA reports)
DEVICE MALFUNCTION ( 59 FDA reports)
FACE OEDEMA ( 59 FDA reports)
MOUTH HAEMORRHAGE ( 59 FDA reports)
MUSCLE DISORDER ( 59 FDA reports)
PELVIC PAIN ( 59 FDA reports)
SHOCK ( 59 FDA reports)
SKIN HYPERPIGMENTATION ( 59 FDA reports)
STEVENS-JOHNSON SYNDROME ( 59 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 59 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 59 FDA reports)
TENDON RUPTURE ( 59 FDA reports)
UMBILICAL HERNIA ( 59 FDA reports)
SEXUAL DYSFUNCTION ( 58 FDA reports)
VENTRICULAR DYSFUNCTION ( 58 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 58 FDA reports)
BODY HEIGHT DECREASED ( 58 FDA reports)
DISEASE RECURRENCE ( 58 FDA reports)
EAR DISCOMFORT ( 58 FDA reports)
INTRACARDIAC THROMBUS ( 58 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 58 FDA reports)
MICTURITION URGENCY ( 58 FDA reports)
MITRAL VALVE CALCIFICATION ( 58 FDA reports)
NASAL SEPTUM DEVIATION ( 58 FDA reports)
NON-CARDIAC CHEST PAIN ( 58 FDA reports)
OEDEMA MOUTH ( 58 FDA reports)
OVARIAN CYST ( 58 FDA reports)
ACCIDENTAL OVERDOSE ( 57 FDA reports)
ANXIETY DISORDER ( 57 FDA reports)
DIABETIC RETINOPATHY ( 57 FDA reports)
HYPOKINESIA ( 57 FDA reports)
LACERATION ( 57 FDA reports)
MAJOR DEPRESSION ( 57 FDA reports)
MALIGNANT MELANOMA ( 57 FDA reports)
NICOTINE DEPENDENCE ( 57 FDA reports)
ODYNOPHAGIA ( 57 FDA reports)
TONGUE DISCOLOURATION ( 57 FDA reports)
TONGUE ULCERATION ( 57 FDA reports)
VENOUS INSUFFICIENCY ( 57 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 56 FDA reports)
SYNOVIAL CYST ( 56 FDA reports)
WOUND INFECTION ( 56 FDA reports)
BREAST MASS ( 56 FDA reports)
BREATH SOUNDS ABNORMAL ( 56 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 56 FDA reports)
MYOSITIS ( 56 FDA reports)
PLEURAL FIBROSIS ( 56 FDA reports)
PSYCHOTIC DISORDER ( 56 FDA reports)
DEAFNESS NEUROSENSORY ( 55 FDA reports)
DIABETIC KETOACIDOSIS ( 55 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 55 FDA reports)
INFUSION RELATED REACTION ( 55 FDA reports)
ISCHAEMIC STROKE ( 55 FDA reports)
SUICIDE ATTEMPT ( 55 FDA reports)
URINE OUTPUT DECREASED ( 55 FDA reports)
WOUND ( 55 FDA reports)
WOUND DRAINAGE ( 55 FDA reports)
WALKING AID USER ( 54 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 54 FDA reports)
BONE MARROW FAILURE ( 54 FDA reports)
DILATATION VENTRICULAR ( 54 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 54 FDA reports)
LOBAR PNEUMONIA ( 54 FDA reports)
ORAL INFECTION ( 54 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 53 FDA reports)
CERVICAL SPINAL STENOSIS ( 53 FDA reports)
ATHEROSCLEROSIS ( 52 FDA reports)
COLITIS ISCHAEMIC ( 52 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 52 FDA reports)
DECREASED ACTIVITY ( 52 FDA reports)
FRACTURE ( 52 FDA reports)
GRANULOMA ( 52 FDA reports)
HOMICIDAL IDEATION ( 52 FDA reports)
MUSCLE ATROPHY ( 52 FDA reports)
MUSCLE CRAMP ( 52 FDA reports)
OCCULT BLOOD POSITIVE ( 52 FDA reports)
OPEN WOUND ( 52 FDA reports)
SEQUESTRECTOMY ( 52 FDA reports)
SINUS HEADACHE ( 51 FDA reports)
SOFT TISSUE DISORDER ( 51 FDA reports)
TONGUE DISORDER ( 51 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 51 FDA reports)
BRONCHOSPASM ( 51 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 51 FDA reports)
CROHN'S DISEASE ( 51 FDA reports)
ENDOCARDITIS ( 51 FDA reports)
EYE INFECTION ( 51 FDA reports)
INGUINAL HERNIA ( 51 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 51 FDA reports)
OSTEOSCLEROSIS ( 51 FDA reports)
PETECHIAE ( 51 FDA reports)
DEVICE FAILURE ( 50 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 50 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 50 FDA reports)
OSTEITIS ( 50 FDA reports)
PANIC DISORDER ( 50 FDA reports)
POLYURIA ( 50 FDA reports)
RENAL TUBULAR NECROSIS ( 50 FDA reports)
VISUAL FIELD DEFECT ( 49 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 49 FDA reports)
APNOEA ( 49 FDA reports)
DIABETIC NEPHROPATHY ( 49 FDA reports)
MYOPATHY ( 49 FDA reports)
NEUROPATHY ( 49 FDA reports)
PAIN OF SKIN ( 49 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 48 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 48 FDA reports)
GRIP STRENGTH DECREASED ( 48 FDA reports)
HERPES SIMPLEX ( 48 FDA reports)
JOINT SPRAIN ( 48 FDA reports)
ONYCHOMYCOSIS ( 48 FDA reports)
PLASMACYTOSIS ( 48 FDA reports)
PNEUMOTHORAX ( 48 FDA reports)
PROSTATOMEGALY ( 48 FDA reports)
PYELONEPHRITIS ( 48 FDA reports)
SINUS POLYP ( 48 FDA reports)
SKIN LACERATION ( 48 FDA reports)
WRIST FRACTURE ( 48 FDA reports)
SNEEZING ( 47 FDA reports)
BRAIN INJURY ( 47 FDA reports)
BRONCHOPNEUMONIA ( 47 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 47 FDA reports)
FOOT DEFORMITY ( 47 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 47 FDA reports)
LUMBAR RADICULOPATHY ( 47 FDA reports)
OESOPHAGEAL DISORDER ( 47 FDA reports)
POLYTRAUMATISM ( 47 FDA reports)
BIPOLAR DISORDER ( 46 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 46 FDA reports)
CHOKING ( 46 FDA reports)
DERMAL CYST ( 46 FDA reports)
DUODENAL ULCER ( 46 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 46 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 46 FDA reports)
INJECTION SITE PRURITUS ( 46 FDA reports)
LIPASE INCREASED ( 46 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 46 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 46 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 46 FDA reports)
PANCREATIC CARCINOMA ( 46 FDA reports)
URINARY HESITATION ( 46 FDA reports)
VAGINAL HAEMORRHAGE ( 45 FDA reports)
BLOOD COUNT ABNORMAL ( 45 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 45 FDA reports)
GOITRE ( 45 FDA reports)
HEPATIC LESION ( 45 FDA reports)
HYDROCEPHALUS ( 45 FDA reports)
HYPOCALCAEMIA ( 45 FDA reports)
PELVIC FRACTURE ( 45 FDA reports)
BLEPHARITIS ( 44 FDA reports)
CHEST X-RAY ABNORMAL ( 44 FDA reports)
FACIAL BONES FRACTURE ( 44 FDA reports)
FACIAL PALSY ( 44 FDA reports)
FAMILY STRESS ( 44 FDA reports)
FULL BLOOD COUNT DECREASED ( 44 FDA reports)
GALLBLADDER OPERATION ( 44 FDA reports)
INJECTION SITE HAEMATOMA ( 44 FDA reports)
INJECTION SITE REACTION ( 44 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 44 FDA reports)
PROCTALGIA ( 44 FDA reports)
PULSE ABSENT ( 44 FDA reports)
SENSATION OF FOREIGN BODY ( 44 FDA reports)
SENSITIVITY OF TEETH ( 44 FDA reports)
TUBERCULOSIS ( 44 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 44 FDA reports)
VITREOUS DETACHMENT ( 44 FDA reports)
SNORING ( 43 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 43 FDA reports)
THERAPY NON-RESPONDER ( 43 FDA reports)
VOCAL CORD PARALYSIS ( 43 FDA reports)
ACUTE SINUSITIS ( 43 FDA reports)
AORTIC VALVE SCLEROSIS ( 43 FDA reports)
APLASTIC ANAEMIA ( 43 FDA reports)
ASPIRATION ( 43 FDA reports)
BLINDNESS TRANSIENT ( 43 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 43 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 43 FDA reports)
CONCUSSION ( 43 FDA reports)
GINGIVAL SWELLING ( 43 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 43 FDA reports)
HYPERPHAGIA ( 43 FDA reports)
INJECTION SITE BRUISING ( 43 FDA reports)
LIBIDO DECREASED ( 43 FDA reports)
LUNG CONSOLIDATION ( 43 FDA reports)
METABOLIC SYNDROME ( 43 FDA reports)
OTITIS MEDIA ( 43 FDA reports)
PARALYSIS ( 43 FDA reports)
PARANOIA ( 43 FDA reports)
ACNE ( 42 FDA reports)
ACUTE PULMONARY OEDEMA ( 42 FDA reports)
CLOSTRIDIAL INFECTION ( 42 FDA reports)
DENTURE WEARER ( 42 FDA reports)
FOREIGN BODY ( 42 FDA reports)
GASTRITIS EROSIVE ( 42 FDA reports)
INITIAL INSOMNIA ( 42 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 42 FDA reports)
PERICARDITIS ( 42 FDA reports)
PHOTOSENSITIVITY REACTION ( 42 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 42 FDA reports)
SPUTUM DISCOLOURED ( 42 FDA reports)
STRESS URINARY INCONTINENCE ( 42 FDA reports)
RETINAL DETACHMENT ( 41 FDA reports)
SENSORY LOSS ( 41 FDA reports)
SHOULDER PAIN ( 41 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 41 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 41 FDA reports)
TONGUE INJURY ( 41 FDA reports)
EAR DISORDER ( 41 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 41 FDA reports)
LABYRINTHITIS ( 41 FDA reports)
NECK INJURY ( 41 FDA reports)
NO ADVERSE EVENT ( 41 FDA reports)
OESOPHAGEAL ULCER ( 41 FDA reports)
PEAU D'ORANGE ( 41 FDA reports)
ABDOMINAL TENDERNESS ( 40 FDA reports)
BONE OPERATION ( 40 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 40 FDA reports)
ENDOTRACHEAL INTUBATION ( 40 FDA reports)
GANGRENE ( 40 FDA reports)
HAEMANGIOMA ( 40 FDA reports)
HEAD DISCOMFORT ( 40 FDA reports)
HUMERUS FRACTURE ( 40 FDA reports)
NASAL DISORDER ( 40 FDA reports)
OESOPHAGEAL STENOSIS ( 40 FDA reports)
ORGAN FAILURE ( 40 FDA reports)
POLYNEUROPATHY ( 40 FDA reports)
RENAL ARTERY STENOSIS ( 40 FDA reports)
SKIN IRRITATION ( 40 FDA reports)
SKIN PLAQUE ( 40 FDA reports)
SOCIAL PROBLEM ( 40 FDA reports)
TROPONIN INCREASED ( 40 FDA reports)
RESPIRATORY TRACT INFECTION ( 39 FDA reports)
SENSATION OF HEAVINESS ( 39 FDA reports)
TRIGGER FINGER ( 39 FDA reports)
UTERINE HAEMORRHAGE ( 39 FDA reports)
VASCULITIS ( 39 FDA reports)
ADRENAL INSUFFICIENCY ( 39 FDA reports)
CALCINOSIS ( 39 FDA reports)
COELIAC DISEASE ( 39 FDA reports)
COMPLETED SUICIDE ( 39 FDA reports)
EYELID DISORDER ( 39 FDA reports)
INJECTION SITE SWELLING ( 39 FDA reports)
MEDICATION RESIDUE ( 39 FDA reports)
NEOPLASM PROGRESSION ( 39 FDA reports)
ORAL INTAKE REDUCED ( 39 FDA reports)
PERITONITIS ( 39 FDA reports)
QUALITY OF LIFE DECREASED ( 39 FDA reports)
RASH MACULO-PAPULAR ( 39 FDA reports)
APPLICATION SITE ERYTHEMA ( 38 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 38 FDA reports)
BREAST CANCER RECURRENT ( 38 FDA reports)
DIZZINESS POSTURAL ( 38 FDA reports)
DRUG PRESCRIBING ERROR ( 38 FDA reports)
EXERCISE LACK OF ( 38 FDA reports)
EYE PRURITUS ( 38 FDA reports)
HAEMORRHAGIC DIATHESIS ( 38 FDA reports)
INTESTINAL ISCHAEMIA ( 38 FDA reports)
MUSCULOSKELETAL DISORDER ( 38 FDA reports)
PROCEDURAL COMPLICATION ( 38 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 38 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 38 FDA reports)
SUDDEN DEATH ( 37 FDA reports)
THINKING ABNORMAL ( 37 FDA reports)
ACCIDENT ( 37 FDA reports)
ACIDOSIS ( 37 FDA reports)
BLOOD CHLORIDE DECREASED ( 37 FDA reports)
BLOOD URIC ACID INCREASED ( 37 FDA reports)
CHONDROMALACIA ( 37 FDA reports)
COLON ADENOMA ( 37 FDA reports)
COSTOCHONDRITIS ( 37 FDA reports)
DELUSION ( 37 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 37 FDA reports)
EXPIRED DRUG ADMINISTERED ( 37 FDA reports)
EYELID PTOSIS ( 37 FDA reports)
HYPERTENSIVE CRISIS ( 37 FDA reports)
LYMPHADENITIS ( 37 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 37 FDA reports)
MUSCLE RIGIDITY ( 37 FDA reports)
NEPHROSCLEROSIS ( 37 FDA reports)
ORAL DISCOMFORT ( 37 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 37 FDA reports)
ANGIOPLASTY ( 36 FDA reports)
BREAST TENDERNESS ( 36 FDA reports)
DENTAL OPERATION ( 36 FDA reports)
DRUG ERUPTION ( 36 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 36 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 36 FDA reports)
GASTRIC POLYPS ( 36 FDA reports)
GOUTY ARTHRITIS ( 36 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 36 FDA reports)
MELANOCYTIC NAEVUS ( 36 FDA reports)
NERVE COMPRESSION ( 36 FDA reports)
PROTEIN URINE PRESENT ( 36 FDA reports)
SKIN INFECTION ( 36 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 36 FDA reports)
VIITH NERVE PARALYSIS ( 36 FDA reports)
SEBORRHOEIC KERATOSIS ( 35 FDA reports)
SINUS ARRHYTHMIA ( 35 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 35 FDA reports)
SPONDYLITIS ( 35 FDA reports)
VAGINAL DISCHARGE ( 35 FDA reports)
ANOSMIA ( 35 FDA reports)
BLOOD DISORDER ( 35 FDA reports)
BREAST HYPERPLASIA ( 35 FDA reports)
BREATH ODOUR ( 35 FDA reports)
CIRCULATORY COLLAPSE ( 35 FDA reports)
DIABETIC COMPLICATION ( 35 FDA reports)
EXERCISE TOLERANCE DECREASED ( 35 FDA reports)
IMMUNOSUPPRESSION ( 35 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 35 FDA reports)
MEDICAL DEVICE COMPLICATION ( 35 FDA reports)
METASTASES TO LYMPH NODES ( 35 FDA reports)
NEUTROPHIL COUNT DECREASED ( 35 FDA reports)
OLFACTORY NERVE DISORDER ( 35 FDA reports)
OPTIC NEURITIS ( 35 FDA reports)
PLANTAR FASCIITIS ( 35 FDA reports)
POOR PERIPHERAL CIRCULATION ( 35 FDA reports)
PULMONARY GRANULOMA ( 35 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 35 FDA reports)
ANGIONEUROTIC OEDEMA ( 34 FDA reports)
APPARENT DEATH ( 34 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 34 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 34 FDA reports)
BRONCHITIS CHRONIC ( 34 FDA reports)
CONJUNCTIVITIS ( 34 FDA reports)
CORONARY ARTERY THROMBOSIS ( 34 FDA reports)
DEAFNESS UNILATERAL ( 34 FDA reports)
DEMENTIA WITH LEWY BODIES ( 34 FDA reports)
DERMATITIS CONTACT ( 34 FDA reports)
EXTREMITY CONTRACTURE ( 34 FDA reports)
EYELID OEDEMA ( 34 FDA reports)
FAECALOMA ( 34 FDA reports)
FORMICATION ( 34 FDA reports)
HAEMOLYTIC ANAEMIA ( 34 FDA reports)
HICCUPS ( 34 FDA reports)
HYPERTONIC BLADDER ( 34 FDA reports)
LIPOMA ( 34 FDA reports)
MARROW HYPERPLASIA ( 34 FDA reports)
MASTECTOMY ( 34 FDA reports)
NO THERAPEUTIC RESPONSE ( 34 FDA reports)
PIGMENTATION DISORDER ( 34 FDA reports)
POOR DENTAL CONDITION ( 34 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 34 FDA reports)
REFLUX OESOPHAGITIS ( 34 FDA reports)
SCAB ( 34 FDA reports)
SINUS OPERATION ( 34 FDA reports)
TENDON DISORDER ( 34 FDA reports)
ULCER HAEMORRHAGE ( 34 FDA reports)
RENAL CANCER ( 33 FDA reports)
RETINAL HAEMORRHAGE ( 33 FDA reports)
RHONCHI ( 33 FDA reports)
SENSORY DISTURBANCE ( 33 FDA reports)
SYNCOPE VASOVAGAL ( 33 FDA reports)
TEMPORAL ARTERITIS ( 33 FDA reports)
TOOTH IMPACTED ( 33 FDA reports)
URINARY TRACT DISORDER ( 33 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 33 FDA reports)
CEREBROVASCULAR DISORDER ( 33 FDA reports)
DEVICE DISLOCATION ( 33 FDA reports)
IMMUNE SYSTEM DISORDER ( 33 FDA reports)
INJECTION SITE IRRITATION ( 33 FDA reports)
NASAL DISCOMFORT ( 33 FDA reports)
NERVE ROOT LESION ( 33 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 33 FDA reports)
ORAL DISORDER ( 33 FDA reports)
PLATELET COUNT INCREASED ( 33 FDA reports)
PROCEDURAL PAIN ( 33 FDA reports)
APATHY ( 32 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 32 FDA reports)
BEDRIDDEN ( 32 FDA reports)
BRONCHITIS ACUTE ( 32 FDA reports)
CHOLECYSTITIS ACUTE ( 32 FDA reports)
DUODENITIS ( 32 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 32 FDA reports)
GASTROINTESTINAL PAIN ( 32 FDA reports)
HYPOAESTHESIA FACIAL ( 32 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 32 FDA reports)
LEUKAEMIA ( 32 FDA reports)
LUNG HYPERINFLATION ( 32 FDA reports)
MUSCLE FATIGUE ( 32 FDA reports)
PULMONARY MASS ( 32 FDA reports)
PURPURA ( 32 FDA reports)
RENAL CELL CARCINOMA ( 32 FDA reports)
TEMPERATURE INTOLERANCE ( 32 FDA reports)
UTERINE POLYP ( 32 FDA reports)
VITAMIN B12 DEFICIENCY ( 32 FDA reports)
RETINOPATHY ( 31 FDA reports)
SARCOIDOSIS ( 31 FDA reports)
SLUGGISHNESS ( 31 FDA reports)
TOURETTE'S DISORDER ( 31 FDA reports)
X-RAY ABNORMAL ( 31 FDA reports)
AORTIC CALCIFICATION ( 31 FDA reports)
APLASIA PURE RED CELL ( 31 FDA reports)
ATROPHIC VULVOVAGINITIS ( 31 FDA reports)
BRAIN NEOPLASM ( 31 FDA reports)
COAGULATION TIME PROLONGED ( 31 FDA reports)
CORONARY ARTERY RESTENOSIS ( 31 FDA reports)
DEVICE BREAKAGE ( 31 FDA reports)
FEELING DRUNK ( 31 FDA reports)
INGROWING NAIL ( 31 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 31 FDA reports)
PANCREATITIS CHRONIC ( 31 FDA reports)
PULPITIS DENTAL ( 31 FDA reports)
AUTONOMIC NEUROPATHY ( 30 FDA reports)
BASEDOW'S DISEASE ( 30 FDA reports)
BLOOD CHLORIDE INCREASED ( 30 FDA reports)
BLOOD CULTURE POSITIVE ( 30 FDA reports)
BONE LOSS ( 30 FDA reports)
BREAST DISORDER ( 30 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 30 FDA reports)
EMBOLISM ( 30 FDA reports)
GENERALISED ERYTHEMA ( 30 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 30 FDA reports)
LIPIDS INCREASED ( 30 FDA reports)
OSTEOMYELITIS CHRONIC ( 30 FDA reports)
RENAL MASS ( 30 FDA reports)
RIGHT ATRIAL DILATATION ( 30 FDA reports)
SKIN ATROPHY ( 30 FDA reports)
STRESS FRACTURE ( 30 FDA reports)
VERTEBROPLASTY ( 30 FDA reports)
SEROMA ( 29 FDA reports)
VASCULAR GRAFT ( 29 FDA reports)
APPLICATION SITE PRURITUS ( 29 FDA reports)
BILIARY DILATATION ( 29 FDA reports)
BRONCHIAL SECRETION RETENTION ( 29 FDA reports)
BRUXISM ( 29 FDA reports)
CARDIAC OUTPUT DECREASED ( 29 FDA reports)
CARDIAC VALVE SCLEROSIS ( 29 FDA reports)
CATHETER RELATED INFECTION ( 29 FDA reports)
COLLAPSE OF LUNG ( 29 FDA reports)
EARLY SATIETY ( 29 FDA reports)
HEPATIC ENCEPHALOPATHY ( 29 FDA reports)
LARGE INTESTINE PERFORATION ( 29 FDA reports)
MENINGIOMA ( 29 FDA reports)
METAMORPHOPSIA ( 29 FDA reports)
MONOCYTE COUNT INCREASED ( 29 FDA reports)
NEOPLASM ( 29 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 29 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 29 FDA reports)
ABSCESS JAW ( 28 FDA reports)
ACCIDENT AT HOME ( 28 FDA reports)
ACUTE PRERENAL FAILURE ( 28 FDA reports)
BLOOD AMYLASE INCREASED ( 28 FDA reports)
BLOOD SODIUM INCREASED ( 28 FDA reports)
BONE FORMATION DECREASED ( 28 FDA reports)
BONE NEOPLASM MALIGNANT ( 28 FDA reports)
BREAST CANCER METASTATIC ( 28 FDA reports)
CARBON DIOXIDE INCREASED ( 28 FDA reports)
FACE INJURY ( 28 FDA reports)
FEMORAL NECK FRACTURE ( 28 FDA reports)
HEARING DISABILITY ( 28 FDA reports)
HUNGER ( 28 FDA reports)
HYPERPLASIA ( 28 FDA reports)
INADEQUATE ANALGESIA ( 28 FDA reports)
LOSS OF EMPLOYMENT ( 28 FDA reports)
MOTOR DYSFUNCTION ( 28 FDA reports)
MULTIPLE ALLERGIES ( 28 FDA reports)
MYASTHENIA GRAVIS ( 28 FDA reports)
NASAL DRYNESS ( 28 FDA reports)
NASAL POLYPS ( 28 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 28 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 28 FDA reports)
PROTEIN TOTAL DECREASED ( 28 FDA reports)
PYURIA ( 28 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 28 FDA reports)
SEBORRHOEIC DERMATITIS ( 28 FDA reports)
TACHYPNOEA ( 28 FDA reports)
VENOUS THROMBOSIS ( 27 FDA reports)
BLOOD MAGNESIUM DECREASED ( 27 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 27 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 27 FDA reports)
CHOLECYSTITIS INFECTIVE ( 27 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 27 FDA reports)
CONVERSION DISORDER ( 27 FDA reports)
DEVICE RELATED SEPSIS ( 27 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 27 FDA reports)
HAEMORRHAGIC STROKE ( 27 FDA reports)
HAIR GROWTH ABNORMAL ( 27 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 27 FDA reports)
INCOHERENT ( 27 FDA reports)
INTESTINAL PERFORATION ( 27 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 27 FDA reports)
MALIGNANT HYPERTENSION ( 27 FDA reports)
NEURODERMATITIS ( 27 FDA reports)
PATHOLOGICAL GAMBLING ( 27 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 27 FDA reports)
PERONEAL NERVE PALSY ( 27 FDA reports)
PLEURISY ( 27 FDA reports)
PRESBYOPIA ( 27 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 27 FDA reports)
ACCIDENT AT WORK ( 26 FDA reports)
AORTIC DILATATION ( 26 FDA reports)
CONDUCTION DISORDER ( 26 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 26 FDA reports)
HAEMATOCRIT ABNORMAL ( 26 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 26 FDA reports)
HYPERPARATHYROIDISM ( 26 FDA reports)
HYPOTONIA ( 26 FDA reports)
ILEUS PARALYTIC ( 26 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 26 FDA reports)
INTESTINAL POLYP ( 26 FDA reports)
IRON DEFICIENCY ( 26 FDA reports)
LUNG INFECTION ( 26 FDA reports)
MACROGLOSSIA ( 26 FDA reports)
METASTATIC NEOPLASM ( 26 FDA reports)
NARCOLEPSY ( 26 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 26 FDA reports)
PRESCRIBED OVERDOSE ( 26 FDA reports)
PROSTATIC DISORDER ( 26 FDA reports)
RADIUS FRACTURE ( 26 FDA reports)
RENAL PAIN ( 26 FDA reports)
SKIN NECROSIS ( 26 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 26 FDA reports)
WEIGHT FLUCTUATION ( 26 FDA reports)
RESPIRATORY TRACT CONGESTION ( 25 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 25 FDA reports)
STENT OCCLUSION ( 25 FDA reports)
STRESS SYMPTOMS ( 25 FDA reports)
SUBCUTANEOUS NODULE ( 25 FDA reports)
ALVEOLOPLASTY ( 25 FDA reports)
CARDIAC ABLATION ( 25 FDA reports)
CARDIAC ENZYMES INCREASED ( 25 FDA reports)
CERVICOBRACHIAL SYNDROME ( 25 FDA reports)
DYSTONIA ( 25 FDA reports)
ENTEROCOCCAL INFECTION ( 25 FDA reports)
ESCHERICHIA INFECTION ( 25 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 25 FDA reports)
HEART RATE ABNORMAL ( 25 FDA reports)
HEMIPLEGIA ( 25 FDA reports)
HYPERURICAEMIA ( 25 FDA reports)
HYPOALBUMINAEMIA ( 25 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 25 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 25 FDA reports)
LIGAMENT SPRAIN ( 25 FDA reports)
NECROSIS ( 25 FDA reports)
NEUROGENIC BLADDER ( 25 FDA reports)
NODAL RHYTHM ( 25 FDA reports)
ORAL HERPES ( 25 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 25 FDA reports)
POSTNASAL DRIP ( 25 FDA reports)
PRODUCT ADHESION ISSUE ( 25 FDA reports)
PULMONARY THROMBOSIS ( 25 FDA reports)
PURULENCE ( 25 FDA reports)
REFLUX LARYNGITIS ( 25 FDA reports)
ABNORMAL FAECES ( 24 FDA reports)
AMMONIA INCREASED ( 24 FDA reports)
ANAPHYLACTIC SHOCK ( 24 FDA reports)
ANURIA ( 24 FDA reports)
APPLICATION SITE RASH ( 24 FDA reports)
ARTERIAL DISORDER ( 24 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 24 FDA reports)
BODY TEMPERATURE DECREASED ( 24 FDA reports)
CARDIAC ANEURYSM ( 24 FDA reports)
DRUG ABUSER ( 24 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 24 FDA reports)
DRUG SCREEN POSITIVE ( 24 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 24 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 24 FDA reports)
EMBOLIC STROKE ( 24 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 24 FDA reports)
HEART VALVE INCOMPETENCE ( 24 FDA reports)
INJECTION SITE EXTRAVASATION ( 24 FDA reports)
INTENTIONAL OVERDOSE ( 24 FDA reports)
JUGULAR VEIN DISTENSION ( 24 FDA reports)
MITRAL VALVE STENOSIS ( 24 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 24 FDA reports)
OESOPHAGEAL PAIN ( 24 FDA reports)
PERFORMANCE STATUS DECREASED ( 24 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 24 FDA reports)
PSEUDOMONAS INFECTION ( 24 FDA reports)
RIGHT VENTRICULAR FAILURE ( 24 FDA reports)
SOFT TISSUE INFLAMMATION ( 24 FDA reports)
SPINAL CORD COMPRESSION ( 24 FDA reports)
THROMBOSIS IN DEVICE ( 24 FDA reports)
TONGUE COATED ( 24 FDA reports)
TRANSFUSION ( 24 FDA reports)
VASCULAR CALCIFICATION ( 24 FDA reports)
VOCAL CORD DISORDER ( 24 FDA reports)
ABSCESS ORAL ( 23 FDA reports)
AFFECTIVE DISORDER ( 23 FDA reports)
ANOXIC ENCEPHALOPATHY ( 23 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 23 FDA reports)
AORTIC VALVE REPLACEMENT ( 23 FDA reports)
CHANGE OF BOWEL HABIT ( 23 FDA reports)
CHEST WALL PAIN ( 23 FDA reports)
CREPITATIONS ( 23 FDA reports)
CYSTOCELE ( 23 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 23 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 23 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 23 FDA reports)
GASTRIC HAEMORRHAGE ( 23 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 23 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 23 FDA reports)
GENITAL HERPES ( 23 FDA reports)
HAEMODYNAMIC INSTABILITY ( 23 FDA reports)
HAEMOLYSIS ( 23 FDA reports)
HEPATIC CONGESTION ( 23 FDA reports)
HIP SURGERY ( 23 FDA reports)
HYPOGONADISM ( 23 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 23 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 23 FDA reports)
LIP PAIN ( 23 FDA reports)
LOCALISED OEDEMA ( 23 FDA reports)
MACULAR OEDEMA ( 23 FDA reports)
MICTURITION DISORDER ( 23 FDA reports)
NAIL DISORDER ( 23 FDA reports)
NEPHROPATHY ( 23 FDA reports)
OCULAR ICTERUS ( 23 FDA reports)
OROPHARYNGEAL BLISTERING ( 23 FDA reports)
PERIPHERAL ISCHAEMIA ( 23 FDA reports)
PITTING OEDEMA ( 23 FDA reports)
PSYCHIATRIC SYMPTOM ( 23 FDA reports)
RECTOCELE ( 23 FDA reports)
ALKALOSIS ( 22 FDA reports)
ANISOCYTOSIS ( 22 FDA reports)
AORTIC VALVE DISEASE ( 22 FDA reports)
AORTIC VALVE STENOSIS ( 22 FDA reports)
APPETITE DISORDER ( 22 FDA reports)
APPLICATION SITE IRRITATION ( 22 FDA reports)
ARTHROPOD BITE ( 22 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 22 FDA reports)
BONE EROSION ( 22 FDA reports)
CATHETER PLACEMENT ( 22 FDA reports)
CATHETER RELATED COMPLICATION ( 22 FDA reports)
CERVICAL DYSPLASIA ( 22 FDA reports)
CHOKING SENSATION ( 22 FDA reports)
DERMATOPHYTOSIS ( 22 FDA reports)
FIBROUS HISTIOCYTOMA ( 22 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 22 FDA reports)
HEPATIC MASS ( 22 FDA reports)
HYPOVENTILATION ( 22 FDA reports)
INFARCTION ( 22 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 22 FDA reports)
MACULAR HOLE ( 22 FDA reports)
MALABSORPTION ( 22 FDA reports)
MAXILLOFACIAL OPERATION ( 22 FDA reports)
METABOLIC ENCEPHALOPATHY ( 22 FDA reports)
MICROCYTIC ANAEMIA ( 22 FDA reports)
MULTIPLE FRACTURES ( 22 FDA reports)
NEURITIS ( 22 FDA reports)
NEUTROPENIC SEPSIS ( 22 FDA reports)
NEUTROPHIL COUNT INCREASED ( 22 FDA reports)
OESOPHAGEAL SPASM ( 22 FDA reports)
PERIODONTAL OPERATION ( 22 FDA reports)
POLYMYALGIA RHEUMATICA ( 22 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 22 FDA reports)
SERUM FERRITIN INCREASED ( 22 FDA reports)
SKIN NEOPLASM EXCISION ( 22 FDA reports)
SKIN PAPILLOMA ( 22 FDA reports)
SKIN WARM ( 22 FDA reports)
URGE INCONTINENCE ( 22 FDA reports)
SECRETION DISCHARGE ( 21 FDA reports)
SKIN REACTION ( 21 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 21 FDA reports)
TOE OPERATION ( 21 FDA reports)
VARICOSE VEIN ( 21 FDA reports)
VITAMIN D DECREASED ( 21 FDA reports)
WOUND DECOMPOSITION ( 21 FDA reports)
YELLOW SKIN ( 21 FDA reports)
ABDOMINAL RIGIDITY ( 21 FDA reports)
ABNORMAL SENSATION IN EYE ( 21 FDA reports)
ACCOMMODATION DISORDER ( 21 FDA reports)
ALCOHOL USE ( 21 FDA reports)
APHTHOUS STOMATITIS ( 21 FDA reports)
ARTERIAL STENOSIS ( 21 FDA reports)
ATRIAL SEPTAL DEFECT ( 21 FDA reports)
BLOOD CREATINE INCREASED ( 21 FDA reports)
BLOOD IRON DECREASED ( 21 FDA reports)
BREAST CANCER IN SITU ( 21 FDA reports)
CALCULUS URETERIC ( 21 FDA reports)
CARDIAC TAMPONADE ( 21 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 21 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 21 FDA reports)
DENTOFACIAL FUNCTIONAL DISORDER ( 21 FDA reports)
ECZEMA ASTEATOTIC ( 21 FDA reports)
EYE OPERATION ( 21 FDA reports)
FEAR OF DEATH ( 21 FDA reports)
FURUNCLE ( 21 FDA reports)
GLOSSITIS ( 21 FDA reports)
IMMOBILE ( 21 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 21 FDA reports)
MACROCYTOSIS ( 21 FDA reports)
METASTASIS ( 21 FDA reports)
MUSCLE INJURY ( 21 FDA reports)
MYOCLONUS ( 21 FDA reports)
NIPPLE PAIN ( 21 FDA reports)
PERIODONTAL INFECTION ( 21 FDA reports)
PERSONALITY CHANGE ( 21 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 21 FDA reports)
PLASMACYTOMA ( 21 FDA reports)
ABDOMINAL ABSCESS ( 20 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 20 FDA reports)
ADENOMYOSIS ( 20 FDA reports)
AEROMONA INFECTION ( 20 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 20 FDA reports)
ANAEMIA POSTOPERATIVE ( 20 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 20 FDA reports)
ASTHENOPIA ( 20 FDA reports)
BLOOD TEST ABNORMAL ( 20 FDA reports)
CERVICAL CORD COMPRESSION ( 20 FDA reports)
CHOLESTASIS ( 20 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 20 FDA reports)
CLUSTER HEADACHE ( 20 FDA reports)
COCCYDYNIA ( 20 FDA reports)
COLECTOMY ( 20 FDA reports)
CORONARY ARTERY SURGERY ( 20 FDA reports)
CYSTITIS INTERSTITIAL ( 20 FDA reports)
DIABETIC FOOT ( 20 FDA reports)
DRUG ABUSE ( 20 FDA reports)
DRUG TOLERANCE ( 20 FDA reports)
FACET JOINT SYNDROME ( 20 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 20 FDA reports)
FLUID INTAKE REDUCED ( 20 FDA reports)
GASTROINTESTINAL INFECTION ( 20 FDA reports)
GASTROINTESTINAL ULCER ( 20 FDA reports)
GENERALISED ANXIETY DISORDER ( 20 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 20 FDA reports)
HEPATOTOXICITY ( 20 FDA reports)
HERPES VIRUS INFECTION ( 20 FDA reports)
HYPERPHOSPHATAEMIA ( 20 FDA reports)
ICHTHYOSIS ( 20 FDA reports)
INJECTION SITE INDURATION ( 20 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 20 FDA reports)
KNEE OPERATION ( 20 FDA reports)
LIGAMENT RUPTURE ( 20 FDA reports)
LUMBAR SPINE FLATTENING ( 20 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 20 FDA reports)
ORAL MUCOSA ATROPHY ( 20 FDA reports)
ORTHODONTIC APPLIANCE USER ( 20 FDA reports)
PANCREATIC DISORDER ( 20 FDA reports)
PANCREATIC ENZYMES INCREASED ( 20 FDA reports)
PARANASAL SINUS BENIGN NEOPLASM ( 20 FDA reports)
PROGRESSIVE SUPRANUCLEAR PALSY ( 20 FDA reports)
PULMONARY ARTERY DILATATION ( 20 FDA reports)
RAYNAUD'S PHENOMENON ( 20 FDA reports)
RENAL HAEMORRHAGE ( 20 FDA reports)
RENAL TRANSPLANT ( 20 FDA reports)
RESORPTION BONE INCREASED ( 20 FDA reports)
SERRATIA INFECTION ( 20 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 20 FDA reports)
TONGUE OEDEMA ( 20 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 20 FDA reports)
URETERAL DISORDER ( 20 FDA reports)
URETHRAL STENOSIS ( 20 FDA reports)
VASODILATATION ( 20 FDA reports)
VENOUS THROMBOSIS LIMB ( 20 FDA reports)
ROTATOR CUFF REPAIR ( 19 FDA reports)
SACROILIITIS ( 19 FDA reports)
THROMBOPHLEBITIS ( 19 FDA reports)
TOOTH DISCOLOURATION ( 19 FDA reports)
UNDERDOSE ( 19 FDA reports)
URINE ANALYSIS ABNORMAL ( 19 FDA reports)
VERTIGO POSITIONAL ( 19 FDA reports)
WOUND HAEMORRHAGE ( 19 FDA reports)
ACCIDENTAL EXPOSURE ( 19 FDA reports)
ADENOCARCINOMA ( 19 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 19 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 19 FDA reports)
AORTIC BRUIT ( 19 FDA reports)
APPENDICITIS ( 19 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 19 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 19 FDA reports)
BLADDER DYSFUNCTION ( 19 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 19 FDA reports)
BUNDLE BRANCH BLOCK ( 19 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 19 FDA reports)
CONNECTIVE TISSUE DISORDER ( 19 FDA reports)
CSF PROTEIN INCREASED ( 19 FDA reports)
CYST ASPIRATION ( 19 FDA reports)
DENTAL PLAQUE ( 19 FDA reports)
DIABETIC COMA ( 19 FDA reports)
EYE DISCHARGE ( 19 FDA reports)
FIBRIN D DIMER INCREASED ( 19 FDA reports)
HELICOBACTER INFECTION ( 19 FDA reports)
ISCHAEMIC HEPATITIS ( 19 FDA reports)
JOINT SURGERY ( 19 FDA reports)
MECHANICAL VENTILATION ( 19 FDA reports)
MENIERE'S DISEASE ( 19 FDA reports)
MUSCLE CONTRACTURE ( 19 FDA reports)
MYELOPATHY ( 19 FDA reports)
NOCTURNAL DYSPNOEA ( 19 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 19 FDA reports)
OCCULT BLOOD ( 19 FDA reports)
OOPHORECTOMY ( 19 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 19 FDA reports)
OTITIS EXTERNA ( 19 FDA reports)
PCO2 DECREASED ( 19 FDA reports)
PERIORBITAL OEDEMA ( 19 FDA reports)
RADICULAR SYNDROME ( 19 FDA reports)
READING DISORDER ( 19 FDA reports)
ABDOMINAL HAEMATOMA ( 18 FDA reports)
ABSCESS DRAINAGE ( 18 FDA reports)
ACROCHORDON ( 18 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 18 FDA reports)
BLOODY DISCHARGE ( 18 FDA reports)
BONE MARROW TRANSPLANT ( 18 FDA reports)
BRAIN COMPRESSION ( 18 FDA reports)
CARDIOVERSION ( 18 FDA reports)
CHEILITIS ( 18 FDA reports)
CHEMOTHERAPY ( 18 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 18 FDA reports)
CRANIAL NERVE DISORDER ( 18 FDA reports)
EAR CONGESTION ( 18 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 18 FDA reports)
ENTEROBACTER INFECTION ( 18 FDA reports)
FISTULA DISCHARGE ( 18 FDA reports)
GLYCOSURIA ( 18 FDA reports)
HAEMORRHAGIC ANAEMIA ( 18 FDA reports)
HYPERAESTHESIA ( 18 FDA reports)
INTESTINAL HAEMORRHAGE ( 18 FDA reports)
LACTIC ACIDOSIS ( 18 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 18 FDA reports)
MOTION SICKNESS ( 18 FDA reports)
NEOPLASM RECURRENCE ( 18 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 18 FDA reports)
OESOPHAGEAL CARCINOMA ( 18 FDA reports)
OVARIAN CANCER ( 18 FDA reports)
PANCREATIC NEOPLASM ( 18 FDA reports)
PARKINSONIAN GAIT ( 18 FDA reports)
PNEUMONIA BACTERIAL ( 18 FDA reports)
POLYARTHRITIS ( 18 FDA reports)
POLYCYTHAEMIA ( 18 FDA reports)
PULMONARY CALCIFICATION ( 18 FDA reports)
RADIATION INJURY ( 18 FDA reports)
RADIOTHERAPY ( 18 FDA reports)
RENAL COLIC ( 18 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 18 FDA reports)
SENSATION OF PRESSURE ( 18 FDA reports)
SPLENIC CALCIFICATION ( 18 FDA reports)
SUBDURAL HAEMORRHAGE ( 18 FDA reports)
THERMAL BURN ( 18 FDA reports)
TRACHEOBRONCHITIS ( 18 FDA reports)
ULNA FRACTURE ( 18 FDA reports)
VEIN DISORDER ( 18 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 18 FDA reports)
RESUSCITATION ( 17 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 17 FDA reports)
SCLERODERMA ( 17 FDA reports)
SEPSIS SYNDROME ( 17 FDA reports)
SJOGREN'S SYNDROME ( 17 FDA reports)
SKIN ODOUR ABNORMAL ( 17 FDA reports)
STREPTOCOCCAL SEPSIS ( 17 FDA reports)
TENDON INJURY ( 17 FDA reports)
TENDON PAIN ( 17 FDA reports)
TINEA PEDIS ( 17 FDA reports)
UMBILICAL HERNIA REPAIR ( 17 FDA reports)
URINE FLOW DECREASED ( 17 FDA reports)
UTERINE CANCER ( 17 FDA reports)
UTERINE DISORDER ( 17 FDA reports)
VENA CAVA FILTER INSERTION ( 17 FDA reports)
ABDOMINAL MASS ( 17 FDA reports)
ACUTE HEPATIC FAILURE ( 17 FDA reports)
AORTIC DISORDER ( 17 FDA reports)
ARTERIAL THROMBOSIS ( 17 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 17 FDA reports)
BRAIN HERNIATION ( 17 FDA reports)
BRAIN OEDEMA ( 17 FDA reports)
CHARLES BONNET SYNDROME ( 17 FDA reports)
CHOLANGITIS ( 17 FDA reports)
COLOSTOMY ( 17 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 17 FDA reports)
EAR NEOPLASM ( 17 FDA reports)
ENDOCARDITIS BACTERIAL ( 17 FDA reports)
EPIGASTRIC DISCOMFORT ( 17 FDA reports)
EXFOLIATIVE RASH ( 17 FDA reports)
FIBROMA ( 17 FDA reports)
GASTROINTESTINAL NECROSIS ( 17 FDA reports)
GINGIVAL ERYTHEMA ( 17 FDA reports)
HEART TRANSPLANT ( 17 FDA reports)
HYPERBILIRUBINAEMIA ( 17 FDA reports)
HYPERKINESIA ( 17 FDA reports)
HYPERMETROPIA ( 17 FDA reports)
HYPOPERFUSION ( 17 FDA reports)
INJECTION SITE DISCOLOURATION ( 17 FDA reports)
INJECTION SITE MASS ( 17 FDA reports)
JAUNDICE CHOLESTATIC ( 17 FDA reports)
KYPHOSCOLIOSIS ( 17 FDA reports)
LEG AMPUTATION ( 17 FDA reports)
LIMB OPERATION ( 17 FDA reports)
METAPLASIA ( 17 FDA reports)
MYDRIASIS ( 17 FDA reports)
MYOPIA ( 17 FDA reports)
NON-SMALL CELL LUNG CANCER ( 17 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 17 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 17 FDA reports)
OVERWEIGHT ( 17 FDA reports)
PALATAL DISORDER ( 17 FDA reports)
PANIC REACTION ( 17 FDA reports)
PATHOGEN RESISTANCE ( 17 FDA reports)
PERIARTHRITIS ( 17 FDA reports)
PERITONEAL DIALYSIS ( 17 FDA reports)
PHLEBITIS ( 17 FDA reports)
POLYMYOSITIS ( 17 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 17 FDA reports)
PYELONEPHRITIS ACUTE ( 17 FDA reports)
ANAL FISSURE ( 16 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 16 FDA reports)
APPLICATION SITE PAIN ( 16 FDA reports)
ARTERIAL STENT INSERTION ( 16 FDA reports)
ASTIGMATISM ( 16 FDA reports)
BIPOLAR I DISORDER ( 16 FDA reports)
BLADDER PROLAPSE ( 16 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 16 FDA reports)
BONE LESION EXCISION ( 16 FDA reports)
CACHEXIA ( 16 FDA reports)
CARDIORENAL SYNDROME ( 16 FDA reports)
CHOROIDAL DETACHMENT ( 16 FDA reports)
DENTAL PULP DISORDER ( 16 FDA reports)
DROOLING ( 16 FDA reports)
EPILEPSY ( 16 FDA reports)
EUTHYROID SICK SYNDROME ( 16 FDA reports)
FOLLICULITIS ( 16 FDA reports)
FOREIGN BODY TRAUMA ( 16 FDA reports)
HAEMOPHILUS INFECTION ( 16 FDA reports)
HAEMOTHORAX ( 16 FDA reports)
HAIR TEXTURE ABNORMAL ( 16 FDA reports)
HEPATOSPLENOMEGALY ( 16 FDA reports)
HISTOPLASMOSIS ( 16 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 16 FDA reports)
HYPOTHERMIA ( 16 FDA reports)
INJECTION SITE NODULE ( 16 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 16 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 16 FDA reports)
JUGULAR VEIN THROMBOSIS ( 16 FDA reports)
LEFT VENTRICULAR FAILURE ( 16 FDA reports)
LIVEDO RETICULARIS ( 16 FDA reports)
LUDWIG ANGINA ( 16 FDA reports)
MEAN CELL VOLUME INCREASED ( 16 FDA reports)
MENINGITIS ( 16 FDA reports)
OCULAR VASCULAR DISORDER ( 16 FDA reports)
OESOPHAGEAL MUCOSAL HYPERPLASIA ( 16 FDA reports)
ORAL FIBROMA ( 16 FDA reports)
PARATHYROID TUMOUR BENIGN ( 16 FDA reports)
PELVIC FLOOR MUSCLE WEAKNESS ( 16 FDA reports)
POST HERPETIC NEURALGIA ( 16 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 16 FDA reports)
PSORIATIC ARTHROPATHY ( 16 FDA reports)
RASH PUSTULAR ( 16 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 16 FDA reports)
ROSACEA ( 16 FDA reports)
SCAN MYOCARDIAL PERFUSION ( 16 FDA reports)
SCAPULA FRACTURE ( 16 FDA reports)
SINUS RHYTHM ( 16 FDA reports)
SPINAL FUSION ACQUIRED ( 16 FDA reports)
SUDDEN CARDIAC DEATH ( 16 FDA reports)
THERAPY CESSATION ( 16 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 16 FDA reports)
TOBACCO ABUSE ( 16 FDA reports)
TRANSAMINASES INCREASED ( 16 FDA reports)
TUBERCULIN TEST POSITIVE ( 16 FDA reports)
VASCULAR GRAFT OCCLUSION ( 16 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 16 FDA reports)
WOUND SECRETION ( 16 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 15 FDA reports)
SHOCK HAEMORRHAGIC ( 15 FDA reports)
SINUSITIS FUNGAL ( 15 FDA reports)
SKIN HAEMORRHAGE ( 15 FDA reports)
SKIN SWELLING ( 15 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 15 FDA reports)
SPLENIC INFARCTION ( 15 FDA reports)
SUICIDAL BEHAVIOUR ( 15 FDA reports)
TERMINAL STATE ( 15 FDA reports)
VARICES OESOPHAGEAL ( 15 FDA reports)
ACTINIC ELASTOSIS ( 15 FDA reports)
ADENOMA BENIGN ( 15 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 15 FDA reports)
AORTIC THROMBOSIS ( 15 FDA reports)
APPLICATION SITE REACTION ( 15 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 15 FDA reports)
AUTOIMMUNE HEPATITIS ( 15 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 15 FDA reports)
BILIARY DYSKINESIA ( 15 FDA reports)
BLADDER MASS ( 15 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 15 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 15 FDA reports)
CALCULUS URINARY ( 15 FDA reports)
CARDIAC FAILURE CHRONIC ( 15 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 15 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 15 FDA reports)
CATATONIA ( 15 FDA reports)
CHAPPED LIPS ( 15 FDA reports)
CHEMICAL POISONING ( 15 FDA reports)
COLONOSCOPY ABNORMAL ( 15 FDA reports)
COR PULMONALE ( 15 FDA reports)
CULTURE URINE POSITIVE ( 15 FDA reports)
DIAPHRAGMATIC HERNIA ( 15 FDA reports)
DYSPLASTIC NAEVUS ( 15 FDA reports)
ECHOCARDIOGRAM ( 15 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 15 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 15 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 15 FDA reports)
HAEMOGLOBIN INCREASED ( 15 FDA reports)
HEART DISEASE CONGENITAL ( 15 FDA reports)
HYPERCHLORHYDRIA ( 15 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 15 FDA reports)
HYPOGLYCAEMIC COMA ( 15 FDA reports)
IMPAIRED FASTING GLUCOSE ( 15 FDA reports)
IMPAIRED SELF-CARE ( 15 FDA reports)
INCISIONAL HERNIA ( 15 FDA reports)
INJECTION SITE URTICARIA ( 15 FDA reports)
KETOACIDOSIS ( 15 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 15 FDA reports)
LIVER INJURY ( 15 FDA reports)
LUNG ADENOCARCINOMA ( 15 FDA reports)
MARITAL PROBLEM ( 15 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 15 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 15 FDA reports)
NAIL DISCOLOURATION ( 15 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 15 FDA reports)
NEUROMA ( 15 FDA reports)
NO ADVERSE EFFECT ( 15 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 15 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 15 FDA reports)
PAROTITIS ( 15 FDA reports)
POSTURE ABNORMAL ( 15 FDA reports)
PROTEIN S DECREASED ( 15 FDA reports)
REFLUX GASTRITIS ( 15 FDA reports)
ANASTOMOTIC ULCER ( 14 FDA reports)
ARTERIOVENOUS FISTULA OCCLUSION ( 14 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 14 FDA reports)
ATRIAL THROMBOSIS ( 14 FDA reports)
B-CELL LYMPHOMA ( 14 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 14 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 14 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 14 FDA reports)
BONE TRIMMING ( 14 FDA reports)
BREAST SWELLING ( 14 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 14 FDA reports)
CARDIOPULMONARY FAILURE ( 14 FDA reports)
CEREBRAL DISORDER ( 14 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 14 FDA reports)
DIURETIC THERAPY ( 14 FDA reports)
DYSGRAPHIA ( 14 FDA reports)
DYSPHEMIA ( 14 FDA reports)
DYSPHORIA ( 14 FDA reports)
EJACULATION FAILURE ( 14 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 14 FDA reports)
EPICONDYLITIS ( 14 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 14 FDA reports)
EYE LASER SURGERY ( 14 FDA reports)
FOOD POISONING ( 14 FDA reports)
FUNGAL SKIN INFECTION ( 14 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 14 FDA reports)
GRANULOCYTOPENIA ( 14 FDA reports)
GRANULOMA ANNULARE ( 14 FDA reports)
HEPATIC NECROSIS ( 14 FDA reports)
HILAR LYMPHADENOPATHY ( 14 FDA reports)
HYPERVENTILATION ( 14 FDA reports)
ILIUM FRACTURE ( 14 FDA reports)
INFECTIOUS PERITONITIS ( 14 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 14 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 14 FDA reports)
INTRAOCULAR LENS IMPLANT ( 14 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 14 FDA reports)
MAMMOGRAM ( 14 FDA reports)
MANDIBULAR PROSTHESIS USER ( 14 FDA reports)
METASTASES TO ABDOMINAL WALL ( 14 FDA reports)
MULTI-ORGAN DISORDER ( 14 FDA reports)
NODULE ON EXTREMITY ( 14 FDA reports)
NONSPECIFIC REACTION ( 14 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ( 14 FDA reports)
OPEN REDUCTION OF FRACTURE ( 14 FDA reports)
PARTNER STRESS ( 14 FDA reports)
POST PROCEDURAL HAEMATOMA ( 14 FDA reports)
POST PROCEDURAL INFECTION ( 14 FDA reports)
PROSTATIC OBSTRUCTION ( 14 FDA reports)
PROSTHESIS IMPLANTATION ( 14 FDA reports)
PROTEIN TOTAL INCREASED ( 14 FDA reports)
PUPIL FIXED ( 14 FDA reports)
RADIATION SKIN INJURY ( 14 FDA reports)
RECTAL ULCER ( 14 FDA reports)
SCAN ABNORMAL ( 14 FDA reports)
SCHIZOPHRENIA ( 14 FDA reports)
SPINAL CORD DISORDER ( 14 FDA reports)
SPINAL OPERATION ( 14 FDA reports)
SPLENECTOMY ( 14 FDA reports)
SUBCUTANEOUS ABSCESS ( 14 FDA reports)
THYROID CYST ( 14 FDA reports)
VENTRICULO-PERITONEAL SHUNT ( 14 FDA reports)
VESTIBULAR DISORDER ( 14 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 13 FDA reports)
SKELETAL INJURY ( 13 FDA reports)
TEARFULNESS ( 13 FDA reports)
TOE AMPUTATION ( 13 FDA reports)
TOE DEFORMITY ( 13 FDA reports)
TROPONIN I INCREASED ( 13 FDA reports)
URINE COLOUR ABNORMAL ( 13 FDA reports)
VENTRICULAR ARRHYTHMIA ( 13 FDA reports)
VITREOUS HAEMORRHAGE ( 13 FDA reports)
VOCAL CORD POLYP ( 13 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 13 FDA reports)
WEIGHT BEARING DIFFICULTY ( 13 FDA reports)
WHEELCHAIR USER ( 13 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 13 FDA reports)
ABSCESS LIMB ( 13 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 13 FDA reports)
ADJUSTMENT DISORDER WITH MIXED ANXIETY AND DEPRESSED MOOD ( 13 FDA reports)
AFFECT LABILITY ( 13 FDA reports)
ANAPHYLACTOID REACTION ( 13 FDA reports)
ANORECTAL DISCOMFORT ( 13 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 13 FDA reports)
ATROPHY ( 13 FDA reports)
AUTOIMMUNE DISORDER ( 13 FDA reports)
BACTERIAL DISEASE CARRIER ( 13 FDA reports)
BACTERIAL TEST POSITIVE ( 13 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 13 FDA reports)
BRADYARRHYTHMIA ( 13 FDA reports)
BREAST CYST ( 13 FDA reports)
BREAST ENLARGEMENT ( 13 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 13 FDA reports)
CARBUNCLE ( 13 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 13 FDA reports)
CERVICITIS ( 13 FDA reports)
CHEST WALL MASS ( 13 FDA reports)
CLOSTRIDIUM COLITIS ( 13 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 13 FDA reports)
CONGENITAL KNEE DEFORMITY ( 13 FDA reports)
DERMATITIS EXFOLIATIVE ( 13 FDA reports)
EPIDERMAL NAEVUS ( 13 FDA reports)
EPIDIDYMITIS ( 13 FDA reports)
EYE ROLLING ( 13 FDA reports)
FISTULA REPAIR ( 13 FDA reports)
GALLBLADDER ENLARGEMENT ( 13 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 13 FDA reports)
GINGIVAL GRAFT ( 13 FDA reports)
GINGIVAL HYPERPLASIA ( 13 FDA reports)
HAEMATOCRIT INCREASED ( 13 FDA reports)
HAIR COLOUR CHANGES ( 13 FDA reports)
HEART VALVE REPLACEMENT ( 13 FDA reports)
HEPATOCELLULAR DAMAGE ( 13 FDA reports)
HERNIA REPAIR ( 13 FDA reports)
HYPERCOAGULATION ( 13 FDA reports)
HYPERTENSIVE EMERGENCY ( 13 FDA reports)
HYPERTROPHY ( 13 FDA reports)
HYPHAEMA ( 13 FDA reports)
HYPOMANIA ( 13 FDA reports)
HYPOPNOEA ( 13 FDA reports)
IATROGENIC INJURY ( 13 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 13 FDA reports)
KLEBSIELLA INFECTION ( 13 FDA reports)
KNEE DEFORMITY ( 13 FDA reports)
MENOPAUSAL SYMPTOMS ( 13 FDA reports)
MENSTRUATION IRREGULAR ( 13 FDA reports)
METASTASES TO THE MEDIASTINUM ( 13 FDA reports)
MICTURITION FREQUENCY DECREASED ( 13 FDA reports)
MUSCLE RUPTURE ( 13 FDA reports)
NEPHRITIS INTERSTITIAL ( 13 FDA reports)
ONYCHOMADESIS ( 13 FDA reports)
OPTIC NERVE CUPPING ( 13 FDA reports)
OSTEOCHONDROSIS ( 13 FDA reports)
PANCREATIC ATROPHY ( 13 FDA reports)
PAPILLOEDEMA ( 13 FDA reports)
PARKINSONISM ( 13 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 13 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 13 FDA reports)
PREGNANCY ( 13 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 13 FDA reports)
PULMONARY HAEMORRHAGE ( 13 FDA reports)
REGURGITATION ( 13 FDA reports)
ABSCESS NECK ( 12 FDA reports)
ADJUSTMENT DISORDER ( 12 FDA reports)
ADRENAL ADENOMA ( 12 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 12 FDA reports)
ALCOHOLIC LIVER DISEASE ( 12 FDA reports)
ALLERGIC COUGH ( 12 FDA reports)
AMBLYOPIA ( 12 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 12 FDA reports)
ANAL SPHINCTER ATONY ( 12 FDA reports)
ANORECTAL DISORDER ( 12 FDA reports)
AREFLEXIA ( 12 FDA reports)
ARTERIOSPASM CORONARY ( 12 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 12 FDA reports)
ARTERIOVENOUS GRAFT SITE INFECTION ( 12 FDA reports)
ARTERIOVENOUS MALFORMATION ( 12 FDA reports)
BLADDER SPASM ( 12 FDA reports)
BLOOD BICARBONATE ABNORMAL ( 12 FDA reports)
BLOOD PH DECREASED ( 12 FDA reports)
BONE INFARCTION ( 12 FDA reports)
BRAIN STEM SYNDROME ( 12 FDA reports)
CANCER PAIN ( 12 FDA reports)
CARDIAC FIBRILLATION ( 12 FDA reports)
CHRONIC FATIGUE SYNDROME ( 12 FDA reports)
COLITIS ULCERATIVE ( 12 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 12 FDA reports)
CONGO-CRIMEAN HAEMORRHAGIC FEVER ( 12 FDA reports)
CORNEAL DYSTROPHY ( 12 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 12 FDA reports)
DYSPLASIA ( 12 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 12 FDA reports)
ENCEPHALITIS ( 12 FDA reports)
ENERGY INCREASED ( 12 FDA reports)
EROSIVE OESOPHAGITIS ( 12 FDA reports)
ERYTHEMA MULTIFORME ( 12 FDA reports)
EXPOSURE TO TOXIC AGENT ( 12 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 12 FDA reports)
GINGIVAL EROSION ( 12 FDA reports)
HEPATITIS ACUTE ( 12 FDA reports)
HOSTILITY ( 12 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 12 FDA reports)
INCISION SITE HAEMORRHAGE ( 12 FDA reports)
INJECTION SITE RASH ( 12 FDA reports)
INJECTION SITE WARMTH ( 12 FDA reports)
IRON OVERLOAD ( 12 FDA reports)
JOINT LOCK ( 12 FDA reports)
KLEBSIELLA TEST POSITIVE ( 12 FDA reports)
LYMPH NODE CALCIFICATION ( 12 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 12 FDA reports)
MEDICAL DEVICE REMOVAL ( 12 FDA reports)
METRORRHAGIA ( 12 FDA reports)
MIOSIS ( 12 FDA reports)
MONOPLEGIA ( 12 FDA reports)
MUCOSAL EROSION ( 12 FDA reports)
MUCOSAL HAEMORRHAGE ( 12 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 12 FDA reports)
MUSCLE HAEMORRHAGE ( 12 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 12 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 12 FDA reports)
OLIGURIA ( 12 FDA reports)
OSTEOMALACIA ( 12 FDA reports)
PANCREATIC MASS ( 12 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 12 FDA reports)
PNEUMONIA KLEBSIELLA ( 12 FDA reports)
POLYPECTOMY ( 12 FDA reports)
POOR PERSONAL HYGIENE ( 12 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 12 FDA reports)
PRESBYOESOPHAGUS ( 12 FDA reports)
RETINAL DISORDER ( 12 FDA reports)
RETINAL VEIN OCCLUSION ( 12 FDA reports)
RETROPERITONEAL HAEMATOMA ( 12 FDA reports)
SCLERAL OPERATION ( 12 FDA reports)
SCRATCH ( 12 FDA reports)
SKIN FISSURES ( 12 FDA reports)
SUNBURN ( 12 FDA reports)
TORSADE DE POINTES ( 12 FDA reports)
TRANSFUSION REACTION ( 12 FDA reports)
VASCULAR DEMENTIA ( 12 FDA reports)
VASCULAR OCCLUSION ( 12 FDA reports)
VOMITING PROJECTILE ( 12 FDA reports)
VULVOVAGINAL PAIN ( 12 FDA reports)
RESPIRATORY RATE DECREASED ( 11 FDA reports)
SCOTOMA ( 11 FDA reports)
SEMEN VOLUME DECREASED ( 11 FDA reports)
SHOULDER DEFORMITY ( 11 FDA reports)
SMOKER ( 11 FDA reports)
SPINAL FUSION SURGERY ( 11 FDA reports)
SPINAL LAMINECTOMY ( 11 FDA reports)
SPLENIC GRANULOMA ( 11 FDA reports)
SPLENIC LESION ( 11 FDA reports)
SPUTUM CULTURE POSITIVE ( 11 FDA reports)
STEATORRHOEA ( 11 FDA reports)
SUBRETINAL FIBROSIS ( 11 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 11 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 11 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 11 FDA reports)
TENSION HEADACHE ( 11 FDA reports)
THROAT CANCER ( 11 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 11 FDA reports)
THYROID CANCER ( 11 FDA reports)
TINEA CRURIS ( 11 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 11 FDA reports)
TRAUMATIC LUNG INJURY ( 11 FDA reports)
URETERIC OBSTRUCTION ( 11 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 11 FDA reports)
URINE ODOUR ABNORMAL ( 11 FDA reports)
VASCULAR CAUTERISATION ( 11 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 11 FDA reports)
VITAMIN B12 INCREASED ( 11 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 11 FDA reports)
ABDOMINAL HERNIA OBSTRUCTIVE ( 11 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 11 FDA reports)
ALVEOLAR OSTEITIS ( 11 FDA reports)
AMPUTATION ( 11 FDA reports)
ANORGASMIA ( 11 FDA reports)
ASTERIXIS ( 11 FDA reports)
BACTERIA STOOL IDENTIFIED ( 11 FDA reports)
BENIGN COLONIC POLYP ( 11 FDA reports)
BILE DUCT CANCER ( 11 FDA reports)
BILE DUCT STENOSIS ( 11 FDA reports)
BILIARY COLIC ( 11 FDA reports)
BILIARY TRACT DISORDER ( 11 FDA reports)
BLEPHAROSPASM ( 11 FDA reports)
BLOOD IRON INCREASED ( 11 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 11 FDA reports)
BONE MARROW OEDEMA ( 11 FDA reports)
BREAKTHROUGH PAIN ( 11 FDA reports)
CALCIPHYLAXIS ( 11 FDA reports)
CATARACT NUCLEAR ( 11 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 11 FDA reports)
CLAUSTROPHOBIA ( 11 FDA reports)
CONTRAST MEDIA REACTION ( 11 FDA reports)
CYSTITIS NONINFECTIVE ( 11 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 11 FDA reports)
DEMYELINATION ( 11 FDA reports)
DENTAL PROSTHESIS USER ( 11 FDA reports)
DIABETIC EYE DISEASE ( 11 FDA reports)
DIVERTICULAR PERFORATION ( 11 FDA reports)
DRUG LEVEL DECREASED ( 11 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 11 FDA reports)
EOSINOPHILIA ( 11 FDA reports)
ESCHERICHIA SEPSIS ( 11 FDA reports)
EYE MOVEMENT DISORDER ( 11 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 11 FDA reports)
FRACTURE NONUNION ( 11 FDA reports)
FRACTURED SACRUM ( 11 FDA reports)
FUNGAEMIA ( 11 FDA reports)
GASTRODUODENITIS ( 11 FDA reports)
GIANT CELL TUMOUR OF TENDON SHEATH ( 11 FDA reports)
GLOBULINS INCREASED ( 11 FDA reports)
GRAVITATIONAL OEDEMA ( 11 FDA reports)
HAEMOCHROMATOSIS ( 11 FDA reports)
HAEMORRHAGE URINARY TRACT ( 11 FDA reports)
HAEMORRHOID OPERATION ( 11 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 11 FDA reports)
HELICOBACTER GASTRITIS ( 11 FDA reports)
HERNIA PAIN ( 11 FDA reports)
HYPERACUSIS ( 11 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 11 FDA reports)
INTESTINAL INFARCTION ( 11 FDA reports)
LABILE HYPERTENSION ( 11 FDA reports)
LARGE INTESTINAL ULCER ( 11 FDA reports)
LASER THERAPY ( 11 FDA reports)
LICHEN PLANUS ( 11 FDA reports)
LIGHT CHAIN ANALYSIS ( 11 FDA reports)
LOOSE STOOLS ( 11 FDA reports)
LOSS OF LIBIDO ( 11 FDA reports)
LOW TURNOVER OSTEOPATHY ( 11 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE 0 ( 11 FDA reports)
LUPUS-LIKE SYNDROME ( 11 FDA reports)
MUSCLE SPASTICITY ( 11 FDA reports)
MYOPATHY TOXIC ( 11 FDA reports)
NEPHROCALCINOSIS ( 11 FDA reports)
OROPHARYNGEAL SWELLING ( 11 FDA reports)
PANCREATIC CYST ( 11 FDA reports)
PNEUMATOSIS INTESTINALIS ( 11 FDA reports)
PROSTATITIS ( 11 FDA reports)
PROTEIN URINE ABSENT ( 11 FDA reports)
PULSE ABNORMAL ( 11 FDA reports)
RASH SCALY ( 11 FDA reports)
ABDOMINAL ADHESIONS ( 10 FDA reports)
ABDOMINAL NEOPLASM ( 10 FDA reports)
ABDOMINAL OPERATION ( 10 FDA reports)
ACCELERATED HYPERTENSION ( 10 FDA reports)
AKATHISIA ( 10 FDA reports)
AMAUROSIS FUGAX ( 10 FDA reports)
ANAESTHETIC COMPLICATION ( 10 FDA reports)
ANKYLOSING SPONDYLITIS ( 10 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 10 FDA reports)
AORTIC ANEURYSM RUPTURE ( 10 FDA reports)
APPENDICECTOMY ( 10 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 10 FDA reports)
BILE DUCT STONE ( 10 FDA reports)
BLADDER PAIN ( 10 FDA reports)
BLEEDING TIME PROLONGED ( 10 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 10 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 10 FDA reports)
BLOOD UREA DECREASED ( 10 FDA reports)
BONE SCAN ABNORMAL ( 10 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 10 FDA reports)
BREAST DISCHARGE ( 10 FDA reports)
BREAST FIBROSIS ( 10 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 10 FDA reports)
BURNS SECOND DEGREE ( 10 FDA reports)
CANDIDURIA ( 10 FDA reports)
CATHETER SITE HAEMORRHAGE ( 10 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 10 FDA reports)
CEREBELLAR ISCHAEMIA ( 10 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 10 FDA reports)
CEREBRAL ARTERY STENOSIS ( 10 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 10 FDA reports)
CLAVICLE FRACTURE ( 10 FDA reports)
COLON POLYPECTOMY ( 10 FDA reports)
COMMINUTED FRACTURE ( 10 FDA reports)
DRESSLER'S SYNDROME ( 10 FDA reports)
DYSPHASIA ( 10 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 10 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 10 FDA reports)
ENTEROCELE ( 10 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 10 FDA reports)
EYE INFLAMMATION ( 10 FDA reports)
EYE INJURY ( 10 FDA reports)
FRACTURE DISPLACEMENT ( 10 FDA reports)
GASTRITIS ATROPHIC ( 10 FDA reports)
GINGIVAL ABSCESS ( 10 FDA reports)
GLUCOSE URINE PRESENT ( 10 FDA reports)
HANGOVER ( 10 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 10 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 10 FDA reports)
INCISION SITE COMPLICATION ( 10 FDA reports)
INCREASED VENTRICULAR AFTERLOAD ( 10 FDA reports)
INJECTION SITE ABSCESS ( 10 FDA reports)
INJECTION SITE VESICLES ( 10 FDA reports)
INTENTIONAL SELF-INJURY ( 10 FDA reports)
INTUSSUSCEPTION ( 10 FDA reports)
LIP BLISTER ( 10 FDA reports)
LIP DRY ( 10 FDA reports)
LOSS OF CONTROL OF LEGS ( 10 FDA reports)
MAMMOGRAM ABNORMAL ( 10 FDA reports)
MELANOSIS COLI ( 10 FDA reports)
MICROALBUMINURIA ( 10 FDA reports)
MIXED HYPERLIPIDAEMIA ( 10 FDA reports)
MONONEURITIS ( 10 FDA reports)
MOUTH CYST ( 10 FDA reports)
NEUROMYOPATHY ( 10 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 10 FDA reports)
OSTEOMYELITIS ACUTE ( 10 FDA reports)
PARAPROTEINAEMIA ( 10 FDA reports)
PATELLA FRACTURE ( 10 FDA reports)
PENIS DISORDER ( 10 FDA reports)
PERITONITIS BACTERIAL ( 10 FDA reports)
PORTAL VEIN THROMBOSIS ( 10 FDA reports)
POSTOPERATIVE ILEUS ( 10 FDA reports)
POSTURING ( 10 FDA reports)
PREMATURE BABY ( 10 FDA reports)
PROTHROMBIN TIME SHORTENED ( 10 FDA reports)
PSYCHOLOGICAL TRAUMA ( 10 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 10 FDA reports)
QRS AXIS ABNORMAL ( 10 FDA reports)
REBOUND EFFECT ( 10 FDA reports)
RECTAL PROLAPSE ( 10 FDA reports)
REHABILITATION THERAPY ( 10 FDA reports)
RENAL ATROPHY ( 10 FDA reports)
RENAL OSTEODYSTROPHY ( 10 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 10 FDA reports)
RHEUMATIC HEART DISEASE ( 10 FDA reports)
SALIVARY HYPERSECRETION ( 10 FDA reports)
SPINAL COLUMN INJURY ( 10 FDA reports)
SPINAL DEFORMITY ( 10 FDA reports)
STARING ( 10 FDA reports)
STREPTOCOCCAL INFECTION ( 10 FDA reports)
STRIDOR ( 10 FDA reports)
SYNOVIAL RUPTURE ( 10 FDA reports)
TONGUE PARALYSIS ( 10 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 10 FDA reports)
TRANSPLANT REJECTION ( 10 FDA reports)
TREATMENT FAILURE ( 10 FDA reports)
TRIGEMINAL NEURALGIA ( 10 FDA reports)
TUMOUR MARKER INCREASED ( 10 FDA reports)
URETERIC CANCER ( 10 FDA reports)
URETHRAL MEATUS STENOSIS ( 10 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 10 FDA reports)
URINE OUTPUT INCREASED ( 10 FDA reports)
VASOSPASM ( 10 FDA reports)
VITAMIN B12 DECREASED ( 10 FDA reports)
VULVOVAGINAL DRYNESS ( 10 FDA reports)
RESPIRATORY ACIDOSIS ( 9 FDA reports)
RETINAL ARTERY OCCLUSION ( 9 FDA reports)
RETINAL TEAR ( 9 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 9 FDA reports)
TACHYARRHYTHMIA ( 9 FDA reports)
TOOTH RESORPTION ( 9 FDA reports)
TUMOUR EMBOLISM ( 9 FDA reports)
URETHRAL DISORDER ( 9 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 9 FDA reports)
URINE ABNORMALITY ( 9 FDA reports)
VAGINAL NEOPLASM ( 9 FDA reports)
VASCULAR RUPTURE ( 9 FDA reports)
ACCIDENTAL NEEDLE STICK ( 9 FDA reports)
AMYLOIDOSIS ( 9 FDA reports)
APPLICATION SITE VESICLES ( 9 FDA reports)
BIOPSY BONE ( 9 FDA reports)
BLADDER DISCOMFORT ( 9 FDA reports)
BLOOD BICARBONATE INCREASED ( 9 FDA reports)
BLOOD CREATININE ABNORMAL ( 9 FDA reports)
BLOOD LACTIC ACID INCREASED ( 9 FDA reports)
BLOOD MAGNESIUM INCREASED ( 9 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 9 FDA reports)
BONE DEFORMITY ( 9 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 9 FDA reports)
BRAIN DEATH ( 9 FDA reports)
BREAST CELLULITIS ( 9 FDA reports)
BREAST LUMP REMOVAL ( 9 FDA reports)
BRONCHIECTASIS ( 9 FDA reports)
CARBON DIOXIDE DECREASED ( 9 FDA reports)
CARDIAC HYPERTROPHY ( 9 FDA reports)
CARTILAGE ATROPHY ( 9 FDA reports)
CATHETER REMOVAL ( 9 FDA reports)
CEREBELLAR INFARCTION ( 9 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 9 FDA reports)
COAGULATION FACTOR DEFICIENCY ( 9 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 9 FDA reports)
CORONARY ARTERY ANEURYSM ( 9 FDA reports)
DENTAL CARE ( 9 FDA reports)
DENTAL IMPRESSION PROCEDURE ( 9 FDA reports)
DIABETIC GASTROPARESIS ( 9 FDA reports)
DRUG EFFECT INCREASED ( 9 FDA reports)
EDENTULOUS ( 9 FDA reports)
ENCEPHALOMALACIA ( 9 FDA reports)
ENDOMETRIAL CANCER ( 9 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 9 FDA reports)
EPIDURAL LIPOMATOSIS ( 9 FDA reports)
EYE REDNESS ( 9 FDA reports)
FUNGAL RASH ( 9 FDA reports)
GROIN INFECTION ( 9 FDA reports)
GUILLAIN-BARRE SYNDROME ( 9 FDA reports)
GUN SHOT WOUND ( 9 FDA reports)
HAIR DISORDER ( 9 FDA reports)
HAND DEFORMITY ( 9 FDA reports)
HEAD TITUBATION ( 9 FDA reports)
HEPATIC NEOPLASM ( 9 FDA reports)
HYPEROSMOLAR STATE ( 9 FDA reports)
HYPERPATHIA ( 9 FDA reports)
HYPERVOLAEMIA ( 9 FDA reports)
HYPOPROTEINAEMIA ( 9 FDA reports)
INCORRECT STORAGE OF DRUG ( 9 FDA reports)
INSULIN RESISTANCE ( 9 FDA reports)
INTERCOSTAL NEURALGIA ( 9 FDA reports)
IRITIS ( 9 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 9 FDA reports)
LARYNGEAL OEDEMA ( 9 FDA reports)
LYMPHATIC DISORDER ( 9 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 9 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 9 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 9 FDA reports)
MASTOIDITIS ( 9 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 9 FDA reports)
MIDDLE EAR EFFUSION ( 9 FDA reports)
MITRAL VALVE REPLACEMENT ( 9 FDA reports)
MUCOUS STOOLS ( 9 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 9 FDA reports)
NAIL GROWTH ABNORMAL ( 9 FDA reports)
NASAL MUCOSAL DISORDER ( 9 FDA reports)
NEPHROTIC SYNDROME ( 9 FDA reports)
NEUROLOGICAL SYMPTOM ( 9 FDA reports)
NEUROSENSORY HYPOACUSIS ( 9 FDA reports)
OBSTRUCTIVE UROPATHY ( 9 FDA reports)
OESOPHAGEAL MASS ( 9 FDA reports)
ONYCHOLYSIS ( 9 FDA reports)
ORAL FUNGAL INFECTION ( 9 FDA reports)
OROPHARYNGEAL PLAQUE ( 9 FDA reports)
OSTEITIS DEFORMANS ( 9 FDA reports)
OTITIS MEDIA ACUTE ( 9 FDA reports)
OXYGEN SUPPLEMENTATION ( 9 FDA reports)
PANCREATIC DUCT OBSTRUCTION ( 9 FDA reports)
PARAPLEGIA ( 9 FDA reports)
PERICARDIAL HAEMORRHAGE ( 9 FDA reports)
PERIPHERAL EMBOLISM ( 9 FDA reports)
PERITONEAL HAEMORRHAGE ( 9 FDA reports)
PHARYNGEAL DISORDER ( 9 FDA reports)
PHOTODERMATOSIS ( 9 FDA reports)
PNEUMONIA FUNGAL ( 9 FDA reports)
PNEUMONIA LEGIONELLA ( 9 FDA reports)
POSTERIOR CAPSULOTOMY ( 9 FDA reports)
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME ( 9 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 9 FDA reports)
PULMONARY INFARCTION ( 9 FDA reports)
PULSE PRESSURE DECREASED ( 9 FDA reports)
PUPILS UNEQUAL ( 9 FDA reports)
PYELOCALIECTASIS ( 9 FDA reports)
RADICULAR CYST ( 9 FDA reports)
RECTAL NEOPLASM ( 9 FDA reports)
RECTAL POLYP ( 9 FDA reports)
RECURRENT CANCER ( 9 FDA reports)
REFRACTORY ANAEMIA ( 9 FDA reports)
ACQUIRED PORPHYRIA ( 8 FDA reports)
ADRENAL MASS ( 8 FDA reports)
ANIMAL BITE ( 8 FDA reports)
AORTIC ATHEROSCLEROSIS ( 8 FDA reports)
AORTIC DISSECTION ( 8 FDA reports)
AORTIC VALVE CALCIFICATION ( 8 FDA reports)
APPENDIX DISORDER ( 8 FDA reports)
ARTHROPOD STING ( 8 FDA reports)
AXILLARY MASS ( 8 FDA reports)
BACTERIA URINE IDENTIFIED ( 8 FDA reports)
BACTERIAL SEPSIS ( 8 FDA reports)
BEREAVEMENT ( 8 FDA reports)
BIOPSY BREAST ( 8 FDA reports)
BIOPSY MUCOSA ABNORMAL ( 8 FDA reports)
BLISTER INFECTED ( 8 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 8 FDA reports)
BLOOD PRESSURE ( 8 FDA reports)
BODY TINEA ( 8 FDA reports)
BREAST CANCER STAGE I ( 8 FDA reports)
BREAST RECONSTRUCTION ( 8 FDA reports)
CAECITIS ( 8 FDA reports)
CALCIUM DEFICIENCY ( 8 FDA reports)
CALCULUS BLADDER ( 8 FDA reports)
CALCULUS URETHRAL ( 8 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 8 FDA reports)
CARDIAC DEATH ( 8 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 8 FDA reports)
CATARACT OPERATION COMPLICATION ( 8 FDA reports)
CATHETER SEPSIS ( 8 FDA reports)
CEREBELLAR ATROPHY ( 8 FDA reports)
CHEST INJURY ( 8 FDA reports)
CHOLESTEROSIS ( 8 FDA reports)
CLOSED FRACTURE MANIPULATION ( 8 FDA reports)
COLON CANCER STAGE I ( 8 FDA reports)
COLONOSCOPY ( 8 FDA reports)
CONNECTIVE TISSUE INFLAMMATION ( 8 FDA reports)
DERMATITIS PSORIASIFORM ( 8 FDA reports)
DEVICE LEAKAGE ( 8 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 8 FDA reports)
DRUG LEVEL INCREASED ( 8 FDA reports)
DYSPNOEA AT REST ( 8 FDA reports)
EFFUSION ( 8 FDA reports)
ENCEPHALITIS POST MEASLES ( 8 FDA reports)
ENZYME ABNORMALITY ( 8 FDA reports)
FACIAL WASTING ( 8 FDA reports)
FOOD ALLERGY ( 8 FDA reports)
FOOD AVERSION ( 8 FDA reports)
GASTRIC CANCER ( 8 FDA reports)
GASTRODUODENAL ULCER ( 8 FDA reports)
GRAFT THROMBOSIS ( 8 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 8 FDA reports)
HAEMARTHROSIS ( 8 FDA reports)
HEPATIC FIBROSIS ( 8 FDA reports)
HEPATOJUGULAR REFLUX ( 8 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 8 FDA reports)
HORDEOLUM ( 8 FDA reports)
HYPOTRICHOSIS ( 8 FDA reports)
INGUINAL HERNIA REPAIR ( 8 FDA reports)
INJECTION SITE BURNING ( 8 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 8 FDA reports)
INTESTINAL DILATATION ( 8 FDA reports)
INTESTINAL ULCER ( 8 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 8 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 8 FDA reports)
INTUBATION ( 8 FDA reports)
IRON METABOLISM DISORDER ( 8 FDA reports)
JOINT CREPITATION ( 8 FDA reports)
JOINT PROSTHESIS USER ( 8 FDA reports)
LARYNGOSPASM ( 8 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 8 FDA reports)
LIMB IMMOBILISATION ( 8 FDA reports)
LIPOMA EXCISION ( 8 FDA reports)
LISTLESS ( 8 FDA reports)
LOWER EXTREMITY MASS ( 8 FDA reports)
LYMPH NODE PAIN ( 8 FDA reports)
MYELOFIBROSIS ( 8 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 8 FDA reports)
OBSTRUCTION ( 8 FDA reports)
ONYCHOCLASIS ( 8 FDA reports)
OPTIC ATROPHY ( 8 FDA reports)
OPTIC NEUROPATHY ( 8 FDA reports)
OSTEOSARCOMA LOCALISED ( 8 FDA reports)
OVARIAN ATROPHY ( 8 FDA reports)
PANCREATIC INSUFFICIENCY ( 8 FDA reports)
PERSONALITY DISORDER ( 8 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 8 FDA reports)
PIGMENTED NAEVUS ( 8 FDA reports)
PLATELET DISORDER ( 8 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 8 FDA reports)
POSTPERICARDIOTOMY SYNDROME ( 8 FDA reports)
PROCEDURAL HYPOTENSION ( 8 FDA reports)
PRODUCT PACKAGING ISSUE ( 8 FDA reports)
PSEUDOMONAL SEPSIS ( 8 FDA reports)
RADIATION EXPOSURE ( 8 FDA reports)
RADICAL MASTECTOMY ( 8 FDA reports)
RASH MORBILLIFORM ( 8 FDA reports)
RENAL ARTERY OCCLUSION ( 8 FDA reports)
SELF-INJURIOUS IDEATION ( 8 FDA reports)
SELF-MEDICATION ( 8 FDA reports)
SEROSITIS ( 8 FDA reports)
SERRATIA BACTERAEMIA ( 8 FDA reports)
SERUM SICKNESS ( 8 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 8 FDA reports)
SLEEP WALKING ( 8 FDA reports)
SMALL INTESTINE CARCINOMA ( 8 FDA reports)
SOFT TISSUE INFECTION ( 8 FDA reports)
SPLEEN DISORDER ( 8 FDA reports)
STASIS DERMATITIS ( 8 FDA reports)
SURGICAL PROCEDURE REPEATED ( 8 FDA reports)
SWEAT DISCOLOURATION ( 8 FDA reports)
TESTICULAR SWELLING ( 8 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 8 FDA reports)
TOOTH REPAIR ( 8 FDA reports)
TOXIC ENCEPHALOPATHY ( 8 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 8 FDA reports)
URINARY TRACT OBSTRUCTION ( 8 FDA reports)
VAGINAL INFECTION ( 8 FDA reports)
VASCULAR BYPASS GRAFT ( 8 FDA reports)
VASCULAR INJURY ( 8 FDA reports)
VENOUS OCCLUSION ( 8 FDA reports)
WEIGHT LOSS POOR ( 8 FDA reports)
WRIST SURGERY ( 8 FDA reports)
YAWNING ( 8 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 7 FDA reports)
RETINOPATHY OF PREMATURITY ( 7 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 7 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 7 FDA reports)
SALMONELLOSIS ( 7 FDA reports)
SCREAMING ( 7 FDA reports)
SCROTAL OEDEMA ( 7 FDA reports)
SEBACEOUS ADENOMA ( 7 FDA reports)
SIALOADENITIS ( 7 FDA reports)
SINUS ARREST ( 7 FDA reports)
SKIN OEDEMA ( 7 FDA reports)
SOMATOFORM DISORDER ( 7 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 7 FDA reports)
SPLINT APPLICATION ( 7 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 7 FDA reports)
TABLET PHYSICAL ISSUE ( 7 FDA reports)
TESTICULAR ATROPHY ( 7 FDA reports)
TESTICULAR PAIN ( 7 FDA reports)
THYROXINE INCREASED ( 7 FDA reports)
TIBIA FRACTURE ( 7 FDA reports)
TOOTH DEPOSIT ( 7 FDA reports)
TORTICOLLIS ( 7 FDA reports)
TRICHORRHEXIS ( 7 FDA reports)
TUMOUR LYSIS SYNDROME ( 7 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 7 FDA reports)
UTERINE PROLAPSE ( 7 FDA reports)
VISUAL BRIGHTNESS ( 7 FDA reports)
VITREOUS DEGENERATION ( 7 FDA reports)
WEST NILE VIRAL INFECTION ( 7 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 7 FDA reports)
ACUTE STRESS DISORDER ( 7 FDA reports)
ADHESION ( 7 FDA reports)
ALVEOLITIS ALLERGIC ( 7 FDA reports)
AMENORRHOEA ( 7 FDA reports)
ANAL HAEMORRHAGE ( 7 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 7 FDA reports)
ANTIBODY TEST POSITIVE ( 7 FDA reports)
APPENDICITIS PERFORATED ( 7 FDA reports)
APPLICATION SITE BURN ( 7 FDA reports)
ARTERIAL INJURY ( 7 FDA reports)
ARTERIAL RUPTURE ( 7 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 7 FDA reports)
BIOPSY LYMPH GLAND ABNORMAL ( 7 FDA reports)
BLADDER NEOPLASM ( 7 FDA reports)
BLADDER OBSTRUCTION ( 7 FDA reports)
BLOOD CREATININE DECREASED ( 7 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 7 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 7 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 7 FDA reports)
BLOOD URINE ( 7 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 7 FDA reports)
BRADYPHRENIA ( 7 FDA reports)
BRAIN DAMAGE ( 7 FDA reports)
BRONCHIAL DISORDER ( 7 FDA reports)
BRONCHOPULMONARY DISEASE ( 7 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 7 FDA reports)
CARDIAC DISCOMFORT ( 7 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 7 FDA reports)
CAROTID ARTERY ATHEROMA ( 7 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 7 FDA reports)
CEREBRAL HAEMATOMA ( 7 FDA reports)
CHOLANGITIS CHRONIC ( 7 FDA reports)
CHOREA ( 7 FDA reports)
CLUMSINESS ( 7 FDA reports)
COAGULATION TEST ABNORMAL ( 7 FDA reports)
COLON CANCER METASTATIC ( 7 FDA reports)
COLON NEOPLASM ( 7 FDA reports)
COLON OPERATION ( 7 FDA reports)
CONJUNCTIVAL ABRASION ( 7 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 7 FDA reports)
CORONARY ANGIOPLASTY ( 7 FDA reports)
DANDRUFF ( 7 FDA reports)
DEVELOPMENTAL DELAY ( 7 FDA reports)
DEVICE OCCLUSION ( 7 FDA reports)
DIAPHRAGMATIC DISORDER ( 7 FDA reports)
DISSOCIATION ( 7 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 7 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 7 FDA reports)
DUODENAL ULCER PERFORATION ( 7 FDA reports)
DYSAESTHESIA ( 7 FDA reports)
EJACULATION DISORDER ( 7 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 7 FDA reports)
ENDOLYMPHATIC HYDROPS ( 7 FDA reports)
ENTERITIS ( 7 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 7 FDA reports)
EXOPHTHALMOS ( 7 FDA reports)
FAECES PALE ( 7 FDA reports)
FEAR OF DISEASE ( 7 FDA reports)
FEMORAL ARTERY ANEURYSM ( 7 FDA reports)
FEMORAL ARTERY OCCLUSION ( 7 FDA reports)
FLIGHT OF IDEAS ( 7 FDA reports)
FOOD CRAVING ( 7 FDA reports)
FOOT OPERATION ( 7 FDA reports)
GASTRIC DILATATION ( 7 FDA reports)
GENERAL SYMPTOM ( 7 FDA reports)
GENITAL RASH ( 7 FDA reports)
GRIMACING ( 7 FDA reports)
H1N1 INFLUENZA ( 7 FDA reports)
HAEMOGLOBIN ABNORMAL ( 7 FDA reports)
HEAT EXHAUSTION ( 7 FDA reports)
HEAT RASH ( 7 FDA reports)
HEPATIC HAEMORRHAGE ( 7 FDA reports)
HYPERCAPNIA ( 7 FDA reports)
HYPERMAGNESAEMIA ( 7 FDA reports)
HYPERNATRAEMIA ( 7 FDA reports)
HYPERTHERMIA ( 7 FDA reports)
ILEOSTOMY ( 7 FDA reports)
INJECTION SITE CELLULITIS ( 7 FDA reports)
INNER EAR DISORDER ( 7 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 7 FDA reports)
JOINT INSTABILITY ( 7 FDA reports)
LABILE BLOOD PRESSURE ( 7 FDA reports)
LARYNGEAL WEB ( 7 FDA reports)
LOCALISED OSTEOARTHRITIS ( 7 FDA reports)
LUNG CANCER METASTATIC ( 7 FDA reports)
LYME DISEASE ( 7 FDA reports)
LYMPH NODE CANCER METASTATIC ( 7 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 7 FDA reports)
LYMPHOPENIA ( 7 FDA reports)
MACULAR SCAR ( 7 FDA reports)
MALABSORPTION FROM INJECTION SITE ( 7 FDA reports)
MALIGNANT MESENTERIC NEOPLASM ( 7 FDA reports)
METABOLIC DISORDER ( 7 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 7 FDA reports)
MUSCULAR DYSTROPHY ( 7 FDA reports)
MYOCARDITIS ( 7 FDA reports)
NAIL BED BLEEDING ( 7 FDA reports)
NEOPLASM PROSTATE ( 7 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 7 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 7 FDA reports)
NIGHT BLINDNESS ( 7 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 7 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 7 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 7 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 7 FDA reports)
OPERATIVE HAEMORRHAGE ( 7 FDA reports)
ORBITAL OEDEMA ( 7 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 7 FDA reports)
OS TRIGONUM SYNDROME ( 7 FDA reports)
PALATAL OEDEMA ( 7 FDA reports)
PANCREATITIS NECROTISING ( 7 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 7 FDA reports)
PARONYCHIA ( 7 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 7 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 7 FDA reports)
PLASMAPHERESIS ( 7 FDA reports)
PLATELET AGGREGATION INCREASED ( 7 FDA reports)
PLATELET COUNT ABNORMAL ( 7 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 7 FDA reports)
POLYCYSTIC OVARIES ( 7 FDA reports)
PORTAL HYPERTENSION ( 7 FDA reports)
POST PROCEDURAL DISCHARGE ( 7 FDA reports)
POTENTIATING DRUG INTERACTION ( 7 FDA reports)
PRECANCEROUS CELLS PRESENT ( 7 FDA reports)
PRODUCT TASTE ABNORMAL ( 7 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 7 FDA reports)
PROTEIN URINE ( 7 FDA reports)
PROTRUSION TONGUE ( 7 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 7 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 7 FDA reports)
PULMONARY VASCULAR DISORDER ( 7 FDA reports)
RECTAL CANCER METASTATIC ( 7 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 6 FDA reports)
ADDISON'S DISEASE ( 6 FDA reports)
ADRENAL NEOPLASM ( 6 FDA reports)
ALCOHOL ABUSE ( 6 FDA reports)
ALCOHOLISM ( 6 FDA reports)
ALLERGIC SINUSITIS ( 6 FDA reports)
ANAEMIA MACROCYTIC ( 6 FDA reports)
APNOEIC ATTACK ( 6 FDA reports)
APPLICATION SITE INFECTION ( 6 FDA reports)
ARTERIAL INSUFFICIENCY ( 6 FDA reports)
ASEPTIC NECROSIS BONE ( 6 FDA reports)
ASPIRATION BREAST ( 6 FDA reports)
ATRIAL NATRIURETIC PEPTIDE INCREASED ( 6 FDA reports)
AUTOMATIC BLADDER ( 6 FDA reports)
BACTERIURIA ( 6 FDA reports)
BASAL GANGLION DEGENERATION ( 6 FDA reports)
BIOPSY BREAST ABNORMAL ( 6 FDA reports)
BIOPSY ENDOMETRIUM ( 6 FDA reports)
BLADDER CANCER RECURRENT ( 6 FDA reports)
BLOOD BLISTER ( 6 FDA reports)
BLOOD GASES ABNORMAL ( 6 FDA reports)
BLOOD IRON ABNORMAL ( 6 FDA reports)
BONE GRAFT ( 6 FDA reports)
BOWEN'S DISEASE ( 6 FDA reports)
BRADYKINESIA ( 6 FDA reports)
BRAIN ABSCESS ( 6 FDA reports)
BREAST CALCIFICATIONS ( 6 FDA reports)
BREAST DISORDER FEMALE ( 6 FDA reports)
BREAST HAEMATOMA ( 6 FDA reports)
BREAST MICROCALCIFICATION ( 6 FDA reports)
BUNION ( 6 FDA reports)
CAESAREAN SECTION ( 6 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 6 FDA reports)
CARDIAC FAILURE ACUTE ( 6 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 6 FDA reports)
CARTILAGE INJURY ( 6 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 6 FDA reports)
CHONDROPATHY ( 6 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 6 FDA reports)
COLON CANCER STAGE III ( 6 FDA reports)
COLON GANGRENE ( 6 FDA reports)
COLONIC OBSTRUCTION ( 6 FDA reports)
COLORECTAL CANCER ( 6 FDA reports)
COMA HEPATIC ( 6 FDA reports)
COMMUNICATION DISORDER ( 6 FDA reports)
COMPARTMENT SYNDROME ( 6 FDA reports)
COMPLEX PARTIAL SEIZURES ( 6 FDA reports)
CORNEAL DISORDER ( 6 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 6 FDA reports)
CRANIOTOMY ( 6 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 6 FDA reports)
CUBITAL TUNNEL SYNDROME ( 6 FDA reports)
CUSHING'S SYNDROME ( 6 FDA reports)
CYANOPSIA ( 6 FDA reports)
CYSTIC FIBROSIS PANCREATIC ( 6 FDA reports)
DEAFNESS BILATERAL ( 6 FDA reports)
DEPENDENCE ( 6 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 6 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 6 FDA reports)
DRUG TOLERANCE INCREASED ( 6 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 6 FDA reports)
DYSPNOEA EXACERBATED ( 6 FDA reports)
DYSTHYMIC DISORDER ( 6 FDA reports)
EAR PRURITUS ( 6 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 6 FDA reports)
EJECTION FRACTION ABNORMAL ( 6 FDA reports)
ENDOMETRIAL ATROPHY ( 6 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 6 FDA reports)
EOSINOPHIL COUNT INCREASED ( 6 FDA reports)
EPIDERMAL NECROSIS ( 6 FDA reports)
EXTRADURAL HAEMATOMA ( 6 FDA reports)
EXTRAVASATION ( 6 FDA reports)
EXTREMITY NECROSIS ( 6 FDA reports)
EYE INFECTION VIRAL ( 6 FDA reports)
FEELING HOT AND COLD ( 6 FDA reports)
FIBULA FRACTURE ( 6 FDA reports)
FOAMING AT MOUTH ( 6 FDA reports)
FOOT AMPUTATION ( 6 FDA reports)
FULL BLOOD COUNT INCREASED ( 6 FDA reports)
GALLBLADDER FISTULA ( 6 FDA reports)
GALLBLADDER PAIN ( 6 FDA reports)
GALLBLADDER POLYP ( 6 FDA reports)
GASTRIC BYPASS ( 6 FDA reports)
GASTRIC INFECTION ( 6 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 6 FDA reports)
GASTROINTESTINAL OEDEMA ( 6 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 6 FDA reports)
GLIOSIS ( 6 FDA reports)
GLOBAL AMNESIA ( 6 FDA reports)
GOUTY TOPHUS ( 6 FDA reports)
HAPTOGLOBIN DECREASED ( 6 FDA reports)
HEART VALVE INSUFFICIENCY ( 6 FDA reports)
HEAT STROKE ( 6 FDA reports)
HEPATIC VEIN THROMBOSIS ( 6 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 6 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 6 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 6 FDA reports)
HEPATORENAL SYNDROME ( 6 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 6 FDA reports)
HYPOPARATHYROIDISM ( 6 FDA reports)
HYPOREFLEXIA ( 6 FDA reports)
ILIAC ARTERY STENOSIS ( 6 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 6 FDA reports)
IMPETIGO ( 6 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 6 FDA reports)
IMPULSE-CONTROL DISORDER ( 6 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 6 FDA reports)
INFECTED SKIN ULCER ( 6 FDA reports)
INFERTILITY ( 6 FDA reports)
INJECTION SITE INFECTION ( 6 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 6 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 6 FDA reports)
IRIS ADHESIONS ( 6 FDA reports)
IUD MIGRATION ( 6 FDA reports)
KIDNEY FIBROSIS ( 6 FDA reports)
LACRIMATION DECREASED ( 6 FDA reports)
LIBIDO INCREASED ( 6 FDA reports)
LIGAMENT DISORDER ( 6 FDA reports)
LIP ULCERATION ( 6 FDA reports)
LISTERIOSIS ( 6 FDA reports)
LIVER TRANSPLANT REJECTION ( 6 FDA reports)
LOGORRHOEA ( 6 FDA reports)
LYMPHOCELE ( 6 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 6 FDA reports)
MADAROSIS ( 6 FDA reports)
MAMMOPLASTY ( 6 FDA reports)
MANDIBULECTOMY ( 6 FDA reports)
MANTLE CELL LYMPHOMA ( 6 FDA reports)
MEDIASTINITIS ( 6 FDA reports)
METASTASES TO STOMACH ( 6 FDA reports)
MICROANGIOPATHY ( 6 FDA reports)
MIGRAINE WITH AURA ( 6 FDA reports)
MODIFIED RADICAL MASTECTOMY ( 6 FDA reports)
MULTIPLE DRUG OVERDOSE ( 6 FDA reports)
MYOCARDIAL FIBROSIS ( 6 FDA reports)
NASAL OEDEMA ( 6 FDA reports)
NEPHRECTOMY ( 6 FDA reports)
NEPHROGENIC ANAEMIA ( 6 FDA reports)
OESTRADIOL DECREASED ( 6 FDA reports)
OPTIC NERVE DISORDER ( 6 FDA reports)
ORAL HAIRY LEUKOPLAKIA ( 6 FDA reports)
ORAL SOFT TISSUE DISORDER ( 6 FDA reports)
ORCHITIS ( 6 FDA reports)
OVARIAN ADHESION ( 6 FDA reports)
PAROTID GLAND ENLARGEMENT ( 6 FDA reports)
PARTIAL SEIZURES ( 6 FDA reports)
PELVIC ADHESIONS ( 6 FDA reports)
PENILE PAIN ( 6 FDA reports)
PENILE SWELLING ( 6 FDA reports)
PERIORBITAL HAEMATOMA ( 6 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 6 FDA reports)
PHARYNGEAL ERYTHEMA ( 6 FDA reports)
PINGUECULA ( 6 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 6 FDA reports)
PLATELET TRANSFUSION ( 6 FDA reports)
PO2 DECREASED ( 6 FDA reports)
POST LAMINECTOMY SYNDROME ( 6 FDA reports)
POST PROCEDURAL OEDEMA ( 6 FDA reports)
PRINZMETAL ANGINA ( 6 FDA reports)
PROCEDURAL HYPERTENSION ( 6 FDA reports)
PROSTATECTOMY ( 6 FDA reports)
PROTEUS INFECTION ( 6 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 6 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 6 FDA reports)
RADICULITIS ( 6 FDA reports)
RESIDUAL URINE ( 6 FDA reports)
RESIDUAL URINE VOLUME ( 6 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS BRONCHIOLITIS ( 6 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 6 FDA reports)
SCROTAL SWELLING ( 6 FDA reports)
SHOULDER OPERATION ( 6 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 6 FDA reports)
SKIN GRAFT ( 6 FDA reports)
SKIN NODULE ( 6 FDA reports)
SKULL FRACTURED BASE ( 6 FDA reports)
SLEEP TERROR ( 6 FDA reports)
SPINAL HAEMANGIOMA ( 6 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 6 FDA reports)
STENT MALFUNCTION ( 6 FDA reports)
STRESS INCONTINENCE ( 6 FDA reports)
STUPOR ( 6 FDA reports)
SUSPICIOUSNESS ( 6 FDA reports)
SYNOVITIS ( 6 FDA reports)
TESTICULAR DISORDER ( 6 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 6 FDA reports)
THERAPY REGIMEN CHANGED ( 6 FDA reports)
THORACOTOMY ( 6 FDA reports)
THYROID MASS ( 6 FDA reports)
THYROXINE FREE INCREASED ( 6 FDA reports)
TINEA INFECTION ( 6 FDA reports)
TONGUE DRY ( 6 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 6 FDA reports)
TRACHEOSTOMY ( 6 FDA reports)
TRANSPLANT FAILURE ( 6 FDA reports)
TRAUMATIC BRAIN INJURY ( 6 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 6 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 6 FDA reports)
VAGINAL LESION ( 6 FDA reports)
VASOCONSTRICTION ( 6 FDA reports)
VENOUS STASIS ( 6 FDA reports)
VISUAL MIDLINE SHIFT SYNDROME ( 6 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 6 FDA reports)
VULVOVAGINAL PRURITUS ( 6 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 6 FDA reports)
WOUND NECROSIS ( 6 FDA reports)
RENAL ARTERY STENT PLACEMENT ( 5 FDA reports)
RENAL NEOPLASM ( 5 FDA reports)
RESPIRATION ABNORMAL ( 5 FDA reports)
RETICULOCYTE COUNT INCREASED ( 5 FDA reports)
SCAN LYMPH NODES ( 5 FDA reports)
SERUM FERRITIN DECREASED ( 5 FDA reports)
SERUM SEROTONIN DECREASED ( 5 FDA reports)
SICCA SYNDROME ( 5 FDA reports)
SKIN CANCER METASTATIC ( 5 FDA reports)
SKIN DISCOMFORT ( 5 FDA reports)
SKIN TURGOR DECREASED ( 5 FDA reports)
SKULL FRACTURE ( 5 FDA reports)
SMALL INTESTINAL RESECTION ( 5 FDA reports)
SOFT TISSUE INJURY ( 5 FDA reports)
SOFT TISSUE NECROSIS ( 5 FDA reports)
SOMATISATION DISORDER ( 5 FDA reports)
SPINAL CORD NEOPLASM ( 5 FDA reports)
SPLENIC ABSCESS ( 5 FDA reports)
SPLENIC RUPTURE ( 5 FDA reports)
STATUS ASTHMATICUS ( 5 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 5 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 5 FDA reports)
SUBSTANCE ABUSE ( 5 FDA reports)
SUFFOCATION FEELING ( 5 FDA reports)
TENOSYNOVITIS ( 5 FDA reports)
TERATOMA ( 5 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 5 FDA reports)
TONGUE BLACK HAIRY ( 5 FDA reports)
TONSILLITIS ( 5 FDA reports)
TOOTH EROSION ( 5 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 5 FDA reports)
TRICUSPID VALVE REPLACEMENT ( 5 FDA reports)
TRISMUS ( 5 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 5 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 5 FDA reports)
URETERIC DILATATION ( 5 FDA reports)
URETERIC STENOSIS ( 5 FDA reports)
URETHRAL HAEMORRHAGE ( 5 FDA reports)
URINE KETONE BODY PRESENT ( 5 FDA reports)
URTICARIA GENERALISED ( 5 FDA reports)
VAGINAL PAIN ( 5 FDA reports)
VASCULAR INSUFFICIENCY ( 5 FDA reports)
VEIN DISCOLOURATION ( 5 FDA reports)
VENOUS HAEMORRHAGE ( 5 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 5 FDA reports)
VERTIGO LABYRINTHINE ( 5 FDA reports)
VICTIM OF CRIME ( 5 FDA reports)
VIRAL CARDIOMYOPATHY ( 5 FDA reports)
VITILIGO ( 5 FDA reports)
VULVOVAGINAL DISCOMFORT ( 5 FDA reports)
ACUTE PSYCHOSIS ( 5 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 5 FDA reports)
ANOGENITAL WARTS ( 5 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 5 FDA reports)
APPLICATION SITE BLEEDING ( 5 FDA reports)
ARACHNOIDITIS ( 5 FDA reports)
ARTERIAL BYPASS OPERATION ( 5 FDA reports)
ARTERIAL REPAIR ( 5 FDA reports)
ARTERIOVENOUS FISTULA ANEURYSM ( 5 FDA reports)
ARTHRITIS BACTERIAL ( 5 FDA reports)
ARTHROSCOPY ( 5 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 5 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 5 FDA reports)
BEHCET'S SYNDROME ( 5 FDA reports)
BENIGN GASTROINTESTINAL NEOPLASM ( 5 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 5 FDA reports)
BIPOLAR II DISORDER ( 5 FDA reports)
BLADDER CATHETERISATION ( 5 FDA reports)
BLEEDING VARICOSE VEIN ( 5 FDA reports)
BLOOD ALCOHOL INCREASED ( 5 FDA reports)
BLOOD BICARBONATE DECREASED ( 5 FDA reports)
BLOOD CREATINE ABNORMAL ( 5 FDA reports)
BLOOD PH INCREASED ( 5 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 5 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 5 FDA reports)
BLOOD VISCOSITY INCREASED ( 5 FDA reports)
BLUE TOE SYNDROME ( 5 FDA reports)
BODY DYSMORPHIC DISORDER ( 5 FDA reports)
BRAIN STEM INFARCTION ( 5 FDA reports)
BREAST CANCER STAGE II ( 5 FDA reports)
BREAST INFECTION ( 5 FDA reports)
BREATH HOLDING ( 5 FDA reports)
BREATH SOUNDS DECREASED ( 5 FDA reports)
CAPILLARY LEAK SYNDROME ( 5 FDA reports)
CARCINOMA IN SITU OF EYE ( 5 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 5 FDA reports)
CARTILAGE HYPERTROPHY ( 5 FDA reports)
CATHETER SITE PAIN ( 5 FDA reports)
CEREBELLAR SYNDROME ( 5 FDA reports)
CEREBRAL THROMBOSIS ( 5 FDA reports)
CERVICAL MYELOPATHY ( 5 FDA reports)
CHRONIC HEPATITIS ( 5 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA TRANSFORMATION ( 5 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 5 FDA reports)
COLONIC STENOSIS ( 5 FDA reports)
COLORECTAL CANCER METASTATIC ( 5 FDA reports)
CONGENITAL EYE NAEVUS ( 5 FDA reports)
CORONARY ARTERY EMBOLISM ( 5 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 5 FDA reports)
DERMATITIS ACNEIFORM ( 5 FDA reports)
DIZZINESS EXERTIONAL ( 5 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 5 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 5 FDA reports)
ENDOMETRIOSIS ( 5 FDA reports)
ERECTION INCREASED ( 5 FDA reports)
ERYTHEMA OF EYELID ( 5 FDA reports)
EXCESSIVE EYE BLINKING ( 5 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 5 FDA reports)
FACIAL PARESIS ( 5 FDA reports)
FAECES HARD ( 5 FDA reports)
FAT TISSUE INCREASED ( 5 FDA reports)
FEEDING DISORDER ( 5 FDA reports)
FEEDING TUBE COMPLICATION ( 5 FDA reports)
FOREIGN BODY ASPIRATION ( 5 FDA reports)
FRACTURE DELAYED UNION ( 5 FDA reports)
FRACTURED COCCYX ( 5 FDA reports)
GAIT DEVIATION ( 5 FDA reports)
GALLOP RHYTHM PRESENT ( 5 FDA reports)
GASTRIC OPERATION ( 5 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 5 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 5 FDA reports)
GINGIVAL CYST ( 5 FDA reports)
GRAFT DYSFUNCTION ( 5 FDA reports)
HAEMANGIOMA OF LIVER ( 5 FDA reports)
HAEMOGLOBINURIA ( 5 FDA reports)
HALLUCINATIONS, MIXED ( 5 FDA reports)
HEPATIC CANCER METASTATIC ( 5 FDA reports)
HEPATIC ENZYME ABNORMAL ( 5 FDA reports)
HEPATIC INFARCTION ( 5 FDA reports)
HEPATITIS B ( 5 FDA reports)
HYPERALBUMINAEMIA ( 5 FDA reports)
HYPERINSULINAEMIA ( 5 FDA reports)
HYPERSEXUALITY ( 5 FDA reports)
HYPERVIGILANCE ( 5 FDA reports)
HYPOCHROMIC ANAEMIA ( 5 FDA reports)
HYPOGEUSIA ( 5 FDA reports)
HYPOSMIA ( 5 FDA reports)
HYPOVOLAEMIC SHOCK ( 5 FDA reports)
IMMUNODEFICIENCY ( 5 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 5 FDA reports)
IMPULSIVE BEHAVIOUR ( 5 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 5 FDA reports)
INDURATION ( 5 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 5 FDA reports)
INJECTION SITE OEDEMA ( 5 FDA reports)
INTENTIONAL MISUSE ( 5 FDA reports)
JOINT INJECTION ( 5 FDA reports)
KLEBSIELLA BACTERAEMIA ( 5 FDA reports)
LABELLED DRUG-FOOD INTERACTION MEDICATION ERROR ( 5 FDA reports)
LABORATORY TEST INTERFERENCE ( 5 FDA reports)
LENTIGO ( 5 FDA reports)
LIFE SUPPORT ( 5 FDA reports)
LIMB DEFORMITY ( 5 FDA reports)
LIPIDS ABNORMAL ( 5 FDA reports)
LIPOMATOUS HYPERTROPHY OF THE INTERATRIAL SEPTUM ( 5 FDA reports)
LUNG OPERATION ( 5 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 5 FDA reports)
LYMPHORRHOEA ( 5 FDA reports)
MACULOPATHY ( 5 FDA reports)
MALIGNANT TUMOUR EXCISION ( 5 FDA reports)
MEDIASTINAL MASS ( 5 FDA reports)
MEGACOLON ( 5 FDA reports)
MENINGITIS BACTERIAL ( 5 FDA reports)
MENSTRUATION DELAYED ( 5 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 5 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 5 FDA reports)
MITRAL VALVE REPAIR ( 5 FDA reports)
MITRAL VALVE SCLEROSIS ( 5 FDA reports)
MORTON'S NEUROMA ( 5 FDA reports)
MUCOSAL ULCERATION ( 5 FDA reports)
MYCETOMA MYCOTIC ( 5 FDA reports)
MYELITIS ( 5 FDA reports)
MYELOMA RECURRENCE ( 5 FDA reports)
NERVE ROOT COMPRESSION ( 5 FDA reports)
NERVE ROOT INJURY LUMBAR ( 5 FDA reports)
NEUROPATHIC ARTHROPATHY ( 5 FDA reports)
NODAL ARRHYTHMIA ( 5 FDA reports)
NYSTAGMUS ( 5 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 5 FDA reports)
OEDEMA GENITAL ( 5 FDA reports)
OESOPHAGEAL DISCOMFORT ( 5 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 5 FDA reports)
ONYCHOPHAGIA ( 5 FDA reports)
OPTIC DISC DISORDER ( 5 FDA reports)
OPTIC NERVE INJURY ( 5 FDA reports)
ORAL SUBMUCOSAL FIBROSIS ( 5 FDA reports)
ORAL TORUS ( 5 FDA reports)
ORTHOSIS USER ( 5 FDA reports)
OSTEOPETROSIS ( 5 FDA reports)
OSTEORADIONECROSIS ( 5 FDA reports)
OVARIAN DISORDER ( 5 FDA reports)
PACEMAKER COMPLICATION ( 5 FDA reports)
PAIN EXACERBATED ( 5 FDA reports)
PAINFUL DEFAECATION ( 5 FDA reports)
PANCREATIC PSEUDOCYST ( 5 FDA reports)
PARAPARESIS ( 5 FDA reports)
PELVIC ABSCESS ( 5 FDA reports)
PERICARDIAL DISEASE ( 5 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 5 FDA reports)
PHARYNGEAL MASS ( 5 FDA reports)
PHLEBITIS SUPERFICIAL ( 5 FDA reports)
PICKWICKIAN SYNDROME ( 5 FDA reports)
PNEUMOMEDIASTINUM ( 5 FDA reports)
PNEUMONIA HAEMOPHILUS ( 5 FDA reports)
PNEUMONIA MYCOPLASMAL ( 5 FDA reports)
POLYP COLORECTAL ( 5 FDA reports)
POST CONCUSSION SYNDROME ( 5 FDA reports)
POSTOPERATIVE INFECTION ( 5 FDA reports)
POSTPARTUM DISORDER ( 5 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 5 FDA reports)
PROCEDURAL DIZZINESS ( 5 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 5 FDA reports)
PRURITUS ANI ( 5 FDA reports)
PULMONARY TOXICITY ( 5 FDA reports)
PUNCTATE KERATITIS ( 5 FDA reports)
RADIATION NEUROPATHY ( 5 FDA reports)
RASH VESICULAR ( 5 FDA reports)
RECTOCELE REPAIR ( 5 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE DECREASED ( 5 FDA reports)
ABDOMINAL SYMPTOM ( 4 FDA reports)
ABORTION INDUCED ( 4 FDA reports)
ABSCESS INTESTINAL ( 4 FDA reports)
ABSCESS MANAGEMENT ( 4 FDA reports)
ACOUSTIC NEUROMA ( 4 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 4 FDA reports)
ACUTE LEUKAEMIA ( 4 FDA reports)
ADRENAL DISORDER ( 4 FDA reports)
AGITATED DEPRESSION ( 4 FDA reports)
AGRANULOCYTOSIS ( 4 FDA reports)
AKINESIA ( 4 FDA reports)
ANAL PRURITUS ( 4 FDA reports)
ANION GAP INCREASED ( 4 FDA reports)
ANTICOAGULANT THERAPY ( 4 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 4 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 4 FDA reports)
APPLICATION SITE DERMATITIS ( 4 FDA reports)
APPLICATION SITE EXCORIATION ( 4 FDA reports)
APPLICATION SITE EXFOLIATION ( 4 FDA reports)
APPLICATION SITE SWELLING ( 4 FDA reports)
ARTERIAL SPASM ( 4 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 4 FDA reports)
ARTHRITIS INFECTIVE ( 4 FDA reports)
ATRIAL HYPERTROPHY ( 4 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 4 FDA reports)
AUTOIMMUNE THYROIDITIS ( 4 FDA reports)
AVULSION FRACTURE ( 4 FDA reports)
AXONAL NEUROPATHY ( 4 FDA reports)
BALANITIS ( 4 FDA reports)
BENIGN CARDIAC NEOPLASM ( 4 FDA reports)
BIFASCICULAR BLOCK ( 4 FDA reports)
BILE DUCT OBSTRUCTION ( 4 FDA reports)
BIOPSY LIVER ABNORMAL ( 4 FDA reports)
BLADDER DISTENSION ( 4 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 4 FDA reports)
BLEPHARAL PAPILLOMA ( 4 FDA reports)
BLOOD CHOLESTEROL ( 4 FDA reports)
BLOOD CORTISOL INCREASED ( 4 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 4 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 4 FDA reports)
BLOOD FOLATE INCREASED ( 4 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 4 FDA reports)
BLOOD SODIUM ABNORMAL ( 4 FDA reports)
BLOOD TRIGLYCERIDES ( 4 FDA reports)
BONE FISTULA ( 4 FDA reports)
BONE MARROW DEPRESSION ( 4 FDA reports)
BONE MARROW DISORDER ( 4 FDA reports)
BOWEL SOUNDS ABNORMAL ( 4 FDA reports)
BRAIN OPERATION ( 4 FDA reports)
BRAIN SCAN ABNORMAL ( 4 FDA reports)
BREAST OPERATION ( 4 FDA reports)
BRONCHIAL INFECTION ( 4 FDA reports)
BURN OESOPHAGEAL ( 4 FDA reports)
BURN OF INTERNAL ORGANS ( 4 FDA reports)
CAMPYLOBACTER GASTROENTERITIS ( 4 FDA reports)
CANCER IN REMISSION ( 4 FDA reports)
CARDIAC INFECTION ( 4 FDA reports)
CARDIAC PACEMAKER REVISION ( 4 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 4 FDA reports)
CAROTID ARTERY STENT INSERTION ( 4 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 4 FDA reports)
CENTRAL OBESITY ( 4 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 4 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 4 FDA reports)
CERVIX CARCINOMA ( 4 FDA reports)
CHALAZION ( 4 FDA reports)
CHEYNE-STOKES RESPIRATION ( 4 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 4 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 4 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 4 FDA reports)
CLUBBING ( 4 FDA reports)
COLITIS MICROSCOPIC ( 4 FDA reports)
COLONIC HAEMORRHAGE ( 4 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 4 FDA reports)
CORNEAL DEPOSITS ( 4 FDA reports)
CORNEAL SCAR ( 4 FDA reports)
CRACKLES LUNG ( 4 FDA reports)
CSF TEST ABNORMAL ( 4 FDA reports)
CULDOPLASTY ( 4 FDA reports)
CULTURE POSITIVE ( 4 FDA reports)
CUSHINGOID ( 4 FDA reports)
CYSTOCELE REPAIR ( 4 FDA reports)
CYSTOPEXY ( 4 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 4 FDA reports)
DEFAECATION URGENCY ( 4 FDA reports)
DEPRESSION SUICIDAL ( 4 FDA reports)
DERMATOMYOSITIS ( 4 FDA reports)
DETOXIFICATION ( 4 FDA reports)
DIABETIC KETOACIDOTIC HYPERGLYCAEMIC COMA ( 4 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 4 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 4 FDA reports)
DIPLEGIA ( 4 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 4 FDA reports)
DRUG EFFECT DELAYED ( 4 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 4 FDA reports)
DRUG LEVEL FLUCTUATING ( 4 FDA reports)
DYSHIDROSIS ( 4 FDA reports)
EAR HAEMORRHAGE ( 4 FDA reports)
EAR IRRIGATION ( 4 FDA reports)
ECZEMA NUMMULAR ( 4 FDA reports)
EJECTION FRACTION ( 4 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 4 FDA reports)
EMBOLISM ARTERIAL ( 4 FDA reports)
ENTEROBACTER PNEUMONIA ( 4 FDA reports)
ENTEROCOCCAL SEPSIS ( 4 FDA reports)
EROSIVE DUODENITIS ( 4 FDA reports)
ERYTHEMA NODOSUM ( 4 FDA reports)
EYE OPERATION COMPLICATION ( 4 FDA reports)
EYELID FUNCTION DISORDER ( 4 FDA reports)
FASCIITIS ( 4 FDA reports)
FEAR OF FALLING ( 4 FDA reports)
FEELING GUILTY ( 4 FDA reports)
FINGER AMPUTATION ( 4 FDA reports)
FLAT AFFECT ( 4 FDA reports)
FOOD INTOLERANCE ( 4 FDA reports)
FUNGAL OESOPHAGITIS ( 4 FDA reports)
FUNGAL SEPSIS ( 4 FDA reports)
GALLBLADDER INJURY ( 4 FDA reports)
GANGLION ( 4 FDA reports)
GASTROENTERITIS RADIATION ( 4 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 4 FDA reports)
GRAFT INFECTION ( 4 FDA reports)
GRANULOCYTE COUNT INCREASED ( 4 FDA reports)
GRIEF REACTION ( 4 FDA reports)
HAEMORRHAGIC DISORDER ( 4 FDA reports)
HAEMOSIDEROSIS ( 4 FDA reports)
HEART SOUNDS ABNORMAL ( 4 FDA reports)
HELICOBACTER TEST POSITIVE ( 4 FDA reports)
HEMIANOPIA HOMONYMOUS ( 4 FDA reports)
HEPATECTOMY ( 4 FDA reports)
HEPATIC PAIN ( 4 FDA reports)
HERPES DERMATITIS ( 4 FDA reports)
HOSPICE CARE ( 4 FDA reports)
HYPERPARATHYROIDISM TERTIARY ( 4 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 4 FDA reports)
HYPERTONIA ( 4 FDA reports)
HYPOCHROMASIA ( 4 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 4 FDA reports)
ILEITIS ( 4 FDA reports)
ILIAC ARTERY OCCLUSION ( 4 FDA reports)
IMPATIENCE ( 4 FDA reports)
INCISIONAL HERNIA, OBSTRUCTIVE ( 4 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 4 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 4 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 4 FDA reports)
INFUSION SITE REACTION ( 4 FDA reports)
INJECTION SITE STINGING ( 4 FDA reports)
INTENTION TREMOR ( 4 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 4 FDA reports)
INTERVERTEBRAL DISC INJURY ( 4 FDA reports)
INTESTINAL OPERATION ( 4 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 4 FDA reports)
INTRAOCULAR PRESSURE DECREASED ( 4 FDA reports)
INTRATHECAL PUMP INSERTION ( 4 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 4 FDA reports)
IUCD COMPLICATION ( 4 FDA reports)
JC VIRUS INFECTION ( 4 FDA reports)
JEJUNECTOMY ( 4 FDA reports)
KIDNEY SMALL ( 4 FDA reports)
KLEBSIELLA SEPSIS ( 4 FDA reports)
LARYNGEAL CANCER ( 4 FDA reports)
LAZINESS ( 4 FDA reports)
LIPID METABOLISM DISORDER ( 4 FDA reports)
LIQUID PRODUCT PHYSICAL ISSUE ( 4 FDA reports)
LITHOTRIPSY ( 4 FDA reports)
LORDOSIS ( 4 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 4 FDA reports)
LUNG TRANSPLANT ( 4 FDA reports)
LUPUS PNEUMONITIS ( 4 FDA reports)
LYMPHADENECTOMY ( 4 FDA reports)
MALIGNANT MELANOMA STAGE IV ( 4 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 4 FDA reports)
MASKED FACIES ( 4 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 4 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 4 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 4 FDA reports)
MEDIASTINAL DISORDER ( 4 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 4 FDA reports)
MICROCYTOSIS ( 4 FDA reports)
MICROVASCULAR ANGINA ( 4 FDA reports)
MUCOSAL DISCOLOURATION ( 4 FDA reports)
MUCOUS MEMBRANE DISORDER ( 4 FDA reports)
MUSCLE ENZYME INCREASED ( 4 FDA reports)
MUSCLE HYPERTROPHY ( 4 FDA reports)
MYCOSIS FUNGOIDES ( 4 FDA reports)
MYELITIS TRANSVERSE ( 4 FDA reports)
NECK MASS ( 4 FDA reports)
NEOPLASM SKIN ( 4 FDA reports)
NEPHRITIS ( 4 FDA reports)
NEPHROPATHY TOXIC ( 4 FDA reports)
NERVE BLOCK ( 4 FDA reports)
NEUROGENIC BOWEL ( 4 FDA reports)
NEUROPATHIC PAIN ( 4 FDA reports)
NEUTROPHILIA ( 4 FDA reports)
NO ADVERSE DRUG EFFECT ( 4 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 4 FDA reports)
NOSOCOMIAL INFECTION ( 4 FDA reports)
OBSTRUCTION GASTRIC ( 4 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 4 FDA reports)
OESOPHAGEAL OEDEMA ( 4 FDA reports)
ORAL MUCOSAL BLISTERING ( 4 FDA reports)
ORBITAL CYST ( 4 FDA reports)
ORTHOSTATIC INTOLERANCE ( 4 FDA reports)
OXYGEN SATURATION ABNORMAL ( 4 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 4 FDA reports)
PANCREAS INFECTION ( 4 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 4 FDA reports)
PANCREATIC INJURY ( 4 FDA reports)
PANCREATICODUODENECTOMY ( 4 FDA reports)
PAPILLOMA VIRAL INFECTION ( 4 FDA reports)
PARANEOPLASTIC SYNDROME ( 4 FDA reports)
PCO2 INCREASED ( 4 FDA reports)
PEDAL PULSE DECREASED ( 4 FDA reports)
PERICARDIAL FIBROSIS ( 4 FDA reports)
PERICARDITIS CONSTRICTIVE ( 4 FDA reports)
PERICARDITIS LUPUS ( 4 FDA reports)
PERONEAL MUSCULAR ATROPHY ( 4 FDA reports)
PHAEOCHROMOCYTOMA ( 4 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 4 FDA reports)
PILOERECTION ( 4 FDA reports)
PNEUMATOSIS CYSTOIDES INTESTINALIS ( 4 FDA reports)
PNEUMOCONIOSIS ( 4 FDA reports)
POISONING ( 4 FDA reports)
POLYMENORRHOEA ( 4 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 4 FDA reports)
POST PROCEDURAL NAUSEA ( 4 FDA reports)
POST PROCEDURAL PAIN ( 4 FDA reports)
POST THROMBOTIC SYNDROME ( 4 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 4 FDA reports)
PREMATURE LABOUR ( 4 FDA reports)
PRESSURE OF SPEECH ( 4 FDA reports)
PRIAPISM ( 4 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 4 FDA reports)
PROSTATE CANCER METASTATIC ( 4 FDA reports)
PROSTATE INFECTION ( 4 FDA reports)
PROSTHESIS USER ( 4 FDA reports)
PRURITUS GENITAL ( 4 FDA reports)
PSYCHOMOTOR RETARDATION ( 4 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 4 FDA reports)
PULMONARY TUBERCULOSIS ( 4 FDA reports)
PULSE PRESSURE INCREASED ( 4 FDA reports)
RADICULAR PAIN ( 4 FDA reports)
RECTAL DISCHARGE ( 4 FDA reports)
RECTAL PERFORATION ( 4 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 4 FDA reports)
RELATIONSHIP BREAKDOWN ( 4 FDA reports)
RENAL CANCER METASTATIC ( 4 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 4 FDA reports)
RENAL VEIN THROMBOSIS ( 4 FDA reports)
RESPIRATORY DEPRESSION ( 4 FDA reports)
RETINAL INJURY ( 4 FDA reports)
RETROGRADE EJACULATION ( 4 FDA reports)
RHEUMATOID FACTOR INCREASED ( 4 FDA reports)
RHINALGIA ( 4 FDA reports)
RHINITIS SEASONAL ( 4 FDA reports)
SALIVARY GLAND CALCULUS ( 4 FDA reports)
SCAN ABDOMEN ABNORMAL ( 4 FDA reports)
SCINTILLATING SCOTOMA ( 4 FDA reports)
SCLERAL HAEMORRHAGE ( 4 FDA reports)
SENSATION OF BLOCK IN EAR ( 4 FDA reports)
SEROTONIN SYNDROME ( 4 FDA reports)
SHIFT TO THE LEFT ( 4 FDA reports)
SIMPLE PARTIAL SEIZURES ( 4 FDA reports)
SKIN WRINKLING ( 4 FDA reports)
SOCIAL FEAR ( 4 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 4 FDA reports)
SPINAL CLAUDICATION ( 4 FDA reports)
SPINAL DECOMPRESSION ( 4 FDA reports)
SPINAL LIGAMENT OSSIFICATION ( 4 FDA reports)
SPINAL PAIN ( 4 FDA reports)
SPINDLE CELL SARCOMA ( 4 FDA reports)
SPLENIC HAEMORRHAGE ( 4 FDA reports)
SPLENIC MARGINAL ZONE LYMPHOMA ( 4 FDA reports)
SPLINTER HAEMORRHAGES ( 4 FDA reports)
SPONDYLOSIS ( 4 FDA reports)
STENT REMOVAL ( 4 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 4 FDA reports)
SUDDEN ONSET OF SLEEP ( 4 FDA reports)
SWEAT GLAND DISORDER ( 4 FDA reports)
SYSTEMIC CANDIDA ( 4 FDA reports)
SYSTOLIC DYSFUNCTION ( 4 FDA reports)
TABLET ISSUE ( 4 FDA reports)
TENDON OPERATION ( 4 FDA reports)
THROAT LESION ( 4 FDA reports)
THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
THYROIDECTOMY ( 4 FDA reports)
THYROIDITIS ( 4 FDA reports)
TONGUE BLISTERING ( 4 FDA reports)
TRICUSPID VALVE DISEASE ( 4 FDA reports)
TROPONIN ( 4 FDA reports)
TROPONIN I ( 4 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 4 FDA reports)
UNEMPLOYMENT ( 4 FDA reports)
URAEMIC ENCEPHALOPATHY ( 4 FDA reports)
URETERAL STENT INSERTION ( 4 FDA reports)
URINARY BLADDER POLYP ( 4 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 4 FDA reports)
URINE ANALYSIS ( 4 FDA reports)
URINE BILIRUBIN INCREASED ( 4 FDA reports)
URTICARIA PAPULAR ( 4 FDA reports)
UTERINE ENLARGEMENT ( 4 FDA reports)
UVEITIS ( 4 FDA reports)
VASCULAR GRAFT COMPLICATION ( 4 FDA reports)
VASCULAR STENOSIS ( 4 FDA reports)
VASCULAR STENT INSERTION ( 4 FDA reports)
VENTRICULAR FAILURE ( 4 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 4 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 4 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 4 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
VITAMIN D ABNORMAL ( 4 FDA reports)
VITH NERVE PARALYSIS ( 4 FDA reports)
VITRECTOMY ( 4 FDA reports)
VULVOVAGINAL ERYTHEMA ( 4 FDA reports)
WHOLE BLOOD TRANSFUSION ( 4 FDA reports)
WOUND COMPLICATION ( 4 FDA reports)
WOUND DEBRIDEMENT ( 4 FDA reports)
WOUND SEPSIS ( 4 FDA reports)
XANTHOPSIA ( 4 FDA reports)
XEROSIS ( 4 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 3 FDA reports)
RENAL TUBULAR ACIDOSIS ( 3 FDA reports)
RENAL VASCULITIS ( 3 FDA reports)
RETINAL DEGENERATION ( 3 FDA reports)
RETINAL OPERATION ( 3 FDA reports)
RETINAL VASCULAR OCCLUSION ( 3 FDA reports)
RETINITIS PIGMENTOSA ( 3 FDA reports)
RHEUMATOID LUNG ( 3 FDA reports)
RHEUMATOID NODULE ( 3 FDA reports)
RHYTHM IDIOVENTRICULAR ( 3 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE DECREASED ( 3 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 3 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 3 FDA reports)
SELF ESTEEM DECREASED ( 3 FDA reports)
SENSATION OF PRESSURE IN EAR ( 3 FDA reports)
SEPTIC EMBOLUS ( 3 FDA reports)
SHOULDER ARTHROPLASTY ( 3 FDA reports)
SHUNT INFECTION ( 3 FDA reports)
SKIN INJURY ( 3 FDA reports)
SLEEP ATTACKS ( 3 FDA reports)
SMALL INTESTINAL STENOSIS ( 3 FDA reports)
SOMATIC DELUSION ( 3 FDA reports)
SPEECH REHABILITATION ( 3 FDA reports)
SPINAL CORD INJURY ( 3 FDA reports)
SPLEEN CONGESTION ( 3 FDA reports)
SPLENIC ARTERY ANEURYSM ( 3 FDA reports)
SPUTUM PURULENT ( 3 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 3 FDA reports)
STAPHYLOCOCCAL MEDIASTINITIS ( 3 FDA reports)
STARVATION ( 3 FDA reports)
STERNAL FRACTURE ( 3 FDA reports)
STITCH ABSCESS ( 3 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 3 FDA reports)
SUPERFICIAL INJURY OF EYE ( 3 FDA reports)
SUPERINFECTION ( 3 FDA reports)
SUPRAPUBIC PAIN ( 3 FDA reports)
SYNOVIAL DISORDER ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 3 FDA reports)
SYSTOLIC HYPERTENSION ( 3 FDA reports)
TACHYCARDIA PAROXYSMAL ( 3 FDA reports)
TERMINAL INSOMNIA ( 3 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 3 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 3 FDA reports)
THROMBOCYTHAEMIA ( 3 FDA reports)
THROMBOTIC STROKE ( 3 FDA reports)
THYROXINE DECREASED ( 3 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 3 FDA reports)
TONGUE BITING ( 3 FDA reports)
TONSILLAR DISORDER ( 3 FDA reports)
TONSILLAR HYPERTROPHY ( 3 FDA reports)
TONSILLECTOMY ( 3 FDA reports)
TOXIC NEUROPATHY ( 3 FDA reports)
TRACHEAL DISORDER ( 3 FDA reports)
TRANSPLANT ( 3 FDA reports)
TRAUMATIC ARTHRITIS ( 3 FDA reports)
TRAUMATIC ARTHROPATHY ( 3 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 3 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 3 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 3 FDA reports)
TYPE II HYPERLIPIDAEMIA ( 3 FDA reports)
UPPER EXTREMITY MASS ( 3 FDA reports)
URETHRAL OBSTRUCTION ( 3 FDA reports)
UROBILINOGEN URINE INCREASED ( 3 FDA reports)
VAGINAL DISORDER ( 3 FDA reports)
VAGINAL ERYTHEMA ( 3 FDA reports)
VARICOSE VEIN OPERATION ( 3 FDA reports)
VENOUS STENOSIS ( 3 FDA reports)
VERTEBRAL INJURY ( 3 FDA reports)
VIIITH NERVE LESION ( 3 FDA reports)
VIRAL LABYRINTHITIS ( 3 FDA reports)
VIRAL LOAD INCREASED ( 3 FDA reports)
VOLVULUS ( 3 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 3 FDA reports)
WALKING DISABILITY ( 3 FDA reports)
WEGENER'S GRANULOMATOSIS ( 3 FDA reports)
WHITE BLOOD CELL DISORDER ( 3 FDA reports)
WHITE BLOOD CELL MORPHOLOGY ABNORMAL ( 3 FDA reports)
5Q MINUS SYNDROME ( 3 FDA reports)
ABDOMINAL INFECTION ( 3 FDA reports)
ABDOMINAL WALL ABSCESS ( 3 FDA reports)
ABNORMAL CLOTTING FACTOR ( 3 FDA reports)
ACANTHOSIS NIGRICANS ( 3 FDA reports)
ACQUIRED CLAW TOE ( 3 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 3 FDA reports)
ALCOHOL INTERACTION ( 3 FDA reports)
ALCOHOL POISONING ( 3 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 3 FDA reports)
ALDOLASE INCREASED ( 3 FDA reports)
ALLERGY TO CHEMICALS ( 3 FDA reports)
ALLOIMMUNISATION ( 3 FDA reports)
AMYLASE INCREASED ( 3 FDA reports)
ANAL CANCER ( 3 FDA reports)
ANAL FISTULA ( 3 FDA reports)
ANAL ULCER ( 3 FDA reports)
ANDROGEN DEFICIENCY ( 3 FDA reports)
ANGIOGRAM ( 3 FDA reports)
ANGIOGRAM ABNORMAL ( 3 FDA reports)
ANIMAL SCRATCH ( 3 FDA reports)
ANOVULATORY CYCLE ( 3 FDA reports)
ANTIANDROGEN THERAPY ( 3 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
AORTIC OCCLUSION ( 3 FDA reports)
APPLICATION SITE DISCHARGE ( 3 FDA reports)
APPLICATION SITE DISCOLOURATION ( 3 FDA reports)
APPLICATION SITE DRYNESS ( 3 FDA reports)
APPLICATION SITE ULCER ( 3 FDA reports)
APPLICATION SITE WARMTH ( 3 FDA reports)
ARM AMPUTATION ( 3 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 3 FDA reports)
ARTERIAL HAEMORRHAGE ( 3 FDA reports)
ASBESTOSIS ( 3 FDA reports)
ASPIRATION PLEURAL CAVITY ( 3 FDA reports)
BELLIGERENCE ( 3 FDA reports)
BENIGN RENAL NEOPLASM ( 3 FDA reports)
BICUSPID AORTIC VALVE ( 3 FDA reports)
BIOPSY COLON ABNORMAL ( 3 FDA reports)
BLADDER PERFORATION ( 3 FDA reports)
BLOOD AMYLASE ABNORMAL ( 3 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 3 FDA reports)
BLOOD CALCIUM ABNORMAL ( 3 FDA reports)
BLOOD COPPER INCREASED ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MM INCREASED ( 3 FDA reports)
BLOOD HOMOCYSTEINE ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN A ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN G ( 3 FDA reports)
BLOOD OSMOLARITY DECREASED ( 3 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 3 FDA reports)
BLOOD THROMBIN ABNORMAL ( 3 FDA reports)
BODY MASS INDEX DECREASED ( 3 FDA reports)
BONE FORMATION TEST ABNORMAL ( 3 FDA reports)
BONE SARCOMA ( 3 FDA reports)
BRAIN MIDLINE SHIFT ( 3 FDA reports)
BRAIN STEM HAEMORRHAGE ( 3 FDA reports)
BREAST INJURY ( 3 FDA reports)
BRONCHOSTENOSIS ( 3 FDA reports)
CALCIUM IONISED INCREASED ( 3 FDA reports)
CAPILLARY DISORDER ( 3 FDA reports)
CARCINOID TUMOUR OF THE PROSTATE ( 3 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 3 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 3 FDA reports)
CARDIAC VALVE VEGETATION ( 3 FDA reports)
CARDIOTOXICITY ( 3 FDA reports)
CAROTID ENDARTERECTOMY ( 3 FDA reports)
CAROTID PULSE INCREASED ( 3 FDA reports)
CATHETER SITE DISCHARGE ( 3 FDA reports)
CATHETER SITE ERYTHEMA ( 3 FDA reports)
CATHETER SITE HAEMATOMA ( 3 FDA reports)
CATHETER SITE RELATED REACTION ( 3 FDA reports)
CATHETER THROMBOSIS ( 3 FDA reports)
CEREBELLAR HAEMORRHAGE ( 3 FDA reports)
CEREBRAL MICROANGIOPATHY ( 3 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 3 FDA reports)
CERULOPLASMIN INCREASED ( 3 FDA reports)
CERVICAL CYST ( 3 FDA reports)
CERVICAL POLYP ( 3 FDA reports)
CERVICAL STRICTURE ( 3 FDA reports)
CHEMICAL BURN OF SKIN ( 3 FDA reports)
CHEST TUBE INSERTION ( 3 FDA reports)
CHOREOATHETOSIS ( 3 FDA reports)
CHRONIC GRANULOMATOUS DISEASE ( 3 FDA reports)
CLONIC CONVULSION ( 3 FDA reports)
CLONUS ( 3 FDA reports)
COAGULATION TIME SHORTENED ( 3 FDA reports)
COCCIDIOIDOMYCOSIS ( 3 FDA reports)
COLITIS COLLAGENOUS ( 3 FDA reports)
COLON INJURY ( 3 FDA reports)
COLOSTOMY CLOSURE ( 3 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 3 FDA reports)
COMPULSIONS ( 3 FDA reports)
CONDYLOMA ACUMINATUM ( 3 FDA reports)
CONGENITAL ANOMALY ( 3 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 3 FDA reports)
CONJUNCTIVAL DISORDER ( 3 FDA reports)
CORONARY ARTERY DISSECTION ( 3 FDA reports)
CORONARY OSTIAL STENOSIS ( 3 FDA reports)
CREATININE RENAL CLEARANCE ( 3 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 3 FDA reports)
CSF GLUCOSE ABNORMAL ( 3 FDA reports)
CULTURE STOOL POSITIVE ( 3 FDA reports)
CULTURE WOUND POSITIVE ( 3 FDA reports)
DEAFNESS TRANSITORY ( 3 FDA reports)
DENTAL IMPLANTATION ( 3 FDA reports)
DEPRESSIVE SYMPTOM ( 3 FDA reports)
DERMATITIS ALLERGIC ( 3 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 3 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 3 FDA reports)
DIABETIC RETINAL OEDEMA ( 3 FDA reports)
DIABETIC ULCER ( 3 FDA reports)
DIASTOLIC HYPERTENSION ( 3 FDA reports)
DISEASE COMPLICATION ( 3 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 3 FDA reports)
DRUG DIVERSION ( 3 FDA reports)
DRUG LEVEL CHANGED ( 3 FDA reports)
DRUG NAME CONFUSION ( 3 FDA reports)
DRUG RESISTANCE ( 3 FDA reports)
DUODENAL OBSTRUCTION ( 3 FDA reports)
ECZEMA EYELIDS ( 3 FDA reports)
EDUCATIONAL PROBLEM ( 3 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 3 FDA reports)
ENCHONDROMATOSIS ( 3 FDA reports)
ENDARTERECTOMY ( 3 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 3 FDA reports)
ENDOPHTHALMITIS ( 3 FDA reports)
ENTEROBACTER SEPSIS ( 3 FDA reports)
ENTEROVESICAL FISTULA ( 3 FDA reports)
EOSINOPHILIC PNEUMONIA ( 3 FDA reports)
EPIGLOTTITIS ( 3 FDA reports)
ERYTHEMA INDURATUM ( 3 FDA reports)
ESSENTIAL TREMOR ( 3 FDA reports)
EXSANGUINATION ( 3 FDA reports)
EXTRADURAL ABSCESS ( 3 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 3 FDA reports)
EYE OEDEMA ( 3 FDA reports)
FACIAL NEURALGIA ( 3 FDA reports)
FACTOR V INHIBITION ( 3 FDA reports)
FACTOR XI DEFICIENCY ( 3 FDA reports)
FAECAL VOLUME INCREASED ( 3 FDA reports)
FALLOT'S TETRALOGY ( 3 FDA reports)
FEELING OF DESPAIR ( 3 FDA reports)
FEELINGS OF WORTHLESSNESS ( 3 FDA reports)
FEMORAL NERVE INJURY ( 3 FDA reports)
FINGER DEFORMITY ( 3 FDA reports)
FLOPPY IRIS SYNDROME ( 3 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 3 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 3 FDA reports)
FUNGUS SPUTUM TEST POSITIVE ( 3 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 3 FDA reports)
GAMMOPATHY ( 3 FDA reports)
GASTRIC PERFORATION ( 3 FDA reports)
GASTROINTESTINAL EROSION ( 3 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 3 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 3 FDA reports)
GASTROINTESTINAL TELANGIECTASIA ( 3 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 3 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 3 FDA reports)
GENITAL HAEMORRHAGE ( 3 FDA reports)
GESTATIONAL DIABETES ( 3 FDA reports)
GLIOBLASTOMA MULTIFORME ( 3 FDA reports)
GLOMERULOSCLEROSIS ( 3 FDA reports)
GLYCOGEN STORAGE DISEASE TYPE II ( 3 FDA reports)
HAEMOGLOBIN ( 3 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 3 FDA reports)
HALLUCINATION, TACTILE ( 3 FDA reports)
HEART TRANSPLANT REJECTION ( 3 FDA reports)
HEMIANOPIA ( 3 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 3 FDA reports)
HEPATIC TRAUMA ( 3 FDA reports)
HEPATOCELLULAR INJURY ( 3 FDA reports)
HEREDITARY ANGIOEDEMA ( 3 FDA reports)
HISTRIONIC PERSONALITY DISORDER ( 3 FDA reports)
HOARSENESS ( 3 FDA reports)
HYDROCELE ( 3 FDA reports)
HYDROURETER ( 3 FDA reports)
HYPERCHLORAEMIA ( 3 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 3 FDA reports)
HYPERMETABOLISM ( 3 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 3 FDA reports)
HYPERTROPHY BREAST ( 3 FDA reports)
HYPERVISCOSITY SYNDROME ( 3 FDA reports)
HYPNOPOMPIC HALLUCINATION ( 3 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 3 FDA reports)
HYPOLIPIDAEMIA ( 3 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 3 FDA reports)
ILIOTIBIAL BAND SYNDROME ( 3 FDA reports)
IMMUNOGLOBULINS INCREASED ( 3 FDA reports)
IMPLANT SITE REACTION ( 3 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 3 FDA reports)
INADEQUATE DIET ( 3 FDA reports)
INCISION SITE ABSCESS ( 3 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 3 FDA reports)
INFERIOR VENA CAVA DILATATION ( 3 FDA reports)
INFUSION SITE EXTRAVASATION ( 3 FDA reports)
INJECTION SITE DISCOMFORT ( 3 FDA reports)
INJECTION SITE INFLAMMATION ( 3 FDA reports)
INJECTION SITE NECROSIS ( 3 FDA reports)
INJECTION SITE PUSTULE ( 3 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 3 FDA reports)
INTESTINAL RESECTION ( 3 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE EXPELLED ( 3 FDA reports)
INTRA-UTERINE DEATH ( 3 FDA reports)
INTRANASAL FUNGAL INFECTION ( 3 FDA reports)
INVESTIGATION ( 3 FDA reports)
INVESTIGATION ABNORMAL ( 3 FDA reports)
IRIS DISORDER ( 3 FDA reports)
ISCHAEMIC NEPHROPATHY ( 3 FDA reports)
JOINT ARTHROPLASTY ( 3 FDA reports)
KERATITIS HERPETIC ( 3 FDA reports)
KETONURIA ( 3 FDA reports)
LACTOSE INTOLERANCE ( 3 FDA reports)
LARYNGEAL MASS ( 3 FDA reports)
LEARNING DISORDER ( 3 FDA reports)
LENS DISORDER ( 3 FDA reports)
LICHENIFICATION ( 3 FDA reports)
LIGAMENT INJURY ( 3 FDA reports)
LIP HAEMORRHAGE ( 3 FDA reports)
LIPASE ABNORMAL ( 3 FDA reports)
LIPOPROTEIN (A) INCREASED ( 3 FDA reports)
LIVER TRANSPLANT ( 3 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 3 FDA reports)
LOW DENSITY LIPOPROTEIN ABNORMAL ( 3 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 3 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 3 FDA reports)
LUNG INJURY ( 3 FDA reports)
LUNG LOBECTOMY ( 3 FDA reports)
MACROANGIOPATHY ( 3 FDA reports)
MACULAR CYST ( 3 FDA reports)
MACULAR PSEUDOHOLE ( 3 FDA reports)
MALIGNANT MELANOMA IN SITU ( 3 FDA reports)
MALLORY-WEISS SYNDROME ( 3 FDA reports)
MATERNAL EXPOSURE BEFORE PREGNANCY ( 3 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 3 FDA reports)
MEDICAL DEVICE PAIN ( 3 FDA reports)
MEDICAL OBSERVATION ABNORMAL ( 3 FDA reports)
MEDICATION TAMPERING ( 3 FDA reports)
MENISCUS REMOVAL ( 3 FDA reports)
METABOLIC ALKALOSIS ( 3 FDA reports)
METASTASES TO PLEURA ( 3 FDA reports)
METATARSALGIA ( 3 FDA reports)
METHAEMOGLOBINAEMIA ( 3 FDA reports)
MONOCYTE COUNT DECREASED ( 3 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 3 FDA reports)
MONOCYTOSIS ( 3 FDA reports)
MONOPARESIS ( 3 FDA reports)
MORBID THOUGHTS ( 3 FDA reports)
MUSCLE SWELLING ( 3 FDA reports)
MYOCARDIAL OEDEMA ( 3 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 3 FDA reports)
MYOGLOBIN URINE PRESENT ( 3 FDA reports)
MYOPATHY STEROID ( 3 FDA reports)
NAIL TINEA ( 3 FDA reports)
NASAL ULCER ( 3 FDA reports)
NATURAL KILLER T CELL COUNT DECREASED ( 3 FDA reports)
NECK DEFORMITY ( 3 FDA reports)
NEPHRITIC SYNDROME ( 3 FDA reports)
NEPHRITIS ALLERGIC ( 3 FDA reports)
NERVE ROOT INJURY ( 3 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 3 FDA reports)
NIGHT CRAMPS ( 3 FDA reports)
NITRITE URINE PRESENT ( 3 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 3 FDA reports)
OCCIPITAL NEURALGIA ( 3 FDA reports)
OEDEMATOUS PANCREATITIS ( 3 FDA reports)
OPISTHOTONUS ( 3 FDA reports)
OPPORTUNISTIC INFECTION ( 3 FDA reports)
OPTIC NERVE INFARCTION ( 3 FDA reports)
ORGASM ABNORMAL ( 3 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 3 FDA reports)
OTORRHOEA ( 3 FDA reports)
OVARIAN CANCER METASTATIC ( 3 FDA reports)
OVARIAN MASS ( 3 FDA reports)
PACEMAKER GENERATED ARRHYTHMIA ( 3 FDA reports)
PANCREATIC CALCIFICATION ( 3 FDA reports)
PANCREATIC HAEMORRHAGE ( 3 FDA reports)
PANIC DISORDER WITHOUT AGORAPHOBIA ( 3 FDA reports)
PARADOXICAL DRUG REACTION ( 3 FDA reports)
PARASOMNIA ( 3 FDA reports)
PEMPHIGOID ( 3 FDA reports)
PENILE SIZE REDUCED ( 3 FDA reports)
PERFORATED ULCER ( 3 FDA reports)
PERICARDIAL DRAINAGE ( 3 FDA reports)
PERICARDIOTOMY ( 3 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 3 FDA reports)
PERITONEAL DISORDER ( 3 FDA reports)
PERNICIOUS ANAEMIA ( 3 FDA reports)
PETIT MAL EPILEPSY ( 3 FDA reports)
PHARYNGEAL OPERATION ( 3 FDA reports)
PHONOPHOBIA ( 3 FDA reports)
PHYSICAL ABUSE ( 3 FDA reports)
PIRIFORMIS SYNDROME ( 3 FDA reports)
PNEUMONIA PARAINFLUENZAE VIRAL ( 3 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 3 FDA reports)
PNEUMOPERITONEUM ( 3 FDA reports)
PO2 INCREASED ( 3 FDA reports)
POIKILOCYTOSIS ( 3 FDA reports)
PORTAL TRIADITIS ( 3 FDA reports)
POST PROCEDURAL VOMITING ( 3 FDA reports)
POSTINFARCTION ANGINA ( 3 FDA reports)
POSTOPERATIVE THROMBOSIS ( 3 FDA reports)
PREMATURE MENOPAUSE ( 3 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 3 FDA reports)
PROCEDURAL NAUSEA ( 3 FDA reports)
PRODUCT COUNTERFEIT ( 3 FDA reports)
PRODUCT ODOUR ABNORMAL ( 3 FDA reports)
PROTEIN S DEFICIENCY ( 3 FDA reports)
PSEUDOCYST ( 3 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 3 FDA reports)
PSYCHOTIC BEHAVIOUR ( 3 FDA reports)
PULMONARY EOSINOPHILIA ( 3 FDA reports)
PULMONARY FUNCTION TEST ( 3 FDA reports)
PULMONARY HILUM MASS ( 3 FDA reports)
PUSTULAR PSORIASIS ( 3 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 3 FDA reports)
RECTAL LESION ( 3 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 3 FDA reports)
RELAPSING FEVER ( 3 FDA reports)
RENAL ARTERIOSCLEROSIS ( 3 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 2 FDA reports)
ABDOMINAL WALL DISORDER ( 2 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 2 FDA reports)
ABNORMAL WEIGHT GAIN ( 2 FDA reports)
ABSCESS BACTERIAL ( 2 FDA reports)
ACARODERMATITIS ( 2 FDA reports)
ACCIDENTAL DEATH ( 2 FDA reports)
ACUTE ENDOCARDITIS ( 2 FDA reports)
ACUTE LUNG INJURY ( 2 FDA reports)
ADENOCARCINOMA PANCREAS ( 2 FDA reports)
ADENOIDECTOMY ( 2 FDA reports)
ADHESIOLYSIS ( 2 FDA reports)
ADNEXA UTERI PAIN ( 2 FDA reports)
ADRENAL SUPPRESSION ( 2 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 2 FDA reports)
AGORAPHOBIA ( 2 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 2 FDA reports)
ALLERGY TEST POSITIVE ( 2 FDA reports)
ALPHA-1 ANTI-TRYPSIN DEFICIENCY ( 2 FDA reports)
ANAEMIA MEGALOBLASTIC ( 2 FDA reports)
ANDROGENS DECREASED ( 2 FDA reports)
ANEURYSM ARTERIOVENOUS ( 2 FDA reports)
ANGIODYSPLASIA ( 2 FDA reports)
ANTERIOR CHAMBER INFLAMMATION ( 2 FDA reports)
ANTI-SS-A ANTIBODY POSITIVE ( 2 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
ANTIBIOTIC THERAPY ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 2 FDA reports)
ANTICONVULSANT TOXICITY ( 2 FDA reports)
APALLIC SYNDROME ( 2 FDA reports)
APPLICATION SITE EROSION ( 2 FDA reports)
APPLICATION SITE HAEMATOMA ( 2 FDA reports)
APPLICATION SITE INFLAMMATION ( 2 FDA reports)
APPLICATION SITE SCAB ( 2 FDA reports)
APPLICATION SITE URTICARIA ( 2 FDA reports)
APRAXIA ( 2 FDA reports)
APTYALISM ( 2 FDA reports)
ARACHNOID CYST ( 2 FDA reports)
ARCUS LIPOIDES ( 2 FDA reports)
ARTERIAL FIBROSIS ( 2 FDA reports)
ARTERIAL STENOSIS LIMB ( 2 FDA reports)
ARTERIOVENOUS FISTULA ( 2 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 2 FDA reports)
ARTERIOVENOUS GRAFT THROMBOSIS ( 2 FDA reports)
ARTERITIS ( 2 FDA reports)
ARTHROSCOPIC SURGERY ( 2 FDA reports)
ARTICULAR CALCIFICATION ( 2 FDA reports)
ASPHYXIA ( 2 FDA reports)
ASPIRATION BONE MARROW ( 2 FDA reports)
ASTHMA EXERCISE INDUCED ( 2 FDA reports)
AURICULAR PERICHONDRITIS ( 2 FDA reports)
B-CELL LYMPHOMA STAGE III ( 2 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 2 FDA reports)
BACTERIA URINE ( 2 FDA reports)
BAND NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 2 FDA reports)
BASILAR ARTERY STENOSIS ( 2 FDA reports)
BENIGN BREAST NEOPLASM ( 2 FDA reports)
BENIGN GASTRIC NEOPLASM ( 2 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 2 FDA reports)
BENIGN SOFT TISSUE NEOPLASM ( 2 FDA reports)
BILATERAL HYDRONEPHROSIS ( 2 FDA reports)
BILE OUTPUT ( 2 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 2 FDA reports)
BILIRUBIN URINE ( 2 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 2 FDA reports)
BIOPSY BREAST NORMAL ( 2 FDA reports)
BIOPSY KIDNEY ( 2 FDA reports)
BIOPSY LIP ( 2 FDA reports)
BIOPSY SKIN ABNORMAL ( 2 FDA reports)
BK VIRUS INFECTION ( 2 FDA reports)
BLADDER DILATATION ( 2 FDA reports)
BLADDER INJURY ( 2 FDA reports)
BLADDER NECROSIS ( 2 FDA reports)
BLADDER NEOPLASM SURGERY ( 2 FDA reports)
BLADDER OPERATION ( 2 FDA reports)
BLADDER SPHINCTER ATONY ( 2 FDA reports)
BLADDER STENOSIS ( 2 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA RECURRENT ( 2 FDA reports)
BLASTOMYCOSIS ( 2 FDA reports)
BLINDNESS TRAUMATIC ( 2 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 2 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 2 FDA reports)
BLOOD GROWTH HORMONE INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 2 FDA reports)
BLOOD KETONE BODY ( 2 FDA reports)
BLOOD OESTROGEN DECREASED ( 2 FDA reports)
BLOOD TESTOSTERONE ABNORMAL ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 2 FDA reports)
BLOOD UREA ABNORMAL ( 2 FDA reports)
BLOOD ZINC DECREASED ( 2 FDA reports)
BONE MARROW TUMOUR CELL INFILTRATION ( 2 FDA reports)
BORDERLINE GLAUCOMA ( 2 FDA reports)
BOREDOM ( 2 FDA reports)
BOTULISM ( 2 FDA reports)
BRACHIAL PLEXOPATHY ( 2 FDA reports)
BREAST ABSCESS ( 2 FDA reports)
BREAST COSMETIC SURGERY ( 2 FDA reports)
BREAST OEDEMA ( 2 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 2 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 2 FDA reports)
BRONCHOPLEURAL FISTULA ( 2 FDA reports)
BRONCHOSCOPY ABNORMAL ( 2 FDA reports)
BUDD-CHIARI SYNDROME ( 2 FDA reports)
BUNION OPERATION ( 2 FDA reports)
BURNING FEET SYNDROME ( 2 FDA reports)
BUTTOCK PAIN ( 2 FDA reports)
CARBON MONOXIDE POISONING ( 2 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 2 FDA reports)
CARCINOID TUMOUR PULMONARY ( 2 FDA reports)
CARCINOMA ( 2 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 2 FDA reports)
CARDIAC PERFORATION ( 2 FDA reports)
CARDIAC SEPTAL DEFECT ( 2 FDA reports)
CARDIAC VALVE ABSCESS ( 2 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 2 FDA reports)
CAROTID ARTERY ANEURYSM ( 2 FDA reports)
CAROTID ARTERY DISSECTION ( 2 FDA reports)
CAROTIDYNIA ( 2 FDA reports)
CASTLEMAN'S DISEASE ( 2 FDA reports)
CATHETER SITE INFECTION ( 2 FDA reports)
CELLULITIS STREPTOCOCCAL ( 2 FDA reports)
CEREBELLAR HAEMATOMA ( 2 FDA reports)
CEREBRAL CYST ( 2 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 2 FDA reports)
CERVIX CARCINOMA STAGE III ( 2 FDA reports)
CERVIX HAEMORRHAGE UTERINE ( 2 FDA reports)
CHEST WALL CYST ( 2 FDA reports)
CHOLESTATIC LIVER INJURY ( 2 FDA reports)
CHROMATOPSIA ( 2 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 2 FDA reports)
CHRONIC GASTROINTESTINAL BLEEDING ( 2 FDA reports)
CHRONIC HEPATIC FAILURE ( 2 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 2 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 2 FDA reports)
COAGULATION FACTOR VIII LEVEL DECREASED ( 2 FDA reports)
COLLATERAL CIRCULATION ( 2 FDA reports)
COLON CANCER RECURRENT ( 2 FDA reports)
COMA SCALE ABNORMAL ( 2 FDA reports)
COMPLEMENT FACTOR C3 INCREASED ( 2 FDA reports)
COMPLEMENT FACTOR DECREASED ( 2 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 2 FDA reports)
CONDUCTIVE DEAFNESS ( 2 FDA reports)
CONGENITAL ANAEMIA ( 2 FDA reports)
CONJUNCTIVAL OEDEMA ( 2 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 2 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 2 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 2 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 2 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 2 FDA reports)
CORNEAL ABRASION ( 2 FDA reports)
CORNEAL OEDEMA ( 2 FDA reports)
CORNEAL REFLEX DECREASED ( 2 FDA reports)
CORNEAL TRANSPLANT ( 2 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 2 FDA reports)
CSF PROTEIN ABNORMAL ( 2 FDA reports)
CSF WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
CYST RUPTURE ( 2 FDA reports)
CYSTITIS HAEMORRHAGIC ( 2 FDA reports)
CYSTITIS KLEBSIELLA ( 2 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 2 FDA reports)
DARK CIRCLES UNDER EYES ( 2 FDA reports)
DEATH OF RELATIVE ( 2 FDA reports)
DECREASED VIBRATORY SENSE ( 2 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 2 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 2 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 2 FDA reports)
DENTAL TREATMENT ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
DEVICE BATTERY ISSUE ( 2 FDA reports)
DEVICE EXPULSION ( 2 FDA reports)
DEVICE INEFFECTIVE ( 2 FDA reports)
DIABETIC GASTROPATHY ( 2 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 2 FDA reports)
DIABETIC VASCULAR DISORDER ( 2 FDA reports)
DIET REFUSAL ( 2 FDA reports)
DIEULAFOY'S VASCULAR MALFORMATION ( 2 FDA reports)
DISABLED RELATIVE ( 2 FDA reports)
DISTRACTIBILITY ( 2 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 2 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 2 FDA reports)
DRUG EFFECT PROLONGED ( 2 FDA reports)
DRUG SCREEN NEGATIVE ( 2 FDA reports)
DRUG THERAPY CHANGED ( 2 FDA reports)
DYSPAREUNIA ( 2 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 2 FDA reports)
EAR INJURY ( 2 FDA reports)
EATING DISORDER SYMPTOM ( 2 FDA reports)
ECLAMPSIA ( 2 FDA reports)
ECTOPIC PREGNANCY ( 2 FDA reports)
ECTROPION ( 2 FDA reports)
EJACULATION DELAYED ( 2 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 2 FDA reports)
ELECTROCUTION ( 2 FDA reports)
EMPYEMA ( 2 FDA reports)
ENCEPHALITIS TOXIC ( 2 FDA reports)
ENCOPRESIS ( 2 FDA reports)
ENDOCRINE DISORDER ( 2 FDA reports)
ENDOMETRIAL CANCER STAGE I ( 2 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 2 FDA reports)
ENDOVENOUS ABLATION ( 2 FDA reports)
ENTEROBACTER BACTERAEMIA ( 2 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 2 FDA reports)
ENTEROCOLITIS ( 2 FDA reports)
ENTEROCUTANEOUS FISTULA ( 2 FDA reports)
ENTHESOPATHY ( 2 FDA reports)
ENTROPION ( 2 FDA reports)
EOSINOPHIL COUNT DECREASED ( 2 FDA reports)
ERYTHRODERMIC PSORIASIS ( 2 FDA reports)
ESCHERICHIA BACTERAEMIA ( 2 FDA reports)
EUSTACHIAN TUBE DISORDER ( 2 FDA reports)
EX-TOBACCO USER ( 2 FDA reports)
EXTRAOCULAR MUSCLE DISORDER ( 2 FDA reports)
EYE EXCISION ( 2 FDA reports)
EYELIDS PRURITUS ( 2 FDA reports)
FACIAL NERVE DISORDER ( 2 FDA reports)
FAMILIAL TREMOR ( 2 FDA reports)
FEELING OF RELAXATION ( 2 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 2 FDA reports)
FEMORAL ARTERY DISSECTION ( 2 FDA reports)
FEMORAL BRUIT ( 2 FDA reports)
FEMORAL PULSE DECREASED ( 2 FDA reports)
FLASHBACK ( 2 FDA reports)
FOOD INTERACTION ( 2 FDA reports)
FROSTBITE ( 2 FDA reports)
FUNGUS STOOL IDENTIFIED ( 2 FDA reports)
FUSARIUM INFECTION ( 2 FDA reports)
FUSOBACTERIUM INFECTION ( 2 FDA reports)
GALLBLADDER CANCER ( 2 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 2 FDA reports)
GAMBLING ( 2 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 2 FDA reports)
GASTRIC MUCOSAL LESION ( 2 FDA reports)
GASTRIC NEOPLASM ( 2 FDA reports)
GASTRIC PH DECREASED ( 2 FDA reports)
GASTROENTERITIS BACTERIAL ( 2 FDA reports)
GASTROENTERITIS SALMONELLA ( 2 FDA reports)
GASTROINTESTINAL ANASTOMOTIC LEAK ( 2 FDA reports)
GASTROINTESTINAL CARCINOMA ( 2 FDA reports)
GASTROINTESTINAL INJURY ( 2 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 2 FDA reports)
GASTROINTESTINAL STENOSIS ( 2 FDA reports)
GASTROINTESTINAL SURGERY ( 2 FDA reports)
GAZE PALSY ( 2 FDA reports)
GENITAL ABSCESS ( 2 FDA reports)
GENITAL BURNING SENSATION ( 2 FDA reports)
GENITAL NEOPLASM MALIGNANT MALE ( 2 FDA reports)
GENITAL PRURITUS FEMALE ( 2 FDA reports)
GENITAL SWELLING ( 2 FDA reports)
GILBERT'S SYNDROME ( 2 FDA reports)
GINGIVAL BLISTER ( 2 FDA reports)
GINGIVAL DISCOLOURATION ( 2 FDA reports)
GLARE ( 2 FDA reports)
GLOBULINS DECREASED ( 2 FDA reports)
GLOMERULONEPHRITIS ( 2 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 2 FDA reports)
GLOSSOPHARYNGEAL NEURALGIA ( 2 FDA reports)
GLUCOSE TOLERANCE TEST ABNORMAL ( 2 FDA reports)
GRAM STAIN POSITIVE ( 2 FDA reports)
GRANULOCYTE COUNT DECREASED ( 2 FDA reports)
GRANULOCYTES ABNORMAL ( 2 FDA reports)
GROIN ABSCESS ( 2 FDA reports)
HAEMATOCRIT ( 2 FDA reports)
HAEMATOSPERMIA ( 2 FDA reports)
HAEMOPHILUS BACTERAEMIA ( 2 FDA reports)
HAEMORRHAGE CORONARY ARTERY ( 2 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 2 FDA reports)
HAEMORRHAGIC INFARCTION ( 2 FDA reports)
HALO VISION ( 2 FDA reports)
HAPTOGLOBIN ( 2 FDA reports)
HEAD AND NECK CANCER ( 2 FDA reports)
HEART VALVE STENOSIS ( 2 FDA reports)
HEPATIC VEIN OCCLUSION ( 2 FDA reports)
HEPATITIS B VIRUS TEST POSITIVE ( 2 FDA reports)
HEPATITIS CHOLESTATIC ( 2 FDA reports)
HEPATITIS D ( 2 FDA reports)
HERNIA HIATUS REPAIR ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN ABNORMAL ( 2 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 2 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 2 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 2 FDA reports)
HYPERPARATHYROIDISM PRIMARY ( 2 FDA reports)
HYPERREFLEXIA ( 2 FDA reports)
HYPERTENSIVE CARDIOMEGALY ( 2 FDA reports)
HYPOCHLORAEMIA ( 2 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 2 FDA reports)
HYPOMENORRHOEA ( 2 FDA reports)
HYPOPITUITARISM ( 2 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 2 FDA reports)
HYPOPLASTIC RIGHT HEART SYNDROME ( 2 FDA reports)
HYPOVITAMINOSIS ( 2 FDA reports)
IGA NEPHROPATHY ( 2 FDA reports)
ILIAC ARTERY THROMBOSIS ( 2 FDA reports)
ILLUSION ( 2 FDA reports)
IMPLANT SITE DISCHARGE ( 2 FDA reports)
IMPLANT SITE ERYTHEMA ( 2 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 2 FDA reports)
INCISION SITE INFECTION ( 2 FDA reports)
INCISION SITE PAIN ( 2 FDA reports)
INCLUSION BODY MYOSITIS ( 2 FDA reports)
INCREASED BRONCHIAL SECRETION ( 2 FDA reports)
INCREASED INSULIN REQUIREMENT ( 2 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 2 FDA reports)
INFECTED BITES ( 2 FDA reports)
INFECTED CYST ( 2 FDA reports)
INFUSION SITE ERYTHEMA ( 2 FDA reports)
INFUSION SITE SCAR ( 2 FDA reports)
INHALATION THERAPY ( 2 FDA reports)
INHIBITORY DRUG INTERACTION ( 2 FDA reports)
INJECTION SITE DISCHARGE ( 2 FDA reports)
INJECTION SITE PAPULE ( 2 FDA reports)
INJECTION SITE SCAR ( 2 FDA reports)
INSTILLATION SITE PAIN ( 2 FDA reports)
INSULIN RESISTANCE SYNDROME ( 2 FDA reports)
INSULIN-LIKE GROWTH FACTOR INCREASED ( 2 FDA reports)
INSULIN-REQUIRING TYPE II DIABETES MELLITUS ( 2 FDA reports)
INTERCEPTED MEDICATION ERROR ( 2 FDA reports)
INTESTINAL FISTULA ( 2 FDA reports)
INTRACRANIAL HAEMATOMA ( 2 FDA reports)
INTRADUCTAL PAPILLARY MUCINOUS NEOPLASM ( 2 FDA reports)
INTRADUCTAL PAPILLOMA OF BREAST ( 2 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 2 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 2 FDA reports)
IODINE UPTAKE DECREASED ( 2 FDA reports)
IRIDECTOMY ( 2 FDA reports)
JOB DISSATISFACTION ( 2 FDA reports)
JOINT DESTRUCTION ( 2 FDA reports)
KELOID SCAR ( 2 FDA reports)
KERATITIS ( 2 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 2 FDA reports)
LANGERHANS' CELL GRANULOMATOSIS ( 2 FDA reports)
LARGE CELL CARCINOMA OF THE RESPIRATORY TRACT STAGE UNSPECIFIED ( 2 FDA reports)
LARYNGEAL ULCERATION ( 2 FDA reports)
LARYNGEAL VENTRICLE PROLAPSE ( 2 FDA reports)
LEFT ATRIAL HYPERTROPHY ( 2 FDA reports)
LEIOMYOMA ( 2 FDA reports)
LEPROSY ( 2 FDA reports)
LEUKAEMIC INFILTRATION ( 2 FDA reports)
LEUKOENCEPHALOPATHY ( 2 FDA reports)
LICHEN SCLEROSUS ( 2 FDA reports)
LIMB CRUSHING INJURY ( 2 FDA reports)
LIMB REDUCTION DEFECT ( 2 FDA reports)
LIP DISCOLOURATION ( 2 FDA reports)
LIP DISORDER ( 2 FDA reports)
LIPODYSTROPHY ACQUIRED ( 2 FDA reports)
LIVER OPERATION ( 2 FDA reports)
LONG QT SYNDROME ( 2 FDA reports)
LOSS OF PROPRIOCEPTION ( 2 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 2 FDA reports)
LOW TENSION GLAUCOMA ( 2 FDA reports)
LOWER MOTOR NEURONE LESION ( 2 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 2 FDA reports)
LUNG ABSCESS ( 2 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 2 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE III ( 2 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 2 FDA reports)
LUNG TRANSPLANT REJECTION ( 2 FDA reports)
LYMPHANGITIS ( 2 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
MALARIA ( 2 FDA reports)
MALIGNANT NEOPLASM OF LACRIMAL DUCT ( 2 FDA reports)
MALIGNANT URINARY TRACT NEOPLASM ( 2 FDA reports)
MALOCCLUSION ( 2 FDA reports)
MASTITIS ( 2 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 2 FDA reports)
MEDICAL DIET ( 2 FDA reports)
MEGAKARYOCYTES ABNORMAL ( 2 FDA reports)
MENINGEAL DISORDER ( 2 FDA reports)
MENINGITIS ASEPTIC ( 2 FDA reports)
MENINGITIS HAEMOPHILUS ( 2 FDA reports)
MENINGITIS VIRAL ( 2 FDA reports)
MENTAL DISABILITY ( 2 FDA reports)
MENTAL RETARDATION ( 2 FDA reports)
MESENTERIC ARTERY STENOSIS ( 2 FDA reports)
METAMYELOCYTE COUNT ( 2 FDA reports)
METAMYELOCYTE COUNT INCREASED ( 2 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 2 FDA reports)
METASTASES TO ADRENALS ( 2 FDA reports)
METASTASES TO NASAL SINUSES ( 2 FDA reports)
METASTASES TO SMALL INTESTINE ( 2 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 2 FDA reports)
MONARTHRITIS ( 2 FDA reports)
MORGANELLA INFECTION ( 2 FDA reports)
MOTOR NEURONE DISEASE ( 2 FDA reports)
MUCOSAL DRYNESS ( 2 FDA reports)
MUIR-TORRE SYNDROME ( 2 FDA reports)
MULTIMORBIDITY ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 2 FDA reports)
MUMPS ( 2 FDA reports)
MUSCLE FIBROSIS ( 2 FDA reports)
MYCOPLASMA INFECTION ( 2 FDA reports)
MYCOTIC ALLERGY ( 2 FDA reports)
MYELOCYTE COUNT ( 2 FDA reports)
MYELOMALACIA ( 2 FDA reports)
MYODESOPSIA ( 2 FDA reports)
MYOFASCITIS ( 2 FDA reports)
MYOTONIC DYSTROPHY ( 2 FDA reports)
MYRINGOTOMY ( 2 FDA reports)
MYXOEDEMA ( 2 FDA reports)
NAIL INFECTION ( 2 FDA reports)
NARCISSISTIC PERSONALITY DISORDER ( 2 FDA reports)
NASAL CAVITY CANCER ( 2 FDA reports)
NASAL NEOPLASM ( 2 FDA reports)
NASAL SEPTAL OPERATION ( 2 FDA reports)
NASAL SEPTUM PERFORATION ( 2 FDA reports)
NASOPHARYNGEAL DISORDER ( 2 FDA reports)
NECROSIS ISCHAEMIC ( 2 FDA reports)
NECROTISING FASCIITIS ( 2 FDA reports)
NEEDLE ISSUE ( 2 FDA reports)
NEOLOGISM ( 2 FDA reports)
NERVOUS SYSTEM SURGERY ( 2 FDA reports)
NEUROTOXICITY ( 2 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 2 FDA reports)
NIPPLE DISORDER ( 2 FDA reports)
NODAL OSTEOARTHRITIS ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 2 FDA reports)
OEDEMA MUCOSAL ( 2 FDA reports)
OESOPHAGEAL DILATATION ( 2 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 2 FDA reports)
OESOPHAGEAL RUPTURE ( 2 FDA reports)
OESOPHAGITIS ULCERATIVE ( 2 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 2 FDA reports)
OLIGODIPSIA ( 2 FDA reports)
OPIATES ( 2 FDA reports)
ORAL BACTERIAL INFECTION ( 2 FDA reports)
ORAL LICHEN PLANUS ( 2 FDA reports)
ORAL MUCOSAL DISORDER ( 2 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 2 FDA reports)
OROANTRAL FISTULA ( 2 FDA reports)
ORTHOSTATIC HYPERTENSION ( 2 FDA reports)
OSTECTOMY ( 2 FDA reports)
OVERGROWTH BACTERIAL ( 2 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 2 FDA reports)
OXYGEN SATURATION ( 2 FDA reports)
PACEMAKER GENERATED RHYTHM ( 2 FDA reports)
PAIN MANAGEMENT ( 2 FDA reports)
PANCREAS LIPOMATOSIS ( 2 FDA reports)
PANCREATIC DUCT DILATATION ( 2 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 2 FDA reports)
PAPILLARY THYROID CANCER ( 2 FDA reports)
PAPULE ( 2 FDA reports)
PARACENTESIS ( 2 FDA reports)
PARATHYROID DISORDER ( 2 FDA reports)
PARATHYROIDECTOMY ( 2 FDA reports)
PARENT-CHILD PROBLEM ( 2 FDA reports)
PAROPHTHALMIA ( 2 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 2 FDA reports)
PCO2 ABNORMAL ( 2 FDA reports)
PELVIC DISCOMFORT ( 2 FDA reports)
PELVIC VENOUS THROMBOSIS ( 2 FDA reports)
PENILE DISCHARGE ( 2 FDA reports)
PENILE HAEMORRHAGE ( 2 FDA reports)
PENILE OEDEMA ( 2 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 2 FDA reports)
PEPTOSTREPTOCOCCUS INFECTION ( 2 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 2 FDA reports)
PERFORMANCE FEAR ( 2 FDA reports)
PERINEAL PAIN ( 2 FDA reports)
PERINEPHRIC COLLECTION ( 2 FDA reports)
PERIPHERAL NERVE INJURY ( 2 FDA reports)
PERIPHERAL PULSE DECREASED ( 2 FDA reports)
PERIRECTAL ABSCESS ( 2 FDA reports)
PERTUSSIS ( 2 FDA reports)
PHARYNGEAL ULCERATION ( 2 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 2 FDA reports)
PHYSIOTHERAPY ( 2 FDA reports)
PITUITARY TUMOUR ( 2 FDA reports)
PITYRIASIS ( 2 FDA reports)
PLASMA CELLS INCREASED ( 2 FDA reports)
PLATELET AGGREGATION ( 2 FDA reports)
PLEURAL HAEMORRHAGE ( 2 FDA reports)
PLEURAL NEOPLASM ( 2 FDA reports)
PLICA SYNDROME ( 2 FDA reports)
PNEUMONIA ASPERGILLUS ( 2 FDA reports)
PNEUMONIA ESCHERICHIA ( 2 FDA reports)
PNEUMONIA SALMONELLA ( 2 FDA reports)
PNEUMONIA VIRAL ( 2 FDA reports)
POLYCHROMASIA ( 2 FDA reports)
POLYCYTHAEMIA VERA ( 2 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 2 FDA reports)
POST-TRAUMATIC HEADACHE ( 2 FDA reports)
POSTOPERATIVE FEVER ( 2 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 2 FDA reports)
POSTOPERATIVE THORACIC PROCEDURE COMPLICATION ( 2 FDA reports)
POSTRENAL FAILURE ( 2 FDA reports)
POVERTY OF THOUGHT CONTENT ( 2 FDA reports)
PROCEDURAL SITE REACTION ( 2 FDA reports)
PROCTITIS ( 2 FDA reports)
PRODUCT FORMULATION ISSUE ( 2 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 2 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 2 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 2 FDA reports)
PRODUCT TAMPERING ( 2 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 2 FDA reports)
PROSTATIC OPERATION ( 2 FDA reports)
PROSTATIC PAIN ( 2 FDA reports)
PROSTATIC SPECIFIC ANTIGEN DECREASED ( 2 FDA reports)
PSEUDODEMENTIA ( 2 FDA reports)
PSEUDOENDOPHTHALMITIS ( 2 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 2 FDA reports)
PUBIC RAMI FRACTURE ( 2 FDA reports)
PUBIS FRACTURE ( 2 FDA reports)
PULMONARY VALVE DISEASE ( 2 FDA reports)
PULMONARY VALVE STENOSIS CONGENITAL ( 2 FDA reports)
PUPILLARY DISORDER ( 2 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 2 FDA reports)
QUADRUPLE VESSEL BYPASS GRAFT ( 2 FDA reports)
RADIATION OESOPHAGITIS ( 2 FDA reports)
RASH FOLLICULAR ( 2 FDA reports)
RECALL PHENOMENON ( 2 FDA reports)
RECTAL ABSCESS ( 2 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 2 FDA reports)
REFLEXES ABNORMAL ( 2 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 2 FDA reports)
REMOVAL OF TRANSPLANTED ORGAN ( 2 FDA reports)
RENAL BRUIT ( 2 FDA reports)
RENAL EMBOLISM ( 2 FDA reports)
RENAL INFARCT ( 2 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 2 FDA reports)
RENAL TUBULAR DISORDER ( 2 FDA reports)
RENAL VESSEL DISORDER ( 2 FDA reports)
REPETITIVE SPEECH ( 2 FDA reports)
RESPIRATORY ALKALOSIS ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 2 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 2 FDA reports)
RETINAL ARTERY EMBOLISM ( 2 FDA reports)
RETINAL EXUDATES ( 2 FDA reports)
RETINAL OEDEMA ( 2 FDA reports)
RETINAL SCAR ( 2 FDA reports)
RETINAL VASCULAR DISORDER ( 2 FDA reports)
RETINOPEXY ( 2 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 2 FDA reports)
REVISION OF INTERNAL FIXATION ( 2 FDA reports)
SACRAL PAIN ( 2 FDA reports)
SCLERAL DISORDER ( 2 FDA reports)
SCROTAL PAIN ( 2 FDA reports)
SECONDARY HYPERTENSION ( 2 FDA reports)
SELF MUTILATION ( 2 FDA reports)
SENILE DEMENTIA ( 2 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 2 FDA reports)
SINUS PERFORATION ( 2 FDA reports)
SKIN BACTERIAL INFECTION ( 2 FDA reports)
SKIN BLEEDING ( 2 FDA reports)
SKIN CHAPPED ( 2 FDA reports)
SKIN SENSITISATION ( 2 FDA reports)
SKIN SQUAMOUS CELL CARCINOMA SURGERY ( 2 FDA reports)
SMEAR CERVIX ABNORMAL ( 2 FDA reports)
SOCIAL PHOBIA ( 2 FDA reports)
SOLAR ELASTOSIS ( 2 FDA reports)
SPERM COUNT DECREASED ( 2 FDA reports)
SPINAL CORD OEDEMA ( 2 FDA reports)
SPINAL X-RAY ABNORMAL ( 2 FDA reports)
SPLENIC HAEMATOMA ( 2 FDA reports)
SPONDYLOLYSIS ( 2 FDA reports)
SPOUSAL ABUSE ( 2 FDA reports)
SPUTUM RETENTION ( 2 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 2 FDA reports)
STATUS EPILEPTICUS ( 2 FDA reports)
STEAL SYNDROME ( 2 FDA reports)
STOMACH MASS ( 2 FDA reports)
STRABISMUS ( 2 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 2 FDA reports)
STRESS ULCER ( 2 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 2 FDA reports)
SUPERIOR VENA CAVAL STENOSIS ( 2 FDA reports)
SURGICAL FAILURE ( 2 FDA reports)
SUTURE INSERTION ( 2 FDA reports)
SUTURE REMOVAL ( 2 FDA reports)
T-CELL LYMPHOMA STAGE IV ( 2 FDA reports)
TACHYPHRENIA ( 2 FDA reports)
TEETH BRITTLE ( 2 FDA reports)
TEMPERATURE REGULATION DISORDER ( 2 FDA reports)
THALAMIC INFARCTION ( 2 FDA reports)
THALAMUS HAEMORRHAGE ( 2 FDA reports)
THIRST DECREASED ( 2 FDA reports)
THORACIC OPERATION ( 2 FDA reports)
THYMOMA ( 2 FDA reports)
THYROID FIBROSIS ( 2 FDA reports)
THYROID GLAND CANCER ( 2 FDA reports)
THYROTOXIC CRISIS ( 2 FDA reports)
THYROXINE ABNORMAL ( 2 FDA reports)
TINEA CAPITIS ( 2 FDA reports)
TONGUE EXFOLIATION ( 2 FDA reports)
TONIC CONVULSION ( 2 FDA reports)
TOOTH MALFORMATION ( 2 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO DECREASED ( 2 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO INCREASED ( 2 FDA reports)
TRANCE ( 2 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 2 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 2 FDA reports)
TRAUMATIC FRACTURE ( 2 FDA reports)
TRAUMATIC HAEMATOMA ( 2 FDA reports)
TRAUMATIC HAEMORRHAGE ( 2 FDA reports)
TRICHIASIS ( 2 FDA reports)
TUNNEL VISION ( 2 FDA reports)
TYPE I HYPERSENSITIVITY ( 2 FDA reports)
ULCERATIVE KERATITIS ( 2 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 2 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 2 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 2 FDA reports)
UNINTENDED PREGNANCY ( 2 FDA reports)
UPPER RESPIRATORY FUNGAL INFECTION ( 2 FDA reports)
URETHRAL PAIN ( 2 FDA reports)
URETHRITIS ( 2 FDA reports)
URINARY BLADDER RUPTURE ( 2 FDA reports)
URINARY CASTS ( 2 FDA reports)
URINARY SEDIMENT PRESENT ( 2 FDA reports)
URINARY SYSTEM X-RAY ( 2 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 2 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
URINARY TRACT INFLAMMATION ( 2 FDA reports)
URINARY TRACT PAIN ( 2 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 2 FDA reports)
UTERINE CYST ( 2 FDA reports)
VACCINATION COMPLICATION ( 2 FDA reports)
VAGINAL BURNING SENSATION ( 2 FDA reports)
VAGINAL CANCER ( 2 FDA reports)
VAGINAL MYCOSIS ( 2 FDA reports)
VAGINAL SWELLING ( 2 FDA reports)
VAGINITIS BACTERIAL ( 2 FDA reports)
VASCULAR ACCESS COMPLICATION ( 2 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 2 FDA reports)
VASCULAR HEADACHE ( 2 FDA reports)
VASCULAR RESISTANCE SYSTEMIC DECREASED ( 2 FDA reports)
VASODILATION PROCEDURE ( 2 FDA reports)
VENTRICULAR DYSKINESIA ( 2 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 2 FDA reports)
VESSEL PUNCTURE SITE REACTION ( 2 FDA reports)
VICTIM OF ELDER ABUSE ( 2 FDA reports)
VIRAEMIA ( 2 FDA reports)
VIRAL MYOCARDITIS ( 2 FDA reports)
VIRAL SINUSITIS ( 2 FDA reports)
VISUAL ACUITY TESTS ABNORMAL ( 2 FDA reports)
VOCAL CORD INFLAMMATION ( 2 FDA reports)
VOLUME BLOOD DECREASED ( 2 FDA reports)
VON HIPPEL-LINDAU DISEASE ( 2 FDA reports)
VULVAL ULCERATION ( 2 FDA reports)
VULVITIS ( 2 FDA reports)
WHITE BLOOD CELL COUNT ( 2 FDA reports)
WISDOM TEETH REMOVAL ( 2 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 2 FDA reports)
XERODERMA ( 2 FDA reports)
RENAL ARTERY THROMBOSIS ( 1 FDA reports)
RENAL CELL CARCINOMA RECURRENT ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE II ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE III ( 1 FDA reports)
RENAL CYST HAEMORRHAGE ( 1 FDA reports)
RENAL HYPERTENSION ( 1 FDA reports)
RENAL ONCOCYTOMA ( 1 FDA reports)
RENAL PAPILLARY NECROSIS ( 1 FDA reports)
RENAL SCAN ABNORMAL ( 1 FDA reports)
RENAL SURGERY ( 1 FDA reports)
RENOVASCULAR HYPERTENSION ( 1 FDA reports)
REOCCLUSION ( 1 FDA reports)
RESPIRATORY DEPTH INCREASED ( 1 FDA reports)
RESPIRATORY FREMITUS ( 1 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 1 FDA reports)
RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
RESPIRATORY TRACT OEDEMA ( 1 FDA reports)
RESTING TREMOR ( 1 FDA reports)
RETINAL DEPOSITS ( 1 FDA reports)
RETINAL ISCHAEMIA ( 1 FDA reports)
RETINAL LASER COAGULATION ( 1 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 1 FDA reports)
RETINOSCHISIS ( 1 FDA reports)
RHEUMATIC FEVER ( 1 FDA reports)
RHEUMATOID FACTOR ( 1 FDA reports)
RIGHT ATRIAL PRESSURE INCREASED ( 1 FDA reports)
ROULEAUX FORMATION ( 1 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 1 FDA reports)
SACCADIC EYE MOVEMENT ( 1 FDA reports)
SALIVA ALTERED ( 1 FDA reports)
SALIVARY GLAND CANCER ( 1 FDA reports)
SALIVARY GLAND MASS ( 1 FDA reports)
SALPINGO-OOPHORECTOMY UNILATERAL ( 1 FDA reports)
SCLERAL DISCOLOURATION ( 1 FDA reports)
SCLERAL HYPERAEMIA ( 1 FDA reports)
SCLERITIS ( 1 FDA reports)
SCLERODACTYLIA ( 1 FDA reports)
SCROTAL ABSCESS ( 1 FDA reports)
SCROTAL HAEMATOCOELE ( 1 FDA reports)
SCROTAL INFECTION ( 1 FDA reports)
SEBACEOUS CYST EXCISION ( 1 FDA reports)
SEBORRHOEA ( 1 FDA reports)
SECONDARY PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SEMEN DISCOLOURATION ( 1 FDA reports)
SEMEN VISCOSITY ABNORMAL ( 1 FDA reports)
SENSATION OF BLOOD FLOW ( 1 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 1 FDA reports)
SEPTIC RASH ( 1 FDA reports)
SERRATIA TEST POSITIVE ( 1 FDA reports)
SERUM SEROTONIN INCREASED ( 1 FDA reports)
SHARED PSYCHOTIC DISORDER ( 1 FDA reports)
SHOCK HYPOGLYCAEMIC ( 1 FDA reports)
SHUNT OCCLUSION ( 1 FDA reports)
SHUNT THROMBOSIS ( 1 FDA reports)
SICKLE CELL TRAIT ( 1 FDA reports)
SIGHT DISABILITY ( 1 FDA reports)
SIMPLE MASTECTOMY ( 1 FDA reports)
SINUS PAIN ( 1 FDA reports)
SKIN CANDIDA ( 1 FDA reports)
SKIN DEPIGMENTATION ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN FRAGILITY ( 1 FDA reports)
SKIN HYPOPIGMENTATION ( 1 FDA reports)
SKIN MASS ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SLEEP PARALYSIS ( 1 FDA reports)
SLOW RESPONSE TO STIMULI ( 1 FDA reports)
SLOW SPEECH ( 1 FDA reports)
SMALL CELL LUNG CANCER EXTENSIVE STAGE ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
SMALL INTESTINAL PERFORATION ( 1 FDA reports)
SMALL INTESTINE CARCINOMA METASTATIC ( 1 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 1 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 1 FDA reports)
SOLILOQUY ( 1 FDA reports)
SPERMATOZOA PROGRESSIVE MOTILITY DECREASED ( 1 FDA reports)
SPINAL CORD DRAINAGE ( 1 FDA reports)
SPINAL CORPECTOMY ( 1 FDA reports)
SPINAL HAEMATOMA ( 1 FDA reports)
SPINAL INFECTION VIRAL ( 1 FDA reports)
SPINAL MENINGEAL CYST ( 1 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 1 FDA reports)
SPIROMETRY ABNORMAL ( 1 FDA reports)
SPLENIC CYST ( 1 FDA reports)
SPLENIC INJURY ( 1 FDA reports)
SPLENIC VEIN OCCLUSION ( 1 FDA reports)
SPLENIC VEIN THROMBOSIS ( 1 FDA reports)
SPLENITIS ( 1 FDA reports)
SPLENORENAL SHUNT ( 1 FDA reports)
SPLINTER ( 1 FDA reports)
SPONDYLOARTHROPATHY ( 1 FDA reports)
SPONTANEOUS HAEMATOMA ( 1 FDA reports)
SPUTUM ABNORMAL ( 1 FDA reports)
SPUTUM INCREASED ( 1 FDA reports)
STAPHYLOCOCCAL IMPETIGO ( 1 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 1 FDA reports)
STENOTROPHOMONAS INFECTION ( 1 FDA reports)
STENOTROPHOMONAS SEPSIS ( 1 FDA reports)
STEROID THERAPY ( 1 FDA reports)
STICKY SKIN ( 1 FDA reports)
STOOLS WATERY ( 1 FDA reports)
STREPTOCOCCAL SEROLOGY POSITIVE ( 1 FDA reports)
STRESS AT WORK ( 1 FDA reports)
STRUCK BY LIGHTNING ( 1 FDA reports)
STUBBORNNESS ( 1 FDA reports)
SUBCLAVIAN ARTERY THROMBOSIS ( 1 FDA reports)
SUBCLAVIAN STEAL SYNDROME ( 1 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 1 FDA reports)
SUBDURAL EMPYEMA ( 1 FDA reports)
SUBMANDIBULAR MASS ( 1 FDA reports)
SUPERFICIAL VEIN PROMINENCE ( 1 FDA reports)
SWEAT GLAND INFECTION ( 1 FDA reports)
SYMPTOM MASKED ( 1 FDA reports)
SYNOVECTOMY ( 1 FDA reports)
SYRINGOMYELIA ( 1 FDA reports)
T-CELL LYMPHOMA ( 1 FDA reports)
TALIPES ( 1 FDA reports)
TANDEM GAIT TEST ABNORMAL ( 1 FDA reports)
TARSAL TUNNEL SYNDROME ( 1 FDA reports)
TELANGIECTASIA ( 1 FDA reports)
TENDON CALCIFICATION ( 1 FDA reports)
THEFT ( 1 FDA reports)
THERAPEUTIC PROCEDURE ( 1 FDA reports)
THERAPY RESPONDER ( 1 FDA reports)
THERMOHYPOAESTHESIA ( 1 FDA reports)
THORACIC HAEMORRHAGE ( 1 FDA reports)
THORACIC OUTLET SYNDROME ( 1 FDA reports)
THORACOPLASTY ( 1 FDA reports)
THREAT OF REDUNDANCY ( 1 FDA reports)
THROMBECTOMY ( 1 FDA reports)
THROMBIN TIME PROLONGED ( 1 FDA reports)
THROMBOEMBOLECTOMY ( 1 FDA reports)
THROMBOEMBOLIC STROKE ( 1 FDA reports)
THROMBOTIC CEREBRAL INFARCTION ( 1 FDA reports)
THYROID CANCER METASTATIC ( 1 FDA reports)
THYROXINE FREE DECREASED ( 1 FDA reports)
TIC ( 1 FDA reports)
TILT TABLE TEST ( 1 FDA reports)
TONGUE HAEMATOMA ( 1 FDA reports)
TONGUE HAEMORRHAGE ( 1 FDA reports)
TONGUE NEOPLASM ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TONSIL CANCER ( 1 FDA reports)
TONSILLAR INFLAMMATION ( 1 FDA reports)
TOOTH INJURY ( 1 FDA reports)
TOXICOLOGIC TEST NORMAL ( 1 FDA reports)
TRABECULECTOMY ( 1 FDA reports)
TRACHEAL STENOSIS ( 1 FDA reports)
TRACHEITIS ( 1 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 1 FDA reports)
TRANSFERRIN SATURATION INCREASED ( 1 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 1 FDA reports)
TRAUMATIC ULCER ( 1 FDA reports)
TRI-IODOTHYRONINE FREE DECREASED ( 1 FDA reports)
TRICUSPID VALVE PROLAPSE ( 1 FDA reports)
TUMOUR EXCISION ( 1 FDA reports)
TUMOUR FLARE ( 1 FDA reports)
TUMOUR HAEMORRHAGE ( 1 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 1 FDA reports)
ULTRASOUND BREAST ABNORMAL ( 1 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 1 FDA reports)
UMBILICAL CORD AROUND NECK ( 1 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
UNDERWEIGHT ( 1 FDA reports)
UP AND DOWN PHENOMENON ( 1 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 1 FDA reports)
UPPER MOTOR NEURONE LESION ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
UPPER RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
URETERAL STENT REMOVAL ( 1 FDA reports)
URETERIC CANCER LOCAL ( 1 FDA reports)
URETEROSCOPY ( 1 FDA reports)
URETHRAL MEATOTOMY ( 1 FDA reports)
URETHRAL PROLAPSE ( 1 FDA reports)
URINARY CALCULUS REMOVAL ( 1 FDA reports)
URINARY CASTS PRESENT ( 1 FDA reports)
URINARY RETENTION POSTOPERATIVE ( 1 FDA reports)
URINE ALCOHOL TEST NEGATIVE ( 1 FDA reports)
URINE AMPHETAMINE POSITIVE ( 1 FDA reports)
URINE KETONE BODY ( 1 FDA reports)
URINE PROTEIN/CREATININE RATIO DECREASED ( 1 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 1 FDA reports)
URINE URIC ACID INCREASED ( 1 FDA reports)
URTICARIA CHRONIC ( 1 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 1 FDA reports)
UTERINE CERVIX ATROPHY ( 1 FDA reports)
UTERINE CONTRACTIONS ABNORMAL ( 1 FDA reports)
UTERINE INFECTION ( 1 FDA reports)
UTERINE LEIOMYOSARCOMA ( 1 FDA reports)
UTERINE NEOPLASM ( 1 FDA reports)
UTERINE PERFORATION ( 1 FDA reports)
VACCINATION FAILURE ( 1 FDA reports)
VAGINAL CANDIDIASIS ( 1 FDA reports)
VAGINAL INFLAMMATION ( 1 FDA reports)
VAGINAL MUCOSAL BLISTERING ( 1 FDA reports)
VAGUS NERVE DISORDER ( 1 FDA reports)
VARICELLA ( 1 FDA reports)
VARICOCELE ( 1 FDA reports)
VASCULAR ANOMALY ( 1 FDA reports)
VASCULAR BYPASS DYSFUNCTION ( 1 FDA reports)
VASCULAR ENCEPHALOPATHY ( 1 FDA reports)
VASCULAR OPERATION ( 1 FDA reports)
VASCULAR SKIN DISORDER ( 1 FDA reports)
VASCULITIC RASH ( 1 FDA reports)
VASCULITIS GASTROINTESTINAL ( 1 FDA reports)
VENA CAVA THROMBOSIS ( 1 FDA reports)
VENIPUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
VENOUS INJURY ( 1 FDA reports)
VENOUS PRESSURE INCREASED ( 1 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 1 FDA reports)
VENOUS RECANALISATION ( 1 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 1 FDA reports)
VENTRICULAR HYPERKINESIA ( 1 FDA reports)
VENTRICULAR INTERNAL DIAMETER ABNORMAL ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT REPAIR ( 1 FDA reports)
VERBAL ABUSE ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
VESTIBULAR NEURONITIS ( 1 FDA reports)
VICTIM OF ABUSE ( 1 FDA reports)
VIRAL DIARRHOEA ( 1 FDA reports)
VIRAL PERICARDITIS ( 1 FDA reports)
VIRAL RASH ( 1 FDA reports)
VIRUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
VISUAL PATHWAY DISORDER ( 1 FDA reports)
VITAL CAPACITY DECREASED ( 1 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 1 FDA reports)
VITAMIN D INCREASED ( 1 FDA reports)
VOCAL CORD PARESIS ( 1 FDA reports)
VOLUME BLOOD INCREASED ( 1 FDA reports)
VON WILLEBRAND'S DISEASE ( 1 FDA reports)
VULVAL ABSCESS ( 1 FDA reports)
VULVAL DISORDER ( 1 FDA reports)
VULVAL HAEMORRHAGE ( 1 FDA reports)
VULVAL OEDEMA ( 1 FDA reports)
VULVAR DYSPLASIA ( 1 FDA reports)
WALLENBERG SYNDROME ( 1 FDA reports)
WANDERING PACEMAKER ( 1 FDA reports)
WEIGHT ( 1 FDA reports)
WHIPLASH INJURY ( 1 FDA reports)
WHITE BLOOD CELLS URINE ( 1 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 1 FDA reports)
WOUND INFECTION FUNGAL ( 1 FDA reports)
WOUND TREATMENT ( 1 FDA reports)
WRIST DEFORMITY ( 1 FDA reports)
X-RAY LIMB ABNORMAL ( 1 FDA reports)
X-RAY OF PELVIS AND HIP ABNORMAL ( 1 FDA reports)
X-RAY WITH CONTRAST UPPER GASTROINTESTINAL TRACT ( 1 FDA reports)
ABDOMINAL BRUIT ( 1 FDA reports)
ABDOMINAL CAVITY DRAINAGE ( 1 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 1 FDA reports)
ABDOMINAL HERNIA REPAIR ( 1 FDA reports)
ABDOMINAL PANNICULECTOMY ( 1 FDA reports)
ABDOMINAL WALL NEOPLASM ( 1 FDA reports)
ABDOMINOPLASTY ( 1 FDA reports)
ABNORMAL CHEST SOUND ( 1 FDA reports)
ABORTION ( 1 FDA reports)
ABORTION SPONTANEOUS COMPLETE ( 1 FDA reports)
ABSCESS RUPTURE ( 1 FDA reports)
ABSCESS SOFT TISSUE ( 1 FDA reports)
ABSTAINS FROM ALCOHOL ( 1 FDA reports)
ACCESSORY MUSCLE ( 1 FDA reports)
ACCIDENTAL POISONING ( 1 FDA reports)
ACHLORHYDRIA ( 1 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 1 FDA reports)
ACINETOBACTER INFECTION ( 1 FDA reports)
ACOUSTIC NEURITIS ( 1 FDA reports)
ACQUIRED CARDIAC SEPTAL DEFECT ( 1 FDA reports)
ACQUIRED HAEMOPHILIA ( 1 FDA reports)
ACROMEGALY ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE MONOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 1 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 1 FDA reports)
ADENOIDAL DISORDER ( 1 FDA reports)
ADENOIDITIS ( 1 FDA reports)
ADENOVIRAL CONJUNCTIVITIS ( 1 FDA reports)
ADNEXA UTERI MASS ( 1 FDA reports)
ADRENALECTOMY ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY CHRONIC ( 1 FDA reports)
ADRENOMEGALY ( 1 FDA reports)
AEROPHAGIA ( 1 FDA reports)
AIR EMBOLISM ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ( 1 FDA reports)
ALBUMIN URINE ABSENT ( 1 FDA reports)
ALBUMIN URINE PRESENT ( 1 FDA reports)
ALBUMINURIA ( 1 FDA reports)
ALCOHOL DETOXIFICATION ( 1 FDA reports)
ALCOHOLIC PANCREATITIS ( 1 FDA reports)
ALKALOSIS HYPOCHLORAEMIC ( 1 FDA reports)
ALLERGY TO ANIMAL ( 1 FDA reports)
ALLERGY TO ARTHROPOD BITE ( 1 FDA reports)
ALPHA-1 ANTI-TRYPSIN ABNORMAL ( 1 FDA reports)
ALVEOLAR PROTEINOSIS ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
AMAUROSIS ( 1 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 1 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 1 FDA reports)
ANAL ABSCESS ( 1 FDA reports)
ANAL DISCOMFORT ( 1 FDA reports)
ANAL POLYP ( 1 FDA reports)
ANALGESIA ( 1 FDA reports)
ANASTOMOTIC COMPLICATION ( 1 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 1 FDA reports)
ANASTOMOTIC LEAK ( 1 FDA reports)
ANASTOMOTIC ULCER HAEMORRHAGE ( 1 FDA reports)
ANEURYSM REPAIR ( 1 FDA reports)
ANION GAP DECREASED ( 1 FDA reports)
ANKLE OPERATION ( 1 FDA reports)
ANOMALOUS PULMONARY VENOUS CONNECTION ( 1 FDA reports)
ANTERIOR DISPLACED ANUS ( 1 FDA reports)
ANTICHOLINERGIC SYNDROME ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABNORMAL ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY INCREASED ( 1 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES ( 1 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANXIETY DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
ANXIETY POSTOPERATIVE ( 1 FDA reports)
AORTIC ANEURYSM REPAIR ( 1 FDA reports)
AORTIC INJURY ( 1 FDA reports)
AORTIC RUPTURE ( 1 FDA reports)
AORTIC SURGERY ( 1 FDA reports)
AORTITIS ( 1 FDA reports)
AORTOGRAM ABNORMAL ( 1 FDA reports)
APICECTOMY ( 1 FDA reports)
APLASIA ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPENDICEAL MUCOCOELE ( 1 FDA reports)
APPLICATION SITE ANAESTHESIA ( 1 FDA reports)
APPLICATION SITE DISCOMFORT ( 1 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 1 FDA reports)
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA ( 1 FDA reports)
ARTERIAL BRUIT ( 1 FDA reports)
ARTERIAL GRAFT ( 1 FDA reports)
ARTERIAL RESTENOSIS ( 1 FDA reports)
ARTERIOGRAM CAROTID ABNORMAL ( 1 FDA reports)
ARTERIOPATHIC DISEASE ( 1 FDA reports)
ARTHRODESIS ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ASPIRATION JOINT ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ABNORMAL ( 1 FDA reports)
ASPIRATION TRACHEAL ( 1 FDA reports)
ASTROCYTOMA ( 1 FDA reports)
ATHEROSCLEROSIS PROPHYLAXIS ( 1 FDA reports)
ATRIAL SEPTAL DEFECT REPAIR ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 1 FDA reports)
ATROPHY OF GLOBE ( 1 FDA reports)
AURA ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
AUTONOMIC FAILURE SYNDROME ( 1 FDA reports)
AVERSION ( 1 FDA reports)
B PRECURSOR TYPE ACUTE LEUKAEMIA ( 1 FDA reports)
B-CELL TYPE ACUTE LEUKAEMIA ( 1 FDA reports)
BABINSKI REFLEX TEST ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACILLUS TEST POSITIVE ( 1 FDA reports)
BACTERIAL ANTIGEN POSITIVE ( 1 FDA reports)
BACTEROIDES BACTERAEMIA ( 1 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
BARBITURATES POSITIVE ( 1 FDA reports)
BARTHOLIN'S CYST ( 1 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 1 FDA reports)
BASAL GANGLIA INFARCTION ( 1 FDA reports)
BASE EXCESS POSITIVE ( 1 FDA reports)
BENIGN COLONIC NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF SKIN ( 1 FDA reports)
BENIGN OVARIAN TUMOUR ( 1 FDA reports)
BENIGN PANCREATIC NEOPLASM ( 1 FDA reports)
BENIGN SALIVARY GLAND NEOPLASM ( 1 FDA reports)
BENIGN UTERINE NEOPLASM ( 1 FDA reports)
BEREAVEMENT REACTION ( 1 FDA reports)
BILIARY CANCER METASTATIC ( 1 FDA reports)
BILIARY CYST ( 1 FDA reports)
BILIARY NEOPLASM ( 1 FDA reports)
BIOPSY ABDOMINAL WALL ABNORMAL ( 1 FDA reports)
BIOPSY CARTILAGE ABNORMAL ( 1 FDA reports)
BIOPSY CERVIX ( 1 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 1 FDA reports)
BIOPSY LUNG ( 1 FDA reports)
BIOPSY STOMACH ABNORMAL ( 1 FDA reports)
BIRTH MARK ( 1 FDA reports)
BISEXUALITY ( 1 FDA reports)
BITE ( 1 FDA reports)
BLADDER CANCER STAGE IV ( 1 FDA reports)
BLADDER NECK OBSTRUCTION ( 1 FDA reports)
BLADDER NECK SUSPENSION ( 1 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 1 FDA reports)
BLADDER PAPILLOMA ( 1 FDA reports)
BLADDER REPAIR ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
BLEEDING TIME ABNORMAL ( 1 FDA reports)
BLEPHARAL PIGMENTATION ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 1 FDA reports)
BLOOD AMYLASE ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE DECREASED ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CARBON MONOXIDE INCREASED ( 1 FDA reports)
BLOOD CHLORIDE ABNORMAL ( 1 FDA reports)
BLOOD CHROMOGRANIN A ( 1 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 1 FDA reports)
BLOOD CORTISOL DECREASED ( 1 FDA reports)
BLOOD CREATININE ( 1 FDA reports)
BLOOD ERYTHROPOIETIN DECREASED ( 1 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 1 FDA reports)
BLOOD GLUCOSE ( 1 FDA reports)
BLOOD HOMOCYSTEINE ABNORMAL ( 1 FDA reports)
BLOOD INSULIN INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 1 FDA reports)
BLOOD PARATHYROID HORMONE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC ( 1 FDA reports)
BLOOD PRESSURE MANAGEMENT ( 1 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO DECREASED ( 1 FDA reports)
BLOODY PERITONEAL EFFLUENT ( 1 FDA reports)
BODY HEIGHT ABNORMAL ( 1 FDA reports)
BODY HEIGHT INCREASED ( 1 FDA reports)
BODY MASS INDEX INCREASED ( 1 FDA reports)
BODY TEMPERATURE ( 1 FDA reports)
BONE CYST ( 1 FDA reports)
BONE DENSITY ABNORMAL ( 1 FDA reports)
BONE DENSITY INCREASED ( 1 FDA reports)
BONE MARROW DONATION ( 1 FDA reports)
BONE MARROW GRANULOMA ( 1 FDA reports)
BONE NEOPLASM ( 1 FDA reports)
BONE SWELLING ( 1 FDA reports)
BORDERLINE LEPROSY ( 1 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 1 FDA reports)
BOVINE TUBERCULOSIS ( 1 FDA reports)
BOWEL PREPARATION ( 1 FDA reports)
BRAIN CANCER METASTATIC ( 1 FDA reports)
BRAIN CONTUSION ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE ( 1 FDA reports)
BRAIN STEM ISCHAEMIA ( 1 FDA reports)
BREAST CANCER MALE ( 1 FDA reports)
BREAST CANCER STAGE III ( 1 FDA reports)
BREAST CANCER STAGE IV ( 1 FDA reports)
BREAST CYST EXCISION ( 1 FDA reports)
BREAST DISCOMFORT ( 1 FDA reports)
BREAST INFLAMMATION ( 1 FDA reports)
BREAST NECROSIS ( 1 FDA reports)
BREAST NEOPLASM ( 1 FDA reports)
BREAST PROSTHESIS USER ( 1 FDA reports)
BREATH ALCOHOL TEST POSITIVE ( 1 FDA reports)
BREATH SOUNDS ABSENT ( 1 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 1 FDA reports)
BREECH PRESENTATION ( 1 FDA reports)
BRONCHIAL HAEMORRHAGE ( 1 FDA reports)
BRONCHIAL HYPERACTIVITY ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHIAL OEDEMA ( 1 FDA reports)
BRONCHIOLITIS ( 1 FDA reports)
BRONCHITIS BACTERIAL ( 1 FDA reports)
BRONCHOGENIC CYST ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
BRONCHOSCOPY ( 1 FDA reports)
BRONCHOSPASM PARADOXICAL ( 1 FDA reports)
BRUNNER'S GLAND HYPERPLASIA ( 1 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 1 FDA reports)
BULLOUS IMPETIGO ( 1 FDA reports)
BULLOUS LUNG DISEASE ( 1 FDA reports)
BURNING MOUTH SYNDROME ( 1 FDA reports)
BURNING SENSATION MUCOSAL ( 1 FDA reports)
BURNS FIRST DEGREE ( 1 FDA reports)
BURNS THIRD DEGREE ( 1 FDA reports)
BUTTERFLY RASH ( 1 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 1 FDA reports)
CALCULUS PROSTATIC ( 1 FDA reports)
CAMPTOCORMIA ( 1 FDA reports)
CANDIDA PNEUMONIA ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 1 FDA reports)
CANDIDA TEST POSITIVE ( 1 FDA reports)
CAPILLARY FRAGILITY ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 15-3 INCREASED ( 1 FDA reports)
CARCINOID SYNDROME ( 1 FDA reports)
CARCINOID TUMOUR OF THE GASTROINTESTINAL TRACT ( 1 FDA reports)
CARDIAC ASSISTANCE DEVICE USER ( 1 FDA reports)
CARDIAC ELECTROPHYSIOLOGIC STUDY ABNORMAL ( 1 FDA reports)
CARDIAC FAILURE HIGH OUTPUT ( 1 FDA reports)
CARDIAC INDEX DECREASED ( 1 FDA reports)
CARDIAC MONITORING ( 1 FDA reports)
CARDIAC PSEUDOANEURYSM ( 1 FDA reports)
CARDIAC STRESS TEST ( 1 FDA reports)
CARDIAC VALVE RUPTURE ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ( 1 FDA reports)
CARDIOSPASM ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CARDITIS ( 1 FDA reports)
CAROTID ANGIOPLASTY ( 1 FDA reports)
CAROTID ARTERY BYPASS ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CARTILAGE NEOPLASM ( 1 FDA reports)
CATARACT CORTICAL ( 1 FDA reports)
CATHETER SITE BRUISE ( 1 FDA reports)
CATHETER SITE CELLULITIS ( 1 FDA reports)
CATHETER SITE OEDEMA ( 1 FDA reports)
CAUSTIC INJURY ( 1 FDA reports)
CAUTERY TO NOSE ( 1 FDA reports)
CELLULITIS PASTEURELLA ( 1 FDA reports)
CENTRAL LINE INFECTION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 1 FDA reports)
CENTRAL VENOUS PRESSURE DECREASED ( 1 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 1 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 1 FDA reports)
CEREBRAL CALCIFICATION ( 1 FDA reports)
CEREBRAL FUNGAL INFECTION ( 1 FDA reports)
CEREBRAL HYPOPERFUSION ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT PROPHYLAXIS ( 1 FDA reports)
CERVICAL NEURITIS ( 1 FDA reports)
CERVICAL SPINE FLATTENING ( 1 FDA reports)
CERVIX CANCER METASTATIC ( 1 FDA reports)
CERVIX CARCINOMA RECURRENT ( 1 FDA reports)
CERVIX DISORDER ( 1 FDA reports)
CERVIX OPERATION ( 1 FDA reports)
CHANGE IN SUSTAINED ATTENTION ( 1 FDA reports)
CHEMICAL EYE INJURY ( 1 FDA reports)
CHILD NEGLECT ( 1 FDA reports)
CHLOROPSIA ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
CHOLELITHOTOMY ( 1 FDA reports)
CHONDRITIS ( 1 FDA reports)
CHONDROCALCINOSIS ( 1 FDA reports)
CHORDAE TENDINAE RUPTURE ( 1 FDA reports)
CHORIORETINAL DISORDER ( 1 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 1 FDA reports)
CHROMOSOME ABNORMALITY ( 1 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA TRANSFORMATION ( 1 FDA reports)
CHRONIC RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
CHRONOTROPIC INCOMPETENCE ( 1 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 1 FDA reports)
CLOSED HEAD INJURY ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 1 FDA reports)
COAGULATION FACTOR XI LEVEL DECREASED ( 1 FDA reports)
COELIAC ARTERY OCCLUSION ( 1 FDA reports)
COELIAC ARTERY STENOSIS ( 1 FDA reports)
COGWHEEL RIGIDITY ( 1 FDA reports)
COLON CANCER STAGE II ( 1 FDA reports)
COLON FISTULA REPAIR ( 1 FDA reports)
COLONIC HAEMATOMA ( 1 FDA reports)
COLONIC PERFORATION POSTOPERATIVE ( 1 FDA reports)
COLOUR BLINDNESS ( 1 FDA reports)
COLOUR VISION TESTS ABNORMAL ( 1 FDA reports)
COMPLEMENT FACTOR ABNORMAL ( 1 FDA reports)
COMPLEMENT FACTOR C4 DECREASED ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
COMPRESSION STOCKINGS APPLICATION ( 1 FDA reports)
COMPUTERISED TOMOGRAM NORMAL ( 1 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 1 FDA reports)
CONGENITAL AORTIC ANOMALY ( 1 FDA reports)
CONGENITAL AORTIC ATRESIA ( 1 FDA reports)
CONGENITAL ATRIAL SEPTAL DEFECT ( 1 FDA reports)
CONGENITAL ECTOPIC BLADDER ( 1 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 1 FDA reports)
CONGENITAL NYSTAGMUS ( 1 FDA reports)
CONGENITAL PULMONARY ARTERY ANOMALY ( 1 FDA reports)
CONGENITAL PULMONARY VALVE ATRESIA ( 1 FDA reports)
CONGENITAL URETERIC ANOMALY ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONJUNCTIVITIS VIRAL ( 1 FDA reports)
CONSTRICTED AFFECT ( 1 FDA reports)
CONTACT LENS INTOLERANCE ( 1 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 1 FDA reports)
COOMBS TEST POSITIVE ( 1 FDA reports)
COR PULMONALE CHRONIC ( 1 FDA reports)
CORNEAL BLEEDING ( 1 FDA reports)
CORNEAL DEGENERATION ( 1 FDA reports)
CORNEAL EROSION ( 1 FDA reports)
CORNEAL THINNING ( 1 FDA reports)
CORONARY ARTERY REOCCLUSION ( 1 FDA reports)
CORONARY BYPASS THROMBOSIS ( 1 FDA reports)
CORONARY REVASCULARISATION ( 1 FDA reports)
CORRECTIVE LENS USER ( 1 FDA reports)
CRANIOCEREBRAL INJURY ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
CROUP NONINFECTIOUS ( 1 FDA reports)
CRUSH INJURY ( 1 FDA reports)
CRYOTHERAPY ( 1 FDA reports)
CRYPTOCOCCOSIS ( 1 FDA reports)
CSF CELL COUNT ABNORMAL ( 1 FDA reports)
CSF CELL COUNT INCREASED ( 1 FDA reports)
CYSTITIS ESCHERICHIA ( 1 FDA reports)
CYSTITIS RADIATION ( 1 FDA reports)
CYSTOSCOPY ( 1 FDA reports)
CYSTOSTOMY ( 1 FDA reports)
CYTOKINE RELEASE SYNDROME ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS TEST ( 1 FDA reports)
DEATH OF SPOUSE ( 1 FDA reports)
DEFICIENCY ANAEMIA ( 1 FDA reports)
DENERVATION ATROPHY ( 1 FDA reports)
DEPENDENCE ON RESPIRATOR ( 1 FDA reports)
DEPENDENT RUBOR ( 1 FDA reports)
DEPERSONALISATION ( 1 FDA reports)
DEPRESSION POSTOPERATIVE ( 1 FDA reports)
DEREALISATION ( 1 FDA reports)
DERMABRASION ( 1 FDA reports)
DERMATILLOMANIA ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DEVICE ADHESION ISSUE ( 1 FDA reports)
DEVICE COMPONENT ISSUE ( 1 FDA reports)
DEVICE CONNECTION ISSUE ( 1 FDA reports)
DEVICE DAMAGE ( 1 FDA reports)
DEVICE INTERACTION ( 1 FDA reports)
DEVICE LEAD DAMAGE ( 1 FDA reports)
DEVICE MIGRATION ( 1 FDA reports)
DEVICE MISUSE ( 1 FDA reports)
DEVICE PACING ISSUE ( 1 FDA reports)
DIABETES MELLITUS MALNUTRITION-RELATED ( 1 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 1 FDA reports)
DIABETIC ENTEROPATHY ( 1 FDA reports)
DIABETIC MICROANGIOPATHY ( 1 FDA reports)
DIALYSIS DEVICE COMPLICATION ( 1 FDA reports)
DIALYSIS DEVICE INSERTION ( 1 FDA reports)
DIAPHRAGMATIC RUPTURE ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE IV ( 1 FDA reports)
DIPHTHERIA ( 1 FDA reports)
DIRECT INFECTION TRANSMISSION ( 1 FDA reports)
DIRECTIONAL DOPPLER FLOW TESTS ABNORMAL ( 1 FDA reports)
DISBACTERIOSIS ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 1 FDA reports)
DISLOCATION OF VERTEBRA ( 1 FDA reports)
DISSOCIATIVE FUGUE ( 1 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DIVERTICULUM DUODENAL ( 1 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 1 FDA reports)
DIVORCED ( 1 FDA reports)
DRUG ADDICT ( 1 FDA reports)
DRUG CLEARANCE DECREASED ( 1 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 1 FDA reports)
DRUG IMPLANTATION ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG LABEL CONFUSION ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 1 FDA reports)
DRUG TOLERANCE DECREASED ( 1 FDA reports)
DRUG USE FOR UNKNOWN INDICATION ( 1 FDA reports)
DRUG WITHDRAWAL HEADACHE ( 1 FDA reports)
DUODENAL NEOPLASM ( 1 FDA reports)
DUODENAL PERFORATION ( 1 FDA reports)
DUODENAL POLYP ( 1 FDA reports)
DUODENAL ULCER, OBSTRUCTIVE ( 1 FDA reports)
DYSCALCULIA ( 1 FDA reports)
DYSKINESIA OESOPHAGEAL ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
EAR OPERATION ( 1 FDA reports)
EARLY MORNING AWAKENING ( 1 FDA reports)
ELBOW DEFORMITY ( 1 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE BIPHASIC ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
ELECTROLYTE DEPLETION ( 1 FDA reports)
ELECTROPHORESIS PROTEIN ABNORMAL ( 1 FDA reports)
ELLIPTOCYTOSIS ( 1 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 1 FDA reports)
EMBOLISM VENOUS ( 1 FDA reports)
EMPHYSEMATOUS CYSTITIS ( 1 FDA reports)
EMPTY SELLA SYNDROME ( 1 FDA reports)
ENCHONDROMA ( 1 FDA reports)
ENDOCARDIAL DISEASE ( 1 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 1 FDA reports)
ENDOMETRIAL CANCER METASTATIC ( 1 FDA reports)
ENDOMETRIAL DISORDER ( 1 FDA reports)
ENDOMETRIAL NEOPLASM ( 1 FDA reports)
ENDOMETRITIS DECIDUAL ( 1 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ABNORMAL ( 1 FDA reports)
ENDOSCOPY ABNORMAL ( 1 FDA reports)
ENDOSCOPY GASTROINTESTINAL ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 1 FDA reports)
ENOPHTHALMOS ( 1 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
EPIDERMAL GROWTH FACTOR RECEPTOR DECREASED ( 1 FDA reports)
EPINEPHRINE INCREASED ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 1 FDA reports)
ERYTHEMA INFECTIOSUM ( 1 FDA reports)
ERYTHROPSIA ( 1 FDA reports)
ESCHAR ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
EWING'S SARCOMA ( 1 FDA reports)
EXECUTIVE DYSFUNCTION ( 1 FDA reports)
EXOMPHALOS ( 1 FDA reports)
EXPLORATIVE LAPAROTOMY ( 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)
EYE INFECTION FUNGAL ( 1 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
EYEBALL RUPTURE ( 1 FDA reports)
EYELID BLEEDING ( 1 FDA reports)
EYELID CYST ( 1 FDA reports)
EYELID IRRITATION ( 1 FDA reports)
EYELID OPERATION ( 1 FDA reports)
EYES SUNKEN ( 1 FDA reports)
FACE CRUSHING ( 1 FDA reports)
FACTOR V LEIDEN MUTATION ( 1 FDA reports)
FALLOPIAN TUBE CYST ( 1 FDA reports)
FALSE NEGATIVE INVESTIGATION RESULT ( 1 FDA reports)
FALSE POSITIVE INVESTIGATION RESULT ( 1 FDA reports)
FANCONI SYNDROME ( 1 FDA reports)
FANCONI SYNDROME ACQUIRED ( 1 FDA reports)
FAT ATROPHY ( 1 FDA reports)
FAT EMBOLISM ( 1 FDA reports)
FAT NECROSIS ( 1 FDA reports)
FIBRIN D DIMER ( 1 FDA reports)
FIBROADENOMA OF BREAST ( 1 FDA reports)
FIBROSARCOMA ( 1 FDA reports)
FIXED ERUPTION ( 1 FDA reports)
FLUID IMBALANCE ( 1 FDA reports)
FLUORIDE INCREASED ( 1 FDA reports)
FLUOROSIS ( 1 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 1 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 1 FDA reports)
FOREIGN BODY IN EYE ( 1 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 1 FDA reports)
FREE THYROXINE INDEX DECREASED ( 1 FDA reports)
FREE THYROXINE INDEX INCREASED ( 1 FDA reports)
FRONTOTEMPORAL DEMENTIA ( 1 FDA reports)
FUCHS' SYNDROME ( 1 FDA reports)
FUNGAL PERITONITIS ( 1 FDA reports)
FUNGAL TEST POSITIVE ( 1 FDA reports)
GALLBLADDER PERFORATION ( 1 FDA reports)
GALLSTONE ILEUS ( 1 FDA reports)
GASTRECTOMY ( 1 FDA reports)
GASTRIC HYPOMOTILITY ( 1 FDA reports)
GASTRIC ULCER PERFORATION ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROENTERITIS PROTEUS ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA HAEMORRHAGIC ( 1 FDA reports)
GASTROINTESTINAL BACTERIAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 1 FDA reports)
GASTROINTESTINAL FISTULA ( 1 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 1 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 1 FDA reports)
GASTROOESOPHAGEAL SPHINCTER INSUFFICIENCY ( 1 FDA reports)
GASTROOESOPHAGITIS ( 1 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
GENITAL PRURITUS MALE ( 1 FDA reports)
GENITALIA EXTERNAL AMBIGUOUS ( 1 FDA reports)
GENITALIA EXTERNAL PAINFUL ( 1 FDA reports)
GESTATIONAL HYPERTENSION ( 1 FDA reports)
GINGIVAL INJURY ( 1 FDA reports)
GINGIVAL OPERATION ( 1 FDA reports)
GLABELLAR REFLEX ABNORMAL ( 1 FDA reports)
GLIOBLASTOMA ( 1 FDA reports)
GLIOMA ( 1 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 1 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 1 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 1 FDA reports)
GLUCAGON SECRETION DISORDER ( 1 FDA reports)
GLUCOSE TOLERANCE INCREASED ( 1 FDA reports)
GLUCOSE URINE ( 1 FDA reports)
GRAFT HAEMORRHAGE ( 1 FDA reports)
GRAFT LOSS ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
HAEMANGIOMA OF SKIN ( 1 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 1 FDA reports)
HAEMATOMA EVACUATION ( 1 FDA reports)
HAEMOGLOBIN URINE ( 1 FDA reports)
HAEMOLYTIC TRANSFUSION REACTION ( 1 FDA reports)
HAEMORRHAGE SUBEPIDERMAL ( 1 FDA reports)
HALITOSIS ( 1 FDA reports)
HALLUCINATION, OLFACTORY ( 1 FDA reports)
HEAD BANGING ( 1 FDA reports)
HEARING AID USER ( 1 FDA reports)
HEART VALVE OPERATION ( 1 FDA reports)
HEMIPLEGIC MIGRAINE ( 1 FDA reports)
HEPATIC ARTERY EMBOLISM ( 1 FDA reports)
HEPATIC CANCER STAGE IV ( 1 FDA reports)
HEPATIC ENZYME ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT RECURRENT ( 1 FDA reports)
HEPATITIS A ( 1 FDA reports)
HEPATITIS A POSITIVE ( 1 FDA reports)
HEPATITIS ALCOHOLIC ( 1 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS C VIRUS TEST POSITIVE ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HEREDITARY HAEMOCHROMATOSIS ( 1 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 1 FDA reports)
HERPES ZOSTER DISSEMINATED ( 1 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 1 FDA reports)
HIGH FREQUENCY ABLATION ( 1 FDA reports)
HIGH TURNOVER OSTEOPATHY ( 1 FDA reports)
HIP DEFORMITY ( 1 FDA reports)
HIPPOCAMPAL SCLEROSIS ( 1 FDA reports)
HIRSUTISM ( 1 FDA reports)
HISTAMINE LEVEL INCREASED ( 1 FDA reports)
HISTONE ANTIBODY POSITIVE ( 1 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HOLMES-ADIE PUPIL ( 1 FDA reports)
HOMELESS ( 1 FDA reports)
HOMOCYSTINAEMIA ( 1 FDA reports)
HOUSE DUST ALLERGY ( 1 FDA reports)
HYDROMETRA ( 1 FDA reports)
HYDROTHORAX ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERALDOSTERONISM ( 1 FDA reports)
HYPERAMYLASAEMIA ( 1 FDA reports)
HYPERCALCIURIA ( 1 FDA reports)
HYPERDYNAMIC LEFT VENTRICLE ( 1 FDA reports)
HYPERGASTRINAEMIA ( 1 FDA reports)
HYPERKERATOSIS LENTICULARIS PERSTANS ( 1 FDA reports)
HYPERLIPASAEMIA ( 1 FDA reports)
HYPERPROLACTINAEMIA ( 1 FDA reports)
HYPERSPLENISM ( 1 FDA reports)
HYPERTRICHOSIS ( 1 FDA reports)
HYPOCHOLESTEROLAEMIA ( 1 FDA reports)
HYPOCOAGULABLE STATE ( 1 FDA reports)
HYPOFIBRINOGENAEMIA ( 1 FDA reports)
HYPOPHONESIS ( 1 FDA reports)
HYPOPHOSPHATAEMIC RICKETS ( 1 FDA reports)
HYPOPROTHROMBINAEMIA ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDERS ( 1 FDA reports)
HYPOTHROMBINAEMIA ( 1 FDA reports)
HYPOTHYROIDIC GOITRE ( 1 FDA reports)
HYPOZINCAEMIA ( 1 FDA reports)
HYSTEROSALPINGO-OOPHORECTOMY ( 1 FDA reports)
IATROGENIC INFECTION ( 1 FDA reports)
IDIOPATHIC URTICARIA ( 1 FDA reports)
IIIRD NERVE PARALYSIS ( 1 FDA reports)
IIIRD NERVE PARESIS ( 1 FDA reports)
ILEAL STENOSIS ( 1 FDA reports)
ILEAL ULCER ( 1 FDA reports)
ILIAC VEIN THROMBOSIS ( 1 FDA reports)
IMPINGEMENT SYNDROME ( 1 FDA reports)
IMPLANT SITE CALCIFICATION ( 1 FDA reports)
IMPLANT SITE HAEMATOMA ( 1 FDA reports)
IMPLANT SITE PAIN ( 1 FDA reports)
IMPLANT SITE SWELLING ( 1 FDA reports)
INCISION SITE HAEMATOMA ( 1 FDA reports)
INCISION SITE OEDEMA ( 1 FDA reports)
INCISIONAL HERNIA REPAIR ( 1 FDA reports)
INCORRECT PRODUCT STORAGE ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFECTION PARASITIC ( 1 FDA reports)
INFECTIVE TENOSYNOVITIS ( 1 FDA reports)
INFUSION SITE CELLULITIS ( 1 FDA reports)
INFUSION SITE RASH ( 1 FDA reports)
INFUSION SITE SWELLING ( 1 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
INGUINAL MASS ( 1 FDA reports)
INJECTION ( 1 FDA reports)
INJECTION SITE ANAESTHESIA ( 1 FDA reports)
INJECTION SITE ATROPHY ( 1 FDA reports)
INJECTION SITE FIBROSIS ( 1 FDA reports)
INJECTION SITE NERVE DAMAGE ( 1 FDA reports)
INJECTION SITE PARAESTHESIA ( 1 FDA reports)
INJECTION SITE PHLEBITIS ( 1 FDA reports)
INJECTION SITE THROMBOSIS ( 1 FDA reports)
INJECTION SITE ULCER ( 1 FDA reports)
INJURY ASPHYXIATION ( 1 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 1 FDA reports)
INSULIN-LIKE GROWTH FACTOR DECREASED ( 1 FDA reports)
INTERCAPILLARY GLOMERULOSCLEROSIS ( 1 FDA reports)
INTERNAL INJURY ( 1 FDA reports)
INTERVERTEBRAL DISCITIS ( 1 FDA reports)
INTESTINAL ANASTOMOSIS COMPLICATION ( 1 FDA reports)
INTESTINAL DIAPHRAGM DISEASE ( 1 FDA reports)
INTESTINAL HYPOMOTILITY ( 1 FDA reports)
INTESTINAL MASS ( 1 FDA reports)
INTRA-AORTIC BALLOON PLACEMENT ( 1 FDA reports)
INTRA-OCULAR INJECTION ( 1 FDA reports)
INTRACRANIAL HYPOTENSION ( 1 FDA reports)
INTRAOCULAR MELANOMA ( 1 FDA reports)
INTRASPINAL ABSCESS ( 1 FDA reports)
INTUBATION COMPLICATION ( 1 FDA reports)
IODINE ALLERGY ( 1 FDA reports)
IRIDOCELE ( 1 FDA reports)
IRIS ATROPHY ( 1 FDA reports)
ISCHAEMIC ULCER ( 1 FDA reports)
JEALOUS DELUSION ( 1 FDA reports)
JOINT ABSCESS ( 1 FDA reports)
JOINT FLUID DRAINAGE ( 1 FDA reports)
KAPOSI'S SARCOMA ( 1 FDA reports)
KERATITIS BACTERIAL ( 1 FDA reports)
KERATOPATHY ( 1 FDA reports)
KERATOPLASTY ( 1 FDA reports)
KERATOSIS FOLLICULAR ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
KIDNEY MALROTATION ( 1 FDA reports)
KIDNEY RUPTURE ( 1 FDA reports)
LACTOBACILLUS INFECTION ( 1 FDA reports)
LARGE INTESTINE CARCINOMA ( 1 FDA reports)
LARYNGEAL DISORDER ( 1 FDA reports)
LARYNGEAL ERYTHEMA ( 1 FDA reports)
LARYNGEAL INFLAMMATION ( 1 FDA reports)
LARYNGEAL PAIN ( 1 FDA reports)
LARYNX IRRITATION ( 1 FDA reports)
LATEX ALLERGY ( 1 FDA reports)
LEG CRUSHING ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LEIOMYOSARCOMA ( 1 FDA reports)
LEUKAEMIA PLASMACYTIC ( 1 FDA reports)
LEUKOPLAKIA ( 1 FDA reports)
LIGAMENT LAXITY ( 1 FDA reports)
LIGHT CHAIN ANALYSIS ABNORMAL ( 1 FDA reports)
LIMB ASYMMETRY ( 1 FDA reports)
LIMB PROSTHESIS USER ( 1 FDA reports)
LIMB SALVAGE THERAPY ( 1 FDA reports)
LIP INJURY ( 1 FDA reports)
LIP SLOUGHING ( 1 FDA reports)
LIPASE ( 1 FDA reports)
LIPASE DECREASED ( 1 FDA reports)
LIPIDS DECREASED ( 1 FDA reports)
LIPOMA OF BREAST ( 1 FDA reports)
LIPOMATOSIS ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LIVER SCAN ABNORMAL ( 1 FDA reports)
LIVER TENDERNESS ( 1 FDA reports)
LOCALISED EXFOLIATION ( 1 FDA reports)
LOOSE ASSOCIATIONS ( 1 FDA reports)
LOOSE BODY IN JOINT ( 1 FDA reports)
LOWER URINARY TRACT SYMPTOMS ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 1 FDA reports)
LUNG WEDGE RESECTION ( 1 FDA reports)
LYMPH GLAND INFECTION ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE ABNORMAL ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
LYMPHOCYTIC LYMPHOMA ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
MACULE ( 1 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 1 FDA reports)
MALIGNANT NEOPLASM OF EYE ( 1 FDA reports)
MASS EXCISION ( 1 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MEAN PLATELET VOLUME INCREASED ( 1 FDA reports)
MEASLES ( 1 FDA reports)
MECHANICAL COMPLICATION OF IMPLANT ( 1 FDA reports)
MEDIASTINAL HAEMATOMA ( 1 FDA reports)
MEDICAL OBSERVATION ( 1 FDA reports)
MEDULLARY THYROID CANCER ( 1 FDA reports)
MENINGIOMA MALIGNANT ( 1 FDA reports)
MENINGOCELE ( 1 FDA reports)
MENOMETRORRHAGIA ( 1 FDA reports)
MESENTERIC ARTERIOSCLEROSIS ( 1 FDA reports)
MESENTERIC OCCLUSION ( 1 FDA reports)
MESOTHELIOMA ( 1 FDA reports)
MESOTHELIOMA MALIGNANT ( 1 FDA reports)
METASTASES TO KIDNEY ( 1 FDA reports)
METASTASES TO MENINGES ( 1 FDA reports)
METASTASES TO SPLEEN ( 1 FDA reports)
METASTATIC CARCINOMA OF THE BLADDER ( 1 FDA reports)
METASTATIC LYMPHOMA ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 1 FDA reports)
MILIA ( 1 FDA reports)
MILK ALLERGY ( 1 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 1 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 1 FDA reports)
MOANING ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MONONEUROPATHY MULTIPLEX ( 1 FDA reports)
MORPHOEA ( 1 FDA reports)
MOUTH BREATHING ( 1 FDA reports)
MOUTH INJURY ( 1 FDA reports)
MOUTH PLAQUE ( 1 FDA reports)
MUCOCUTANEOUS RASH ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MULTIPLE ENDOCRINE ADENOMATOSIS TYPE II ( 1 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 1 FDA reports)
MURPHY'S SIGN POSITIVE ( 1 FDA reports)
MUSCLE NECROSIS ( 1 FDA reports)
MYASTHENIA GRAVIS CRISIS ( 1 FDA reports)
MYASTHENIC SYNDROME ( 1 FDA reports)
MYCOTOXICOSIS ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME UNCLASSIFIABLE ( 1 FDA reports)
MYELOID LEUKAEMIA ( 1 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 1 FDA reports)
MYOCARDIAL CALCIFICATION ( 1 FDA reports)
MYOCARDIAL RUPTURE ( 1 FDA reports)
MYOKYMIA ( 1 FDA reports)
MYOSITIS OSSIFICANS ( 1 FDA reports)
NAIL BED INFECTION ( 1 FDA reports)
NAIL HYPERTROPHY ( 1 FDA reports)
NAIL INJURY ( 1 FDA reports)
NAIL OPERATION ( 1 FDA reports)
NASAL FLARING ( 1 FDA reports)
NASAL OPERATION ( 1 FDA reports)
NASAL SEPTUM DISORDER ( 1 FDA reports)
NEGATIVE THOUGHTS ( 1 FDA reports)
NEGATIVISM ( 1 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NEOPLASM OF APPENDIX ( 1 FDA reports)
NERVE ROOT INJURY CERVICAL ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA ( 1 FDA reports)
NEUROGENIC SHOCK ( 1 FDA reports)
NEUROSIS ( 1 FDA reports)
NEUTROPENIC COLITIS ( 1 FDA reports)
NEUTROPHIL PELGER-HUET ANOMALY PRESENT ( 1 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 1 FDA reports)
NITRITE URINE ( 1 FDA reports)
NOCARDIOSIS ( 1 FDA reports)
NODAL MARGINAL ZONE B-CELL LYMPHOMA ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 1 FDA reports)
NORMAL DELIVERY ( 1 FDA reports)
NUCLEATED RED CELLS ( 1 FDA reports)
OBSTRUCTIVE CHRONIC BRONCHITIS WITH ACUTE EXACERBATION ( 1 FDA reports)
OCCUPATIONAL PHYSICAL PROBLEM ( 1 FDA reports)
OCULAR HYPERTENSION ( 1 FDA reports)
OCULAR MYASTHENIA ( 1 FDA reports)
OCULAR TOXICITY ( 1 FDA reports)
OEDEMA DUE TO HEPATIC DISEASE ( 1 FDA reports)
OESOPHAGEAL DILATION PROCEDURE ( 1 FDA reports)
OESOPHAGEAL INFECTION ( 1 FDA reports)
OESOPHAGEAL NEOPLASM ( 1 FDA reports)
OESOPHAGEAL STENT INSERTION ( 1 FDA reports)
OESOPHAGOENTEROSTOMY ( 1 FDA reports)
OESOPHAGOSCOPY ABNORMAL ( 1 FDA reports)
OLIGOHYDRAMNIOS ( 1 FDA reports)
OLIGOMENORRHOEA ( 1 FDA reports)
ONYCHALGIA ( 1 FDA reports)
ONYCHORRHEXIS ( 1 FDA reports)
OPEN ANGLE GLAUCOMA ( 1 FDA reports)
OPHTHALMOLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
OPTIC NERVE SHEATH HAEMORRHAGE ( 1 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 1 FDA reports)
ORAL ADMINISTRATION COMPLICATION ( 1 FDA reports)
ORAL DYSAESTHESIA ( 1 FDA reports)
ORAL NEOPLASM ( 1 FDA reports)
ORAL PAPILLOMA ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
ORCHIDECTOMY ( 1 FDA reports)
ORGAN TRANSPLANT ( 1 FDA reports)
ORGANISING PNEUMONIA ( 1 FDA reports)
ORGASMIC SENSATION DECREASED ( 1 FDA reports)
OROPHARYNGEAL CANCER STAGE UNSPECIFIED ( 1 FDA reports)
OROPHARYNGEAL SPASM ( 1 FDA reports)
OROPHARYNGITIS FUNGAL ( 1 FDA reports)
ORTHOPEDIC PROCEDURE ( 1 FDA reports)
OSTEOCALCIN INCREASED ( 1 FDA reports)
OSTEODYSTROPHY ( 1 FDA reports)
OSTEOPOROSIS POSTMENOPAUSAL ( 1 FDA reports)
OSTEOPOROTIC FRACTURE ( 1 FDA reports)
OSTEOSARCOMA METASTATIC ( 1 FDA reports)
OVARIAN CANCER RECURRENT ( 1 FDA reports)
OVARIAN CYSTECTOMY ( 1 FDA reports)
OVARIAN FIBROMA ( 1 FDA reports)
OXYGEN SATURATION IMMEASURABLE ( 1 FDA reports)
PAIN THRESHOLD DECREASED ( 1 FDA reports)
PAINFUL ERECTION ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PALPABLE PURPURA ( 1 FDA reports)
PANCREAS TRANSPLANT ( 1 FDA reports)
PANCREATIC CARCINOMA STAGE IV ( 1 FDA reports)
PANCREATIC SPHINCTEROTOMY ( 1 FDA reports)
PANCREATITIS RELAPSING ( 1 FDA reports)
PANCREATITIS VIRAL ( 1 FDA reports)
PAPILLARY MUSCLE DISORDER ( 1 FDA reports)
PARALYSIS FLACCID ( 1 FDA reports)
PARANASAL CYST ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PATIENT-DEVICE INCOMPATIBILITY ( 1 FDA reports)
PECTUS EXCAVATUM ( 1 FDA reports)
PEDAL PULSE ABNORMAL ( 1 FDA reports)
PELVIC FLOOR REPAIR ( 1 FDA reports)
PELVIC HAEMATOMA ( 1 FDA reports)
PELVIC HAEMORRHAGE ( 1 FDA reports)
PELVIC INFECTION ( 1 FDA reports)
PELVIC MASS ( 1 FDA reports)
PELVIC PROLAPSE ( 1 FDA reports)
PENILE PROSTHESIS INSERTION ( 1 FDA reports)
PEPTIC ULCER REACTIVATED ( 1 FDA reports)
PERIANAL ABSCESS ( 1 FDA reports)
PERICARDIAL CALCIFICATION ( 1 FDA reports)
PERICARDIAL RUB ( 1 FDA reports)
PERIHEPATIC DISCOMFORT ( 1 FDA reports)
PERINEAL ABSCESS ( 1 FDA reports)
PERINEPHRIC EFFUSION ( 1 FDA reports)
PERIORBITAL DISORDER ( 1 FDA reports)
PERIPHERAL NERVE OPERATION ( 1 FDA reports)
PERIPORTAL OEDEMA ( 1 FDA reports)
PERISTALSIS VISIBLE ( 1 FDA reports)
PERITONEAL CLOUDY EFFLUENT ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERITONEAL NEOPLASM ( 1 FDA reports)
PERIVASCULAR DERMATITIS ( 1 FDA reports)
PERSECUTORY DELUSION ( 1 FDA reports)
PERSEVERATION ( 1 FDA reports)
PEYRONIE'S DISEASE ( 1 FDA reports)
PH URINE DECREASED ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 1 FDA reports)
PHARYNGEAL CYST ( 1 FDA reports)
PHARYNGEAL HAEMATOMA ( 1 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 1 FDA reports)
PHARYNGEAL INFLAMMATION ( 1 FDA reports)
PHARYNGEAL LEUKOPLAKIA ( 1 FDA reports)
PHARYNGEAL NEOPLASM ( 1 FDA reports)
PHARYNGITIS BACTERIAL ( 1 FDA reports)
PHARYNGOLARYNGEAL DISCOMFORT ( 1 FDA reports)
PHENYLKETONURIA ( 1 FDA reports)
PHIMOSIS ( 1 FDA reports)
PHLEBOTHROMBOSIS ( 1 FDA reports)
PHOSPHORUS METABOLISM DISORDER ( 1 FDA reports)
PHOTOCOAGULATION ( 1 FDA reports)
PHOTOSENSITIVITY ALLERGIC REACTION ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PILONIDAL CYST ( 1 FDA reports)
PLACENTA PRAEVIA ( 1 FDA reports)
PLACENTAL DISORDER ( 1 FDA reports)
PLASMA PROTEIN METABOLISM DISORDER ( 1 FDA reports)
PLASTIC SURGERY ( 1 FDA reports)
PLEURAL ADHESION ( 1 FDA reports)
PLEURAL CALCIFICATION ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PLEURAL INFECTION ( 1 FDA reports)
PLEURODESIS ( 1 FDA reports)
PNEUMATOSIS ( 1 FDA reports)
PNEUMATURIA ( 1 FDA reports)
PNEUMOCEPHALUS ( 1 FDA reports)
PNEUMOCOCCAL SEPSIS ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMONIA ADENOVIRAL ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
POLYARTERITIS NODOSA ( 1 FDA reports)
POLYGLANDULAR DISORDER ( 1 FDA reports)
POLYMYALGIA ( 1 FDA reports)
POLYOMAVIRUS TEST POSITIVE ( 1 FDA reports)
POLYSUBSTANCE ABUSE ( 1 FDA reports)
PORPHYRIA NON-ACUTE ( 1 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 1 FDA reports)
PORTAL VEIN STENOSIS ( 1 FDA reports)
PORTOPULMONARY HYPERTENSION ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 1 FDA reports)
POST COITAL BLEEDING ( 1 FDA reports)
POST PROCEDURAL BILE LEAK ( 1 FDA reports)
POST PROCEDURAL DIARRHOEA ( 1 FDA reports)
POST PROCEDURAL DRAINAGE ( 1 FDA reports)
POST PROCEDURAL SWELLING ( 1 FDA reports)
POSTOPERATIVE ABSCESS ( 1 FDA reports)
POSTOPERATIVE ADHESION ( 1 FDA reports)
POSTOPERATIVE HERNIA ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
PRE-ECLAMPSIA ( 1 FDA reports)
PRECANCEROUS SKIN LESION ( 1 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 1 FDA reports)
PRESBYACUSIS ( 1 FDA reports)
PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PRODUCT DEPOSIT ( 1 FDA reports)
PRODUCT OUTER PACKAGING ISSUE ( 1 FDA reports)
PRODUCT SIZE ISSUE ( 1 FDA reports)
PROGRESSIVE MASSIVE FIBROSIS ( 1 FDA reports)
PROPHYLAXIS ( 1 FDA reports)
PROSTATE CANCER RECURRENT ( 1 FDA reports)
PROSTATIC HAEMORRHAGE ( 1 FDA reports)
PROSTATIC MASS ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN ( 1 FDA reports)
PROSTATISM ( 1 FDA reports)
PROTEIN C DEFICIENCY ( 1 FDA reports)
PROTEIN S INCREASED ( 1 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME RATIO ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 1 FDA reports)
PSEUDARTHROSIS ( 1 FDA reports)
PSEUDOMENINGOCELE ( 1 FDA reports)
PSEUDOPHAKIA ( 1 FDA reports)
PSOAS ABSCESS ( 1 FDA reports)
PSYCHOSEXUAL DISORDER ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE ABNORMAL ( 1 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE DECREASED ( 1 FDA reports)
PULMONARY ARTERIOPATHY ( 1 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 1 FDA reports)
PULMONARY CAVITATION ( 1 FDA reports)
PULMONARY HYPOPLASIA ( 1 FDA reports)
PULMONARY SARCOIDOSIS ( 1 FDA reports)
PULMONARY VALVE STENOSIS ( 1 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
PUNCTURE SITE REACTION ( 1 FDA reports)
PURPLE GLOVE SYNDROME ( 1 FDA reports)
PYELECTASIA ( 1 FDA reports)
PYODERMA GANGRENOSUM ( 1 FDA reports)
PYOGENIC GRANULOMA ( 1 FDA reports)
PYOMYOSITIS ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
RADIAL NERVE INJURY ( 1 FDA reports)
RADIAL NERVE PALSY ( 1 FDA reports)
RADIATION DYSPHAGIA ( 1 FDA reports)
RADIATION PNEUMONITIS ( 1 FDA reports)
RADICAL NECK DISSECTION ( 1 FDA reports)
RADICULITIS BRACHIAL ( 1 FDA reports)
RATHKE'S CLEFT CYST ( 1 FDA reports)
REACTION TO AZO-DYES ( 1 FDA reports)
REACTION TO FOOD ADDITIVE ( 1 FDA reports)
REACTION TO PRESERVATIVES ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
RECTOSIGMOID CANCER ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RED BLOOD CELL MORPHOLOGY ABNORMAL ( 1 FDA reports)
RED BLOOD CELL TARGET CELLS PRESENT ( 1 FDA reports)
REFRACTION DISORDER ( 1 FDA reports)
REGURGITATION OF FOOD ( 1 FDA reports)
REMOVAL OF FOREIGN BODY FROM OESOPHAGUS ( 1 FDA reports)
RENAL APLASIA ( 1 FDA reports)