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

ANXIETY ( 2218 FDA reports)
NAUSEA ( 2158 FDA reports)
PAIN ( 2019 FDA reports)
DEPRESSION ( 2016 FDA reports)
DRUG INEFFECTIVE ( 1884 FDA reports)
HEADACHE ( 1843 FDA reports)
FATIGUE ( 1821 FDA reports)
DIZZINESS ( 1782 FDA reports)
DYSPNOEA ( 1562 FDA reports)
INSOMNIA ( 1560 FDA reports)
COMPLETED SUICIDE ( 1504 FDA reports)
FALL ( 1497 FDA reports)
ASTHENIA ( 1412 FDA reports)
VOMITING ( 1392 FDA reports)
DIARRHOEA ( 1366 FDA reports)
SOMNOLENCE ( 1286 FDA reports)
PYREXIA ( 1268 FDA reports)
WEIGHT INCREASED ( 1256 FDA reports)
CONVULSION ( 1236 FDA reports)
CONFUSIONAL STATE ( 1170 FDA reports)
TREMOR ( 1081 FDA reports)
MALAISE ( 1071 FDA reports)
PAIN IN EXTREMITY ( 1046 FDA reports)
CHEST PAIN ( 1044 FDA reports)
WEIGHT DECREASED ( 996 FDA reports)
ARTHRALGIA ( 993 FDA reports)
PNEUMONIA ( 969 FDA reports)
DIABETES MELLITUS ( 968 FDA reports)
SUICIDAL IDEATION ( 965 FDA reports)
BACK PAIN ( 955 FDA reports)
HYPERTENSION ( 950 FDA reports)
FEELING ABNORMAL ( 903 FDA reports)
DRUG INTERACTION ( 892 FDA reports)
OEDEMA PERIPHERAL ( 887 FDA reports)
OVERDOSE ( 868 FDA reports)
CARDIAC ARREST ( 847 FDA reports)
ABDOMINAL PAIN ( 838 FDA reports)
AGITATION ( 812 FDA reports)
CONSTIPATION ( 809 FDA reports)
HYPOTENSION ( 798 FDA reports)
DEATH ( 766 FDA reports)
GAIT DISTURBANCE ( 755 FDA reports)
LOSS OF CONSCIOUSNESS ( 738 FDA reports)
CONDITION AGGRAVATED ( 725 FDA reports)
SUICIDE ATTEMPT ( 704 FDA reports)
RASH ( 699 FDA reports)
ANAEMIA ( 690 FDA reports)
HYPOAESTHESIA ( 686 FDA reports)
VISION BLURRED ( 675 FDA reports)
HYPERHIDROSIS ( 649 FDA reports)
DECREASED APPETITE ( 645 FDA reports)
TYPE 2 DIABETES MELLITUS ( 637 FDA reports)
RESPIRATORY ARREST ( 635 FDA reports)
MUSCLE SPASMS ( 635 FDA reports)
PARAESTHESIA ( 632 FDA reports)
ABDOMINAL PAIN UPPER ( 626 FDA reports)
URINARY TRACT INFECTION ( 609 FDA reports)
DEHYDRATION ( 595 FDA reports)
PRURITUS ( 573 FDA reports)
MEMORY IMPAIRMENT ( 565 FDA reports)
BLOOD PRESSURE INCREASED ( 543 FDA reports)
CARDIO-RESPIRATORY ARREST ( 521 FDA reports)
BALANCE DISORDER ( 511 FDA reports)
MYALGIA ( 507 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 499 FDA reports)
DYSPHAGIA ( 499 FDA reports)
COUGH ( 496 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 493 FDA reports)
MYOCARDIAL INFARCTION ( 484 FDA reports)
MUSCULAR WEAKNESS ( 481 FDA reports)
PALPITATIONS ( 476 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 473 FDA reports)
TACHYCARDIA ( 471 FDA reports)
AGGRESSION ( 470 FDA reports)
BLOOD GLUCOSE INCREASED ( 470 FDA reports)
AMNESIA ( 464 FDA reports)
INJURY ( 464 FDA reports)
NERVOUSNESS ( 458 FDA reports)
IRRITABILITY ( 455 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 442 FDA reports)
HEART RATE INCREASED ( 442 FDA reports)
CEREBROVASCULAR ACCIDENT ( 439 FDA reports)
PULMONARY EMBOLISM ( 431 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 427 FDA reports)
SPEECH DISORDER ( 421 FDA reports)
RENAL FAILURE ( 420 FDA reports)
DISORIENTATION ( 416 FDA reports)
PANIC ATTACK ( 416 FDA reports)
HALLUCINATION ( 415 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 414 FDA reports)
RENAL FAILURE ACUTE ( 407 FDA reports)
CHILLS ( 400 FDA reports)
DRUG TOXICITY ( 391 FDA reports)
NEUROPATHY PERIPHERAL ( 391 FDA reports)
ERYTHEMA ( 388 FDA reports)
DRY MOUTH ( 379 FDA reports)
DISTURBANCE IN ATTENTION ( 378 FDA reports)
NECK PAIN ( 375 FDA reports)
SLEEP DISORDER ( 374 FDA reports)
PANCREATITIS ( 368 FDA reports)
DEEP VEIN THROMBOSIS ( 367 FDA reports)
DYSARTHRIA ( 363 FDA reports)
BRONCHITIS ( 359 FDA reports)
CONTUSION ( 358 FDA reports)
SYNCOPE ( 352 FDA reports)
DRUG DEPENDENCE ( 351 FDA reports)
LETHARGY ( 350 FDA reports)
ABNORMAL BEHAVIOUR ( 348 FDA reports)
INTENTIONAL OVERDOSE ( 345 FDA reports)
CRYING ( 343 FDA reports)
EMOTIONAL DISTRESS ( 342 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 339 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 336 FDA reports)
DYSKINESIA ( 336 FDA reports)
MENTAL DISORDER ( 335 FDA reports)
SEPSIS ( 333 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 332 FDA reports)
OSTEOARTHRITIS ( 331 FDA reports)
PSYCHOTIC DISORDER ( 331 FDA reports)
RESPIRATORY FAILURE ( 330 FDA reports)
NEUTROPENIA ( 323 FDA reports)
STRESS ( 321 FDA reports)
COMA ( 318 FDA reports)
DELIRIUM ( 318 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 317 FDA reports)
MIGRAINE ( 317 FDA reports)
HYPERGLYCAEMIA ( 316 FDA reports)
DRUG DOSE OMISSION ( 314 FDA reports)
HAEMOGLOBIN DECREASED ( 314 FDA reports)
THROMBOCYTOPENIA ( 314 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 311 FDA reports)
ABDOMINAL DISTENSION ( 310 FDA reports)
RESTLESSNESS ( 309 FDA reports)
SINUSITIS ( 304 FDA reports)
ALOPECIA ( 302 FDA reports)
HYPERLIPIDAEMIA ( 302 FDA reports)
CARDIAC DISORDER ( 298 FDA reports)
RHABDOMYOLYSIS ( 296 FDA reports)
ANGER ( 295 FDA reports)
INFLUENZA LIKE ILLNESS ( 293 FDA reports)
DYSPEPSIA ( 291 FDA reports)
MUSCULOSKELETAL PAIN ( 289 FDA reports)
CHEST DISCOMFORT ( 288 FDA reports)
MENTAL STATUS CHANGES ( 288 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 285 FDA reports)
HYPERSENSITIVITY ( 285 FDA reports)
ASTHMA ( 282 FDA reports)
SEDATION ( 282 FDA reports)
ATRIAL FIBRILLATION ( 281 FDA reports)
NIGHTMARE ( 280 FDA reports)
BLOOD PRESSURE DECREASED ( 279 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 279 FDA reports)
INTENTIONAL DRUG MISUSE ( 276 FDA reports)
HYPONATRAEMIA ( 274 FDA reports)
SWELLING ( 274 FDA reports)
VISUAL IMPAIRMENT ( 274 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 274 FDA reports)
CELLULITIS ( 273 FDA reports)
CHOLELITHIASIS ( 273 FDA reports)
DEPRESSED MOOD ( 272 FDA reports)
MANIA ( 272 FDA reports)
TINNITUS ( 269 FDA reports)
COGNITIVE DISORDER ( 268 FDA reports)
OFF LABEL USE ( 265 FDA reports)
ANOREXIA ( 264 FDA reports)
DYSGEUSIA ( 263 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 263 FDA reports)
OSTEOPOROSIS ( 260 FDA reports)
ABNORMAL DREAMS ( 258 FDA reports)
DRUG EFFECT DECREASED ( 253 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 253 FDA reports)
SWELLING FACE ( 253 FDA reports)
WITHDRAWAL SYNDROME ( 253 FDA reports)
ROAD TRAFFIC ACCIDENT ( 252 FDA reports)
INFECTION ( 251 FDA reports)
OBESITY ( 251 FDA reports)
OSTEONECROSIS OF JAW ( 251 FDA reports)
TREATMENT NONCOMPLIANCE ( 249 FDA reports)
BIPOLAR DISORDER ( 248 FDA reports)
BRADYCARDIA ( 248 FDA reports)
MULTIPLE DRUG OVERDOSE ( 248 FDA reports)
DRUG ABUSE ( 246 FDA reports)
INCORRECT DOSE ADMINISTERED ( 244 FDA reports)
OSTEOMYELITIS ( 244 FDA reports)
FLUSHING ( 243 FDA reports)
SEROTONIN SYNDROME ( 243 FDA reports)
BONE DISORDER ( 242 FDA reports)
HAEMORRHAGE ( 240 FDA reports)
POISONING ( 240 FDA reports)
GRAND MAL CONVULSION ( 238 FDA reports)
EPILEPSY ( 237 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 236 FDA reports)
MEDICATION ERROR ( 234 FDA reports)
NASOPHARYNGITIS ( 231 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 231 FDA reports)
ABDOMINAL DISCOMFORT ( 228 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 228 FDA reports)
VERTIGO ( 225 FDA reports)
HYPOKALAEMIA ( 223 FDA reports)
JOINT SWELLING ( 222 FDA reports)
FEAR ( 221 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 221 FDA reports)
MOOD SWINGS ( 220 FDA reports)
PLEURAL EFFUSION ( 220 FDA reports)
RESTLESS LEGS SYNDROME ( 220 FDA reports)
INJECTION SITE PAIN ( 219 FDA reports)
CATARACT ( 218 FDA reports)
URINARY RETENTION ( 218 FDA reports)
BONE PAIN ( 217 FDA reports)
PARANOIA ( 215 FDA reports)
BLOOD CREATININE INCREASED ( 213 FDA reports)
HYPOGLYCAEMIA ( 213 FDA reports)
GASTRITIS ( 211 FDA reports)
PAIN IN JAW ( 211 FDA reports)
DIPLOPIA ( 209 FDA reports)
FIBROMYALGIA ( 208 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 207 FDA reports)
PULMONARY OEDEMA ( 207 FDA reports)
URTICARIA ( 206 FDA reports)
PLATELET COUNT DECREASED ( 205 FDA reports)
ARTHRITIS ( 203 FDA reports)
URINARY INCONTINENCE ( 203 FDA reports)
ARRHYTHMIA ( 202 FDA reports)
HYPOTHYROIDISM ( 200 FDA reports)
ILL-DEFINED DISORDER ( 200 FDA reports)
INFLUENZA ( 200 FDA reports)
PRODUCT QUALITY ISSUE ( 200 FDA reports)
SPINAL OSTEOARTHRITIS ( 199 FDA reports)
BURNING SENSATION ( 196 FDA reports)
LEUKOPENIA ( 196 FDA reports)
EMOTIONAL DISORDER ( 195 FDA reports)
IMPAIRED HEALING ( 195 FDA reports)
THROMBOSIS ( 195 FDA reports)
APHASIA ( 194 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 192 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 191 FDA reports)
HEPATIC STEATOSIS ( 190 FDA reports)
TARDIVE DYSKINESIA ( 190 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 190 FDA reports)
CARDIOMEGALY ( 189 FDA reports)
CORONARY ARTERY DISEASE ( 187 FDA reports)
PNEUMONIA ASPIRATION ( 186 FDA reports)
UNRESPONSIVE TO STIMULI ( 186 FDA reports)
RECTAL HAEMORRHAGE ( 185 FDA reports)
VISUAL ACUITY REDUCED ( 184 FDA reports)
COORDINATION ABNORMAL ( 184 FDA reports)
ABASIA ( 183 FDA reports)
OEDEMA ( 183 FDA reports)
HYPERSOMNIA ( 178 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 176 FDA reports)
NEPHROLITHIASIS ( 176 FDA reports)
MOBILITY DECREASED ( 175 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 175 FDA reports)
THINKING ABNORMAL ( 175 FDA reports)
SLEEP APNOEA SYNDROME ( 173 FDA reports)
DRUG HYPERSENSITIVITY ( 173 FDA reports)
DIABETIC NEUROPATHY ( 172 FDA reports)
PANCYTOPENIA ( 172 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 170 FDA reports)
HEPATIC ENZYME INCREASED ( 170 FDA reports)
BLOOD SODIUM DECREASED ( 169 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 169 FDA reports)
OROPHARYNGEAL PAIN ( 169 FDA reports)
OSTEONECROSIS ( 169 FDA reports)
LIVER DISORDER ( 168 FDA reports)
TOOTH EXTRACTION ( 167 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 165 FDA reports)
DELUSION ( 163 FDA reports)
ANGINA PECTORIS ( 161 FDA reports)
HALLUCINATION, AUDITORY ( 161 FDA reports)
DYSURIA ( 160 FDA reports)
NERVOUS SYSTEM DISORDER ( 160 FDA reports)
HOT FLUSH ( 159 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 159 FDA reports)
BREAST CANCER ( 158 FDA reports)
HYPOXIA ( 158 FDA reports)
MOOD ALTERED ( 158 FDA reports)
MOVEMENT DISORDER ( 158 FDA reports)
MULTIPLE SCLEROSIS ( 158 FDA reports)
VIRAL INFECTION ( 156 FDA reports)
ATAXIA ( 155 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 155 FDA reports)
DYSTONIA ( 155 FDA reports)
FLATULENCE ( 155 FDA reports)
OXYGEN SATURATION DECREASED ( 155 FDA reports)
HEAD INJURY ( 154 FDA reports)
INJECTION SITE ERYTHEMA ( 154 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 153 FDA reports)
RENAL IMPAIRMENT ( 153 FDA reports)
EYE PAIN ( 151 FDA reports)
HAEMATOCHEZIA ( 151 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 151 FDA reports)
GALLBLADDER DISORDER ( 150 FDA reports)
ANHEDONIA ( 149 FDA reports)
BLINDNESS ( 149 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 149 FDA reports)
POLLAKIURIA ( 149 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 148 FDA reports)
DYSPHONIA ( 147 FDA reports)
EPISTAXIS ( 147 FDA reports)
ARTHROPATHY ( 146 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 146 FDA reports)
LIMB INJURY ( 146 FDA reports)
UNEVALUABLE EVENT ( 146 FDA reports)
DRUG LEVEL INCREASED ( 145 FDA reports)
ERECTILE DYSFUNCTION ( 145 FDA reports)
MAJOR DEPRESSION ( 145 FDA reports)
MUSCLE TWITCHING ( 145 FDA reports)
DENTAL CARIES ( 144 FDA reports)
SKIN DISCOLOURATION ( 144 FDA reports)
ECONOMIC PROBLEM ( 143 FDA reports)
HAEMATURIA ( 143 FDA reports)
LYMPHADENOPATHY ( 143 FDA reports)
MUSCLE RIGIDITY ( 142 FDA reports)
MYOCLONUS ( 142 FDA reports)
STATUS EPILEPTICUS ( 141 FDA reports)
SCHIZOPHRENIA ( 140 FDA reports)
DIABETIC KETOACIDOSIS ( 140 FDA reports)
FEELING HOT ( 140 FDA reports)
EAR PAIN ( 139 FDA reports)
EATING DISORDER ( 139 FDA reports)
MENTAL IMPAIRMENT ( 138 FDA reports)
SWOLLEN TONGUE ( 138 FDA reports)
HAEMORRHOIDS ( 137 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 135 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 135 FDA reports)
PALLOR ( 135 FDA reports)
ACCIDENTAL OVERDOSE ( 133 FDA reports)
CHOLECYSTITIS CHRONIC ( 133 FDA reports)
HAEMATOCRIT DECREASED ( 133 FDA reports)
GLAUCOMA ( 131 FDA reports)
INCONTINENCE ( 131 FDA reports)
CYSTITIS ( 130 FDA reports)
STOMATITIS ( 130 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 129 FDA reports)
RHINORRHOEA ( 129 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 129 FDA reports)
DYSSTASIA ( 127 FDA reports)
DEFORMITY ( 126 FDA reports)
NIGHT SWEATS ( 126 FDA reports)
DECREASED INTEREST ( 125 FDA reports)
ENCEPHALOPATHY ( 125 FDA reports)
HIP FRACTURE ( 125 FDA reports)
RHEUMATOID ARTHRITIS ( 125 FDA reports)
SINUS TACHYCARDIA ( 124 FDA reports)
GASTROINTESTINAL DISORDER ( 123 FDA reports)
DISEASE PROGRESSION ( 122 FDA reports)
INFLAMMATION ( 122 FDA reports)
MITRAL VALVE INCOMPETENCE ( 122 FDA reports)
HYPERCHOLESTEROLAEMIA ( 120 FDA reports)
HYPERKALAEMIA ( 120 FDA reports)
STAPHYLOCOCCAL INFECTION ( 120 FDA reports)
TOOTH FRACTURE ( 118 FDA reports)
DIVERTICULUM ( 118 FDA reports)
BLOOD GLUCOSE DECREASED ( 117 FDA reports)
HYPOPHAGIA ( 117 FDA reports)
PANCREATITIS ACUTE ( 117 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 117 FDA reports)
TYPE 1 DIABETES MELLITUS ( 116 FDA reports)
HEPATIC FAILURE ( 116 FDA reports)
HEPATITIS ( 116 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 115 FDA reports)
MULTI-ORGAN FAILURE ( 115 FDA reports)
MYDRIASIS ( 115 FDA reports)
TOOTH DISORDER ( 115 FDA reports)
WHEEZING ( 115 FDA reports)
BLOOD POTASSIUM DECREASED ( 114 FDA reports)
HALLUCINATION, VISUAL ( 114 FDA reports)
JOINT INJURY ( 114 FDA reports)
BLOOD UREA INCREASED ( 113 FDA reports)
FEELING JITTERY ( 113 FDA reports)
INCREASED APPETITE ( 113 FDA reports)
CANDIDIASIS ( 112 FDA reports)
HAEMATEMESIS ( 112 FDA reports)
HEART RATE DECREASED ( 112 FDA reports)
RENAL FAILURE CHRONIC ( 112 FDA reports)
SCAR ( 111 FDA reports)
ASPIRATION ( 111 FDA reports)
HAEMATOMA ( 111 FDA reports)
NEOPLASM MALIGNANT ( 111 FDA reports)
NEURALGIA ( 111 FDA reports)
ORTHOSTATIC HYPOTENSION ( 111 FDA reports)
CARDIOMYOPATHY ( 110 FDA reports)
EMPHYSEMA ( 110 FDA reports)
HYPOTONIA ( 110 FDA reports)
LUNG DISORDER ( 110 FDA reports)
BLISTER ( 109 FDA reports)
CARDIAC FAILURE ( 109 FDA reports)
CARPAL TUNNEL SYNDROME ( 109 FDA reports)
CYANOSIS ( 109 FDA reports)
GRANULOCYTOPENIA ( 109 FDA reports)
NASAL CONGESTION ( 109 FDA reports)
TOOTH LOSS ( 109 FDA reports)
DRY EYE ( 108 FDA reports)
INJECTION SITE HAEMATOMA ( 108 FDA reports)
FEBRILE NEUTROPENIA ( 107 FDA reports)
HERPES ZOSTER ( 107 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 107 FDA reports)
SENSORY DISTURBANCE ( 107 FDA reports)
RENAL CYST ( 106 FDA reports)
CYTOLYTIC HEPATITIS ( 106 FDA reports)
GASTROENTERITIS ( 106 FDA reports)
HEART RATE IRREGULAR ( 106 FDA reports)
POOR QUALITY SLEEP ( 106 FDA reports)
COLITIS ( 105 FDA reports)
HEMIPARESIS ( 105 FDA reports)
RESPIRATORY DISTRESS ( 105 FDA reports)
STEVENS-JOHNSON SYNDROME ( 105 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 104 FDA reports)
RIB FRACTURE ( 104 FDA reports)
SEPTIC SHOCK ( 103 FDA reports)
FOOT FRACTURE ( 103 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 103 FDA reports)
HIATUS HERNIA ( 102 FDA reports)
RASH PRURITIC ( 102 FDA reports)
SURGERY ( 101 FDA reports)
ATELECTASIS ( 101 FDA reports)
FUNGAL INFECTION ( 100 FDA reports)
IMPAIRED DRIVING ABILITY ( 100 FDA reports)
RENAL DISORDER ( 100 FDA reports)
SKIN EXFOLIATION ( 100 FDA reports)
SKIN LESION ( 100 FDA reports)
PREGNANCY ( 99 FDA reports)
PULMONARY HYPERTENSION ( 99 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 99 FDA reports)
LUNG NEOPLASM ( 99 FDA reports)
MYOCARDIAL ISCHAEMIA ( 99 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 98 FDA reports)
TOOTHACHE ( 98 FDA reports)
RESPIRATORY DEPRESSION ( 97 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 97 FDA reports)
DRY SKIN ( 97 FDA reports)
MIDDLE INSOMNIA ( 97 FDA reports)
CROHN'S DISEASE ( 96 FDA reports)
EJECTION FRACTION DECREASED ( 96 FDA reports)
INJECTION SITE HAEMORRHAGE ( 96 FDA reports)
PATHOLOGICAL GAMBLING ( 96 FDA reports)
BLOOD URINE PRESENT ( 95 FDA reports)
MUCOSAL INFLAMMATION ( 95 FDA reports)
OESOPHAGITIS ( 95 FDA reports)
RASH MACULAR ( 95 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 94 FDA reports)
SALIVARY HYPERSECRETION ( 94 FDA reports)
CIRCULATORY COLLAPSE ( 94 FDA reports)
DISEASE RECURRENCE ( 94 FDA reports)
DYSPNOEA EXERTIONAL ( 94 FDA reports)
ORAL PAIN ( 94 FDA reports)
HAEMOPTYSIS ( 93 FDA reports)
OSTEOPENIA ( 93 FDA reports)
PSORIASIS ( 93 FDA reports)
APATHY ( 92 FDA reports)
BODY TEMPERATURE INCREASED ( 92 FDA reports)
IRRITABLE BOWEL SYNDROME ( 92 FDA reports)
LEUKOCYTOSIS ( 92 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 91 FDA reports)
ILEUS ( 91 FDA reports)
PRODUCTIVE COUGH ( 91 FDA reports)
PSYCHIATRIC SYMPTOM ( 91 FDA reports)
VISUAL DISTURBANCE ( 91 FDA reports)
BLOOD CALCIUM DECREASED ( 90 FDA reports)
FEMUR FRACTURE ( 90 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 89 FDA reports)
DYSLIPIDAEMIA ( 89 FDA reports)
EYE DISORDER ( 89 FDA reports)
GASTRIC DISORDER ( 89 FDA reports)
ORAL CANDIDIASIS ( 89 FDA reports)
SHOCK ( 89 FDA reports)
PULMONARY CONGESTION ( 88 FDA reports)
ADVERSE EVENT ( 88 FDA reports)
DRUG ABUSER ( 88 FDA reports)
IMPAIRED WORK ABILITY ( 88 FDA reports)
MOUTH ULCERATION ( 88 FDA reports)
PERICARDIAL EFFUSION ( 88 FDA reports)
ARTERIOSCLEROSIS ( 87 FDA reports)
COLONIC POLYP ( 87 FDA reports)
DROOLING ( 87 FDA reports)
PRESYNCOPE ( 87 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 87 FDA reports)
RESPIRATORY DISORDER ( 86 FDA reports)
FLUID RETENTION ( 86 FDA reports)
HEPATITIS C ( 86 FDA reports)
EUPHORIC MOOD ( 85 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 85 FDA reports)
CORONARY ARTERY OCCLUSION ( 84 FDA reports)
DISABILITY ( 84 FDA reports)
HOMICIDAL IDEATION ( 84 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 84 FDA reports)
PREMATURE BABY ( 83 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 83 FDA reports)
AKATHISIA ( 83 FDA reports)
CEREBRAL ATROPHY ( 83 FDA reports)
DRUG ADMINISTRATION ERROR ( 83 FDA reports)
EYE SWELLING ( 83 FDA reports)
FEELING DRUNK ( 83 FDA reports)
INTENTIONAL SELF-INJURY ( 83 FDA reports)
MULTIPLE MYELOMA ( 83 FDA reports)
ABORTION SPONTANEOUS ( 82 FDA reports)
FORMICATION ( 82 FDA reports)
INTENTIONAL MISUSE ( 82 FDA reports)
INTESTINAL OBSTRUCTION ( 82 FDA reports)
NEUTROPHIL COUNT DECREASED ( 82 FDA reports)
SPINAL COLUMN STENOSIS ( 82 FDA reports)
VAGINAL HAEMORRHAGE ( 82 FDA reports)
SKIN DISORDER ( 81 FDA reports)
TOOTH ABSCESS ( 81 FDA reports)
DRUG INTOLERANCE ( 81 FDA reports)
MALNUTRITION ( 81 FDA reports)
MUSCLE DISORDER ( 81 FDA reports)
BLOOD POTASSIUM INCREASED ( 80 FDA reports)
CARDIAC MURMUR ( 80 FDA reports)
HOSPITALISATION ( 80 FDA reports)
PANIC DISORDER ( 80 FDA reports)
PRURITUS GENERALISED ( 80 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 80 FDA reports)
SENSORY LOSS ( 80 FDA reports)
SUDDEN DEATH ( 79 FDA reports)
TENDONITIS ( 79 FDA reports)
UPPER LIMB FRACTURE ( 79 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 79 FDA reports)
BLOOD BILIRUBIN INCREASED ( 79 FDA reports)
BRAIN OEDEMA ( 79 FDA reports)
FEELING OF DESPAIR ( 79 FDA reports)
PARKINSONISM ( 79 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 78 FDA reports)
DEPENDENCE ( 78 FDA reports)
DIABETIC COMA ( 78 FDA reports)
GASTRIC ULCER ( 78 FDA reports)
INTERSTITIAL LUNG DISEASE ( 78 FDA reports)
PARKINSON'S DISEASE ( 78 FDA reports)
DRUG SCREEN POSITIVE ( 77 FDA reports)
EXCORIATION ( 77 FDA reports)
JAUNDICE ( 77 FDA reports)
DEMENTIA ( 76 FDA reports)
HYDRONEPHROSIS ( 76 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 76 FDA reports)
AGRANULOCYTOSIS ( 75 FDA reports)
LUNG INFECTION ( 75 FDA reports)
NEUTROPHIL COUNT INCREASED ( 75 FDA reports)
PARALYSIS ( 75 FDA reports)
RADICULOPATHY ( 75 FDA reports)
SKIN ULCER ( 75 FDA reports)
RASH GENERALISED ( 74 FDA reports)
VENTRICULAR TACHYCARDIA ( 74 FDA reports)
ANGINA UNSTABLE ( 74 FDA reports)
COLD SWEAT ( 74 FDA reports)
LIBIDO DECREASED ( 74 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 73 FDA reports)
GINGIVAL BLEEDING ( 73 FDA reports)
HYPERTHERMIA ( 73 FDA reports)
INCOHERENT ( 73 FDA reports)
LIP SWELLING ( 73 FDA reports)
MUSCLE ATROPHY ( 73 FDA reports)
SCIATICA ( 73 FDA reports)
RESPIRATORY TRACT INFECTION ( 72 FDA reports)
TACHYPNOEA ( 72 FDA reports)
DEAFNESS ( 72 FDA reports)
EYELID PTOSIS ( 72 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 72 FDA reports)
CAESAREAN SECTION ( 71 FDA reports)
HAEMODIALYSIS ( 71 FDA reports)
MUSCLE TIGHTNESS ( 71 FDA reports)
ABDOMINAL PAIN LOWER ( 70 FDA reports)
CARDIOVASCULAR DISORDER ( 70 FDA reports)
HYPOTHERMIA ( 70 FDA reports)
METABOLIC ACIDOSIS ( 70 FDA reports)
MULTIPLE INJURIES ( 70 FDA reports)
SINUS DISORDER ( 70 FDA reports)
RASH ERYTHEMATOUS ( 69 FDA reports)
RETCHING ( 69 FDA reports)
AFFECT LABILITY ( 69 FDA reports)
FEELING COLD ( 69 FDA reports)
HYPOAESTHESIA ORAL ( 69 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 69 FDA reports)
PNEUMONITIS ( 69 FDA reports)
ANKLE FRACTURE ( 68 FDA reports)
CHOLESTASIS ( 68 FDA reports)
DEVICE RELATED INFECTION ( 68 FDA reports)
PHOTOPHOBIA ( 68 FDA reports)
THROAT IRRITATION ( 68 FDA reports)
RHINITIS ALLERGIC ( 67 FDA reports)
SLUGGISHNESS ( 67 FDA reports)
ULCER ( 67 FDA reports)
CEREBRAL HAEMORRHAGE ( 67 FDA reports)
CHOKING ( 67 FDA reports)
CHOLECYSTITIS ( 67 FDA reports)
COGWHEEL RIGIDITY ( 67 FDA reports)
LOWER LIMB FRACTURE ( 67 FDA reports)
MIOSIS ( 67 FDA reports)
PAROSMIA ( 67 FDA reports)
CHROMATURIA ( 66 FDA reports)
DRUG PRESCRIBING ERROR ( 66 FDA reports)
FAECAL INCONTINENCE ( 66 FDA reports)
ORAL INFECTION ( 66 FDA reports)
PANIC REACTION ( 66 FDA reports)
PLATELET COUNT INCREASED ( 66 FDA reports)
ROTATOR CUFF SYNDROME ( 66 FDA reports)
THYROID DISORDER ( 66 FDA reports)
TOBACCO USER ( 66 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 65 FDA reports)
BACK INJURY ( 65 FDA reports)
HEPATOTOXICITY ( 65 FDA reports)
MENSTRUAL DISORDER ( 65 FDA reports)
METASTASES TO BONE ( 65 FDA reports)
PHARYNGITIS ( 65 FDA reports)
BRADYPHRENIA ( 64 FDA reports)
HYPOMANIA ( 64 FDA reports)
NO THERAPEUTIC RESPONSE ( 64 FDA reports)
NOCTURIA ( 64 FDA reports)
PREMATURE LABOUR ( 64 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 63 FDA reports)
PYELONEPHRITIS ( 63 FDA reports)
RASH MACULO-PAPULAR ( 63 FDA reports)
SOMNAMBULISM ( 63 FDA reports)
SPINAL FRACTURE ( 63 FDA reports)
APNOEA ( 63 FDA reports)
BEDRIDDEN ( 63 FDA reports)
DECUBITUS ULCER ( 63 FDA reports)
DISSOCIATION ( 63 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 63 FDA reports)
EOSINOPHILIA ( 63 FDA reports)
INJECTION SITE REACTION ( 63 FDA reports)
OEDEMA MOUTH ( 63 FDA reports)
ASCITES ( 62 FDA reports)
BACTERIAL INFECTION ( 62 FDA reports)
DRUG LEVEL DECREASED ( 62 FDA reports)
EAR INFECTION ( 62 FDA reports)
FLANK PAIN ( 62 FDA reports)
JOINT SPRAIN ( 62 FDA reports)
LARYNGITIS ( 62 FDA reports)
LOCALISED INFECTION ( 62 FDA reports)
OCULAR HYPERAEMIA ( 62 FDA reports)
POST PROCEDURAL COMPLICATION ( 62 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 62 FDA reports)
SINUS BRADYCARDIA ( 61 FDA reports)
TOXIC SKIN ERUPTION ( 61 FDA reports)
DIFFICULTY IN WALKING ( 61 FDA reports)
ELECTROLYTE IMBALANCE ( 61 FDA reports)
LUNG INFILTRATION ( 61 FDA reports)
MENSTRUATION IRREGULAR ( 61 FDA reports)
METASTASES TO LIVER ( 61 FDA reports)
PARTIAL SEIZURES ( 61 FDA reports)
PHOTOSENSITIVITY REACTION ( 61 FDA reports)
AMENORRHOEA ( 60 FDA reports)
HYPERTHYROIDISM ( 60 FDA reports)
INADEQUATE ANALGESIA ( 60 FDA reports)
INITIAL INSOMNIA ( 60 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 60 FDA reports)
MYOCARDITIS ( 60 FDA reports)
ORAL DISORDER ( 60 FDA reports)
TRANSAMINASES INCREASED ( 60 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 59 FDA reports)
BLADDER DISORDER ( 59 FDA reports)
DRUG ERUPTION ( 59 FDA reports)
FACIAL PAIN ( 59 FDA reports)
HYPOVOLAEMIA ( 59 FDA reports)
JOINT DISLOCATION ( 59 FDA reports)
POLYDIPSIA ( 59 FDA reports)
ACCIDENTAL EXPOSURE ( 58 FDA reports)
DIVERTICULITIS ( 58 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 58 FDA reports)
DRUG TOLERANCE ( 58 FDA reports)
EXOSTOSIS ( 58 FDA reports)
EYE IRRITATION ( 58 FDA reports)
ILEUS PARALYTIC ( 58 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 58 FDA reports)
PETIT MAL EPILEPSY ( 58 FDA reports)
SEXUAL DYSFUNCTION ( 58 FDA reports)
TENDERNESS ( 58 FDA reports)
RASH PAPULAR ( 57 FDA reports)
RENAL PAIN ( 57 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 57 FDA reports)
THYROID NEOPLASM ( 57 FDA reports)
ADVERSE DRUG REACTION ( 57 FDA reports)
ATRIAL SEPTAL DEFECT ( 57 FDA reports)
BLOOD ALBUMIN DECREASED ( 57 FDA reports)
CATATONIA ( 57 FDA reports)
HAND FRACTURE ( 57 FDA reports)
HEAD DISCOMFORT ( 57 FDA reports)
HYPERAESTHESIA ( 57 FDA reports)
HYPOKINESIA ( 57 FDA reports)
LUMBAR SPINAL STENOSIS ( 57 FDA reports)
MELAENA ( 57 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 57 FDA reports)
ALCOHOL USE ( 56 FDA reports)
ALCOHOLISM ( 56 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 56 FDA reports)
FOOT DEFORMITY ( 56 FDA reports)
HEPATOMEGALY ( 56 FDA reports)
NYSTAGMUS ( 56 FDA reports)
PHARYNGEAL OEDEMA ( 56 FDA reports)
POLYNEUROPATHY ( 56 FDA reports)
SINUS CONGESTION ( 56 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 56 FDA reports)
TEARFULNESS ( 56 FDA reports)
VENTRICULAR FIBRILLATION ( 56 FDA reports)
PROCEDURAL PAIN ( 55 FDA reports)
RALES ( 55 FDA reports)
VITAMIN D DEFICIENCY ( 55 FDA reports)
CARDIOGENIC SHOCK ( 55 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 55 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 55 FDA reports)
FRACTURE ( 55 FDA reports)
ISCHAEMIA ( 55 FDA reports)
MASS ( 55 FDA reports)
METABOLIC ENCEPHALOPATHY ( 55 FDA reports)
ABSCESS ( 54 FDA reports)
BREAST PAIN ( 54 FDA reports)
CEREBRAL INFARCTION ( 54 FDA reports)
CHRONIC SINUSITIS ( 54 FDA reports)
CONJUNCTIVITIS ( 54 FDA reports)
DEPERSONALISATION ( 54 FDA reports)
DISCOMFORT ( 54 FDA reports)
LIMB DISCOMFORT ( 54 FDA reports)
LUNG NEOPLASM MALIGNANT ( 54 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 54 FDA reports)
MOTOR DYSFUNCTION ( 54 FDA reports)
PATHOLOGICAL FRACTURE ( 54 FDA reports)
ECCHYMOSIS ( 53 FDA reports)
LACERATION ( 53 FDA reports)
SKIN BURNING SENSATION ( 53 FDA reports)
STOMACH DISCOMFORT ( 52 FDA reports)
THIRST ( 52 FDA reports)
ACUTE RESPIRATORY FAILURE ( 52 FDA reports)
COMPRESSION FRACTURE ( 52 FDA reports)
EXPOSED BONE IN JAW ( 52 FDA reports)
FEELING GUILTY ( 52 FDA reports)
GLOSSODYNIA ( 52 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 52 FDA reports)
JAW DISORDER ( 52 FDA reports)
LABORATORY TEST ABNORMAL ( 52 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 52 FDA reports)
PERSONALITY CHANGE ( 52 FDA reports)
POLYP ( 52 FDA reports)
ANAPHYLACTIC REACTION ( 51 FDA reports)
BIPOLAR I DISORDER ( 51 FDA reports)
BODY TEMPERATURE DECREASED ( 51 FDA reports)
CHOLECYSTECTOMY ( 51 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 51 FDA reports)
MYELODYSPLASTIC SYNDROME ( 51 FDA reports)
MYOPATHY ( 51 FDA reports)
ORAL INTAKE REDUCED ( 51 FDA reports)
PERIPHERAL COLDNESS ( 51 FDA reports)
SENSATION OF HEAVINESS ( 51 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 51 FDA reports)
VAGINAL INFECTION ( 50 FDA reports)
WOUND ( 50 FDA reports)
ABNORMAL SENSATION IN EYE ( 50 FDA reports)
AORTIC ANEURYSM ( 50 FDA reports)
BACTERAEMIA ( 50 FDA reports)
BRONCHOPNEUMONIA ( 50 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 50 FDA reports)
ECZEMA ( 50 FDA reports)
FACE OEDEMA ( 50 FDA reports)
BREAST MASS ( 49 FDA reports)
BRUXISM ( 49 FDA reports)
CYST ( 49 FDA reports)
DIALYSIS ( 49 FDA reports)
DRUG DISPENSING ERROR ( 49 FDA reports)
GENERALISED OEDEMA ( 49 FDA reports)
GOUT ( 49 FDA reports)
INFUSION RELATED REACTION ( 49 FDA reports)
PELVIC PAIN ( 49 FDA reports)
SCOLIOSIS ( 49 FDA reports)
TENSION ( 49 FDA reports)
SKIN LACERATION ( 48 FDA reports)
SPINAL DISORDER ( 48 FDA reports)
SUICIDAL BEHAVIOUR ( 48 FDA reports)
EYE MOVEMENT DISORDER ( 48 FDA reports)
FISTULA ( 48 FDA reports)
GASTROINTESTINAL PAIN ( 48 FDA reports)
GROIN PAIN ( 48 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 48 FDA reports)
OSTEOSCLEROSIS ( 48 FDA reports)
ACCIDENT ( 47 FDA reports)
ACIDOSIS ( 47 FDA reports)
BRADYKINESIA ( 47 FDA reports)
CLUMSINESS ( 47 FDA reports)
ERUCTATION ( 47 FDA reports)
GINGIVAL INFECTION ( 47 FDA reports)
H1N1 INFLUENZA ( 47 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 47 FDA reports)
PERONEAL NERVE PALSY ( 47 FDA reports)
POLYURIA ( 47 FDA reports)
PRESCRIBED OVERDOSE ( 47 FDA reports)
PULSE ABSENT ( 47 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 47 FDA reports)
TOOTH INFECTION ( 47 FDA reports)
TORSADE DE POINTES ( 47 FDA reports)
SYNOVIAL CYST ( 46 FDA reports)
THYROID CANCER ( 46 FDA reports)
BASAL CELL CARCINOMA ( 46 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 46 FDA reports)
HYSTERECTOMY ( 46 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 46 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 46 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 46 FDA reports)
PAIN OF SKIN ( 46 FDA reports)
ACNE ( 45 FDA reports)
BLOOD CHLORIDE DECREASED ( 45 FDA reports)
CERVICOBRACHIAL SYNDROME ( 45 FDA reports)
DYSPHORIA ( 45 FDA reports)
HALLUCINATIONS, MIXED ( 45 FDA reports)
HYPERAMMONAEMIA ( 45 FDA reports)
HYPERPHAGIA ( 45 FDA reports)
KIDNEY INFECTION ( 45 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 45 FDA reports)
SPINAL COMPRESSION FRACTURE ( 45 FDA reports)
PUPIL FIXED ( 44 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 44 FDA reports)
THROAT TIGHTNESS ( 44 FDA reports)
TROPONIN INCREASED ( 44 FDA reports)
UTERINE LEIOMYOMA ( 44 FDA reports)
AFFECTIVE DISORDER ( 44 FDA reports)
AORTIC VALVE INCOMPETENCE ( 44 FDA reports)
BLOOD PRESSURE ABNORMAL ( 44 FDA reports)
CAROTID ARTERY STENOSIS ( 44 FDA reports)
CHOLECYSTITIS ACUTE ( 44 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 44 FDA reports)
FLAT AFFECT ( 44 FDA reports)
GINGIVAL SWELLING ( 44 FDA reports)
HEPATIC CIRRHOSIS ( 44 FDA reports)
HYPERTONIA ( 44 FDA reports)
HYPOACUSIS ( 44 FDA reports)
MASTICATION DISORDER ( 44 FDA reports)
NERVE INJURY ( 44 FDA reports)
NODULE ( 44 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 43 FDA reports)
BONE MARROW FAILURE ( 43 FDA reports)
BRONCHOSPASM ( 43 FDA reports)
BURSITIS ( 43 FDA reports)
CONCUSSION ( 43 FDA reports)
FACIAL BONES FRACTURE ( 43 FDA reports)
HYPERKERATOSIS ( 43 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 43 FDA reports)
MICTURITION URGENCY ( 43 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 43 FDA reports)
PROSTATE CANCER ( 43 FDA reports)
RESPIRATORY RATE INCREASED ( 43 FDA reports)
SELF-MEDICATION ( 43 FDA reports)
SPLENOMEGALY ( 43 FDA reports)
VASCULITIS ( 43 FDA reports)
WRIST FRACTURE ( 43 FDA reports)
SNORING ( 42 FDA reports)
THERAPY NON-RESPONDER ( 42 FDA reports)
THERMAL BURN ( 42 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 42 FDA reports)
WRONG DRUG ADMINISTERED ( 42 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 42 FDA reports)
DEBRIDEMENT ( 42 FDA reports)
GASTROENTERITIS VIRAL ( 42 FDA reports)
HOSTILITY ( 42 FDA reports)
LIBIDO INCREASED ( 42 FDA reports)
PERSECUTORY DELUSION ( 42 FDA reports)
ABDOMINAL HERNIA ( 41 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 41 FDA reports)
CHANGE OF BOWEL HABIT ( 41 FDA reports)
CHEST X-RAY ABNORMAL ( 41 FDA reports)
DEREALISATION ( 41 FDA reports)
GALACTORRHOEA ( 41 FDA reports)
HUNGER ( 41 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 41 FDA reports)
INJECTION SITE PRURITUS ( 41 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 41 FDA reports)
PARAPLEGIA ( 41 FDA reports)
SEQUESTRECTOMY ( 41 FDA reports)
SPUTUM DISCOLOURED ( 41 FDA reports)
TONGUE DISORDER ( 41 FDA reports)
PRIMARY SEQUESTRUM ( 40 FDA reports)
PROTHROMBIN TIME PROLONGED ( 40 FDA reports)
RESPIRATORY ACIDOSIS ( 40 FDA reports)
SOPOR ( 40 FDA reports)
STRESS FRACTURE ( 40 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 40 FDA reports)
VISUAL FIELD DEFECT ( 40 FDA reports)
ASTIGMATISM ( 40 FDA reports)
AZOTAEMIA ( 40 FDA reports)
CEREBRAL ISCHAEMIA ( 40 FDA reports)
CORONARY ARTERY STENOSIS ( 40 FDA reports)
DILATATION VENTRICULAR ( 40 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 40 FDA reports)
FAECES DISCOLOURED ( 40 FDA reports)
FRUSTRATION ( 40 FDA reports)
GOITRE ( 40 FDA reports)
HYPERVENTILATION ( 40 FDA reports)
MUSCULOSKELETAL DISORDER ( 40 FDA reports)
AMMONIA INCREASED ( 39 FDA reports)
BONE LOSS ( 39 FDA reports)
COAGULOPATHY ( 39 FDA reports)
EOSINOPHIL COUNT INCREASED ( 39 FDA reports)
HERNIA ( 39 FDA reports)
IRON DEFICIENCY ANAEMIA ( 39 FDA reports)
LIPASE INCREASED ( 39 FDA reports)
MUSCLE STRAIN ( 39 FDA reports)
NEUROTOXICITY ( 39 FDA reports)
RHINITIS ( 39 FDA reports)
STILLBIRTH ( 39 FDA reports)
TRIGEMINAL NEURALGIA ( 39 FDA reports)
PURPURA ( 38 FDA reports)
PURULENT DISCHARGE ( 38 FDA reports)
TORTICOLLIS ( 38 FDA reports)
URINE OUTPUT DECREASED ( 38 FDA reports)
ANAPHYLACTIC SHOCK ( 38 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 38 FDA reports)
BREAST CANCER FEMALE ( 38 FDA reports)
CATARACT OPERATION ( 38 FDA reports)
HAEMANGIOMA ( 38 FDA reports)
HEMIPLEGIA ( 38 FDA reports)
HEPATIC CYST ( 38 FDA reports)
HEPATIC ENCEPHALOPATHY ( 38 FDA reports)
LACTIC ACIDOSIS ( 38 FDA reports)
LOGORRHOEA ( 38 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 38 FDA reports)
OVARIAN CYST ( 38 FDA reports)
PERIODONTITIS ( 38 FDA reports)
PNEUMOTHORAX ( 38 FDA reports)
APPLICATION SITE ERYTHEMA ( 37 FDA reports)
AREFLEXIA ( 37 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 37 FDA reports)
BLEPHARITIS ( 37 FDA reports)
BLOOD TEST ABNORMAL ( 37 FDA reports)
CARDIAC VALVE DISEASE ( 37 FDA reports)
DISINHIBITION ( 37 FDA reports)
DIVERTICULUM INTESTINAL ( 37 FDA reports)
FACE INJURY ( 37 FDA reports)
FAECALOMA ( 37 FDA reports)
HYPERBILIRUBINAEMIA ( 37 FDA reports)
INJECTION SITE SWELLING ( 37 FDA reports)
INTRA-UTERINE DEATH ( 37 FDA reports)
LACRIMATION INCREASED ( 37 FDA reports)
LIVER INJURY ( 37 FDA reports)
LYMPHOMA ( 37 FDA reports)
MENINGITIS ASEPTIC ( 37 FDA reports)
NEUROPATHY ( 37 FDA reports)
ORTHOPNOEA ( 37 FDA reports)
PHOTOPSIA ( 37 FDA reports)
PROTEIN URINE PRESENT ( 37 FDA reports)
SUBDURAL HAEMATOMA ( 37 FDA reports)
TIC ( 36 FDA reports)
ANGIOEDEMA ( 36 FDA reports)
BODY HEIGHT DECREASED ( 36 FDA reports)
BONE DEBRIDEMENT ( 36 FDA reports)
BONE LESION ( 36 FDA reports)
DECREASED ACTIVITY ( 36 FDA reports)
HEPATITIS ACUTE ( 36 FDA reports)
HYPERREFLEXIA ( 36 FDA reports)
HYPOALBUMINAEMIA ( 36 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 36 FDA reports)
KETOACIDOSIS ( 36 FDA reports)
LISTLESS ( 36 FDA reports)
NICOTINE DEPENDENCE ( 36 FDA reports)
ORAL DISCOMFORT ( 36 FDA reports)
ATRIOVENTRICULAR BLOCK ( 35 FDA reports)
BACK DISORDER ( 35 FDA reports)
BLADDER CANCER ( 35 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 35 FDA reports)
COLON CANCER ( 35 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 35 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 35 FDA reports)
GASTRIC PH DECREASED ( 35 FDA reports)
GINGIVAL DISORDER ( 35 FDA reports)
GUN SHOT WOUND ( 35 FDA reports)
HEPATOCELLULAR DAMAGE ( 35 FDA reports)
HYPOCALCAEMIA ( 35 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 35 FDA reports)
METASTASES TO LUNG ( 35 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 35 FDA reports)
OPTIC NEURITIS ( 35 FDA reports)
OTITIS MEDIA ( 35 FDA reports)
STUPOR ( 35 FDA reports)
PROTEINURIA ( 34 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 34 FDA reports)
SNEEZING ( 34 FDA reports)
SUBSTANCE ABUSE ( 34 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 34 FDA reports)
URINE ODOUR ABNORMAL ( 34 FDA reports)
VENTRICULAR HYPERTROPHY ( 34 FDA reports)
AGORAPHOBIA ( 34 FDA reports)
BLEPHAROSPASM ( 34 FDA reports)
BLOOD CALCIUM INCREASED ( 34 FDA reports)
DERMATITIS ( 34 FDA reports)
EYELID DISORDER ( 34 FDA reports)
FLUID OVERLOAD ( 34 FDA reports)
HEPATIC NECROSIS ( 34 FDA reports)
HYPOPHOSPHATAEMIA ( 34 FDA reports)
HYPOVENTILATION ( 34 FDA reports)
IMPULSIVE BEHAVIOUR ( 34 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 34 FDA reports)
MENORRHAGIA ( 34 FDA reports)
METABOLIC DISORDER ( 34 FDA reports)
MITRAL VALVE PROLAPSE ( 34 FDA reports)
OVERWEIGHT ( 34 FDA reports)
PARAESTHESIA ORAL ( 34 FDA reports)
ADRENAL INSUFFICIENCY ( 33 FDA reports)
ASPHYXIA ( 33 FDA reports)
BONE DENSITY DECREASED ( 33 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 33 FDA reports)
DEPRESSION SUICIDAL ( 33 FDA reports)
DERMAL CYST ( 33 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 33 FDA reports)
ESSENTIAL HYPERTENSION ( 33 FDA reports)
EYELID OEDEMA ( 33 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 33 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 33 FDA reports)
GENERALISED ANXIETY DISORDER ( 33 FDA reports)
GINGIVAL PAIN ( 33 FDA reports)
GYNAECOMASTIA ( 33 FDA reports)
HICCUPS ( 33 FDA reports)
HIP ARTHROPLASTY ( 33 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 33 FDA reports)
KNEE ARTHROPLASTY ( 33 FDA reports)
LOCAL SWELLING ( 33 FDA reports)
NEUROGENIC BLADDER ( 33 FDA reports)
ORAL HERPES ( 33 FDA reports)
PEPTIC ULCER ( 33 FDA reports)
PERIPHERAL ISCHAEMIA ( 33 FDA reports)
PULMONARY FIBROSIS ( 33 FDA reports)
QUALITY OF LIFE DECREASED ( 33 FDA reports)
SKIN PAPILLOMA ( 33 FDA reports)
UROSEPSIS ( 33 FDA reports)
VIITH NERVE PARALYSIS ( 33 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 32 FDA reports)
TACHYPHRENIA ( 32 FDA reports)
TRISMUS ( 32 FDA reports)
ATRIAL TACHYCARDIA ( 32 FDA reports)
BLOOD PH DECREASED ( 32 FDA reports)
COMMUNICATION DISORDER ( 32 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 32 FDA reports)
DEMYELINATION ( 32 FDA reports)
DERMATITIS EXFOLIATIVE ( 32 FDA reports)
EXPIRED DRUG ADMINISTERED ( 32 FDA reports)
FIBROSIS ( 32 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 32 FDA reports)
HAEMOLYTIC ANAEMIA ( 32 FDA reports)
LIGAMENT RUPTURE ( 32 FDA reports)
MEDICATION RESIDUE ( 32 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 32 FDA reports)
NEOPLASM PROGRESSION ( 32 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 32 FDA reports)
OPEN WOUND ( 32 FDA reports)
PERIODONTAL DISEASE ( 32 FDA reports)
POISONING DELIBERATE ( 32 FDA reports)
APHONIA ( 31 FDA reports)
BLOOD AMYLASE INCREASED ( 31 FDA reports)
CONGENITAL ANOMALY ( 31 FDA reports)
DERMATITIS ALLERGIC ( 31 FDA reports)
ESCHERICHIA INFECTION ( 31 FDA reports)
FEMORAL NECK FRACTURE ( 31 FDA reports)
GRIP STRENGTH DECREASED ( 31 FDA reports)
INJECTION SITE NODULE ( 31 FDA reports)
ISCHAEMIC STROKE ( 31 FDA reports)
JAW OPERATION ( 31 FDA reports)
LABILE BLOOD PRESSURE ( 31 FDA reports)
LOBAR PNEUMONIA ( 31 FDA reports)
LYMPHOEDEMA ( 31 FDA reports)
METABOLIC SYNDROME ( 31 FDA reports)
MULTIPLE FRACTURES ( 31 FDA reports)
MUSCLE SPASTICITY ( 31 FDA reports)
NECK MASS ( 31 FDA reports)
NON-CARDIAC CHEST PAIN ( 31 FDA reports)
PSEUDOMONAS INFECTION ( 31 FDA reports)
RASH PUSTULAR ( 31 FDA reports)
RESPIRATORY RATE DECREASED ( 31 FDA reports)
SELF-INJURIOUS IDEATION ( 31 FDA reports)
SKIN HYPERTROPHY ( 31 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 31 FDA reports)
UNDERDOSE ( 31 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 31 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 30 FDA reports)
SARCOIDOSIS ( 30 FDA reports)
SCAB ( 30 FDA reports)
SCREAMING ( 30 FDA reports)
SEBORRHOEIC DERMATITIS ( 30 FDA reports)
SKIN REACTION ( 30 FDA reports)
SLEEP TALKING ( 30 FDA reports)
SOCIAL PROBLEM ( 30 FDA reports)
TOXIC ENCEPHALOPATHY ( 30 FDA reports)
WALKING AID USER ( 30 FDA reports)
WOUND INFECTION ( 30 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 30 FDA reports)
ANXIETY DISORDER ( 30 FDA reports)
ATRIAL FLUTTER ( 30 FDA reports)
BILIARY COLIC ( 30 FDA reports)
BLINDNESS TRANSIENT ( 30 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 30 FDA reports)
BLOOD DISORDER ( 30 FDA reports)
BRAIN DEATH ( 30 FDA reports)
BRAIN INJURY ( 30 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 30 FDA reports)
CLOSTRIDIAL INFECTION ( 30 FDA reports)
COMPLEX PARTIAL SEIZURES ( 30 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 30 FDA reports)
DUODENAL ULCER ( 30 FDA reports)
GUILLAIN-BARRE SYNDROME ( 30 FDA reports)
HERPES SIMPLEX ( 30 FDA reports)
HYDROCEPHALUS ( 30 FDA reports)
HYPERCALCAEMIA ( 30 FDA reports)
HYPERMETROPIA ( 30 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 30 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 30 FDA reports)
NECK INJURY ( 30 FDA reports)
NEOPLASM ( 30 FDA reports)
NEUROMYOPATHY ( 30 FDA reports)
PERICARDITIS ( 30 FDA reports)
PHLEBITIS ( 30 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 30 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 29 FDA reports)
BILE DUCT OBSTRUCTION ( 29 FDA reports)
BLOOD BICARBONATE DECREASED ( 29 FDA reports)
BONE NEOPLASM MALIGNANT ( 29 FDA reports)
CHEILITIS ( 29 FDA reports)
CREPITATIONS ( 29 FDA reports)
DIABETIC NEPHROPATHY ( 29 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 29 FDA reports)
ENURESIS ( 29 FDA reports)
EXTRASYSTOLES ( 29 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 29 FDA reports)
LIGAMENT SPRAIN ( 29 FDA reports)
LOSS OF EMPLOYMENT ( 29 FDA reports)
MEDICAL DEVICE COMPLICATION ( 29 FDA reports)
NARCOLEPSY ( 29 FDA reports)
PERSONALITY DISORDER ( 29 FDA reports)
PETECHIAE ( 29 FDA reports)
PHYSICAL ASSAULT ( 29 FDA reports)
RESPIRATORY TRACT CONGESTION ( 29 FDA reports)
SENSITIVITY OF TEETH ( 29 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 29 FDA reports)
WEIGHT FLUCTUATION ( 29 FDA reports)
RENAL COLIC ( 28 FDA reports)
TRAUMATIC BRAIN INJURY ( 28 FDA reports)
ABSCESS JAW ( 28 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 28 FDA reports)
APPLICATION SITE IRRITATION ( 28 FDA reports)
APPLICATION SITE RASH ( 28 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 28 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 28 FDA reports)
BILIARY DYSKINESIA ( 28 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 28 FDA reports)
BLOOD SODIUM INCREASED ( 28 FDA reports)
BONE SCAN ABNORMAL ( 28 FDA reports)
BOWEN'S DISEASE ( 28 FDA reports)
DIABETIC RETINOPATHY ( 28 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 28 FDA reports)
DYSPHEMIA ( 28 FDA reports)
GINGIVITIS ( 28 FDA reports)
HEPATITIS FULMINANT ( 28 FDA reports)
HYDROPS FOETALIS ( 28 FDA reports)
HYPERKINESIA ( 28 FDA reports)
HYPERNATRAEMIA ( 28 FDA reports)
HYPERPROLACTINAEMIA ( 28 FDA reports)
LIFE SUPPORT ( 28 FDA reports)
METASTASES TO SPINE ( 28 FDA reports)
NEURITIS ( 28 FDA reports)
OBSESSIVE THOUGHTS ( 28 FDA reports)
ABORTION INDUCED ( 27 FDA reports)
ACUTE SINUSITIS ( 27 FDA reports)
ANOXIC ENCEPHALOPATHY ( 27 FDA reports)
ANURIA ( 27 FDA reports)
APHAGIA ( 27 FDA reports)
APPLICATION SITE PRURITUS ( 27 FDA reports)
BILIARY TRACT DISORDER ( 27 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 27 FDA reports)
BLOOD MAGNESIUM DECREASED ( 27 FDA reports)
BLOOD PROLACTIN INCREASED ( 27 FDA reports)
CEREBRAL DISORDER ( 27 FDA reports)
CONVERSION DISORDER ( 27 FDA reports)
DYSGRAPHIA ( 27 FDA reports)
EAR DISCOMFORT ( 27 FDA reports)
ENDOMETRIOSIS ( 27 FDA reports)
ENTEROCOCCAL INFECTION ( 27 FDA reports)
EYE HAEMORRHAGE ( 27 FDA reports)
HEARING IMPAIRED ( 27 FDA reports)
HYPERTENSIVE CRISIS ( 27 FDA reports)
INJECTION SITE IRRITATION ( 27 FDA reports)
INTESTINAL ISCHAEMIA ( 27 FDA reports)
JOINT STIFFNESS ( 27 FDA reports)
LABYRINTHITIS ( 27 FDA reports)
MYOSITIS ( 27 FDA reports)
OESOPHAGEAL DISORDER ( 27 FDA reports)
OSTEORADIONECROSIS ( 27 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 27 FDA reports)
PLASMACYTOSIS ( 27 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 27 FDA reports)
SELF ESTEEM DECREASED ( 27 FDA reports)
SENSATION OF PRESSURE ( 27 FDA reports)
SKIN INDURATION ( 27 FDA reports)
SKIN IRRITATION ( 27 FDA reports)
SKIN TIGHTNESS ( 27 FDA reports)
STENT PLACEMENT ( 27 FDA reports)
PRODUCT ADHESION ISSUE ( 26 FDA reports)
PROTEIN TOTAL DECREASED ( 26 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 26 FDA reports)
RENAL TUBULAR NECROSIS ( 26 FDA reports)
SEASONAL ALLERGY ( 26 FDA reports)
SPINAL FUSION SURGERY ( 26 FDA reports)
SPINAL HAEMANGIOMA ( 26 FDA reports)
TEMPERATURE INTOLERANCE ( 26 FDA reports)
ABORTION ( 26 FDA reports)
ACCIDENTAL DEATH ( 26 FDA reports)
ACUTE CORONARY SYNDROME ( 26 FDA reports)
ANIMAL BITE ( 26 FDA reports)
BACTERIAL SEPSIS ( 26 FDA reports)
CARDIAC FLUTTER ( 26 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 26 FDA reports)
DENTAL OPERATION ( 26 FDA reports)
DERMATITIS BULLOUS ( 26 FDA reports)
DIABETIC COMPLICATION ( 26 FDA reports)
DILATATION ATRIAL ( 26 FDA reports)
EOSINOPHIL COUNT DECREASED ( 26 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 26 FDA reports)
IMMUNODEFICIENCY ( 26 FDA reports)
INJECTION SITE MASS ( 26 FDA reports)
MENISCUS LESION ( 26 FDA reports)
MOUTH HAEMORRHAGE ( 26 FDA reports)
OPEN REDUCTION OF FRACTURE ( 26 FDA reports)
OPTIC NERVE CUPPING ( 26 FDA reports)
PLEURISY ( 26 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 25 FDA reports)
BLOOD IRON DECREASED ( 25 FDA reports)
BONE FRAGMENTATION ( 25 FDA reports)
BREAST CANCER METASTATIC ( 25 FDA reports)
BREATH ODOUR ( 25 FDA reports)
BRONCHITIS CHRONIC ( 25 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 25 FDA reports)
ENCEPHALITIS ( 25 FDA reports)
EXERCISE TOLERANCE DECREASED ( 25 FDA reports)
EYE NAEVUS ( 25 FDA reports)
GASTRIC HAEMORRHAGE ( 25 FDA reports)
HYPERACUSIS ( 25 FDA reports)
LARYNGEAL OEDEMA ( 25 FDA reports)
LEG AMPUTATION ( 25 FDA reports)
MONOCYTE COUNT INCREASED ( 25 FDA reports)
MULTIPLE ALLERGIES ( 25 FDA reports)
MYELOMA RECURRENCE ( 25 FDA reports)
NEPHROPATHY ( 25 FDA reports)
OSTEOLYSIS ( 25 FDA reports)
PANCREATITIS CHRONIC ( 25 FDA reports)
PROCTALGIA ( 25 FDA reports)
PROSTATOMEGALY ( 25 FDA reports)
SENSATION OF FOREIGN BODY ( 25 FDA reports)
SINUS HEADACHE ( 25 FDA reports)
SPINAL CORD COMPRESSION ( 25 FDA reports)
SPUTUM CULTURE POSITIVE ( 25 FDA reports)
STRESS URINARY INCONTINENCE ( 25 FDA reports)
VESICAL FISTULA ( 25 FDA reports)
POSTURE ABNORMAL ( 24 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 24 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 24 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 24 FDA reports)
TALIPES ( 24 FDA reports)
VAGINAL DISCHARGE ( 24 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 24 FDA reports)
APPARENT DEATH ( 24 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 24 FDA reports)
BREAST TENDERNESS ( 24 FDA reports)
COSTOCHONDRITIS ( 24 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 24 FDA reports)
ENDODONTIC PROCEDURE ( 24 FDA reports)
FIBRIN D DIMER INCREASED ( 24 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 24 FDA reports)
GENERALISED ERYTHEMA ( 24 FDA reports)
HAEMODYNAMIC INSTABILITY ( 24 FDA reports)
HEPATIC LESION ( 24 FDA reports)
HUMERUS FRACTURE ( 24 FDA reports)
HYPERPARATHYROIDISM ( 24 FDA reports)
HYPOAESTHESIA FACIAL ( 24 FDA reports)
IMMUNE SYSTEM DISORDER ( 24 FDA reports)
NAIL DISORDER ( 24 FDA reports)
NERVE COMPRESSION ( 24 FDA reports)
NEUROLOGICAL SYMPTOM ( 24 FDA reports)
OCULOGYRIC CRISIS ( 24 FDA reports)
OSTEITIS ( 24 FDA reports)
PLEURITIC PAIN ( 24 FDA reports)
POLYDACTYLY ( 24 FDA reports)
POLYSUBSTANCE ABUSE ( 24 FDA reports)
BLADDER PAIN ( 23 FDA reports)
BLOOD LACTIC ACID INCREASED ( 23 FDA reports)
BLOOD UREA DECREASED ( 23 FDA reports)
CARDIOPULMONARY FAILURE ( 23 FDA reports)
CEREBROVASCULAR DISORDER ( 23 FDA reports)
COELIAC DISEASE ( 23 FDA reports)
CULTURE URINE POSITIVE ( 23 FDA reports)
DENTAL FISTULA ( 23 FDA reports)
DEPRESSIVE SYMPTOM ( 23 FDA reports)
HAND DEFORMITY ( 23 FDA reports)
HERPES VIRUS INFECTION ( 23 FDA reports)
HYPERCAPNIA ( 23 FDA reports)
INGROWING NAIL ( 23 FDA reports)
INJECTION SITE INDURATION ( 23 FDA reports)
LUMBAR RADICULOPATHY ( 23 FDA reports)
MELANOCYTIC NAEVUS ( 23 FDA reports)
NASAL DISCOMFORT ( 23 FDA reports)
ONYCHOMYCOSIS ( 23 FDA reports)
PLANTAR FASCIITIS ( 23 FDA reports)
PSYCHOMOTOR RETARDATION ( 23 FDA reports)
RENAL INJURY ( 23 FDA reports)
RETINOPATHY ( 23 FDA reports)
THERAPY CESSATION ( 23 FDA reports)
TONGUE DISCOLOURATION ( 23 FDA reports)
VITAMIN D DECREASED ( 23 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 23 FDA reports)
RAYNAUD'S PHENOMENON ( 22 FDA reports)
RESORPTION BONE INCREASED ( 22 FDA reports)
SHOULDER PAIN ( 22 FDA reports)
STREPTOCOCCAL INFECTION ( 22 FDA reports)
STRESS SYMPTOMS ( 22 FDA reports)
TENDON RUPTURE ( 22 FDA reports)
TONGUE BITING ( 22 FDA reports)
ABDOMINAL TENDERNESS ( 22 FDA reports)
APPENDICITIS ( 22 FDA reports)
BARRETT'S OESOPHAGUS ( 22 FDA reports)
BLINDNESS UNILATERAL ( 22 FDA reports)
BRAIN NEOPLASM ( 22 FDA reports)
BREAST CANCER IN SITU ( 22 FDA reports)
CERVICAL DYSPLASIA ( 22 FDA reports)
CERVICAL SPINAL STENOSIS ( 22 FDA reports)
DIABETIC FOOT ( 22 FDA reports)
DIZZINESS POSTURAL ( 22 FDA reports)
FACIAL PALSY ( 22 FDA reports)
FAMILY STRESS ( 22 FDA reports)
FOOD CRAVING ( 22 FDA reports)
GALLBLADDER OPERATION ( 22 FDA reports)
GRAFT VERSUS HOST DISEASE ( 22 FDA reports)
HEPATITIS CHOLESTATIC ( 22 FDA reports)
INCREASED TENDENCY TO BRUISE ( 22 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 22 FDA reports)
MEGACOLON ( 22 FDA reports)
MENINGIOMA ( 22 FDA reports)
PARKINSONIAN GAIT ( 22 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 22 FDA reports)
ACTINOMYCOSIS ( 21 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 21 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 21 FDA reports)
BREAST CANCER RECURRENT ( 21 FDA reports)
DEAFNESS UNILATERAL ( 21 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 21 FDA reports)
DRUG RESISTANCE ( 21 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 21 FDA reports)
ENTEROCOLITIS ( 21 FDA reports)
EYE DISCHARGE ( 21 FDA reports)
GASTRIC POLYPS ( 21 FDA reports)
GASTROINTESTINAL CARCINOMA ( 21 FDA reports)
INJECTION SITE RASH ( 21 FDA reports)
JOINT CONTRACTURE ( 21 FDA reports)
LACUNAR INFARCTION ( 21 FDA reports)
LIP HAEMORRHAGE ( 21 FDA reports)
LOSS OF LIBIDO ( 21 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 21 FDA reports)
MENOPAUSE ( 21 FDA reports)
MONOCLONAL GAMMOPATHY ( 21 FDA reports)
MONOCYTE COUNT DECREASED ( 21 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 21 FDA reports)
MUSCLE CONTRACTURE ( 21 FDA reports)
MUTISM ( 21 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 21 FDA reports)
NASAL SEPTUM DEVIATION ( 21 FDA reports)
NODAL RHYTHM ( 21 FDA reports)
POSTNASAL DRIP ( 21 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 21 FDA reports)
PULMONARY THROMBOSIS ( 21 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 21 FDA reports)
SPONDYLOLISTHESIS ( 21 FDA reports)
TENDON DISORDER ( 21 FDA reports)
TOBACCO ABUSE ( 21 FDA reports)
TOOTH INJURY ( 21 FDA reports)
UMBILICAL HERNIA ( 21 FDA reports)
VARICOSE VEIN ( 21 FDA reports)
VITREOUS FLOATERS ( 21 FDA reports)
REFLUX OESOPHAGITIS ( 20 FDA reports)
ROSACEA ( 20 FDA reports)
SCLERODERMA ( 20 FDA reports)
SECRETION DISCHARGE ( 20 FDA reports)
SKIN INFECTION ( 20 FDA reports)
SYNCOPE VASOVAGAL ( 20 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 20 FDA reports)
TOE AMPUTATION ( 20 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 20 FDA reports)
URINARY HESITATION ( 20 FDA reports)
URINARY TRACT DISORDER ( 20 FDA reports)
VERTIGO POSITIONAL ( 20 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 20 FDA reports)
APLASIA PURE RED CELL ( 20 FDA reports)
APPLICATION SITE REACTION ( 20 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 20 FDA reports)
BRUGADA SYNDROME ( 20 FDA reports)
BUNION ( 20 FDA reports)
CAROTID ARTERY DISEASE ( 20 FDA reports)
CAROTID ARTERY OCCLUSION ( 20 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 20 FDA reports)
COMPULSIVE SHOPPING ( 20 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 20 FDA reports)
CYSTITIS HAEMORRHAGIC ( 20 FDA reports)
DENTURE WEARER ( 20 FDA reports)
DEVICE FAILURE ( 20 FDA reports)
EAR DISORDER ( 20 FDA reports)
FAILURE TO THRIVE ( 20 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 20 FDA reports)
GINGIVAL EROSION ( 20 FDA reports)
HYPERAMYLASAEMIA ( 20 FDA reports)
HYPOMAGNESAEMIA ( 20 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 20 FDA reports)
INFARCTION ( 20 FDA reports)
INGUINAL HERNIA ( 20 FDA reports)
KYPHOSIS ( 20 FDA reports)
LIP DISORDER ( 20 FDA reports)
METRORRHAGIA ( 20 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 20 FDA reports)
MYOCLONIC EPILEPSY ( 20 FDA reports)
OLIGURIA ( 20 FDA reports)
PAINFUL RESPIRATION ( 20 FDA reports)
PATELLA FRACTURE ( 20 FDA reports)
PERIORBITAL OEDEMA ( 20 FDA reports)
PHOBIA ( 20 FDA reports)
PO2 DECREASED ( 20 FDA reports)
POLYCYSTIC OVARIES ( 20 FDA reports)
POLYTRAUMATISM ( 20 FDA reports)
ABDOMINAL MASS ( 19 FDA reports)
ABSCESS LIMB ( 19 FDA reports)
ACCIDENTAL POISONING ( 19 FDA reports)
ACROCHORDON ( 19 FDA reports)
ALCOHOL POISONING ( 19 FDA reports)
ANORGASMIA ( 19 FDA reports)
ARTHROPOD BITE ( 19 FDA reports)
ASTERIXIS ( 19 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 19 FDA reports)
BREATH SOUNDS ABNORMAL ( 19 FDA reports)
CALCINOSIS ( 19 FDA reports)
DERMATITIS CONTACT ( 19 FDA reports)
DETOXIFICATION ( 19 FDA reports)
EAR HAEMORRHAGE ( 19 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 19 FDA reports)
EROSIVE OESOPHAGITIS ( 19 FDA reports)
GLOSSITIS ( 19 FDA reports)
HAEMOTHORAX ( 19 FDA reports)
HANGOVER ( 19 FDA reports)
HEPATOSPLENOMEGALY ( 19 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 19 FDA reports)
INJECTION SITE URTICARIA ( 19 FDA reports)
INTRACRANIAL ANEURYSM ( 19 FDA reports)
JUDGEMENT IMPAIRED ( 19 FDA reports)
MALABSORPTION ( 19 FDA reports)
MONOPLEGIA ( 19 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 19 FDA reports)
OCULAR ICTERUS ( 19 FDA reports)
ORAL CAVITY FISTULA ( 19 FDA reports)
ORTHOPEDIC PROCEDURE ( 19 FDA reports)
OTITIS EXTERNA ( 19 FDA reports)
PERIORBITAL HAEMATOMA ( 19 FDA reports)
PERITONITIS ( 19 FDA reports)
SKIN EROSION ( 19 FDA reports)
SKIN WARM ( 19 FDA reports)
TENDON INJURY ( 19 FDA reports)
THERAPY REGIMEN CHANGED ( 19 FDA reports)
TONGUE PARALYSIS ( 19 FDA reports)
UTERINE CANCER ( 19 FDA reports)
VENTRICULAR HYPOKINESIA ( 19 FDA reports)
POSTICTAL STATE ( 18 FDA reports)
PROCEDURAL COMPLICATION ( 18 FDA reports)
PROSTATIC DISORDER ( 18 FDA reports)
ROTATOR CUFF REPAIR ( 18 FDA reports)
SKIN PLAQUE ( 18 FDA reports)
THOUGHT BLOCKING ( 18 FDA reports)
TIBIA FRACTURE ( 18 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 18 FDA reports)
TUBERCULOSIS ( 18 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 18 FDA reports)
VITAMIN B12 DEFICIENCY ( 18 FDA reports)
ABNORMAL FAECES ( 18 FDA reports)
ACUTE PULMONARY OEDEMA ( 18 FDA reports)
ALCOHOL ABUSE ( 18 FDA reports)
ANAL HAEMORRHAGE ( 18 FDA reports)
ANGIOPATHY ( 18 FDA reports)
BENIGN COLONIC NEOPLASM ( 18 FDA reports)
BILIARY DILATATION ( 18 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 18 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 18 FDA reports)
BRADYPNOEA ( 18 FDA reports)
CEREBELLAR SYNDROME ( 18 FDA reports)
DEVELOPMENTAL DELAY ( 18 FDA reports)
DEVICE BREAKAGE ( 18 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 18 FDA reports)
EPIGASTRIC DISCOMFORT ( 18 FDA reports)
ERYSIPELAS ( 18 FDA reports)
FIBULA FRACTURE ( 18 FDA reports)
FOOD AVERSION ( 18 FDA reports)
GAMMOPATHY ( 18 FDA reports)
GLYCOSURIA ( 18 FDA reports)
GRAVITATIONAL OEDEMA ( 18 FDA reports)
GRIMACING ( 18 FDA reports)
HOMICIDE ( 18 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 18 FDA reports)
HYPOVOLAEMIC SHOCK ( 18 FDA reports)
INJECTION SITE WARMTH ( 18 FDA reports)
KNEE OPERATION ( 18 FDA reports)
LYMPHOPENIA ( 18 FDA reports)
MUSCLE CRAMP ( 18 FDA reports)
MUSCLE RUPTURE ( 18 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 18 FDA reports)
PANCREATIC DISORDER ( 18 FDA reports)
PARAPARESIS ( 18 FDA reports)
PARESIS ( 18 FDA reports)
ADHESION ( 17 FDA reports)
ALVEOLITIS ( 17 FDA reports)
ANGIONEUROTIC OEDEMA ( 17 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 17 FDA reports)
BREAST ABSCESS ( 17 FDA reports)
BREAST CALCIFICATIONS ( 17 FDA reports)
BREAST CYST ( 17 FDA reports)
CLAUSTROPHOBIA ( 17 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 17 FDA reports)
DEVICE MALFUNCTION ( 17 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 17 FDA reports)
DYSTHYMIC DISORDER ( 17 FDA reports)
ENGRAFTMENT SYNDROME ( 17 FDA reports)
FOOD ALLERGY ( 17 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 17 FDA reports)
GALLBLADDER INJURY ( 17 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 17 FDA reports)
GINGIVAL RECESSION ( 17 FDA reports)
HEART DISEASE CONGENITAL ( 17 FDA reports)
HEAT STROKE ( 17 FDA reports)
HEPATIC PAIN ( 17 FDA reports)
HERNIA REPAIR ( 17 FDA reports)
HYPERSEXUALITY ( 17 FDA reports)
IMPAIRED SELF-CARE ( 17 FDA reports)
INTRAOCULAR LENS IMPLANT ( 17 FDA reports)
JAW FRACTURE ( 17 FDA reports)
LEUKAEMIA ( 17 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 17 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 17 FDA reports)
ODYNOPHAGIA ( 17 FDA reports)
OESOPHAGEAL ULCER ( 17 FDA reports)
PANCREATIC CYST ( 17 FDA reports)
PANCREATIC PSEUDOCYST ( 17 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 17 FDA reports)
PRIAPISM ( 17 FDA reports)
PURULENCE ( 17 FDA reports)
RADICULITIS LUMBOSACRAL ( 17 FDA reports)
RIGHT VENTRICULAR FAILURE ( 17 FDA reports)
SKIN CANCER ( 17 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 17 FDA reports)
WHEELCHAIR USER ( 17 FDA reports)
YELLOW SKIN ( 17 FDA reports)
PRESBYOPIA ( 16 FDA reports)
PROSTATITIS ( 16 FDA reports)
PYELONEPHRITIS ACUTE ( 16 FDA reports)
RADIATION INJURY ( 16 FDA reports)
RADIUS FRACTURE ( 16 FDA reports)
SERUM FERRITIN INCREASED ( 16 FDA reports)
SKELETAL INJURY ( 16 FDA reports)
SKIN HYPERPIGMENTATION ( 16 FDA reports)
SKIN OEDEMA ( 16 FDA reports)
SUDDEN CARDIAC DEATH ( 16 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 16 FDA reports)
ULCER HAEMORRHAGE ( 16 FDA reports)
URINE COLOUR ABNORMAL ( 16 FDA reports)
VARICES OESOPHAGEAL ( 16 FDA reports)
WOUND SECRETION ( 16 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 16 FDA reports)
AGEUSIA ( 16 FDA reports)
ANEURYSM ( 16 FDA reports)
APHTHOUS STOMATITIS ( 16 FDA reports)
APLASTIC ANAEMIA ( 16 FDA reports)
ATONIC SEIZURES ( 16 FDA reports)
BASEDOW'S DISEASE ( 16 FDA reports)
BLADDER SPASM ( 16 FDA reports)
BLOOD CHLORIDE INCREASED ( 16 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 16 FDA reports)
BRAIN HERNIATION ( 16 FDA reports)
BREAST ENLARGEMENT ( 16 FDA reports)
CALCULUS BLADDER ( 16 FDA reports)
CLEFT LIP AND PALATE ( 16 FDA reports)
CLONUS ( 16 FDA reports)
COLITIS ISCHAEMIC ( 16 FDA reports)
DENTAL CARE ( 16 FDA reports)
DISSOCIATIVE DISORDER ( 16 FDA reports)
EJACULATION DISORDER ( 16 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 16 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 16 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 16 FDA reports)
EMBOLISM ( 16 FDA reports)
ENCEPHALITIS HERPES ( 16 FDA reports)
FACET JOINT SYNDROME ( 16 FDA reports)
FURUNCLE ( 16 FDA reports)
GASTRIC BYPASS ( 16 FDA reports)
GASTROINTESTINAL NECROSIS ( 16 FDA reports)
GESTATIONAL DIABETES ( 16 FDA reports)
GRANULOMA ( 16 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 16 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 16 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 16 FDA reports)
HYPOPNOEA ( 16 FDA reports)
INAPPROPRIATE AFFECT ( 16 FDA reports)
JUGULAR VEIN THROMBOSIS ( 16 FDA reports)
KLEBSIELLA INFECTION ( 16 FDA reports)
MACULAR DEGENERATION ( 16 FDA reports)
MARITAL PROBLEM ( 16 FDA reports)
MICROCYTIC ANAEMIA ( 16 FDA reports)
ORAL MUCOSA EROSION ( 16 FDA reports)
PAROTID GLAND ENLARGEMENT ( 16 FDA reports)
PELVIC FRACTURE ( 16 FDA reports)
PENIS DISORDER ( 16 FDA reports)
PNEUMONIA BACTERIAL ( 16 FDA reports)
POOR PERIPHERAL CIRCULATION ( 16 FDA reports)
ASTEATOSIS ( 15 FDA reports)
ASTHENOPIA ( 15 FDA reports)
BLOOD CREATINE INCREASED ( 15 FDA reports)
BLOOD CULTURE POSITIVE ( 15 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 15 FDA reports)
BLOOD URINE ( 15 FDA reports)
BRAIN DAMAGE ( 15 FDA reports)
CACHEXIA ( 15 FDA reports)
CARDIAC FAILURE CHRONIC ( 15 FDA reports)
CARDIOTOXICITY ( 15 FDA reports)
CAROTID BRUIT ( 15 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 15 FDA reports)
COLLAPSE OF LUNG ( 15 FDA reports)
DRY THROAT ( 15 FDA reports)
DUODENITIS ( 15 FDA reports)
EDENTULOUS ( 15 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 15 FDA reports)
FEBRILE BONE MARROW APLASIA ( 15 FDA reports)
FLIGHT OF IDEAS ( 15 FDA reports)
FLUID INTAKE REDUCED ( 15 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 15 FDA reports)
GAMBLING ( 15 FDA reports)
GASTROINTESTINAL INFECTION ( 15 FDA reports)
GLOBULINS INCREASED ( 15 FDA reports)
HAEMORRHAGIC ANAEMIA ( 15 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 15 FDA reports)
HEAD TITUBATION ( 15 FDA reports)
HEPATITIS TOXIC ( 15 FDA reports)
HEPATOCELLULAR INJURY ( 15 FDA reports)
KELOID SCAR ( 15 FDA reports)
LIP OEDEMA ( 15 FDA reports)
LYMPHOCYTOSIS ( 15 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 15 FDA reports)
NO ADVERSE EVENT ( 15 FDA reports)
OROPHARYNGEAL BLISTERING ( 15 FDA reports)
PCO2 DECREASED ( 15 FDA reports)
PERFORMANCE STATUS DECREASED ( 15 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 15 FDA reports)
PLEURAL FIBROSIS ( 15 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 15 FDA reports)
POTENTIATING DRUG INTERACTION ( 15 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 15 FDA reports)
RASH MORBILLIFORM ( 15 FDA reports)
RENAL CANCER ( 15 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 15 FDA reports)
SUDDEN ONSET OF SLEEP ( 15 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 15 FDA reports)
TREATMENT FAILURE ( 15 FDA reports)
URGE INCONTINENCE ( 15 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 15 FDA reports)
URINOMA ( 15 FDA reports)
VOLVULUS ( 15 FDA reports)
VOMITING PROJECTILE ( 15 FDA reports)
WEIGHT LOSS POOR ( 15 FDA reports)
WOUND COMPLICATION ( 15 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 14 FDA reports)
PREMENSTRUAL SYNDROME ( 14 FDA reports)
PROSTATE CANCER METASTATIC ( 14 FDA reports)
PSORIATIC ARTHROPATHY ( 14 FDA reports)
PULMONARY INFARCTION ( 14 FDA reports)
RADIOTHERAPY ( 14 FDA reports)
RECTAL PROLAPSE ( 14 FDA reports)
RETROGNATHIA ( 14 FDA reports)
SCOTOMA ( 14 FDA reports)
SINUS POLYP ( 14 FDA reports)
SJOGREN'S SYNDROME ( 14 FDA reports)
SKIN NECROSIS ( 14 FDA reports)
SLEEP TERROR ( 14 FDA reports)
SOCIAL PHOBIA ( 14 FDA reports)
SQUAMOUS CELL CARCINOMA ( 14 FDA reports)
TONGUE BLISTERING ( 14 FDA reports)
TOOTH REPAIR ( 14 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 14 FDA reports)
VENOOCCLUSIVE DISEASE ( 14 FDA reports)
VENTRICULAR ARRHYTHMIA ( 14 FDA reports)
AKINESIA ( 14 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 14 FDA reports)
ANAEMIA MACROCYTIC ( 14 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 14 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 14 FDA reports)
ATROPHY ( 14 FDA reports)
AURA ( 14 FDA reports)
BLADDER CANCER RECURRENT ( 14 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 14 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 14 FDA reports)
BOWEL SOUNDS ABNORMAL ( 14 FDA reports)
BREAST OPERATION ( 14 FDA reports)
CARDIAC TAMPONADE ( 14 FDA reports)
CEREBRAL THROMBOSIS ( 14 FDA reports)
CHOREOATHETOSIS ( 14 FDA reports)
CLOSTRIDIUM COLITIS ( 14 FDA reports)
COLITIS ULCERATIVE ( 14 FDA reports)
CONDUCTION DISORDER ( 14 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 14 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 14 FDA reports)
CULTURE POSITIVE ( 14 FDA reports)
DYSHIDROSIS ( 14 FDA reports)
DYSPHASIA ( 14 FDA reports)
EPICONDYLITIS ( 14 FDA reports)
EYE PRURITUS ( 14 FDA reports)
FOOD INTOLERANCE ( 14 FDA reports)
FOOD POISONING ( 14 FDA reports)
GASTRITIS HAEMORRHAGIC ( 14 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 14 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 14 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 14 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 14 FDA reports)
HAIR TEXTURE ABNORMAL ( 14 FDA reports)
HEPATIC NEOPLASM ( 14 FDA reports)
HEPATITIS B ( 14 FDA reports)
HEPATORENAL SYNDROME ( 14 FDA reports)
HORDEOLUM ( 14 FDA reports)
HYPOGONADISM ( 14 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 14 FDA reports)
ILLUSION ( 14 FDA reports)
IMMUNOSUPPRESSION ( 14 FDA reports)
IMPATIENCE ( 14 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 14 FDA reports)
LEUKODYSTROPHY ( 14 FDA reports)
MASTECTOMY ( 14 FDA reports)
MORBID THOUGHTS ( 14 FDA reports)
MUSCLE HAEMORRHAGE ( 14 FDA reports)
NEONATAL DISORDER ( 14 FDA reports)
NOSOCOMIAL INFECTION ( 14 FDA reports)
OCCULT BLOOD POSITIVE ( 14 FDA reports)
OESOPHAGEAL PAIN ( 14 FDA reports)
PAPILLOEDEMA ( 14 FDA reports)
PCO2 INCREASED ( 14 FDA reports)
PERITONITIS BACTERIAL ( 14 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 14 FDA reports)
PORTAL HYPERTENSION ( 14 FDA reports)
ACUTE HEPATIC FAILURE ( 13 FDA reports)
AORTIC STENOSIS ( 13 FDA reports)
APPENDICECTOMY ( 13 FDA reports)
ATHEROSCLEROSIS ( 13 FDA reports)
ATROPHIC VULVOVAGINITIS ( 13 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 13 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 13 FDA reports)
BRAIN OPERATION ( 13 FDA reports)
BRONCHITIS ACUTE ( 13 FDA reports)
BULBAR PALSY ( 13 FDA reports)
CARDIAC ENZYMES INCREASED ( 13 FDA reports)
CARDIAC FAILURE ACUTE ( 13 FDA reports)
CATHETER PLACEMENT ( 13 FDA reports)
CHONDROPATHY ( 13 FDA reports)
CHRONIC FATIGUE SYNDROME ( 13 FDA reports)
CLONIC CONVULSION ( 13 FDA reports)
COMPARTMENT SYNDROME ( 13 FDA reports)
COMPULSIONS ( 13 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 13 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 13 FDA reports)
CORNEAL OEDEMA ( 13 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 13 FDA reports)
DRUG SCREEN NEGATIVE ( 13 FDA reports)
ENDOCARDITIS ( 13 FDA reports)
ENERGY INCREASED ( 13 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 13 FDA reports)
EYE INJURY ( 13 FDA reports)
FANCONI SYNDROME ACQUIRED ( 13 FDA reports)
FAT NECROSIS ( 13 FDA reports)
FOLATE DEFICIENCY ( 13 FDA reports)
GALLBLADDER POLYP ( 13 FDA reports)
GASTRIC CANCER ( 13 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 13 FDA reports)
HAEMORRHAGIC DIATHESIS ( 13 FDA reports)
HYPERPYREXIA ( 13 FDA reports)
HYPOPROTEINAEMIA ( 13 FDA reports)
HYPOREFLEXIA ( 13 FDA reports)
IMPRISONMENT ( 13 FDA reports)
INJECTION SITE BRUISING ( 13 FDA reports)
INJURY ASPHYXIATION ( 13 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 13 FDA reports)
INTERMITTENT CLAUDICATION ( 13 FDA reports)
INTESTINAL PERFORATION ( 13 FDA reports)
INTRACARDIAC THROMBUS ( 13 FDA reports)
LIP EROSION ( 13 FDA reports)
LOCALISED OEDEMA ( 13 FDA reports)
LUNG ABSCESS ( 13 FDA reports)
LYMPH NODE PALPABLE ( 13 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 13 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 13 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 13 FDA reports)
METASTASES TO LYMPH NODES ( 13 FDA reports)
MUSCLE FATIGUE ( 13 FDA reports)
MUSCLE INJURY ( 13 FDA reports)
MYOPIA ( 13 FDA reports)
NARCOTIC INTOXICATION ( 13 FDA reports)
NEGATIVE THOUGHTS ( 13 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 13 FDA reports)
NEUTROPHILIA ( 13 FDA reports)
OESOPHAGEAL STENOSIS ( 13 FDA reports)
ORAL SURGERY ( 13 FDA reports)
OVARIAN CANCER METASTATIC ( 13 FDA reports)
PANCREATIC INSUFFICIENCY ( 13 FDA reports)
PARAPROTEINAEMIA ( 13 FDA reports)
PEAU D'ORANGE ( 13 FDA reports)
PHIMOSIS ( 13 FDA reports)
PIGMENTATION DISORDER ( 13 FDA reports)
PITTING OEDEMA ( 13 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 13 FDA reports)
QUADRIPLEGIA ( 13 FDA reports)
RHINALGIA ( 13 FDA reports)
SCRATCH ( 13 FDA reports)
SICK SINUS SYNDROME ( 13 FDA reports)
SLEEP-RELATED EATING DISORDER ( 13 FDA reports)
STEM CELL TRANSPLANT ( 13 FDA reports)
STEREOTYPY ( 13 FDA reports)
SYNOVITIS ( 13 FDA reports)
THORACIC OUTLET SYNDROME ( 13 FDA reports)
THROMBOSIS IN DEVICE ( 13 FDA reports)
TOOTH EROSION ( 13 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 13 FDA reports)
VESTIBULAR DISORDER ( 13 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 13 FDA reports)
PRE-ECLAMPSIA ( 12 FDA reports)
PROTEIN TOTAL INCREASED ( 12 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 12 FDA reports)
PSYCHOLOGICAL TRAUMA ( 12 FDA reports)
PULMONARY GRANULOMA ( 12 FDA reports)
PUPILLARY DISORDER ( 12 FDA reports)
RETINAL DETACHMENT ( 12 FDA reports)
SEBORRHOEIC KERATOSIS ( 12 FDA reports)
SHOCK HAEMORRHAGIC ( 12 FDA reports)
SKIN FIBROSIS ( 12 FDA reports)
SKIN FISSURES ( 12 FDA reports)
SKIN HAEMORRHAGE ( 12 FDA reports)
SMEAR CERVIX ABNORMAL ( 12 FDA reports)
SOFT TISSUE DISORDER ( 12 FDA reports)
SOMATOFORM DISORDER ( 12 FDA reports)
STARING ( 12 FDA reports)
THROMBOPHLEBITIS ( 12 FDA reports)
TONGUE ULCERATION ( 12 FDA reports)
TRANSFUSION ( 12 FDA reports)
TUMOUR INVASION ( 12 FDA reports)
TWIN PREGNANCY ( 12 FDA reports)
URINE AMPHETAMINE POSITIVE ( 12 FDA reports)
URINE OUTPUT INCREASED ( 12 FDA reports)
VARICOCELE ( 12 FDA reports)
VENOUS THROMBOSIS ( 12 FDA reports)
VENOUS THROMBOSIS LIMB ( 12 FDA reports)
VENTRICULAR DYSFUNCTION ( 12 FDA reports)
ABDOMINAL ADHESIONS ( 12 FDA reports)
ANAL FISSURE ( 12 FDA reports)
ANOGENITAL WARTS ( 12 FDA reports)
AORTIC DISORDER ( 12 FDA reports)
APNOEIC ATTACK ( 12 FDA reports)
APPLICATION SITE BURN ( 12 FDA reports)
APPLICATION SITE VESICLES ( 12 FDA reports)
AUTOIMMUNE THYROIDITIS ( 12 FDA reports)
BK VIRUS INFECTION ( 12 FDA reports)
BLADDER CATHETERISATION ( 12 FDA reports)
BONE FORMATION DECREASED ( 12 FDA reports)
BREAKTHROUGH PAIN ( 12 FDA reports)
CALCIUM IONISED INCREASED ( 12 FDA reports)
CATHETERISATION CARDIAC ( 12 FDA reports)
CHEST INJURY ( 12 FDA reports)
CHOLESTEROSIS ( 12 FDA reports)
COLONIC STENOSIS ( 12 FDA reports)
CORNEAL ABRASION ( 12 FDA reports)
CYSTITIS INTERSTITIAL ( 12 FDA reports)
CYSTOCELE ( 12 FDA reports)
DEFAECATION URGENCY ( 12 FDA reports)
DEVICE LEAKAGE ( 12 FDA reports)
DIASTOLIC DYSFUNCTION ( 12 FDA reports)
DROP ATTACKS ( 12 FDA reports)
DYSAESTHESIA ( 12 FDA reports)
EJACULATION FAILURE ( 12 FDA reports)
ENZYME ABNORMALITY ( 12 FDA reports)
EPILEPTIC AURA ( 12 FDA reports)
FACIAL PARESIS ( 12 FDA reports)
FATTY LIVER ALCOHOLIC ( 12 FDA reports)
FRACTURE NONUNION ( 12 FDA reports)
GALLBLADDER ENLARGEMENT ( 12 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 12 FDA reports)
GASTRITIS EROSIVE ( 12 FDA reports)
GINGIVAL ERYTHEMA ( 12 FDA reports)
HAEMOGLOBIN INCREASED ( 12 FDA reports)
HAIR GROWTH ABNORMAL ( 12 FDA reports)
HYPERAEMIA ( 12 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 12 FDA reports)
HYPOTONIA NEONATAL ( 12 FDA reports)
INFERTILITY FEMALE ( 12 FDA reports)
INJECTION SITE EXTRAVASATION ( 12 FDA reports)
INTESTINAL ULCER ( 12 FDA reports)
IRITIS ( 12 FDA reports)
ISCHAEMIC HEPATITIS ( 12 FDA reports)
LARYNGOSPASM ( 12 FDA reports)
LEARNING DISORDER ( 12 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 12 FDA reports)
LIP DRY ( 12 FDA reports)
LIP PAIN ( 12 FDA reports)
LOW SET EARS ( 12 FDA reports)
MALIGNANT MELANOMA ( 12 FDA reports)
MENIERE'S DISEASE ( 12 FDA reports)
MICROALBUMINURIA ( 12 FDA reports)
MICTURITION DISORDER ( 12 FDA reports)
NEONATAL ASPIRATION ( 12 FDA reports)
NONSPECIFIC REACTION ( 12 FDA reports)
PERIARTHRITIS ( 12 FDA reports)
PERICARDIAL DISEASE ( 12 FDA reports)
PERIOSTITIS ( 12 FDA reports)
PLEUROTHOTONUS ( 12 FDA reports)
ACCOMMODATION DISORDER ( 11 FDA reports)
ACUTE PRERENAL FAILURE ( 11 FDA reports)
ADENOMA BENIGN ( 11 FDA reports)
APPETITE DISORDER ( 11 FDA reports)
APPLICATION SITE PAIN ( 11 FDA reports)
ASPIRATION PLEURAL CAVITY ( 11 FDA reports)
BACTERIAL TEST POSITIVE ( 11 FDA reports)
BLOOD IRON INCREASED ( 11 FDA reports)
BONE FORMATION INCREASED ( 11 FDA reports)
BONE MARROW DISORDER ( 11 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 11 FDA reports)
CALCULUS URETERIC ( 11 FDA reports)
CARDIAC OPERATION ( 11 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 11 FDA reports)
CERVICITIS HUMAN PAPILLOMA VIRUS ( 11 FDA reports)
CHOREA ( 11 FDA reports)
CLAVICLE FRACTURE ( 11 FDA reports)
CORNEAL DISORDER ( 11 FDA reports)
CORONARY ARTERY RESTENOSIS ( 11 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 11 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 11 FDA reports)
DRUG EFFECT INCREASED ( 11 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 11 FDA reports)
DYSMORPHISM ( 11 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 11 FDA reports)
EJACULATION DELAYED ( 11 FDA reports)
EJECTION FRACTION ABNORMAL ( 11 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 11 FDA reports)
ERYTHEMA MULTIFORME ( 11 FDA reports)
EXCESSIVE EYE BLINKING ( 11 FDA reports)
FOAMING AT MOUTH ( 11 FDA reports)
FULGURATION ( 11 FDA reports)
FULL BLOOD COUNT DECREASED ( 11 FDA reports)
GANGRENE ( 11 FDA reports)
HEPATIC CONGESTION ( 11 FDA reports)
HILAR LYMPHADENOPATHY ( 11 FDA reports)
HIP DYSPLASIA ( 11 FDA reports)
HOMELESS ( 11 FDA reports)
HORMONE LEVEL ABNORMAL ( 11 FDA reports)
HYPERPHOSPHATAEMIA ( 11 FDA reports)
HYPERTRANSAMINASAEMIA ( 11 FDA reports)
IATROGENIC INJURY ( 11 FDA reports)
IMPETIGO ( 11 FDA reports)
INJECTION SITE DISCOLOURATION ( 11 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 11 FDA reports)
INTUBATION ( 11 FDA reports)
LARGE INTESTINE PERFORATION ( 11 FDA reports)
LIMB CRUSHING INJURY ( 11 FDA reports)
LUNG CANCER METASTATIC ( 11 FDA reports)
LUNG CONSOLIDATION ( 11 FDA reports)
MITRAL VALVE DISEASE ( 11 FDA reports)
NEPHRITIS ( 11 FDA reports)
NEPHRITIS INTERSTITIAL ( 11 FDA reports)
NIGHT BLINDNESS ( 11 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 11 FDA reports)
OROPHARYNGEAL PLAQUE ( 11 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 11 FDA reports)
PERIVASCULAR DERMATITIS ( 11 FDA reports)
PHARYNGEAL ERYTHEMA ( 11 FDA reports)
PITUITARY TUMOUR ( 11 FDA reports)
PREMATURE DELIVERY ( 11 FDA reports)
PRODUCT TASTE ABNORMAL ( 11 FDA reports)
PULMONARY TUBERCULOSIS ( 11 FDA reports)
QUADRIPARESIS ( 11 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 11 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 11 FDA reports)
RENAL TUBULAR ACIDOSIS ( 11 FDA reports)
RESPIRATION ABNORMAL ( 11 FDA reports)
RESUSCITATION ( 11 FDA reports)
SACROILIITIS ( 11 FDA reports)
SINUS ARRHYTHMIA ( 11 FDA reports)
SPINAL DECOMPRESSION ( 11 FDA reports)
STEATORRHOEA ( 11 FDA reports)
STRABISMUS ( 11 FDA reports)
STRESS INCONTINENCE ( 11 FDA reports)
SUBILEUS ( 11 FDA reports)
SUSPICIOUSNESS ( 11 FDA reports)
TENOSYNOVITIS ( 11 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 11 FDA reports)
ULCERATIVE KERATITIS ( 11 FDA reports)
VENOUS OCCLUSION ( 11 FDA reports)
VESTIBULAR NEURONITIS ( 11 FDA reports)
X-RAY DENTAL ( 11 FDA reports)
POSTOPERATIVE INFECTION ( 10 FDA reports)
PRESSURE OF SPEECH ( 10 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 10 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 10 FDA reports)
PULMONARY MASS ( 10 FDA reports)
SHOULDER ARTHROPLASTY ( 10 FDA reports)
SHOULDER OPERATION ( 10 FDA reports)
SKIN MASS ( 10 FDA reports)
SKIN ODOUR ABNORMAL ( 10 FDA reports)
SMOKER ( 10 FDA reports)
SPINAL CORD DISORDER ( 10 FDA reports)
STREPTOCOCCAL SEPSIS ( 10 FDA reports)
STRESS AT WORK ( 10 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 10 FDA reports)
THYROIDITIS ( 10 FDA reports)
TOE DEFORMITY ( 10 FDA reports)
TONSILLITIS ( 10 FDA reports)
TRIGGER FINGER ( 10 FDA reports)
UTERINE DISORDER ( 10 FDA reports)
VASCULAR RUPTURE ( 10 FDA reports)
VASODILATATION ( 10 FDA reports)
VENOUS INSUFFICIENCY ( 10 FDA reports)
VOCAL CORD NEOPLASM ( 10 FDA reports)
WOUND HAEMORRHAGE ( 10 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 10 FDA reports)
ABDOMINAL INJURY ( 10 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 10 FDA reports)
ADDISON'S DISEASE ( 10 FDA reports)
ADJUSTMENT DISORDER ( 10 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 10 FDA reports)
ALVEOLOPLASTY ( 10 FDA reports)
ANION GAP INCREASED ( 10 FDA reports)
ANORECTAL DISORDER ( 10 FDA reports)
APTYALISM ( 10 FDA reports)
BENIGN GASTRIC NEOPLASM ( 10 FDA reports)
BINGE EATING ( 10 FDA reports)
BLADDER DISCOMFORT ( 10 FDA reports)
BLOOD COUNT ABNORMAL ( 10 FDA reports)
BLOOD CREATININE ABNORMAL ( 10 FDA reports)
BLOOD CREATININE DECREASED ( 10 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 10 FDA reports)
BLOOD URIC ACID INCREASED ( 10 FDA reports)
BONE GRAFT ( 10 FDA reports)
BREAST CANCER STAGE I ( 10 FDA reports)
BREAST SWELLING ( 10 FDA reports)
BRONCHIAL SECRETION RETENTION ( 10 FDA reports)
BRONCHIECTASIS ( 10 FDA reports)
CAECITIS ( 10 FDA reports)
CARTILAGE INJURY ( 10 FDA reports)
CATHETER RELATED INFECTION ( 10 FDA reports)
CENTRAL OBESITY ( 10 FDA reports)
CEREBRAL CYST ( 10 FDA reports)
CORONARY ARTERY THROMBOSIS ( 10 FDA reports)
CRANIAL NERVE DISORDER ( 10 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 10 FDA reports)
DIABETES INSIPIDUS ( 10 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 10 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 10 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 10 FDA reports)
EMBOLISM VENOUS ( 10 FDA reports)
ENDOTRACHEAL INTUBATION ( 10 FDA reports)
EYE INFECTION BACTERIAL ( 10 FDA reports)
FAECES PALE ( 10 FDA reports)
FINGER DEFORMITY ( 10 FDA reports)
FOETAL HEART RATE ABNORMAL ( 10 FDA reports)
FOLLICULITIS ( 10 FDA reports)
GAZE PALSY ( 10 FDA reports)
HAEMORRHAGIC STROKE ( 10 FDA reports)
HEART RATE ABNORMAL ( 10 FDA reports)
HELMINTHIC INFECTION ( 10 FDA reports)
HEPATIC FIBROSIS ( 10 FDA reports)
HIP SURGERY ( 10 FDA reports)
HIRSUTISM ( 10 FDA reports)
IMMOBILE ( 10 FDA reports)
IMPAIRED FASTING GLUCOSE ( 10 FDA reports)
IMPULSE-CONTROL DISORDER ( 10 FDA reports)
INCISION SITE COMPLICATION ( 10 FDA reports)
INJECTION SITE INFLAMMATION ( 10 FDA reports)
INTESTINAL POLYP ( 10 FDA reports)
INTRAOCULAR PRESSURE FLUCTUATION ( 10 FDA reports)
JOINT EFFUSION ( 10 FDA reports)
KIDNEY ENLARGEMENT ( 10 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 10 FDA reports)
LEFT ATRIAL DILATATION ( 10 FDA reports)
LEGAL PROBLEM ( 10 FDA reports)
LIMB MALFORMATION ( 10 FDA reports)
LIPIDS INCREASED ( 10 FDA reports)
LOOSE TOOTH ( 10 FDA reports)
LOSS OF CONTROL OF LEGS ( 10 FDA reports)
LOW TURNOVER OSTEOPATHY ( 10 FDA reports)
LOWER EXTREMITY MASS ( 10 FDA reports)
MACULOPATHY ( 10 FDA reports)
MAMMOPLASTY ( 10 FDA reports)
METASTASES TO MENINGES ( 10 FDA reports)
METASTATIC NEOPLASM ( 10 FDA reports)
MICROTIA ( 10 FDA reports)
MOUTH INJURY ( 10 FDA reports)
MYASTHENIA GRAVIS ( 10 FDA reports)
NASAL DRYNESS ( 10 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 10 FDA reports)
NON-SMALL CELL LUNG CANCER ( 10 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 10 FDA reports)
OESOPHAGEAL OPERATION ( 10 FDA reports)
OPTIC ATROPHY ( 10 FDA reports)
ORCHITIS ( 10 FDA reports)
ORGAN FAILURE ( 10 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 10 FDA reports)
PAPULE ( 10 FDA reports)
PARADOXICAL DRUG REACTION ( 10 FDA reports)
PARONYCHIA ( 10 FDA reports)
PHYSICAL DISABILITY ( 10 FDA reports)
PLATELET COUNT ABNORMAL ( 10 FDA reports)
PLATELET DISORDER ( 10 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 10 FDA reports)
POLYDIPSIA PSYCHOGENIC ( 10 FDA reports)
PORTAL VEIN THROMBOSIS ( 10 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 9 FDA reports)
ACARODERMATITIS ( 9 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 9 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 9 FDA reports)
ACUTE PSYCHOSIS ( 9 FDA reports)
ADENOMYOSIS ( 9 FDA reports)
AGITATION NEONATAL ( 9 FDA reports)
AMBLYOPIA ( 9 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 9 FDA reports)
ANAESTHETIC COMPLICATION ( 9 FDA reports)
ANISOCYTOSIS ( 9 FDA reports)
AXILLARY PAIN ( 9 FDA reports)
BIPOLAR II DISORDER ( 9 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 9 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 9 FDA reports)
BREAST RECONSTRUCTION ( 9 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 9 FDA reports)
CARBON DIOXIDE DECREASED ( 9 FDA reports)
CARDIOVERSION ( 9 FDA reports)
CATAPLEXY ( 9 FDA reports)
CATHETER SITE INFECTION ( 9 FDA reports)
CEREBRAL PALSY ( 9 FDA reports)
CERVICITIS ( 9 FDA reports)
CHOKING SENSATION ( 9 FDA reports)
CHOLANGITIS ( 9 FDA reports)
CLEFT PALATE ( 9 FDA reports)
COMA SCALE ABNORMAL ( 9 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 9 FDA reports)
CONGENITAL CARDIOVASCULAR ANOMALY ( 9 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 9 FDA reports)
CORONARY ARTERY BYPASS ( 9 FDA reports)
CRYOGLOBULINAEMIA ( 9 FDA reports)
CYSTITIS NONINFECTIVE ( 9 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 9 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 9 FDA reports)
DELUSION OF GRANDEUR ( 9 FDA reports)
DEMENTIA WITH LEWY BODIES ( 9 FDA reports)
DENTAL DISCOMFORT ( 9 FDA reports)
DIPLEGIA ( 9 FDA reports)
DYSENTERY ( 9 FDA reports)
DYSMENORRHOEA ( 9 FDA reports)
DYSPLASIA ( 9 FDA reports)
ESCHERICHIA TEST POSITIVE ( 9 FDA reports)
ESSENTIAL TREMOR ( 9 FDA reports)
FEBRILE CONVULSION ( 9 FDA reports)
FEEDING DISORDER ( 9 FDA reports)
FEEDING DISORDER NEONATAL ( 9 FDA reports)
FEELINGS OF WORTHLESSNESS ( 9 FDA reports)
FRACTURED COCCYX ( 9 FDA reports)
FUNGAEMIA ( 9 FDA reports)
FUNGAL RASH ( 9 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 9 FDA reports)
GALLOP RHYTHM PRESENT ( 9 FDA reports)
HAEMOLYSIS ( 9 FDA reports)
HEART INJURY ( 9 FDA reports)
HELICOBACTER INFECTION ( 9 FDA reports)
HEPATIC ENZYME ABNORMAL ( 9 FDA reports)
HERNIA PAIN ( 9 FDA reports)
HYPOCHLORAEMIA ( 9 FDA reports)
IMPACTED FRACTURE ( 9 FDA reports)
IMPLANT SITE SWELLING ( 9 FDA reports)
INCORRECT STORAGE OF DRUG ( 9 FDA reports)
INJECTION SITE NECROSIS ( 9 FDA reports)
IRREGULAR SLEEP PHASE ( 9 FDA reports)
KUSSMAUL RESPIRATION ( 9 FDA reports)
KYPHOSCOLIOSIS ( 9 FDA reports)
LIMB DEFORMITY ( 9 FDA reports)
LIMB OPERATION ( 9 FDA reports)
LOCALISED OSTEOARTHRITIS ( 9 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 9 FDA reports)
MASKED FACIES ( 9 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 9 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 9 FDA reports)
MEAN CELL VOLUME INCREASED ( 9 FDA reports)
MENINGITIS ( 9 FDA reports)
METASTASES TO THYROID ( 9 FDA reports)
MICROANGIOPATHY ( 9 FDA reports)
MUCOSAL EROSION ( 9 FDA reports)
NECROSIS ( 9 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 9 FDA reports)
NEPHROTIC SYNDROME ( 9 FDA reports)
NERVE BLOCK ( 9 FDA reports)
NERVE ROOT LESION ( 9 FDA reports)
NEURODEVELOPMENTAL DISORDER ( 9 FDA reports)
NIKOLSKY'S SIGN ( 9 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 9 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE I ( 9 FDA reports)
ONYCHALGIA ( 9 FDA reports)
ORAL TORUS ( 9 FDA reports)
PANCREATIC CARCINOMA ( 9 FDA reports)
PARASOMNIA ( 9 FDA reports)
PARATHYROIDECTOMY ( 9 FDA reports)
PERITONEAL EFFUSION ( 9 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 9 FDA reports)
POLYHYDRAMNIOS ( 9 FDA reports)
PORTAL VEIN OCCLUSION ( 9 FDA reports)
POST HERPETIC NEURALGIA ( 9 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 9 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 9 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 9 FDA reports)
PROTHROMBIN TIME SHORTENED ( 9 FDA reports)
PSYCHOTIC BEHAVIOUR ( 9 FDA reports)
PULMONARY HAEMORRHAGE ( 9 FDA reports)
RASH VESICULAR ( 9 FDA reports)
RECTOCELE ( 9 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 9 FDA reports)
REGURGITATION ( 9 FDA reports)
RETINAL HAEMORRHAGE ( 9 FDA reports)
RETINAL TEAR ( 9 FDA reports)
RIGHT ATRIAL DILATATION ( 9 FDA reports)
SIALOADENITIS ( 9 FDA reports)
SLEEP WALKING ( 9 FDA reports)
SOMATIC DELUSION ( 9 FDA reports)
SOMATISATION DISORDER ( 9 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 9 FDA reports)
SUBCUTANEOUS ABSCESS ( 9 FDA reports)
TENSION HEADACHE ( 9 FDA reports)
TOOTH DISCOLOURATION ( 9 FDA reports)
TRACHEOBRONCHITIS ( 9 FDA reports)
TRAUMATIC HAEMATOMA ( 9 FDA reports)
TUNNEL VISION ( 9 FDA reports)
ULNA FRACTURE ( 9 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 9 FDA reports)
VASCULAR PSEUDOANEURYSM ( 9 FDA reports)
VENA CAVA THROMBOSIS ( 9 FDA reports)
VULVOVAGINAL PRURITUS ( 9 FDA reports)
WEIGHT ABNORMAL ( 9 FDA reports)
WHITE BLOOD CELL DISORDER ( 9 FDA reports)
WOUND DRAINAGE ( 9 FDA reports)
YAWNING ( 9 FDA reports)
PRODUCT COUNTERFEIT ( 8 FDA reports)
PRODUCT FORMULATION ISSUE ( 8 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 8 FDA reports)
REFLUX GASTRITIS ( 8 FDA reports)
RENAL ATROPHY ( 8 FDA reports)
RENAL TUBULAR DISORDER ( 8 FDA reports)
SKIN CANDIDA ( 8 FDA reports)
SOMNOLENCE NEONATAL ( 8 FDA reports)
SPINAL PAIN ( 8 FDA reports)
SPLENIC INJURY ( 8 FDA reports)
SPONDYLITIS ( 8 FDA reports)
SUBCUTANEOUS NODULE ( 8 FDA reports)
SUTURE RELATED COMPLICATION ( 8 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 8 FDA reports)
TACHYARRHYTHMIA ( 8 FDA reports)
TELANGIECTASIA ( 8 FDA reports)
THEFT ( 8 FDA reports)
TONIC CLONIC MOVEMENTS ( 8 FDA reports)
TRANSVERSE PRESENTATION ( 8 FDA reports)
TRAUMATIC LUNG INJURY ( 8 FDA reports)
TROPONIN I INCREASED ( 8 FDA reports)
UNINTENDED PREGNANCY ( 8 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 8 FDA reports)
UPPER EXTREMITY MASS ( 8 FDA reports)
URINE KETONE BODY PRESENT ( 8 FDA reports)
VAGINAL CANDIDIASIS ( 8 FDA reports)
VAGINAL DISORDER ( 8 FDA reports)
VASCULAR GRAFT OCCLUSION ( 8 FDA reports)
VENOUS INJURY ( 8 FDA reports)
VERTEBROPLASTY ( 8 FDA reports)
VITAMIN B12 DECREASED ( 8 FDA reports)
VOCAL CORD INFLAMMATION ( 8 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 8 FDA reports)
ACCIDENT AT WORK ( 8 FDA reports)
ACQUIRED PORPHYRIA ( 8 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 8 FDA reports)
ADRENAL ADENOMA ( 8 FDA reports)
ADVERSE REACTION ( 8 FDA reports)
ALLODYNIA ( 8 FDA reports)
ANAEMIA POSTOPERATIVE ( 8 FDA reports)
ANKYLOGLOSSIA CONGENITAL ( 8 FDA reports)
AORTIC VALVE DISEASE ( 8 FDA reports)
APGAR SCORE LOW ( 8 FDA reports)
APPLICATION SITE DERMATITIS ( 8 FDA reports)
APPLICATION SITE DISCOLOURATION ( 8 FDA reports)
APPLICATION SITE SCAB ( 8 FDA reports)
ARTERIAL INJURY ( 8 FDA reports)
ARTERIAL INSUFFICIENCY ( 8 FDA reports)
ARTERIAL THROMBOSIS ( 8 FDA reports)
ARTERITIS ( 8 FDA reports)
ASPERGILLOSIS ( 8 FDA reports)
ASPIRATION BRONCHIAL ( 8 FDA reports)
AUTOIMMUNE DISORDER ( 8 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 8 FDA reports)
BILE DUCT STONE ( 8 FDA reports)
BONE OPERATION ( 8 FDA reports)
BREAST CANCER STAGE II ( 8 FDA reports)
BREAST LUMP REMOVAL ( 8 FDA reports)
BRONCHIOLITIS ( 8 FDA reports)
BUNDLE BRANCH BLOCK ( 8 FDA reports)
BUNION OPERATION ( 8 FDA reports)
BUTTOCK PAIN ( 8 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 8 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 8 FDA reports)
CEREBELLAR ATROPHY ( 8 FDA reports)
CEREBRAL HAEMATOMA ( 8 FDA reports)
CHAPPED LIPS ( 8 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 8 FDA reports)
COLON ADENOMA ( 8 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 8 FDA reports)
COMA HEPATIC ( 8 FDA reports)
CONJUNCTIVITIS VIRAL ( 8 FDA reports)
CONVULSION NEONATAL ( 8 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 8 FDA reports)
DELUSIONAL PERCEPTION ( 8 FDA reports)
DENGUE FEVER ( 8 FDA reports)
DEVICE DISLOCATION ( 8 FDA reports)
DEVICE OCCLUSION ( 8 FDA reports)
DIABETIC GASTROPARESIS ( 8 FDA reports)
DISSOCIATIVE FUGUE ( 8 FDA reports)
DIVERTICULAR PERFORATION ( 8 FDA reports)
DOPAMINE DYSREGULATION SYNDROME ( 8 FDA reports)
DROWNING ( 8 FDA reports)
DRUG DIVERSION ( 8 FDA reports)
DRUG INTERACTION POTENTIATION ( 8 FDA reports)
EARLY SATIETY ( 8 FDA reports)
ELECTRIC SHOCK ( 8 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 8 FDA reports)
EMOTIONAL POVERTY ( 8 FDA reports)
ENCEPHALITIS POST MEASLES ( 8 FDA reports)
ENDOCARDITIS BACTERIAL ( 8 FDA reports)
EXANTHEM ( 8 FDA reports)
EXPOSURE DURING BREAST FEEDING ( 8 FDA reports)
EXTREMITY CONTRACTURE ( 8 FDA reports)
EYE INFECTION ( 8 FDA reports)
EYE INFLAMMATION ( 8 FDA reports)
FANCONI SYNDROME ( 8 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 8 FDA reports)
FOREIGN BODY ( 8 FDA reports)
FRACTURE DISPLACEMENT ( 8 FDA reports)
FRACTURED SACRUM ( 8 FDA reports)
GASTROINTESTINAL INJURY ( 8 FDA reports)
GASTROSTOMY ( 8 FDA reports)
GINGIVAL ULCERATION ( 8 FDA reports)
GRUNTING ( 8 FDA reports)
HALLUCINATION, TACTILE ( 8 FDA reports)
HEPATIC TRAUMA ( 8 FDA reports)
HYPERCHLORHYDRIA ( 8 FDA reports)
HYPERTENSIVE HEART DISEASE ( 8 FDA reports)
HYPERVOLAEMIA ( 8 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 8 FDA reports)
INCREASED BRONCHIAL SECRETION ( 8 FDA reports)
INDURATION ( 8 FDA reports)
INFUSION SITE MASS ( 8 FDA reports)
INFUSION SITE PAIN ( 8 FDA reports)
INSULIN RESISTANCE ( 8 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 8 FDA reports)
INTERVERTEBRAL DISCITIS ( 8 FDA reports)
INTESTINAL HAEMORRHAGE ( 8 FDA reports)
IRON DEFICIENCY ( 8 FDA reports)
JAW CYST ( 8 FDA reports)
JOINT ARTHROPLASTY ( 8 FDA reports)
JOINT PROSTHESIS USER ( 8 FDA reports)
LIVE BIRTH ( 8 FDA reports)
LIVEDO RETICULARIS ( 8 FDA reports)
LIVER TENDERNESS ( 8 FDA reports)
LIVER TRANSPLANT REJECTION ( 8 FDA reports)
MEAN CELL VOLUME DECREASED ( 8 FDA reports)
MENSTRUATION DELAYED ( 8 FDA reports)
METAMORPHOPSIA ( 8 FDA reports)
MUCOSAL DRYNESS ( 8 FDA reports)
MUCOUS MEMBRANE DISORDER ( 8 FDA reports)
MUCOUS STOOLS ( 8 FDA reports)
MYCOPLASMA INFECTION ( 8 FDA reports)
NEGATIVISM ( 8 FDA reports)
NEPHROSCLEROSIS ( 8 FDA reports)
NIPPLE PAIN ( 8 FDA reports)
NODAL ARRHYTHMIA ( 8 FDA reports)
NORMAL NEWBORN ( 8 FDA reports)
OBSTRUCTIVE UROPATHY ( 8 FDA reports)
OCCULT BLOOD ( 8 FDA reports)
OEDEMA GENITAL ( 8 FDA reports)
OESOPHAGEAL CARCINOMA ( 8 FDA reports)
OESOPHAGEAL SPASM ( 8 FDA reports)
OPTIC NERVE DISORDER ( 8 FDA reports)
ORAL FUNGAL INFECTION ( 8 FDA reports)
OROPHARYNGEAL SWELLING ( 8 FDA reports)
OVARIAN CANCER ( 8 FDA reports)
OVERGROWTH BACTERIAL ( 8 FDA reports)
PANCREATIC NECROSIS ( 8 FDA reports)
PANNICULITIS ( 8 FDA reports)
PARANOID PERSONALITY DISORDER ( 8 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 8 FDA reports)
PHARYNGEAL INFLAMMATION ( 8 FDA reports)
PITUITARY TUMOUR BENIGN ( 8 FDA reports)
PNEUMATOSIS INTESTINALIS ( 8 FDA reports)
POLYARTHRITIS ( 8 FDA reports)
POLYMEDICATION ( 8 FDA reports)
POLYP COLORECTAL ( 8 FDA reports)
ABDOMINAL INFECTION ( 7 FDA reports)
ABDOMINAL RIGIDITY ( 7 FDA reports)
AMPUTATION ( 7 FDA reports)
ANAL ABSCESS ( 7 FDA reports)
ANAL SPHINCTER ATONY ( 7 FDA reports)
ANGIOPLASTY ( 7 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 7 FDA reports)
ANTIBODY TEST POSITIVE ( 7 FDA reports)
ANTISOCIAL BEHAVIOUR ( 7 FDA reports)
AORTIC CALCIFICATION ( 7 FDA reports)
APRAXIA ( 7 FDA reports)
ARM AMPUTATION ( 7 FDA reports)
ARTERIAL DISORDER ( 7 FDA reports)
ASEPTIC NECROSIS BONE ( 7 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 7 FDA reports)
B-CELL LYMPHOMA ( 7 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 7 FDA reports)
BED REST ( 7 FDA reports)
BELLIGERENCE ( 7 FDA reports)
BICYTOPENIA ( 7 FDA reports)
BIOPSY BONE MARROW ( 7 FDA reports)
BLADDER DILATATION ( 7 FDA reports)
BLADDER HYPERTROPHY ( 7 FDA reports)
BLADDER PROLAPSE ( 7 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 7 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 7 FDA reports)
BLOOD KETONE BODY ( 7 FDA reports)
BLOOD OSMOLARITY DECREASED ( 7 FDA reports)
BLOOD PH INCREASED ( 7 FDA reports)
BODY DYSMORPHIC DISORDER ( 7 FDA reports)
BRACHIAL PLEXOPATHY ( 7 FDA reports)
BREAST DISCHARGE ( 7 FDA reports)
BREAST DISORDER ( 7 FDA reports)
BURNOUT SYNDROME ( 7 FDA reports)
CALCIFICATION METASTATIC ( 7 FDA reports)
CALCIUM DEFICIENCY ( 7 FDA reports)
CALCULUS URINARY ( 7 FDA reports)
CARDIAC HYPERTROPHY ( 7 FDA reports)
CARDIAC PACEMAKER INSERTION ( 7 FDA reports)
CATARACT NUCLEAR ( 7 FDA reports)
CATHETER RELATED COMPLICATION ( 7 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 7 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 7 FDA reports)
CHOLANGITIS CHRONIC ( 7 FDA reports)
COLOUR BLINDNESS ( 7 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 7 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 7 FDA reports)
CRANIOCEREBRAL INJURY ( 7 FDA reports)
CUSHING'S SYNDROME ( 7 FDA reports)
DENTAL NECROSIS ( 7 FDA reports)
DIAPHRAGMATIC INJURY ( 7 FDA reports)
DIET REFUSAL ( 7 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 7 FDA reports)
EAR CONGESTION ( 7 FDA reports)
EARLY MORNING AWAKENING ( 7 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 7 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 7 FDA reports)
ELEVATED MOOD ( 7 FDA reports)
ENTERITIS ( 7 FDA reports)
ENTERITIS INFECTIOUS ( 7 FDA reports)
ERECTION INCREASED ( 7 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 7 FDA reports)
EXCESSIVE MASTURBATION ( 7 FDA reports)
EXCITABILITY ( 7 FDA reports)
EXOMPHALOS ( 7 FDA reports)
EXOPHTHALMOS ( 7 FDA reports)
FACIAL DYSMORPHISM ( 7 FDA reports)
FALLOT'S TETRALOGY ( 7 FDA reports)
FEAR OF FALLING ( 7 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 7 FDA reports)
FLASHBACK ( 7 FDA reports)
FRACTURE DELAYED UNION ( 7 FDA reports)
GASTRIC PERFORATION ( 7 FDA reports)
GASTROENTERITIS RADIATION ( 7 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 7 FDA reports)
GASTROINTESTINAL NEOPLASM ( 7 FDA reports)
GINGIVAL OEDEMA ( 7 FDA reports)
HAEMANGIOMA OF LIVER ( 7 FDA reports)
HAIR COLOUR CHANGES ( 7 FDA reports)
HEART TRANSPLANT ( 7 FDA reports)
HEPATOJUGULAR REFLUX ( 7 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 7 FDA reports)
HOARSENESS ( 7 FDA reports)
HYPERAMMONAEMIC ENCEPHALOPATHY ( 7 FDA reports)
HYPERCOAGULATION ( 7 FDA reports)
HYPHAEMA ( 7 FDA reports)
HYPOCHONDRIASIS ( 7 FDA reports)
HYPOPHOSPHATASIA ( 7 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 7 FDA reports)
INFUSION SITE ERYTHEMA ( 7 FDA reports)
INJECTION SITE BURNING ( 7 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 7 FDA reports)
INJURY CORNEAL ( 7 FDA reports)
INTESTINAL DILATATION ( 7 FDA reports)
INTESTINAL FISTULA ( 7 FDA reports)
INTRACRANIAL HYPOTENSION ( 7 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 7 FDA reports)
IRON METABOLISM DISORDER ( 7 FDA reports)
JAUNDICE NEONATAL ( 7 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 7 FDA reports)
KERATOCONUS ( 7 FDA reports)
KLEBSIELLA TEST POSITIVE ( 7 FDA reports)
LEUKOENCEPHALOPATHY ( 7 FDA reports)
LIGAMENT INJURY ( 7 FDA reports)
LIP BLISTER ( 7 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 7 FDA reports)
METASTASES TO PERITONEUM ( 7 FDA reports)
MITOCHONDRIAL CYTOPATHY ( 7 FDA reports)
MOANING ( 7 FDA reports)
MONOPARESIS ( 7 FDA reports)
MOTOR NEURONE DISEASE ( 7 FDA reports)
MULTI-ORGAN DISORDER ( 7 FDA reports)
NAIL BED TENDERNESS ( 7 FDA reports)
NASAL POLYPS ( 7 FDA reports)
NEONATAL TACHYPNOEA ( 7 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 7 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 7 FDA reports)
OBSTRUCTION ( 7 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 7 FDA reports)
ONYCHOMADESIS ( 7 FDA reports)
OSTEOMALACIA ( 7 FDA reports)
PAIN EXACERBATED ( 7 FDA reports)
PAINFUL DEFAECATION ( 7 FDA reports)
PANCREATITIS RELAPSING ( 7 FDA reports)
PARTNER STRESS ( 7 FDA reports)
PERITONEAL DIALYSIS ( 7 FDA reports)
PERITONEAL DISORDER ( 7 FDA reports)
PNEUMOCOCCAL BACTERAEMIA ( 7 FDA reports)
PNEUMONIA MYCOPLASMAL ( 7 FDA reports)
PORPHYRIA ( 7 FDA reports)
PORPHYRIA NON-ACUTE ( 7 FDA reports)
POST PROCEDURAL SWELLING ( 7 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 7 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 7 FDA reports)
PRODUCT TAMPERING ( 7 FDA reports)
PROSTRATION ( 7 FDA reports)
PROTEUS INFECTION ( 7 FDA reports)
PSEUDOEPITHELIOMATOUS HYPERPLASIA ( 7 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 7 FDA reports)
PURPURA SENILE ( 7 FDA reports)
PYURIA ( 7 FDA reports)
QRS AXIS ABNORMAL ( 7 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 7 FDA reports)
RECTAL POLYP ( 7 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 7 FDA reports)
RETINAL DEGENERATION ( 7 FDA reports)
RETROPERITONEAL HAEMATOMA ( 7 FDA reports)
RHONCHI ( 7 FDA reports)
SALMONELLOSIS ( 7 FDA reports)
SEGMENTED HYALINISING VASCULITIS ( 7 FDA reports)
SEROMA ( 7 FDA reports)
SERUM SEROTONIN INCREASED ( 7 FDA reports)
SKIN SWELLING ( 7 FDA reports)
SKULL FRACTURE ( 7 FDA reports)
SLEEP PARALYSIS ( 7 FDA reports)
SLOW RESPONSE TO STIMULI ( 7 FDA reports)
SOCIAL FEAR ( 7 FDA reports)
SPINA BIFIDA ( 7 FDA reports)
SPLENIC INFARCTION ( 7 FDA reports)
SUPERINFECTION ( 7 FDA reports)
SURGICAL FAILURE ( 7 FDA reports)
SYSTEMIC CANDIDA ( 7 FDA reports)
THALASSAEMIA BETA ( 7 FDA reports)
THROAT CANCER ( 7 FDA reports)
THROMBOCYTOPENIC PURPURA ( 7 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 7 FDA reports)
TINEA PEDIS ( 7 FDA reports)
TONGUE COATED ( 7 FDA reports)
TONIC CONVULSION ( 7 FDA reports)
TUBERCULIN TEST POSITIVE ( 7 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 7 FDA reports)
UTERINE POLYP ( 7 FDA reports)
UVEITIS ( 7 FDA reports)
VESTIBULITIS ( 7 FDA reports)
VIRAL LABYRINTHITIS ( 7 FDA reports)
VIRAL SINUSITIS ( 7 FDA reports)
VOCAL CORD DISORDER ( 7 FDA reports)
WOUND DEHISCENCE ( 7 FDA reports)
POSTOPERATIVE ADHESION ( 6 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 6 FDA reports)
PRIMARY MEDIASTINAL LARGE B-CELL LYMPHOMA STAGE II ( 6 FDA reports)
PROCEDURAL VOMITING ( 6 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 6 FDA reports)
PROTRUSION TONGUE ( 6 FDA reports)
PUPILS UNEQUAL ( 6 FDA reports)
PYOGENIC GRANULOMA ( 6 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 6 FDA reports)
RADICAL MASTECTOMY ( 6 FDA reports)
READING DISORDER ( 6 FDA reports)
RECTAL FISSURE ( 6 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 6 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 6 FDA reports)
SERRATIA INFECTION ( 6 FDA reports)
SKIN ATROPHY ( 6 FDA reports)
SKIN STRIAE ( 6 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 6 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 6 FDA reports)
SOFT TISSUE INJURY ( 6 FDA reports)
SPINAL OPERATION ( 6 FDA reports)
SPLEEN DISORDER ( 6 FDA reports)
SPUTUM ABNORMAL ( 6 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 6 FDA reports)
STRESS ULCER ( 6 FDA reports)
SUBACUTE ENDOCARDITIS ( 6 FDA reports)
SUBDURAL HAEMORRHAGE ( 6 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 6 FDA reports)
SURGICAL PROCEDURE REPEATED ( 6 FDA reports)
SWEAT GLAND DISORDER ( 6 FDA reports)
TACHYCARDIA PAROXYSMAL ( 6 FDA reports)
TARSAL TUNNEL SYNDROME ( 6 FDA reports)
TERMINAL INSOMNIA ( 6 FDA reports)
TESTICULAR SWELLING ( 6 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE FOR UNAPPROVED INDICATION ( 6 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 6 FDA reports)
THROMBOCYTOSIS ( 6 FDA reports)
TONGUE DRY ( 6 FDA reports)
TONGUE HAEMORRHAGE ( 6 FDA reports)
TONGUE INJURY ( 6 FDA reports)
TREMOR NEONATAL ( 6 FDA reports)
UMBILICAL HERNIA REPAIR ( 6 FDA reports)
URETHRAL DISORDER ( 6 FDA reports)
URINE ABNORMALITY ( 6 FDA reports)
URTICARIA GENERALISED ( 6 FDA reports)
UTERINE ENLARGEMENT ( 6 FDA reports)
UTERINE HAEMORRHAGE ( 6 FDA reports)
VAGINITIS BACTERIAL ( 6 FDA reports)
VASCULAR CALCIFICATION ( 6 FDA reports)
VASCULAR DEMENTIA ( 6 FDA reports)
VASCULAR INJURY ( 6 FDA reports)
VEIN DISORDER ( 6 FDA reports)
VIRAL MYOCARDITIS ( 6 FDA reports)
WEIGHT BEARING DIFFICULTY ( 6 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 6 FDA reports)
ABSCESS DRAINAGE ( 6 FDA reports)
ABSCESS NECK ( 6 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 6 FDA reports)
ADRENAL MASS ( 6 FDA reports)
ADRENAL NEOPLASM ( 6 FDA reports)
ALCOHOL INTERACTION ( 6 FDA reports)
AMOEBIASIS ( 6 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 6 FDA reports)
ANKYLOSING SPONDYLITIS ( 6 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 6 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 6 FDA reports)
APALLIC SYNDROME ( 6 FDA reports)
APLASIA ( 6 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 6 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 6 FDA reports)
ARTERIOSPASM CORONARY ( 6 FDA reports)
ASPERGILLOSIS ORAL ( 6 FDA reports)
AUTOIMMUNE HEPATITIS ( 6 FDA reports)
AUTONOMIC NEUROPATHY ( 6 FDA reports)
BILIARY CYST ( 6 FDA reports)
BLADDER DYSFUNCTION ( 6 FDA reports)
BLOOD ALCOHOL INCREASED ( 6 FDA reports)
BLOOD BICARBONATE INCREASED ( 6 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 6 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 6 FDA reports)
BLOOD MAGNESIUM INCREASED ( 6 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 6 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 6 FDA reports)
BONE MARROW OEDEMA ( 6 FDA reports)
BONE NEOPLASM ( 6 FDA reports)
BRADYARRHYTHMIA ( 6 FDA reports)
BRADYCARDIA NEONATAL ( 6 FDA reports)
BRAIN MASS ( 6 FDA reports)
BREAST CELLULITIS ( 6 FDA reports)
BRONCHIAL OBSTRUCTION ( 6 FDA reports)
CAPILLARY DISORDER ( 6 FDA reports)
CARCINOID TUMOUR OF THE APPENDIX ( 6 FDA reports)
CARDITIS ( 6 FDA reports)
CASTLEMAN'S DISEASE ( 6 FDA reports)
CATARACT CONGENITAL ( 6 FDA reports)
CATHETER SITE PAIN ( 6 FDA reports)
CELL DEATH ( 6 FDA reports)
CERUMEN IMPACTION ( 6 FDA reports)
CHOLANGITIS ACUTE ( 6 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 6 FDA reports)
COAGULATION TIME PROLONGED ( 6 FDA reports)
COLON CANCER METASTATIC ( 6 FDA reports)
CONGENITAL NOSE MALFORMATION ( 6 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 6 FDA reports)
CSF PROTEIN INCREASED ( 6 FDA reports)
DACRYOSTENOSIS CONGENITAL ( 6 FDA reports)
DEAFNESS BILATERAL ( 6 FDA reports)
DERMATITIS ACNEIFORM ( 6 FDA reports)
DIABETIC ULCER ( 6 FDA reports)
DISEASE COMPLICATION ( 6 FDA reports)
DISSOCIATIVE IDENTITY DISORDER ( 6 FDA reports)
DUODENAL ULCER PERFORATION ( 6 FDA reports)
DYSLALIA ( 6 FDA reports)
EAR INFECTION FUNGAL ( 6 FDA reports)
EFFUSION ( 6 FDA reports)
ENTEROCOCCAL SEPSIS ( 6 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 6 FDA reports)
EPIDERMAL NECROSIS ( 6 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 6 FDA reports)
EYE OPERATION ( 6 FDA reports)
EYE ROLLING ( 6 FDA reports)
FACIAL NEURALGIA ( 6 FDA reports)
FALSE POSITIVE INVESTIGATION RESULT ( 6 FDA reports)
FOETAL DISORDER ( 6 FDA reports)
FOOD INTERACTION ( 6 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 6 FDA reports)
GASTRIC INFECTION ( 6 FDA reports)
GASTRIC LAVAGE ( 6 FDA reports)
GENITAL CANDIDIASIS ( 6 FDA reports)
GINGIVAL ABSCESS ( 6 FDA reports)
GRANDIOSITY ( 6 FDA reports)
HAEMATOCRIT INCREASED ( 6 FDA reports)
HAEMOCHROMATOSIS ( 6 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 6 FDA reports)
HEART VALVE INCOMPETENCE ( 6 FDA reports)
HELICOBACTER GASTRITIS ( 6 FDA reports)
HEPATIC INFECTION ( 6 FDA reports)
HEPATIC MASS ( 6 FDA reports)
HEPATITIS VIRAL ( 6 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 6 FDA reports)
HODGKIN'S DISEASE ( 6 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 6 FDA reports)
HYDROCELE ( 6 FDA reports)
HYPERCALCIURIA ( 6 FDA reports)
HYPERLACTACIDAEMIA ( 6 FDA reports)
HYPERLIPASAEMIA ( 6 FDA reports)
HYPERTRICHOSIS ( 6 FDA reports)
HYPERVIGILANCE ( 6 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 6 FDA reports)
INCISION SITE INFECTION ( 6 FDA reports)
INCISIONAL DRAINAGE ( 6 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 6 FDA reports)
INFUSION SITE EXTRAVASATION ( 6 FDA reports)
INFUSION SITE INFECTION ( 6 FDA reports)
INJECTION SITE ABSCESS ( 6 FDA reports)
INJECTION SITE ANAESTHESIA ( 6 FDA reports)
INJECTION SITE DISCOMFORT ( 6 FDA reports)
INJECTION SITE VESICLES ( 6 FDA reports)
INTESTINAL MASS ( 6 FDA reports)
JOINT CREPITATION ( 6 FDA reports)
LABORATORY TEST INTERFERENCE ( 6 FDA reports)
LEFT VENTRICULAR FAILURE ( 6 FDA reports)
LEGIONELLA INFECTION ( 6 FDA reports)
LEIOMYOMA ( 6 FDA reports)
LEUKOARAIOSIS ( 6 FDA reports)
LEUKOPLAKIA ( 6 FDA reports)
LICHENOID KERATOSIS ( 6 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 6 FDA reports)
LUPUS-LIKE SYNDROME ( 6 FDA reports)
LYMPHADENECTOMY ( 6 FDA reports)
MALIGNANT HYPERTENSION ( 6 FDA reports)
MAMMOGRAM ABNORMAL ( 6 FDA reports)
MENINGISM ( 6 FDA reports)
MENOPAUSAL SYMPTOMS ( 6 FDA reports)
METASTASIS ( 6 FDA reports)
MICROCEPHALY ( 6 FDA reports)
MICTURITION FREQUENCY DECREASED ( 6 FDA reports)
MITRAL VALVE STENOSIS ( 6 FDA reports)
MYOCARDIAL FIBROSIS ( 6 FDA reports)
NASAL ULCER ( 6 FDA reports)
NEOPLASM SKIN ( 6 FDA reports)
NERVE ROOT COMPRESSION ( 6 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 6 FDA reports)
NEUTROPENIC SEPSIS ( 6 FDA reports)
OESOPHAGEAL ACHALASIA ( 6 FDA reports)
OESOPHAGEAL RUPTURE ( 6 FDA reports)
OESOPHAGOGASTRIC FUNDOPLASTY ( 6 FDA reports)
ON AND OFF PHENOMENON ( 6 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 6 FDA reports)
OVARIAN CYST RUPTURED ( 6 FDA reports)
PANCREATIC NEOPLASM ( 6 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 6 FDA reports)
PERICARDITIS CONSTRICTIVE ( 6 FDA reports)
PERIPHERAL EMBOLISM ( 6 FDA reports)
PHARYNGEAL DISORDER ( 6 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 6 FDA reports)
PO2 INCREASED ( 6 FDA reports)
POLYCYTHAEMIA ( 6 FDA reports)
POOR DENTAL CONDITION ( 6 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 6 FDA reports)
POST CONCUSSION SYNDROME ( 6 FDA reports)
POST LAMINECTOMY SYNDROME ( 6 FDA reports)
POST PROCEDURAL INFECTION ( 6 FDA reports)
POST PROCEDURAL MYOCARDIAL INFARCTION ( 6 FDA reports)
POST-THORACOTOMY PAIN SYNDROME ( 6 FDA reports)
ABDOMINAL ABSCESS ( 5 FDA reports)
ABNORMAL CLOTTING FACTOR ( 5 FDA reports)
ACANTHOSIS ( 5 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 5 FDA reports)
ADNEXA UTERI MASS ( 5 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 5 FDA reports)
ALLERGY TEST POSITIVE ( 5 FDA reports)
ALLERGY TO METALS ( 5 FDA reports)
ALOPECIA AREATA ( 5 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 5 FDA reports)
ANAL FISTULA ( 5 FDA reports)
ANAL PRURITUS ( 5 FDA reports)
ANKLE OPERATION ( 5 FDA reports)
ANORECTAL DISCOMFORT ( 5 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 5 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 5 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 5 FDA reports)
AORTIC VALVE CALCIFICATION ( 5 FDA reports)
AORTIC VALVE SCLEROSIS ( 5 FDA reports)
APPLICATION SITE EXFOLIATION ( 5 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 5 FDA reports)
ARTERIAL HAEMORRHAGE ( 5 FDA reports)
ARTERIAL STENOSIS ( 5 FDA reports)
ARTHRITIS BACTERIAL ( 5 FDA reports)
ARTHRITIS INFECTIVE ( 5 FDA reports)
ARTHROFIBROSIS ( 5 FDA reports)
ASPERGER'S DISORDER ( 5 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 5 FDA reports)
AXILLARY MASS ( 5 FDA reports)
AZOOSPERMIA ( 5 FDA reports)
BACTERIAL DISEASE CARRIER ( 5 FDA reports)
BENIGN ANORECTAL NEOPLASM ( 5 FDA reports)
BILE DUCT STENOSIS ( 5 FDA reports)
BIOPSY LIVER ( 5 FDA reports)
BLADDER OBSTRUCTION ( 5 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 5 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 5 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 5 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 5 FDA reports)
BLOOD URIC ACID DECREASED ( 5 FDA reports)
BODY TEMPERATURE ( 5 FDA reports)
BONE ATROPHY ( 5 FDA reports)
BRAIN CONTUSION ( 5 FDA reports)
BULIMIA NERVOSA ( 5 FDA reports)
BURNS SECOND DEGREE ( 5 FDA reports)
BURSITIS INFECTIVE ( 5 FDA reports)
CALCULUS URETHRAL ( 5 FDA reports)
CANDIDURIA ( 5 FDA reports)
CARBON MONOXIDE POISONING ( 5 FDA reports)
CARDIAC OUTPUT DECREASED ( 5 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 5 FDA reports)
CAROTID ARTERY ANEURYSM ( 5 FDA reports)
CENTRAL LINE INFECTION ( 5 FDA reports)
CEPHALO-PELVIC DISPROPORTION ( 5 FDA reports)
CEREBELLAR ATAXIA ( 5 FDA reports)
CERVIX CARCINOMA ( 5 FDA reports)
CERVIX CERCLAGE PROCEDURE ( 5 FDA reports)
CHLAMYDIAL INFECTION ( 5 FDA reports)
CHONDROCALCINOSIS ( 5 FDA reports)
CHONDROMALACIA ( 5 FDA reports)
CHORDAE TENDINAE RUPTURE ( 5 FDA reports)
CHROMATOPSIA ( 5 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 5 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 5 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 5 FDA reports)
COAGULATION FACTOR X LEVEL DECREASED ( 5 FDA reports)
COLONIC OBSTRUCTION ( 5 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 5 FDA reports)
CONFABULATION ( 5 FDA reports)
CONGENITAL HYPOTHYROIDISM ( 5 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 5 FDA reports)
CORTICAL LAMINAR NECROSIS ( 5 FDA reports)
CRANIAL NERVE PARALYSIS ( 5 FDA reports)
CREUTZFELDT-JAKOB DISEASE ( 5 FDA reports)
CRYPTORCHISM ( 5 FDA reports)
CULTURE TISSUE SPECIMEN POSITIVE ( 5 FDA reports)
DECEREBRATION ( 5 FDA reports)
DIABETIC EYE DISEASE ( 5 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 5 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 5 FDA reports)
DISLOCATION OF VERTEBRA ( 5 FDA reports)
DIZZINESS EXERTIONAL ( 5 FDA reports)
DRUG LEVEL CHANGED ( 5 FDA reports)
DRUG TOLERANCE INCREASED ( 5 FDA reports)
DYSPAREUNIA ( 5 FDA reports)
EAR OPERATION ( 5 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 5 FDA reports)
EMBOLIC STROKE ( 5 FDA reports)
EMPYEMA ( 5 FDA reports)
ENTEROBACTER INFECTION ( 5 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 5 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 5 FDA reports)
ERYTHEMA NODOSUM ( 5 FDA reports)
ERYTHEMA OF EYELID ( 5 FDA reports)
ESCHERICHIA SEPSIS ( 5 FDA reports)
EXFOLIATIVE RASH ( 5 FDA reports)
EYE EXCISION ( 5 FDA reports)
EYE OEDEMA ( 5 FDA reports)
FACIAL SPASM ( 5 FDA reports)
FEAR OF DEATH ( 5 FDA reports)
FEAR OF DISEASE ( 5 FDA reports)
FEEDING TUBE COMPLICATION ( 5 FDA reports)
FISTULA DISCHARGE ( 5 FDA reports)
FOREARM FRACTURE ( 5 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 5 FDA reports)
GALLBLADDER CANCER ( 5 FDA reports)
GASTRIC NEOPLASM ( 5 FDA reports)
GINGIVAL HYPERPLASIA ( 5 FDA reports)
HAEMOBILIA ( 5 FDA reports)
HAIR DISORDER ( 5 FDA reports)
HALO VISION ( 5 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 5 FDA reports)
HIV INFECTION ( 5 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 5 FDA reports)
HYPERTONIC BLADDER ( 5 FDA reports)
HYPOSPADIAS ( 5 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 5 FDA reports)
INJECTION SITE CELLULITIS ( 5 FDA reports)
INJECTION SITE DYSAESTHESIA ( 5 FDA reports)
INJECTION SITE INFECTION ( 5 FDA reports)
INJECTION SITE STINGING ( 5 FDA reports)
INJECTION SITE ULCER ( 5 FDA reports)
INTERCOSTAL NEURALGIA ( 5 FDA reports)
INTERNAL HERNIA ( 5 FDA reports)
INTESTINAL INFARCTION ( 5 FDA reports)
JARISCH-HERXHEIMER REACTION ( 5 FDA reports)
JAUNDICE CHOLESTATIC ( 5 FDA reports)
JEALOUS DELUSION ( 5 FDA reports)
JOINT FLUID DRAINAGE ( 5 FDA reports)
JOINT LOCK ( 5 FDA reports)
JUGULAR VEIN DISTENSION ( 5 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 5 FDA reports)
LICHEN PLANUS ( 5 FDA reports)
LIPOMA ( 5 FDA reports)
LIVER TRANSPLANT ( 5 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
LUNG INJURY ( 5 FDA reports)
LYMPHADENITIS ( 5 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 5 FDA reports)
LYMPHOCYTIC INFILTRATION ( 5 FDA reports)
MACULAR OEDEMA ( 5 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 5 FDA reports)
MANDIBULAR PROSTHESIS USER ( 5 FDA reports)
MARROW HYPERPLASIA ( 5 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 5 FDA reports)
MECHANICAL VENTILATION ( 5 FDA reports)
MEDIASTINAL BIOPSY ( 5 FDA reports)
MEDIASTINAL MASS ( 5 FDA reports)
MENINGOCELE ( 5 FDA reports)
MENTAL RETARDATION ( 5 FDA reports)
METAL POISONING ( 5 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 5 FDA reports)
MITRAL VALVE CALCIFICATION ( 5 FDA reports)
MORPHOEA ( 5 FDA reports)
MOUTH BREATHING ( 5 FDA reports)
MYOPERICARDITIS ( 5 FDA reports)
NAIL BED INFLAMMATION ( 5 FDA reports)
NAIL DYSTROPHY ( 5 FDA reports)
NEONATAL RESPIRATORY FAILURE ( 5 FDA reports)
NEOPLASM RECURRENCE ( 5 FDA reports)
NODULE ON EXTREMITY ( 5 FDA reports)
NOSE DEFORMITY ( 5 FDA reports)
NUCHAL RIGIDITY ( 5 FDA reports)
ONYCHOCLASIS ( 5 FDA reports)
ORAL MUCOSAL BLISTERING ( 5 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 5 FDA reports)
ORGANISING PNEUMONIA ( 5 FDA reports)
OSTEITIS DEFORMANS ( 5 FDA reports)
OSTEOCHONDROSIS ( 5 FDA reports)
OSTEOPOROTIC FRACTURE ( 5 FDA reports)
OXYGEN SUPPLEMENTATION ( 5 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 5 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 5 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 5 FDA reports)
PARKINSONIAN REST TREMOR ( 5 FDA reports)
PATHOGEN RESISTANCE ( 5 FDA reports)
PEMPHIGOID ( 5 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 5 FDA reports)
PERIPHERAL NERVE DECOMPRESSION ( 5 FDA reports)
PERIPHERAL NERVE INJURY ( 5 FDA reports)
PHARYNGEAL ULCERATION ( 5 FDA reports)
PHOBIA OF DRIVING ( 5 FDA reports)
PILOERECTION ( 5 FDA reports)
PLACENTAL DISORDER ( 5 FDA reports)
PLASMA CELL DISORDER ( 5 FDA reports)
PLASMACYTOMA ( 5 FDA reports)
PLEURAL DISORDER ( 5 FDA reports)
PNEUMATOSIS CYSTOIDES INTESTINALIS ( 5 FDA reports)
PNEUMONIA KLEBSIELLA ( 5 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 5 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 5 FDA reports)
PNEUMONIA VIRAL ( 5 FDA reports)
POST-TRAUMATIC NECK SYNDROME ( 5 FDA reports)
PRECANCEROUS CELLS PRESENT ( 5 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 5 FDA reports)
PROPIONIBACTERIUM INFECTION ( 5 FDA reports)
PRURIGO ( 5 FDA reports)
PSYCHOMOTOR AGITATION ( 5 FDA reports)
PTERYGIUM ( 5 FDA reports)
PULMONARY SARCOIDOSIS ( 5 FDA reports)
PULSE ABNORMAL ( 5 FDA reports)
PULSE PRESSURE INCREASED ( 5 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 5 FDA reports)
RADICULAR PAIN ( 5 FDA reports)
RASH SCALY ( 5 FDA reports)
RASH SCARLATINIFORM ( 5 FDA reports)
RED BLOOD CELL ABNORMALITY ( 5 FDA reports)
RENAL HAEMORRHAGE ( 5 FDA reports)
RESPIRATORY DYSKINESIA ( 5 FDA reports)
RETINAL EXUDATES ( 5 FDA reports)
SALIVARY DUCT OBSTRUCTION ( 5 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 5 FDA reports)
SEBORRHOEA ( 5 FDA reports)
SECONDARY PROGRESSIVE MULTIPLE SCLEROSIS ( 5 FDA reports)
SEPSIS NEONATAL ( 5 FDA reports)
SINUS OPERATION ( 5 FDA reports)
SKIN WRINKLING ( 5 FDA reports)
SPLENIC CYST ( 5 FDA reports)
SPONDYLITIC MYELOPATHY ( 5 FDA reports)
SPONDYLOLYSIS ( 5 FDA reports)
STATUS ASTHMATICUS ( 5 FDA reports)
STERNAL FRACTURE ( 5 FDA reports)
STOMACH MASS ( 5 FDA reports)
SUBACUTE COMBINED CORD DEGENERATION ( 5 FDA reports)
SUBMANDIBULAR MASS ( 5 FDA reports)
SUFFOCATION FEELING ( 5 FDA reports)
SUNBURN ( 5 FDA reports)
TEMPERATURE REGULATION DISORDER ( 5 FDA reports)
TENOSYNOVITIS STENOSANS ( 5 FDA reports)
THALAMIC INFARCTION ( 5 FDA reports)
TONGUE OEDEMA ( 5 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO DECREASED ( 5 FDA reports)
TRAUMATIC SHOCK ( 5 FDA reports)
TUBO-OVARIAN ABSCESS ( 5 FDA reports)
URINARY TRACT OBSTRUCTION ( 5 FDA reports)
URINE FLOW DECREASED ( 5 FDA reports)
VICTIM OF CRIME ( 5 FDA reports)
VIRAL CARDIOMYOPATHY ( 5 FDA reports)
VON WILLEBRAND'S DISEASE ( 5 FDA reports)
VULVA CYST ( 5 FDA reports)
WALKING DISABILITY ( 5 FDA reports)
WATER INTOXICATION ( 5 FDA reports)
WRIST SURGERY ( 5 FDA reports)
POSTMENOPAUSE ( 4 FDA reports)
POSTPARTUM DEPRESSION ( 4 FDA reports)
POSTPARTUM DISORDER ( 4 FDA reports)
PROCTOCOLITIS ( 4 FDA reports)
PSYCHOTIC DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 4 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 4 FDA reports)
PULMONARY MYCOSIS ( 4 FDA reports)
PUNCTATE KERATITIS ( 4 FDA reports)
PUSTULAR PSORIASIS ( 4 FDA reports)
RADIAL NERVE PALSY ( 4 FDA reports)
RADICAL HYSTERECTOMY ( 4 FDA reports)
RADICULITIS ( 4 FDA reports)
REBOUND EFFECT ( 4 FDA reports)
RECTAL ABSCESS ( 4 FDA reports)
RECTOSIGMOID CANCER ( 4 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 4 FDA reports)
REFLEXES ABNORMAL ( 4 FDA reports)
RENAL ARTERY STENOSIS ( 4 FDA reports)
RENAL LIPOMATOSIS ( 4 FDA reports)
REPETITIVE SPEECH ( 4 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 4 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 4 FDA reports)
RETROVIRAL INFECTION ( 4 FDA reports)
RHEUMATOID FACTOR INCREASED ( 4 FDA reports)
RHINITIS SEASONAL ( 4 FDA reports)
ROCKY MOUNTAIN SPOTTED FEVER ( 4 FDA reports)
ROTAVIRUS INFECTION ( 4 FDA reports)
SCAPULA FRACTURE ( 4 FDA reports)
SCEDOSPORIUM INFECTION ( 4 FDA reports)
SENILE DEMENTIA ( 4 FDA reports)
SERUM FERRITIN DECREASED ( 4 FDA reports)
SEXUALLY INAPPROPRIATE BEHAVIOUR ( 4 FDA reports)
SHOCK HYPOGLYCAEMIC ( 4 FDA reports)
SIMPLE PARTIAL SEIZURES ( 4 FDA reports)
SINOBRONCHITIS ( 4 FDA reports)
SKIN CHAPPED ( 4 FDA reports)
SKIN DESQUAMATION ( 4 FDA reports)
SKIN DISCOMFORT ( 4 FDA reports)
SOLILOQUY ( 4 FDA reports)
SPLENIC GRANULOMA ( 4 FDA reports)
SPLENIC HAEMORRHAGE ( 4 FDA reports)
SPUTUM DECREASED ( 4 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 4 FDA reports)
STRIDOR ( 4 FDA reports)
SUPERFICIAL VEIN PROMINENCE ( 4 FDA reports)
SYMBLEPHARON ( 4 FDA reports)
T-CELL LYMPHOMA ( 4 FDA reports)
TABLET ISSUE ( 4 FDA reports)
TEETH BRITTLE ( 4 FDA reports)
TEMPORAL ARTERITIS ( 4 FDA reports)
TEMPORAL LOBE EPILEPSY ( 4 FDA reports)
TESTICULAR PAIN ( 4 FDA reports)
THERMOHYPOAESTHESIA ( 4 FDA reports)
THROAT LESION ( 4 FDA reports)
THROMBECTOMY ( 4 FDA reports)
TINEA VERSICOLOUR ( 4 FDA reports)
TOOTH DECALCIFICATION ( 4 FDA reports)
TOOTH IMPACTED ( 4 FDA reports)
TOURETTE'S DISORDER ( 4 FDA reports)
TRACHEOSTOMY ( 4 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 4 FDA reports)
TRICHORRHEXIS ( 4 FDA reports)
TRICUSPID VALVE STENOSIS ( 4 FDA reports)
TUMOUR LYSIS SYNDROME ( 4 FDA reports)
URETHRAL STENOSIS ( 4 FDA reports)
URETHRITIS ( 4 FDA reports)
URINARY BLADDER RUPTURE ( 4 FDA reports)
URINE ANALYSIS ABNORMAL ( 4 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 4 FDA reports)
VASCULAR GRAFT ( 4 FDA reports)
VASCULAR INSUFFICIENCY ( 4 FDA reports)
VASCULAR STENT INSERTION ( 4 FDA reports)
VASOCONSTRICTION ( 4 FDA reports)
VIRAEMIA ( 4 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 4 FDA reports)
VOCAL CORD POLYP ( 4 FDA reports)
VULVOVAGINAL DISCOMFORT ( 4 FDA reports)
VULVOVAGINAL DRYNESS ( 4 FDA reports)
X-RAY ABNORMAL ( 4 FDA reports)
XANTHOPSIA ( 4 FDA reports)
ABDOMINAL SYMPTOM ( 4 FDA reports)
ABSCESS ORAL ( 4 FDA reports)
ACUTE ABDOMEN ( 4 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 4 FDA reports)
AGONAL RHYTHM ( 4 FDA reports)
ALLERGIC RESPIRATORY SYMPTOM ( 4 FDA reports)
AMNIOCENTESIS ABNORMAL ( 4 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 4 FDA reports)
ANAPHYLACTOID REACTION ( 4 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY ( 4 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 4 FDA reports)
ARTERECTOMY ( 4 FDA reports)
ARTERIAL BYPASS OPERATION ( 4 FDA reports)
ARTERIAL STENT INSERTION ( 4 FDA reports)
ARTHROPOD STING ( 4 FDA reports)
ATRIAL THROMBOSIS ( 4 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 4 FDA reports)
BEHCET'S SYNDROME ( 4 FDA reports)
BENIGN CONGENITAL HYPOTONIA ( 4 FDA reports)
BILE DUCT CANCER ( 4 FDA reports)
BILE DUCT STENT INSERTION ( 4 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 4 FDA reports)
BIOPSY LIP ( 4 FDA reports)
BIOPSY SKIN ABNORMAL ( 4 FDA reports)
BITE ( 4 FDA reports)
BLADDER SPHINCTER ATONY ( 4 FDA reports)
BLEEDING TIME PROLONGED ( 4 FDA reports)
BLOOD CORTISOL DECREASED ( 4 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 4 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 4 FDA reports)
BONE DECALCIFICATION ( 4 FDA reports)
BONE MARROW TRANSPLANT ( 4 FDA reports)
BORDERLINE OVARIAN TUMOUR ( 4 FDA reports)
BRAIN NATRIURETIC PEPTIDE DECREASED ( 4 FDA reports)
BRAIN NEOPLASM BENIGN ( 4 FDA reports)
BREAST HYPERPLASIA ( 4 FDA reports)
BREAST INFECTION ( 4 FDA reports)
CAMPTODACTYLY CONGENITAL ( 4 FDA reports)
CARCINOID TUMOUR PULMONARY ( 4 FDA reports)
CARDIAC DISCOMFORT ( 4 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 4 FDA reports)
CAROTID ARTERY STENT INSERTION ( 4 FDA reports)
CATHETER SITE HAEMORRHAGE ( 4 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 4 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 4 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 4 FDA reports)
CEREBRAL HYPERPERFUSION SYNDROME ( 4 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 4 FDA reports)
CERVIX DISORDER ( 4 FDA reports)
CHEMICAL BURN OF GASTROINTESTINAL TRACT ( 4 FDA reports)
CHEMICAL POISONING ( 4 FDA reports)
CHEST WALL PAIN ( 4 FDA reports)
CHORIOAMNIONITIS ( 4 FDA reports)
CHORIORETINAL ATROPHY ( 4 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 4 FDA reports)
CLEFT LIP ( 4 FDA reports)
COAGULATION FACTOR VII LEVEL DECREASED ( 4 FDA reports)
COLONIC FISTULA ( 4 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 4 FDA reports)
COMA BLISTER ( 4 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 4 FDA reports)
CONGENITAL PULMONARY HYPERTENSION ( 4 FDA reports)
CONNECTIVE TISSUE DISORDER ( 4 FDA reports)
CONSTRICTED AFFECT ( 4 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 4 FDA reports)
CORNEAL DEPOSITS ( 4 FDA reports)
CORNEAL OPACITY ( 4 FDA reports)
CORONARY OSTIAL STENOSIS ( 4 FDA reports)
CORRECTIVE LENS USER ( 4 FDA reports)
CREATININE URINE INCREASED ( 4 FDA reports)
CSF PRESSURE INCREASED ( 4 FDA reports)
CYSTIC LYMPHANGIOMA ( 4 FDA reports)
CYSTITIS BACTERIAL ( 4 FDA reports)
DANDRUFF ( 4 FDA reports)
DEATH NEONATAL ( 4 FDA reports)
DEVICE COMPONENT ISSUE ( 4 FDA reports)
DEVICE DAMAGE ( 4 FDA reports)
DIAPHRAGMATIC HERNIA ( 4 FDA reports)
DRESSLER'S SYNDROME ( 4 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 4 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 4 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 4 FDA reports)
DYSLOGIA ( 4 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 4 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 4 FDA reports)
ENAMEL ANOMALY ( 4 FDA reports)
ENANTHEMA ( 4 FDA reports)
ENTEROCOLITIS BACTERIAL ( 4 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 4 FDA reports)
EUSTACHIAN TUBE DISORDER ( 4 FDA reports)
EXERCISE LACK OF ( 4 FDA reports)
EXSANGUINATION ( 4 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 4 FDA reports)
FAECES HARD ( 4 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 4 FDA reports)
FEELING HOT AND COLD ( 4 FDA reports)
FEMALE GENITAL OPERATION ( 4 FDA reports)
FEMORAL ARTERY ANEURYSM ( 4 FDA reports)
FOETAL GROWTH RETARDATION ( 4 FDA reports)
FOETAL HYPOKINESIA ( 4 FDA reports)
FOREIGN BODY ASPIRATION ( 4 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 4 FDA reports)
FREEZING PHENOMENON ( 4 FDA reports)
FUNGAL SKIN INFECTION ( 4 FDA reports)
GALLBLADDER NECROSIS ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE DECREASED ( 4 FDA reports)
GASTROINTESTINAL MALFORMATION ( 4 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 4 FDA reports)
GASTROOESOPHAGITIS ( 4 FDA reports)
GAUCHER'S DISEASE ( 4 FDA reports)
GENERAL SYMPTOM ( 4 FDA reports)
GINGIVAL BLISTER ( 4 FDA reports)
GLIOMA ( 4 FDA reports)
GRANULOCYTE COUNT INCREASED ( 4 FDA reports)
GRIEF REACTION ( 4 FDA reports)
HAEMATOTOXICITY ( 4 FDA reports)
HAEMODILUTION ( 4 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 4 FDA reports)
HAEMORRHAGE URINARY TRACT ( 4 FDA reports)
HAEMORRHAGIC DISORDER ( 4 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 4 FDA reports)
HALLUCINATION, OLFACTORY ( 4 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 4 FDA reports)
HELLP SYNDROME ( 4 FDA reports)
HEPATITIS B CORE ANTIGEN POSITIVE ( 4 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 4 FDA reports)
HUNTINGTON'S DISEASE ( 4 FDA reports)
HYPERCHLORAEMIA ( 4 FDA reports)
HYPERINSULINISM ( 4 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 4 FDA reports)
HYPOCHROMASIA ( 4 FDA reports)
HYPOPHYSITIS ( 4 FDA reports)
INCISION SITE HAEMORRHAGE ( 4 FDA reports)
INCISION SITE PAIN ( 4 FDA reports)
INFANTILE APNOEIC ATTACK ( 4 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 4 FDA reports)
INFECTIVE ANEURYSM ( 4 FDA reports)
INFERTILITY ( 4 FDA reports)
INFUSION SITE SWELLING ( 4 FDA reports)
INHIBITORY DRUG INTERACTION ( 4 FDA reports)
INJECTION SITE ATROPHY ( 4 FDA reports)
INJECTION SITE SCAR ( 4 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 4 FDA reports)
INTESTINAL ADENOCARCINOMA ( 4 FDA reports)
INTESTINAL STENOSIS ( 4 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 4 FDA reports)
INVESTIGATION ABNORMAL ( 4 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 4 FDA reports)
JOINT INJECTION ( 4 FDA reports)
JOINT WARMTH ( 4 FDA reports)
KERATITIS ( 4 FDA reports)
KIDNEY FIBROSIS ( 4 FDA reports)
LACTOSE INTOLERANCE ( 4 FDA reports)
LATEX ALLERGY ( 4 FDA reports)
LEUKOCYTURIA ( 4 FDA reports)
LIP DISCOLOURATION ( 4 FDA reports)
LIPODYSTROPHY ACQUIRED ( 4 FDA reports)
LONG QT SYNDROME ( 4 FDA reports)
LOOSE ASSOCIATIONS ( 4 FDA reports)
LOSS OF PROPRIOCEPTION ( 4 FDA reports)
LOW BIRTH WEIGHT BABY ( 4 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 4 FDA reports)
MACROCYTOSIS ( 4 FDA reports)
MACROGLOSSIA ( 4 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 4 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 4 FDA reports)
MENTAL DISABILITY ( 4 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 4 FDA reports)
METASTATIC CARCINOMA OF THE BLADDER ( 4 FDA reports)
MICROVASCULAR ANGINA ( 4 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 4 FDA reports)
MITOCHONDRIAL DNA DELETION ( 4 FDA reports)
MITRAL VALVE REPLACEMENT ( 4 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 4 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 4 FDA reports)
MOTION SICKNESS ( 4 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 4 FDA reports)
MUSCLE ABSCESS ( 4 FDA reports)
MUSCLE ENZYME INCREASED ( 4 FDA reports)
MUSCLE NECROSIS ( 4 FDA reports)
MYELITIS TRANSVERSE ( 4 FDA reports)
NASAL DISORDER ( 4 FDA reports)
NASAL TURBINATE ABNORMALITY ( 4 FDA reports)
NEPHRECTOMY ( 4 FDA reports)
NEURODERMATITIS ( 4 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 4 FDA reports)
NEUROSIS ( 4 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 4 FDA reports)
OBSTRUCTION GASTRIC ( 4 FDA reports)
OCCIPITAL NEURALGIA ( 4 FDA reports)
OCULAR VASCULAR DISORDER ( 4 FDA reports)
OESOPHAGEAL ATRESIA ( 4 FDA reports)
OESOPHAGEAL DILATATION ( 4 FDA reports)
OOPHORECTOMY ( 4 FDA reports)
OPTIC DISC DISORDER ( 4 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 4 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 4 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 4 FDA reports)
ORGASM ABNORMAL ( 4 FDA reports)
OVARIAN INFECTION ( 4 FDA reports)
OVARIAN MASS ( 4 FDA reports)
OXYGEN SATURATION ABNORMAL ( 4 FDA reports)
PALATAL DISORDER ( 4 FDA reports)
PANCREATIC DUCT DILATATION ( 4 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 4 FDA reports)
PAPILLOMA ( 4 FDA reports)
PAPILLOMA VIRAL INFECTION ( 4 FDA reports)
PARATHYROID TUMOUR BENIGN ( 4 FDA reports)
PAROTITIS ( 4 FDA reports)
PAROXYSMAL ARRHYTHMIA ( 4 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 4 FDA reports)
PATIENT-DEVICE INCOMPATIBILITY ( 4 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 4 FDA reports)
PELVIC ABSCESS ( 4 FDA reports)
PELVIC FLUID COLLECTION ( 4 FDA reports)
PELVIC NEOPLASM ( 4 FDA reports)
PELVIC PROLAPSE ( 4 FDA reports)
PENILE PAIN ( 4 FDA reports)
PERICARDITIS MALIGNANT ( 4 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 4 FDA reports)
PERITONEAL ADHESIONS ( 4 FDA reports)
PERITONSILLAR ABSCESS ( 4 FDA reports)
PERNICIOUS ANAEMIA ( 4 FDA reports)
PLACENTAL INFARCTION ( 4 FDA reports)
PLACENTAL INSUFFICIENCY ( 4 FDA reports)
PLASMAPHERESIS ( 4 FDA reports)
PLATELET AGGREGATION INCREASED ( 4 FDA reports)
PLATYBASIA ( 4 FDA reports)
POIKILOCYTOSIS ( 4 FDA reports)
POLYMENORRHOEA ( 4 FDA reports)
POOR PERSONAL HYGIENE ( 4 FDA reports)
POOR VENOUS ACCESS ( 4 FDA reports)
PORTAL TRIADITIS ( 4 FDA reports)
POST PROCEDURAL PAIN ( 4 FDA reports)
ABDOMINAL WALL DISORDER ( 3 FDA reports)
ABNORMAL LABOUR ( 3 FDA reports)
ABORTION THREATENED ( 3 FDA reports)
ABSCESS INTESTINAL ( 3 FDA reports)
ACINETOBACTER INFECTION ( 3 FDA reports)
ACQUIRED CLAW TOE ( 3 FDA reports)
ACQUIRED MACROGLOSSIA ( 3 FDA reports)
ACROMEGALY ( 3 FDA reports)
ACTINIC KERATOSIS ( 3 FDA reports)
ACUPUNCTURE ( 3 FDA reports)
ACUTE LEUKAEMIA ( 3 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 3 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 3 FDA reports)
ADENOCARCINOMA ( 3 FDA reports)
ADRENAL DISORDER ( 3 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 3 FDA reports)
AGNOSIA ( 3 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 3 FDA reports)
ALBUMIN GLOBULIN RATIO INCREASED ( 3 FDA reports)
ALBUMIN URINE PRESENT ( 3 FDA reports)
ALLERGY TO ARTHROPOD BITE ( 3 FDA reports)
ALLERGY TO CHEMICALS ( 3 FDA reports)
ALVEOLAR PROTEINOSIS ( 3 FDA reports)
AMAUROSIS FUGAX ( 3 FDA reports)
AMINO ACID LEVEL INCREASED ( 3 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 3 FDA reports)
ANAEMIA OF PREGNANCY ( 3 FDA reports)
ANALGESIC DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
ANASTOMOTIC COMPLICATION ( 3 FDA reports)
ANEURYSM RUPTURED ( 3 FDA reports)
ANOSMIA ( 3 FDA reports)
ANOXIA ( 3 FDA reports)
ANTI-HBC ANTIBODY POSITIVE ( 3 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 3 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 3 FDA reports)
ANTITHROMBIN III DECREASED ( 3 FDA reports)
AORTIC ANEURYSM RUPTURE ( 3 FDA reports)
AORTIC DISSECTION ( 3 FDA reports)
APOPTOSIS ( 3 FDA reports)
APPARENT LIFE THREATENING EVENT ( 3 FDA reports)
APPENDICITIS PERFORATED ( 3 FDA reports)
ARRHYTHMIA NEONATAL ( 3 FDA reports)
ARTERIOVENOUS FISTULA ( 3 FDA reports)
ARTERIOVENOUS FISTULA, ACQUIRED ( 3 FDA reports)
ARTERIOVENOUS MALFORMATION ( 3 FDA reports)
ARTHRODESIS ( 3 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 3 FDA reports)
ASBESTOSIS ( 3 FDA reports)
ASOCIAL BEHAVIOUR ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 3 FDA reports)
ASPIRATION JOINT ( 3 FDA reports)
AURICULAR SWELLING ( 3 FDA reports)
AUTOMATISM ( 3 FDA reports)
AXONAL NEUROPATHY ( 3 FDA reports)
B-LYMPHOCYTE COUNT DECREASED ( 3 FDA reports)
BASAL GANGLION DEGENERATION ( 3 FDA reports)
BASOPHIL COUNT INCREASED ( 3 FDA reports)
BENCE JONES PROTEINURIA ( 3 FDA reports)
BENIGN BREAST NEOPLASM ( 3 FDA reports)
BILIARY FIBROSIS ( 3 FDA reports)
BILIARY NEOPLASM ( 3 FDA reports)
BIOPSY BREAST ABNORMAL ( 3 FDA reports)
BIOPSY TONGUE ABNORMAL ( 3 FDA reports)
BLADDER IRRITATION ( 3 FDA reports)
BLADDER NEOPLASM ( 3 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE I ( 3 FDA reports)
BLOOD ALBUMIN INCREASED ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 3 FDA reports)
BLOOD AMYLASE ABNORMAL ( 3 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 3 FDA reports)
BLOOD BLISTER ( 3 FDA reports)
BLOOD CAFFEINE INCREASED ( 3 FDA reports)
BLOOD ETHANOL INCREASED ( 3 FDA reports)
BLOOD FOLATE DECREASED ( 3 FDA reports)
BLOOD GLUCOSE ( 3 FDA reports)
BLOOD HIV RNA INCREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 3 FDA reports)
BLOOD PROLACTIN DECREASED ( 3 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO DECREASED ( 3 FDA reports)
BLUE TOE SYNDROME ( 3 FDA reports)
BODY MASS INDEX INCREASED ( 3 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 3 FDA reports)
BONE INFARCTION ( 3 FDA reports)
BONE INFECTION ( 3 FDA reports)
BOVINE TUBERCULOSIS ( 3 FDA reports)
BRAIN HYPOXIA ( 3 FDA reports)
BRAIN SCAN ABNORMAL ( 3 FDA reports)
BRAIN STEM SYNDROME ( 3 FDA reports)
BRONCHOPNEUMOPATHY ( 3 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 3 FDA reports)
BURNS THIRD DEGREE ( 3 FDA reports)
BUTTERFLY RASH ( 3 FDA reports)
CANDIDA SEPSIS ( 3 FDA reports)
CARBON DIOXIDE INCREASED ( 3 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 3 FDA reports)
CARDIAC PERFORATION ( 3 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 3 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 3 FDA reports)
CEREBELLAR HAEMORRHAGE ( 3 FDA reports)
CEREBRAL ASPERGILLOSIS ( 3 FDA reports)
CEREBRAL HAEMORRHAGE NEONATAL ( 3 FDA reports)
CERVICAL CYST ( 3 FDA reports)
CHILD ABUSE ( 3 FDA reports)
CHOLINERGIC SYNDROME ( 3 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 3 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 3 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 3 FDA reports)
COAGULATION TEST ABNORMAL ( 3 FDA reports)
COGNITIVE DETERIORATION ( 3 FDA reports)
COLECTOMY ( 3 FDA reports)
COLONOSCOPY ( 3 FDA reports)
COLONOSCOPY ABNORMAL ( 3 FDA reports)
COLORECTAL CANCER METASTATIC ( 3 FDA reports)
COLOSTOMY ( 3 FDA reports)
CONFUSIONAL AROUSAL ( 3 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 3 FDA reports)
CONGENITAL FOOT MALFORMATION ( 3 FDA reports)
CONGENITAL HAND MALFORMATION ( 3 FDA reports)
CONGENITAL JAW MALFORMATION ( 3 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 3 FDA reports)
CONJUNCTIVAL IRRITATION ( 3 FDA reports)
COR PULMONALE ( 3 FDA reports)
CORNEAL LESION ( 3 FDA reports)
CORONARY ARTERY SURGERY ( 3 FDA reports)
CROSS SENSITIVITY REACTION ( 3 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 3 FDA reports)
DACTYLITIS ( 3 FDA reports)
DEAFNESS NEUROSENSORY ( 3 FDA reports)
DEAFNESS TRANSITORY ( 3 FDA reports)
DEATH OF FRIEND ( 3 FDA reports)
DEATH OF RELATIVE ( 3 FDA reports)
DELIRIUM TREMENS ( 3 FDA reports)
DELIVERY ( 3 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 3 FDA reports)
DEPENDENCE ON RESPIRATOR ( 3 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 3 FDA reports)
DERMOID CYST ( 3 FDA reports)
DIABETIC HYPERGLYCAEMIC COMA ( 3 FDA reports)
DISTRACTIBILITY ( 3 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 3 FDA reports)
DOUBLE OUTLET RIGHT VENTRICLE ( 3 FDA reports)
DRUG EFFECT DELAYED ( 3 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 3 FDA reports)
DRUG LEVEL FLUCTUATING ( 3 FDA reports)
DRUG THERAPY CHANGED ( 3 FDA reports)
DRY SOCKET ( 3 FDA reports)
DUODENOGASTRIC REFLUX ( 3 FDA reports)
DURAL TEAR ( 3 FDA reports)
DYSCHEZIA ( 3 FDA reports)
EAR DEFORMITY ACQUIRED ( 3 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 3 FDA reports)
ELECTROCARDIOGRAM RR INTERVAL PROLONGED ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 3 FDA reports)
ELECTROCARDIOGRAM U-WAVE ABNORMALITY ( 3 FDA reports)
ENCEPHALITIS VIRAL ( 3 FDA reports)
ENCOPRESIS ( 3 FDA reports)
ENDOMETRIAL ABLATION ( 3 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 3 FDA reports)
EPIDERMOLYSIS BULLOSA ( 3 FDA reports)
EPIDIDYMITIS ( 3 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 3 FDA reports)
ERYTHROPENIA ( 3 FDA reports)
ESCHAR ( 3 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 3 FDA reports)
EXTRAVASATION BLOOD ( 3 FDA reports)
EYELID CYST ( 3 FDA reports)
EYELID EROSION ( 3 FDA reports)
EYELIDS PRURITUS ( 3 FDA reports)
FAECAL VOMITING ( 3 FDA reports)
FAECALITH ( 3 FDA reports)
FALLOPIAN TUBE DISORDER ( 3 FDA reports)
FALSE NEGATIVE INVESTIGATION RESULT ( 3 FDA reports)
FAMILIAL TREMOR ( 3 FDA reports)
FEAR OF EATING ( 3 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 3 FDA reports)
FIXED ERUPTION ( 3 FDA reports)
FLUID INTAKE RESTRICTION ( 3 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 3 FDA reports)
FOETAL HEART RATE DECREASED ( 3 FDA reports)
FOETAL VALPROATE SYNDROME ( 3 FDA reports)
FRONTOTEMPORAL DEMENTIA ( 3 FDA reports)
GALLBLADDER OEDEMA ( 3 FDA reports)
GALLBLADDER PAIN ( 3 FDA reports)
GASTRIC DILATATION ( 3 FDA reports)
GASTRIC OPERATION ( 3 FDA reports)
GASTROENTERITIS SALMONELLA ( 3 FDA reports)
GASTROINTESTINAL PERFORATION ( 3 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 3 FDA reports)
GENITAL BURNING SENSATION ( 3 FDA reports)
GENITAL EROSION ( 3 FDA reports)
GIGANTISM ( 3 FDA reports)
GLIOBLASTOMA MULTIFORME ( 3 FDA reports)
GLIOSIS ( 3 FDA reports)
GLOMERULONEPHRITIS ( 3 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 3 FDA reports)
GLUCOSE URINE PRESENT ( 3 FDA reports)
GLYCOGEN STORAGE DISEASE TYPE V ( 3 FDA reports)
GRAFT THROMBOSIS ( 3 FDA reports)
GRIP STRENGTH ( 3 FDA reports)
HAEMORRHAGIC INFARCTION ( 3 FDA reports)
HEAD BANGING ( 3 FDA reports)
HEART SOUNDS ABNORMAL ( 3 FDA reports)
HEMIANOPIA ( 3 FDA reports)
HEPATITIS A ( 3 FDA reports)
HEPATITIS ALCOHOLIC ( 3 FDA reports)
HEREDITARY ANGIOEDEMA ( 3 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 3 FDA reports)
HIP DEFORMITY ( 3 FDA reports)
HOSPICE CARE ( 3 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 3 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 3 FDA reports)
HYPERTENSIVE EMERGENCY ( 3 FDA reports)
HYPERTHERMIA MALIGNANT ( 3 FDA reports)
HYPERTONIA NEONATAL ( 3 FDA reports)
HYPERURICAEMIA ( 3 FDA reports)
HYPOCOMPLEMENTAEMIA ( 3 FDA reports)
HYPOMENORRHOEA ( 3 FDA reports)
HYPOPERFUSION ( 3 FDA reports)
HYPOPROTHROMBINAEMIA ( 3 FDA reports)
HYPOTRICHOSIS ( 3 FDA reports)
ILEAL PERFORATION ( 3 FDA reports)
ILEITIS ( 3 FDA reports)
ILLITERACY ( 3 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 3 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 3 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 3 FDA reports)
INCISION SITE ERYTHEMA ( 3 FDA reports)
INDIFFERENCE ( 3 FDA reports)
INFECTIOUS PERITONITIS ( 3 FDA reports)
INFUSION SITE INDURATION ( 3 FDA reports)
INFUSION SITE INFLAMMATION ( 3 FDA reports)
INFUSION SITE REACTION ( 3 FDA reports)
INJECTION SITE DISCHARGE ( 3 FDA reports)
INJECTION SITE INJURY ( 3 FDA reports)
INJECTION SITE PAPULE ( 3 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 3 FDA reports)
INTENTION TREMOR ( 3 FDA reports)
INTERMITTENT EXPLOSIVE DISORDER ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 3 FDA reports)
INTERVERTEBRAL DISC INJURY ( 3 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 3 FDA reports)
INTESTINAL OPERATION ( 3 FDA reports)
INTRATHECAL PUMP INSERTION ( 3 FDA reports)
INTUSSUSCEPTION ( 3 FDA reports)
JOB DISSATISFACTION ( 3 FDA reports)
JOINT HYPEREXTENSION ( 3 FDA reports)
JOINT MANIPULATION ( 3 FDA reports)
KNEE DEFORMITY ( 3 FDA reports)
LABILE HYPERTENSION ( 3 FDA reports)
LAGOPHTHALMOS ( 3 FDA reports)
LAPAROTOMY ( 3 FDA reports)
LARGE INTESTINAL ULCER ( 3 FDA reports)
LATENT TUBERCULOSIS ( 3 FDA reports)
LAZINESS ( 3 FDA reports)
LDL/HDL RATIO DECREASED ( 3 FDA reports)
LEARNING DISABILITY ( 3 FDA reports)
LENTIGO ( 3 FDA reports)
LEUCINE AMINOPEPTIDASE INCREASED ( 3 FDA reports)
LEUKOPLAKIA ORAL ( 3 FDA reports)
LICHEN SCLEROSUS ( 3 FDA reports)
LIGAMENT DISORDER ( 3 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 3 FDA reports)
LIP EXFOLIATION ( 3 FDA reports)
LIP ULCERATION ( 3 FDA reports)
LIPIDS ABNORMAL ( 3 FDA reports)
LIPOATROPHY ( 3 FDA reports)
LIPOEDEMA ( 3 FDA reports)
LIVIDITY ( 3 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 3 FDA reports)
LOOSE STOOLS ( 3 FDA reports)
LORDOSIS ( 3 FDA reports)
LOWER LIMB DEFORMITY ( 3 FDA reports)
LUPUS NEPHRITIS ( 3 FDA reports)
LUPUS VASCULITIS ( 3 FDA reports)
MACULE ( 3 FDA reports)
MAGNESIUM DEFICIENCY ( 3 FDA reports)
MALE ORGASMIC DISORDER ( 3 FDA reports)
MARASMUS ( 3 FDA reports)
MASTOIDITIS ( 3 FDA reports)
MAXILLOFACIAL OPERATION ( 3 FDA reports)
MEDIASTINITIS ( 3 FDA reports)
MEDICAL OBSERVATION ABNORMAL ( 3 FDA reports)
METASTASES TO OVARY ( 3 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 3 FDA reports)
MICROCYTOSIS ( 3 FDA reports)
MICROGNATHIA ( 3 FDA reports)
MIXED HYPERLIPIDAEMIA ( 3 FDA reports)
MONOCYTE PERCENTAGE ABNORMAL ( 3 FDA reports)
MONONEUROPATHY ( 3 FDA reports)
MONONUCLEOSIS SYNDROME ( 3 FDA reports)
MUSCLE HYPERTROPHY ( 3 FDA reports)
MUSCLE SWELLING ( 3 FDA reports)
MUSCULAR DYSTROPHY ( 3 FDA reports)
MYOCARDIAL STRAIN ( 3 FDA reports)
MYOSCLEROSIS ( 3 FDA reports)
NAIL BED BLEEDING ( 3 FDA reports)
NAIL DISCOLOURATION ( 3 FDA reports)
NAIL INFECTION ( 3 FDA reports)
NASAL MUCOSAL DISORDER ( 3 FDA reports)
NASAL SEPTUM DISORDER ( 3 FDA reports)
NASAL SEPTUM ULCERATION ( 3 FDA reports)
NEEDLE ISSUE ( 3 FDA reports)
NEONATAL RESPIRATORY DEPRESSION ( 3 FDA reports)
NEPHROCALCINOSIS ( 3 FDA reports)
NEPHROPATHY TOXIC ( 3 FDA reports)
NIPPLE DISORDER ( 3 FDA reports)
NITRITE URINE PRESENT ( 3 FDA reports)
NOCTURNAL DYSPNOEA ( 3 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 3 FDA reports)
NORMAL TENSION GLAUCOMA ( 3 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 3 FDA reports)
OCULAR DISCOMFORT ( 3 FDA reports)
OESOPHAGEAL MASS ( 3 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 3 FDA reports)
OESOPHAGITIS ULCERATIVE ( 3 FDA reports)
ONCOLOGIC COMPLICATION ( 3 FDA reports)
OPISTHOTONUS ( 3 FDA reports)
OPSOCLONUS MYOCLONUS ( 3 FDA reports)
OPTIC NERVE INJURY ( 3 FDA reports)
OPTIC NEUROPATHY ( 3 FDA reports)
ORAL PRURITUS ( 3 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 3 FDA reports)
OTITIS MEDIA ACUTE ( 3 FDA reports)
OVARIAN GRANULOSA-THECA CELL TUMOUR ( 3 FDA reports)
PANCREATIC CALCIFICATION ( 3 FDA reports)
PANCREATIC MASS ( 3 FDA reports)
PATIENT ISOLATION ( 3 FDA reports)
PELVIC CONGESTION ( 3 FDA reports)
PELVIC DISCOMFORT ( 3 FDA reports)
PELVIC PERITONEAL ADHESIONS ( 3 FDA reports)
PERICARDIAL HAEMORRHAGE ( 3 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 3 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED ( 3 FDA reports)
PHLEBITIS SUPERFICIAL ( 3 FDA reports)
PHLEBOTOMY ( 3 FDA reports)
PICA ( 3 FDA reports)
PNEUMOCOCCAL SEPSIS ( 3 FDA reports)
PNEUMONIA FUNGAL ( 3 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 3 FDA reports)
POLYMYALGIA RHEUMATICA ( 3 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 3 FDA reports)
POOR SUCKING REFLEX ( 3 FDA reports)
PORIOMANIA ( 3 FDA reports)
PORPHYRIA ACUTE ( 3 FDA reports)
POSITIVE ROMBERGISM ( 3 FDA reports)
POST PROCEDURAL BILE LEAK ( 3 FDA reports)
POST PROCEDURAL HAEMATOMA ( 3 FDA reports)
POSTICTAL PARALYSIS ( 3 FDA reports)
POSTOPERATIVE FEVER ( 3 FDA reports)
PRECANCEROUS SKIN LESION ( 3 FDA reports)
PREGNANCY WITH IMPLANT CONTRACEPTIVE ( 3 FDA reports)
PRESBYOESOPHAGUS ( 3 FDA reports)
PRINZMETAL ANGINA ( 3 FDA reports)
PROCEDURAL NAUSEA ( 3 FDA reports)
PRODUCT COATING ISSUE ( 3 FDA reports)
PRODUCT COLOUR ISSUE ( 3 FDA reports)
PRODUCT ODOUR ABNORMAL ( 3 FDA reports)
PRODUCT RECONSTITUTION ISSUE ( 3 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 3 FDA reports)
PROTEIN URINE ( 3 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 3 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 3 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 3 FDA reports)
PSEUDODEMENTIA ( 3 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 3 FDA reports)
PSEUDOMONAL SEPSIS ( 3 FDA reports)
PUBIS FRACTURE ( 3 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 3 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 3 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 3 FDA reports)
PULMONARY SEPSIS ( 3 FDA reports)
PULMONARY TOXICITY ( 3 FDA reports)
PULSE PRESSURE DECREASED ( 3 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 3 FDA reports)
PYONEPHROSIS ( 3 FDA reports)
RECTAL CANCER ( 3 FDA reports)
RECTAL DISCHARGE ( 3 FDA reports)
RECTAL LESION ( 3 FDA reports)
RECTAL POLYPECTOMY ( 3 FDA reports)
RECURRENT CANCER ( 3 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 3 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 3 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 3 FDA reports)
RENAL ARTERY OCCLUSION ( 3 FDA reports)
RENAL CELL CARCINOMA ( 3 FDA reports)
RENAL TRANSPLANT ( 3 FDA reports)
RESIDUAL URINE ( 3 FDA reports)
RESPIRATORY FATIGUE ( 3 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS BRONCHIOLITIS ( 3 FDA reports)
RETICULIN INCREASED ( 3 FDA reports)
RETICULOCYTE COUNT ABNORMAL ( 3 FDA reports)
RETINAL ARTERY THROMBOSIS ( 3 FDA reports)
RETROPERITONEAL FIBROSIS ( 3 FDA reports)
RETROPERITONEAL NEOPLASM ( 3 FDA reports)
RHEUMATOID LUNG ( 3 FDA reports)
SALIVA ALTERED ( 3 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 3 FDA reports)
SALPINGO-OOPHORECTOMY ( 3 FDA reports)
SCAR EXCISION ( 3 FDA reports)
SCAR PAIN ( 3 FDA reports)
SCHIZOPHRENIA, DISORGANISED TYPE ( 3 FDA reports)
SCHIZOPHRENIFORM DISORDER ( 3 FDA reports)
SCIATIC NERVE INJURY ( 3 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 3 FDA reports)
SELF MUTILATION ( 3 FDA reports)
SENSE OF OPPRESSION ( 3 FDA reports)
SENSORIMOTOR DISORDER ( 3 FDA reports)
SEPSIS SYNDROME ( 3 FDA reports)
SEPTIC ENCEPHALOPATHY ( 3 FDA reports)
SERRATIA SEPSIS ( 3 FDA reports)
SEXUAL ABUSE ( 3 FDA reports)
SHOPLIFTING ( 3 FDA reports)
SINUS ARREST ( 3 FDA reports)
SINUSITIS BACTERIAL ( 3 FDA reports)
SINUSITIS FUNGAL ( 3 FDA reports)
SKIN DEGENERATIVE DISORDER ( 3 FDA reports)
SKIN INJURY ( 3 FDA reports)
SKULL FRACTURED BASE ( 3 FDA reports)
SMALL CELL LUNG CANCER EXTENSIVE STAGE ( 3 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 3 FDA reports)
SMALL FOR DATES BABY ( 3 FDA reports)
SMALL INTESTINAL PERFORATION ( 3 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 3 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 3 FDA reports)
SPINAL CORD INJURY ( 3 FDA reports)
SPINAL CORD INJURY CERVICAL ( 3 FDA reports)
SPINAL DEFORMITY ( 3 FDA reports)
SPINAL LAMINECTOMY ( 3 FDA reports)
SPINAL X-RAY ABNORMAL ( 3 FDA reports)
SPLEEN CONGESTION ( 3 FDA reports)
SPONDYLOARTHROPATHY ( 3 FDA reports)
SPUTUM RETENTION ( 3 FDA reports)
STENOTROPHOMONAS INFECTION ( 3 FDA reports)
STENT OCCLUSION ( 3 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 3 FDA reports)
STRESS CARDIOMYOPATHY ( 3 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 3 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 3 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 3 FDA reports)
SUDDEN UNEXPLAINED DEATH IN EPILEPSY ( 3 FDA reports)
SUPERINFECTION LUNG ( 3 FDA reports)
SUPRAPUBIC PAIN ( 3 FDA reports)
SYSTEMIC SCLEROSIS ( 3 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 3 FDA reports)
TENDON PAIN ( 3 FDA reports)
TESTICULAR CYST ( 3 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 3 FDA reports)
THORACOTOMY ( 3 FDA reports)
THROMBOCYTHAEMIA ( 3 FDA reports)
THYROIDECTOMY ( 3 FDA reports)
TONGUE EXFOLIATION ( 3 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 3 FDA reports)
TOOTH MALFORMATION ( 3 FDA reports)
TOXOPLASMOSIS ( 3 FDA reports)
TRACHEITIS ( 3 FDA reports)
TRANSPLANT FAILURE ( 3 FDA reports)
TRANSPLANT REJECTION ( 3 FDA reports)
TRICHIASIS ( 3 FDA reports)
TRICUSPID VALVE DISEASE ( 3 FDA reports)
TRIGEMINAL NERVE ABLATION ( 3 FDA reports)
TRISOMY 21 ( 3 FDA reports)
TROUSSEAU'S SYNDROME ( 3 FDA reports)
TUBERCULOSIS GASTROINTESTINAL ( 3 FDA reports)
TUMOUR MARKER INCREASED ( 3 FDA reports)
TUMOUR NECROSIS ( 3 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 3 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 3 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 3 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 3 FDA reports)
UPPER MOTOR NEURONE LESION ( 3 FDA reports)
URETERIC OBSTRUCTION ( 3 FDA reports)
URETHRAL HAEMORRHAGE ( 3 FDA reports)
URINARY BLADDER POLYP ( 3 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 3 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 3 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 3 FDA reports)
URINE KETONE BODY ( 3 FDA reports)
UTEROVAGINAL PROLAPSE ( 3 FDA reports)
VAGINAL MYCOSIS ( 3 FDA reports)
VAGINITIS ATROPHIC ( 3 FDA reports)
VARICELLA VIRUS TEST POSITIVE ( 3 FDA reports)
VASCULAR OCCLUSION ( 3 FDA reports)
VASCULAR PURPURA ( 3 FDA reports)
VENOUS STASIS ( 3 FDA reports)
VERBAL ABUSE ( 3 FDA reports)
VICTIM OF ABUSE ( 3 FDA reports)
VICTIM OF SEXUAL ABUSE ( 3 FDA reports)
VISUAL ACUITY REDUCED TRANSIENTLY ( 3 FDA reports)
VULVAL ABSCESS ( 3 FDA reports)
VULVAL ULCERATION ( 3 FDA reports)
VULVOVAGINAL PAIN ( 3 FDA reports)
WAXY FLEXIBILITY ( 3 FDA reports)
WEIGHT GAIN POOR ( 3 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 3 FDA reports)
WHOLE BLOOD TRANSFUSION ( 3 FDA reports)
WOUND DEBRIDEMENT ( 3 FDA reports)
WOUND INFECTION FUNGAL ( 3 FDA reports)
XANTHOGRANULOMA ( 3 FDA reports)
POSTURING ( 2 FDA reports)
PREALBUMIN DECREASED ( 2 FDA reports)
PRECOCIOUS PUBERTY ( 2 FDA reports)
PREGNANCY AFTER POST COITAL CONTRACEPTION ( 2 FDA reports)
PRESBYACUSIS ( 2 FDA reports)
PROCEDURAL SITE REACTION ( 2 FDA reports)
PRODUCT CONTAINER ISSUE ( 2 FDA reports)
PRODUCT LABEL ISSUE ( 2 FDA reports)
PRODUCT OUTER PACKAGING ISSUE ( 2 FDA reports)
PRODUCT SHAPE ISSUE ( 2 FDA reports)
PRODUCT SIZE ISSUE ( 2 FDA reports)
PROLONGED PREGNANCY ( 2 FDA reports)
PROSTHESIS IMPLANTATION ( 2 FDA reports)
PROTEUS TEST POSITIVE ( 2 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 2 FDA reports)
PROTHROMBIN TIME RATIO ABNORMAL ( 2 FDA reports)
PSEUDARTHROSIS ( 2 FDA reports)
PSEUDOCYST ( 2 FDA reports)
PSEUDOLYMPHOMA ( 2 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 2 FDA reports)
PSEUDOMONONUCLEOSIS ( 2 FDA reports)
PSEUDOPHAKIA ( 2 FDA reports)
PSYCHOSOMATIC DISEASE ( 2 FDA reports)
PULMONARY VALVE DISEASE ( 2 FDA reports)
PULMONARY VASCULAR DISORDER ( 2 FDA reports)
PYELECTASIA ( 2 FDA reports)
PYELONEPHRITIS CHRONIC ( 2 FDA reports)
PYODERMA ( 2 FDA reports)
PYODERMA GANGRENOSUM ( 2 FDA reports)
RADIAL PULSE ABNORMAL ( 2 FDA reports)
RADIATION SKIN INJURY ( 2 FDA reports)
RADICULAR CYST ( 2 FDA reports)
RADICULAR SYNDROME ( 2 FDA reports)
RASMUSSEN ENCEPHALITIS ( 2 FDA reports)
RECTAL TENESMUS ( 2 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 2 FDA reports)
REFRACTORINESS TO PLATELET TRANSFUSION ( 2 FDA reports)
REMOVAL OF RENAL TRANSPLANT ( 2 FDA reports)
RENAL FUNCTION TEST ( 2 FDA reports)
RENAL HYPERTROPHY ( 2 FDA reports)
RENAL NEOPLASM ( 2 FDA reports)
RENAL VESSEL DISORDER ( 2 FDA reports)
RENIN DECREASED ( 2 FDA reports)
RESPIRATORY ALKALOSIS ( 2 FDA reports)
RESPIRATORY RATE ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 2 FDA reports)
RETICULOCYTE COUNT DECREASED ( 2 FDA reports)
RETICULOCYTE COUNT INCREASED ( 2 FDA reports)
RETINAL DISORDER ( 2 FDA reports)
RETINAL VEIN OCCLUSION ( 2 FDA reports)
RETINITIS ( 2 FDA reports)
REVERSIBLE ISCHAEMIC NEUROLOGICAL DEFICIT ( 2 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 2 FDA reports)
ROULEAUX FORMATION ( 2 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 2 FDA reports)
SALIVARY GLAND MASS ( 2 FDA reports)
SALIVARY GLAND NEOPLASM ( 2 FDA reports)
SALMONELLA TEST POSITIVE ( 2 FDA reports)
SCHIZOPHRENIA SIMPLE ( 2 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 2 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 2 FDA reports)
SECONDARY SEXUAL CHARACTERISTICS ABSENCE ( 2 FDA reports)
SEIZURE LIKE PHENOMENA ( 2 FDA reports)
SEMINOMA ( 2 FDA reports)
SEPTOPLASTY ( 2 FDA reports)
SERONEGATIVE ARTHRITIS ( 2 FDA reports)
SERUM SICKNESS ( 2 FDA reports)
SEXUAL ASSAULT VICTIM ( 2 FDA reports)
SHIFT TO THE LEFT ( 2 FDA reports)
SHUNT OCCLUSION ( 2 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 2 FDA reports)
SKIN BACTERIAL INFECTION ( 2 FDA reports)
SKIN GRAFT ( 2 FDA reports)
SKIN HYPOPIGMENTATION ( 2 FDA reports)
SKIN INFLAMMATION ( 2 FDA reports)
SKIN NODULE ( 2 FDA reports)
SKIN TEST POSITIVE ( 2 FDA reports)
SPIDER NAEVUS ( 2 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 2 FDA reports)
SPLENECTOMY ( 2 FDA reports)
SPLENIC VEIN THROMBOSIS ( 2 FDA reports)
SPUTUM INCREASED ( 2 FDA reports)
STAG HORN CALCULUS ( 2 FDA reports)
STAPHYLOCOCCAL IDENTIFICATION TEST POSITIVE ( 2 FDA reports)
STARVATION ( 2 FDA reports)
STASIS SYNDROME ( 2 FDA reports)
STENT REMOVAL ( 2 FDA reports)
STOMATITIS HAEMORRHAGIC ( 2 FDA reports)
STOOL ANALYSIS ABNORMAL ( 2 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 2 FDA reports)
SUDDEN HEARING LOSS ( 2 FDA reports)
SUPERINFECTION BACTERIAL ( 2 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 2 FDA reports)
SUPRANUCLEAR PALSY ( 2 FDA reports)
SUTURE INSERTION ( 2 FDA reports)
SUTURE RUPTURE ( 2 FDA reports)
SYMPTOM MASKED ( 2 FDA reports)
SYPHILIS ( 2 FDA reports)
SYSTOLIC HYPERTENSION ( 2 FDA reports)
T-CELL TYPE ACUTE LEUKAEMIA ( 2 FDA reports)
TANGENTIALITY ( 2 FDA reports)
TERATOGENICITY ( 2 FDA reports)
TERMINAL STATE ( 2 FDA reports)
TESTICULAR FAILURE ( 2 FDA reports)
TESTICULAR NEOPLASM ( 2 FDA reports)
TESTIS CANCER ( 2 FDA reports)
THALASSAEMIA TRAIT ( 2 FDA reports)
THREATENED LABOUR ( 2 FDA reports)
THROMBIN TIME SHORTENED ( 2 FDA reports)
THROMBOTIC STROKE ( 2 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
THYROID ATROPHY ( 2 FDA reports)
THYROID GLAND CANCER ( 2 FDA reports)
THYROID MASS ( 2 FDA reports)
THYROTOXIC CRISIS ( 2 FDA reports)
THYROXINE DECREASED ( 2 FDA reports)
THYROXINE FREE DECREASED ( 2 FDA reports)
TINEA INFECTION ( 2 FDA reports)
TOBACCO WITHDRAWAL SYMPTOMS ( 2 FDA reports)
TONGUE NEOPLASM ( 2 FDA reports)
TONGUE SPASM ( 2 FDA reports)
TONSILLAR HYPERTROPHY ( 2 FDA reports)
TONSILLECTOMY ( 2 FDA reports)
TOTAL BILE ACIDS INCREASED ( 2 FDA reports)
TOXIC NEUROPATHY ( 2 FDA reports)
TOXIC SHOCK SYNDROME ( 2 FDA reports)
TRACHEAL DISORDER ( 2 FDA reports)
TRANCE ( 2 FDA reports)
TRANSFERRIN DECREASED ( 2 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 2 FDA reports)
TRANSFERRIN SATURATION INCREASED ( 2 FDA reports)
TRANSFUSION REACTION ( 2 FDA reports)
TRANSIENT TACHYPNOEA OF THE NEWBORN ( 2 FDA reports)
TRANSPLANT ( 2 FDA reports)
TRAUMATIC LIVER INJURY ( 2 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 2 FDA reports)
TRICHOMONIASIS ( 2 FDA reports)
TRICHOTILLOMANIA ( 2 FDA reports)
TROPONIN T INCREASED ( 2 FDA reports)
TUMOUR PAIN ( 2 FDA reports)
UHTHOFF'S PHENOMENON ( 2 FDA reports)
ULNAR NERVE PALSY ( 2 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 2 FDA reports)
UMBILICAL HERNIA PERFORATION ( 2 FDA reports)
UNEQUAL LEG LENGTH ACQUIRED ( 2 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 2 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 2 FDA reports)
URETHRAL ATROPHY ( 2 FDA reports)
URETHRAL OBSTRUCTION ( 2 FDA reports)
URETHRAL OPERATION ( 2 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 2 FDA reports)
URINARY CASTS ( 2 FDA reports)
URINARY TRACT PAIN ( 2 FDA reports)
URINE SODIUM INCREASED ( 2 FDA reports)
UTERINE PROLAPSE ( 2 FDA reports)
VACCINATION COMPLICATION ( 2 FDA reports)
VAGINAL CYST ( 2 FDA reports)
VAGINAL ODOUR ( 2 FDA reports)
VASCULITIS NECROTISING ( 2 FDA reports)
VASOSPASM ( 2 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 2 FDA reports)
VENOUS STENOSIS ( 2 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 2 FDA reports)
VESSEL PERFORATION ( 2 FDA reports)
VIRAL LOAD INCREASED ( 2 FDA reports)
VIRAL RASH ( 2 FDA reports)
VISCERAL CONGESTION ( 2 FDA reports)
VISUAL BRIGHTNESS ( 2 FDA reports)
VISUAL TRACKING TEST ABNORMAL ( 2 FDA reports)
VITAMIN E DEFICIENCY ( 2 FDA reports)
VITRECTOMY ( 2 FDA reports)
VITREOUS DETACHMENT ( 2 FDA reports)
VOCAL CORD CYST ( 2 FDA reports)
VOMITING IN PREGNANCY ( 2 FDA reports)
VULVAL CANCER ( 2 FDA reports)
VULVAL DISORDER ( 2 FDA reports)
WEST NILE VIRAL INFECTION ( 2 FDA reports)
WHIPLASH INJURY ( 2 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 2 FDA reports)
WOUND NECROSIS ( 2 FDA reports)
XANTHOCHROMIA ( 2 FDA reports)
XANTHOMA ( 2 FDA reports)
XEROSIS ( 2 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 2 FDA reports)
ABDOMINAL WALL ABSCESS ( 2 FDA reports)
ACANTHOMA ( 2 FDA reports)
ACCIDENTAL NEEDLE STICK ( 2 FDA reports)
ACETABULUM FRACTURE ( 2 FDA reports)
ACID BASE BALANCE ABNORMAL ( 2 FDA reports)
ACINETOBACTER TEST POSITIVE ( 2 FDA reports)
ACNE CYSTIC ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 2 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 2 FDA reports)
ACUTE STRESS DISORDER ( 2 FDA reports)
ADMINISTRATION SITE REACTION ( 2 FDA reports)
ADRENAL CORTICAL INSUFFICIENCY ( 2 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 2 FDA reports)
ALBUMINURIA ( 2 FDA reports)
ALCOHOLIC PANCREATITIS ( 2 FDA reports)
ALCOHOLIC SEIZURE ( 2 FDA reports)
ALDOLASE INCREASED ( 2 FDA reports)
ALPERS' DISEASE ( 2 FDA reports)
ALPHA-1 ANTI-TRYPSIN INCREASED ( 2 FDA reports)
ALVEOLAR OSTEITIS ( 2 FDA reports)
ALVEOLITIS ALLERGIC ( 2 FDA reports)
AMINOACIDURIA ( 2 FDA reports)
AMNESTIC DISORDER ( 2 FDA reports)
AMPHETAMINES POSITIVE ( 2 FDA reports)
ANAL CANCER ( 2 FDA reports)
ANAL STENOSIS ( 2 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 2 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 2 FDA reports)
ANEURYSM REPAIR ( 2 FDA reports)
ANGIOMYOLIPOMA ( 2 FDA reports)
ANTERIOR CHAMBER CLEAVAGE SYNDROME ( 2 FDA reports)
ANTEROGRADE AMNESIA ( 2 FDA reports)
ANTIBODY TEST ABNORMAL ( 2 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 2 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 2 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 2 FDA reports)
AORTIC INJURY ( 2 FDA reports)
AORTIC VALVE STENOSIS ( 2 FDA reports)
APPENDIX DISORDER ( 2 FDA reports)
APPLICATION SITE BURNING ( 2 FDA reports)
APPLICATION SITE DRYNESS ( 2 FDA reports)
APPLICATION SITE PARAESTHESIA ( 2 FDA reports)
APPLICATION SITE PERSPIRATION ( 2 FDA reports)
APPLICATION SITE SWELLING ( 2 FDA reports)
APPLICATION SITE URTICARIA ( 2 FDA reports)
ARTERIOSCLEROSIS MOENCKEBERG-TYPE ( 2 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 2 FDA reports)
ARTHROSCOPY ( 2 FDA reports)
ASTHMATIC CRISIS ( 2 FDA reports)
ATRIOVENTRICULAR SEPTAL DEFECT ( 2 FDA reports)
ATROPHY OF TONGUE PAPILLAE ( 2 FDA reports)
ATYPICAL FEMUR FRACTURE ( 2 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 2 FDA reports)
AVULSION FRACTURE ( 2 FDA reports)
BACTERIAL CULTURE POSITIVE ( 2 FDA reports)
BARTHOLIN'S CYST ( 2 FDA reports)
BASILAR MIGRAINE ( 2 FDA reports)
BASOPHIL PERCENTAGE INCREASED ( 2 FDA reports)
BENIGN BONE NEOPLASM ( 2 FDA reports)
BENIGN HEPATIC NEOPLASM ( 2 FDA reports)
BENIGN HYDATIDIFORM MOLE ( 2 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 2 FDA reports)
BENIGN MUSCLE NEOPLASM ( 2 FDA reports)
BEZOAR ( 2 FDA reports)
BICUSPID AORTIC VALVE ( 2 FDA reports)
BILATERAL HYDRONEPHROSIS ( 2 FDA reports)
BILIRUBIN URINE ( 2 FDA reports)
BINOCULAR EYE MOVEMENT DISORDER ( 2 FDA reports)
BLADDER CANCER STAGE 0, WITH CANCER IN SITU ( 2 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 2 FDA reports)
BLINDNESS CORTICAL ( 2 FDA reports)
BLISTER INFECTED ( 2 FDA reports)
BLOOD ALDOSTERONE DECREASED ( 2 FDA reports)
BLOOD ALDOSTERONE INCREASED ( 2 FDA reports)
BLOOD BILIRUBIN DECREASED ( 2 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 2 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 2 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 2 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE DECREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 2 FDA reports)
BLOOD INSULIN INCREASED ( 2 FDA reports)
BLOOD KETONE BODY DECREASED ( 2 FDA reports)
BLOOD LACTIC ACID DECREASED ( 2 FDA reports)
BLOOD LUTEINISING HORMONE INCREASED ( 2 FDA reports)
BLOOD OSMOLARITY INCREASED ( 2 FDA reports)
BLOOD PRESSURE ( 2 FDA reports)
BLOOD PROLACTIN ABNORMAL ( 2 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 2 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 2 FDA reports)
BLOODY DISCHARGE ( 2 FDA reports)
BLUNTED AFFECT ( 2 FDA reports)
BODY TINEA ( 2 FDA reports)
BONE CYST ( 2 FDA reports)
BONE DEFORMITY ( 2 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 2 FDA reports)
BONE FISTULA ( 2 FDA reports)
BONE MARROW DEPRESSION ( 2 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 2 FDA reports)
BONE SWELLING ( 2 FDA reports)
BORDETELLA INFECTION ( 2 FDA reports)
BRACHIAL PLEXUS INJURY ( 2 FDA reports)
BRAIN STEM HAEMORRHAGE ( 2 FDA reports)
BRAIN STEM INFARCTION ( 2 FDA reports)
BREAST ATROPHY ( 2 FDA reports)
BREAST DYSPLASIA ( 2 FDA reports)
BREAST ENGORGEMENT ( 2 FDA reports)
BREATH HOLDING ( 2 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 2 FDA reports)
BRONCHIAL INFECTION ( 2 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 2 FDA reports)
BRONCHITIS VIRAL ( 2 FDA reports)
BRONCHOSCOPY ABNORMAL ( 2 FDA reports)
BRONCHOSPASM PARADOXICAL ( 2 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 2 FDA reports)
BURKITT'S LYMPHOMA ( 2 FDA reports)
BURN OESOPHAGEAL ( 2 FDA reports)
BURSA CALCIFICATION ( 2 FDA reports)
BURSITIS INFECTIVE STAPHYLOCOCCAL ( 2 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 2 FDA reports)
CANCER PAIN ( 2 FDA reports)
CAPILLARY PERMEABILITY INCREASED ( 2 FDA reports)
CARCINOMA ( 2 FDA reports)
CARDIAC ABLATION ( 2 FDA reports)
CARDIAC ASSISTANCE DEVICE USER ( 2 FDA reports)
CARDIAC ASTHMA ( 2 FDA reports)
CARDIAC DEATH ( 2 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 2 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 2 FDA reports)
CARDIOSPASM ( 2 FDA reports)
CAROTID ARTERY THROMBOSIS ( 2 FDA reports)
CATHETER SITE INFLAMMATION ( 2 FDA reports)
CATHETER SITE OEDEMA ( 2 FDA reports)
CATHETER SITE PHLEBITIS ( 2 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 2 FDA reports)
CAUDA EQUINA SYNDROME ( 2 FDA reports)
CELL MARKER INCREASED ( 2 FDA reports)
CENTRAL-ALVEOLAR HYPOVENTILATION ( 2 FDA reports)
CEREBELLAR INFARCTION ( 2 FDA reports)
CEREBRAL HAEMORRHAGE TRAUMATIC ( 2 FDA reports)
CEREBROSCLEROSIS ( 2 FDA reports)
CERULOPLASMIN INCREASED ( 2 FDA reports)
CERVICAL CORD COMPRESSION ( 2 FDA reports)
CERVICAL MYELOPATHY ( 2 FDA reports)
CERVICAL POLYP ( 2 FDA reports)
CERVICAL SPINE FLATTENING ( 2 FDA reports)
CERVIX HAEMORRHAGE UTERINE ( 2 FDA reports)
CHANGE IN SUSTAINED ATTENTION ( 2 FDA reports)
CHEILOSIS ( 2 FDA reports)
CHEMICAL BURN OF SKIN ( 2 FDA reports)
CHOLECYSTITIS INFECTIVE ( 2 FDA reports)
CHOLELITHIASIS OBSTRUCTIVE ( 2 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
CHRONIC HEPATITIS ( 2 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 2 FDA reports)
CHRONOTROPIC INCOMPETENCE ( 2 FDA reports)
CIRCULATING ANTICOAGULANT ( 2 FDA reports)
CLEAR CELL SARCOMA OF THE KIDNEY ( 2 FDA reports)
CLUTTERING ( 2 FDA reports)
COCCIDIOIDOMYCOSIS ( 2 FDA reports)
COCCYDYNIA ( 2 FDA reports)
COLON CANCER STAGE IV ( 2 FDA reports)
COMEDONE ( 2 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 2 FDA reports)
COMPULSIVE SEXUAL BEHAVIOUR ( 2 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 2 FDA reports)
CONGENITAL BLADDER ANOMALY ( 2 FDA reports)
CONGENITAL EYE DISORDER ( 2 FDA reports)
CONGENITAL MULTIPLEX ARTHROGRYPOSIS ( 2 FDA reports)
CONGENITAL NAIL DISORDER ( 2 FDA reports)
CONGENITAL URINARY TRACT OBSTRUCTION ( 2 FDA reports)
CONJUNCTIVAL PALLOR ( 2 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 2 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 2 FDA reports)
CONTRAST MEDIA ALLERGY ( 2 FDA reports)
COOMBS TEST POSITIVE ( 2 FDA reports)
COR PULMONALE ACUTE ( 2 FDA reports)
COR PULMONALE CHRONIC ( 2 FDA reports)
CORD BLOOD TRANSPLANT THERAPY ( 2 FDA reports)
CORNEAL REFLEX DECREASED ( 2 FDA reports)
CORONARY ANGIOPLASTY ( 2 FDA reports)
CORROSIVE GASTRITIS ( 2 FDA reports)
CORYNEBACTERIUM INFECTION ( 2 FDA reports)
CRANIOFACIAL DYSOSTOSIS ( 2 FDA reports)
CREST SYNDROME ( 2 FDA reports)
CRUSH INJURY ( 2 FDA reports)
CSF CELL COUNT INCREASED ( 2 FDA reports)
CSF NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
CSF TEST ABNORMAL ( 2 FDA reports)
CSF WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
CULTURE THROAT POSITIVE ( 2 FDA reports)
CUSHINGOID ( 2 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 2 FDA reports)
CUTANEOUS VASCULITIS ( 2 FDA reports)
CYANOSIS NEONATAL ( 2 FDA reports)
CYCLIC VOMITING SYNDROME ( 2 FDA reports)
CYST RUPTURE ( 2 FDA reports)
CYSTITIS ESCHERICHIA ( 2 FDA reports)
CYTOGENETIC ABNORMALITY ( 2 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 2 FDA reports)
DARK CIRCLES UNDER EYES ( 2 FDA reports)
DAYDREAMING ( 2 FDA reports)
DEATH OF COMPANION ( 2 FDA reports)
DEJA VU ( 2 FDA reports)
DELUSION OF REFERENCE ( 2 FDA reports)
DENTAL IMPLANTATION ( 2 FDA reports)
DENTAL TREATMENT ( 2 FDA reports)
DERMATITIS ATOPIC ( 2 FDA reports)
DERMATOPHYTOSIS ( 2 FDA reports)
DEVICE ADHESION ISSUE ( 2 FDA reports)
DEVICE CONNECTION ISSUE ( 2 FDA reports)
DEVICE DEPOSIT ISSUE ( 2 FDA reports)
DEVICE ELECTRICAL FINDING ( 2 FDA reports)
DEVICE INEFFECTIVE ( 2 FDA reports)
DEVICE INTERACTION ( 2 FDA reports)
DEVICE MISUSE ( 2 FDA reports)
DEVICE PACING ISSUE ( 2 FDA reports)
DEVICE RELATED SEPSIS ( 2 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 2 FDA reports)
DIABETIC BLINDNESS ( 2 FDA reports)
DIABETIC VASCULAR DISORDER ( 2 FDA reports)
DIAPHRAGMALGIA ( 2 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 2 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 2 FDA reports)
DISBACTERIOSIS ( 2 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 2 FDA reports)
DNA ANTIBODY POSITIVE ( 2 FDA reports)
DRUG ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE ( 2 FDA reports)
DRUG DELIVERY DEVICE IMPLANTATION ( 2 FDA reports)
DRUG DETOXIFICATION ( 2 FDA reports)
DRUG EFFECT PROLONGED ( 2 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 2 FDA reports)
DRUG-INDUCED LIVER INJURY ( 2 FDA reports)
DUODENAL OBSTRUCTION ( 2 FDA reports)
DUPUYTREN'S CONTRACTURE ( 2 FDA reports)
DYSACUSIS ( 2 FDA reports)
DYSPNOEA AT REST ( 2 FDA reports)
EAR CANAL STENOSIS ( 2 FDA reports)
EAR INJURY ( 2 FDA reports)
EAR NEOPLASM MALIGNANT ( 2 FDA reports)
EAR PRURITUS ( 2 FDA reports)
EATING DISORDER SYMPTOM ( 2 FDA reports)
EDUCATIONAL PROBLEM ( 2 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 2 FDA reports)
ELECTROCARDIOGRAM PQ INTERVAL PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE BIPHASIC ( 2 FDA reports)
ELECTROCONVULSIVE THERAPY ( 2 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 2 FDA reports)
ENDOMETRIAL CANCER ( 2 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 2 FDA reports)
ENDOPHTHALMITIS ( 2 FDA reports)
ENGRAFT FAILURE ( 2 FDA reports)
ENTEROBACTER BACTERAEMIA ( 2 FDA reports)
ENTEROBACTER TEST POSITIVE ( 2 FDA reports)
ENTEROSTOMY ( 2 FDA reports)
EOSINOPHILIC OESOPHAGITIS ( 2 FDA reports)
EOSINOPHILIC PNEUMONIA ACUTE ( 2 FDA reports)
ERYTHEMA ELEVATUM DIUTINUM ( 2 FDA reports)
ERYTHEMA INFECTIOSUM ( 2 FDA reports)
EUSTACHIAN TUBE OBSTRUCTION ( 2 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 2 FDA reports)
EXPOSURE TO EXTREME TEMPERATURE ( 2 FDA reports)
EXTERNAL EAR PAIN ( 2 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 2 FDA reports)
EXTRAVASATION ( 2 FDA reports)
EXTRUSION OF DEVICE ( 2 FDA reports)
FACTITIOUS DISORDER ( 2 FDA reports)
FACTOR V LEIDEN MUTATION ( 2 FDA reports)
FASCIITIS ( 2 FDA reports)
FAT EMBOLISM ( 2 FDA reports)
FAT REDISTRIBUTION ( 2 FDA reports)
FEMORAL ARTERY OCCLUSION ( 2 FDA reports)
FEVER NEONATAL ( 2 FDA reports)
FIBROMA ( 2 FDA reports)
FIBROUS HISTIOCYTOMA ( 2 FDA reports)
FLAIL CHEST ( 2 FDA reports)
FLAT ANTERIOR CHAMBER OF EYE ( 2 FDA reports)
FOETAL DEATH ( 2 FDA reports)
FOETAL GROWTH RESTRICTION ( 2 FDA reports)
FOETAL MALFORMATION ( 2 FDA reports)
FOOT AMPUTATION ( 2 FDA reports)
FOOT OPERATION ( 2 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 2 FDA reports)
FORCEPS DELIVERY ( 2 FDA reports)
FOREIGN BODY IN EYE ( 2 FDA reports)
FRACTURE MALUNION ( 2 FDA reports)
FUNGAL CYSTITIS ( 2 FDA reports)
FUNGAL OESOPHAGITIS ( 2 FDA reports)
GALLBLADDER OBSTRUCTION ( 2 FDA reports)
GANGLION ( 2 FDA reports)
GAS GANGRENE ( 2 FDA reports)
GASTRIC ATONY ( 2 FDA reports)
GASTRIC MUCOSAL LESION ( 2 FDA reports)
GASTRITIS VIRAL ( 2 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 2 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 2 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 2 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 2 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 2 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 2 FDA reports)
GENITAL HAEMORRHAGE ( 2 FDA reports)
GENITAL HERPES ( 2 FDA reports)
GENITAL PAIN ( 2 FDA reports)
GILBERT'S SYNDROME ( 2 FDA reports)
GINGIVAL ATROPHY ( 2 FDA reports)
GLOBULINS DECREASED ( 2 FDA reports)
GLOMERULOSCLEROSIS ( 2 FDA reports)
GLOSSOPTOSIS ( 2 FDA reports)
GRAFT DYSFUNCTION ( 2 FDA reports)
GRANULOCYTES MATURATION ARREST ( 2 FDA reports)
GRANULOCYTOSIS ( 2 FDA reports)
GRANULOMA SKIN ( 2 FDA reports)
HAEMARTHROSIS ( 2 FDA reports)
HAEMATOSPERMIA ( 2 FDA reports)
HAEMOCONCENTRATION ( 2 FDA reports)
HAEMOPHILUS INFECTION ( 2 FDA reports)
HAEMORRHOID OPERATION ( 2 FDA reports)
HAEMOSIDEROSIS ( 2 FDA reports)
HAIRY CELL LEUKAEMIA ( 2 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 2 FDA reports)
HEAD CIRCUMFERENCE ( 2 FDA reports)
HEAD DEFORMITY ( 2 FDA reports)
HEAD LAG ABNORMAL ( 2 FDA reports)
HEART VALVE INSUFFICIENCY ( 2 FDA reports)
HEMIVERTEBRA ( 2 FDA reports)
HEPATIC ADENOMA ( 2 FDA reports)
HEPATIC HAEMORRHAGE ( 2 FDA reports)
HEPATIC INFARCTION ( 2 FDA reports)
HEPATIC INFECTION BACTERIAL ( 2 FDA reports)
HEPATIC INFILTRATION EOSINOPHILIC ( 2 FDA reports)
HEPATIC ISCHAEMIA ( 2 FDA reports)
HEPATIC RUPTURE ( 2 FDA reports)
HEPATIC VEIN THROMBOSIS ( 2 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 2 FDA reports)
HERPES ZOSTER DISSEMINATED ( 2 FDA reports)
HIDRADENITIS ( 2 FDA reports)
HIGH FREQUENCY ABLATION ( 2 FDA reports)
HIGH RISK SEXUAL BEHAVIOUR ( 2 FDA reports)
HISTOPLASMOSIS ( 2 FDA reports)
HODGKIN'S DISEASE STAGE II ( 2 FDA reports)
HOFFMANN'S SIGN ( 2 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 2 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 2 FDA reports)
HYPERGLYCAEMIC SEIZURE ( 2 FDA reports)
HYPEROSMOLAR STATE ( 2 FDA reports)
HYPERPLASIA ( 2 FDA reports)
HYPERPROTEINAEMIA ( 2 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 2 FDA reports)
HYPERTROPHY ( 2 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 2 FDA reports)
HYPOGLYCAEMIC COMA ( 2 FDA reports)
HYPOMETABOLISM ( 2 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 2 FDA reports)
HYPOTONIC URINARY BLADDER ( 2 FDA reports)
HYPOVITAMINOSIS ( 2 FDA reports)
ILIAC ARTERY STENOSIS ( 2 FDA reports)
IMMUNOGLOBULINS INCREASED ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 2 FDA reports)
INCORRECT DRUG DOSAGE FORM ADMINISTERED ( 2 FDA reports)
INFANTILE COLIC ( 2 FDA reports)
INFECTED NEOPLASM ( 2 FDA reports)
INFLAMMATORY MARKER INCREASED ( 2 FDA reports)
INFLUENZA A VIRUS TEST POSITIVE ( 2 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
INFUSION SITE ANAESTHESIA ( 2 FDA reports)
INFUSION SITE HAEMATOMA ( 2 FDA reports)
INFUSION SITE IRRITATION ( 2 FDA reports)
INFUSION SITE RASH ( 2 FDA reports)
INFUSION SITE WARMTH ( 2 FDA reports)
INHALATION THERAPY ( 2 FDA reports)
INJECTION SITE OEDEMA ( 2 FDA reports)
INSOMNIA RELATED TO ANOTHER MENTAL CONDITION ( 2 FDA reports)
INTERTRIGO ( 2 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 2 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 2 FDA reports)
INTESTINAL RESECTION ( 2 FDA reports)
INTESTINAL STRANGULATION ( 2 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 2 FDA reports)
INTRADUCTAL PAPILLOMA OF BREAST ( 2 FDA reports)
INTRAOCULAR PRESSURE TEST ( 2 FDA reports)
IRIDECTOMY ( 2 FDA reports)
IRIDOCYCLITIS ( 2 FDA reports)
IRIS ADHESIONS ( 2 FDA reports)
IRIS CYST ( 2 FDA reports)
JOINT ANKYLOSIS ( 2 FDA reports)
KIDNEY MALFORMATION ( 2 FDA reports)
KLEPTOMANIA ( 2 FDA reports)
LARGE INTESTINE CARCINOMA ( 2 FDA reports)
LARYNGEAL DISORDER ( 2 FDA reports)
LARYNGOMALACIA ( 2 FDA reports)
LASER THERAPY ( 2 FDA reports)
LENNOX-GASTAUT SYNDROME ( 2 FDA reports)
LEUKAEMOID REACTION ( 2 FDA reports)
LIBIDO DISORDER ( 2 FDA reports)
LIFE EXPECTANCY SHORTENED ( 2 FDA reports)
LIPOMATOSIS ( 2 FDA reports)
LIPOSARCOMA ( 2 FDA reports)
LOCKED-IN SYNDROME ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION BACTERIAL ( 2 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 2 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 2 FDA reports)
LUNG LOBECTOMY ( 2 FDA reports)
LUNG OPERATION ( 2 FDA reports)
LYME DISEASE ( 2 FDA reports)
LYMPHOCELE ( 2 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 2 FDA reports)
MACROSOMIA ( 2 FDA reports)
MACULAR REFLEX ABNORMAL ( 2 FDA reports)
MADAROSIS ( 2 FDA reports)
MALE SEXUAL DYSFUNCTION ( 2 FDA reports)
MALOCCLUSION ( 2 FDA reports)
MASTOCYTOSIS ( 2 FDA reports)
MATERNAL EXPOSURE BEFORE PREGNANCY ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 2 FDA reports)
MECONIUM STAIN ( 2 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 2 FDA reports)
MEDICAL DEVICE PAIN ( 2 FDA reports)
MEDICAL DIET ( 2 FDA reports)
MEGACOLON ACQUIRED ( 2 FDA reports)
MEIGE'S SYNDROME ( 2 FDA reports)
MELANOSIS COLI ( 2 FDA reports)
MENDELSON'S SYNDROME ( 2 FDA reports)
MENINGITIS BACTERIAL ( 2 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 2 FDA reports)
MENINGITIS MENINGOCOCCAL ( 2 FDA reports)
MENINGITIS VIRAL ( 2 FDA reports)
MENOPAUSAL DISORDER ( 2 FDA reports)
MERYCISM ( 2 FDA reports)
MESOTHELIOMA MALIGNANT ( 2 FDA reports)
METABOLIC ALKALOSIS ( 2 FDA reports)
METAPLASIA ( 2 FDA reports)
METASTASES TO ADRENALS ( 2 FDA reports)
MICROLITHIASIS ( 2 FDA reports)
MIDDLE EAR EFFUSION ( 2 FDA reports)
MIGRAINE WITH AURA ( 2 FDA reports)
MIGRAINE WITHOUT AURA ( 2 FDA reports)
MITOCHONDRIAL DNA DEPLETION ( 2 FDA reports)
MITRAL VALVE DISEASE MIXED ( 2 FDA reports)
MIXED LIVER INJURY ( 2 FDA reports)
MOLLUSCUM CONTAGIOSUM ( 2 FDA reports)
MONARTHRITIS ( 2 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 2 FDA reports)
MONOCYTOSIS ( 2 FDA reports)
MORAXELLA INFECTION ( 2 FDA reports)
MUMPS ( 2 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 2 FDA reports)
MYELOPATHY ( 2 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 2 FDA reports)
MYOGLOBIN URINE PRESENT ( 2 FDA reports)
MYOKYMIA ( 2 FDA reports)
N-TERMINAL PROHORMONE BRAIN NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
NAIL GROWTH ABNORMAL ( 2 FDA reports)
NAIL HYPERTROPHY ( 2 FDA reports)
NAIL PITTING ( 2 FDA reports)
NARCISSISTIC PERSONALITY DISORDER ( 2 FDA reports)
NARROW ANTERIOR CHAMBER ANGLE ( 2 FDA reports)
NASAL INFLAMMATION ( 2 FDA reports)
NASAL OEDEMA ( 2 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 2 FDA reports)
NEONATAL TACHYCARDIA ( 2 FDA reports)
NEOPLASM PROSTATE ( 2 FDA reports)
NEUROENDOCRINE CARCINOMA ( 2 FDA reports)
NEUROFIBROMA ( 2 FDA reports)
NEUROGENIC BOWEL ( 2 FDA reports)
NEUROLOGICAL INFECTION ( 2 FDA reports)
NEUROPATHIC PAIN ( 2 FDA reports)
NEUROPSYCHIATRIC SYNDROME ( 2 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 2 FDA reports)
NO ADVERSE DRUG EFFECT ( 2 FDA reports)
NODAL OSTEOARTHRITIS ( 2 FDA reports)
NON-CONSUMMATION ( 2 FDA reports)
NONKETOTIC HYPERGLYCINAEMIA ( 2 FDA reports)
OCULAR HYPERTENSION ( 2 FDA reports)
OCULOCEPHALOGYRIC REFLEX ABSENT ( 2 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 2 FDA reports)
OESOPHAGEAL IRRITATION ( 2 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 2 FDA reports)
OESOPHAGOBRONCHIAL FISTULA ( 2 FDA reports)
OESOPHAGOSTOMY ( 2 FDA reports)
OESTRADIOL INCREASED ( 2 FDA reports)
OILY SKIN ( 2 FDA reports)
OLIGODIPSIA ( 2 FDA reports)
OLIGOMENORRHOEA ( 2 FDA reports)
OPEN ANGLE GLAUCOMA ( 2 FDA reports)
OPIATES POSITIVE ( 2 FDA reports)
OPPORTUNISTIC INFECTION ( 2 FDA reports)
ORAL FIBROMA ( 2 FDA reports)
ORAL MUCOSAL DISORDER ( 2 FDA reports)
ORAL NEOPLASM ( 2 FDA reports)
ORAL SOFT TISSUE DISORDER ( 2 FDA reports)
OROPHARYNGEAL SPASM ( 2 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 2 FDA reports)
OVARIAN ENLARGEMENT ( 2 FDA reports)
OVARIAN GERM CELL TERATOMA BENIGN ( 2 FDA reports)
OVARIAN NEOPLASM ( 2 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 2 FDA reports)
PALLIATIVE CARE ( 2 FDA reports)
PANCOAST'S TUMOUR ( 2 FDA reports)
PANCREATIC ENLARGEMENT ( 2 FDA reports)
PANCREATITIS NECROTISING ( 2 FDA reports)
PARAKERATOSIS ( 2 FDA reports)
PARESIS ANAL SPHINCTER ( 2 FDA reports)
PEDAL PULSE ABNORMAL ( 2 FDA reports)
PELVIC ORGAN INJURY ( 2 FDA reports)
PELVIC VENOUS THROMBOSIS ( 2 FDA reports)
PENILE PROSTHESIS INSERTION ( 2 FDA reports)
PENOSCROTAL FUSION ( 2 FDA reports)
PEPTIC ULCER PERFORATION ( 2 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 2 FDA reports)
PERFORATION BILE DUCT ( 2 FDA reports)
PERIANAL ABSCESS ( 2 FDA reports)
PERICARDIAL EXCISION ( 2 FDA reports)
PERIDIVERTICULAR ABSCESS ( 2 FDA reports)
PERINEAL ABSCESS ( 2 FDA reports)
PERINEAL INFECTION ( 2 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 2 FDA reports)
PERIPHERAL PARALYSIS ( 2 FDA reports)
PERIPHERAL PULSE DECREASED ( 2 FDA reports)
PERIRENAL HAEMATOMA ( 2 FDA reports)
PERTUSSIS ( 2 FDA reports)
PHAEOCHROMOCYTOMA ( 2 FDA reports)
PHONOPHOBIA ( 2 FDA reports)
PHYSIOTHERAPY ( 2 FDA reports)
PICKWICKIAN SYNDROME ( 2 FDA reports)
PIERRE ROBIN SYNDROME ( 2 FDA reports)
PILONIDAL CYST ( 2 FDA reports)
PINGUECULA ( 2 FDA reports)
PITYRIASIS ROSEA ( 2 FDA reports)
PLASTIC SURGERY TO THE FACE ( 2 FDA reports)
PLATELET TRANSFUSION ( 2 FDA reports)
PLEURAL ADHESION ( 2 FDA reports)
PLEURAL CALCIFICATION ( 2 FDA reports)
PNEUMOCEPHALUS ( 2 FDA reports)
PNEUMOCONIOSIS ( 2 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 2 FDA reports)
PNEUMONIA HAEMOPHILUS ( 2 FDA reports)
PNEUMONIA LEGIONELLA ( 2 FDA reports)
PNEUMOPERITONEUM ( 2 FDA reports)
POLYCHROMASIA ( 2 FDA reports)
POLYMYOSITIS ( 2 FDA reports)
PORPHYRINS URINE INCREASED ( 2 FDA reports)
POST PROCEDURAL DISCHARGE ( 2 FDA reports)
POST PROCEDURAL HYPOTHYROIDISM ( 2 FDA reports)
POST-TRAUMATIC AMNESTIC DISORDER ( 2 FDA reports)
5'NUCLEOTIDASE INCREASED ( 1 FDA reports)
ABDOMINAL HAEMATOMA ( 1 FDA reports)
ABDOMINAL OPERATION ( 1 FDA reports)
ABDOMINAL PANNICULECTOMY ( 1 FDA reports)
ABDOMINAL SEPSIS ( 1 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 1 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 1 FDA reports)
ABSTAINS FROM ALCOHOL ( 1 FDA reports)
ACALCULIA ( 1 FDA reports)
ACANTHOSIS NIGRICANS ( 1 FDA reports)
ACHLORHYDRIA ( 1 FDA reports)
ACHOLIA ( 1 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 1 FDA reports)
ACTIVATION SYNDROME ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ADENOCARCINOMA PANCREAS ( 1 FDA reports)
ADENOIDITIS ( 1 FDA reports)
ADENOVIRAL HEPATITIS ( 1 FDA reports)
ADJUSTMENT DISORDER WITH ANXIETY ( 1 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 1 FDA reports)
ADJUSTMENT DISORDER WITH MIXED ANXIETY AND DEPRESSED MOOD ( 1 FDA reports)
ADJUSTMENT DISORDER WITH MIXED DISTURBANCE OF EMOTION AND CONDUCT ( 1 FDA reports)
ADNEXA UTERI CYST ( 1 FDA reports)
ADNEXA UTERI PAIN ( 1 FDA reports)
ADRENAL CARCINOMA ( 1 FDA reports)
ADRENAL HAEMORRHAGE ( 1 FDA reports)
AEROPHAGIA ( 1 FDA reports)
AGITATION POSTOPERATIVE ( 1 FDA reports)
AIDS RELATED COMPLICATION ( 1 FDA reports)
AIR EMBOLISM ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ALBUMIN URINE ( 1 FDA reports)
ALCOHOL INTOLERANCE ( 1 FDA reports)
ALCOHOL PROBLEM ( 1 FDA reports)
ALCOHOLIC LIVER DISEASE ( 1 FDA reports)
ALLERGIC RESPIRATORY DISEASE ( 1 FDA reports)
ALLERGIC SINUSITIS ( 1 FDA reports)
ALLERGY TO ARTHROPOD STING ( 1 FDA reports)
ALOPECIA EFFLUVIUM ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN AMNIOTIC FLUID INCREASED ( 1 FDA reports)
ALPHA 2 GLOBULIN DECREASED ( 1 FDA reports)
AMIMIA ( 1 FDA reports)
AMMONIA ABNORMAL ( 1 FDA reports)
AMYLASE INCREASED ( 1 FDA reports)
AMYLOIDOSIS ( 1 FDA reports)
ANAEMIA MEGALOBLASTIC ( 1 FDA reports)
ANAESTHESIA ( 1 FDA reports)
ANAESTHESIA REVERSAL ( 1 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 1 FDA reports)
ANAL DISCOMFORT ( 1 FDA reports)
ANAL EROSION ( 1 FDA reports)
ANAL INJURY ( 1 FDA reports)
ANAL PROLAPSE ( 1 FDA reports)
ANASTOMOTIC LEAK ( 1 FDA reports)
ANASTOMOTIC STENOSIS ( 1 FDA reports)
ANASTOMOTIC ULCER ( 1 FDA reports)
ANGIODERMATITIS ( 1 FDA reports)
ANHIDROSIS ( 1 FDA reports)
ANIMAL SCRATCH ( 1 FDA reports)
ANION GAP ( 1 FDA reports)
ANION GAP DECREASED ( 1 FDA reports)
ANOGENITAL DYSPLASIA ( 1 FDA reports)
ANORECTAL CELLULITIS ( 1 FDA reports)
ANOREXIA NERVOSA ( 1 FDA reports)
ANOSOGNOSIA ( 1 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 1 FDA reports)
ANTI-ERYTHROCYTE ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBS ANTIBODY ( 1 FDA reports)
ANTICHOLINERGIC SYNDROME ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABNORMAL ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTIGLIADIN ANTIBODY POSITIVE ( 1 FDA reports)
ANTISOCIAL PERSONALITY DISORDER ( 1 FDA reports)
AORTA HYPOPLASIA ( 1 FDA reports)
AORTIC BYPASS ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
AORTIC ELONGATION ( 1 FDA reports)
AORTIC EMBOLUS ( 1 FDA reports)
AORTIC VALVE REPLACEMENT ( 1 FDA reports)
AORTITIS ( 1 FDA reports)
APICAL GRANULOMA ( 1 FDA reports)
APPLICATION SITE ANAESTHESIA ( 1 FDA reports)
APPLICATION SITE BLEEDING ( 1 FDA reports)
APPLICATION SITE EROSION ( 1 FDA reports)
APPLICATION SITE HAEMATOMA ( 1 FDA reports)
APPLICATION SITE INFLAMMATION ( 1 FDA reports)
APPLICATION SITE PAPULES ( 1 FDA reports)
APPLICATION SITE SCAR ( 1 FDA reports)
ARACHNOID CYST ( 1 FDA reports)
ARTERIAL RUPTURE ( 1 FDA reports)
ARTERIAL STENOSIS LIMB ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 1 FDA reports)
ARTERIOVENOUS GRAFT SITE HAEMATOMA ( 1 FDA reports)
ARTHRITIS REACTIVE ( 1 FDA reports)
ARTICULAR CALCIFICATION ( 1 FDA reports)
ARTIFICIAL ANUS ( 1 FDA reports)
ASPERGILLUS TEST POSITIVE ( 1 FDA reports)
ASPERMIA ( 1 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 1 FDA reports)
ATELECTASIS NEONATAL ( 1 FDA reports)
ATHEROSCLEROSIS OBLITERANS ( 1 FDA reports)
ATHETOSIS ( 1 FDA reports)
ATONIC URINARY BLADDER ( 1 FDA reports)
ATYPICAL MYCOBACTERIAL LYMPHADENITIS ( 1 FDA reports)
AUTISM ( 1 FDA reports)
AUTISM SPECTRUM DISORDER ( 1 FDA reports)
AUTOIMMUNE PANCREATITIS ( 1 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 1 FDA reports)
AUTOMATIC BLADDER ( 1 FDA reports)
AUTONOMIC FAILURE SYNDROME ( 1 FDA reports)
AV DISSOCIATION ( 1 FDA reports)
AVERSION ( 1 FDA reports)
B-CELL LYMPHOMA RECURRENT ( 1 FDA reports)
BACILLUS TEST POSITIVE ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BACTERIA URINE NO ORGANISM OBSERVED ( 1 FDA reports)
BACTERIAL FOOD POISONING ( 1 FDA reports)
BALINT'S SYNDROME ( 1 FDA reports)
BARBITURATES POSITIVE ( 1 FDA reports)
BASAL GANGLIA STROKE ( 1 FDA reports)
BASE EXCESS ( 1 FDA reports)
BASE EXCESS INCREASED ( 1 FDA reports)
BASE EXCESS NEGATIVE ( 1 FDA reports)
BASOPHIL PERCENTAGE DECREASED ( 1 FDA reports)
BENCE JONES PROTEIN URINE PRESENT ( 1 FDA reports)
BENIGN NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF BLADDER ( 1 FDA reports)
BENIGN NEOPLASM OF SKIN ( 1 FDA reports)
BENIGN OESOPHAGEAL NEOPLASM ( 1 FDA reports)
BENIGN OVARIAN TUMOUR ( 1 FDA reports)
BENIGN RENAL NEOPLASM ( 1 FDA reports)
BENIGN SALIVARY GLAND NEOPLASM ( 1 FDA reports)
BEREAVEMENT REACTION ( 1 FDA reports)
BETA 2 MICROGLOBULIN URINE INCREASED ( 1 FDA reports)
BIFASCICULAR BLOCK ( 1 FDA reports)
BILATERAL ORCHIDECTOMY ( 1 FDA reports)
BILIARY ANASTOMOSIS COMPLICATION ( 1 FDA reports)
BILIARY TRACT INFECTION ( 1 FDA reports)
BIOPSY ARTERY ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BIOPSY LUNG ( 1 FDA reports)
BISEXUALITY ( 1 FDA reports)
BLADDER DISTENSION ( 1 FDA reports)
BLADDER IRRIGATION ( 1 FDA reports)
BLADDER MALPOSITION ACQUIRED ( 1 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 1 FDA reports)
BLADDER STENOSIS ( 1 FDA reports)
BLAST CELL COUNT INCREASED ( 1 FDA reports)
BLASTOCYSTIS INFECTION ( 1 FDA reports)
BLEEDING VARICOSE VEIN ( 1 FDA reports)
BLINDNESS HYSTERICAL ( 1 FDA reports)
BLOOD 25-HYDROXYCHOLECALCIFEROL DECREASED ( 1 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 1 FDA reports)
BLOOD AMYLASE DECREASED ( 1 FDA reports)
BLOOD ARSENIC INCREASED ( 1 FDA reports)
BLOOD BICARBONATE ABNORMAL ( 1 FDA reports)
BLOOD CALCIUM ABNORMAL ( 1 FDA reports)
BLOOD CANNABINOIDS INCREASED ( 1 FDA reports)
BLOOD CARBON MONOXIDE ABNORMAL ( 1 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 1 FDA reports)
BLOOD COPPER INCREASED ( 1 FDA reports)
BLOOD CREATINE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
BLOOD CREATININE ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD GASTRIN INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD INSULIN DECREASED ( 1 FDA reports)
BLOOD LACTIC ACID ( 1 FDA reports)
BLOOD LUTEINISING HORMONE ABNORMAL ( 1 FDA reports)
BLOOD LUTEINISING HORMONE DECREASED ( 1 FDA reports)
BLOOD MERCURY ( 1 FDA reports)
BLOOD OESTROGEN ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ABNORMAL ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 1 FDA reports)
BLOOD SMEAR TEST ABNORMAL ( 1 FDA reports)
BLOOD SODIUM ABNORMAL ( 1 FDA reports)
BLOOD TESTOSTERONE FREE INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE ( 1 FDA reports)
BLOOD TRIGLYCERIDES ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BLOOD URIC ACID ABNORMAL ( 1 FDA reports)
BODY HEIGHT BELOW NORMAL ( 1 FDA reports)
BONE CALLUS EXCESSIVE ( 1 FDA reports)
BONE EROSION ( 1 FDA reports)
BONE MARROW GRANULOMA ( 1 FDA reports)
BONE MARROW ISCHAEMIA ( 1 FDA reports)
BONE MARROW LEUKAEMIC CELL INFILTRATION ( 1 FDA reports)
BONE MARROW TOXICITY ( 1 FDA reports)
BONE MARROW TRANSPLANT REJECTION ( 1 FDA reports)
BOREDOM ( 1 FDA reports)
BOWEL PREPARATION ( 1 FDA reports)
BRAIN CANCER METASTATIC ( 1 FDA reports)
BRAIN MALFORMATION ( 1 FDA reports)
BRAIN MIDLINE SHIFT ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE ( 1 FDA reports)
BRAIN STEM STROKE ( 1 FDA reports)
BREAST CANCER STAGE IV ( 1 FDA reports)
BREAST DISCOLOURATION ( 1 FDA reports)
BREAST DISCOMFORT ( 1 FDA reports)
BREAST DISORDER FEMALE ( 1 FDA reports)
BREAST DISORDER MALE ( 1 FDA reports)
BREAST INFLAMMATION ( 1 FDA reports)
BREAST MALFORMATION ( 1 FDA reports)
BREAST NEOPLASM ( 1 FDA reports)
BREATH ALCOHOL TEST POSITIVE ( 1 FDA reports)
BREATH SOUNDS ( 1 FDA reports)
BRIEF PSYCHOTIC DISORDER WITH MARKED STRESSORS ( 1 FDA reports)
BRONCHIAL CARCINOMA ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHIAL HAEMORRHAGE ( 1 FDA reports)
BRONCHIAL NEOPLASM ( 1 FDA reports)
BRONCHIAL OEDEMA ( 1 FDA reports)
BRONCHITIS BACTERIAL ( 1 FDA reports)
BRONCHITIS CHEMICAL ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
BRONCHOPLEURAL FISTULA ( 1 FDA reports)
BRONCHOSTENOSIS ( 1 FDA reports)
BUCCOGLOSSAL SYNDROME ( 1 FDA reports)
BULLOUS LUNG DISEASE ( 1 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 1 FDA reports)
BURN DRESSING ( 1 FDA reports)
BURN INFECTION ( 1 FDA reports)
BURNING FEET SYNDROME ( 1 FDA reports)
BURNS FIRST DEGREE ( 1 FDA reports)
BURNS FOURTH DEGREE ( 1 FDA reports)
BURSA DISORDER ( 1 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 1 FDA reports)
CAFE AU LAIT SPOTS ( 1 FDA reports)
CAFFEINE CONSUMPTION ( 1 FDA reports)
CALCIPHYLAXIS ( 1 FDA reports)
CAMPBELL DE MORGAN SPOTS ( 1 FDA reports)
CAPSULE PHYSICAL ISSUE ( 1 FDA reports)
CARBOHYDRATE METABOLISM DISORDER ( 1 FDA reports)
CARBON DIOXIDE ABNORMAL ( 1 FDA reports)
CARCINOID TUMOUR ( 1 FDA reports)
CARCINOID TUMOUR OF THE GASTROINTESTINAL TRACT ( 1 FDA reports)
CARCINOMA IN SITU ( 1 FDA reports)
CARDIAC FIBRILLATION ( 1 FDA reports)
CARDIAC FUNCTION DISTURBANCE POSTOPERATIVE ( 1 FDA reports)
CARDIAC INDEX DECREASED ( 1 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 1 FDA reports)
CARDIAC SEPTAL DEFECT ( 1 FDA reports)
CARDIAC STRESS TEST ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CARDIORENAL SYNDROME ( 1 FDA reports)
CARDIOVASCULAR FUNCTION TEST ABNORMAL ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 1 FDA reports)
CATHETER REMOVAL ( 1 FDA reports)
CATHETER SITE CELLULITIS ( 1 FDA reports)
CATHETER SITE DISCHARGE ( 1 FDA reports)
CATHETER SITE ERYTHEMA ( 1 FDA reports)
CATHETER SITE HAEMATOMA ( 1 FDA reports)
CATHETER THROMBOSIS ( 1 FDA reports)
CAUDAL REGRESSION SYNDROME ( 1 FDA reports)
CAUSTIC INJURY ( 1 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 1 FDA reports)
CD4/CD8 RATIO DECREASED ( 1 FDA reports)
CELLULITIS STREPTOCOCCAL ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFLAMMATION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM STIMULATION ( 1 FDA reports)
CENTRAL VENOUS PRESSURE DECREASED ( 1 FDA reports)
CEREBELLAR ISCHAEMIA ( 1 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
CEREBRAL ARTERY STENOSIS ( 1 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 1 FDA reports)
CEREBRAL CALCIFICATION ( 1 FDA reports)
CEREBRAL HYPOPERFUSION ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CERULOPLASMIN ( 1 FDA reports)
CERULOPLASMIN DECREASED ( 1 FDA reports)
CHALAZION ( 1 FDA reports)
CHARCOT-LEYDEN CRYSTALS ( 1 FDA reports)
CHEMICAL INJURY ( 1 FDA reports)
CHEMOTHERAPY ( 1 FDA reports)
CHEYNE-STOKES RESPIRATION ( 1 FDA reports)
CHITOTRIOSIDASE DECREASED ( 1 FDA reports)
CHOLANGIOGRAM ABNORMAL ( 1 FDA reports)
CHOLEDOCHAL CYST ( 1 FDA reports)
CHORIORETINOPATHY ( 1 FDA reports)
CHOROIDAL EFFUSION ( 1 FDA reports)
CHROMOSOME ABNORMALITY ( 1 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 1 FDA reports)
CIRRHOSIS ALCOHOLIC ( 1 FDA reports)
CITROBACTER INFECTION ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 1 FDA reports)
COAGULATION FACTOR DECREASED ( 1 FDA reports)
COAGULATION FACTOR INCREASED ( 1 FDA reports)
COARCTATION OF THE AORTA ( 1 FDA reports)
COLECTOMY TOTAL ( 1 FDA reports)
COLITIS EROSIVE ( 1 FDA reports)
COLITIS HERPES ( 1 FDA reports)
COLITIS MICROSCOPIC ( 1 FDA reports)
COLLAGEN DISORDER ( 1 FDA reports)
COLLATERAL CIRCULATION ( 1 FDA reports)
COLON INJURY ( 1 FDA reports)
COLON NEOPLASM ( 1 FDA reports)
COLON POLYPECTOMY ( 1 FDA reports)
COLORECTAL CANCER ( 1 FDA reports)
COLOSTOMY CLOSURE ( 1 FDA reports)
COLOUR VISION TESTS ABNORMAL ( 1 FDA reports)
COMPLICATED MIGRAINE ( 1 FDA reports)
COMPLICATION OF DELIVERY ( 1 FDA reports)
COMPLICATION OF DEVICE REMOVAL ( 1 FDA reports)
COMPLICATION OF PREGNANCY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LUNG ( 1 FDA reports)
COMPULSIVE LIP BITING ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 1 FDA reports)
CONDUCTIVE DEAFNESS ( 1 FDA reports)
CONFUSION POSTOPERATIVE ( 1 FDA reports)
CONGENITAL ANOMALY IN OFFSPRING ( 1 FDA reports)
CONGENITAL AORTIC ANOMALY ( 1 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 1 FDA reports)
CONGENITAL CORONARY ARTERY MALFORMATION ( 1 FDA reports)
CONGENITAL HIP DEFORMITY ( 1 FDA reports)
CONGENITAL HYDROCEPHALUS ( 1 FDA reports)
CONGENITAL NEUROLOGICAL DISORDER ( 1 FDA reports)
CONGENITAL ORAL MALFORMATION ( 1 FDA reports)
CONGENITAL PANCREATIC ANOMALY ( 1 FDA reports)
CONJUNCTIVAL OEDEMA ( 1 FDA reports)
CONJUNCTIVAL PIGMENTATION ( 1 FDA reports)
CONTRAST MEDIA REACTION ( 1 FDA reports)
COPROPORPHYRINOGEN INCREASED ( 1 FDA reports)
CORNEAL BLEEDING ( 1 FDA reports)
CORNEAL DYSTROPHY ( 1 FDA reports)
CORNEAL ENDOTHELIITIS ( 1 FDA reports)
CORNEAL EROSION ( 1 FDA reports)
CORNEAL NEOVASCULARISATION ( 1 FDA reports)
CORNEAL ULCER ( 1 FDA reports)
CORONARY ARTERY ANEURYSM ( 1 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 1 FDA reports)
CORONARY ARTERY REOCCLUSION ( 1 FDA reports)
COXIELLA INFECTION ( 1 FDA reports)
COXSACKIE VIRAL INFECTION ( 1 FDA reports)
CRANIAL NERVE INFECTION ( 1 FDA reports)
CRANIAL NEUROPATHY ( 1 FDA reports)
CRANIOPHARYNGIOMA ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
CREATINE URINE INCREASED ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
CREATININE URINE DECREASED ( 1 FDA reports)
CRYPTOGENIC CIRRHOSIS ( 1 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 1 FDA reports)
CRYSTAL URINE PRESENT ( 1 FDA reports)
CRYSTALLURIA ( 1 FDA reports)
CSF CULTURE POSITIVE ( 1 FDA reports)
CSF GLUCOSE INCREASED ( 1 FDA reports)
CSF LACTATE INCREASED ( 1 FDA reports)
CSF PROTEIN ABNORMAL ( 1 FDA reports)
CSF PROTEIN DECREASED ( 1 FDA reports)
CSF VOLUME INCREASED ( 1 FDA reports)
CUBITAL TUNNEL SYNDROME ( 1 FDA reports)
CULTURE WOUND POSITIVE ( 1 FDA reports)
CYANOPSIA ( 1 FDA reports)
CYANOSIS CENTRAL ( 1 FDA reports)
CYCLOTHYMIC DISORDER ( 1 FDA reports)
CYST REMOVAL ( 1 FDA reports)
CYSTITIS KLEBSIELLA ( 1 FDA reports)
CYSTITIS RADIATION ( 1 FDA reports)
CYSTOSCOPY ABNORMAL ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 1 FDA reports)
CYTOMEGALOVIRUS GASTROINTESTINAL INFECTION ( 1 FDA reports)
DEATH OF PET ( 1 FDA reports)
DECREASED EYE CONTACT ( 1 FDA reports)
DEFORMITY THORAX ( 1 FDA reports)
DELAYED DELIVERY ( 1 FDA reports)
DELUSIONAL DISORDER, JEALOUS TYPE ( 1 FDA reports)
DENERVATION ATROPHY ( 1 FDA reports)
DERMABRASION ( 1 FDA reports)
DERMATITIS DIAPER ( 1 FDA reports)
DERMATITIS EXFOLIATIVE GENERALISED ( 1 FDA reports)
DERMATITIS INFECTED ( 1 FDA reports)
DERMATITIS PSORIASIFORM ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DERMATOSIS ( 1 FDA reports)
DEVICE ISSUE ( 1 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 1 FDA reports)
DIABETIC DYSLIPIDAEMIA ( 1 FDA reports)
DIABETIC FOOT INFECTION ( 1 FDA reports)
DIABETIC GANGRENE ( 1 FDA reports)
DIABETIC GASTROPATHY ( 1 FDA reports)
DIABETIC KETOACIDOTIC HYPERGLYCAEMIC COMA ( 1 FDA reports)
DIABETIC NEUROPATHIC ULCER ( 1 FDA reports)
DIALYSIS DEVICE COMPLICATION ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DIFFUSE CUTANEOUS MASTOCYTOSIS ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA RECURRENT ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE II ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE IV ( 1 FDA reports)
DISEASE PRODROMAL STAGE ( 1 FDA reports)
DISSOCIATIVE AMNESIA ( 1 FDA reports)
DISTAL INTESTINAL OBSTRUCTION SYNDROME ( 1 FDA reports)
DISUSE SYNDROME ( 1 FDA reports)
DIVERTICULUM DUODENAL ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY POSITIVE ( 1 FDA reports)
DREAMY STATE ( 1 FDA reports)
DRUG INTERACTION INHIBITION ( 1 FDA reports)
DRUG LEVEL THERAPEUTIC ( 1 FDA reports)
DRUG NAME CONFUSION ( 1 FDA reports)
DRUG TOLERANCE DECREASED ( 1 FDA reports)
DRUG WITHDRAWAL HEADACHE ( 1 FDA reports)
DRUG WITHDRAWAL MAINTENANCE THERAPY ( 1 FDA reports)
DRY GANGRENE ( 1 FDA reports)
DUODENAL PERFORATION ( 1 FDA reports)
DUODENAL SCARRING ( 1 FDA reports)
DUODENAL ULCER, OBSTRUCTIVE ( 1 FDA reports)
DYSLEXIA ( 1 FDA reports)
DYSMORPHOPHOBIA ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
DYSPRAXIA ( 1 FDA reports)
EAR NEOPLASM ( 1 FDA reports)
EBSTEIN'S ANOMALY ( 1 FDA reports)
ECHOLALIA ( 1 FDA reports)
ECLAMPSIA ( 1 FDA reports)
ECTHYMA ( 1 FDA reports)
ECTOPIC PREGNANCY ( 1 FDA reports)
ECZEMA VESICULAR ( 1 FDA reports)
ELDER ABUSE ( 1 FDA reports)
ELECTROCARDIOGRAM ( 1 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 1 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 1 FDA reports)
EMPTY SELLA SYNDROME ( 1 FDA reports)
ENCEPHALITIS POST VARICELLA ( 1 FDA reports)
ENDOCARDIAL FIBROSIS ( 1 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 1 FDA reports)
ENDOCRINE PANCREATIC DISORDER ( 1 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 1 FDA reports)
ENDOMETRITIS ( 1 FDA reports)
ENDOSCOPY GASTROINTESTINAL ABNORMAL ( 1 FDA reports)
ENDOSCOPY SMALL INTESTINE ABNORMAL ( 1 FDA reports)
ENDOTOXIC SHOCK ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
ENTEROCOLONIC FISTULA ( 1 FDA reports)
ENTEROVESICAL FISTULA ( 1 FDA reports)
ENTEROVIRUS TEST POSITIVE ( 1 FDA reports)
ENTHESOPATHY ( 1 FDA reports)
EOSINOPENIA ( 1 FDA reports)
EOSINOPHIL PERCENTAGE ABNORMAL ( 1 FDA reports)
EOSINOPHIL PERCENTAGE DECREASED ( 1 FDA reports)
EOSINOPHILIC MYOCARDITIS ( 1 FDA reports)
EPIDERMOLYSIS ( 1 FDA reports)
EPIGLOTTITIS ( 1 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 1 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 1 FDA reports)
EROSIVE DUODENITIS ( 1 FDA reports)
ERYTHEMA ANNULARE ( 1 FDA reports)
ERYTHEMA INDURATUM ( 1 FDA reports)
ERYTHRODERMIC PSORIASIS ( 1 FDA reports)
ERYTHROSIS ( 1 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 1 FDA reports)
EVAN'S SYNDROME ( 1 FDA reports)
EWING'S SARCOMA ( 1 FDA reports)
EXCESSIVE SKIN ( 1 FDA reports)
EXERCISE TEST ABNORMAL ( 1 FDA reports)
EXHIBITIONISM ( 1 FDA reports)
EXPLORATIVE LAPAROTOMY ( 1 FDA reports)
EXTERNAL EAR INFLAMMATION ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
EXTRAOCULAR MUSCLE DISORDER ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EXTUBATION ( 1 FDA reports)
EYE DEGENERATIVE DISORDER ( 1 FDA reports)
EYE LASER SURGERY ( 1 FDA reports)
EYEGLASSES THERAPY ( 1 FDA reports)
EYELID INFECTION ( 1 FDA reports)
EYELID IRRITATION ( 1 FDA reports)
EYES SUNKEN ( 1 FDA reports)
FACIAL ASYMMETRY ( 1 FDA reports)
FACTOR II DEFICIENCY ( 1 FDA reports)
FACTOR XI DEFICIENCY ( 1 FDA reports)
FAECAL VOLUME INCREASED ( 1 FDA reports)
FAILURE OF IMPLANT ( 1 FDA reports)
FAT TISSUE INCREASED ( 1 FDA reports)
FEAR OF WEIGHT GAIN ( 1 FDA reports)
FEBRILE INFECTION ( 1 FDA reports)
FEELING OF RELAXATION ( 1 FDA reports)
FEMALE ORGASMIC DISORDER ( 1 FDA reports)
FEMALE SEXUAL AROUSAL DISORDER ( 1 FDA reports)
FEMALE STERILISATION ( 1 FDA reports)
FEMORAL NERVE PALSY ( 1 FDA reports)
FEMORAL PULSE ABNORMAL ( 1 FDA reports)
FEMORAL PULSE DECREASED ( 1 FDA reports)
FIBRINOLYSIS ( 1 FDA reports)
FIBROADENOMA OF BREAST ( 1 FDA reports)
FINE MOTOR DELAY ( 1 FDA reports)
FLAVOBACTERIUM INFECTION ( 1 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 1 FDA reports)
FOETAL ANTICONVULSANT SYNDROME ( 1 FDA reports)
FOETAL CEREBROVASCULAR DISORDER ( 1 FDA reports)
FOETAL HEART RATE DECELERATION ( 1 FDA reports)
FOETAL MOVEMENTS DECREASED ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III ( 1 FDA reports)
FOLLICULAR THYROID CANCER ( 1 FDA reports)
FONTANELLE BULGING ( 1 FDA reports)
FOREIGN BODY REACTION ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
FRONTAL LOBE EPILEPSY ( 1 FDA reports)
FULL BLOOD COUNT INCREASED ( 1 FDA reports)
FUNGAL TEST POSITIVE ( 1 FDA reports)
FUNGUS BODY FLUID IDENTIFIED ( 1 FDA reports)
GALACTOCELE ( 1 FDA reports)
GALLBLADDER PERFORATION ( 1 FDA reports)
GASTRECTOMY ( 1 FDA reports)
GASTRIC BANDING ( 1 FDA reports)
GASTRIC CANCER RECURRENT ( 1 FDA reports)
GASTRIC FISTULA ( 1 FDA reports)
GASTRIC HYPOMOTILITY ( 1 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 1 FDA reports)
GASTRIC OUTLET OBSTRUCTION ( 1 FDA reports)
GASTRIC PH INCREASED ( 1 FDA reports)
GASTRIC STENOSIS ( 1 FDA reports)
GASTRIC VARICES HAEMORRHAGE ( 1 FDA reports)
GASTRODUODENAL HAEMORRHAGE ( 1 FDA reports)
GASTRODUODENITIS ( 1 FDA reports)
GASTROENTERITIS BACTERIAL ( 1 FDA reports)
GASTROENTERITIS EOSINOPHILIC ( 1 FDA reports)
GASTROENTERITIS STAPHYLOCOCCAL ( 1 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 1 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 1 FDA reports)
GASTROINTESTINAL TRACT MUCOSAL DISCOLOURATION ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
GASTROSTOMY TUBE INSERTION ( 1 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
GENERALISED NON-CONVULSIVE EPILEPSY ( 1 FDA reports)
GENITAL DISCHARGE ( 1 FDA reports)
GENITAL DISCOMFORT ( 1 FDA reports)
GENITAL ERYTHEMA ( 1 FDA reports)
GENITAL HYPOAESTHESIA ( 1 FDA reports)
GENITAL INFECTION BACTERIAL ( 1 FDA reports)
GENITAL LESION ( 1 FDA reports)
GENITAL ULCERATION ( 1 FDA reports)
GINGIVAL DISCOLOURATION ( 1 FDA reports)
GINGIVAL HYPERTROPHY ( 1 FDA reports)
GINGIVAL INJURY ( 1 FDA reports)
GINGIVAL OPERATION ( 1 FDA reports)
GINGIVAL PRURITUS ( 1 FDA reports)
GLABELLAR REFLEX ABNORMAL ( 1 FDA reports)
GLIOBLASTOMA ( 1 FDA reports)
GLOBAL AMNESIA ( 1 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 1 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 1 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 1 FDA reports)
GLOMERULONEPHRITIS CHRONIC ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 1 FDA reports)
GLUCOSE TOLERANCE TEST ABNORMAL ( 1 FDA reports)
GLUTAMATE DEHYDROGENASE INCREASED ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN DECREASED ( 1 FDA reports)
GONORRHOEA ( 1 FDA reports)
GOUTY TOPHUS ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
GRANULOCYTES ABNORMAL ( 1 FDA reports)
GROSS MOTOR DELAY ( 1 FDA reports)
GROWTH OF EYELASHES ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
GUTTATE PSORIASIS ( 1 FDA reports)
HAEMANGIOMA OF SKIN ( 1 FDA reports)
HAEMODIALYSIS-INDUCED SYMPTOM ( 1 FDA reports)
HAEMODYNAMIC TEST ABNORMAL ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HAEMOGLOBINOPATHY ( 1 FDA reports)
HAEMOGLOBINURIA ( 1 FDA reports)
HAEMORRHAGIC ASCITES ( 1 FDA reports)
HAEMORRHAGIC CYST ( 1 FDA reports)
HAEMORRHOID INFECTION ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HEAD AND NECK CANCER ( 1 FDA reports)
HEAD LAG ( 1 FDA reports)
HEARING AID USER ( 1 FDA reports)
HEART RATE ( 1 FDA reports)
HEART TRANSPLANT REJECTION ( 1 FDA reports)
HEART VALVE REPLACEMENT ( 1 FDA reports)
HEAT EXPOSURE INJURY ( 1 FDA reports)
HEAT RASH ( 1 FDA reports)
HEAT THERAPY ( 1 FDA reports)
HELICOBACTER TEST POSITIVE ( 1 FDA reports)
HEMIANOPIA HETERONYMOUS ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HEMICEPHALALGIA ( 1 FDA reports)
HEPATIC HYDROTHORAX ( 1 FDA reports)
HEPATIC VEIN OCCLUSION ( 1 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS C VIRUS TEST POSITIVE ( 1 FDA reports)
HEPATITIS GRANULOMATOUS ( 1 FDA reports)
HEPATO-LENTICULAR DEGENERATION ( 1 FDA reports)
HEPATOBILIARY DISEASE ( 1 FDA reports)
HEPATOBILIARY SCAN ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HERNIA GANGRENOUS ( 1 FDA reports)
HERPES PHARYNGITIS ( 1 FDA reports)
HERPES ZOSTER OTICUS ( 1 FDA reports)
HIP SWELLING ( 1 FDA reports)
HISTOLOGY ABNORMAL ( 1 FDA reports)
HISTONE ANTIBODY POSITIVE ( 1 FDA reports)
HISTRIONIC PERSONALITY DISORDER ( 1 FDA reports)
HIV TEST POSITIVE ( 1 FDA reports)
HYPERALDOSTERONISM ( 1 FDA reports)
HYPERCAPNIC ENCEPHALOPATHY ( 1 FDA reports)
HYPERDYNAMIC LEFT VENTRICLE ( 1 FDA reports)
HYPERDYNAMIC PRECORDIUM ( 1 FDA reports)
HYPEREMESIS GRAVIDARUM ( 1 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 1 FDA reports)
HYPEREXPLEXIA ( 1 FDA reports)
HYPERINSULINAEMIA ( 1 FDA reports)
HYPERKERATOSIS PALMARIS AND PLANTARIS ( 1 FDA reports)
HYPERSPLENISM ( 1 FDA reports)
HYPERTELORISM OF ORBIT ( 1 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 1 FDA reports)
HYPERTROPHIC OSTEOARTHROPATHY ( 1 FDA reports)
HYPERURICOSURIA ( 1 FDA reports)
HYPNOPOMPIC HALLUCINATION ( 1 FDA reports)
HYPOAESTHESIA EYE ( 1 FDA reports)
HYPOALDOSTERONISM ( 1 FDA reports)
HYPOCAPNIA ( 1 FDA reports)
HYPOCHROMIC ANAEMIA ( 1 FDA reports)
HYPOGEUSIA ( 1 FDA reports)
HYPOGLYCAEMIC ENCEPHALOPATHY ( 1 FDA reports)
HYPOHIDROSIS ( 1 FDA reports)
HYPOKALAEMIC SYNDROME ( 1 FDA reports)
HYPOKINESIA NEONATAL ( 1 FDA reports)
HYPOLIPIDAEMIA ( 1 FDA reports)
HYPOSOMNIA ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 1 FDA reports)
HYPOTONIC-HYPORESPONSIVE EPISODE ( 1 FDA reports)
HYPOURICAEMIA ( 1 FDA reports)
HYPOVENTILATION NEONATAL ( 1 FDA reports)
ICHTHYOSIS ( 1 FDA reports)
ICHTHYOSIS ACQUIRED ( 1 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 1 FDA reports)
IGA NEPHROPATHY ( 1 FDA reports)
ILIAC ARTERY THROMBOSIS ( 1 FDA reports)
ILIUM FRACTURE ( 1 FDA reports)
ILLOGICAL THINKING ( 1 FDA reports)
IMMATURE RESPIRATORY SYSTEM ( 1 FDA reports)
IMMOBILISATION PROLONGED ( 1 FDA reports)
IMMUNE TOLERANCE INDUCTION ( 1 FDA reports)
IMMUNOGLOBULINS DECREASED ( 1 FDA reports)
IMPAIRED INSULIN SECRETION ( 1 FDA reports)
IMPETIGO HERPETIFORMIS ( 1 FDA reports)
IMPINGEMENT SYNDROME ( 1 FDA reports)
IMPLANT SITE CALCIFICATION ( 1 FDA reports)
IMPLANT SITE EFFUSION ( 1 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 1 FDA reports)
IMPLANT SITE INFECTION ( 1 FDA reports)
IMPLANT SITE IRRITATION ( 1 FDA reports)
IMPLANT SITE PAIN ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
INBORN ERROR OF METABOLISM ( 1 FDA reports)
INCISION SITE CELLULITIS ( 1 FDA reports)
INCISION SITE OEDEMA ( 1 FDA reports)
INCISION SITE PRURITUS ( 1 FDA reports)
INCISIONAL HERNIA REPAIR ( 1 FDA reports)
INCORRECT PRODUCT STORAGE ( 1 FDA reports)
INDUCED LABOUR ( 1 FDA reports)
INFANT ( 1 FDA reports)
INFANTILE SPASMS ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS ( 1 FDA reports)
INFERTILITY MALE ( 1 FDA reports)
INFUSION SITE DISCOLOURATION ( 1 FDA reports)
INFUSION SITE NECROSIS ( 1 FDA reports)
INFUSION SITE URTICARIA ( 1 FDA reports)
INGUINAL HERNIA REPAIR ( 1 FDA reports)
INGUINAL HERNIA STRANGULATED ( 1 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
INJECTION SITE CYST ( 1 FDA reports)
INJECTION SITE EXFOLIATION ( 1 FDA reports)
INJECTION SITE FIBROSIS ( 1 FDA reports)
INJECTION SITE NERVE DAMAGE ( 1 FDA reports)
INSTILLATION SITE ERYTHEMA ( 1 FDA reports)
INSTILLATION SITE IRRITATION ( 1 FDA reports)
INSULIN C-PEPTIDE DECREASED ( 1 FDA reports)
INTELLIGENCE TEST ABNORMAL ( 1 FDA reports)
INTERCOSTAL RETRACTION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 1 FDA reports)
INTERSTITIAL GRANULOMATOUS DERMATITIS ( 1 FDA reports)
INTESTINAL CYST ( 1 FDA reports)
INTESTINAL ULCER PERFORATION ( 1 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE EXPELLED ( 1 FDA reports)
INTRACRANIAL HAEMATOMA ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
INTRAOCULAR MELANOMA ( 1 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 1 FDA reports)
INTRAPARTUM HAEMORRHAGE ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 1 FDA reports)
JAPAN COMA SCALE ABNORMAL ( 1 FDA reports)
JEJUNAL ULCER ( 1 FDA reports)
JOB CHANGE ( 1 FDA reports)
JOINT ABSCESS ( 1 FDA reports)
JOINT INSTABILITY ( 1 FDA reports)
KAOLIN CEPHALIN CLOTTING TIME PROLONGED ( 1 FDA reports)
KAPOSI'S SARCOMA ( 1 FDA reports)
KERATOSIS FOLLICULAR ( 1 FDA reports)
KETONURIA ( 1 FDA reports)
KIDNEY SMALL ( 1 FDA reports)
KLEBSIELLA SEPSIS ( 1 FDA reports)
LACK OF SATIETY ( 1 FDA reports)
LACRIMAL DISORDER ( 1 FDA reports)
LACRIMATION DECREASED ( 1 FDA reports)
LACTATION DISORDER ( 1 FDA reports)
LARGE CELL CARCINOMA OF THE RESPIRATORY TRACT STAGE UNSPECIFIED ( 1 FDA reports)
LARGE CELL LUNG CANCER STAGE IV ( 1 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 1 FDA reports)
LARYNGEAL OBSTRUCTION ( 1 FDA reports)
LARYNGEAL ULCERATION ( 1 FDA reports)
LARYNGITIS FUNGAL ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 1 FDA reports)
LEIOMYOSARCOMA METASTATIC ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LHERMITTE'S SIGN ( 1 FDA reports)
LICE INFESTATION ( 1 FDA reports)
LID LAG ( 1 FDA reports)
LIGAMENT CALCIFICATION ( 1 FDA reports)
LIGHT CHAIN ANALYSIS ABNORMAL ( 1 FDA reports)
LIMB ASYMMETRY ( 1 FDA reports)
LIMB SALVAGE THERAPY ( 1 FDA reports)
LINEAR IGA DISEASE ( 1 FDA reports)
LIP INJURY ( 1 FDA reports)
LIP NEOPLASM ( 1 FDA reports)
LIP NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 1 FDA reports)
LIPASE ABNORMAL ( 1 FDA reports)
LIPIDOSIS ( 1 FDA reports)
LIPOHYPERTROPHY ( 1 FDA reports)
LIPOSUCTION ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LIVER SARCOIDOSIS ( 1 FDA reports)
LOSS OF DREAMING ( 1 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN ABNORMAL ( 1 FDA reports)
LOWRY-WOOD SYNDROME ( 1 FDA reports)
LUDWIG ANGINA ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG CYST BENIGN ( 1 FDA reports)
LUNG HYPERINFLATION ( 1 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 1 FDA reports)
LUNG NEOPLASM SURGERY ( 1 FDA reports)
LUNG TRANSPLANT ( 1 FDA reports)
LUNG TRANSPLANT REJECTION ( 1 FDA reports)
LUPUS ENCEPHALITIS ( 1 FDA reports)
LUPUS ENTERITIS ( 1 FDA reports)
LUTEAL PHASE DEFICIENCY ( 1 FDA reports)
LYMPH GLAND INFECTION ( 1 FDA reports)
LYMPH NODE PAIN ( 1 FDA reports)
LYMPHANGIOLEIOMYOMATOSIS ( 1 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 1 FDA reports)
LYMPHANGITIS ( 1 FDA reports)
LYMPHATIC DISORDER ( 1 FDA reports)
LYMPHATIC DUCT RUPTURE ( 1 FDA reports)
LYMPHATIC OBSTRUCTION ( 1 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
LYMPHOHISTIOCYTOSIS ( 1 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 1 FDA reports)
MACRODACTYLY ( 1 FDA reports)
MACULAR ISCHAEMIA ( 1 FDA reports)
MALABSORPTION FROM INJECTION SITE ( 1 FDA reports)
MALIGNANT ASCITES ( 1 FDA reports)
MALIGNANT MELANOMA STAGE I ( 1 FDA reports)
MALIGNANT MELANOMA STAGE III ( 1 FDA reports)
MALLORY-WEISS SYNDROME ( 1 FDA reports)
MAMMARY DUCT ECTASIA ( 1 FDA reports)
MARBURG'S VARIANT MULTIPLE SCLEROSIS ( 1 FDA reports)
MASS EXCISION ( 1 FDA reports)
MASTITIS ( 1 FDA reports)
MASTOID DISORDER ( 1 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 1 FDA reports)
MEDICAL DEVICE REMOVAL ( 1 FDA reports)
MEDICAL DEVICE SITE REACTION ( 1 FDA reports)
MEGAKARYOCYTES ABNORMAL ( 1 FDA reports)
MEGAKARYOCYTES DECREASED ( 1 FDA reports)
MELANOSIS ( 1 FDA reports)
MENINGEAL NEOPLASM ( 1 FDA reports)
MENINGITIS CHEMICAL ( 1 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 1 FDA reports)
MENINGOMYELOCELE ( 1 FDA reports)
MENINGORADICULITIS ( 1 FDA reports)
MENISCAL DEGENERATION ( 1 FDA reports)
MENOMETRORRHAGIA ( 1 FDA reports)
MENOPAUSE DELAYED ( 1 FDA reports)
MESENTERIC LYMPHADENOPATHY ( 1 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 1 FDA reports)
METABOLIC FUNCTION TEST ABNORMAL ( 1 FDA reports)
METANEPHRINE URINE INCREASED ( 1 FDA reports)
METAPNEUMOVIRUS INFECTION ( 1 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 1 FDA reports)
METASTASES TO REPRODUCTIVE ORGAN ( 1 FDA reports)
METASTASES TO SPLEEN ( 1 FDA reports)
METATARSALGIA ( 1 FDA reports)
METHAEMOGLOBINAEMIA ( 1 FDA reports)
MIGRATION OF IMPLANT ( 1 FDA reports)
MILD MENTAL RETARDATION ( 1 FDA reports)
MILIA ( 1 FDA reports)
MINERAL DEFICIENCY ( 1 FDA reports)
MISSED LABOUR ( 1 FDA reports)
MITOCHONDRIAL TOXICITY ( 1 FDA reports)
MITRAL VALVE SCLEROSIS ( 1 FDA reports)
MOLE EXCISION ( 1 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MOROSE ( 1 FDA reports)
MORTON'S NEUROMA ( 1 FDA reports)
MUCOCUTANEOUS CANDIDIASIS ( 1 FDA reports)
MUCOPOLYSACCHARIDOSIS I ( 1 FDA reports)
MUCOSAL ULCERATION ( 1 FDA reports)
MULTIPLE CHEMICAL SENSITIVITY ( 1 FDA reports)
MUNCHAUSEN'S SYNDROME ( 1 FDA reports)
MYCOPLASMA SEROLOGY POSITIVE ( 1 FDA reports)
MYCOPLASMA TEST POSITIVE ( 1 FDA reports)
MYCOSIS FUNGOIDES ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
MYELOFIBROSIS ( 1 FDA reports)
MYELOID LEUKAEMIA ( 1 FDA reports)
MYOCARDIAL CALCIFICATION ( 1 FDA reports)
MYOCARDIAL HAEMORRHAGE ( 1 FDA reports)
MYOCARDITIS POST INFECTION ( 1 FDA reports)
MYODESOPSIA ( 1 FDA reports)
MYOGLOBINAEMIA ( 1 FDA reports)
MYOGLOBINURIA ( 1 FDA reports)
MYOMECTOMY ( 1 FDA reports)
MYOPATHY TOXIC ( 1 FDA reports)
NAIL INJURY ( 1 FDA reports)
NASAL OBSTRUCTION ( 1 FDA reports)
NASAL OPERATION ( 1 FDA reports)
NASAL POLYPECTOMY ( 1 FDA reports)
NASAL SINUS DRAINAGE ( 1 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 1 FDA reports)
NECROTISING COLITIS ( 1 FDA reports)
NECROTISING FASCIITIS ( 1 FDA reports)
NECROTISING FASCIITIS STAPHYLOCOCCAL ( 1 FDA reports)
NECROTISING RETINITIS ( 1 FDA reports)
NEEDLE TRACK MARKS ( 1 FDA reports)
NEONATAL ASPHYXIA ( 1 FDA reports)
NEONATAL HYPONATRAEMIA ( 1 FDA reports)
NEONATAL HYPOXIA ( 1 FDA reports)
NEOPLASM OF THYMUS ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NERVE DEGENERATION ( 1 FDA reports)
NEURODEGENERATIVE DISORDER ( 1 FDA reports)
NEUROENDOCRINE TUMOUR ( 1 FDA reports)
NEUROGLYCOPENIA ( 1 FDA reports)
NEUROLOGIC NEGLECT SYNDROME ( 1 FDA reports)
NEUROMA ( 1 FDA reports)
NEUROMUSCULAR BLOCK PROLONGED ( 1 FDA reports)
NEUROSURGERY ( 1 FDA reports)
NEUTRALISING ANTIBODIES POSITIVE ( 1 FDA reports)
NEUTROPENIC INFECTION ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NIEMANN-PICK DISEASE ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
NON-HIGH-DENSITY LIPOPROTEIN CHOLESTEROL INCREASED ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
NOREPINEPHRINE INCREASED ( 1 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 1 FDA reports)
NUCLEATED RED CELLS ( 1 FDA reports)
OBESITY SURGERY ( 1 FDA reports)
OEDEMA MUCOSAL ( 1 FDA reports)
OESOPHAGEAL NEOPLASM ( 1 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 1 FDA reports)
OESOPHAGEAL PERFORATION ( 1 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 1 FDA reports)
OESOPHAGOENTEROSTOMY ( 1 FDA reports)
OESTRADIOL DECREASED ( 1 FDA reports)
OLFACTORY TEST ABNORMAL ( 1 FDA reports)
ONYCHOPHAGIA ( 1 FDA reports)
ONYCHORRHEXIS ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
OPHTHALMOPLEGIA ( 1 FDA reports)
OPPOSITIONAL DEFIANT DISORDER ( 1 FDA reports)
OPTIC NERVE CUP/DISC RATIO DECREASED ( 1 FDA reports)
OPTIC NERVE SHEATH HAEMORRHAGE ( 1 FDA reports)
ORAL MUCOSAL ERUPTION ( 1 FDA reports)
ORAL SUBMUCOSAL FIBROSIS ( 1 FDA reports)
OROMANDIBULAR DYSTONIA ( 1 FDA reports)
OROPHARYNGITIS FUNGAL ( 1 FDA reports)
ORTHOSTATIC INTOLERANCE ( 1 FDA reports)
ORTHOSTATIC TREMOR ( 1 FDA reports)
OSTEOGENESIS IMPERFECTA ( 1 FDA reports)
OSTEOMA ( 1 FDA reports)
OSTEOMYELITIS CHRONIC ( 1 FDA reports)
OSTEOPETROSIS ( 1 FDA reports)
OVARIAN EPITHELIAL CANCER ( 1 FDA reports)
OVARIAN FAILURE ( 1 FDA reports)
OVULATION PAIN ( 1 FDA reports)
PACEMAKER GENERATED RHYTHM ( 1 FDA reports)
PAGET'S DISEASE OF THE BREAST ( 1 FDA reports)
PAGET-SCHROETTER SYNDROME ( 1 FDA reports)
PALATAL OEDEMA ( 1 FDA reports)
PANCREAS INFECTION ( 1 FDA reports)
PANCREATECTOMY ( 1 FDA reports)
PANCREATIC DUCT STENOSIS ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANCREATIC LEAK ( 1 FDA reports)
PANCREATITIS VIRAL ( 1 FDA reports)
PAPILLARY THYROID CANCER ( 1 FDA reports)
PARACENTESIS ( 1 FDA reports)
PARANEOPLASTIC ENCEPHALOMYELITIS ( 1 FDA reports)
PARAPSORIASIS ( 1 FDA reports)
PARATHYROID DISORDER ( 1 FDA reports)
PARATHYROID GLAND ENLARGEMENT ( 1 FDA reports)
PARATHYROID HAEMORRHAGE ( 1 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 1 FDA reports)
PARKINSONIAN CRISIS ( 1 FDA reports)
PARTIAL SEIZURES WITH SECONDARY GENERALISATION ( 1 FDA reports)
PASSIVE SMOKING ( 1 FDA reports)
PATIENT RESTRAINT ( 1 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 1 FDA reports)
PELVIC ADHESIONS ( 1 FDA reports)
PELVIC MASS ( 1 FDA reports)
PENILE DYSPLASIA ( 1 FDA reports)
PENILE EXFOLIATION ( 1 FDA reports)
PENILE HAEMORRHAGE ( 1 FDA reports)
PENILE OPERATION ( 1 FDA reports)
PENILE WART ( 1 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 1 FDA reports)
PERCUSSION TEST ABNORMAL ( 1 FDA reports)
PERFORMANCE FEAR ( 1 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 1 FDA reports)
PERICARDIAL RUB ( 1 FDA reports)
PERINEAL PAIN ( 1 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 1 FDA reports)
PERIPHERAL NERVE DESTRUCTION ( 1 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIRECTAL ABSCESS ( 1 FDA reports)
PERITONEAL ABSCESS ( 1 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 1 FDA reports)
PERITONEAL EFFLUENT ABNORMAL ( 1 FDA reports)
PERITONEAL FIBROSIS ( 1 FDA reports)
PERSEVERATION ( 1 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 1 FDA reports)
PEYRONIE'S DISEASE ( 1 FDA reports)
PH BODY FLUID ABNORMAL ( 1 FDA reports)
PHANTOM PAIN ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 1 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 1 FDA reports)
PHARYNGEAL INJURY ( 1 FDA reports)
PHARYNGITIS BACTERIAL ( 1 FDA reports)
PHLEBOLITH ( 1 FDA reports)
PHOTOCOAGULATION ( 1 FDA reports)
PHYSICAL ABUSE ( 1 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PIGMENTATION LIP ( 1 FDA reports)
PITUITARY ENLARGEMENT ( 1 FDA reports)
PITUITARY HAEMORRHAGE ( 1 FDA reports)
PITUITARY TUMOUR RECURRENT ( 1 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 1 FDA reports)
PLACENTA PRAEVIA HAEMORRHAGE ( 1 FDA reports)
PLAGIOCEPHALY ( 1 FDA reports)
PLASMA CELLS INCREASED ( 1 FDA reports)
PLATELET AGGREGATION ( 1 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 1 FDA reports)
PLATELET AGGREGATION DECREASED ( 1 FDA reports)
PLATELET MORPHOLOGY ABNORMAL ( 1 FDA reports)
PLEUROPERICARDITIS ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 1 FDA reports)
PNEUMONECTOMY ( 1 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 1 FDA reports)
PNEUMONIA INFLUENZAL ( 1 FDA reports)
POLYCYTHAEMIA VERA ( 1 FDA reports)
POLYMYALGIA ( 1 FDA reports)
POLYPECTOMY ( 1 FDA reports)
POOR WEIGHT GAIN NEONATAL ( 1 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 1 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 1 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 1 FDA reports)
POST PROCEDURAL DIARRHOEA ( 1 FDA reports)
POST PROCEDURAL PNEUMONIA ( 1 FDA reports)
POST THROMBOTIC SYNDROME ( 1 FDA reports)
POST TRANSPLANT DISTAL LIMB SYNDROME ( 1 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
POST-TRAUMATIC HEADACHE ( 1 FDA reports)
POST-TRAUMATIC OSTEOPOROSIS ( 1 FDA reports)
POST-TRAUMATIC PAIN ( 1 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 1 FDA reports)
POSTOPERATIVE ABSCESS ( 1 FDA reports)
POSTPARTUM STRESS DISORDER ( 1 FDA reports)
POSTPERICARDIOTOMY SYNDROME ( 1 FDA reports)
POVERTY OF THOUGHT CONTENT ( 1 FDA reports)
PRE-EXISTING CONDITION IMPROVED ( 1 FDA reports)
PRE-EXISTING DISEASE ( 1 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 1 FDA reports)
PREGNANCY TEST FALSE POSITIVE ( 1 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 1 FDA reports)
PREMATURE AGEING ( 1 FDA reports)
PREMATURE EJACULATION ( 1 FDA reports)
PRESCRIPTION FORM TAMPERING ( 1 FDA reports)
PRIMARY IMMUNODEFICIENCY SYNDROME ( 1 FDA reports)
PROCALCITONIN INCREASED ( 1 FDA reports)
PROCEDURAL HYPERTENSION ( 1 FDA reports)
PROCTITIS ( 1 FDA reports)
PRODUCT COMMINGLING ( 1 FDA reports)
PRODUCT CONTAMINATION ( 1 FDA reports)
PRODUCT DEPOSIT ( 1 FDA reports)
PRODUCT EXPIRATION DATE ISSUE ( 1 FDA reports)
PRODUCT LABEL CONFUSION ( 1 FDA reports)
PRODUCT LABEL ON WRONG PRODUCT ( 1 FDA reports)
PRODUCT PHYSICAL ISSUE ( 1 FDA reports)
PROGESTERONE DECREASED ( 1 FDA reports)
PROPHYLAXIS ( 1 FDA reports)
PROPOFOL INFUSION SYNDROME ( 1 FDA reports)
PROSTATE INFECTION ( 1 FDA reports)
PROSTATIC OPERATION ( 1 FDA reports)
PROSTATIC PAIN ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN ABNORMAL ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN DECREASED ( 1 FDA reports)
PROTEIN C DECREASED ( 1 FDA reports)
PROTEIN C DEFICIENCY ( 1 FDA reports)
PROTEIN DEFICIENCY ANAEMIA ( 1 FDA reports)
PROTEIN S DEFICIENCY ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PROTHROMBIN CONSUMPTION TIME PROLONGED ( 1 FDA reports)
PSEUDO LYMPHOMA ( 1 FDA reports)
PSEUDOPHAEOCHROMOCYTOMA ( 1 FDA reports)
PSEUDOPORPHYRIA ( 1 FDA reports)
PSYCHIATRIC EVALUATION ( 1 FDA reports)
PSYCHOGENIC ERECTILE DYSFUNCTION ( 1 FDA reports)
PSYCHOGENIC PAIN DISORDER ( 1 FDA reports)
PSYCHOSOCIAL SUPPORT ( 1 FDA reports)
PUBIC PAIN ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY ARTERY STENOSIS ( 1 FDA reports)
PULMONARY CAVITATION ( 1 FDA reports)
PULMONARY DYSMATURITY SYNDROME ( 1 FDA reports)
PULMONARY HYPOPLASIA ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PULPITIS DENTAL ( 1 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
PURPLE GLOVE SYNDROME ( 1 FDA reports)
PYELOCALIECTASIS ( 1 FDA reports)
PYLORIC STENOSIS ( 1 FDA reports)
PYLOROPLASTY ( 1 FDA reports)
PYROGLUTAMATE INCREASED ( 1 FDA reports)
RADIAL PULSE ( 1 FDA reports)
RADIATION PNEUMONITIS ( 1 FDA reports)
RADICULITIS CERVICAL ( 1 FDA reports)
RADICULOTOMY ( 1 FDA reports)
RADIOISOTOPE SCAN ABNORMAL ( 1 FDA reports)
RASH FOLLICULAR ( 1 FDA reports)
RECTAL CRAMPS ( 1 FDA reports)
RECTAL PERFORATION ( 1 FDA reports)
RECTAL SPASM ( 1 FDA reports)
RECTAL ULCER ( 1 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 1 FDA reports)
RECTOCELE REPAIR ( 1 FDA reports)
RED BLOOD CELL ROULEAUX FORMATION PRESENT ( 1 FDA reports)
RED BLOOD CELL SPHEROCYTES PRESENT ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH DECREASED ( 1 FDA reports)
REFLEX TEST ABNORMAL ( 1 FDA reports)
REFRACTION DISORDER ( 1 FDA reports)
REFRACTORY ANAEMIA ( 1 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 1 FDA reports)
REGRESSIVE BEHAVIOUR ( 1 FDA reports)
RELAPSING FEVER ( 1 FDA reports)
RENAL ADENOMA ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE II ( 1 FDA reports)
RENAL NECROSIS ( 1 FDA reports)
RENAL TUBULAR ATROPHY ( 1 FDA reports)
REPRODUCTIVE TRACT DISORDER ( 1 FDA reports)
RESPIRATORY FUME INHALATION DISORDER ( 1 FDA reports)
RESPIRATORY MONILIASIS ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS TEST POSITIVE ( 1 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
RESPIRATORY TRACT MALFORMATION ( 1 FDA reports)
RETINAL ANEURYSM ( 1 FDA reports)
RETINAL ARTERY OCCLUSION ( 1 FDA reports)
RETINAL ARTERY SPASM ( 1 FDA reports)
RETINAL ARTERY STENOSIS ( 1 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 1 FDA reports)
RETINAL VASCULAR OCCLUSION ( 1 FDA reports)
RETINAL VASCULITIS ( 1 FDA reports)
RETINITIS PIGMENTOSA ( 1 FDA reports)
RETINOGRAM ABNORMAL ( 1 FDA reports)
RETINOPATHY HYPERTENSIVE ( 1 FDA reports)
RETROGRADE AMNESIA ( 1 FDA reports)
RETROGRADE EJACULATION ( 1 FDA reports)
RETROPERITONEAL EFFUSION ( 1 FDA reports)
RETROPLACENTAL HAEMATOMA ( 1 FDA reports)
REVERSIBLE AIRWAYS OBSTRUCTION ( 1 FDA reports)
RHABDOMYOMA ( 1 FDA reports)
RHEUMATIC HEART DISEASE ( 1 FDA reports)
RHEUMATOID NODULE ( 1 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 1 FDA reports)
ROSEOLOVIRUS TEST POSITIVE ( 1 FDA reports)
RUSSELL'S VIPER VENOM TIME ABNORMAL ( 1 FDA reports)
SACCADIC EYE MOVEMENT ( 1 FDA reports)
SALIVA DISCOLOURATION ( 1 FDA reports)
SALIVARY GLAND CALCULUS ( 1 FDA reports)
SALIVARY GLAND DISORDER ( 1 FDA reports)
SALIVARY GLAND PAIN ( 1 FDA reports)
SALPINGITIS ( 1 FDA reports)
SARCOMA ( 1 FDA reports)
SCAN ABDOMEN ABNORMAL ( 1 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 1 FDA reports)
SCHIZOID PERSONALITY DISORDER ( 1 FDA reports)
SCIATIC NERVE NEUROPATHY ( 1 FDA reports)
SCLERAL DISORDER ( 1 FDA reports)
SCLERAL HYPERAEMIA ( 1 FDA reports)
SCLEREMA ( 1 FDA reports)
SCLERITIS ( 1 FDA reports)
SCLEROTHERAPY ( 1 FDA reports)
SCROTAL CANCER ( 1 FDA reports)
SCROTAL MASS ( 1 FDA reports)
SCROTAL SWELLING ( 1 FDA reports)
SEDATIVE THERAPY ( 1 FDA reports)
SEIZURE CLUSTER ( 1 FDA reports)
SEMEN DISCOLOURATION ( 1 FDA reports)
SEMEN VOLUME DECREASED ( 1 FDA reports)
SEMEN VOLUME INCREASED ( 1 FDA reports)
SENSATION OF BLOOD FLOW ( 1 FDA reports)
SENSORY INTEGRATIVE DYSFUNCTION ( 1 FDA reports)
SEPTIC EMBOLUS ( 1 FDA reports)
SEPTO-OPTIC DYSPLASIA ( 1 FDA reports)
SEROLOGY POSITIVE ( 1 FDA reports)
SERRATIA TEST POSITIVE ( 1 FDA reports)
SEXUAL RELATIONSHIP CHANGE ( 1 FDA reports)
SEXUAL TRANSMISSION OF INFECTION ( 1 FDA reports)
SEXUALLY TRANSMITTED DISEASE ( 1 FDA reports)
SHUNT ANEURYSM ( 1 FDA reports)
SHUNT INFECTION ( 1 FDA reports)
SHUNT STENOSIS ( 1 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 1 FDA reports)
SIGNET-RING CELL CARCINOMA ( 1 FDA reports)
SILICOSIS ( 1 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 1 FDA reports)
SINGLE PHOTON EMISSION COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
SKELETON DYSPLASIA ( 1 FDA reports)
SKIN LESION EXCISION ( 1 FDA reports)
SKIN SENSITISATION ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SKIN TURGOR DECREASED ( 1 FDA reports)
SKULL MALFORMATION ( 1 FDA reports)
SLEEP PHASE RHYTHM DISTURBANCE ( 1 FDA reports)
SLOW SPEECH ( 1 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
SMALL INTESTINAL RESECTION ( 1 FDA reports)
SMALL INTESTINAL STENOSIS ( 1 FDA reports)
SMALL INTESTINE CARCINOMA ( 1 FDA reports)
SMALL INTESTINE CARCINOMA METASTATIC ( 1 FDA reports)
SMALL INTESTINE ULCER ( 1 FDA reports)
SMOKING CESSATION THERAPY ( 1 FDA reports)
SODIUM RETENTION ( 1 FDA reports)
SPASTIC PARALYSIS ( 1 FDA reports)
SPECIFIC GRAVITY URINE ABNORMAL ( 1 FDA reports)
SPECIFIC GRAVITY URINE DECREASED ( 1 FDA reports)
SPERM ANALYSIS ABNORMAL ( 1 FDA reports)
SPERMATOCELE ( 1 FDA reports)
SPERMATOZOA MORPHOLOGY ABNORMAL ( 1 FDA reports)
SPERMATOZOA PROGRESSIVE MOTILITY ABNORMAL ( 1 FDA reports)
SPERMATOZOA PROGRESSIVE MOTILITY DECREASED ( 1 FDA reports)
SPIDER VEIN ( 1 FDA reports)
SPINAL COLUMN INJURY ( 1 FDA reports)
SPINAL CORD OEDEMA ( 1 FDA reports)
SPINAL X-RAY ( 1 FDA reports)
SPINE MALFORMATION ( 1 FDA reports)
SPLENIC LESION ( 1 FDA reports)
SPONTANEOUS PENILE ERECTION ( 1 FDA reports)
SPOUSAL ABUSE ( 1 FDA reports)
SPUTUM PURULENT ( 1 FDA reports)
ST. LOUIS ENCEPHALITIS ( 1 FDA reports)
STAB WOUND ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STENOTROPHOMONAS TEST POSITIVE ( 1 FDA reports)
STRONGYLOIDIASIS ( 1 FDA reports)
SUBCLAVIAN ARTERY EMBOLISM ( 1 FDA reports)
SUDDEN INFANT DEATH SYNDROME ( 1 FDA reports)
SUPERFICIAL INJURY OF EYE ( 1 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 1 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 1 FDA reports)
SYNDACTYLY ( 1 FDA reports)
SYNOVIAL DISORDER ( 1 FDA reports)
SYRINGE ISSUE ( 1 FDA reports)
SYRINGOMYELIA ( 1 FDA reports)
SYSTOLIC DYSFUNCTION ( 1 FDA reports)
T-LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
TABLET PHYSICAL ISSUE ( 1 FDA reports)
TANDEM GAIT TEST ( 1 FDA reports)
TENDON CALCIFICATION ( 1 FDA reports)
TENDON OPERATION ( 1 FDA reports)
TESTICULAR ATROPHY ( 1 FDA reports)
TESTICULAR DISORDER ( 1 FDA reports)
TESTICULAR RETRACTION ( 1 FDA reports)
TESTICULAR SEMINOMA (PURE) ( 1 FDA reports)
THERAPEUTIC PROCEDURE ( 1 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
THERAPY RESPONDER ( 1 FDA reports)
THROMBOLYSIS ( 1 FDA reports)
THYMOMA ( 1 FDA reports)
THYMUS DISORDER ( 1 FDA reports)
THYMUS ENLARGEMENT ( 1 FDA reports)
THYROID ADENOMA ( 1 FDA reports)
THYROIDITIS CHRONIC ( 1 FDA reports)
THYROIDITIS SUBACUTE ( 1 FDA reports)
THYROXINE FREE INCREASED ( 1 FDA reports)
TILT TABLE TEST ( 1 FDA reports)
TINEA CRURIS ( 1 FDA reports)
TOE OPERATION ( 1 FDA reports)
TONGUE HAEMATOMA ( 1 FDA reports)
TONSILLAR DISORDER ( 1 FDA reports)
TOOTH DEPOSIT ( 1 FDA reports)
TOOTH HYPOPLASIA ( 1 FDA reports)
TOOTH RESORPTION ( 1 FDA reports)
TOXIC ANTERIOR SEGMENT SYNDROME ( 1 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 1 FDA reports)
TRACHEAL STENOSIS ( 1 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 1 FDA reports)
TRANSAMINASES ABNORMAL ( 1 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 1 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 1 FDA reports)
TRAUMATIC ARTHRITIS ( 1 FDA reports)
TRAUMATIC INTRACRANIAL HAEMORRHAGE ( 1 FDA reports)
TRICUSPID VALVE PROLAPSE ( 1 FDA reports)
TRYPTASE INCREASED ( 1 FDA reports)
TUMOUR EXCISION ( 1 FDA reports)
TUMOUR FLARE ( 1 FDA reports)
TYMPANIC MEMBRANE HYPERAEMIA ( 1 FDA reports)
TYPE III HYPERLIPIDAEMIA ( 1 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 1 FDA reports)
ULNAR NEURITIS ( 1 FDA reports)
ULTRAFILTRATION FAILURE ( 1 FDA reports)
ULTRASOUND ANTENATAL SCREEN ABNORMAL ( 1 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 1 FDA reports)
UMBILICAL CORD SHORT ( 1 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
UNEMPLOYMENT ( 1 FDA reports)
UNEQUAL LIMB LENGTH ( 1 FDA reports)
UNIVENTRICULAR HEART ( 1 FDA reports)
UNWANTED AWARENESS DURING ANAESTHESIA ( 1 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 1 FDA reports)
UPPER LIMB DEFORMITY ( 1 FDA reports)
URETERIC DILATATION ( 1 FDA reports)
URETERIC STENOSIS ( 1 FDA reports)
URETHRAL MEATUS STENOSIS ( 1 FDA reports)
URETHRAL PAIN ( 1 FDA reports)
URETHROTOMY ( 1 FDA reports)
URINARY SEDIMENT PRESENT ( 1 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
URINARY TRACT INFECTION VIRAL ( 1 FDA reports)
URINARY TRACT INJURY ( 1 FDA reports)
URINE ALCOHOL TEST POSITIVE ( 1 FDA reports)
URINE CALCIUM INCREASED ( 1 FDA reports)
URINE DELTA AMINOLEVULINATE ( 1 FDA reports)
URINE ELECTROPHORESIS ABNORMAL ( 1 FDA reports)
URINE OSMOLARITY DECREASED ( 1 FDA reports)
URINE PHOSPHATE INCREASED ( 1 FDA reports)
URINE POTASSIUM DECREASED ( 1 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 1 FDA reports)
URINE SODIUM DECREASED ( 1 FDA reports)
URINE URIC ACID ( 1 FDA reports)
UROBILINOGEN URINE INCREASED ( 1 FDA reports)
UROGENITAL DISORDER ( 1 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 1 FDA reports)
UTERINE CARCINOMA IN SITU ( 1 FDA reports)
UTERINE CYST ( 1 FDA reports)
UTERINE DILATION AND CURETTAGE ( 1 FDA reports)
UTERINE MASS ( 1 FDA reports)
UTERINE NEOPLASM ( 1 FDA reports)
VACUUM EXTRACTOR DELIVERY ( 1 FDA reports)
VAGINAL CANCER ( 1 FDA reports)
VAGINAL EROSION ( 1 FDA reports)
VAGINAL FISTULA ( 1 FDA reports)
VAGINAL OPERATION ( 1 FDA reports)
VAGINAL PROLAPSE ( 1 FDA reports)
VAGINAL REMOVAL OF INTRAUTERINE FOREIGN BODY ( 1 FDA reports)
VAGINAL SWELLING ( 1 FDA reports)
VARIANT CREUTZFELDT-JAKOB DISEASE ( 1 FDA reports)
VASCULAR BYPASS GRAFT ( 1 FDA reports)
VASCULAR GRAFT COMPLICATION ( 1 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 1 FDA reports)
VASCULAR NEOPLASM ( 1 FDA reports)
VASCULAR OPERATION ( 1 FDA reports)
VASCULAR PARKINSONISM ( 1 FDA reports)
VASCULAR RESISTANCE SYSTEMIC INCREASED ( 1 FDA reports)
VASCULITIS CEREBRAL ( 1 FDA reports)
VASODILATION PROCEDURE ( 1 FDA reports)
VELOPHARYNGEAL INCOMPETENCE ( 1 FDA reports)
VENA CAVA EMBOLISM ( 1 FDA reports)
VENA CAVA FILTER INSERTION ( 1 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 1 FDA reports)
VENTRICLE RUPTURE ( 1 FDA reports)
VENTRICULAR ASYSTOLE ( 1 FDA reports)
VENTRICULAR FAILURE ( 1 FDA reports)
VENTRICULO-PERITONEAL SHUNT ( 1 FDA reports)
VERBIGERATION ( 1 FDA reports)
VERTEBRAL ARTERY THROMBOSIS ( 1 FDA reports)
VERTEBRAL INJURY ( 1 FDA reports)
VESICOURETERIC REFLUX ( 1 FDA reports)
VIBRATION TEST ABNORMAL ( 1 FDA reports)
VICTIM OF SPOUSAL ABUSE ( 1 FDA reports)
VIRAL DIARRHOEA ( 1 FDA reports)
VIRAL LOAD DECREASED ( 1 FDA reports)
VIRAL MUTATION IDENTIFIED ( 1 FDA reports)
VIRAL MYOSITIS ( 1 FDA reports)
VIRAL OESOPHAGITIS ( 1 FDA reports)
VIRAL PERICARDITIS ( 1 FDA reports)
VITAL CAPACITY DECREASED ( 1 FDA reports)
VITAMIN B12 INCREASED ( 1 FDA reports)
VITAMIN K DECREASED ( 1 FDA reports)
VITAMIN K DEFICIENCY ( 1 FDA reports)
VOCAL CORD ATROPHY ( 1 FDA reports)
VOCAL CORD PARALYSIS ( 1 FDA reports)
VOLVULUS OF BOWEL ( 1 FDA reports)
VOMITING NEONATAL ( 1 FDA reports)
VOMITING PSYCHOGENIC ( 1 FDA reports)
VULVITIS ( 1 FDA reports)
VULVOVAGINAL ERYTHEMA ( 1 FDA reports)
VULVOVAGINITIS ( 1 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 1 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 1 FDA reports)
WEANING FAILURE ( 1 FDA reports)
WEGENER'S GRANULOMATOSIS ( 1 FDA reports)
WEIGHT CONTROL ( 1 FDA reports)
WHITE BLOOD CELL COUNT ( 1 FDA reports)
WHITE BLOOD CELLS URINE ( 1 FDA reports)
WOUND ABSCESS ( 1 FDA reports)
X-LINKED CHROMOSOMAL DISORDER ( 1 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
ZINC DEFICIENCY ( 1 FDA reports)
ZYGOMYCOSIS ( 1 FDA reports)