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

NAUSEA ( 19 FDA reports)
HYPOTENSION ( 16 FDA reports)
DIZZINESS ( 12 FDA reports)
FATIGUE ( 12 FDA reports)
PAIN IN EXTREMITY ( 12 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 11 FDA reports)
VOMITING ( 11 FDA reports)
ASTHENIA ( 10 FDA reports)
HEADACHE ( 10 FDA reports)
COUGH ( 9 FDA reports)
HYPERTENSION ( 8 FDA reports)
INJURY ( 8 FDA reports)
PAIN ( 8 FDA reports)
ABDOMINAL PAIN UPPER ( 7 FDA reports)
ANAEMIA ( 7 FDA reports)
ATRIAL FIBRILLATION ( 7 FDA reports)
DRUG INEFFECTIVE ( 7 FDA reports)
FEELING ABNORMAL ( 7 FDA reports)
HYPERHIDROSIS ( 7 FDA reports)
MUSCLE SPASMS ( 7 FDA reports)
URINARY TRACT INFECTION ( 7 FDA reports)
ABDOMINAL PAIN ( 6 FDA reports)
ANXIETY ( 6 FDA reports)
ARTERIAL THROMBOSIS ( 6 FDA reports)
ATELECTASIS ( 6 FDA reports)
CARDIAC ARREST ( 6 FDA reports)
CONVULSION ( 6 FDA reports)
DIARRHOEA ( 6 FDA reports)
DYSPNOEA ( 6 FDA reports)
GASTRIC ULCER ( 6 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
INTESTINAL ISCHAEMIA ( 6 FDA reports)
OROPHARYNGEAL PAIN ( 6 FDA reports)
POLYCYTHAEMIA ( 6 FDA reports)
RECTAL HAEMORRHAGE ( 6 FDA reports)
RENAL FAILURE ACUTE ( 6 FDA reports)
SPINAL COLUMN STENOSIS ( 6 FDA reports)
VERTIGO ( 6 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 5 FDA reports)
BLOOD PRESSURE INCREASED ( 5 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 5 FDA reports)
EROSIVE OESOPHAGITIS ( 5 FDA reports)
HEART RATE DECREASED ( 5 FDA reports)
ILL-DEFINED DISORDER ( 5 FDA reports)
INSOMNIA ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 5 FDA reports)
IRRITABILITY ( 5 FDA reports)
MALAISE ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
PERIPHERAL ISCHAEMIA ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
TENOSYNOVITIS ( 5 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 5 FDA reports)
BACK PAIN ( 4 FDA reports)
BLINDNESS UNILATERAL ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 4 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
CATARACT ( 4 FDA reports)
CHEST DISCOMFORT ( 4 FDA reports)
COAGULOPATHY ( 4 FDA reports)
DEEP VEIN THROMBOSIS ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
EYE IRRITATION ( 4 FDA reports)
HEART RATE IRREGULAR ( 4 FDA reports)
IRITIS ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 4 FDA reports)
PROTEINURIA ( 4 FDA reports)
RHABDOMYOLYSIS ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
SYNCOPE ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
ULCERATIVE KERATITIS ( 4 FDA reports)
VIRAL INFECTION ( 4 FDA reports)
ABASIA ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
BLOOD GLUCOSE DECREASED ( 3 FDA reports)
CARDIOMEGALY ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CORNEAL ABRASION ( 3 FDA reports)
DRY EYE ( 3 FDA reports)
ECONOMIC PROBLEM ( 3 FDA reports)
ERUCTATION ( 3 FDA reports)
ESCHERICHIA INFECTION ( 3 FDA reports)
EYE INJURY ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
LATEX ALLERGY ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
LIVEDO RETICULARIS ( 3 FDA reports)
MULTIPLE INJURIES ( 3 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
NEUROPATHY PERIPHERAL ( 3 FDA reports)
OSTEOPOROSIS ( 3 FDA reports)
PERIPHERAL COLDNESS ( 3 FDA reports)
POOR QUALITY SLEEP ( 3 FDA reports)
PRESYNCOPE ( 3 FDA reports)
PULSE ABSENT ( 3 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 3 FDA reports)
SEBORRHOEIC KERATOSIS ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
STRESS ( 3 FDA reports)
UNEVALUABLE EVENT ( 3 FDA reports)
URINARY RETENTION ( 3 FDA reports)
UVEITIS ( 3 FDA reports)
ANGIOMYOLIPOMA ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CULTURE URINE POSITIVE ( 2 FDA reports)
CYST ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
EPIGASTRIC DISCOMFORT ( 2 FDA reports)
EYELID PTOSIS ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
GOITRE ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
INTRAOCULAR LENS IMPLANT ( 2 FDA reports)
ONYCHOMYCOSIS ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PHARYNGEAL DISORDER ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
PRODUCT ODOUR ABNORMAL ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
RALES ( 2 FDA reports)
TENDERNESS ( 2 FDA reports)
TREMOR ( 2 FDA reports)
ULCER ( 2 FDA reports)
URINE ODOUR ABNORMAL ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ACUTE STRESS DISORDER ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
APPLICATION SITE BURN ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASTHENOPIA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BREAST DISORDER ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
CAPILLARY DISORDER ( 1 FDA reports)
CARDIAC FIBRILLATION ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORNEAL EROSION ( 1 FDA reports)
CORNEAL OPACITY ( 1 FDA reports)
CRYING ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
EJACULATION DISORDER ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
EYELIDS PRURITUS ( 1 FDA reports)
FALL ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GENITAL PRURITUS FEMALE ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HAND FRACTURE ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYPERKERATOSIS ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCORRECT PRODUCT STORAGE ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
MACULAR ISCHAEMIA ( 1 FDA reports)
MELANOCYTIC NAEVUS ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
NAIL DYSTROPHY ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OCULAR DISCOMFORT ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PRURITUS ANI ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PURPURA ( 1 FDA reports)
RASH ( 1 FDA reports)
RESIDUAL URINE ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
SEASONAL ALLERGY ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TELANGIECTASIA ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRI-IODOTHYRONINE FREE INCREASED ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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