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

PARAESTHESIA ( 6 FDA reports)
DRUG DOSE OMISSION ( 5 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 5 FDA reports)
BREAST CANCER ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
ESCHERICHIA INFECTION ( 4 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
HYPOREFLEXIA ( 4 FDA reports)
STAPHYLOCOCCAL INFECTION ( 4 FDA reports)
THROAT IRRITATION ( 4 FDA reports)
BREAST RECONSTRUCTION ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 3 FDA reports)
WRONG DRUG ADMINISTERED ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
CARPAL TUNNEL SYNDROME ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 2 FDA reports)
HIATUS HERNIA ( 2 FDA reports)
MACULAR DEGENERATION ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MOVEMENT DISORDER ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
PAIN ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
RASH ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TREMOR ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ADRENAL ADENOMA ( 1 FDA reports)
ADRENOMEGALY ( 1 FDA reports)
ANDROGEN DEFICIENCY ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BIOPSY LYMPH GLAND ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBRAL CALCIFICATION ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DUODENAL NEOPLASM ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GENITAL HERPES ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HAND FRACTURE ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MITRAL VALVE CALCIFICATION ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MULTIPLE CHEMICAL SENSITIVITY ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OESOPHAGEAL SPASM ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ONYCHOMYCOSIS ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
POSTNASAL DRIP ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
TENDON PAIN ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT FLUCTUATION ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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