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

DEATH ( 10 FDA reports)
DYSPNOEA ( 9 FDA reports)
DEHYDRATION ( 7 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 6 FDA reports)
PNEUMONIA ( 6 FDA reports)
URTICARIA ( 5 FDA reports)
ANGIOEDEMA ( 5 FDA reports)
ORAL DISCOMFORT ( 4 FDA reports)
HYPOAESTHESIA ORAL ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 4 FDA reports)
TACHYCARDIA ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
FAECES DISCOLOURED ( 3 FDA reports)
COUGH ( 3 FDA reports)
CYANOSIS ( 3 FDA reports)
DUODENAL ULCER ( 3 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
GRANULOMA ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRUG THERAPY ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 1 FDA reports)
GASTRIC ULCER PERFORATION ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOGLOBINURIA ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PERICARDIAL DISEASE ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SCAR ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
TREMOR ( 1 FDA reports)
ADHESION ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)

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