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

VOMITING ( 6 FDA reports)
NAUSEA ( 4 FDA reports)
AMNESIA ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DEATH ( 4 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
WOUND SECRETION ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
SWELLING ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
RASH ( 2 FDA reports)
BLOOD GLUCOSE FALSE POSITIVE ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
DEVICE INTERACTION ( 2 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GOUT ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
ILEUS ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
PYODERMA GANGRENOSUM ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
CHILLS ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)

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