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VISION BLURRED ( 2 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 2 FDA reports)
PAIN ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
DEAFNESS BILATERAL ( 2 FDA reports)
BRADYCARDIA ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FISTULA DISCHARGE ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
RECTAL ABSCESS ( 1 FDA reports)
SUBDURAL HAEMORRHAGE ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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