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

HYPOKALAEMIA ( 5 FDA reports)
ASTHENIA ( 4 FDA reports)
HYPONATRAEMIA ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
VOMITING ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
AMNESIA ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG ABUSER ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
FALL ( 2 FDA reports)
APPLICATION SITE ERYTHEMA ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
ATAXIA ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
MASS ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
PAIN ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)

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