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

GASTRIC ULCER ( 7 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 6 FDA reports)
RENAL FAILURE ACUTE ( 6 FDA reports)
HEPATIC ENZYME INCREASED ( 5 FDA reports)
HYPERTENSION ( 5 FDA reports)
LIPASE INCREASED ( 5 FDA reports)
BLOOD AMYLASE INCREASED ( 5 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 5 FDA reports)
DIARRHOEA ( 4 FDA reports)
ANAEMIA ( 3 FDA reports)
RENAL TUBULAR DISORDER ( 3 FDA reports)
MALAISE ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
EATING DISORDER ( 3 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
METAPLASIA ( 2 FDA reports)
MELAENA ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
APHASIA ( 2 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
HEMISENSORY NEGLECT ( 1 FDA reports)
HYPERAMYLASAEMIA ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
ILEUS ( 1 FDA reports)
LIP EROSION ( 1 FDA reports)
HAEMATOMA EVACUATION ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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