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

PYREXIA ( 7 FDA reports)
CHILLS ( 7 FDA reports)
ASTHENIA ( 6 FDA reports)
MULTI-ORGAN FAILURE ( 6 FDA reports)
HYPOTENSION ( 4 FDA reports)
VOMITING ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
UNRESPONSIVE TO STIMULI ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
BLOOD SODIUM INCREASED ( 3 FDA reports)
RENAL PAIN ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 3 FDA reports)
APHASIA ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
MENTAL STATUS CHANGES ( 3 FDA reports)
METABOLIC ALKALOSIS ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
CALCIPHYLAXIS ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
SKIN GRAFT INFECTION ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DEATH ( 1 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)

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