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

SHOCK ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
RASH ( 2 FDA reports)
MALAISE ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
EOSINOPHIL COUNT DECREASED ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
COMA ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CALCIUM IONISED DECREASED ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAPTOGLOBIN INCREASED ( 1 FDA reports)
HYPOCHROMASIA ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PERIDIVERTICULITIS ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ANURIA ( 1 FDA reports)
ANION GAP DECREASED ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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