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

PYREXIA ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
TESTIS CANCER ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
PUPIL FIXED ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
OTITIS MEDIA ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
CATHETER SITE PAIN ( 2 FDA reports)
CHILLS ( 2 FDA reports)
DEATH ( 2 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
INJURY ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MANTLE CELL LYMPHOMA ( 1 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
ASCITES ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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