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

PERITONITIS ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 3 FDA reports)
PYREXIA ( 2 FDA reports)
ASCITES ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
CHILLS ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
FALL ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INFUSION SITE CELLULITIS ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
AXILLARY MASS ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
AURA ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
POSTICTAL HEADACHE ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
URGE INCONTINENCE ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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