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

PLATELET COUNT DECREASED ( 4 FDA reports)
TUMOUR LYSIS SYNDROME ( 3 FDA reports)
ANAEMIA ( 3 FDA reports)
ATRIAL FLUTTER ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 3 FDA reports)
SEPSIS ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
PLEURAL HAEMORRHAGE ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
HYPOCALCAEMIA ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GLIOBLASTOMA MULTIFORME ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL PERFORATION ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
ILEUS ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INTERNAL HERNIA ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEATH ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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