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

DECREASED APPETITE ( 12 FDA reports)
DIARRHOEA ( 8 FDA reports)
STOMATITIS ( 5 FDA reports)
MALAISE ( 5 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 5 FDA reports)
INFUSION RELATED REACTION ( 4 FDA reports)
ANAEMIA ( 4 FDA reports)
INTERSTITIAL LUNG DISEASE ( 4 FDA reports)
RASH ( 4 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 4 FDA reports)
COLITIS ISCHAEMIC ( 3 FDA reports)
PROTEIN TOTAL DECREASED ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
METASTASES TO LIVER ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
DERMATITIS ACNEIFORM ( 3 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 3 FDA reports)
MELAENA ( 3 FDA reports)
BLOOD ALBUMIN DECREASED ( 3 FDA reports)
SEBORRHOEIC DERMATITIS ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
EOSINOPHIL COUNT ABNORMAL ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
HYPOTHYROIDISM ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
HAEMATOCRIT ABNORMAL ( 3 FDA reports)
HAEMOGLOBIN ABNORMAL ( 3 FDA reports)
HEPATITIS B ( 3 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 3 FDA reports)
ACIDOSIS ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
EAR DISCOMFORT ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DEATH ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
PARONYCHIA ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
COUGH ( 1 FDA reports)

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