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

NEUTROPHIL COUNT DECREASED ( 15 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 12 FDA reports)
PLATELET COUNT DECREASED ( 11 FDA reports)
FEBRILE NEUTROPENIA ( 9 FDA reports)
NAUSEA ( 9 FDA reports)
ANAEMIA ( 7 FDA reports)
HAEMOGLOBIN DECREASED ( 7 FDA reports)
PYREXIA ( 7 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 6 FDA reports)
RENAL DISORDER ( 6 FDA reports)
SEPSIS ( 6 FDA reports)
CONSTIPATION ( 5 FDA reports)
INSOMNIA ( 5 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 5 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
HYPOALBUMINAEMIA ( 4 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 4 FDA reports)
PROTEIN URINE PRESENT ( 4 FDA reports)
STOMATITIS ( 4 FDA reports)
VOMITING ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD CHLORIDE DECREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
GLUCOSE URINE PRESENT ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
METASTASES TO PLEURA ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 3 FDA reports)
PROTEIN TOTAL DECREASED ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 2 FDA reports)
ANTITHROMBIN III DECREASED ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BREAST CANCER METASTATIC ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CATARACT SUBCAPSULAR ( 2 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DIPLEGIA ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
ENDOTOXAEMIA ( 2 FDA reports)
ENGRAFT FAILURE ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
HAEMATOTOXICITY ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
LUNG INFECTION ( 2 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
METASTASES TO LUNG ( 2 FDA reports)
METASTASES TO SPINE ( 2 FDA reports)
MONOCYTE COUNT ABNORMAL ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PAIN ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PHLEBITIS ( 2 FDA reports)
PULMONARY TUBERCULOSIS ( 2 FDA reports)
RECALL PHENOMENON ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SPINAL COMPRESSION FRACTURE ( 2 FDA reports)
SPINAL CORD COMPRESSION ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
UROBILIN URINE PRESENT ( 2 FDA reports)
VENOOCCLUSIVE DISEASE ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEATH ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HYPERPLASIA ( 1 FDA reports)
ILEUS ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MALAISE ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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