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

CEREBRAL INFARCTION ( 5 FDA reports)
FOLLICULITIS ( 5 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 5 FDA reports)
NASOPHARYNGITIS ( 5 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 4 FDA reports)
CONVULSION ( 4 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 4 FDA reports)
ANOREXIA ( 3 FDA reports)
BLOOD CALCIUM INCREASED ( 3 FDA reports)
BLOOD UREA DECREASED ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
LACUNAR INFARCTION ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 3 FDA reports)
MALAISE ( 3 FDA reports)
MELAENA ( 3 FDA reports)
PAIN ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
BK VIRUS INFECTION ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 2 FDA reports)
CEREBRAL ASPERGILLOSIS ( 2 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
ENCEPHALITIS HERPES ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HERPES ZOSTER DISSEMINATED ( 2 FDA reports)
INFECTION ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 2 FDA reports)
VIRAL HAEMORRHAGIC CYSTITIS ( 2 FDA reports)
VOMITING ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
APPLICATION SITE SWELLING ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CYST ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATIC HAEMORRHAGE ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
RENAL NEOPLASM ( 1 FDA reports)
SPLENECTOMY ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)

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