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

NEUTROPENIA ( 6 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 4 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 4 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
ASCITES ( 3 FDA reports)
NEUTROPHIL COUNT DECREASED ( 3 FDA reports)
ILEUS ( 3 FDA reports)
HYPERNATRAEMIA ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
HYPERPHOSPHATAEMIA ( 2 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
ENGRAFTMENT SYNDROME ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
OVARIAN CANCER RECURRENT ( 2 FDA reports)
HAEMOCONCENTRATION ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
HYPERCHLORAEMIA ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
CANDIDURIA ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
INFECTION ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
MONOCYTE COUNT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)

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