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

KIDNEY TRANSPLANT REJECTION ( 6 FDA reports)
HYPERTENSION ( 4 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 3 FDA reports)
BILE DUCT STONE ( 3 FDA reports)
BILIARY SPHINCTEROTOMY ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
CHOLANGITIS SUPPURATIVE ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
THYMOMA ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
BILIARY DRAINAGE ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
HEMIANOPIA ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
FIBROADENOMA OF BREAST ( 1 FDA reports)
GINGIVAL HYPERTROPHY ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
HIRSUTISM ( 1 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
CATHETER REMOVAL ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
PERIODONTITIS ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 1 FDA reports)
ACNE ( 1 FDA reports)
TUMOUR EXCISION ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)

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