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

PNEUMONIA ( 9 FDA reports)
OSTEOMYELITIS ( 7 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 6 FDA reports)
BLOOD ALBUMIN DECREASED ( 6 FDA reports)
PSEUDARTHROSIS ( 6 FDA reports)
TRANSPLANT REJECTION ( 6 FDA reports)
DRUG HYPERSENSITIVITY ( 6 FDA reports)
STERNAL FRACTURE ( 6 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 5 FDA reports)
OPPORTUNISTIC INFECTION ( 5 FDA reports)
RESPIRATORY DISORDER ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
STAPHYLOCOCCAL INFECTION ( 5 FDA reports)
EOSINOPHIL COUNT INCREASED ( 4 FDA reports)
TRANSPLANT ( 4 FDA reports)
HYPERGLYCAEMIA ( 4 FDA reports)
LYMPHATIC DUCT RUPTURE ( 4 FDA reports)
RENAL IMPAIRMENT ( 4 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 4 FDA reports)
CONVULSION ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 4 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 4 FDA reports)
PNEUMOTHORAX ( 4 FDA reports)
ENTEROCOLITIS ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
CHYLOTHORAX ( 3 FDA reports)
FOREIGN BODY TRAUMA ( 2 FDA reports)
DIFFUSE PANBRONCHIOLITIS ( 2 FDA reports)
PYOTHORAX ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
LYMPHANGIOLEIOMYOMATOSIS ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
LUNG TRANSPLANT REJECTION ( 1 FDA reports)
INTERLEUKIN LEVEL INCREASED ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
VOMITING ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LUNG ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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