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

URINOMA ( 4 FDA reports)
STAPHYLOCOCCAL INFECTION ( 4 FDA reports)
LYMPHOCELE ( 4 FDA reports)
CELLULITIS ( 4 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
KIDNEY SMALL ( 1 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
MALIGNANT ASCITES ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
PAIN ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PERITONEAL NEOPLASM ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
RENAL ABSCESS ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
ACINETOBACTER BACTERAEMIA ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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