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

SEPTIC SHOCK ( 12 FDA reports)
DRUG INEFFECTIVE ( 11 FDA reports)
SERUM SICKNESS ( 9 FDA reports)
GRAFT VERSUS HOST DISEASE ( 8 FDA reports)
URINARY TRACT INFECTION ( 8 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 7 FDA reports)
DRUG INTERACTION ( 6 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 5 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 5 FDA reports)
ASPERGILLOSIS ( 4 FDA reports)
CYTOLYTIC HEPATITIS ( 4 FDA reports)
HYPERGLYCAEMIA ( 4 FDA reports)
LIVER DISORDER ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 3 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 3 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 3 FDA reports)
HEPATIC ENCEPHALOPATHY ( 3 FDA reports)
HEPATORENAL SYNDROME ( 3 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
MEDICATION ERROR ( 3 FDA reports)
METABOLIC ENCEPHALOPATHY ( 3 FDA reports)
PANCREATITIS NECROTISING ( 3 FDA reports)
PEARSON'S SYNDROME ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
RENAL TUBULAR DISORDER ( 3 FDA reports)
ABDOMINAL MASS ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ASCITES ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MYELOPATHY ( 2 FDA reports)
NEUROPATHY ( 2 FDA reports)
ORAL MUCOSAL DISORDER ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PELIOSIS HEPATIS ( 2 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SKIN MASS ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CIRCUMORAL OEDEMA ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
ENCEPHALITIS CYTOMEGALOVIRUS ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
IMMUNOLOGY TEST ABNORMAL ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
LARYNGEAL CANCER ( 1 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
NAIL INJURY ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
RASH ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THYROID CANCER ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)

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