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

ASTHENIA ( 8 FDA reports)
HAEMOGLOBIN DECREASED ( 6 FDA reports)
HYPERSENSITIVITY ( 6 FDA reports)
DEHYDRATION ( 5 FDA reports)
VOMITING ( 5 FDA reports)
EOSINOPHILIA ( 4 FDA reports)
MALAISE ( 4 FDA reports)
MYELOPATHY ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
RASH ( 4 FDA reports)
RASH ERYTHEMATOUS ( 4 FDA reports)
RASH PRURITIC ( 4 FDA reports)
ABASIA ( 3 FDA reports)
ANAEMIA ( 3 FDA reports)
ANAPHYLACTIC REACTION ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 3 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
INFUSION RELATED REACTION ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
ORAL INTAKE REDUCED ( 3 FDA reports)
PALLOR ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 2 FDA reports)
FAILURE TO THRIVE ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LOBAR PNEUMONIA ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
OSTEOMYELITIS ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
URETERAL NECROSIS ( 2 FDA reports)
URINARY FISTULA ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABSCESS INTESTINAL ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
COUGH ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
INJURY ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NOCARDIOSIS ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL CANCER METASTATIC ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL NEOPLASM ( 1 FDA reports)
REOCCLUSION ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
URINARY SEDIMENT PRESENT ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VASCULAR GRAFT COMPLICATION ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)

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