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

RASH ( 7 FDA reports)
LEUKOPENIA ( 5 FDA reports)
BLOOD BILIRUBIN INCREASED ( 5 FDA reports)
WOUND INFECTION ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
TRANSAMINASES INCREASED ( 4 FDA reports)
ANXIETY ( 4 FDA reports)
MUCOSAL INFLAMMATION ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
CANDIDIASIS ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
HYPOTONIA ( 3 FDA reports)
VASCULAR OCCLUSION ( 3 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
TACHYPNOEA ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 3 FDA reports)
CYTOMEGALOVIRUS TEST ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 3 FDA reports)
PURPURA ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PETECHIAE ( 3 FDA reports)
PAIN ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
DRUG LEVEL INCREASED ( 3 FDA reports)
NEUROLOGICAL SYMPTOM ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
MELAENA ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
ILEUS ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
DIVERTICULAR PERFORATION ( 2 FDA reports)
PERITONITIS ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ENCEPHALITIS VIRAL ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATIC NEOPLASM ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANCREATITIS CHRONIC ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEATH ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
SHOCK ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
SWELLING ( 1 FDA reports)
CONGENITAL AORTIC STENOSIS ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
HEART DISEASE CONGENITAL ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
VENTRICULAR DRAINAGE ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)

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