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

STEVENS-JOHNSON SYNDROME ( 10 FDA reports)
JAUNDICE ( 9 FDA reports)
MULTI-ORGAN FAILURE ( 8 FDA reports)
PLATELET COUNT DECREASED ( 8 FDA reports)
PNEUMONIA ( 8 FDA reports)
RENAL FAILURE ACUTE ( 8 FDA reports)
RESPIRATORY FAILURE ( 8 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 6 FDA reports)
BLOOD BILIRUBIN INCREASED ( 5 FDA reports)
DEATH ( 5 FDA reports)
FEBRILE NEUTROPENIA ( 5 FDA reports)
HAEMATEMESIS ( 5 FDA reports)
HEPATIC FAILURE ( 5 FDA reports)
PROTHROMBIN TIME PROLONGED ( 5 FDA reports)
RECTAL HAEMORRHAGE ( 5 FDA reports)
RIGHT VENTRICULAR FAILURE ( 5 FDA reports)
ACUTE MONOCYTIC LEUKAEMIA ( 4 FDA reports)
AGRANULOCYTOSIS ( 4 FDA reports)
BRADYCARDIA ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
ERYTHEMA ( 4 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
HEPATIC ENZYME INCREASED ( 4 FDA reports)
HYPONATRAEMIA ( 4 FDA reports)
LUNG INFECTION ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 3 FDA reports)
ANAEMIA ( 3 FDA reports)
BACTERIAL INFECTION ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DRUG LEVEL DECREASED ( 3 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 3 FDA reports)
EPILEPSY ( 3 FDA reports)
FUNGUS CULTURE POSITIVE ( 3 FDA reports)
HELLP SYNDROME ( 3 FDA reports)
HEPATOTOXICITY ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 3 FDA reports)
ABSCESS ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
AGITATION POSTOPERATIVE ( 2 FDA reports)
ALVEOLITIS ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 2 FDA reports)
ERYTHROPENIA ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPOCOAGULABLE STATE ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
ILEUS ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
PEMPHIGOID ( 2 FDA reports)
PURULENCE ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RENAL TRANSPLANT ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
STEM CELL TRANSPLANT ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ACIDOSIS ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANURIA ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CENTRAL VENOUS PRESSURE DECREASED ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMORRHAGIC ASCITES ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOFIBRINOGENAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
INFECTION ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PERITONEAL DIALYSIS ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PURPURA ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)

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