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

TOXIC EPIDERMAL NECROLYSIS ( 6 FDA reports)
INFECTION ( 6 FDA reports)
STEVENS-JOHNSON SYNDROME ( 5 FDA reports)
HYPOKALAEMIA ( 5 FDA reports)
VOMITING ( 4 FDA reports)
GENERALISED OEDEMA ( 4 FDA reports)
VENTRICULAR TACHYCARDIA ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
PULMONARY CONGESTION ( 3 FDA reports)
ASCITES ( 3 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
ILEUS ( 3 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PERIPHERAL EMBOLISM ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
MUCOUS MEMBRANE DISORDER ( 2 FDA reports)
MALAISE ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
HYPOCALCAEMIA ( 2 FDA reports)
BLOOD PH INCREASED ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HEPATITIS A ( 1 FDA reports)
INFLUENZA SEROLOGY POSITIVE ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ABSCESS ( 1 FDA reports)

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