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

PNEUMONIA ( 14 FDA reports)
TORSADE DE POINTES ( 9 FDA reports)
CARDIAC ARREST ( 9 FDA reports)
HYPOALBUMINAEMIA ( 9 FDA reports)
ANAEMIA ( 8 FDA reports)
THROMBOCYTOPENIA ( 8 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 8 FDA reports)
BLOOD BILIRUBIN INCREASED ( 8 FDA reports)
NEUTROPENIA ( 8 FDA reports)
BLOOD CALCIUM DECREASED ( 6 FDA reports)
OEDEMA ( 6 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
SPINAL COMPRESSION FRACTURE ( 4 FDA reports)
BLOOD UREA INCREASED ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 4 FDA reports)
LEUKOPENIA ( 4 FDA reports)
VENTRICULAR TACHYCARDIA ( 3 FDA reports)
LEUKOENCEPHALOPATHY ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
OSTEOPOROSIS ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
EXTRASYSTOLES ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
CONVULSIONS LOCAL ( 1 FDA reports)
CONJUNCTIVAL OEDEMA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
CHLOROMA ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM NEOPLASM ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
CAPILLARY LEAK SYNDROME ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
SCLERAL HAEMORRHAGE ( 1 FDA reports)
SCLERAL OEDEMA ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
BLAST CELLS PRESENT ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
ASCITES ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
ACUTE LEUKAEMIA ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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