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

CEREBRAL INFARCTION ( 7 FDA reports)
DEATH ( 7 FDA reports)
GASTRIC CANCER ( 7 FDA reports)
RENAL IMPAIRMENT ( 7 FDA reports)
HYPOGLYCAEMIC COMA ( 5 FDA reports)
PLATELET COUNT DECREASED ( 5 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
RESPIRATORY FAILURE ( 4 FDA reports)
SPINAL COMPRESSION FRACTURE ( 4 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BONE MARROW FAILURE ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
INJURY ( 3 FDA reports)
OSTEONECROSIS ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
RASH ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ARTERIAL RUPTURE ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
CACHEXIA ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
GRANULOCYTE COUNT DECREASED ( 2 FDA reports)
GRANULOCYTOPENIA ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HEPATIC CONGESTION ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HYPERURICAEMIA ( 2 FDA reports)
HYPOPROTEINAEMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
MALAISE ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
PANCREATIC ENZYMES INCREASED ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
SPONDYLITIS ( 2 FDA reports)
SWELLING ( 2 FDA reports)
THROMBOPHLEBITIS ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
FALL ( 1 FDA reports)
FASCIITIS ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
NECROTISING FASCIITIS ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
RADIATION SKIN INJURY ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
TESTICULAR SWELLING ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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