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

HAEMORRHAGE ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
INFECTIOUS PERITONITIS ( 2 FDA reports)
HYDROTHORAX ( 2 FDA reports)
HEART VALVE INCOMPETENCE ( 2 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
GASTRIC NEOPLASM ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
DEATH ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TUMOUR HAEMORRHAGE ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
VASCULAR PURPURA ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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