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

CARDIAC FAILURE ( 7 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 6 FDA reports)
ATRIAL FIBRILLATION ( 5 FDA reports)
DIZZINESS ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
TACHYARRHYTHMIA ( 5 FDA reports)
ANAEMIA ( 4 FDA reports)
ANGINA PECTORIS ( 4 FDA reports)
CEREBRAL INFARCTION ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
MITRAL VALVE INCOMPETENCE ( 4 FDA reports)
AMAUROSIS FUGAX ( 3 FDA reports)
BALANCE DISORDER ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
DRY MOUTH ( 3 FDA reports)
FLATULENCE ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
LOCALISED INFECTION ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
OSTEOARTHRITIS ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 3 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 3 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 3 FDA reports)
ACANTHOMA ( 2 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BASAL CELL CARCINOMA ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
COMA HEPATIC ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
GASTROINTESTINAL INFECTION ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HIP ARTHROPLASTY ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
MALIGNANT NEOPLASM OF AMPULLA OF VATER ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PANCREATIC CARCINOMA ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
POLYNEUROPATHY ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PROSTATIC ADENOMA ( 2 FDA reports)
RADICULAR SYNDROME ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
ROSACEA ( 2 FDA reports)
SICCA SYNDROME ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
SOFT TISSUE DISORDER ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
TARSAL TUNNEL SYNDROME ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
VENTRICULAR HYPERTROPHY ( 2 FDA reports)
VITAL CAPACITY DECREASED ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADENOMA BENIGN ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
AORTIC ATHEROSCLEROSIS ( 1 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD IRON INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC ADENOMA ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
IRON METABOLISM DISORDER ( 1 FDA reports)
MALAISE ( 1 FDA reports)
METASTASES TO PERITONEUM ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PENILE OEDEMA ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use