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

MYOCARDIAL INFARCTION ( 11 FDA reports)
FATIGUE ( 6 FDA reports)
RHABDOMYOLYSIS ( 6 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 5 FDA reports)
CHROMATURIA ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 4 FDA reports)
LIVER TENDERNESS ( 4 FDA reports)
MUSCLE CRAMP ( 4 FDA reports)
OEDEMA ( 4 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
MUSCLE DISORDER ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST DISORDER ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHRONIC SINUSITIS ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONDUCTIVE DEAFNESS ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEATH ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GOITRE ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LOW TURNOVER OSTEOPATHY ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
OTITIS MEDIA ACUTE ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PELVIC PROLAPSE ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POST HERPETIC NEURALGIA ( 1 FDA reports)
PYURIA ( 1 FDA reports)
REFLUX LARYNGITIS ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THIRST ( 1 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WOUND SEPSIS ( 1 FDA reports)

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