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

FALL ( 7 FDA reports)
HEADACHE ( 7 FDA reports)
NAUSEA ( 7 FDA reports)
DEATH ( 6 FDA reports)
HYPERTENSION ( 6 FDA reports)
PYREXIA ( 6 FDA reports)
CONTUSION ( 5 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
DRUG INTERACTION ( 5 FDA reports)
STOMACH DISCOMFORT ( 5 FDA reports)
WEIGHT DECREASED ( 5 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
BLOOD BILIRUBIN INCREASED ( 4 FDA reports)
HEMIPARESIS ( 4 FDA reports)
NEPHROLITHIASIS ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
ARTERIAL INSUFFICIENCY ( 3 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BLOOD ALBUMIN DECREASED ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
CHROMATURIA ( 3 FDA reports)
EPIGASTRIC DISCOMFORT ( 3 FDA reports)
EXCORIATION ( 3 FDA reports)
FAECES PALE ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
GALLBLADDER DISORDER ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
HUNGER ( 3 FDA reports)
HYPOGLYCAEMIA ( 3 FDA reports)
HYPOPHAGIA ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
JAUNDICE CHOLESTATIC ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
OSTEOPOROSIS ( 3 FDA reports)
SCAN ABDOMEN ABNORMAL ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 3 FDA reports)
ALBUMIN URINE PRESENT ( 2 FDA reports)
BLOOD COUNT ABNORMAL ( 2 FDA reports)
BLOOD CREATINE INCREASED ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 2 FDA reports)
HAEMORRHOIDS ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
NEPHROTIC SYNDROME ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PAIN ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
THALAMIC INFARCTION ( 2 FDA reports)
THERAPEUTIC PROCEDURE ( 2 FDA reports)
TINEA VERSICOLOUR ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
URINARY TRACT DISORDER ( 2 FDA reports)
URINE ANALYSIS ABNORMAL ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DELAYED EFFECTS OF RADIATION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EMPYEMA ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANCREATIC MASS ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RETINAL INJURY ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
URETERIC OBSTRUCTION ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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