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

HEPATIC FUNCTION ABNORMAL ( 16 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 13 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 12 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 12 FDA reports)
INTERSTITIAL LUNG DISEASE ( 9 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 8 FDA reports)
BLOOD GLUCOSE INCREASED ( 7 FDA reports)
ANAEMIA ( 6 FDA reports)
CARDIAC FAILURE ( 6 FDA reports)
PLATELET COUNT DECREASED ( 6 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 5 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 5 FDA reports)
HAEMATURIA ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
MYOCARDIAL INFARCTION ( 5 FDA reports)
URINARY RETENTION ( 5 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
ECZEMA ( 4 FDA reports)
HYPOGLYCAEMIA ( 4 FDA reports)
MACULAR DEGENERATION ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
VOMITING ( 4 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 3 FDA reports)
BLOOD AMYLASE ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
COUGH ( 3 FDA reports)
DEAFNESS ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DRUG ERUPTION ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
LOW DENSITY LIPOPROTEIN ABNORMAL ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
PROSTATIC HAEMORRHAGE ( 3 FDA reports)
PROTEIN TOTAL DECREASED ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
TESTICULAR NEOPLASM ( 3 FDA reports)
TINNITUS ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
BLADDER TAMPONADE ( 2 FDA reports)
BLOOD ALDOSTERONE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CHEILITIS ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
GENITAL HAEMORRHAGE ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 2 FDA reports)
PAIN ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PLASMACYTOMA ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
RASH ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
TONGUE DISCOLOURATION ( 2 FDA reports)
TREMOR ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
BALANITIS ( 1 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN DECREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 1 FDA reports)
BLOOD CHOLINESTERASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEFICIENCY ANAEMIA ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
IRON BINDING CAPACITY UNSATURATED INCREASED ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PRODUCT TASTE ABNORMAL ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
REGURGITATION ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RETINAL NEOVASCULARISATION ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TESTICULAR ATROPHY ( 1 FDA reports)
TONGUE PARALYSIS ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use