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

ALANINE AMINOTRANSFERASE INCREASED ( 14 FDA reports)
JAUNDICE ( 14 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 12 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 11 FDA reports)
BLOOD BILIRUBIN INCREASED ( 10 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 10 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 9 FDA reports)
LIVER DISORDER ( 9 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 8 FDA reports)
PLATELET COUNT DECREASED ( 8 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 7 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 7 FDA reports)
BLOOD CREATININE INCREASED ( 5 FDA reports)
ASCITES ( 4 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 4 FDA reports)
HEPATIC FAILURE ( 4 FDA reports)
MALAISE ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
SENSATION OF HEAVINESS ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
AMMONIA INCREASED ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BONE MARROW DISORDER ( 2 FDA reports)
CARDIAC FAILURE CHRONIC ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DISSEMINATED TUBERCULOSIS ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
FALL ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
HEPATIC ATROPHY ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATITIS B ( 2 FDA reports)
HYPERCAPNIA ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
IMMUNOGLOBULINS INCREASED ( 2 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RHEUMATOID LUNG ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
STRESS SYMPTOMS ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
VOMITING ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
COMA ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
DEATH ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LUNG ABSCESS ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
OSTEOMALACIA ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PAIN ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
SINUS ARREST ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TREMOR ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)

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