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

ASPARTATE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
ASCITES ( 4 FDA reports)
ATELECTASIS ( 4 FDA reports)
BLOOD BILIRUBIN INCREASED ( 4 FDA reports)
HEPATIC ENCEPHALOPATHY ( 4 FDA reports)
ANOREXIA ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
MUCOSAL INFLAMMATION ( 3 FDA reports)
PERITONITIS BACTERIAL ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
HEPATITIS B ( 2 FDA reports)
KLEBSIELLA INFECTION ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
MALAISE ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ADJUSTMENT DISORDER ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANGIOGRAM ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
AORTIC ATHEROSCLEROSIS ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BILIRUBIN URINE ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CELLS IN URINE ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
COUGH ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIARRHOEA INFECTIOUS ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
FALL ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 1 FDA reports)
HAEMANGIOMA OF LIVER ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMOGLOBIN URINE PRESENT ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HBV DNA INCREASED ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERTENSIVE EMERGENCY ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INTESTINAL STOMA COMPLICATION ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MACULOPATHY ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NITRITE URINE PRESENT ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PORTAL VEIN THROMBOSIS ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PSYCHOMOTOR AGITATION ( 1 FDA reports)
PULMONARY CALCIFICATION ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RASH ( 1 FDA reports)
RED BLOOD CELLS URINE ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
SCAR ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SMALL INTESTINAL PERFORATION ( 1 FDA reports)
SOFT TISSUE DISORDER ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
SPONDYLOARTHROPATHY ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)

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