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

HEPATIC FAILURE ( 20 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 11 FDA reports)
ASCITES ( 11 FDA reports)
WEIGHT DECREASED ( 10 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 8 FDA reports)
HEPATIC ENCEPHALOPATHY ( 8 FDA reports)
HEPATITIS B ( 8 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 8 FDA reports)
BLOOD BILIRUBIN INCREASED ( 7 FDA reports)
FANCONI SYNDROME ACQUIRED ( 7 FDA reports)
HEPATIC CIRRHOSIS ( 7 FDA reports)
ANOREXIA ( 6 FDA reports)
OSTEOPOROSIS ( 6 FDA reports)
PROTHROMBIN TIME PROLONGED ( 6 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 5 FDA reports)
BLOOD CREATININE INCREASED ( 5 FDA reports)
DEPRESSION ( 5 FDA reports)
LIVER TRANSPLANT ( 5 FDA reports)
MUSCULAR WEAKNESS ( 5 FDA reports)
PANCREATITIS ACUTE ( 5 FDA reports)
PORTAL VEIN THROMBOSIS ( 5 FDA reports)
RENAL IMPAIRMENT ( 5 FDA reports)
ADJUSTMENT DISORDER ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 4 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 4 FDA reports)
BONE PAIN ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
GAIT DISTURBANCE ( 4 FDA reports)
HYPOPHOSPHATAEMIA ( 4 FDA reports)
METABOLIC ACIDOSIS ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
OSTEOMALACIA ( 4 FDA reports)
RENAL TUBULAR DISORDER ( 4 FDA reports)
VARICES OESOPHAGEAL ( 4 FDA reports)
VIRAL MUTATION IDENTIFIED ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BLOOD UREA DECREASED ( 3 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DRUG RESISTANCE ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 3 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 3 FDA reports)
LUNG INFECTION ( 3 FDA reports)
METASTASES TO LUNG ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
OLIGURIA ( 3 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 3 FDA reports)
PATHOGEN RESISTANCE ( 3 FDA reports)
PERITONITIS BACTERIAL ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ABORTION INDUCED ( 2 FDA reports)
AMINO ACID LEVEL INCREASED ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLEEDING VARICOSE VEIN ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD LACTIC ACID INCREASED ( 2 FDA reports)
BLOOD URIC ACID INCREASED ( 2 FDA reports)
BONE METABOLISM DISORDER ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 2 FDA reports)
GLYCOSURIA ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HBV DNA INCREASED ( 2 FDA reports)
HEPATIC ATROPHY ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT RECURRENT ( 2 FDA reports)
HEPATITIS CHOLESTATIC ( 2 FDA reports)
HEPATORENAL SYNDROME ( 2 FDA reports)
HYPERLACTACIDAEMIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
MYOPATHY TOXIC ( 2 FDA reports)
NEPHROTIC SYNDROME ( 2 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
TRANSPLANT REJECTION ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
COMA HEPATIC ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEATH ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
FANCONI SYNDROME ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GRAFT INFECTION ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMORRHAGIC ASCITES ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERSPLENISM ACQUIRED ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LIVER TRANSPLANT REJECTION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN FRAGILITY ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VIRAL LOAD INCREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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