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

HEPATIC ENCEPHALOPATHY ( 48 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 38 FDA reports)
DIARRHOEA ( 35 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 33 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 27 FDA reports)
HEPATIC FAILURE ( 24 FDA reports)
RASH ( 23 FDA reports)
ASCITES ( 22 FDA reports)
PYREXIA ( 19 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 18 FDA reports)
DECREASED APPETITE ( 18 FDA reports)
BLOOD BILIRUBIN INCREASED ( 15 FDA reports)
PLATELET COUNT DECREASED ( 13 FDA reports)
LIVER DISORDER ( 12 FDA reports)
MALAISE ( 12 FDA reports)
HEPATITIS B ( 11 FDA reports)
HYPERTENSION ( 11 FDA reports)
LIVER CARCINOMA RUPTURED ( 11 FDA reports)
PLEURAL EFFUSION ( 11 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 11 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 10 FDA reports)
BLOOD URIC ACID INCREASED ( 10 FDA reports)
FATIGUE ( 10 FDA reports)
ALOPECIA ( 9 FDA reports)
DYSPNOEA ( 9 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 9 FDA reports)
HYPERAMMONAEMIA ( 9 FDA reports)
AMMONIA INCREASED ( 8 FDA reports)
ANAEMIA ( 8 FDA reports)
CONSTIPATION ( 8 FDA reports)
NAUSEA ( 8 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 7 FDA reports)
RENAL IMPAIRMENT ( 7 FDA reports)
OEDEMA PERIPHERAL ( 6 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 6 FDA reports)
PORTAL VEIN THROMBOSIS ( 6 FDA reports)
STOMATITIS ( 6 FDA reports)
ABDOMINAL PAIN ( 5 FDA reports)
AMYLASE INCREASED ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 5 FDA reports)
BLOOD PRESSURE INCREASED ( 5 FDA reports)
DYSPHONIA ( 5 FDA reports)
FLUSHING ( 5 FDA reports)
GASTRIC ULCER ( 5 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
HEPATIC ENZYME INCREASED ( 5 FDA reports)
HYPONATRAEMIA ( 5 FDA reports)
JAUNDICE ( 5 FDA reports)
LIVER ABSCESS ( 5 FDA reports)
PNEUMONIA ASPIRATION ( 5 FDA reports)
TOXIC ENCEPHALOPATHY ( 5 FDA reports)
WEIGHT DECREASED ( 5 FDA reports)
ABDOMINAL DISTENSION ( 4 FDA reports)
ARTHRALGIA ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
CONTRALATERAL BREAST CANCER ( 4 FDA reports)
DELIRIUM ( 4 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
ERYTHEMA ( 4 FDA reports)
FACE OEDEMA ( 4 FDA reports)
HAEMORRHAGIC ASCITES ( 4 FDA reports)
HYPOPHOSPHATAEMIA ( 4 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 4 FDA reports)
LIPASE INCREASED ( 4 FDA reports)
MUSCLE ATROPHY ( 4 FDA reports)
OSTEOPOROSIS ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
ACUTE HEPATIC FAILURE ( 3 FDA reports)
BLOOD AMYLASE INCREASED ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
DEATH ( 3 FDA reports)
DEEP VEIN THROMBOSIS ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
HAEMOBILIA ( 3 FDA reports)
HYPOGLYCAEMIA ( 3 FDA reports)
HYPOTHYROIDISM ( 3 FDA reports)
INFECTION ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 3 FDA reports)
METABOLIC ACIDOSIS ( 3 FDA reports)
NAIL RIDGING ( 3 FDA reports)
OSTEOMALACIA ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
PURPURA ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
SHOCK HAEMORRHAGIC ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
TUMOUR HAEMORRHAGE ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ADVERSE DRUG REACTION ( 2 FDA reports)
APPLICATION SITE BLEEDING ( 2 FDA reports)
AZOTAEMIA ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
FANCONI SYNDROME ACQUIRED ( 2 FDA reports)
GASTROINTESTINAL NECROSIS ( 2 FDA reports)
HEPATIC CIRRHOSIS ( 2 FDA reports)
HYPERCREATININAEMIA ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 2 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 2 FDA reports)
MULTIPLE FRACTURES ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
PAIN ( 2 FDA reports)
PAIN OF SKIN ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
SCROTAL ULCER ( 2 FDA reports)
SKIN HYPERTROPHY ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANTI-HBE ANTIBODY POSITIVE ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD UREA ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BRAIN STEM INFARCTION ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
COMA HEPATIC ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
DEVICE DIFFICULT TO USE ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HEPATIC INFARCTION ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LYMPHANGITIS ( 1 FDA reports)
MALLORY-WEISS SYNDROME ( 1 FDA reports)
MELAENA ( 1 FDA reports)
METASTASES TO PERITONEUM ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
TINEA PEDIS ( 1 FDA reports)
TUMOUR RUPTURE ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use