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

VOMITING ( 8 FDA reports)
DIARRHOEA ( 6 FDA reports)
HEADACHE ( 6 FDA reports)
LIPODYSTROPHY ACQUIRED ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
ASTHENIA ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
HEPATIC CIRRHOSIS ( 4 FDA reports)
HEPATIC STEATOSIS ( 4 FDA reports)
LIVER DISORDER ( 4 FDA reports)
ANAEMIA ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
HEPATOTOXICITY ( 3 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 3 FDA reports)
NEPHROLITHIASIS ( 3 FDA reports)
RASH ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
CACHEXIA ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
SKIN ATROPHY ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL OBESITY ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
ADRENAL SUPPRESSION ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASEPTIC NECROSIS BONE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG EFFECT INCREASED ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HEPATIC ECHINOCOCCIASIS ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERLACTACIDAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
KAPOSI'S SARCOMA ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIPOHYPERTROPHY ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MITOCHONDRIAL CYTOPATHY ( 1 FDA reports)
MITOCHONDRIAL TOXICITY ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
OBESITY ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PAROTID GLAND ENLARGEMENT ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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