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

NAUSEA ( 24 FDA reports)
HEPATITIS ( 23 FDA reports)
ASTHENIA ( 22 FDA reports)
VOMITING ( 22 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 21 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 21 FDA reports)
FATIGUE ( 20 FDA reports)
HYPERHIDROSIS ( 18 FDA reports)
PYREXIA ( 18 FDA reports)
HEPATIC ENZYME INCREASED ( 15 FDA reports)
CHROMATURIA ( 14 FDA reports)
JAUNDICE ( 13 FDA reports)
CHILLS ( 12 FDA reports)
ABDOMINAL PAIN ( 11 FDA reports)
BLOOD BILIRUBIN INCREASED ( 10 FDA reports)
HEADACHE ( 10 FDA reports)
ABDOMINAL PAIN UPPER ( 9 FDA reports)
ANOREXIA ( 9 FDA reports)
MALAISE ( 9 FDA reports)
MYALGIA ( 9 FDA reports)
PAIN ( 9 FDA reports)
FEELING ABNORMAL ( 8 FDA reports)
ACUTE HEPATIC FAILURE ( 7 FDA reports)
AUTOIMMUNE HEPATITIS ( 7 FDA reports)
BACK PAIN ( 7 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 7 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 7 FDA reports)
CHEST DISCOMFORT ( 7 FDA reports)
COAGULOPATHY ( 7 FDA reports)
FAECES PALE ( 7 FDA reports)
INFLUENZA ( 7 FDA reports)
INSOMNIA ( 7 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 7 FDA reports)
NASAL CONGESTION ( 7 FDA reports)
NASAL DISCOMFORT ( 7 FDA reports)
OCULAR ICTERUS ( 7 FDA reports)
SKIN DISCOLOURATION ( 7 FDA reports)
IMMUNOLOGY TEST ABNORMAL ( 5 FDA reports)
NEUTROPENIA ( 5 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 4 FDA reports)
MUSCULAR WEAKNESS ( 4 FDA reports)
BLOOD GLUCOSE DECREASED ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
COLD SWEAT ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
RASH ( 3 FDA reports)
SYNCOPE VASOVAGAL ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
ALOPECIA ( 2 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
CHOLESTATIC LIVER INJURY ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
FEELING JITTERY ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
PAPILLOEDEMA ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PHOTOPSIA ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
URINE ANALYSIS ABNORMAL ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
VISUAL FIELD DEFECT ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ASTHMA ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CATARACT ( 1 FDA reports)
COUGH ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYPERTRANSAMINASAEMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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