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

PRURITUS ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
MALAISE ( 4 FDA reports)
LIVER INJURY ( 4 FDA reports)
PRODUCT QUALITY ISSUE ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
VOMITING ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
IMPAIRED WORK ABILITY ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CRYING ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
ANGER ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
INJURY ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
MENOPAUSAL SYMPTOMS ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
RASH ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
ASCITES ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)

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