Generic Medicine Info
Pre-existing hepatic disease or hepatic impairment including ALT or AST ≥2 times the upper limit of normal (ULN), history of autoimmune hepatitis.
Special Precautions
Patient w/ previous or current depressive disorders, severe active infection, TB. Pregnancy and lactation. Monitoring Parameters Monitor serum transaminases (ALT and AST) and bilirubin levels prior to initiation, monthly during treatment, and up to 4 mth after last dose.
Adverse Reactions
Hypersensitivity reactions e.g. anaphylaxis, angioedema, urticaria, rash, pruritus), dermatitis, eczema, psoriasis, skin exfoliation, acne, erythema, dry skin, toxic skin eruption; lymphadenopathy, lymphadenitis, non-infectious colitis; nasopharyngitis, upper resp tract infection, pneumonia, bronchitis, viral infection, influenza, laryngitis, tonsillitis, pharyngitis, folliculitis, anaemia, depression, oropharyngeal pain, diarrhoea, pyrexia, increased ALT/AST.
Potentially Fatal: Autoimmune hepatitis; hepatic failure.
Drug Interactions
May reduce the therapeutic effect of live vaccines.
CIMS Class
ATC Classification
L04AC01 - daclizumab ; Belongs to the class of interleukin inhibitors. Used as immunosuppressants.
Disclaimer: This information is independently developed by CIMS based on daclizumab from various references and is provided for your reference only. Therapeutic uses, prescribing information and product availability may vary between countries. Please refer to CIMS Product Monographs for specific and locally approved prescribing information. Although great effort has been made to ensure content accuracy, CIMS shall not be held responsible or liable for any claims or damages arising from the use or misuse of the information contained herein, its contents or omissions, or otherwise. Copyright © 2021 CIMS. All rights reserved. Powered by CIMSAsia.com
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