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Monkeypox: Bavarian Nordic Jynneos vaccine gets USFDA emergency use nod
For those aged 18 years and older determined to be at high risk of monkeypox infection, the authorization allows for a fraction of the Jynneos dose to be administered between the layers of the skin.
New Delhi: The U.S. drug regulator has authorized Bavarian Nordic's Jynneos vaccine for emergency use through intradermal injection in individuals aged 18 years and older who are determined to be at high risk of monkeypox infection.
Read also: In talks with Bavarian Nordic for import of monkeypox vaccine: Serum institute CEO
Ruchika Sharma joined Medical Dialogue as an Correspondent for the Business Section in 2019. She covers all the updates in the Pharmaceutical field, Policy, Insurance, Business Healthcare, Medical News, Health News, Pharma News, Healthcare and Investment. She has completed her B.Com from Delhi University and then pursued postgraduation in M.Com. She can be contacted at editorial@medicaldialogues.in Contact no. 011-43720751