
DCGI accepts 3 COVID injections for children matured over 5 years

The authorization has actually been provided to covaxin, ZyCov-D and also Corbevax
The Drugs Controller General of India (DCGI) has actually accepted 3 COVID-19 injections for youngsters that are aged over 5 years.
The health regulatory authority has actually offered the Emergency Use Authorisation (EUA) by ZyCov-D by Zydus Lifesciences, which is a 2 dosage vaccination. It will certainly be provided to those aged 12 years and also over.
Apart from it, the DCGI has actually likewise accepted Covaxin made by Bharat Biotech and also Corbevax by Biological E.
While Covaxin has actually been accepted for youngsters matured in between 6 and also 12 years, Corbevax has actually been accepted for those that comes from the five-to-12 year age.
Mahima Datla, Managing Director, Biological E. Limited, claimed, “As many of us would be aware, the SEC had already given a positive recommendation for our vaccine’s use in the 5-12 age group. In continuation of the same, we were very happy to receive the formal approval from the DCGI making this an extremely safe and effective intervention available, particularly for the age groups 5 years onwards. This is a great opportunity to get back to some level of normalcy in our continuing fight against the prevalent pandemic situation as CORBEVAX is the first indigenous COVID-19 vaccine in the country that addresses the vaccination needs of all age groups from 5 years and above.”
Dr Krishna Ella, Chairman and also Managing Director, Bharat Biotech, claimed, “We have established COVAXIN as an universal vaccine for adults and children. Safety of the vaccine is critical for children and we are glad to share that COVAXIN has now proven data for safety and immunogenicity in children. We have achieved our goal of developing a safe and efficacious COVID-19 vaccine for adults and children.”
Speaking on the development, Dr Sharvil Patel, Managing Director, Zydus Lifesciences claimed, “The approval of a two-dose regimen for ZyCoV-D is a welcome development. This will increase the compliance for the vaccine and reduce the overall time required for vaccination to improve immunity against the virus. It will also help in administering the vaccine in a larger population in a shorter time which is always desirable in the midst of a pandemic.”
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