“In Case Of Adverse Events…”: What Covaxin Consent Form Says

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Covaxin has been developed by Hyderabad-based Bharat Biotech.

New Delhi:

As India’s vaccination drive began today with Covid shots to health workers, those receiving Bharat Biotech’s Covaxin were asked to sign consent forms that assured compensation if any adverse effect was found linked to the vaccine.

Recipients of Covaxin have to sign a consent form before being vaccinated because its use has been allowed by the government in “clinical trial mode”.

The form says “COVAXINTM” is being offered under restricted use in an emergency situation and has been permitted in “public interest” as an abundant precaution. It also explains that the clinical efficacy of the vaccine is yet to be established and it is still in Phase 3 trials.

“The Bharat Biotech COVID-19 Vaccine (COVAXINTM) is a vaccine with approval for restricted use in emergency situation that may prevent COVID-19. In phase 1 and phase 2 clinical trials, COVAXINT has demonstrated the ability to produce antibodies against COVID-19. However, the clinical efficacy of COVAXIN is yet to be established and it is still being studied in phase 3 clinical trial. Hence, it is important to appreciate that receiving the vaccine does not mean that other precautions related to Covid-19 need not be followed,” the form states.

“In case of any adverse events or serious adverse events, you will be provided medically recognized standard of care in the government designated and authorized centers/hospitals. The compensation for serious adverse event will be paid by sponsor (BBIL) if the (adverse effect) is proven to be causally related to the vaccine.”

The declaration says: “I further emphasize that any information provided by me prior to taking the vaccine will be archived in the database maintained by the immunization program of the government and privacy as well as confidentiality of the information provided by you will be maintained.”

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The recipients will also be handed over a factsheet and a form to report adverse effects, in which they have to note down symptoms like fever, pain within seven days.

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Two-dose vaccines Covaxin and Serum Institute of India (SII)’s Covishield – developed by Oxford-AstraZeneca — were cleared for emergency use earlier this month and will be administered to crores beginning today.

The clearance to Bharat Biotech’s Covaxin, even though it has yet to clear final-stage trials, has been criticized by opposition parties and a section of scientists.

Recipients will not get to choose which vaccine to take.

In Delhi, for example, six central government hospitals will administer only Covaxin — AIIMS, Safdarjung, Ram Manohar Lohia hospital, Kalawati Saran Children Hospital, ESI Hospital Basaidarapur and ESI Hospital Rohini. The remaining 75 Sites, which include Delhi government and private hospitals, will receive Covishield shots.

In a statement, the Indian Medical Association (IMA), said yesterday that it endorsed the safety and efficacy of both Covaxin and Covishield and added that the “misinformation around vaccines on social sites is unfortunate and more harmful than the disease itself.”

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