Quantcast
Sunday, June 23, 2024

FDA Proposes Easing Restrictions on LGBT Blood Donors

'... the agency believes the implementation of the proposed individual risk-based questions will not compromise the safety or availability of the blood supply...'

(Dmytro “Henry” AleksandrovHeadline USA) The Food and Drug Administration [FDA] proposed new guidelines on Friday that would remove the restriction that homosexual and bisexual men in monogamous relationships abstain from sex before donating blood.

The new guidelines state that time-based deferrals for men who have sex with men [MSM] and women who have sex with MSM would be eliminated, according to the Gateway Pundit.

“The U.S. Food and Drug Administration today announced it is proposing a change from time-based deferrals to assessing blood donor eligibility using gender-inclusive, individual risk-based questions to reduce the risk of transfusion-transmitted HIV,” the agency said in a Friday statement.

“These draft recommendations are based on the FDA’s careful review of available information, including data from other countries with similar HIV epidemiology that have instituted this approach, as well as ongoing surveillance of the U.S. blood supply.”

“Based on the available data, the agency believes the implementation of the proposed individual risk-based questions will not compromise the safety or availability of the blood supply,” the agency continued.

CNBC reported that during the AIDS crisis in the 1980s, the FDA banned men who had sex with other men from ever donating blood again but then eased the rule in 2015, making it possible for homosexual and bisexual males to donate blood if they had not engaged in sexual activity throughout the previous year.

Because there were not enough blood donors in 2020, the FDA even further eased restrictions in Apr. 2020, allowing homosexual and bisexual people who did not have sex within the past three months to donate blood.

“Whether it’s for someone involved in a car accident, or for an individual with a life-threatening illness, blood donations save lives every day,” FDA Commissioner Robert M. Califf, M.D., said.

“Maintaining a safe and adequate supply of blood and blood products in the U.S. is paramount for the FDA, and this proposal for an individual risk assessment, regardless of gender or sexual orientation, will enable us to continue using the best science to do so.”

Peter Marks, M.D., Ph.D., director of the FDA’s Center for Biologics Evaluation and Research, agrees.

“Our approach to this work has always been, and will continue to be, based on the best available science and data. Over the years, this data-driven process has enabled us to revise our policies thereby increasing those eligible to donate blood while maintaining appropriate safeguards to protect recipients,” he said.

“We will continue to follow the best available scientific evidence to maintain an adequate supply of blood and minimize the risk of transmitting infectious diseases and are committed to finalizing this draft guidance as quickly as possible.”

Copyright 2024. No part of this site may be reproduced in whole or in part in any manner other than RSS without the permission of the copyright owner. Distribution via RSS is subject to our RSS Terms of Service and is strictly enforced. To inquire about licensing our content, use the contact form at https://headlineusa.com/advertising.
- Advertisement -

TRENDING NOW

TRENDING NOW