FDA
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FDA delays meeting on COVID-19 vaccines for kids under 5
Federal health regulators on Friday delayed next week's public meeting to review Pfizer’s COVID-19 vaccine for children under 5, saying…
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As omicron surges, the FDA has expanded access to Pfizer boosters for more teens
The U.S. is expanding COVID-19 boosters as it confronts the omicron surge, with the Food and Drug Administration allowing extra…
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FDA approves first injectable PrEP medication to lower HIV risk
FDA approves first injectable PrEP medication to lower HIV risk Updated: 11:43 PM EST Dec 21, 2021 The U.S. Food…
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Cincy News
FDA authorizes monoclonal antibody treatment for newborns
Newborns and younger pediatric patients who have tested positive for COVID-19 can now receive monoclonal antibody treatments that were previously…
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Pfizer seeking FDA emergency use authorization for COVID-19 antiviral pill
There's another potential game-changer in the fight against this pandemic.Pfizer has now applied for Food and Drug Administration emergency authorization…
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Cincy News
FDA considers black box warning for all breast implants
CINCINNATI — A rash and joint pain may have saved Lily McBreen's life by getting her to the doctor in…
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What is it, and why is it raising concerns?
I LOOKED INTO WHY IT IS CAUSING CONCERN. DELTA 8 THC PRODUCTS ARE BEING SOLD ONLINE AND IN STORES IN…
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Ohio doctor expresses relief after FDA recommends Pfizer’s COVID-19 vaccine for children
The U.S. Food and Drug Administration's advisory panel has voted to allow emergency use authorization of Pfizer's shot in kids…
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FDA OKs mixing and matching COVID-19 vaccines; backs Moderna, J&J boosters
U.S. regulators on Wednesday signed off on extending COVID-19 boosters to Americans who got the Moderna or Johnson & Johnson…
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Cincy News
FDA authorizes e-cigarette products for first time in history
For the first time in history, the FDA authorized three e-cigarette products: the Vuse Solo device and its pods. The…
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President Biden discusses COVID-19 vaccines
Vaccine advisers to the Food and Drug Administration are meeting Thursday morning to discuss whether to authorize boosters of Moderna's…
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Merck seeks FDA emergency use authorization for antiviral COVID-19 treatment
Merck said Monday it is seeking U.S. Food and Drug Administration emergency use authorization for its experimental antiviral COVID-19 treatment,…
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Cincy News
FDA advises not to use certain artnaturals hand sanitizers
The U.S. Food and Drug Administration has warned consumers against using a particular hand sanitizer after tests revealed it contained…
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