Federal Appeals Court Revived the FDA Approval of Mifepristone Temporarily with Restrictions
A Louisiana federal appeals court’s 3 judge panel has revived the FDA’s approval of the abortion pill Mifepristone with temporary restrictions.
Abortion Pills Get Mixed Signals from the Federal Courts
7pm: A Texas federal judge announced he would suspend approval of the medicated abortion pill but gives the Department of Justice a week for an appeal. 7:35pm A Washington state…
FDA Approved First Over-The-Counter Opioid Overdose Antidote
The Food & Drug Administration has approved the first over-the-counter opioid overdose antidote, Narcan.
FDA Approved a Breakthrough Alzheimer’s Drug
The Food & Drug Administration have approved Eisai’s Alzheimer’s drug Leqembi. The drug is a breakthrough drug which is used to slow down cognitive decline in the early stage of…
U.S. Pharmacies Can Now Carry Abortion Pills
The FDA announced that United States pharmacies, if they agree to certain rules, can now sell abortion pills if they have a prescription for the pills.
FDA Investigating Whether Lucky Charms Are Making People Sick
The Food and Drug Administration is investigating whether Lucky Charms are making people sick. The FDA have received over 100 complaints of people getting sick after eating the General Mills…
FDA Authorized Second Booster Shot for People 50 and Older
The FDA has authorized a second booster shot of the Pfizer-BioNTech or Moderna Covid-19 vaccine for people 50 and older, if their last booster was more than 40 months ago.
Moderna Asked the FDA to Authorize A Second Booster of the Covid-19 Vaccine
Moderna has asked the FDA to authorize a second booster of their Covid-19 vaccine for all adults.
FDA Has Recalled More Baby Formula
The Food and Drug Administration has recalled more baby formula to include Similac PM after a second infant has died from a bacterial infection. Research shows 4 reports of Cronobacter…
More Then a 1,000 Dead Rodents and Birds Were Found in a Family Dollar Distribution Center
West Memphis, AR: The FDA discovered a 1,000 dead rodents and birds in a Family Dollar distribution center. The FDA inspection has resulted in the temporary closing of over 400…
FDA Warns People to Not Use Similac and Other Baby Formulas Cause of Bacterial Infections
The FDA warns customers after Abbott Nutrition recalled Similac, Alimentum and ElsCare infant formulas because of reports of bacterial infections. One infant died and 3 others had bacterial infections.
FDA Approves New Monoclonal Antibodies Against Omicron Variant
The FDA has authorized a new Covid-19 monoclonal antibodies that work against the omicron variant. The antibodies are laboratory made proteins that mimic the immune system’s ability to fight harmful…
FDA Approves Mixing Moderna and Johnson and Johnson’s Booster Shots
10/20/2021-The FDA approved mixing the Covid-19 booster shots of Moderna’s and Johnson and Johnson’s vaccines.
White House Plans 28 Million Vaccine Doses for Children
10/20/2021-Washington, DC, the White House released a plan for 28 million children (5-11) to get Covid-19 vaccines within weeks of FDA approval.
FDA Panel Voted Unanimously for Johnson and Johnson’s Booster Shot
10/15/2021-The FDA panel has voted unanimously in support of the Johnson and Johnson booster shot for all Americans, who 2 months before got the first shot.
FDA Delays Moderna Vaccine for Children
10/15/2021-The FDA delays the Moderna Covid-19 vaccine for children to review the increased risk of Myocarditis side effect.
FDA Panel Recommend Moderna Booster for Elderly and High Risk Adults
10/14/2021-An FDA advisory panel voted to recommend a booster shot of the Moderna Coronavirus vaccine for the elderly and high risk adults.
FDA Asked Food Companies to Use Less Salt
10/13/2021-The FDA has asked food manufacturers to use less salt in their food products.
FDA Questioned the Strength of the Johnson and Johnson Booster
10/13/2021-The FDA questioned the strength of the evidence that Johnson and Johnson provided for their Covid-19 booster shot. They believe that the test used by the company wasn’t sensitive enough,…