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Ozempic, Zepbound and Food and Drug Administration
Drug makers can’t make knockoff weight-loss drugs anymore—and they’re mad
With the resolution, compounding pharmacies are no longer able to produce tirzepatide. And the FDA highlighted the point to the drug makers, writing in bold that the agency "reminds compounders of the legal restrictions on making copies of FDA-approved drugs."
Why Ozempic, Zepbound, and other weight-loss drug dupes carry risks
Poor purity can cause patients to experience fever, chills, nausea, skin irritation, infections and low blood pressure.
Buyer beware: Off-brand Ozempic, Zepbound and other weight loss products carry undisclosed risks for consumers
In just a few years, brand-name injectable drugs such as Ozempic, Wegovy, Mounjaro and Zepbound have rocketed to fame as billion-dollar annual sellers for weight loss as well as to control blood sugar levels and reduce the risk of heart disease.
Ozempic and prescription weight loss drugs: How they work, what they cost, side effects, and everything to know
A highly effective class of weight loss drug has taken the world by storm, as medications like Ozempic, Wegovy, and Zepbound become household names. These drugs, originally meant to treat diabetes, have become widely known for their slimming side effects.
2h
US FDA approves Pfizer's drug for rare bleeding disorder
The U.S. Food and Drug Administration approved Pfizer's once-a-week injection for the two main types of a rare bleeding ...
11d
on MSN
FDA issues recalls on at least 16 food and drug items in September. Here's a list
The FDA has removed the following items from store shelves this September, including pet food, baby powder and Lactaid.
2d
U.S. Food and Drug Administration (FDA) accepts New Drug Application for elinzanetant
Bayer today announced that the U.S. Food and Drug Administration (FDA) has accepted the company’s New Drug Application (NDA) ...
STAT
2d
Q&A: How the FDA is approaching AI in clinical trials and drug development
The FDA's Tala Fakhouri discusses the agency's approach to the regulation of AI in clinical trials in a new interview.
JD Supra
3d
GLP-1 Drugs: FDA Removes Lilly’s Zepbound® and Mounjaro® (tirzepatide injection) from its Drug Shortage List
On October 2, 2024, the U.S. Food and Drug Administration (FDA) determined the shortage of the tirzepatide injection, a glucagon-like peptide ...
Business Wire
13d
U.S. Food and Drug Administration Approves Bristol Myers Squibb’s COBENFY™ (xanomeline and trospium chloride), a First-In-Class Muscarinic Agonist for the Treat…
U.S. FDA Approves Bristol Myers Squibb’s COBENFY, a First-In-Class Muscarinic Agonist for the Treatment of Schizophrenia in ...
NBC New York
15d
FDA issues recall notices over 2 brands of pet food due to salmonella and listeria risk
Amid an ongoing pet
food
recall, the U.S.
Food
and Drug
Administration
(FDA) is urging pet owners not to give their ...
agdaily
3d
10 careers in food science: Driving innovation and sustainability in the food industry
Careers in food science not only focus on improving food quality but also on addressing challenges like food security, waste ...
WHYY
2d
Philadelphia health providers and patients seek a new treatment roadmap for sickle cell disease after drug recall
Voxelotor, which was sold under the brand name Oxbryta, was suddenly pulled from the market over safety concerns from ...
SCOTUSblog
7d
Food and Drug Administration v. R.J. Reynolds Vapor Co.
Issue: Whether a manufacturer may file a petition for review in a circuit (other than the U.S. Court of Appeals for the District of Columbia Circuit) where it neither resides nor has its principal ...
1d
on MSN
FDA approves the first at-home test for COVID-19 and the flu, no prescription needed
The Food and Drug Administration has granted authorization of a COVID-19 and flu test that can be used without a prescription ...
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