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FDA recalls more than 7,000 bottles of antidepressant

FDA recalls more than 7,000 bottles of antidepressant over a possible cancerous chemical

The FDA is recalling more than 7,000 bottles of the antidepressant duloxetine due to a possible cancer-causing chemical.

People on MSN · 13h

FDA Has Recalled Thousands of Bottles of Antidepressant Duloxetine: Here’s Why

The U.S. Food and Drug Administration has recalled thousands of bottles of the antidepressant Duloxetine for potentially cancer-causing chemicals in the medication.

WPIX New York City, NY on MSN · 15h

FDA issues recall for antidepressant drug

The Federal Drug Administration issued a recall on Tuesday for a common medicine for depression. Over 7,000 bottles of Duloxetine were recalled due to the elevated presence of Nitrosamine, an ingredient believed to be cancerous,

FDA, RSV and Pfizer

MedPage Today on MSN · 18h

FDA Expands Approval of RSV Vaccine Abrysvo to Include All At-Risk Adults

The FDA expanded the approval of the bivalent RSV prefusion F (RSVpreF) vaccine (Abrysvo) to include the prevention of lower respiratory tract disease (LRTD) caused by respiratory syncytial virus (RSV) in high-risk adults ages 18 to 59 years, Pfizer announced on Tuesday.

Wall Street Journal · 17h

Pfizer Receives Expanded FDA Approval for RSV Vaccine

Abrysvo is the first vaccine for the respiratory syncytial virus that is indicated for adults younger than 50, the drugmaker said.

Business Insider · 1d

Pfizer announces FDA approval of Abrysvo

Pfizer (PFE) announced that the U.S. FDA has approved Abrysvo, the company’s bivalent RSV prefusion F vaccine, for the prevention of

ENDPOINTS NEWS6m

Novo Nordisk petitions FDA to stop semaglutide compounding over safety risks

Novo Nordisk is continuing its crusade against compounded versions of its blockbuster weight loss drugs by petitioning the ...

Acsh.org11h

The Anniversary of FDA's Landmark Approval of Genetically Engineered Human Insulin: A Cautionary Tale

Often, they do not. Next Tuesday, October 29 th, marks the 42nd anniversary of one of biotechnology's most significant ...

19hon MSN

FDA and CBP Seize $76 Million in Illegal Vapes From China

Roughly 3 million units were confiscated in the operation as part of a federal crackdown on illegal e-cigarettes.

21hon MSN

Novo Nordisk asks FDA to ban compounding pharmacies from making Ozempic, Wegovy copies

The Danish drugmaker Novo Nordisk contends that semaglutide, the active ingredient in Ozempic and Wegovy, is too complex for ...

Managed Healthcare Executive7m

FDA Approves Stelara Biosimilar Selardsi for Additional Formulation

This week’s approval expands Seldardsi indications to treat adults with Crohn’s disease and ulcerative colitis.

16hon MSN

FDA says this weight loss drug shortage is over, but patients worry about cost and availability

Some patients fear tirzepatide, sold by Eli Lilly under the brand names Zepbound and Mounjaro, will be hard to get and prohibitively expensive once compounding pharmacies are no longer producing it.

14h

Novo Nordisk asks FDA to block compounding pharmacies from making Ozempic copycats

Novo Nordisk wants the Food and Drug Administration (FDA) to prevent compounding pharmacies from manufacturing their own ...

19h

FDA Appoints New Head of Medical Devices

Diane Zuckerman is president of the National Center for Health Research, a nonprofit that monitors FDA device policy. Speaking to the Times, she said she said Tarver is focused on patient safety and ...

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FDA recalls more than 7,000 bottles of antidepressant

FDA, RSV and Pfizer

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