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FDA recalls more than 7,000 bottles of antidepressant

FDA Duloxetine recall flags 7,100+ bottles of generic Cymbalta antidepressants

A Duloxetine recall by the FDA has flagged more than 7,100 bottles of the Cymbalta generic drug due to a cancerous chemical.

USA TODAY on MSN · 2h

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.

WPIX New York City, NY on MSN · 19h

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,

E. Coli, McDonald's and FDA

Hosted on MSN · 13m

FDA eyes McDonald's supplier's onions as source of E. Coli outbreak

The FDA said Thursday that it's investigating whether McDonald’s supplier Taylor Farms is the possible source of the E. coli outbreak linked to Quarter Pounders hamburgers.

The Washington Post · 1d

What to know about E. coli causes, symptoms amid McDonald’s-linked outbreak

One person died and 10 were hospitalized in an E. coli outbreak in 10 states, which health officials linked to the McDonald’s burgers.

Yahoo · 14h

FDA identifies possible sources of McDonald's E. coli outbreak

The FDA is looking into two possibilities as the source of an E. coli outbreak linked to McDonald's Quarter Pounder burgers. CBS News Colorado reporter Karen Morfitt has the latest.

FDA, Novo Nordisk

Yahoo · 16h

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 versions of the company’s popular weight loss drug Wegovy and diabetes treatment Ozempic,

Hosted on MSN · 21h

Novo Nordisk asks US to stop compounding pharmacies from making weight-loss drug copies

Novo Nordisk on Tuesday asked the U.S. Food and Drug Administration to ban compounding pharmacies from making copycat versions of its popular weight-loss and diabetes drugs, which it said were too complex for those manufacturers to produce safely.

CBS News on MSN · 20h

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.

BioSpace2h

GLP-1 Prescriptions for Type 1 Diabetes Spike Despite Lack of FDA Approval: Study

While the regulator has not approved their use in type 1 diabetes, off-label prescribing for GLP-1 receptor agonists has ...

Managed Healthcare Executive3h

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.

Richmond3h

New FDA rules require plain language for mammograms

In September, the U.S. Food and Drug Administration released new rules that require a summary be sent directly to patients ...

ENDPOINTS NEWS3h

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.org15h

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 ...

22hon 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.

MedPage Today22h

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 ...

23h

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

E. Coli, McDonald's and FDA

FDA, Novo Nordisk

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