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Zepbound, Sleep Apnea and FDA Approval
The shortage of popular weight loss drug tirzepatide is over, FDA says. Patients could see higher costs as a result.
The weight loss medication tirzepatide (Mounjaro and Zepbound) is no longer in shortage, according to the FDA. Access to cheaper versions could end.
Lilly Rises on FDA Approval of Weight-Loss Drug Zepbound for Sleep Apnea
Key Takeaways Eli Lilly's Zepbound has been approved by the Food and Drug Administration (FDA) as a treatment for adults with sleep apnea and obesity, the drugmaker said after the bell Friday.Trials of the Lilly drug found that it helped reduce the number of breathing disruptions in an average night of sleep.
Popular Weight Loss Drug Zepbound Gains FDA Approval to Treat Sleep Apnea
The FDA has approved Eli Lilly's Zepbound to treat moderate to severe obstructive sleep apnea in adults with obesity.
FDA issues highest-level recall for Costco eggs
FDA issues urgent salmonella warning for Costco eggs
The Food and Drug Administration has escalated its warning regarding certain eggs distributed to Costco locations, potentially linked to salmonella exposure.
FDA raises Costco egg recall alert to higher level over salmonella concerns
The FDA has raised the recall alert level to a high level for Costco eggs because of the risk of severe illness or death due to salmonella poisoning,
Costco egg recall now classified as highest risk level, FDA says
(CNN) - The Food and Drug Administration said a recall of organic eggs sold at Costco is now classified at the highest risk level for potential salmonella contamination. The upgraded level means there is “a reasonable probability” that a recalled product “will cause serious adverse health consequences or death.”
FDA, AVITA Medical and GO Mini
FDA approves new medication for type 2 diabetes
Patients who have a family history of medullary thyroid carcinoma and multiple endocrine neoplasia syndrome Type 2 are not encouraged to use the drug because of possible complications.
Avita Medical Says FDA Approved Recell GO Mini
Avita Medical said the U.S. Food and Drug Administration has approved the company's premarket approval supplement for Recell Go mini, a system to treat smaller wounds. The Recell Go mini is a line extension of the Recall Go system,
Avita Medical discloses FDA premarket approval for ECELL GO mini
AVITA Medical (RCEL) announced that the FDA has approved its premarket approval, PMA, supplement for RECELL GO mini. As a
2h
on MSN
Zepbound Weight Loss Medication Approved by FDA to Treat Sleep Apnea
The Food and Drug Administration (FDA) announced the approval of the weight loss drug Zepbound, generically known as ...
1d
on MSN
FDA approves first medication for obstructive sleep apnea, which also promotes weight loss
The FDA approved a new drug treatment for obstructive sleep apnea that improves the condition through weight loss. Sleep ...
1d
US FDA approves Hikma's generic version of Novo's diabetes drug Victoza
The U.S. Food and Drug Administration on Monday approved Hikma Pharmaceuticals' generic version of Novo Nordisk's diabetes ...
The Indianapolis Star
5d
Which foods are considered 'healthy?' FDA issues new label criteria
"We know food labeling can be a powerful tool for change," James Jones, the
FDA
's deputy commissioner for human foods, said ...
21h
on MSN
FDA approves GLP-1 generic for Type 2 diabetes
The U.S. Food and Drug Administration (FDA) has approved a generic daily injectable for the GLP-1 medication for patients who ...
4h
on MSN
The FDA’s new rules for ‘healthy’ labels force design best practices
New labeling may prevent unhealthy foods from passing as healthful choices, but experts say it’s only the first step toward ...
1d
on MSN
FDA says decongestant in many cold medicines doesn’t work. So what does?
The most popular nasal decongestant on U.S. pharmacy shelves may not be there much longer. The Food and Drug Administration ...
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