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FDA approves an at-home flu vaccine
FDA approves first flu vaccine that can be self-administered at home
The US Food and Drug Administration on Friday approved the first flu vaccine that does not have to be administered by a health care provider, but it won’t be available in time for this respiratory virus season.
FDA approves first nasal spray flu vaccine for use at home
The Food and Drug Administration on Friday approved the first at-home flu vaccine, a nasal spray that consumers with a prescription will be able to order online starting next year. Health experts say the convenience of the spray — FluMist — could lead to increased flu vaccination rates.
FDA approves FluMist for upcoming flu season
The Food and Drug Administration announced on Friday an approval of a new self- and caregiver-administered nose spray against the flu.
1d
on MSN
Nationwide Snack Recall Update As FDA Sets Highest Risk Level
The snacks now have a Class I risk level, meaning there is a "reasonable probability" they could cause "serious adverse ...
1h
FDA approves Apple Watch function that can help detect sleep apnea
The Food and Drug Administration has approved an Apple Watch function that can help detect sleep apnea. Here's how it works.
6h
FDA issues recall for milk; Ohio, Kentucky, Indiana among states included
A brand of milk has been recalled in 27 states including Ohio, Kentucky and Indiana. Lactaid, a brand of lactose-free dairy ...
2d
on MSN
Drugmakers to stop making controversial fentanyl lollipops, FDA says
Drugmaker Cephalon had the FDA's approval to market these drugs, old under brand names like Actiq, as a sweetened lozenge on ...
12h
Fudge Recall Update As FDA Sets Risk Level Over Mold
The Canadian-based firm Authentik Fudge initiated the recall of the Chocolate Fudge with Nuts products in August.
1d
US FDA approves Zevra's treatment for rare genetic disease
The U.S. Food and Drug Administration approved Zevra Therapeutics' drug for a rare and fatal genetic disorder, making it the ...
STAT
1d
FDA’s new head of device safety held senior role at company troubled by safety warnings
“Olympus’ continued failure to meet FDA requirements demonstrates a troubling disregard for patient safety,” said Jeffrey ...
The American Journal of Managed Care
1d
FDA Approves Amivantamab for EGFR-Positive NSCLC With Exon 19 Deletion, Exon 21 L858R Substitution
The FDA approval of amivantamab-vmjw (Rybrevant) in combination with chemotherapy is the first targeted treatment to cut ...
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