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McDonald's, Escherichia coli and US FDA
E. coli infections tied to McDonald's burgers rise to 75, US FDA says
The number of people infected by the E. coli outbreak tied to McDonald's Quarter Pounder hamburgers increased to 75 from 49, the U.S. Food and Drug Administration said on Friday.
US FDA Says 75 People Taken Ill From McDonald's E.coli Outbreak
(Reuters) -The U.S. Food and Drug Administration said on Friday that 75 persons have been infected from the E.coli outbreak linked to McDonald's Quarter Pounder hamburgers. The infections had killed one person, sickened 49 and hospitalized 10 across the U.S. West and Midwest, the CDC had said on Oct. 22.
McDonald’s outbreak news: What to know about E. coli cases, onions, recalls, more
Seventy-five people across 13 states have fallen ill in an E. coli outbreak attributed to McDonald's Quarter Pounders.
FDA recalls thousands of antidepressant bottles
FDA recalls duloxetine, antidepressant known as Cymbalta, over possible cancerous chemical
The U.S. Food and Drug Administration has recalled over 7,000 bottles of the antidepressant duloxetine, which is commonly sold under the name Cymbalta. According to the FDA, the drug was recalled because it had the "presence" of N-nitroso-duloxetine, a nitrosamine, which is a chemical that could increase the risk of cancer.
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.
FDA Has Recalled Thousands of Bottles of Antidepressant Duloxetine, Sold Under Brand Name Cymbalta: Here’s Why
The Duloxetine Delayed-Release Capsules' voluntary recall began on Oct. 10 after the FDA deemed the medication the second-highest risk classification. Over 7,100 bottles of Duloxetine were recalled, including 500 delayed-release 20mg capsules. The lot number is 220128, and the expiration date is 12/2024, per the FDA report.
Iterum, FDA and Orlynvah
US FDA approves Iterum's treatment for urinary infection
The U.S. Food and Drug Administration has approved Iterum Therapeutics' oral antibiotic to treat a type of urinary tract infection (UTI) in adult women, the health regulator said on Friday.
Iterum Therapeutics announces FDA approval of Orlynvah
Iterum Therapeutics (ITRM) plc announced that the U.S. Food and Drug Administration has approved Iterum’s new drug application for
Iterum Therapeutics Shares Soar on FDA's Orlynvah Approval
Shares of Iterum Therapeutics surged after federal regulators approved the use of its urinary tract infection treatment Orlynvah. The stock was up 64% at $1.92 around noon ET, closer to where it started the year.
2h
on MSN
As FDA probes source of national E. coli outbreak, California firm recalls onion products
Salinas-based international food production giant Taylor Farms had announced a recall on four onion products 'due to ...
6h
on MSN
FDA eyes McDonald's supplier's onions as source of E. Coli outbreak
McDonald's said Thursday that Taylor Farms is the supplier of the onions served on Quarter Pounders, which were pulled from ...
dvm360
1h
FDA: Off-label use of aspirin in lactating dairy cattle is prohibited
Vazalore is currently the only FDA-approved human aspirin that may be used in food-producing animals under certain conditions ...
TCTMD
29m
Michelle Tarver Named New FDA Director of Medical Devices
Tarver, an ophthalmologist, replaces longtime CDRH Director Jeff Shuren, who announced his retirement in July.
FierceBiotech
4h
FDA approves Medtronic's Affera all-in-one pulsed field ablation system
Less than a year after obtaining an FDA approval for its first foray into pulsed field ablation, Medtronic has done it again.
JD Supra
1h
FDA Finalizes Guidance on Use of Part 11 Electronic Systems, Records and Signatures in Clinical Investigations
On October 1, 2024, the US Food and Drug Administration (FDA) finalized its guidance on the use of electronic records in clinical investigations ...
1h
MrBeast's Lunchly Meal Brand Reportedly Hit By FDA Complaints, Claims of Mold
The brand was launched last month by Logan Paul, KSI, and MrBeast.
MedPage Today
1d
FDA Warns Companies Over Products Made With Amniotic Fluid
These warning letters are the latest in a series of FDA efforts to crack down on companies selling birth-tissue-derived ...
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