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McDonald's, E.coli and US FDA
E. coli infections tied to McDonald's burgers rise to 75, US FDA says
Oct 25 (Reuters) - The number of people infected by the E. coli outbreak tied to McDonald's (MCD.N) 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 E.Coli outbreak linked to California farm, FDA investigating
The FDA is investigating Taylor Farms out of Salinas, California for their onions which may be linked to the recent McDonald's E. Coli outbreak across the country.
Iterum Therapeutics Gets FDA Approval Of Orlynvah
FDA Approves Novel Treatment for UTIs
The FDA approved oral sulopenem etzadroxil and probenecid (Orlynvah) to treat uncomplicated urinary tract infections (uUTIs) caused by certain bacteria in women with limited or no alternative oral antibacterial treatment options, the agency said Friday.
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. The drug has been approved to treat uncomplicated UTIs,
Iterum Therapeutics Gets FDA Approval Of Orlynvah For Treatment Of Urinary Tract Infections
This is the first approved indication for Orlynvah and the first FDA-approved product for Iterum. "We are so pleased to have achieved this historic milestone and would like to thank all the patients,
FDA recalls over 7,000 bottles of antidepressant
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 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.
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.
8h
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 ...
Managed Healthcare Executive
29m
FDA Approves IV Form of Stelara Biosimilar Selardsi
This week’s approval expands Seldardsi indications to treat adults with Crohn’s disease and ulcerative colitis.
dvm360
7h
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 ...
Cure Today
1d
FDA Accepts New Drug Application for Pixclara for Glioma Imaging
Pixclara, a glioma-imaging agent, has been granted priority review by the
FDA
with a decision deadline of April 26, 2025.
TCTMD
6h
Michelle Tarver Named New FDA Director of Medical Devices
Tarver, an ophthalmologist, replaces longtime CDRH Director Jeff Shuren, who announced his retirement in July.
JD Supra
7h
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 ...
7h
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.
FierceBiotech
10h
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.
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