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FDA eyes McDonald's supplier's onions
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.
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.
FDA recalls over 7,000 bottles of antidepressant
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 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 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 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 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
13h
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
5h
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.
FiercePharma
12h
After prior rejection, Iterum nabs long-sought FDA nod for oral UTI drug Orlynvah
Despite recent concerns from the FDA about potential off-label use and antimicrobial resistance, Dublin-based Iterum ...
dvm360
12h
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
11h
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
12h
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 ...
12h
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
15h
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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