No evidence Tyson Foods received FDA approval to add insects to human food | Fact check
There is no evidence Tyson Foods started putting insects in food for humans. The FDA doesn't have specific regulations for ...
WATE 6 On Your Side on MSN11h
1 in 8 adults has taken Ozempic or other GLP-1 drug: Survey
The majority — 62 percent — said they were using the drugs to treat a chronic condition like diabetes or heart disease while ...
U.S. Food and Drug Administration Accepts Bristol Myers Squibb’s Application for Subcutaneous Nivolumab (nivolumab and hyaluronidase)
U.S. Food and Drug Administration Accepts Bristol Myers Squibb’s Application for Subcutaneous Nivolumab (nivolumab and hyaluronidase) ...
According to the DEA, getting illegal pills as easy as ordering food
The Drug Enforcement Administration is working to crack down on dangerous drugs invading communities around the United States ...
According to the DEA, getting illegal pills as as easy as ordering food
The Drug Enforcement Administration is working to crack down on dangerous drugs invading communities around the United States ...
WXOW17h
1 in 8 adults in the US has taken Ozempic or another GLP-1 drug, KFF survey finds
About 1 in 8 adults in the United States has used a GLP-1 drug like Ozempic or Mounjaro at some point in their life, and half of them – about ...
pna18h
Pangasinan export-quality products get exposure in int'l food expo
Pangasinan has joined the International Food Exhibition (IFEX) Philippines as a province for the first time to help small and ...
devdiscourse14h
Zydus Secures USFDA Approval for Generic Arthritis Drug in the United States
Zydus Lifesciences received US FDA approval to market Dexamethasone tablets, a generic arthritis medication. Dexamethasone treats arthritis, immune system disorders, and other conditions, with annual ...
c-span26d
Food and Drug Administration Oversight Hearing, Part 1
Food and Drug Administration (FDA) Commissioner Dr. Robert Califf testified on oversight matters before the House Oversight and Accountabili… read more Food and Drug Administration (FDA ...
Center for Food Safety15d
U.S. Food and Drug Administration (FDA) announces fluorinated polyethylene petition filing
U.S. Food and Drug Administration (FDA) announced the filing of a food additive petition that asks FDA to remove its approval ...
c-span26d
Food and Drug Administration Oversight Hearing, Part 1
Food and Drug Administration (FDA) Commissioner Dr. Robert Califf testified on oversight matters before the House Oversight and Accountabili… read more Food and Drug Administration (FDA ...
The Valdosta Daily Times11d
The U.S. Food & Drug Administration (FDA) Approves Updated LUPKYNIS® (voclosporin) Label to include Long-Term Data from the AURORA Clinical Program
(NASDAQ: AUPH) (Aurinia or the Company) today announced that the FDA has approved a label update for LUPKYNIS. The updated label no longer includes language indicating that the safety and efficacy of ...