Synonyms that are in the dictionary are marked in green. Synonyms that are not in the dictionary are marked in red.
Antonyms that are in the dictionary are marked in green. Antonyms that are not in the dictionary are marked in red.
Among other things, the lawsuit contends that the U.S. Food and Drug Administration has continued with burdensome and unnecessary regulations.
Source: https://crosscut.com/politics/2023/04/gov-inslee-buys-3-year-supply-abortion-pills-case-ban
CAPLYTA is the only U.S. Food and Drug Administration (FDA) approved treatment for depressive episodes associated with bipolar I or II disorder (bipolar depression) in adults as monotherapy and as adjunctive therapy with lithium or valproate.
C.) has been trying to pull her party back to the center on abortion, going so far as to suggest the U.S. Food and Drug Administration ignore the ruling by federal Judge Matthew Kacsmaryk that would rescind the agency’s approval of the abortion pill.
Source: https://jezebel.com/abortion-isnt-even-a-top-5-issue-for-republican-primary-1850337590
FRIDAY, May 19, 2023 (HealthDay News) -- Patients with Crohn’s disease have a new treatment option, following U.S. Food and Drug Administration approval of a pill called Rinvoq (upadacitinib).
In 1996, the U.S. Food and Drug Administration approved the use of the zero-calorie artificial fat Olestra.
In January, the U.S. Food and Drug Administration approved Leqembi for people with mild cognitive decline after it was shown to reduce plaque by a statistically significant amount.
Source: https://www.dailyherald.com/entlife/20230903/updates-in-time-for-world-alzheimers-month
In most cases, medication is advised and the ''acompañante'' is able to provide a combination of two abortion pills, misoprostol and mifepristone, both considered safe by the World Health Organization and the U.S. Food and Drug Administration.
Source: https://www.startribune.com/activists-network-in-mexico-helps-u-s-women-get-abortions/600263902/
June 16 (Reuters) - The U.S. Food and Drug Administration (FDA) said on Friday it has advised manufacturers that are updating their COVID-19 vaccines to develop monovalent shots to target the XBB.1.5 subvariant.
Stratford Care USA, Inc has recalled 62 brands of Omega-3 supplements for cats and dogs over concern for "potentially elevated levels of Vitamin A," according to a from the U.S. Food and Drug Administration published Friday.
Source: https://abcnews.go.com/Health/60-omega-3-dog-cat-supplements-recalled-stratford/story?id=97857635
Teropavimab and zinlirvimab are investigational compounds and are not approved by the U.S. Food and Drug Administration or any other regulatory authority for any use.
The company’s Covid-19 vaccine was one of the first approved by the U.S. Food and Drug Administration (FDA).
Source: https://investorplace.com/2023/09/undervalued-biotech-stocks-to-buy/
The cost of a generic drug is as much as 85% lower, on average, than the cost of brand-name products, according to the U.S. Food and Drug Administration.
Source: https://www.moneytalksnews.com/slideshows/10-ways-to-save-on-prescription-drugs/
The New Jersey facility has been under scrutiny by the U.S. Food and Drug Administration since 2019 when inspectors found quality control data had been deleted and not appropriately audited, Reuters has reported.
Source: https://www.insurancejournal.com/news/east/2023/10/03/742591.htm
The updated recommendations reflect recent clinical trial results and U.S. Food and Drug Administration (FDA) approval of teplizumab and provide healthcare professionals with new guidance on the use of teplizumab to delay the progression of the disease.
The U.S. Food and Drug Administration approved mifepristone in 2000 to end pregnancy, when used in combination with a second drug, misoprostol.
The U.S. Food and Drug Administration has approved the first over-the-counter naloxone nasal spray (also known as Narcan).
The U.S. Food and Drug Administration issued the warning.
Source: https://247wallst.com/consumer-products/2023/02/19/starbucks-frappuccino-scare/
The U.S. Food and Drug Administration on Wednesday issued warnings to three infant formula makers to correct their manufacturing processes to better catch bacterial contamination, but added it does not expect any impact on the supply.
Source: https://www.insurancejournal.com/news/national/2023/08/31/738583.htm
The U.S. Food and Drug Administration said it has received reports of seven illnesses in at least five states possibly linked to contaminated puree.
THOUSAND OAKS, Calif. /PRNewswire/ -- Amgen (NASDAQ:AMGN) today announced that the U.S. Food and Drug Administration (FDA) has accepted and granted Priority Review for the Company's Biologics License Application (BLA) for tarlatamab.