Por: 10 WBNS Nation December 24, 2022
WASHINGTON — The Food and Drug Administration announced Friday that it will overhaul packaging labels for the emergency contraceptive pill, Plan B, that women can take after having sex to prevent a pregnancy. The federal agency said it will remove references on the contraception's packaging that claim, without scientific evidence, that the pill prevents a fertilized egg from implanting in the womb. The new labels are intended to further... + full article
CNBC USA Politics January 24, 2023
Mifepristone (Mifeprex) and Misoprostol, the two drugs used in a medication abortion, are seen at the Women's Reproductive Clinic, which provides legal medication abortion services, in Santa Teresa, New Mexico, on June 17, 2022.Robyn Beck AFP Getty ImagesThe Food and Drug... + más
Abortion pill maker GenBioPro sues West Virginia, argues FDA rules preempt state ban | CNBC
Abortion pill is the most common method to end a pregnancy in the U.S., CDC says | CNBC
ABC7 USA Health January 04, 2023
The abortion drug mifepristone is safe enough that local pharmacies can provide the drug so long as it's prescribed by a certified healthcare provider and if that pharmacy meets certain requirements, according to new rules published Tuesday by the US Food and Drug... + más
FDA says it will greenlight pharmacies to fill prescriptions for abortion pill | ABC7
Will Pharmacies Really Make Abortion Pills More Accessible? | Time
ABC7 USA World January 04, 2023
by the U.S. Food and Drug Administration.If pharmacies jump on board, the FDA action could dramatically expand access to the drug in states where it's already legal. Doctors, for example, might be more willing to get certified to prescribe the drug because they would no... + más
FDA will greenlight pharmacies to fill prescriptions for abortion pill, agency says | ABC7
Politico USA Health December 30, 2022
The FDA’s collaboration with Biogen, the maker of a controversial Alzheimer’s drug, before it granted the product accelerated approval was “atypical” and ran afoul of the agency’s protocol for documenting interactions with drug companies, according to a joint House... + más
Alzheimer's drug approval by FDA 'rife with irregularities,' probe finds | Los Angeles Times
Probe: Alzheimer's drug approval 'rife with irregularities' | ABC News
ABC News USA Health December 20, 2022
WASHINGTON -- The lack of clear direction and priorities at the U.S. Food and Drug Administration's tobacco division has hampered its ability to regulate electronic cigarettes and other products, according to an expert panel assembled to examine problems at the agency.A... + más
Panel warns FDA’s beleaguered tobacco unit lacks direction | Associated Press
Panel warns FDA’s beleaguered tobacco unit lacks direction | WPLG Local 10
WPLG Local 10 USA Politics December 20, 2022
WASHINGTON – The lack of clear direction and priorities at the U.S. Food and Drug Administration's tobacco division has hampered its ability to regulate electronic cigarettes and other products, according to an expert panel assembled to examine problems at the agency.A... + más
Panel warns FDA’s beleaguered tobacco unit lacks direction | ABC News
Associated Press USA Politics December 19, 2022
WASHINGTON (AP) — The lack of clear direction and priorities at the U.S. Food and Drug Administration’s tobacco division has hampered its ability to regulate electronic cigarettes and other products, according to an expert panel assembled to examine problems at the agency.A... + más
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