Por: ABC News Life May 13, 2023
Women have suffered for centuries with hot flashes, one of the , without many treatment options.Now, the U.S. Food and Drug Administration has approved a first-of-its-kind drug, fezolinetant, sold under the brand name Veozah, to treat moderate to severe hot flashes during menopause.The drug, a pill taken once a day, is hormone-free, which makes it promising for women who cannot take hormone treatment because of other underlying health concerns,... + full article
WPTV USA Nation May 13, 2023
When a woman gets older, her period will eventually stop — a natural menopausal transition that can leave many women struggling with symptoms for years.One of the most common symptoms are hot flashes, and there haven't been many treatment options — until now.On Friday,... + más
FDA approves first-of-its-kind drug to treat hot flashes | ABC News
FDA approves first-of-its-kind drug to treat hot flashes | ABC7
ABC7 USA World May 13, 2023
, without many treatment options.Now, the U.S. Food and Drug Administration has approved a first-of-its-kind drug, fezolinetant, sold under the brand name Veozah, to treat moderate to severe hot flashes during menopause.The drug, a pill taken once a day, is hormone-free, which... + más
FDA approves drug called Veozah to treat hot flashes resulting from menopause | CBS News
CBS News USA Politics May 12, 2023
The Food and Drug Administration announced Friday it has approved a new kind of drug to treat moderate to severe hot flashes caused by , which could offer relief to millions of women who do not want to take hormone therapy to treat their symptoms.Drugmaker Astellas says the... + más
Time USA Health April 12, 2023
When a Texas district judge ruled on Apr. 7 that mifepristone, a drug for inducing abortion, —decades after it was granted—the decision didn’t just threaten abortion access. It raised deeper questions about the U.S. Food and Drug Administration (FDA)’s authority and the... + más
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Now that a Texas judge has ruled that the U.S. Food and Drug Administration (FDA)’s , what happens to the supply of the drug? The judge gave the Department of Justice (DOJ), which represents the FDA, until Apr. 14 to file an appeal before the suspension of the drug takes... + más
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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
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ABC News USA Health September 30, 2022
WASHINGTON -- A much-debated drug for Lou Gehrig’s disease won U.S. approval Thursday, a long-sought victory for patients that is likely to renew questions about the scientific rigor behind government reviews of experimental medicines.Amylyx Pharmaceuticals said the Food and... + más
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