President-elect Donald Trump nominated many leading healthcare experts who opposed coronavirus-era lockdowns, focused on ending chronic illness, and want to overhaul America’s healthcare bureaucracies.
Robert F. Kennedy Jr. said he would clear out “entire departments” at the Food and Drug Administration (FDA) during an interview on Wednesday previewing his plans in the upcoming Trump administration.
The first over-the-counter birth control pill approved in the U.S. is headed to stores in the coming weeks and will also be available online.
The U.S. Centers for Disease Control and Prevention (CDC) said on Tuesday it is communicating with Chinese health officials about the explosion of pediatric respiratory diseases and pneumonia in northern China.
Vice President Kamala Harris mistakenly credited a nonexistent federal agency with approving mifepristone, a drug used in a two-drug medication abortion regimen.
Walgreens agreed not to sell abortion pills by mail in 20 conservative-led states after Republican attorneys general warned against doing so.
Several Democrat state attorneys general filed a lawsuit against the FDA challenging the agency’s restrictions on mifepristone.
As soon as Friday, a district judge could issue a ruling potentially blocking the use of the abortion medication mifepristone across the United States.
The U.S. Food and Drug Administration issued new guidance easing restrictions on gay men donating blood.
The Food and Drug Administration (FDA) is planning to lift more restrictions on donating blood for gay and bisexual men in monogamous relationships, even if they have not abstained from sex for 90 days.
Senator Marsha Blackburn of Tennessee is calling on the Food and Drug Administration (FDA) to investigate the use of puberty blocking drugs on minors.
The state of Florida is suing the Food and Drug Administration (FDA) over records requests regarding a program designed to import cheaper drugs from Canada.
Pfizer announced Wednesday it has completed an emergency submission to the U.S. Food and Drug Administration (FDA) to administer its three-dose coronavirus vaccine to children under the age of 5.
Chinese government media outlets condemned the U.S. baby formula market, in some cases citing American media, this weekend for not allowing more imports amid a crippling shortage that has resulted in infant hospitalizations nationwide.
The Food and Drug Administration (FDA) has reached an agreement with Abbott Nutrition on a plan to restart production at the Michigan baby formula plant to combat the shortage crisis.
The U.S. Food and Drug Administration (FDA) ruled on Thursday to limit the authorized use of the Johnson & Johnson coronavirus vaccine.
Four Senate Republicans bailed out Senate Majority Leader Chuck Schumer (D-NY) on Monday by voting to advance the nomination of Dr. Robert Califf as the head of the Food and Drug Administration.
President Joe Biden sounded the alarm about the rise in coronavirus cases on Tuesday, but made no mention of existing or future treatments for the virus.
The U.S. Food and Drug Administration (FDA) is expected to meet Tuesday and consider a proposal to extend coronavirus vaccinations making 28 million younger children down to age five eligible for the shots in November.
The Food and Drug Administration (FDA) has now approved the Moderna and Johnson & Johnson booster shots for the vulnerable.
Joe Biden specifically condemned reports that claimed Southwest Airlines employees protested the mandates last weekend which led to major service delays.
A meeting in March with Dr. Anthony Fauci and Centers for Disease Control and Prevention (CDC) Director Rochelle Walensky raises questions of “outside influence” regarding President Joe Biden’s federal vaccine mandate, Breitbart News has learned exclusively.
The FDA approved Pfizer coronavirus booster shots on Wednesday for senior citizens and those at high risk for coronavirus.
Scott Gottlieb, the former commissioner of the Food and Drug Administration (FDA), admitted during an interview on Face the Nation that the six foot social distancing rule recommended by public health officials for months on end was actually “arbitrary in and of itself,” and he noted that “nobody knows where it came from.”
Bad news for President Joe Biden piled up right after he left the White House early on Friday for a long weekend at the beach.
A Food and Drug Administration (FDA) panel voted Friday afternoon to reject a plan to provide Pfizer-BioNTech coronavirus booster vaccines for most Americans due to a lack of data showing the additional doses are safe and effective.
Pfizer prefaced its upcoming presentation to the Food and Drug Administration (FDA) to discuss its application for Chinese coronavirus booster shots by asserting data shows vaccine efficacy wanes over time.
Throughout his presidency, Joe Biden has constantly repeated the mantra that he would “follow the science” on coronavirus policy, but two Food and Drug Administration (FDA) officials have just resigned in protest of what they claim is the Biden administration perpetuating an atmosphere of pressure and intimidation to push the coronavirus booster shots.
Data from the Centers for Disease Control and Prevention (CDC) has demonstrated what anonymous administration officials described to Politico as a “worrying drop” in coronavirus vaccine efficacy over time, leading to the Biden administration’s conclusion to push vaccine booster shots.
The vast majority of Americans oppose being forced or coerced into getting a vaccine for the Chinese coronavirus, a Convention of States Action/Trafalgar Group survey released this week found.
The Food and Drug Administration (FDA) on Monday added warning labels to Johnson & Johnson’s single-dose vaccine for the Chinese coronavirus over links to a rare neurological condition.
Dr. Anthony Fauci, chief medical adviser to President Joe Biden, dismissed the fact that the Food and Drug Administration (FDA) has not yet approved vaccines for the Chinese coronavirus as merely a “technical issue.”
Pfizer representatives will meet with top U.S. health officials Monday to outline their plans to request federal authorization of a third dose of its coronavirus vaccine. The head-to-head comes as President Joe Biden’s chief medical adviser conceded “it is entirely conceivable, maybe likely” booster shots will be needed.
The Food and Drug Administration (FDA) on Monday approved what it described as a “first-of-its-kind” treatment for Alzheimer’s disease, which it says “targets the fundamental pathophysiology of the disease.”
OTTAWA, Ontario (AP) – Plans to distribute the first 300,000 doses of the Johnson & Johnson COVID-19 vaccine in Canada next week are on hold after Health Canada learned part of them were manufactured at a Maryland facility that messed up the ingredients in 15 million doses bound for the U.S. market.
Israel is planning to expand its turbo-speed coronavirus vaccination drive to children, pending approval by the U.S. Food and Drug Administration (FDA), Prime Minister Benjamin Netanyahu said on Tuesday.
The Biden-Harris administration announced a reversal of Trump’s decision to end taxpayer funding for experiments using aborted babies.
The FDA lifted restrictions on abortion-inducing drugs, allowing for dispensation through telemedicine and the mail during the pandemic.
The president defended the “extraordinary” results of the vaccine but lamented the company’s vaccine would never recover its reputation after the pause was announced by federal regulators.
U.S. health agencies on Tuesday will issue a joint call for Washington to begin an “immediate pause” in the rollout of Johnson & Johnson’s single-dose coronavirus vaccine.
