Janet Woodcock and Coronavirus

Selected healthcare news for the person - Janet Woodcock, and the healthcare topic - Coronavirus We have 137 shared news items for this connection to-date.

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5/12/2021 FDA Approves COVID Vaccine for Ages 12 to 15 ... Inc. All rights reserved. Terms of Use.MedicineNet does not provide medical advice, diagnosis or treatment. See additional information . home / coronavirus (covid-19) center / coronavirus a-z list / fda approves covid vaccine for ages 12 ... of normalcy and to ending the pandemic," Acting FDA Commissioner Janet Woodcock said in a statement released Monday.The FDA's authorization is not the final step in bringing Pfizer's vaccine to younger children. A U.S ...
4/26/2021 More Than 100 Legislators Call On FDA To Enforce Safety Measures For Chemical Abortions ... Janet Woodcock said her agency would stop enforcing a restriction that required women using abortion pills to obtain the first drug in the two-dose regimen, mifepristone, in person from a medical provider. The FDA will now allow women to obtain the pills by mail during the coronavirus pandemic.‚AuThe FDA should not remove or weaken the existing REMS [Risk Evaluation and Mitigation Strategies] on mifepristone when the insufficient data ...
4/24/2021 Over 100 GOP Lawmakers Call On FDA To Keep Abortion Drug Restrictions | The Daily Caller ... Janet Woodcock highlighting President Joe Biden‚Aos administration‚Aos plans to lift the FDA‚Aos restrictions on abortion drugs, allowing the abortion pills to be delivered by mail during the coronavirus pandemic.‚AuThe FDA should not remove or weaken the existing [risk evaluation and mitigation strategy] on mifepristone when the insufficient data available suggests that mifepristone endangers women‚Aos health,‚Au the letter said . ‚AuRequests to remove the in-person ...
4/24/2021 CDC, FDA lift pause on using J&J's coronavirus vaccine, add safety warning ... vaccine outweigh its known and potential risks in individuals 18 years of age and older,‚Au acting FDA Commissioner Dr. Janet Woodcock said in a statement.‚AuWe are confident that this vaccine continues to meet ... in certain groups. The CDC took into consideration deaths from coronavirus and the likelihood that people would get vaccinated more quickly if the Janssen vaccine was in the mix.‚AuWhen resuming vaccination among all persons ...
4/24/2021 Over 100 GOP Lawmakers Warn of ‚ÄòDire Consequences‚Äô as Biden Admin Pushes Abortion by Mail ... Janet Woodcock highlighting the plans to allow the abortifacient drug mifepristone to be delivered by mail during the coronavirus pandemic.‚AuThe FDA should not remove or weaken the existing [risk evaluation and mitigation strategy] on mifepristone when the insufficient data available suggests that mifepristone endangers women‚Aos health,‚Au the letter said. Advertisement - story continues below‚AuRequests to remove the in-person requirements for chemical abortion look the other way ...
4/24/2021 The US is resuming its rollout of Johnson & Johnson's vaccine after a pause to investigate blood clots Yahoo News ... Melissa Mendez in Reading, Pennsylvania. Ben Hasty/MediaNews Group/Reading Eagle/Getty Images The US will resume using Johnson & Johnson's coronavirus vaccine.The decision came after a CDC committee voted to recommend using the shots ... of the vaccines in preventing COVID-19 outweigh the risks.Janet Woodcock, acting administrator of the Food and Drug Administration, told reporters on Friday that regulators had "full confidence that this vaccine's known and potential ...
4/24/2021 Over 100 GOP lawmakers call on FDA to keep abortion drug restrictions ... Janet Woodcock highlighting President Joe Biden‚Aos administration‚Aos plans to lift the FDA‚Aos restrictions on abortion drugs, allowing the abortion pills to be delivered by mail during the coronavirus pandemic.‚AuThe FDA should not remove or weaken the existing [risk evaluation and mitigation strategy] on mifepristone when the insufficient data available suggests that mifepristone endangers women‚Aos health,‚Au the letter said . ‚AuRequests to remove the in-person ...
4/24/2021 One-dose shots get green light after U.S. pause ... Federal health officials on Friday evening lifted an 11-day pause on the use of the single-shot Johnson & Johnson coronavirus vaccine after an extensive safety review by the Centers for Disease Control and Prevention ... not a decision the agencies reached lightly," FDA acting Commissioner Janet Woodcock told reporters.CDC Director Dr. Rochelle Walensky added that the pause should increase confidence in vaccine safety, showing "that we are taking every ...
4/24/2021 CDC, FDA lift pause on using J&J's coronavirus vaccine, add safety warning Share on Facebook CDC, FDA lift pause on using J&J‚Aos coronavirus vaccine, add safety warningThe US Centers for Disease Control and Prevention and Food and Drug Administration lifted their recommended pause on ... years of age and older,‚Au acting FDA Commissioner Dr. Janet Woodcock said in a statement.‚AuWe are confident that this vaccine continues to meet our standards for safety, effectiveness and quality. We recommend people ...
4/24/2021 CDC, FDA lift pause on using J&J's coronavirus vaccine, add safety warning - Local News 8 ... for Disease Control and Prevention and Food and Drug Administration lifted their recommended pause on use of Johnson & Johnson‚Aos coronavirus vaccine Friday and said the label will be updated to warn of blood clot ... years of age and older,‚Au acting FDA Commissioner Dr. Janet Woodcock said in a statement.‚AuWe are confident that this vaccine continues to meet our standards for safety, effectiveness and quality. We recommend people ...
4/24/2021 Nearly 1,200 New Covid-19 Cases As Johnson and Johnson Vaccines Resume ‚Äì CBS Baltimore CBS Local Filed Under: Baltimore. Native Americans , coronavirus in Maryland , covid vaccinations BALTIMORE (WJZ)‚Ai Nearly 1,200 new Covid-19 cases were confirmed in Maryland Saturday and 15 more people have died from the coronavirus. This comes ... benefits outweigh its known and potential risks,‚Au said Dr. Janet Woodcock, acting FDA commisioner.The vaccine now has a warning label for rare and severe blood clots. Six women experienced them after getting the ...
4/23/2021 Coronavirus: CDC advisory panel meeting Friday to discuss Johnson & Johnson vaccine ‚Äì HOT 105! ... 19 Vaccine outweigh its known and potential risks in individuals 18 years of age and older,‚Au acting FDA Commissioner Janet Woodcock said in a statement. ‚AuWe are confident that this vaccine continues to meet ... in patients who got the Pfizer or Moderna vaccines. Related: Coronavirus: US health agencies call for pause in use of Johnson & Johnson vaccine‚AuThis is a really rare event,‚Au Dr. Anthony Fauci, the nation ...
4/23/2021 Johnson & Johnson Coronavirus Vaccine Rollout Resumes Business Insider The US will resume using Johnson & Johnson's coronavirus vaccine. The decision came after a CDC committee voted to recommend using the shots. The US paused its rollout on April 13, citing concerns over rare blood ... of the vaccines in preventing COVID-19 outweigh the risks.Janet Woodcock, acting administrator of the Food and Drug Administration, told reporters on Friday that regulators had "full confidence that this vaccine's known and potential ...
4/23/2021 Health Officials: Johnson & Johnson Vaccinations Could Restart Soon Yahoo News Federal health officials said the pause on Johnson & Johnson coronavirus vaccinations could soon be lifted, in interviews with the New York Times over the past week.The Centers for Disease Control and Prevention and Food ... additional cases of the clotting disorder.Acting FDA commissioner Dr. Janet Woodcock said that while a small number of cases were discovered, the rate of the clotting disorder was not higher ‚Auin terms of the ...
4/22/2021 Vaccination campaign slows in past week | Washington Examiner Washington Examiner ... Janet Woodcock.BIDEN SAYS CORONAVIRUS DEATHS AMONG SENIORS ARE DOWN 80% AS HE LAUNCHES NEW VACCINATION PHASEThe single-shot vaccine was also crucial to getting shots into the arms of people who are homebound, live long distances from vaccination sites, or are generally reluctant to get a COVID-19 vaccine. Public confidence in the shot plummeted from 52% to 37% after the administration announced the pause, according to a ...
4/16/2021 FDA walks back ‚Äòerror and ambiguity‚Äô-filled HHS proposal to exempt 91 devices from premarket review | FierceBiotech FierceBiotech ... coronavirus pandemic, in a bid to increase the availability of much-needed personal protective equipment, as well as tools like thermometers, ventilators and remote patient monitoring technologies.In a follow-up notice , however, the FDA and HHS officially rescinded the proposal to exempt the group of 84 devices‚Aiall of which are Class II, except for one unclassified device‚Aifrom premarket review.It was signed by Janet Woodcock, acting commissioner ...
4/14/2021 FDA approves removing in-person requirement for abortion pill amid pandemic ... coronavirus pandemic.In a letter sent Monday to two physician organizations The American College of Obstetricians and Gynecologists and the Society for Maternal-Fetal Medicine, Acting Commissioner of Food and Drugs Janet Woodcock said the FDA would "exercise enforcement discretion" concerning the in-person requirement for dispensing mifepristone, the first of two-drug regimen to end an early pregnancy. AdvertisementWoodcock said a review of relevant literature found there does ...
4/14/2021 FDA approves removing in-person requirement for abortion pill amid pandemic - UPI.com April 13 (UPI) -- The Biden administration has approved for abortion medication to be dispensed through the mail during the coronavirus pandemic.In a letter sent Monday to two physician organizations The American College of Obstetricians and Gynecologists and the Society for Maternal-Fetal Medicine, Acting Commissioner of Food and Drugs Janet Woodcock said the FDA would "exercise enforcement discretion" concerning the in-person requirement for dispensing mifepristone, the first of ...
4/14/2021 Johnson & Johnson Vaccine: Health Officials Call for Pause Due to Rare Blood Clot Occurrences ... Janet Woodcock, she'd like to stress that the blood clot occurrences seem to be extremely rare.Nevertheless, she added that COVID-19 safety is a top priority for the federal governments and they are taking all reports of adverse events after vaccination very seriously. It was also Woodcock who said that the investigation would move fast and could include in days.ALSO READ: Universal Coronavirus Vaccine: Research Ongoing for Possible ...
4/13/2021 Biden Administration to Lift Restrictions on Telemedicine Abortions mHealth Intelligence Policy News Biden Administration to Lift Restrictions on Telemedicine Abortions The administration has announced that it will allow healthcare providers to prescribe abortion-inducing drugs via telehealth without an in-person exam for the remainder of the public health emergency. The Biden Administration is supporting the use of telehealth to facilitate medication abortions during the coronavirus pandemic.Acting US Food and Drug Administration Commissioner Janet Woodcock told Gynecologists this week ...
4/13/2021 FDA ends restrictions on mailing abortion pills during pandemic The Hill FDA ends restrictions on mailing abortion pills during pandemic By Justine Coleman - 04/13/21 12:19 PM EDT © Getty ImagesThe Food and Drug Administration (FDA) on Monday ended restrictions on mailing abortion pills during the pandemic, after the Trump administration moved to keep the decades-old requirement for in-person pickup of the drug amid the public health emergency surrounding the coronavirus pandemic.Acting FDA Commissioner Janet Woodcock sent a letter ...
4/13/2021 Johnson & Johnson vaccine should be paused in U.S. after 'extremely rare' blood clots, FDA and CDC say NBC News ... coronavirus outbreak"We are recommending this pause while we work together to fully understand these events, and also so we can get information out to health care providers and vaccine recipients," Dr. Janet Woodcock, acting FDA commissioner, said during a briefing Tuesday.The review is expected to be completed quickly, lasting "a matter of days," officials said.The clots are considered extremely rare. Overall, more than 6.8 million people in ...
4/13/2021 Concerns over rare clotting disorders halt use of Johnson & Johnson's COVID-19 vaccine See all of our coverage of the coronavirus outbreak‚AuWhile these events are very rare, we‚Aore recommending a pause in the use of the J&J COVID-19 vaccine in order to prepare the health care system to recognize and treat patients appropriately and to report severe events they may be seeing,‚Au FDA acting Commissioner Janet Woodcock said at a press conference. J&J announced it had decided ...
4/13/2021 US pauses use of J&J vaccine, rollout delayed in Europe J vaccine, rollout delayed in Europe April 14 2021 01:03 AM & Johnson's Janssen coronavirus disease (COVID-19) vaccine. (REUTERS) & Johnson (J&J)‚Aos coronavirus (Covid-19) vaccine for at least a few days after six ... United States. Acting US Food and Drug Administration (FDA) Commissioner Janet Woodcock said the agency expected the pause to be a matter of days, and was aimed at providing information to healthcare providers on how ...
4/13/2021 Biden Administration Lifts Restrictions On Abortion Pills Despite Risks, Allows Them To Be Delivered By Mail President Joe Biden‚Aos administration is lifting the Food and Drug Administration‚Aos former restrictions on abortion drugs, allowing the abortion pills to be delivered by mail during the coronavirus pandemic. Acting FDA Commissioner Janet Woodcock said Monday that sending the drugs by mail will not increase risks for women and will protect those who want the drugs from COVID-19, Politico reported. The same day, the FDA recommended a ...