Janet Woodcock and Johnson & Johnson

Selected healthcare news for the person - Janet Woodcock, and the company - Johnson & Johnson. We have 419 shared news items for this connection to-date.

Please provide a valid email address.

Selected Headlines

Date Headline (link) Source Relevant Snippet
12/9/2021 FDA authorizes Pfizer booster for 16- and 17-year-olds Becker's Hospital Review ... measures like masking and avoiding large crowds and poorly ventilated spaces, remain our most effective methods for fighting COVID-19," Janet Woodcock, MD, acting commissioner of the FDA, said in a Dec. 9 news release ... the second dose.As of Dec. 9, the Moderna and Johnson & Johnson vaccines are not authorized for anyone younger than 18.More research is required before a decision is made about boosters for younger children ...
11/28/2021 Who Would Be the Best FDA Commissioner for Biotech Investors? | Nasdaq Nasdaq ... the next Food and Drug Administration (FDA) Commissioner, despite some expectations that the choice would be the current acting commissioner Janet Woodcock. Both had seemed well qualified for the position.In this Motley Fool Live ... companies in the industries.10 stocks we like better than Johnson & JohnsonWhen our award-winning analyst team has a stock tip, it can pay to listen. After all, the newsletter they have run for ...
10/21/2021 U.S. FDA clears Moderna, J&J COVID-19 boosters, backs use of different vaccine for boost Yahoo News ... Johnson & Johnson, and said Americans can choose a different shot from their original inoculation as a booster.That means all three vaccines authorized in the United States can also be given as boosters to some groups."The availability of these authorized boosters is important for continued protection against COVID-19 disease," acting FDA Commissioner Janet Woodcock said in a statement. She noted that data suggests vaccine effectiveness may wane over ...
10/21/2021 FDA authorizes ‚Äòmixing and matching‚Äô Moderna and J&J booster shots On Wednesday, the Food and Drug Administration (‚AuFDA‚Au) authorized boosters of the Moderna and Johnson & Johnson COVID-19 vaccines, giving its approval for people to ‚Aumix and match‚Au booster shots. The agency granted ... advisory committee recommended their authorization last week. Acting FDA Commissioner Janet Woodcock said: ‚AuToday‚Aos actions demonstrate our commitment to public health in proactively fighting against the COVID-19 pandemic. As the pandemic continues to ...
10/21/2021 FDA authorizes ‚Äòmixing and matching‚Äô Moderna and J&J booster shots On Wednesday, the Food and Drug Administration (‚AuFDA‚Au) authorized boosters of the Moderna and Johnson & Johnson COVID-19 vaccines, giving its approval for people to ‚Aumix and match‚Au booster shots. The agency granted ... advisory committee recommended their authorization last week. Acting FDA Commissioner Janet Woodcock said: ‚AuToday‚Aos actions demonstrate our commitment to public health in proactively fighting against the COVID-19 pandemic. As the pandemic continues to ...
10/21/2021 FDA authorizes ‚Äòmixing and matching‚Äô Moderna and J&J booster shots On Wednesday, the Food and Drug Administration (‚AuFDA‚Au) authorized boosters of the Moderna and Johnson & Johnson COVID-19 vaccines, giving its approval for people to ‚Aumix and match‚Au booster shots. The agency granted ... advisory committee recommended their authorization last week. Acting FDA Commissioner Janet Woodcock said: ‚AuToday‚Aos actions demonstrate our commitment to public health in proactively fighting against the COVID-19 pandemic. As the pandemic continues to ...
10/21/2021 FDA authorizes ‚Äòmixing and matching‚Äô Moderna and J&J booster shots On Wednesday, the Food and Drug Administration (‚AuFDA‚Au) authorized boosters of the Moderna and Johnson & Johnson COVID-19 vaccines, giving its approval for people to ‚Aumix and match‚Au booster shots. The agency granted ... advisory committee recommended their authorization last week. Acting FDA Commissioner Janet Woodcock said: ‚AuToday‚Aos actions demonstrate our commitment to public health in proactively fighting against the COVID-19 pandemic. As the pandemic continues to ...
10/21/2021 FDA authorizes ‚Äòmixing and matching‚Äô Moderna and J&J booster shots On Wednesday, the Food and Drug Administration (‚AuFDA‚Au) authorized boosters of the Moderna and Johnson & Johnson COVID-19 vaccines, giving its approval for people to ‚Aumix and match‚Au booster shots. The agency granted ... advisory committee recommended their authorization last week. Acting FDA Commissioner Janet Woodcock said: ‚AuToday‚Aos actions demonstrate our commitment to public health in proactively fighting against the COVID-19 pandemic. As the pandemic continues to ...
10/8/2021 Biden close to naming new FDA head | wgrz.com ... Janet Woodcock,Former FDA officials,coming weeks" data-t1-publisher="[email protected]" COVID shots for younger kids: Answering top questions parents may haveIn the coming weeks, the agency will decide on the scope of booster shots for adults who received the Moderna and Johnson & Johnson vaccines. Regulators will also rule on whether Pfizer's vaccine is safe and effective for children as young as 5.That comes atop other high ...
10/8/2021 Biden close to naming new FDA head | kcentv.com ... Janet Woodcock,Former FDA officials,coming weeks" data-t1-publisher="[email protected]" COVID shots for younger kids: Answering top questions parents may haveIn the coming weeks, the agency will decide on the scope of booster shots for adults who received the Moderna and Johnson & Johnson vaccines. Regulators will also rule on whether Pfizer's vaccine is safe and effective for children as young as 5.That comes atop other high ...
8/19/2021 Will Johnson & Johnson COVID-19 vaccine recipients need booster too? ... to Americans who received both doses of an mRNA COVID-19 vaccine , but for the nearly 14 million who received Johnson & Johnson‚Aos one-dose jab, the details are not yet clear. CLICK HERE TO ... Dr. Rochelle Walensky, Dr. Anthony Fauci, the FDA‚Aos Dr. Janet Woodcock and others, said. ‚AuAdministration of the J&J vaccine did not begin in the U.S. until March 2021, and we expect more data ...
8/15/2021 CDC approval of Covid booster shot provides assist for some Individuals ... they‚Aore absolutely vaccinated. Nevertheless, there may be nonetheless one hitch: immunocompromised individuals who obtained their earlier shot from the Johnson & Johnson vaccine won‚Aot be eligible for a booster shot. The Meals and Drug ... are significantly in danger for extreme illness,‚Au mentioned Dr. Janet Woodcock, the appearing FDA commissioner, in a press release associated to the announcement. ‚AuAfter a radical overview of the obtainable information, the FDA decided ...
8/13/2021 FDA authorizes Covid-19 booster shots, but only for the immunocompromised - MedCity News MedCity News ... Johnson & Johnson, remains unchanged. The update comes ahead of a scheduled Friday meeting of the Centers for Disease Control and Prevention‚Aos Advisory Committee on Immunization Practices, which will discuss clinical recommendations about vaccination of immunocompromised people.Janet Woodcock, the FDA‚Aos acting commissioner, said in the announcement that the agency updated the emergency authorizations because immunocompromised people have a harder time fighting off infection, putting them at particularly high ...
7/16/2021 UPDATE 1-U.S. FDA sets January target to decide on approval of Pfizer's COVID-19 shot Yahoo News ... Janet Woodcock said on Twitter. (https://bit.ly/36Ixfkm) "Quite to the contrary, the review of this BLA (biologics license application) has been ongoing, is among the highest priorities of the agency, and the agency intends to complete the review far in advance of the PDUFA Goal Date." The vaccine is among the three being used in the United States under the FDA's emergency use authorization, alongside shots from Johnson & Johnson ...
7/16/2021 U.S. FDA sets January target to decide on approval of Pfizer's COVID-19 shot - Netscape News ... Janet Woodcock said on Twitter. (https://bit.ly/36Ixfkm)"Quite to the contrary, the review of this BLA (biologics license application) has been ongoing, is among the highest priorities of the agency, and the agency intends to complete the review far in advance of the PDUFA Goal Date."The vaccine is among the three being used in the United States under the FDA's emergency use authorization, alongside shots from Johnson & Johnson ...
6/10/2021 FDA hopes to extend shelf life of J&J's soon-to-expire COVID-19 vaccine LA Times The Biden administration is encouraging states to hold on to hundreds of thousands of soon-to-expire COVID-19 vaccine doses from Johnson & Johnson, given the possibility that additional data will show the shots are viable beyond their expiration date at month‚Aos end.Dr. Janet Woodcock , acting commissioner of the Food and Drug Administration, told state officials during a White House call Tuesday that they could store expired doses ...
6/10/2021 Unused Johnson & Johnson Covid Doses Are Piling Up as FDA Waits to See if Shelf Life Can Be Extended Unused Johnson & Johnson Covid Doses Pile Up as FDA Awaits Shelf Life Study By:√C Vaccine Johnson & Johnson Shutterstock.jpg Johnson & Johnson's COVID vaccine is one dose./Shutterstock The Biden administration is encouraging states to hold ... beyond their expiration date at month√¢¬A¬os end.Dr. Janet Woodcock, acting commissioner of the Food and Drug Administration, told state officials during a White House call Tuesday that they could store expired doses ...
5/11/2021 FDA gives Pfizer nod to provide COVID vaccine to younger teens ... Johnson & Johnson, have not been available to minors because studies are still underway. ‚AuToday‚Aos action allows for a younger population to be protected from COVID-19, bringing us closer to returning to a sense of normalcy and to ending the pandemic,‚Au Acting FDA Commissioner Dr. Janet Woodcock said in a prepared statement Monday. ‚AuParents and guardians can rest assured that the agency undertook a rigorous and thorough review ...
5/10/2021 News Updates: Mask-Wearing Guidelines Could Ease as Vaccinations Rise | Barron's ... approved the Pfizer-BioNTech Covid-19 vaccine for use in children 12 to 15 years old . Acting FDA commissioner Dr. Janet Woodcock said it ‚Aubrings us closer to returning to a sense of normalcy.‚Au ... among 3,000 children between 12 and 17 years old, while Johnson & Johnson is administering its shots to 16- and 17-year-olds. Moderna and J&J vaccines are currently approved for people 18 and older ...
4/25/2021 CDC and FDA resume Johnson & Johnson vaccine | WKRN News 2 WASHINGTON (NEXSTAR) ‚Ai After 11 days, the FDA and the CDC say the Johnson & Johnson/Jansen vaccine is once again a recommended option, for those seeking a vaccine.‚AuWe‚Aore confident that the Jansen covid-19 vaccine meets our robust standards for safety effectiveness and quality,‚Au Acting FDA Commissioner Janet Woodcock said.The federal agencies recommended the pause after six cases of a rare blood clotting disorder, out of ...
4/25/2021 CDC and FDA resume Johnson & Johnson vaccine | RochesterFirst WASHINGTON (NEXSTAR) ‚Ai After 11 days, the FDA and the CDC say the Johnson & Johnson/Jansen vaccine is once again a recommended option, for those seeking a vaccine.‚AuWe‚Aore confident that the Jansen covid-19 vaccine meets our robust standards for safety effectiveness and quality,‚Au Acting FDA Commissioner Janet Woodcock said.The federal agencies recommended the pause after six cases of a rare blood clotting disorder, out of ...
4/25/2021 Maryland Resumes Johnson & Johnson COVID Vaccinations After CDC, FDA Lift Pause CBS Local Maryland has begun to administer the Johnson & Johnson vaccine again after the Food & Drug Administration, along with the U.S. Centers for Disease Control & Prevention, lifted the pause on the one-shot covid-19 vaccine on ... benefits outweigh its known and potential risks,‚Au said Dr. Janet Woodcock, acting FDA commissioner.The vaccine now has a warning label for rare and severe blood clots. Six women experienced them after getting the ...
4/24/2021 US to resume J&J COVID vaccinations despite rare clot risk Star Tribune U.S. health officials lifted an 11-day pause on COVID-19 vaccinations using Johnson & Johnson's single-dose shot on Friday, after scientific advisers decided its benefits outweigh a rare risk of blood clot.The government ... not a decision the agencies reached lightly," FDA Acting Commissioner Janet Woodcock told reporters late Friday.CDC Director Dr. Rochelle Walensky added that the pause should increase confidence in vaccine safety, showing "that we are ...
4/24/2021 US to resume J&J COVID vaccinations despite rare clot risk ... LAURAN NEERGAARD and MIKE STOBBE Associated PressU.S. health officials lifted an 11-day pause on COVID-19 vaccinations using Johnson & Johnson‚Aos single-dose shot on Friday, after scientific advisers decided its benefits outweigh ... a decision the agencies reached lightly,‚Au FDA Acting Commissioner Janet Woodcock told reporters late Friday.CDC Director Dr. Rochelle Walensky added that the pause should increase confidence in vaccine safety, showing ‚Authat we are ...
4/24/2021 FDA lifts Johnson & Johnson COVID-19 vaccine pause following safety review ... Johnson & Johnson COVID-19 vaccine on Friday following an 11-day review and the recommendation of a panel of experts who determined it met safety standards despite rare instances of severe blood clots. ‚AuWe have concluded that the known and potential benefits of the Janssen COVID-19 Vaccine outweigh its known and potential risks in individuals 18 years of age and older,‚Au Acting FDA Commissioner Janet Woodcock said in ...