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FDA Strengthens Warning Over Severe Condition Linked to J&J COVID Vaccine
Published on December 17, 2021
U.S. drug regulators this week formally strengthened a warning to Americans regarding a severe condition linked to Johnson & Johnson’s COVID-19 vaccine.
Blood clots and low blood platelet levels, known as thrombosis with thrombocytopenia syndrome (TTS), are now listed as a contraindication, or a medical reason for somebody not to get the shot.
“Do not administer” the vaccine to individuals with a history of the set of conditions following the vaccine or any other adenovirus-vectored COVID-19 vaccine, the Food and Drug Administration (FDA) says in an updated fact sheet (pdf) for health care providers administering vaccines.
TTS has been reported in “a wide range of individuals 18 years and older” since administration of the Johnson & Johnson (J&J) vaccine began earlier this year, regulators say.
The highest reporting rate, approximately 1 case per 100,000 doses administered, has occurred in women aged 30 to 49.
About 15 percent of the TTS cases have been fatal.
“Currently available evidence supports a causal relationship between TTS and the Janssen COVID-19 Vaccine,” the FDA says in its updated fact sheets.
Janssen is a subsidiary of J&J.
J&J did not respond to a request for comment.
In the spring, U.S. health officials recommended a nationwide pause in administration of the vaccine due to TTS cases appearing among people who had gotten it.
The pause was lifted in April.
The FDA and Centers for Disease Control and Prevention (CDC) said at the time that officials were confident the vaccine was safe and effective in preventing COVID-19.
The FDA said that the available data showed the known and potential benefits outweigh its known and potential risks.
Paul Stoffels, J&J’s chief scientific officer, said when the pause was lifted that the company would work with health authorities worldwide “to educate health care professionals and the public to ensure this very rare event can be identified early and treated effectively.”
COVID-19 is the disease caused by the CCP (Chinese Communist Party) virus. Three COVID-19 vaccines are available for use in the United States. J&J’s is by far the least used. Just 17.2 million doses have been administered as of Dec. 15, compared to 185.8 million doses of Moderna’s vaccine and 283 million doses of the Pfizer-BioNTech vaccine.
A study in November found J&J vaccine recipients had a higher risk of blood clots when compared to recipients of the other two shots.
Currently, there are no restrictions in place on administration of the J&J jab.
The two contraindications, TTS and severe allergic reaction, typically only apply once a person has suffered an adverse event.
The CDC’s vaccine advisory panel is meeting Thursday to hear presentations from the CDC on J&J’s vaccine.
A draft agenda says that one presentation will be on TTS. Another will go over updates to the risk-benefit assessment for the vaccine.
Members of the panel will vote in the afternoon on updated recommendations for use. They may potentially narrow the populations who can get the shot.
The panel is meeting “to hear the latest information on vaccines and disease epidemiology,” Jasmine Reed, a CDC spokeswoman, told The Epoch Times in an email.
There is no indication FDA experts will participate in the meeting and a spokeswoman for the agency did not respond to a request for comment.
Bold emphasis added
https://principia-scientific.com/fda-strengthens-warning-over-severe-condition-linked-to-jj-covid-vaccine/?utm_source=feedburner&utm_medium=email
Thanks to: https://principia-scientific.com
CDC Warns Americans NOT to Get J&J Shot Over Blood Clot Risk
Date: December 17, 2021Author: Nwo Report
CDC advisers back use of Pfizer, Moderna vaccines over Johnson & Johnson
Source: Zero Hedge
Update (1631ET): A panel of health advisors to the Centers for Disease Control and Prevention voted Thursday unanimously that adults seeking boosters should go with Pfizer-BioNTech or Moderna vaccine rather than Johnson & Johnson vaccine.
The Advisory Committee on Immunization Practices voted 15-0 that the mRNA vaccines are “preferred” to the J&J vaccine because they’re the safest and most effective vaccines.
CDC Director Rochelle Walensky is expected to decide whether to adopt the panel’s advice as agency policy later today.
Johnson & Johnson’s COVID-19 vaccine has been linked to rare forms of blood clotting.
* * *
Authored by Zachary Stieber via The Epoch Times,
A panel of experts who advise the Centers for Disease Control and Prevention (CDC) on vaccines is meeting Thursday to discuss updates to a severe condition linked to Johnson & Johnson’s COVID-19 vaccine.
The syndrome is a combination of blood clots and low blood platelet levels.
Concern over patients getting the syndrome after getting the vaccine led to a near-nationwide pause in administering the shot in the spring, but the pause was lifted after the Food and Drug Administration (FDA) determined the benefits of the vaccine outweighed its risks.
Since then, more evidence has emerged linking the syndrome to the vaccine.
Researchers with the CDC last month found people who got the Johnson & Johnson (J&J) shot were far more likely to experience the syndrome when compared to people who got a Moderna or Pfizer COVID-19 vaccine.
The reporting rate to the Vaccine Adverse Event Reporting System (VAERS), a system run by the CDC and the FDA, was 3.55 per million doses administered for the Johnson & Johnson vaccine, compared to 0.0057 per million doses administered after one of the other vaccines.
The rate was the highest among women aged 30 to 39.
Read more
https://nworeport.me/2021/12/17/cdc-warns-americans-not-to-get-jj-shot-over-blood-clot-risk/
Thanks to: https://nworeport.me
Published on December 17, 2021
U.S. drug regulators this week formally strengthened a warning to Americans regarding a severe condition linked to Johnson & Johnson’s COVID-19 vaccine.
Blood clots and low blood platelet levels, known as thrombosis with thrombocytopenia syndrome (TTS), are now listed as a contraindication, or a medical reason for somebody not to get the shot.
“Do not administer” the vaccine to individuals with a history of the set of conditions following the vaccine or any other adenovirus-vectored COVID-19 vaccine, the Food and Drug Administration (FDA) says in an updated fact sheet (pdf) for health care providers administering vaccines.
TTS has been reported in “a wide range of individuals 18 years and older” since administration of the Johnson & Johnson (J&J) vaccine began earlier this year, regulators say.
The highest reporting rate, approximately 1 case per 100,000 doses administered, has occurred in women aged 30 to 49.
About 15 percent of the TTS cases have been fatal.
“Currently available evidence supports a causal relationship between TTS and the Janssen COVID-19 Vaccine,” the FDA says in its updated fact sheets.
Janssen is a subsidiary of J&J.
J&J did not respond to a request for comment.
In the spring, U.S. health officials recommended a nationwide pause in administration of the vaccine due to TTS cases appearing among people who had gotten it.
The pause was lifted in April.
The FDA and Centers for Disease Control and Prevention (CDC) said at the time that officials were confident the vaccine was safe and effective in preventing COVID-19.
The FDA said that the available data showed the known and potential benefits outweigh its known and potential risks.
Paul Stoffels, J&J’s chief scientific officer, said when the pause was lifted that the company would work with health authorities worldwide “to educate health care professionals and the public to ensure this very rare event can be identified early and treated effectively.”
COVID-19 is the disease caused by the CCP (Chinese Communist Party) virus. Three COVID-19 vaccines are available for use in the United States. J&J’s is by far the least used. Just 17.2 million doses have been administered as of Dec. 15, compared to 185.8 million doses of Moderna’s vaccine and 283 million doses of the Pfizer-BioNTech vaccine.
A study in November found J&J vaccine recipients had a higher risk of blood clots when compared to recipients of the other two shots.
Currently, there are no restrictions in place on administration of the J&J jab.
The two contraindications, TTS and severe allergic reaction, typically only apply once a person has suffered an adverse event.
The CDC’s vaccine advisory panel is meeting Thursday to hear presentations from the CDC on J&J’s vaccine.
A draft agenda says that one presentation will be on TTS. Another will go over updates to the risk-benefit assessment for the vaccine.
Members of the panel will vote in the afternoon on updated recommendations for use. They may potentially narrow the populations who can get the shot.
The panel is meeting “to hear the latest information on vaccines and disease epidemiology,” Jasmine Reed, a CDC spokeswoman, told The Epoch Times in an email.
There is no indication FDA experts will participate in the meeting and a spokeswoman for the agency did not respond to a request for comment.
Bold emphasis added
https://principia-scientific.com/fda-strengthens-warning-over-severe-condition-linked-to-jj-covid-vaccine/?utm_source=feedburner&utm_medium=email
Thanks to: https://principia-scientific.com
CDC Warns Americans NOT to Get J&J Shot Over Blood Clot Risk
Date: December 17, 2021Author: Nwo Report
CDC advisers back use of Pfizer, Moderna vaccines over Johnson & Johnson
Source: Zero Hedge
Update (1631ET): A panel of health advisors to the Centers for Disease Control and Prevention voted Thursday unanimously that adults seeking boosters should go with Pfizer-BioNTech or Moderna vaccine rather than Johnson & Johnson vaccine.
The Advisory Committee on Immunization Practices voted 15-0 that the mRNA vaccines are “preferred” to the J&J vaccine because they’re the safest and most effective vaccines.
CDC Director Rochelle Walensky is expected to decide whether to adopt the panel’s advice as agency policy later today.
Johnson & Johnson’s COVID-19 vaccine has been linked to rare forms of blood clotting.
* * *
Authored by Zachary Stieber via The Epoch Times,
A panel of experts who advise the Centers for Disease Control and Prevention (CDC) on vaccines is meeting Thursday to discuss updates to a severe condition linked to Johnson & Johnson’s COVID-19 vaccine.
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The panel will listen to presentations by CDC officials on thrombosis with thrombocytopenia syndrome (TTS), which U.S. drug regulators say has a “causal relationship” with the jab, according to a draft agenda for the meeting.The syndrome is a combination of blood clots and low blood platelet levels.
Concern over patients getting the syndrome after getting the vaccine led to a near-nationwide pause in administering the shot in the spring, but the pause was lifted after the Food and Drug Administration (FDA) determined the benefits of the vaccine outweighed its risks.
Since then, more evidence has emerged linking the syndrome to the vaccine.
Researchers with the CDC last month found people who got the Johnson & Johnson (J&J) shot were far more likely to experience the syndrome when compared to people who got a Moderna or Pfizer COVID-19 vaccine.
The reporting rate to the Vaccine Adverse Event Reporting System (VAERS), a system run by the CDC and the FDA, was 3.55 per million doses administered for the Johnson & Johnson vaccine, compared to 0.0057 per million doses administered after one of the other vaccines.
The rate was the highest among women aged 30 to 39.
Read more
https://nworeport.me/2021/12/17/cdc-warns-americans-not-to-get-jj-shot-over-blood-clot-risk/
Thanks to: https://nworeport.me
