Flying Eze and its trusted partners need your
permission to store and access cookies, unique identifiers, personal data, and information on your
browsing behaviour on this device. This only applies to Flying Eze. You don’t have to accept, and
you
can change your preferences at any time via the Privacy Options link at the bottom of this screen. If
you don’t accept, you may will still see some personalised ads and content.
Cookies, device identifiers, or other information can be stored or accessed on
your device for the purposes presented to you.
Ads and content can be personalised based on a profile. More data can be added
to better personalise ads and content. Ad and content performance can be
measured. Insights about audiences who saw the ads and content can be derived.
Data can be used to build or improve user experience, systems and software.
Precise geolocation and information about device characteristics can be used.
If you don’t want to accept, please select Read More option below where you can also see how and
why your data may be used. You can also see where we or our partners claim a legitimate interest and
object to the processing of your data.
The U.S. Food and Drug Administration and the U.S. Centers for Disease Control and Prevention said in a Twitter thread that the pause has been recommended “out of an abundance of caution”
“Right now, these adverse events appear to be extremely rare,” the FDA wrote on Twitter. “Treatment of this specific type of blood clot is different from the treatment that might typically be administered.”
Today FDA and @CDCgov issued a statement regarding the Johnson & Johnson #COVID19 vaccine. We are recommending a pause in the use of this vaccine out of an abundance of caution.
All the six recipients were women between the ages of 18 and 48. One woman died and a second woman in Nebraska has been hospitalized in critical condition, the NYT reported.
The CDC will convene a meeting of the Advisory Committee on Immunization Practices (ACIP) on Wednesday to further review these cases and assess their potential significance. The FDA will then review that analysis as it also investigates these cases, it said in a statement.
A press conference will be held at 10 a.m. EDT where officials will provide further detail on the pause.
The company’s shares were down 3 per cent before the opening bell.
The move from the U.S. regulators comes less than a week after Europe’s drug regulator said it was reviewing rare blood clots in four people in the United States who received the shot.
Canada has also approved the one-shot Johnson and Johnson vaccine, however, deliveries to the country are not expected to begin until the end of April.
Canada also moved to change recommendations for use of the AstraZeneca vaccine after the reports of very rare blood clots in some recipients, although there have been no such reports in the country.