OKLAHOMA CITY (KFOR) – Following a suggestion by the Meals and Drug Administration, state leaders in Oklahoma say they’re asking all vaccine websites throughout the state to cease utilizing the Johnson & Johnson COVID-19 vaccine.
On Tuesday, the FDA and the Facilities for Illness Management and Prevention issued a press release, calling for a pause in the usage of the Johnson & Johnson single shot COVID-19 vaccine out of an abundance of warning.
Up to now, officers say greater than 6.8 million doses of the Johnson & Johnson COVID-19 vaccine have been administered in america.
Well being leaders say they’re investigating after six folks developed a uncommon and extreme kind of blood clot after receiving the Johnson & Johnson vaccine.
Officers say the CDC will maintain a meting of the Advisory Committee on Immunization Practices on Wednesday to additional assessment the instances. The FDA will then assessment that evaluation.
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“Till that course of is full, we’re recommending this pause. That is necessary to make sure that the well being care supplier group is conscious of the potential for these hostile occasions and may plan as a result of distinctive remedy required with such a blood clot,” the FDA posted on Twitter.
Shortly after the announcement, the Oklahoma State Division of Well being mentioned it was asking all vaccine websites within the state to cease giving the Johnson & Johnson vaccine till the federal company’s investigation is full.
“Out of an abundance of warning, we now have requested all of our vaccine websites to pause the usage of the Johnson & Johnson vaccine instantly whereas we collect extra data,” mentioned Well being Commissioner Dr. Lance Frye. “The sort of potential hostile response following administration of the Johnson & Johnson vaccine is extraordinarily uncommon and has occurred in lower than one in each million recipients. Nonetheless, the well being and security of Oklahomans stays our prime precedence. We really feel it greatest to pause administration of this vaccine in alignment with the CDC and FDA’s suggestion till extra information on this potential hostile response is out there.”
Up to now, Oklahoma has administered 62,000 doses of the Johnson & Johnson vaccine.
Oklahomans who’ve acquired the Johnson & Johnson vaccine who develop extreme headache, belly ache, leg ache or shortness of breath inside three weeks after their vaccination ought to contact their healthcare supplier.
If in case you have already scheduled an appointment for the Johnson & Johnson vaccine, OSDH is working with these suppliers to supply Pfizer and Moderna vaccines as alternate options.
“This pause can have minimal affect on Oklahoma’s vaccine effort,” mentioned Deputy Commissioner Reed. “Right now’s motion demonstrates the sensitivity of our monitoring system and our dedication to take any potential hostile response very severely. After the administration of tens of hundreds of thousands of doses throughout the nation, the Moderna and Pfizer vaccine have confirmed to be extraordinarily protected. We proceed to encourage all Oklahomans to get their shot to guard themselves and family members.”
Officers say after subsequent week’s allocation is available in, the state can have over 500,000 doses of Moderna and Pfizer vaccine accessible.
“We have now loads of the Pfizer and Moderna vaccine readily available to make sure that each Oklahoman who needs a vaccine can get one,” mentioned Deputy Commissioner Keith Reed. “Security of each Oklahoman is paramount, which is why we’re pausing Johnson & Johnson vaccine administration whereas that is studied additional. We have now no cause to consider any Oklahomans have been affected by this uncommon response, however will proceed to gather data and work carefully with our companions to make sure Oklahomans are protected.”
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