FDA doesn't see increased risk of stroke for seniors who received Pfizer's omicron booster
- The FDA has not identified a stroke risk in seniors who received the Pfizer booster after reviewing multiple federal databases.
- The FDA also reached out to regulators in Europe and Israel, who did not report an increased risk of stroke.
- Preliminary CDC data indicated a possible stroke risk following simultaneous administration of the Pfizer Covid booster and the flu vaccine.
- FDA is launching a study to look into this possibility.
The Food and Drug Administration hasn't found an increased risk of stroke for seniors who've received Pfizer's omicron booster shot, a federal health official said Thursday.
The FDA launched an extensive review of federal data after investigators at the Centers for Disease Control and Prevention detected a possible risk of stroke for seniors who received Pfizer's booster.
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The CDC's Vaccine Safety Datalink, which monitors serious reactions to vaccines, showed a possible risk of stroke in late November. The FDA independently looked at data from the Centers for Medicare and Medicaid Services and its Vaccine Adverse Event Reporting System.
"So far the data that we have seen suggests the absence of a safety risk for the bivalent boosters in age 65 years and older," Richard Forshee, deputy director of the FDA's biostatistics office, told the agency's independent vaccine committee.
The FDA reviewed CMS data from 4.25 million seniors who received Pfizer's omicron booster and did not identify any increased stroke risk. The agency's review of VAERS data also did not find an increased risk.
The Department of Veterans Affairs has also conducted preliminary review of its database and did not identify an increased stroke risk, Forshee said. The FDA also reached out to international partners and Pfizer to find out what they observed in their data.
"We contacted a number of our international regulatory agencies, and various countries in Europe as well as Israel have indicated no increased risk of stroke on their surveillance systems," Forshee told the FDA committee.
"We also contacted Pfizer and they consulted their global safety database and they did not see any increase or a signal for ischemic stroke in their systems," Forshee added.
CDC investigators found that 130 seniors suffered strokes in the 21 days after receiving Pfizer's booster among about 550,000 recipients in the VSD database. One man in his 70s died a month after the stroke which was his likely cause of death, according to data presented Thursday.
Dr. Nicola Klein, the main investigator of the CDC's Vaccine Safety Datalink, said a statistical signal indicating a potential stroke risk was first identified in late November and has persisted through January, though the signal's strength has eased somewhat.
"I will say that in the data from just a couple days ago it has attenuated substantially and actually has not signaled this past week for the first time," Klein told the FDA panel of vaccine advisors.
However, the investigators ran small analysis that indicated seniors who received both the Pfizer omicron booster and a high-dose or adjuvanted flu vaccine on the same day may have a higher risk of stroke, though the data is preliminary.
Although the FDA has not identified a stroke risk, the agency is launching a study to examine potential safety concerns that may arise from administering the Covid omicron shots at the same time as the high-dose or adjuvant flu shots, Forshee said. The study will help the agency prepare for the vaccine campaign in the 2023-2024 respiratory virus season, he said.