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The pause in April was a recommendation by the CDC and FDA “out of an abundance of caution.”

After initial reports that six women between the ages of 18 and 48 developed a rare blood clot within one to three weeks of vaccination, health authorities learned of nine additional cases in women and one in a man. Authorities reviewed the data and resumed the rollout of the J&J shot 10 days later, but with a warning added to its label about the risk for a rare blood-clotting disorder. “A review of all available data at this time shows that the J&J/Janssen COVID-19 Vaccine’s known and potential benefits outweigh its known and potential risks,” the CDC said in a statement.

“Pauses are common and allow health authorities to assess the situation and communicate with healthcare providers on recognizing symptoms and treating patients appropriately,” says Dr. Zucker. “A pause doesn’t mean that there isn’t an important role for this vaccine.”

If you’ve already gotten the J&J vaccine, don’t panic.

“The risk of these severe adverse events from the J&J vaccine remains extremely low. The risk of getting COVID-19 in the United States is higher,” says Dr. Zucker.

The CDC recommends contacting your healthcare provider and seeking medical treatment if you develop any of the following symptoms:

The J&J vaccine uses a different technology from the first two vaccines approved in the U.S.

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