#childsafety | Johnson & Johnson COVID-19 Vaccine Side Effects: What to Know


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The J&J vaccine has mostly mild side effects that can be managed with rest or an over-the-counter pain reliever. Michael Ciaglo/Getty Images
  • The most common side effects seen with the J&J COVID-19 vaccine are pain at the injection site, headache, and flu-like symptoms.
  • There have been fewer cases of allergic reactions to the J&J vaccine compared with the Moderna-NIAID and Pfizer-BioNTech vaccines.
  • The FDA will continue to monitor the safety of the J&J vaccine as it’s rolled out to the American public.

In February 2021, the Food and Drug Administration (FDA) issued an emergency approval for the one-dose COVID-19 vaccine developed by Johnson & Johnson’s subsidiary company Janssen Biotech.

As with the two mRNA vaccines approved in December, the J&J vaccine has mostly mild side effects that can be managed with rest or an over-the-counter pain reliever.

So far, there have been fewer cases of allergic reactions to the J&J vaccine compared with the Moderna-NIAID and Pfizer-BioNTech vaccines, although J&J reported in February that two clinical trial participants had a severe allergic reaction after receiving its vaccine.

The FDA will continue to monitor the safety of the J&J vaccine as it’s rolled out to the American public.

Before the FDA issued the Emergency Use Authorization (EUA) for the J&J COVID-19 vaccine, scientists from the agency reviewed data from the company’s phase 3 clinical trials.

Dr. Bruce Y. Lee, executive director of Public Health Computational and Operations Research and professor of health policy and management at CUNY Graduate School of Public Health and Health Policy, says the side effects seen in those trials fall into two main categories.

“First are the injection site reactions. That’s usually pain, redness of the skin ,or swelling at the injection site,” he said.

“And then there are systemic side effects — flu-like symptoms such as fatigue, muscle aches, nausea, and potentially fever.”

Data from the clinical trials showed that around half of the people who received the vaccine had a local reaction. Pain at the injection site was the most commonly reported one, occurring in almost all cases.

Local side effects began on average 2 days after vaccination. Pain and redness lasted for 2 days on average and swelling for 3 days on average.

The onset and duration of local side effects varied, but less than 3 percent of people had side effects that lasted longer than 7 days.

Severe local side effects were uncommon, with less than 1 percent of people having severe pain. A small number of people had reddening of the skin near the injection site or swelling.

All of these local side effects were reported more often among people 18 to 59 years of age compared to those 60 years of age or older.

Systemic side effects occurred in about 55 percent of people who received the vaccine.

The most commonly reported ones were headache, fatigue, and muscle pain, and in smaller numbers of people, nausea and fever.

These began on average 2 days after vaccination. Fatigue, headache, and muscle ache lasted on average 2 days. Nausea and fever lasted on average 1 day.

The onset and duration of systemic side effects varied, although fewer than 2 percent of people experienced systemic side effects lasting longer than 7 days.

Less than 2 percent of the systemic side effects were severe, with the most common being fatigue, muscle pain, and fever.

All of the systemic side effects were reported more frequently among younger adults compared to older adults. The one exception was nausea, which occurred at about the same rate in both groups.

Around one-fifth of people reported using a medication to relieve their pain or fever within 1 week of their vaccination. This was more common among younger adults.

While it can be difficult to compare the efficacy of vaccines tested in different clinical trials under different conditions, Katelyn Jetelina, PhD, an assistant professor at University of Texas Health School of Public Health in Dallas, says side effects are easier to compare.

“Because the clinical trials were large and randomized,” she said, “we are confident that these side effects aren’t due to individual variation, but rather closer to the ‘true’ experience for vaccinated adults.”

The type of side effects seen with the J&J vaccine are in line with those experienced by people who received one of the mRNA vaccines.

However, “in the clinical trials [for the J&J vaccine], fewer people reported side effects, relative to Pfizer or Moderna, especially if we compare J&J to the second dose of Pfizer or Moderna,” Jetelina said.

Over 80 percent of people who received the Moderna-NIAID vaccine experienced local reactions after either dose. It was about the same for the Pfizer-BioNTech vaccine. This is higher than seen with the J&J vaccine.

For the Moderna-NIAID vaccine, about 55 percent of people experienced systemic reactions after the first dose — similar to the J&J vaccine — but 80 percent experienced them after the second dose.

The Pfizer-BioNTech vaccine also had a higher rate of systemic reactions than the J&J vaccine, especially after the second dose.

Lee says the stronger side effects after the second dose of the mRNA vaccines is “probably because your immune system is primed from receiving the first dose.”

Clinical trials provide important information about the safety of vaccines, but the federal government continues to monitor vaccines after they’re approved.

This includes monitoring vaccines through the V-safe smartphone app and the Vaccine Adverse Event Reporting System, both of which allow the general public to report side effects they experience after a vaccine.

“Any time you have an adverse event from a vaccine, it’s important to report it,” said Lee, “because we really want to see how the vaccine behaves in a broader population and over time.”



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