Out of an abundance of caution, the CDC and FDA announced a recommendation [ncdhhs.us4.list-manage.com] to pause use of the Johnson & Johnson COVID-19 vaccine. Therefore, NCDHHS is following the recommendation of the CDC and FDA and has asked vaccinating providers to pause the administration of the J&J COVID-19 vaccine until we learn more.
These adverse events appear to be extremely rare. The vast majority of people who receive the J&J shot will only experience the expected temporary reactions like soreness of arm and feeling achy or tired for a day or two. Mild headaches and flu-like symptoms in the first few days after a vaccination can be expected and are not associated with this more severe concern. While it is extremely rare that someone would have a severe adverse reaction, people who have received the J&J vaccine and develop severe headache, abdominal pain, leg pain or shortness of breath within three weeks of their vaccination should contact their health care provider and mention they’ve received the J&J vaccine.
Specific instructions for providers who were planning to administer the Janssen (Johnson & Johnson) vaccine
The community event doses of Janssen (Johnson & Johnson) have already shipped/arrived for the week of April 12. When you receive the Janssen (Johnson & Johnson) vaccine, please immediately implement the following CDC operational guidance until further notice:
If you have any questions, please submit a ticket to the CVMS Help Desk Portal or call the COVID-19 Vaccine Provider Help Center at (877) 873-6247 and select option 1 for COVID-19 questions (Monday – Friday 7:00 AM – 7:00 PM ET and Saturday – Sunday 10:00 AM – 6:00 PM ET).