Tips for Navigating COVID-19 in the Winter: Stay Vigilant. Stay Safe.
In a special video, Mass General's Rochelle Walensky, MD, MPH, addresses common questions about navigating COVID-19 during the winter months.
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Patient EducationJan | 14 | 2021
In December, the FDA approved two COVID vaccines (Pfizer/BioNTech and Moderna) for Emergency Use Authorization and they are now being distributed across the country. There have been a small number of allergic reactions reported upon initial rollout both in the United States and in the U.K. Aleena Banerji, MD, clinical director, Allergy and Clinical Immunology at Massachusetts General Hospital, Kim Blumenthal, MD, MSc, quality and safety officer for Allergy at Massachusetts General Hospital, Rebecca Saff, MD, PhD, training program director of Allergy and Clinical Immunology at Massachusetts General Hospital, and Anna Wolfson, MD, director of Quality Assurance and Improvement of Allergic and Clinical Immunology at Massachusetts General Hospital, and colleagues in the Allergy & Clinical Immunology departments at Mass General and Brigham and Women’s Hospital offer guidance and answers to common questions regarding these initial reports of allergic reaction.
On December 9, 2020, it was reported that two patients in the U.K. had an allergic reaction after getting the COVID-19 vaccine. As of December 28, 2020, at least 10 allergic reactions to the Pfizer/BioNTech and two allergic reactions to Moderna vaccines have been reported. Very little information about the cause of these reactions are known, but to date all patients have recovered. While we still need more information to understand the risk of allergic reactions to the COVID-19 vaccine, currently the concern is low due to the small number of reactions reported among the individuals who have been vaccinated.
In the vaccine trials, only patients with a history of severe adverse reaction associated with a vaccine or severe allergic reaction to any component of the vaccine were excluded.
We suggest allergy/immunology consultation if you have the following issues:
No, increased rates of reaction to the COVID-19 vaccine in patients with food, drug, latex venom allergy from the clinical trial data have not been reported. Patients with allergic conditions, such as food, drug, latex, venom or other allergic disorders, were not excluded. Patients with a history an anaphylaxis history of an unrelated medication or food are advised to be observed for 30 minutes after vaccination.
Polyethylene glycol (PEG) is a common, water-soluble ingredient in a wide variety of commercial products including some vaccines and more than 1,000 FDA approved medications. It is the primary ingredient in commonly used colonoscopy preparations (Golytely) or constipation treatment (Miralax) as well as in IV medications such as PEGylated medications. It is also in ultrasound gel and depot steroid injections such as methylprednisolone acetate. Reactions to PEG are rare but anaphylaxis has been reported. PEG is the main component allergists suspect may be causing the rare anaphylaxis cases to the Pfizer/BioNTech and Moderna vaccines.
Yes. In the U.S. the FDA reviews data from development of the vaccine and clinical trial data before approving the vaccine for use. Both vaccines that received Emergency Use Authorization from the FDA have been shown in clinical studies to be more than 94% effective. As people receive the vaccine, the FDA continues to closely monitor its safety and effectiveness.
Similar to medications or antibiotics, people can be allergic to vaccines. However, allergic reactions to vaccines are rare. Allergic reactions to vaccines most often start within minutes following the vaccination and are characterized by the same symptoms as allergic reactions to foods or medications. This can include skin symptoms (urticaria, swelling, itching), respiratory symptoms (cough, difficulty breathing, wheezing) or more severe symptoms like a reduction in blood pressure or anaphylaxis.
Sometimes vaccines can cause local reactions that begin in the hours following vaccination or even the next day. The site of vaccination (usually the arm) can become inflamed, red and painful. The reaction can last several days. Although these reactions can be quite worrisome, they are not felt to be an allergic reaction. There is generally no risk of an allergic reaction with any subsequent vaccinations people may receive. Consultation with an allergist is not necessary.
Different components of vaccines including gelatin, egg and excipients can cause vaccine allergy. Some people may be allergic to the rubber stopper on the vial or syringe rather than the vaccine itself. However, most manufacturers have moved away from latex rubber stoppers and now use synthetic rubber-like materials. Overall, allergic reactions to these components remain very rare.
If an allergic reaction occurs, depending on the symptoms that occur, a person can be treated immediately with antihistamines or epinephrine (if severe symptoms). It is important that the person suffering from the allergic reaction be referred to an allergist for further evaluation. Most of the time, allergy skin testing can confirm the allergy to the vaccine, and the resulting information can be very helpful for future vaccination. Testing in this case will include skin testing to the common inactive ingredients in the mRNA vaccines (PEG and polysorbates). In general, most patients allergic to one vaccine can receive other vaccinations without problems.
If you have an allergic reaction with the first dose, we suggest allergy evaluation before the second dose. If you have a large local reaction with symptoms of pain, burning or swelling at the site of injection, this usually does not require allergy evaluation before the second dose. Other reactions may require a longer observation period or skin testing assessment.
Local injection site pain, itching, redness and swelling can occur and is not felt to be an allergic reaction. Delayed reactions with pain, redness and swelling at the injection site have been seen up to 7 to 10 days after vaccination. These delayed reactions are also not allergic reactions and do not impact the ability of the patient to receive the second dose of vaccine. In fact, these delayed reactions are a sign that your immune system is working well.
Based on what we know so far from the clinical trial data and personal experience, most individuals will have mild, short-term side effects after getting a COVID-19 vaccine including fever, fatigue, headache, muscle pain and joint pain and this may be worse after the second dose. The current COVID-19 vaccines are different from other vaccinations with the need for a second dose within 3 to 4 weeks. We do not have data to answer this question yet but we are working to understand this exact issue. We hope to have more information as more individuals receive the second injection.
Acetaminophen, like Tylenol, and NSAIDs, like Ibuprofen, are very effective in managing post-vaccine adverse effects including fever, muscle aches and local injection site pain. However, there are data showing meloxicam can decrease antibody responses in mice. The CDC does not recommend pre-vaccine administration of acetaminophen or NSAIDs.
A full list of trials can be found on the National Institute of Allergy and Infectious Diseases website.
If you want to learn more about vaccines and the COVID-19 vaccine, Galit Alter, PhD, MGH Research Scholar at Mass General Research Institute offers additional information on the science behind vaccines in the videos below:
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In a special video, Mass General's Rochelle Walensky, MD, MPH, addresses common questions about navigating COVID-19 during the winter months.
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