The most common side effects of ZOSTAVAX are:
- Redness, pain, itching, swelling, hard lump, warmth, or bruising where the shot was given
Additional side effects reported with ZOSTAVAX are:
- Allergic reactions, which may be serious and may include difficulty in breathing or swallowing
- Hives at the injection site
- Joint pain
- Muscle pain
- Rash at the injection site
- Swollen glands near the injection site (may last a few days to a few weeks)
You should tell your health care professional if you have any new or unusual symptoms after you receive ZOSTAVAX.
Still have questions about Shingles and ZOSTAVAX, the Shingles vaccine? Check out the Shingles FAQs.
ZOSTAVAX is a vaccine used for adults 50 years of age or older to prevent Shingles (also known as zoster).
Important Safety Information
- ZOSTAVAX does not protect everyone, so some people who get the vaccine may still get Shingles.
- You should not get ZOSTAVAX if you are allergic to any of its ingredients, including gelatin or neomycin, have a weakened immune system, take high doses of steroids, or are pregnant or plan to become pregnant. You should not get ZOSTAVAX to prevent chickenpox.
- Talk to your health care professional if you plan to get ZOSTAVAX (Zoster Vaccine Live) at the same time as PNEUMOVAX®23 (Pneumococcal Vaccine Polyvalent) because it may be better to get these vaccines at least 4 weeks apart.
- Possible side effects include redness, pain, itching, swelling, hard lump, warmth, or bruising at the injection site, as well as headache.
- ZOSTAVAX (Zoster Vaccine Live) contains a weakened chickenpox virus. Tell your health care professional if you will be in close contact with newborn infants, someone who may be pregnant and has not had chickenpox or been vaccinated against chickenpox, or someone who has problems with their immune system. Your health care professional can tell you what situations you may need to avoid.
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch, or call 1-800-FDA-1088.
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