During a system upgrade from Friday, Dec. 5, through Sunday, Dec. 7, the AAFP website, on-demand courses and CME purchases will be unavailable.

  • Birth Through Age 18 Immunization Schedule

    This version of the adult immunization schedule has been adopted by the American Academy of Family Physicians.

    The CDC's 2025 immunization schedules, which are not endorsed by the AAFP, can be found here.

    Schedule Based on Age Group

    Schedule Based on Medical Indication

    Notes

    Minimum age: 6 months

    Universal vaccination for ages 6-23 months; Risk-based single-dose for 2-18 years (with access upon request for families seeking protection

    Routine Vaccination

    Age 6 months–23 months

    • Unvaccinated (i.e., never received any COVID-19 vaccine doses)
      • 2 doses Moderna Spikevax 0, 4–8 weeks
    • Incomplete initial vaccination series:
      • 1 dose Moderna: complete initial series with 1 dose 4–8 weeks after most recent dose of Spikevax
      • 1 dose Pfizer-BioNTech: complete initial series with 2 doses Moderna Spikevax 8 weeks apart (administer dose 1 4–8 weeks after most recent dose)
      • 2 doses Pfizer-BioNTech: complete initial series with 1 dose Moderna Spikevax at least 8 weeks after the most recent dose
    • Completed initial vaccination series:
      • 1 dose Moderna Spikevax at least 8 weeks after the most recent dose

    Special situations

    Age 2–18 years in the following risk groups*: persons at high risk of severe COVID-19, residents of long-term care facilities or other congregate settings, persons who have never been vaccinated against COVID-19, persons whose household contacts are at high risk for severe COVID-19:

    • Ages 2–4 years: 1 dose of Moderna Spikevax regardless of previous vaccination status at least 8 weeks after the most recent dose
    • Ages 5-11 years: 1 dose of Moderna Spikevax or Pfizer-BioNTech Comirnaty regardless of previous vaccination status at least 8 weeks after the most recent dose
    • Ages 12–18 years:
      • 1 dose of Moderna Spikevax, Pfizer-BioNTech Comirnaty, or Novavax Nuvaxovid regardless of previous vaccination status at least 8 weeks after the most recent dose
      • 1 dose of Moderna mNexspike regardless of previous vaccination status at least 12 weeks after the last dose was received.

    Children 2 through 18 years of age not included in the risk groups above whose parent or guardian desires their protection from COVID-19 should be offered a single dose of age-appropriate COVID-19 vaccine.

    Use any available COVID-19 vaccine appropriate by age and health status that is approved by the FDA through a biologics license application. The most updated version of the COVID-19 vaccine that is available should be used. *Refer to the AAFPs 2025-26 COVID-19 Vaccinations Clinical Guidance for more information on risk groups, https://www.aafp.org/family-physician/patient-care/prevention-wellness/immunizations-vaccines.html.

    Persons who are moderately or severely immunocompromised. People eligible for additional doses include those who are receiving active cancer treatment for tumors or cancers of the blood, those who received an organ transplant and are taking medicine to suppress the immune system, those who received a hematopoietic cell transplant within the last 2 years or are taking medicine to suppress the immune system, those with moderate or severe primary immunodeficiency (such as DiGeorge syndrome, Wiskott-Aldrich syndrome), those with advanced or untreated HIV infection, and those with active treatment with high-dose corticosteroids or other drugs that may suppress an immune response. For revaccination guidance for children with hematologic malignancy post-hematopoietic cell transplant or CAR T-cell therapy, refer to: https://doi.org/10.1111/tid.14109.

    Age 6 months–4 years moderately or severely immunocompromised

    • Unvaccinated:
      • 4 doses (3-dose initial series Moderna Spikevax at 0, 4 weeks, and at least 4 weeks after dose 2, followed by 1 dose Moderna Spikevax 6 months later [minimum interval 2 months]). May administer additional doses.*
    • Incomplete initial 3-dose vaccination series:
      • Previous vaccination with Moderna
        • 1 dose Moderna: complete initial series with 2 doses Moderna Spikevax at least 4 weeks apart (administer dose 1 Moderna Spikevax 4 weeks after most recent dose), followed by 1 dose Moderna Spikevax 6 months later (minimum interval 2 months). May administer additional doses of Moderna Spikevax.**
        • 2 doses Moderna: complete initial series with 1 dose Moderna Spikevax at least 4 weeks after most recent dose, followed by 1 dose Moderna Spikevax 6 months later (minimum interval 2 months). May administer additional doses of Moderna Spikevax.*
      • Previous vaccination with Pfizer-BioNTech
        • 1 dose Pfizer-BioNTech: complete initial series with 2 doses Moderna Spikevax at least 8 weeks apart (administer dose 1 Moderna Spikevax 4 weeks after most recent dose), followed by 1 dose Moderna Spikevax 6 months later (minimum interval 2 months). May administer additional doses of Moderna Spikevax.*
        • 2 doses Pfizer-BioNTech: complete initial series with 1 dose Moderna Spikevax at least 8 weeks after most recent dose, followed by 1 dose Moderna Spikevax 6 months later (minimum interval 2 months).
      • Previously completed initial 3-dose vaccination series with:
        • 3 or more doses Moderna: 2 doses Moderna Spikevax 6 months apart (minimum interval 2 months). Administer dose 1 at least 8 weeks after the most recent dose. May administer additional doses of Moderna Spikevax.*
        • 3 or more doses Pfizer-BioNTech: 2 doses Moderna Spikevax 6 months apart (minimum interval 2 months). Administer dose 1 at least 8 weeks after the most recent dose. May administer additional doses of Moderna Spikevax.*

    Age 5–11 years moderately or severely immunocompromised

    Use vaccine from the same manufacturer for all doses in the initial vaccination series.

    • Unvaccinated:
      • 4 doses (3-dose initial series Moderna Spikevax at 0, 4 weeks, and at least 4 weeks after dose 2, followed by 1 dose Moderna Spikevax or Pfizer-BioNTech 6 months later [minimum interval 2 months]). May administer additional doses.*
      • 4 doses (3-dose initial series Pfizer-BioNTech at 0, 3 weeks, and at least 4 weeks after dose 2, followed by 1 dose Moderna Spikevax or Pfizer-BioNTech 6 months later [minimum interval 2 months]). May administer additional doses.*
    • Incomplete initial 3-dose vaccination series:
    • Previous vaccination with Moderna
      • 1 dose Moderna Spikevax: complete initial series with 2 doses Moderna a Spikevax t least 4 weeks apart (administer dose 1 Moderna Spikevax 4 weeks after most recent dose), followed by 1 dose Moderna Spikevax or Pfizer-BioNTech 6 months later (minimum interval 2 months). May administer additional doses of Moderna Spikevax or Pfizer-BioNTech.*
      • 2 doses Moderna Spikevax: complete initial series with 1 dose Moderna Spikevax at least 4 weeks after most recent dose, followed by 1 dose Moderna Spikevax or Pfizer BioNTech 6 months later (minimum interval 2 months). May administer additional doses of Moderna Spikevax or Pfizer-BioNTech.*
    • Previous vaccination with Pfizer-BioNTech
      • 1 dose Pfizer-BioNTech: complete initial series with 2 doses Pfizer-BioNTech at least 4 weeks apart (administer dose 1 Pfizer-BioNTech 3 weeks after most recent dose), followed by 1 dose Moderna Spikevax or Pfizer-BioNTech 6 months later (minimum interval 2 months). May administer additional doses of Moderna or PfizerBioNTech.*
      • 2 doses Pfizer-BioNTech: complete initial series with 1 dose Pfizer-BioNTech at least 4 weeks after most recent dose, followed by 1 dose Moderna Spikevax or Pfizer-BioNTech 6 months later (minimum interval 2 months). May administer additional doses of Moderna Spikevax or Pfizer-BioNTech.*
    • Completed initial 3-dose vaccination series with: 
      • 3 or more doses Moderna or 3 or more doses PfizerBioNTech: 2 doses Moderna or Pfizer-BioNTech 6 months apart (minimum interval 2 months). Administer dose 1 at least 8 weeks after the most recent dose. May administer additional doses of Moderna or Pfizer-BioNTech.*

    Age 12–18 years moderately or severely immunocompromised

    Use vaccine from the same manufacturer for all doses in the initial vaccination series. Either Moderna product (Spikevax or mNEXSPIKE) can be used unless otherwise specified.

    • Unvaccinated:
      • 4 doses (3-dose initial series Moderna at 0, 4 weeks, and at least 4 weeks after dose 2, followed by 1 dose Moderna or Novavax or Pfizer-BioNTech 6 months later [minimum interval 2 months]). May administer additional doses of Moderna or Novavax or Pfizer-BioNTech.*
      • 4 doses (3-dose initial series Pfizer-BioNTech at 0, 3 weeks, and at least 4 weeks after dose 2, followed by 1 dose Moderna or Novavax or Pfizer-BioNTech 6 months later [minimum interval 2 months]). May administer additional doses of Moderna or Novavax or Pfizer-BioNTech.*
      • 3 doses (2-dose initial series Novavax at 0, 3 weeks, followed by 1 dose Moderna or Novavax or Pfizer-BioNTech 6 months later [minimum interval 2 months]). May administer additional doses of Moderna or Novavax or Pfizer-BioNTech.*
    • Incomplete initial vaccination series:
      • Previous vaccination with Moderna
        • 1 dose Moderna: complete initial series with 2 doses Moderna at least 4 weeks apart (administer dose 1 Moderna 4 weeks after most recent dose), followed by 1 dose Moderna or Novavax or Pfizer-BioNTech 6 months later (minimum interval 2 months). May administer additional doses of Moderna or Novavax or PfizerBioNTech.*
        • 2 doses Moderna: complete initial series with 1 dose Moderna at least 4 weeks after most recent dose, followed by 1 dose Moderna or Novavax or Pfizer-BioNTech 6 months later (minimum interval 2 months). May administer additional doses of Moderna or Novavax or Pfizer-BioNTech.*
      • Previous vaccination with Pfizer-BioNTech
        • 1 dose Pfizer-BioNTech: complete initial series with 2 doses Pfizer-BioNTech at least 4 weeks apart (administer dose 1 Pfizer-BioNTech 3 weeks after most recent dose), followed by 1 dose Moderna or Novavax or PfizerBioNTech 6 months later (minimum interval 2 months). May administer additional doses of Moderna or Novavax or Pfizer-BioNTech.*
        • 2 doses Pfizer-BioNTech: complete initial series with 1 dose Pfizer-BioNTech at least 4 weeks after most recent dose, followed by 1 dose Moderna or Novavax or Pfizer-BioNTech 6 months later (minimum interval 2 months). May administer additional doses of Moderna or Novavax or Pfizer-BioNTech.*
      • Previous vaccination with Novavax
        • 1 dose Novavax: complete initial series with 1 dose Novavax at least 3 weeks after most recent dose, followed by 1 dose Moderna or Novavax or Pfizer-BioNTech 6 months later (minimum interval 2 months). May administer additional doses of Moderna or Novavax or Pfizer-BioNTech.*
      • Completed initial 3-dose vaccination series with:
        • 3 or more doses Moderna or 3 or more doses PfizerBioNTech: 2 doses Moderna or Novavax or Pfizer-BioNTech 6 months apart (minimum interval 2 months). Administer dose 1 at least 8 weeks after the most recent dose. May administer additional doses of Moderna or Novavax or Pfizer-BioNTech.*
        • 2 or more doses Novavax: 2 doses Moderna or Novavax or Pfizer-BioNTech 6 months apart (minimum interval 2 months). Administer dose 1 at least 8 weeks after the most recent dose. May administer additional doses of Moderna or Novavax or Pfizer-BioNTech.*

    *Additional doses of COVID-19 vaccine for moderately or severely immunocompromised: based on shared clinical decision making and administered at least 2 months after the most recent dose.

    Minimum Age: 9 years 

    Routine Vaccination

    • Age 9-16 years living in areas with endemic dengue AND have laboratory confirmation of previous dengue infection
      • 3-dose series administered at 0, 6, and 12 months
    • Endemic areas include Puerto Rico, American Samoa, US Virgin Islands, Federated States of Micronesia, Republic of Marshall Islands, and the Republic of Palau.
    • Dengue vaccine should not be administered to children traveling to or visiting endemic dengue areas.

    Minimum Age: 6 weeks [4 years for Kinrix or Quadracel]

    Routine vaccination

    5-dose series (3-dose primary series at age 2, 4, and 6 months, followed by booster doses at ages 15–18 months and 4–6 years

    • Prospectively: Dose 4 may be administered as early as age 12 months if at least 6 months have elapsed since dose 3.
    • Retrospectively: A 4th dose that was inadvertently administered as early as age 12 months may be counted if at least 4 months have elapsed since dose 3.

    Catch-up vaccination

    • Dose 5 is not necessary if dose 4 was administered at age 4 years or older and at least 6 months after dose 3.
    • For other catch-up guidance, see Catch Up Schedule

    Special Situations

    • Children younger than age 7 years with a contraindication specific to the pertussis component of DTaP: May administer Td for all recommended remaining doses in place of DTaP. Encephalopathy within 7 days of vaccination when not attributable to another identifiable cause is the only contraindication specific to the pertussis component of DTaP. For additional information, see www.cdc.gov/pertussis/hcp/vaccine-recommendations/td-offlabel.html.
    • Wound management in children younger than age 7 years with history of 3 or more doses of tetanus-toxoid containing vaccine: For all wounds except clean and minor wounds, administer DTaP if more than 5 years since last dose of tetanus-toxoid-containing vaccine. For detailed information, see www.cdc.gov/mmwr/volumes/67/rr/rr6702a1.htm.

    Minimum Age: 6 weeks

    Routine vaccination

    • ActHIB, Hiberix, Pentacel, or Vaxelis: 4-dose series (3-dose primary series at age 2, 4, and 6 months, followed by a booster dose* at age 12–15 months)
      • *Vaxelis is not recommended for use as a booster dose. A different Hib-containing vaccine should be used for the booster dose.
    • PedvaxHIB: 3-dose series (2-dose primary series at age 2 and 4 months, followed by a booster dose at age 12–15months)

    Catch-up Vaccination

    • Dose 1 at age 7–11 months: Administer dose 2 at least 4 weeks later and dose 3 (final dose) at age 12–15 months or 8 weeks after dose 2 (whichever is later).
    • Dose 1 at age 12–14 months: Administer dose 2 (final dose) at least 8 weeks after dose 1.
    • Dose 1 before age 12 months and dose 2 before age15 months: Administer dose 3 (final dose) at least 8 weeks after dose 2.
    • 2 doses of PedvaxHIB before age 12 months: Administer dose 3 (final dose) at age 12–59 months and at least 8 weeks after dose 2.
    • 1 dose administered at age 15 months or older: No further doses needed
    • Unvaccinated at age 15–59 months: Administer 1 dose
    • Previously unvaccinated children age 60 months or older who are not considered high risk: Do not require catch-up vaccination
    • For other catch-up guidance, see Catch Up Schedule. Vaxelis can be used for catch-up vaccination in children less than age 5 years. Follow the catch-up schedule even if Vaxelis is used for one or more doses. For detailed information on use of Vaxelis® see www.cdc.gov/mmwr/volumes/69/wr/mm6905a5.htm.

    Special Situations

    • Chemotherapy or radiation treatment:
      • Unvaccinated or only 1 dose before age 12 months: 2 doses, 8 weeks apart
      • 2 or more doses before age 12 months: 1 dose at least 8 weeks after previous dose

    Doses administered within 14 days of starting therapy or during therapy should be repeated at least 3 months after therapy completion.

    Age 12–59 months

    • Hematopoietic stem cell transplant (HSCT):
      • 3-dose series 4 weeks apart starting 6 to 12 months after successful transplant, regardless of Hib vaccination history
    • Anatomic or functional asplenia (including sickle cell disease):
      • Unvaccinated or only 1 dose before age 12 months: 2 doses, 8 weeks apart
      • 2 or more doses before age 12 months:1 dose at least 8 weeks after previous dose

    Persons age 5 years or older

    • Unvaccinated*
      • 1 dose

    Persons age 15 months or older

    • Elective splenectomy:
      • Unvaccinated*
        • 1 dose (preferably at least 14 days before procedure)
    • HIV infection:
      • Unvaccinated or only 1 dose before age 12 months: 2 doses, 8 weeks apart
      • 2 or more doses before age 12 months:1 dose at least 8 weeks after previous dose

    Persons age 5–18 years

    • Unvaccinated*
      • 1 dose
    • Immunoglobulin deficiency, early component complement deficiency:
      • Unvaccinated or only 1 dose before age 12 months: 2 doses, 8 weeks apart
      • 2 or more doses before age 12 months: 1 dose at least 8 weeks after previous dose

    *Unvaccinated = Less than routine series (through age 14 months) OR no doses (age 15 months or older)

    Minimum age: 12 months for routine vaccination

    Routine vaccination

    2-dose series (minimum interval: 6 months) at age 12–23 months

    Catch-up vaccination

    • Unvaccinated persons through age 18 years should complete a 2-dose series (minimum interval: 6 months).
    • Persons who previously received 1 dose at age 12 months or older should receive dose 2 at least 6 months after dose 1.
    • Adolescents age 18 years or older may receive HepA-HepB (Twinrix) as a 3-dose series (0, 1, and 6 months) or 4-dose series (3 doses at 0, 7, and 21–30 days, followed by a booster dose at 12 months).

    International travel

    • Persons traveling to or working in countries with high or intermediate endemic hepatitis A (www.cdc.gov/travel/):
      • Infants age 6–11 months: 1 dose before departure; revaccinate with 2 doses (separated by at least 6 months) between age 12–23 months.
      • Unvaccinated age 12 months or older: Administer dose 1 as soon as travel is considered.

    Minimum age: birth

    Routine Vaccination

    • Mother is HBsAg-negative
      • 3-dose series at age 0, 1–2, 6–18 months (use monovalent HepB vaccine for doses administered before age 6 weeks)
        • Birth weight ≥2,000 grams: 1 dose within 24 hours of birth if medically stable
        • Birth weight <2,000 grams: 1 dose at chronological age 1 month or hospital discharge (whichever is earlier and even if weight is still <2,000 grams
      • Infants who did not receive a birth dose should begin the series as soon as possible (see Table 2 for minimum intervals).
      • Administration of 4 doses is permitted when a combination vaccine containing HepB is used after the birth dose.
      • Minimum intervals (see Table 2): when 4 doses are administered, substitute “dose 4” for “dose 3” in these calculations.
      • Final (3rd or 4th) dose: age 6–18 months (minimum age 24 weeks)
    • Mother is HBsAg-positive
      • Birth dose (monovalent HepB vaccine only): administer HepB vaccine and hepatitis B immune globulin (HBIG) (in separate limbs) within 12 hours of birth, regardless of birth weight.
      • Birth weight <2000 grams: administer 3 additional dosesof HepB vaccine beginning at age 1 month (total of 4 doses).
      • Final (3rd or 4th) dose: administer at age 6 months (minimum age 24 weeks)
      • Test for HBsAg and anti-HBs at age 9–12 months. If HepB series is delayed, test 1–2 months after final dose. Do not test before age 9 months.
    • Mother is HBsAg-unknown If other evidence suggestive of maternal hepatitis B infection exists (e.g., presence of HBV DNA, HBeAg-positive, or mother known to have chronic hepatitis B infection), manage infant as if mother is HBsAg-positive.
      • Birth dose (monovalent HepB vaccine only):
        • Birth weight ≥2,000 grams: administer HepB vaccine within 12 hours of birth. Determine mother’s HBsAg status as soon as possible. If mother is determined to be HBsAg-positive, administer HBIG as soon as possible (in separatelimb), but no later than 7 days of age.
        • Birth weight <2,000 grams: administer HepB vaccine and HBIG (in separate limbs) within 12 hours of birth. Administer 3 additional doses of HepB vaccine beginning at age 1 month (total of 4 doses).
      • Final (3rd or 4th) dose: administer at age 6 months (minimum age 24 weeks)
      • If mother is determined to be HBsAg-positive or if status remains unknown, test for HBsAg and anti-HBs at age 9–12 months. If HepB series is delayed, test 1–2 months after final dose. Do not test before age 9 months.

    Catch-up Vaccination

    • Unvaccinated persons should complete a 3-dose series at 0, 1–2, 6 months. See Catch Up Schedule for minimum intervals.
    • Adolescents age 11–15 years may use an alternative 2-dose schedule with at least 4 months between doses (adult formulation Recombivax HB only).
    • Adolescents age 18 years may receive:
      • Heplisav-B: 2-dose series at least 4 weeks apart
      • PreHevbrio: 3-dose series at 0, 1, and 6 months
      • HepA-HepB (Twinrix): 3-dose series (0, 1, and 6 months) or 4-dose series (3 doses at 0, 7, and 21–30 days, followed by a booster dose at 12 months).

    Special Situations

    Revaccination is not generally recommended for persons with a normal immune status who were vaccinated as infants, children, adolescents, or adults.

    Post-vaccination serology testing and revaccination (if anti-HBs <10mlU/mL) is recommended for certain populations, including:

    • Infants born to HBsAg-positive mothers
    • Persons who are predialysis or on maintenance dialysis
    • Other immunocompromised persons
    • For detailed revaccination recommendations, see www.cdc.gov/vaccines/hcp/acip-recs/vacc-specific/hepb.html.

    Note: PreHevbrio is not recommended in pregnancy due to lack of safety data in pregnant persons.

    Minimum Age: 9 years

    Routine and catch-up vaccination

    HPV vaccination routinely recommended at age 11–12 years (can start at age 9 years) and catch-up HPV vaccination recommended for all persons through age 18 years if not adequately vaccinated

    • 2- or 3-dose series depending on age at initial vaccination:
      • Age 9–14 years at initial vaccination: 2-dose series at 0, 6–12 months (minimum interval: 5 months; repeat dose if administered too soon)
      • Age 15 years or older at initial vaccination: 3-dose series at 0, 1–2 months, 6 months (minimum intervals: dose 1 to dose 2: 4 weeks / dose 2 to dose 3: 12 weeks / dose 1 to dose3: 5 months; repeat dose if administered too soon)
    • No additional dose recommended when any HPV vaccine series of any valency has been completed using recommended dosing intervals.

    Special situations

    • Immunocompromising conditions, including HIV infection: 3-dose series, even for those who initiate vaccination at age 9 through 14 years.
    • History of sexual abuse or assault: Start at age 9 years
    • Pregnancy: Pregnancy testing not needed before vaccination; HPV vaccination not recommended until after pregnancy; no intervention needed if vaccinated while pregnant.

    Minimum Age:

    • 6 months [IIV3],
    • 2 years [LAIV3]
    • 9 years [recombinant influenza vaccine, Flublok RIV3]

    Routine Vaccination

    • Use any influenza vaccine appropriate for age and health status annually. All marketed U.S. vaccines are trivalent this season (2025-26).
      • Age 6 months–8 years who have received fewer than 2 influenza vaccine doses before July 1, or whose influenza vaccination history is unknown: 2 doses, separated by at least 4 weeks. Administer dose 2 even if the child turns 9 years between receipt of dose 1 and dose 2.
      • Age 6 months–8 years who have received at least 2 influenza vaccine doses before July 1: 1 dose
      • Age 9 years or older: 1 dose
      • Age 18 years solid organ transplant recipients receiving immunosuppressive medications: high-dose inactivated (HD-IIV3) and adjuvanted inactivated (aIIV3) influenza vaccines are acceptable options. No preference over other age-appropriate IIV3 or RIV3.
    • For the 2025-2026 season, see www.cdc.gov/mmwr/volumes/74/wr/mm7432a2.htm.

    Special Situations

    Close contacts (e.g., household contacts) of severely immunosuppressed persons who require a protected environment: should not receive LAIV3. If LAIV3 is given, they should avoid contact with or caring for such immunosuppressed persons for 7 days after vaccination.

    Note: Persons with an egg allergy can receive any influenza vaccine (egg-based and non-egg-based) appropriate for age and health status.

    Minimum Age: 12 Months for routine vaccination
    Routine
    Vaccination

    • 2-dose series at age 12–15 months, age 4–6 years
    • MMR or MMRV* may be administered

    Note: For dose 1 in children age 12–47 months, it is recommended to administer MMR and varicella vaccines separately. MMRV may be used if parents or caregivers express a preference.

    Catch-up Vaccination

    • Unvaccinated children and adolescents: 2-dose series at least 4 weeks apart
    • The maximum age for use of MMRV* is 12 years.
    • Minimum interval between MMRV* doses: 3 month

    Special Situations

    • International travel
      • Infants age 6–11 months: 1 dose before departure; revaccinate with 2-dose series at age 12–15 months (12 months for children in high-risk areas) and dose 2 as early as 4 weeks later.
      • - Unvaccinated children age 12 months or older: 2-dose series at least 4 weeks apart before departure

    In mumps outbreak settings, for information about additional doses of MMR (including 3rd dose of MMR), see www.cdc.gov/mmwr/volumes/67/wr/mm6701a7.htm

    *Note: If MMRV is used, the minimum interval between MMRV doses is 3 months.

    Minimum Age:

    • 2 months [MenACWY-CRM, Menveo]
    • 2 years [MenACWY-TT, MenQuadfi],
    • 10 years [MenACWY-TT/MenB-FHbp, Penbraya]

    Routine Vaccination

    2-dose series at age 11–12 years; 16 years

    Catch-up Vaccination

    • Age 13–15 years: 1 dose now and booster at age 16–18 years (minimum interval: 8 weeks)
    • Age 16–18 years: 1 dose

    Special situations

    Anatomic or functional asplenia (including sickle cell disease), HIV infection, persistent complement component deficiency, complement inhibitor (e.g., eculizumab, ravulizumab) use:

    • Menveo*
      • Dose 1 at age 2 months: 4-dose series (additional 3 doses at age 4, 6, and 12 months)
      • Dose 1 at age 3–6 months: 3- or 4-dose series (dose 2 [and dose 3 if applicable] at least 8 weeks after previous dose until a dose is received at age 7 months or older, followed by an additional dose at least 12 weeks later and after age 12 months)
      • Dose 1 at age 7–23 months: 2-dose series (dose 2 at least 12 weeks after dose 1 and after age 12 months)
      • Dose 1 at age 24 months or older: 2-dose series at least 8 weeks apart
    • MenQuadfi
      • Dose 1 at age 24 months or older: 2-dose series at least 8 weeks apart

    Travel to countries with hyperendemic or epidemic meningococcal disease, including countries in the African meningitis belt or during the Hajj:

    • Children less than age 24 months:
      • Menveo* (age 2-23 months)
        • Dose 1 at age 2 months: 4-dose series (additional 3 doses at age 4, 6, and 12 months)
        • Dose 1 at age 3–6 months: 3- or 4-dose series (dose 2 [and dose 3 if applicable] at least 8 weeks after previous dose until a dose is received at age 7 months or older, followed by an additional dose at least 12 weeks later and after age 12 months)
        • Dose 1 at age 7–23 months: 2-dose series (dose 2 at least 12 weeks after dose 1 and after age 12 months)

    Children age 2 years or older: 1 dose Menveo* or MenQuadfi

    First-year college students who live in residential housing (if not previously vaccinated at age 16 years or older) or military recruits:

    • 1 dose Menveo* or MenQuadfi®

    Adolescent vaccination of children who received MenACWY prior to age 10 years:

    • Children for whom boosters are recommended because of an ongoing increased risk of meningococcal disease (e.g., those with complement component deficiency, HIV, or asplenia): Follow the booster schedule for persons at increased risk.
    • Children for whom boosters are not recommended (e.g., a healthy child who received a single dose for travel to a country where meningococcal disease is endemic): Administer MenACWY according to the recommended adolescent schedule with dose 1 at age 11–12 years and dose 2 at age 16 years.

    *Menveo has two formulations: lyophilized and liquid. The liquid formulation should not be used before age 10 years. See www.cdc.gov/vaccines/vpd/mening/downloads/menveo-single-vial-presentation.pdf.

    Note: For MenACWY booster dose recommendations for groups listed under “Special situations” and in an outbreak setting and additional meningococcal vaccination information, see www.cdc.gov/mmwr/volumes/69/rr/rr6909a1.htm.

    Children age 10 years or older may receive a single dose of Penbraya as an alternative to separate administration of MenACWY and MenB when both vaccines would be given on the same clinic day and a single injection with Penbraya is preferred (see “Meningococcal serogroup B vaccination” section below for more information).

    Minimum Age: 10 years [MenB-4C, Bexsero; MenBF-Hbp, Trumenba; MenACWY-TT/MenB-FHbp, Penbraya])

    Shared clinical decision-making

    Adolescents not at increased risk age 16–23 years (preferred age 16–18 years)* based on shared clinical decision-making.

    • Bexsero or Trumenba (use same brand for all doses): 2-dose series at least 6 months apart (if dose 2 is administered earlier than 6 months, administer dose 3 at least 4 months after dose 2)
    • To optimize rapid protection (e.g., for students starting college in less than 6 months), a 3-dose series (0, 1–2, 6 months) may be administered.

    For additional information on shared clinical decision-making for MenB, see www.cdc.gov/vaccines/media/pdfs/2025/03/2024-isd-job-aid-scdm-menb-508-remediated.pdf

    Special situations

    Anatomic or functional asplenia (including sickle cell disease), persistent complement component deficiency, complement inhibitor (e.g., eculizumab, ravulizumab) use:

    • Bexsero or Trumenba (use same brand for all doses including booster doses): 3-dose series at 0, 1–2, 6 months (if dose 2 was administered at least 6 months after dose 1, dose 3 not needed; if dose 3 is administered earlier than 4 months after dose 2, a 4th dose should be administered at least 4 months after dose 3)

    For MenB booster dose recommendations for groups listed under “Special situations” and in an outbreak setting and additional meningococcal vaccination information, see www.cdc.gov/mmwr/volumes/69/rr/rr6909a1.htm.

    Note: MenB vaccines may be administered simultaneously with MenACWY vaccines if indicated, but at a different anatomic site, if feasible.

    Children age 10 years or older may receive a dose of Penbraya (MenACWY–TT/MenB–FHbp) as an alternative to separate administration of MenACWY and MenB when both vaccines would be given on the same clinic day. For age-eligible children not at increased risk, if Penbraya is used for dose 1 MenB, MenB-FHbp (Trumenba) should be administered for dose 2 MenB. For age-eligible children at increased risk of meningococcal disease, Penbraya may be used for additional MenACWY and MenB doses (including booster doses) if both would be given on the same clinic day and at least 6 months have elapsed since most recent Penbraya dose.

    Minimum Age: 18 years

    Special Situations

    • Age 18 years and at risk for mpox infection: complete 2-dose series, 28 days apart.
      • Persons who are gay, bisexual, and other MSM, transgender or nonbinary people who in the past 6 months have had:
        • A new diagnosis of at least 1 sexually transmitted disease
        • More than 1 sex partner
        • Sex at a commercial sex venue
        • Sex in association with a large public event in a geographic area where mpox transmission is occurring
      • Persons who are sexual partners of the persons described above
      • Persons who anticipate experiencing any of the situations described above
    • Pregnancy: There is currently no ACIP recommendation for Jynneos use in pregnancy due to lack of safety data in pregnant persons. Pregnant persons with any risk factor described above may receive Jynneos.

    For detailed information, visit https://publications.aap.org/ redbook/book/755/chapter/14079669/Mpox

    Minimum Age:

    • 6 weeks [PCV15], [PCV 20]

    • 2 years [PPSV23])

    Routine Vaccination with PCV

    4-dose series at 2, 4, 6, 12-15 months

    Catch-up vaccination

    • Healthy children ages 2-4 years with any incomplete* PCV series: 1 dose PCV
    • For other catch-up guidance, see Catch-up Schedule.

    Note: For children without risk conditions, PCV20 is not indicated if they have received 4 doses of PCV13 or PCV15 or another age appropriate complete PCV series.

    Special situations

    Children and adolescents with cerebrospinal fluid leak; chronic heart disease; chronic kidney disease (excluding maintenance dialysis and nephrotic syndrome); chronic liver disease; chronic lung disease (including moderate persistent or severe persistent asthma); cochlear implant; or diabetes mellitus:

    Age 2-5 years

    • Any incomplete* PCV series with:
      • 3 PCV doses: 1 dose PCV (at least 8 weeks after the most recent PCV dose)
      • Less than 3 PCV doses: 2 doses PCV (at least 8 weeks after the most recent dose and administered at least 8 weeks apart)
    • Completed recommended PCV series but have not received PPSV23
      • Previously received at least 1 dose of PCV20: no further PCV or PPSV23 doses needed
      • Not previously received PCV20: administer 1 dose PCV20 OR 1 dose PPSV23 at least 8 weeks after the most recent PCV dose.

    Age 6–18 years

    • Not previously received any dose of PCV13, PCV15, or PCV20: administer 1 dose of PCV15 or PCV20. If PCV15 is used and no previous receipt of PPSV23, administer 1 dose of PPSV23 at least 8 weeks after the PCV15 dose.**
    • Received PCV before age 6 years but have not received PPSV23
      • Not previously received PCV20: administer 1 dose PCV20 OR 1 dose PPSV23 at least 8 weeks after the most recent PCV dose.
    • Received PCV13 only at or after age 6 years: administer 1 dose PCV20 OR 1 dose PPSV23 at least 8 weeks after the most recent PCV13 dose
    • Received 1 dose PCV13 and 1 dose PPSV23 at or after age 6 years: no further doses of any PCV or PPSV23 indicated.

    Children and adolescents on maintenance dialysis, or with immunocompromising conditions such as nephrotic syndrome; congenital or acquired asplenia or splenic dysfunction; congenital or acquired immunodeficiencies; diseases and conditions treated with immunosuppressive drugs or radiation therapy, including malignant neoplasms, leukemias, lymphomas, Hodgkin disease, and solid organ transplant; HIV infection; or sickle cell disease or other hemoglobinopathies:

    Age 2–5 years

    • Any incomplete* PCV series:
      • 3 PCV doses: 1 dose PCV (at least 8 weeks after the most recent PCV dose)
      • Less than 3 PCV doses: 2 doses PCV (at least 8 weeks after the most recent dose and administered at least 8 weeks apart)
    • Completed recommended PCV series but have not received PPSV23
      • Previously received at least 1 dose of PCV20: no further PCV or PPSV23 doses needed
      • Not previously received PCV20: administer 1 dose PCV20 OR 1 dose PPSV23 at least 8 weeks after the most recent PCV dose. If PPSV23 is used, administer 1 dose of PCV20 or dose 2 PPSV23 at least 5 years after dose 1 PPSV23.

    Age 6–18 years

    • Not previously received any dose of PCV13, PCV15, or PCV20: administer 1 dose of PCV15 or 1 dose of PCV20. If PCV15 is used and no previous receipt of PPSV23, administer 1 dose of PPSV23 at least 8 weeks after the PCV15 dose.**
    • Received PCV before age 6 years but have not received PPSV23
      • Previously received at least 1 dose of PCV20: no additional dose of PCV or PPSV23
      • Not previously received PCV20: administer 1 dose PCV20 OR 1 dose PPSV23 at least 8 weeks after the most recent PCV dose. If PPSV23 is used, administer either PCV20 or dose 2 PPSV23 at least 5 years after dose 1 PPSV23.
    • Received PCV13 only at or after age 6 years: administer 1 dose PCV20 OR 1 dose PPSV23 at least 8 weeks after the most recent PCV13 dose. If PPSV23 is used, administer 1 dose of PCV20 or dose 2 PPSV23 at least 5 years after dose 1 PPSV23.
    • Received 1 dose PCV13 and 1 dose PPSV23 at or after age 6 years: administer 1 dose PCV20 OR 1 dose PPSV23 at least 8 weeks after the most recent PCV13 dose and at least 5 years after dose 1 PPSV23.
    • Pregnancy: no recommendation for PCV or PPSV23 due to limited data. Summary of existing data on pneumococcal vaccination during pregnancy can be found at www.cdc.gov/mmwr/volumes/72/rr/rr7203a1.htm

    For guidance on determining which pneumococcal vaccines a patient needs and when, please refer to the mobile app, which can be downloaded here: www.cdc.gov/pneumococcal/hcp/vaccine-recommendations/app.html

    *Incomplete series = Not having received all doses in either the recommended series or an age-appropriate catch-up series. See Table 2 in ACIP pneumococcal recommendations at stacks.cdc.gov/view/cdc/133252

    **When both PCV15 and PPSV23 are indicated, administer all doses of PCV15 first. PCV15 and PPSV23 should not be administered during the same visit.

    Minimum Age: 6 weeks

    Routine Vaccination

    • 4-dose series at ages 2, 4, 6-18 months, 4-6 years; administer the final dose on or after age 4 years and at least 6 months after the previous dose.
    • 4 or more doses of IPV can be administered before age 4 years when a combination vaccine containing IPV is used. However, a dose is still recommended on or after age 4 years and at least 6 months after the previous dose.

    Catch-up Vaccination

    In the first 6 months of life, use minimum ages and intervals only for travel to a polio-endemic region or during an outbreak.

    Adolescents age 18 years known or suspected to be unvaccinated or incompletely vaccinated: administer remaining doses (1, 2, or 3 IPV doses) to complete a 3-dose primary series.* Unless there are specific reasons to believe they were not vaccinated, most persons aged 18 years or older born and raised in the United States can assume they were vaccinated against polio as children.

    Series containing oral poliovirus vaccine (OPV), either mixed OPV-IPV or OPV-only series:

    • Total number of doses needed to complete the series is the same as that recommended for the U.S. IPV schedule. See www.cdc.gov/mmwr/volumes/66/wr/mm6601a6.htm?s_%20cid=mm6601a6_w.
    • Only trivalent OPV (tOPV) counts toward the U.S. vaccination requirements.
      • Doses of OPV administered before April 1, 2016, should be counted (unless specifically noted as administered during a campaign).
      • Doses of OPV administered on or after April 1, 2016, should not be counted.
      • For guidance to assess doses documented as “OPV,” see www.cdc.gov/mmwr/volumes/66/wr/mm6606a7.htm?s_cid=mm6606a7_w.
      • For other catch-up guidance, see Catch up schedule.

    Special Situations

    Adolescents aged 18 years at increased risk of exposure to poliovirus and completed primary series*: may administer one lifetime IPV booster

    *Note: Complete primary series consist of at least 3 doses of IPV or trivalent oral poliovirus vaccine (tOPV) in any combination.

    For detailed information, see www.cdc.gov/vaccines/vpd/polio/hcp/recommendations.html

    Routine Immunization

    • Pregnant at 32 weeks 0 days through 36 weeks and 6 days gestation from September through January in most of the continental United States*: 1 dose Abrysvo. Administer RSV vaccine regardless of previous RSV infection.
      • Either maternal RSV vaccination with Abrysvo or infant immunization with nirsevimab or clesrovimab (RSV monoclonal antibody) is recommended to prevent severe respiratory syncytial virus disease in infants.
    • All other pregnant persons: RSV vaccine not recommended
    • Subsequent pregnancies: additional doses not recommended. No data are available to inform whether additional doses are needed in subsequent pregnancies. If vaccine was not provided during the current pregnancy, the infant should receive nirsevimab or clesrovimab.

    *Note: Providers in jurisdictions with RSV seasonality that differs from most of the continental United States (e.g., Alaska, jurisdictions with tropical climate) should follow guidance from public health authorities (e.g., CDC, health departments) or regional medical centers on timing of administration based on local RSV seasonality.

    Minimum age: birth (monoclonal antibody) *Note: “RSV monoclonol antibody” refers to either Nirsevimab or Clesrovimab.

    Routine Immunization

    • Infants born October - March in most of the continental United States*
      • Mother did not receive RSV vaccine OR mother’s RSV vaccination status is unknown: administer 1 dose RSV monoclonol antibody within 1 week of birth in hospital or outpatient setting
      • Mother received RSV vaccine less than 14 days prior to delivery: administer 1 dose RSV monoclonol antibody within 1 week of birth in hospital or outpatient setting
      • Mother received RSV vaccine at least 14 days prior to delivery: RSV monoclonol antibody not needed but can be considered in rare circumstances at the discretion of health care providers (see special populations and situations at www.cdc.gov/vaccines/vpd/rsv/hcp/child-faqs.html)
    • Infants born April–September in most of the continental United States*
      • Mother did not receive RSV vaccine OR mother’s RSV vaccination status is unknown: administer 1 dose RSV monoclonol antibody shortly before start of RSV season*
      • Mother received RSV vaccine less than 14 days prior to delivery: administer 1 dose RSV monoclonol antibody shortly before start of RSV season*
      • Mother received RSV vaccine at least 14 days prior to delivery: RSV monoclonol antibody not needed but can be considered in rare circumstances at the discretion of health care providers (see special populations and situations at www.cdc.gov/vaccines/vpd/rsv/hcp/child-faqs.html)
    • Infants with prolonged birth hospitalization** (e.g., for prematurity) discharged October through March should be immunized shortly before or promptly after discharge.

    Special Situations

    • Infants <8 months entering first season without maternal protection should receive nirsevimab or clesrovimab (new product in 2025-26). Any licensed product may be used where indicated.
    • Ages 8–19 months with chronic lung disease of prematurity requiring medical support (e.g., chronic corticosteroid therapy, diuretic therapy, or supplemental oxygen) any time during the 6-month period before the start of the second RSV season; severe immunocompromise; cystic fibrosis with either weight for length <10th percentile or manifestation of severe lung disease (e.g., previous hospitalization for pulmonary exacerbation in the first year of life or abnormalities on chest imaging that persist when stable)**:
      • 1 dose RSV monoclonol antibody shortly before start of second RSV season*
    • Ages 8–19 months who are American Indian or Alaska Native:
      • 1 dose nirsevimab shortly before start of second RSV season*
    • Age-eligible and undergoing cardiac surgery with cardiopulmonary bypass**: 1 additional dose of RSV monoclonol antibody after surgery. For additional details, see special populations and situations at www.cdc.gov/vaccines/vpd/rsv/hcp/child-faqs.html

    *Note: While the timing of the onset and duration of RSV season may vary, administration of RSV monoclonol antibody is recommended October through March in most of the continental United States (optimally October through November or within 1 week of birth). Providers in jurisdictions with RSV seasonality that differs from most of the continental United States (e.g., Alaska, jurisdiction with tropical climate) should follow guidance from public health authorities (e.g., CDC, health departments) or regional medical centers on timing of administration based on local RSV seasonality

    Minimum age: 6 weeks

    Routine Vaccination

    • Rotarix: 2-dose series at age 2 and 4 months
    • RotaTeq®: 3-dose series at age 2, 4, and 6 months
    • If any dose in the series is either RotaTeq® or unknown, default to 3-dose series.

    Catch-up Vaccination

    • Do not start the series on or after age 15 weeks, 0 days.
    • The maximum age for the final dose is 8 months, 0 days.
    • For other catch-up guidance, see Catch Up Schedule.

    Minimum Age: 11 years for routine vaccination, 7 years for |catch-up vaccination

    Routine Vaccination

    • Age 11–12 years: 1 dose Tdap (adolescent booster)
    • Pregnancy: 1 dose Tdap during each pregnancy, preferably in early part of gestational weeks 27–36.

    Note: Tdap may be administered regardless of the interval since the last tetanus- and diphtheria-toxoid-containing vaccine.

    Catch-up vaccination

    • Age 13–18 years who have not received Tdap: 1 dose Tdap (adolescent booster)
    • Age 7–18 years not fully vaccinated* with DTaP: 1 dose Tdap as part of the catch-up series (preferably the first dose); if additional doses are needed, use Td or Tdap.
    • Tdap administered at age 7–10 years:
      • Age 7–9 years who receive Tdap should receive the adolescent Tdap booster dose at age 11–12 years.
      • Age 10 years who receive Tdap do not need the adolescent Tdap booster dose at age 11–12 years.
    • DTaP inadvertently administered on or after age 7 years:
      • Age 7–9 years: DTaP may count as part of catch-up series. Administer adolescent Tdap booster dose at age 11–12 years.
      • Age 10–18 years: Count dose of DTaP as the adolescent Tdap booster dose.
    • For other catch-up guidance, see Catch Up Schedule.

    Special situations

    Wound management in persons age 7 years or older with history of 3 or more doses of tetanus-toxoid-containing vaccine: For clean and minor wounds, administer Tdap or Td if more than 10 years since last dose of tetanus-toxoid-containing vaccine; for all other wounds, administer Tdap or Td if more than 5 years since last dose of tetanus-toxoid-containing vaccine. Tdap is preferred for persons age 11 years or older who have not previously received Tdap or whose Tdap history is unknown. If a tetanus-toxoid-containing vaccine is indicated for a pregnant adolescent, use Tdap.

    For detailed information, see www.cdc.gov/mmwr/volumes/69/wr/mm6903a5.htm.

    *Fully vaccinated = 5 valid doses of DTaP OR 4 valid doses of DTaP if dose 4 was administered at age 4 years or older

    Minimum Age: 12 months

    Routine Vaccination

    • 2-dose series at age 12-15 months, 4-6 years
    • VAR or MMRV may be administered*
    • Dose 2 may be administered as early as 3 months after dose 1 (a dose inadvertently administered after at least 4 weeks may be counted as valid).

    *Note: For dose 1 in children age 12-47 months, it is recommended to administer MMR and varicella vaccines separately. MMRV may be used if parents or caregivers express a preference.

    Catch-up vaccination

    • Ensure persons age 7–18 years without evidence of immunity (see MMWR at www.cdc.gov/mmwr/pdf/rr/rr5604.pdf) have a 2-dose series:
      • Age 7–12 years: Routine interval: 3 months (a dose inadvertently administered after at least 4 weeks may be counted as valid)
      • Age 13 years and older: Routine interval: 4–8 weeks (minimum interval: 4 weeks)
      • The maximum age for use of MMRV is 12 years.

    Catch-up Schedule

    Children Ages 4 months Through 6 years
    Minimum Interval Between Doses
    Vaccine Minimum Age for Dose 1 Dose 1 to 2  Dose 2 to 3 Dose 3 to 4 Dose 4 to 5
    Hepatitis B Birth 4 Weeks 8 weeks and at least 16 weeks after first dose; minimum age for the final dose is 24 weeks    
    Rotavirus 6 weeks; maximum age for first dose is 14 weeks, 6 days. 4 weeks 4 weeks; maximum age for final dose is 8 months, 0 days    
    Diphtheria, tetanus, and acellular pertussis 6 weeks  4 weeks 4 weeks 6 monhts 6 months; 5th dose is not necessary if the fourth dose was administered at age 4 years or older and at least 6 months after dose 3
    Haemophilus influenzae type b 6 weeks

    No further doses needed if first dose was administered at age 15 months or older.

    4 weeks if first dose was administered before the 1st birthday.

    8 weeks (as final dose) if first dose was administered at age 12 through 14 months.

    No further doses needed if previous dose was administered at age 15 months or older

    4 weeks if current age is younger than 12 months and first dose was administered at younger than age 7 months and at least 1 previous dose was PRP-T (ActHib, Pentacel, Hiberix), Vaxelis or unknown

    8 weeks and age 12 through 59 months (as final dose) if:

    current age is younger than 12 months and first dose was administered at age 7 through 11 months; OR

    • if current age is 12 through 59 months and first dose was administered before the 1st birthday and second dose was administered at younger than 15 months; OR
    • if both doses were PedvaxHIB and were administered before the 1st birthday
    8 weeks (as final dose). This dose only necessary for children age 12 through 59 months who received 3 doses before the 1st birthday.  
    Pneumococcal conjugate 6 Week

    No further doses needed for healthy children if first dose was administered at age 24 months or older

    4 weeks if first dose was administered before the 1st birthday

    8 weeks (as final dose for healthy children) if first dose was administered at the 1st birthday or after

    No further doses needed for healthy children if previous dose was administered at age 24 months or older

    4 weeks if current age is younger than 12 months and previous dose was administered at <7 months old

    8 weeks (as final dose for healthy children)

    • if previous dose was administered between 7-11 months (wait until at least 12 months old); OR
    • if current age is 12 months or older and at least 1 dose was administered before age 12 months
    8 weeks (as final dose); This dose is only necessary for children age 12 through 59 months regardless of risk, or age 60 through 71 months with any risk, who received 3 doses before age 12 months.  
    Inactivated poliovirus 6 weeks 4 weeks

    4 weeks if current age is <4 years

    6 months (as final dose) if current age is 4 years or older

    6 months (minimum age 4 years for final dose)  
    Measles, mumps, rubella 12 months 4 weeks      
    Varicella 12 months 3 months      
    Hepatitis A 12 months 6 months      
    Meningococcal ACWY

    2 months MenACWY-CRM

    2 years MenACWY-TT

    8 weeks See Notes See notes  
    Children and adolescents age 7 through 18 years
    Meningococcal ACWY N/A 8 Weeks      
    Tetanus, diphtheria; tetanus, diphtheria, and acellular pertussis 7 years 4 Weeks

    4 weeks if first dose of DTaP/DT was administered before the 1st birthday

    6 months (as final dose) if first dose of DTaP/DT or Tdap/Td was administered at or after the 1st birthday

    6 months if first dose of DTaP/DT was administered before the 1st birthday  
    HPV 9 years Routine dosing intervals are recommended.      
    Hepatitis A N/A 6 months      
    Hepatitis B N/A 4 weeks * weeks and at least 16 weeks after first dose    
    Inactivated poliovirus N/A 4 weeks 6 months; A fourth dose is not necessary if the third dose was administered at age 4 years or older and at least 6 months after the previous dose. A fourth dose of IPV is indicated if all previous doses were administered at <4 years OR if the third dose was administered <6 months after the second dose.  
    Measles, mumps, rubella N/A 4 weeks      
    Varicella N/A

    3 months if younger than age 13 years.

    4 weeks if age 13 years or older

         
    Dengue 9 years 6 months 6 months    

    Appendix: Contraindications and Precautions to Commonly Used Vaccines

    When a contraindication is present, a vaccine should NOT be administered. Vaccination providers should check FDA-approved prescribing information for the most complete and updated information, including contraindications, warnings, and precautions. 

     

    Vaccines and other Immunizing Agents Contraindicated or Not Recommended Precautions
    COVID-19 mRNA vaccines
    [Pfizer-BioNTech, Moderna] 
    Severe allergic reaction (e.g., anaphylaxis) after a previous dose or to a component of an mRNA COVID-19 vaccine
    • Diagnosed non-severe allergy (e.g., urticaria beyond the injection site) to a component of an mRNA COVID-19 vaccine; or non-severe, immediate (onset less than 4 hours) allergic reaction after administration of a previous dose of an mRNA COVID-19 vaccine
    • Myocarditis or pericarditis within 3 weeks after a dose of any COVID-19 vaccine
    • Multisystem inflammatory syndrome in children (MIS-C) or multisystem inflammatory syndrome in adults (MIS-A)
    • Moderate or severe acute illness, with or without fever
    COVID-19 protein subunit vaccines [Novavax]
    Severe allergic reaction (e.g., anaphylaxis) after a previous dose or to a component of a Novavax COVID-19 vaccine
    • Diagnosed non-severe allergy (e.g., urticaria beyond the injection site) to a component of Novavax COVID-19 vaccine; or non-severe, immediate (onset less than 4 hours) allergic reaction after administration of a previous dose of a Novavax COVID-19 vaccine
    • Myocarditis or pericarditis within 3 weeks after a dose of any COVID-19 vaccine
    • Multisystem inflammatory syndrome in children (MIS-C) or multisystem inflammatory syndrome in adults (MIS-A)
    • Moderate or severe acute illness, with or without fever
    Influenza, egg-based, inactivated injectable (IIV3)

    Severe allergic reaction (e.g., anaphylaxis) after previous dose of any influenza vaccine (i.e., any egg-based IIV, ccIIV, RIV, or LAIV of any valency)

    Severe allergic reaction (e.g., anaphylaxis) to any vaccine component (excluding egg)

    • Guillain-Barré syndrome (GBS) within 6 weeks after a previous dose of any type of influenza vaccine
    • Moderate or severe acute illness with or without fever
    Influenza, cell culture-based inactivated injectable (ccIIV3) [Flucelvax] Severe allergic reaction (e.g., anaphylaxis) to any ccIIV of any valency, or to any component of ccIIV3
    • Guillain-Barré syndrome (GBS) within 6 weeks after a previous dose of any type of influenza vaccine
    • Persons with a history of severe allergic reaction (e.g., anaphylaxis) after a previous dose of any egg-based IIV, RIV, or LAIV of any valency. If using ccIIV4, administer in medical setting under supervision of health care provider who can recognize and manage severe allergic reactions. May consult an allergist.
    • Moderate or severe acute illness with or without fever
    Influenza, recombinant injectable (RIV3) [Flublok] Severe allergic reaction (e.g., anaphylaxis) to any RIV of any valency, or to any component of RIV3
    • Guillain-Barré syndrome (GBS) within 6 weeks after a previous dose of any type of influenza vaccine
    • Persons with a history of severe allergic reaction (e.g., anaphylaxis) after a previous dose of any egg-based IIV, ccIIV, or LAIV of any valency. If using RIV3, administer in medical setting under supervision of health care provider who can recognize and manage severe allergic reactions. May consult an allergist.
    • Moderate or severe acute illness with or without fever
    Influenza, live attenuated (LAIV3) [Flumist]
    • Severe allergic reaction (e.g., anaphylaxis) after previous dose of any influenza vaccine (i.e., any egg-based IIV, ccIIV, RIV, or LAIV of any valency)
    • Severe allergic reaction (e.g., anaphylaxis) to any vaccine component3 (excluding egg)
    • Children age 2 –4 years with a history of asthma or wheezing
    • Anatomic or functional asplenia
    • Immunocompromised due to any cause including, but not limited to, medications and HIV infection
    • Close contacts or caregivers of severely immunosuppressed persons who require a protected environment
    • Pregnancy
    • Cochlear implant
    • Active communication between the cerebrospinal fluid (CSF) and the oropharynx, nasopharynx, nose, ear or any other cranial CSF leak
    • Children and adolescents receiving aspirin or salicylate-containing medications
    • Received influenza antiviral medications oseltamivir or zanamivir within the previous 48 hours, peramivir within the previous 5 days, or baloxavir within the previous 17 days
    • Guillain-Barré syndrome (GBS) within 6 weeks after a previous dose of any type of influenza vaccine
    • Asthma in persons age 5 years old or older
    • Persons with underlying medical conditions other than those listed under contraindications that might predispose to complications after wild-type influenza virus infection, e.g., chronic pulmonary, cardiovascular (except isolated hypertension), renal, hepatic, neurologic, hematologic, or metabolic disorders (including diabetes mellitus)
    • Moderate or severe acute illness with or without fever
    Dengue (DEN4CYD)
    • Severe allergic reaction (e.g., anaphylaxis) after a previous dose or to a vaccine component
    • Severe immunodeficiency (e.g., hematologic and solid tumors, receipt of chemotherapy, congenital immunodeficiency, long-term immunosuppressive therapy or patients with HIV infection who are severely immunocompromised)
    • Lack of laboratory confirmation of a previous dengue infection
    • Pregnancy
    • HIV infection without evidence of severe immunosuppression
    • Moderate or severe acute illness with or without fever
    Diphtheria, tetanus, pertussis (DTaP)
    • Severe allergic reaction (e.g., anaphylaxis) after a previous dose or to a vaccine component
    • Encephalopathy (e.g., coma, decreased level of consciousness, prolonged seizures) not attributable to another identifiable cause within 7 days of administration of previous dose of DTP or DTaP
    • Guillain-Barré syndrome (GBS) within 6 weeks after previous dose of tetanus-toxoid–containing vaccine
    • History of Arthus-type hypersensitivity reactions after a previous dose of diphtheria-toxoid–containing or tetanus-toxoid–containing vaccine; defer vaccination until at least 10 years have elapsed since the last tetanus-toxoid-containing vaccine
    • For DTaP only: Progressive neurologic disorder, including infantile spasms, uncontrolled epilepsy, progressive encephalopathy; defer DTaP until neurologic status clarified and stabilized
    • Moderate or severe acute illness with or without fever
    Haemophilus influenzae type b (Hib)
    • Severe allergic reaction (e.g., anaphylaxis) after a previous dose or to a vaccine component
    • Younger than age 6 weeks
    Moderate or severe acute illness with or without fever
    Hepatitis A (HepA) Severe allergic reaction (e.g., anaphylaxis) after a previous dose or to a vaccine component including neomycin Moderate or severe acute illness with or without fever
    Hepatitis B (HepB)
    • Severe allergic reaction (e.g., anaphylaxis) after a previous dose or to a vaccine component including yeast
    • Pregnancy: Heplisav-B and PreHevbrio is not recommended due to lack of safety data in pregnant persons. Use other hepatitis B vaccines if HepB is indicated
    Moderate or severe acute illness with or without fever
    Hepatitis A-Hepatitis B vaccine (HepA-HepB) [Twinrix] Severe allergic reaction (e.g., anaphylaxis) after a previous dose or to a vaccine component including neomycin and yeast Moderate or severe acute illness with or without fever
    HPV
    • Severe allergic reaction (e.g., anaphylaxis) after a previous dose or to a vaccine component
    • Pregnancy: HPV vaccination not recommended
    Moderate or severe acute illness with or without fever
    Measles, mumps, rubella (MMR) 
    Measles, mumps, rubella, and varicella (MMRV)
    • Severe allergic reaction (e.g., anaphylaxis) after a previous dose or to a vaccine component
    • Severe immunodeficiency (e.g., hematologic and solid tumors, receipt of chemotherapy, congenital immunodeficiency, long-term immunosuppressive therapy or patients with HIV infection who are severely immunocompromised)
    • Pregnancy
    • Family history of altered immunocompetence, unless verified clinically or by laboratory testing as immunocompetent
    • Recent (≤11 months) receipt of antibody-containing blood product (specific interval depends on product)
    • History of thrombocytopenia or thrombocytopenic purpura
    • Need for tuberculin skin testing or interferon-gamma release assay (IGRA) testing
    • Moderate or severe acute illness with or without fever
    • For MMRV only: Personal or family (i.e., sibling or parent) history of seizures of any etiology
    Meningococcal ACWY (MenACWY)
    MenACWY-CRM [Menveo]
    MenACWY-TT [MenQuadfi]
    • Severe allergic reaction (e.g., anaphylaxis) after a previous dose or to a vaccine component
    • For Men ACWY-CRM only: severe allergic reaction to any diphtheria toxoid- or CRM197-containing vaccine
    • For MenACWY-TT only: severe allergic reaction to a tetanus toxoid-containing vaccine
    • For MenACWY-CRM only: Preterm birth if younger than age 9 months
    • Moderate or severe acute illness with or without fever
    Meningococcal B (MenB)
    MenB-4C [Bexsero]
    MenB-FHbp [Trumenba]
    Severe allergic reaction (e.g., anaphylaxis) after a previous dose or to a vaccine component
    • Pregnancy
    • For MenB-4C only: Latex sensitivity
    • Moderate or severe acute illness with or without fever
    Mpox [Jynneos]

    Severe allergic reaction (e.g., anaphylaxis) after a previous dose or to a vaccine component

    • Moderate or severe acute illness with or without fever
    • Simultaneous administration of mpox vaccine with COVID-19 vaccine (due to a hypothetical increased risk for myocarditis/pericarditis following vaccination)

     

     

    Pneumococcal conjugate (PCV)
    • Severe allergic reaction (e.g., anaphylaxis) after a previous dose or to a vaccine component
    • Severe allergic reaction (e.g., anaphylaxis) to any diphtheria-toxoid-containing vaccine or its component
    Moderate or severe acute illness with or without fever
    Pneumococcal polysaccharide (PPSV23)

    Severe allergic reaction (e.g., anaphylaxis) after a previous dose or to a vaccine component

    Moderate or severe acute illness with or without fever
    Poliovirus vaccine, inactivated (IPV)

    Severe allergic reaction (e.g., anaphylaxis) after a previous dose or to a vaccine component

    • Pregnancy
    • Moderate or severe acute illness with or without fever
    RSV monoclonal antibody (RSV-mAb)

    Severe allergic reaction (e.g., anaphylaxis) after a previous dose or to a vaccine component

    Moderate or severe acute illness with or without fever
    Respiratory syncytial virus vaccine (RSV)

    Severe allergic reaction (e.g., anaphylaxis) after a previous dose or to a vaccine component

    Moderate or severe acute illness with or without fever
    Rotavirus (RV)
    RV1 [Rotarix]
    RV5 [RotaTeq]
    • Severe allergic reaction (e.g., anaphylaxis) after a previous dose or to a vaccine component3
    • Severe combined immunodeficiency (SCID)
    • History of intussusception
    • Altered immunocompetence other than SCID
    • Chronic gastrointestinal disease
    • RV1 only: Spina bifida or bladder exstrophy
    • Moderate or severe acute illness with or without fever
    Tetanus, diphtheria, and acellular pertussis (Tdap)
    Tetanus, diphtheria (Td)
    • Severe allergic reaction (e.g., anaphylaxis) after a previous dose or to a vaccine component
    • For Tdap only: Encephalopathy (e.g., coma, decreased level of consciousness, prolonged seizures) not attributable to another identifiable cause within 7 days of administration of previous dose of DTP, DTaP, or Tdap
    • Guillain-Barré syndrome (GBS) within 6 weeks after a previous dose of tetanus-toxoid-containing vaccine
    • History of Arthus-type hypersensitivity reactions after a previous dose of diphtheria-toxoid-containing or tetanus-toxoid-containing vaccine; defer vaccination until at least 10 years have elapsed since the last tetanus-toxoid-containing vaccine
    • For Tdap only: Progressive or unstable neurological disorder, uncontrolled seizures, or progressive encephalopathy until a treatment regimen has been established and the condition has stabilized
    • Moderate or severe acute illness with or without fever
    Varicella (VAR)
    Measles, mumps, rubella, and varicella (MMRV)
    • Severe allergic reaction (e.g., anaphylaxis) after a previous dose or to a vaccine component
    • Severe immunodeficiency (e.g., hematologic and solid tumors, receipt of chemotherapy, congenital immunodeficiency, long-term immunosuppressive therapy or patients with HIV infection who are severely immunocompromised)
    • Pregnancy
    • Family history of altered immunocompetence, unless verified clinically or by laboratory testing as immunocompetent
    • Recent (≤11 months) receipt of antibody-containing blood product (specific interval depends on product)
    • Receipt of specific antiviral drugs (acyclovir, famciclovir, or valacyclovir) 24 hours before vaccination (avoid use of these antiviral drugs for 14 days after vaccination)
    • Use of aspirin or aspirin-containing products
    • Moderate or severe acute illness with or without fever
    • If using MMRV, see MMR/MMRV for additional precautions