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.
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
Age 6 months–23 months
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:
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
Age 5–11 years moderately or severely immunocompromised
Use vaccine from the same manufacturer for all doses in the initial vaccination series.
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.
*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
Minimum Age: 6 weeks [4 years for Kinrix or Quadracel]
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
Minimum Age: 6 weeks
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
Persons age 5 years or older
Persons age 15 months or older
Persons age 5–18 years
*Unvaccinated = Less than routine series (through age 14 months) OR no doses (age 15 months or older)
Minimum age: 12 months for routine vaccination
2-dose series (minimum interval: 6 months) at age 12–23 months
Minimum age: birth
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:
Note: PreHevbrio is not recommended in pregnancy due to lack of safety data in pregnant persons.
Minimum Age: 9 years
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
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.
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.
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-dose series at age 11–12 years; 16 years
Anatomic or functional asplenia (including sickle cell disease), HIV infection, persistent complement component deficiency, complement inhibitor (e.g., eculizumab, ravulizumab) use:
Travel to countries with hyperendemic or epidemic meningococcal disease, including countries in the African meningitis belt or during the Hajj:
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:
Adolescent vaccination of children who received MenACWY prior to age 10 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])
Adolescents not at increased risk age 16–23 years (preferred age 16–18 years)* based on shared clinical decision-making.
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
Anatomic or functional asplenia (including sickle cell disease), persistent complement component deficiency, complement inhibitor (e.g., eculizumab, ravulizumab) use:
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.
Special Situations
For detailed information, visit https://publications.aap.org/ redbook/book/755/chapter/14079669/Mpox
Minimum Age:
6 weeks [PCV15], [PCV 20]
Routine Vaccination with PCV
4-dose series at 2, 4, 6, 12-15 months
Catch-up vaccination
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
Age 6–18 years
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
Age 6–18 years
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
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:
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
*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.
*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
Note: Tdap may be administered regardless of the interval since the last tetanus- and diphtheria-toxoid-containing vaccine.
Catch-up vaccination
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
*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.
| 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
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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)
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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 |
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| Dengue | 9 years | 6 months | 6 months | ||
| 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
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| 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
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| 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) |
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| 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 |
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| Influenza, recombinant injectable (RIV3) [Flublok] | Severe allergic reaction (e.g., anaphylaxis) to any RIV of any valency, or to any component of RIV3 |
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| Influenza, live attenuated (LAIV3) [Flumist] |
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| Dengue (DEN4CYD) |
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| Diphtheria, tetanus, pertussis (DTaP) |
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| Haemophilus influenzae type b (Hib) |
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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) |
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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 |
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Moderate or severe acute illness with or without fever |
| Measles, mumps, rubella (MMR) Measles, mumps, rubella, and varicella (MMRV) |
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| Meningococcal ACWY (MenACWY) MenACWY-CRM [Menveo] MenACWY-TT [MenQuadfi] |
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| Meningococcal B (MenB) MenB-4C [Bexsero] MenB-FHbp [Trumenba] |
Severe allergic reaction (e.g., anaphylaxis) after a previous dose or to a vaccine component |
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| Mpox [Jynneos] | Severe allergic reaction (e.g., anaphylaxis) after a previous dose or to a vaccine component |
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| Pneumococcal conjugate (PCV) |
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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 |
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| 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] |
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| Tetanus, diphtheria, and acellular pertussis (Tdap) Tetanus, diphtheria (Td) |
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| Varicella (VAR) Measles, mumps, rubella, and varicella (MMRV) |
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