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Meningococcal B and ABCWY vaccines: Bexsero, Trumenba, Penbraya and Penmenvy

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Vaccine School · Childhood and adolescent

A pharmacist-focused lesson on serogroup B meningococcal vaccines (Bexsero, Trumenba) and the pentavalent MenABCWY vaccines (Penbraya, Penmenvy): shared clinical decision-making at 16 to 23 years, risk-based vaccination, products that are not interchangeable, dosing and booster intervals, preparation, storage, contraindications, safety, pregnancy and counseling. Unreviewed draft.

Content current as of October 11, 2026. AI-assisted draft; not yet reviewed by a licensed pharmacist. Current CDC schedules: immunization schedules.

The disease and why it matters

Serogroups B, C and Y cause the majority of meningococcal disease in the United States; the disease is uncommon but very serious, and its two most common syndromes are meningitis and septicemia. [1]

Even when treated, meningococcal disease kills 10 to 15 of every 100 infected people, and about 10 to 20 of every 100 survivors suffer disabilities such as hearing loss, brain damage, kidney damage, loss of limbs, nervous system problems or severe scars from skin grafts. [2]

In recent years between 20 and 50 cases of serogroup B meningococcal disease occurred each year among 16- through 23-year-old people in the United States, most commonly affecting young adults who attend a four-year university, are freshmen, live in on-campus housing or participate in sororities or fraternities. [3]

Video and figures

Video

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Meningococcus - VEC Vaccine Notes | Vaccine Education Center at Children’s Hospital of Philadelphia
Channel: Vaccine Education Center at CHOP · Uploaded April 15, 2026 · Confirmed available October 12, 2026 · Open on YouTubeRxEvidence has not checked every statement in this video.

Get CE credit

  • CDC You Call the Shots: Meningococcal module (CDC TRAIN course WB4594R) — CDC · Free (CDC states no fees for its CE activities) · accredited by CDC, jointly accredited by ACCME, ACPE and ANCC; pharmacy UAN JA4008229-0000-22-061-H06-P. CDC's listing shows credit expiring 6/15/2026, so confirm on CDC TRAIN that credit is still available · link confirmed October 11, 2026

RxEvidence is not an accredited continuing education provider and does not award CE credit. These are links to activities offered by others.

Products available

CDC lists two MenB vaccines (Bexsero and Trumenba), which protect against serogroup B only, and two MenABCWY vaccines (Penbraya and Penmenvy), which protect against serogroups A, B, C, W and Y; MenABCWY vaccine is an option for people getting MenACWY and MenB vaccines at the same visit. [4]

Serogroup B-containing meningococcal vaccines, from FDA product pages and prescribing information
VaccineManufacturerFDA-approved useInitial U.S. approval
Bexsero (MenB-4C)GlaxoSmithKline Biologicals SA [5]Active immunization to prevent invasive disease caused by N. meningitidis serogroup B in individuals aged 10 through 25 years [6]2015 [6]
Trumenba (MenB-FHbp)Pfizer Inc. [7]Active immunization to prevent invasive disease caused by N. meningitidis serogroup B in individuals 10 through 25 years of age [7]2014 [7]
Penbraya (MenACWY-TT/MenB-FHbp)Pfizer Ireland Pharmaceuticals [8]Active immunization to prevent invasive disease caused by N. meningitidis serogroups A, B, C, W and Y in individuals 10 through 25 years of age [9]2023 [9]
Penmenvy (MenACWY/MenB, GSK)GlaxoSmithKline Biologicals [10]Active immunization to prevent invasive disease caused by N. meningitidis serogroups A, B, C, W and Y in individuals 10 through 25 years of age [11]2025 [11]

CDC says that Penbraya includes Trumenba and that Penmenvy includes Bexsero; for later doses after a MenABCWY dose, give Trumenba for additional MenB doses when Penbraya was used, and Bexsero when Penmenvy was used, in each case when MenACWY is not indicated. [12]

CDC's child and adolescent schedule notes (July 2, 2025) name only Penbraya among the MenABCWY vaccines, whereas FDA lists Penmenvy as approved (letter dated February 14, 2025) and CDC's March 2026 recommendations page names both products; the schedule notes pre-date or do not address Penmenvy, and the pages opened do not say which. [13] [10] [12]

Label currency as posted by FDA: the Trumenba page is marked content current as of 06/20/2024 (label revised 6/2024), the Bexsero page 08/20/2024 (label 08/2024), the Penbraya page 11/21/2024 (label 11/2024) and the Penmenvy page 08/01/2025 (label 08/2025). [14] [7] [5] [6] [8] [9] [10] [11]

Bexsero 0.5-mL doses are supplied as single-dose prefilled TIP-LOK syringes packaged without needles; Trumenba as a 0.5-mL single-dose prefilled syringe; Penbraya as a kit with a vial of lyophilized MenACWY component, a prefilled syringe containing the MenB component and a vial adapter. [6] [7] [9]

Who should get it

CDC / ACIP (meningococcal vaccine recommendations page, March 30, 2026)

As of March 30, 2026

For adolescents and young adults not at increased risk, CDC recommends a shared clinical decision-making process to decide if MenB vaccination is appropriate; those who want it should receive 2 doses 6 months apart, and the preferred age for vaccination is 16 through 18 years. People with MenB-relevant risk factors are recommended to receive MenB vaccine (3-dose primary series, with boosters) from 10 years of age. [12] [3]

CDC VIS (January 31, 2025 edition)

As of January 31, 2025

The VIS says MenB vaccines are recommended for people 10 years or older who are at increased risk for serogroup B disease (including outbreak, damaged or removed spleen, complement component deficiency, complement inhibitors and microbiologists), and may also be given to anyone 16 through 23 years old for short-term protection, with 16 through 18 years the preferred age. [2]

The CDC risk-indications page lists these factors for MenB vaccination: complement component deficiency, functional or anatomic asplenia (including sickle cell disease), complement inhibitors (for example Soliris and Ultomiris), microbiologists routinely exposed to N. meningitidis, and being part of a community experiencing a serogroup B outbreak; unlike MenACWY, HIV is not among the MenB indications on that page. [15]

CDC's adult schedule notes (July 2, 2025) say adolescents and young adults age 16 to 23 years (16 to 18 preferred) not at increased risk may be vaccinated based on shared clinical decision-making, and recommend MenB for adults with asplenia, persistent complement component deficiency, complement inhibitor use or routine exposure to N. meningitidis as microbiologists. [16]

The FDA-approved age range for Bexsero, Trumenba, Penbraya and Penmenvy is 10 through 25 years, so use in adults older than 25 years (for example an asplenic adult) is a CDC recommendation beyond the labeled age range; the label of each product states the 10 through 25 year indication. [6] [7] [9] [11]

CDC: January 2026 schedule revision and its legal status (meningococcal)

As of June 11, 2026

On January 5, 2026 the CDC Acting Director approved a revised childhood and adolescent schedule that changed the recommendation type for hepatitis A, meningococcal ACWY and RSV vaccines from a full recommendation for all children to a risk-based recommendation for children at high risk, with shared clinical decision-making for other children; the schedule's first category (recommended for all children) lists measles, mumps, rubella, polio, pertussis, tetanus, diphtheria, Hib, pneumococcal disease, HPV and varicella. A federal district court stayed that schedule on March 16, 2026 and reverted it to the version as of May 2025, and CDC's schedule page continues to show the July 2, 2025 addendum edition. [17] [18] [19]

American Academy of Pediatrics 2026 schedule (endorsed by AAFP, ACOG, AMA, IDSA, APhA and others)

As of January 26, 2026

The AAP published its own 2026 schedule on January 26, 2026, which continues to recommend routine immunization for protection against 18 diseases, including RSV, hepatitis A, hepatitis B, rotavirus, influenza and meningococcal disease, and differs from the schedule recently issued by CDC; the AAP schedule is formally endorsed by 12 organizations, including AAFP, ACOG, AMA, IDSA and the American Pharmacists Association. [20]

Dosing and schedule, including catch-up

MenB and MenABCWY dosing from the FDA prescribing information
VaccineSchedule in the label
BexseroTwo doses (0.5 mL) at 0 and 6 months; if the second dose is given earlier than 6 months after the first, give a third dose at least 4 months after the second. Three-dose schedule: 0, 1-2 and 6 months. [6]
TrumenbaTwo doses (0.5 mL) at 0 and 6 months; if the second dose is given earlier than 6 months after the first, give a third dose at least 4 months after the second. Three-dose schedule: 0, 1-2 and 6 months. [7]
PenbrayaTwo doses (approximately 0.5 mL each) 6 months apart. [9]
PenmenvyTwo doses (approximately 0.5 mL each) 6 months apart. [11]

CDC's notes for people at increased risk give a 3-dose primary series at 0, 1 to 2 and 6 months with the same brand for all doses including boosters (dose 3 not needed if dose 2 was given at least 6 months after dose 1; if dose 3 is given earlier than 4 months after dose 2, give a 4th dose at least 4 months after dose 3), then a booster one year after the primary series and every 2 to 3 years if risk remains. [16]

For shared clinical decision-making, CDC's notes list a 2-dose series at least 6 months apart (if dose 2 is given earlier than 6 months, give dose 3 at least 4 months after dose 2); to optimize rapid protection (for example students starting college in less than 6 months) a 3-dose series (0, 1 to 2, 6 months) may be given. [13]

CDC says MenB vaccine protective antibodies decrease quickly (within 1 to 2 years) after vaccination, and during a serogroup B outbreak a booster is recommended for previously vaccinated people at increased risk if a year or more has passed since the most recent MenB vaccine; public health authorities may recommend a booster after 6 months in some outbreaks. [4] [12]

The minimum interval between MenABCWY doses is 6 months; MenABCWY vaccine can be used only when both MenACWY and MenB vaccines are indicated at the same visit, and otherwise MenACWY and MenB vaccines should be given separately as appropriate. [12]

CDC and the labels on interchangeability

As of December 9, 2024

CDC says both MenB vaccine products need more than 1 dose for maximum protection and individuals should receive the same vaccine product for all doses; its shared clinical decision-making job aid says MenB-4C and MenB-FHbp are not interchangeable. [12] [3]

FDA labels (Bexsero 08/2024; Trumenba 6/2024)

As of August 20, 2024

The Bexsero label says sufficient data are not available on the safety and effectiveness of using Bexsero and other meningococcal group B vaccines interchangeably, and the Trumenba label says the same for Trumenba. [6] [7]

Administration

  • Bexsero: shake the syringe immediately before use to form a homogeneous suspension; do not use if it cannot be resuspended or if particulate matter or discoloration is found; give as a 0.5-mL intramuscular injection. [6]
  • Trumenba: shake the syringe vigorously to obtain a homogenous white suspension; do not use if it cannot be re-suspended; inject each 0.5 mL dose intramuscularly with the preferred site the deltoid muscle of the upper arm; do not mix with any other vaccine in the same syringe. [7]
  • Penbraya: reconstitute the lyophilized MenACWY component with the MenB component using the vial adapter (shake the MenB syringe vigorously first and do not use if it cannot be resuspended; swirl until the powder dissolves, less than 1 minute); after reconstitution, administer immediately or store between 2 and 30 °C and use within 4 hours, discarding unused vaccine after 4 hours. [9]
  • Penmenvy: reconstitute the lyophilized MenACWY component with the MenB component, administer intramuscularly, and administer immediately after reconstitution. [11]
  • MenB vaccines may be given simultaneously with MenACWY vaccines if indicated, at a different anatomic site if feasible. [16]

Storage and handling

  • Bexsero: store refrigerated at 36 to 46 °F (2 to 8 °C); do not freeze (discard if frozen); protect from light; do not use after the expiration date. [6]
  • Trumenba: upon receipt store refrigerated at 2 to 8 °C (36 to 46 °F); store syringes horizontally (laying flat) to minimize re-dispersion time; do not freeze (discard if frozen). [7]
  • Penbraya: before reconstitution store refrigerated at 2 to 8 °C in the original carton, horizontally, to minimize resuspension time (a white deposit and clear supernatant may be seen in the MenB syringe); do not freeze (discard if the carton has been frozen). [9]
  • Penmenvy: before reconstitution store refrigerated, away from the freezer compartment, at 36 to 46 °F (2 to 8 °C) in the original carton to protect from light; do not freeze (discard if the carton has been frozen); use immediately after reconstitution. [11]

Contraindications and precautions

Contraindications and precautions
VaccineStatementSource
MenB (Bexsero, Trumenba)Severe allergic reaction (e.g., anaphylaxis) after a previous dose or to a vaccine component; pregnancy is listed as a precaution; for Bexsero only, latex sensitivity; moderate or severe acute illness with or without fever. [21]CDC appendix
MenABCWY (Penbraya)Severe allergic reaction after a previous dose or to a vaccine component; severe allergic reaction to a tetanus toxoid-containing vaccine; moderate or severe acute illness with or without fever. [21]CDC appendix
Bexsero labelSevere allergic reaction (e.g., anaphylaxis) to any component of Bexsero or after a previous dose of Bexsero. [6]FDA label
Trumenba labelSevere allergic reaction (e.g., anaphylaxis) to any component of Trumenba. [7]FDA label
Penbraya labelSevere allergic reaction (e.g., anaphylaxis) to any component of Penbraya. [9]FDA label
Penmenvy labelSevere allergic reaction (e.g., anaphylaxis) to a previous dose of Penmenvy, to any component of the vaccine, or to any other diphtheria toxoid-containing vaccine. [11]FDA label

The CDC appendix lists the Penbraya severe-allergy statement as tetanus toxoid-containing vaccine, whereas the Penmenvy label lists any other diphtheria toxoid-containing vaccine; the two MenABCWY vaccines therefore have different cross-reactivity contraindications. [21] [11]

Safety and adverse events

Most commonly reported solicited adverse reactions in the clinical trials, from the prescribing information
VaccineReactions reported
BexseroPain at the injection site (87%-92%), fatigue (45%-49%), headache (37%-41%), nausea (11%-13%), erythema (10%-15%), myalgia (10%-14%) and swelling (10%-14%) (10% or more). [6]
TrumenbaIn adolescents and young adults: pain at the injection site (85% or more), fatigue (60% or more), headache (55% or more) and muscle pain (35% or more). [7]
PenbrayaAfter dose 1 and dose 2 respectively (15% or more): pain at the injection site (89% and 84%), fatigue (52% and 48%), headache (47% and 40%), muscle pain (26% and 23%), injection site redness (26% and 23%), injection site swelling (25% and 24%), joint pain (20% and 18%) and chills (20% and 16%). [9]
PenmenvyAfter dose 1 and dose 2 respectively (10% or more), in individuals aged 10 through 25 years: pain at the injection site (92% and 88%), fatigue (51% and 42%), headache (42% and 36%), myalgia (15% and 12%), nausea (15% and 10%), erythema (13% and 12%) and swelling (13% and 12%). [11]

Syncope can occur with injectable vaccines including all four products, and procedures should be in place to avoid injury from fainting; appropriate medical treatment must be immediately available to manage anaphylaxis. [6] [7] [9] [11]

Guillain-Barré syndrome (GBS) has been reported in temporal relationship following another U.S.-licensed meningococcal quadrivalent polysaccharide conjugate vaccine, and the decision to give Penbraya or Penmenvy to people with a history of GBS should take into account expected benefits and potential risks. [9] [11]

Vaccination may not protect all recipients, and Bexsero and Penmenvy may not provide protection against all meningococcal serogroup B strains. [6] [11]

Trumenba pediatric use: safety and effectiveness have not been established in children younger than 10 years, and in a clinical study 90% of infants younger than 12 months vaccinated with a reduced-dosage formulation had fever. [7]

Special populations

Pregnancy: CDC says to delay MenB vaccination until after pregnancy due to lack of safety data in pregnant women, but MenB may be given if the person is at increased risk and the benefits of vaccination outweigh the potential risks. [16]

The labels state that available human data on Bexsero, Trumenba, Penbraya and Penmenvy administered to pregnant women are insufficient to inform vaccine-associated risks in pregnancy; Pfizer maintains a pregnancy exposure registry for Penbraya. [6] [7] [9] [11]

Lactation: for Bexsero, available data are not sufficient to assess the effects on the breastfed infant or on milk production or excretion, and the benefits of breastfeeding should be considered with the mother's clinical need for the vaccine. [6]

Complement deficiency and complement inhibitors: people with certain complement deficiencies and people receiving treatment that inhibits terminal complement activation (for example eculizumab) are at increased risk for invasive disease caused by serogroup B even if they develop antibodies after vaccination; CDC says patients taking complement inhibitors may still contract meningococcal disease despite being fully vaccinated and up to date with boosters or receiving antimicrobial prophylaxis. [6] [15]

Altered immunocompetence: some individuals with altered immunocompetence may have reduced immune responses to Bexsero, Trumenba and Penbraya, and immunocompromised persons, including those receiving immunosuppressive therapy, may have reduced immune responses to Penmenvy. [6] [7] [9] [11]

Geriatric use: for Bexsero, safety and effectiveness have not been established in adults older than 65 years. [6]

Counseling pearls for the pharmacy counter

  • For best protection, more than 1 dose of a MenB vaccine is needed, and the same vaccine must be used for all doses. [2]
  • MenB vaccines are safe and effective but offer only short-term protection (1 to 2 years) to those vaccinated, and protect against most strains of serogroup B circulating in the United States. [3]
  • MenB vaccine does not protect against serogroups A, C, W and Y; a different meningococcal vaccine is available for those serogroups. [2]
  • Tell the vaccination provider about an allergic reaction after a previous dose or any severe, life-threatening allergy, and about pregnancy or breastfeeding; MenB vaccination should be postponed for pregnant women unless the woman is at increased risk and the benefits are considered to outweigh the potential risks. [2]
  • A low risk of exposure or infection does not mean a person cannot get a MenB vaccine; it is one consideration in shared clinical decision-making. [3]
  • Completing the series matters: the labels advise informing recipients of the importance of completing the immunization series and of reporting adverse reactions. [6] [7]

Common patient questions

Can a patient start with Bexsero and finish with Trumenba?

No. CDC says to use the same MenB product for all doses, and the labels say data are not available on using MenB vaccines interchangeably. [12] [6]

A healthy 17-year-old asks about MenB vaccine. Is it recommended?

CDC recommends a shared clinical decision-making process for adolescents and young adults not at increased risk; if they want the vaccine, give 2 doses 6 months apart (16 through 18 years is the preferred age). [12]

A student starts college in 4 months. Can the series be sped up?

Yes. CDC says people desiring more rapid protection against serogroup B (for example students with less than 6 months before college entry) may receive a 3-dose series (0, 1 to 2, 6 months). [12]

Which vaccine for a patient who needs both MenACWY and MenB today?

CDC gives two options: administer the individual vaccines at different anatomical injection sites, or administer a MenABCWY vaccine instead. [12]

Does a patient on eculizumab need MenB vaccine?

Yes, complement inhibitors are listed among the indications for MenB vaccination, but vaccines and antimicrobial prophylaxis likely provide incomplete protection, so these patients should seek care immediately for symptoms. [15] [1]

References

  1. Centers for Disease Control and Prevention. Clinical overview of meningococcal disease. Page dated March 30, 2026. Accessed October 11, 2026. https://www.cdc.gov/meningococcal/hcp/clinical/index.html. Accessed October 11, 2026.
  2. Centers for Disease Control and Prevention. Meningococcal B vaccine: what you need to know. Vaccine Information Statement, January 31, 2025. Accessed October 11, 2026. https://www.cdc.gov/vaccines/hcp/current-vis/meningococcal-b.html. Accessed October 11, 2026.
  3. Centers for Disease Control and Prevention. Shared clinical decision-making: meningococcal B vaccination (job aid, 12/09/24). Accessed October 11, 2026. https://www.cdc.gov/vaccines/media/pdfs/2025/03/2024-isd-job-aid-scdm-menb-508-remediated.pdf. Accessed October 11, 2026.
  4. Centers for Disease Control and Prevention. Types of meningococcal vaccines. Page dated March 30, 2026. Accessed October 11, 2026. https://www.cdc.gov/meningococcal/vaccines/types.html. Accessed October 11, 2026.
  5. U.S. Food and Drug Administration. BEXSERO product page (content current as of 08/20/2024). Accessed October 11, 2026. https://www.fda.gov/vaccines-blood-biologics/vaccines/bexsero. Accessed October 11, 2026.
  6. BEXSERO (meningococcal group B vaccine), injectable suspension for intramuscular use: prescribing information, revised 08/2024. GlaxoSmithKline Biologicals. U.S. Food and Drug Administration. Accessed October 11, 2026. https://www.fda.gov/media/90996/download?attachment. Accessed October 11, 2026.
  7. TRUMENBA (meningococcal group B vaccine), suspension for intramuscular injection: prescribing information, revised 6/2024. Pfizer Inc. U.S. Food and Drug Administration. Accessed October 11, 2026. https://www.fda.gov/media/89936/download?attachment. Accessed October 11, 2026.
  8. U.S. Food and Drug Administration. PENBRAYA product page (content current as of 11/21/2024). Accessed October 11, 2026. https://www.fda.gov/vaccines-blood-biologics/vaccines/penbraya. Accessed October 11, 2026.
  9. PENBRAYA (meningococcal groups A, B, C, W, and Y vaccine), suspension for intramuscular injection: prescribing information, revised 11/2024. Pfizer Ireland Pharmaceuticals. U.S. Food and Drug Administration. Accessed October 11, 2026. https://www.fda.gov/media/173223/download?attachment. Accessed October 11, 2026.
  10. U.S. Food and Drug Administration. PENMENVY product page (content current as of 08/01/2025). Accessed October 11, 2026. https://www.fda.gov/vaccines-blood-biologics/penmenvy. Accessed October 11, 2026.
  11. PENMENVY (meningococcal groups A, B, C, W, and Y vaccine) for injectable suspension, for intramuscular use: prescribing information, revised 08/2025. GlaxoSmithKline Biologicals. U.S. Food and Drug Administration. Accessed October 11, 2026. https://www.fda.gov/media/185479/download?attachment. Accessed October 11, 2026.
  12. Centers for Disease Control and Prevention. Meningococcal vaccine recommendations (for health care providers). Page dated March 30, 2026. Accessed October 11, 2026. https://www.cdc.gov/meningococcal/hcp/vaccine-recommendations/index.html. Accessed October 11, 2026.
  13. Centers for Disease Control and Prevention. Child and adolescent immunization schedule notes: recommendations for ages 18 years or younger, United States, 2025. July 2, 2025. Accessed October 11, 2026. https://www.cdc.gov/vaccines/hcp/imz-schedules/child-adolescent-notes.html. Accessed October 11, 2026.
  14. U.S. Food and Drug Administration. Trumenba product page (content current as of 06/20/2024). Accessed October 11, 2026. https://www.fda.gov/vaccines-blood-biologics/vaccines/trumenba. Accessed October 11, 2026.
  15. Centers for Disease Control and Prevention. Meningococcal vaccine risk indications. Page dated March 16, 2026. Accessed October 11, 2026. https://www.cdc.gov/meningococcal/hcp/vaccine-recommendations/risk-indications.html. Accessed October 11, 2026.
  16. Centers for Disease Control and Prevention. Adult immunization schedule notes: recommendations for ages 19 years or older, United States, 2025. July 2, 2025. Accessed October 11, 2026. https://www.cdc.gov/vaccines/hcp/imz-schedules/adult-notes.html. Accessed October 11, 2026.
  17. Congressional Research Service. The 2026 Childhood Immunization Schedule (R48982). June 11, 2026. Accessed October 11, 2026. https://www.congress.gov/crs_external_products/R/PDF/R48982/R48982.1.pdf. Accessed October 11, 2026.
  18. Centers for Disease Control and Prevention. CDC acts on Presidential Memorandum to update childhood immunization schedule. News release, January 5, 2026. Accessed October 11, 2026. https://www.cdc.gov/media/releases/2026/2026-cdc-acts-on-presidential-memorandum-to-update-childhood-immunization-schedule.html. Accessed October 11, 2026.
  19. Centers for Disease Control and Prevention. Healthcare professionals: immunization schedules. Accessed October 11, 2026. https://www.cdc.gov/vaccines/hcp/imz-schedules/index.html. Accessed October 11, 2026.
  20. American Academy of Pediatrics. AAP releases recommended childhood and adolescent immunization schedule for 2026. HealthyChildren.org news. Accessed October 11, 2026. https://healthychildren.org/English/news/Pages/AAPs-recommended-childhood-and-adolescent-immunization-schedule-for-2026.aspx. Accessed October 11, 2026.
  21. Centers for Disease Control and Prevention. Child and adolescent immunization schedule appendix: contraindications and precautions (July 2, 2025 edition). Accessed October 11, 2026. https://www.cdc.gov/vaccines/hcp/imz-schedules/child-adolescent-appendix.html. Accessed October 11, 2026.

For professional education. Check current labeling and guidance before acting. Not medical advice.

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