Haemophilus influenzae type b (Hib) Vaccines
About Hib Disease
Hib disease is a serious illness caused by the bacteria Haemophilus influenzae type b (Hib). These bacteria most commonly affect children younger than 5 years old. Adults 65 years or older, people who are American Indian or Alaska Native, and people with certain medical conditions are also at increased risk. People can spread the bacteria by coughing or sneezing while in close contact with others.
Hib bacteria can cause mild illness, such as an ear infection or bronchitis, or more severe illness such as pneumonia, meningitis, and infections of the bloodstream. Severe Hib infection, also called invasive Hib disease, requires treatment in a hospital and can sometimes result in death.
There are safe and effective vaccines that can protect against Hib disease.
Available Vaccines
There are 5 Hib vaccines approved for use in the United States: 3 single antigen vaccines and 2 combination vaccines.
Who Should Get Hib Vaccine
CDC recommends Hib vaccination for all children younger than 5 years old. Children need multiple (3 or 4) shots of a Hib vaccine. CDC recommends shots at the following ages:
- 2 months
- 4 months
- 6 months (if needed; depends on vaccine)
- 12 through 15 months
Older children and adults usually do not need a Hib vaccine. However, CDC recommends Hib vaccination for people with certain medical conditions.
For more information, see Who should get a Hib vaccine.
Vaccine Information Statements (VISs) are information sheets produced by CDC that explain both the benefits and risks of a vaccine.
Haemophilus influenzae type b (Hib) Vaccine
Talk with your
healthcare provider
about vaccines.
They can answer questions and
offer advice based on your
specific health needs.
Child and Adult Immunization Schedules
Get CDC’s official recommended immunization schedules for children, adolescents, and adults.
Manufacturer Package Inserts
Severe allergic reactions following vaccination are rare, but can be life threatening.
Symptoms of a severe allergic reaction can include hives, swelling of the face and throat, difficulty breathing, a fast heartbeat, dizziness, and weakness.
If such reactions occur, call 9-1-1 and get the person to the nearest hospital.
- Redness, warmth, or swelling at the site of injection
- Fever
- irritability
Who should not get a single antigen Hib vaccine
This vaccine is not intended for use in children younger than 6 weeks old.
People should not get a single antigen Hib vaccine if they:
- Have had a severe life-threatening allergic reaction after a previous dose or to any component of a Hib vaccine
- Have had a severe allergic reaction to latex
People should talk to their healthcare provider before getting a single antigen Hib vaccine if they:
- Are experiencing a moderate or severe acute illness with or without a fever
In some cases, the healthcare provider may decide to postpone Hib vaccination to a future visit.
- Redness, warmth, or swelling at the site of injection
- Fever
- Irritability
Who should not get a combination vaccine with Hib
This vaccine is not intended for use in children younger than 6 weeks old.
People should not get the combination vaccine with Hib if they:
- Have had a severe life-threatening allergic reaction after a previous dose or to any component of a combination vaccine with Hib
- Developed encephalopathy (e.g., coma, decreased level of consciousness, prolonged seizures) within 7 days of a previous dose of DTP (Diphtheria, Tetanus, and Pertussis) or DTaP (Diphtheria, Tetanus, and acellular Pertussis).
People should talk to their healthcare provider before getting a combination vaccine with Hib if they:
- Developed a condition called Guillain-Barré syndrome (GBS) within 6 weeks of getting a vaccine containing tetanus-toxoid
- Have a history of Arthus-type hypersensitivity reaction (i.e., severe injection site pain, swelling, and redness) after a previous dose of vaccine that protects against tetanus or diphtheria.
- Are pregnant
In some cases, the healthcare provider may decide to postpone Hib vaccination to a future visit.
More information about contraindications and precautions.
The Vaccine Adverse Event Reporting System (VAERS) is an early warning system, co-managed by CDC and FDA, that monitors for potential vaccine safety problems.
Healthcare providers and vaccine manufacturers are required by law to report certain adverse events following vaccination to VAERS; patients and caregivers can also submit reports.
For more information, see Report an Adverse Event to VAERS.
Hib Vaccination: What Everyone Should Know
What everyone should know about Hib and the vaccines that can protect against it.
Who Should Not Get Vaccinated?
Some people should not get certain vaccines or should wait before getting them. Read the CDC Guidelines for each vaccine.
Hib Vaccine – ACIP Recommendations
Official guidance on Hib vaccine from the Advisory Committee on Immunization Practices (ACIP).
Hib Information for Healthcare Professionals
Information for healthcare professionals about Hib vaccination and recommendations.
Findings from vaccine safety monitoring systems and scientific studies have shown that Hib vaccines have a favorable safety profile—the body of scientific evidence overwhelmingly supports their safety.
- A study of the safety of Hib vaccines (PedvaxHIB, ActHIB, Hiberix, Pentacel) in VAERS did not find any new or unexpected safety concerns and reconfirmed the safety of Hib vaccines.
- An observational study using Vaccine Safety Datalink records did not find an increased risk for seizures, meningitis/encephalitis/myelitis, allergic reactions, or fever among children younger than 1 year old.
Which adverse events are considered “serious?”
By the Code of Federal Regulations (CFR) Title 21 outcomes:
- Death
- A life-threatening adverse event
- A persistent or significant disability or incapacity
- A congenital anomaly or birth defect
- Hospitalization, or prolongation of existing hospitalization
Learn more about adverse events.
CDC and FDA monitor the safety of vaccines after they are approved or authorized. If a problem is found with a vaccine, CDC and FDA will inform health officials, health care providers, and the public.
CDC uses 3 systems to monitor vaccine safety:
- The Vaccine Adverse Event Reporting System (VAERS): an early warning system, co-managed by CDC and FDA, to monitor for potential vaccine safety problems. Anyone can report possible vaccine side effects to VAERS.
- The Vaccine Safety Datalink (VSD): a collaboration between CDC and 13 healthcare organizations that conducts vaccine safety monitoring and research.
- The Clinical Immunization Safety Assessment (CISA) Project: a partnership between CDC and several medical research centers that provides expert consultation and conducts clinical research on vaccine-associated health risks.
Related Scientific Articles
Oliver SE, Moore KL. Licensure of a Diphtheria and Tetanus Toxoids and Acellular Pertussis, Inactivated Poliovirus, Haemophilus influenzae Type b Conjugate, and Hepatitis B Vaccine, and Guidance for Use in Infants. MMWR Morb Mortal Wkly Rep. 2020 Feb 7;69:136-139.
Moro PL, Jankosky C, Menschik D, Lewis P, Duffy J, Stewart B, et al. Adverse events following Haemophilus influenzae type b (Hib) vaccines in the Vaccine Adverse Event Reporting System (VAERS), 1990-2013. J Pediatr. 2015 Apr;166(4):992-7.
Nelson JC, Yu O, Dominguez-Islas CP, Cook AJ, Peterson D, Greene SK. Adapting group sequential methods to observational postlicensure vaccine safety surveillance: Results of a pentavalent combination DTaP-IPV-Hib vaccine safety study. Am J Epidemiol. 2013 Jan 15;177(2):131-41.
Rinderknecht S, Bryant KA, Nolan T, Pavia-Ruz N, Doniz CA, Weber MA, et al. The safety profile of Haemophilus influenzae type b-Neisseria meningitidis serogroups C and Y tetanus toxoid conjugate vaccine (HibMenCY). Hum Vaccin Immunother. 2012 Mar;8(3):304-11.
CDC. Prevention and Control of Haemophilus influenzae type b Disease: Recommendations of the Advisory Committee on Immunization Practices (ACIP). MMWR. 2014;63(No. RR-1):1-14.
Guerra FA, Blatter MM, Greenberg DP, Pichichero M, Noriega FR. Pentacel Study Group. Safety and immunogenicity of a pentavalent vaccine compared with separate administration of licensed equivalent vaccines in US infants and toddlers and persistence of antibodies before a preschool booster dose: A randomized, clinical trial. Pediatrics. 2009 Jan;123(1):301-12.
Black S, Greenberg DP. A combined diphtheria, tetanus, five-component acellular pertussis, poliovirus, and Haemophilus influenzae type b vaccine. Expert Rev Vaccines 2005 Dec;4(6):793-805.
Davis RL, Black S, Shinefield H, Mahoney L, Zavitkovsky A, Lewis E, et al. Post-marketing evaluation of the short term safety of COMVAX. Vaccine. 2004 Jan 2;22(3-4):536-43.
Holmes SJ, Fritzell B, Guito KP, Esbenshade JF, Blatter MM, Reisinger KS, et al. Immunogenicity of Haemophilus influenzae type b polysaccharide-tetanus toxoid conjugate vaccine in infants. Am J Dis Child. 1993 Aug;147(8):832-6.
Decker MD, Edwards KM, Bradley R, Palmer P. Comparative trial in infants of four conjugate Haemophilus influenzae type b vaccines. J Pediatr. 1992 Feb;120(2 Pt 1):184-9.
Fritzell B, Plotkin S. Efficacy and safety of a Haemophilus influenzae type b capsular polysaccharide-tetanus protein conjugate vaccine. J Pediatr. 1992 Sep;121(3):355-62.