Prevnar 20 (PCV20)
Pronunciation: PREV-nar twenty.
- Generic name
- Pneumococcal 20-valent Conjugate Vaccine
- Drug class
- Pneumococcal conjugate vaccine (PCV20)
- Form
- Suspension for injection, 0.5 mL single-dose pre-filled syringe
- Route
- Intramuscular injection
- Legal status
- Prescription-only, administered by a healthcare professional
Availability and supply rules vary by country
Trade names by country: United States · United Kingdom · Canada · Australia
Australia: Prevenar 20 (5) · Full directory
What Pneumococcal 20-valent Conjugate Vaccine is and how it works
Prevnar 20 / Prevenar 20 is a vaccine that helps protect against invasive disease, pneumonia, and (in young children) middle-ear infections caused by 20 different types (serotypes) of the bacterium Streptococcus pneumoniae. It works by training the immune system to recognise and fight these specific pneumococcal serotypes before a real infection takes hold. (1) (2)
This vaccine is given as an injection by a doctor, nurse, or pharmacist, following an age-based schedule -- it is not something you take or dose yourself. It has no boxed warning, but like all vaccines it carries a small risk of allergic reaction, so it is given where medical treatment for a severe reaction is immediately available.
Mechanism of action: how Pneumococcal 20-valent Conjugate Vaccine works
Prevnar 20/Prevenar 20 is a 20-valent pneumococcal conjugate vaccine: purified capsular polysaccharides from 20 S. pneumoniae serotypes are each individually conjugated to CRM197, a non-toxic carrier protein derived from diphtheria toxin, to elicit a T-cell-dependent immune response with stronger and longer-lasting antibody production (including in infants) than an unconjugated polysaccharide vaccine. (1)
What Pneumococcal 20-valent Conjugate Vaccine is used for
Prevention of invasive pneumococcal disease (infants through adults)
Used for active immunisation to help prevent invasive disease (such as bacteraemia, meningitis, and bacteraemic pneumonia) caused by the 20 S. pneumoniae serotypes covered by the vaccine, in people 6 weeks of age and older. (1) (4)
Prevention of pneumonia in adults
Used in adults 18 years and older to help prevent pneumonia caused by the covered S. pneumoniae serotypes. (1) (3)
Prevention of middle-ear infection (otitis media) in young children
Used in children 6 weeks through 5 years of age to help prevent acute middle-ear infections caused by 7 of the covered S. pneumoniae serotypes. (1) (3)
Before taking Pneumococcal 20-valent Conjugate Vaccine
Do not take / not appropriate for
- This vaccine should not be given to anyone who has had a severe allergic reaction (such as anaphylaxis) to a previous dose of Prevnar 20/Prevenar 20, to any of its components, or to diphtheria toxoid (the carrier protein used in this and some other vaccines). (all countries) (1) (2)
- Vaccination is generally deferred (postponed, not cancelled) during an acute severe febrile illness -- your immunisation provider will decide when it is safe to proceed. (all countries) (2)
Tell your clinician about
- Any past severe allergic reaction to this vaccine, an earlier pneumococcal vaccine, or to diphtheria-toxoid-containing vaccines.
- Whether your baby was born prematurely -- the timing of vaccination and a period of monitoring afterwards may need individual consideration.
- Any bleeding disorder, or if you take a blood thinner, since an intramuscular injection needs extra care in these situations.
- Any condition or treatment that weakens the immune system, which may mean the vaccine works less well and needs individualised advice.
- Whether you are pregnant, plan to become pregnant, or are breastfeeding.
How to take Pneumococcal 20-valent Conjugate Vaccine
- This is a vaccine given as an injection into a muscle (the thigh in infants, the upper arm in older children and adults) by a doctor, nurse, or pharmacist -- it is never self-administered.
- The number of doses and the timing between them depend on the age at which the immunisation series is started and any prior pneumococcal vaccination -- your immunisation provider follows the age-based schedule below.
- Appropriate medical treatment must be available at the point of vaccination in case of a rare severe allergic reaction.
Procedures and treatment changes
Tell the treating team before surgery, procedures, or any medicine change. Do not alter treatment without the responsible clinician. (1) (2) (3) (4) (5) (6)
Missed dose
If a scheduled dose in the immunisation series is missed or delayed, contact your immunisation provider to arrange the next dose as soon as practical -- there is no need to restart the whole series, but your provider will confirm the right next step for your age and history.
Overdose
An overdose is not applicable in the usual sense for a single-dose pre-filled syringe given by a healthcare professional. If you have concerns about vaccine administration or develop concerning symptoms afterwards, contact your immunisation provider or seek medical attention. (1)
Side effects
Side effects and their urgency vary; report severe, persistent, or concerning symptoms.
In infants and young children: irritability, drowsiness, injection-site pain, decreased appetite, and redness or swelling at the injection site; fever is also common.
What to notice: In infants and young children: irritability, drowsiness, injection-site pain, decreased appetite, and redness or swelling at the injection site; fever is also common.
What to do: Discuss persistent or troublesome symptoms with the treating clinician or pharmacist. (1) (2)
In older children and adults: pain at the injection site, muscle pain, fatigue, and headache; joint pain and injection-site swelling are also common in adults.
What to notice: In older children and adults: pain at the injection site, muscle pain, fatigue, and headache; joint pain and injection-site swelling are also common in adults.
What to do: Discuss persistent or troublesome symptoms with the treating clinician or pharmacist. (1) (2)
Most of these reactions are mild to moderate and resolve within 1-3 days.
What to notice: Most of these reactions are mild to moderate and resolve within 1-3 days.
What to do: Discuss persistent or troublesome symptoms with the treating clinician or pharmacist. (2)
Serious warnings
Signs of a severe allergic reaction (anaphylaxis) — emergency
Symptoms: Swelling of the face, lips, tongue, or throat; difficulty breathing; widespread rash or hives; dizziness or collapse, usually within minutes of the injection.
Action: This is why vaccination is given where medical treatment for anaphylaxis is immediately available. Seek emergency help immediately if symptoms develop after leaving the clinic. (1) (2)
Apnoea (pauses in breathing) in infants born prematurely — high caution
Symptoms: Pauses in breathing observed in some very premature infants following intramuscular vaccination.
Action: Discuss timing of vaccination with your infant's clinician if they were born prematurely -- a period of respiratory monitoring after the injection may be considered for very premature infants. (1) (2)
Interactions
- This vaccine can generally be given at the same visit as other routinely recommended vaccines, using separate injection sites and syringes, per official immunisation schedules -- your immunisation provider will confirm what is appropriate for your age and history. (1)
- In people with a weakened immune system (for example, from a medical condition or immunosuppressive treatment), the immune response to the vaccine may be reduced -- this does not necessarily mean it should not be given, but timing and expectations should be discussed with your clinician. (2)
Pregnancy, breastfeeding, kidney/liver function, age
Pregnancy
No adequate and well-controlled studies of this vaccine exist in pregnant women in the sources reviewed; animal reproduction data did not show evidence of fetal harm, but vaccination in pregnancy should be discussed with your clinician. (1) (2) (3) (4) (5) (6)
Breastfeeding
It is not known whether this vaccine passes into human breast milk; discuss with your clinician if you are breastfeeding. (1) (2) (3) (4) (5) (6)
Children
Authorised from 6 weeks of age; the number and timing of doses depends on the age the series is started (see how-to-take). Also helps prevent otitis media (ear infection) in children 6 weeks through 5 years for the serotypes covered. (1) (2) (3) (4) (5) (6)
Elderly
Included in the adult single-dose recommendation (18 years and older); no upper age limit is described in the sources reviewed. (1) (2) (3) (4) (5) (6)
Hepatic_impairment
No specific guidance identified in the sources reviewed for this vaccine. (1) (2) (3) (4) (5) (6)
Renal_impairment
No specific guidance identified in the sources reviewed for this vaccine. (1) (2) (3) (4) (5) (6)
Source_ids
US-DAILYMED-PREVNAR20-2026,UK-EMC-PREVENAR20-2026 (1) (2) (3) (4) (5) (6)
Monitoring
Before starting
- Review of allergy history to this vaccine, diphtheria-toxoid-containing vaccines, or any component
- Confirmation of prior pneumococcal vaccination history to determine the correct dose/schedule
- For infants born prematurely, review of respiratory status before deciding on timing
During treatment
- Brief observation period after the injection is standard practice for any vaccine, to watch for an immediate allergic reaction.
- For some very premature infants, a period of respiratory monitoring after vaccination may be considered.
Storage
Stored and handled by healthcare providers in a refrigerator at 2C to 8C, protected from light, and not frozen -- this is a clinic-administered product, not one that patients store at home.
Professional information
Clinician-facing context only, sourced from the current US FDA prescribing information and UK SmPC; verify against the current full label/product monograph before administering.
United States / United Kingdom / European Union / Canada / Australia
Indication: Infant series (from 6 weeks of age)
Dose summary: 4-dose series at approximately 2, 4, 6, and 12-15 months; alternative 3-dose infant series (2 primary doses plus a booster at 11-15 months) also described in the UK SmPC.
Renal context: Not applicable -- this is a vaccine, not renally dosed. (1) (2)
United States / United Kingdom / European Union / Canada / Australia
Indication: Adults 18 years and older
Dose summary: Single 0.5 mL intramuscular dose, preferably in the deltoid muscle.
Renal context: Not applicable -- this is a vaccine, not renally dosed. (1) (2)
Hepatic guidance
No hepatic-specific guidance identified in the sources reviewed.
Overdose note
Not applicable in the conventional sense for a single-dose pre-filled syringe administered by a healthcare professional. (1)
Frequently asked questions
Is Prevnar 20 / Prevenar 20 available in the US, UK, Europe, Canada, Australia, and New Zealand?
It is authorised in the United States (as Prevnar 20), the United Kingdom, European Union, and Australia (as Prevenar 20 -- originally Apexxnar in the EU), and Canada (as Prevnar 20). Its status in New Zealand could not be confirmed: a direct search of Medsafe's own records found only a data sheet for the older Prevenar 13 vaccine, which remains the pneumococcal vaccine on New Zealand's National Immunisation Schedule as of this research date, with no Prevenar 20 record located. (1) (2) (3) (4) (5) (6)
Does Prevnar 20 / Prevenar 20 have a boxed warning?
No. This vaccine does not carry a boxed warning (the FDA's strongest safety warning). It does carry standard vaccine precautions, including a warning about apnoea in some infants born prematurely and the need for anaphylaxis treatment to be immediately available. (1)
How is the number of doses decided?
It depends on the age the series is started and whether earlier pneumococcal vaccine doses were already given. Infants starting on schedule from 6 weeks of age typically receive 4 doses; children starting later need fewer catch-up doses; adults 18 years and older need only a single dose. Your immunisation provider follows the official age-based schedule to decide. (1) (4)
What is the mechanism of action of Pneumococcal 20-valent Conjugate Vaccine?
Prevnar 20/Prevenar 20 is a 20-valent pneumococcal conjugate vaccine: purified capsular polysaccharides from 20 S. pneumoniae serotypes are each individually conjugated to CRM197, a non-toxic carrier protein derived from diphtheria toxin, to elicit a T-cell-dependent immune response with stronger and longer-lasting antibody production (including in infants) than an unconjugated polysaccharide vaccine. (1)
References
- PREVNAR 20 (Pneumococcal 20-valent Conjugate Vaccine) suspension for intramuscular injection -- full prescribing informationU.S. Food and Drug Administration / DailyMed (NIH), full prescribing information, Pfizer Inc. · United States · accessed 2026-07-30 · source 1
- Prevenar 20 suspension for injection in pre-filled syringe -- Summary of Product Characteristicselectronic medicines compendium (emc), United Kingdom -- Pfizer Limited · United Kingdom · accessed 2026-07-30 · source 2
- Prevenar 20 (previously Apexxnar) -- EPAR medicine overviewEuropean Medicines Agency (EMA), EPAR · European Union · accessed 2026-07-30 · source 3
- PREVNAR 20 (Pneumococcal 20-valent Conjugate Vaccine [Diphtheria CRM197 Protein]) -- Product MonographHealth Canada, Drug Product Database / Summary Basis of Decision, Pfizer Canada · Canada · accessed 2026-07-30 · source 4
- Prevenar 20 pneumococcal polysaccharide conjugate vaccine -- ARTG entry 376353 / AusPARTherapeutic Goods Administration (TGA), Australia · Australia · accessed 2026-07-30 · source 5
- Medsafe site search for 'prevenar'/'Prevnar 20' data sheetsMedsafe (New Zealand regulator) -- direct site search · New Zealand · accessed 2026-07-30 · source 6
Brand names by country
Single-ingredient Pneumococcal 20-valent Conjugate Vaccine names are shown separately by country. Product availability, strengths, and supply rules can change; combination products are not included here.
Priority countries
United States
- Prevnar 20 (1)FDA approved currently labeled · 0.5 mL single-dose pre-filled syringe · Pfizer Inc.
United Kingdom
- Prevenar 20 (2)MHRA licensed emc smpc confirmed · 0.5 mL single-dose pre-filled syringe · Pfizer Limited
Canada
- Prevnar 20 (4)Health Canada approved 2023-07-21 confirmed · 0.5 mL single-dose pre-filled syringe · Pfizer Canada
Australia
- Prevenar 20 (5)TGA ARTG registered 2022-12-02 confirmed · 0.5 mL single-dose pre-filled syringe · Pfizer Australia Pty Ltd
View brands in additional countries.
European Union
Prevenar 20 (previously Apexxnar) (3)