Diphtheria / Tetanus / Poliomyelitis (inactivated) vaccine (adsorbed) suspension for injection 0.5ml pre-filled syringes
Requires a prescription from a doctor or prescriber
Official documents, adverse reaction reporting, and safety monitoring
Report a side effect
Submit a Yellow Card report to the MHRA
Official medicine documents
Yellow Card
Report side effects (MHRA)
Drug safety updates
MHRA alerts for Diphtheria + Tetanus + Poliomyelitis vaccine
Safety monitoring data
Yellow Card reports
The MHRA Yellow Card scheme collects reports of suspected side effects from healthcare professionals and patients. View the Drug Analysis Profile (iDAP) for real-world adverse reaction data.
View Drug Analysis Profile
Browse all Drug Analysis Profiles A–Z
Browse all iDAP reports
Interactive Drug Analysis Profiles for all medicines
Report a side effect
Submit a Yellow Card report to the MHRA
Data from the MHRA Yellow Card scheme. A reported reaction does not necessarily mean the medicine caused it. Contains public sector information licensed under the Open Government Licence v3.0.
EudraVigilance
The European Medicines Agency (EMA) collects suspected adverse reaction reports from across the EU/EEA through the EudraVigilance system. Search for safety data on this medicine.
Search EudraVigilance database
Browse substances A–Z in the European adverse reaction database
About EudraVigilance
Learn about EU pharmacovigilance and safety monitoring
EudraVigilance data is published by the European Medicines Agency (EMA). A suspected adverse reaction is not necessarily caused by the medicine.
2 branded products available
MHRA licensed products
View all licensed products for Diphtheria + Tetanus + Poliomyelitis vaccine on the MHRA register
Revaxis vaccine suspension for injection 0.5ml pre-filled syringes
Revaxis vaccine suspension for injection 0.5ml pre-filled syringes
This is the NHS Drug Tariff indicative price used for reimbursement purposes. It may not reflect the price paid by patients or pharmacies.
View full Drug TariffSource: NHS Drug Tariff via NHSBSA. Derived from dm+d VMPP (Virtual Medicinal Product Pack) pricing data. Contains public sector information licensed under the Open Government Licence v3.0.
Therapeutically similar medicines
Similarity is based on WHO Anatomical Therapeutic Chemical (ATC) classification and on a factual NHS dm+d therapeutic-grouping code prefix. Source data: NHS dm+d via TRUD (OGL v3.0), WHO ATC/DDD Index.
NHS prescribing volume and spending trends
Check stock at pharmacies and supply information
Pharmacy stock checkers
Search for this medicine at major UK pharmacy chains. These links open the retailer's own website — results depend on their current online catalogue.
Supply & safety information
Official UK regulator monitoring and safety alerts
Pharmacy links redirect to the retailer's own search and do not represent real-time stock levels. Shortage and safety information sourced from MHRA drug safety updates (gov.uk, Crown Copyright under OGL v3.0).
Codes for healthcare professionals and prescribing systems
These codes are used by healthcare IT systems and prescribers to identify this medicine.
NHS UK identifiers
Browse tools
SNOMED CT and dm+d codes from NHS TRUD (Technology Reference data Update Distribution), licensed under the Open Government Licence v3.0. ATC codes from the WHO Collaborating Centre for Drug Statistics Methodology (whocc.no).
Active and completed clinical studies from ClinicalTrials.gov
Source: ClinicalTrials.gov, a database of the U.S. National Library of Medicine (NLM), National Institutes of Health (NIH). Data accessed via ClinicalTrials.gov API v2. Trial information is provided for research purposes and does not constitute medical advice.
Academic studies and reviews for this medicine's active substance
Showing the 50 most relevant studies.
Reviews & meta-analyses: 32 · Randomised trials: 11 · 1995–2026
Showing the 50 most relevant studies, sorted by most relevant.
Maggi S, Fulöp T, De Vita E, et al.
2025
- Dementia
- Vaccination
- Pneumococcal Vaccines
ImportanceDementia is a highly prevalent issue in older people. Whilst the prevention of dementia is a public health priority, the role of vaccinations is still largely unexplored.ObjectiveThe aim of this systematic review is to evaluate whether common adult vaccinations are associated with a reduced risk of dementia.Data sourcesPubMed, Embase and Web of Science were searched from inception to 1 January 2025.Study selectionObservational studies comparing dementia and mild cognitive impairment incidence between vaccinated and unvaccinated adults aged ≥50 years.Data extraction and synthesisFour reviewers independently extracted data and assessed study quality using the Newcastle-Ottawa Scale. Risk ratios (RRs) and 95% confidence intervals (CIs) were pooled using a random-effects model.Main outcomes and measuresIncidence of dementia, including its subtypes.ResultsTwenty-one studies (n = 104 031 186 participants) were included. Vaccination against herpes zoster was associated with a reduced risk of any dementia (RR 0.76, 95% CI 0.69-0.83) and Alzheimer's disease (RR 0.53, 95% CI 0.44-0.64). Influenza vaccination was linked to a reduction in dementia risk (RR 0.87, 95% CI 0.77-0.99), as was pneumococcal vaccination (RR 0.64, 95% CI 0.47-0.87) for Alzheimer's disease. Tetanus, diphtheria, pertussis (Tdap) vaccination was also associated with a significant reduction for any dementia (RR 0.67, 95% CI 0.54-0.83).Conclusions and relevanceAdult vaccinations, particularly against herpes zoster, influenza, pneumococcus and Tdap, are associated with a lower risk of dementia. Vaccination strategies should be incorporated into public health initiatives for dementia prevention.Registrationhttps://osf.io/x3d4f/.
Abstract licence: CC BY
Rojas M, Florencia Lución M, Becker Feijó R, et al.
2025
- Vaccination
- Immunization Programs
- Vaccination Coverage
This review aimed to characterize adolescent vaccination schedules in publicly funded national immunization programs in Latin America and the Caribbean. The initial review identified vaccine type, target age and gender, dose schedule, and vaccination coverage rate (VCR) across 50 countries/territories in the region. A systematic review from January 2010-October 2023 was then conducted to identify primary data collection studies reporting VCRs. Overall, 42 webpages and 23 primary studies were identified. Among 47 countries/territories with ≥1 vaccine for adolescent immunization, human papillomavirus (HPV) vaccine was included in 45, tetanus component vaccines in 43, and meningococcal vaccines in 10. Catch-up vaccination for hepatitis B in 17, and yellow fever in all 13 endemic countries/territories. VCRs were primarily available for HPV. The findings of this review underscore the need to prioritize adolescent vaccination, improve accessibility, and strengthen tracking infrastructure to ensure comprehensive protection of this age group across the region.
Abstract licence: Public domain
Protano C, Valeriani F, Vitale K, et al.
2024
Background: Many human activities release harmful substances, contaminating the air, water, and soil. Since exposure to environmental pollutants is currently unavoidable, it is important to verify how these compounds may influence individual immune responses to vaccines. Methods: This review was conducted in accordance with the PRISMA statement. The protocol was registered on the PROSPERO platform with the following ID: CRD42024582592. We evaluated all observational, semi-experimental, and experimental studies written in both Italian and English that reported possible effects of exposure to environmental pollutants on the production of vaccine-induced antibodies. Results: Forty-two studies were included. The effects of pollutants were examined mainly in terms of antibody production in relation to mumps, measles and rubella, diphtheria and tetanus, hepatitis A and B, Haemophilus influenzae type B, influenza, tuberculosis, pertussis, Japanese encephalitis, poliomyelitis, and COVID-19 vaccines. Perfluorinated compounds were the most studied pollutants. Conclusions: Correlations between exposure to pollutants and reductions in antibody production were found in quite all the selected studies, suggesting that pollution control policies could contribute to increase the efficacy of vaccination campaigns. However, the heterogeneity of the examined studies did not allow us to perform a meta-analysis, and the literature on each type of vaccine or pollutant is still too limited to generate robust evidence. In order to confirm the findings of the present systematic review, and in the perspective of establishing possible exposure limit values for each type of pollutant, further research in this field is required.
Abstract licence: CC BY
Terekhov RP, Svotin AA, Korochkina MD, et al.
2025
- Poliomyelitis
- Poliovirus Vaccine, Inactivated
- Poliovirus Vaccines
Poliomyelitis, preventable only through vaccination, remains a global health concern, with wild poliovirus transmission and the emergence of vaccine-derived polioviruses. The risk of further deterioration of the situation jeopardizes efforts to eradicate polio, which has been a long-term goal for the whole world. In this systematic review, an analysis of randomized clinical trials was carried out to comprehensively assess the immunogenicity and safety of various polio immunization methods in infants. Geometric mean neutralizing antibody titers (GMT) data collected after 28-31 days after immunization were used to calculate the geometric mean titer ratio (GMR), the analysis of which showed that both inactivated polio vaccine (IPV) and Sabin strain-based inactivated polio vaccine (sIPV) as primary vaccination induce high antibody rates. Average GMR rates (CI = 0.05) for the 3 types of polio were 83.08, 33.60, and 166.30 for IPV and 234.35, 44.04, and 163.13 for sIPV, with fractional IPV showing similar results. One or two doses of IPV were insufficient to induce protection levels of antibodies against type 2 poliovirus. The novel oral polio vaccine type 2 (nOPV2) and trivalent oral polio vaccine (tOPV) also demonstrated immunogenicity in establishing immunity comparable to the inactivated vaccine; the latter exhibited an average GMR of 50.75 for serotype 2. High antibody levels were also induced by combined vaccine schedules, with sIPV-sIPV-bOPV (GMR of 1,172.7 for type 1 and 887.6 for type 3) and IPV combinations with diphtheria-tetanus-whole-cell pertussis, hepatitis B and Haemophilus influenzae type b (351.2, 258.8, and 573.6 for the 3 types) or pentavalent rotavirus vaccine (354.6, 117.7, and 540.9 for the 3 types) establishing particularly high antibody levels. Analysis of adverse events presented all vaccines to be well-tolerated and safe, with a tendency for combination vaccines to have a higher frequency of local reactions and fever. While the studies presented a diverse landscape with some existing areas of concern, this review provides structured evidence supporting the safety and immunogenicity of existing polio vaccines, as well as highlighting the interchangeability of different vaccination approaches in infants. Future research should aim to provide detailed reporting of adverse events in order to facilitate more comprehensive assessment of vaccine immunogenicity and, therefore, efficacy.
Abstract licence: CC BY
Halliday R, Morais B, Bouaddi O, et al.
2025
- Transients and Migrants
- Vaccine-Preventable Diseases
- Whooping Cough
BackgroundMigrants in Europe often face barriers to vaccination, increasing their vulnerability to vaccine-preventable diseases (VPDs). Despite policies promoting catch-up immunisation on arrival, data on VPD burden and outcomes among migrants remain limited. This systematic review synthesises evidence on the prevalence, incidence, mortality, and outcomes of VPDs in migrants across EU/EEA countries, UK, and Switzerland.MethodsWe searched Medline, Embase, Global Health, and grey literature sources (including websites of national public health organisations and agencies) for primary studies and reports on VPD cases among migrants (foreign-born individuals) in 32 European countries, published between January 2010 and April 2024. Data on demographics, VPD type, vaccination status, and outcomes were extracted. We focused on diphtheria, measles, mumps, pertussis, rubella, and tetanus. Study quality was assessed using Joanna Briggs Institute tools.ResultsFifty-seven studies met inclusion criteria, reporting 1950 VPD cases in migrants across 16 countries (2010-2024). Most studies were in Germany (n = 12), Spain (n = 11), Switzerland (n = 8), Greece (n = 6), and the UK (n = 7). Reported cases included: measles (n = 992; 50.8 %), diphtheria (n = 546; 28.0 %), pertussis (n = 267; 13.7 %), and mumps (n = 137; 7.0 %). No cases of rubella or tetanus were reported. Migrants affected mainly included asylum seekers (n = 23 studies), refugees (n = 6), labour migrants (n = 2). Six studies from Greece, Germany, and Spain accounted for 1942 cases (99.6 %). Over half of diphtheria cases (n = 307; 55.4 %) occurred in reception centres. Diphtheria primarily affected adolescents and adults (n = 10 studies), while measles cases were mostly in children. Migrants from the Eastern Mediterranean and Africa were disproportionately affected by diphtheria. Non-EU/EEA European migrants (WHO EUR), mainly from Bosnia and Herzegovina and Serbia, accounted for most measles cases (87 %), and non-European migrants were from Somalia (n = 112), Afghanistan (n = 94), Eritrea (n = 76), and Syria (n = 64). Vaccination status was unknown or unreported in over 60 % of cases. Five VPD related deaths were reported of which 4/5 were due to measles.ConclusionMigrants are at increased risk of VPDs due to gaps in vaccination. Strengthening catch-up vaccination, particularly in adolescents and adults, and improving data collection are essential next steps.
Abstract licence: CC BY
Niyati R, Rezahosseini O, Ekenberg C, et al.
2025
Background: Co-administration of vaccines can impact the immune response and safety. We aim to systematically review the current scientific literature and find evidence regarding the immunogenicity and safety of pneumococcal vaccines co-administered with common vaccines that are recommended for travelers, including hepatitis A, hepatitis B, yellow fever, tetanus, diphtheria, and acellular pertussis (Tdap), Japanese encephalitis, rabies, typhoid, or meningococcal (MCV) vaccine in adults (18 years or older). Methods: We followed the PRISMA 2020 guidelines and used the PICOS process to select the keywords. We searched PubMed, Web of Science, Scopus, EMBASE, and Google from 1 January 2000 to 30 June 2024. We included randomized controlled trials, non-randomized controlled trials, observational studies, case series, and case reports in adults, all published in English. Results: Out of 598 articles screened, 6 studies were included in our study. Three studies involved immunocompetent individuals, and three involved immunocompromised individuals. Co-administration of pneumococcal vaccine with Tdap or Hepatitis A in immunocompetent individuals was safe and immunogenic. Similar findings were reported for immunocompromised individuals when pneumococcal vaccines were co-administered with Tdap, hepatitis A, and hepatitis B. However, no reports investigated the co-administration of yellow fever, rabies, Japanese encephalitis, and typhoid. Two non-randomized studies in immunocompromised individuals had a high risk of bias. Conclusions: The studies collectively indicate that the co-administration of pneumococcal vaccines with Hepatitis A and Tdap vaccines in adult immunocompetent and immunocompromised individuals is safe and immunogenic. However, a knowledge gap remains, and further high-quality studies are needed, particularly due to the limited number of studies and the potential risk of bias.
Abstract licence: CC BY
Baiocchi C, Bhardwaj M
2025
- Parents
- Disease Outbreaks
- Vaccination Refusal
BackgroundParental vaccine hesitancy is a growing concern, and Europe has witnessed significant outbreaks of Vaccine-Preventable Diseases (VPDs) over the past two decades. Unvaccinated children are at increased risk of contracting VPDs, and the incidence of several VPDs has been on the rise. Vaccine hesitancy is a serious global health challenge. Nevertheless, the specific association between intentionally unvaccinated children and VPD outbreaks in Europe remains inadequately explored. This rapid systematic review aims to identify and examine studies focused on VPD outbreaks in Europe that involve intentionally non-vaccinated children and the factors associated with vaccine hesitancy.MethodsA rapid systematic review was conducted with a comprehensive search of electronic databases, including Medline, Embase, and Academic Search Elite. The population, exposure and outcome (PEO) framework was used to formulate the research question, inclusion and exclusion criteria. Publications from 2010 to and including August 2023 were included.ResultsOf the 330 studies initially identified, a total of nine were included in the final review. The included studies indicated that unvaccinated children due to parental refusal are contributing to outbreaks of measles, diphtheria and tetanus in the European region.ConclusionThis systematic review provides compelling evidence of an association between intentionally unvaccinated children-those unvaccinated due to parental refusal-and outbreaks of vaccine-preventable diseases (VPDs). The findings strongly suggest that this group contributes significantly to VPD outbreaks within the European region. To deepen our understanding, further research is needed to compare the role of intentionally unvaccinated children with that of other unvaccinated groups (e.g., those unvaccinated due to medical contraindications, immunosuppression, or limited access to healthcare) in the emergence and spread of VPDs.
Abstract licence: CC BY-NC-ND
Sun J, Jin X, Li H, et al.
2026
OBJECTIVE: This study aims to systematically review the published economic evaluations of vaccines included in China’s National Immunization Program (NIP), synthesise the current evidence base, and assess their cost-effectiveness. METHODS: A comprehensive search was conducted across PubMed, Web of Science, Embase, CNKI, CSTJ, and Wanfang Data for cost-benefit analyses (CBA), cost-effectiveness analyses (CEA), and cost-utility analyses (CUA) related to NIP vaccines in China, from database inception to 14 July 2025. Studies were screened following the PRISMA guidelines. The study’s reporting quality was assessed using the CHEERS 2022 checklist, while methodological quality was evaluated using the QHES instrument. RESULTS: A total of 41 studies were included and demonstrated an overall moderate methodological quality (mean CHEERS score: 66.42; mean QHES score: 70.63). The included studies covered a range of NIP-targeted vaccines, including hepatitis B, measles, tuberculosis, diphtheria-pertussis-tetanus, hepatitis A, and meningococcal vaccines, with hepatitis B receiving the greatest research focus (n = 32). Most evaluations were conducted from a societal or healthcare system perspective. The majority of studies reported benefit-cost ratios (BCR) greater than 1 or incremental cost-effectiveness ratios (ICER) below the per capita GDP threshold, indicating substantial economic value. Despite variations in model structures, baseline parameters, and assumptions, all studies consistently concluded that NIP vaccines are cost-effective compared with no vaccination. Hepatitis B vaccination, particularly when combined with maternal transmission prevention strategies, demonstrated exceptionally high net benefits at both national and subnational levels. CONCLUSION: NIP vaccines in China offer substantial economic value; however, interpretation of the findings may be influenced by methodological heterogeneity and the use of GDP per capita-based cost-effectiveness thresholds, and the adoption of standardised evaluation methods is essential to support policy optimisation and sustainability.
Abstract licence: CC BY-NC-ND
Barnidge IT, Ferreira AJF, Kovats S, et al.
2026
Terekhov RP, Svotin AA, Korochkina MD, et al.
2025
Sources: aggregated from Europe PMC (EMBL-EBI), OpenAlex, Crossref, PubMed and other open scholarly databases. Retracted articles are excluded. Study information is provided for research purposes and does not constitute medical advice.
Scientific data (pharmacology, interactions, ADME) is not yet available for this medicine. Clinical sections are sourced from the NHS dm+d database.