Safety and utilisation of AZD1222 (ChAdOx1 nCoV-19) COVID-19 vaccine: a UK post-authorisation active surveillance study
ObjectivesTo monitor the safety and utilisation of AZD1222 under real-world use in the UK.DesignA non-interventional post-authorisation active surveillance study.SettingVaccination sites in the UK.ParticipantsA total of 17 945 participants were eligible and provided consent to participate in the stu...
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| Vydané v: | BMJ open Ročník 15; číslo 5; s. e093366 |
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England
British Medical Journal Publishing Group
02.05.2025
BMJ Publishing Group LTD BMJ Publishing Group |
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| Abstract | ObjectivesTo monitor the safety and utilisation of AZD1222 under real-world use in the UK.DesignA non-interventional post-authorisation active surveillance study.SettingVaccination sites in the UK.ParticipantsA total of 17 945 participants were eligible and provided consent to participate in the study between 1 March 2021 and 6 April 2023. Participants were followed up at weeks 1, 4 and 14 and at months 6, 9, 12 and 18 after the first dose of AZD1222 vaccination and prompted to complete electronic data capture forms. A total of 11 219 participants submitted a Follow-Up 1 form and 5189 participants submitted a Follow-Up 7 form (at 18 months).Primary and secondary outcome measuresThe safety of AZD1222, including the identification, assessment and quantification of serious adverse events (SAEs) and adverse events of special interest (AESI), was examined. The utilisation of AZD1222 was described and characterised, including populations with missing information.ResultsThe majority of participants were women (n=10 845; 60.4%) and the median age (IQR) was 50 (43, 62) years. Most participants were from white ethnic groups (n=13 112; 73.1%). Headache and fatigue had the highest reported incidence rate (421.28 cases per 1000 person years and 386.00 cases per 1000 person years, respectively). The most frequently reported AESI was anosmia (6.25 cases per 1000 person years). An increased Observed versus Expected (O:E) ratio was seen for anaphylaxis (O:E 7.38 (95% CI 2.80 to 11.95); based on 10 observed cases (expected cases: 1.36)) and anosmia and/or ageusia (O:E 39.23 (95% CI 29.13 to 49.32), based on 58 observed cases (expected cases: 1.48)).ConclusionsThe most frequent vaccinee-reported adverse events (AEs) were headache and fatigue. An increased O:E ratio was seen for the AEs of anaphylaxis and anosmia and/or ageusia. No safety signals were identified throughout the course of this study.Trial registration numberThis study is registered with the HMA-EMA Catalogue of RWD studies (EUPAS44035). |
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| AbstractList | ObjectivesTo monitor the safety and utilisation of AZD1222 under real-world use in the UK.DesignA non-interventional post-authorisation active surveillance study.SettingVaccination sites in the UK.ParticipantsA total of 17 945 participants were eligible and provided consent to participate in the study between 1 March 2021 and 6 April 2023. Participants were followed up at weeks 1, 4 and 14 and at months 6, 9, 12 and 18 after the first dose of AZD1222 vaccination and prompted to complete electronic data capture forms. A total of 11 219 participants submitted a Follow-Up 1 form and 5189 participants submitted a Follow-Up 7 form (at 18 months).Primary and secondary outcome measuresThe safety of AZD1222, including the identification, assessment and quantification of serious adverse events (SAEs) and adverse events of special interest (AESI), was examined. The utilisation of AZD1222 was described and characterised, including populations with missing information.ResultsThe majority of participants were women (n=10 845; 60.4%) and the median age (IQR) was 50 (43, 62) years. Most participants were from white ethnic groups (n=13 112; 73.1%). Headache and fatigue had the highest reported incidence rate (421.28 cases per 1000 person years and 386.00 cases per 1000 person years, respectively). The most frequently reported AESI was anosmia (6.25 cases per 1000 person years). An increased Observed versus Expected (O:E) ratio was seen for anaphylaxis (O:E 7.38 (95% CI 2.80 to 11.95); based on 10 observed cases (expected cases: 1.36)) and anosmia and/or ageusia (O:E 39.23 (95% CI 29.13 to 49.32), based on 58 observed cases (expected cases: 1.48)).ConclusionsThe most frequent vaccinee-reported adverse events (AEs) were headache and fatigue. An increased O:E ratio was seen for the AEs of anaphylaxis and anosmia and/or ageusia. No safety signals were identified throughout the course of this study.Trial registration numberThis study is registered with the HMA-EMA Catalogue of RWD studies (EUPAS44035). To monitor the safety and utilisation of AZD1222 under real-world use in the UK. A non-interventional post-authorisation active surveillance study. Vaccination sites in the UK. A total of 17 945 participants were eligible and provided consent to participate in the study between 1 March 2021 and 6 April 2023. Participants were followed up at weeks 1, 4 and 14 and at months 6, 9, 12 and 18 after the first dose of AZD1222 vaccination and prompted to complete electronic data capture forms. A total of 11 219 participants submitted a Follow-Up 1 form and 5189 participants submitted a Follow-Up 7 form (at 18 months). The safety of AZD1222, including the identification, assessment and quantification of serious adverse events (SAEs) and adverse events of special interest (AESI), was examined. The utilisation of AZD1222 was described and characterised, including populations with missing information. The majority of participants were women (n=10 845; 60.4%) and the median age (IQR) was 50 (43, 62) years. Most participants were from white ethnic groups (n=13 112; 73.1%). Headache and fatigue had the highest reported incidence rate (421.28 cases per 1000 person years and 386.00 cases per 1000 person years, respectively). The most frequently reported AESI was anosmia (6.25 cases per 1000 person years). An increased Observed versus Expected (O:E) ratio was seen for anaphylaxis (O:E 7.38 (95% CI 2.80 to 11.95); based on 10 observed cases (expected cases: 1.36)) and anosmia and/or ageusia (O:E 39.23 (95% CI 29.13 to 49.32), based on 58 observed cases (expected cases: 1.48)). The most frequent vaccinee-reported adverse events (AEs) were headache and fatigue. An increased O:E ratio was seen for the AEs of anaphylaxis and anosmia and/or ageusia. No safety signals were identified throughout the course of this study. This study is registered with the HMA-EMA Catalogue of RWD studies (EUPAS44035). To monitor the safety and utilisation of AZD1222 under real-world use in the UK.OBJECTIVESTo monitor the safety and utilisation of AZD1222 under real-world use in the UK.A non-interventional post-authorisation active surveillance study.DESIGNA non-interventional post-authorisation active surveillance study.Vaccination sites in the UK.SETTINGVaccination sites in the UK.A total of 17 945 participants were eligible and provided consent to participate in the study between 1 March 2021 and 6 April 2023. Participants were followed up at weeks 1, 4 and 14 and at months 6, 9, 12 and 18 after the first dose of AZD1222 vaccination and prompted to complete electronic data capture forms. A total of 11 219 participants submitted a Follow-Up 1 form and 5189 participants submitted a Follow-Up 7 form (at 18 months).PARTICIPANTSA total of 17 945 participants were eligible and provided consent to participate in the study between 1 March 2021 and 6 April 2023. Participants were followed up at weeks 1, 4 and 14 and at months 6, 9, 12 and 18 after the first dose of AZD1222 vaccination and prompted to complete electronic data capture forms. A total of 11 219 participants submitted a Follow-Up 1 form and 5189 participants submitted a Follow-Up 7 form (at 18 months).The safety of AZD1222, including the identification, assessment and quantification of serious adverse events (SAEs) and adverse events of special interest (AESI), was examined. The utilisation of AZD1222 was described and characterised, including populations with missing information.PRIMARY AND SECONDARY OUTCOME MEASURESThe safety of AZD1222, including the identification, assessment and quantification of serious adverse events (SAEs) and adverse events of special interest (AESI), was examined. The utilisation of AZD1222 was described and characterised, including populations with missing information.The majority of participants were women (n=10 845; 60.4%) and the median age (IQR) was 50 (43, 62) years. Most participants were from white ethnic groups (n=13 112; 73.1%). Headache and fatigue had the highest reported incidence rate (421.28 cases per 1000 person years and 386.00 cases per 1000 person years, respectively). The most frequently reported AESI was anosmia (6.25 cases per 1000 person years). An increased Observed versus Expected (O:E) ratio was seen for anaphylaxis (O:E 7.38 (95% CI 2.80 to 11.95); based on 10 observed cases (expected cases: 1.36)) and anosmia and/or ageusia (O:E 39.23 (95% CI 29.13 to 49.32), based on 58 observed cases (expected cases: 1.48)).RESULTSThe majority of participants were women (n=10 845; 60.4%) and the median age (IQR) was 50 (43, 62) years. Most participants were from white ethnic groups (n=13 112; 73.1%). Headache and fatigue had the highest reported incidence rate (421.28 cases per 1000 person years and 386.00 cases per 1000 person years, respectively). The most frequently reported AESI was anosmia (6.25 cases per 1000 person years). An increased Observed versus Expected (O:E) ratio was seen for anaphylaxis (O:E 7.38 (95% CI 2.80 to 11.95); based on 10 observed cases (expected cases: 1.36)) and anosmia and/or ageusia (O:E 39.23 (95% CI 29.13 to 49.32), based on 58 observed cases (expected cases: 1.48)).The most frequent vaccinee-reported adverse events (AEs) were headache and fatigue. An increased O:E ratio was seen for the AEs of anaphylaxis and anosmia and/or ageusia. No safety signals were identified throughout the course of this study.CONCLUSIONSThe most frequent vaccinee-reported adverse events (AEs) were headache and fatigue. An increased O:E ratio was seen for the AEs of anaphylaxis and anosmia and/or ageusia. No safety signals were identified throughout the course of this study.This study is registered with the HMA-EMA Catalogue of RWD studies (EUPAS44035).TRIAL REGISTRATION NUMBERThis study is registered with the HMA-EMA Catalogue of RWD studies (EUPAS44035). Objectives To monitor the safety and utilisation of AZD1222 under real-world use in the UK.Design A non-interventional post-authorisation active surveillance study.Setting Vaccination sites in the UK.Participants A total of 17 945 participants were eligible and provided consent to participate in the study between 1 March 2021 and 6 April 2023. Participants were followed up at weeks 1, 4 and 14 and at months 6, 9, 12 and 18 after the first dose of AZD1222 vaccination and prompted to complete electronic data capture forms. A total of 11 219 participants submitted a Follow-Up 1 form and 5189 participants submitted a Follow-Up 7 form (at 18 months).Primary and secondary outcome measures The safety of AZD1222, including the identification, assessment and quantification of serious adverse events (SAEs) and adverse events of special interest (AESI), was examined. The utilisation of AZD1222 was described and characterised, including populations with missing information.Results The majority of participants were women (n=10 845; 60.4%) and the median age (IQR) was 50 (43, 62) years. Most participants were from white ethnic groups (n=13 112; 73.1%). Headache and fatigue had the highest reported incidence rate (421.28 cases per 1000 person years and 386.00 cases per 1000 person years, respectively). The most frequently reported AESI was anosmia (6.25 cases per 1000 person years). An increased Observed versus Expected (O:E) ratio was seen for anaphylaxis (O:E 7.38 (95% CI 2.80 to 11.95); based on 10 observed cases (expected cases: 1.36)) and anosmia and/or ageusia (O:E 39.23 (95% CI 29.13 to 49.32), based on 58 observed cases (expected cases: 1.48)).Conclusions The most frequent vaccinee-reported adverse events (AEs) were headache and fatigue. An increased O:E ratio was seen for the AEs of anaphylaxis and anosmia and/or ageusia. No safety signals were identified throughout the course of this study.Trial registration number This study is registered with the HMA-EMA Catalogue of RWD studies (EUPAS44035). |
| Author | Lane, Samantha Morris, Denise Roy, Debabrata Davies, Miranda Aurelius, Taylor Fry, Catherine Evans, Alison Dhanda, Sandeep Shakir, Saad |
| Author_xml | – sequence: 1 givenname: Alison orcidid: 0000-0003-1878-2429 surname: Evans fullname: Evans, Alison email: alison.evans@dsru.org organization: University of Portsmouth, Portsmouth, UK – sequence: 2 givenname: Debabrata orcidid: 0000-0003-2803-6323 surname: Roy fullname: Roy, Debabrata organization: University of Portsmouth, Portsmouth, UK – sequence: 3 givenname: Miranda orcidid: 0000-0003-2949-8378 surname: Davies fullname: Davies, Miranda organization: University of Portsmouth, Portsmouth, UK – sequence: 4 givenname: Sandeep surname: Dhanda fullname: Dhanda, Sandeep organization: University of Portsmouth, Portsmouth, UK – sequence: 5 givenname: Denise surname: Morris fullname: Morris, Denise organization: University of Portsmouth, Portsmouth, UK – sequence: 6 givenname: Taylor surname: Aurelius fullname: Aurelius, Taylor organization: University of Portsmouth, Portsmouth, UK – sequence: 7 givenname: Samantha orcidid: 0000-0001-7532-1149 surname: Lane fullname: Lane, Samantha organization: University of Portsmouth, Portsmouth, UK – sequence: 8 givenname: Catherine orcidid: 0000-0002-5307-1297 surname: Fry fullname: Fry, Catherine organization: University of Portsmouth, Portsmouth, UK – sequence: 9 givenname: Saad surname: Shakir fullname: Shakir, Saad organization: University of Portsmouth, Portsmouth, UK |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/40316343$$D View this record in MEDLINE/PubMed |
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| CitedBy_id | crossref_primary_10_1016_j_vaccine_2025_127597 crossref_primary_10_1007_s40264_025_01579_w crossref_primary_10_1007_s40278_025_82285_4 |
| Cites_doi | 10.1136/bmj.n1114 10.1016/j.vaccine.2022.11.031 10.1136/bmjopen-2020-045343 10.1007/s13577-021-00512-4 10.1136/jnnp.2005.073221 10.1136/bmj.n513 10.1093/ije/dyv098 10.1016/j.vaccine.2022.08.007 10.1016/S1473-3099(21)00404-7 10.1002/jmv.28771 10.1016/j.eclinm.2019.10.001 10.3399/bjgp13X668456 10.1016/j.jclinepi.2007.11.008 10.1177/014107680409701204 10.1136/bmjebm-2020-111507 10.1002/9781444300710 10.1258/jrsm.97.12.571 |
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| DOI | 10.1136/bmjopen-2024-093366 |
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| Notes | Original research ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 The Drug Safety Research Unit (DSRU) is an independent academic institution which works in association with the University of Portsmouth. All authors have no competing interest to declare. This study (EUPAS44035) was conducted with support from AstraZeneca UK Limited. Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise. |
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| References | Willame, Dodd, Durán (R18) 2023; 41 Redwood, Gill (R24) 2013; 63 Moynihan, Sanders, Michaleff (R19) 2021; 11 Dhanda, Osborne, Lynn (R3) 2022; 27 Gallagher, Thomas, Hamilton (R16) 2004; 97 Latinovic, Gulliford, Ridsdale (R15) 2006; 77 Laffan, Rees, Yadavalli (R17) 2022; 40 Kadambari, Vanderslott (R26) 2021; 21 Watson, Caster, Rochon (R22) 2019; 17 Kashte, Gulbake, El-Amin Iii (R2) 2021; 34 Pottegård, Lund, Karlstad (R9) 2021; 373 Razai, Osama, McKechnie (R25) 2021; 372 Herrett, Gallagher, Bhaskaran (R27) 2015; 44 von Elm, Altman, Egger (R10) 2008; 61 Riad, Schulz-Weidner, Dziedzic (R20) 2023; 95 Watson (2025081404365665000_15.5.e093366.22) 2019; 17 2025081404365665000_15.5.e093366.27 2025081404365665000_15.5.e093366.21 2025081404365665000_15.5.e093366.24 2025081404365665000_15.5.e093366.23 2025081404365665000_15.5.e093366.4 2025081404365665000_15.5.e093366.3 Kashte (2025081404365665000_15.5.e093366.2) 2021; 34 2025081404365665000_15.5.e093366.1 2025081404365665000_15.5.e093366.8 2025081404365665000_15.5.e093366.7 2025081404365665000_15.5.e093366.6 2025081404365665000_15.5.e093366.5 Riad (2025081404365665000_15.5.e093366.20) 2023; 95 Laffan (2025081404365665000_15.5.e093366.17) 2022; 40 Razai (2025081404365665000_15.5.e093366.25) 2021; 372 2025081404365665000_15.5.e093366.15 2025081404365665000_15.5.e093366.14 Willame (2025081404365665000_15.5.e093366.18) 2023; 41 2025081404365665000_15.5.e093366.16 2025081404365665000_15.5.e093366.11 2025081404365665000_15.5.e093366.10 2025081404365665000_15.5.e093366.13 2025081404365665000_15.5.e093366.12 Moynihan (2025081404365665000_15.5.e093366.19) 2021; 11 Kadambari (2025081404365665000_15.5.e093366.26) 2021; 21 Pottegård (2025081404365665000_15.5.e093366.9) 2021; 373 |
| References_xml | – volume: 373 year: 2021 ident: R9 article-title: Arterial events, venous thromboembolism, thrombocytopenia, and bleeding after vaccination with Oxford-AstraZeneca ChAdOx1-S in Denmark and Norway: population based cohort study publication-title: BMJ doi: 10.1136/bmj.n1114 – volume: 41 start-page: 251 year: 2023 ident: R18 article-title: Background rates of 41 adverse events of special interest for COVID-19 vaccines in 10 European healthcare databases - an ACCESS cohort study publication-title: Vaccine (Auckl) doi: 10.1016/j.vaccine.2022.11.031 – volume: 11 year: 2021 ident: R19 article-title: Impact of COVID-19 pandemic on utilisation of healthcare services: a systematic review publication-title: BMJ Open doi: 10.1136/bmjopen-2020-045343 – volume: 34 start-page: 711 year: 2021 ident: R2 article-title: COVID-19 vaccines: rapid development, implications, challenges and future prospects publication-title: Hum Cell doi: 10.1007/s13577-021-00512-4 – volume: 77 start-page: 385 year: 2006 ident: R15 article-title: Headache and migraine in primary care: consultation, prescription, and referral rates in a large population publication-title: J Neurol Neurosurg Psychiatry doi: 10.1136/jnnp.2005.073221 – volume: 372 year: 2021 ident: R25 article-title: Covid-19 vaccine hesitancy among ethnic minority groups publication-title: BMJ doi: 10.1136/bmj.n513 – volume: 44 start-page: 827 year: 2015 ident: R27 article-title: Data Resource Profile: Clinical Practice Research Datalink (CPRD) publication-title: Int J Epidemiol doi: 10.1093/ije/dyv098 – volume: 40 start-page: 5585 year: 2022 ident: R17 article-title: Thrombosis with thrombocytopenia after AZD1222 (ChAdOx1 nCov-19) vaccination: Case characteristics and associations publication-title: Vaccine (Auckl) doi: 10.1016/j.vaccine.2022.08.007 – volume: 21 start-page: 1204 year: 2021 ident: R26 article-title: Lessons about COVID-19 vaccine hesitancy among minority ethnic people in the UK publication-title: Lancet Infect Dis doi: 10.1016/S1473-3099(21)00404-7 – volume: 95 year: 2023 ident: R20 article-title: Oral side effects of COVID-19 vaccines in 32 European countries: Analysis of EudraVigilance reports publication-title: J Med Virol doi: 10.1002/jmv.28771 – volume: 17 year: 2019 ident: R22 article-title: Reported adverse drug reactions in women and men: Aggregated evidence from globally collected individual case reports during half a century publication-title: EClinicalMedicine doi: 10.1016/j.eclinm.2019.10.001 – volume: 63 start-page: 342 year: 2013 ident: R24 article-title: Under-representation of minority ethnic groups in research--call for action publication-title: Br J Gen Pract doi: 10.3399/bjgp13X668456 – volume: 61 start-page: 344 year: 2008 ident: R10 article-title: The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: guidelines for reporting observational studies publication-title: J Clin Epidemiol doi: 10.1016/j.jclinepi.2007.11.008 – volume: 97 start-page: 571 year: 2004 ident: R16 article-title: Incidence of fatigue symptoms and diagnoses presenting in UK primary care from 1990 to 2001 publication-title: J R Soc Med doi: 10.1177/014107680409701204 – volume: 27 start-page: 1 year: 2022 ident: R3 article-title: Postmarketing studies: can they provide a safety net for COVID-19 vaccines in the UK? publication-title: BMJ Evid Based Med doi: 10.1136/bmjebm-2020-111507 – ident: 2025081404365665000_15.5.e093366.1 – ident: 2025081404365665000_15.5.e093366.8 doi: 10.1002/9781444300710 – ident: 2025081404365665000_15.5.e093366.10 doi: 10.1016/j.jclinepi.2007.11.008 – volume: 17 year: 2019 ident: 2025081404365665000_15.5.e093366.22 article-title: Reported adverse drug reactions in women and men: Aggregated evidence from globally collected individual case reports during half a century publication-title: EClinicalMedicine doi: 10.1016/j.eclinm.2019.10.001 – volume: 40 start-page: 5585 year: 2022 ident: 2025081404365665000_15.5.e093366.17 article-title: Thrombosis with thrombocytopenia after AZD1222 (ChAdOx1 nCov-19) vaccination: Case characteristics and associations publication-title: Vaccine (Auckl) doi: 10.1016/j.vaccine.2022.08.007 – ident: 2025081404365665000_15.5.e093366.12 – ident: 2025081404365665000_15.5.e093366.5 – ident: 2025081404365665000_15.5.e093366.14 – volume: 11 year: 2021 ident: 2025081404365665000_15.5.e093366.19 article-title: Impact of COVID-19 pandemic on utilisation of healthcare services: a systematic review publication-title: BMJ Open doi: 10.1136/bmjopen-2020-045343 – volume: 95 year: 2023 ident: 2025081404365665000_15.5.e093366.20 article-title: Oral side effects of COVID-19 vaccines in 32 European countries: Analysis of EudraVigilance reports publication-title: J Med Virol doi: 10.1002/jmv.28771 – ident: 2025081404365665000_15.5.e093366.24 doi: 10.3399/bjgp13X668456 – ident: 2025081404365665000_15.5.e093366.15 doi: 10.1136/jnnp.2005.073221 – ident: 2025081404365665000_15.5.e093366.21 – volume: 373 year: 2021 ident: 2025081404365665000_15.5.e093366.9 article-title: Arterial events, venous thromboembolism, thrombocytopenia, and bleeding after vaccination with Oxford-AstraZeneca ChAdOx1-S in Denmark and Norway: population based cohort study publication-title: BMJ doi: 10.1136/bmj.n1114 – ident: 2025081404365665000_15.5.e093366.23 – ident: 2025081404365665000_15.5.e093366.16 doi: 10.1258/jrsm.97.12.571 – ident: 2025081404365665000_15.5.e093366.11 – ident: 2025081404365665000_15.5.e093366.4 – ident: 2025081404365665000_15.5.e093366.13 – ident: 2025081404365665000_15.5.e093366.6 – volume: 372 year: 2021 ident: 2025081404365665000_15.5.e093366.25 article-title: Covid-19 vaccine hesitancy among ethnic minority groups publication-title: BMJ doi: 10.1136/bmj.n513 – ident: 2025081404365665000_15.5.e093366.3 doi: 10.1136/bmjebm-2020-111507 – ident: 2025081404365665000_15.5.e093366.27 doi: 10.1093/ije/dyv098 – ident: 2025081404365665000_15.5.e093366.7 – volume: 21 start-page: 1204 year: 2021 ident: 2025081404365665000_15.5.e093366.26 article-title: Lessons about COVID-19 vaccine hesitancy among minority ethnic people in the UK publication-title: Lancet Infect Dis doi: 10.1016/S1473-3099(21)00404-7 – volume: 34 start-page: 711 year: 2021 ident: 2025081404365665000_15.5.e093366.2 article-title: COVID-19 vaccines: rapid development, implications, challenges and future prospects publication-title: Hum Cell doi: 10.1007/s13577-021-00512-4 – volume: 41 start-page: 251 year: 2023 ident: 2025081404365665000_15.5.e093366.18 article-title: Background rates of 41 adverse events of special interest for COVID-19 vaccines in 10 European healthcare databases - an ACCESS cohort study publication-title: Vaccine (Auckl) doi: 10.1016/j.vaccine.2022.11.031 |
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| Snippet | ObjectivesTo monitor the safety and utilisation of AZD1222 under real-world use in the UK.DesignA non-interventional post-authorisation active surveillance... To monitor the safety and utilisation of AZD1222 under real-world use in the UK. A non-interventional post-authorisation active surveillance study. Vaccination... To monitor the safety and utilisation of AZD1222 under real-world use in the UK.OBJECTIVESTo monitor the safety and utilisation of AZD1222 under real-world use... Objectives To monitor the safety and utilisation of AZD1222 under real-world use in the UK.Design A non-interventional post-authorisation active surveillance... |
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| SubjectTerms | Adult Aged Breastfeeding & lactation ChAdOx1 nCoV-19 - adverse effects Clinical medicine COVID-19 - prevention & control COVID-19 vaccines COVID-19 Vaccines - administration & dosage COVID-19 Vaccines - adverse effects Drug Utilization Epidemiology Family physicians Female Headache - chemically induced Headache - epidemiology Humans Immunization Male Middle Aged Non-pharmacological intervention Original Research Pandemics Product Surveillance, Postmarketing Public health Regulatory agencies Safety SARS-CoV-2 Surveillance United Kingdom - epidemiology Vaccination |
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| Title | Safety and utilisation of AZD1222 (ChAdOx1 nCoV-19) COVID-19 vaccine: a UK post-authorisation active surveillance study |
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