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Gidengil C, Goetz MB, Maglione M, et al. Safety of Vaccines Used for Routine Immunization in the United States: An Update [Internet]. Rockville (MD): Agency for Healthcare Research and Quality (US); 2021 May. (Comparative Effectiveness Review, No. 244.)

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Safety of Vaccines Used for Routine Immunization in the United States: An Update [Internet].

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Appendix BList of Excluded Studies

Note: after each reference is the aspect of the eligibility criteria the study failed to meet for inclusion.

1.
Polio vaccine and congenital defects. British Medical Journal. 1967 Feb 25;1(5538):510. PMID: 6017538. Study design [PubMed: 6017538]
2.
Pneumococcal polysaccharide vaccine. Recommendation of the Immunization Practices Advisory Committee. Annals of Internal Medicine. 1982 Feb;96(2):203–5. PMID: 6277218. Study design [PubMed: 6277218]
3.
Pneumococcal vaccine. Health and Public Policy Committee, American College of Physicians. Annals of Internal Medicine. 1986 Jan;104(1):118–20. PMID: 3940479. Study design [PubMed: 3940479]
4.
Immunization during pregnancy. ACOG technical bulletin number 160--October 1991. International Journal of Gynaecology & Obstetrics. 1993 Jan;40(1):69–79. PMID: 8094357. Study design [PubMed: 8094357]
5.
Facts about pertussis and DTP vaccine. EPI Newsletter. 1994 Jun;16(3):5. PMID: 12345538. Study design [PubMed: 12345538]
6.
Erratum: Safety and efficacy of high-dose rhesus-human reassortant rotavirus vaccines - Report of the National Multicenter Trial (Pediatrics (1996) 97 (7–13)). Pediatrics. 1996 1996;98(1):A38. PMID: 1996204872. Study design [PubMed: 8545227]
7.
From the Centers for Disease Control and Prevention. Status report on the Childhood Immunization Initiative: national, state, and urban area vaccination coverage levels among children aged 19–35 months--United States, 1996. JAMA. 1997 Aug 27;278(8):622–3. PMID: 9272882. Outcome [PubMed: 9272882]
8.
WHO meeting on maternal and neonatal pneumococcal immunization. Weekly Epidemiological Record. 1998 Jun 19;73(25):187–8. PMID: 9648498. Study design [PubMed: 9648498]
9.
From the Centers for Disease Control and Prevention. Withdrawal of rotavirus vaccine recommendation. JAMA. 1999 Dec 8;282(22):2113–4. PMID: 10591321. Study design [PubMed: 10591321]
10.
Measles immunization in HIV-infected children. American Academy of Pediatrics. Committee on Infectious Diseases and Committee on Pediatric AIDS. Pediatrics. 1999 May;103(5 Pt 1):1057–60. PMID: 10224192. Study design [PubMed: 10224192]
11.
Infections and vaccinations as risk factors for childhood type I (insulin-dependent) diabetes mellitus: a multicentre case-control investigation. EURODIAB Substudy 2 Study Group. Diabetologia. 2000 Jan;43(1):47–53. PMID: 10663215. Publication year [PubMed: 10663215]
12.
Pneumococcal vaccination for elderly subjects: license extension. Still no proof of clinical efficacy. Prescrire International. 2000 Aug;9(48):106–9. PMID: 11067718. Study design [PubMed: 11067718]
13.
The safety of inactivated influenza vaccine in adults and children with asthma. N Engl J Med. 2001 Nov 22;345(21):1529–36. doi: 10.1056/NEJMoa011961. PMID: 11794219. Publication year [PubMed: 11794219] [CrossRef]
14.
Erratum: Intussusception among infants given an oral rotavirus vaccine (New England Journal of Medicine (Feb. 22, 2001) 344 (564–72)). New England Journal of Medicine. 2001 17;344(20):1564. PMID: 2001174517. Study design [PubMed: 11207352]
15.
7-valent pneumococcal conjugate vaccine: new preparation. Prevents rare invasive infections in infants. Prescrire International. 2002 Feb;11(57):7–10. PMID: 11985376. Study design [PubMed: 11985376]
16.
Rotavirus vaccine ready for licensing. WHO Drug Information. 2004 2004;18(2):129–30. PMID: 2004362555. Study design
17.
CDC’s advisory committee recommends new vaccine to prevent rotavirus. Indian Journal of Medical Sciences. 2006 Feb;60(2):89–90. PMID: 16538799. Study design [PubMed: 16538799]
18.
Global Advisory Committee on Vaccine Safety, 1–2 December 2005. Weekly Epidemiological Record. 2006 Jan 13;81(2):15–9. PMID: 16671243. Study design [PubMed: 16671243]
19.
Global Advisory Committee on Vaccine Safety, 6–7 June 2006. Weekly Epidemiological Record. 2006 Jul 14;81(28):273–8. PMID: 16841398. Publication type [PubMed: 16841398]
20.
New rotavirus vaccine is likely on its way. Child Health Alert. 2006 Feb;24:1. PMID: 16526105. Study design [PubMed: 16526105]
21.
Infant immunisation with a pneumococcal conjugate vaccine: from the age of two months, for all infants. Prescrire International. 2006 Dec;15(86):227–33. PMID: 17167934. Study design [PubMed: 17167934]
22.
RotaTeq: A new oral rotavirus vaccine. Medical Letter on Drugs and Therapeutics. 2006 31;48(1240):61–3. PMID: 2008221795 MEDLINE PMID 16874281 (http://www​.ncbi.nlm.nih​.gov/pubmed/16874281). Study design [PubMed: 16874281]
23.
New rotavirus vaccines safe and effective in large clinical trials. Gastroenterology. 2006 Mar;130(3):627–8. PMID: WOS:000236210100001. Study design
24.
Global Advisory Committee on Vaccine Safety, 12–13 June 2007. Weekly Epidemiological Record. 2007 Jul 20;82(28–29):252–9. PMID: 17642098. Publication type [PubMed: 17642098]
25.
Rotavirus vaccine and intussusception. WHO Drug Information. 2007 2007;21(1):8. PMID: 2008001204. Study design
26.
Safety updates on rotavirus vaccine. Expert Review of Vaccines. 2007 Apr;6(2):130-. PMID: WOS:000245821400005. Study design
27.
Erratum: Safety and immunogenicity of a fully liquid vaccine containing five-component pertussis-diphtheria-tetanus-inactivated poliomyelitis- Haemophilus influenzae type b conjugate vaccines administered at two, four, six and 18 months of age (Clinical Journal of Infectious Diseases and Medical Microbiology (2007) 18, 4, (241–248)). Canadian Journal of Infectious Diseases and Medical Microbiology. 2007 September/October;18(5):318. PMID: 2007589433. Outcome [PMC free article: PMC2533632] [PubMed: 18923741]
28.
Global Advisory Committee on Vaccine Safety, 12–13 December 2007. Weekly Epidemiological Record. 2008 Jan 25;83(4):37–44. PMID: 18219807. Publication type [PubMed: 18219807]
29.
Adjuvanted hepatitis B vaccine: new drug. Patients with renal failure: similar response rate but fewer boosters needed. Prescrire International. 2008 Dec;17(98):234–6. PMID: 19422145. Study design [PubMed: 19422145]
30.
Global Advisory Committee on Vaccine Safety, 17–18 December 2008. Weekly Epidemiological Record. 2009 Jan 30;84(5):37–40. PMID: 19180768. Publication type [PubMed: 19180768]
31.
Global Advisory Committee on Vaccine Safety, report of meeting held 17–18 June 2009. Weekly Epidemiological Record. 2009 Aug 7;84(32):325–32. PMID: 19860024. Publication type [PubMed: 19860024]
32.
Updated recommendations of the Advisory Committee on Immunization Practices (ACIP) regarding routine poliovirus vaccination. MMWR Morb Mortal Wkly Rep. 2009 Aug 7;58(30):829–30. PMID: 19661857. Outcome [PubMed: 19661857]
33.
Risk levels for febrile seizures with combined measles-mumps-rubella-varicella vaccine. Expert Review of Vaccines. 2010 Aug;9(8):810-. PMID: WOS:000281104800004. Study design
34.
Herpes zoster vaccine (Zostavax) revisited. Medical Letter on Drugs and Therapeutics. 2010 31;52(1339):41. PMID: 2010390996 MEDLINE PMID 20508580 (http://www​.ncbi.nlm.nih​.gov/pubmed/20508580). Study design [PubMed: 20508580]
35.
Canadian Society of Allergy and Clinical Immunology Annual Scientific Meeting 2010. Allergy, Asthma and Clinical Immunology. 2010;6(2):2010–11. Publication type
36.
Pneumococcal immunization in older adults. Clinical Geriatrics. 2010 June;18(6):13–4. PMID: 2010389740. Publication type
37.
Adverse effects of papillomavirus vaccination: 2009 data. Prescrire International. 2010 Jun;19(107):124. PMID: 20738043. Study design [PubMed: 20738043]
38.
FDA panel recommends continued use of rotarix and rotateq vaccines viral DNA contamination. Formulary. 2010 May;45(5):167. PMID: 2010397508. Outcome
39.
Updated recommendations for prevention of invasive pneumococcal disease among adults using the 23-valent pneumococcal polysaccharide vaccine (PPSV23). MMWR Morb Mortal Wkly Rep. 2010 Sep 3;59(34):1102–6. PMID: 20814406. Outcome [PubMed: 20814406]
40.
Benefits and risks of vaccination against papillomavirus human ORIGINAL (NON-ENGLISH) TITLE Beneficios y riesgos de la vacunacion contra el virus del papiloma humano. Ginecologia y Obstetricia de Mexico. 2011 December;79(12):803–7. PMID: 2012155624 MEDLINE PMID 22384535 (http://www​.ncbi.nlm.nih​.gov/pubmed/22384535). Not in English [PubMed: 22384535]
41.
Safety of rotavirus vaccines: postmarketing surveillance in the WHO Region of the Americas. Weekly Epidemiological Record. 2011 Feb 18;86(8):66–72. PMID: 21337810. Study design [PubMed: 21337810]
42.
Rotavirus vaccination and risk of intussusception: Investigation of a possible safety signal. Australian Prescriber. 2011 April;34(2):47. PMID: 2011237396. Outcome
43.
Use of 13-valent pneumococcal conjugate vaccine and 23-valent pneumococcal polysaccharide vaccine for adults with immunocompromising conditions: recommendations of the Advisory Committee on Immunization Practices (ACIP). MMWR Morb Mortal Wkly Rep. 2012 Oct 12;61(40):816–9. PMID: 23051612. Outcome [PubMed: 23051612]
44.
Safety and Immunogenicity of Tetanus, Diphtheria, and Acellular Pertussis Immunization During Pregnancy in Mothers and Infants: A Randomized Clinical Trial EDITORIAL COMMENT. Obstetrical & Gynecological Survey. 2014 Sep;69(9):517–9. PMID: WOS:000342571300001. Duplicate
45.
GEN-004 pneumococcal vaccine development stopped after clinical trial failure. Human Vaccines & Immunotherapeutics. 2015 Dec;11(12):2748-. PMID: WOS:000367066700011. Study design
46.
Erratum: eff ectiveness of the ten-valent pneumococcal Haemophilus infl uenzae protein D conjugate vaccine (PHiD-CV10) against invasive pneumococcal disease: a cluster randomised trial(Lancet (2013) 381 (214–22)). Lancet. 2015;385(9983):2152. doi: 10.1016/S0140-6736%2815%2961023-6. PMID: CN-01102786. Intervention [PubMed: 23158882] [CrossRef]
47.
Adjuvanted A/H1N1 (2009) influenza vaccination during pregnancy: description of a prospective cohort and spontaneously reported pregnancy-related adverse reactions in the Netherlands. Essentially MIDIRS. 2015;6(1):44-. PMID: 101113317. Language: English. Entry Date: 20150224. Revision Date: 20190711. Publication Type: Article. Intervention
48.
IPVS Policy statement on safety of HPV vaccines. Papillomavirus Research. 2016;2:9–10. doi: 10.1016/j.pvr.2015.11.001. Study design [PMC free article: PMC5886868] [PubMed: 29074192] [CrossRef]
49.
Influenza vaccination during pregnancy. Prescrire international. 2016;25(168):51. Duplicate [PubMed: 27042735]
50.
A universal influenza vaccine candidate enters clinical trials. Human Vaccines & Immunotherapeutics. 2016;12(9):2218-. PMID: WOS:000384217200012. Study design
51.
Therapeutic HPV vaccine GTL001 initiated US-based clinical trials. Human Vaccines & Immunotherapeutics. 2016 Jan;12(1):4-. PMID: WOS:000375931700010. Study design
52.
Immune responses in U.S. military personnel who received meningococcal conjugate vaccine (MenACWY) concomitantly with other vaccines were higher than in personnel who received MenACWY alone. Clinical and vaccine immunology. 23 (8) (pp 672–680), 2016. Date of publication: august 2016. 2016. doi: 10.1128/CVI.00267-16. PMID: CN-01194015. Comparator [PMC free article: PMC4979175] [PubMed: 27280619] [CrossRef]
53.
Universal influenza vaccine enters Phase 2 clinical trial. Human Vaccines & Immunotherapeutics. 2017;13(12):2753-. doi: 10.1080/21645515.2017.1327109. PMID: WOS:000418052100009. Intervention [CrossRef]
54.
Clinical effect of different pneumococcal vaccination schedules in patients with chronic obstructive pulmonary disease (COPD): long-term follow-up results. European respiratory journal. 2017;50. doi: 10.1183/1393003.congress-2017.PA4954. PMID: CN-01932385. Publication type [CrossRef]
55.
Is inadvertent HPV vaccination in pregnancy safe? Contemporary OB/GYN. 2017;62(2):14–6. PMID: 121310940. Language: English. Entry Date: 20170221. Revision Date: 20170223. Publication Type: Article. Journal Subset: Biomedical. Duplicate
56.
Safety and immunogenicity of an upper-range release titer measles-mumps-rubella vaccine in children vaccinated at 12 to 15 months of age: a phase III, randomized study. Human Vaccines and Immunotherapeutics. 2018;14(12):2921–31. doi: 10.1080/21645515.2018.1502527. Intervention [PMC free article: PMC6343620] [PubMed: 30118386] [CrossRef]
57.
Immunogenicity and safety of measles-mumps-rubella vaccine at two different potency levels administered to healthy children aged 12–15months: A phase III, randomized, non-inferiority trial. Vaccine. 2018;36(38):5781–8. doi: 10.1016/j.vaccine.2018.07.076. Duplicate [PubMed: 30104117] [CrossRef]
58.
HBSAG-1018, a two-dose hepatitis b vaccine, is well tolerated and effective in diabetic patients aged 60 years or older. Diabetes. 2018;Conference: 78th Scientific Sessions of the American Diabetes Association, ADA 2018. United States. 67(Supplement 1):LB60. PMID: CN-01921465. Participants
59.
Comparison of reported adverse events of premature and term born infants following childhood vaccinations in the Netherlands. Drug safety. 2018;Conference: 18th Annual Meeting of the International Society of Pharmacovigilance, ISoP 2018. Switzerland. 41(11):1198. doi: 10.1007/s40264-018-0719-2. PMID: CN-01923149. Comparator [CrossRef]
60.
Effect of HBIG combined with hepatitis B vaccineon blocking HBV transmission between motherand infant and its effect on immune cells. Experimental and therapeutic medicine. 2018;15(1):919–23. doi: 10.3892/etm.2017.5474. PMID: CN-01643730. Comparator [PMC free article: PMC5772875] [PubMed: 29399100] [CrossRef]
61.
Recently approved HEPLISAV-B shows a lower proportion of subjects with non-and low response compared with ENGERIX-B [hepatitis B vaccine (recombinant)] in pooled analysis of trials. Hepatology (baltimore, md.). 2018;Conference: 69th Annual Meeting of the American Association for the Study of Liver Diseases, AASLD 2018. United States. 68(Supplement 1):231A–2A. doi: 10.1002/hep.30257. PMID: CN-01923131. Publication type [CrossRef]
62.
Immunogenicity and safety of measles-mumps-rubella vaccine at two different potency levels administered to healthy children aged 12–15 months: a phase III, randomized, non-inferiority trial. Vaccine. 2018;36(38):5781–8. doi: 10.1016/j.vaccine.2018.07.076. PMID: CN-01655596. Duplicate [PubMed: 30104117] [CrossRef]
63.
A second dose of a measles-mumps-rubella vaccine administered to healthy four-to-six-year-old children: a phase III, observer-blind, randomized, safety and immunogenicity study comparing GSK MMR and MMR II with and without DTaP-IPV and varicella vaccines co-administration. Human Vaccines and Immunotherapeutics. 2019;15(4):786–99. doi: 10.1080/21645515.2018.1554971. Intervention [PMC free article: PMC6605865] [PubMed: 30785357] [CrossRef]
64.
The Efficacy and Safety of Tipapkinogen Sovacivec Therapeutic HPV Vaccine in Cervical Intraepithelial Neoplasia Grades 2 and 3: Randomized Controlled Phase II Trial with 2.5 Years of Follow-up. Obstetrical & Gynecological Survey. 2019 Sep;74(9):529–30. PMID: WOS:000493546800012. Intervention [PubMed: 30955915]
65.
Erratum: comparison of the Impact of Pneumococcal Conjugate Vaccine 10 or Pneumococcal Conjugate Vaccine 13 on Invasive Pneumococcal Disease in Equivalent Populations(Clinical Infectious Diseases (2017) 65 (1780–1789) DOI: 10.1093/cid/ciy857). Clinical infectious diseases. 2019;68(1):175-. doi: 10.1093/cid/ciy316. PMID: CN-01966677. Study design [PMC free article: PMC5848315] [PubMed: 29020171] [CrossRef]
66.
Corrigendum: use of UV treated milk powder to increase vaccine efficacy in the elderly (Frontiers in Immunology (2018) 9 (2254) DOI: 10.3389/fimmu.2018.02254). Frontiers in immunology. 2019;10(MAR). doi: 10.3389/fimmu.2019.00427. PMID: CN-02003452. Intervention [PMC free article: PMC6200024] [PubMed: 30386327] [CrossRef]
67.
Correction: effect of recombinant zoster vaccine on incidence of herpes zoster after autologous stem cell transplantation: a randomized clinical trial (JAMA - Journal of the American Medical Association (2019) 322L: 2 (123–133) DOI: 10.1001/jama.2019.9053). JAMA - journal of the american medical association. 2019;322(8):785-. doi: 10.1001/jama.2019.11467. PMID: CN-02011114. Participants [PMC free article: PMC6618796] [PubMed: 31287523] [CrossRef]
68.
Correction to Safety and efficacy of inactivated varicella zoster virus vaccine in immunocompromised patients with malignancies: a two-arm, randomised, double-blind, phase 3 trial (The Lancet Infectious Diseases (2019) 19(9) (1001–1012), (S147330991930310X), (10.1016/S1473-3099(19)30310-X)). Lancet infectious diseases. 2019;19(10):e337. doi: 10.1016/S1473-3099(19)30469-4. PMID: CN-02003928. Publication type [PubMed: 31399378] [CrossRef]
69.
Postlicensure Safety Surveillance of Recombinant Zoster Vaccine (Shingrix) - United States, October 2017–June 2018. MMWR. Morbidity and mortality weekly report. 2019;68(4):91–4. doi: 10.15585/mmwr.mm6804a4. PMID: CN-01966755. Duplicate [PMC free article: PMC6400583] [PubMed: 30703077] [CrossRef]
70.
Large Cohort Study Shows No Link Between MMR and ASD. ASHA Leader. 2019;24(5):12-. doi: 10.1044/leader.NIB1.24052019.12. PMID: 136191240. Language: English. Entry Date: 20190504. Revision Date: 20190520. Publication Type: Article. Study design [CrossRef]
71.
Erratum to: 13-valent pneumococcal conjugate vaccine (PCV13) is immunogenic and safe in children 6–17 years of age with sickle cell disease previously vaccinated with 23-valent pneumococcal polysaccharide vaccine (PPSV23): Results of a phase 3 study: PCV13 in Pre-PPSV23-Vaccinated SCD Children (Pediatric Blood & Cancer, (2015), 62, 8, (1427–1436), 10.1002/pbc.25502). Pediatric Blood and Cancer. 2019;66(2). doi: 10.1002/pbc.27554. Publication type [PubMed: 25810327] [CrossRef]
72.
Measles-mumps-rubella vaccine (MMR): No link with autism. Prescrire International. 2020;29(215):125–6. Publication type
73.
Efficacy, duration of protection, birth outcomes, and infant growth associated with influenza vaccination in pregnancy: a pooled analysis of three randomised controlled trials. The lancet respiratory medicine. 2020;8(6):597–608. doi: 10.1016/S2213-2600(19)30479-5. PMID: CN-02182518. Intervention [PMC free article: PMC7284303] [PubMed: 32526188] [CrossRef]
74.
Aaby P, Benn C, Nielsen J, et al. Testing the hypothesis that diphtheria-tetanus-pertussis vaccine has negative non-specific and sex-differential effects on child survival in high-mortality countries. BMJ Open. 2012;2(3). PMID: 2012335376. Study design [PMC free article: PMC3364456] [PubMed: 22619263]
75.
Aaby P, Benn CS. Non-specific and sex-differential effects of routine vaccines: what evidence is needed to take these effects into consideration in low-income countries? Human Vaccines. 2011 Jan 1;7(1):120–4. PMID: 21278492. Outcome [PubMed: 21278492]
76.
Aaby P, Jensen H, Samb B, et al. Differences in female-male mortality after high-titre measles vaccine and association with subsequent vaccination with diphtheria-tetanus-pertussis and inactivated poliovirus: reanalysis of West African studies. Lancet. 2003 Jun 28;361(9376):2183–8. PMID: 12842371. Study design [PubMed: 12842371]
77.
Aaby P, Knudsen K, Whittle H, et al. Long-term survival after Edmonston-Zagreb measles vaccination in Guinea-Bissau: increased female mortality rate. Journal of Pediatrics. 1993 Jun;122(6):904–8. PMID: 8501567. Study design [PubMed: 8501567]
78.
Aaby P, Martins C, Bale C, et al. Sex Differences in the Effect of Vaccines on the Risk of Hospitalization Due to Measles in Guinea-Bissau. Pediatric Infectious Disease Journal. 2010 Apr;29(4):324–8. PMID: WOS:000276565600008. Study design [PubMed: 19934785]
79.
Aaby P, Martins CL, Garly ML, et al. Non-specific effects of standard measles vaccine at 4.5 and 9 months of age on childhood mortality: randomised controlled trial. British Medical Journal. 2010 Nov;341. PMID: WOS:000285090100006. Outcome [PMC free article: PMC2994348] [PubMed: 21118875]
80.
Aaby P, Mogensen SW, Rodrigues A, et al. Evidence of Increase in Mortality After the Introduction of Diphtheria-Tetanus-Pertussis Vaccine to Children Aged 6–35 Months in Guinea-Bissau: A Time for Reflection? Frontiers in Public Health. 2018 Mar;6:10. doi: 10.3389/fpubh.2018.00079. PMID: WOS:000429556900001. Comparator [PMC free article: PMC5868131] [PubMed: 29616207] [CrossRef]
81.
Aaby P, Nielsen J, Benn CS, et al. Sex-differential and non-specific effects of routine vaccinations in a rural area with low vaccination coverage: an observational study from Senegal. Transactions of the Royal Society of Tropical Medicine and Hygiene. 2015 Jan;109(1):77–84. doi: 10.1093/trstmh/tru186. PMID: WOS:000350102400012. Outcome [PubMed: 25573112] [CrossRef]
82.
Aaby P, Ravn H, Roth A, et al. Early diphtheria-tetanus-pertussis vaccination associated with higher female mortality and no difference in male mortality in a cohort of low birthweight children: an observational study within a randomised trial. Archives of Disease in Childhood. 2012 Aug;97(8):685–91. PMID: 22331681. Intervention [PMC free article: PMC3409557] [PubMed: 22331681]
83.
Aaby P, Roth A, Ravn H, et al. Randomized Trial of BCG Vaccination at Birth to Low-Birth-Weight Children: Beneficial Nonspecific Effects in the Neonatal Period? Journal of Infectious Diseases. 2011 Jul;204(2):245–52. PMID: WOS:000292562200013. Intervention [PubMed: 21673035]
84.
Aagaard L, Hansen EW, Hansen EH. Adverse events following immunization in children: Retrospective analysis of spontaneous reports over a decade. European Journal of Clinical Pharmacology. 2011 March;67(3):283–8. PMID: 2011203245 MEDLINE PMID 21079934 (http://www​.ncbi.nlm.nih​.gov/pubmed/21079934). Study design [PubMed: 21079934]
85.
Aagaard L, Weber CB, Hansen EH. Adverse drug reactions in the paediatric population in denmark: A retrospective analysis of reports made to the danish medicines agency from 1998 to 2007. Drug Safety. 2010 2010;33(4):327–39. PMID: 2010179689 MEDLINE PMID 20297864 (http://www​.ncbi.nlm.nih​.gov/pubmed/20297864). Study design [PubMed: 20297864]
86.
Aalst Mv, Garrido HMG, van der Leun J, et al. Immunogenicity of the Currently Recommended Pneumococcal Vaccination Schedule in Patients With Inflammatory Bowel Disease. Clinical Infectious Diseases. 2020;70(4):595–604. doi: 10.1093/cid/ciz226. PMID: 141534929. Language: English. Entry Date: 20200206. Revision Date: 20200207. Publication Type: Article. Comparator [PubMed: 30899961] [CrossRef]
87.
Aavitsland P, Bjune G, Aasen S, et al. Adverse events following vaccine or placebo injection in an efficacy trial of an outer membrane vesicle vaccine against group B meningococcal disease in Norwegian secondary schools 1988–1991. NIPH Annals. 1991 Dec;14(2):133–4; discussion 6–7. PMID: 1812426. Intervention [PubMed: 1812426]
88.
Abarca K, Ibanez I, de la Fuente P, et al. Immunogenicity and tolerability of a paediatric presentation of a virosomal hepatitis A vaccine in Chilean children aged 1–16 years. Vaccine. 2011 08;29(48):8855–62. PMID: 2011659714 MEDLINE PMID 21983354 (http://www​.ncbi.nlm.nih​.gov/pubmed/21983354). Study design [PubMed: 21983354]
89.
Abbas KM, van Zandvoort K, Brisson M, et al. Effects of updated demography, disability weights, and cervical cancer burden on estimates of human papillomavirus vaccination impact at the global, regional, and national levels: a PRIME modelling study. The Lancet Global Health. 2020;8(4):e536–e44. doi: 10.1016/S2214-109X(20)30022-X. Intervention [PMC free article: PMC7083230] [PubMed: 32105613] [CrossRef]
90.
Abbott KC, Yuan CM, Lee JL. Nothing to sneeze at: Efficacy and cost-effectiveness of the influenza vaccine in patients receiving long-term dialysis. American Journal of Kidney Diseases. 2011 May;57(5):651–3. PMID: 2011205912 MEDLINE PMID 21496725 (http://www​.ncbi.nlm.nih​.gov/pubmed/21496725). Outcome [PubMed: 21496725]
91.
Abd AK, Kadhim DJ, Younus MM. Assessment of causality, severity and seriousness of adverse event following immunization in Iraq: A retrospective study based on Iraqi pharmacovigilance database. Iraqi Journal of Pharmaceutical Sciences. 2019;28(2):142–50. doi: 10.31351/vol28iss2pp142-150. Comparator [CrossRef]
92.
Abdelnour A, Silas PE, Lamas MRV, et al. Safety of a quadrivalent meningococcal serogroups A, C, W and Y conjugate vaccine (MenACWY-CRM) administered with routine infant vaccinations: Results of an open-label, randomized, phase 3b controlled study in healthy infants. Vaccine. 2014;32(8):965–72. doi: 10.1016/j.vaccine.2013.12.034. Duplicate [PubMed: 24397906] [CrossRef]
93.
Abedi GR, Mutuc JD, Lawler J, et al. Adverse events following a third dose of measles, mumps, and rubella vaccine in a mumps outbreak. Vaccine. 2012 Nov 19;30(49):7052–8. doi: 10.1016/j.vaccine.2012.09.053. PMID: 23041123. Study design [PubMed: 23041123] [CrossRef]
94.
Aberdein J, Heyderman R, Gordon S, et al. MODIFICATION OF ADULT PNEUMOCOCCAL CARRIAGE BY VACCINATION: EFFECT OF 7-CONJUGATE VACCINE ON CARRIAGE IN MALAWIAN ADULTS, RESULTS FROM A RANDOMISED CONTROLLED TRIAL. Journal of Infection. 2015 Dec;71(6):687-. doi: 10.1016/j.jinf.2015.09.028. PMID: WOS:000368480600019. Intervention [CrossRef]
95.
Ablin JN, Aloush V, Brill A, et al. Influenza vaccination is safe and effective in patients suffering from fibromyalgia syndrome. Reumatismo. 2015;67(2):57–61. doi: 10.4081/reumatismo.2015.823. Intervention [PubMed: 26492963] [CrossRef]
96.
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Cruz-Valdez A, Valdez-Zapata G, Patel SS, et al. MF59-adjuvanted influenza vaccine (FLUAD) elicits higher immune responses than a non-adjuvanted influenza vaccine (Fluzone): A randomized, multicenter, Phase III pediatric trial in Mexico. Human vaccines & immunotherapeutics. 2018;14(2):386–95. doi: 10.1080/21645515.2017.1373227. Intervention [PMC free article: PMC5806633] [PubMed: 28925801] [CrossRef]
1179.
Cruz-Valdez A, Valdez-Zapata G, Patel SS, et al. MF59-adjuvanted influenza vaccine (FLUAD®) elicits higher immune responses than a non-adjuvanted influenza vaccine (Fluzone®): A randomized, multicenter, Phase III pediatric trial in Mexico. Human Vaccines and Immunotherapeutics. 2018;14(2):386–95. doi: 10.1080/21645515.2017.1373227. Duplicate [PMC free article: PMC5806633] [PubMed: 28925801] [CrossRef]
1180.
Cserti-Gazdewich CM, Pendergrast JM, Reis M. Postvaccination hyperhemolysis coinciding with remission of Epstein Barr virus (EBV)-associated immune thrombocytopenic purpura (ITP). American Journal of Hematology. 2009 September;84(9):612–3. PMID: 2009465276 MEDLINE PMID 19610018 (http://www​.ncbi.nlm.nih​.gov/pubmed/19610018). Study design [PubMed: 19610018]
1181.
Ctri. Vitamin D supplementation and responses to vaccines in infants. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2013/04/003566. 2013. PMID: CN-01860091. Intervention
1182.
Ctri. A clinical trial to study the effect and safety of Rotavirus Vaccine against Severe Rotavirus Gastroenteritis in healthy Indian Infants. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2013/05/003667. 2013. PMID: CN-01882050. Intervention
1183.
Ctri. Clinical Study to assess safety and immune response of DTP-HB-HIB vaccination by Disposable Syringe Jet Injector as compared to Needle Syringe method in Indian infants. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2013/05/003670. 2013. PMID: CN-01882056. Comparator
1184.
Ctri. Clinical Study to assess safety and immune response of MMR subcutaneous vaccination by Disposable Syringe Jet Injector as compared to Needle Syringe method in 15–18 month old children. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2013/05/003702. 2013. PMID: CN-01880348. Comparator
1185.
Ctri. To assess potential hazards, including immediate adverse events after bivalent and quadrivalent HPV vaccines immunizations in healthy Indian women aged 18–25 years. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2013/11/004140. 2013. PMID: CN-01816244. Intervention
1186.
Ctri. Clinical Study to assess the immune response and safety of Measles, Mumps and Rubella (MMR) vaccine (Live) (Freeze-dried) of M/s Cadila Healthcare Ltd. in healthy pediatric subjects aged 15–18 months. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2014/01/004339. 2014. PMID: CN-01845215. Intervention
1187.
Ctri. Treatment of enteric infections to improve response to oral poliovirus vaccine. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2014/05/004588. 2014. PMID: CN-01839723. Intervention
1188.
Ctri. A study to test the safety of a new trivalent seasonal influenza vaccine in healthy volunteers. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2014/10/005107. 2014. PMID: CN-01870787. Intervention
1189.
Ctri. A clinical trial to study the efficacy and safety of a New Fully Liquid six in one vaccine ( DTwP-HepB-Hib-IPV) with a five in one vaccine (DTwP-HepB-Hib) given along with a polio vaccine. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2015/02/005578. 2015. PMID: CN-01831453. Comparator
1190.
Ctri. Clinical study to compare the immune response and safety of Measles vaccine manufactured by Cadila healthcare Ltd. with Measles vaccine manufactured by Serum Institute of India Ltd. in children 9–12 months of age. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2015/05/005739. 2015. PMID: CN-01847677. Intervention
1191.
Ctri. Clinical study to evaluate and compare the immunogenicity and safety of Tetanus vaccine of Cadila Healthcare Ltd. vs Tetanus vaccine of Serum Institute of India Ltd. in healthy subjects and subjects with clean minor wounds. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2015/05/005740. 2015. PMID: CN-01847682. Comparator
1192.
Ctri. Clinical study to compare immune response and safety of DPT vaccine of Cadila Healthcare Ltd. with DPT vaccine of Serum Institute of India Ltd. in healthy children. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2015/05/005768. 2015. PMID: CN-01847701. Intervention
1193.
Ctri. Study of a Single Dose or Two Doses of a Quadrivalent Influenza Vaccine in Subjects Aged 6 Months or Older in India. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2015/05/005770. 2015. PMID: CN-01847702. Outcome
1194.
Ctri. Clinical study to compare the immune response and safety of Measles, Mumps and Rubella (MMR) vaccine manufactured by Cadila Healthcare Ltd. with MMR vaccine manufactured by Serum Institute of India Ltd. in children 15–18 months of age. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2015/05/005784. 2015. PMID: CN-01845295. Intervention
1195.
Ctri. A clinical study on Pentavalent vaccine. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2015/06/005837. 2015. PMID: CN-01884221. Intervention
1196.
Ctri. A randomized, open label, multicenter study to evaluate the immunogenicity and safety of BBILs trivalent type 1, 2 & 3 oral polio vaccine. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2015/06/005856. 2015. PMID: CN-01884208. Intervention
1197.
Ctri. A clinical trial to compare the effectiveness of licensed live and inactivated influenza vaccines administered as nasal spray and injection respectively in children. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2015/06/005902. 2015. PMID: CN-01884085. Intervention
1198.
Ctri. Clinical trial on Rotavirus vaccine to check consistency of different lots of vaccines manufactured and to check vaccine interference with other childhood vaccines given under universal immunization program in India. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2015/07/006034. 2015. PMID: CN-01830599. Intervention
1199.
Ctri. Clinical study to compare the immune response and safety of Chicken Pox vaccine manufactured by Cadila Healthcare Ltd. with another Chicken Pox vaccine marketed in India in children 1–12 years of age. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2015/07/006059. 2015. PMID: CN-01830586. Intervention
1200.
Ctri. Clinical study to compare the immune response and safety of trivalent flu vaccine manufactured by Cadila Healthcare Ltd. with a trivalent flu vaccine marketed in India in healthy adults. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2015/09/006208. 2015. PMID: CN-01799190. Intervention
1201.
Ctri. Clinical study to compare the immune response and safety of tetravalent flu vaccine manufactured by Cadila Healthcare Ltd. with a trivalent flu vaccine marketed in India in healthy adults. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2015/09/006209. 2015. PMID: CN-01799189. Intervention
1202.
Ctri. A study on the maternal and infant factors determining the performance of Rotavirus vaccines in African, Indian and European infants. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2015/11/006354. 2015. PMID: CN-01840902. Outcome
1203.
Ctri. Randomized open label study to compare immunogenicity and safety of ROTAVAC® and ROTARIX® rotavirus vaccine. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2015/12/006428. 2015. PMID: CN-01808072. Intervention
1204.
Ctri. A clinical trial to study the safety and effectiveness of Serum Institute of India’s Pneumococcal Conjugate Vaccine in Healthy Indian Toddlers. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2015/12/006456. 2015. PMID: CN-01807965. Intervention
1205.
Ctri. A clinical trial to study the optimal dose of Hepatitis B vaccine in Human Immunodeficiency Virus (HIV) infected children. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2016/01/006495. 2016. PMID: CN-01855633. Intervention
1206.
Ctri. A Clinical trial to Compare the Immunogenicity and Safety of HBI Pentavalent (DTwP-Hb-Hib[Liquid]) Combination Vaccine with Pentavac SD® Vaccine in Healthy Infants. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2016/01/006541. 2016. PMID: CN-01855759. Intervention
1207.
Ctri. Comparative evaluation of immunogenicity of bivalent oral poliovirus vaccine (bOPV) and monovalent oral poliovirus vaccine type 1 (mOPV1) with a dose of inactivated polio vaccine (IPV) at week 14. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2016/04/006826. 2016. PMID: CN-01797274. Intervention
1208.
Ctri. A clinical trial to study the effect of reduced and alternate dose schedule of already approved pneumococcal conjugate vaccine. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2016/06/007042. 2016. PMID: CN-01818356. Intervention
1209.
Ctri. A multicenter, open label, comparative study to evaluate the immunogenicity and reactogenicity of a new fully liquid pentavalent DTwP-Hib-IPV vaccine (EasyfourPolTM, Panacea Biotec Ltd.)in Healthy Infants. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2016/07/007078. 2016. PMID: CN-01841039. Intervention
1210.
Ctri. A clinical trial to assess the safety and protective efficacy of Biological Es Measles-Rubella Vaccine in 9–12 months old Infants in India. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2016/07/007109. 2016. PMID: CN-01841373. Intervention
1211.
Ctri. clinical study of Meninigococcal vaccine for comparison of immunogenecity and safety with Menomune vaccine. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2016/11/007477. 2016. PMID: CN-01852556. Intervention
1212.
Ctri. Comparative evaluation of immunogenicity of various schedules and delivery options to provide fractional Dose Inactivated Poliovirus Vaccine in routine immunization. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2017/02/007793. 2017. PMID: CN-01818897. Intervention
1213.
Ctri. Clinical study to compare the immune response and safety of vaccine for prevention of Measles and Rubella diseases (MR vaccine) manufactured by Cadila Healthcare Ltd. with MR vaccine manufactured by Serum Institute of India Ltd. in children 9–12 months of age. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2017/05/008701. 2017. PMID: CN-01884318. Intervention
1214.
Ctri. A study to find out the effectiveness of measles, mumps, rubella(mmr) vaccine in the treatment of common warts and to compare its efficacy with formic acid treatment of common warts. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2017/07/009041. 2017. PMID: CN-01888935. Intervention
1215.
Ctri. Clinical study to evaluate the immune response and safety of four valent flu vaccine manufactured by Cadila Healthcare Ltd. in healthy children aged 6 months to 17 years. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2017/08/009204. 2017. PMID: CN-01891876. Intervention
1216.
Ctri. A study to determine the optimum timing of Hepatitis B vaccination during treatment of Acute Lymphoblastic leukemia( a type of blood cancer). http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2017/08/009402. 2017. PMID: CN-01891644. Outcome
1217.
Ctri. A clinical trial to describe the safety and immunogenicity of 13 valent pneumococcal conjugate vaccine formulated in multidose vials when given with routine pediatric vaccines in healthy infants in India. Title intended for the lay public in easily understood language. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2017/08/009492. 2017. PMID: CN-01891614. Intervention
1218.
Ctri. Comparison of immunogenicity, safety and tolerability of Single Dose of Hepatitis A (Live) Vaccine obtained by Freeze-dried process from Sinopharm against BiovacTM-A (Freeze-dried Live Attenuated Vaccine from Wockhardt)in Healthy Indian Children. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2017/09/009760. 2017. PMID: CN-01892697. Intervention
1219.
Ctri. Beneficial non-specific effects of BCG-Green signal and zero dose polio on neonatal survival in babies less than 2000 gram. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2018/08/015424. 2018. PMID: CN-01907868. Intervention
1220.
Ctri. A study to compare SB12 (proposed eculizumab biosimilar) with Soliris® in patients with the disease Paroxysmal Nocturnal Haemoglobinuria. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2019/05/019148. 2019. PMID: CN-01969220. Intervention
1221.
Ctri. A clinical study to assess the safety,tolerability & over all immune response of BEs Pneumococcal conjugate vaccine when administered in a three dose schedule. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2020/02/023129. 2020. PMID: CN-02166885. Intervention
1222.
Ctri. A clinical study to evaluate immune responses and adverse events of the 6-in-one SHAN6® vaccine in children. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID=CTRI​/2020/04/024843. 2020. PMID: CN-02167826. Intervention
1223.
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1225.
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1226.
Cullen G, Baden RP, Cheifetz AS. Vaccination in inflammatory bowel disease. American Journal of Gastroenterology. 2011 Jan;106(1):168. PMID: 21212760. Study design [PubMed: 21212760]
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Cunningham AL, Heineman T. Vaccine profile of herpes zoster (HZ/su) subunit vaccine. Expert Review of Vaccines. 2017;16(7):661–70. doi: 10.1080/14760584.2017.1329012. Intervention [PubMed: 28486850] [CrossRef]
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Esposito S, Corona F, Barzon L, et al. Immunogenicity, safety and tolerability of a bivalent human papillomavirus vaccine in adolescents with juvenile idiopathic arthritis. Expert Rev Vaccines. 2014 Nov;13(11):1387–93. doi: 10.1586/14760584.2014.943195. PMID: 25066387. Intervention [PubMed: 25066387] [CrossRef]
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Esposito S, Daleno C, Picciolli I, et al. Immunogenicity and safety of intradermal influenza vaccine in children. Vaccine. 2011 Oct 13;29(44):7606–10. PMID: 21855592. Study design [PubMed: 21855592]
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Esposito S, Marchisio P, Ansaldi F, et al. A randomized clinical trial assessing immunogenicity and safety of a double dose of virosomal-adjuvanted influenza vaccine administered to unprimed children aged 6–35 months. Vaccine. 2010 Aug 31;28(38):6137–44. PMID: 20670909. Study design [PubMed: 20670909]
1592.
Esposito S, Mastrolia MV, Ghio L, et al. Influenza immunization in hemodialyzed or kidney transplanted adolescents and young adults. Expert review of vaccines. 2014;13(8):1059–66. doi: 10.1586/14760584.2014.935768. Intervention [PubMed: 24972949] [CrossRef]
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Esposito S, Meregalli E, Daleno C, et al. An open-label, randomized clinical trial assessing immunogenicity, safety and tolerability of pandemic influenza A/H1N1 MF59-adjuvanted vaccine administered sequentially or simultaneously with seasonal virosomal-adjuvanted influenza vaccine to paediatric kidney transplant recipients. Nephrology Dialysis Transplantation. 2011 Jun;26(6):2018–24. PMID: 20974645. Study design [PMC free article: PMC7313880] [PubMed: 20974645]
1594.
Esposito S, Principi N. Influenza vaccination in young children. The Lancet Infectious Diseases. 2011 September;11(9):656–7. PMID: 2011460533. Participants [PubMed: 21867946]
1595.
Esposito S, Prymula R, Zuccotti GV, et al. A phase 2 randomized controlled trial of a multicomponent meningococcal serogroup B vaccine, 4CMenB, in infants (II). Human vaccines & immunotherapeutics. 2014;10(7):2005–14. doi: 10.4161/hv.29218. Participants [PMC free article: PMC4186018] [PubMed: 25424810] [CrossRef]
1596.
Esposito S, Prymula R, Zuccotti GV, et al. A phase 2 randomized controlled trial of a multicomponent meningococcal serogroup B vaccine, 4CMenB, in infants (II): Effects of variations of the OMV and protein content on immunogenicity and reactogenicity. Human Vaccines and Immunotherapeutics. 2014;10(7):2005–14. doi: 10.4161/hv.29218. Duplicate [PMC free article: PMC4186018] [PubMed: 25424810] [CrossRef]
1597.
Esposito S, Pugni L, Bosis S, et al. Immunogenicity, safety and tolerability of heptavalent pneumococcal conjugate vaccine administered at 3, 5 and 11 months post-natally to pre- and full-term infants. Vaccine. 2005 Feb 25;23(14):1703–8. PMID: 15705475. Study design [PubMed: 15705475]
1598.
Esposito S, Pugni L, Daleno C, et al. Influenza A/H1N1 MF59-adjuvanted vaccine in preterm and term children aged 6 to 23 months. Pediatrics. 2011 May;127(5):e1161–8. PMID: 21464195. Study design [PubMed: 21464195]
1599.
Esposito S, Salvini F, Menni F, et al. Preliminary data on immunogenicity, safety and tolerability of trivalent inactivated influenza vaccine in children with inborn errors of metabolism at risk of decompensation. Vaccine. 2013;31(45):5149–51. doi: 10.1016/j.vaccine.2013.08.058. Comparator [PubMed: 24012567] [CrossRef]
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Esposito S, Selicorni A, Daleno C, et al. Immunogenicity, safety and tolerability of monovalent 2009 pandemic influenza A/H1N1 MF59-adjuvanted vaccine in children and adolescents with Williams or Cornelia De Lange syndrome. Human Vaccines. 2011 Jun;7(6):613–7. PMID: 21508673. Study design [PubMed: 21508673]
1601.
Esposito S, Tagliaferri L, Daleno C, et al. Pandemic influenza A/H1N1 vaccine administered sequentially or simultaneously with seasonal influenza vaccine to HIV-infected children and adolescents. Vaccine. 2011 Feb 11;29(8):1677–82. PMID: 21199699. Study design [PubMed: 21199699]
1602.
Esposito S, Tansey S, Thompson A, et al. Safety and immunogenicity of a 13-valent pneumococcal conjugate vaccine compared to those of a 7-valent pneumococcal conjugate vaccine given as a three-dose series with routine vaccines in healthy infants and toddlers. Clinical & Vaccine Immunology: CVI. 2010 Jun;17(6):1017–26. PMID: 20427630. Study design [PMC free article: PMC2884425] [PubMed: 20427630]
1603.
Estcourt MJ, Marsh JA, Campbell DE, et al. Protocol for Pertussis Immunisation and Food Allergy (PIFA): a case-control study of the association between pertussis vaccination in infancy and the risk of IgE-mediated food allergy among Australian children. BMJ open. 2018;8(1):e020232. doi: 10.1136/bmjopen-2017-020232. Study design [PMC free article: PMC5878256] [PubMed: 29391374] [CrossRef]
1604.
Esteghamati A, Keshtkar A, Heshmat R, et al. Adverse reactions following immunization with MMR vaccine in children at selected provinces of Iran. Archives of Iranian Medicine. 2011 Mar;14(2):91–5. PMID: 21361714. Study design [PubMed: 21361714]
1605.
Esteves K. Safety of oral poliomyelitis vaccine: results of a WHO enquiry. Bulletin of the World Health Organization. 1988;66(6):739–46. PMID: 3266113. Intervention [PMC free article: PMC2491155] [PubMed: 3266113]
1606.
Esteves-Jaramillo A, Koehler T, Jeanfreau R, et al. Immunogenicity and safety of a quadrivalent meningococcal tetanus toxoid-conjugate vaccine (MenACYW-TT) in >=56-year-olds: A Phase III randomized study. Vaccine. 2020;38(28):4405–11. doi: 10.1016/j.vaccine.2020.04.067. Duplicate [PubMed: 32387012] [CrossRef]
1607.
Estívariz CF, Anand A, Gary HE, et al. Immunogenicity of three doses of bivalent, trivalent, or type 1 monovalent oral poliovirus vaccines with a 2 week interval between doses in Bangladesh: an open-label, non-inferiority, randomised, controlled trial. The lancet. Infectious diseases. 2015;15(8):898–904. doi: 10.1016/S1473-3099(15)00094-8. PMID: CN-01085325. Duplicate [PMC free article: PMC10406135] [PubMed: 26093980] [CrossRef]
1608.
Estivariz CF, Anand A, Gary HE, Jr., et al. Immunogenicity of three doses of bivalent, trivalent, or type 1 monovalent oral poliovirus vaccines with a 2 week interval between doses in Bangladesh: an open-label, non-inferiority, randomised, controlled trial. The Lancet. Infectious diseases. 2015;15(8):898–904. doi: 10.1016/S1473-3099(15)00094-8. Intervention [PMC free article: PMC10406135] [PubMed: 26093980] [CrossRef]
1609.
Estivariz CF, Molnar Z, Venczel L, et al. Paralytic poliomyelitis associated with Sabin monovalent and bivalent oral polio vaccines in Hungary. American Journal of Epidemiology. 2011 Aug 1;174(3):316–25. PMID: 21685412. Study design [PubMed: 21685412]
1610.
Etsano A, Damisa E, Shuaib F, et al. Environmental Isolation of Circulating Vaccine-Derived Poliovirus After Interruption of Wild Poliovirus Transmission - Nigeria, 2016. Mmwr-Morbidity and Mortality Weekly Report. 2016 Aug;65(30):770–3. PMID: WOS:000386699800004. Intervention [PubMed: 27490081]
1611.
Etzion O, Novack V, Perl Y, et al. Comparison Between Sci-B-Vac (TM) (Third Generation Vaccine) and Engerix-B Vaccines for Hepatitis B Virus in Patients With Inflammatory Bowel Diseases Treated With Immunosuppressive Medications. Randomized Control Trial. Gastroenterology. 2015 Apr;148(4):S269–S. PMID: WOS:000360115800222. Intervention
1612.
Etzion O, Novack V, Perl Y, et al. Sci-B-VacTM Vs ENGERIX-B Vaccines for Hepatitis B Virus in Patients with Inflammatory Bowel Diseases: A Randomised Controlled Trial. Journal of Crohn’s & colitis. 2016;10(8):905–12. doi: 10.1093/ecco-jcc/jjw046. Intervention [PMC free article: PMC5007589] [PubMed: 26928962] [CrossRef]
1613.
EU/EEA EO. A Study to Evaluate Safety and Immune Response of Novartis Meningococcal ACWY Conjugate Vaccine In US Adolescents and Adults. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2014-003504-79-Outside-EU/EEA. 2014. PMID: CN-01819851. Comparator
1614.
EU/EEA EO. The administration of adjuvanted Trivalent Influenza Vaccine (aTIV) has come to result in a more immunogenic and effective response compared with conventional influenza vaccines in elderly and adults. The aim of this study is to evaluate safety and immunogenicity of Novartis aTIV in Children 6 to <72 months of age, Mexican population, in comparison to Fluzone, a non adjuvanted Trivalent Influenza Vaccine (TIV). http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2014-004248-36-Outside-EU/EEA. 2014. PMID: CN-01861140. Intervention
1615.
EU/EEA EO. A phase II study, performed over a period of approximately 20 months, at one study site in Colombia in a population of subjects 18 to 40 years of age. Its aim was to evaluate the immunogenicity, safety and tolerability of H5N1 adjuvanted vaccine given either sequentially, concomitantly or using extemporaneous mixing with a seasonal trivalent influenza vaccine (Agrippal). http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2014-004515-37-Outside-EU/EEA. 2014. PMID: CN-01864500. Participants
1616.
EU/EEA EO. Safety and Immunogenicity of Two 0.25 mL or 0.5 mL Doses of Two Different Influenza Vaccines in Healthy Children Aged 6 to <60 Months. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2014-004543-12-Outside-EU/EEA. 2014. PMID: CN-01836657. Intervention
1617.
EU/EEA EO. Immunogenicity and safety of BoostrixTM using a new syringe in 10 to 15-year-old adolescents. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2013-003768-30-Outside-EU/EEA. 2015. PMID: CN-01895031. Intervention
1618.
EU/EEA EO. A study to evaluate consistency and immunogenicity of 3 lots of GSK Biologicals’ Hib conjugate vaccine versus ActHIB and Pentacel administered at 2, 4, 6 and 15–18 months of age in healthy infants. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2013-004194-27-Outside-EU/EEA. 2015. PMID: CN-01843321. Comparator
1619.
EU/EEA EO. Immunogenicity and safety study of GSK Biologicals’ Infanrix hexa™ when administered in healthy infants at 2, 4 and 6 months of age. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2013-004304-19-Outside-EU/EEA. 2015. PMID: CN-01814367. Intervention
1620.
EU/EEA EO. A study to compare the immunogenicity of GSK Biologicals’ 10Pn-PD-DiT 4-dose presentation to the licensed 1-dose Synflorix™ (10Pn-PD-DiT) vaccine when co-administered with DTPw-combination vaccine in healthy infants. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2014-000750-11-Outside-EU/EEA. 2015. PMID: CN-01879407. Intervention
1621.
EU/EEA EO. An Immunogenicity and Safety Study of GARDASIL™ in Chinese Female Subjects Aged 9 to 45 Years and Male Subjects Aged 9 to 15 Years. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2014-004581-16-Outside-EU/EEA. 2015. PMID: CN-01862280. Intervention
1622.
EU/EEA EO. This is a study to assess the safety and immune (antibody) response of a CSL inactivated influenza virus vaccine in a healthy paediatric, adult and senior adult populations. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2015-000177-12-Outside-EU/EEA. 2015. PMID: CN-01821117. Intervention
1623.
EU/EEA EO. Study to evaluate the immunogenicity and safety of GSK Biologicals’ thimerosal-free TIV Flu vaccine versus a licensed comparator in children. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2015-001258-13-Outside-EU/EEA. 2015. PMID: CN-01854743. Intervention
1624.
EU/EEA EO. Booster vaccination with pneumococcal vaccine GSK1024850A or Prevenar™ co-administered with Hiberix™ in children primed with the same vaccines. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2015-001506-34-Outside-EU/EEA. 2015. PMID: CN-01845374. Intervention
1625.
EU/EEA EO. An open, phase IIIb, randomized, multicentric clinical trial to compare the immunogenicity, safety and reactogenicity of GlaxoSmithKline (GSK) Biologicals’ DTPa-IPV vaccine versus co-administration of GSK Biologicals’ DTPa vaccine and Sanofi-Pasteurs’ IPV vaccine at different injection sites, to healthy children at 2, 4 and 6 months of age. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2015-001508-71-Outside-EU/EEA. 2015. PMID: CN-01841220. Intervention
1626.
EU/EEA EO. Immunogenicity and safety of GlaxoSmithKline Biologicals’ Havrix administered on a 0, 6-month schedule concomitantly with Merck and Company, Inc. M-M-R II and Merck and Company, Inc. VARIVAX to healthy children 15 months of age. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2015-001509-15-Outside-EU/EEA. 2015. PMID: CN-01851599. Comparator
1627.
EU/EEA EO. Study to evaluate the efficacy of GSK Biologicals’ quadrivalent influenza vaccine, GSK2282512A, (FLU Q-QIV) when administered in children 3 to 8 years of age. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2015-001514-97-Outside-EU/EEA. 2015. PMID: CN-01878256. Comparator
1628.
EU/EEA EO. Study to compare the reactogenicity and evaluate the safety and immunogenicity of GSK Biologicals combined hepatitis A / hepatitis B vaccine administered according to a 0, 6 month schedule versus Twinrix™ Junior administered according to a 0, 1, 6 month schedule in healthy children between 1 to 11 years old. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2015-001515-12-Outside-EU/EEA. 2015. PMID: CN-01816937. Comparator
1629.
EU/EEA EO. Study to evaluate the immunogenicity, safety, and reactogenicity of TWINRIX ADULT containing 720 ELISA units of hepatitis A antigen and 20 µg of hepatitis B surface antigen, administered following a two-dose (0, 6 months) schedule in healthy children between the ages of 1 and 11 years. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2015-001516-35-Outside-EU/EEA. 2015. PMID: CN-01860119. Comparator
1630.
EU/EEA EO. Immunogenicity and safety study of GlaxoSmithKline Biologicals’ Havrix administered on a 0, 6-month schedule concomitantly with GlaxoSmithKline Biologicals’ Infanrix and Aventis Pasteur’s Ac-tHIB in healthy children 15 months of age. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2015-001530-25-Outside-EU/EEA. 2015. PMID: CN-01807540. Comparator
1631.
EU/EEA EO. Study to compare the immunogenicity of GlaxoSmithKline Biologicals’ thiomersal-free 2-dose Engerix™-B and 3-dose preservative-free Engerix™-B vaccines administered according to a 0, 6 month and 0, 1, 6 month schedule, respectively, and to evaluate safety and reactogenicity of each vaccine in healthy adolescent volunteers (11 to 15 years). http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2015-001531-20-Outside-EU/EEA. 2015. PMID: CN-01870881. Intervention
1632.
EU/EEA EO. Study to evaluate the immunogenicity, reactogenicity and safety of two doses of GlaxoSmithKline (GSK) Biologicals’ oral live attenuated human rotavirus (HRV) liquid vaccine, when given to healthy infants, in Philippines. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2015-001544-11-Outside-EU/EEA. 2015. PMID: CN-01872781. Participants
1633.
EU/EEA EO. Study to evaluate the safety of Rotarix™ in Chinese children. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2015-001547-37-Outside-EU/EEA. 2015. PMID: CN-01841652. Participants
1634.
EU/EEA EO. A phase II study to assess the safety and immunogenicity of GlaxoSmithKline Biologicals’ rotavirus vaccine, RIX4414 when administered to HIV infected infants in South Africa. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2015-001484-39-Outside-EU/EEA. 2015. PMID: CN-01855362. Intervention
1635.
EU/EEA EO. Immunogenicity and safety study of Infanrix hexa in healthy infants born to mothers vaccinated with Boostrix™ during pregnancy or immediately post-delivery. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2014-001117-41-Outside-EU/EEA. 2016. PMID: CN-01879672. Intervention
1636.
EU/EEA EO. Immunogenicity and safety of the diphtheria, tetanus, pertussis and inactivated poliovirus (DPT-IPV) vaccine Squarekids™ co-administered with GSK Biologicals’ human rotavirus (HRV) vaccine Rotarix™ (444563) in healthy infants. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2014-005282-78-Outside-EU/EEA. 2016. PMID: CN-01859228. Participants
1637.
EU/EEA EO. Immunogenicity and safety study of GlaxoSmithKline (GSK) Biologicals’ Boostrix™ vaccine and the Chinese DT vaccine, when administered as booster vaccination in healthy children aged 6–8 years. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2016-000644-34-Outside-EU/EEA. 2016. PMID: CN-01878659. Intervention
1638.
EU/EEA EO. Immunogenicity and reactogenicity of a booster dose of GlaxoSmithKline Biologicals’ GSK2036874A vaccine in healthy toddlers. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2016-000645-31-Outside-EU/EEA. 2016. PMID: CN-01881245. Intervention
1639.
EU/EEA EO. This study will evaluate the immunogenicity, reactogenicity and safety of the routine infant vaccines Pediarix, Hiberix and Prevenar 13 when co-administered with GlaxoSmithKline (GSK) Biologicals’ liquid human rotavirus vaccine (HRV) as compared to GSK’s licensed lyophilized vaccine. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2016-003210-27-Outside-EU/EEA. 2017. PMID: CN-01893303. Intervention
1640.
EU/EEA EO. Safety and Immunogenicity of Novartis Meningococcal Group B Vaccine When Administered Concomitantly With Novartis MenACWY Conjugate Vaccine to Healthy Infants. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2016-005117-44-Outside-EU/EEA. 2017. PMID: CN-01875841. Participants
1641.
Euctr BE. Immunogenicity and Lot-to-Lot Consistency Study of a Quadrivalent Influenza Vaccine in Adult and Elderly Subjects. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2014-000785-21-BE. 2014. PMID: CN-01858964. Comparator
1642.
Euctr BE. A vaccine study in healthy adults to evaluate the safety and immune response of a licensed oral polio vaccine containing 3 polio vaccine strains. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2015-003324-32-BE. 2015. PMID: CN-01879744. Comparator
1643.
Euctr BE. A vaccine study in healthy adults to evaluate the safety and immune response of a licensed oral polio vaccine containing the polio vaccine 2 strain. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2015-003325-33-BE. 2015. PMID: CN-01858456. Intervention
1644.
Euctr BE. A study to evaluate the reactogenicity, safety and immunogenicity of GlaxoSmithKline (GSK) Biologicals’ investigational supra-seasonal universal influenza vaccines - inactivated (SUIVs) (GSK3816302A) in healthy adults aged 18 to 39 years. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2017-001584-20-BE. 2017. PMID: CN-01884767. Intervention
1645.
Euctr BE. A Double-blind Randomized Controlled Trial to Assess the Lot-to-lot Consistency of Sci-B-Vac™ in Adults. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2017-001820-22-BE. 2018. PMID: CN-01910029. Comparator
1646.
Euctr BE. Safety and Immunogenicity of V114 in Recipients of Allo-HSCT. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2018-000066-11-BE. 2018. PMID: CN-01906746. Intervention
1647.
Euctr BE. A phase 2 vaccine study in healthy adults to evaluate the safety and immunogenicity of two oral polio type 2 vaccine candidates. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2018-001684-22-BE. 2018. PMID: CN-01906884. Participants
1648.
Euctr CZ. Immunogenicity and Safety of Meningococcal MenABCWY Vaccine, and of rMenB+OMV NZ and MenACWY Administered Concomitantly in the Same Arm or in 2 Different Arms, or Alone. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2017-005128-12-CZ. 2018. PMID: CN-01905435. Intervention
1649.
Euctr DE. Antibody persistence for GlaxoSmithKline (GSK) Biologicals’ HPV-16/18 L1 VLP AS04 vaccine (GSK-580299) administered in healthy adults and adolescents, 6.5 years after first vaccination in the primary study. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2014-000060-17-DE. 2014. PMID: CN-01820270. Participants
1650.
Euctr DE. Safety and immunogenicity study of GSK Biologicals’ Quadrivalent Influenza Vaccine (GSK2321138A) manufactured with a new process in adults and children. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2014-000955-10-DE. 2014. PMID: CN-01797196. Comparator
1651.
Euctr DE. A blinded study to compare the safety and immune response in children and adolescents aged 3–17 years between Abbott’s Candidate Quadrivalant Influenza and Trivalent Influenza Vaccine. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2015-005482-23-DE. 2016. PMID: CN-01842151. Intervention
1652.
Euctr DE. Evaluation of immunogenicity and safety of two formulations of human rotavirus (HRV) vaccine, in healthy infants starting at age 6–12 weeks. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2016-000598-19-DE. 2016. PMID: CN-01832734. Intervention
1653.
Euctr DE. A Clinical Study to Assess the Safety and Immunogenicity of the Tetanus, Diphtheria and Pertussis Vaccine SIIPL Tdap in Comparison with Boostrix® in Healthy Adults, Adolescents and Children. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2019-002706-46-DE. 2019. PMID: CN-02169317. Intervention
1654.
Euctr DK. Safety and efficay of 3 new low dose polio vaccines with adjuvant compared to a full dose polio vaccine without adjuvant. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2014-000052-29-DK. 2014. PMID: CN-01847542. Intervention
1655.
Euctr EE. Clinical Study in Elderly to Evaluate the Safety, Immunogenicity and Efficacy of Investigational Flu Vaccine Compared to an Approved non-Flu Vaccine. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2015-000728-27-EE. 2015. PMID: CN-01808513. Comparator
1656.
Euctr ES. Evaluation of immunogenicity and safety of a booster dose of Infanrix hexa? in healthy infants born to mothers vaccinated with Boostrix? during pregnancy or immediately post-delivery. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2014-001120-30-ES. 2016. PMID: CN-01818149. Participants
1657.
Euctr ES. Study to assess the immunogenicity and safety of GSK’s investigational vaccine (GSK3277511A) when given to healthy smokers and ex-smokers after Shingrix vaccination. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2018-002977-24-ES. 2019. PMID: CN-02068172. Intervention
1658.
Euctr ES. Clinical trial in children from 12 to 35 months of the flu vaccine to estimate efficacy against influenza and other respiratory infections. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2019-001186-33-ES. 2019. PMID: CN-02068634. Intervention
1659.
Euctr FI. Safety and Immunogenicity of Repeated Exposure to an Adjuvanted Quadrivalent Subunit Influenze Virus Vaccine Compared to Non-Adjuvanted Comparator Influenza Vaccine in Children Vaccinated in Trial V118_05. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2014-002599-95-FI. 2014. PMID: CN-01864823. Participants
1660.
Euctr FI. A Phase II Study of the Immunogenicity and Safety of an Investigational Quadrivalent Meningococcal Conjugate Vaccines in Healthy Toddlers. http://www​.who.int/trialsearch/Trial2​.aspx?TrialID​=EUCTR2014-004367-20-FI. 2014. PMID: CN-01838326. Comparator
1661.
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