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The reporting sensitivities of two passive surveillance systems for vaccine adverse events.
Am J Public Health. 1995 Dec;85(12):1706-9. doi: 10.2105/ajph.85.12.1706.
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Surveillance for adverse events following immunization (AEFI) for 7 years using a computerised vaccination system.
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Evaluating the safety profile of the CoronaVac in adult and older adult populations: A phase IV prospective observational study in Brazil.
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Otorhinolaryngologic complications after COVID-19 vaccination, vaccine adverse event reporting system (VAERS).
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Autoimmune disorders reported following COVID-19 vaccination: A disproportionality analysis using the WHO database.
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Acute thrombocytopenic purpura following measles, mumps and rubella vaccination. A report on 23 patients.
Acta Paediatr. 1993 Mar;82(3):267-70. doi: 10.1111/j.1651-2227.1993.tb12657.x.
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The Vaccine Adverse Event Reporting System (VAERS).
Vaccine. 1994 May;12(6):542-50. doi: 10.1016/0264-410x(94)90315-8.
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A 7-year survey of disorders attributed to vaccination in North West Thames region.
Lancet. 1983 Apr 2;1(8327):753-7. doi: 10.1016/s0140-6736(83)92037-8.
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History of convulsions and use of pertussis vaccine.
J Pediatr. 1985 Aug;107(2):175-9. doi: 10.1016/s0022-3476(85)80120-7.
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Diphtheria-tetanus-pertussis immunization and sudden infant death syndrome.
Am J Public Health. 1987 Aug;77(8):945-51. doi: 10.2105/ajph.77.8.945.

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