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Vaccine-related adverse events in Cuban children, 1999-2008
Belkys M Galindo1, Damarys Concepción, Miguel A Galindo
1Pedro Kourí Tropical Medicine Institute (IPK), Havana, Cuba. bgalindo@ipk.sld.cu
Insights
Cuba
Area of Science:
- Public Health
- Epidemiology
- Vaccinology
Background:
- Cuba's National Immunization Program, established in 1962, administers 11 vaccines against 13 diseases.
- A national vaccine adverse event surveillance system was launched in 1999 to monitor immunization safety.
Purpose of the Study:
- To describe adverse events following vaccination in children under 16 in Cuba.
- To assess vaccine safety and identify potential program errors from 1999 to 2008.
Main Methods:
- A retrospective descriptive study of vaccine adverse events reported between January 1999 and December 2008.
- Analysis included event type, severity, vaccine type, and investigation outcomes of severe events.
Main Results:
- Over 45 million vaccine doses administered, with 26,159 adverse events reported (57.8 per 100,000 doses).
- The 0-5 year age group had the highest adverse event rate. DTwP vaccine showed the highest event rate. Common events included fever and injection site reactions. Rare severe events were infrequent.
Conclusions:
- Low rates of severe vaccine-associated adverse events confirm the safety and benefits of Cuba's immunization program.
- Comprehensive surveillance and expert analysis support informed decision-making for program success.
Abstract:
INTRODUCTION Cuba has implemented an effective National Immunization Program since 1962. The schedule, administered primarily to children, comprises 11 vaccines (8 domestically produced) protecting against 13 diseases. In 1999 Cuba launched a national vaccine adverse event surveillance system to monitor and assess the safety of the immunization program, its vaccination procedures and the products administered. OBJECTIVES Describe adverse events following vaccination reported in children aged <16 years in Cuba from 1999 through 2008. METHODS A retrospective descriptive study was conducted of adverse events following vaccination reported from January 1999 through December 2008. Variables used: year, number of adverse events, province, type of vaccine, type and severity of adverse events (common minor, rare, severe), vaccination program errors, number of deaths, and final results of investigations of severe events. Percentages and rates per dose administered were calculated. Adverse event rates were calculated per 100,000 doses administered and by percentages of individual effects among events reported. RESULTS A total of 45,237,532 vaccine doses were administered, and 26,159 vaccine-associated adverse events were reported (overall rate: 57.8 per 100,000 doses). The group aged 0-5 years reported the highest rate of vaccine-associated adverse events (82/100,000 doses). The DTwP vaccine exhibited the highest rate of adverse events. Common minor events were: fever (17,538), reactions at injection site (4470) and systemic side effects (2422). Rare events (by WHO definition) reported were: persistent crying (2666), hypotonic-hyporesponsive episodes (3), encephalopathy (2) and febrile seizures (112). Severe events included: anaphylaxis (2), respiratory distress (1), multiple organ failure (1), sudden death (1), vaccine-associated paralytic poliomyelitis (2), toxic shock syndrome (3), and sepsis (1). The 10 deaths and 3 cases of disability were investigated by an expert commission, which concluded that 8 of the 13 severe events were vaccination-related. CONCLUSIONS Low rates of severe vaccine-associated adverse events observed in this study underline the low risk of vaccination relative to its demonstrated benefits in Cuba. Decision-making for the continued success of the National Immunization Program is supported by reliable information from comprehensive national surveillance with standarized reporting, along with multidisciplinary expert analysis of rare and severe adverse events and program errors. KEYWORDS Immunization; immunization programs; vaccines; vaccination; product surveillance, postmarketing; adverse drug event; communicable disease control; Cuba.
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