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Article

The Tolerability of the Dengue Vaccine TAK-003 (Qdenga®) in German Travelers: The Results of a Prospective Survey

Berlin Centre for Travel & Tropical Medicine, Friedrichstrasse 134, 10117 Berlin, Germany
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Author to whom correspondence should be addressed.
Trop. Med. Infect. Dis. 2025, 10(12), 352; https://doi.org/10.3390/tropicalmed10120352
Submission received: 1 October 2025 / Revised: 6 December 2025 / Accepted: 15 December 2025 / Published: 16 December 2025
(This article belongs to the Section Travel Medicine)

Abstract

Background: The global incidence of dengue has markedly increased over the last decades. Consequently, the risk of infection has increased significantly, resulting in record numbers of imported cases in various European countries and elsewhere in 2024. Methods: In early 2023, TAK-003, a novel, live attenuated vaccine against dengue, became available in Germany. At the Berlin Centre for Travel & Tropical Medicine, we delivered 56,459 doses during the first 24 months of its availability, from February 2023 to February 2025. To obtain data on the tolerability of the vaccine in travelers, an active follow-up survey was initiated. Results: In total, 30,306 (53.7%) vaccinees agreed to being contacted. Of these, 11,827 (39.0%) completed an anonymous questionnaire ≥ 4 weeks after the vaccination. Overall, 6856 (58.0%) were female, and 565 (4.8%) reported having had a prior dengue infection. The average age was 38.3 years (range 4–86 years). An endemic area had been visited by 6309 subjects before answering the questionnaire, and among these, 46 (0.7%) reported a dengue infection while abroad. All cases were mild, and no complications were reported. TAK-003 was applied with other vaccines in 7363 (62.3%) travelers. Local adverse reactions, mostly local pain, were reported by 5263 (47.5%) subjects. Systemic reactions were reported by 4891 subjects (41.4%) and were most frequently fatigue, myalgia, and flu-like symptoms. The majority of adverse events manifested in the second week after vaccination (median 8 days) and were mostly limited to a duration of 1–3 days. A macular exanthema was described by 1844 subjects (15.6%), typically during the second week after the vaccination. Conclusions: Side effects were frequently reported but generally well tolerated. Age groups above 50 years showed a decline in reactogenicity. Co-vaccination was frequent and led to an increase in systemic adverse events. Denominator data of the study population suggest a strong reporting bias towards adverse events. This survey adds evidence of the chronology and characteristics of adverse events associated with TAK-003 and may support decision making when vaccinating dengue-naïve travelers.
Keywords: dengue; live attenuated vaccine; traveler vaccination; adverse event; side effect dengue; live attenuated vaccine; traveler vaccination; adverse event; side effect

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MDPI and ACS Style

Jelinek, T.; Kramm, J.; Wagner, M.; Jelinek, C. The Tolerability of the Dengue Vaccine TAK-003 (Qdenga®) in German Travelers: The Results of a Prospective Survey. Trop. Med. Infect. Dis. 2025, 10, 352. https://doi.org/10.3390/tropicalmed10120352

AMA Style

Jelinek T, Kramm J, Wagner M, Jelinek C. The Tolerability of the Dengue Vaccine TAK-003 (Qdenga®) in German Travelers: The Results of a Prospective Survey. Tropical Medicine and Infectious Disease. 2025; 10(12):352. https://doi.org/10.3390/tropicalmed10120352

Chicago/Turabian Style

Jelinek, Tomas, Juliane Kramm, Maik Wagner, and Claudia Jelinek. 2025. "The Tolerability of the Dengue Vaccine TAK-003 (Qdenga®) in German Travelers: The Results of a Prospective Survey" Tropical Medicine and Infectious Disease 10, no. 12: 352. https://doi.org/10.3390/tropicalmed10120352

APA Style

Jelinek, T., Kramm, J., Wagner, M., & Jelinek, C. (2025). The Tolerability of the Dengue Vaccine TAK-003 (Qdenga®) in German Travelers: The Results of a Prospective Survey. Tropical Medicine and Infectious Disease, 10(12), 352. https://doi.org/10.3390/tropicalmed10120352

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