Getting a flu shot and COVID-19 shot at the same time is safe and has no increased risk of adverse effects. New research, published in the Annals of Internal Medicine, evaluating the 90-day risks for adverse events after coadministration of COVID-19 and influenza vaccines versus receipt of only the flu vaccine, showed no statistically significant risks at any level of severity.
For the study, 2.5 million adults were either administered a flu shot only, or coadministered same-day COVID-19 and influenza vaccines. The effects were then assessed against three tiers of severity (serious or life-threatening, clinically significant, and less severe or self-limiting) for 90 days during 3 updated COVID-19 vaccine formulation periods (bivalent, XBB-adapted, and KP-adapted). No outcome showed a statistically significant difference between flu vaccine only and flu and COVID-19 vaccine coadministration.
Overall, the study’s findings that same-day coadministration of COVID-19 and influenza vaccines was not associated with increased risk for adverse events during the 90 days of follow-up across 3 updated-formulation periods support the short-term safety of coadministration in older adults. The findings also may help inform ongoing vaccine policy discussions and individual risk–benefit assessments.
The authors note that these results should be considered in the context of the risks for SARS-CoV-2 infection itself, which continues to cause substantial morbidity and mortality in the U.S., with an estimated 879,000 hospitalizations and 101,000 deaths during the 2023 to 2024 surveillance period. Additionally, the nearly 300 recruits infected with the flu in the Lackland AFB outbreak, resulting in at least four hospitalizations and one death, show the need for population immunity.
For ongoing updates on the current status and risk of COVID-19, influenza, and other communicable diseases, see TAG’s monthly updated Communicable Disease Risk Matrix.
COVID Risk Matrix

Influenza


Public Health News
- The Health and Human Services (HHS) has declared a termination of the COVID-19 Emergency Use Authorization (EUA) declarations for drugs, biological products, and medical devices, concluding that the circumstances that justified these emergency authorities no longer exist and FDA-approved, cleared, and licensed products are now widely available through traditional regulatory pathways. The terminations will take effect following advance notice, with drugs and biological products terminating in 12 months and medical devices in 180 days. During the transition, HHS and FDA will continue working with manufacturers on appropriate regulatory pathways for products seeking traditional approval, clearance, or licensure.
- The Michigan Department of Health and Human Services (MDHHS) is investigating a sudden and large increase of  Cyclospora infections (cyclosporiasis) across numerous counties in Michigan. Although the state typically has 50 cases in a full year, there have been more than 225 cases of cyclosporiasis reported since June 22. With no common point of exposure yet identified and outbreaks in recent years having resulted from eating contaminated fresh produce, officials are advising that all produce be thoroughly washed, in restaurants or at home.
- There is another report of cyclosporiasis cases in the US. The CDC is reporting at least 145 cases in 17 states; these do not include the cases in Michigan. Investigations to determine the source of the infection are underway. TAG will continue to follow this as it develops.
- In Indonesia, 170 cases and 21 deaths due to leptospirosis have been reported, likely tied to intense rain and flooding that have occurred in the first half of 2026. Leptospira is a bacterium often transmitted  via rodent urine, which then contaminates and survives in moist environments and stagnant water, including drains, ponds, slow-flowing rivers, and puddles, for as long as months.Â


