What Happens If You Give the Wrong Vaccine?

Vaccine administration errors are uncommon events. Healthcare systems maintain protocols to address these situations, ensuring patient well-being is prioritized. This article provides information on what happens when such an error occurs, including potential outcomes and necessary steps.

Understanding Vaccine Administration Errors

A “wrong vaccine” error refers to various scenarios beyond receiving a completely different vaccine product. These incidents typically stem from human error during administration, not issues with the vaccine product itself. For instance, an error might involve giving a measles vaccine when a mumps vaccine was indicated.

Further examples include providing a vaccine formulated for a different age group, like an adult dose to a child, or vice-versa. Errors can also involve an incorrect dosage, where too much or too little of the vaccine is given. Additionally, administering an expired vaccine or using an incorrect route of administration, such as injecting subcutaneously instead of intramuscularly, or at the wrong anatomical site, constitute administration errors.

Potential Health Consequences

Most vaccine administration errors result in no serious harm, with reactions often limited to mild, temporary effects like local soreness, redness, or a low-grade fever. The primary concern is often ineffective vaccination, meaning the individual may not develop adequate protection against the intended disease.

When an incorrect vaccine type or age-specific formulation is given, it might lead to increased local or systemic side effects, or simply be ineffective. For example, a live attenuated vaccine (e.g., measles, mumps, rubella, or varicella) carries a risk of causing a mild form of the disease if administered to an immunocompromised individual. In such cases, non-live vaccines are generally safe, though they might be less effective in stimulating an immune response.

An incorrect dose, particularly an under-dose, typically leads to insufficient immunity, making re-vaccination necessary. An over-dose may increase typical vaccine side effects like fever or body aches, but rarely causes severe harm. If an expired vaccine is given, the main risk is reduced potency, meaning it may not provide adequate protection, but it is generally not harmful.

An incorrect route or site of administration can result in increased local reactions, such as the formation of a granuloma, which is a small area of inflammation. This can also reduce the vaccine’s efficacy or lead to increased systemic side effects, depending on the specific vaccine and the route chosen. Overall, serious adverse events from vaccine administration errors are exceedingly rare, and most incidents are benign or can be easily corrected.

Immediate Actions and Follow-Up Care

Should an individual or caregiver suspect a vaccine administration error has occurred, contacting a healthcare provider immediately is important. This includes reaching out to the clinic, doctor’s office, or hospital where the vaccine was administered without delay. It is important to avoid attempting any home remedies or self-medication without professional medical guidance.

When contacting the provider, provide details like the date and time of vaccination, the vaccine name (if known), and any symptoms. The healthcare provider will evaluate the situation to determine next steps, which may involve monitoring health, additional testing, or re-vaccination. Following medical advice is important for appropriate care.

Reporting and Learning from Errors

Reporting vaccine administration errors, even minor ones, serves a broader public health purpose. This practice identifies error patterns, informing improvements in vaccine administration and enhancing patient safety. National reporting systems document such incidents, contributing to a comprehensive understanding of vaccine safety.

In the United States, the Vaccine Adverse Event Reporting System (VAERS) collects reports of adverse events and administration errors following vaccination. Healthcare professionals, vaccine manufacturers, and the public can submit reports. Each reported error contributes to a safer vaccination landscape by providing data that informs training, refines protocols, and strengthens oversight, reducing future occurrences.