Adverse Reactions Following Vaccination and Reporting Vaccine Adverse
Events
Vaccines are intended to produce active immunity to specific antigens. An
adverse reaction is an untoward effect caused by a vaccine that is
extraneous to the vaccine’s primary purpose of producing immunity. Adverse
reactions are also called vaccine side effects. A vaccine adverse event
refers to any medical event that occurs following vaccination. An adverse
event could be a true adverse reaction or just a coincidental event, with
further research needed to distinguish between them.
Acute vaccine adverse reactions fall into three general categories: local,
systemic, and allergic. The most common type of adverse reactions are local
reactions, such as pain, swelling, and redness at the site of injection.
Local reactions may occur with up to 80% of vaccine doses, depending on the
type of vaccine. Local adverse reactions generally occur within a few hours
of the injection and are usually mild and self-limited. On rare occasions,
local reactions may be very exaggerated or severe.
Some of these reactions,
referred to as Arthus reactions, are most frequently seen with diphtheria
and tetanus toxoids. Arthus reactions are not allergic reactions. Arthus
reactions are believed to be due to very high titers of antibody, usually
caused by too many doses of toxoid.
Systemic adverse reactions are more generalized events and include fever,
malaise, myalgias (muscle pain), headache, loss of appetite, and others.
These symptoms are nonspecific; they may occur in vaccinated persons
because of the vaccine or may be caused by something unrelated to the
vaccine.
Systemic adverse reactions were relatively frequent with DTP vaccine, which
contained a whole-cell pertussis component. However, comparison of the
frequency of systemic adverse events among vaccine and placebo recipients
shows they are less common with inactivated vaccines currently in use,
including acellular pertussis vaccine.
Systemic adverse reactions may occur following receipt of live attenuated
vaccines. Live attenuated vaccines must replicate in order to produce
immunity. The adverse reactions that follow live attenuated vaccines, such
as fever or rash, represent symptoms produced from viral replication and
are similar to a mild form of the natural disease. Systemic adverse
reactions following live vaccines are usually mild, and occur 3–21 days
after the vaccine was given (i.e., after an incubation period of the
vaccine virus). LAIV replicates in the mucous membranes of the nose and
throat, not in the lungs. As a result, LAIV may cause upper respiratory
symptoms (like a cold) but not influenza-like symptoms.
A third type of acute vaccine adverse reactions are allergic reactions.
Allergic reactions may be caused by the vaccine antigen itself or some
other component of the vaccine, such as cell culture material, stabilizer,
preservative, or antibiotic used to inhibit bacterial growth. Severe
allergic reactions (anaphylaxis) may be life-threatening. Fortunately, they
are rare. The risk of an allergic reaction can be decreased by good
screening prior to vaccination. All providers who administer vaccines must
have an emergency protocol and supplies to treat anaphylaxis.
Reporting Vaccine Adverse Events
Providers should report any clinically significant adverse event that
occurs after the administration of any vaccine licensed in the United
States to the Vaccine Adverse Event Reporting System (VAERS), which
includes reporting from both public and private sectors. Providers should
report a clinically significant adverse event even if they are unsure
whether a vaccine caused the event. The telephone number to call for
answers to questions and to obtain VAERS forms is (800) 822-7967, or visit
the VAERS website at http://vaers.hhs.gov. VAERS accepts reports of adverse
reactions through their online system.
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Adverse Reactions Following Vaccination and Reporting Vaccine Adverse Events
Sunday, January 6, 2019
Adverse Reactions Following Vaccination and Reporting Vaccine Adverse Events
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