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BOOSTRIX
Tetanus Toxoid, Reduced Diphtheria Toxoid And Acellular Pertussis Vaccine, Adsorbed
$66.00
1 syringes
BrandBranded medicine· By GlaxoSmithKline
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About BOOSTRIX
Overview
BOOSTRIX is a noninfectious vaccine supplied in prefilled syringes. It is used as a booster to protect people aged 10 years and older against tetanus, diphtheria and pertussis (whooping cough). It is also indicated during the third trimester of pregnancy to help prevent whooping cough in infants younger than 2 months. It stimulates protective antibodies against tetanus and diphtheria toxins, while antibodies against pertussis can pass through the placenta to help protect the infant.
What it treats
- Booster immunization against tetanus, diphtheria and pertussis (whooping cough) in people aged 10 years and older. - Immunization during the third trimester of pregnancy to help prevent pertussis in infants younger than 2 months.
Safety information
Side effects
Common side effects in people aged 10 to 64 include pain, redness and swelling at the injection site, headache, tiredness and stomach or bowel symptoms. Adolescents aged 10 to 18 may also have swelling that increases the size of the injected arm. In adults aged 65 and older, injection-site pain was the most common reported side effect. Contact your doctor before vaccination if you have had Guillain-Barré syndrome within six weeks of a previous tetanus-containing vaccine, as another such vaccine, including BOOSTRIX, may increase the risk of this condition. Also tell your doctor about any progressive or unstable neurological condition, which is a reason to postpone vaccination, or any previous Arthus-type reaction, an immune-related hypersensitivity reaction, after a tetanus-containing vaccine. This history affects whether you should receive BOOSTRIX.
Before taking this medicine
BOOSTRIX should not be given to anyone who has had a severe allergic reaction, such as anaphylaxis, to any ingredient in BOOSTRIX or after a previous vaccine containing tetanus, diphtheria or pertussis components. It should also not be given to anyone who developed encephalopathy (a serious disturbance of brain function) within 7 days after a previous pertussis-containing vaccine. Vaccination should be deferred in people with progressive or unstable neurological conditions. Tell the clinician if Guillain-Barré syndrome occurred within 6 weeks after a previous tetanus-containing vaccine, as the risk may be increased with BOOSTRIX. Also tell the clinician about any previous Arthus-type reaction (a severe local immune reaction) after a tetanus-containing vaccine, as this requires vaccination to be delayed.
Using BOOSTRIX
Dosing
Dosing is set by your prescriber. Each health care professional may prescribe medication differently according to a patient's medical history and condition, so follow the directions on your prescription label and speak to your doctor or pharmacist before changing anything.
Storage
Store in the original carton to protect it from light. Check the pack for whether it must be refrigerated before first use. Keep all medicines out of the sight and reach of children.
Clinical information on this page is summarised from the US FDA label BOOSTRIX (TETANUS TOXOID, REDUCED DIPHTHERIA TOXOID AND ACELLULAR PERTUSSIS VACCINE, ADSORBED) SUSPENSION [GLAXOSMITHKLINE BIOLOGICALS SA] (DailyMed, retrieved 19 September 2026).
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