Leaflet BOOSTRIX suspension for injection in pre-filled syringe

Product code:
W67291001
Quantity:
1
Indicated for:
prevention of diphtheria, tetanus and pertussis
Route of administration:
injectable
ATC
J07AJ52 — Antiinfectives for systemic use | Bacterial vaccines | Pertussis vaccines

Precautions:

Anaphylaxis

Risk of severe allergic reaction. Seek urgent medical help if serious symptoms occur.

Additional monitoring

This medicine is subject to additional monitoring.

Refrigerated storage

Store in the refrigerator as instructed in the leaflet.

Protect from light

Store protected from light.

The diphtheria, tetanus, pertussis (DTP) vaccine is used to prevent diphtheria, tetanus, and whooping cough, three serious infectious diseases caused by bacteria. The vaccine contains diphtheria and tetanus toxoids, as well as inactivated or purified components of Bordetella pertussis, which stimulate the immune system to produce specific antibodies against these pathogens.

The vaccine is administered intramuscularly, usually in multiple doses, according to recommended vaccination schedules for infants, children, and adolescents. Booster doses are required at regular intervals to maintain immunity.

Common side effects include pain at the injection site, mild fever, fatigue, and irritability. In rare cases, severe allergic reactions may occur.

The DTP vaccine is an essential measure for protecting public health, helping to reduce the incidence and severity of these infectious diseases and prevent the severe complications associated with them.

General data about BOOSTRIX

Substance:
diphtheria, tetanus, pertussis vaccine
Date of latest medicines list:
01-02-2021
Product code:
W67291001
Pharmaceutical form:
suspension for injection in pre-filled syringe
Quantity:
1
Product type:
Original
Prescription status:
P-RF — Medicines dispensed with a medical prescription that is retained by the pharmacy and cannot be renewed.

Marketing authorisation

Manufacturer:
GLAXOSMITHKLINE BIOLOGICALS SA - BELGIA
Holder:
GLAXOSMITHKLINE (GSK) S.R.L. - ROMANIA
Number:
12980/2020/01
Shelf life:
3 years