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Boostrix Polio

Boostrix Polio

Manufacturer:

GlaxoSmithKline

Distributor:

Zuellig
Concise Prescribing Info
Contents
Diphtheria, tetanus, pertussis (acellular, component) & poliomyelitis (inactivated) vaccine [adsorbed, reduced antigen(s) content]
Indications/Uses
Booster vaccination against diphtheria, tetanus, pertussis (DTP) & poliomyelitis for individuals ≥3 yr. Passive protection against pertussis in early infancy following maternal immunisation during pregnancy.
Dosage/Direction for Use
Single 0.5 mL dose by deep IM inj, preferably in the deltoid region. Pregnant women Administer during 2nd or 3rd trimester in accordance w/ official recommendations.
Contraindications
Hypersensitivity to any component of the vaccine, to neomycin or polymyxin, or after previous administration of DTP or poliomyelitis vaccines. Encephalopathy of unknown aetiology occurring w/in 7 days following previous vaccination w/ pertussis-containing vaccine. Transient thrombocytopenia or neurological complications following an earlier immunisation against diphtheria &/or tetanus. Postpone vaccination in subjects suffering from acute severe febrile illness.
Special Precautions
Do not administer intravascularly. Appropriate medical treatment & supervision should always be readily available in case of rare anaphylactic reactions following vaccination. If any of the following occurs in temporal relation to receipt of pertussis-containing vaccine, the decision to give doses of pertussis-containing vaccine should be carefully considered: Temp ≥40°C w/in 48 hr of vaccination, not due to another identifiable cause; collapse or shock-like state w/in 48 hr of vaccination; persistent, inconsolable crying lasting ≥3 hr w/in 48 hr of vaccination; convulsions w/ or w/o fever, occurring w/in 3 days of vaccination. Childn w/ new onset or progressive severe neurological disorders; individuals w/ thrombocytopenia or a bleeding disorder; immunosuppressed patients. Protective immune response may not be elicited in all vaccinees. Lactation. Safety & efficacy in childn <3 yr have not been established.
Adverse Reactions
Pain, redness, swelling at inj site. Pyrexia, inj site pruritus, induration. Individuals 10-93 yr: Fatigue; headache. GI disorders; inj site haematoma, warmth numbness. Individuals 4-8 yr: Somnolence. Anorexia; irritability; headache; extensive swelling of vaccinated limb, inj site haemorrhage.
Drug Interactions
May be administered concomitantly w/ MMR, varicella, & HPV vaccine. If to be given at the same time as other vaccines or Ig, the products should be given at separate sites. Response may not be adequately achieved if given w/ immunosuppressive therapy.
MIMS Class
Vaccines, Antisera & Immunologicals
ATC Classification
J07CA02 - diphtheria-pertussis-poliomyelitis-tetanus ; Belongs to the class of combined bacterial and viral vaccines.
Presentation/Packing
Form
Boostrix Polio vaccine susp for inj
Packing/Price
(pre-filled syringe) 0.5 mL x 1's
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