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PENTAXIM VACCINE

Product Information

Registration Status: Active

SIN14795P

PENTAXIM VACCINE is approved to be sold in Singapore with effective from 2015-05-06. It is marketed by SANOFI-AVENTIS SINGAPORE PTE LTD, with the registration number of SIN14795P.

This product contains PENTAXIM Conjugated To Tetanus Protein (Prp-T) 18 - 30mcg,(Freeze-Dried Powder) Haemophilus Influenzae Type-B Polysaccharide (Polyribosylribitol Phosphate) 10mcg,Diptheria Toxoid Minimum 30IU,Filamentous Haemagglutinin 25mcg,Pertussis Toxoid 25mcg,Poliovirus (Inactivated) Type 1 (Mahoney) 40 DU,Poliovirus (Inactivated) Type 2 (Mef-1) 8 DU,Poliovirus (Inactivated) Type 3 (Saukett) 32 DU, and Tetanus Toxoid Minimum 40IU in the form of INJECTION, POWDER, FOR SUSPENSION. It is approved for INTRAMUSCULAR use.

This product is manufactured by Sanofi Pasteur S.A. in FRANCE, and MLE in ITALY.

It is a Prescription Only Medicine that can only be obtained from a doctor or a dentist, or a pharmacist with a prescription from a Singapore-registered doctor or dentist.

Product Reference
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Source of information: Drugbank (External Link). Last updated on: 3rd July 18. *Trade Name used in the content below may not be the same as the HSA-registered product.



Source of information: Drugbank (External Link). Last updated on: 3rd July 18. *Trade Name used in the content below may not be the same as the HSA-registered product.



Source of information: Drugbank (External Link). Last updated on: 3rd July 18. *Trade Name used in the content below may not be the same as the HSA-registered product.


Description

Bordetella pertussis filamentous hemagglutinin antigen (formaldehyde inactivated) is a vaccine that contains inactivated acellular pertussis antigen that is isolated from Bordetella pertussis culture.

Active Ingredient/Synonyms

Bordetella pertussis filamentous hemagglutinin vaccine, inactivated | Filamentous haemagglutinin | Filamentous haemagglutinin adsorbed | Bordetella pertussis filamentous hemagglutinin antigen (formaldehyde inactivated) |


Source of information: Drugbank (External Link). Last updated on: 3rd July 18. *Trade Name used in the content below may not be the same as the HSA-registered product.



Source of information: Drugbank (External Link). Last updated on: 3rd July 18. *Trade Name used in the content below may not be the same as the HSA-registered product.



Source of information: Drugbank (External Link). Last updated on: 3rd July 18. *Trade Name used in the content below may not be the same as the HSA-registered product.



Source of information: Drugbank (External Link). Last updated on: 3rd July 18. *Trade Name used in the content below may not be the same as the HSA-registered product.



Source of information: Drugbank (External Link). Last updated on: 3rd July 18. *Trade Name used in the content below may not be the same as the HSA-registered product.


Description

Clostridium tetani toxoid antigen (formaldehyde inactivated) is a vaccine for intramuscular injection. It is used for active immunization of children 7 years of age or older, and adults, for prevention of tetanus. The toxoid in the Clostridium tetani culture is grown and detoxified followed by purification via ammonium sulfate filtration and precipation.

Active Ingredient/Synonyms

Tetanus toxoid | Tetanus toxoid adsorbed | tetanus toxoid vaccine, inactivated | Clostridium tetani toxoid antigen (formaldehyde inactivated) |


Source of information: Drugbank (External Link). Last updated on: 3rd July 18. *Trade Name used in the content below may not be the same as the HSA-registered product.

References

  1. Health Science Authority of Singapore - Reclassified POM
  2. Drugbank

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