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Products » Items » Pentaxim°


Contraindicated

No available information
Pentaxim° :
Type Medicine Withdrawn
Originator B
Agent UPO
Distributor UPO
Laboratory Sanofi Pasteur
Responsible Party Sanofi Pasteur SA
Origin France
Manufacturer Sanofi Pasteur SA
Origin France
ATC J07CA06

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Pentaxim° :

Revision Date :


Effect Frequency
Anaphylactic reactions Not known
Anaphylactic shock Not known
Angioedema (Angioneurotic oedema) (Quincke oedema) Not known
Appetite lost Very Common
Convulsion Not known
Crying abnormal Very Common
Cyanosis Rare
Diarrhoea (Diarrhea) Common
Erythema Not known
Extensive swelling of vaccinated limb Not known
Face oedema Not known
Fever Very Common
Hypotonic-hyporesponsive episode Not known
Immediate hypersensitivity reaction Not known
Inconsolable crying Uncommon
Injection site erythema Very Common
Injection site induration Common
Injection site oedema Very Common
Injection site pain Very Common
Injection site reaction Not known
Injection site redness Uncommon
Injection site tenderness Not known
Injection site warmth Not known
Insomnia Common
Irritability Very Common
Nervousness Very Common
Purpura Rare
Skin Eruption Not known
Sleep disorder (Sleep disturbance) Common
Somnolence Very Common
Urticaria Not known
Vomiting Very Common

Different Units By MoH Code

Revision Date : 01/05/2002

Pentaxim°  MoH 568 :
Form Powder and solvent for suspension for injection
Packaging Pre-filled Syringe + Vial
Package Size 1+1x0.5ml
Strength multicompo
Storage Condition 2-8°C Do not freeze
Stratum N/A
NSSF ✘
Quarantine ✘
Reg. Number 148166/03
Submission date 01/01/2003
Registration Year 2006
Withdrawn Date 07/04/2021

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