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Products » Items » Dultavax


Contraindicated

No available information
Dultavax :
Type Medicine Non Marketed
Originator B
Agent UPO
Distributor UPO
Laboratory Sanofi Pasteur
Responsible Party Sanofi Pasteur SA
Origin France
Manufacturer Sanofi Pasteur SA
Origin France
ATC J07CA01

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Dultavax :

Revision Date : 25/02/2015


Effect Frequency
Abdominal pain Not known
Allergic reaction Not known
Anaphylactic reactions Not known
Anaphylactic shock Not known
Angioedema (Angioneurotic oedema) (Quincke oedema) Not known
Arthralgia (Pain joint) (Joint ache) Rare
Asthenia Not known
Cephalea Common
Chills Not known
Convulsion Not known
Diarrhoea (Diarrhea) Not known
Erythema Not known
Extensive swelling of vaccinated limb Not known
Face oedema Not known
Guillain-Barre syndrome Not known
Hyperthermia Common
Hypoesthesia Not known
Hypotension Not known
Immediate hypersensitivity reaction Not known
Influenza-like symptoms Not known
Injection site erythema Not known
Injection site induration Not known
Injection site nodule Not known
Injection site oedema Not known
Injection site pain Not known
Injection site reaction Not known
Injection site warmth Not known
Lymphadenopathy Uncommon
Malaise Uncommon
Myalgia Uncommon
Nausea Common
Pallor Not known
Paraesthesia (paresthesia) Not known
Pruritus Not known
Skin rash Not known
Urticaria Not known
Vasovagal reaction Not known
Vertigo Common
Vomiting Common

Different Units By MoH Code

Revision Date : 01/06/2004

Dultavax  MoH 5674 :
Form Suspension for injection
Packaging Pre-filled Syringe
Package Size 1 x0.5ml
Strength multicompo
Storage Condition 2-8°C Do not freeze
NSSF ✘
Quarantine ✘
Reg. Number 219501/09
Submission date 01/01/2009
Registration Year 2010
Archived Date 2019

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