Cervarix

Pays: Union européenne

Langue: anglais

Source: EMA (European Medicines Agency)

Achète-le

Ingrédients actifs:

human papillomavirus1 type 16 L1 protein, human papillomavirus type 18 L1 protein

Disponible depuis:

GlaxoSmithKline Biologicals S.A.

Code ATC:

J07BM02

DCI (Dénomination commune internationale):

human papillomavirus vaccine [types 16, 18] (recombinant, adjuvanted, adsorbed)

Groupe thérapeutique:

Vaccines

Domaine thérapeutique:

Papillomavirus Infections; Uterine Cervical Dysplasia; Immunization

indications thérapeutiques:

Cervarix is a vaccine for use from the age of 9 years for the prevention of premalignant ano-genital lesions (cervical, vulvar, vaginal and anal) and cervical and anal cancers causally related to certain oncogenic Human Papillomavirus (HPV) types. See sections 4.4 and 5.1 for important information on the data that support this indication.The use of Cervarix should be in accordance with official recommendations.

Descriptif du produit:

Revision: 39

Statut de autorisation:

Authorised

Date de l'autorisation:

2007-09-20

Notice patient

                                36
B. PACKAGE LEAFLET
37
PACKAGE LEAFLET: INFORMATION FOR THE USER
CERVARIX SUSPENSION FOR INJECTION IN A VIAL
Human Papillomavirus vaccine [Types 16, 18] (Recombinant, adjuvanted,
adsorbed)
READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU START RECEIVING THIS
VACCINE BECAUSE IT CONTAINS
IMPORTANT INFORMATION FOR YOU.
-
Keep this leaflet. You may need to read it again.
-
If you have any further questions, ask your doctor or pharmacist.
-
This medicine has been prescribed for you only. Do not pass it on to
others.
-
If you get any side effects, talk to your doctor or pharmacist. This
includes any possible side
effects not listed in this leaflet. See section 4.
WHAT IS IN THIS LEAFLET:
1.
What Cervarix is and what it is used for
2.
What you need to know before you receive Cervarix
3.
How Cervarix is given
4.
Possible side effects
5.
How to store Cervarix
6.
Contents of the pack and other information
1.
WHAT CERVARIX IS AND WHAT IT IS USED FOR
Cervarix is a vaccine intended to protect from the age of 9 years
against the diseases caused by
infection with Human Papillomaviruses (HPV).
These diseases include:
-
cervical cancer (cancer of the cervix i.e. lower part of the uterus or
womb) and anal cancer,
-
precancerous cervical, vulvar, vaginal and anal lesions (changes in
genital or anal cells that have a
risk of turning into cancer).
The Human Papillomavirus (HPV) types contained in the vaccine (HPV
types 16 and 18) are
responsible for approximately 70% of cervical cancers, 90% of anal
cancers, 70% of HPV-related pre-
cancerous lesions of the vulva and vagina and 78% of HPV-related
pre-cancerous lesions of the anus.
Other HPV types can also cause ano-genital cancers. Cervarix does not
protect against all HPV types.
When a female or a male individual is vaccinated with Cervarix, the
immune system (the body’s
natural defence system) will make antibodies against HPV types 16 and
18.
Cervarix is not infectious and so, it cannot cause HPV related
diseases.
Cervarix is not used to treat HPV related diseases already present a
                                
                                Lire le document complet
                                
                            

Résumé des caractéristiques du produit

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Cervarix suspension for injection in pre-filled syringe
Cervarix suspension for injection in a vial
Cervarix suspension for injection in multidose container
Human Papillomavirus vaccine [Types 16, 18] (Recombinant, adjuvanted,
adsorbed)
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
1 dose (0.5 ml) contains:
Human Papillomavirus
1
type 16 L1 protein
2,3,4
20 micrograms
Human Papillomavirus
1
type 18 L1 protein
2,3,4
20 micrograms
1
Human Papillomavirus = HPV
2
adjuvanted by AS04 containing:
3-
_O_
-desacyl-4’- monophosphoryl lipid A (MPL)
3
50 micrograms
3
adsorbed on aluminium hydroxide, hydrated (Al(OH)
3
)
0.5 milligrams Al
3+
in total
4
L1 protein in the form of non-infectious virus-like particles (VLPs)
produced by recombinant DNA
technology using a Baculovirus expression system which uses Hi-5
Rix4446 cells derived from
_Trichoplusia ni_
.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Suspension for injection.
Turbid white suspension.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Cervarix is a vaccine for use from the age of 9 years for the
prevention of premalignant ano-genital
lesions (cervical, vulvar, vaginal and anal) and cervical and anal
cancers causally related to certain
oncogenic Human Papillomavirus (HPV) types. See sections 4.4 and 5.1
for important information on
the data that support this indication.
The use of Cervarix should be in accordance with official
recommendations.
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Posology
The vaccination schedule depends on the age of the subject.
3
AGE AT THE TIME OF THE FIRST
INJECTION
IMMUNIZATION AND SCHEDULE
9 to and including 14 years*
Two doses each of 0.5 ml. The second dose given
between 5 and 13 months after the first dose
From 15 years and above
Three doses each of 0.5 ml at 0, 1, 6 months**
*If the second vaccine dose is administered before the 5
th
month after the first dose, a third dose
should always be administered.
**If flexibility
                                
                                Lire le document complet
                                
                            

Documents dans d'autres langues

Notice patient Notice patient bulgare 23-05-2023
Rapport public d'évaluation Rapport public d'évaluation bulgare 18-08-2016
Notice patient Notice patient espagnol 23-05-2023
Rapport public d'évaluation Rapport public d'évaluation espagnol 18-08-2016
Notice patient Notice patient tchèque 23-05-2023
Rapport public d'évaluation Rapport public d'évaluation tchèque 18-08-2016
Notice patient Notice patient danois 23-05-2023
Rapport public d'évaluation Rapport public d'évaluation danois 18-08-2016
Notice patient Notice patient allemand 23-05-2023
Rapport public d'évaluation Rapport public d'évaluation allemand 18-08-2016
Notice patient Notice patient estonien 23-05-2023
Rapport public d'évaluation Rapport public d'évaluation estonien 18-08-2016
Notice patient Notice patient grec 23-05-2023
Notice patient Notice patient français 23-05-2023
Rapport public d'évaluation Rapport public d'évaluation français 18-08-2016
Notice patient Notice patient italien 23-05-2023
Rapport public d'évaluation Rapport public d'évaluation italien 18-08-2016
Notice patient Notice patient letton 23-05-2023
Rapport public d'évaluation Rapport public d'évaluation letton 18-08-2016
Notice patient Notice patient lituanien 23-05-2023
Rapport public d'évaluation Rapport public d'évaluation lituanien 18-08-2016
Notice patient Notice patient hongrois 23-05-2023
Rapport public d'évaluation Rapport public d'évaluation hongrois 18-08-2016
Notice patient Notice patient maltais 23-05-2023
Rapport public d'évaluation Rapport public d'évaluation maltais 18-08-2016
Notice patient Notice patient néerlandais 23-05-2023
Rapport public d'évaluation Rapport public d'évaluation néerlandais 18-08-2016
Notice patient Notice patient polonais 23-05-2023
Rapport public d'évaluation Rapport public d'évaluation polonais 18-08-2016
Notice patient Notice patient portugais 23-05-2023
Rapport public d'évaluation Rapport public d'évaluation portugais 18-08-2016
Notice patient Notice patient roumain 23-05-2023
Rapport public d'évaluation Rapport public d'évaluation roumain 18-08-2016
Notice patient Notice patient slovaque 23-05-2023
Rapport public d'évaluation Rapport public d'évaluation slovaque 18-08-2016
Notice patient Notice patient slovène 23-05-2023
Rapport public d'évaluation Rapport public d'évaluation slovène 18-08-2016
Notice patient Notice patient finnois 23-05-2023
Rapport public d'évaluation Rapport public d'évaluation finnois 18-08-2016
Notice patient Notice patient suédois 23-05-2023
Rapport public d'évaluation Rapport public d'évaluation suédois 18-08-2016
Notice patient Notice patient norvégien 23-05-2023
Notice patient Notice patient islandais 23-05-2023
Notice patient Notice patient croate 23-05-2023
Rapport public d'évaluation Rapport public d'évaluation croate 18-08-2016

Afficher l'historique des documents