Silgard

Țară: Uniunea Europeană

Limbă: engleză

Sursă: EMA (European Medicines Agency)

Cumpara asta acum

Prospect Prospect (PIL)
02-04-2019

Ingredient activ:

human papillomavirus type 6 L1 protein, human papillomavirus type 11 L1 protein, human papillomavirus type 16 L1 protein, human papillomavirus type 18 L1 protein

Disponibil de la:

Merck Sharp Dohme Ltd

Codul ATC:

J07BM01

INN (nume internaţional):

human papillomavirus vaccine [types 6, 11, 16, 18] (recombinant, adsorbed)

Grupul Terapeutică:

Vaccines

Zonă Terapeutică:

Papillomavirus Infections; Uterine Cervical Dysplasia; Condylomata Acuminata; Immunization

Indicații terapeutice:

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

Rezumat produs:

Revision: 33

Statutul autorizaţiei:

Withdrawn

Data de autorizare:

2006-09-19

Prospect

                                36
B. PACKAGE LEAFLET
(VIAL)
Medicinal product no longer authorised
37
PACKAGE LEAFLET: INFORMATION FOR THE USER
SILGARD, SUSPENSION FOR INJECTION
Human Papillomavirus Vaccine [Types 6, 11, 16, 18] (Recombinant,
adsorbed)
READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU OR YOUR CHILD ARE
VACCINATED.
-
Keep this leaflet. You may need to read it again.
-
If you have any further questions, please ask your doctor or
pharmacist.
-
If any of the side effects gets serious, or if you notice any side
effects not listed in this leaflet,
please tell your doctor or pharmacist. See section 4.
WHAT IS IN THIS LEAFLET
1.
What Silgard is and what it is used for
2.
What you need to know before you receive Silgard
3.
How Silgard is given
4.
Possible side effects
5.
How to store Silgard
6.
Contents of the pack and other information
1.
WHAT SILGARD IS AND WHAT IT IS USED FOR
Silgard is a vaccine. Vaccination with Silgard is intended to protect
against diseases caused by Human
Papillomavirus (HPV) types 6, 11, 16, and 18.
These diseases include pre-cancerous lesions of the female genitals
(cervix, vulva, and vagina); pre-
cancerous lesions of the anus and genital warts in males and females;
cervical and anal cancers. HPV
types 16 and 18 are responsible for approximately 70% of cervical
cancer cases, 75-80% of anal
cancer cases; 70% of HPV-related pre-cancerous lesions of the vulva
and vagina; 75% of HPV related
pre-cancerous lesions of the anus. HPV types 6 and 11 are responsible
for approximately 90% of
genital wart cases.
Silgard is intended to prevent these diseases. The vaccine is not used
to treat HPV related diseases.
Silgard does not have any effect in individuals who already have a
persistent infection or disease
associated with any of the HPV types in the vaccine. However, in
individuals who are already infected
with one or more of the vaccine HPV types, Silgard can still protect
against diseases associated with
the other HPV types in the vaccine.
Silgard cannot cause the diseases it protects against.
Silgard produces type-spec
                                
                                Citiți documentul complet
                                
                            

Caracteristicilor produsului

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
Medicinal product no longer authorised
2
1.
NAME OF THE MEDICINAL PRODUCT
Silgard, suspension for injection.
Silgard, suspension for injection in a pre-filled syringe.
Human Papillomavirus Vaccine [Types 6, 11, 16, 18] (Recombinant,
adsorbed).
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
1 dose (0.5 ml) contains approximately:
Human Papillomavirus
1
Type 6 L1 protein
2,3
20 micrograms
Human Papillomavirus
1
Type 11 L1 protein
2,3
40 micrograms
Human Papillomavirus
1
Type 16 L1 protein
2,3
40 micrograms
Human Papillomavirus
1
Type 18 L1 protein
2,3
20 micrograms.
1
Human Papillomavirus = HPV.
2
L1 protein in the form of virus-like particles produced in yeast cells
(_Saccharomyces cerevisiae_
CANADE 3C-5 (Strain 1895)) by recombinant DNA technology.
3
adsorbed on amorphous aluminium hydroxyphosphate sulphate adjuvant
(0.225 milligrams Al).
For a full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Silgard, suspension for injection.
Silgard, suspension for injection in a pre-filled syringe.
Prior to agitation, Silgard may appear as a clear liquid with a white
precipitate. After thorough
agitation, it is a white, cloudy liquid.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Silgard is a vaccine for use from the age of 9 years for the
prevention of:
–
premalignant genital lesions (cervical, vulvar and vaginal),
premalignant anal lesions, cervical
cancers and anal cancers causally related to certain oncogenic Human
Papillomavirus (HPV)
types
–
genital warts (condyloma acuminata) causally related to specific HPV
types.
See sections 4.4 and 5.1 for important information on the data that
support this indication.
The use of Silgard should be in accordance with official
recommendations.
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Posology
_Individuals 9 to and including 13 years of age_
Silgard can be administered according to a 2-dose schedule (0.5 ml at
0, 6 months) (see section 5.1).
If the second vaccine dose is administered earlier than 6 months after
the f
                                
                                Citiți documentul complet
                                
                            

Documente în alte limbi

Prospect Prospect bulgară 02-04-2019
Caracteristicilor produsului Caracteristicilor produsului bulgară 02-04-2019
Raport public de evaluare Raport public de evaluare bulgară 02-04-2019
Prospect Prospect spaniolă 02-04-2019
Caracteristicilor produsului Caracteristicilor produsului spaniolă 02-04-2019
Raport public de evaluare Raport public de evaluare spaniolă 02-04-2019
Prospect Prospect cehă 02-04-2019
Caracteristicilor produsului Caracteristicilor produsului cehă 02-04-2019
Raport public de evaluare Raport public de evaluare cehă 02-04-2019
Prospect Prospect daneză 02-04-2019
Caracteristicilor produsului Caracteristicilor produsului daneză 02-04-2019
Raport public de evaluare Raport public de evaluare daneză 02-04-2019
Prospect Prospect germană 02-04-2019
Caracteristicilor produsului Caracteristicilor produsului germană 02-04-2019
Raport public de evaluare Raport public de evaluare germană 02-04-2019
Prospect Prospect estoniană 02-04-2019
Caracteristicilor produsului Caracteristicilor produsului estoniană 02-04-2019
Raport public de evaluare Raport public de evaluare estoniană 02-04-2019
Prospect Prospect greacă 02-04-2019
Caracteristicilor produsului Caracteristicilor produsului greacă 02-04-2019
Raport public de evaluare Raport public de evaluare greacă 02-04-2019
Prospect Prospect franceză 02-04-2019
Caracteristicilor produsului Caracteristicilor produsului franceză 02-04-2019
Raport public de evaluare Raport public de evaluare franceză 02-04-2019
Prospect Prospect italiană 02-04-2019
Caracteristicilor produsului Caracteristicilor produsului italiană 02-04-2019
Raport public de evaluare Raport public de evaluare italiană 02-04-2019
Prospect Prospect letonă 02-04-2019
Caracteristicilor produsului Caracteristicilor produsului letonă 02-04-2019
Raport public de evaluare Raport public de evaluare letonă 02-04-2019
Prospect Prospect lituaniană 02-04-2019
Caracteristicilor produsului Caracteristicilor produsului lituaniană 02-04-2019
Raport public de evaluare Raport public de evaluare lituaniană 02-04-2019
Prospect Prospect maghiară 02-04-2019
Caracteristicilor produsului Caracteristicilor produsului maghiară 02-04-2019
Raport public de evaluare Raport public de evaluare maghiară 02-04-2019
Prospect Prospect malteză 02-04-2019
Caracteristicilor produsului Caracteristicilor produsului malteză 02-04-2019
Raport public de evaluare Raport public de evaluare malteză 02-04-2019
Prospect Prospect olandeză 02-04-2019
Caracteristicilor produsului Caracteristicilor produsului olandeză 02-04-2019
Raport public de evaluare Raport public de evaluare olandeză 02-04-2019
Prospect Prospect poloneză 02-04-2019
Caracteristicilor produsului Caracteristicilor produsului poloneză 02-04-2019
Raport public de evaluare Raport public de evaluare poloneză 02-04-2019
Prospect Prospect portugheză 02-04-2019
Caracteristicilor produsului Caracteristicilor produsului portugheză 02-04-2019
Raport public de evaluare Raport public de evaluare portugheză 02-04-2019
Prospect Prospect română 02-04-2019
Caracteristicilor produsului Caracteristicilor produsului română 02-04-2019
Raport public de evaluare Raport public de evaluare română 02-04-2019
Prospect Prospect slovacă 02-04-2019
Caracteristicilor produsului Caracteristicilor produsului slovacă 02-04-2019
Raport public de evaluare Raport public de evaluare slovacă 02-04-2019
Prospect Prospect slovenă 02-04-2019
Caracteristicilor produsului Caracteristicilor produsului slovenă 02-04-2019
Raport public de evaluare Raport public de evaluare slovenă 02-04-2019
Prospect Prospect finlandeză 02-04-2019
Caracteristicilor produsului Caracteristicilor produsului finlandeză 02-04-2019
Raport public de evaluare Raport public de evaluare finlandeză 02-04-2019
Prospect Prospect suedeză 02-04-2019
Caracteristicilor produsului Caracteristicilor produsului suedeză 02-04-2019
Raport public de evaluare Raport public de evaluare suedeză 02-04-2019
Prospect Prospect norvegiană 02-04-2019
Caracteristicilor produsului Caracteristicilor produsului norvegiană 02-04-2019
Prospect Prospect islandeză 02-04-2019
Caracteristicilor produsului Caracteristicilor produsului islandeză 02-04-2019
Prospect Prospect croată 02-04-2019
Caracteristicilor produsului Caracteristicilor produsului croată 02-04-2019
Raport public de evaluare Raport public de evaluare croată 02-04-2019

Vizualizați istoricul documentelor