Twinrix Paediatric

Nchi: Umoja wa Ulaya

Lugha: Kiingereza

Chanzo: EMA (European Medicines Agency)

Nunua Sasa

Taarifa za kipeperushi Taarifa za kipeperushi (PIL)
07-02-2024
Tabia za bidhaa Tabia za bidhaa (SPC)
07-02-2024

Viambatanisho vya kazi:

hepatitis A virus (inactivated), hepatitis B surface antigen

Inapatikana kutoka:

GlaxoSmithKline Biologicals S.A.

ATC kanuni:

J07BC20

INN (Jina la Kimataifa):

hepatitis A (inactivated) and hepatitis B (rDNA) (HAB) vaccine (adsorbed)

Kundi la matibabu:

Vaccines

Eneo la matibabu:

Immunization; Hepatitis B; Hepatitis A

Matibabu dalili:

Twinrix Paediatric is indicated for use in non-immune infants, children and adolescents from one year up to and including 15 years who are at risk of both hepatitis-A and hepatitis-B infection.

Bidhaa muhtasari:

Revision: 23

Idhini hali ya:

Authorised

Idhini ya tarehe:

1997-02-10

Taarifa za kipeperushi

                                18
B. PACKAGE LEAFLET
19
PACKAGE LEAFLET: INFORMATION FOR THE USER
TWINRIX PAEDIATRIC, SUSPENSION FOR INJECTION IN PRE-FILLED SYRINGE
Hepatitis A (inactivated) and hepatitis B (rDNA) (HAB) vaccine
(adsorbed)
READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU START/ YOUR CHILD STARTS
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 your pharmacist.
-
This vaccine has been prescribed for you/ your child only. Do not pass
it on to others.
-
If you get / your child gets any side effects, talk to your doctor or
pharmacist. This includes any
possible side effects not listed in this leaflet. See section 4.
This leaflet has been written assuming the person receiving the
vaccine is reading it, but it can be given
to adolescents and children so you may be reading it for your child.
WHAT IS IN THIS LEAFLET
1.
What Twinrix Paediatric is and what it is used for
2.
What you need to know before you receive Twinrix Paediatric
3.
How Twinrix Paediatric is given
4.
Possible side effects
5.
How to store Twinrix Paediatric
6.
Contents of the pack and other information
1.
WHAT TWINRIX PAEDIATRIC IS AND WHAT IT IS USED FOR
Twinrix Paediatric is a vaccine used in infants, children and
adolescents from 1 year up to and
including 15 years to prevent two diseases: hepatitis A and hepatitis
B. The vaccine works by causing
the body to produce its own protection (antibodies) against these
diseases.
•
HEPATITIS A:
Hepatitis A is an infectious disease, which can affect the liver. This
disease is
caused by the hepatitis A virus. The hepatitis A virus can be passed
from person to person in
food and drink, or by swimming in water contaminated by sewage.
Symptoms of hepatitis A
begin 3 to 6 weeks after coming into contact with the virus. These
consist of nausea (feeling
sick), fever and aches and pains. After a few days the whites of eyes
and skin may become
yellowish (jaundice). The severity and type of symptoms can va
                                
                                Soma hati kamili
                                
                            

Tabia za bidhaa

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Twinrix Paediatric, suspension for injection in pre-filled syringe
_ _
Hepatitis A (inactivated) and hepatitis B (rDNA) (HAB) vaccine
(adsorbed).
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
1 dose (0.5 ml) contains:
Hepatitis A virus (inactivated)
1,2
360 ELISA Units
Hepatitis B surface antigen
3,4
10 micrograms
1
Produced on human diploid (MRC-5) cells
2
Adsorbed on aluminium hydroxide, hydrated
0.025 milligrams Al
3+
3
Produced in yeast cells (
_Saccharomyces_
_cerevisiae_
) by recombinant DNA technology
4
Adsorbed on aluminium phosphate
0.2 milligrams Al
3+
The vaccine may contain traces of neomycin which is used during the
manufacturing process (see
section 4.3).
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
Twinrix Paediatric is indicated for use in non immune infants,
children and adolescents from 1 year up
to and including 15 years who are at risk of both hepatitis A and
hepatitis B infection.
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Posology
- Dosage
The dose of 0.5 ml (360 ELISA Units HA/10 µg HBsAg) is recommended
for infants, children and
adolescents from 1 year up to and including 15 years of age.
- Primary vaccination schedule
The standard primary course of vaccination with Twinrix Paediatric
consists of three doses, the first
administered at the elected date, the second one month later and the
third six months after the first
dose. The recommended schedule should be adhered to. Once initiated,
the primary course of
vaccination should be completed with the same vaccine.
- Booster dose
In situations where a booster dose of hepatitis A and/or hepatitis B
is desired, a monovalent or combined
vaccine can be given. The safety and immunogenicity of Twinrix
Paediatric administered as a booster
3
dose following a three-dose primary course have not been evaluated.
Long-term antibody persistence data f
                                
                                Soma hati kamili
                                
                            

Nyaraka katika lugha zingine

Taarifa za kipeperushi Taarifa za kipeperushi Kibulgaria 07-02-2024
Tabia za bidhaa Tabia za bidhaa Kibulgaria 07-02-2024
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kibulgaria 15-04-2008
Taarifa za kipeperushi Taarifa za kipeperushi Kihispania 07-02-2024
Tabia za bidhaa Tabia za bidhaa Kihispania 07-02-2024
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kihispania 15-04-2008
Taarifa za kipeperushi Taarifa za kipeperushi Kicheki 07-02-2024
Tabia za bidhaa Tabia za bidhaa Kicheki 07-02-2024
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kicheki 15-04-2008
Taarifa za kipeperushi Taarifa za kipeperushi Kidenmaki 07-02-2024
Tabia za bidhaa Tabia za bidhaa Kidenmaki 07-02-2024
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kidenmaki 15-04-2008
Taarifa za kipeperushi Taarifa za kipeperushi Kijerumani 07-02-2024
Tabia za bidhaa Tabia za bidhaa Kijerumani 07-02-2024
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kijerumani 15-04-2008
Taarifa za kipeperushi Taarifa za kipeperushi Kiestonia 07-02-2024
Tabia za bidhaa Tabia za bidhaa Kiestonia 07-02-2024
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kiestonia 15-04-2008
Taarifa za kipeperushi Taarifa za kipeperushi Kigiriki 07-02-2024
Tabia za bidhaa Tabia za bidhaa Kigiriki 07-02-2024
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kigiriki 15-04-2008
Taarifa za kipeperushi Taarifa za kipeperushi Kifaransa 07-02-2024
Tabia za bidhaa Tabia za bidhaa Kifaransa 07-02-2024
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kifaransa 15-04-2008
Taarifa za kipeperushi Taarifa za kipeperushi Kiitaliano 07-02-2024
Tabia za bidhaa Tabia za bidhaa Kiitaliano 07-02-2024
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kiitaliano 15-04-2008
Taarifa za kipeperushi Taarifa za kipeperushi Kilatvia 07-02-2024
Tabia za bidhaa Tabia za bidhaa Kilatvia 07-02-2024
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kilatvia 15-04-2008
Taarifa za kipeperushi Taarifa za kipeperushi Kilithuania 07-02-2024
Tabia za bidhaa Tabia za bidhaa Kilithuania 07-02-2024
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kilithuania 15-04-2008
Taarifa za kipeperushi Taarifa za kipeperushi Kihungari 07-02-2024
Tabia za bidhaa Tabia za bidhaa Kihungari 07-02-2024
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kihungari 15-04-2008
Taarifa za kipeperushi Taarifa za kipeperushi Kimalta 07-02-2024
Tabia za bidhaa Tabia za bidhaa Kimalta 07-02-2024
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kimalta 15-04-2008
Taarifa za kipeperushi Taarifa za kipeperushi Kiholanzi 07-02-2024
Tabia za bidhaa Tabia za bidhaa Kiholanzi 07-02-2024
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kiholanzi 15-04-2008
Taarifa za kipeperushi Taarifa za kipeperushi Kipolandi 07-02-2024
Tabia za bidhaa Tabia za bidhaa Kipolandi 07-02-2024
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kipolandi 15-04-2008
Taarifa za kipeperushi Taarifa za kipeperushi Kireno 07-02-2024
Tabia za bidhaa Tabia za bidhaa Kireno 07-02-2024
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kireno 15-04-2008
Taarifa za kipeperushi Taarifa za kipeperushi Kiromania 07-02-2024
Tabia za bidhaa Tabia za bidhaa Kiromania 07-02-2024
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kiromania 15-04-2008
Taarifa za kipeperushi Taarifa za kipeperushi Kislovakia 07-02-2024
Tabia za bidhaa Tabia za bidhaa Kislovakia 07-02-2024
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kislovakia 15-04-2008
Taarifa za kipeperushi Taarifa za kipeperushi Kislovenia 07-02-2024
Tabia za bidhaa Tabia za bidhaa Kislovenia 07-02-2024
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kislovenia 15-04-2008
Taarifa za kipeperushi Taarifa za kipeperushi Kifinlandi 07-02-2024
Tabia za bidhaa Tabia za bidhaa Kifinlandi 07-02-2024
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kifinlandi 15-04-2008
Taarifa za kipeperushi Taarifa za kipeperushi Kiswidi 07-02-2024
Tabia za bidhaa Tabia za bidhaa Kiswidi 07-02-2024
Ripoti ya Tathmini ya umma Ripoti ya Tathmini ya umma Kiswidi 15-04-2008
Taarifa za kipeperushi Taarifa za kipeperushi Kinorwe 07-02-2024
Tabia za bidhaa Tabia za bidhaa Kinorwe 07-02-2024
Taarifa za kipeperushi Taarifa za kipeperushi Kiaisilandi 07-02-2024
Tabia za bidhaa Tabia za bidhaa Kiaisilandi 07-02-2024
Taarifa za kipeperushi Taarifa za kipeperushi Kroeshia 07-02-2024
Tabia za bidhaa Tabia za bidhaa Kroeshia 07-02-2024