Twinrix Paediatric

国家: 欧盟

语言: 英文

来源: EMA (European Medicines Agency)

现在购买

资料单张 资料单张 (PIL)
07-02-2024
产品特点 产品特点 (SPC)
07-02-2024
公众评估报告 公众评估报告 (PAR)
15-04-2008

有效成分:

hepatitis A virus (inactivated), hepatitis B surface antigen

可用日期:

GlaxoSmithKline Biologicals S.A.

ATC代码:

J07BC20

INN(国际名称):

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

治疗组:

Vaccines

治疗领域:

Immunization; Hepatitis B; Hepatitis A

疗效迹象:

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.

產品總結:

Revision: 23

授权状态:

Authorised

授权日期:

1997-02-10

资料单张

                                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
                                
                                阅读完整的文件
                                
                            

产品特点

                                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
                                
                                阅读完整的文件
                                
                            

其他语言的文件

资料单张 资料单张 保加利亚文 07-02-2024
产品特点 产品特点 保加利亚文 07-02-2024
公众评估报告 公众评估报告 保加利亚文 15-04-2008
资料单张 资料单张 西班牙文 07-02-2024
产品特点 产品特点 西班牙文 07-02-2024
公众评估报告 公众评估报告 西班牙文 15-04-2008
资料单张 资料单张 捷克文 07-02-2024
产品特点 产品特点 捷克文 07-02-2024
公众评估报告 公众评估报告 捷克文 15-04-2008
资料单张 资料单张 丹麦文 07-02-2024
产品特点 产品特点 丹麦文 07-02-2024
公众评估报告 公众评估报告 丹麦文 15-04-2008
资料单张 资料单张 德文 07-02-2024
产品特点 产品特点 德文 07-02-2024
公众评估报告 公众评估报告 德文 15-04-2008
资料单张 资料单张 爱沙尼亚文 07-02-2024
产品特点 产品特点 爱沙尼亚文 07-02-2024
公众评估报告 公众评估报告 爱沙尼亚文 15-04-2008
资料单张 资料单张 希腊文 07-02-2024
产品特点 产品特点 希腊文 07-02-2024
公众评估报告 公众评估报告 希腊文 15-04-2008
资料单张 资料单张 法文 07-02-2024
产品特点 产品特点 法文 07-02-2024
公众评估报告 公众评估报告 法文 15-04-2008
资料单张 资料单张 意大利文 07-02-2024
产品特点 产品特点 意大利文 07-02-2024
公众评估报告 公众评估报告 意大利文 15-04-2008
资料单张 资料单张 拉脱维亚文 07-02-2024
产品特点 产品特点 拉脱维亚文 07-02-2024
公众评估报告 公众评估报告 拉脱维亚文 15-04-2008
资料单张 资料单张 立陶宛文 07-02-2024
产品特点 产品特点 立陶宛文 07-02-2024
公众评估报告 公众评估报告 立陶宛文 15-04-2008
资料单张 资料单张 匈牙利文 07-02-2024
产品特点 产品特点 匈牙利文 07-02-2024
公众评估报告 公众评估报告 匈牙利文 15-04-2008
资料单张 资料单张 马耳他文 07-02-2024
产品特点 产品特点 马耳他文 07-02-2024
公众评估报告 公众评估报告 马耳他文 15-04-2008
资料单张 资料单张 荷兰文 07-02-2024
产品特点 产品特点 荷兰文 07-02-2024
公众评估报告 公众评估报告 荷兰文 15-04-2008
资料单张 资料单张 波兰文 07-02-2024
产品特点 产品特点 波兰文 07-02-2024
公众评估报告 公众评估报告 波兰文 15-04-2008
资料单张 资料单张 葡萄牙文 07-02-2024
产品特点 产品特点 葡萄牙文 07-02-2024
公众评估报告 公众评估报告 葡萄牙文 15-04-2008
资料单张 资料单张 罗马尼亚文 07-02-2024
产品特点 产品特点 罗马尼亚文 07-02-2024
公众评估报告 公众评估报告 罗马尼亚文 15-04-2008
资料单张 资料单张 斯洛伐克文 07-02-2024
产品特点 产品特点 斯洛伐克文 07-02-2024
公众评估报告 公众评估报告 斯洛伐克文 15-04-2008
资料单张 资料单张 斯洛文尼亚文 07-02-2024
产品特点 产品特点 斯洛文尼亚文 07-02-2024
公众评估报告 公众评估报告 斯洛文尼亚文 15-04-2008
资料单张 资料单张 芬兰文 07-02-2024
产品特点 产品特点 芬兰文 07-02-2024
公众评估报告 公众评估报告 芬兰文 15-04-2008
资料单张 资料单张 瑞典文 07-02-2024
产品特点 产品特点 瑞典文 07-02-2024
公众评估报告 公众评估报告 瑞典文 15-04-2008
资料单张 资料单张 挪威文 07-02-2024
产品特点 产品特点 挪威文 07-02-2024
资料单张 资料单张 冰岛文 07-02-2024
产品特点 产品特点 冰岛文 07-02-2024
资料单张 资料单张 克罗地亚文 07-02-2024
产品特点 产品特点 克罗地亚文 07-02-2024