Tritanrix HepB

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)
07-01-2014
产品特点 产品特点 (SPC)
07-01-2014
公众评估报告 公众评估报告 (PAR)
07-01-2014

有效成分:

Diphtheria toxoid, hepatitis B surface antigen, Bordetella pertussis (inactivated), tetanus toxoid

可用日期:

GlaxoSmithKline Biologicals S.A.

ATC代码:

J07CA05

INN(国际名称):

diphtheria (D), tetanus (T), pertussis (whole cell) (Pw) and hepatitis B (rDNA) (HBV) vaccine (adsorbed)

治疗组:

Vaccines

治疗领域:

Hepatitis B; Tetanus; Immunization; Whooping Cough; Diphtheria

疗效迹象:

Tritanrix HepB is indicated for active immunisation against diphtheria, tetanus, pertussis and hepatitis B (HBV) in infants from six weeks onwards (see section 4.2).

產品總結:

Revision: 15

授权状态:

Withdrawn

授权日期:

1996-07-19

资料单张

                                Medicinal product no longer authorised
31
B. PACKAGE LEAFLET
Medicinal product no longer authorised
32
PACKAGE LEAFLET: INFORMATION FOR THE USER
TRITANRIX HEPB SUSPENSION FOR INJECTION
Diphtheria (D), tetanus (T), pertussis (whole cell) (Pw) and hepatitis
B (rDNA) (HBV) vaccine (adsorbed)
READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOUR CHILD STARTS RECEIVING
THIS VACCINE.
-
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 your child. Do not pass it on to
others.
-
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.
IN THIS LEAFLET
:
1.
What Tritanrix HepB is and what it is used for
2.
Before your child receives Tritanrix HepB
3.
How Tritanrix HepB is given
4.
Possible side effects
5.
How to store Tritanrix HepB
6.
Further information
1.
WHAT TRITANRIX HEPB IS AND WHAT IT IS USED FOR
Tritanrix HepB is a vaccine used in children to prevent four diseases:
diphtheria, tetanus (lockjaw), pertussis
(whooping cough) and hepatitis B. The vaccine works by causing the
body to produce its own protection
(antibodies) against these diseases.
•
DIPHTHERIA
: Diphtheria mainly affects the airways and sometimes the skin.
Generally the airways
become inflamed (swollen) causing severe breathing difficulties and
sometimes suffocation. The bacteria
also release a toxin (poison), which can cause nerve damage, heart
problems, and even death.
•
TETANUS
(Lockjaw): Tetanus bacteria enter the body through cuts, scratches or
wounds in the skin.
Wounds that are especially prone to infection are burns, fractures,
deep wounds or wounds contaminated
with soil, dust, horse manure/dung or wood splinters. The bacteria
release a toxin (poison), which can
cause muscle stiffness, painful muscle spasms, fits and even death.
The muscle spasms can be strong
enough to cause bone fractures of the spine.
•
PERTUSSIS
(Whooping cough): Pertussis is a hig
                                
                                阅读完整的文件
                                
                            

产品特点

                                Medicinal product no longer authorised
1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
_ _
Medicinal product no longer authorised
2
1.
NAME OF THE MEDICINAL PRODUCT
Tritanrix HepB, suspension for injection
Diphtheria (D), tetanus (T), pertussis (whole cell) (Pw) and hepatitis
B (rDNA) (HBV) vaccine (adsorbed)
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
1 dose (0.5 ml) contains:
Diphtheria toxoid
1
not less than 30 IU
Tetanus toxoid
1
not less than 60 IU
_Bordetella pertussis _
(inactivated)
2
not less than 4 IU
Hepatitis B surface antigen
2,3
10 micrograms
1
Adsorbed on aluminium hydroxide, hydrated
0.26 milligrams Al
3+
2
Adsorbed on aluminium phosphate
0.37 milligrams Al
3+
3
Produced in yeast cells (
_Saccharomyces cerevisiae_
) by recombinant DNA technology
For a full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Suspension for injection.
Turbid white suspension.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Tritanrix HepB is indicated for active immunisation against
diphtheria, tetanus, pertussis and hepatitis B
(HBV) in infants from 6 weeks onwards (see
section 4.2).
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
_Posology _
The recommended dose is 0.5 ml.
Primary vaccination:
The primary vaccination schedule consists of three doses within the
first six months of life. Where HBV
vaccine is not given at birth, the combined vaccine can be
administered beginning as early as 8 weeks of age.
Where there is
a high endemicity of HBV, the practice to administer HBV vaccine at
birth should be
continued. In these circumstances, vaccination with the combined
vaccine should start at 6 weeks of age.
Three vaccine doses must be administered at intervals of at least 4
weeks.
When Tritanrix HepB is given according to the 6-10-14 weeks schedule,
it is recommended to
administer a dose of HBV vaccine at birth to improve protection.
In the case of children born of known HBV carrier mothers the
immunoprophylactic measures for hepatitis B
should not be modified. This may require separate vaccination with HBV
and DTPw
                                
                                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 07-01-2014
产品特点 产品特点 保加利亚文 07-01-2014
公众评估报告 公众评估报告 保加利亚文 07-01-2014
资料单张 资料单张 西班牙文 07-01-2014
产品特点 产品特点 西班牙文 07-01-2014
公众评估报告 公众评估报告 西班牙文 07-01-2014
资料单张 资料单张 捷克文 07-01-2014
产品特点 产品特点 捷克文 07-01-2014
公众评估报告 公众评估报告 捷克文 07-01-2014
资料单张 资料单张 丹麦文 07-01-2014
产品特点 产品特点 丹麦文 07-01-2014
公众评估报告 公众评估报告 丹麦文 07-01-2014
资料单张 资料单张 德文 07-01-2014
产品特点 产品特点 德文 07-01-2014
公众评估报告 公众评估报告 德文 07-01-2014
资料单张 资料单张 爱沙尼亚文 07-01-2014
产品特点 产品特点 爱沙尼亚文 07-01-2014
公众评估报告 公众评估报告 爱沙尼亚文 07-01-2014
资料单张 资料单张 希腊文 07-01-2014
产品特点 产品特点 希腊文 07-01-2014
公众评估报告 公众评估报告 希腊文 07-01-2014
资料单张 资料单张 法文 07-01-2014
产品特点 产品特点 法文 07-01-2014
公众评估报告 公众评估报告 法文 07-01-2014
资料单张 资料单张 意大利文 07-01-2014
产品特点 产品特点 意大利文 07-01-2014
公众评估报告 公众评估报告 意大利文 07-01-2014
资料单张 资料单张 拉脱维亚文 07-01-2014
产品特点 产品特点 拉脱维亚文 07-01-2014
公众评估报告 公众评估报告 拉脱维亚文 07-01-2014
资料单张 资料单张 立陶宛文 07-01-2014
产品特点 产品特点 立陶宛文 07-01-2014
公众评估报告 公众评估报告 立陶宛文 07-01-2014
资料单张 资料单张 匈牙利文 07-01-2014
产品特点 产品特点 匈牙利文 07-01-2014
公众评估报告 公众评估报告 匈牙利文 07-01-2014
资料单张 资料单张 马耳他文 07-01-2014
产品特点 产品特点 马耳他文 07-01-2014
公众评估报告 公众评估报告 马耳他文 07-01-2014
资料单张 资料单张 荷兰文 07-01-2014
产品特点 产品特点 荷兰文 07-01-2014
公众评估报告 公众评估报告 荷兰文 07-01-2014
资料单张 资料单张 波兰文 07-01-2014
产品特点 产品特点 波兰文 07-01-2014
公众评估报告 公众评估报告 波兰文 07-01-2014
资料单张 资料单张 葡萄牙文 07-01-2014
产品特点 产品特点 葡萄牙文 07-01-2014
公众评估报告 公众评估报告 葡萄牙文 07-01-2014
资料单张 资料单张 罗马尼亚文 07-01-2014
产品特点 产品特点 罗马尼亚文 07-01-2014
公众评估报告 公众评估报告 罗马尼亚文 07-01-2014
资料单张 资料单张 斯洛伐克文 07-01-2014
产品特点 产品特点 斯洛伐克文 07-01-2014
公众评估报告 公众评估报告 斯洛伐克文 07-01-2014
资料单张 资料单张 斯洛文尼亚文 07-01-2014
产品特点 产品特点 斯洛文尼亚文 07-01-2014
公众评估报告 公众评估报告 斯洛文尼亚文 07-01-2014
资料单张 资料单张 芬兰文 07-01-2014
产品特点 产品特点 芬兰文 07-01-2014
公众评估报告 公众评估报告 芬兰文 07-01-2014
资料单张 资料单张 瑞典文 07-01-2014
产品特点 产品特点 瑞典文 07-01-2014
公众评估报告 公众评估报告 瑞典文 07-01-2014
资料单张 资料单张 挪威文 07-01-2014
产品特点 产品特点 挪威文 07-01-2014
资料单张 资料单张 冰岛文 07-01-2014
产品特点 产品特点 冰岛文 07-01-2014