Praluent

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)
15-02-2024
产品特点 产品特点 (SPC)
15-02-2024
公众评估报告 公众评估报告 (PAR)
04-01-2024

有效成分:

Alirocumab

可用日期:

Sanofi Winthrop Industrie

ATC代码:

C10AX14

INN(国际名称):

alirocumab

治疗组:

Lipid modifying agents

治疗领域:

Dyslipidemias

疗效迹象:

Primary hypercholesterolaemia and mixed dyslipidaemiaPraluent is indicated in adults with primary hypercholesterolaemia (heterozygous familial and non-familial) or mixed dyslipidaemia, as an adjunct to diet:in combination with a statin or statin with other lipid lowering therapies in patients unable to reach LDL-C goals with the maximum tolerated dose of a statin or,alone or in combination with other lipid-lowering therapies in patients who are statin-intolerant, or for whom a statin is contraindicated.Established atherosclerotic cardiovascular disease Praluent is indicated in adults with established atherosclerotic cardiovascular disease to reduce cardiovascular risk by lowering LDL-C levels, as an adjunct to correction of other risk factors:in combination with the maximum tolerated dose of a statin with or without other lipid-lowering therapies or,alone or in combination with other lipid-lowering therapies in patients who are statin-intolerant, or for whom a statin is contraindicated.For study results with respect to effects on LDL-C, cardiovascular events and populations studied see section 5.1.

產品總結:

Revision: 21

授权状态:

Authorised

授权日期:

2015-09-23

资料单张

                                53
B. PACKAGE LEAFLET
54
PACKAGE LEAFLET: INFORMATION FOR THE USER
PRALUENT 75 MG SOLUTION FOR INJECTION IN A PRE-FILLED PEN
PRALUENT 150 MG SOLUTION FOR INJECTION IN A PRE-FILLED PEN
PRALUENT 300 MG SOLUTION FOR INJECTION IN A PRE-FILLED PEN
alirocumab
READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU START USING THIS
MEDICINE 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, pharmacist or
nurse.
-
This medicine has been prescribed for you only. Do not pass it on to
others. It may harm them, even if
their signs of illness are the same as yours.
-
If you get any side effects, talk to your doctor, pharmacist or nurse.
This includes any possible side
effects not listed in this leaflet. See section 4.
WHAT IS IN THIS LEAFLET
1.
What Praluent is and what it is used for
2.
What you need to know before you use Praluent
3.
How to use Praluent
4.
Possible side effects
5.
How to store Praluent
6.
Contents of the pack and other information
1.
WHAT PRALUENT IS AND WHAT IT IS USED FOR
WHAT PRALUENT IS
•
Praluent contains the active substance alirocumab.
•
Praluent is a monoclonal antibody (a type of specialised protein
designed to attach to a target
substance in the body). Monoclonal antibodies are proteins that
recognise and bind to other unique
proteins. Alirocumab binds to PCSK9.
HOW PRALUENT WORKS
Praluent helps lower your levels of “bad” cholesterol (also called
“LDL cholesterol”). Praluent blocks a
protein called PCSK9.
•
PCSK9 is a protein secreted by liver cells.
•
“Bad” cholesterol is normally removed from your blood by binding
to specific “receptors” (docking
stations) in your liver.
•
PCSK9 lowers the number of these receptors in the liver – this
causes your “bad” cholesterol to be
higher than it should.
•
By blocking PCSK9, Praluent increases the number of receptors
available to help remove the “bad”
cholesterol – this lowers your “bad” cholesterol levels.
WHAT PRALUEN
                                
                                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
Praluent 75 mg solution for injection in pre-filled pen
Praluent 150 mg solution for injection in pre-filled pen
Praluent 75 mg solution for injection in pre-filled syringe
Praluent 150 mg solution for injection in pre-filled syringe
Praluent 300 mg solution for injection in pre-filled pen
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Praluent 75 mg solution for injection in pre-filled pen
Each single-use pre-filled pen contains 75 mg alirocumab in 1 ml
solution.
Praluent 75 mg solution for injection in pre-filled syringe
Each single-use pre-filled syringe contains 75 mg alirocumab in 1 ml
solution.
Praluent 150 mg solution for injection in pre-filled pen
Each single-use pre-filled pen contains 150 mg alirocumab in 1 ml
solution.
Praluent 150 mg solution for injection in pre-filled syringe
Each single-use pre-filled syringe contains 150 mg alirocumab in 1 ml
solution.
Praluent 300 mg solution for injection in pre-filled pen
Each single-use pre-filled pen contains 300 mg alirocumab in 2 ml
solution.
Alirocumab is a human IgG1 monoclonal antibody produced in Chinese
Hamster Ovary cells by
recombinant DNA technology.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Solution for injection (injection)
Clear, colourless to pale yellow solution.
pH: 5.7 – 6.3
Osmolality:
Praluent 75 mg solution for injection
293 - 439 mOsm/kg
Praluent 150 mg solution for injection
383 - 434 mOsm/kg
Praluent 300 mg solution for injection
383 – 434 mOsm/kg
3
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Primary hypercholesterolaemia and mixed dyslipidaemia
Praluent is indicated in adults with primary hypercholesterolaemia
(heterozygous familial and non-familial)
or mixed dyslipidaemia, and in paediatric patients 8 years of age and
older with heterozygous familial
hypercholesterolaemia (HeFH) as an adjunct to diet:
-
in combination with a statin or statin with other lipid lowering
therapies in patients unable to reach
LDL-C goals
                                
                                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 15-02-2024
产品特点 产品特点 保加利亚文 15-02-2024
公众评估报告 公众评估报告 保加利亚文 04-01-2024
资料单张 资料单张 西班牙文 15-02-2024
产品特点 产品特点 西班牙文 15-02-2024
公众评估报告 公众评估报告 西班牙文 04-01-2024
资料单张 资料单张 捷克文 15-02-2024
产品特点 产品特点 捷克文 15-02-2024
公众评估报告 公众评估报告 捷克文 04-01-2024
资料单张 资料单张 丹麦文 15-02-2024
产品特点 产品特点 丹麦文 15-02-2024
公众评估报告 公众评估报告 丹麦文 04-01-2024
资料单张 资料单张 德文 15-02-2024
产品特点 产品特点 德文 15-02-2024
公众评估报告 公众评估报告 德文 04-01-2024
资料单张 资料单张 爱沙尼亚文 15-02-2024
产品特点 产品特点 爱沙尼亚文 15-02-2024
公众评估报告 公众评估报告 爱沙尼亚文 04-01-2024
资料单张 资料单张 希腊文 15-02-2024
产品特点 产品特点 希腊文 15-02-2024
公众评估报告 公众评估报告 希腊文 04-01-2024
资料单张 资料单张 法文 15-02-2024
产品特点 产品特点 法文 15-02-2024
公众评估报告 公众评估报告 法文 04-01-2024
资料单张 资料单张 意大利文 15-02-2024
产品特点 产品特点 意大利文 15-02-2024
公众评估报告 公众评估报告 意大利文 04-01-2024
资料单张 资料单张 拉脱维亚文 15-02-2024
产品特点 产品特点 拉脱维亚文 15-02-2024
公众评估报告 公众评估报告 拉脱维亚文 04-01-2024
资料单张 资料单张 立陶宛文 15-02-2024
产品特点 产品特点 立陶宛文 15-02-2024
公众评估报告 公众评估报告 立陶宛文 04-01-2024
资料单张 资料单张 匈牙利文 15-02-2024
产品特点 产品特点 匈牙利文 15-02-2024
公众评估报告 公众评估报告 匈牙利文 04-01-2024
资料单张 资料单张 马耳他文 15-02-2024
产品特点 产品特点 马耳他文 15-02-2024
公众评估报告 公众评估报告 马耳他文 04-01-2024
资料单张 资料单张 荷兰文 15-02-2024
产品特点 产品特点 荷兰文 15-02-2024
公众评估报告 公众评估报告 荷兰文 04-01-2024
资料单张 资料单张 波兰文 15-02-2024
产品特点 产品特点 波兰文 15-02-2024
公众评估报告 公众评估报告 波兰文 04-01-2024
资料单张 资料单张 葡萄牙文 15-02-2024
产品特点 产品特点 葡萄牙文 15-02-2024
公众评估报告 公众评估报告 葡萄牙文 04-01-2024
资料单张 资料单张 罗马尼亚文 15-02-2024
产品特点 产品特点 罗马尼亚文 15-02-2024
公众评估报告 公众评估报告 罗马尼亚文 04-01-2024
资料单张 资料单张 斯洛伐克文 15-02-2024
产品特点 产品特点 斯洛伐克文 15-02-2024
公众评估报告 公众评估报告 斯洛伐克文 04-01-2024
资料单张 资料单张 斯洛文尼亚文 15-02-2024
产品特点 产品特点 斯洛文尼亚文 15-02-2024
公众评估报告 公众评估报告 斯洛文尼亚文 04-01-2024
资料单张 资料单张 芬兰文 15-02-2024
产品特点 产品特点 芬兰文 15-02-2024
公众评估报告 公众评估报告 芬兰文 04-01-2024
资料单张 资料单张 瑞典文 15-02-2024
产品特点 产品特点 瑞典文 15-02-2024
公众评估报告 公众评估报告 瑞典文 04-01-2024
资料单张 资料单张 挪威文 15-02-2024
产品特点 产品特点 挪威文 15-02-2024
资料单张 资料单张 冰岛文 15-02-2024
产品特点 产品特点 冰岛文 15-02-2024
资料单张 资料单张 克罗地亚文 15-02-2024
产品特点 产品特点 克罗地亚文 15-02-2024
公众评估报告 公众评估报告 克罗地亚文 04-01-2024

搜索与此产品相关的警报

查看文件历史