Ilaris

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)
25-08-2023
产品特点 产品特点 (SPC)
25-08-2023
公众评估报告 公众评估报告 (PAR)
17-05-2017

有效成分:

Canakinumab

可用日期:

Novartis Europharm Limited

ATC代码:

L04AC08

INN(国际名称):

canakinumab

治疗组:

Interleukin inhibitors,

治疗领域:

Cryopyrin-Associated Periodic Syndromes; Arthritis, Juvenile Rheumatoid; Arthritis, Gouty

疗效迹象:

Periodic fever syndromesIlaris is indicated for the treatment of the following autoinflammatory periodic fever syndromes in adults, adolescents and children aged 2 years and older:Cryopyrin-associated periodic syndromesIlaris is indicated for the treatment of cryopyrin-associated periodic syndromes (CAPS) including:Muckle-Wells syndrome (MWS),Neonatal-onset multisystem inflammatory disease (NOMID) / chronic infantile neurological, cutaneous, articular syndrome (CINCA),Severe forms of familial cold autoinflammatory syndrome (FCAS) / familial cold urticaria (FCU) presenting with signs and symptoms beyond cold-induced urticarial skin rash.Tumour necrosis factor receptor associated periodic syndrome (TRAPS)Ilaris is indicated for the treatment of tumour necrosis factor (TNF) receptor associated periodic syndrome (TRAPS).Hyperimmunoglobulin D syndrome (HIDS)/mevalonate kinase deficiency (MKD)Ilaris is indicated for the treatment of hyperimmunoglobulin D syndrome (HIDS)/mevalonate kinase deficiency (MKD).Familial Mediterranean fever (FMF)Ilaris is indicated for the treatment of Familial Mediterranean Fever (FMF). Ilaris should be given in combination with colchicine, if appropriate.Ilaris is also indicated for the treatment of:Still’s diseaseIlaris is indicated for the treatment of active Still’s disease including adult-onset Still’s disease (AOSD) and systemic juvenile idiopathic arthritis (SJIA) in patients aged 2 years and older who have responded inadequately to previous therapy with non-steroidal anti-inflammatory drugs (NSAIDs) and systemic corticosteroids. Ilaris can be given as monotherapy or in combination with methotrexate.Gouty arthritisIlaris is indicated for the symptomatic treatment of adult patients with frequent gouty arthritis attacks (at least 3 attacks in the previous 12 months) in whom non-steroidal anti-inflammatory drugs (NSAIDs) and colchicine are contraindicated, are not tolerated, or do not provide an adequate response, and in whom repeated courses of corticosteroids are not appropriate.

產品總結:

Revision: 30

授权状态:

Authorised

授权日期:

2009-10-23

资料单张

                                65
B. PACKAGE LEAFLET
66
PACKAGE LEAFLET: INFORMATION FOR THE USER
ILARIS 150 MG POWDER FOR SOLUTION FOR INJECTION
canakinumab
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 Ilaris is and what it is used for
2.
What you need to know before you use Ilaris
3.
How to use Ilaris
4.
Possible side effects
5.
How to store Ilaris
6.
Contents of the pack and other information
1.
WHAT ILARIS IS AND WHAT IT IS USED FOR
WHAT ILARIS IS
Ilaris contains the active substance canakinumab, a monoclonal
antibody that belongs to a group of
medicines called interleukin inhibitors. It blocks the activity of a
substance called interleukin-1 beta
(IL-1 beta) in the body, which is present at increased levels in
inflammatory diseases.
WHAT ILARIS IS USED FOR
Ilaris is used for treatment of the following inflammatory diseases:
-
Periodic fever syndromes:
•
Cryopyrin-associated periodic syndromes (CAPS),
•
Tumour necrosis factor receptor associated periodic syndrome (TRAPS),
•
Hyperimmunoglobulin D syndrome (HIDS)/mevalonate kinase deficiency
(MKD),
•
Familial Mediterranean fever (FMF).
-
Still’s disease including adult onset Still’s disease (AOSD) and
systemic juvenile idiopathic
arthritis (SJIA)
-
Gouty arthritis
More information on each of these diseases is given below.
67
Periodic fever syndromes
Ilaris is used in adults and children aged 2 years and older to treat
the following:
-
Cryopyrin-associated periodic syndromes (CAPS) – this is a group of
auto-inflammatory
diseases, which include:
                                
                                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
Ilaris 150 mg powder for solution for injection
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
One vial contains 150 mg of canakinumab*.
After reconstitution, each ml of solution contains 150 mg canakinumab.
* human monoclonal antibody produced in mouse myeloma Sp2/0 cells by
recombinant DNA
technology
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Powder for solution for injection.
The powder is white.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Periodic fever syndromes
Ilaris is indicated for the treatment of the following
autoinflammatory periodic fever syndromes in
adults, adolescents and children aged 2 years and older:
_Cryopyrin-associated periodic syndromes _
Ilaris is indicated for the treatment of cryopyrin-associated periodic
syndromes (CAPS) including:
•
Muckle-Wells syndrome (MWS),
•
Neonatal-onset multisystem inflammatory disease (NOMID) / chronic
infantile neurological,
cutaneous, articular syndrome (CINCA),
•
Severe forms of familial cold autoinflammatory syndrome (FCAS) /
familial cold urticaria
(FCU) presenting with signs and symptoms beyond cold-induced
urticarial skin rash.
_Tumour necrosis factor receptor associated periodic syndrome (TRAPS)
_
Ilaris is indicated for the treatment of tumour necrosis factor (TNF)
receptor associated periodic
syndrome (TRAPS).
_Hyperimmunoglobulin D syndrome (HIDS)/mevalonate kinase deficiency
(MKD) _
Ilaris is indicated for the treatment of hyperimmunoglobulin D
syndrome (HIDS)/mevalonate kinase
deficiency (MKD).
_Familial Mediterranean fever (FMF) _
Ilaris is indicated for the treatment of Familial Mediterranean Fever
(FMF). Ilaris should be given in
combination with colchicine, if appropriate.
3
Ilaris is also indicated for the treatment of:
Still’s disease
Ilaris is indicated for the treatment of active Still’s disease
including adult-onset Still’s disease
(AOSD) and systemic juvenile idiopathic arthritis (SJIA) in patients
aged 2 years
                                
                                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 25-08-2023
产品特点 产品特点 保加利亚文 25-08-2023
公众评估报告 公众评估报告 保加利亚文 17-05-2017
资料单张 资料单张 西班牙文 25-08-2023
产品特点 产品特点 西班牙文 25-08-2023
公众评估报告 公众评估报告 西班牙文 17-05-2017
资料单张 资料单张 捷克文 25-08-2023
产品特点 产品特点 捷克文 25-08-2023
公众评估报告 公众评估报告 捷克文 17-05-2017
资料单张 资料单张 丹麦文 25-08-2023
产品特点 产品特点 丹麦文 25-08-2023
公众评估报告 公众评估报告 丹麦文 17-05-2017
资料单张 资料单张 德文 25-08-2023
产品特点 产品特点 德文 25-08-2023
公众评估报告 公众评估报告 德文 17-05-2017
资料单张 资料单张 爱沙尼亚文 25-08-2023
产品特点 产品特点 爱沙尼亚文 25-08-2023
公众评估报告 公众评估报告 爱沙尼亚文 17-05-2017
资料单张 资料单张 希腊文 25-08-2023
产品特点 产品特点 希腊文 25-08-2023
公众评估报告 公众评估报告 希腊文 17-05-2017
资料单张 资料单张 法文 25-08-2023
产品特点 产品特点 法文 25-08-2023
公众评估报告 公众评估报告 法文 17-05-2017
资料单张 资料单张 意大利文 25-08-2023
产品特点 产品特点 意大利文 25-08-2023
公众评估报告 公众评估报告 意大利文 17-05-2017
资料单张 资料单张 拉脱维亚文 25-08-2023
产品特点 产品特点 拉脱维亚文 25-08-2023
公众评估报告 公众评估报告 拉脱维亚文 17-05-2017
资料单张 资料单张 立陶宛文 25-08-2023
产品特点 产品特点 立陶宛文 25-08-2023
公众评估报告 公众评估报告 立陶宛文 17-05-2017
资料单张 资料单张 匈牙利文 25-08-2023
产品特点 产品特点 匈牙利文 25-08-2023
公众评估报告 公众评估报告 匈牙利文 17-05-2017
资料单张 资料单张 马耳他文 25-08-2023
产品特点 产品特点 马耳他文 25-08-2023
公众评估报告 公众评估报告 马耳他文 17-05-2017
资料单张 资料单张 荷兰文 25-08-2023
产品特点 产品特点 荷兰文 25-08-2023
公众评估报告 公众评估报告 荷兰文 17-05-2017
资料单张 资料单张 波兰文 25-08-2023
产品特点 产品特点 波兰文 25-08-2023
公众评估报告 公众评估报告 波兰文 17-05-2017
资料单张 资料单张 葡萄牙文 25-08-2023
产品特点 产品特点 葡萄牙文 25-08-2023
公众评估报告 公众评估报告 葡萄牙文 17-05-2017
资料单张 资料单张 罗马尼亚文 25-08-2023
产品特点 产品特点 罗马尼亚文 25-08-2023
公众评估报告 公众评估报告 罗马尼亚文 17-05-2017
资料单张 资料单张 斯洛伐克文 25-08-2023
产品特点 产品特点 斯洛伐克文 25-08-2023
公众评估报告 公众评估报告 斯洛伐克文 17-05-2017
资料单张 资料单张 斯洛文尼亚文 25-08-2023
产品特点 产品特点 斯洛文尼亚文 25-08-2023
公众评估报告 公众评估报告 斯洛文尼亚文 17-05-2017
资料单张 资料单张 芬兰文 25-08-2023
产品特点 产品特点 芬兰文 25-08-2023
公众评估报告 公众评估报告 芬兰文 17-05-2017
资料单张 资料单张 瑞典文 25-08-2023
产品特点 产品特点 瑞典文 25-08-2023
公众评估报告 公众评估报告 瑞典文 17-05-2017
资料单张 资料单张 挪威文 25-08-2023
产品特点 产品特点 挪威文 25-08-2023
资料单张 资料单张 冰岛文 25-08-2023
产品特点 产品特点 冰岛文 25-08-2023
资料单张 资料单张 克罗地亚文 25-08-2023
产品特点 产品特点 克罗地亚文 25-08-2023
公众评估报告 公众评估报告 克罗地亚文 17-05-2017

搜索与此产品相关的警报

查看文件历史