Mimpara

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)
10-10-2023
产品特点 产品特点 (SPC)
10-10-2023
公众评估报告 公众评估报告 (PAR)
05-09-2017

有效成分:

cinacalcet hydrochloride

可用日期:

Amgen Europe B.V.

ATC代码:

H05BX01

INN(国际名称):

cinacalcet

治疗组:

Calcium homeostasis

治疗领域:

Hypercalcemia; Parathyroid Neoplasms; Hyperparathyroidism

疗效迹象:

Secondary hyperparathyroidismAdultsTreatment of secondary hyperparathyroidism (HPT) in adult patients with end stage renal disease (ESRD) on maintenance dialysis therapy.Paediatric populationTreatment of secondary hyperparathyroidism (HPT) in children aged 3 years and older with end stage renal disease (ESRD) on maintenance dialysis therapy in whom secondary HPT is not adequately controlled with standard of care therapy.Mimpara may be used as part of a therapeutic regimen including phosphate binders and/or Vitamin D sterols, as appropriate.Parathyroid carcinoma and primary hyperparathyroidism in adults.Reduction of hypercalcaemia in adult patients with:parathyroid carcinoma;primary HPT for whom parathyroidectomy would be indicated on the basis of serum calcium levels (as defined by relevant treatment guidelines), but in whom parathyroidectomy is not clinically appropriate or is contraindicated.

產品總結:

Revision: 25

授权状态:

Authorised

授权日期:

2004-10-22

资料单张

                                71
B. PACKAGE LEAFLET
72
PACKAGE LEAFLET: INFORMATION FOR THE PATIENT
MIMPARA 30 MG FILM-COATED TABLETS
MIMPARA 60 MG FILM-COATED TABLETS
MIMPARA 90 MG FILM-COATED TABLETS
Cinacalcet
READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU START TAKING 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 Mimpara is and what it is used for
2.
What you need to know before you take Mimpara
3.
How to take Mimpara
4.
Possible side effects
5.
How to store Mimpara
6.
Contents of the pack and other information
1.
WHAT MIMPARA IS AND WHAT IT IS USED FOR
Mimpara works by controlling the levels of parathyroid hormone (PTH),
calcium and phosphorous in
your body. It is used to treat problems with organs called parathyroid
glands. The parathyroids are four
small glands in the neck, near the thyroid gland, that produce
parathyroid hormone (PTH).
Mimpara is used in adults:
•
to treat secondary hyperparathyroidism in adults with serious kidney
disease who need dialysis
to clear their blood of waste products.
•
to reduce high levels of calcium in the blood (hypercalcaemia) in
adult patients with parathyroid
cancer.
•
to reduce high levels of calcium in the blood (hypercalcaemia) in
adult patients with primary
hyperparathyroidism when removal of the gland is not possible.
Mimpara is used in children aged 3 years to less than 18 years of age:
•
to treat secondary hyperparathyroidism in patients with serious kidney
disease who need
dialysis to clear their blood of waste products, whose condition is
not controlled with other
treatments.
In primary and secondary hyperpa
                                
                                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
Mimpara 30 mg film-coated tablets
Mimpara 60 mg film-coated tablets
Mimpara 90 mg film-coated tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Mimpara 30 mg film-coated tablets
Each tablet contains 30 mg cinacalcet (as hydrochloride).
_Excipient with known effect _
Each tablet contains 2.74 mg of lactose.
Mimpara 60 mg film-coated tablets
Each tablet contains 60 mg cinacalcet (as hydrochloride).
_Excipient with known effect _
Each tablet contains 5.47 mg of lactose.
Mimpara 90 mg film-coated tablets
Each tablet contains 90 mg cinacalcet (as hydrochloride).
_Excipient with known effect _
Each tablet contains 8.21 mg of lactose.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Film-coated tablet (tablet).
Mimpara 30 mg film-coated tablets
Light green, oval (approximately 9.7 mm long and 6.0 mm wide),
film-coated tablet marked “AMG”
on one side and “30” on the other.
Mimpara 60 mg film-coated tablets
Light green, oval (approximately 12.2 mm long and 7.6 mm wide),
film-coated tablet marked “AMG”
on one side and “60” on the other.
Mimpara 90 mg film-coated tablets
Light green, oval (approximately 13.9 mm long and 8.7 mm wide),
film-coated tablet marked “AMG”
on one side and “90” on the other.
3
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Secondary hyperparathyroidism
_Adults _
Treatment of secondary hyperparathyroidism (HPT) in adult patients
with end-stage renal disease
(ESRD) on maintenance dialysis therapy.
_Paediatric population _
Treatment of secondary hyperparathyroidism (HPT) in children aged 3
years and older with end-stage
renal disease (ESRD) on maintenance dialysis therapy in whom secondary
HPT is not adequately
controlled with standard of care therapy (see section 4.4).
Mimpara may be used as part of a therapeutic regimen including
phosphate binders and/or Vitamin D
sterols, as appropriate (see section 5.1).
Parathyroid carcinoma and primary hyperparathyroidism in adult
                                
                                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 10-10-2023
产品特点 产品特点 保加利亚文 10-10-2023
公众评估报告 公众评估报告 保加利亚文 05-09-2017
资料单张 资料单张 西班牙文 10-10-2023
产品特点 产品特点 西班牙文 10-10-2023
公众评估报告 公众评估报告 西班牙文 05-09-2017
资料单张 资料单张 捷克文 10-10-2023
产品特点 产品特点 捷克文 10-10-2023
公众评估报告 公众评估报告 捷克文 05-09-2017
资料单张 资料单张 丹麦文 10-10-2023
产品特点 产品特点 丹麦文 10-10-2023
公众评估报告 公众评估报告 丹麦文 05-09-2017
资料单张 资料单张 德文 10-10-2023
产品特点 产品特点 德文 10-10-2023
公众评估报告 公众评估报告 德文 05-09-2017
资料单张 资料单张 爱沙尼亚文 10-10-2023
产品特点 产品特点 爱沙尼亚文 10-10-2023
公众评估报告 公众评估报告 爱沙尼亚文 05-09-2017
资料单张 资料单张 希腊文 10-10-2023
产品特点 产品特点 希腊文 10-10-2023
公众评估报告 公众评估报告 希腊文 05-09-2017
资料单张 资料单张 法文 10-10-2023
产品特点 产品特点 法文 10-10-2023
公众评估报告 公众评估报告 法文 05-09-2017
资料单张 资料单张 意大利文 10-10-2023
产品特点 产品特点 意大利文 10-10-2023
公众评估报告 公众评估报告 意大利文 05-09-2017
资料单张 资料单张 拉脱维亚文 10-10-2023
产品特点 产品特点 拉脱维亚文 10-10-2023
公众评估报告 公众评估报告 拉脱维亚文 05-09-2017
资料单张 资料单张 立陶宛文 10-10-2023
产品特点 产品特点 立陶宛文 10-10-2023
公众评估报告 公众评估报告 立陶宛文 05-09-2017
资料单张 资料单张 匈牙利文 10-10-2023
产品特点 产品特点 匈牙利文 10-10-2023
公众评估报告 公众评估报告 匈牙利文 05-09-2017
资料单张 资料单张 马耳他文 10-10-2023
产品特点 产品特点 马耳他文 10-10-2023
公众评估报告 公众评估报告 马耳他文 05-09-2017
资料单张 资料单张 荷兰文 10-10-2023
产品特点 产品特点 荷兰文 10-10-2023
公众评估报告 公众评估报告 荷兰文 05-09-2017
资料单张 资料单张 波兰文 10-10-2023
产品特点 产品特点 波兰文 10-10-2023
公众评估报告 公众评估报告 波兰文 05-09-2017
资料单张 资料单张 葡萄牙文 10-10-2023
产品特点 产品特点 葡萄牙文 10-10-2023
公众评估报告 公众评估报告 葡萄牙文 05-09-2017
资料单张 资料单张 罗马尼亚文 10-10-2023
产品特点 产品特点 罗马尼亚文 10-10-2023
公众评估报告 公众评估报告 罗马尼亚文 05-09-2017
资料单张 资料单张 斯洛伐克文 10-10-2023
产品特点 产品特点 斯洛伐克文 10-10-2023
公众评估报告 公众评估报告 斯洛伐克文 05-09-2017
资料单张 资料单张 斯洛文尼亚文 10-10-2023
产品特点 产品特点 斯洛文尼亚文 10-10-2023
公众评估报告 公众评估报告 斯洛文尼亚文 05-09-2017
资料单张 资料单张 芬兰文 10-10-2023
产品特点 产品特点 芬兰文 10-10-2023
公众评估报告 公众评估报告 芬兰文 05-09-2017
资料单张 资料单张 瑞典文 10-10-2023
产品特点 产品特点 瑞典文 10-10-2023
公众评估报告 公众评估报告 瑞典文 05-09-2017
资料单张 资料单张 挪威文 10-10-2023
产品特点 产品特点 挪威文 10-10-2023
资料单张 资料单张 冰岛文 10-10-2023
产品特点 产品特点 冰岛文 10-10-2023
资料单张 资料单张 克罗地亚文 10-10-2023
产品特点 产品特点 克罗地亚文 10-10-2023
公众评估报告 公众评估报告 克罗地亚文 05-09-2017

搜索与此产品相关的警报

查看文件历史