Xermelo

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)
12-12-2022
产品特点 产品特点 (SPC)
12-12-2022
公众评估报告 公众评估报告 (PAR)
20-10-2017

有效成分:

telotristat etiprate

可用日期:

SERB SAS

ATC代码:

A16A

INN(国际名称):

telotristat ethyl

治疗组:

Other alimentary tract and metabolism products

治疗领域:

Carcinoid Tumor; Neuroendocrine Tumors

疗效迹象:

Xermelo is indicated for the treatment of carcinoid syndrome diarrhoea in combination with somatostatin analogue (SSA) therapy in adults inadequately controlled by SSA therapy.

產品總結:

Revision: 15

授权状态:

Authorised

授权日期:

2017-09-17

资料单张

                                23
B. PACKAGE LEAFLET
24
PACKAGE LEAFLET: INFORMATION FOR THE PATIENT
XERMELO 250 MG FILM-COATED TABLETS
telotristat ethyl
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 or pharmacist.
-
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 Xermelo is and what it is used for
2.
What you need to know before you take Xermelo
3.
How to take Xermelo
4.
Possible side effects
5.
How to store Xermelo
6.
Contents of the pack and other information
1.
WHAT XERMELO IS AND WHAT IT IS USED FOR
WHAT XERMELO IS
This medicine contains the active substance telotristat ethyl.
WHAT XERMELO IS USED FOR
This medicine is used in adults with a condition called ‘carcinoid
syndrome’. This is when a tumour,
called a ‘neuroendocrine tumour’, releases a substance called
serotonin into your bloodstream.
Your doctor will prescribe this medicine if your diarrhoea is not well
controlled with injections of
other medicines called ‘somatostatin analogues’ (lanreotide or
octreotide). You should keep having
injections of these other medicines when taking Xermelo.
HOW XERMELO WORKS
When the tumour releases too much serotonin into your bloodstream you
can get diarrhoea.
This medicine works by reducing the amount of serotonin made by the
tumour. It will reduce your
diarrhoea.
2.
WHAT YOU NEED TO KNOW BEFORE YOU TAKE XERMELO
DO NOT TAKE XERMELO
-
if you are allergic to telotristat or any of the other ingredients of
this medicine (listed in
section 6).
WARNINGS AND PRECAUTIONS
Talk to your doctor or pharmacist before taking Xermelo:
•
if you have liver problems. This is because this m
                                
                                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
Xermelo 250 mg film-coated tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each film-coated tablet contains telotristat etiprate equivalent to
250 mg telotristat ethyl.
Excipient with known effect
Each tablet contains 168 mg of lactose.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Film-coated tablet.
White to off-white film-coated oval tablets (approximately 17 mm long
by 7.5 mm wide) with ‘T-E’
debossed on one side and ‘250’ debossed on the other side.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Xermelo is indicated for the treatment of carcinoid syndrome diarrhoea
in combination with
somatostatin analogue (SSA) therapy in adults inadequately controlled
by SSA therapy.
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Posology
The recommended dose is 250 mg three times daily (tid).
Available data suggest that clinical response is usually achieved
within 12 weeks of treatment.
It is recommended to reassess the benefit of continued therapy in a
patient not responding within this
time period.
Based on the high inter-subject variability observed, accumulation in
a subset of patients with
carcinoid syndrome cannot be excluded. Therefore, intake of higher
doses is not recommended (see
section 5.2).
_Missed doses _
In the event of a missed dose, patients should take their subsequent
dose at the next scheduled time
point. Patients should not take a double dose to make up for a missed
dose.
_ _
_Special population _
_ _
_Elderly _
_ _
No specific dose recommendations are available for elderly patients
(see section 5.2).
_ _
3
_Renal impairment _
_ _
No change in dose is required in patients with mild, moderate or
severe renal impairment; who are not
requiring dialysis (see section 5.2). As a precautionary measure, it
is recommended that patients with
severe renal impairment will be monitored for signs of reduced
tolerability.
The use of Xermelo is not recommended in patients with end-stage renal
disease
                                
                                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 12-12-2022
产品特点 产品特点 保加利亚文 12-12-2022
公众评估报告 公众评估报告 保加利亚文 20-10-2017
资料单张 资料单张 西班牙文 12-12-2022
产品特点 产品特点 西班牙文 12-12-2022
公众评估报告 公众评估报告 西班牙文 20-10-2017
资料单张 资料单张 捷克文 12-12-2022
产品特点 产品特点 捷克文 12-12-2022
公众评估报告 公众评估报告 捷克文 20-10-2017
资料单张 资料单张 丹麦文 12-12-2022
产品特点 产品特点 丹麦文 12-12-2022
公众评估报告 公众评估报告 丹麦文 20-10-2017
资料单张 资料单张 德文 12-12-2022
产品特点 产品特点 德文 12-12-2022
公众评估报告 公众评估报告 德文 20-10-2017
资料单张 资料单张 爱沙尼亚文 12-12-2022
产品特点 产品特点 爱沙尼亚文 12-12-2022
公众评估报告 公众评估报告 爱沙尼亚文 20-10-2017
资料单张 资料单张 希腊文 12-12-2022
产品特点 产品特点 希腊文 12-12-2022
公众评估报告 公众评估报告 希腊文 20-10-2017
资料单张 资料单张 法文 12-12-2022
产品特点 产品特点 法文 12-12-2022
公众评估报告 公众评估报告 法文 20-10-2017
资料单张 资料单张 意大利文 12-12-2022
产品特点 产品特点 意大利文 12-12-2022
公众评估报告 公众评估报告 意大利文 20-10-2017
资料单张 资料单张 拉脱维亚文 12-12-2022
产品特点 产品特点 拉脱维亚文 12-12-2022
公众评估报告 公众评估报告 拉脱维亚文 20-10-2017
资料单张 资料单张 立陶宛文 12-12-2022
产品特点 产品特点 立陶宛文 12-12-2022
公众评估报告 公众评估报告 立陶宛文 20-10-2017
资料单张 资料单张 匈牙利文 12-12-2022
产品特点 产品特点 匈牙利文 12-12-2022
公众评估报告 公众评估报告 匈牙利文 20-10-2017
资料单张 资料单张 马耳他文 12-12-2022
产品特点 产品特点 马耳他文 12-12-2022
公众评估报告 公众评估报告 马耳他文 20-10-2017
资料单张 资料单张 荷兰文 12-12-2022
产品特点 产品特点 荷兰文 12-12-2022
公众评估报告 公众评估报告 荷兰文 20-10-2017
资料单张 资料单张 波兰文 12-12-2022
产品特点 产品特点 波兰文 12-12-2022
公众评估报告 公众评估报告 波兰文 20-10-2017
资料单张 资料单张 葡萄牙文 12-12-2022
产品特点 产品特点 葡萄牙文 12-12-2022
公众评估报告 公众评估报告 葡萄牙文 20-10-2017
资料单张 资料单张 罗马尼亚文 12-12-2022
产品特点 产品特点 罗马尼亚文 12-12-2022
公众评估报告 公众评估报告 罗马尼亚文 20-10-2017
资料单张 资料单张 斯洛伐克文 12-12-2022
产品特点 产品特点 斯洛伐克文 12-12-2022
公众评估报告 公众评估报告 斯洛伐克文 20-10-2017
资料单张 资料单张 斯洛文尼亚文 12-12-2022
产品特点 产品特点 斯洛文尼亚文 12-12-2022
公众评估报告 公众评估报告 斯洛文尼亚文 20-10-2017
资料单张 资料单张 芬兰文 12-12-2022
产品特点 产品特点 芬兰文 12-12-2022
公众评估报告 公众评估报告 芬兰文 20-10-2017
资料单张 资料单张 瑞典文 12-12-2022
产品特点 产品特点 瑞典文 12-12-2022
公众评估报告 公众评估报告 瑞典文 20-10-2017
资料单张 资料单张 挪威文 12-12-2022
产品特点 产品特点 挪威文 12-12-2022
资料单张 资料单张 冰岛文 12-12-2022
产品特点 产品特点 冰岛文 12-12-2022
资料单张 资料单张 克罗地亚文 12-12-2022
产品特点 产品特点 克罗地亚文 12-12-2022
公众评估报告 公众评估报告 克罗地亚文 20-10-2017

搜索与此产品相关的警报

查看文件历史