Capecitabine Teva

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)
01-02-2024
产品特点 产品特点 (SPC)
01-02-2024
公众评估报告 公众评估报告 (PAR)
29-07-2020

有效成分:

capecitabine

可用日期:

Teva Pharma B.V.

ATC代码:

L01BC06

INN(国际名称):

capecitabine

治疗组:

Antineoplastic agents

治疗领域:

Colonic Neoplasms; Breast Neoplasms; Colorectal Neoplasms; Stomach Neoplasms

疗效迹象:

Capecitabine Teva is indicated for the adjuvant treatment of patients following surgery of stage III (Dukes’ stage C) colon cancer.Capecitabine Teva is indicated for the treatment of metastatic colorectal cancer.Capecitabine Teva is indicated for first‑line treatment of advanced gastric cancer in combination with a platinum‑based regimen.Capecitabine Teva in combination with docetaxel is indicated for the treatment of patients with locally advanced or metastatic breast cancer after failure of cytotoxic chemotherapy. Previous therapy should have included an anthracycline. Capecitabine Teva is also indicated as monotherapy for the treatment of patients with locally advanced or metastatic breast cancer after failure of taxanes and an anthracycline containing chemotherapy regimen or for whom further anthracycline therapy is not indicated.

產品總結:

Revision: 15

授权状态:

Authorised

授权日期:

2012-04-20

资料单张

                                40
B. PACKAGE LEAFLET
41
PACKAGE LEAFLET: INFORMATION FOR THE USER
_ _
CAPECITABINE TEVA 150 MG FILM-COATED TABLETS
CAPECITABINE TEVA 500 MG FILM-COATED TABLETS
capecitabine
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 or pharmacist. This
includes any possible side
effects not listed in this leaflet. See section 4.
WHAT IS IN THIS LEAFLET
1.
What Capecitabine Teva is and what it is used for
2.
What you need to know before you take Capecitabine Teva
3.
How to take Capecitabine Teva
4.
Possible side effects
5.
How to store Capecitabine Teva
6.
Contents of the pack and other information
1.
WHAT CAPECITABINE TEVA IS AND WHAT IT IS USED FOR
Capecitabine Teva belongs to the group of medicines called "cytostatic
medicines", which stop the
growth of cancer cells. Capecitabine Teva contains capecitabine, which
itself is not a cytostatic
medicine. Only after being absorbed by the body is it changed into an
active anti-cancer medicine
(more in tumour tissue than in normal tissue).
Capecitabine Teva is used in the treatment of colon, rectal, gastric,
or breast cancers. Furthermore,
Capecitabine Teva is used to prevent new occurrence of colon cancer
after complete removal of the
tumour by surgery.
Capecitabine Teva may be used either alone or in combination with
other medicines.
2.
WHAT YOU NEED TO KNOW BEFORE YOU TAKE CAPECITABINE TEVA
_ _
DO NOT TAKE CAPECITABINE TEVA_ _
-
if you are allergic to capecitabine or any of the other ingredients of
this medicine (listed in
section 6). You must inform your doctor if you know that you have an
allergy or over-reaction
to this medicine,
-
if you previously have had severe reactions to fluor
                                
                                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
Capecitabine Teva 150 mg film-coated tablets
Capecitabine Teva 500 mg film-coated tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Capecitabine Teva 150 mg film-coated tablets
Each film-coated tablet contains 150 mg capecitabine.
Capecitabine Teva 500 mg film-coated tablets
Each film-coated tablet contains 500 mg capecitabine.
Excipient with known effect
_Capecitabine Teva 150 mg film-coated tablets _
Each film-coated tablet contains 15.6 mg lactose.
_Capecitabine Teva 500 mg film-coated tablets _
Each film-coated tablet contains 52.0 mg lactose.
For the full list of excipients, see section 6.1.
_ _
3.
PHARMACEUTICAL FORM
Film-coated tablet
Capecitabine Teva 150 mg film-coated tablets
The film-coated tablets are oval biconvex light peach, 11.5 mm x 5.4
mm with inscription “C” on one
side and “150”on the other side.
Capecitabine Teva 500 mg film-coated tablets
The film-coated tablets are oval biconvex light peach, 16.0 mm x 8.5
mm with inscription “C” on one
side and “500”on the other side.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Capecitabine Teva is indicated for the treatment of:
-
for the adjuvant treatment of patients following surgery of stage III
(Dukes’ stage C) colon cancer
(see section 5.1).
-
metastatic colorectal cancer (see section 5.1).
-
first-line treatment of advanced gastric cancer in combination with a
platinum-based regimen (see
section 5.1).
-
in combination with docetaxel (see section 5.1) for the treatment of
patients with locally advanced
or metastatic breast cancer after failure of cytotoxic chemotherapy.
Previous therapy should have
included an anthracycline.
-
as monotherapy for the treatment of patients with locally advanced or
metastatic breast cancer after
failure of taxanes and an anthracycline containing chemotherapy
regimen or for whom further
anthracycline therapy is not indicated.
3
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Capecitabine Teva should only be prescribed by
                                
                                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 01-02-2024
产品特点 产品特点 保加利亚文 01-02-2024
公众评估报告 公众评估报告 保加利亚文 29-07-2020
资料单张 资料单张 西班牙文 01-02-2024
产品特点 产品特点 西班牙文 01-02-2024
公众评估报告 公众评估报告 西班牙文 29-07-2020
资料单张 资料单张 捷克文 01-02-2024
产品特点 产品特点 捷克文 01-02-2024
公众评估报告 公众评估报告 捷克文 29-07-2020
资料单张 资料单张 丹麦文 01-02-2024
产品特点 产品特点 丹麦文 01-02-2024
公众评估报告 公众评估报告 丹麦文 29-07-2020
资料单张 资料单张 德文 01-02-2024
产品特点 产品特点 德文 01-02-2024
公众评估报告 公众评估报告 德文 29-07-2020
资料单张 资料单张 爱沙尼亚文 01-02-2024
产品特点 产品特点 爱沙尼亚文 01-02-2024
公众评估报告 公众评估报告 爱沙尼亚文 29-07-2020
资料单张 资料单张 希腊文 01-02-2024
产品特点 产品特点 希腊文 01-02-2024
公众评估报告 公众评估报告 希腊文 29-07-2020
资料单张 资料单张 法文 01-02-2024
产品特点 产品特点 法文 01-02-2024
公众评估报告 公众评估报告 法文 29-07-2020
资料单张 资料单张 意大利文 01-02-2024
产品特点 产品特点 意大利文 01-02-2024
公众评估报告 公众评估报告 意大利文 29-07-2020
资料单张 资料单张 拉脱维亚文 01-02-2024
产品特点 产品特点 拉脱维亚文 01-02-2024
公众评估报告 公众评估报告 拉脱维亚文 29-07-2020
资料单张 资料单张 立陶宛文 01-02-2024
产品特点 产品特点 立陶宛文 01-02-2024
公众评估报告 公众评估报告 立陶宛文 29-07-2020
资料单张 资料单张 匈牙利文 01-02-2024
产品特点 产品特点 匈牙利文 01-02-2024
公众评估报告 公众评估报告 匈牙利文 29-07-2020
资料单张 资料单张 马耳他文 01-02-2024
产品特点 产品特点 马耳他文 01-02-2024
公众评估报告 公众评估报告 马耳他文 29-07-2020
资料单张 资料单张 荷兰文 01-02-2024
产品特点 产品特点 荷兰文 01-02-2024
公众评估报告 公众评估报告 荷兰文 29-07-2020
资料单张 资料单张 波兰文 01-02-2024
产品特点 产品特点 波兰文 01-02-2024
公众评估报告 公众评估报告 波兰文 29-07-2020
资料单张 资料单张 葡萄牙文 01-02-2024
产品特点 产品特点 葡萄牙文 01-02-2024
公众评估报告 公众评估报告 葡萄牙文 29-07-2020
资料单张 资料单张 罗马尼亚文 01-02-2024
产品特点 产品特点 罗马尼亚文 01-02-2024
公众评估报告 公众评估报告 罗马尼亚文 29-07-2020
资料单张 资料单张 斯洛伐克文 01-02-2024
产品特点 产品特点 斯洛伐克文 01-02-2024
公众评估报告 公众评估报告 斯洛伐克文 29-07-2020
资料单张 资料单张 斯洛文尼亚文 01-02-2024
产品特点 产品特点 斯洛文尼亚文 01-02-2024
公众评估报告 公众评估报告 斯洛文尼亚文 29-07-2020
资料单张 资料单张 芬兰文 01-02-2024
产品特点 产品特点 芬兰文 01-02-2024
公众评估报告 公众评估报告 芬兰文 29-07-2020
资料单张 资料单张 瑞典文 01-02-2024
产品特点 产品特点 瑞典文 01-02-2024
公众评估报告 公众评估报告 瑞典文 29-07-2020
资料单张 资料单张 挪威文 01-02-2024
产品特点 产品特点 挪威文 01-02-2024
资料单张 资料单张 冰岛文 01-02-2024
产品特点 产品特点 冰岛文 01-02-2024
资料单张 资料单张 克罗地亚文 01-02-2024
产品特点 产品特点 克罗地亚文 01-02-2024

搜索与此产品相关的警报