Avastin

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)
17-03-2023
产品特点 产品特点 (SPC)
17-03-2023
公众评估报告 公众评估报告 (PAR)
27-07-2017

有效成分:

bevacizumab

可用日期:

Roche Registration GmbH

ATC代码:

L01FG01

INN(国际名称):

bevacizumab

治疗组:

Antineoplastic agents

治疗领域:

Carcinoma, Non-Small-Cell Lung; Breast Neoplasms; Ovarian Neoplasms; Colorectal Neoplasms; Carcinoma, Renal Cell

疗效迹象:

Bevacizumab in combination with fluoropyrimidine-based chemotherapy is indicated for treatment of adult patients with metastatic carcinoma of the colon or rectum.Bevacizumab in combination with paclitaxel is indicated for first-line treatment of adult patients with metastatic breast cancer. For further information as to human epidermal growth factor receptor 2 (HER2) status.Bevacizumab in combination with capecitabine is indicated for first-line treatment of adult patients with metastatic breast cancer in whom treatment with other chemotherapy options including taxanes or anthracyclines is not considered appropriate. Patients who have received taxane and anthracycline-containing regimens in the adjuvant setting within the last 12 months should be excluded from treatment with Avastin in combination with capecitabine. For further information as to HER2 status.Bevacizumab, in addition to platinum-based chemotherapy, is indicated for first-line treatment of adult patients with unresectable advanced, metastatic or recurrent non-small cell lung cancer other than predominantly squamous cell histology.Bevacizumab, in combination with erlotinib, is indicated for first-line treatment of adult patients with unresectable advanced, metastatic or recurrent non-squamous non-small cell lung cancer with Epidermal Growth Factor Receptor (EGFR) activating mutations.Bevacizumab in combination with interferon alfa-2a is indicated for first line treatment of adult patients with advanced and/or metastatic renal cell cancer.Bevacizumab, in combination with carboplatin and paclitaxel is indicated for the front-line treatment of adult patients with advanced (International Federation of Gynecology and Obstetrics (FIGO) stages III B, III C and IV) epithelial ovarian, fallopian tube, or primary peritoneal cancer.Bevacizumab, in combination with carboplatin and gemcitabine, is indicated for treatment of adult patients with first recurrence of platinum-sensitive epithelial ovarian, fallopian tube or primary peritoneal cancer who have not received prior therapy with bevacizumab or other VEGF inhibitors or VEGF receptor–targeted agents.Bevacizumab in combination with paclitaxel, topotecan, or pegylated liposomal doxorubicin is indicated for the treatment of adult patients with platinum-resistant recurrent epithelial ovarian, fallopian tube, or primary peritoneal cancer who received no more than two prior chemotherapy regimens and who have not received prior therapy with bevacizumab or other VEGF inhibitors or VEGF receptor–targeted agents.Bevacizumab, in combination with paclitaxel and cisplatin or, alternatively, paclitaxel and topotecan in patients who cannot receive platinum therapy, is indicated for the treatment of adult patients with persistent, recurrent, or metastatic carcinoma of the cervix.

產品總結:

Revision: 63

授权状态:

Authorised

授权日期:

2005-01-12

资料单张

                                66
B. PACKAGE LEAFLET
67
PACKAGE LEAFLET: INFORMATION FOR THE USER
AVASTIN 25 MG/ML CONCENTRATE FOR SOLUTION FOR INFUSION
bevacizumab
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.
●
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 Avastin is and what it is used for
2.
What you need to know before you use Avastin
3.
How to use Avastin
4.
Possible side effects
5.
How to store Avastin
6.
Contents of the pack and other information
1.
WHAT AVASTIN IS AND WHAT IT IS USED FOR
Avastin contains the active substance bevacizumab, which is a
humanised monoclonal antibody (a
type of protein that is normally made by the immune system to help
defend the body from infection
and cancer). Bevacizumab binds selectively to a protein called human
vascular endothelial growth
factor (VEGF), which is found on the lining of blood and lymph vessels
in the body. The VEGF
protein causes blood vessels to grow within tumours, these blood
vessels provide the tumour with
nutrients and oxygen. Once bevacizumab is bound to VEGF, tumour growth
is prevented by blocking
the growth of the blood vessels which provide the nutrients and oxygen
to the tumour.
Avastin is a medicine used for the treatment of adult patients with
advanced cancer in the large bowel,
i.e., in the colon or rectum. Avastin will be administered in
combination with chemotherapy treatment
containing a fluoropyrimidine medicine.
Avastin is also used for the treatment of adult patients with
metastatic breast cancer. When used for
patients with breast cancer, it will be administered with a
chemotherapy medicinal product called
paclitaxel or capecitabine.
Avastin is also used for the treatment of adult patients with advanced
non-small cell lun
                                
                                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
Avastin 25 mg/ml concentrate for solution for infusion.
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each ml of concentrate contains 25 mg of bevacizumab*.
Each 4 ml vial contains 100 mg of bevacizumab.
Each 16 ml vial contains 400 mg of bevacizumab.
For dilution and other handling recommendations, see section 6.6.
*Bevacizumab is a recombinant humanised monoclonal antibody produced
by DNA technology in
Chinese Hamster Ovary cells.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Concentrate for solution for infusion.
Clear to slightly opalescent, colourless to pale brown liquid.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Bevacizumab in combination with fluoropyrimidine-based chemotherapy is
indicated for treatment of
adult patients with metastatic carcinoma of the colon or rectum.
Bevacizumab in combination with paclitaxel is indicated for first-line
treatment of adult patients with
metastatic breast cancer. For further information as to human
epidermal growth factor receptor 2
(HER2) status, please refer to section 5.1.
Bevacizumab in combination with capecitabine is indicated for
first-line treatment of adult patients
with metastatic breast cancer in whom treatment with other
chemotherapy options including taxanes or
anthracyclines is not considered appropriate. Patients who have
received taxane and anthracycline-
containing regimens in the adjuvant setting within the last 12 months
should be excluded from
treatment with Avastin in combination with capecitabine. For further
information as to HER2 status,
please refer to section 5.1.
Bevacizumab, in addition to platinum-based chemotherapy, is indicated
for first-line treatment of adult
patients with unresectable advanced, metastatic or recurrent non-small
cell lung cancer other than
predominantly squamous cell histology.
Bevacizumab, in combination with erlotinib, is indicated for
first-line treatment of adult patients with
unresectable advanced, meta
                                
                                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 17-03-2023
产品特点 产品特点 保加利亚文 17-03-2023
公众评估报告 公众评估报告 保加利亚文 27-07-2017
资料单张 资料单张 西班牙文 17-03-2023
产品特点 产品特点 西班牙文 17-03-2023
公众评估报告 公众评估报告 西班牙文 27-07-2017
资料单张 资料单张 捷克文 17-03-2023
产品特点 产品特点 捷克文 17-03-2023
公众评估报告 公众评估报告 捷克文 27-07-2017
资料单张 资料单张 丹麦文 17-03-2023
产品特点 产品特点 丹麦文 17-03-2023
公众评估报告 公众评估报告 丹麦文 27-07-2017
资料单张 资料单张 德文 17-03-2023
产品特点 产品特点 德文 17-03-2023
公众评估报告 公众评估报告 德文 27-07-2017
资料单张 资料单张 爱沙尼亚文 17-03-2023
产品特点 产品特点 爱沙尼亚文 17-03-2023
公众评估报告 公众评估报告 爱沙尼亚文 27-07-2017
资料单张 资料单张 希腊文 17-03-2023
产品特点 产品特点 希腊文 17-03-2023
公众评估报告 公众评估报告 希腊文 27-07-2017
资料单张 资料单张 法文 17-03-2023
产品特点 产品特点 法文 17-03-2023
公众评估报告 公众评估报告 法文 27-07-2017
资料单张 资料单张 意大利文 17-03-2023
产品特点 产品特点 意大利文 17-03-2023
公众评估报告 公众评估报告 意大利文 27-07-2017
资料单张 资料单张 拉脱维亚文 17-03-2023
产品特点 产品特点 拉脱维亚文 17-03-2023
公众评估报告 公众评估报告 拉脱维亚文 27-07-2017
资料单张 资料单张 立陶宛文 17-03-2023
产品特点 产品特点 立陶宛文 17-03-2023
公众评估报告 公众评估报告 立陶宛文 27-07-2017
资料单张 资料单张 匈牙利文 17-03-2023
产品特点 产品特点 匈牙利文 17-03-2023
公众评估报告 公众评估报告 匈牙利文 27-07-2017
资料单张 资料单张 马耳他文 17-03-2023
产品特点 产品特点 马耳他文 17-03-2023
公众评估报告 公众评估报告 马耳他文 27-07-2017
资料单张 资料单张 荷兰文 17-03-2023
产品特点 产品特点 荷兰文 17-03-2023
公众评估报告 公众评估报告 荷兰文 27-07-2017
资料单张 资料单张 波兰文 17-03-2023
产品特点 产品特点 波兰文 17-03-2023
公众评估报告 公众评估报告 波兰文 27-07-2017
资料单张 资料单张 葡萄牙文 17-03-2023
产品特点 产品特点 葡萄牙文 17-03-2023
公众评估报告 公众评估报告 葡萄牙文 27-07-2017
资料单张 资料单张 罗马尼亚文 17-03-2023
产品特点 产品特点 罗马尼亚文 17-03-2023
公众评估报告 公众评估报告 罗马尼亚文 27-07-2017
资料单张 资料单张 斯洛伐克文 17-03-2023
产品特点 产品特点 斯洛伐克文 17-03-2023
公众评估报告 公众评估报告 斯洛伐克文 27-07-2017
资料单张 资料单张 斯洛文尼亚文 17-03-2023
产品特点 产品特点 斯洛文尼亚文 17-03-2023
公众评估报告 公众评估报告 斯洛文尼亚文 27-07-2017
资料单张 资料单张 芬兰文 17-03-2023
产品特点 产品特点 芬兰文 17-03-2023
公众评估报告 公众评估报告 芬兰文 27-07-2017
资料单张 资料单张 瑞典文 17-03-2023
产品特点 产品特点 瑞典文 17-03-2023
公众评估报告 公众评估报告 瑞典文 27-07-2017
资料单张 资料单张 挪威文 17-03-2023
产品特点 产品特点 挪威文 17-03-2023
资料单张 资料单张 冰岛文 17-03-2023
产品特点 产品特点 冰岛文 17-03-2023
资料单张 资料单张 克罗地亚文 17-03-2023
产品特点 产品特点 克罗地亚文 17-03-2023
公众评估报告 公众评估报告 克罗地亚文 27-07-2017

搜索与此产品相关的警报

查看文件历史