Navelbine

国家: 马耳他

语言: 英文

来源: Medicines Authority

现在购买

下载 资料单张 (PIL)
06-06-2024
下载 产品特点 (SPC)
06-06-2024

有效成分:

VINORELBINE TARTRATE

可用日期:

Pierre Fabre Medicament 45 Place Abel Gance, 92100 Boulogne, France

ATC代码:

L01CA04

INN(国际名称):

VINORELBINE TARTRATE 10 mg/ml

药物剂型:

CONCENTRATE FOR SOLUTION FOR INFUSION

组成:

VINORELBINE TARTRATE 10 mg/ml

处方类型:

POM

治疗领域:

ANTINEOPLASTIC AGENTS

授权状态:

Withdrawn

授权日期:

2006-11-23

资料单张

                                Page 1 of 5 
 
CORE PATIENT INFORMATION LEAFLET: 
 
Package Leaflet: Information for the user 
 
NAVELBINE® 10MG/ML CONCENTRATE FOR SOLUTION FOR INFUSION 
Vinorelbine (as tartrate) 
 
 
READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU ARE GIVEN 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. 
- 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 NAVELBINE is and what it is used for 
2. What you need to know before you are given NAVELBINE 
3. How NAVELBINE is given 
4. Possible side effects 
5. How to store NAVELBINE 
6. Contents of the pack and other information 
 
1. WHAT NAVELBINE IS AND WHAT IT IS USED FOR 
 
NAVELBINE contains the active substance Vinorelbine (as
tartrate), and belongs to a family of 
medicines called the vinca alkaloid, family used to treat
cancer. 
NAVELBINE is used to treat some types of prostate cancer,
lung cancer and some types of breast 
cancer in patients over 18 years old. 
 
2. WHAT YOU NEED TO KNOW BEFORE YOU ARE GIVEN NAVELBINE 
 
DO NOT USE NAVELBINE: 
- If you are allergic to Vinorelbine, or to any of
the related family of cancer drugs called the 
vincaalkaloids, or any of the other ingredients of this
medicine (listed in section 6). 
- If you are breast feeding. 
- If you have a low white blood cell and/or platelet count, or
a severe infection current or recent 
(within 2 weeks). 
- If you plan to receive a yellow fever
vaccination or have just had one. 
 
WARNINGS AND PRECAUTIONS 
Talk to your doctor or pharmacist before you are given NAVELBINE
if: 
- You have a history of heart attack or severe chest pain. 
- You have received 
                                
                                阅读完整的文件
                                
                            

产品特点

                                Page 1 of 11 
 
SUMMARY OF PRODUCT CHARACTERISTICS 
 
 
1. NAME OF THE MEDICINAL PRODUCT 
 
Navelbine 10mg/ml, concentrate for solution for infusion 
 
2. QUALITATIVE AND QUANTITATIVE COMPOSITION 
 
ACTIVE 
INGREDIENT 
 
FORMULATION 
 
 
10 mg/1ml 
50 mg/5 ml 
vinorelbine tartrate (mg) 
13.85 
69.25 
equivalent to vinorelbine 
(INN) base (mg) 
10.00 
50.00 
 
For the full list of excipients refer to section 6.1. 
 
3. PHARMACEUTICAL FORM 
 
Concentrate for solution for infusion. 
Navelbine is a clear colourless to pale yellow solution with a
pH range from 3.3 to 3.8. 
 
4. CLINICAL PARTICULARS 
 
4.1. THERAPEUTIC INDICATIONS 
 
- Navelbine is indicated as single agent or in combination for the
first line treatment of stage 3 or 4 
Non-small cell lung cancer 
- Navelbine is indicated in the treatment of stage 3 or
4 advanced breast cancer relapsing or 
refractory to an anthracycline containing regimen. 
 
4.2. POSOLOGY AND METHOD OF ADMINISTRATION 
 
Strictly intravenous administration after appropriate dilution. 
Intra-thecal administration of Navelbinemay be fatal. 
Instructions for use and handling: see section 6.6. 
 
It is recommended to infuse Navelbine over 6-10 minutes after
dilution in 20-50 ml of sodium 
chloride 9 mg/ml (0.9%) solution for injection or in
glucose solution for injection 5%. 
 
Administration should always be followed with at least 250 ml of an
isotonic solution infusion to 
flush the vein. 
 
- NON-SMALL CELL LUNG CANCER AND ADVANCED BREAST CANCER 
In monotherapy the usual dose given is 25-30 mg/m² once weekly. 
In combination chemotherapy the usual dose (25-30 mg/m²) is
usually maintained, while the 
frequency of administration is reduced e.g. day 1 and 5 every 3
weeks or day 1 and 8 every 3 weeks 
according to treatment protocol. 
Page 2 of 11 
 
 
- ADMINISTRATION IN THE ELDERLY 
Clinical experience has not identified re
                                
                                阅读完整的文件
                                
                            

搜索与此产品相关的警报

查看文件历史