Methylthioninium chloride Proveblue

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)
14-03-2024
产品特点 产品特点 (SPC)
14-03-2024
公众评估报告 公众评估报告 (PAR)
07-05-2018

有效成分:

methylthioninium chloride

可用日期:

Provepharm SAS

ATC代码:

V03AB17

INN(国际名称):

methylthioninium chloride

治疗组:

All other therapeutic products

治疗领域:

Methemoglobinemia

疗效迹象:

Acute symptomatic treatment of medicinal and chemical products- induced methaemoglobinaemia.Methylthioninium chloride Proveblue is indicated in adults, children and adolescents (aged 0 to 17 years old).

產品總結:

Revision: 26

授权状态:

Authorised

授权日期:

2011-05-06

资料单张

                                20
B. PACKAGE LEAFLET
21
PACKAGE LEAFLET: INFORMATION FOR THE USER
_ _
METHYLTHIONINIUM CHLORIDE PROVEBLUE 5 MG/ML SOLUTION FOR INJECTION
methylthioninium chloride
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 nurse.
-
If you get any side effects, talk to your doctor or nurse. This
includes any possible side effects
not listed in this leaflet. See section 4.
WHAT IS IN THIS LEAFLET
1.
What Methylthioninium chloride Proveblue is and what it is used for
2.
What you need to know before you are given Methylthioninium chloride
Proveblue
3.
How Methylthioninium chloride Proveblue is given
4.
Possible side effects
5.
How to store Methylthioninium chloride Proveblue
6.
Contents of the pack and other information
1.
WHAT METHYLTHIONINIUM CHLORIDE PROVEBLUE IS AND WHAT IT IS USED FOR
Methylthioninium chloride (also called methylene blue) belongs to a
group of medicines called
antidotes.
Methylthioninium chloride Proveblue will be given to you or your child
(0-17 years old) to treat
problems with your blood resulting from exposure to some medicines or
chemicals that can cause a
disease called methaemoglobinaemia.
In methaemoglobinaemia, your blood contains too much methaemoglobin
(an abnormal form of
haemoglobin that is not able to transport oxygen around your body
effectively). This medicine will
help your haemoglobin return to normal and restore the transport of
oxygen in the blood.
2.
WHAT YOU NEED TO KNOW BEFORE YOU ARE GIVEN METHYLTHIONINIUM CHLORIDE
PROVEBLUE
_ _
YOU MUST NOT BE GIVEN METHYLTHIONINIUM CHLORIDE PROVEBLUE
-
if you are allergic to methylthioninium chloride or other thiazine
dyes
-
if your body does not produce enough of the enzyme G6PD
(glucose-6-phosphate
dehydrogenase)
-
if your body does not produce enough of the enzyme NADPH (nicotinamide
adenine
dinucleotide phosphate) reductase
-
if your blood disorder has been caused b
                                
                                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
Methylthioninium chloride Proveblue 5 mg/ml solution for injection
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each ml of solution contains 5 mg methylthioninium chloride.
Each 10 ml ampoule contains 50 mg methylthioninium chloride.
Each 2 ml ampoule contains 10 mg methylthioninium chloride.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Solution for injection (injection)
Clear dark blue solution with a pH value between 3.0 and 4.5
Osmolality is usually between 10 and 15 mOsm/kg.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Acute symptomatic treatment of medicinal and chemical products-induced
methaemoglobinaemia.
Methylthioninium chloride Proveblue is indicated in adults, children
and adolescents (aged 0 to
17 years old).
_ _
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Methylthioninium chloride Proveblue
is for administration by a healthcare professional.
Posology
_ _
_Adults _
_ _
The usual dose is 1 to 2 mg per kg body weight, i.e. 0.2-0.4 ml per kg
body weight, given over a
period of 5 minutes.
A repeat dose (1 to 2 mg/kg body weight, i.e. 0.2-0.4 ml/kg body
weight) may be given one hour after
the first dose in cases of persistent or recurrent symptoms or if
methaemoglobin levels remain
significantly higher than the normal clinical range.
Treatment does not usually exceed one day.
The maximum recommended cumulative dose for the course of treatment is
7 mg/kg and should not be
exceeded, since Methylthioninium chloride administered above the
maximum dose may cause
methaemoglobinaemia in susceptible patients.
In the case of aniline- or dapsone-induced methaemaglobinaemia, the
maximum recommended
cumulative dose for the course of treatment is 4 mg/kg (see section
4.4).
Too limited data are available to support a continuous infusion dose
recommendation.
_ _
_ _
_ _
3
Special populations
_ _
_Elderly _
_ _
No dose adjustment is necessary.
_Renal impairment _
_ _
In infants above 3 months, children and 
                                
                                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 14-03-2024
产品特点 产品特点 保加利亚文 14-03-2024
公众评估报告 公众评估报告 保加利亚文 07-05-2018
资料单张 资料单张 西班牙文 14-03-2024
产品特点 产品特点 西班牙文 14-03-2024
公众评估报告 公众评估报告 西班牙文 07-05-2018
资料单张 资料单张 捷克文 14-03-2024
产品特点 产品特点 捷克文 14-03-2024
公众评估报告 公众评估报告 捷克文 07-05-2018
资料单张 资料单张 丹麦文 14-03-2024
产品特点 产品特点 丹麦文 14-03-2024
公众评估报告 公众评估报告 丹麦文 07-05-2018
资料单张 资料单张 德文 14-03-2024
产品特点 产品特点 德文 14-03-2024
公众评估报告 公众评估报告 德文 07-05-2018
资料单张 资料单张 爱沙尼亚文 14-03-2024
产品特点 产品特点 爱沙尼亚文 14-03-2024
公众评估报告 公众评估报告 爱沙尼亚文 07-05-2018
资料单张 资料单张 希腊文 14-03-2024
产品特点 产品特点 希腊文 14-03-2024
公众评估报告 公众评估报告 希腊文 07-05-2018
资料单张 资料单张 法文 14-03-2024
产品特点 产品特点 法文 14-03-2024
公众评估报告 公众评估报告 法文 07-05-2018
资料单张 资料单张 意大利文 14-03-2024
产品特点 产品特点 意大利文 14-03-2024
公众评估报告 公众评估报告 意大利文 07-05-2018
资料单张 资料单张 拉脱维亚文 14-03-2024
产品特点 产品特点 拉脱维亚文 14-03-2024
公众评估报告 公众评估报告 拉脱维亚文 07-05-2018
资料单张 资料单张 立陶宛文 14-03-2024
产品特点 产品特点 立陶宛文 14-03-2024
公众评估报告 公众评估报告 立陶宛文 07-05-2018
资料单张 资料单张 匈牙利文 14-03-2024
产品特点 产品特点 匈牙利文 14-03-2024
公众评估报告 公众评估报告 匈牙利文 07-05-2018
资料单张 资料单张 马耳他文 14-03-2024
产品特点 产品特点 马耳他文 14-03-2024
公众评估报告 公众评估报告 马耳他文 07-05-2018
资料单张 资料单张 荷兰文 14-03-2024
产品特点 产品特点 荷兰文 14-03-2024
公众评估报告 公众评估报告 荷兰文 07-05-2018
资料单张 资料单张 波兰文 14-03-2024
产品特点 产品特点 波兰文 14-03-2024
公众评估报告 公众评估报告 波兰文 07-05-2018
资料单张 资料单张 葡萄牙文 14-03-2024
产品特点 产品特点 葡萄牙文 14-03-2024
公众评估报告 公众评估报告 葡萄牙文 07-05-2018
资料单张 资料单张 罗马尼亚文 14-03-2024
产品特点 产品特点 罗马尼亚文 14-03-2024
公众评估报告 公众评估报告 罗马尼亚文 07-05-2018
资料单张 资料单张 斯洛伐克文 14-03-2024
产品特点 产品特点 斯洛伐克文 14-03-2024
公众评估报告 公众评估报告 斯洛伐克文 07-05-2018
资料单张 资料单张 斯洛文尼亚文 14-03-2024
产品特点 产品特点 斯洛文尼亚文 14-03-2024
公众评估报告 公众评估报告 斯洛文尼亚文 07-05-2018
资料单张 资料单张 芬兰文 14-03-2024
产品特点 产品特点 芬兰文 14-03-2024
公众评估报告 公众评估报告 芬兰文 07-05-2018
资料单张 资料单张 瑞典文 14-03-2024
产品特点 产品特点 瑞典文 14-03-2024
公众评估报告 公众评估报告 瑞典文 07-05-2018
资料单张 资料单张 挪威文 14-03-2024
产品特点 产品特点 挪威文 14-03-2024
资料单张 资料单张 冰岛文 14-03-2024
产品特点 产品特点 冰岛文 14-03-2024
资料单张 资料单张 克罗地亚文 14-03-2024
产品特点 产品特点 克罗地亚文 14-03-2024
公众评估报告 公众评估报告 克罗地亚文 07-05-2018

搜索与此产品相关的警报