MELPHALAN RAZ 50 MG

国家: 以色列

语言: 英文

来源: Ministry of Health

现在购买

下载 产品特点 (SPC)
02-08-2023
下载 公众评估报告 (PAR)
04-04-2021

有效成分:

MELPHALAN AS HYDROCHLORIDE

可用日期:

RAZ PHARMACEUTICS LTD, ISRAEL

ATC代码:

L01AA03

药物剂型:

POWDER AND SOLVENT FOR SOLUTION FOR INJECTION/INFUSION

组成:

MELPHALAN AS HYDROCHLORIDE 50 MG

给药途径:

I.V

处方类型:

Not required

厂商:

TILLOMED LABORATORIES LIMITED, UK

治疗领域:

MELPHALAN

疗效迹象:

For the palliative treatment of multiple myeloma and for the palliation of non resectable epithelial cancer of the ovary.

授权日期:

2020-12-06

产品特点

                                SUMMARY OF PRODUCT CHARACTERISTICS
1. Name of the medicinal product
MELPHALAN RAZ 50 MG
2. Qualitative and quantitative composition
Each vial of powder contains melphalan hydrochloride equivalent to 50
mg melphalan.
Each vial of solvent contains 10 ml of solvent.
Each ml of the reconstituted solution contains 5 mg melphalan.
Excipient(s) with known effect:
Each vial of solvent contains 0.4243 g ethanol and 6.2148 g propylene
glycol.
Each vial of solvent contains 53.5 mg sodium.
For the full list of excipients, see section 6.1.
3. Pharmaceutical form
Powder and solvent for solution for injection/infusion.
Powder: White to pale yellow lyophilized powder/cake.
Solvent: A clear colourless solution
.
4. Clinical particulars
4.1Therapeutic indications
For the palliative treatment of multiple myeloma and for the
palliation of non resectable epithelial cancer of the ovary.
4.2 Posology and method of administration
Melphalan is a cytotoxic drug which falls into the general class of
alkylating agents. It should be prescribed only by
physicians experienced in the management of malignant disease with
such agents.
Since melphalan is myelosuppressive, frequent blood counts are
essential during therapy and the dosage should be
delayed or adjusted if necessary (See section 4.4)
P
osology
P
arenteral administration:
For intravenous administration, it is recommended that MELPHALAN RAZ
50 MG solution is injected slowly into a
fast-running infusion solution via a swabbed injection port.
If direct injection into a fast-running infusion is not appropriate,
MELPHALAN RAZ 50 MG solution may be
administered diluted in an infusion bag.
Melphalan is not compatible with infusion solutions containing
dextrose, and it is recommended that ONLY Sodium
Chloride intravenous infusion 0.9% w/v is used.
When further diluted in an infusion solution, MELPHALAN RAZ 50 MG has
reduced stability and the rate of
degradation increases rapidly with rise in temperature. If
administration occurs at a room temperature of
approximately 25°C, the total time from
                                
                                阅读完整的文件
                                
                            

搜索与此产品相关的警报