CYTARABINE INJECTION BP SOLUTION

国家: 加拿大

语言: 英文

来源: Health Canada

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06-12-2017

有效成分:

CYTARABINE

可用日期:

SANDOZ CANADA INCORPORATED

ATC代码:

L01BC01

INN(国际名称):

CYTARABINE

剂量:

100MG

药物剂型:

SOLUTION

组成:

CYTARABINE 100MG

给药途径:

INTRATHECAL

每包单位数:

1/5/10/20ML

处方类型:

Prescription

治疗领域:

ANTINEOPLASTIC AGENTS

產品總結:

Active ingredient group (AIG) number: 0108854005; AHFS:

授权状态:

CANCELLED PRE MARKET

授权日期:

2019-08-01

产品特点

                                _ _
_Cytarabine Injection BP _
_Page 1 of 41_
PRODUCT MONOGRAPH
PR
CYTARABINE INJECTION BP
100 mg / mL
(100 mg / 1 mL, 500 mg / 5 mL, 1 g / 10 mL, 2 g / 20 mL)
Antileukemic Agent
Sandoz Canada Inc.
145, Jules-Léger
Boucherville, Quebec
J4B 7K8
Date of Revision:
December 06, 2017
Submission Control No: 199911
_ _
_Cytarabine Injection BP _
_Page 2 of 41_
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
......................................................... 3
SUMMARY PRODUCT INFORMATION
.......................................................................
3
INDICATIONS AND CLINICAL USE
.............................................................................
3
CONTRAINDICATIONS
..................................................................................................
3
WARNINGS AND PRECAUTIONS
.................................................................................
4
ADVERSE REACTIONS
...................................................................................................
9
DRUG INTERACTIONS
.................................................................................................
13
DOSAGE AND ADMINISTRATION
.............................................................................
14
OVERDOSAGE
...............................................................................................................
21
ACTION AND CLINICAL PHARMACOLOGY
........................................................... 21
STORAGE AND STABILITY
.........................................................................................
23
SPECIAL HANDLING INSTRUCTIONS
......................................................................
23
DOSAGE FORMS, COMPOSITION AND PACKAGING
............................................ 24
PART II: SCIENTIFIC INFORMATION
...............................................................................
25
PHARMACEUTICAL INFORMATION
.........................................................................
25
DETAILED PHARMACOLOGY
..................
                                
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