PEMETREXED DISODIUM FOR INJECTION Poudre pour solution

국가: 캐나다

언어: 프랑스어

출처: Health Canada

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Download 제품 특성 요약 (SPC)
24-08-2018

유효 성분:

Pémétrexed (Hémipentahydrate de pémétrexed disodique)

제공처:

MARCAN PHARMACEUTICALS INC

ATC 코드:

L01BA04

INN (국제 이름):

PEMETREXED

복용량:

500MG

약제 형태:

Poudre pour solution

구성:

Pémétrexed (Hémipentahydrate de pémétrexed disodique) 500MG

관리 경로:

Intraveineuse

패키지 단위:

50ML

처방전 유형:

Prescription

치료 영역:

ANTINEOPLASTIC AGENTS

제품 요약:

Numéro de groupe d'ingrédients actifs (GIA) :0150104001; AHFS:

승인 상태:

APPROUVÉ

승인 날짜:

2018-02-02

제품 특성 요약

                                Page 1 of 61
PRODUCT MONOGRAPH
PR
PEMETREXED DISODIUM FOR INJECTION
Mfr. Std.
500 mg pemetrexed per vial (as pemetrexed disodium hemipentahydrate)
Sterile Lyophilized Powder
Antineoplastic Agent
Marcan Pharmaceuticals Inc.
Date of Preparation:
2 Gurdwara Road, Suite #112
August 24, 2018
Ottawa, ON, K2E 1A2
Control # 218069
Page 2 of 61
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
......................................................... 3
SUMMARY PRODUCT INFORMATION
........................................................................
3
INDICATIONS AND CLINICAL USE
.............................................................................
3
CONTRAINDICATIONS
...................................................................................................
4
WARNINGS AND PRECAUTIONS
.................................................................................
4
ADVERSE REACTIONS
...................................................................................................
7
DRUG
INTERACTIONS..................................................................................................
20
DOSAGE AND
ADMINISTRATION..............................................................................
19
OVERDOSAGE
................................................................................................................
24
ACTION AND CLINICAL PHARMACOLOGY
............................................................ 25
STORAGE AND STABILITY
.........................................................................................
27
SPECIAL HANDLING INSTRUCTIONS
.......................................................................
27
DOSAGE FORMS, COMPOSITION AND PACKAGING
............................................. 27
PART II: SCIENTIFIC
INFORMATION...............................................................................
28
PHARMACEUTICAL INFORMATION
.........................................................................
28
CLINICAL TRIALS
......................................
                                
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