IMOGAM RABIES PASTEURIZED SOLUTION

国: カナダ

言語: 英語

ソース: Health Canada

即購入

製品の特徴 製品の特徴 (SPC)
12-10-2016

有効成分:

RABIES IMMUNOGLOBULIN (HUMAN)

から入手可能:

SANOFI PASTEUR LIMITED

ATCコード:

J06BB05

INN(国際名):

RABIES IMMUNOGLOBULIN

投薬量:

150UNIT

医薬品形態:

SOLUTION

構図:

RABIES IMMUNOGLOBULIN (HUMAN) 150UNIT

投与経路:

INTRAMUSCULAR

パッケージ内のユニット:

2ML

処方タイプ:

Schedule D

治療領域:

SERUMS

製品概要:

Active ingredient group (AIG) number: 0110666002; AHFS:

認証ステータス:

CANCELLED POST MARKET

承認日:

2022-03-31

製品の特徴

                                SANOFI PASTEUR
SECTION 1.3.1
194 – IMOGAM
® RABIES PASTEURIZED
PRODUCT MONOGRAPH
Product Monograph Template – Schedule D
Page
1 of 21
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
IMOGAM
® RABIES PASTEURIZED
RABIES IMMUNE GLOBULIN, PASTEURIZED (HUMAN)
Solution for Injection (150 IU/mL)
2.0 mL vials and 10.0 mL vials
Passive Immunizing Agent for the Prevention of Rabies
ATC: Code J06BB05
Manufactured by:
DATE OF REVISION:
SANOFI PASTEUR SA
November 2015
Lyon, France
Distributed by:
DATE OF APPROVAL:
SANOFI PASTEUR LIMITED
December 9, 2015
Toronto, Ontario, Canada
SUBMISSION CONTROL NO: 177025
SANOFI PASTEUR
SECTION 1.3.1
194 – IMOGAM
® RABIES PASTEURIZED
PRODUCT MONOGRAPH
Product Monograph Template – Schedule D
Page
2 of 21
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
........................................................... 3
SUMMARY PRODUCT INFORMATION
......................................................................................
3
DESCRIPTION
.................................................................................................................................
3
INDICATIONS AND CLINICAL USE
...........................................................................................
3
CONTRAINDICATIONS
.................................................................................................................
8
WARNINGS AND PRECAUTIONS
...............................................................................................
8
ADVERSE REACTIONS
.................................................................................................................
9
DRUG INTERACTIONS
................................................................................................................
10
DOSAGE AND
ADMINISTRATION............................................................................................
10
OVERDOSAGE
..............................................................................................................................
12

                                
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