GADOPENTETATE DIMEGLUMINE INJECTION, USP 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)
08-10-2014

有効成分:

GADOPENTETATE DIMEGLUMINE

から入手可能:

JUBILANT DRAXIMAGE INC. DBA JUBILANT RADIOPHARMA

ATCコード:

V08CA01

INN(国際名):

GADOPENTETIC ACID

投薬量:

469MG

医薬品形態:

SOLUTION

構図:

GADOPENTETATE DIMEGLUMINE 469MG

投与経路:

INTRAVENOUS

パッケージ内のユニット:

5/10/15/20ML

処方タイプ:

Ethical

治療領域:

OTHER DIAGNOSTIC AGENTS

製品概要:

Active ingredient group (AIG) number: 0123846001; AHFS:

認証ステータス:

CANCELLED PRE MARKET

承認日:

2022-05-17

製品の特徴

                                JUBILANT DRAXIMAGE INC.
MODULE 1 ADMINISTRATIVE
GADOPENTETATE DIMEGLUMINE INJECTION, USP
1.3.1 PRODUCT MONOGRAPH
1
PRODUCT MONOGRAPH
GADOPENTETATE DIMEGLUMINE INJECTION, USP
469 mg/mL (0.5 mmol/mL)
For Intravenous Use
THERAPEUTIC CLASSIFICATION
Contrast Enhancement Agent
for Magnetic Resonance Imaging (MRI)
Jubilant DraxImage Inc.
Date of Preparation:
16751 Trans Canada Hwy
September 12, 2014
Kirkland, Quebec
H9H 4J4
Canada
http://www. draximage.com
Submission Control No.: 160553
JUBILANT DRAXIMAGE INC.
MODULE 1 ADMINISTRATIVE
GADOPENTETATE DIMEGLUMINE INJECTION, USP
1.3.1 PRODUCT MONOGRAPH
2
TABLE OF CONTENTS
1.3.1
PRODUCT MONOGRAPH – NON-ANNOTATED ....... ERROR! BOOKMARK NOT
DEFINED.
PART I: HEALTH PROFESSIONAL INFORMATION
......................................................... 4
ACTION
AND
CLINICAL
PHARMACOLOGY
......................................................................
4
INDICATIONS
AND
CLINICAL
USE
.....................................................................................
5
CONTRAINDICATIONS
..........................................................................................................
5
WARNINGS
...............................................................................................................................
6
_General
...................................................................................................................................
7_
_Nephrogenic Systemic Fibrosis (NSF)
....................................................................................
7_
_Hypersensitivity Reactions
......................................................................................................
8_
_Injection Site
Reactions...........................................................................................................
8_
_Sickle
Erythrocytes..................................................................................................................
9_
_Renal
Impairment....................................................................
                                
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