LEFLUNOMIDE TABLET

国: カナダ

言語: 英語

ソース: Health Canada

即購入

ダウンロード 製品の特徴 (SPC)
11-07-2023

有効成分:

LEFLUNOMIDE

から入手可能:

PRO DOC LIMITEE

ATCコード:

L04AK01

INN(国際名):

LEFLUNOMIDE

投薬量:

10MG

医薬品形態:

TABLET

構図:

LEFLUNOMIDE 10MG

投与経路:

ORAL

パッケージ内のユニット:

30

処方タイプ:

Prescription

治療領域:

DISEASE-MODIFYING ANTIRHEUMATIC AGENTS

製品概要:

Active ingredient group (AIG) number: 0140182001; AHFS:

認証ステータス:

APPROVED

承認日:

2016-01-14

製品の特徴

                                _ _
_Leflunomide (Leflunomide Tablets) _
_Page 1 of 79 _
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
Pr
LEFLUNOMIDE
Leflunomide Tablets
Film-coated Tablets, 10 mg and 20 mg, Oral
BP
Antirheumatic, Immunomodulator Agent
ATC Code: L04AA13
Pro Doc Ltée
2925 boul. Industriel
Laval, Québec
H7L 3W9
Date of Initial Authorization:
NOV 26, 2013
Date of Revision:
JUL 11, 2023
Submission Control Number: 276418
_ _
_Leflunomide (Leflunomide Tablets) _
_Page 2 of 79 _
RECENT MAJOR LABEL CHANGES
7 WARNINGS AND PRECAUTIONS
07/2023
TABLE OF CONTENTS
SECTIONS OR SUBSECTIONS THAT ARE NOT APPLICABLE AT THE TIME OF
AUTHORIZATION ARE NOT LISTED.
RECENT MAJOR LABEL CHANGES
...........................................................................................
2
TABLE OF CONTENTS
............................................................................................................
2
PART I: HEALTH PROFESSIONAL INFORMATION
.....................................................................
4
1
INDICATIONS
..............................................................................................................
4
1.1 Pediatrics
......................................................................................................................
4
1.2
Geriatrics
.......................................................................................................................
4
2
CONTRAINDICATIONS
.................................................................................................
4
4
DOSAGE AND ADMINISTRATION
.................................................................................
5
4.2
Recommended Dose and Dosage Adjustment
............................................................. 5
4.4
Administration
..............................................................................................................
6
4.5
Missed Dose
..................................................................................................................
6
5
OVERDOSAGE
...................
                                
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