TEVA-SIMVASTATIN TABLET

国: カナダ

言語: 英語

ソース: Health Canada

有効成分:

SIMVASTATIN

から入手可能:

TEVA CANADA LIMITED

ATCコード:

C10AA01

INN（国際名）:

SIMVASTATIN

投薬量:

10MG

医薬品形態:

TABLET

構図:

SIMVASTATIN 10MG

投与経路:

ORAL

パッケージ内のユニット:

100/500

処方タイプ:

Prescription

治療領域:

HMG-COA REDUCTASE INHIBITORS

製品概要:

Active ingredient group (AIG) number: 0122415004; AHFS:

認証ステータス:

APPROVED

承認日:

2004-03-19

製品の特徴

_TEVA-SIMVASTATIN Page 1 of 60 _
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
Pr
TEVA-SIMVASTATIN
Simvastatin Tablets
Tablets, 5 mg, 10 mg, 20 mg, 40 mg and 80 mg, Oral
USP
Lipid Metabolism Regulator
Teva Canada Limited
Date of Initial Authorization:
30 Novopharm Court
April 30, 2010
Toronto, ON
M1B 2K9
Date of Revision:
Canada
February 20, 2024
www.tevacanada.com
Submission Control Number: 279407
_TEVA-SIMVASTATIN Page 2 of 60 _
RECENT MAJOR LABEL CHANGES
7 Warnings and Precautions, Musculoskeletal
02/2024
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
..............................................................................................
5
4
DOSAGE AND ADMINISTRATION
..............................................................................
5
4.1
Dosing Considerations
.........................................................................................
5
4.2
Recommended Dose and Dosage Adjustment
..................................................... 6
4.4
Administration
.....................................................................................................
8
4.5
Missed Dose
...................................................................................