FOSAMAX 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)
24-09-2010

有効成分:

ALENDRONIC ACID (ALENDRONATE SODIUM)

から入手可能:

MERCK CANADA INC

ATCコード:

M05BA04

INN(国際名):

ALENDRONIC ACID

投薬量:

10MG

医薬品形態:

TABLET

構図:

ALENDRONIC ACID (ALENDRONATE SODIUM) 10MG

投与経路:

ORAL

パッケージ内のユニット:

28

処方タイプ:

Prescription

治療領域:

BONE RESORPTION INHIBITORS

製品概要:

Active ingredient group (AIG) number: 0150323003; AHFS:

認証ステータス:

CANCELLED POST MARKET

承認日:

2011-11-10

製品の特徴

                                _ _
_Product Monograph – FOSAMAX_
_®_
_ _
_Page 1 of 50_
PRODUCT MONOGRAPH
FOSAMAX
®
alendronate sodium tablets
5 MG, 10 MG, 40 MG AND 70 MG ALENDRONATE
alendronate sodium oral solution
70 MG/75 ML ALENDRONATE
Bone Metabolism Regulator
MERCK FROSST CANADA LTD.
16711 Trans Canada Highway
Kirkland QC H9H 3L1
Canada
www.merckfrosst.com
DATE OF REVISION:
SEPTEMBER 10, 2010
SUBMISSION CONTROL NO: 139605
FOSAMAX
®
is a Registered Trademark of Merck Sharp & Dohme Corp., a subsidiary
of
MERCK & CO., INC.
Used
under license.
_ _
_Product Monograph – FOSAMAX_
_®_
_ _
_Page 2 of 50_
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
..................................................................................................13
DOSAGE AND
ADMINISTRATION..............................................................................15
OVERDOSAGE
................................................................................................................16
ACTION AND CLINICAL PHARMACOLOGY
............................................................16
STORAGE AND
STABILITY..........................................................................................21
DOSAGE FORMS, COMPOSITION AND PACKAGING
.............................................21
PART II: SCIENTIFIC INFORMATION
...............................................................................23
PHARMACEUTICAL
INFORMATION
                                
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