PMS-RISEDRONATE PLUS CALCIUM TABLET

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)
14-06-2016

有効成分:

RISEDRONATE SODIUM (RISEDRONATE SODIUM HEMIPENTAHYDRATE); CALCIUM (CALCIUM CARBONATE)

から入手可能:

PHARMASCIENCE INC

ATCコード:

M05BB02

INN(国際名):

RISEDRONIC ACID AND CALCIUM, SEQUENTIAL

投薬量:

35MG; 500MG

医薬品形態:

TABLET

構図:

RISEDRONATE SODIUM (RISEDRONATE SODIUM HEMIPENTAHYDRATE) 35MG; CALCIUM (CALCIUM CARBONATE) 500MG

投与経路:

ORAL

パッケージ内のユニット:

100

処方タイプ:

Prescription

治療領域:

BONE RESORPTION INHIBITORS

製品概要:

Active ingredient group (AIG) number: 0251633001; AHFS:

認証ステータス:

APPROVED

承認日:

2011-02-17

製品の特徴

                                PRODUCT MONOGRAPH
PR PMS-RISEDRONATE PLUS CALCIUM
Risedronate Sodium (as the hemi-pentahydrate) 35 mg Tablets, House
Standard
BONE METABOLISM REGULATOR
and
Calcium Carbonate 1250 mg Caplets, House Standard
(Equivalent to 500 mg elemental calcium)
MINERAL SUPPLEMENT
PHARMASCIENCE INC.
DATE OF REVISION:
6111 Royalmount Avenue, Suite 100,
June 08, 2016
Montreal QC, H4P 2T4
www.pharmascience.com
Control Number: 195294
_ _
_pms-RISEDRONATE PLUS CALCIUM - Product Monograph Page 2 of 38_
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
.............................................................. 3
SUMMARY PRODUCT INFORMATION
...............................................................................
3
INDICATIONS AND CLINICAL USE
.....................................................................................
3
CONTRAINDICATIONS
..........................................................................................................
4
WARNINGS AND PRECAUTIONS
.........................................................................................
5
ADVERSE
REACTIONS...........................................................................................................
7
DRUG INTERACTIONS
.........................................................................................................
10
DOSAGE AND ADMINISTRATION
.....................................................................................
13
OVERDOSAGE
.......................................................................................................................
15
ACTION AND CLINICAL PHARMACOLOGY
................................................................... 15
STORAGE AND STABILITY
.................................................................................................
19
DOSAGE FORMS, COMPOSITION AND PACKAGING
.................................................... 20
PART II: SCIENTIFIC INFORMATION
....................................................................................
21
PHARMACEUTICAL
INFORMA
                                
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製品の特徴 製品の特徴 フランス語 08-06-2016