M-PILOCARPINE 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)
10-05-2021

有効成分:

PILOCARPINE HYDROCHLORIDE

から入手可能:

MANTRA PHARMA INC

ATCコード:

N07AX01

INN(国際名):

PILOCARPINE

投薬量:

5MG

医薬品形態:

TABLET

構図:

PILOCARPINE HYDROCHLORIDE 5MG

投与経路:

ORAL

パッケージ内のユニット:

15G/50G

処方タイプ:

Prescription

治療領域:

PARASYMPATHOMEMETIC (CHOLINERGIC) AGENTS

製品概要:

Active ingredient group (AIG) number: 0107358009; AHFS:

認証ステータス:

APPROVED

承認日:

2020-02-06

製品の特徴

                                _M-Pilocarpine Product Monograph_
_Page 1 of 30_
PRODUCT MONOGRAPH
PR
M-PILOCARPINE
PILOCARPINE HYDROCHLORIDE TABLETS, USP
5 MG
CHOLINOMIMETIC AGENT
Mantra Pharma Inc.
9150 Leduc Blvd, Suite 201
Brossard, QC, Canada
J4Y 0E3
Date of Revision:
May 10, 2021
Submission Control No.: 250828
_M-Pilocarpine Product Monograph _
_ _
_Page 2 of 30_
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
...................................................... 3
SUMMARY PRODUCT INFORMATION
.....................................................................
3
INDICATIONS AND CLINICAL USE
...........................................................................
3
CONTRAINDICATIONS
................................................................................................
3
WARNINGS AND PRECAUTIONS
..............................................................................
3
ADVERSE REACTIONS
................................................................................................
6
DRUG INTERACTIONS
...............................................................................................
10
DOSAGE AND ADMINISTRATION
...........................................................................
10
OVERDOSAGE
.............................................................................................................
11
ACTION AND CLINICAL PHARMACOLOGY
......................................................... 12
STORAGE AND STABILITY
......................................................................................
16
DOSAGE FORMS, COMPOSITION AND PACKAGING
.......................................... 16
PART II: SCIENTIFIC INFORMATION
.............................................................................
17
PHARMACEUTICAL INFORMATION
......................................................................
17
CLINICAL TRIALS
.......................................................................................................
18
DETAILED PHARMACOLOGY
.................................................
                                
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