PMS-METOPROLOL-L TABLET

Ország: Kanada

Nyelv: angol

Forrás: Health Canada

Aktív összetevők:

METOPROLOL TARTRATE

Beszerezhető a:

PHARMASCIENCE INC

ATC-kód:

C07AB02

INN (nemzetközi neve):

METOPROLOL

Adagolás:

50MG

Gyógyszerészeti forma:

TABLET

Összetétel:

METOPROLOL TARTRATE 50MG

Az alkalmazás módja:

ORAL

db csomag:

100/500/1000

Recept típusa:

Prescription

Terápiás terület:

BETA-ADRENERGIC BLOCKING AGENTS

Termék összefoglaló:

Active ingredient group (AIG) number: 0111923002; AHFS:

Engedélyezési státusz:

APPROVED

Engedély dátuma:

1997-03-10

Termékjellemzők

PRODUCT MONOGRAPH
PR
PMS-METOPROLOL-L
Metoprolol Tartrate Tablets, USP
25 mg, 50 mg and 100 mg
Β-ADRENERGIC RECEPTOR BLOCKING AGENT
PHARMASCIENCE INC.
6111 Royalmount Ave., Suite 100
Montréal, Canada
H4P 2T4
DATE OF REVISION:
September 24, 2020
www.pharmascience.com
SUBMISSION CONTROL NO: 240530
_pms-METOPROLOL-L Product Monograph _
_Page 2 of 39_
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
..................................................................................................11
DRUG INTERACTIONS
..................................................................................................13
DOSAGE AND ADMINISTRATION
..............................................................................17
OVERDOSAGE
................................................................................................................20
ACTION AND CLINICAL PHARMACOLOGY
............................................................21
STORAGE AND STABILITY
..........................................................................................24
DOSAGE FORMS, COMPOSITION AND PACKAGING
.............................................25
PART II: SCIENTIFIC INFORMATION
...............................................................................26
PHARMACEUTICAL INFORMATION
..........................................................................26
DETAILED PHARMACOLOGY
.....................................................................................27
TOXICOLOGY
...............................