Država: Kanada
Jezik: angleščina
Source: Health Canada
CARVEDILOL
DOMINION PHARMACAL
C07AG02
CARVEDILOL
6.25MG
TABLET
CARVEDILOL 6.25MG
ORAL
100
Prescription
BETA-ADRENERGIC BLOCKING AGENTS
Active ingredient group (AIG) number: 0122683004; AHFS:
APPROVED
2004-02-18
PRODUCT MONOGRAPH PR DOM-CARVEDILOL Carvedilol Tablets, House Standard 3.125, 6.25, 12.5 and 25 mg CONGESTIVE HEART FAILURE AGENT DOMINION PHARMACAL 6111 Royalmount Ave., Suite 100 Montréal, Québec H4P 2T4 DATE OF REVISION: September 1 2016 SUBMISSION CONTROL NO.: 197191 _ _ _Dom-CARVEDILOL 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 ...................................................................................................3 WARNINGS AND PRECAUTIONS ..................................................................................4 ADVERSE REACTIONS ....................................................................................................9 DRUG INTERACTIONS ..................................................................................................15 DOSAGE AND ADMINISTRATION ..............................................................................17 OVERDOSAGE ................................................................................................................19 ACTION AND CLINICAL PHARMACOLOGY ............................................................20 STORAGE AND STABILITY ..........................................................................................23 DOSAGE FORMS, COMPOSITION AND PACKAGING ..............................................23 PART II: SCIENTIFIC INFORMATION ...............................................................................25 PHARMACEUTICAL INFORMATION ..........................................................................25 CLINICAL TRIALS ..........................................................................................................26 DETAILED PHARMACOLOGY ....................... Preberite celoten dokument