TEVA-FENTANYL PATCH

Valsts: Kanāda

Valoda: angļu

Klimata pārmaiņas: Health Canada

Aktīvā sastāvdaļa:

FENTANYL

Pieejams no:

TEVA CANADA LIMITED

ATĶ kods:

N02AB03

SNN (starptautisko nepatentēto nosaukumu):

FENTANYL

Deva:

25MCG

Zāļu forma:

PATCH

Kompozīcija:

FENTANYL 25MCG

Ievadīšanas:

TRANSDERMAL

Vienības iepakojumā:

5

Receptes veids:

Narcotic (CDSA I)

Ārstniecības joma:

OPIATE AGONISTS

Produktu pārskats:

Active ingredient group (AIG) number: 0123302014; AHFS:

Autorizācija statuss:

APPROVED

Autorizācija datums:

2006-07-04

Produkta apraksts

_ _
_TEVA-FENTANYL (12, 25, 50, 75 and 100 mcg/h) _
_ Page 1 of 60_
PRODUCT MONOGRAPH
N
TEVA-FENTANYL
FENTANYL TRANSDERMAL SYSTEM
PATCH, 12 MCG/H, 25 MCG/H, 50 MCG/H, 75 MCG/H AND 100 MCG/H
Opioid Analgesic
Teva Canada Limited
30 Novopharm Court
Toronto, Ontario
Canada M1B 2K9
www.tevacanada.com
Date of Revision:
June 10, 2022
Submission
Control No: 257888
_ _
_TEVA-FENTANYL (12, 25, 50, 75 and 100 mcg/h) _
_ Page 2 of 60_
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............................................................................................
18
DRUG INTERACTIONS
............................................................................................
21
DOSAGE AND ADMINISTRATION
.........................................................................
23
OVERDOSAGE
.........................................................................................................
30
ACTION AND CLINICAL
PHARMACOLOGY.........................................................
31
STORAGE AND STABILITY
....................................................................................
34
SPECIAL HANDLING INSTRUCTIONS
................................................................... 34
DOSAGE FORMS, COMPOSITION AND PACKAGING
.......................................... 35
PART II: SCIENTIFIC INFORMATION
..........................................................................
37
PHARMACEUTICAL INFORMATION
.....................................................................
37
CLINICAL TRIALS
......................