ABSTRAL TABLET

Kraj: Kanada

Język: angielski

Źródło: Health Canada

Składnik aktywny:

FENTANYL (FENTANYL CITRATE)

Dostępny od:

PALADIN LABS INC.

Kod ATC:

N02AB03

INN (International Nazwa):

FENTANYL

Dawkowanie:

200MCG

Forma farmaceutyczna:

TABLET

Skład:

FENTANYL (FENTANYL CITRATE) 200MCG

Droga podania:

SUBLINGUAL

Sztuk w opakowaniu:

10/30

Typ recepty:

Narcotic (CDSA I)

Dziedzina terapeutyczna:

OPIATE AGONISTS

Podsumowanie produktu:

Active ingredient group (AIG) number: 0123302017; AHFS:

Status autoryzacji:

CANCELLED POST MARKET

Data autoryzacji:

2018-06-29

Charakterystyka produktu

_ _
_ABSTRAL Product Monograph _
_Page 1 of 64_
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
_ _
N
ABSTRAL
®
Fentanyl citrate sublingual tablets
100 mcg, 200 mcg, 300 mcg, 400 mcg, 600 mcg and 800 mcg fentanyl as
fentanyl citrate
Opioid Analgesic
Paladin Labs Inc.
100 Alexis Nihon Blvd, Suite 600
St-Laurent, Quebec H4M 2P2
Date of Preparation:
March 8, 2018
Version 7.0
Submission Control No: 210630
_ _
®
Registered trademark of Strakan International Limited
_ _
_ _
_ABSTRAL Product Monograph Page 2 of 64_
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
.........................................................3
SUMMARY PRODUCT INFORMATION
........................................................................3
INDICATIONS AND CLINICAL USE
..............................................................................3
CONTRAINDICATIONS
...................................................................................................4
WARNINGS AND PRECAUTIONS
..................................................................................6
ADVERSE REACTIONS
..................................................................................................15
DRUG INTERACTIONS
..................................................................................................22
DOSAGE AND ADMINISTRATION
..............................................................................23
OVERDOSAGE
................................................................................................................30
ACTION AND CLINICAL PHARMACOLOGY
............................................................31
STORAGE AND STABILITY
..........................................................................................36
SPECIAL HANDLING INSTRUCTIONS
.......................................................................36
DOSAGE FORMS, COMPOSITION AND PACKAGING
.............................................36
PART II: SCIENTIFIC INFORMATION
...........................................................