PHL-TERBINAFINE TABLET

País: Canadà

Idioma: anglès

Font: Health Canada

ingredients actius:

TERBINAFINE (TERBINAFINE HYDROCHLORIDE)

Disponible des:

PHARMEL INC

Codi ATC:

D01BA02

Designació comuna internacional (DCI):

TERBINAFINE

Dosis:

250MG

formulario farmacéutico:

TABLET

Composición:

TERBINAFINE (TERBINAFINE HYDROCHLORIDE) 250MG

Vía de administración:

ORAL

Unidades en paquete:

100

tipo de receta:

Prescription

Área terapéutica:

ALLYLAMINES

Resumen del producto:

Active ingredient group (AIG) number: 0132855002; AHFS:

Estat d'Autorització:

CANCELLED POST MARKET

Data d'autorització:

2016-10-25

Fitxa tècnica

PRODUCT MONOGRAPH
PR
PHL-TERBINAFINE
Terbinafine Tablets, USP
250 mg Terbinafine, as Terbinafine Hydrochloride
ANTIFUNGAL AGENT
PHARMEL INC.
6111 Royalmount Ave., Suite 100
Montréal, Québec
H4P 2T4
DATE OF REVISION:
October 03, 2016
SUBMISSION CONTROL NO.: 197968
_ _
_phl-TERBINAFINE Product Monograph _
_Page 2 of 42_
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
.........................................................................................................7
DRUG INTERACTIONS
........................................................................................................
10
DOSAGE AND ADMINISTRATION
....................................................................................
13
OVERDOSAGE
.....................................................................................................................
13
ACTION AND CLINICAL PHARMACOLOGY
................................................................... 14
STORAGE AND STABILITY
................................................................................................
15
DOSAGE FORMS, COMPOSITION AND PACKAGING
..................................................... 15
PART II: SCIENTIFIC INFORMATION
...........................................................................
16
PHARMACEUTICAL INFORMATION
................................................................................
16
CLINICAL TRIALS
..........................................................................................