PMS-FLUCONAZOLE TABLET

Valsts: Kanāda

Valoda: angļu

Klimata pārmaiņas: Health Canada

Nopērc to tagad

Lejuplādēt Produkta apraksts (SPC)
16-05-2023

Aktīvā sastāvdaļa:

FLUCONAZOLE

Pieejams no:

PHARMASCIENCE INC

ATĶ kods:

J02AC01

SNN (starptautisko nepatentēto nosaukumu):

FLUCONAZOLE

Deva:

50MG

Zāļu forma:

TABLET

Kompozīcija:

FLUCONAZOLE 50MG

Ievadīšanas:

ORAL

Vienības iepakojumā:

50

Receptes veids:

Prescription

Ārstniecības joma:

AZOLES

Produktu pārskats:

Active ingredient group (AIG) number: 0122529001; AHFS:

Autorizācija statuss:

APPROVED

Autorizācija datums:

2002-06-05

Produkta apraksts

                                _pms-FLUCONAZOLE – Product Monograph _
_ _
_Page 1 of 56_
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
PMS-FLUCONAZOLE
Fluconazole Tablets
Tablets, 50 mg and 100 mg, Oral
House Standard
Antifungal Agent
PHARMASCIENCE INC.
6111 Royalmount Ave., Suite 100
Montréal, Québec
H4P 2T4
www.pharmascience.com
Date of Initial Authorization:
June 5, 2002
Date of Revision:
May 16, 2023
Submission Control Number: 273867
_pms-FLUCONAZOLE – Product Monograph _
_ _
_Page 2 of 56_
RECENT MAJOR LABEL CHANGES
7 WARNINGS AND PRECAUTIONS
10/2022
9 DRUG INTERACTIONS
05/2023
TABLE OF CONTENTS
SECTIONS OR SUBSECTIONS THAT ARE NOT APPLICABLE AT THE TIME OF
AUTHORIZATION ARE NOT LISTED.
RECENT MAJOR LABEL CHANGES
.........................................................................................
2
TABLE OF CONTENTS
...........................................................................................................
2
PART I: HEALTH PROFESSIONAL INFORMATION
................................................................... 4
1
INDICATIONS
............................................................................................................
4
1.1
Pediatrics (<18 years of age)
..................................................................................
4
1.2
Geriatrics
.................................................................................................................
4
2
CONTRAINDICATIONS
..............................................................................................
5
4
DOSAGE AND ADMINISTRATION
..............................................................................
5
4.1
Dosing Considerations
............................................................................................
5
4.2
Recommended Dose and Dosage Adjustment
....................................................... 5
4.5
Missed Dose
............................................................................................................
8
5
OVERDOSAGE
....................................
                                
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