KALYDECO GRANULES

Country: Kanada

Lingwa: Ingliż

Sors: Health Canada

Ixtrih issa

Ingredjent attiv:

IVACAFTOR

Disponibbli minn:

VERTEX PHARMACEUTICALS (CANADA) INCORPORATED

Kodiċi ATC:

R07AX02

INN (Isem Internazzjonali):

IVACAFTOR

Dożaġġ:

75MG

Għamla farmaċewtika:

GRANULES

Kompożizzjoni:

IVACAFTOR 75MG

Rotta amministrattiva:

ORAL

Unitajiet fil-pakkett:

56 PACKETS

Tip ta 'preskrizzjoni:

Prescription

Żona terapewtika:

Cystic Fibrosis Transmembrane Conductance Regulator Potentiators

Sommarju tal-prodott:

Active ingredient group (AIG) number: 0153450003; AHFS:

L-istatus ta 'awtorizzazzjoni:

APPROVED

Data ta 'l-awtorizzazzjoni:

2015-06-12

Karatteristiċi tal-prodott

                                _ _
_Pr_
_KALYDECO_
_®_
_ (ivacaftor) Tablets and Granules _
_Page 1 of 43_
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
KALYDECO
®
Ivacaftor Tablets
Tablets: 150 mg, Oral
Ivacaftor Granules
Granules: 13.4 mg per packet, 25 mg per packet, 50 mg per packet, and
75 mg per packet,
Oral
Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Potentiator
ATC R07AX02
Vertex Pharmaceuticals (Canada) Incorporated
20 Bay Street, Suite 1520
Toronto, Ontario
M5J 2N8
Date of Initial Authorization:
Nov 26, 2012
Date of Revision:
Nov 27, 2023
Submission Control Number: 273575
_ _
_KALYDECO (ivacaftor) Tablets and Granules _
_Page 2 of 43_
RECENT MAJOR LABEL CHANGES
1 Indications
11/2023
1 Indications, 1.1 Pediatrics
11/2023
4 Dosage and Administration
11/2023
7 Warnings and Precautions
11/2023
7 Warnings and Precautions, 7.1.3 Pediatrics
11/2023
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
....................................................................................................
4
1.2
Geriatrics
....................................................................................................
4
2
CONTRAINDICATIONS
......................................................................................
4
4
DOSAGE AND ADMINISTRATION
.................................................................... 4
4.1
Dosing
Considerations................................................................................
4
4.2
Recommended Dose and Dosage Adjustment
.........................................
                                
                                Aqra d-dokument sħiħ
                                
                            

Dokumenti f'lingwi oħra

Karatteristiċi tal-prodott Karatteristiċi tal-prodott Franċiż 27-11-2023

Fittex twissijiet relatati ma 'dan il-prodott