ACH-LACOSAMIDE TABLET

Země: Kanada

Jazyk: angličtina

Zdroj: Health Canada

Koupit nyní

Aktivní složka:

LACOSAMIDE

Dostupné s:

ACCORD HEALTHCARE INC

ATC kód:

N03AX18

INN (Mezinárodní Name):

LACOSAMIDE

Dávkování:

200MG

Léková forma:

TABLET

Složení:

LACOSAMIDE 200MG

Podání:

ORAL

Jednotky v balení:

15G/50G

Druh předpisu:

Prescription

Terapeutické oblasti:

MISCELLANEOUS ANTICONVULSANTS

Přehled produktů:

Active ingredient group (AIG) number: 0152810004; AHFS:

Stav Autorizace:

APPROVED

Datum autorizace:

2019-06-10

Charakteristika produktu

                                _Product Monograph_
_-ACH-LACOSAMIDE _
_ Page 1 of 42_
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
ACH-LACOSAMIDE
lacosamide tablets
Tablets, 50 mg, 100 mg, 150 mg, 200 mg, Oral
Antiepileptic
ATC Code: N03AX18
Accord Healthcare Inc.
3535 boul. St. Charles, Suite 704
Kirkland, QC, H9H 5B9
Canada
Date of Initial Authorization:
June 10, 2019
Date of Revision:
January 24, 2023
Submission Control Number: 269505
_Product Monograph_
_-ACH-LACOSAMIDE _
_ Page 2 of 42_
RECENT MAJOR LABEL CHANGES
7 Warnings and Precautions, 7.1.1 Pregnant Women
12/2022
7 Warnings and Precautions, 7.1.2 Breast-feeding
12/2022
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
......................................................... 4
4.4
Administration
....................................................................................
                                
                                Přečtěte si celý dokument
                                
                            

Dokumenty v jiných jazycích

Charakteristika produktu Charakteristika produktu francouzština 24-01-2023

Vyhledávejte upozornění související s tímto produktem

Zobrazit historii dokumentů