NOVORAPID SOLUTION

Country: Kanada

Tungumál: enska

Heimild: Health Canada

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Vara einkenni Vara einkenni (SPC)
12-08-2021

Virkt innihaldsefni:

INSULIN ASPART

Fáanlegur frá:

NOVO NORDISK CANADA INC

ATC númer:

A10AB05

INN (Alþjóðlegt nafn):

INSULIN ASPART

Skammtar:

100UNIT

Lyfjaform:

SOLUTION

Samsetning:

INSULIN ASPART 100UNIT

Stjórnsýsluleið:

SUBCUTANEOUS

Einingar í pakka:

10 ML

Gerð lyfseðils:

Schedule D

Lækningarsvæði:

INSULINS

Vörulýsing:

Active ingredient group (AIG) number: 0144802001; AHFS:

Leyfisstaða:

APPROVED

Leyfisdagur:

2001-07-18

Vara einkenni

                                _ _
_Product Monograph Master Template _
_Template Date: September 2020 _
_NovoRapid_
_® _
_Insulin Aspart _
_Page 1 of 52_
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
NOVORAPID
®
Insulin Aspart
Solution for Injection, 100 Units/mL, Subcutaneous Injection
Professed Standard
Anti-diabetic Agent
ATC code: A10AB05
fast-acting
Novo Nordisk Canada Inc.
101-2476 Argentia Road
Mississauga, Ontario
L5N 6M1 Canada
Date of Initial Authorization:
APR 06, 2018
Date of Revision:
AUG 12, 2021
Submission Control Number: 251029
_ _
_Product Monograph Master Template _
_Template Date: September 2020 _
_NovoRapid_
_® _
_Insulin Aspart _
_Page 2 of 52_
RECENT MAJOR LABEL CHANGES
4.4 Administration
03/2021
7 Warnings and Precautions
03/2021
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
1
INDICATIONS.............................................................................................................
4
1.1
Pediatrics
..........................................................................................................
4
1.2
Geriatrics...........................................................................................................
4
2
CONTRAINDICATIONS
..............................................................................................
4
3
SERIOUS WARNINGS AND PRECAUTIONS
BOX..................................................... 4
4
DOSAGE AND ADMINISTRATION
.............................................................................
5
4.1
Dosing Considerations
.......................................................................................
5
4.2
Recommended Dose and Dosage Adjustment
................................................... 5
4.4
Administration.........................
                                
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