GLUCAGON KIT

Riik: Kanada

keel: inglise

Allikas: Health Canada

Toimeaine:

GLUCAGON (RECOMBINANT DNA ORIGIN)

Saadav alates:

ELI LILLY CANADA INC

ATC kood:

H04AA01

INN (Rahvusvaheline Nimetus):

GLUCAGON

Annus:

1MG

Ravimvorm:

KIT

Koostis:

GLUCAGON (RECOMBINANT DNA ORIGIN) 1MG

Manustamisviis:

INTRAMUSCULAR

Ühikuid pakis:

1 ML

Retsepti tüüp:

Schedule D

Terapeutiline ala:

GLYCOGENOLYTIC AGENTS

Toote kokkuvõte:

Active ingredient group (AIG) number: 0142861001; AHFS:

Volitamisolek:

CANCELLED POST MARKET

Loa andmise kuupäev:

2023-12-18

Toote omadused

GLUCACON (rDNA Origin) Product Monograph
Page 1 of 32
PRODUCT MONOGRAPH
GLUCAGON
GLUCAGON FOR INJECTION, RDNA ORIGIN
1 MG GLUCAGON PER VIAL
Sterile Lyophilized Powder and Diluent
Hyperglycemic Agent
©
Eli Lilly Canada Inc.
3650 Danforth Avenue
Toronto, Ontario
M1N 2E8
1-888-545-5972
Date of Approval:
July 9, 2012
www.lilly.ca
Submission Control No: 139332
GLUCACON (rDNA Origin) Product Monograph
Page 2 of 32
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
......................................................... 3
SUMMARY PRODUCT INFORMATION
..............................................................................
3
INDICATIONS AND CLINICAL USE
...................................................................................
3
CONTRAINDICATIONS
.........................................................................................................
4
ADVERSE REACTIONS
.........................................................................................................
6
DRUG INTERACTION
............................................................................................................
8
DOSAGE AND ADMINISTRATION
.....................................................................................
9
OVERDOSAGE
......................................................................................................................
11
ACTION AND CLINICAL PHARMACOLOGY
.................................................................. 12
STORAGE AND STABILITY
...............................................................................................
13
DOSAGE FORMS, COMPOSITION AND PACKAGING
................................................... 13
PART II: SCIENTIFIC INFORMATION
..............................................................................
14
PHARMACEUTICAL INFORMATION
...............................................................................
14
CLINICAL TRIALS
...........................................................................................................