TOUJEO SOLOSTAR SOLUTION

Ország: Kanada

Nyelv: angol

Forrás: Health Canada

Aktív összetevők:

INSULIN GLARGINE

Beszerezhető a:

SANOFI-AVENTIS CANADA INC

ATC-kód:

A10AE04

INN (nemzetközi neve):

INSULIN GLARGINE

Adagolás:

300UNIT

Gyógyszerészeti forma:

SOLUTION

Összetétel:

INSULIN GLARGINE 300UNIT

Az alkalmazás módja:

SUBCUTANEOUS

db csomag:

3X1.5ML/ 5X1.5ML

Recept típusa:

Schedule D

Terápiás terület:

INSULINS

Termék összefoglaló:

Active ingredient group (AIG) number: 0147062002; AHFS:

Engedélyezési státusz:

APPROVED

Engedély dátuma:

2015-05-28

Termékjellemzők

_Page 1 of 88 _
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
TOUJEO
® SOLOSTAR
®
TOUJEO
® DOUBLESTAR
®
Insulin glargine (rDNA origin)
Solution for injection 300 U/mL
Antidiabetic Agent
Long-acting Recombinant Human Insulin Analogue
sanofi-aventis Canada Inc.
2905 Place Louis R.-Renaud
Laval, Quebec H7V 0A3
Date of Initial Approval:
May 28, 2015
Submission Control No: 228382
Date of Revision:
May 12, 2020
_Page 2 of 88 _
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
................................................ 3
SUMMARY PRODUCT INFORMATION
..........................................................................
3
DESCRIPTION
.....................................................................................................................
3
INDICATIONS AND CLINICAL USE
................................................................................
3
CONTRAINDICATIONS
.....................................................................................................
4
WARNINGS AND
PRECAUTIONS....................................................................................
4
ADVERSE REACTIONS
...................................................................................................
11
DRUG INTERACTIONS
....................................................................................................
19
DOSAGE AND ADMINISTRATION
................................................................................
20
OVERDOSAGE
..................................................................................................................
24
ACTION AND CLINICAL PHARMACOLOGY
.............................................................. 24
STORAGE AND
STABILITY............................................................................................
27
SPECIAL HANDLING INSTRUCTIONS
.........................................................................
27
DOSAGE FORMS, COMPOSITION AND PACKAGING
............................................... 29
PART II: SCIENTIFIC