TEVA-SALBUTAMOL STERINEBS P.F. SOLUTION

Šalis: Kanada

kalba: anglų

Šaltinis: Health Canada

Veiklioji medžiaga:

SALBUTAMOL (SALBUTAMOL SULFATE)

Prieinama:

TEVA CANADA LIMITED

ATC kodas:

R03AC02

INN (Tarptautinis Pavadinimas):

SALBUTAMOL

Dozė:

2MG

Vaisto forma:

SOLUTION

Sudėtis:

SALBUTAMOL (SALBUTAMOL SULFATE) 2MG

Vartojimo būdas:

INHALATION

Vienetai pakuotėje:

2.5ML UNIT DOSES(CARTON 20)

Recepto tipas:

Prescription

Gydymo sritis:

SELECTIVE BETA 2-ADRENERGIC AGONISTS

Produkto santrauka:

Active ingredient group (AIG) number: 0108887001; AHFS:

Autorizacija statusas:

APPROVED

Leidimo data:

2012-07-05

Prekės savybės

PRODUCT MONOGRAPH
PR
TEVA-SALBUTAMOL STERINEBS
TM P.F.
Salbutamol Sulphate Solution
1 mg / mL (2.5 mg / 2.5 mL) salbutamol per ampoule
2 mg / mL (5 mg / 2.5 mL) salbutamol per ampoule
Bronchodilator
(beta
2
-adrenergic agonist)
Teva Canada Limited
30 Novopharm Court
Toronto, Ontario
M1B 2K9
Canada
www.tevacanada.com
Submission Control No: 254982
Date of Revision::
Dec. 21, 2021
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
......................................................... 3
SUMMARY
PRODUCT
INFORMATION
.............................................................................
3
INDICATIONS
AND
CLINICAL
USE
......................................................................................
3
CONTRAINDICATIONS
...........................................................................................................
3
WARNINGS
AND
PRECAUTIONS
..........................................................................................
4
ADVERSE
REACTIONS
...........................................................................................................
7
DRUG
INTERACTIONS
............................................................................................................
9
DOSAGE
AND
ADMINISTRATION
......................................................................................
10
OVERDOSAGE
........................................................................................................................
12
ACTION
AND
CLINICAL
PHARMACOLOGY
.....................................................................
12
STORAGE
AND
STABILITY
..................................................................................................
14
DOSAGE
FORMS,
COMPOSITION
AND
PACKAGING ...................................................... 14
PART II: SCIENTIFIC INFORMATION
...............................................................................
15
PHARMACEUTICAL
INFORMATION..................................................................................
15
CLINICAL
TRIAL