ORCIPRENALINE SYRUP

País: Canadá

Idioma: inglés

Fuente: Health Canada

Ingredientes activos:

ORCIPRENALINE SULFATE

Disponible desde:

AA PHARMA INC

Código ATC:

R03CB03

Designación común internacional (DCI):

ORCIPRENALINE

Dosis:

2MG

formulario farmacéutico:

SYRUP

Composición:

ORCIPRENALINE SULFATE 2MG

Vía de administración:

ORAL

Unidades en paquete:

250ML

tipo de receta:

Prescription

Área terapéutica:

SELECTIVE BETA 2-ADRENERGIC AGONISTS

Resumen del producto:

Active ingredient group (AIG) number: 0102598001; AHFS:

Estado de Autorización:

APPROVED

Fecha de autorización:

1997-11-10

Ficha técnica

_ORCIPRENALINE (Orciprenaline Sulfate Syrup) _
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_Page 1 of 23 _
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
ORCIPRENALINE
Orciprenaline Sulfate Syrup
Syrup 2 mg/mL and Oral
House Standard
Beta-Adrenergic Agonist
Bronchodilator
AA PHARMA INC.
1165 Creditstone Road, Unit #1
Vaughan, Ontario
L4K 4N7
www.aapharma.ca
Submission Control Number: 267347
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Date of Initial Authorization:
April
17, 2014
Date of Revision:
OCT
11,
2022
_ORCIPRENALINE (Orciprenaline Sulfate Syrup) _
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_ Page 2 of 23 _
RECENT MAJOR LABEL CHANGES
7 Warnings and Precautions
10/2022
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
.....................................................................................
5
4.1
Dosing Considerations
......................................................................................................
5
4.2
Recommended Dose and Dosage Adjustment
................................................................ 5
4.4
Administration
.............................................