PMS-PREDNISOLONE SOLUTION

Ülke: Kanada

Dil: İngilizce

Kaynak: Health Canada

şimdi satın al

Indir Ürün özellikleri (SPC)
30-11-2022

Aktif bileşen:

PREDNISOLONE (PREDNISOLONE SODIUM PHOSPHATE)

Mevcut itibaren:

PHARMASCIENCE INC

ATC kodu:

H02AB06

INN (International Adı):

PREDNISOLONE

Doz:

5MG

Farmasötik formu:

SOLUTION

Kompozisyon:

PREDNISOLONE (PREDNISOLONE SODIUM PHOSPHATE) 5MG

Uygulama yolu:

ORAL

Paketteki üniteler:

120 ML

Reçete türü:

Prescription

Terapötik alanı:

ADRENALS

Ürün özeti:

Active ingredient group (AIG) number: 0106287004; AHFS:

Yetkilendirme durumu:

APPROVED

Yetkilendirme tarihi:

2002-03-08

Ürün özellikleri

                                PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
PMS-PREDNISOLONE
Prednisolone Oral Solution
Solution, 5 mg / 5 mL Prednisolone (as Prednisolone Sodium Phosphate),
Oral
House Standard
Glucocorticoid / Anti-Inflammatory
PHARMASCIENCE INC.
6111 Royalmount Ave., Suite 100
Montréal, Québec
H4P 2T4
www.pharmascience.com
Submission Control Number: 265215
Date of Initial Authorization
MAR 8, 2002
Date of Revision:
NOV 30, 2022
_pms-PREDNISOLONE Product Monograph _
_Page 2 of 33_
RECENT MAJOR LABEL CHANGES
2 CONTRAINDICATIONS
12/2020
7 WARNINGS AND PRECAUTIONS
12/2020
7 WARNINGS AND PRECAUTIONS, Endocrine and Metabolism
11/2022
7 WARNINGS AND PRECAUTIONS, 7.1.1 Pregnant Women
11/2022
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
2
CONTRAINDICATIONS........................................................................................................
4
4
DOSAGE AND ADMINISTRATION
.......................................................................................
4
4.1
Dosing Considerations
.............................................................................................4
4.2
Recommended Dose and Dosage
Adjustment...........................................................4
4.4
Administration.........................................................................................................5
4.5
Missed Dos
                                
                                Belgenin tamamını okuyun
                                
                            

Diğer dillerdeki belgeler

Ürün özellikleri Ürün özellikleri Fransızca 30-11-2022

Bu ürünle ilgili arama uyarıları

Belge geçmişini görüntüleyin