METHYLPREDNISOLONE SODIUM SUCCINATE FOR INJECTION POWDER FOR SOLUTION

Țară: Canada

Limbă: engleză

Sursă: Health Canada

Ingredient activ:

METHYLPREDNISOLONE (METHYLPREDNISOLONE SODIUM SUCCINATE)

Disponibil de la:

TEVA CANADA LIMITED

Codul ATC:

H02AB04

INN (nume internaţional):

METHYLPREDNISOLONE

Dozare:

40MG

Forma farmaceutică:

POWDER FOR SOLUTION

Compoziție:

METHYLPREDNISOLONE (METHYLPREDNISOLONE SODIUM SUCCINATE) 40MG

Calea de administrare:

INTRAMUSCULAR

Unități în pachet:

1ML

Tip de prescriptie medicala:

Prescription

Zonă Terapeutică:

ADRENALS

Rezumat produs:

Active ingredient group (AIG) number: 0106290002; AHFS:

Statutul autorizaţiei:

APPROVED

Data de autorizare:

2014-04-02

Caracteristicilor produsului

_Methylprednisolone Sodium Succinate for Injection Page 1 of 42 _
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
METHYLPREDNISOLONE SODIUM SUCCINATE
FOR INJECTION
Methylprednisolone Sodium Succinate for Injection
Sterile Powder for Solution, 40mg, 125mg, 500 mg, 1 g Vials,
intravenous or intramuscular
USP
Glucocorticoid
Teva Canada Limited
Date of Initial Authorization:
30 Novopharm Court
MAY 06, 2014
Toronto, ON
M1B 2K9
Date of Revision:
Canada
September 23, 2022
www.tevacanada.com
Submission Control Number: 263266
_Methylprednisolone Sodium Succinate for Injection Page 2 of 42 _
RECENT MAJOR LABEL CHANGES
WARNINGS AND PRECAUTIONS, SPECIAL POPULATIONS, PEDIATRICS
09/2022
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
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2
PART I: HEALTH PROFESSIONAL
INFORMATION........................................................................
4
1 INDICATIONS
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4
1.1 Pediatrics
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5
1.2 Geriatrics
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5
2
CONTRAINDICATIONS............................................................................................................
5
4 DOSAGE AND ADMINISTRATION
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6
4.1 Dosing Considerations
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6
4.2 Recommended Dose and Dosage Adjustment
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