SOLU-CORTEF POWDER FOR SOLUTION

Land: Canada

Taal: Engels

Bron: Health Canada

Werkstoffen:

HYDROCORTISONE (HYDROCORTISONE SODIUM SUCCINATE)

Beschikbaar vanaf:

PFIZER CANADA ULC

ATC-code:

H02AB09

INN (Algemene Internationale Benaming):

HYDROCORTISONE

Dosering:

500MG

farmaceutische vorm:

POWDER FOR SOLUTION

Samenstelling:

HYDROCORTISONE (HYDROCORTISONE SODIUM SUCCINATE) 500MG

Toedieningsweg:

INTRAMUSCULAR

Eenheden in pakket:

4ML-VIAL

Prescription-type:

Prescription

Therapeutisch gebied:

ADRENALS

Product samenvatting:

Active ingredient group (AIG) number: 0106344011; AHFS:

Autorisatie-status:

APPROVED

Autorisatie datum:

2001-04-10

Productkenmerken

_Solu-Cortef (Hydrocortisone sodium succinate) _
_Page 1 of 38_
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
SOLU-CORTEF*
Hydrocortisone sodium succinate for injection USP
Sterile Powder and Diluent
100 mg, 250 mg, 500 mg and 1 g Act-O-Vials†
Glucocorticoid
Pfizer Canada ULC
17,300 Trans-Canada Highway
Kirkland, Québec H9J 2M5
Date of Initial Authorization:
September 24, 2003
Date of Revision:
September 18, 2023
Submission Control Number: 274957
*
®
Pfizer Enterprises SARL
Pfizer Canada ULC, Licensee
†
®
Pharmacia & Upjohn Company LLC
Pfizer Canada ULC, Licensee
©
Pfizer Canada ULC 2023
_ _
_Solu-Cortef (Hydrocortisone sodium succinate) _
_Page 2 of 38_
RECENT MAJOR LABEL CHANGES
7 WARNINGS AND PRECAUTIONS, OTHER
09/2023
8 ADVERSE REACTIONS, 8.1 ADVERSE REACTIONS
OVERVIEW
09/2023
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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6
1.2
Geriatrics
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6
2
CONTRAINDICATIONS
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6
4
DOSAGE AND ADMINISTRATION
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7
4.1
Dosing Considerations
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7
4.2
Recom