CAMBIA POWDER FOR SOLUTION

Country: Kanada

Tungumál: enska

Heimild: Health Canada

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Vara einkenni Vara einkenni (SPC)
06-12-2021

Virkt innihaldsefni:

DICLOFENAC POTASSIUM

Fáanlegur frá:

ARALEZ PHARMACEUTICALS CANADA INC

ATC númer:

M01AB05

INN (Alþjóðlegt nafn):

DICLOFENAC

Skammtar:

50MG

Lyfjaform:

POWDER FOR SOLUTION

Samsetning:

DICLOFENAC POTASSIUM 50MG

Stjórnsýsluleið:

ORAL

Einingar í pakka:

3/9

Gerð lyfseðils:

Prescription

Lækningarsvæði:

OTHER NONSTEROIDAL ANTIIMFLAMMATORY AGENTS

Vörulýsing:

Active ingredient group (AIG) number: 0122516001; AHFS:

Leyfisstaða:

APPROVED

Leyfisdagur:

2012-03-14

Vara einkenni

                                _ _
_CAMBIA_
_®_
_ (diclofenac potassium) Product Monograph _
_Page 1 of 33_
PRODUCT MONOGRAPH
PR
CAMBIA
®
Diclofenac potassium powder for oral solution
50 mg
Nonsteroidal Anti-Inflammatory Drug (NSAID)
Aralez Pharmaceuticals Canada Inc.*
6733 Mississauga Road, Suite 800
Mississauga, Ontario
L5N 6J5
www.miravohealthcare.com
Date of Revision:
December 6, 2021
Submission Control No: 253454
*Doing business as (d/b/a) Miravo Healthcare
_ _
_CAMBIA_
_® _
_(diclofenac potassium) Product Monograph _
_Page 2 of 33_
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
..........................................................3
SUMMARY PRODUCT INFORMATION
........................................................................3
INDICATIONS AND CLINICAL USE
..............................................................................3
CONTRAINDICATIONS
...................................................................................................4
WARNINGS AND PRECAUTIONS
..................................................................................5
ADVERSE REACTIONS
..................................................................................................15
DRUG INTERACTIONS
..................................................................................................18
DOSAGE AND ADMINISTRATION
..............................................................................22
OVERDOSAGE
................................................................................................................23
ACTION AND CLINICAL PHARMACOLOGY
............................................................23
STORAGE AND STABILITY
..........................................................................................25
DOSAGE FORMS, COMPOSITION AND PACKAGING
.............................................25
PART II: SCIENTIFIC INFORMATION
................................................................................26
PHARMACEUTICAL INFORMATION
...............................................................
                                
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