ACT DICLO-MISO TABLET (ENTERIC-COATED)

Šalis: Kanada

kalba: anglų

Šaltinis: Health Canada

Veiklioji medžiaga:

DICLOFENAC SODIUM; MISOPROSTOL

Prieinama:

ACTAVIS PHARMA COMPANY

ATC kodas:

M01AB55

INN (Tarptautinis Pavadinimas):

DICLOFENAC, COMBINATIONS

Dozė:

50MG; 200MCG

Vaisto forma:

TABLET (ENTERIC-COATED)

Sudėtis:

DICLOFENAC SODIUM 50MG; MISOPROSTOL 200MCG

Vartojimo būdas:

ORAL

Vienetai pakuotėje:

100/250/500

Recepto tipas:

Prescription

Gydymo sritis:

OTHER NONSTEROIDAL ANTIIMFLAMMATORY AGENTS

Produkto santrauka:

Active ingredient group (AIG) number: 0222885003; AHFS:

Autorizacija statusas:

CANCELLED POST MARKET

Leidimo data:

2019-08-08

Prekės savybės

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_Page 1 of 54_
PRODUCT MONOGRAPH
PR
ACT_ _DICLO-MISO
Diclofenac sodium and Misoprostol Enteric-coated Tablets, USP
50 mg diclofenac/200 mcg misoprostol
and
75 mg diclofenac/200 mcg misoprostol
NSAID with a
Mucosal Protective Agent
Actavis Pharma Company
6733 Mississauga Road, Suite 400
Mississauga, ON
Canada, L5N 6J5
Date of Revision:
December 09, 2015
Submission Control No: 190014
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_Page 2 of 54_
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
.................................................................................................
17
DRUG INTERACTIONS
.................................................................................................
21
DOSAGE AND ADMINISTRATION
.............................................................................
25
OVERDOSAGE
...............................................................................................................
26
ACTION AND CLINICAL PHARMACOLOGY
........................................................... 27
STORAGE AND STABILITY
.........................................................................................
30
DOSAGE FORMS, COMPOSITION AND PACKAGING
............................................ 30
PART II: SCIENTIFIC INFORMATION
..............................................................................
32
PHARMACEUTICAL INFORMATION
.........................................................................
32
CLINICAL TRIALS
........................................................................