ACT DICLO-MISO TABLET (ENTERIC-COATED)

Krajina: Kanada

Jazyk: angličtina

Zdroj: Health Canada

Kúpte ho teraz

Aktívna zložka:

DICLOFENAC SODIUM; MISOPROSTOL

Dostupné z:

ACTAVIS PHARMA COMPANY

ATC kód:

M01AB55

INN (Medzinárodný Name):

DICLOFENAC, COMBINATIONS

Dávkovanie:

75MG; 200MCG

Forma lieku:

TABLET (ENTERIC-COATED)

Zloženie:

DICLOFENAC SODIUM 75MG; MISOPROSTOL 200MCG

Spôsob podávania:

ORAL

Počet v balení:

100/250/500

Typ predpisu:

Prescription

Terapeutické oblasti:

OTHER NONSTEROIDAL ANTIIMFLAMMATORY AGENTS

Prehľad produktov:

Active ingredient group (AIG) number: 0222885004; AHFS:

Stav Autorizácia:

CANCELLED POST MARKET

Dátum Autorizácia:

2019-08-08

Súhrn charakteristických

                                _ _
_ _
_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
_ _
_ _
_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
........................................................................
                                
                                Prečítajte si celý dokument
                                
                            

Dokumenty v iných jazykoch

Súhrn charakteristických Súhrn charakteristických francúzština 04-12-2015