Voltaren Emulgel 20mg/g gel for external use

Land: Armenia

Språk: engelsk

Kilde: Դեղերի և բժշկական տեխնոլոգիաների փորձագիտական կենտրոնի գործունեության Հայաստանի Հանրապետությունում

Preparatomtale Preparatomtale (SPC)
22-08-2018

Aktiv ingrediens:

diclofenac (diclofenac diethylamine)

Tilgjengelig fra:

Novartis Consumer Health S.A.

ATC-kode:

M02AA15

INN (International Name):

diclofenac (diclofenac diethylamine)

Dosering :

20mg/g

Legemiddelform:

gel for external use

Enheter i pakken:

50g laminated tube, 100g laminated tube

Resept typen:

OTC

Autorisasjon status:

Registered

Autorisasjon dato:

2015-09-04

Preparatomtale

                                Novartis Consumer Health SA
CH-1260 Nyon, Switzerland
Global Regulatory Affairs
VOLTAREN ®EMULGEL®
Gel
Diclofenac diethylamine 2.32%
F.AADI01
REGIONAL SUMMARY OF PRODUCT CHARACTERISTICS (SMPC)
Property of Novartis Consumer Health
Confidential
May not be used, divulged, published or otherwise disclosed
without the consent of Novartis Consumer Health
Novartis Consumer Health SA
CONFIDENTIAL
Page 2
EU-rSmPC
Voltaren Forte 2.32% gel
TABLE OF CONTENTS
1
NAME OF THE MEDICINAL PRODUCT
.......................................................................
3
2
QUALITATIVE AND QUANTITATIVE COMPOSITION
............................................. 3
3
PHARMACEUTICAL FORM
............................................................................................
3
4
CLINICAL PARTICULARS
..............................................................................................
3
4.1
Therapeutic indications
............................................................................................
3
4.2
Posology and method of administration
.................................................................. 3
4.3
Contraindications
.....................................................................................................
4
4.4
Special warnings and precautions for use
................................................................ 5
4.5
Interaction with other medicinal products and other forms of
interaction .............. 5
4.6
Pregnancy and lactation
...........................................................................................
5
4.7
Effects on ability to drive and use machines
........................................................... 5
4.8
Undesirable effects
..................................................................................................
5
4.9
Overdose
..................................................................................................................
6
5
PHARMACOLOGICAL PROPERTIES
............................................................................
6
                                
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Informasjon til brukeren Informasjon til brukeren russisk 22-08-2018

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