Voltaren Emulgel 20mg/g gel for external use

Valsts: Armēnija

Valoda: angļu

Klimata pārmaiņas: Դեղերի և բժշկական տեխնոլոգիաների փորձագիտական կենտրոնի գործունեության Հայաստանի Հանրապետությունում

Lietošanas instrukcija Lietošanas instrukcija (PIL)
11-09-2015
Produkta apraksts Produkta apraksts (SPC)
22-08-2018

Aktīvā sastāvdaļa:

diclofenac (diclofenac diethylamine)

Pieejams no:

Novartis Consumer Health S.A.

ATĶ kods:

M02AA15

SNN (starptautisko nepatentēto nosaukumu):

diclofenac (diclofenac diethylamine)

Deva:

20mg/g

Zāļu forma:

gel for external use

Vienības iepakojumā:

50g laminated tube, 100g laminated tube

Receptes veids:

OTC

Autorizācija statuss:

Registered

Autorizācija datums:

2015-09-04

Produkta apraksts

                                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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