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Voltadol® 24 hour pain patch 140 mg active ingredient-containing patch, 5 ST

Product information "Voltadol® 24 hour pain patch 140 mg active ingredient-containing patch"

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Voltadol® 24 Hour Pain Relief Patch is a non-prescription medicine containing the active ingredient diclofenac in the form of 140 mg diclofenac sodium per patch containing the active ingredient. Voltadol® 24 Hour Pain Relief Patch is an analgesic medicine.

It belongs to the group of non-steroidal anti-inflammatory drugs (NSAIDs). Voltadol 24 Hour Pain Patch is used for the local, symptomatic short-term treatment (max. 7 days) of pain in acute strains, sprains or bruises of the arms and legs as a result of blunt injuries in adolescents aged 16 and over and adults.

Voltadol 24-hour pain plaster is a white, 10 cm x 14 cm, self-adhesive plaster containing the active ingredient and made of non-woven fabric on one side and paper on the other. After removing the protective film, the adhesive film is transparent.


Dosage form

plaster

Application

The recommended dose is one plaster containing the active ingredient once a day. Apply one plaster containing the active ingredient to the painful area. The maximum daily dose is one plaster containing the active ingredient, even if more than one injured area needs to be treated. Only treat one painful area at a time.

Duration of use: Do not use Voltadol 24 hour pain plasters for more than 7 days. If you need this medicine for more than 7 days to treat pain or if your symptoms worsen, consult your doctor.

Route of administration: For application to the skin.

Instructions for use:

  1. Cut open the sachet along the dotted line and remove the plaster containing the active ingredient.

Apply the plaster:

  1. Remove one of the two protective films.
  2. Apply the plaster to the area to be treated and remove the remaining protective film.
  3. Press the plaster lightly with the palm of your hand until it adheres completely to the skin.

Remove the plaster:

  1. Moisten the plaster with water, detach one corner of the plaster and carefully pull it off the skin.
  2. To remove plaster residue, wash the affected area with water by gently rubbing it with circular movements of the fingers.

Notes: If necessary, the plaster containing the active ingredient can be held in place with a mesh bandage. Only apply the plaster containing the active ingredient to intact, healthy skin. Do not apply the plaster containing the active ingredient together with an air-impermeable (occlusive) bandage. Do not wear the plaster when bathing or showering. Do not share the plaster containing the active ingredient.

Ingredients

  • The active ingredient is: diclofenac sodium. 140 mg diclofenac sodium is contained in each active ingredient-containing plaster.
  • The other ingredients are: backing layer: polyester non-woven fabric; adhesive layer: polyacrylate dispersion, tributyl citrate, butyl hydroxyanisole (E320); protective film: paper, silicone-coated on one side.
Stück: 5
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Anwendungshinweise

Art der Anwendung: LogImport.sisx.AAD.Nur auf gesunder Haut Nicht beim Baden oder Duschen tragen Nicht mit Okklusivverband Pflaster nicht teilen
Anwendungsgebiet: LogImport.sisx.AGD.Lokale Kurzzeitbehandlung von Schmerzen bei stumpfen Traumen Zerrung, Verstauchung oder Prellung
Dosierung: LogImport.sisx.DOD.Personen ab 16 Jahren 1mal tgl für max 7 Tage ein Pflaster auf die schmerzende Stelle aufkleben MTD 1 Pflaster, es kann nur eine schmerzende Stelle behandelt werden Möglichst kurzzeitig anwenden! Für Kinder und Jugendliche unter 16 J
Eigenschaften und Wirksamkeit: LogImport.sisx.EWD.Topisches nichtsteroidales Antiphlogistikum
Gegenanzeigen: LogImport.sisx.GAD.Analgetika-Asthma, aktives peptisches Ulkus, verletzte Haut
Nebenwirkungen: LogImport.sisx.NWD.Lokale Reaktionen, Hautausschlag, Überempfindlichkeitsreaktionen, Asthma Risiko für systemische NW von Diclofenac gering
Besondere Warnhinweise zur sicheren Anwendung: LogImport.sisx.WHD.Nicht auf den Augen oder auf Schleimhäuten anwenden Nach Entfernen des Pflasters direktes Sonnenlicht oder UV-Strahlung meiden Vorsicht bei Nieren-, Herz-, Leberschäden, Ulcus pepticum, Darmentzündungen oder hämorrhagischer Diathese
Wechselwirkungen: LogImport.sisx.WWD.Gleichzeitig keine anderen Diclofenac-haltigen Arzneimittel oder andere NSARs topisch oder systemisch anwenden
Schwangerschaft und Stillperiode: LogImport.sisx.SSTD.Strenge Indikationsstellung im 1 und 2 Trimenon Gegenanzeige im 3 Trimenon Vorsicht in der Stillzeit, nicht auf der Brust stillender Mütter und nicht auf großen Hautbereichen oder über einen längeren Zeitraum anwenden

Schwangerschaftshinweise

Anwendung verboten
Anwendung nur bei zwingender oder vitaler Indikation

Stillzeithinweise

Stillen nur bei zwingender oder vitaler Indikation
Stillen unter sorgfältiger Kontrolle möglich

Piktogramme

Vorsicht Photosensibilität, übermäßige UV-Strahlung meiden
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