dermauk-img-product-betesil

Potent, practical medicated plaster with a uniform metered dose delivered directly to the affected area

Active Ingredients:
Betamethasone valerate 2.250 mg per 7.5 cm x 10 cm medicated plaster (corresponding to 1.845 mg of betamethasone)

A medicated corticosteroid plaster for the treatment of chronic, localised inflammatory skin disorders in adults.

Betesil® is indicated in adults for the treatment of inflammatory skin disorders which do not respond to treatment with less potent corticosteroids, such as eczema, lichenification, lichen planus, granuloma annulare, palmoplantar pustulosis and mycosis fungoides.

Due to its particular pharmaceutical form, Betesil® is suitable for chronic plaque psoriasis localized in difficult to treat areas (e.g. knees, elbows and anterior face of the tibia on an area not greater than 5% of the body surface).

Betesil® contains 2.250 mg Betamethasone Valerate (corresponding to 1.845 mg of betamethasone).

Betesil® provides a localised, uniform concentration of Betamethasone valerate(1)

Potent Action:

  • Anti-inflammatory
  • Anti-itch(5)
  • Vasoconstrictive(5)

Advantages of Betesil® Medicated Plaster

Betesil® Application Guide Video

Watch our application guide video which provides some helpful advice for patients on how best to use Betesil®, including a variety of cutting and application techniques.

(For Healthcare Professionals and Patients)

For Healthcare Professionals

Arrange a Demonstration

Arrange a demonstration, this can be arranged either face to face within your department or digitally. (for healthcare professionals)

Betesil® Resources

Browse our latest product information and expert-led advice.

FAQs

Legal Category: (POM) Prescription Only Medicine
Precautions to be taken before handling or administering the medicinal product.
Cleanse and carefully dry the area to be treated before each application so that the medicated plaster adheres well to the skin.
 
Open the sachet containing the medicated plaster and cut the plaster, if necessary, so that it fits the area to be treated. Peel off the protective film and apply the adhesive medicated part to the area concerned.
 
Any unused part of the plaster should be put back into the sachet so that it keeps and can be used at the next application, always within one month.
 
The medicated plaster must not be removed and reused.
 
Once the medicated plaster has been applied, the skin must not come in contact with water. It is advisable to take a bath or have a shower between applications.
Furthermore, if the medicated plaster is applied to particularly mobile parts (e.g. an elbow or knee) and its edges start to lift, it is advisable to apply the adhesive strips for securing dressings included in the medicinal product pack.
 
Never cover the medicated plaster completely with occlusive material or dressing.
Children aged <18 years

Do not use on patients under 18 years of age.

1 plaster per plaque every 24 hours.

6 plasters/day maximum.

Adhesive strips included for securing dressings if required.

Betesil® comes in boxes of 4 and 8. 

Box of 4 or 8 medicated plasters (10 x 7.5 cm)

30 days until plaque improves, then if needed continue treatment with a less potent corticosteroid

Additional Information

Betesil® contains 2.250 mg Betamethasone Valerate (corresponding to 1.845 mg of betamethasone).

Each medicated plaster is packed individually in a paper/polyethylene/aluminium/ethylene-methacrylic acid copolymer sachet.

Each box includes adhesive strips for securing dressings.

The Summary of Product Characteristics, which may be downloaded below, is the most up to date version. Due to the timing of regulatory changes this may vary from the document on the MHRA website.

If you have any queries, please contact us on +44 (0)191 375 9020

Click the button below to view the Abbreviated prescribing information

Below you will find a button to download the Betesil® Patient Information Leaflet.

If you have any queries, please contact us on +44 (0)191 375 9020

Betamethasone valerate 2.250 mg per 7.5 cm x 10 cm medicated plaster
(corresponding to 1.845 mg of betamethasone)

Adverse Events

Adverse events should be reported. Reporting forms and information can be found at https://yellowcard.mhra.gov.uk

Adverse events should also be reported to Derma UK on +44 (0)191 375 9020.

References

  1. Derma UK Ltd., ‘Summary of Betesil® Product Characteristics (SmPC).’ 2021
  2. Naldi L et al., ‘Efficacy and Safety of the Betamethasone Valerate 0,1% Plaster in Mild-to-Moderate Chronic Plaque Psoriasis: A Randomized, Parallel-Group, Active-Controlled, Phase III Study.’ American Journal of Clinical Dermatology, vol. 12, no 3, 2011, pp. 191-2011.
  3. Pacifico A et al., ‘A new formulation of an occlusive dressing containing betamethasone valerate 0.1% in the treatment of mild to moderate psoriasis.’ Journal of European Academy of Dermatology and Venereology, no 20, 2006, pp. 153-157.
  4. Ortonne JP, et al., ‘Betamethasone valerate dressing is non-inferior to calcipotriol-betamethasone dipropionate ointment in the treatment of patients with mild-to-moderate chronic plaque psoriasis: results of a randomized assessor-blinded multicentre trial.’ Journal of European Academy of Dermatology and Venereology, vol. 28, no 9, 2014, pp. 1226-34.
  5. National Institute for Health and Care Excellence, Topical corticosteroids, National Institute for Health and Care Excellence, https://bnf.nice.org.uk/treatment-summary/topical-corticosteroids.html, (accessed 24th November 2021).

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