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Traumeel S

Traumeel S ®


Traumeel S® is produced in Germany and marketed by Biologische Heilmittel Heel GmbH for more than 60 years and marketed in Greece by A.S.K. Pharmaceutical, as an OTC medicine supporting two convenient formulations: tablets and ointment.1

Traumeel S® consists of an innovative formula of 14 herbal and mineral ingredients and is effective in relieving symptoms of pain and edema that may result from minor injuries such as sprains, muscle strains and bruises.1


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Characteristics

Natural relief for musculoskeletal injuries and inflammation.


Aconitum Napellus
Hamamelis Virginiana
Achillea Millefolium
Bellis Perennis
Atropa Belladonna
Arnica Montana

Improves vasotonia and stabilization of vassal permeability, elimination of venous stasis.2-8



Calendula Officinalis
Arnica Montana
Echinacea Purpurea
Hypericum Perforatum

Acts analgesic and against neuralgia.2-8



Echinacea Angustifolia
Echinacea Purpurea
Mercuro Amidonitrate
Calcium Sulfide
Hamamelis Virginiana

Acts anti-inflammatory through regulation of the inflammatory cytokine network.2-8



Aconitum Napellus
Arnica Montana
Chamomilla Recutita
Symphytum Officinale

Stimulation of wound healing, formation of osseous callous.2-8


Suitability


High risk patients and the elderly.

Patients receiving other medicines or are undergoing treatment.

Persons with contraindications to conventional treatment.

Athletes


Health professionals


  • Traumeel S Leaflet
  • Citations
Traumeel S Leaflet
Citations

1.Traumeel S ointment License Number: 27961/17 / 27-6-2018, Traumeel S tablet: 27953/17 / 27-6-2018

2.Cesnulevicius K. The bioregulatory approach to work-related musculoskeletal disorders: using the multicomponent ultra low-dose medication Traumeel to target the multiple pathopshysiological processes of the disease. Alternative Therapies Health Med 2011;17(2)Suppl:S8-S17.

3.Heine H, Andrȁ F.Zum antiinflammatorischen Wirkmechanismus eines Antihomotoxikum compositum. {The anti-inflammatory action mechanism of a antihomotoxic composita remedy }. Ȁrztezeitschrift fur Naturheilverfahren 2002;43:96-104.

4.Gonza’lez de Vega C, Speed C, Wolfarth B et al.Traumeel vs. diclofenac for reducing pain and improving ankle mobility after acute ankle sprain: A multicenter, randomized, blinded, controlled and non-inferiority trial. Int J Clin Pract 2013;67(10):979-989.

5.Zenner S, Weiser M. Oral treatment of traumatic, inflammatory and degenarative conditions with a homeopathic remedy. Biol Ther 1997;XV(1):22-26.

6.Eming SA, Krieg T, Davidson JM. Inflammation in wound repair: molecular and cellular mechanisms. J Invest Dermatol 2007 Mar;127(3):514-525.

7.Porozov S, Cahalon L, Weiser M et al. Inhibition of IL-1β and TNF-alpha secretion from resting and activated human immunocytes by the homeopathic medication Traumeel S. Clin Dev Immunol 2004 June;11(2):143-149.

8. Lussignoli S, Bertani S, Metelmann H et al. Effect of Traumeel S, a homeopathic formulation, on blood-induced inflammation in rats. Compliment Ther Med 1999 Dec;7(4):225-230.

9. Arora S, Harris T, Sherer C et al. Clinical safety of a homeopathic preparation. Biomed Ther 2000;XVIII(2):222-225.

10. Zenner S, Metelmann H. Therapy experiences with a homeopathic ointment : Results of drug surveillance conducted on 3.422  patients. Biol Ther 1994;XII(3):204-211.

11. Orizola AJ, Vargas F. The efficacy of Traumeel vs. diclofenac and placebo ointment in tendinous pain in elite athletes: a randomized controlled trial. Med Sci Sports Med Excer 2007;39(5 Suppl):S79, Abstract 858.

Report side effects


  • How can I report side effects?
How can I report side effects?

Healthcare professionals are asked to report any suspected adverse reactions via the National Organization of Medicines. If you are a patient and you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in the package leaflet. You can report adverse reactions with the following options :

1) Electronic submission through EOF’s website http://www.eof.gr/web/guest/yellowgeneral

2) Dispatching the Yellow card in hard copy via mail to EOF to the Department of Adverse Reactions (Mesogeion 284, Cholargos 15562)

3) Communication with the Department of Adverse Reactions via telephone : 213.20.40.380-337

4) Submission of the yellow card via fax at 210.6549.585

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