S Drops - Drops
TRAUMEEL S DROPS are for the temporary relief of muscular pain, joint pain, sports injuries and bruising.
Traumeel' S is indicated in injuries such as sprains, dislocations, contusions, effusions of blood and effusions into a joints, fractures, post-operative and post-traumatic oedema and swelling of the soft tissues; inflammatory processes and degenerative processes associated with inflammation on the various organs and tissues, including, in particular, on the support and mobility apparatus (tendovaginitis, styloiditis, epicondylitis, bursitis, scapulohumeral periarthritis; arthrosis of the hip, knee and small joints; commotion cerebri acuta.Traumeel' S is contraindicated in patients with a known hypersensitivity to one of the active ingredients or excipients, to Arnica, Chamomilla, Achillea millefolium or to other plants of the daisy (compositae) family. As a matter of principle, Echinacea should not be used in progressive, systemic diseases such as tuberculosis, leukaemia or leukaemia-like diseases, inflammatory diseases of the connective tissue (collagen disease), autoimmune diseases, multiple sclerosis, AIDS, HIV infections or other chronic viral diseases.
Ingredients: Each 50 ml contains: Arnica montana, radix 3X, 5 ml; Aconitum napellus 3X, Chamomilla 3X, Belladonna 4X, Symphytum officinale 8X, 2.5 ml each; Bellis perennis 2X, Calendula officinalis 2X, Echinacea angustifolia 2X, Echinacea purpurea 2X, Hamamelis virginiana 2X, Hypericum perforatum 3X, Millefolium 3X, Hepar sulphuris calcareum 8X, Mercurius solubilis 8X, 1 ml each. Inactive ingredients: Ethanol, purified water USP.
Traumeel' S should not be administered for pain for more than 10 days for adults or 5 days for children unless directed by a medical practitioner. If pain persists or worsens, if new symptoms occur, or if redness or swelling is present, the patient should consult a medical practitioner because these could be signs of a serious condition. Traumeel' S should not be administered to children for the pain of arthritis unless directed by a medical practitioner. If you are pregnant or breast feeding your baby consult your doctor, pharmacist or other health care professional for advice before taking this medicine.
The dosage schedules listed below can be used as a general guide for the administration of Traumeel' S. Traumeel' S shows individual differences in clinical response. Therefore, the dosage for each patient should be individualised according to the patient's response to therapy. The frequency of administration of the oral (Tablets, Oral Drops) and topical (Ointment, Gel) dosage forms may be increased to 5 times daily for the treatment of acute symptoms in both children and adults, unless otherwise directed by a medical practitioner. The oral dosag forms of Traumeel' S should be administered at least 30 minutes after meals and when the oral cavity is free of food material. For best results treatment with Traumeel' S should be initiated immediately following injury or at the first sign of symptoms. Traumeel' S may be administered until symptoms disappear. However, if symptoms persist or worsen, a medical practitioner should be consulted (see Warnings). Always tell your health care professional if you are taking any other medicine. In the event of over dosage, consult your doctor or pharmacist. If neither is available, contact the nearest poison control centre. Adults and children above 11 years: 10 drops orally 3 times daily, for swelling of the soft tissues, 30 drops 3 times daily. Hold in mouth 10-15 seconds before swallowing. Infants and children to 11 years: Due to its alcohol conten (35 % v/v ethyl alcohol), a medical practitioner should be consulted before using Traumeel' S Oral Drops for children below 12 years. For best results, Traumeel' S Oral Drops should be administered on an empty stomach. Traumeel' S may be added to clear, non-sparkling water prior to administration.