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Proprietary name and dosage form:

MERCURIUS-HEEL®S TABLETS

Composition: 1 tablet cont.: Mercurius solubilis Hahnemanni D10 90 mg; Hepar sulfuris    D8 30 mg; Lachesis mutus D12 30 mg; Phytolacca americana D4 30 mg; Ailanthus altissima D3 30 mg; Echinacea angustifolia D3 30 mg; Atropa belladonna D4 60 mg.
Indications: This medicine is prepared in accordance with homeopathic principles and is proposed for use in furuncles, carbuncles and other suppurations, including, e.g. those in the (peri)tonsillar tissue.
Contraindications: Hypersensitivity to one of the active ingredients or excipients, or hypersensitivity to members of the Compositae family. Principally contraindicated for patients with progressive systemic disease such as tuberculosis, leukose, collagen disorders, multiple sclerosis, AIDS, HIV infection, and other autoimmune disorders.
Warnings: This preparation contains natural lactose. Although the quantity of lactose present is probably not sufficient to cause discomfort, a health professional should be consulted in strong cases of lactose intolerance. A temporary aggravation of the existing symptoms is possible after taking a homeopathic preparation.
Interactions: No interactions studies have been performed.
Pregnancy and lactation: If you are pregnant or breast feeding your baby please consult your doctor, pharmacist or other health care professional for advice before taking this medicine.
Dosage and directions for use: Adults and children over 3 years of age: Dissolve 1 tablet in the mouth 3 times daily. In acute disorders, 1 tablet every 15 minutes for 8 doses. Infants: Half the adult dose. Crush the tablet and administer it dissolved in a little water or milk.
It is recommended not to eat or drink 15 minutes before or after taking the medication.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 hospital or poison control centre.
Side Effects and Special Precautions: Side Effects
Increased flow of saliva may occur after taking this medication; in such an event, do not continue therapy with this preparation. Hypersensitivity reactions may occur in individual cases. The following have been observed among patients taking medication containing preparations from rudbeckia: rashes, itching, facial swelling (rare), acute respiratory distress, vertigo, and acute hypotension. Not all side effects reported for this medicine are included in this leaflet.  Should your general health worsen or if you experience untoward effects while taking this medicine, please consult your doctor, pharmacist or other health care professional for advice.
Registration number: U5501 (Act 101/1965).
Disclaimer: This medicine has not been evaluated by the Medicines Control Council. This medicine is not intended to diagnose, treat, cure or prevent any disease.