Informations for option: Hirudoid Gel, show other option

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1. Hirudoid Gel
2. Hirudoid Gel

SUMMARY OF PRODUCT CHARACTERISTICS

1    NAME OF THE MEDICINAL PRODUCT

Hirudoid Gel

2.    QUALITATIVE AND QUANTITATIVE COMPOSITION

Heparinoid 0.3% w/w (Equivalent to 25,000 Units per 100g gel).

3.    PHARMACEUTICAL FORM

Topical gel.

4.    CLINICAL PARTICULARS

4.1    Therapeutic indications

Hirudoid is indicated for the treatment of superficial thrombophlebitis and the soothing relief of superficial bruising and haematoma.

4.2    Posology and method of administration

Adults, the elderly and children over 5 years of age:

Two to six inches (5-15 cm) to be applied, as a thin layer, up to four times a day to the affected area. Recommended when its cooling effect and rapid action are required.

4.3    Contraindications

Not to be used on large areas of skin, broken skin, sensitive areas of skin or mucous membranes. Not to be used in individuals with a known sensitivity to any active or inactive component of the formulation. Not to be used in children under 5 years of age.

4.4    Special warnings and precautions for use

For external use only. If symptoms persist or worsen, seek medical advice. Do not exceed the stated dose.

4.5    Interactions with other medicinal products and other forms of interaction

None known.

4.6    Pregnancy and lactation

There is no evidence to suggest that Hirudoid should not be used during pregnancy and lactation.

4.7    Effects on ability to drive and use machines

None.

4.8    Undesirable effects

None known.

Reporting of suspected adverse reactions

Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via the Yellow Card Scheme at: www.mhra.gov.uk/yellowcard

4.9    Overdose

In the absence of any reports of the accidental ingestion of Hirudoid, no specific advice is available. General supportive measures may be appropriate.

5.    PHARMACOLOGICAL PROPERTIES

5.1    Pharmacodynamic properties

Heparinoid is recognised as having: a weak inhibitory effect on PGE₂ synthesis and an indirect effect on LTB₄ production (based on in vitro studies), anti-coagulant activity (as a heparinoid), thrombolytic activity (through potentiation of urokinase activity), anti-exudatory activity (through inhibition of hyaluronidase).

5.2 Pharmacokinetic properties

Radiochemical studies of absorption following cutaneous application of heparinoid (mucopolysaccharide polysulphate) have shown that between 0.3 and 4% of the mucopolysaccharide administered is absorbed by various tissues (other than the treated area) within the first 8 hours. Typically between 1.7% and 4.6% will be absorbed within 2 to 4 days. Animal studies have also shown that mucopolysaccharide is bound intracellularly within the subcutis. Peak serum concentrations following cutaneous application are below the threshold of physiological relevance for coagulation. Mucopolysaccharide is excreted in the urine partly unchanged and partly as depolymerized, shorter chain length molecules.

5.3 Preclinical safety data

None stated

6. PHARMACEUTICAL PARTICULARS

6.1 List of excipients

Isopropyl alcohol Polyacrylic acid Propylene glycol Purified water Sodium hydroxide

6.2 Incompatibilities

None.

Shelf life

01/05/2015