European Union herbal monograph on Linum usitatissimum L., semen

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10 March 2015 EMA/HMPC/377675/2014 Committee on Herbal Medicinal Products (HMPC) European Union herbal monograph on Linum usitatissimum L., semen Final Initial assessment Discussion in Working Party on European Union monographs and May 2005 European Union list (MLWP) June 2005 September 2005 Adoption by Committee on Herbal Medicinal Products (HMPC) for 20 September 2005 release for consultation End of consultation (deadline for comments). 31 January 2006 Rediscussion in MLWP May 2006 July 2006 Adoption by HMPC 13 July 2006 Monograph (EMEA/HMPC/340849/2005) AR (EMEA/HMPC/167395/2006) List of references (EMEA/HMPC/167397/2006) Overview of comments received during the public consultation (EMEA/HMPC/66042/2006) HMPC Opinion (EMEA/HMPC/353205/2006) First systematic review Discussion in MLWP July 2014 September 2014 Adoption by HMPC 10 March 2015 Keywords Herbal medicinal products; HMPC; European Union herbal monographs; wellestablished medicinal use; traditional use; Linum usitatissimum L., semen; Lini semen; linseed 30 Churchill Place Canary Wharf London E14 5EU United Kingdom Telephone +44 (0)20 3660 6000 Facsimile +44 (0)20 3660 5555 Send a question via our website www.ema.europa.eu/contact An agency of the European Union European Medicines Agency, 2015. Reproduction is authorised provided the source is acknowledged.

BG (bulgarski): Ленено семе CS (čeština): lněné semeno DA (dansk): Hørfrø DE (Deutsch): Leinsamen EL (elliniká): Σπέρματα λιναριού- λίνου σπέρμα EN (English): Linseed ES (español): Lino, semilla de ET (eesti keel): linaseeme FI (suomi): pellava, siemen FR (français): Lin (graine de) HU (magyar): Lenmag HR (hrvatski): laneno sjeme IT (italiano): Lino seme LT (lietuvių kalba): Linų sėmenys LV (latviešu valoda): Linu sēklas MT (Malti): Żerriegħa tal-kittien NL (Nederlands): Lijnzaad PL (polski): Nasienie lnu PT (português): Linho, semente RO (română): sămânţă de in SK (slovenčina): Semeno ľanu SL (slovenščina): seme navadnega lana SV (svenska): Linfrö IS (íslenska): NO (norsk): Linfrø

European Union herbal monograph on Linum usitatissimum L., semen 1. Name of the medicinal product To be specified for the individual finished product. 2. Qualitative and quantitative composition 1,2 With regard to the marketing authorisation application of Article 10(a) of Directive 2001/83/EC as amended Linum usitatissimum L., semen (linseed) i) Herbal substance As defined in the Ph. Eur. monograph ii) Herbal preparations not applicable With regard to the registration application of Article 16d(1) of Directive 2001/83/EC as amended Linum usitatissimum L., semen (linseed) i) Herbal substance As defined in the Ph. Eur. monograph ii) Herbal preparations not applicable 3. Pharmaceutical form Herbal substance for oral use. The pharmaceutical form should be described by the European Pharmacopoeia full standard term. Herbal substance for oral use. The pharmaceutical form should be described by the European Pharmacopoeia full standard term. 4. Clinical particulars 4.1. Therapeutic indications Herbal medicinal product for the treatment of habitual constipation or in conditions in which easy defaecation with soft stool is desirable. Traditional herbal medicinal product used as a demulcent preparation for the symptomatic relief of mild gastrointestinal discomfort. The product is a traditional herbal medicinal product for use in the specified indication exclusively based upon long-standing use. 1 The declaration of the active substance(s) for an individual finished product should be in accordance with relevant herbal quality guidance. 2 The material complies with the Ph. Eur. monograph (ref.: 0095). EMA/HMPC/377675/2014 Page 3/8

4.2. Posology and method of administration Posology Adolescents, adults and elderly Single dose 10-15 g, Daily dose: 2-3 times daily The use in children under 12 years of age is not recommended (see section 4.4 Special warnings and precautions for use ). Duration of use If the constipation does not resolve within 3 days, a doctor or a pharmacist should be consulted. Method of administration Oral use. Take 10-15 g seeds with 150 ml water, milk, fruit juice or similar aqueous liquid 2-3 times daily; then maintain adequate fluid intake. The product should be taken during the day at least ½ to 1 hour before or after intake of other medicines. The effect starts 12-24 hours later. Warning: not to be taken immediately prior to bedtime. Posology Adolescents, adults and elderly Single dose 5 10 g in 250 ml water Daily dose: up to three times during the day The use in children under 12 years of age is not recommended (see section 4.4 Special warnings and precautions for use ). Duration of use If the symptoms persist for longer than 1 week during the use of the medicinal product, a doctor or a qualified health care practitioner should be consulted. Method of administration Oral use. For a mucilaginous preparation, soak 5-10 g whole or broken seeds in 250 ml water for at least <x min> and take this half an hour before eating. At the time of consumption the process of swelling has to be accomplished [length has to be specified for the individual product]. The mucilaginous preparations may be consumed with or without the seeds. 4.3. Contraindications Hypersensitivity to the active substance. Linseed should not be used by patients with a sudden change in bowel habit that persists for more than 2 weeks, undiagnosed rectal bleeding and failure to defaecate following the use of a laxative. Hypersensitivity to the active substance. This product should not be taken by patients, who have difficulty in swallowing or any throat problems. Linseed should also not be used by patients suffering from abnormal constrictions in the gastro-intestinal tract, with diseases of the oesophagus and cardia or existing intestinal blockage (ileus), paralysis (ileus) of the intestine or megacolon. EMA/HMPC/377675/2014 Page 4/8

This product should not be taken by patients, who have difficulty swallowing or any throat problems. 4.4. Special warnings and precautions for use The use is not recommended in children under 12 years due to insufficient data on safety and efficacy. If abdominal pain occurs or in cases of any irregularity of frequency of faeces, the use of linseed should be discontinued and medical advice must be sought. Taking this herbal substance without adequate fluid, may cause it to swell and block the throat or oesophagus and may cause choking. Intestinal obstruction may occur if adequate fluid intake is not maintained. If experiencing chest pain, vomiting, or difficulty in swallowing or breathing after taking this herbal substance, immediate medical attention should be sought. The use in children under 12 years of age has not been established due to lack of adequate data. The treatment of debilitated patients and elderly should be supervised. Investigations in healthy women suggest that long term use of linseed may have an oestrogenic effect, and its use is therefore not recommended in women with hormonally dependent tumours. The treatment of debilitated patients and elderly should be supervised. Investigations in healthy women suggest that long term use of linseed may have an oestrogenic effect, and its use is therefore not recommended in women with hormonally dependent tumours. 4.5. Interactions with other medicinal products and other forms of interaction Enteral absorption of concomitantly administered medicines may be delayed by bulk forming laxatives such as linseed. For this reason the product should be taken at least ½ to 1 hour before or after intake of other medicinal products. Enteral absorption of concomitantly administered medicines may be delayed by a demulcent preparation of linseed. For this reason the product should not be taken ½ to 1 hour before or after intake of other medicinal products. In order to decrease the risk of gastrointestinal obstruction (ileus), linseed should be used together with medicinal products known to inhibit peristaltic movement (e.g. opioids, loperamide) only under medical supervision. EMA/HMPC/377675/2014 Page 5/8

4.6. Fertility, pregnancy and lactation There are no reports of any harmful or deleterious effects during pregnancy and lactation. Investigations in healthy women suggest that linseed may have an oestrogenic effect. Safety during pregnancy and lactation has not been established. In the absence of sufficient data, the use during pregnancy and lactation is not recommended. There are no reports of any harmful or deleterious effects during pregnancy and lactation. Investigations in healthy women suggest that linseed may have an oestrogenic effect. Safety during pregnancy and lactation has not been established. In the absence of sufficient data, the use during pregnancy and lactation is not recommended. 4.7. Effects on ability to drive and use machines Not relevant. Not relevant. 4.8. Undesirable effects Meteorism, occurring with the use of the product, is common. Reactions of hypersensitivity including anaphylaxis-like reactions may occur very rarely. If other adverse reactions not mentioned above occur, a doctor or a pharmacist should be consulted. Meteorism, occurring with the use of the product, is common. Reactions of hypersensitivity including anaphylaxis-like reactions may occur very rarely. If other adverse reactions not mentioned above occur, a doctor or a qualified health care practitioner should be consulted. 4.9. Overdose Overdose with linseed may cause abdominal discomfort, flatulence and possibly intestinal obstruction. Adequate fluid intake should be maintained and management should be symptomatic. No case of overdose has been reported. EMA/HMPC/377675/2014 Page 6/8

5. Pharmacological properties 5.1. Pharmacodynamic properties Pharmacotherapeutic group: Bulk Producers Proposed ATC code: A 06 AC Not required as per Article 16c(1)(a)(iii) of Directive 2001/83/EC as amended. The active ingredient linseed consists of the dried, ripe seeds of Linum usitatissimum L. The seeds contain nearly 25 % of bulk materials (3-6 % of mucilage, 4-7 % of alimentary fibres). The laxative effects of linseed have long been recognised empirically and shown in animal and clinical investigations. These effects are attributed to the bulk materials and in particular to the mucilage that binds with water and swells to form a demulcent gel in the intestine. Water is held back in the intestine due to the swelling of the mucilage. Faeces become softer. The volume of the intestinal content increases and causes a stretch stimulus, which results in a decrease in transit time. The swollen mass of mucilage forms a lubrication layer facilitating the transit of intestinal content. Progress of action: Linseed usually acts within 12 to 24 hours. Sometimes the maximum effect is not reached before 2 or 3 days. Broken seeds do not always cause a stretch stimulus because the increase in volume may already start in the stomach. Whole or bruised seeds have a delayed increase in volume. The use in conditions, in which easy defaecation with soft stool is desirable, is scientifically substantiated on the basis of the laxative effects but there are no special data available. 5.2. Pharmacokinetic properties One part of the bulk materials in linseed is defaecated, the other part is fermented in the colon by bacteria. This process of fermentation can produce gas and flatulence. The predominant products of fermentation are short chain fatty acids (SCFA), which are mainly resorbed. Not required as per Article 16c(1)(a)(iii) of Directive 2001/83/EC as amended. EMA/HMPC/377675/2014 Page 7/8

5.3. Preclinical safety data Tests on reproductive toxicity, genotoxicity and carcinogenicity have not been performed. Not required as per Article 16c(1)(a)(iii) of Directive 2001/83/EC as amended, unless necessary for the safe use of the product. Tests on reproductive toxicity, genotoxicity and carcinogenicity have not been performed. 6. Pharmaceutical particulars Not applicable. Not applicable. 7. Date of compilation/last revision 10 March 2015 EMA/HMPC/377675/2014 Page 8/8