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Draft Community Herbal Monograph On Sisymbrium Officinale (L.) Scop., Herba

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EUROPEAN MEDICINES AGENCY

SCIENCE MEDICINES HEALTH

15 January 2014

EMA/HMPC/280193/2013

Committee on Herbal Medicinal Products (HMPC)

Community herbal monograph on Sisymbrium officinale (L.) Scop., herba

Herbal medicinal products; HMPC; Community herbal monographs; traditional use; Sisymbrium officinale (L.) Scop., herba; Sisymbrii officinalis herba; hedge mustard


BG (balgarski): MtApw^ ^ene6Ha, ^at

CS (cestina): kvët hulevníku lékarského

DA (dansk): rank vejsennep

DE (Deutsch): Wegraukenkraut

EL (elliniká): Ziaupßpiou ^appaKEUTiKOÙ àv0oç

EN (English): hedge mustard

ES (espanol): Erísimo, partes aéreas floridas de

ET (eesti keel): uniloogaürt

FI (suomi): rohtopernaruoho, verso

FR (français): Erysimum (parties aériennes

fleuries d')

HU (magyar): szapora zsombor HR (hrvatska): zelen divlje gorusice IT (italiano): erisimo, parti aeree_


LT (lietuviq kalba): vaistiniq pikuliq ziedai

LV (latviesu valoda): ärstniedbas zodzenes ziedi

MT (malti): mustarda

NL (nederlands): heeskruid

PL (polski): kwiat stulisza lekarskiego

PT (portugués): rinchao flor

RO (romana):

SK (slovencina): vnat' horcicníka SL (slovenscina): cved navadnega sebenika SV (svenska): vägsenap IS (íslenska):

NO (norsk): veisennep


Draft

Discussion in Working Party on Community monographs and Community list (MLWP)

January 2012 May 2013 July 2013 September 2013

Adoption by Committee on Herbal Medicinal Products (HMPC) for release for consultation

12 November 2013

End of consultation (deadline for comments). Comments should be provided using this template to hmpc.secretariat@ema.europa.eu

15 April 2013

Rediscussion in Working Party on Community monographs and Community list (MLWP)

Adoption by Committee on Herbal Medicinal Products (HMPC)

Keywords

An agency of the European Union


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© European Medicines Agency, 2014. Reproduction is authorised provided the source is acknowledged.

Community herbal monograph on Sisymbrium officinale (L.) Scop., herba

1.    Name of the medicinal product

To be specified for the individual finished product.

2.    Qualitative and quantitative composition1, 2

Well-established use

Traditional use

With regard to the registration application of Article 16d(1) of Directive 2001/83/EC as amended

Sisymbrium officinale (L.) Scop., herba (hedge

mustard)

i)    Herbal substance Not applicable.

ii)    Herbal preparations

a)    Dry extract (DER 3.5-5.5:1), extraction solvent water

b)    Dry extract (DER 6-8:1), extraction solvent water

3. Pharmaceutical form

Well-established use

Traditional use

Herbal preparations for oromucosal use (in a solid dosage form).

Herbal preparation for oral use (in a liquid dosage form).

The pharmaceutical form should be described by the European Pharmacopoeia full standard term.

1    The material complies with the French Pharmacopoeia monograph (Pharmacopée française 1998 Érysimum, Sisymbrium officinale)

2    The declaration of the active substance(s) for an individual finished product should be in accordance with relevant herbal quality guidance.

4. Clinical particulars

4.1. Therapeutic indications

Well-established use

Traditional use

Traditional herbal medicinal product for the relief of throat irritation such as hoarseness and dry cough.

The product is a traditional herbal medicinal product for use in the specified indication exclusively based upon long-standing use.

4.2. Posology and method of administration

Well-established use

Traditional use

Posology Single dose Oromucosal use

Adolescents, adults and elderly

a)    Dry extract (DER 3.5-5.5:1), extraction solvent water: 10 mg, 10 - 12 times daily

b)    Dry extract (DER 6-8:1), extraction solvent water: 7.5 - 10 mg, 10 - 12 times daily

Children 6 - 11 years of age

a)    Dry extract (DER 3.5-5.5:1), extraction solvent water: 10 mg, 5 - 6 times daily

b)    Dry extract (DER 6-8:1), extraction solvent water: 7.5 - 10 mg, 5 - 6 times daily

The oromucosal use in children under 6 years of age is not recommended (see section 4.4 'Special warnings and precautions for use').

Tablet/lozenge to dissolve in the mouth without chewing.

Oral use

Adolescents, adults and elderly

b) Dry extract (DER 6-8:1), extraction solvent

water: 82.5 mg, 3 - 4 times daily

Children 3 - 11 years of age

b) Dry extract (DER 6-8:1), extraction solvent

water: 27.5 mg, 3 - 4 times daily

The oral use in children under 3 years of age is not

Well-established use

Traditional use

recommended (see section 4.4 'Special warnings and precautions for use').

Duration of use

If the symptoms persist 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.

Oromucosal use.

4.3. Contraindications

Well-established use

Traditional use

Hypersensitivity to the active substance.

4.4. Special warnings and precautions for use

Well-established use

Traditional use

If the symptoms worsen during the use of the medicinal product, a doctor or a qualified health care practitioner should be consulted.

If dyspnoea, fever or purulent sputum occurs, a doctor or a qualified health care practitioner should be consulted immediately.

Herbal preparations a) and b)

The oromucosal use in children under 6 years of age is not recommended because of the pharmaceutical form (solid dosage form) and due to lack of adequate data.

Herbal preparation b)

The oral use in children under 3 years of age is not recommended due to lack of adequate data and because medical advice should be sought.

4.5. Interactions with other medicinal products and other forms of interaction

Well-established use

Traditional use

Not known.

4.6. Fertility, pregnancy and lactation

Well-established use

Traditional use

Safety during pregnancy and lactation has not been established. In the absence of sufficient data, the use during pregnancy and lactation is not recommended.

No fertility data available.

4.7. Effects on ability to drive and use machines

Well-established use

Traditional use

No studies on the effect on the ability to drive and use machines have been performed.

4.8. Undesirable effects

Well-established use

Traditional use

None known.

If adverse reactions occur, a doctor or a qualified health care practitioner should be consulted.

4.9. Overdose

Well-established use

Traditional use

No case of overdose has been reported.

5. Pharmacological properties

5.1. Pharmacodynamic properties

Well-established use

Traditional use

Not required as per Article 16c(1)(a)(iii) of Directive 2001/83/EC as amended.

5.2. Pharmacokinetic properties

Well-established use

Traditional use

Not required as per Article 16c(1)(a)(iii) of Directive 2001/83/EC as amended.

5.3. Preclinical safety data

Well-established use

Traditional use

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

Well-established use

Traditional use

Not applicable.

7. Date of compilation/last revision

15 January 2014

Page 6/6

Community herbal monograph on Sisymbrium officinale (L.) Scop., herba

EMA/HMPC/280193/2013