Helixor® M (Helixor® M)

Composition Pharmacodynamics Indications Carefully Contraindications Dosing and Administration Side effects Form release / dosage
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Dosage form: & nbspsubcutaneous homeopathic solution
Composition:Per 1 ml:

Name

preparation:

Components

Amount,

mg

Helixor® M

0.01 mg / ml

Active component:

Viscum album subspecies album ex herba recente D3

0.01 mg

Excipients:

Sodium chloride

9 mg

Water for injections

up to 1.0 ml

Helixor® M

0.1 mg / ml

Active ingredient:

Viscum album subspecies album ex herba recente D2

0.1 mg

Excipients:

Sodium chloride

9 mg

Water for injections

up to 1.0 ml

Helixor® M

1 mg / ml

Active ingredient:

Viscum album subspecies album ex herba, recente D1

1.0 mg

Excipients:

Sodium chloride

9 mg

Water for injections

up to 1.0 ml

Helixor® M

5 mg / ml

Active ingredient:

Viscum album subspecies album ex herba recente D1

5.0 mg

Excipients:

Sodium chloride

8.9 mg

Water for injections

up to 1.0 ml

Helixor® M

10 mg / ml

Active component:


Viscum album subspecies album ex herba recente�?

10.0 mg

Excipients:


Sodium chloride

8.9 mg

Water for injections

up to 1.0 ml

Helixor® M

20 mg / ml

Active component:


Viscum album subspecies album ex herba recente�?

20.0 mg

Excipients:


Sodium chloride

8.8 mg

Water for injections

up to 1.0 ml

Helixor® M

30 mg / ml

Active component:


Viscum album subspecies album ex herba recente�?

30.0 mg

Excipients:


Sodium chloride

8.7 mg

Water for injections

up to 1.0 ml

Helixor® M

50 mg / ml

Active component:


Viscum album subspecies album ex herba recente�?

50.0 mg

Excipients:


Sodium chloride

8.55 mg

Water for injections

up to 1.0 ml

Helixor® M 100 mg / 2 ml

Active component:


Viscum album subspecies album ex herba recente�?

100.0 mg

Excipients:


Sodium chloride

17.1 mg

Water for injections

up to 2.0 ml
Note. Viscum album subspecies album ex herba recente tincture homeopathic matrix (�?) are prepared in accordance with NAV, 2001 p. 49, and homeopathic dilutions D1, D2, D3 are prepared in accordance with 23b.

* SAW - German Homoeopathic Pharmacopoeia;

** DAB - German Pharmacopeia.

Description:A clear, colorless, odorless solution (Helixor® M 0.01 mg / ml, 0.1 mg / ml, 1 mg / ml); clear solution of light yellow color, odorless (Helixor® M 5 mg / ml; 10 mg / ml); transparent solution of yellow color, odorless (Helixor® M 20 mg / ml, 30 mg / ml), a clear solution of a brownish-yellow color, odorless (Helixor® M 50 mg / ml, 100 mg / 2 ml).
Pharmacotherapeutic group:homeopathic remedy
ATX: & nbsp
  • Not assigned
    • Indications:

    The drug is used according to the prescription of a homeopathic doctor in accordance with the rules of the homeopathic method of treatment.

    Contraindications:Hypersensitivity to the components of the drug.
    Pregnancy and lactation:

    The drug is not recommended for use during pregnancy and during breastfeeding (due to the lack of data from special studies).

    Dosing and Administration:

    The dosage regimen and the course of treatment are determined by the homeopath physician.

    Side effects:Possible allergic reactions, nausea, skin rashes after taking the drug. In these cases, the drug should be discontinued.
    Overdose:

    Data on overdose are absent.

    Interaction:Use of the drug does not exclude the use of other drugs.
    Effect on the ability to drive transp. cf. and fur:Does not affect.
    Form release / dosage:The solution for subcutaneous administration is homeopathic, 0.01 mg / ml, 0.1 mg / ml, 1 mg / ml, 5 mg / ml, 10 mg / ml, 20 mg / ml, 30 mg / ml, 50 mg / ml, 100 mg / 2 ml.
    Packaging:

    1.0 ml (for dosage: 0.01 mg / ml, 0.1 mg / ml, 1 mg / ml, 5 mg / ml, 10 mg / ml, 20 mg / ml; 30 mg / ml; 50 mg / ml) or 2.0 ml (for a dosage of 100 mg / 2 ml) in an ampoule of colorless glass of hydrolytic class 1 with a red dot and a notch.

    Packing of 3 ampoules: 3 ampoules and 3 cardboard tubes for accurate opening; The ampoules are placed together with the instruction for use in a cardboard box with a cardboard separator.

    Packing of 8 ampoules: 8 ampoules are placed together with the instructions for use in a cardboard box with a cardboard separator.

    Packing of 50 ampoules: 26 ampoules are placed in one cardboard separator, 24 ampoules and 2 cardboard tubes are placed in the second cardboard separator.

    Both cardboard splitters are placed together with the instructions for use in a cardboard box.

    Storage conditions:

    In a dry, the dark place at a temperature of 5 to 25 ° C.

    Keep out of the reach of children.

    Shelf life:

    2 years (Helixor® M 1mg / ml; Helixor® M 5 mg / ml; Helixor® M 10 mg / ml; Helixor® M 20 mg / ml; Helixor® M 30 mg / ml; Helixor® M 50 mg / ml; Helixor® M 100 mg / 2 ml).

    3 years (Helixor® M 0.01 mg / ml, Helixor® M 0.1 mg / ml).

    Terms of leave from pharmacies:On prescription
    Registration number:LS-000395
    Date of registration:05.04.2012
    The owner of the registration certificate:Heliksor Heilmittel GmbH & Co. KG. KGHeliksor Heilmittel GmbH & Co. KG. KG Germany
    Manufacturer: & nbsp
    Representation: & nbspNaturvita, LLCNaturvita, LLCRussia
    Information update date: & nbsp09.03.2016
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