Air-sea (Avia-mori)

Composition Pharmacodynamics Indications Carefully Contraindications Dosing and Administration Side effects Form release / dosage
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homeopathic tablets

Composition:

Active components: Veratrum album (Veratrum albumum) C200, Anamirta cocculus (Cocculus) (Anamirta cocculus (Kokkulyus)) C200, Natrium tetraboracicum (Borax) (Sodium tetraboracicum (Borax)).

Excipients: lactose, microcrystalline cellulose, magnesium stearate.

Description:

Tablets are flat-cylindrical with a bevel, white or almost white.

Pharmacotherapeutic group:Homeopathic Remedy
Pharmacodynamics:

Increases the stability of the vestibular analyzer to kinetic effects (changes in speed and direction of acceleration), as well as other sensory influences, typical for traffic in transport. Reduces the vegetative response of the body to these effects, reduces the recovery time of the functional state after kinetic effects, including a number of indicators of operator activity (in particular, volume and stability of attention). The drug reduces vestibular and vegetative disorders in sensitive individuals associated with travel in the transport (dizziness, nausea, vomiting, weakness, sweating).

Indications:

The drug is used to prevent and treat "sea" disease, with low resistance to motion sickness in air and road transport, including those performing operator functions.

Contraindications:

Increased individual sensitivity to the components of the drug, children under 6 years.

Pregnancy and lactation:

The use of the drug during pregnancy and during lactation is possible after consultation with a doctor.

Dosing and Administration:

Adults and children over 6 years of 1 tablet per reception (keep in your mouth until completely dissolved - not during meals).

The first intake of the drug is carried out 1 hour before landing in the vehicle. The tablets are then taken every 30 minutes during the stay in the vehicle, but not more than 5 times a day.

Side effects:

With the use of the drug for the indicated indications and in the indicated dosages of side effect to the present time is not revealed. Possible reactions of increased individual sensitivity to the components of the drug.

Overdose:

There have been no cases of overdose to date.

Interaction:

Cases of incompatibility with other medicines are not registered.

Special instructions:

The composition of the drug includes lactose, and therefore it is not recommended to appoint patients with congenital galactosemia, glucose malabsorption syndrome or galactose,or with congenital lactase insufficiency.

Form release / dosage:Tablets are homeopathic.
Packaging:

For 20 tablets in a planar cell packaging made of polyvinylchloride film and aluminum foil.

For 1 or 2 contour mesh packages along with the instruction for medical use are placed in a pack of cardboard.
Storage conditions:

At a temperature of no higher than 25 ° C.

Keep out of the reach of children.

Store the drug until fully used in the package provided by the manufacturer.
Shelf life:

3 years

Do not use after the expiration date.

Terms of leave from pharmacies:Without recipe
Registration number:P N001567 / 01
Date of registration:03.11.2009 / 24.11.2015
Expiration Date:Unlimited
The owner of the registration certificate:NPF Materia Medica Holding, OOO NPF Materia Medica Holding, OOO Russia
Manufacturer: & nbsp
Information update date: & nbsp21.01.2017
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