Dineksan - instructions for use, doses, side effects, contraindications

aromatic oils: 0.04 g - fennel ordinary fruit oil: 0.0096 g - anise star fruit oil: 0.0136 g - peppermint mint oil partially demented oil: 0.0156 g - Peppermint mint oil: 0.0012 g.

Description:

White color, fragrant, soft, homogeneous gel.

Pharmacotherapeutic group:Local anesthetic

ATX: & nbsp

N.01.B.B Amides

N.01.B.B.02 Lidocaine

C.01.B.B.01 Lidocaine

C.01.B.B Antiarrhythmic drugs Ib class

Pharmacodynamics:

Dinexan has a local anesthetic effect. Lidocaine suppresses carrying out not only pain impulses, but also impulses of other modalities. With topical application dilates blood vessels, does not have a locally irritating effect.

Indications:

It is used to anesthetize inflammatory diseases of the oral mucosa (mechanical damage to the integrity of the mucosa, burns, gingivitis, stomatitis,herpetic lesions). Irritations of mucous and worn while wearing dentures. For surface anesthesia at the injection site, removal of calculus.

Contraindications:

Individual intolerance to the drug. Children's age (up to 12 years).

Pregnancy and lactation:Pregnant and lactating women are appointed by the doctor if the benefit to the mother exceeds the risk to the fetus or the baby.

Dosing and Administration:Locally. Gel (in the amount of the size of a pea) is applied with light rubbing 2-3 times a day on painful and inflamed areas of the oral mucosa. In case of insufficient anesthesia, repeat the procedure or application 2-3 minutes later. The maximum dose for adults for 12 hours is 40 mg of lidocaine (2 g of gel). At unpleasant sensations during an accustoming to new prostheses it is recommended to put a thin layer of gel on a prosthesis, the sky and a gum.

Side effects:Usually the gel is well tolerated. Rarely: allergic reactions to the components of the drug.

Very rarely: local allergic and non-allergic reactions (burning, local edema, local erythema), changes in taste (dysgeusia), numbness.

Anaphylactic reaction.

Overdose:Cases of overdose were not observed.When systemic reactions occur, symptomatic treatment is recommended.

Interaction:Not described.

Effect on the ability to drive transp. cf. and fur:

Does not have a negative effect.

Form release / dosage:

Gel for topical use, 2%.

Packaging:

For 10 grams in an aluminum tube with a protective membrane and a screw cap. The lid is equipped with a device for piercing the protective membrane. The tube with instruction for use is packaged in a cardboard box.

Storage conditions:

At a temperature not higher than 25 ° C, out of the reach of children.

Shelf life:

Shelf life 5 years.

Open vials can be used for 3 months.

Do not use after the expiration date on the package.

Terms of leave from pharmacies:Without recipe

Registration number:P N 015576/01

Date of registration:23.09.2011

The owner of the registration certificate:Krojssler Chemical Factory and Co. GmbHKrojssler Chemical Factory and Co. GmbH Germany

Manufacturer: & nbsp

KREUSSLER CHEMISCHE FABRIK & CO., GmbH

Representation: & nbspDENIS Farm Distribution, Inc.DENIS Farm Distribution, Inc.

Information update date: & nbsp31.05.2016

Illustrated instructions

Instructions

Dineksan (Dineksan)