Stadaglycin

Overdose

No overdose data available.

Contraindications

Increased sensitivity to the components of the drug.

Use with caution in children under 4 years old.

Incompatibilities

Reduces the need for ophthalmic drugs containing glucocorticosteroids.

Stadaglycin price

We have no data on the cost of the drug.
However, we will provide data for each active ingredient

Pharmaceutical form

Drops of eye

Undesirable effects

The transient symptoms of local irritation: impaired visual perception, burning in the eye, conjunctiva edema, a foreign body sensation, dry eyes, lacrimation, barley in the century. The defeat of the epithelium of the cornea.

Therapeutic indications

Allergic conjunctivitis, allergic keratitis, keratoconjunctivitis, irritation of the mucous membrane of the eyes due to allergic reactions (environmental factors, occupational hazards, household chemicals, cosmetics, ophthalmological dosage forms, plant pollen and animal dandruff).

Pharmacotherapeutic group

  • Temporal cell membrane stabilizers

Pharmacodynamic properties

Prevents the degradation of fat cells and the separation of histamine, bradikinin, leukotrienes from them (including.h. slowly responding substance) and other biologically active substances. Most effective in preventive use.

Pharmacokinetic properties

Absorption through the mucous membrane of the eyes is negligible. System bioavailability is less than 0.1%. T1/2 - 5-10 minutes.

Special precautions for storage

In a place protected from direct sunlight, at a temperature not exceeding 25 ° C .

Keep out of the reach of children.

Shelf life of the drug Stadaglytsin

eye drops 20 mg / ml - 3 years. After opening the bottle, use for 4 weeks.

slanging for 20 mg / ml - 3 years.

Do not apply after the expiration date indicated on the package.

Nature and contents of container

Drops of eye 1 ml
sodium cromoglycate 20 mg
auxiliary substances : 0.1 mg of chloride benzalkonium, 1.5 mg of 2H dynatrium salt2O edetinic acid, sodium chloride, sodium dihydrophosphate dihydrate, sodium monogydrophosphate dodecahydrate, sorbitol, water for injection  

in polyethylene vials of polyethylene 5 or 10 ml; in a cardboard pack of 1 bottle-camera.

Spray for nasal use 0.14 ml
sodium cromoglycate 2.8 mg
auxiliary substances : 0.014 mg benzalkonia chloride, 0.21 mg of dynatrium salt 2H2O edetinic acid, sodium chloride, sodium dihydrophosphate dihydrate, sodium monogydrophosphate dodecahydrate, sorbitol, water for injection  

in polyethylene bottles of 15 ml; in a pack of cardboard 1 bottle.

Qualitative and quantitative composition

Sodium Cromoglycate

Dosage (Posology) and method of administration

Eye drops : conjunctivally. Adults and children over 4 years old - 1 drop in each eye up to 4 times a day.

If it is necessary to use for a long time, treatment is carried out under the supervision of a doctor.

The abolition of the drug should be carried out gradually over 1 week.

Spray for nasal use : intranasally, by introducing the spray hole of the micro-disper into the nose and pressing the spray mechanism.

Adults and children from 5 years old - 1 dose per night 3-4 times a day (1 dose corresponds to one pressure on the spray mechanism).

If necessary, the daily dose is increased, but the frequency of use should not exceed 6 times a day.

Treatment continues until the patient is exposed to allergens (domestic dust, fungal spores, floral pollen, etc.d.).

ATC - Anatomical and therapeutic chemical classification

R01AC01 Cromoglycyanic acid