Clinical and pharmacological group: & nbsp

Beta-blockers

Included in the formulation
  • Arutimol
    drops d / eye 
    VALEANT, LLC     Russia
  • Glaoutam
    drops d / eye 
  • Okumed®
    drops d / eye 
  • Okumol
    drops d / eye 
  • Okupres-E®
    drops d / eye 
  • Oftan® Timogel
    gel d / eye 
    Santen, AO     Finland
  • Ofthan® Timolol
    drops d / eye 
    Santen, AO     Finland
  • Timolol
    drops d / eye 
  • Timolol
    drops d / eye 
    UPDATE OF PFC, CJSC     Russia
  • Timolol
    drops d / eye 
  • Timolol
    drops d / eye 
    BELMEDPREPARATY, RUP     Republic of Belarus
  • Timolol
    drops d / eye 
  • Timolol Solofarma
    drops d / eye 
    GROTEKS, LLC     Russia
  • Timolol-Akos
    drops d / eye 
    SYNTHESIS, OJSC     Russia
  • Timolol-Betalek
    drops d / eye 
    BETA-LEK, LLC     Russia
  • Timolol-DIA
    drops d / eye 
  • Timolol-Lens®
    drops d / eye 
    LENS-PHARM, LLC     Russia
  • Timolol-MEZ
    drops d / eye 
  • Timolol-POS®
    drops d / eye 
  • Timolol-Teva
    drops d / eye 
  • Timololong®
    drops d / eye 
    FIRN M, ZAO     Russia
  • Included in the list (Order of the Government of the Russian Federation No. 2782-r of 30.12.2014):

    ONLS

    VED

    Minimal chemist's assortment

    АТХ:

    S.01.E.D.   Beta-blockers

    S.01.E.D.01   Timolol

    Pharmacodynamics:

    A non-selective β-adrenoreceptor blocker when inserted into the conjunctival sac inhibits the adenylylcyclase ciliary tissue system that transports sodium ions from the blood into the intraocular fluid, which leads to a decrease in intraocular pressure.

    Does not affect the refraction, accommodation and the size of the pupil.

    Pharmacokinetics:

    After the installation in the conjunctival sac, the therapeutic effect develops after 1-2 hours and lasts for 8-24 hours.

    Absorption into the total blood flow is insignificant - the drug does not have a systemic effect.

    Indications:

    It is used for the treatment of glaucoma and with an acute increase in ophthalmotonus.

    VII.H40-H42.H40.0   Suspicion of glaucoma

    VII.H40-H42.H40.1   Primary open angle glaucoma

    VII.H40-H42.H40.2   Primary angle-closure glaucoma

    VII.H40-H42.H40.3   Glaucoma secondary posttraumatic

    VII.H40-H42.H40.4   Glaucoma secondary due to inflammatory disease of the eye

    VII.H40-H42.H40.5   Glaucoma secondary due to other eye diseases

    Contraindications:

    Dystrophy of the cornea, atrophic rhinitis, sinus bradycardia, severe heart failure, individual intolerance.

    Carefully:

    Pregnancy and lactation.

    Pregnancy and lactation:

    Recommendations for FDA - Category B. It is used in pregnancy and lactation.

    Dosing and Administration:

    Installation in the conjunctival cavity 1 drop 2 times / day.

    The highest daily dose: 1 drop.

    The highest single dose: 2 drops.

    Side effects:

    Reducing tear, "dry eye syndrome."

    Allergic reactions.

    Overdose:

    Cases of overdose are not described.

    Treatment is symptomatic.

    Interaction:

    To enhance the effect and duration of the drug, a combination with pilocarpine, carbonic anhydrase inhibitors, adrenomimetics and taufon is possible.

    Special instructions:

    Persons using contact eye correction should remove their lenses before installing the drug and dress no earlier than 15 minutes.

    Instructions
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