The instruction for medical use
of OFTOLIK medicine
the Trade name
Mezhdunarodnoye the unlicensed name
Is not present
the Dosage form
of the Drop eye
of 1 ml of solution contains
active agents: polyvinyl alcohol – 14.00 mg, povidone – 6.00 mg,
excipients: a benzalkoniya chloride, dinatrium edetat, sodium chloride, water for injections.
Transparent solution from colourless till slightly yellowish color.
Drugs for treatment of diseases of eyes others. Artificial tears and other indifferent drugs.
The ATX S01XA20 code
Pharmacokinetics Concentration properties of drug in plasma after burying two drops Oftolik in each eye remains below a limit of quantitative definition (10 ng/ml) in 4 hours after use. It allows to draw a conclusion that system absorption of drug from the surface of an eye when using eye drops Oftolik low.
Polyvinyl alcohol and povidone render the greasing effect that reduces dryness of a surface of an eye and irritation. These substances, easily covering the surface of an eye, prevent emergence of dry sites on it. Polyvinyl alcohol has the properties similar to properties of the mucin which is produced a conjunctiva. It calms an eye, does its surface smooth due to increase in density of a plaintive film.
Has protective action on a cornea at hyposecretion of plaintive liquid, increases duration of action of eye drops and protects a cornea from their irritant action.
– the burning sensation, irritations and discomfort caused by dryness of a surface of an eye
– as tear substitutes in case of disturbances of functions of lacrimal glands
– a syndrome of a dry eye or any other the disturbances demanding mitigation and moistening of a cornea
the Route of administration and doses
On 1-2 drop 3-4 times a day in both eyes.
The course of treatment is established by the doctor.
Wash up hands before digging drops in eyes.
Stir up a bottle and remove a cover. Make sure that the tip of the pipette does not touch skin or the surface of an eye not to allow hit of bacteria
Cast away the head back, remove a hand a lower eyelid, turn a bottle and dig a drop in the lower conjunctival sac
– local allergic reactions
of the Contraindication
– hypersensitivity to drug components
– a sharp phase of a corrosive burn of eyes are possible
– the children’s age up to 8 years
Polyvinyl alcohol reacts with group of secondary hydroxides, characteristic of complex substances (formation of ester). Substance breaks up in strong acid and is softened or dissolved in weak acids and alkalis. Substance is incompatible with the high-concentrated inorganic salts, especially with sulfates or with phosphates, loss the draft of 5% of polyvinyl alcohol can be caused by reaction with phosphates. Formation of gel from polyvinyl alcohol can be caused by reaction with borax.
Solution of povidone is compatible to many inorganic salts, natural and synthetic pitches and other substances. Forms a product of molecular connection when mixing with sulfatiatsily, salicylates, phenobarbital, tannin and other substances. Reduces efficiency of the means similar to a tiomersal.
not to use if after use of drops color shades change or there is a turbidity in eyes.
It is necessary to stop use of drops and to consult with the doctor if:
– when using drops the pain arises or amplifies
– the sight worsens
– symptoms remain on an extent more, than 72 hours
– remain redness and irritation of eyes.
Drops contain a benzalkoniya chloride therefore it is impossible to put on contact lenses within 20 minutes after use of drops.
To use drops within a month after opening of a bottle.
After burying it is necessary to close immediately and densely a bottle.
Use in pediatrics
Considering lack of experience of use of drug for children up to 8 years, use of this drug at this age group is not recommended.
Use at pregnancy and a lactation
is not studied. Use at pregnancy and a lactation is possible only when the advantage for mother exceeds potential risk for a fruit and the child.
Features of influence of medicine on ability to run the vehicle or potentially dangerous mechanisms As right after burying possible short-term decrease in visual acuity, before driving or work with mechanisms it is necessary to wait until the visual acuity completely is restored.
Cases of overdose of drug are not known
the Form of release and packing
of the Drop eye.
On 10 ml of drug in plastic bottles droppers.
On 1 bottle dropper together with the screw-on cap in which there is a device for opening of a bottle and with the instruction for medical use in the state and Russian languages place in a cardboard pack.
To Store storage conditions in the place protected from light at a temperature not above 25 °C.
Not to freeze.
To store out of children’s reach!
A period of storage
the use Period after opening of a bottle of 45 days.
Not to use after the expiry date specified on packing!
of Proizvoditel SENTISS FARM Pvt. Ltd.
212/D-1, Greene Park, New Delhi, India
At the plant: Villidzh Khera Nikhla, Tekhsil Nalagarkh, Region of Solan, Himachal Pradesh 174,101, India
Name and country of the owner of the registration certificate
of SENTISS FARMA of Pvt. Ltd., India
the Address of the organization accepting in the territory of the Republic of Kazakhstan claims from consumers on quality of products: Republic of Kazakhstan, 050000, Almaty, Bogenbay St. of the Batyr 132, office 309 Ph./fax: +7 (7272) 96-45-99Email: firstname.lastname@example.org