Voltaren® Ofta (Drops) Instructions for Use
Marketing Authorization Holder
Alcon Pharmaceuticals LLC (Russia)
Manufactured By
Excelvision (France)
ATC Code
S01BC03 (Diclofenac)
Active Substance
Diclofenac (Rec.INN registered by WHO)
Dosage Form
| Voltaren® Ofta | Ophthalmic drops 0.1%: bottle 5 ml with dropper. |
Dosage Form, Packaging, and Composition
Ophthalmic drops 0.1% in the form of a clear light yellow solution.
| 1 ml | |
| Diclofenac sodium | 1 mg |
Excipients: benzalkonium chloride, disodium edetate, hydroxypropyl-gamma-cyclodextrin, hydrochloric acid 1M, propylene glycol, trometamol, tyloxapol, purified water.
5 ml – polypropylene bottles (1) with dropper – cardboard packs.
5 ml – polypropylene dropper bottles (1) with dropper – cardboard packs.
Clinical-Pharmacological Group
NSAIDs for topical use in ophthalmology
Pharmacotherapeutic Group
NSAID
Pharmacological Action
NSAID, a phenylacetic acid derivative. It has anti-inflammatory and analgesic effects. The mechanism of action is due to non-selective inhibition of COX-1 and COX-2 activity, which leads to suppression of prostaglandin synthesis.
When used topically in ophthalmology, it reduces swelling and pain in inflammatory processes of non-infectious etiology.
The use of diclofenac does not affect wound healing time.
Pharmacokinetics
The time to reach Cmax in the cornea and conjunctiva is 30 minutes after instillation; it penetrates into the anterior chamber of the eye. It does not penetrate into the systemic circulation in therapeutically significant concentrations.
Indications
Inhibition of miosis during cataract surgery; inflammatory process after surgical intervention; prevention and treatment of cystoid macular edema after surgical removal of cataract; inflammatory processes of non-infectious origin (including conjunctivitis, keratoconjunctivitis, corneal erosion, post-traumatic inflammation of the conjunctiva and cornea); pain syndrome during excimer laser intervention; photophobia after keratotomy.
ICD codes
| ICD-10 code | Indication |
| H10 | Conjunctivitis |
| H16.2 | Keratoconjunctivitis (including that caused by external influence) |
| H18.8 | Other specified disorders of cornea |
| H57.1 | Eye pain |
| S05 | Injury of eye and orbit |
| T81.8 | Other complications of procedures, not elsewhere classified |
| ICD-11 code | Indication |
| 9A60.5 | Vernal keratoconjunctivitis |
| 9A60.Z | Conjunctivitis, unspecified |
| 9A73 | Exposure keratitis |
| 9A74 | Neurotrophic keratitis |
| 9A78.Z | Other diseases of cornea, unspecified |
| 9A7Y | Other specified diseases of cornea |
| 9C22.Y | Other specified deformity of the eyeball |
| MC18 | Eye pain |
| NA06.Z | Injury of eye and orbit, unspecified |
| NE81.Z | Injury or harm arising from a medical procedure, not elsewhere classified, unspecified |
Dosage Regimen
| The method of application and dosage regimen for a specific drug depend on its form of release and other factors. The optimal dosage regimen is determined by the doctor. It is necessary to strictly adhere to the compliance of the dosage form of a specific drug with the indications for use and dosage regimen. |
The frequency and duration of use are determined individually.
For inhibition of intraoperative miosis, the drug is instilled into the conjunctival sac for 2 hours at 30-minute intervals (a total of 4 times) before surgery.
For prevention of cystoid macular edema, instill 1 drop 3-4 times/day for 2 weeks after surgery.
For other indications – 1 drop 3-4 times/day depending on the severity of the condition. The course of treatment can last from 1 to 2 weeks.
Adverse Reactions
Local reactions eye burning, blurred vision (immediately after instillation), corneal opacity (leukoma), iritis.
Gastrointestinal system nausea, vomiting.
Allergic reactions eye itching, hyperemia, angioedema of the face, fever, chills, photosensitivity, skin rash (predominantly erythematous, urticaria), erythema multiforme exudativum.
Contraindications
Disorders of hematopoiesis of unclear origin; erosive and ulcerative processes in the gastrointestinal tract in the acute stage; hypersensitivity to acetylsalicylic acid or other NSAIDs; hypersensitivity to diclofenac and excipients of the used drug.
With caution: epithelial herpetic keratitis (including in history); bronchial asthma induced by taking acetylsalicylic acid; diseases causing blood clotting disorders (including hemophilia, prolonged bleeding time, tendency to bleed, hemorrhagic diathesis, use of anticoagulants); pregnancy; lactation period (breastfeeding); children and adolescents under 18 years of age; elderly age.
Use in Pregnancy and Lactation
Use during pregnancy and lactation (breastfeeding) is possible in cases where the potential benefit to the mother outweighs the potential risk to the fetus or newborn.
Use in Hepatic Impairment
Use with particular caution in patients with a history of liver disease.
Use in Renal Impairment
Use with particular caution in patients with a history of kidney disease.
Pediatric Use
Use with caution in children and adolescents under 18 years of age.
Geriatric Use
Use with caution in elderly patients.
Special Precautions
Intended for topical use only and is not administered subconjunctivally or into the anterior chamber of the eye.
The anti-inflammatory effect of diclofenac may mask the symptoms of infections. If an infection is present or there is a threat of its development, local antibacterial treatment is prescribed simultaneously with the use of diclofenac.
In patients with bronchial asthma combined with rhinitis or chronic sinusitis, since the risk of allergic reactions when using acetylsalicylic acid or NSAIDs is increased, the use of diclofenac may cause bronchospasm.
Effect on the ability to drive vehicles and mechanisms
During treatment with the drug, caution must be exercised when driving vehicles and engaging in other potentially hazardous activities that require increased concentration and speed of psychomotor reactions.
Drug Interactions
Instillation of NSAIDs, including Diclofenac, into the conjunctival cavity together with corticosteroids in patients with severe corneal inflammation can lead to progression of corneal damage (caution is required when used concomitantly).
If simultaneous use with other eye drops – antibiotics and beta-blockers – is necessary, the interval between instillations should be at least 5 minutes to prevent washing out of the active substances by subsequent doses.
Theoretically, it is possible that the use of diclofenac in the form of eye drops together with drugs that reduce blood clotting, or in patients with reduced blood clotting, the bleeding time may increase.
Storage Conditions
Store at 2°C (36°F) to 30°C (86°F). Keep in original packaging, protected from light. Keep out of reach of children.
Dispensing Status
Rx Only
Important Safety Information
This information is for educational purposes only and does not replace professional medical advice. Always consult your doctor before use. Dosage and side effects may vary. Use only as prescribed.
Medical Disclaimer