Betoptik C, eye drops 0.25% 5 ml

Betaxolol is a selective beta 1 -adrenoblocker without intrinsic sympathomimetic activity. It has no membrane stabilizing (local anesthetic) effect.

When used topically, betaxolol reduces intraocular pressure by reducing intraocular fluid production.

The onset of hypotensive effect is observed 30 min after injection, the maximum effect occurs after 2 h. After single instillation the effect on ophthalmotonus lasts for 12 hours.

Betaxolol (in comparison with other beta-adrenoblockers) does not cause reduction of blood flow in the optic nerve.

Betoptic does not cause myosis, accommodation spasm, hemeralopia, the effect of “shrouds” in front of the eyes (unlike myotics).

Indications

To reduce intraocular pressure as monotherapy or in combination with other drugs for:

Open angle glaucoma.
Ocular hypertension.

Pharmacological effect

Betaxolol is a selective beta 1-blocker without intrinsic sympathomimetic activity. Does not have a membrane-stabilizing (local anesthetic) effect.

When applied topically, betaxolol reduces intraocular pressure due to a decrease in the production of intraocular fluid.

The onset of the hypotensive effect is observed 30 minutes after instillation, the maximum effect develops after 2 hours. After a single instillation, the effect on ophthalmotonus persists for 12 hours.

Betaxolol (compared to other beta-blockers) does not cause a decrease in blood flow in the optic nerve.

Betoptik does not cause miosis, accommodation spasm, hemeralopia, or a “veil” effect before the eyes (unlike miotics).

Special instructions

Diabetes mellitus

Beta-blockers should be prescribed with caution to patients with a tendency to hypoglycemia and patients with diabetes mellitus, since these drugs may mask the symptoms of acute hypoglycemia.

Thyrotoxicosis

Beta blockers may mask some symptoms of hyperthyroidism (eg, tachycardia). In patients with suspected thyrotoxicosis, beta-blockers should not be abruptly discontinued, as this may cause an increase in symptoms.

Muscle weakness

Beta blockers may cause symptoms similar to those of myasthenia gravis (eg, diplopia, ptosis, general weakness).

Surgery

Before a planned operation, beta-blockers should be gradually (not all at once!) withdrawn 48 hours before general anesthesia, because during anesthesia, they can reduce the sensitivity of the myocardium to sympathetic stimulation necessary for cardiac function.

Pulmonology

Caution should be exercised when prescribing beta-blockers to patients with severe respiratory failure. Despite the fact that clinical studies have shown no effect of betaxolol on respiratory function, the possibility of hypersensitivity to the drug should not be excluded.

Risk of developing an anaphylactic reaction

Patients taking beta-blockers may have a history of atopy or anaphylactic reactions. In case of repeated reactions, such patients may not be sensitive to the usual doses of adrenaline (epinephrine) needed to relieve anaphylaxis.

The drug should be used with caution in patients with Raynaud’s syndrome and pheochromocytoma. When administered locally, beta blockers can enter the systemic circulation and have the same side effects as when administered systemically. Cases of severe respiratory and cardiovascular disorders have been described, including death from bronchospasm in patients with bronchial asthma and death from heart failure.

Betoptic C has a minimal effect on blood pressure and heart rate. However, caution should be exercised when prescribing it to patients with atrioventricular block or heart failure. Treatment should be stopped when the first signs of decompensation of the cardiovascular system appear.

The drug contains the preservative benzalkonium chloride, which can be absorbed by contact lenses (soft). Before using the drug, the lenses should be removed and put back no earlier than 15 minutes after using the drug.

Do not touch the tip of the dropper bottle to any surface to avoid contamination of the dropper bottle and its contents. The bottle must be closed after each use.

Impact on the ability to drive vehicles and operate machinery

Patients whose vision clarity is temporarily reduced after instillation of the drug are not recommended to engage in activities that require increased attention and reaction until it is restored.

Active ingredient

Betaxolol

Composition

1 ml – betaxolol hydrochloride 2.8 mg, which corresponds to the content of betaxolol 2.5 mg

Excipients:

benzalkonium chloride,

mannitol,

carbomer 974Р,

polystyrene sulfonic acid,

boric acid,

disodium edetate,

N-lauroylsarcosine,

hydrochloric acid and/or sodium hydroxide solution (to maintain pH level),

purified water.

Pregnancy

There is no sufficient experience with the use of the drug Betoptik S during pregnancy and lactation.

The use of the drug during pregnancy and lactation (breastfeeding) is possible only if the expected benefit to the mother outweighs the potential risk to the fetus or child.

Contraindications

Individual hypersensitivity to the components of the drug.
Sinus bradycardia.
AV block II and III degrees.
Cardiogenic shock.
Heart failure (including history).
Sick sinus syndrome in patients with artificial pacemaker.
Children under 18 years of age.

With caution:

Thyrotoxicosis.
Myasthenia gravis.
Diabetes mellitus.
Raynaud’s syndrome.
Pheochromocytoma.
Concomitant use of oral beta-blockers.

Side Effects

Local

Transient discomfort in the eyes, blurred vision, pinpoint keratitis, decreased sensitivity of the cornea, sensation of a foreign body in the eye, photophobia, lacrimation, itching, burning, dry eyes, redness of the eyes, anisocoria, pain in the eye, decreased visual acuity, allergic reactions.

From the side of the central nervous system

Dizziness, nausea, drowsiness, insomnia, headache, depression.

From the cardiovascular system

Bradycardia, cardiac conduction disturbances and heart failure.

From the respiratory system

Dyspnea, bronchospasm, bronchial asthma, respiratory failure.

Other

Alopecia (eyelashes, scalp), muscle weakness, myalgia, eyelid disorders.

Interaction

In patients receiving Betoptic S eye drops and concomitantly taking other beta-blockers orally, the risk of side effects (both systemic and local) may be higher due to a possible additive effect. Such patients should be under close medical supervision.

When combined with drugs that deplete catecholamines, increased effects such as decreased blood pressure and bradycardia may occur.

Caution should be exercised when using betaxolol and adrenergic psychotropic drugs together due to the risk of potentiation of side effects.

With the simultaneous use of betaxolol and drugs that affect atrioventricular conduction (such as quinidine antiarrhythmics, amiodarone, cardiac glycosides, calcium channel blockers, parasympathomimetics), an additive effect may develop – bradycardia, atrioventricular block, arterial hypotension.

If necessary, can be used in combination with other local ophthalmic drugs. In this case, the interval between their use should be at least 10 minutes.

Overdose

If excess amounts of the drug get into your eyes, rinse your eyes with warm water.

Storage conditions

At 8–30 °C

Shelf life

2 years

Manufacturer

Alcon-Couvreur, Belgium