Skip to main content

AK-Beta Side Effects

Generic name: levobunolol ophthalmic

Medically reviewed by Drugs.com. Last updated on Sep 11, 2023.

Note: This document contains side effect information about levobunolol ophthalmic. Some dosage forms listed on this page may not apply to the brand name AK-Beta.

Applies to levobunolol ophthalmic: ophthalmic solution.

Serious side effects of AK-Beta

Along with its needed effects, levobunolol ophthalmic (the active ingredient contained in AK-Beta) may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.

Check with your doctor immediately if any of the following side effects occur while taking levobunolol ophthalmic:

More common

Less common

Rare

Incidence not determined

Other side effects of AK-Beta

Some side effects of levobunolol ophthalmic may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects.

Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:

Incidence not determined

For Healthcare Professionals

Applies to levobunolol ophthalmic: ophthalmic solution.

General

The most commonly reported side effects were ocular burning/stinging, blepharoconjunctivitis, eye irritation, and eye pain.[Ref]

Ocular

Very common (10% or more): Eye irritation, eye pain

Common (1% to 10%): Blepharitis, conjunctivitis

Rare (less than 0.1%): Iridocyclitis

Frequency not reported: Conjunctival/ocular hyperemia, allergic conjunctivitis, decreased corneal reflex, keratitis, blurred vision, punctate keratitis, eye/eyelids pruritus, eye/eyelid edema, eye discharge, increased lacrimation, dry eye, choroidal detachment following filtration surgery, corneal erosion, diplopia, ptosis, corneal calcification, decreased corneal sensitivity, blepharoptosis, eye allergy, foreign body sensation[Ref]

Respiratory

Frequency not reported: Asthma, dyspnea, throat irritation, nasal discomfort, bronchospasm (predominantly in patients with pre-existing bronchospastic disease), cough, respiratory failure, nasal congestion[Ref]

Cardiovascular

Frequency not reported: Raynaud's phenomenon, syncope, bradycardia, atrioventricular block, palpitations, hypotension, arrhythmia, cardiac arrest, cardiac failure, chest pain, congestive heart failure, cold hands and feet[Ref]

Hypersensitivity

Frequency not reported: Anaphylactic reaction, systemic allergic reactions including angioedema[Ref]

Nervous system

Rare (less than 0.1%): Transient ataxia

Frequency not reported: Confusion, dizziness, somnolence, lethargy, headache, memory loss, cerebral ischemia, cerebrovascular accident, increases in signs and symptoms of myasthenia gravis, paresthesia, dysgeusia[Ref]

Gastrointestinal

Frequency not reported: Nausea, abdominal pain, diarrhea, dry mouth, dyspepsia, vomiting[Ref]

Genitourinary

Frequency not reported: Decreased libido, sexual dysfunction, impotence[Ref]

Musculoskeletal

Frequency not reported: Myalgia[Ref]

Psychiatric

Frequency not reported: Depression, insomnia, nightmares[Ref]

Other

Frequency not reported: Edema, fatigue, asthenia[Ref]

Dermatologic

Frequency not reported: Stevens-Johnson syndrome, urticaria, contact dermatitis (including allergic contact dermatitis), rash, skin exfoliation, lichenoid keratosis, pruritus, erythema of eyelid, eyelid eczema, alopecia, psoriasiform rash, exacerbation of psoriasis[Ref]

Metabolic

Frequency not reported: Hypoglycemia, masked symptoms of hypoglycemia in insulin-dependent diabetics[Ref]

References

1. Product Information. Betagan (levobunolol ophthalmic). Allergan Inc. 2022.

2. Cerner Multum, Inc. UK Summary of Product Characteristics.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Some side effects may not be reported. You may report them to the FDA.