Akten Side Effects
Generic name: lidocaine ophthalmic
Medically reviewed by Drugs.com. Last updated on Oct 11, 2023.
Note: This document provides detailed information about Akten Side Effects associated with lidocaine ophthalmic. Some dosage forms listed on this page may not apply specifically to the brand name Akten.
Applies to lidocaine ophthalmic: ophthalmic gel/jelly.
Serious side effects of Akten
Along with its needed effects, lidocaine ophthalmic (the active ingredient contained in Akten) 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 or nurse immediately if any of the following side effects occur while taking lidocaine ophthalmic:
More common
- blurred vision or other changes in vision
- burning feeling at site of application
- redness of the white part of eyes or inside of eyelids
Other side effects of Akten
Some side effects of lidocaine 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:
More common
For healthcare professionals
Applies to lidocaine ophthalmic: ophthalmic gel.
Ocular
- Frequency not reported: Conjunctival hyperemia, corneal epithelial changes[Ref]
Nervous system
- Frequency not reported: Headache[Ref]
Local
- Frequency not reported: Burning upon instillation[Ref]
References
1. (2008) "Product Information. Akten (lidocaine ophthalmic)." Akorn Inc
More about Akten (lidocaine ophthalmic)
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Further information
Akten side effects can vary depending on the individual. 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.