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Besivance Side Effects

Generic name: besifloxacin ophthalmic

Medically reviewed by Drugs.com. Last updated on Oct 18, 2023.

Note: This document provides detailed information about Besivance Side Effects associated with besifloxacin ophthalmic. Some dosage forms listed on this page may not apply specifically to the brand name Besivance.

Applies to besifloxacin ophthalmic: ophthalmic suspension.

Serious side effects of Besivance

Along with its needed effects, besifloxacin ophthalmic (the active ingredient contained in Besivance) 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 besifloxacin ophthalmic:

Less common

  • blurred vision
  • eye pain
  • itching of the eye
  • red, sore eyes
  • swelling of the eye or eyelid

Other side effects of Besivance

Some side effects of besifloxacin 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:

Less common

For healthcare professionals

Applies to besifloxacin ophthalmic: ophthalmic suspension.

Ocular

Nervous system

Other

Respiratory

Psychiatric

Cardiovascular

Dermatologic

Gastrointestinal

Local

Metabolic

Musculoskeletal

References

1. Cerner Multum, Inc. "Australian Product Information."

2. (2009) "Product Information. Besivance (besifloxacin ophthalmic)." Bausch and Lomb Americas, Inc.

Further information

Besivance 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.