Beremagene Geperpavec Topical Side Effects
Medically reviewed by Drugs.com. Last updated on May 12, 2024.
Applies to beremagene geperpavec topical: topical application gel/jelly.
Other side effects
Some side effects of beremagene geperpavec topical 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:
Serious side effects
Along with its needed effects, beremagene geperpavec topical may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.
For healthcare professionals
Applies to beremagene geperpavec topical: topical gel.
General adverse events
The most common adverse reactions occurring in greater than 5% of patients included itching, chills, redness, rash, cough, and runny nose.[Ref]
Dermatologic
- Very common (10% or more): Itching (10%)
- Common (1% to 10%): Rash, redness[Ref]
Immunologic
- Very common (10% or more): Anti-drug antibodies to COL7 or human type VII collagen (72%; significance unknown), anti-herpes-simplex virus type 1 antibody formation (75%; in patients who were seronegative at baseline)[Ref]
Other
- Very common (10% or more): Chills (10%)[Ref]
Respiratory
- Common (1% to 10%): Cough, runny nose[Ref]
References
1. (2023) "Product Information. Vyjuvek (beremagene geperpavec topical)." Krystal Biotech Inc.
More about beremagene geperpavec topical
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Further information
Beremagene geperpavec topical 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.
Note: Medication side effects may be underreported. If you are experiencing side effects that are not listed, submit a report to the FDA by following this guide.
