Who have Labyrinthine fistula with Chantix - from FDA reports


There is no Labyrinthine fistula reported by people who take Chantix yet. This review analyzes which people have Labyrinthine fistula with Chantix. It is created by eHealthMe based on reports from FDA, and is updated regularly.

How to use this study: bring a copy to your health teams to ensure drug risks and benefits are fully discussed and understood.


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On Feb, 18, 2019

No report is found.

Do you have Labyrinthine fistula while taking Chantix?


You are not alone:




Related studies

Chantix

Chantix has active ingredients of varenicline tartrate. It is often used in quit smoking. (latest outcomes from Chantix 81,345 users)

Labyrinthine Fistula

Labyrinthine fistula (an abnormal opening in the bony capsule of the inner ear) has been reported by people with high blood cholesterol, birth control, ankylosing spondylitis, weight loss, muscle spasticity (latest reports from 15 Labyrinthine fistula patients).


Drugs that are associated with Labyrinthine fistula
Labyrinthine fistula
Could your condition cause Labyrinthine fistula
Labyrinthine fistula
Chantix side effects

Browse by gender and age

Female: 0-1 2-9 10-19 20-29 30-39 40-49 50-59 60+

Male: 0-1 2-9 10-19 20-29 30-39 40-49 50-59 60+


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What would happen?

Predict new side effects and undetected conditions when you take Chantix and have Labyrinthine fistula




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NOTE: The study is based on active ingredients and brand name. Other drugs that have the same active ingredients (e.g. generic drugs) are NOT considered.

WARNING: Please DO NOT STOP MEDICATIONS without first consulting a physician since doing so could be hazardous to your health.

DISCLAIMER: All material available on eHealthMe.com is for informational purposes only, and is not a substitute for medical advice, diagnosis, or treatment provided by a qualified healthcare provider. All information is observation-only, and has not been supported by scientific studies or clinical trials unless otherwise stated. Different individuals may respond to medication in different ways. Every effort has been made to ensure that all information is accurate, up-to-date, and complete, but no guarantee is made to that effect. The use of the eHealthMe site and its content is at your own risk.

You may report adverse side effects to the FDA at http://www.fda.gov/medwatch/ or 1-800-FDA-1088 (1-800-332-1088).

If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.

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