Review: could Augmentin Xr cause Ibs?


Summary

There is no Ibs reported by people who take Augmentin xr yet. We study 2,148 people who have side effects while taking Augmentin xr from FDA and social media. Find out below who they are, when they have Ibs and more.

You are not alone

Join a support group for people who take Augmentin xr and have Ibs >>>

Personalized health information

On eHealthMe you can find out what patients like me (same gender, age) reported their drugs and conditions on FDA and social media since 1977. Our tools are free and anonymous. 86 million people have used us. 300+ peer-reviewed medical journals have referenced our original studies. Start now >>>

Augmentin Xr

Augmentin xr has active ingredients of amoxicillin; clavulanate potassium. It is often used in sinusitis. (latest outcomes from Augmentin xr 394 users)

Ibs

Ibs (irritable bowel syndrome -chronic abdominal pain, discomfort, bloating) has been reported by people with breathing difficulty, pain, abdominal pain upper, chest pain, depression (latest reports from 15,024 Ibs patients).

On Jul, 25, 2016

No report is found.

Do you have Ibs when taking Augmentin xr?

Browse all side effects of Augmentin xr

a b c d e f g h i j k l m n o p q r s t u v w x y z

Drugs that are associated with Ibs

Ibs

Could your condition cause Ibs

Ibs

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.