Who have Joint crepitation with Zetia - from FDA reports

Joint crepitation is found among people who take Zetia, especially for people who are female, 60+ old also take medication Lantus, and have Abdominal pain. This study is created by eHealthMe based on reports of 38,016 people who have side effects when taking Zetia 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.

Peer to Peer mobile support

Peer support for this study is available on our Ginger Health app. It's free, anonymous and secure. The app is ideal for people taking multiple medications or having multiple conditions.

On Feb, 06, 2019

38,016 people reported to have side effects when taking Zetia.
Among them, 11 people (0.03%) have Joint crepitation

Number of reports submitted per year:

Gender of people who have Joint crepitation when taking Zetia *:

female: 63.64 %
male: 36.36 %

Age of people who have Joint crepitation when taking Zetia *:

Top conditions involved for these people *:

Resorption Bone Increased: 1 person, 9.09%
Prostate Cancer: 1 person, 9.09%
Indigestion: 1 person, 9.09%
Gastrointestinal Disorder (functional problems of gastrointestinal tract): 1 person, 9.09%
Breast Cancer: 1 person, 9.09%
Ankylosing Spondylitis (type of arthritis affecting the spine): 1 person, 9.09%
Abdominal Pain: 1 person, 9.09%

Top co-used drugs for these people *:

Top other side effects for these people *:

Joint Pain: 9 people, 81.82%
Weakness: 5 people, 45.45%
Oedema Peripheral (superficial swelling): 4 people, 36.36%
Blood Glucose Increased: 4 people, 36.36%
Rashes (redness): 4 people, 36.36%
Abdominal Pain: 3 people, 27.27%
Nervous System Disorder (a general class of medical conditions affecting the nervous system): 3 people, 27.27%
Extrapyramidal Disorder (involuntary muscle spasms in the face and neck): 3 people, 27.27%
Pain In Extremity: 3 people, 27.27%
Pain: 3 people, 27.27%

* Approximation only. Some reports may have incomplete information.

Do you have Joint crepitation while taking Zetia?

You are not alone:

Related studies

Zetia

Zetia has active ingredients of ezetimibe. It is often used in high blood cholesterol. (latest outcomes from Zetia 38,963 users)

Joint crepitation

Joint crepitation has been reported by people with rheumatoid arthritis, osteoporosis, high blood pressure, urinary tract infection, osteopenia (latest reports from 2,553 Joint crepitation patients).

Drugs that are associated with Joint crepitation

Joint crepitation (906 drugs)

Could your condition cause Joint crepitation

Joint crepitation (592 conditions)

Zetia side effects

Zetia side effects (38,028 reports)

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+

Browse all side effects of Zetia

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

Compare Zetia to similar drugs:

What would happen?

Predict new side effects and undetected conditions when you take Zetia and have Joint crepitation

FDA reports used in this study

Want to find out more about the FDA reports used in the study? You can request them from FDA.

Recent updates

Recent general studies

Recent personal studies

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.