Celebrex and Supraventricular tachycardia - from FDA reports

Supraventricular tachycardia is found among people who take Celebrex, especially for people who are female, 60+ old , have been taking the drug for 2 - 5 years, also take medication Fosamax, and have Metastases to bone. This study is created by eHealthMe based on reports of 106,010 people who have side effects when taking Celebrex 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.

Who is eHealthMe: we are a data analysis company who specializes in health care industry. Our original studies have been referenced on 500+ peer-reviewed medical publications, including The Lancet, Mayo Clinic Proceedings, and EANO. On eHealthMe, you can research drugs and monitor them (see testimonials).

On Oct, 15, 2018

106,010 people reported to have side effects when taking Celebrex.
Among them, 95 people (0.09%) have Supraventricular tachycardia

Number of reports submitted per year:

Could Celebrex cause Supraventricular tachycardia?

Time on Celebrex when people have Supraventricular tachycardia *:

Gender of people who have Supraventricular tachycardia when taking Celebrex *:

  • female: 75.82 %
  • male: 24.18 %

Age of people who have Supraventricular tachycardia when taking Celebrex *:

Top conditions involved for these people *:

  1. Metastases To Bone (cancer spreads to bone): 10 people, 10.53%
  2. Osteoporosis (bones weak and more likely to break): 9 people, 9.47%
  3. Multiple Myeloma (cancer of the plasma cells): 7 people, 7.37%
  4. High Blood Cholesterol: 6 people, 6.32%
  5. Back Pain: 4 people, 4.21%

Click here to view more results or personalize the results to your gender and age

Top co-used drugs for these people *:

  1. Fosamax: 18 people, 18.95%
  2. Zometa: 16 people, 16.84%
  3. Ambien: 14 people, 14.74%
  4. Vioxx: 13 people, 13.68%
  5. Aspirin: 13 people, 13.68%

Click here to view more results or personalize the results to your gender and age

Top other side effects for these people *:

  1. Breathing Difficulty: 33 people, 34.74%
  2. Chest Pain: 32 people, 33.68%
  3. Atrial Fibrillation/flutter (atrial fibrillation and flutter are abnormal heart rhythms in which the atria, or upper chambers of the heart, are out of sync with the ventricles): 31 people, 32.63%
  4. High Blood Pressure: 31 people, 32.63%
  5. Joint Pain: 27 people, 28.42%

Click here to view more results or personalize the results to your gender and age

* Approximation only. Some reports may have incomplete information.

FDA reports used in this study

Do you have Supraventricular tachycardia while taking Celebrex?

You are not alone:

Related studies


Celebrex has active ingredients of celecoxib. It is often used in arthritis. (latest outcomes from Celebrex 108,955 users)

Supraventricular tachycardia

Supraventricular tachycardia (rapid heart rhythm originating at or above the atrioventricular node) has been reported by people with high blood pressure, osteoporosis, diabetes, depression, pain (latest reports from 11,776 Supraventricular tachycardia patients).

Drugs that are associated with Supraventricular tachycardia
Supraventricular tachycardia (1,662 drugs)
Could your condition cause Supraventricular tachycardia
Supraventricular tachycardia (1,212 conditions)
Celebrex side effects
Browse all side effects of Celebrex
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

Related publications that referenced our studies

What would happen?

Predict new side effects and undetected conditions when you take Celebrex and have Supraventricular tachycardia

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.