Veltassa and Upper limb fracture - a phase IV clinical study of FDA data
Summary:
Upper limb fracture is reported as a side effect among people who take Veltassa (patiromer sorbitex calcium), especially for people who are female, 60+ old, have been taking the drug for 1 - 6 months also take Lasix, and have Hyperkalemia.
The phase IV clinical study analyzes which people have Upper limb fracture when taking Veltassa. It is created by eHealthMe based on reports of 15,647 people who have side effects when taking Veltassa from the FDA, and is updated regularly.
What is Veltassa?
Veltassa has active ingredients of patiromer sorbitex calcium. eHealthMe is studying from 15,649 Veltassa users. Check the latest studies of Veltassa.
What is Upper limb fracture?
Upper limb fracture is found to be associated with 1,133 drugs and 1,073 conditions by eHealthMe. Check the latest studies of Upper limb fracture.
15,647 people reported to have side effects when taking Veltassa.
Among them, 25 people (0.16%) have Upper limb fracture.

Among these 25 people:
How long have people been on Veltassa when they have Upper limb fracture? *
- < 1 month: 0.0 %
- 1 - 6 months: 100 %
- 6 - 12 months: 0.0 %
- 1 - 2 years: 0.0 %
- 2 - 5 years: 0.0 %
- 5 - 10 years: 0.0 %
- 10+ years: 0.0 %
What is the gender of people who have Upper limb fracture when taking Veltassa? *
- female: 58.33 %
- male: 41.67 %
What is the age of people who have Upper limb fracture when taking Veltassa? *
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 0.0 %
- 20-29: 0.0 %
- 30-39: 0.0 %
- 40-49: 0.0 %
- 50-59: 5.26 %
- 60+: 94.74 %
What are other drugs people take besides Veltassa? *
- Lasix: 7 people, 28.00%
- Linzess: 3 people, 12.00%
- Colace: 3 people, 12.00%
- Fish Oil: 3 people, 12.00%
- Humalog: 3 people, 12.00%
- Vaccinium Macrocarpon: 2 people, 8.00%
- Brimonidine: 2 people, 8.00%
- Lantus: 2 people, 8.00%
- Lantus Solostar: 2 people, 8.00%
- Amlodipine: 2 people, 8.00%
What are other side effects people have besides Upper limb fracture? *
- Fall: 13 people, 52.00%
- Flatulence (flatus expelled through the anus): 2 people, 8.00%
- Acute Upper Airway Obstruction (blockage occurs in the upper airway): 2 people, 8.00%
- Blood Potassium Decreased: 2 people, 8.00%
- Death: 2 people, 8.00%
- Therapeutic Response Decreased (less preventive response): 1 person, 4.00%
- Clavicle Fracture: 1 person, 4.00%
- Constipation: 1 person, 4.00%
- Cough: 1 person, 4.00%
- Dizziness: 1 person, 4.00%
What are the existing conditions these people have? *
- Hyperkalemia (damage to or disease of the kidney): 20 people, 80.00%
- High Blood Pressure: 2 people, 8.00%
- Renal Disorder (kidney disease): 1 person, 4.00%
- Cardiac Disorder: 1 person, 4.00%
* Approximation only. Some reports may have incomplete information.
Do you take Veltassa and have Upper limb fracture?
- Check whether Upper limb fracture is associated with a drug or a condition
- Predict drug outcomes for up to one year with AI
- Get an AI agent to monitor your drugs continuously
Related studies:
Effectiveness of, long term effects of, and alternative drugs to Veltassa:
- Veltassa (15,649 reports)
Upper limb fracture treatments and more:
- Upper limb fracture (25,219 reports)
How severe was Upper limb fracture and when was it recovered:
Expand to all the drugs that have ingredients of patiromer sorbitex calcium:
Sub-studies 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 Veltassa:
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 zBrowse all the drugs that are associated with Upper limb fracture:
- Upper limb fracture (1,133 drugs)
Browse all the conditions that are associated with Upper limb fracture:
- Upper limb fracture (1,073 conditions)
How the study uses the data?
The study uses data from the FDA. It is based on patiromer sorbitex calcium (the active ingredients of Veltassa) and Veltassa (the brand name). Other drugs that have the same active ingredients (e.g. generic drugs) are not considered. Dosage of drugs is not considered in the study.
How to use the study?
DO NOT STOP MEDICATIONS without first consulting your doctor. If there are any serious or long term adverse effects discovered in the study, discuss the study with your doctor to ensure that proper medication management will be in place if applicable.
Who is eHealthMe?
With medical big data and proven AI/ML algorithms, eHealthMe provides a platform for everyone to run phase IV clinical trials. We study millions of patients and 5,000 more each day. Results of our real-world drug study have been referenced on 800+ peer-reviewed medical publications, including The Lancet, Mayo Clinic Proceedings, and Nature. Our analysis results are available to researchers, health care professionals, patients (testimonials), and software developers (open API).
WARNING, DISCLAIMER, USE FOR PUBLICATION
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. Our phase IV clinical studies alone cannot establish cause-effect relationship. 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.
If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.
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