Filspari and Dyspepsia aggravated - a phase IV clinical study of FDA data
Summary:
Dyspepsia aggravated is reported as a side effect among people who take Filspari (sparsentan), especially for people who are female, 60+ old, have been taking the drug for < 1 month also take Tylenol, and have Iga nephropathy.
The phase IV clinical study analyzes which people have Dyspepsia aggravated when taking Filspari. It is created by eHealthMe based on reports of 1,185 people who have side effects when taking Filspari from the FDA, and is updated regularly.
What is Filspari?
Filspari has active ingredients of sparsentan. eHealthMe is studying from 1,185 Filspari users. Check the latest studies of Filspari.
What is Dyspepsia aggravated?
Dyspepsia aggravated (indigestion) is found to be associated with 1,898 drugs and 513 conditions by eHealthMe. Check the latest studies of Dyspepsia aggravated.
1,185 people reported to have side effects when taking Filspari.
Among them, 35 people (2.95%) have Dyspepsia aggravated.

Among these 35 people:
How long have people been on Filspari when they have Dyspepsia aggravated? *
- < 1 month: 66.67 %
- 1 - 6 months: 33.33 %
- 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 Dyspepsia aggravated when taking Filspari? *
- female: 67.65 %
- male: 32.35 %
What is the age of people who have Dyspepsia aggravated when taking Filspari? *
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 0.0 %
- 20-29: 7.14 %
- 30-39: 3.57 %
- 40-49: 32.14 %
- 50-59: 21.43 %
- 60+: 35.71 %
What are other drugs people take besides Filspari? *
- Tylenol: 5 people, 14.29%
- Tarpeyo: 4 people, 11.43%
- Pepcid: 4 people, 11.43%
- Metoprolol Succinate: 4 people, 11.43%
- Sodium Bicarbonate: 3 people, 8.57%
- Farxiga: 3 people, 8.57%
- Losartan Potassium: 3 people, 8.57%
- Lokelma: 3 people, 8.57%
- Rosuvastatin Calcium: 3 people, 8.57%
- Latanoprost: 3 people, 8.57%
What are other side effects people have besides Dyspepsia aggravated? *
- Dizziness: 8 people, 22.86%
- Headache (pain in head): 8 people, 22.86%
- High Blood Pressure: 6 people, 17.14%
- Hypotension (abnormally low blood pressure): 6 people, 17.14%
- Weight Increased: 5 people, 14.29%
- Diarrhea: 5 people, 14.29%
- Fatigue (feeling of tiredness): 5 people, 14.29%
- Peripheral Swelling: 4 people, 11.43%
- Weakness: 4 people, 11.43%
- Nausea (feeling of having an urge to vomit): 4 people, 11.43%
What are the existing conditions these people have? *
- Iga Nephropathy (kidney disease- condition prevents the kidneys from filtering waste): 27 people, 77.14%
- Chronic Kidney Disease: 7 people, 20.00%
- Haematuria (presence of blood in urine): 3 people, 8.57%
* Approximation only. Some reports may have incomplete information.
Do you take Filspari and have Dyspepsia aggravated?
- Check whether Dyspepsia aggravated 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 Filspari:
- Filspari (1,185 reports)
Dyspepsia aggravated treatments and more:
- Dyspepsia aggravated (114 reports)
How severe was Dyspepsia aggravated and when was it recovered:
Expand to all the drugs that have ingredients of sparsentan:
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 Filspari:
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 Dyspepsia aggravated:
- Dyspepsia aggravated (1,898 drugs)
Browse all the conditions that are associated with Dyspepsia aggravated:
- Dyspepsia aggravated (513 conditions)
How the study uses the data?
The study uses data from the FDA. It is based on sparsentan (the active ingredients of Filspari) and Filspari (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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