Allopurinol sodium and Hyperkalemia - a phase IV clinical study of FDA data
Summary:
Hyperkalemia is reported as a side effect among people who take Allopurinol sodium (allopurinol sodium), especially for people who are male, 60+ old, also take Furosemide, and have High blood pressure.
The phase IV clinical study analyzes which people have Hyperkalemia when taking Allopurinol sodium. It is created by eHealthMe based on reports of 836 people who have side effects when taking Allopurinol sodium from the FDA, and is updated regularly.
What is Allopurinol sodium?
Allopurinol sodium has active ingredients of allopurinol sodium. It is often used in gout. eHealthMe is studying from 864 Allopurinol sodium users. Check the latest studies of Allopurinol sodium.
What is Hyperkalemia?
Hyperkalemia (damage to or disease of the kidney) is found to be associated with 1,954 drugs and 2,940 conditions by eHealthMe. Check the latest studies of Hyperkalemia.
eHealthMe: drug outcomes in the real world
eHealthMe runs one of the largest post-marketing drug safety studies in the world. We study millions of patients and 5,000 more each day. Our data-driven phase IV clinical trials have been referenced on 800+ peer-reviewed medical publications including The Lancet, Mayo Clinic Proceedings, and Nature. Tools to study our phase IV findings are available to the public, anonymous and free >>>.
836 people reported to have side effects when taking Allopurinol sodium.
Among them, 23 people (2.75%) have Hyperkalemia.

Among these 23 people:
What is the gender of people who have Hyperkalemia when taking Allopurinol sodium? *
- female: 34.78 %
- male: 65.22 %
What is the age of people who have Hyperkalemia when taking Allopurinol sodium? *
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 0.0 %
- 20-29: 0.0 %
- 30-39: 0.0 %
- 40-49: 5 %
- 50-59: 15 %
- 60+: 80 %
What are other drugs people take besides Allopurinol sodium? *
- Lasix: 7 people, 30.43%
- Furosemide: 7 people, 30.43%
- Aspirin: 6 people, 26.09%
- Aldactone: 5 people, 21.74%
- Omeprazole: 4 people, 17.39%
- Aranesp: 4 people, 17.39%
- Valtrex: 4 people, 17.39%
- Pentostatin: 3 people, 13.04%
- Decadron: 3 people, 13.04%
- Rituxan: 3 people, 13.04%
What are other side effects people have besides Hyperkalemia? *
- Acute Kidney Failure: 11 people, 47.83%
- Hypotension (abnormally low blood pressure): 6 people, 26.09%
- Haemoglobin Decreased: 5 people, 21.74%
- Weakness: 4 people, 17.39%
- Blood Creatinine Increased: 4 people, 17.39%
- 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): 3 people, 13.04%
- Upper Gastrointestinal Haemorrhage (upper gastrointestinal bleeding): 3 people, 13.04%
- Dehydration (dryness resulting from the removal of water): 3 people, 13.04%
- Ischaemic Cardiomyopathy (weakness in the muscle of the heart due to inadequate oxygen delivery to the myocardium with coronary artery disease): 3 people, 13.04%
- Blood Urea Increased: 3 people, 13.04%
What are the existing conditions these people have? *
- High Blood Pressure: 6 people, 26.09%
- Chronic Lymphocytic Leukaemia (cancer in which the bone marrow makes too many lymphocytes (a type of white blood cell)): 3 people, 13.04%
- Hypertensive Heart Disease: 2 people, 8.70%
- Prostate Cancer: 2 people, 8.70%
- Osteoarthritis (a joint disease caused by cartilage loss in a joint): 2 people, 8.70%
- Essential Hypertension (primary hypertension): 2 people, 8.70%
- Type 2 Diabetes: 2 people, 8.70%
- Hyperuricaemia (level of uric acid in the blood that is abnormally high): 2 people, 8.70%
- Urination - Excessive Volume: 1 person, 4.35%
- Cardiac Failure: 1 person, 4.35%
* Approximation only. Some reports may have incomplete information.
Do you take Allopurinol sodium and have Hyperkalemia?
- Check whether Hyperkalemia is associated with a drug or a condition
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Related studies:
Effectiveness of, long term effects of, and alternative drugs to Allopurinol sodium:
- Allopurinol sodium (864 reports)
Hyperkalemia treatments and more:
- Hyperkalemia (78,084 reports)
How severe was Hyperkalemia and when was it recovered:
Expand to all the drugs that have ingredients of allopurinol sodium:
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 Allopurinol sodium:
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 Hyperkalemia:
- Hyperkalemia (1,954 drugs)
Browse all the conditions that are associated with Hyperkalemia:
- Hyperkalemia (2,940 conditions)
How the study uses the data?
The study uses data from the FDA. It is based on allopurinol sodium (the active ingredients of Allopurinol sodium) and Allopurinol sodium (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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