Uloric and Procardia drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Uloric (febuxostat) and Procardia (nifedipine). Common drug interactions include insomnia among females and chronic kidney disease among males.
The phase IV clinical study analyzes what interactions people have when they take Uloric and Procardia. It is created by eHealthMe based on reports of 14 people who take the same drugs from the FDA, and is updated regularly.
What is Uloric?
Uloric has active ingredients of febuxostat. It is often used in gout. eHealthMe is studying from 8,067 Uloric users. Check the latest studies of Uloric.
What is Procardia?
Procardia has active ingredients of nifedipine. It is often used in high blood pressure. eHealthMe is studying from 15,151 Procardia users. Check the latest studies of Procardia.
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 >>>.
14 people who take Uloric and Procardia together, and have interactions are studied.

What are the common drug interactions of Uloric and Procardia, by gender? *:
female:
- Insomnia (sleeplessness)
- Renal failure (kidney dysfunction)
- Blood cholesterol increased
- Hypersensitivity
- Nephrolithiasis (calculi in the kidneys)
- Peripheral swelling
- Pruritus (severe itching of the skin)
- Rash
- Renal failure chronic (long lasting kidney dysfunction)
- Renal injury (kidney injury)
male:
- Chronic kidney disease
- Renal failure (kidney dysfunction)
- Renal injury (kidney injury)
- Nephrogenic anaemia (anaemia due to kidney disease)
- Death
- Hyperparathyroidism secondary (an abnormally high concentration of parathyroid hormone in the blood, resulting in weakening of the bones through loss of calcium-secondary)
- Renal tubular necrosis (death of kidney tubules)
What are the common drug interactions of Uloric and Procardia, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
n/a
30-39:
n/a
40-49:
n/a
50-59:
- Hyperparathyroidism secondary (an abnormally high concentration of parathyroid hormone in the blood, resulting in weakening of the bones through loss of calcium-secondary)
- Nephrogenic anaemia (anaemia due to kidney disease)
- Renal failure (kidney dysfunction)
- Blood cholesterol increased
- Nephrolithiasis (calculi in the kidneys)
- Chronic kidney disease
60+:
- Chronic kidney disease
- Renal failure (kidney dysfunction)
- Renal injury (kidney injury)
- Death
- Hypersensitivity
- Pruritus (severe itching of the skin)
- Rash
- Renal failure chronic (long lasting kidney dysfunction)
- Tubulointerstitial nephritis (a form of nephritis affecting the interstitium of the kidneys surrounding the tubules)
What are the existing conditions these people have? *
- Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 4 people, 28.57%
- Narcolepsy (brain's inability to regulate sleep-wake cycles normally): 2 people, 14.29%
- Hyperkalemia (damage to or disease of the kidney): 2 people, 14.29%
- Type 2 Diabetes: 1 person, 7.14%
- Tetanus (infection of the nervous system with the potentially deadly bacteria): 1 person, 7.14%
- Rickets (softening of bones): 1 person, 7.14%
- Indigestion: 1 person, 7.14%
- Hyperuricaemia (level of uric acid in the blood that is abnormally high): 1 person, 7.14%
- Hyperparathyroidism (an abnormally high concentration of parathyroid hormone in the blood, resulting in weakening of the bones through loss of calcium): 1 person, 7.14%
- Hyperlipidaemia (presence of excess lipids in the blood): 1 person, 7.14%
* Approximation only. Some reports may have incomplete information.
Do you take Uloric and Procardia?
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Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
Browse all drug interactions of Uloric and Procardia:
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 zSub-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 Uloric:
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 side effects of Procardia:
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 interactions between Uloric and drugs from A to Z:
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 interactions between Procardia and drugs from A to Z:
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 zHow the study uses the data?
The study uses data from the FDA. It is based on febuxostat and nifedipine (the active ingredients of Uloric and Procardia, respectively), and Uloric and Procardia (the brand names). 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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