Uloric and Zanaflex drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Uloric (febuxostat) and Zanaflex (tizanidine hydrochloride). Common drug interactions include vomiting among females and chronic kidney disease among males.
The phase IV clinical study analyzes what interactions people have when they take Uloric and Zanaflex. It is created by eHealthMe based on reports of 26 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 Zanaflex?
Zanaflex has active ingredients of tizanidine hydrochloride. It is often used in muscle spasms. eHealthMe is studying from 17,476 Zanaflex users. Check the latest studies of Zanaflex.
26 people who take Uloric and Zanaflex together, and have interactions are studied.

What are the common drug interactions of Uloric and Zanaflex, by gender? *:
female:
- Vomiting
- Back injury
- Dizziness
- Drug administration error
- Fall
- Formication (a sensation that exactly resembles that of small insects crawling on (or under) the skin)
- Injection site erythema (redness at injection site)
- Injection site extravasation (flow of (blood or lymph) from injection site)
- Injection site rash
- Injection site urticaria (rash of round, red welts on the skin at injection site)
male:
- Chronic kidney disease
- Renal failure (kidney dysfunction)
- Atrial flutter (an abnormal heart rhythm that occurs in the atria of the heart)
- Benign prostatic hyperplasia (benign enlargement of the prostate)
- Bradycardia (abnormally slow heart action)
- Constipation
- Death
- Diabetes mellitus (diabetes, caused by a deficiency of the pancreatic hormone insulin)
- Diarrhoea
- Dizziness
What are the common drug interactions of Uloric and Zanaflex, 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:
- Drug administration error
- Injection site extravasation (flow of (blood or lymph) from injection site)
- Retching (strong involuntary effort to vomit)
- Vomiting
- Drug intolerance (drug sensitivity)
- Injection site pain
- Nausea (feeling of having an urge to vomit)
50-59:
- Chronic kidney disease
- Renal failure (kidney dysfunction)
- Back injury
- Dizziness
- Fall
- Formication (a sensation that exactly resembles that of small insects crawling on (or under) the skin)
- Injection site erythema (redness at injection site)
- Injection site rash
- Injection site urticaria (rash of round, red welts on the skin at injection site)
- Pruritus (severe itching of the skin)
60+:
- Chronic kidney disease
- Hyperparathyroidism secondary (an abnormally high concentration of parathyroid hormone in the blood, resulting in weakening of the bones through loss of calcium-secondary)
- Fatigue (feeling of tiredness)
- Feeding disorder (when children refuse to eat certain food groups)
- Hypertension (high blood pressure)
- Hypotension (abnormally low blood pressure)
- Hypoxia (low oxygen in tissues)
- Intestinal obstruction
- Mental status changes (general changes in brain function, such as confusion, amnesia (memory loss), loss of alertness, loss of orientation)
- Renal impairment (severely reduced kidney function)
What are the existing conditions these people have? *
- Multiple Myeloma (cancer of the plasma cells): 5 people, 19.23%
- High Blood Cholesterol: 4 people, 15.38%
- High Blood Pressure: 4 people, 15.38%
- Depression: 3 people, 11.54%
- Diabetes: 3 people, 11.54%
- Fluid Retention (an abnormal accumulation of fluid in the blood): 3 people, 11.54%
- Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 3 people, 11.54%
- Hyperkalemia (damage to or disease of the kidney): 2 people, 7.69%
- Gastric Ulcer (stomach ulcer): 2 people, 7.69%
- Headache (pain in head): 2 people, 7.69%
* Approximation only. Some reports may have incomplete information.
Do you take Uloric and Zanaflex?
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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 Zanaflex:
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 Zanaflex:
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 Zanaflex 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 tizanidine hydrochloride (the active ingredients of Uloric and Zanaflex, respectively), and Uloric and Zanaflex (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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