Flexeril and Kayexalate drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Flexeril (cyclobenzaprine hydrochloride) and Kayexalate (sodium polystyrene sulfonate). Common drug interactions include diabetic vascular disorder among females and abdominal pain among males.
The phase IV clinical study analyzes what interactions people have when they take Flexeril and Kayexalate. It is created by eHealthMe based on reports of 18 people who take the same drugs from the FDA, and is updated regularly.
What is Flexeril?
Flexeril has active ingredients of cyclobenzaprine hydrochloride. It is often used in muscle spasms. eHealthMe is studying from 38,308 Flexeril users. Check the latest studies of Flexeril.
What is Kayexalate?
Kayexalate has active ingredients of sodium polystyrene sulfonate. eHealthMe is studying from 5,004 Kayexalate users. Check the latest studies of Kayexalate.
18 people who take Flexeril and Kayexalate together, and have interactions are studied.

What are the common drug interactions of Flexeril and Kayexalate, by gender? *:
female:
- Diabetic vascular disorder (diseases of the blood vessels due to diabetes)
- Diastolic dysfunction
- Diverticulum intestinal (a pouch that is attached to the first part of the small intestine)
- Dizziness
- Drug effect decreased
- Drug intolerance (drug sensitivity)
- Dyspnoea at rest (difficult or laboured breathing during rest)
- Erythema infectiosum (infection that results in a mild rash on the face, trunk, and limbs)
- Essential hypertension (primary hypertension)
- Failure to thrive (inadequate weight gain and physical growth in children)
male:
- Abdominal pain
- Agitation (state of anxiety or nervous excitement)
- Death
- Dehydration (dryness resulting from the removal of water)
- Delirium (wild excitement)
- Depression
- Diabetes mellitus (diabetes, caused by a deficiency of the pancreatic hormone insulin)
- Diabetic ketoacidosis (diabetic ketoacidosis (dka) is high concentrations of ketone bodies)
- Diarrhoea
- Disorientation (disability in which the senses of time, direction, and recognition of people and places)
What are the common drug interactions of Flexeril and Kayexalate, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
n/a
30-39:
- Blood pressure increased
- 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)
- Nephrogenic anaemia (anaemia due to kidney disease)
- Nephrogenic fibrosing dermopathy (involves fibrosis of skin, joints, eyes due to kidney disease)
- Oedema peripheral (superficial swelling)
- Pruritus (severe itching of the skin)
- Renal failure (kidney dysfunction)
- Superior vena caval occlusion (obstruction of blood flow through the superior vena cava)
- Thrombosis (formation of a blood clot inside a blood vessel)
40-49:
- Nephrogenic systemic fibrosis (involves fibrosis of skin, joints, eyes due to kidney disease)
50-59:
- Delirium (wild excitement)
- Depression
- Diabetes mellitus (diabetes, caused by a deficiency of the pancreatic hormone insulin)
- Diabetic ketoacidosis (diabetic ketoacidosis (dka) is high concentrations of ketone bodies)
- Diarrhoea
- Disorientation (disability in which the senses of time, direction, and recognition of people and places)
- Dysphagia (a condition in which swallowing is difficult or painful)
- Ecchymosis (a discoloration of the skin resulting from bleeding underneath)
- Excoriation (to tear or wear off the skin of)
- Flank pain (a distressing sensation experienced around the lower back and the upper abdomen)
60+:
- Dyspnoea (difficult or laboured respiration)
- Vomiting
- Hyperbilirubinaemia (excess of bilirubin in the blood)
- Hyperkalaemia (damage to or disease of the kidney)
- Hypotension (abnormally low blood pressure)
- Ischaemic hepatitis (decreased blood supply to the liver resulting in injury to liver cells)
- Mitral valve incompetence (inefficient heart valve)
- Multi-organ failure (multisystem organ failure)
- Nausea (feeling of having an urge to vomit)
- Platelet count decreased
What are the existing conditions these people have? *
- Nausea (feeling of having an urge to vomit): 4 people, 22.22%
- High Blood Pressure: 4 people, 22.22%
- Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 4 people, 22.22%
- Depression: 4 people, 22.22%
- Diabetes: 3 people, 16.67%
- Stress And Anxiety: 3 people, 16.67%
- Back Pain: 3 people, 16.67%
- Hyperlipidaemia (presence of excess lipids in the blood): 3 people, 16.67%
- Oedema Peripheral (superficial swelling): 3 people, 16.67%
- Neuropathy Peripheral (surface nerve damage): 3 people, 16.67%
* Approximation only. Some reports may have incomplete information.
Do you take Flexeril and Kayexalate?
- Personalize this study to your gender, age, symptoms and drugs
- Predict drug outcomes for up to one year with AI
- Get an AI agent to monitor your drugs continuously
Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
- Flexeril (38,308 reports)
- Kayexalate (5,004 reports)
Browse all drug interactions of Flexeril and Kayexalate:
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 Flexeril:
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 Kayexalate:
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 Flexeril 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 Kayexalate 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 cyclobenzaprine hydrochloride and sodium polystyrene sulfonate (the active ingredients of Flexeril and Kayexalate, respectively), and Flexeril and Kayexalate (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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