Cefotaxime and Kayexalate drug interactions - a phase IV clinical study of FDA data

Summary:

Drug interactions are reported among people who take Cefotaxime (cefotaxime sodium) and Kayexalate (sodium polystyrene sulfonate). Common drug interactions include eosinophilia among females and urine output decreased among males.

The phase IV clinical study analyzes what interactions people have when they take Cefotaxime and Kayexalate. It is created by eHealthMe based on reports of 11 people who take the same drugs from the FDA, and is updated regularly.

What is Cefotaxime?

Cefotaxime has active ingredients of cefotaxime sodium. eHealthMe is studying from 7,559 Cefotaxime users. Check the latest studies of Cefotaxime.

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.



On Aug, 08, 2026

11 people who take Cefotaxime and Kayexalate together, and have interactions are studied.

Cefotaxime and Kayexalate drug interactions.

What are the common drug interactions of Cefotaxime and Kayexalate, by gender? *:

female:

  1. Eosinophilia (eosinophil count in the peripheral blood exceeds)
  2. Hepatocellular injury (liver injury)
  3. Rash generalised (rash on most of body parts)
  4. Dyspnoea (difficult or laboured respiration)
  5. Meningitis aseptic (a condition that causes the membranes covering your brain and spinal cord to become inflamed)
  6. Tumour lysis syndrome (a group of metabolic complications that can occur after treatment of cancer, these complications are caused by the breakdown products of dying cancer cells)

male:

  1. Urine output decreased
  2. Abdominal distension
  3. Blood osmolarity decreased
  4. Blood osmolarity increased
  5. Blood parathyroid hormone increased
  6. Blood phosphorus decreased
  7. Blood potassium decreased
  8. Blood sodium decreased
  9. Blood urea increased
  10. Carbon dioxide increased

What are the common drug interactions of Cefotaxime 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:

n/a

40-49:

n/a

50-59:

  1. Cardiac arrest
  2. Cardiac failure
  3. Cerebral ischaemia (insufficient blood flow to the brain to meet metabolic demand)
  4. Disease progression
  5. Nervous system disorder (a general class of medical conditions affecting the nervous system)
  6. Osteitis (a general term for inflammation of bone)
  7. Pneumonia
  8. Procedural site reaction

60+:

  1. Eosinophilia (eosinophil count in the peripheral blood exceeds)
  2. Hepatocellular injury (liver injury)
  3. Peripheral arterial occlusive disease (reproducible ischemic muscle pain)
  4. Thrombophlebitis (swelling (inflammation) of a vein caused by a blood clot)
  5. Tumour lysis syndrome (a group of metabolic complications that can occur after treatment of cancer, these complications are caused by the breakdown products of dying cancer cells)
  6. Linear iga disease (a rare, idiopathic or drug-induced autoimmune blistering disease of skin)
  7. Rash generalised (rash on most of body parts)
  8. Toxic skin eruption (skin breakdown due to toxic substance)
  9. Balance disorder
  10. Dyspnoea (difficult or laboured respiration)

What are the existing conditions these people have? *

  1. Respiratory Tract Infection: 1 person, 9.09%
  2. Rashes (redness): 1 person, 9.09%
  3. Pneumonia: 1 person, 9.09%
  4. Pain: 1 person, 9.09%
  5. Insulin-Requiring Type 2 Diabetes Mellitus: 1 person, 9.09%
  6. Infection: 1 person, 9.09%
  7. Immunodeficiency Disorders: 1 person, 9.09%
  8. Hypouricaemia (level of uric acid in the blood that is abnormally high): 1 person, 9.09%
  9. Hypotension (abnormally low blood pressure): 1 person, 9.09%
  10. Hypopituitarism (diminished hormone secretion by the pituitary gland, causing dwarfism in children and premature aging in adults): 1 person, 9.09%

* Approximation only. Some reports may have incomplete information.

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Related studies:

Effectiveness of, side effects of, and alternative drugs to the 2 drugs:

Browse all drug interactions of Cefotaxime 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 z

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 Cefotaxime:

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 z

Browse 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 z

Browse all interactions between Cefotaxime 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 z

Browse 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 z

How the study uses the data?

The study uses data from the FDA. It is based on cefotaxime sodium and sodium polystyrene sulfonate (the active ingredients of Cefotaxime and Kayexalate, respectively), and Cefotaxime 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.

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