Cefotaxime sodium and Lymphocyte count decreased - a phase IV clinical study of FDA data

Summary:

Lymphocyte count decreased is reported as a side effect among people who take Cefotaxime sodium (cefotaxime sodium), especially for people who are male, 30-39 old, have been taking the drug for < 1 month also take Myfortic, and have Diarrhea.

The phase IV clinical study analyzes which people have Lymphocyte count decreased when taking Cefotaxime sodium. It is created by eHealthMe based on reports of 2,548 people who have side effects when taking Cefotaxime sodium from the FDA, and is updated regularly.

What is Cefotaxime sodium?

Cefotaxime sodium has active ingredients of cefotaxime sodium. eHealthMe is studying from 2,549 Cefotaxime sodium users. Check the latest studies of Cefotaxime sodium.

What is Lymphocyte count decreased?

Lymphocyte count decreased is found to be associated with 1,208 drugs and 1,325 conditions by eHealthMe. Check the latest studies of Lymphocyte count decreased.

On Jul, 16, 2026

2,548 people reported to have side effects when taking Cefotaxime sodium.
Among them, 16 people (0.63%) have Lymphocyte count decreased.

Could Cefotaxime sodium cause Lymphocyte count decreased?

Among these 16 people:

How long have people been on Cefotaxime sodium when they have Lymphocyte count decreased? *

What is the gender of people who have Lymphocyte count decreased when taking Cefotaxime sodium? *

female: 12.5 %
male: 87.5 %

What is the age of people who have Lymphocyte count decreased when taking Cefotaxime sodium? *

What are other drugs people take besides Cefotaxime sodium? *

Myfortic: 11 people, 68.75%
Scopolamine: 7 people, 43.75%
Insulin: 5 people, 31.25%
Ciclosporin: 5 people, 31.25%
Chymotrypsin: 4 people, 25.00%
Cobamamide: 4 people, 25.00%
Imipenem And Cilastatin: 4 people, 25.00%
Zyvox: 4 people, 25.00%
Micafungin Sodium: 3 people, 18.75%
Amphotericin B: 2 people, 12.50%

What are other side effects people have besides Lymphocyte count decreased? *

Neutrophil Count Increased (excess than normal number of neutrophil a type of blood cell): 12 people, 75.00%
Haemoglobin Decreased: 11 people, 68.75%
Blood Urea Increased: 10 people, 62.50%
Blood Glucose Increased: 7 people, 43.75%
Anaemia (lack of blood): 7 people, 43.75%
Diarrhea: 6 people, 37.50%
Fever: 5 people, 31.25%
Thrombocytopenia (decrease of platelets in blood): 5 people, 31.25%
Diabetes: 4 people, 25.00%
Hyperuricaemia (level of uric acid in the blood that is abnormally high): 4 people, 25.00%

What are the existing conditions these people have? *

Diarrhea: 9 people, 56.25%
High Blood Pressure: 8 people, 50.00%
Productive Cough: 8 people, 50.00%
Pain: 7 people, 43.75%
Urination - Excessive Volume: 7 people, 43.75%
Weakness: 4 people, 25.00%
Anaemia (lack of blood): 4 people, 25.00%
Blood Disorder: 4 people, 25.00%
Blood Pressure Abnormal: 4 people, 25.00%
Dizziness: 4 people, 25.00%

* Approximation only. Some reports may have incomplete information.

Do you take Cefotaxime sodium and have Lymphocyte count decreased?

- Check whether Lymphocyte count decreased is associated with a drug or a condition
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Related studies:

Effectiveness of, long term effects of, and alternative drugs to Cefotaxime sodium:

Cefotaxime sodium (2,549 reports)

Browse all side effects of Cefotaxime sodium:

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Browse all the drugs that are associated with Lymphocyte count decreased:

Lymphocyte count decreased (1,208 drugs)

Browse all the conditions that are associated with Lymphocyte count decreased:

Lymphocyte count decreased (1,325 conditions)

How the study uses the data?

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