Cefdinir and Blood urea increased - a phase IV clinical study of FDA data

Summary:

Blood urea increased is reported as a side effect among people who take Cefdinir (cefdinir), especially for people who are male, 60+ old, have been taking the drug for < 1 month also take Protonix, and have Nausea and vomiting.

The phase IV clinical study analyzes which people have Blood urea increased when taking Cefdinir. It is created by eHealthMe based on reports of 8,699 people who have side effects when taking Cefdinir from the FDA, and is updated regularly.

What is Cefdinir?

Cefdinir has active ingredients of cefdinir. It is often used in sinusitis. eHealthMe is studying from 9,210 Cefdinir users. Check the latest studies of Cefdinir.

What is Blood urea increased?

Blood urea increased is found to be associated with 1,623 drugs and 1,990 conditions by eHealthMe. Check the latest studies of Blood urea increased.

On Jul, 08, 2026

8,699 people reported to have side effects when taking Cefdinir.
Among them, 23 people (0.26%) have Blood urea increased.

Could Cefdinir cause Blood urea increased?

Among these 23 people:

How long have people been on Cefdinir when they have Blood urea increased? *

What is the gender of people who have Blood urea increased when taking Cefdinir? *

female: 40.91 %
male: 59.09 %

What is the age of people who have Blood urea increased when taking Cefdinir? *

What are other drugs people take besides Cefdinir? *

What are other side effects people have besides Blood urea increased? *

Thrombocytopenia (decrease of platelets in blood): 16 people, 69.57%
Blood Glucose Increased: 13 people, 56.52%
Haemoglobin Decreased: 10 people, 43.48%
Hypokalemia (low potassium): 8 people, 34.78%
Dizziness: 7 people, 30.43%
Pleural Effusion (water on the lungs): 7 people, 30.43%
Electrocardiogram St Segment Depression: 7 people, 30.43%
Enlarged Heart: 7 people, 30.43%
Lymphocyte Count Decreased: 7 people, 30.43%
Stress And Anxiety: 7 people, 30.43%

What are the existing conditions these people have? *

Nausea And Vomiting: 8 people, 34.78%
Thrombosis (formation of a blood clot inside a blood vessel): 7 people, 30.43%
High Blood Pressure: 7 people, 30.43%
Anaesthesia: 7 people, 30.43%
Atrial Fibrillation/flutter (atrial fibrillation and flutter are abnormal heart rhythms in which the atria, or upper chambers of the heart, are out of sync with the ventricles): 7 people, 30.43%
Bacterial Infection: 7 people, 30.43%
Blood Glucose Increased: 7 people, 30.43%
Cardiac Disorder: 7 people, 30.43%
Constipation: 7 people, 30.43%
Diarrhea: 7 people, 30.43%

* Approximation only. Some reports may have incomplete information.

Do you take Cefdinir and have Blood urea increased?

- Check whether Blood urea increased is associated with a drug or a condition
- Predict drug outcomes for up to one year with AI
- Get an AI agent to monitor your drugs continuously

Related studies:

Effectiveness of, long term effects of, and alternative drugs to Cefdinir:

Cefdinir (9,210 reports)

Browse all side effects of Cefdinir:

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 the drugs that are associated with Blood urea increased:

Blood urea increased (1,623 drugs)

Browse all the conditions that are associated with Blood urea increased:

Blood urea increased (1,990 conditions)

How the study uses the data?

The study uses data from the FDA. It is based on cefdinir (the active ingredients of Cefdinir) and Cefdinir (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.