Cefobid and Prothrombin time abnormal - a phase IV clinical study of FDA data

Summary:

We study 2,129 people who take Cefobid (cefoperazone sodium) or have Prothrombin time abnormal. No report of Prothrombin time abnormal is found in people who take Cefobid.

The phase IV clinical study is created by eHealthMe based on reports from the FDA, and is updated regularly.

What is Cefobid?

Cefobid has active ingredients of cefoperazone sodium. eHealthMe is studying from 1,317 Cefobid users. Check the latest studies of Cefobid.

What is Prothrombin Time Abnormal?

Prothrombin time abnormal is found to be associated with 133 drugs and 301 conditions by eHealthMe. Check the latest studies of Prothrombin time abnormal.

On Jul, 08, 2026

No report is found.

Do you take Cefobid and have Prothrombin time abnormal?

- Check whether Prothrombin time abnormal 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 Cefobid:

Cefobid (1,317 reports)

Browse all side effects of Cefobid:

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Browse all the drugs that are associated with Prothrombin time abnormal:

Prothrombin time abnormal

Browse all the conditions that are associated with Prothrombin time abnormal:

Prothrombin time abnormal

How the study uses the data?

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