Cefazolin and Respiratory rate increased - a phase IV clinical study of FDA data

Summary:

Respiratory rate increased is reported as a side effect among people who take Cefazolin (cefazolin sodium), especially for people who are female, 60+ old, have been taking the drug for < 1 month also take Propofol, and have Breast infection.

The phase IV clinical study analyzes which people have Respiratory rate increased when taking Cefazolin. It is created by eHealthMe based on reports of 15,127 people who have side effects when taking Cefazolin from the FDA, and is updated regularly.

What is Cefazolin?

Cefazolin has active ingredients of cefazolin sodium. It is often used in infection. eHealthMe is studying from 15,157 Cefazolin users. Check the latest studies of Cefazolin.

What is Respiratory rate increased?

Respiratory rate increased (excess breathing rate/min) is found to be associated with 882 drugs and 1,060 conditions by eHealthMe. Check the latest studies of Respiratory rate increased.

On Jul, 23, 2026

15,127 people reported to have side effects when taking Cefazolin.
Among them, 24 people (0.16%) have Respiratory rate increased.

Could Cefazolin cause Respiratory rate increased?

Among these 24 people:

How long have people been on Cefazolin when they have Respiratory rate increased? *

What is the gender of people who have Respiratory rate increased when taking Cefazolin? *

female: 54.17 %
male: 45.83 %

What is the age of people who have Respiratory rate increased when taking Cefazolin? *

What are other drugs people take besides Cefazolin? *

What are other side effects people have besides Respiratory rate increased? *

Hypotension (abnormally low blood pressure): 6 people, 25.00%
Chills (felling of cold): 5 people, 20.83%
Heart Rate Increased: 5 people, 20.83%
Nausea (feeling of having an urge to vomit): 5 people, 20.83%
Oxygen Saturation Decreased: 5 people, 20.83%
Dyspnea (difficult or laboured breathing): 5 people, 20.83%
High Blood Pressure: 4 people, 16.67%
Arrhythmias (irregular heartbeat): 4 people, 16.67%
Hypoaesthesia (reduced sense of touch or sensation): 4 people, 16.67%
Agitation (state of anxiety or nervous excitement): 4 people, 16.67%

What are the existing conditions these people have? *

Pain: 2 people, 8.33%
Breast Infection: 2 people, 8.33%
Wound Infection: 1 person, 4.17%
Epidural Anaesthesia: 1 person, 4.17%
Analgesic Effect: 1 person, 4.17%
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): 1 person, 4.17%
Cellulitis (infection under the skin): 1 person, 4.17%
Clonic Convulsion (long lasting seizure): 1 person, 4.17%
Diabetes Insipidus (diabetes caused by a deficiency of the pituitary hormone vasopressin, which regulates kidney function): 1 person, 4.17%
General Anaesthesia: 1 person, 4.17%

* Approximation only. Some reports may have incomplete information.

Do you take Cefazolin and have Respiratory rate increased?

- Check whether Respiratory rate 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 Cefazolin:

Cefazolin (15,157 reports)

Browse all side effects of Cefazolin:

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 Respiratory rate increased:

Respiratory rate increased (882 drugs)

Browse all the conditions that are associated with Respiratory rate increased:

Respiratory rate increased (1,060 conditions)

How the study uses the data?

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