Propofol and Blood lactic acid increased - a phase IV clinical study of FDA data

Summary:

Blood lactic acid increased is reported as a side effect among people who take Propofol (propofol), especially for people who are female, 20-29 old, have been taking the drug for < 1 month also take Midazolam, and have Status epilepticus.

The phase IV clinical study analyzes which people have Blood lactic acid increased when taking Propofol. It is created by eHealthMe based on reports of 37,986 people who have side effects when taking Propofol from the FDA, and is updated regularly.

What is Propofol?

Propofol has active ingredients of propofol. It is often used in colonoscopy abnormal. eHealthMe is studying from 38,224 Propofol users. Check the latest studies of Propofol.

What is Blood lactic acid increased?

Blood lactic acid increased is found to be associated with 536 drugs and 727 conditions by eHealthMe. Check the latest studies of Blood lactic acid increased.

On Jul, 09, 2026

37,986 people reported to have side effects when taking Propofol.
Among them, 181 people (0.48%) have Blood lactic acid increased.

Could Propofol cause Blood lactic acid increased?

Among these 181 people:

How long have people been on Propofol when they have Blood lactic acid increased? *

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What is the gender of people who have Blood lactic acid increased when taking Propofol? *

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What is the age of people who have Blood lactic acid increased when taking Propofol? *

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* Approximation only. Some reports may have incomplete information.

Do you take Propofol and have Blood lactic acid increased?

- Check whether Blood lactic acid increased is associated with a drug or a condition
- Predict drug outcomes for up to one year with AI
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Related studies:

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

Propofol (38,224 reports)

Blood lactic acid increased treatments and more:

Blood lactic acid increased (7,184 reports)

How severe was Blood lactic acid increased and when was it recovered:

Blood lactic acid increased in Propofol

Expand to all the drugs that have ingredients of propofol:

Blood lactic acid increased and drugs with ingredients of propofol (187 reports)

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 Propofol:

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 lactic acid increased:

Blood lactic acid increased (536 drugs)

Browse all the conditions that are associated with Blood lactic acid increased:

Blood lactic acid increased (727 conditions)

How the study uses the data?

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