Prezista and Blood lactate dehydrogenase increased - a phase IV clinical study of FDA data

Summary:

Blood lactate dehydrogenase increased is reported as a side effect among people who take Prezista (darunavir ethanolate), especially for people who are female, 40-49 old, have been taking the drug for < 1 month also take Norvir, and have Depression.

The phase IV clinical study analyzes which people have Blood lactate dehydrogenase increased when taking Prezista. It is created by eHealthMe based on reports of 12,243 people who have side effects when taking Prezista from the FDA, and is updated regularly.

What is Prezista?

Prezista has active ingredients of darunavir ethanolate. It is often used in hiv infection. eHealthMe is studying from 12,363 Prezista users. Check the latest studies of Prezista.

What is Blood lactate dehydrogenase increased?

Blood lactate dehydrogenase increased is found to be associated with 1,264 drugs and 2,012 conditions by eHealthMe. Check the latest studies of Blood lactate dehydrogenase increased.

On Jul, 18, 2026

12,243 people reported to have side effects when taking Prezista.
Among them, 17 people (0.14%) have Blood lactate dehydrogenase increased.

Could Prezista cause Blood lactate dehydrogenase increased?

Among these 17 people:

How long have people been on Prezista when they have Blood lactate dehydrogenase increased? *

What is the gender of people who have Blood lactate dehydrogenase increased when taking Prezista? *

female: 52.94 %
male: 47.06 %

What is the age of people who have Blood lactate dehydrogenase increased when taking Prezista? *

What are other drugs people take besides Prezista? *

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

Gamma-Glutamyltransferase Increased: 10 people, 58.82%
Aspartate Aminotransferase Increased: 7 people, 41.18%
Rashes (redness): 6 people, 35.29%
Liver Function Test Abnormal: 6 people, 35.29%
Pruritus Generalised (generalized itching): 5 people, 29.41%
Leukocytosis (increased white blood cells): 5 people, 29.41%
Fever: 5 people, 29.41%
Eosinophilia (eosinophil count in the peripheral blood exceeds): 5 people, 29.41%
Enanthema (rash formed inside the body): 5 people, 29.41%
Conjunctivitis (pink eye): 5 people, 29.41%

What are the existing conditions these people have? *

Depression: 3 people, 17.65%
Diabetes: 2 people, 11.76%
High Blood Pressure: 2 people, 11.76%
Sleep Disorder: 1 person, 5.88%
Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 1 person, 5.88%
Cerebral Toxoplasmosis (parasitic disease of brain caused by the protozoan toxoplasma gondii): 1 person, 5.88%
Crohn's Disease (a condition that causes inflammation of the gastrointestinal tract): 1 person, 5.88%
Drug Dependence: 1 person, 5.88%
Fibromyalgia (a long-term condition which causes pain all over the body): 1 person, 5.88%
Heart Attack: 1 person, 5.88%

* Approximation only. Some reports may have incomplete information.

Do you take Prezista and have Blood lactate dehydrogenase increased?

- Check whether Blood lactate dehydrogenase 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 Prezista:

Prezista (12,363 reports)

Browse all side effects of Prezista:

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 lactate dehydrogenase increased:

Blood lactate dehydrogenase increased (1,264 drugs)

Browse all the conditions that are associated with Blood lactate dehydrogenase increased:

Blood lactate dehydrogenase increased (2,012 conditions)

How the study uses the data?

The study uses data from the FDA. It is based on darunavir ethanolate (the active ingredients of Prezista) and Prezista (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.