Cymbalta and High density lipoprotein increased - a phase IV clinical study of FDA data

Summary:

High density lipoprotein increased is reported as a side effect among people who take Cymbalta (duloxetine hydrochloride), especially for people who are female, 50-59 old, have been taking the drug for 1 - 6 months also take Jakafi, and have Primary myelofibrosis.

The phase IV clinical study analyzes which people have High density lipoprotein increased when taking Cymbalta. It is created by eHealthMe based on reports of 145,249 people who have side effects when taking Cymbalta from the FDA, and is updated regularly.

What is Cymbalta?

Cymbalta has active ingredients of duloxetine hydrochloride. It is often used in depression. eHealthMe is studying from 154,973 Cymbalta users. Check the latest studies of Cymbalta.

What is High density lipoprotein increased?

High density lipoprotein increased is found to be associated with 194 drugs and 354 conditions by eHealthMe. Check the latest studies of High density lipoprotein increased.

On Jul, 19, 2026

145,249 people reported to have side effects when taking Cymbalta.
Among them, 53 people (0.04%) have High density lipoprotein increased.

Could Cymbalta cause High density lipoprotein increased?

Among these 53 people:

How long have people been on Cymbalta when they have High density lipoprotein increased? *

What is the gender of people who have High density lipoprotein increased when taking Cymbalta? *

female: 86.11 %
male: 13.89 %

What is the age of people who have High density lipoprotein increased when taking Cymbalta? *

What are other drugs people take besides Cymbalta? *

What are other side effects people have besides High density lipoprotein increased? *

Low Density Lipoprotein Increased (cholesterol increased in blood): 31 people, 58.49%
Pain: 31 people, 58.49%
High Blood Cholesterol: 30 people, 56.60%
Alanine Aminotransferase Increased: 28 people, 52.83%
Aspartate Aminotransferase Increased: 28 people, 52.83%
Joint Pain: 27 people, 50.94%
Nausea (feeling of having an urge to vomit): 24 people, 45.28%
Bronchitis (inflammation of the mucous membrane in the bronchial tubes): 23 people, 43.40%
Head Injury: 23 people, 43.40%
Fall: 23 people, 43.40%

What are the existing conditions these people have? *

Primary Myelofibrosis (primary disorder of the bone marrow): 18 people, 33.96%
Polycythaemia Vera (blood disorder in which the bone marrow makes too many red blood cells): 15 people, 28.30%
Neuropathy Peripheral (surface nerve damage): 15 people, 28.30%
Bronchitis (inflammation of the mucous membrane in the bronchial tubes): 15 people, 28.30%
Pelvic Pain: 15 people, 28.30%
Rheumatoid Arthritis (a chronic progressive disease causing inflammation in the joints): 11 people, 20.75%
Muscle Spasms (muscle contraction): 7 people, 13.21%
Pain: 6 people, 11.32%
Diabetes: 4 people, 7.55%
Suicidal Ideation: 3 people, 5.66%

* Approximation only. Some reports may have incomplete information.

Do you take Cymbalta and have High density lipoprotein increased?

- Check whether High density lipoprotein 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 Cymbalta:

Cymbalta (154,973 reports)

Browse all side effects of Cymbalta:

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 High density lipoprotein increased:

High density lipoprotein increased (194 drugs)

Browse all the conditions that are associated with High density lipoprotein increased:

High density lipoprotein increased (354 conditions)

How the study uses the data?

The study uses data from the FDA. It is based on duloxetine hydrochloride (the active ingredients of Cymbalta) and Cymbalta (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.