Vistaril and Hypertriglyceridaemia - a phase IV clinical study of FDA data

Summary:

Hypertriglyceridaemia is reported as a side effect among people who take Vistaril (hydroxyzine hydrochloride), especially for people who are male, 40-49 old, also take Seroquel, and have Depression.

The phase IV clinical study analyzes which people have Hypertriglyceridaemia when taking Vistaril. It is created by eHealthMe based on reports of 8,641 people who have side effects when taking Vistaril from the FDA, and is updated regularly.

What is Vistaril?

Vistaril has active ingredients of hydroxyzine hydrochloride. It is often used in stress and anxiety. eHealthMe is studying from 9,565 Vistaril users. Check the latest studies of Vistaril.

What is Hypertriglyceridaemia?

Hypertriglyceridaemia (excess of triglycerides in the blood) is found to be associated with 755 drugs and 763 conditions by eHealthMe. Check the latest studies of Hypertriglyceridaemia.

On Aug, 10, 2026

8,641 people reported to have side effects when taking Vistaril.
Among them, 12 people (0.14%) have Hypertriglyceridaemia.

Could Vistaril cause Hypertriglyceridaemia?

Among these 12 people:

What is the gender of people who have Hypertriglyceridaemia when taking Vistaril? *

female: 41.67 %
male: 58.33 %

What is the age of people who have Hypertriglyceridaemia when taking Vistaril? *

What are other drugs people take besides Vistaril? *

What are other side effects people have besides Hypertriglyceridaemia? *

Dizziness: 5 people, 41.67%
High Blood Pressure: 5 people, 41.67%
High Blood Cholesterol: 4 people, 33.33%
Weakness: 4 people, 33.33%
Hyperglycemia (high blood sugar): 4 people, 33.33%
Headache (pain in head): 4 people, 33.33%
Pain In Extremity: 4 people, 33.33%
Diabetes: 4 people, 33.33%
Major Depression (a mood state that goes well beyond temporarily feeling sad or blue. it is a serious medical illness that affects one's thoughts, feelings): 3 people, 25.00%
Joint Pain: 3 people, 25.00%

What are the existing conditions these people have? *

Depression: 5 people, 41.67%
Pain: 4 people, 33.33%
Diabetes: 4 people, 33.33%
Nausea (feeling of having an urge to vomit): 3 people, 25.00%
Hyperlipidaemia (presence of excess lipids in the blood): 2 people, 16.67%
Constipation: 2 people, 16.67%
Bipolar Disorder (mood disorder): 2 people, 16.67%
Neuropathy Peripheral (surface nerve damage): 2 people, 16.67%
Lipodystrophy Acquired (a regional loss of subcutaneous adipose tissue which usually starts in the face, extends downward acquired): 2 people, 16.67%
Hypertonic Bladder (bladder-storage function that causes a sudden urge to urinate): 2 people, 16.67%

* Approximation only. Some reports may have incomplete information.

Do you take Vistaril and have Hypertriglyceridaemia?

- Check whether Hypertriglyceridaemia 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 Vistaril:

Vistaril (9,565 reports)

Browse all side effects of Vistaril:

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 Hypertriglyceridaemia:

Hypertriglyceridaemia (755 drugs)

Browse all the conditions that are associated with Hypertriglyceridaemia:

Hypertriglyceridaemia (763 conditions)

Related publications that referenced our studies

Ate? ?, Arikan MF, Kaplan M, Altay M, "Hydroxyzine induced pancytopenia and petechial rashes: a rare complication", Journal Of Contemporary Medicine, 2017 Jan .
Ate? ?, Arikan MF, Kaplan M, Altay M, "Hydroxyzine induced pancytopenia and petechial rashes: a rare complication", Journal Of Contemporary Medicine, 2017 Jan .

How the study uses the data?

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