Atarax and Prempro drug interactions - a phase IV clinical study of FDA data

Summary:

Drug interactions are reported among people who take Atarax (hydroxyzine hydrochloride) and Prempro (estrogens, conjugated; medroxyprogesterone acetate). Common drug interactions include kidney infection among females and myelodysplastic syndrome among males.

The phase IV clinical study analyzes what interactions people have when they take Atarax and Prempro. It is created by eHealthMe based on reports of 34 people who take the same drugs from the FDA, and is updated regularly.

What is Atarax?

Atarax has active ingredients of hydroxyzine hydrochloride. It is often used in stress and anxiety. eHealthMe is studying from 23,553 Atarax users. Check the latest studies of Atarax.

What is Prempro?

Prempro has active ingredients of estrogens, conjugated; medroxyprogesterone acetate. It is often used in menopause. eHealthMe is studying from 42,950 Prempro users. Check the latest studies of Prempro.



On Jul, 24, 2026

34 people who take Atarax and Prempro together, and have interactions are studied.

Atarax and Prempro drug interactions.

What are the common drug interactions of Atarax and Prempro, by gender? *:

female:

  1. Kidney infection
  2. Pain
  3. Post procedural cellulitis (post procedural bacterial infection of the skin and soft tissues)
  4. Seroma (a tumour like collection of serum in the tissues)
  5. Vaginal cyst
  6. Vaginal haemorrhage (vaginal bleeding)
  7. Fatigue (feeling of tiredness)
  8. Headache (pain in head)
  9. Renal disorder (kidney disease)
  10. Night sweats (sweating in night)

male:

  1. Myelodysplastic syndrome (a group of conditions that occur when the blood-forming cells in the bone marrow are damaged)

What are the common drug interactions of Atarax and Prempro, by age (0-1 to 60+)? *:

0-1:

n/a

2-9:

n/a

10-19:

n/a

20-29:

n/a

30-39:

n/a

40-49:

  1. Alanine aminotransferase increased
  2. Aspartate aminotransferase increased
  3. Blood cholesterol increased
  4. Blood glucose increased
  5. Blood triglycerides increased
  6. Cardiovascular disorder (heart diseases)
  7. Cystitis (inflammation of the wall of the bladder)
  8. Dehydration (dryness resulting from the removal of water)
  9. Diabetes mellitus (diabetes, caused by a deficiency of the pancreatic hormone insulin)
  10. Diabetes mellitus inadequate control

50-59:

  1. Kidney infection
  2. Sinusitis (inflammation of sinus)
  3. Abdominal pain
  4. Breast cancer stage ii
  5. Deformity (disfigurement)
  6. Nausea (feeling of having an urge to vomit)
  7. Pain
  8. Post procedural cellulitis (post procedural bacterial infection of the skin and soft tissues)
  9. Seroma (a tumour like collection of serum in the tissues)
  10. Vaginal cyst

60+:

  1. Drug ineffective
  2. Cold sweat
  3. Fatigue (feeling of tiredness)
  4. Malaise (a feeling of general discomfort or uneasiness)
  5. Skin irritation
  6. Night sweats (sweating in night)
  7. Vulvovaginal pruritus (vulvovaginal severe itching)
  8. Back pain
  9. Bundle branch block left (absence of transmission of electric impulses from the atrioventricular (av) bundle of his to the left ventricle)
  10. Cardiac failure congestive

What are the existing conditions these people have? *

  1. Immunodeficiency Common Variable: 9 people, 26.47%
  2. Menopausal Symptoms: 6 people, 17.65%
  3. Hypothyroidism (abnormally low activity of the thyroid gland, resulting in retardation of growth and mental development): 4 people, 11.76%
  4. Urticaria (rash of round, red welts on the skin that itch intensely): 3 people, 8.82%
  5. Type 2 Diabetes: 3 people, 8.82%
  6. Atopy (a genetic disposition to develop an allergic reaction): 3 people, 8.82%
  7. Osteoporosis (bones weak and more likely to break): 2 people, 5.88%
  8. Migraine (headache): 2 people, 5.88%
  9. Hypersensitivity: 2 people, 5.88%
  10. Hepatitis C: 2 people, 5.88%

* Approximation only. Some reports may have incomplete information.

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Related studies:

Effectiveness of, side effects of, and alternative drugs to the 2 drugs:

Browse all drug interactions of Atarax and Prempro:

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

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 Atarax:

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 side effects of Prempro:

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 interactions between Atarax and drugs from A to Z:

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 interactions between Prempro and drugs from A to Z:

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

Related publications that referenced our studies


How the study uses the data?

The study uses data from the FDA. It is based on hydroxyzine hydrochloride and estrogens, conjugated; medroxyprogesterone acetate (the active ingredients of Atarax and Prempro, respectively), and Atarax and Prempro (the brand names). 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.



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