Vistaril and Minipress drug interactions - from FDA reports
Drug interactions are reported among people who take Vistaril and Minipress together. This study is created by eHealthMe based on reports of 11 people who take Vistaril and Minipress from FDA, and is updated regularly.
eHealthMe is a health data analysis company based in Mountain View, California. eHealthMe monitors and analyzes the outcomes of drugs and supplements that are currently on the market. The results are readily available to health care professionals and consumers.
eHealthMe has released original studies on market drugs and worked with leading universities and institutions such as IBM, London Health Science Centre, Mayo Clinic, Northwestern University and VA. eHealthMe studies have now been referenced in over 500 peer-reviewed medical publications.
How we gather our data?
Healthcare data is obtained from a number of sources including the Food and Drug Administration (FDA). This information is aggregated and used to produce personalized reports that patients can reference.
The information that eHealthMe collects includes:
- Side effects (including severity and how people recover from them)
- Associated conditions or symptoms
- Drug effectiveness
- Demographic data regarding drug use
How the study uses the data?
The study is based on hydroxyzine hydrochloride and prazosin hydrochloride (the active ingredients of Vistaril and Minipress, respectively), and Vistaril and Minipress (the brand names). Other drugs that have the same active ingredients (e.g. generic drugs) are not considered.
What is Vistaril?
Vistaril has active ingredients of hydroxyzine hydrochloride. It is often used in stress and anxiety. (latest outcomes from Vistaril 7,312 users)
What is Minipress?
Minipress has active ingredients of prazosin hydrochloride. It is often used in post-traumatic stress disorder. (latest outcomes from Minipress 1,745 users)
How to use the study?
Patients can bring a copy of the report to their healthcare provider to ensure that all drug risks and benefits are fully discussed and understood. It is recommended that patients use the information presented as a part of a broader decision-making process.
11 people who take Vistaril, Minipress are studied.
Number of reports submitted per year:
Most common drug interactions over time *:
< 1 month:
1 - 6 months:
6 - 12 months:
1 - 2 years:
2 - 5 years:
5 - 10 years:
Most common drug interactions by gender *:
Most common drug interactions by age *:
* Approximation only. Some reports may have incomplete information.
Do you take Vistaril and Minipress?
- Personalize this study to your gender and age
- Subscribe to monitor Vistaril and Minipress
- Subscribe to monitor Vistaril
- Subscribe to monitor Minipress
You are not alone:
- Connect with people like you who take Vistaril and Minipress
- Use your healthcare experience to help people like you, and be rewarded
Related publications that referenced our studies
- Ateş İ, Arikan MF, Kaplan M, Altay M, "Hydroxyzine induced pancytopenia and petechial rashes: a rare complication", Journal Of Contemporary Medicine, 2013 Jan .
Browse interactions by gender and age
Interactions between Vistaril and drugs from A to Za 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
Interactions between Minipress and drugs from A to Za 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 drug interactions of Vistaril and Minipressa 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
What would happen?
FDA reports used in this study
- Want to find out more about the FDA reports used in the study? You can request them from FDA.
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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, and has not been supported by scientific studies or clinical trials unless otherwise stated. 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.
You may report adverse side effects to the FDA at http://www.fda.gov/medwatch/ or 1-800-FDA-1088 (1-800-332-1088).
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