Minipress and Restoril drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Minipress (prazosin hydrochloride) and Restoril (temazepam). Common drug interactions include vomiting among females and blood triglycerides increased among males.
The phase IV clinical study analyzes what interactions people have when they take Minipress and Restoril. It is created by eHealthMe based on reports of 17 people who take the same drugs from the FDA, and is updated regularly.
What is Minipress?
Minipress has active ingredients of prazosin hydrochloride. It is often used in post-traumatic stress disorder. eHealthMe is studying from 2,213 Minipress users. Check the latest studies of Minipress.
What is Restoril?
Restoril has active ingredients of temazepam. It is often used in insomnia. eHealthMe is studying from 13,522 Restoril users. Check the latest studies of Restoril.
17 people who take Minipress and Restoril together, and have interactions are studied.

What are the common drug interactions of Minipress and Restoril, by gender? *:
female:
- Vomiting
- Angina unstable (chest pain due to ischemia of the heart muscle- unstable)
- Arthralgia (joint pain)
- Coronary artery disease (plaque building up along the inner walls of the arteries of the heart, which narrows the arteries and restricts blood flow to the heart)
- Fatigue (feeling of tiredness)
- Fibromyalgia (a long-term condition which causes pain all over the body)
- Joint crepitation
- Joint stiffness
- Muscle spasms (muscle contraction)
- Night sweats (sweating in night)
male:
- Blood triglycerides increased
- Granulocytopenia (lack of granulocyte)
- Hyperphagia (an abnormal appetite for food)
- Loss of consciousness
- Nausea (feeling of having an urge to vomit)
- Retching (strong involuntary effort to vomit)
- Somnolence (a state of near-sleep, a strong desire for sleep)
- Weight increased
- Back pain
- Fatigue (feeling of tiredness)
What are the common drug interactions of Minipress and Restoril, 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:
- Amino acid level decreased
- Withdrawal syndrome (a discontinuation syndrome is a set of symptoms occurred due to discontinuation of substance)
50-59:
- Granulocytopenia (lack of granulocyte)
- Blood cholesterol increased
- Blood glucose increased
- Blood triglycerides increased
- Haematocrit decreased
- Haemoglobin decreased
- Overdose
- Lymphocyte count increased
- Neutrophil count decreased (less than normal number of neutrophil a type of blood cell)
- Red blood cell count decreased
60+:
- Vomiting
- Angina unstable (chest pain due to ischemia of the heart muscle- unstable)
- Peptic ulcer
- Ulcer
- Anaemia (lack of blood)
- Bacteraemia (presence of bacteria in the blood)
- Candidiasis (candidiasis or thrush is a fungal infection)
- Cellulitis (infection under the skin)
- Difficulty in walking
- Dry skin
What are the existing conditions these people have? *
- Narcolepsy (brain's inability to regulate sleep-wake cycles normally): 5 people, 29.41%
- Stress And Anxiety: 3 people, 17.65%
- Rheumatoid Arthritis (a chronic progressive disease causing inflammation in the joints): 2 people, 11.76%
- Nausea (feeling of having an urge to vomit): 2 people, 11.76%
- Joint Pain: 2 people, 11.76%
- Sinus Disorder (disease of sinus): 1 person, 5.88%
- Panic Disorder: 1 person, 5.88%
- Pain: 1 person, 5.88%
- Multiple Sclerosis (a nervous system disease that affects your brain and spinal cord. it damages the myelin sheath): 1 person, 5.88%
- Migraine (headache): 1 person, 5.88%
* Approximation only. Some reports may have incomplete information.
Do you take Minipress and Restoril?
- Personalize this study to your gender, age, symptoms and drugs
- Predict drug outcomes for up to one year with AI
- Get an AI agent to monitor your drugs continuously
Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
Browse all drug interactions of Minipress and Restoril:
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 zSub-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 Minipress:
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 zBrowse all side effects of Restoril:
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 zBrowse all interactions between Minipress 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 zBrowse all interactions between Restoril 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 zHow the study uses the data?
The study uses data from the FDA. It is based on prazosin hydrochloride and temazepam (the active ingredients of Minipress and Restoril, respectively), and Minipress and Restoril (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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