Belsomra and Therapeutic response delayed - a phase IV clinical study of FDA data
Summary:
Therapeutic response delayed is reported as a side effect among people who take Belsomra (suvorexant), especially for people who are female, 60+ old, have been taking the drug for < 1 month also take Eliquis, and have Sleep disorder.
The phase IV clinical study analyzes which people have Therapeutic response delayed when taking Belsomra. It is created by eHealthMe based on reports of 12,886 people who have side effects when taking Belsomra from the FDA, and is updated regularly.
What is Belsomra?
Belsomra has active ingredients of suvorexant. It is often used in insomnia. eHealthMe is studying from 12,961 Belsomra users. Check the latest studies of Belsomra.
What is Therapeutic response delayed?
Therapeutic response delayed (late preventive response) is found to be associated with 237 drugs and 366 conditions by eHealthMe. Check the latest studies of Therapeutic response delayed.
12,886 people reported to have side effects when taking Belsomra.
Among them, 15 people (0.12%) have Therapeutic response delayed.

Among these 15 people:
How long have people been on Belsomra when they have Therapeutic response delayed? *
- < 1 month: 75 %
- 1 - 6 months: 25 %
- 6 - 12 months: 0.0 %
- 1 - 2 years: 0.0 %
- 2 - 5 years: 0.0 %
- 5 - 10 years: 0.0 %
- 10+ years: 0.0 %
What is the gender of people who have Therapeutic response delayed when taking Belsomra? *
- female: 60 %
- male: 40 %
What is the age of people who have Therapeutic response delayed when taking Belsomra? *
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 0.0 %
- 20-29: 0.0 %
- 30-39: 0.0 %
- 40-49: 0.0 %
- 50-59: 0.0 %
- 60+: 100 %
What are other drugs people take besides Belsomra? *
- Wellbutrin: 1 person, 6.67%
- Remeron: 1 person, 6.67%
- Prolia: 1 person, 6.67%
- Premarin: 1 person, 6.67%
- Melatonin: 1 person, 6.67%
- Insulin: 1 person, 6.67%
- Eliquis: 1 person, 6.67%
What are other side effects people have besides Therapeutic response delayed? *
- Drug Ineffective: 7 people, 46.67%
- Adverse Event: 4 people, 26.67%
- Drowsiness: 4 people, 26.67%
- Memory Loss: 4 people, 26.67%
- Feeling Abnormal: 4 people, 26.67%
- Depressed Level Of Consciousness: 3 people, 20.00%
- Dizziness: 3 people, 20.00%
- Middle Insomnia (difficulty returning to sleep after awakening either in the middle of the night): 3 people, 20.00%
- Initial Insomnia (feeling of inadequate or poor-quality sleep): 2 people, 13.33%
- Head Discomfort: 1 person, 6.67%
What are the existing conditions these people have? *
- Sleep Disorder: 1 person, 6.67%
* Approximation only. Some reports may have incomplete information.
Do you take Belsomra and have Therapeutic response delayed?
- Check whether Therapeutic response delayed 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 Belsomra:
- Belsomra (12,961 reports)
Therapeutic response delayed treatments and more:
- Therapeutic response delayed (2,950 reports)
How severe was Therapeutic response delayed and when was it recovered:
Expand to all the drugs that have ingredients of suvorexant:
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 Belsomra:
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 the drugs that are associated with Therapeutic response delayed:
- Therapeutic response delayed (237 drugs)
Browse all the conditions that are associated with Therapeutic response delayed:
- Therapeutic response delayed (366 conditions)
How the study uses the data?
The study uses data from the FDA. It is based on suvorexant (the active ingredients of Belsomra) and Belsomra (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.
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