Desonide and Temazepam drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Desonide (desonide) and Temazepam (temazepam). Common drug interactions include bone density decreased among females and chronic kidney disease among males.
The phase IV clinical study analyzes what interactions people have when they take Desonide and Temazepam. It is created by eHealthMe based on reports of 46 people who take the same drugs from the FDA, and is updated regularly.
What is Desonide?
Desonide has active ingredients of desonide. It is often used in rosacea. eHealthMe is studying from 5,484 Desonide users. Check the latest studies of Desonide.
What is Temazepam?
Temazepam has active ingredients of temazepam. It is often used in insomnia. eHealthMe is studying from 42,106 Temazepam users. Check the latest studies of Temazepam.
46 people who take Desonide and Temazepam together, and have interactions are studied.

What are the common drug interactions of Desonide and Temazepam, by gender? *:
female:
- Bone density decreased
- Brain oedema (excess accumulation of fluid in the intracellular or extracellular spaces of the brain)
- Bronchitis (inflammation of the mucous membrane in the bronchial tubes)
- Cerebral haemorrhage (bleeding within the brain)
- Concussion (short loss of normal brain function in response to a head injury)
- Constipation
- Contusion (a type of hematoma of tissue in which capillaries)
- Death
- Decreased appetite
- Defaecation urgency (a sudden compelling urge to defecate)
male:
- Chronic kidney disease
- Emotional distress
- Blood potassium increased
- Dysmorphism (difference of body structure that is suggestive of a congenital disorder)
- Multiple fractures
- Overdose
- Renal failure (kidney dysfunction)
- Atrial fibrillation (fibrillation of the muscles of the atria of the heart)
- Avulsion fracture (bone fracture)
- Bone loss
What are the common drug interactions of Desonide and Temazepam, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
n/a
30-39:
- Aphthous stomatitis (mouth ulcer)
- Aspartate aminotransferase increased
- Blood alkaline phosphatase increased
- Blood sodium increased
- Burning sensation
- Constipation
- Defaecation urgency (a sudden compelling urge to defecate)
- Dermatitis (inflammation of the skin resulting from direct irritation by an external agent or an allergic reaction to it)
- Diarrhoea
- Dyspepsia (indigestion)
40-49:
- Diabetic ketoacidosis (diabetic ketoacidosis (dka) is high concentrations of ketone bodies)
- Pneumonia
- Renal injury (kidney injury)
50-59:
- Emotional distress
- Pain
- Asthenia (weakness)
- Bone density decreased
- Chronic kidney disease
- Rib fracture
- Anxiety
- Anhedonia (inability to experience pleasure from activities usually found enjoyable)
- Atrophy (wasting away of a part of the body)
- Dysmorphism (difference of body structure that is suggestive of a congenital disorder)
60+:
- Abdominal discomfort
- Blood potassium increased
- Surgery
- Balance disorder
- Bladder disorder
- Blindness
- Blood cholesterol increased
- Brain oedema (excess accumulation of fluid in the intracellular or extracellular spaces of the brain)
- Bronchitis (inflammation of the mucous membrane in the bronchial tubes)
- Cardiac disorder
What are the existing conditions these people have? *
- Rheumatoid Arthritis (a chronic progressive disease causing inflammation in the joints): 10 people, 21.74%
- Diabetes: 9 people, 19.57%
- Pain: 6 people, 13.04%
- Narcolepsy (brain's inability to regulate sleep-wake cycles normally): 6 people, 13.04%
- Hiv Infection: 6 people, 13.04%
- High Blood Cholesterol: 6 people, 13.04%
- Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 6 people, 13.04%
- Arthritis (form of joint disorder that involves inflammation of one or more joints): 5 people, 10.87%
- Cataplexy (loss of muscle tone accompanied by full conscious awareness): 5 people, 10.87%
- Skin Disorder (skin disease): 4 people, 8.70%
* Approximation only. Some reports may have incomplete information.
Do you take Desonide and Temazepam?
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Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
Browse all drug interactions of Desonide and Temazepam:
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 Desonide:
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 Temazepam:
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 Desonide 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 Temazepam 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 desonide and temazepam (the active ingredients of Desonide and Temazepam, respectively), and Desonide and Temazepam (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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