Suboxone and Fluticasone propionate drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Suboxone (buprenorphine hydrochloride; naloxone hydrochloride) and Fluticasone propionate (fluticasone propionate). Common drug interactions include decreased appetite among females and renal failure among males.
The phase IV clinical study analyzes what interactions people have when they take Suboxone and Fluticasone propionate. It is created by eHealthMe based on reports of 31 people who take the same drugs from the FDA, and is updated regularly.
What is Suboxone?
Suboxone has active ingredients of buprenorphine hydrochloride; naloxone hydrochloride. It is often used in opiate withdrawal. eHealthMe is studying from 31,249 Suboxone users. Check the latest studies of Suboxone.
What is Fluticasone propionate?
Fluticasone propionate has active ingredients of fluticasone propionate. It is often used in allergies. eHealthMe is studying from 35,174 Fluticasone propionate users. Check the latest studies of Fluticasone propionate.
31 people who take Suboxone and Fluticasone propionate together, and have interactions are studied.

What are the common drug interactions of Suboxone and Fluticasone Propionate, by gender? *:
female:
- Decreased appetite
- Delirium (wild excitement)
- Drug diversion
- Drug ineffective
- Dysgeusia (disorder of the sense of taste)
- Dyspnoea (difficult or laboured respiration)
- Endometriosis (appearance of endometrial tissue outside the uterus and causing pelvic pain)
- Fibula fracture
- Food allergy
- Fungal infection
male:
- Renal failure (kidney dysfunction)
- Anxiety
- Abortion spontaneous (naturally occurring miscarriage)
- Cough
- Dysgeusia (disorder of the sense of taste)
- Activities of daily living impaired
- Agitation (state of anxiety or nervous excitement)
- Anhedonia (inability to experience pleasure from activities usually found enjoyable)
- Arthritis (form of joint disorder that involves inflammation of one or more joints)
- Ataxia (loss of full control of bodily movements)
What are the common drug interactions of Suboxone and Fluticasone Propionate, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
- Ear pruritus (pruritus or itching is ""the unpleasant skin sensation that frequently provokes scratching"" in ear)
- Injection site pain
- Erythema (redness of the skin)
- Rash pruritic (redness with itching)
- Swelling
30-39:
- Pneumonia
- Renal disorder (kidney disease)
- Restless legs syndrome (a powerful urge to move your legs)
- Urinary tract infection
- Uterine leiomyoma (uterine benign tumour derived from smooth muscle)
- Weight decreased
- Arthralgia (joint pain)
- Synovial cyst (cyst of joint filled with synovial fluid)
- Tardive dyskinesia (a disorder that involves involuntary movements)
- Weight increased
40-49:
- Renal failure (kidney dysfunction)
50-59:
- Constipation
- Dermatitis contact (skin reaction (dermatitis) resulting from exposure to allergens)
- Dizziness
- Headache (pain in head)
- Hypoaesthesia (reduced sense of touch or sensation)
- Infusion related reaction
- Infusion site pain
- Neck pain
- Oedema peripheral (superficial swelling)
- Pain in extremity
60+:
- Chronic kidney disease
- Death
- Renal failure (kidney dysfunction)
What are the existing conditions these people have? *
- Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 7 people, 22.58%
- Pain: 6 people, 19.35%
- Narcolepsy (brain's inability to regulate sleep-wake cycles normally): 5 people, 16.13%
- Nausea (feeling of having an urge to vomit): 3 people, 9.68%
- Drowsiness: 3 people, 9.68%
- Cystic Fibrosis (disease of the secretary glands): 3 people, 9.68%
- Cough: 3 people, 9.68%
- Constipation: 3 people, 9.68%
- Cataplexy (loss of muscle tone accompanied by full conscious awareness): 3 people, 9.68%
- Asthma: 3 people, 9.68%
* Approximation only. Some reports may have incomplete information.
Do you take Suboxone and Fluticasone propionate?
- 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:
- Suboxone (31,249 reports)
- Fluticasone propionate (35,174 reports)
Browse all drug interactions of Suboxone and Fluticasone propionate:
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 Suboxone:
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 Fluticasone propionate:
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 Suboxone 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 Fluticasone propionate 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 zRelated publications that referenced our studies
- Lehrer, S., & Rheinstein, P. H. , "Alzheimer’s Disease and Intranasal Fluticasone Propionate in the FDA MedWatch Adverse Events Database", Journal of Alzheimer's disease reports, (Preprint), 1-5., 2018 Jan .
- Lehrer, S., & Rheinstein, P. H. , "Alzheimer’s Disease and Intranasal Fluticasone Propionate in the FDA MedWatch Adverse Events Database", Journal of Alzheimer's disease reports, (Preprint), 1-5., 2018 Jan .
How the study uses the data?
The study uses data from the FDA. It is based on buprenorphine hydrochloride; naloxone hydrochloride and fluticasone propionate (the active ingredients of Suboxone and Fluticasone propionate, respectively), and Suboxone and Fluticasone propionate (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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