Suboxone and Ideomotor apraxia - from FDA reports
Ideomotor apraxia is reported only by a few people who take Suboxone. We study 17,654 people who have side effects while taking Suboxone from FDA. Among them, 3 have Ideomotor apraxia. Find out below who they are, when they have Ideomotor apraxia and more.
How to use this study: bring a copy to your health teams to ensure drug risks and benefits are fully discussed and understood.
Who is eHealthMe: we are a data analysis company who specializes in health care industry. Our original studies have been referenced on 500+ peer-reviewed medical publications, including The Lancet, Mayo Clinic Proceedings, and EANO. On eHealthMe, you can research drugs and monitor them (see testimonials). If you find eHealthMe useful, please help us to spread the words below or leave us a testimonial.
17,654 people reported to have side effects when taking Suboxone.
Among them, 3 people (0.02%) have Ideomotor apraxia
Number of reports submitted per year:
Time on Suboxone when people have Ideomotor apraxia *:
- < 1 month: 66.67 %
- 1 - 6 months: 0.0 %
- 6 - 12 months: 0.0 %
- 1 - 2 years: 0.0 %
- 2 - 5 years: 33.33 %
- 5 - 10 years: 0.0 %
- 10+ years: 0.0 %
Gender of people who have Ideomotor apraxia when taking Suboxone *:
- female: 33.33 %
- male: 66.67 %
Top conditions involved for these people *:
- Drug Dependence: 1 person, 33.33%
Top co-used drugs for these people *:
- Nicotine: 1 person, 33.33%
Top other side effects for these people *:
- Speech Impairment (Adult) (inability to speak (adult)): 2 people, 66.67%
- Incoherent (talking in a confused and unclear way): 2 people, 66.67%
- Hyperhidrosis (abnormally increased sweating): 2 people, 66.67%
- Fatigue (feeling of tiredness): 2 people, 66.67%
- Encephalopathy (functioning of the brain is affected by some agent or condition): 2 people, 66.67%
* Approximation only. Some reports may have incomplete information.
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.
Do you have Ideomotor apraxia while taking Suboxone?
- Check whether a drug or a condition causes Ideomotor apraxia
- Subscribe to monitor Ideomotor apraxia in Suboxone
You are not alone:
Suboxone has active ingredients of buprenorphine hydrochloride; naloxone hydrochloride. It is often used in opiate withdrawal. (latest outcomes from Suboxone 19,719 users)
Ideomotor apraxia (deficits in their ability to plan or complete motor actions that rely on semantic memory) has been reported by people with depression, pain, high blood pressure, rheumatoid arthritis, multiple sclerosis (latest reports from 1,186 Ideomotor apraxia patients).
Drugs that are associated with Ideomotor apraxiaIdeomotor apraxia (772 drugs)
Could your condition cause Ideomotor apraxiaIdeomotor apraxia (576 conditions)
Suboxone side effects
- Suboxone side effects (17,658 reports)
Browse all side effects of Suboxonea 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?
Recent general studies
- Senna Alexandrina and Budesonide drug interaction - 2 seconds ago
- Will you have Necrosis with Aredia? - 5 seconds ago
- Will you have Memory Loss with Luvox? - 5 seconds ago
- Will you have Temporal Memory Loss with Luvox? - 5 seconds ago
- Will you have Sudden Memory Loss with Luvox? - 6 seconds ago
Recent personal studies
- A study for a 38 year old woman who takes Prazosin Hydrochloride, Ranitidine, Cymbalta, Hydroxyzine, Atenolol, Lamictal, Omeprazole, Dexilant - 19 minutes ago
- A study for a 49 year old woman who takes Armodafinil, Wellbutrin Xl - 50 minutes ago
- A study for a 53 year old man who takes Gleevec - 2 hours ago
- A study for a 54 year old woman who takes Xanax Xr, Premarin, Synthroid, Tramadol - 2 hours ago
- A study for a 46 year old woman who takes Ambien, Probiotic, Nexium, Xanax - 5 hours ago
NOTE: The study is based on active ingredients and brand name. Other drugs that have the same active ingredients (e.g. generic drugs) are NOT considered.
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, 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).
If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.