Disorientation: disability in which the senses of time, direction, and recognition of people and places.
This is a real world study of Disorientation (Confusion) among people who take Oxycodone And Acetaminophen, Xyrem. The study is created by eHealthMe based on 3 reports from FDA and social media.
Get a free personalized report of your drugs: we study for you 352 million drug outcomes from FDA and social media. Start to use eHealthMe >>>
What are the drugs
Oxycodone and acetaminophen (latest outcomes from 2,764 users) has active ingredients of acetaminophen; oxycodone hydrochloride. It is often used in pain.
Xyrem (latest outcomes from 3,883 users) has active ingredients of sodium oxybate. It is often used in narcolepsy.
On Aug, 24, 2014: 3 people reported to have Disorientation when taking Oxycodone And Acetaminophen, Xyrem are studied.
Gender of people who have Disorientation when taking the drugs * :
Age of people who have Disorientation when taking the drugs * :
Severity of Disorientation when taking the drugs ** :
How people recovered from Disorientation ** :
* Approximation only. Some reports may have incomplete information.
** Reports from social media are used.
More about the drug combination: Oxycodone And Acetaminophen, Xyrem drug interactions
You can also:
NOTE: The study is based on active ingredients. Other drugs that have the same active ingredients are also 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.