A study for a 43-year old woman who takes Lorazepam, Nucynta
Summary: 5 female patients aged 43 (±5) who take the same drugs are studied.
This is a personalized study for a 43 year old female patient who has Insomnia, Pain. The study is created by eHealthMe based on reports from FDA and social media.
On Mar, 28, 2015: 5 females aged 43 (±5) who take Lorazepam, Nucynta are studied
Information of the patient in this study:
Conditions: Insomnia, Pain
- Lorazepam - 0.5MG (lorazepam)
- Nucynta - EQ 75MG BASE (tapentadol hydrochloride)
eHealthMe real world results:
Drug effectiveness over time :
Most common drug interactions over time * :
|< 1 month||1 - 6 months||6 - 12 months||1 - 2 years||2 - 5 years||5 - 10 years||10+ years||not specified|
|Pain In Extremity|
|Poor Quality Sleep|
* Some reports may have incomplete information.
How to use the study: print a copy of the study and bring it to your health teams to ensure drug risks and benefits are fully discussed and understood.
You can also:
- Check your drugs or symptoms
- Post a comment: or see what other people said about the study
- Join a related support group
You are not alone! Join a related mobile support group on :
- support group for people who have Insomnia
- support group for people who have Pain
- support group for people who take Lorazepam
- support group for people who take Nucynta
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Related drug interaction studies:
- Nucynta and Lorazepam drug interactions (54 reports)
Drug effectiveness in real world:
- Lorazepam for Insomnia reported by 107 people (updated 6 days ago)
- Nucynta for Pain reported by 49 people (updated 24 minutes ago)
Complete drug side effects:
- Insomnia (101 drugs in 7,074 reports) (updated 16 hours ago)
- Pain (221 drugs in 10,465 reports) (updated 2 days ago)
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.
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You may report adverse side effects to the FDA at http://www.fda.gov/medwatch/ or 1-800-FDA-1088 (1-800-332-1088).
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