Back to Results
First PageMeta Content
Organochlorides / Lactams / Hypnotics / Sanofi / Intermezzo / Zolpidem / Eszopiclone / Zopiclone / Insomnia / Chemistry / Nonbenzodiazepines / Organic chemistry


FDA Drug Safety Communication: Risk of next-morning impairment after use of insomnia drugs; FDA requires lower recommended doses for certain drugs containing zolpidem (Ambien, Ambien CR, Edluar, and Zolpimist)
Add to Reading List

Open Document

File Size: 187,93 KB

Share Result on Facebook

Country

United States / /

IndustryTerm

immediate‐release products / treatment of insomnia / zolpidem‐containing products / certain immediate‐release zolpidem products / Online Regular Mail / extended‐release products / outpatient retail pharmacies / prescribing the lower doses―5 mg for immediate‐release products / /

MedicalCondition

insomnia / headache / zolpidem‐containing insomnia / Drowsiness / widely prescribed insomnia / patient’s insomnia / prescription insomnia / /

Organization

U.S. Food and Drug Administration / FDA / /

/

Product

secobarbital sodium / butabarbital sodium / Restoril / Benadryl / Placidyl / Doral / Butisol sodium / estazolam / Lunesta / Rozerem / zolpidem tartrate / Prosom / ethchlorvynol / temazepam / Sonata / Unisom / doxepin hydrochloride / triazolam / Ambien CR / Ambien / Dalmane / flurazepam hydrochloride / Halcion / zolpidem / zaleplon / /

ProvinceOrState

Maryland / /

PublishedMedium

the Medication Guide / /

Technology

simulation / /

SocialTag