Original research
      
 by 
            Darwish, Mona et al
      
    Release Date
2008
          Geography
USA
          Language of Resource
English
          Full Text Available
No
          Open Access / OK to Reproduce
                    No
                            
        Peer Reviewed
Yes
          Objective
FBT is indicated for the management of breakthrough pain (a transient flare of pain on a background of chronic pain otherwise controlled by treatment with opioids) in patients with cancer who are already receiving and who are tolerant to opioid therapy for their underlying persistent cancer pain. This study assessed the bioequivalence of a single 400-μg dose of FBT following buccal (i.e. above a molar tooth between the upper gum and cheek) and sublingual (i.e. placed under the tongue) placement in order to provide an alternative option to patients.
          Findings/Key points
Conclusion: The results of this study support sublingual FBT placement as a viable alternative to buccal placement in patients who may require an alternate administration site.
          Design/methods
n=90
          Keywords
Clinical guidance
          About prescribers
          Chronic pain
              
            



