A Prospective Safety Surveillance Study of Fentanyl Iontophoretic Transdermal System (40 Mcg)
Stopped Study was terminated at the request of the company due to the recall of marketed product in Europe.
Conditions
Interventions
- DRUG: fentanyl iontophoretic transdermal system (40mcg) No Placebo
- DRUG: IV PCA with standard of care opioid analgesia
Sponsor
Alza Corporation, DE, USA