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Fentanyl transdermal system: US FDA label indications

US FDA labelNot medical advice

The product name above is taken from the label's own indications text; the source record has no brand or generic name field.

Indications and usage (label excerpt)

INDICATIONS AND USAGE Fentanyl transdermal system is indicated for management of persistent , moderate to severe chronic pain that: requires continuous, around-the-clock opioid administration for an extended period of time, and cannot be managed by other means such as non-steroidal analgesics, opioid combination products, or immediate-release opioids. Fentanyl transdermal system should ONLY be used in patients who are already receiving opioid therapy, who have demonstrated opioid tolerance, and who require a total daily dose at least equivalent to fentanyl transdermal system 25 mcg/hr (see DOSAGE AND ADMINISTRATION ). Patients who are considered opioid-tolerant are those who have been taking, for a week or longer, at least 60 mg of morphine daily, or at least 30 mg of oral oxycodone daily, or at least 8 mg of oral hydromorphone daily, or an equianalgesic dose of another opioid. Because serious or life-threatening hypoventilation could result, fentanyl transdermal system is contraindicated for use on an as needed basis (i.e., prn), for the management of post-operative or acute pain, or in patients who are not opioid-tolerant or who require opioid analgesia for a short period of time (see BOX WARNING and CONTRAINDICATIONS ). An evaluation of the appropriateness and adequacy of treating with immediate-release opioids is advisable prior to initiating therapy with any modified-release opioid. Prescribers should individualize treatment in every case, initiating therapy at the appro…

Warnings (label excerpt)

WARNINGS Fentanyl transdermal system is intended for transdermal use (on intact skin) only. Do not use a fentanyl transdermal system if the pouch seal is broken or the system is cut, damaged, or changed in any way. The safety of fentanyl transdermal system has not been established in children under 2 years of age. Fentanyl transdermal system should be administered to children only if they are opioid-tolerant and 2 years of age or older (see PRECAUTIONS - Pediatric Use ). Fentanyl transdermal system is ONLY for use in patients who are already tolerant to opioid therapy of comparable potency. Use in non-opioid tolerant patients may lead to fatal respiratory depression. Overestimating the fentanyl transdermal system dose when converting patients from another opioid medication can result in fatal overdose with the first dose. The mean half-life is approximately 20 to 27 hours. Therefore, patients who have experienced serious adverse events, including overdose, will require monitoring for a…

Excerpts are shortened. Read the full label, and ask a pharmacist or prescriber about any medicine. Full label on DailyMed(opens in a new tab) For products sold in Canada, see the Health Canada Drug Product Database(opens in a new tab).

Trials whose interventions mention this drug

Canadian trials first. Showing 50 of 57. A match on the drug name does not mean the trial studied this specific product.

50 trials, recruiting first
PhaseCountries
Fentanyl Sublingual Spray for the Treatment of Acute Procedure-related Pain in a Monitored Setting
NCT02138409
WithdrawnPhase 3INSYS Therapeutics Inc2017-12-30
Nasal Fentanyl for Chronic Cancer Pain
NCT01906073
WithdrawnPhase 3Norwegian University of Science and Technology2017-01
Ischemic Pain Control With Analgesic Methods Clinical Trial
NCT02841488
Unknown statusPhase 3University of Sao Paulo General Hospital2016-09
Does Intraoperative Methadone Prevent Postoperative Pain in Bariatric Surgery?
NCT02775474
CompletedPhase 4BrazilUniversity of Sao Paulo General Hospital2016-06
Remifentanil vs Fentanyl During Cardiac Surgery and Chronic Thoracic Pain
NCT02031016
CompletedPhase 4NetherlandsSt. Antonius Hospital2014-02
Prospective Randomized Trial Comparing the Effectiveness of Continuous Paravertebral Infusion of Local Anesthetics Versus Intravenous Patient-controlled Analgesia on Acute and Chronic Neuropathic Pain After VATS Lobectomy
NCT01703351
CompletedPhase 2South KoreaYonsei University2012-10-04
Use of Fentanyl Patch in Partial Doses Than the Original
NCT01403363
Unknown statusNot applicableIsraelMeir Medical Center2012-03
The Effectiveness and Tolerability of Fentanyl Matrix in Chronic Non-cancer Pain; Assessment of Patient's Pain Treatment Goal Achievement
NCT01688583
CompletedSouth KoreaJanssen Korea, Ltd., Korea2011-12
Sedation in Endoscopic Retrograde Cholangiopancreatography (ERCP) With or Without Opioids
NCT01304342
CompletedNot applicableGreeceUniversity of Athens2011-02
Dexmedetomidine Versus Fentanyl Following Pressure Equalization Tube Placement
NCT01188551
CompletedPhase 2, Phase 3United StatesNationwide Children's Hospital2011-01
Nasal Fentanyl for Patient Controlled Treatment of Pain in Cancer
NCT01248611
CompletedPhase 1, Phase 2NorwaySt. Olavs Hospital2011-01
The Effect of Choice of Intraoperative Opioid on Postoperative Pain
NCT01542645
CompletedPhase 4United StatesEndeavor Health2010-09
Gabapentin Versus Transdermal Fentanyl Matrix for Chronic Neuropathic Pain
NCT01127100
CompletedPhase 4South KoreaSeoul National University Hospital2010-05
Postoperative Analgesia Impact of Narcotic Free Anesthesia
NCT01544959
CompletedNot applicableCanadaUniversité de Sherbrooke2010-01
Prospective Study About Clinical and Pharmacogenetic Safety of Opioid Use for Chronic Pain
NCT00916890
SuspendedPhase 4ItalyFondazione IRCCS Policlinico San Matteo di Pavia2009-02
A Confirmatory Study of Fentanyl in Participants With Osteoarthritis or Low Back Pain
NCT01008618
CompletedPhase 3JapanJanssen Pharmaceutical K.K.2009-01
An Efficacy and Safety Study of Fentanyl Transdermal Patch in Filipino Participants With Osteoarthritis and Chronic Low Back Pain
NCT01795898
CompletedPhase 4PhilippinesJanssen Pharmaceutica2009-01
Fentanyl Buccal Tablets Versus Immediate Release Oxycodone for Breakthrough Pain in Patients With Chronic Pain
NCT00813488
CompletedPhase 3United StatesCephalon2008-12
An Efficacy and Safety Study of Fentanyl in Participants With Chronic Pain
NCT00788372
CompletedPhase 3JapanJanssen Pharmaceutical K.K.2008-11
Observational Study Investigating the Effectiveness of Fentanyl Matrix in Relieving Pain and Improving Function in Patients With Osteoarthritis of the Knee or Hip
NCT01119885
CompletedJanssen Korea, Ltd., Korea2008-08
An Efficacy and Safety Study of Transdermal Therapeutic System (TTS)-Fentanyl in Severe Chronic Low Back Pain
NCT01774903
CompletedPhase 4ThailandJanssen-Cilag Ltd.,Thailand2008-08
Long-term Extension Study of BEMA™ Fentanyl
NCT00696137
CompletedPhase 3BioDelivery Sciences International2008-06
Matrifen® for Therapy of Severe Chronic Pain®
NCT00699335
CompletedGermanyNycomed2008-06
Study on Impact of Fentanyl Matrix on Improvement of Pain and Functioning in Spinal Disorder-related Pain
NCT00797017
CompletedJanssen Korea, Ltd., Korea2008-05
Fentanyl Sublingual Spray in Treating Patients With Breakthrough Cancer Pain
NCT00538850
CompletedPhase 3United StatesINSYS Therapeutics Inc2007-10
Studying Fentanyl in Patients With Cancer
NCT00899951
TerminatedUnited StatesSidney Kimmel Comprehensive Cancer Center at Johns Hopkins2007-10
Efficacy and Safety of Fentanyl Buccal Tablets Compared With Oxycodone for the Management of Break Through Pain
NCT00463047
CompletedPhase 3United StatesCephalon2007-07
Open-Label Study to Evaluate the Effect of Treatment With Fentanyl Buccal Tablets on Pain Anxiety Symptoms When Used for the Management of Breakthrough Pain
NCT00387010
TerminatedPhase 3United StatesCephalon2006-12
Study to Evaluate the Efficacy and Safety of OraVescent Fentanyl Citrate Treatment for the Management of Breakthrough Pain in Opioid-Tolerant Patients With Noncancer-Related Chronic Pain
NCT00343733
CompletedPhase 3United StatesCephalon2006-08
Study of the Safety of BEMA™ Fentanyl Use for Breakthrough Pain in Cancer Subjects on Chronic Opioid Therapy
NCT00293020
CompletedPhase 3United StatesBioDelivery Sciences International2006-02
Opioid Rotation Versus Combination for Chronic Uncontrolled Cancer Pain
NCT00478101
CompletedPhase 2Gachon University Gil Medical Center2006-02
Fentanyl Transdermal Patch With CHADD™ for Breakthrough Pain in Patients With Moderate to Severe Non-Malignant Pain
NCT00278824
TerminatedPhase 2United StatesZARS Pharma Inc.2006-01
Efficacy and Safety Study of Fentanyl Transdermal Patch for Treatment of Chronic Pain
NCT01902524
CompletedPhase 4South KoreaJanssen Korea, Ltd., Korea2005-10
Study to Evaluate the Efficacy and Safety of ORAVESCENT Fentanyl Citrate for Management of Breakthrough Pain
NCT00214942
CompletedPhase 3United StatesCephalon2005-09
Study to Evaluate the Efficacy and Safety of ORAVESCENT Fentanyl Citrate for the Management of Breakthrough Pain
NCT00214955
CompletedPhase 3United StatesCephalon2005-09
Fentanyl Transdermal Matrix Patch ZR-02-01 to Treat Moderate to Severe Cancer Pain
NCT00126789
TerminatedPhase 3United StatesZARS Pharma Inc.2005-08
Fentanyl Transdermal Matrix Patch ZR-02-01 to Treat Chronic, Moderate to Severe Non-Malignant Pain
NCT00126763
TerminatedPhase 3United StatesZARS Pharma Inc.2005-07
Phase III Clinical Trial of Fentanyl Transdermal Matrix Patch, in the Management of Chronic Intractable Pain- Assessment of Effectiveness, Safety and Pharmacokinetics
NCT00216684
CompletedPhase 3Janssen Pharmaceutical K.K.2005-05
Evaluating the Safety and Tolerability of OraVescent Fentanyl for Opioid Tolerant Patients With Noncancer Related Breakthrough Pain
NCT00228605
CompletedPhase 3United StatesCephalon2005-03
Efficacy and Safety of FITpatch Compared to Standard Opioid Treatment in Cancer Pain (FT-015-IN)
NCT00279344
CompletedPhase 3Nycomed2004-09
Fentanyl Transdermal Matrix Patch ZR-02-01 to Treat Chronic, Moderate to Severe Osteoarthritis (OA) Pain
NCT00108771
CompletedPhase 2United StatesZARS Pharma Inc.2004-04
An Efficacy and Safety Study of Transdermal Therapeutic System (TTS)-Fentanyl in Thai Participants With Chronic Non-Malignant Pain
NCT01816243
CompletedPhase 4ThailandJanssen-Cilag Ltd.,Thailand2004-04
Efficacy of Transdermal Fentanyl for Chronic Neuropathic Pain
NCT00181246
CompletedNot applicableJohns Hopkins University2003-10
A Study to Evaluate the Safety and Effectiveness of Fentanyl-TTS Compared to Weak Opioids in Patients With Moderate to Severe Chronic Cancer Pain Previously Treated With NSAIDS (Non-steroidal Anti-inflammatory Drugs).
NCT00576017
CompletedPhase 4Janssen-Cilag, S.A.2003-10
Evaluation of the Efficacy and Safety of Fentanyl Delivered by Adhesive Skin Patch in Out-Patients With Chronic Cancer Pain
NCT00236327
TerminatedPhase 4Janssen Cilag S.A.S.2003-06
A Study to Evaluate the Safety of D-TRANS Fentanyl With Naltrexone in Adult Patients With Chronic Pain and Who Are Opioid Tolerant
NCT00650182
CompletedPhase 2Alza Corporation, DE, USA2003-01
Duragesic® (Fentanyl Transdermal System) Functionality Trial in Chronic Low Back Pain
NCT00237341
CompletedPhase 4PriCara, Unit of Ortho-McNeil, Inc.2002-06
A Study to Assess the Safety, Dose Conversion, and Dose Individualization of Duragesic® (Fentanyl Transdermal Patch) in the Treatment of Children With Chronic Pain Requiring Narcotic Pain Relief Therapy
NCT00271466
CompletedPhase 3Johnson & Johnson Pharmaceutical Research & Development, L.L.C.2000-02
A 15-day Study to Assess the Safety and Clinical Utility of Duragesic (Fentanyl Transdermal Patch) in the Treatment of Children With Continuous Pain Requiring Narcotic Pain Relief Therapy
NCT00271414
CompletedPhase 3Janssen Pharmaceutica N.V., Belgium1999-03
A Study to Assess the Safety and Effectiveness of Durogesic (Fentanyl Transdermal Patch) in the Treatment of Children With Chronic Pain Requiring Long-term Narcotic Pain Relief Therapy
NCT00271453
CompletedPhase 3Johnson & Johnson Pharmaceutical Research & Development, L.L.C.1996-02

Source: openFDA drug label (US FDA), snapshot October 2026. Not a Health Canada Product Monograph.