Suboxone.com - Contact a Clinical Liaison

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IMPORTANT INFORMATION:

On December 8, 2006, Federal legislation was passed allowing physicians to treat up to 100 opioid dependent patients with Suboxone at any given time—a significant increase from the previous limit of 30 patients.

There may be doctors in your area participating in a study to measure opioid dependence treatment outcomes. Patients who meet the eligibility requirements to participate in this study can receive up to $225 in compensation to complete surveys about their treatment.

NOTE: This study is only open to patients not currently under the care of a physician for opioid dependence and are seeking a treatment provider.

Please call 1-866-455-8876 between 9:00 AM to 7:30 PM EST to get more information.

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Prescribing Information -- Site Map

Contact a Clinical Liaison

For Healthcare Professional Use Only

Due to patient privacy regulations, Clinical Liaisons are not able to work directly with patients or individuals seeking treatment. If you need assistance or would like additional information, please contact the Suboxone Help Line at
877-782-6966 or 877-SUBOXONE or access the physician locator.

Your Reckitt Benckiser Clinical Liaison can provide valuable services including:

Information about opioid dependence treatment and Suboxone
Assistance in setting up your practice to treat with Suboxone
Assistance in connecting with counseling providers
Answers to your questions

To have a Clinical Liaison contact you, please provide your information below.

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Please check here if you would like to receive future educational information and materials on opioid dependence and its treatment from Reckitt Benckiser Pharmaceuticals.

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Home -- About SUBOXONE -- Treating Opioid Dependence -- SUBOXONE Certification -- Pharmacists -- Resources

Important Safety Information

SUBOXONE® (buprenorphine HCl/naloxone HCl dihydrate sublingual tablets) (CIII) is indicated for the treatment of opioid dependence.

It is extremely dangerous to take benzodiazepines or other depressants while taking SUBOXONE. A serious overdose and death may occur if benzodiazepines, sedatives, tranquilizers, antidepressants, or alcohol are taken at the same time as SUBOXONE.

SUBOXONE has potential for abuse and produces dependence of the opioid type, with a milder withdrawal syndrome than full agonists.

Cytolytic hepatitis and hepatitis with jaundice have been observed in the addicted population receiving buprenorphine.

Allergic reactions including bronchospasm, angioneurotic edema, and anaphylactic shock have been reported in patients taking buprenorphine.

There are no adequate and well-controlled studies of SUBOXONE (a Category C medication) in pregnancy.

Caution should be exercised when driving cars or operating machinery.

Always store buprenorphine-containing medications safely and out of the reach and sight of children. Destroy any unused medication appropriately.

The most commonly reported adverse events with SUBOXONE include: headache (36%, placebo 22%), withdrawal syndrome (25%, placebo 37%), pain (22%, placebo 19%), insomnia (14%, placebo 16%), nausea (15%, placebo 11%), and constipation (12%, placebo 3%). Please see full Prescribing Information for a complete list.

To report an adverse event caused by taking SUBOXONE, please call 1-877-782-6966. You are also encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch, or call 1-800-FDA-1088.