Suboxone.com - Resource Kit

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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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Resource Kit

The Resource Kit contains important educational information about opioid dependence/addiction and its treatment. These materials are for patients with opioid dependence and their family members and friends.

You can order your free Resource Kit by providing your mailing information below. If you wish, you also may sign up to receive future information from Reckitt Benckiser Pharmaceuticals about treating opioid dependence with SUBOXONE (buprenorphine/naloxone). SUBOXONE is a prescription medicine that is used in a doctor's office to treat opioid dependence.

We want you to know how we will use your information. Your information will only be used by Reckitt Benckiser Pharmaceuticals Inc. for purposes relating to the Company's programs, products, and services and not for any other purpose. We invite you to review the Reckitt Benckiser Privacy Policy by clicking here.

To order your free Resource Kit on opioid dependence and its treatment, please fill out the information below.

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If at any time in the future you would like to stop receiving educational materials from Reckitt Benckiser Pharmaceuticals, please call 1-866-455-TURN or e-mail suboxone.unsubscribe@dsuccess.com.

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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.

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