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Buprenorphine Hydrochloride
Buprenorphine Hydrochloride
assisted treatment (MAT) in patients with addiction to morphine, heroin and other opiates. The
medication was approved for clinical use in October 2002 by the Food and Drug Administration
(FDA), making it relatively new when compared to methadone use in the U.S. over the past four
decades. Buprenorphine provides multiple benefits to the provider and patient when compared
to those of traditional methadone treatment. The first is improved accessibility to the medication
whereas buprenorphine is the first drug to treat opioid dependency that may be prescribed and
dispensed by a qualified MD in their office. Patients with dependency to morphine, heroin and
other opiates may have had to wait for long periods of time before methadone clinics had
available space to treat them thus delaying treatment. As stated in the Drug Addiction Treatment
Act of 2000 (Data 2000), qualified clinicians may prescribe Buprenorphine in the office,
community hospital, health department or correctional facility. The ability of the provider to
directly prescribe and dispense Buprenorphine allows greater patient contact and monitoring by
the physician thereby reducing medication non-compliance in the patient thru regular contact.
The qualified provider may also treat a greater number of patients with opioid dependency while
fewer withdrawal symptoms of its own. Buprenorphine effects are also considered non-sedating
providing a greater sense of normalcy for the patient. This non-sedating effect is desirable in
treating the hospitalized patient for pain as well. Opioid related respiratory depression is a life-
threatening adverse effect that may be significantly reduced by choosing buprenorphine in place
evaluated on an individual patient basis when considering buprenorphine in the line of treatment
Urban, Equal Access System. The American Journal on Addictions, 22: 285291, 2013.
0391.2012.12004.x