The proportion of U.S. adults prescribed Neurontin and other drugs
in the same family of medicines climbed from 1.2 percent in 2002 to
3.9 percent by 2015, a period that also saw a surge in opioid
overdoses and deaths. The family of medicines, known as
gabapentinoids, includes gabapentin (Neurontin, Gralise, Horizant)
and pregabalin.
“Nearly one in 25 adults takes a gabapentinoid during a year, which
matters because we have little data to support much use of this drug
class and minimal data to support the long-term safety of the
medications,” said study author Dr. Michael Johansen of the Heritage
College of Osteopathic Medicine at Ohio University in Athens.
“My suspicion is that much of the use is driven by attempting to
treat chronic pain with a non-opioid medication,” Johansen said by
email.
U.S. deaths from opioids including heroin and prescription drugs
like oxycodone, hydrocodone and methadone have more than quadrupled
since 1999, according to the Centers for Disease Control and
Prevention in Atlanta. Today, more than six in 10 drug overdose
deaths involve opioids.
Amid this worsening opioid epidemic, the CDC has urged physicians to
prescribe other drugs for pain including acetaminophen and
nonsteroidal anti-inflammatory drugs (NSAIDs) as well as
gabapentinoids.
Gabapentin and pregabalin both have won U.S. Food and Drug
Administration (FDA) approval for treating partial seizures and a
type of nerve pain caused by shingles. A version of gabapentin has
also been approved for restless leg syndrome, and pregabalin has
additional approvals for fibromyalgia and nerve pain related to
diabetes and spinal cord injuries.
While the FDA doesn’t allow drug companies to promote these
medicines for other conditions, doctors are free to prescribe the
drugs for off-label, or unapproved, uses.
Off-label use of gabapentinoids has been controversial, however,
because these drugs can be addictive, they haven’t been proven
effective for many common unapproved uses and there’s limited
long-term safety data, Johansen writes in JAMA Internal Medicine.
For his study, Johansen reviewed survey data from a nationally
representative sample of 346,177 adults, including details on any
medical conditions and prescriptions.
Overall, more than four out of five of prescriptions for
gabapentinoids were for gabapentin, the analysis found.
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Prescription growth was concentrated among older adults, diabetics,
people with multiple chronic health problems and patients already
taking opioids or benzodiazepines like Valium and Xanax.
One limitation of the study is that it relied on participants to
accurately report on any drug use, and it’s possible that some
people did not disclose opioid use. The study didn’t include
prescription records or information on drug costs.
“The use of gabapentinoids specifically seems to be outpacing any
proven efficacy and the potential significant harms like addiction
and overdose are only beginning to be investigated,” said Dr.
Christopher Goodman, a researcher at the University of South
Carolina School of Medicine in Columbia who wasn’t involved in the
study.
While some patients may benefit from these drugs, they should
consider other approaches to pain management like exercise, physical
therapy and yoga that may be safer and still provide some relief,
Goodman said by email.
Side effects of gabapentinoids include sedation, dizziness and
trouble thinking, Dr. Chad Brummett, an opioid researcher at the
University of Michigan in Ann Arbor who wasn’t involved in the
study, said by email. The risks are worse at higher doses.
Mixing these drugs with opioids and benzodiazapines may make them
even more dangerous, said Marissa Seamans, a researcher at the Johns
Hopkins Bloomberg School of Public Health in Baltimore who wasn’t
involved in the study.
“Gabapentinoids are increasingly prescribed to patients with opioids
and benzodiazapines, which increases the risk of respiratory
depression and death,” Seamans said by email. “Clinicians and
patients need to carefully monitor the dosage of these medicines,
their interactions, and potentially fatal side effects.”
SOURCE: http://bit.ly/2Ar8g2m JAMA Internal Medicine, online January
2, 2018.
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