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Table of Contents
allodynia - pain in response to something that should not cause pain,
like a light touch
central nervous system - the brain and spinal cord
central pain - abnormal pain arising from damage to the central
nervous system chronic -
long lasting, persistent double
blind - scientific technique used to eliminate bias in a study, where
neither the study participant nor the experimenter (doctor) knows which of
two treatments the participant is receiving
epilepsy - disorder of the nervous system in which abnormal
electrical activity causes seizures
FDA - Food & Drug Administration; US government agency responsible
for approving and regulating medications
GABA - a neurotransmitter; thought to play a role in spinal cord
injuries; some drugs work by affecting the transmission of GABA
narcotic - class of drugs derived from the opium plant -
or created synthetically for the same effect; used as pain-killers
neuron - nerve cell
neuropathic - abnormal pain caused by damage to the nervous system
neurotransmitter - chemical that carries a message between neurons
opioid - narcotic
peripheral pain - pain arising from the outer - or peripheral - nervous
system, the ends of the nerves
placebo - a fake medicine - which has no effect - used in scientific
studies as a control
post-herpetic neuralgia - abnormal pain which results from nerve damage
due to herpes zoster - also known as shingles prospective
study - type of scientific study which looks forward in time; generally,
participants are divided into groups, receive treatments, and the results
are evaluated randomized -
technique used in a scientific study where participants are randomly
assigned to one of two groups; used to control the effects of age, gender,
etc. on the study outcome
refractory - not responsive to treatment
retrospective study - scientific study which uses medical records to
look at events that occurred in the past |
Not many people are thrilled about taking medication on a daily basis,
especially one with side effects. Yet for people suffering through
daily, chronic pain the choices are limited. Is the relief worth the
side effects? Will the drug even work? These are some of the
issues that become part of daily living for many people.
The drug Neurontin - generically known as gabapentin -
is one of the most widely prescribed drugs on the market. Bringing in
more than $2 billion in annual revenue for Pfizer, its manufacturer, it is a
high-profile drug with a bit of a storied past. Originally designed -
and approved - as an anti-epilepsy drug, it has since been FDA approved to
treat post-herpetic neuralgia, a painful type of neuropathic pain that some
people develop after having shingles. But with billions of dollars of
sales, it is clear that Neurontin is being prescribed for more uses than
just those two. In fact, a large portion of Neurontin sales are from
what are known as off-label uses. Once a drug is approved by the FDA,
doctors are allowed to prescribe the drug not only for the approved use, but
for other uses for which they think the drug might be effective.
This is an important, and necessary, part of medicine.
Many drug benefits were discovered by prescribing them off-label, including
the heart related benefits of aspirin. Unfortunately, as will be
discussed later, this is also where Neurontin's checkered past comes into
play. Pfizer (actually Parke-Davis, a division of Warner-Lambert,
which Pfizer acquired) is being accused of illegally marketing Neurontin and
encouraging doctors to prescribe it off-label.
What Is Neurontin?
Neurontin was designed to look like a
neurotransmitter known as GABA. GABA is an important
neurotransmitter, and several types of drugs, including sedatives, work by
affecting how GABA attaches to other chemicals at the molecular level.
In addition, the role of GABA in spinal cord injuries is thought to be
important and is being investigated by spinal cord injury researchers.
What is surprising is that no one knows how Neurontin
works. No one can explain how it offers pain relief or acts as an
anti-convulsant. Despite looking like GABA, it does not affect how
GABA attaches - or binds - in the brain, it doesn't affect how GABA is
processed, and it isn't converted into GABA by the body. In addition,
gabapentin does not affect dopamine or serotonin, other common
neurotransmitters. The substance was also tested to see if it would
bind to many different types of sites at the molecular level, but it does
not. In a study involving a rat brain, the drug was found to attach to
certain areas, but the connection between those sites and how the drug might
work is not clear. Adding to the mystery is the fact that gabapentin
itself is barely absorbed by the human body and is fairly quickly eliminated
through the kidneys and urine.
Does It Work?
Despite the unknowns, there is growing evidence that Neurontin does indeed
offer some level of relief for some types of neuropathic pain. Setting
aside the anti-epileptic effects of the drug, Pfizer's literature on
Neurontin cites two randomized, double-blind, placebo controlled studies on
the use of Neurontin for managing postherpetic neuralgia. The studies
involved 563 patients who were experiencing pain at least 3 months after
their bout with shingles. The patients were given either Neurontin or
a placebo for a several week period (dosage was ramped up to 3600mg/day).
Both studies showed a significant reduction in reported pain throughout the
treatment for those receiving the drug. In fact, around 30% of the
participants receiving the drug reported a 50% or greater improvement in
their pain.
However, there are many types of pain, and is
postherpetic neuralgia similar to SM pain? Fortunately, Neurontin has
also been shown to help pain associated with spinal cord injuries. In
a study published in 2003 (Spine 28(4):341-6), 31 patients with neuropathic
pain due to spinal cord injury were given Neurontin over an 8 week period.
The patients were divided into two groups based on whether they had been
experiencing pain for less than or more than 6 months. Despite the
fact that they tried other types of pain medicines to no avail, Neurontin
did reduce the pain for both groups. On a scale of 0-10, the average
pain score for the less than 6 month group dropped from 7.3 to 3 over the
course of the treatment. While the other group also responded to the
drug, the average score only dropped from 7.6 to 5. So while this
study shows Neurontin can provide relief for SCI related pain, getting
started early on the drug may be important.
Another study demonstrating the effects of
Neurontin on a wide variety of neuropathic pain was published in the journal
Pain in 2002 (Pain 99(3):557-66). This double-blind, randomized,
placebo controlled study looked at over 300 people suffering from
neuropathic pain due to a number of different causes. Over an 8-week
period, the participants either received Neurontin or a placebo. The
results showed a significant difference in the pain relief between the group
receiving the drug and the placebo group.
Of special interest to the CM/SM community is growing
evidence which shows that Neurontin can reduce the brutal consequences of
allodynia. This type of pain - feeling pain from things that shouldn't
be painful - can be especially limiting and difficult to deal with. In
well established rat models, gabapentin - along with other, similar drugs -
has been shown to dramatically reduce allodynia. As more and more
rigorous studies are published showing the beneficial effects of Neurontin,
attention will likely turn to how it works. And once the exact
mechanisms are understood, it should become clearer who the drug can benefit
the most. What
About Side Effects?
A drug's effectiveness is only half the equation. In order to be
useful, any side effects caused by the drug must be minor enough to be
tolerated or the drug is essentially worthless. Narcotics are powerful
pain relievers, but also have very strong side effects. In narcotic
studies, it is not unusual for more than 20% of participants to drop out
because of side effects. In addition, drug tolerance and addiction
pose even bigger challenges to the effective use of a narcotics for pain
relief. What are the side effects of Neurontin like, are they as bad
as narcotics'?
In a postherpetic neuralgia study cited by Pfizer, the most
common side effects of Neurontin were sleepiness, dizziness, numbness, and
bruising. Twenty-eight percent of participants reported experiencing
dizziness and 21% sleepiness. Because of this, more than 3% of
participants experienced accidental injuries versus just 1% of the control
group. In addition to the most common effects, there are a wide range
of less common side effects which nonetheless did not occur in the placebo
group. These range from dry mouth to rashes to blurred vision to
stomach problems to cognitive impairment.
Similar side effects are listed in other published
gabapentin studies but are usually characterized as mild to moderate.
Overall, the drug is considered very safe with few and infrequent serious
medical side effects. One reason for this is that the body metabolizes
very little of the drug itself and the drug doesn't stay in the body for
very long. Addiction to the drug has not been studied adequately to
make a determination if it is a problem.
Anecdotally, people contacted by this publication with
experience taking Neurontin present a mixed view. Most encountered
some side effects with sleepiness and cognitive impairment being most
prominent. Several people stopped taking the drug because of the side
effects, but one person who stayed on it for awhile became used to the side
effects and after a period of time was able to function normally.
As mentioned in
Community News, Pfizer is seeking approval for a follow-on drug
which is intended to help control neuropathic pain with even less side
effects than Neurontin.
Things To Be Aware Of
As with any drug, there are a number of
precautions, or things to be aware of, when either taking or considering
Neurontin:
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Naproxen -
Studies show that when gabapentin is taken with Naproxen (the active
ingredient in Alleve), the amount of gabapentin absorbed is 12%-15% higher
than usual.
-
Morphine -
A study showed that morphine given 2 hours before gabapentin increased the
absorption of gabapentin by 44%. The morphine absorption was not
effected.
-
Antacids -
Maalox has been shown to inhibit the action of gabapentin. It is
recommended that gabapentin be taken at least 2 hours after Maalox.
-
Oral
Contraceptives - Studies have shown that gabapentin does not interfere
with the effectiveness of two common oral contraceptives.
-
Pregnancy
- Rat studies have shown that gabapentin is toxic to fetuses. Effects
were seen at dosage levels of 1-4 times the daily maximum dose of 3600
mg/day. No effect was seen at 1/2 the daily dose level (for people).
In addition, when rats were given the drug before and during mating, there
were adverse effects at doses 1-5 times the daily human dose. There
are no studies involving pregnant women.
-
Nursing -
Gabapentin is secreted into breast milk. The effects on a nursing baby
are unknown.
-
Pediatric -
The drug is not FDA approved as a pain treatment for children under 12.
In a study of children between the age of 3-12 (with epilepsy), behavioral
problems were seen, including hostility, aggression, and other emotional
problems
-
Dosage -
People with kidney problems may need to take a lower dose of the drug
Please note the above is not an inclusive list. More information about
precautions can be found from the manufacturer or a doctor or pharmacist.
The Controversy
Despite it's apparent effectiveness, Neurontin is a controversial drug.
The controversy stems from a highly publicized whistleblower lawsuit filed
by a former employee, David Franklin, Ph.D.
Franklin - who has since been joined by the Justice
Department - claims that Parke-Davis (later acquired by Pfizer in a merger
with Warner Lambert) broke the law by marketing Neurontin for off-label
uses. While such prescriptions are allowed, drug companies are not
allowed to promote them.
Franklin was employed as a medical liaison,
someone with scientific credentials who is supposed to answer doctor's
medical and technical questions. Franklin claims that there was a
company wide campaign to push Neurontin for uses - such as treating bipolar
disorder - for which there was no evidence that the drug worked. In
addition, he claims that doctors were paid money to put their names on
articles they didn't write, and were often flown to vacation-style getaway
locations for 'education' sessions.
NBC's Dateline show conducted a year long investigation
and aired an extensive interview with Franklin. Dateline was able to
obtain internal Parke-Davis documents which they claim show a systematic
push to promote Neurontin for off-label uses. During the interview,
recorded voice messages were played that certainly seem incriminating.
Franklin claims that the evidence shows that the company put sales ahead of
good medicine.
Pfizer denies the claim and it should be pointed out
that as a whistleblower, Franklin stands to gain financially from a
successful lawsuit. Pfizer did not return a request to comment on any
aspect of Neurontin, the controversy, or their new drug application.
The Bottom Line
Despite the controversy, Neurontin does appear to be effective in helping
some people deal with neuropathic pain. The side effects are not
severe from a medical perspective, but can still be too much from a
patient's perspective. Like so many aspects of Daily Living for people
with Chiari and syringomyelia, there are no easy answers when it comes to
Neurontin. For some it may be a blessing, for some yet another waste
of time, but for everyone, it is at least worth knowing about.
Sources:
Pfizer, Inc. web site and drug literature
Serpell, MG. Gabapentin in neuropathic pain syndromes. Pain Oct,
2002 99(3): 557-66.
Ahn SH et.al. Gabapentin effect on neuropathic pain compared among patients
with spinal cord injury and different duration of symptoms. Spine Feb, 15
2003 28(4): 341-6.
FDA web site
MSNBC web site, Dateline interview with David Franklin
Theo Emery (AP), Whistleblower's lawsuit could shake up the drug industry,
8/9/03
Back to Table of Contents |
Key Points
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Neurontin is one of the most
widely prescribed drugs on the market with annual sales of over $2 billion
-
Considered an anti-epilepsy drug (AED),
is currently FDA approved for treating epilepsy and post-herpetic
neuralgia
-
Widely prescribed 'off-label' for
treating other types of pain and other disorders
-
Not approved as a pain treatment
for children under 12
-
Rigorous studies have shown it
offers some relief for some types of neuropathic pain
-
May be especially useful in
helping allodynia
-
How it works is not known
-
Considered very safe with few
medically serious side effects; very little of the drug is actually
absorbed by the body
-
Some common side effects are
sleepiness, dizziness, balance problems, numbness, skin problems
-
There is controversy around
the alleged illegal promotion of Neurontin for off-label uses
Neurontin
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Manufactured by Pfizer, Inc.
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Generic name - gabapentin
-
Formula is C9H17NO2
-
Formula is read as
1-(aminomethyl)cyclohexaneacetic acid
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Comes in capsules, tablets, and an
oral slution in strengths of 100mg, 300mg, 400mg, 600mg, and 800mg
-
Half-life (meaning how long before
half the drug is eliminated from the body) is 5-7 hours
-
Maximum recommended daily dose is
3600mg/day. Patients generally start at a low dose and increase the
dosage over time.
Source: Pfizer, Inc. |