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Gabapentin has been shown to be well tolerated and effective
in the management of postherpetic neuralgia (PHN) pain. This study looked
at whether the occurrence and frequency of adverse events with gabapentin
correlates with increasing doses of the drug. Gabapentin was begun at 300
mg/d and increased to maintenance doses of 1800 to 3600 mg/d by day 12 to
24. The study included data from 603 patients with PHN: 358 patients received
gabapentin and 245 received placebo. The 3 most common adverse events were
dizziness, drowsiness, and peripheral edema. In this analysis, the incidence
of peripheral edema was increased when gabapentin was given at 1800 mg/d
or more. Dizziness and drowsiness, the other most commonly occurring adverse
events, were transient and did not occur more frequently or worsen with
dosages of 1800 mg/d or greater. Based on these findings, it does not appear
that safety concerns should limit the dosage of gabapentin to achieve optimal
efficacy. Parsons B. Tive L. Huang S. “Gabapentin: a pooled analysis
of adverse events from three clinical trials in patients with postherpetic
neuralgia.” American Journal Geriatric Pharmacotherapy. 2(3):157-62,
2004 Sep.
www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=15561647
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