Gabapentin 800 mg is a prescription medication available in capsule form in the United States. Neurontin is one brand of gabapentin, and the FDA-approved labeling lists 800 mg, 300 mg, and 400 mg capsule strengths.
In the United States, Neurontin (gabapentin) is indicated for the management of postherpetic neuralgia in adults and as adjunctive therapy for partial-onset seizures, with or without secondary generalization, in adults and pediatric patients 3 years and older with epilepsy.
Gabapentin may cause side effects such as dizziness, sleepiness, and problems with coordination. Patients should be cautious when driving or operating machinery until they know how the medication affects them. The FDA also warns about respiratory depression, particularly when gabapentin is used with central nervous system depressants such as opioids or in people with underlying respiratory impairment.
Gabapentin should not be stopped abruptly without medical guidance. Rapid or sudden discontinuation may increase the risk of seizures and has also been associated with withdrawal symptoms and suicidal thoughts or behavior. Dose adjustments may be necessary for patients with reduced kidney function.
Gabapentin 800 mg should be used only according to the directions provided by a qualified healthcare professional. This information is intended for general educational purposes and does not replace advice from a doctor or pharmacist.
