Gabapentin

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Sections available in full article Name, Class of drug, Description, Uses, Administration, Do not mix with, Routes of administration, Dosage, Timing of administration, Pharmocokinetics, Normal, Physiological, variations, Pathological variations, Precautions, Use with care, Interactions, Adverse reactions, Sources, Publications,
Contributors Mr Simon Platt BVMS DipACVIM (Neurology) DipECVN MRCVS RCVS Specialist in Veterinary Neurology
Mr Ian Battersby BVSc DSAM DipECVIM-CA MRCVS RCVS and European Specialist in Small Animal Medicine

Name

Gabapentin

Class of drug

  • Anti-epileptic drug (GABA[gamma-aminobutyric acid] agonist) - analog of GABA.

Uses

Action

  • Gabapentin inhibits tonic hindlimb extension in the electroshock seizure model.
  • Also inhibits clonic seizures induced by pentylenetetrazol.
  • Efficacy in both these tests parallels that of valproic acid Sodium valproate and distinguishes it from phenytoin Phenytoin and carbamazepine in humans.
  • Despite its design as a GABA agonist, gabapentin does not mimic GABA when iontophoretically applied to neurons in primary culture.
  • Does not bind to GABA A or B receptors.
  • Appears to act by a novel mechanism; increases promoted release of GABA by an unknown mechanism.
  • Has not been found consistently to reduce sustained repetitive firing of action potentials nor to significantly affect any Ca2+ channel current.

Indications

  • Adjunctive treatment of generalized seizures that are considered refractory to phenobarbitone Phenobarbital and potassium bromide Potassium bromide.
  • Adjunctive gabapentin therapy will reduce frequency of generalized seizures Seizures in over approximately 45% of idiopathic epileptic Epilepsy: idiopathic dogs refractory to phenobarbitone and potassium bromide therapy.
  • Adjunctive treatment of partial seizures Seizures with or without secondary generalization not satisfactorily controlled with other anti-epileptics Therapeutics: nervous system.
  • Neuropathic pain.

Adverse reactions

Effects of overdosage

  • Most common adverse effects are:
    • Somnolence.
    • Dizziness.
    • Ataxia.
    • Fatigue.
  • Effects usually are mild to moderately severe but resolve within 2 weeks of onset during continued treatment.
  • Overall, well tolerated.

Reporting of reactions

  • Severe ataxia.
  • Lethargy.

Treatment

  • Drug removal.

Antidote for overdose

  • None.

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