What They Treat
| Condition | Gabapentin | Pregabalin |
|---|---|---|
| Neuropathic pain (diabetic, post-herpetic) | Yes | Yes (more evidence) |
| Epilepsy (adjunct) | Yes | Yes |
| Generalised anxiety disorder | Off-label | Licensed in UK/EU |
| Fibromyalgia | Off-label | Yes (licensed in some countries) |
| Restless legs syndrome | Off-label | Off-label |
| Alcohol withdrawal | Sometimes | Off-label |
Common Side Effects
- Dizziness (very common, especially when starting)
- Sedation and cognitive slowing ('gabapentin fog')
- Weight gain
- Blurred vision
- Coordination problems / falls risk in elderly
- Peripheral oedema (ankle swelling)
Dosing Schedule (Gabapentin)
| Week | Dose | Timing |
|---|---|---|
| Week 1 | 300 mg | Night only |
| Week 2 | 300 mg | Twice daily |
| Week 3+ | 300 mg | Three times daily |
| Titrate if needed | Up to 3600 mg/day | In divided doses (max 1200 mg/dose) |
Dependence, tolerance, and how to stop safely
Both gabapentin and pregabalin carry a risk of physical dependence, particularly at higher doses and with prolonged use. The UK Medicines and Healthcare products Regulatory Agency (MHRA) reclassified both drugs as Class C controlled substances in 2019 because of misuse potential and a rising number of deaths – particularly in combination with opioids, benzodiazepines, or alcohol, all of which amplify CNS depression.
Tolerance can develop over weeks to months: the dose that initially controlled pain may need to be increased to maintain the same effect. This is distinct from addiction (compulsive use despite harm) but is medically significant because abrupt stopping can cause a withdrawal syndrome resembling benzodiazepine withdrawal: anxiety, insomnia, sweating, tremor, palpitations, and rarely seizures.
The recommended approach to stopping is a slow taper – typically reducing by no more than 10–25% of the current dose per week, or even more slowly in patients who have been on high doses for years. There is no universally agreed protocol; always discuss tapering with your prescriber rather than stopping abruptly.
Drug interactions to watch
The most dangerous interaction is with other central nervous system depressants:
- Opioids: The combination dramatically increases the risk of fatal respiratory depression. Coroners in the UK and USA have consistently identified this combination in overdose deaths. If you are prescribed both, keep doses as low as effective, and ensure family members know where any naloxone (opioid reversal agent) is kept.
- Benzodiazepines: Combined sedation risk; avoid alcohol on this combination.
- Alcohol: Potentiates sedation; driving risk significantly increased.
- Morphine (for gabapentin specifically): Morphine increases gabapentin blood levels by about 44% – a dose reduction of gabapentin may be needed when morphine is added.
What blood tests are needed on gabapentinoids?
Gabapentin and pregabalin are excreted unchanged by the kidneys. In chronic kidney disease (CKD), doses must be reduced proportionally to eGFR – otherwise drug accumulates and sedation/toxicity worsen. A baseline creatinine and eGFR should be checked before starting and monitored annually (or more often if CKD is present or progressing). There are no liver function tests required as these drugs are not hepatically metabolised.
References
Sources cited on this page. PubMed links open the original abstract.
- Wiffen PJ, Derry S, Bell RF, et al. Gabapentin for chronic neuropathic pain in adults. Cochrane Database Syst Rev. 2017;6:CD007938. PMID 28597471 · doi:10.1002/14651858.CD007938.pub4
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