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Galantamine explained

Reading time: 4 minutes Last reviewed: 8th May 2026 Clinically reviewed by The Dementia Service

In plain English

Galantamine is a Cholinesterase Inhibitor licensed for mild to moderate Alzheimer's Disease. It has a dual mechanism: it inhibits acetylcholinesterase and modulates nicotinic receptors. This page covers dosing, side effects and how Galantamine compares with other options.

What Galantamine is

Galantamine (Reminyl XL, also generic) is a Cholinesterase Inhibitor with a dual mechanism. It increases acetylcholine levels by inhibiting the enzyme acetylcholinesterase, and it also modulates nicotinic acetylcholine receptors, which may add a second mechanism for cognitive benefit.

Galantamine is licensed in the UK for mild to moderate Alzheimer's Disease, under NICE TA217.

Dosing

Galantamine is available as modified-release once-daily capsules and as an oral solution. The standard titration:

Take with breakfast. Capsules should not be opened or crushed; the oral solution is available for those who cannot swallow capsules.

Galantamine is metabolised through the liver and partly excreted by the kidneys; dose adjustment is needed in moderate hepatic or renal impairment.

Effectiveness

Galantamine has similar efficacy to Donepezil and Rivastigmine across head-to-head and meta-analytic comparisons. About 60 per cent of people who tolerate Galantamine experience meaningful benefit in attention, memory and daily function over 6 to 12 months.

Side effects

The side effect profile is similar to other Cholinesterase Inhibitors. Most are gastrointestinal and transient:

Galantamine may have a slightly higher rate of mortality in patients with significant cardiovascular disease compared with Donepezil in some studies, although the absolute risk is small. Discuss with your prescriber if you have multiple cardiovascular conditions.

When Galantamine may be preferred

When to switch

If Galantamine is poorly tolerated, switching to Donepezil or to a Rivastigmine patch is reasonable. Switching is usually a direct cross-over with appropriate dose adjustment, under prescriber guidance.

Monitoring and review

A three-month review after reaching the target dose is standard, followed by 6- to 12-monthly reviews. The review assesses tolerability, response, pulse and blood pressure, and whether to continue, switch or add Memantine.

Before starting

The standard pre-prescribing checks for any Cholinesterase Inhibitor apply: Electrocardiogram, medication review, history of asthma or active peptic ulcer, history of seizures, kidney and liver function.

Frequently asked questions

Is Galantamine better than Donepezil?

No clear evidence of superiority on either side. The two have similar effectiveness; choice depends on tolerability, dosing preference and individual response.

When do I take Galantamine?

Once daily with breakfast. Avoid taking on an empty stomach as this increases the risk of nausea.

What if I miss a dose?

Take when remembered if within several hours. If close to the next dose, skip the missed dose. Do not double up.

Can I drive on Galantamine?

Galantamine itself does not prevent driving. The underlying dementia diagnosis requires DVLA notification. See driving and the DVLA.

Is Galantamine available on the NHS?

Yes. NICE TA217 recommends Galantamine for mild to moderate Alzheimer's Disease. It is available on NHS prescription.

What to do next

  1. Confirm an Electrocardiogram has been performed before starting.
  2. Diary the four-week review for dose increase.
  3. Note any side effects in the first month to share at the review.

References

  1. NICE TA217.
  2. BNF Galantamine monograph.
  3. Birks J. Cholinesterase inhibitors for Alzheimer's Disease. Cochrane Database 2018.
  4. Electronic Medicines Compendium. Reminyl XL summary of product characteristics.