Galantamine

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Revision as of 06:15, 30 September 2020 by Ctol2 (talk | contribs) (Pharmacokinetics)

Galantamine Hydrobromide is a reversible inhibitor of acetylcholinesterase. It also has an intrinsic action on nicotinic receptors. It is used for the treatment of mild to moderate dementia in Alzheimer’s disease.

Generic Name 藥名 HA Code 藥物代碼 Classification藥物分類
Galantamine HBR Prolonged Release Cap 8mg GALA04 P1S1S3
Galantamine HBR Prolonged Release Cap 16mg GALA05 P1S1S3
Galantamine HBR Prolonged Release Cap 24mg GALA06 P1S1S3

Mechanism of Action

Acetylcholinesterase inhibiting drug

Dosage

By Oral: initially 4 mg twice daily for 4 weeks increased to 8 mg twice daily for 4 weeks; maintenance 8-12 mg twice daily according to response and tolerance.

A modified-release preparation is also available for once-daily use. Clinical benefit should be assessed on a regular basis.

Reductions in dose may be necessary in patients with hepatic or renal impairment.

Side Effects

Common side effects include

  • Nausea and vomiting
  • difficulty sleeping
  • aggression
  • Loss of appetite
  • Diarrhoea
  • Feeling tired
  • Muscle cramps

These effects usually last 1 – 3 weeks and then lessen

Serious side effects may include:

  • Abnormal heart rhythms
  • Difficulty emptying urine from the bladder
  • seizures

Pharmacokinetics

Oral bioavailability Donepezil hydrochloride is rapidly and well absorbed from the gastrointestinal tract with an oral bioavailability of about 90%. Plasma protein binding is about 18%.
Onset of action Peak plasma levels in about one hour after ingestion from immediate-release preparations; 4 to 5 hours after a dose of modified-release formulations
Metabolism Partially metabolized by CYP2D6, CYP3A4
Elimination half-life 7 to 8 hours

Drug Management

Monitoring

  • acetylcholinesterase inhibitor may increase gastric acid secretion, so patients should be monitored closely for GI bleeding, especially those receiving concurrent NSAID drugs.
  • check body weight regularly
  • monitor the cognitive, global functions, and ADL activities
  • monitor the sleeping quality

Drug interaction

Hepatic metabolism of donepezil via the cytochrome P450 will be affected by drugs that inhibit the isoenzyme CYP3A4 and CYP2D6 Interactions do not generally apply to steroid used for topical action including inhalation, unless specified.

Drugs given with donepezil Potential Effect
CYP2D6 inhibitors:

SSRI, such as Paroxetine, Quinidine, Amitriptyline

May increase plasma-donepezil concentration, increasing the risk of severe adverse reactions.
CYP3A4 inhibitors:

Erythromycin, Itraconazole, Ketoconazole

May increase plasma-donepezil concentration, increasing the risk of severe adverse reactions
CYP3A4 inducers & CYP2D6 inducers:

Rifampicin, Phenytoin, Carbamazepine

May reduce plasma-donepezil concentration

Caution

  • Cardiovascular conduction disorders such as sick-sinus syndrome
  • Susceptibility to peptic ulcers
  • Asthma, chronic obstructive pulmonary disease
  • People who have a predisposition to seizures
  • Concomitant antipsychotic treatment – increased risk of neuroleptic malignant syndrome

Contraindications

patients with severe impairment (creatinine clearance less than 9ml/minute. Patients with known hypersensitivity to galantamine hydrobromide

Hepatic impairment

  • no dose adjustment of galantamine is necessary in mild hepatic impairment.
  • For immediate-release tablet, in moderate impairment, initially 4mg once daily, preferably in the morning, for at least one week, then 4 mg twice daily for at least 4 weeks. Maximum 8 mg twice daily. Avoid in severe impairment
  • For modified-release capsules in moderate impairment, initially 8 mg on alternate days, preferably in the morning for 1 week, then 8 mg once daily for 4 weeks. Maximum 16 mg daily. Avoid in severe impairment

Renal impairment

  • No dose adjustment is necessary for galantamine in mild or moderate renal impairment.
  • Avoid if eGFR less than 9ml/minute/1.73m2

Effects on ability to drive and use machinery

Donepezil can cause fatigue, dizziness and muscles, mainly when initiating or increasing the dose. The treating doctor should routinely evaluate the ability of patients on donepezil to continue driving or operating complex machines.

FAQ

How should Galantamine be taken?

Galantamine comes in three forms: as 8mg and 12mg tablets; as Galatamine XL in 8mg, 16mg and 24mg prolonged release capsules; and as an oral solution 4mg/ml. Tablets and oral solution should be administered twice a day, preferably with morning and evening meals. Drink plenty of liquids to keep yourself hydrated.

What should I avoid while taking?

Avoid abruptly discontinue the medication.

What happen if I overdose?

Contact your primary care doctor. If emergency situation, call 999

What happen if I miss a dose?

Take it as soon as you remember. If it is near the time of the next dose, skip the missed dose. Take your next dose at the regular time. Do not double the dose to catch up.