Galantamine: Difference between revisions

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!style="text-align: left"| Onset of action
!style="text-align: left"| 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
|Peak plasma levels in about one hour after ingestion from immediate-release preparations; 4 to 5 hours after a dose of modified-release formulations
|-
!style="text-align: left"| Metabolism
!style="text-align: left"| Metabolism
|Partially metabolized by CYP2D6, CYP3A4  
|Partially metabolized by CYP2D6, CYP3A4  

Revision as of 23:43, 29 September 2020


Introduction

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