Amisulpride

Description
Amisulpride measured by LC-MS/MS
Clinical details

Amisulpride (aminosultopride) is an atypical antipsychotic drug that has been in clinical use since 1992. It is supplied as the free base in 50, 100, 200 and 400 mg tablets or capsules for oral administration, as well as a 50 mg/mL solution for parenteral injection. It is readily absorbed following oral administration and is largely excreted unchanged. Its plasma half-life is ca. 12 h. Adverse reactions include somnolence, hypotension, dystonia, akathisia and extrapyramidal effects. Oral maintenance doses for adults range from 50-400 mg/d. Amisulpride assay is useful in assessing adherence and in the diagnosis of acute poisoning. A target plasma concentration range of 100-400 µg/L during effective therapy has been suggested.

Related condition
Reference range

100-400

Units

µg/L

Testing site
Synnovis : Reference Services : Blackfriars Hub
Laboratory
Therapeutic Drug Monitoring
Sample type and volume required

4 mL of ETDA whole blood is preferred (pre-dose or ‘rough’ sample). Serum or plasma can be used if required, but please avoid gel-separator tubes.

Storage and transport

Please refrigerate (if possible) if not sending immediately. Send by first class post.

Turnaround time

5 working days

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