Wikia

Psychology Wiki

Levomepromazine

Talk0
34,135pages on
this wiki
Revision as of 02:51, November 14, 2010 by J36Bot (Talk | contribs)

(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)

Assessment | Biopsychology | Comparative | Cognitive | Developmental | Language | Individual differences | Personality | Philosophy | Social |
Methods | Statistics | Clinical | Educational | Industrial | Professional items | World psychology |

Biological: Behavioural genetics · Evolutionary psychology · Neuroanatomy · Neurochemistry · Neuroendocrinology · Neuroscience · Psychoneuroimmunology · Physiological Psychology · Psychopharmacology (Index, Outline)


Levomepromazine chemical structure
Levomepromazine

(2R)-3-(2-Methoxyphenothiazine-10-yl-)-N,N,2-trimethylpropanamine
IUPAC name
CAS number
60-99-1
ATC code

N05AA02

PubChem
72287
DrugBank
[1]
Chemical formula {{{chemical_formula}}}
Molecular weight 328.47 g/mol
Bioavailability approx. 50 to 60%
Metabolism Hepatic
Elimination half-life ~ 20 hours
Excretion In feces and urine (metabolites), unchanged drug only 1%
Pregnancy category Only if clearly needed
Legal status Rx-only (n.a. in the USA)
Routes of administration Oral, seldom intramuscular

Levomepromazine in Germany and Methotrimeprazine in America (Sold as Nosinan Nozinan, Levoprome) is an aliphatic phenothiazine neuroleptic drug. It is a low-potency antipsychotic (approximately half as potent as chlorpromazine) with strong analgesic and antiemetic properties.

Serious side effects include tardive dyskinesia, akathisia, and the potentially fatal neuroleptic malignant syndrome. As is typical of phenothiazine antipsychotics, levomepromazine is a "dirty drug": it exerts its effects by blocking a variety of receptors, including adrenergic receptors, dopamine receptors, histamine receptors, muscarinic acetylcholine receptors, and serotonin receptors.

Currently, levomepromazine is not registered in the USA, although some American physicians are conducting studies regarding the strong analgesic effect of levomepromazine.[How to reference and link to summary or text] In Europe it has been marketed for decades as Neurocil and Nozinan. Nozinan is also available in Canada.

IndicationsEdit

Levomepromazine is used for the treatment of psychosis, particular those of schizophrenia, and manic phases of bipolar disorder. It should be used only with caution in the treatment of agitated depressions, as it can cause akathisia as a side effect, which could worsen the agitation.

Levomepromazine is also used at lower doses for the treatment of nausea.

Adverse effectsEdit

The most common side effect is akathisia.[How to reference and link to summary or text] Levomepromazine has prominent sedative and anticholinergic/sympatholytic effects (dry mouth, hypotension, sinus tachycardia, night sweats) and may cause weight gain. These side effects normally preclude prescribing the drug in doses needed for full remission of schizophrenia, so it has to be combined with a more potent antipsychotic. In any case, blood pressure and EKG should be monitored regularly.

A rare but life-threatening side effect is neuroleptic malignant syndrome (NMS). The symptoms of NMS include muscle stiffness and fever.

PharmacokineticsEdit

  • Absorption, and other characteristics : Levomepromazine has an incomplete oral bioavailability, because it undergoes considerable first-pass-metabolism in the liver. It has a half-life of approximately 20 hours (15 to 30 hours). Maximum plasma levels are reached 1 to 4 hours after oral dosing. After i.m.-doses maximum plasma levels are seen after 30 to 90 minutes.
  • Distribution : The approximate distribution volume is 30 l/kg. Levomepromazine is lipophilic and easily crosses the blood-brain barrier and the placenta, and can also be found in the milk of breast-feeding mothers. Liquor concentration usually exceeds the plasma concentrations.
  • Metabolism : Levomepromazine is metabolized in the liver to a sulfoxide, a glucuronide, and a demethylated metabolite.
  • Elimination : Drug elimination (as metabolites, only 1% of unchanged levomepromazine is recovered) is relatively slow. The metabolites are found in feces and urine.

Mechanism of actionEdit

Levomepromazine blocks the following postsynaptic receptors:

The mode of action explains the particular pharmacological effects of levomepromazine.

InteractionsEdit

Dosages of concomitantly administered opioids should be reduced by approximately half, because levomepromazine amplifies the therapeutic actions and side-effects of opioids. Combination with tramadol (Ultram) is associated with increased risk of seizures.

Additive sedative effects and confusional states may emerge if levomepromazine is given with benzodiazepines or barbiturates. This may be avoided by using the lowest dose possible with the substances in question.

Exert particular caution in combining levomepromazine with other anticholinergic drugs (tricyclic antidepressants and antiparkinsonian-agents): Particularly the elderly may develop delirium, high fever, severe obstipation, even ileus and glaucoma. Reduce both the dose of levomepromazine and the dose of the other drug. If possible, avoid such combinations.

Caffeine and/or stimulantes of the ephedrine/amphetamine type may counteract the specific actions of levomepromazine. Concomitant use of these substances should be avoided.

Coffee and black tea should be avoided because they decrease the absorption of levomepromazine considerably. The same is true for antacids; these should be given 1 to 2 hours before or after oral administration of levomepromazine.

ReferencesEdit

Template:Dopamine antagonists

This page uses Creative Commons Licensed content from Wikipedia (view authors).

Around Wikia's network

Random Wiki