From Wikipedia, the free encyclopedia
Mr. Ibrahem/Levomepromazine
Clinical data
Trade namesNozinan, Levoprome, Detenler, Hirnamin, Levotomin, Neurocil, others
AHFS/ Drugs.com International Drug Names
Pregnancy
category
  • Only if needed
Routes of
administration
By mouth, IV, SC, IM [1]
Drug class Typical antipsychotic
Legal status
Legal status
  • AU: S4 (Prescription only)
  • UK: POM (Prescription only)
Pharmacokinetic data
Bioavailability~50–60%
Metabolism Liver
Onset of action0.5 to 3 hr [2]
Elimination half-life~20 hours
Duration of action8 hr [2]
ExcretionIn feces and urine (metabolites), unchanged drug only 1%
Identifiers
  • (2R)-3-(2-Methoxyphenothiazine-10-yl-)-N,N,2-trimethylpropanamine
Chemical and physical data
FormulaC19H24N2OS
Molar mass328.47 g·mol−1
3D model ( JSmol)
  • O(c2cc1N(c3c(Sc1cc2)cccc3)C[C@H](C)CN(C)C)C
  • InChI=1S/C19H24N2OS/c1-14(12-20(2)3)13-21-16-7-5-6-8-18(16)23-19-10-9-15(22-4)11-17(19)21/h5-11,14H,12-13H2,1-4H3/t14-/m1/s1 checkY
  • Key:VRQVVMDWGGWHTJ-CQSZACIVSA-N checkY
 ☒NcheckY  (what is this?)   (verify)

Levomepromazine, also known as methotrimeprazine, is a medication used for schizophrenia and palliative care. [1] In palliative care it is used for restlessness, pain, and vomiting. [1] It may be used by mouth or by injection. [1] Effects generally begin around 0.5 to 3 hours and last for 8 hours. [2]

Side effects may include low blood pressure with standing, sleepiness, dry mouth, liver problems, and dystonia. [2] [1] Serious side effect may include priapism, QT prolongation, and neuroleptic malignant syndrome. [2] [1] [3] It is an antipsychotic of the phenothiazine type. [2] It works by blocking a variety of receptors, including adrenergic, dopamine, histamine, muscarinic acetylcholine, and serotonin. [2]

Levomepromazine was patented in 1954 and come into medical use in the United State in 1957. [4] It is available as a generic medication. [1] In the United Kingdom 84 tablets of 25 mg costs the NHS about £20 as of 2020. [1] It has been widely used; [2] though is no longer commercially available in the United States. [5]

References

  1. ^ a b c d e f g h i j BNF (80 ed.). BMJ Group and the Pharmaceutical Press. September 2020 – March 2021. p. 460. ISBN  978-0-85711-369-6.{{ cite book}}: CS1 maint: date format ( link)
  2. ^ a b c d e f g h i Dietz, I; Schmitz, A; Lampey, I; Schulz, C (19 January 2013). "Evidence for the use of Levomepromazine for symptom control in the palliative care setting: a systematic review". BMC palliative care. 12: 2. doi: 10.1186/1472-684X-12-2. PMID  23331515.{{ cite journal}}: CS1 maint: unflagged free DOI ( link)
  3. ^ "Levomepromazine Hydrochloride 25mg/ml Solution for Injection - Summary of Product Characteristics (SmPC) - (emc)". www.medicines.org.uk. Archived from the original on 28 August 2021. Retrieved 13 August 2021.
  4. ^ Buschmann, Helmut; Holenz, Jörg; Párraga, Antonio; Torrens, Antoni; Vela, José Miguel; Díaz, José Luis (16 April 2007). Antidepressants, Antipsychotics, Anxiolytics, 2 Volume Set: From Chemistry and Pharmacology to Clinical Application. John Wiley & Sons. p. 502. ISBN  978-3-527-31058-6. Archived from the original on 28 August 2021. Retrieved 13 August 2021.
  5. ^ "Drugs@FDA: FDA-Approved Drugs". www.accessdata.fda.gov. Archived from the original on 24 March 2021. Retrieved 13 August 2021.
From Wikipedia, the free encyclopedia
Mr. Ibrahem/Levomepromazine
Clinical data
Trade namesNozinan, Levoprome, Detenler, Hirnamin, Levotomin, Neurocil, others
AHFS/ Drugs.com International Drug Names
Pregnancy
category
  • Only if needed
Routes of
administration
By mouth, IV, SC, IM [1]
Drug class Typical antipsychotic
Legal status
Legal status
  • AU: S4 (Prescription only)
  • UK: POM (Prescription only)
Pharmacokinetic data
Bioavailability~50–60%
Metabolism Liver
Onset of action0.5 to 3 hr [2]
Elimination half-life~20 hours
Duration of action8 hr [2]
ExcretionIn feces and urine (metabolites), unchanged drug only 1%
Identifiers
  • (2R)-3-(2-Methoxyphenothiazine-10-yl-)-N,N,2-trimethylpropanamine
Chemical and physical data
FormulaC19H24N2OS
Molar mass328.47 g·mol−1
3D model ( JSmol)
  • O(c2cc1N(c3c(Sc1cc2)cccc3)C[C@H](C)CN(C)C)C
  • InChI=1S/C19H24N2OS/c1-14(12-20(2)3)13-21-16-7-5-6-8-18(16)23-19-10-9-15(22-4)11-17(19)21/h5-11,14H,12-13H2,1-4H3/t14-/m1/s1 checkY
  • Key:VRQVVMDWGGWHTJ-CQSZACIVSA-N checkY
 ☒NcheckY  (what is this?)   (verify)

Levomepromazine, also known as methotrimeprazine, is a medication used for schizophrenia and palliative care. [1] In palliative care it is used for restlessness, pain, and vomiting. [1] It may be used by mouth or by injection. [1] Effects generally begin around 0.5 to 3 hours and last for 8 hours. [2]

Side effects may include low blood pressure with standing, sleepiness, dry mouth, liver problems, and dystonia. [2] [1] Serious side effect may include priapism, QT prolongation, and neuroleptic malignant syndrome. [2] [1] [3] It is an antipsychotic of the phenothiazine type. [2] It works by blocking a variety of receptors, including adrenergic, dopamine, histamine, muscarinic acetylcholine, and serotonin. [2]

Levomepromazine was patented in 1954 and come into medical use in the United State in 1957. [4] It is available as a generic medication. [1] In the United Kingdom 84 tablets of 25 mg costs the NHS about £20 as of 2020. [1] It has been widely used; [2] though is no longer commercially available in the United States. [5]

References

  1. ^ a b c d e f g h i j BNF (80 ed.). BMJ Group and the Pharmaceutical Press. September 2020 – March 2021. p. 460. ISBN  978-0-85711-369-6.{{ cite book}}: CS1 maint: date format ( link)
  2. ^ a b c d e f g h i Dietz, I; Schmitz, A; Lampey, I; Schulz, C (19 January 2013). "Evidence for the use of Levomepromazine for symptom control in the palliative care setting: a systematic review". BMC palliative care. 12: 2. doi: 10.1186/1472-684X-12-2. PMID  23331515.{{ cite journal}}: CS1 maint: unflagged free DOI ( link)
  3. ^ "Levomepromazine Hydrochloride 25mg/ml Solution for Injection - Summary of Product Characteristics (SmPC) - (emc)". www.medicines.org.uk. Archived from the original on 28 August 2021. Retrieved 13 August 2021.
  4. ^ Buschmann, Helmut; Holenz, Jörg; Párraga, Antonio; Torrens, Antoni; Vela, José Miguel; Díaz, José Luis (16 April 2007). Antidepressants, Antipsychotics, Anxiolytics, 2 Volume Set: From Chemistry and Pharmacology to Clinical Application. John Wiley & Sons. p. 502. ISBN  978-3-527-31058-6. Archived from the original on 28 August 2021. Retrieved 13 August 2021.
  5. ^ "Drugs@FDA: FDA-Approved Drugs". www.accessdata.fda.gov. Archived from the original on 24 March 2021. Retrieved 13 August 2021.

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