Chemistry:Prochlorperazine

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Short description: Medication for nausea, psychosis, and anxiety
Prochlorperazine
Prochlorperazine.svg
Clinical data
Trade namesCompazine, Stemetil, others
AHFS/Drugs.comMonograph
MedlinePlusa682116
License data
Pregnancy
category
  • AU: C
Routes of
administration		Oral administration, rectal administration, intramuscular injection, intravenous injection (IV)
Drug classTypical antipsychotic
ATC code
Legal status
Legal status
Pharmacokinetic data
BioavailabilityUnknown, but presumed substantial
Protein binding91–99%
MetabolismMainly Liver (CYP2D6 and/or CYP3A4)
Elimination half-life4–8 hours, differs with the method of administration
ExcretionBile duct, (colored) inactive metabolites in urine
Identifiers
CAS Number
PubChem CID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
Chemical and physical data
FormulaC20H24ClN3S
Molar mass373.94 g·mol−1
3D model (JSmol)
  (verify)

Prochlorperazine, formerly[3] sold under the brand name Compazine among others, is a medication used to treat nausea, migraines, schizophrenia, psychosis and anxiety.[4][5][6][7] It is a less preferred medication for anxiety.[4] It may be taken by mouth, rectally, injection into a vein, or injection into a muscle.[4]

Common side effects include sleepiness, blurry vision, low blood pressure, and dizziness.[4] Serious side effects may include movement disorders including tardive dyskinesia and neuroleptic malignant syndrome.[4] Use in pregnancy and breastfeeding is generally not recommended.[8] It is a typical antipsychotic which is believed to work by reducing the action of dopamine in the brain.[4]

Prochlorperazine was approved for medical use in the United States in 1956.[4] It is available as a generic medication.[5] In 2020, it was the 355th most commonly prescribed medication in the United States, with more than 600 thousand prescriptions.[9][10]

Medical uses

Vomiting

Prochlorperazine is used to prevent vomiting caused by chemotherapy, radiation therapy and in the pre- and postoperative setting.[11] A 2015 Cochrane review found no differences in efficacy among drugs commonly used for this purpose in emergency rooms.[12]

Migraine

Prochlorperazine, generally by intravenous, is used to treat migraine.[13][14] Such use is recommended by The American Headache Society.[6] A 2019 systematic review found prochlorperazine was nearly three times as likely as metoclopramide to relieve headache within 60 minutes of administration.[13]

Labyrinthitis

In the UK prochlorperazine maleate has been used for labyrinthitis, which include not only nausea and vertigo, but spatial and temporal 'jerking' and distortion.[15]

Side effects

Sedation is very common, and extrapyramidal side effects are common and include restlessness, dystonic reactions, pseudoparkinsonism, and akathisia; the extrapyramidal symptoms can affect 2% of people at low doses, whereas higher doses may affect as many as 40% of people.[16][17]

Prochlorperazine can also cause a life-threatening condition called neuroleptic malignant syndrome (NMS). Some symptoms of NMS include high fever, stiff muscles, neck muscle spasm, confusion, irregular pulse or blood pressure, fast heart rate (tachycardia), sweating, abnormal heart rhythms (arrhythmias). Research from the Veterans Administration and United States Food and Drug Administration show injection site reactions. Adverse effects are similar in children.[11]

Warning

The FDA approved label for prochlorperazine includes a warning for increased risk of mortality in elderly patients with dementia related psychosis.[18]

Discontinuation

The British National Formulary recommends a gradual withdrawal when discontinuing antipsychotics to avoid acute withdrawal syndrome or rapid relapse.[19] Symptoms of withdrawal commonly include nausea, vomiting, and loss of appetite.[20] Other symptoms may include restlessness, increased sweating, and trouble sleeping.[20] Less commonly there may be a feeling of the world spinning, numbness, or muscle pains.[20] Symptoms generally resolve after a short period of time.[20]

There is tentative evidence that discontinuation of antipsychotics can result in psychosis.[21] It may also result in reoccurrence of the condition that is being treated.[22] Rarely tardive dyskinesia can occur when the medication is stopped.[20]

Pharmacology

Prochlorperazine
Site Ki (nM) Species Ref
5-HT1A 5,888 Human [23]
5-HT2A 7.24 Human [23]
5-HT2C 123 Human [23]
5-HT3 1349 Human [23]
5-HT6 148 Human [23]
5-HT7 6,760 Human [23]
α1 24 Human [24]
α2 1700 Human [24]
M1 776 Human [23]
M2 1413 Human [23]
D1 251 Human [23]
D2 2.24 Human [23]
D3 1.82 Human [23]
D4 5.37 Human [23]
H1 6.03 Human [25]
H3 17,378 Human [25]
H4 17783 Human [25]
DAT 589 Human [23]
NET 600 Rat [26]

Prochlorperazine is thought to exert its antipsychotic effects by blocking dopamine receptors.[27]

Prochlorperazine is analogous to chlorpromazine; both of these agents antagonize dopaminergic D2 receptors in various pathways of the central nervous system. This D2 blockade results in antipsychotic, antiemetic and other effects. Hyperprolactinemia is a side effect of dopamine antagonists as blockade of D2 receptors within the tuberoinfundibular pathway results in increased plasma levels of prolactin due to increased secretion by lactotrophs in the anterior pituitary.

Following intramuscular injection, the antiemetic action is evident within 5 to 10 minutes and lasts for 3 to 4 hours. Rapid action is also noted after buccal treatment. With oral dosing, the start of action is delayed but the duration somewhat longer (approximately 6 hours).

Society and culture

In the United Kingdom, prochlorperazine is available for the treatment of nausea caused by migraine as a tablet dissolved in the mouth, and in Australia as a tablet swallowed whole. In the UK, it is available via a prescription and as a pharmacy medicine, meaning it does not require a prescription but is only available after talking with a pharmacist.[28][29]

Marketing

Prochlorperazine is available as tablets, suppositories, and in an injectable form.[30]

As of September 2017 it was marketed under the trade names Ametil, Antinaus, Buccastem, Bukatel, Chlormeprazine, Chloropernazine, Compazine, Compro, Daolin, Dhaperazine, Emedrotec, Emetiral, Eminorm, Lotamin, Mitil, Mormal, Nautisol, Novamin, Novomit, Proazine, Procalm, Prochlorperazin, Prochlorperazine, Prochlorpérazine, Prochlorperazinum, Prochlozine, Proclorperazina, Promat, Promin, Promtil, Roumin, Scripto-metic, Seratil, Stemetil, Steremal, Vergon, Vestil, and Volimin.[30][31]

It was also marketed at that time as a combination drug for humans with paracetamol as Vestil-A, as a combination drug for veterinary use, with isopropamide as Darbazine.[30]

Research

Alexza Pharmaceuticals studied an inhaled form of prochlorperazine for the treatment of migraine through Phase II trials under the development name AT-001; development was discontinued in 2011.[32]

Synthesis

Thieme Synthesis:[33] Patent:[34]

The alkylation of 2-chlorophenothiazine (1) and 1-(3-Chloropropyl)-4-methylpiperazine [104-16-5] (2) in the presence of sodamide gives Prochlorperazine (3); or by alkylation of 2-Chloro-10-(3-chloropropyl)phenothiazine [2765-59-5] (4) and 1-methylpiperazine (5).

References

  1. ↑ "Prochlorperazine 3 mg Buccal Tablets - Summary of Product Characteristics (SmPC)". 9 December 2019. https://www.medicines.org.uk/emc/product/5227/smpc. 
  2. ↑ "Buccastem M Buccal Tablets - Summary of Product Characteristics (SmPC)". 9 December 2019. https://www.medicines.org.uk/emc/product/478/smpc. 
  3. ↑ "Side Effects of Compazine (Prochlorperazine), Warnings, Uses". https://www.rxlist.com/compazine-side-effects-drug-center.htm. 
  4. ↑ 4.0 4.1 4.2 4.3 4.4 4.5 4.6 "Prochlorperazine Monograph for Professionals". American Society of Health-System Pharmacists. https://www.drugs.com/monograph/prochlorperazine.html. 
  5. ↑ 5.0 5.1 British national formulary : BNF 76 (76 ed.). Pharmaceutical Press. 2018. pp. 385–386. ISBN 9780857113382. 
  6. ↑ 6.0 6.1 "Management of Adults With Acute Migraine in the Emergency Department: The American Headache Society Evidence Assessment of Parenteral Pharmacotherapies". Headache 56 (6): 911–940. June 2016. doi:10.1111/head.12835. PMID 27300483. 
  7. ↑ "Prochlorperazine". StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing. March 2022. https://www.ncbi.nlm.nih.gov/books/NBK537083/. 
  8. ↑ "Prochlorperazine Use During Pregnancy". https://www.drugs.com/pregnancy/prochlorperazine.html. 
  9. ↑ "The Top 300 of 2020". https://clincalc.com/DrugStats/Top300Drugs.aspx. 
  10. ↑ "Prochlorperazine - Drug Usage Statistics". https://clincalc.com/DrugStats/Drugs/Prochlorperazine. 
  11. ↑ 11.0 11.1 "The Safety of Prochlorperazine in Children: A Systematic Review and Meta-Analysis". Drug Safety 39 (6): 509–516. June 2016. doi:10.1007/s40264-016-0398-9. PMID 26884326. 
  12. ↑ "Drugs for the treatment of nausea and vomiting in adults in the emergency department setting". The Cochrane Database of Systematic Reviews 2018 (9): CD010106. September 2015. doi:10.1002/14651858.CD010106.pub2. PMID 26411330. 
  13. ↑ 13.0 13.1 "The Efficacy and Safety of Prochlorperazine in Patients With Acute Migraine: A Systematic Review and Meta-Analysis". Headache 59 (5): 682–700. May 2019. doi:10.1111/head.13527. PMID 30990883. 
  14. ↑ "Acute Treatment Therapies for Pediatric Migraine: A Qualitative Systematic Review". Headache 56 (1): 49–70. January 2016. doi:10.1111/head.12746. PMID 26790849. 
  15. ↑ "Assessment and treatment of dizziness". Journal of Neurology, Neurosurgery, and Psychiatry 69 (5): 706–707. November 2000. doi:10.1136/jnnp.69.5.706. PMID 11184241. 
  16. ↑ "Antipsychotics". Psychiatric Side Effects of Prescription and Over-The-Counter Medications. American Psychiatric Publishing. 1998. pp. 1946. ISBN 9780880488686. https://books.google.com/books?id=K7kevbILCuQC&pg=PA1946. 
  17. ↑ "Procot Side Effects in Detail". https://www.drugs.com/sfx/procot-side-effects.html. 
  18. ↑ "Prochlorperazine Maleate Tablets, USP". https://dailymed.nlm.nih.gov/dailymed/fda/fdaDrugXsl.cfm?setid=2fd7803f-fb1f-4f00-86ad-c2436b569e6d&type=display#:~:text=WARNINGS-,Increased%20Mortality%20in%20Elderly%20Patients%20with%20Dementia-Related%20Psychosis,psychosis%20(see%20BOXED%20WARNING).. 
  19. ↑ Joint Formulary Committee, BMJ, ed (March 2009). "4.2.1". British National Formulary (57 ed.). United Kingdom: Royal Pharmaceutical Society of Great Britain. p. 192. ISBN 978-0-85369-845-6. "Withdrawal of antipsychotic drugs after long-term therapy should always be gradual and closely monitored to avoid the risk of acute withdrawal syndromes or rapid relapse." 
  20. ↑ 20.0 20.1 20.2 20.3 20.4 Adverse Syndromes and Psychiatric Drugs: A Clinical Guide. OUP Oxford. 2004. pp. 207–216. ISBN 9780198527480. https://books.google.com/books?id=CWR7DwAAQBAJ&pg=PA207. 
  21. ↑ "Does antipsychotic withdrawal provoke psychosis? Review of the literature on rapid onset psychosis (supersensitivity psychosis) and withdrawal-related relapse". Acta Psychiatrica Scandinavica 114 (1): 3–13. July 2006. doi:10.1111/j.1600-0447.2006.00787.x. PMID 16774655. 
  22. ↑ Adherence to Antipsychotics in Sc. Springer Science & Business Media. 2013. p. 85. ISBN 9788847026797. https://books.google.com/books?id=odE-AgAAQBAJ&pg=PA85. 
  23. ↑ 23.00 23.01 23.02 23.03 23.04 23.05 23.06 23.07 23.08 23.09 23.10 23.11 23.12 "Research on adverse drug events. I. Muscarinic M3 receptor binding affinity could predict the risk of antipsychotics to induce type 2 diabetes". Methods and Findings in Experimental and Clinical Pharmacology 27 (5): 289–304. June 2005. doi:10.1358/mf.2005.27.5.908643. PMID 16082416. 
  24. ↑ 24.0 24.1 "Antagonism by neuroleptics of neurotransmitter receptors of normal human brain in vitro". European Journal of Pharmacology 103 (3–4): 197–204. August 1984. doi:10.1016/0014-2999(84)90478-3. PMID 6149136. 
  25. ↑ 25.0 25.1 25.2 "Interactions of recombinant human histamine H1R, H2R, H3R, and H4R receptors with 34 antidepressants and antipsychotics". Naunyn-Schmiedeberg's Archives of Pharmacology 385 (2): 145–170. February 2012. doi:10.1007/s00210-011-0704-0. PMID 22033803. 
  26. ↑ "Blockade by antidepressants and related compounds of biogenic amine uptake into rat brain synaptosomes: most antidepressants selectively block norepinephrine uptake". European Journal of Pharmacology 104 (3–4): 277–286. September 1984. doi:10.1016/0014-2999(84)90403-5. PMID 6499924. 
  27. ↑ Desk Reference of Clinical Pharmacology. 2007. 
  28. ↑ "Buccastem M - Summary of Product Characteristics (SPC) - (eMC)". UK Electronic Medicines Compendium. 16 February 2016. https://www.medicines.org.uk/emc/medicine/22797. 
  29. ↑ "Medicines information". NHS Choices. http://www.nhs.uk/conditions/Medicinesinfo/Pages/Introduction.aspx. 
  30. ↑ 30.0 30.1 30.2 "Prochlorperazine international brands". Drugs.com. https://www.drugs.com/international/prochlorperazine.html. 
  31. ↑ "Compazine (Prochlorperazine) Patient Information: Side Effects and Drug Images at RxList". https://www.rxlist.com/compazine-drug/patient-images-side-effects.htm. 
  32. ↑ "Inhaled drug therapy development for the treatment of migraine". Expert Opinion on Pharmacotherapy 17 (13): 1733–1743. September 2016. doi:10.1080/14656566.2016.1203901. PMID 27416108. 
  33. ↑ J. Gen. Chem. USSR (Engl. Transl.), vol. 32, p. 1915 - 1919,1892 – 1895.
  34. ↑ GB780193 idem Horclois Raymond Jacques, U.S. Patent 2,902,484 (1959 to Rhone Poulenc Sa).

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