Escitalopram

Source: Wikipedia, the free encyclopedia.

Escitalopram
Clinical data
Pronunciation/ˌɛsəˈtæləˌpræm/ pronunciation
Trade namesCipralex, Lexapro, others[1]
AHFS/Drugs.comMonograph
MedlinePlusa603005
License data
Pregnancy
category
  • AU: C
Routes of
administration
By mouth
Drug classSelective serotonin reuptake inhibitor (SSRI)
ATC code
Legal status
Legal status
Pharmacokinetic data
Bioavailability80%
Protein binding~56%
MetabolismLiver, specifically the enzymes CYP3A4 and CYP2C19
MetabolitesDesmethylcitalopram, didesmethylcitalopram
Elimination half-life27–32 hours
Identifiers
  • (S)-1-[3-(Dimethylamino)propyl]-1-(4-fluorophenyl)-1,3-dihydroisobenzofuran-5-carbonitrile
JSmol)
  • Fc1ccc(cc1)[C@@]3(OCc2cc(C#N)ccc23)CCCN(C)C
  • InChI=1S/C20H21FN2O/c1-23(2)11-3-10-20(17-5-7-18(21)8-6-17)19-9-4-15(13-22)12-16(19)14-24-20/h4-9,12H,3,10-11,14H2,1-2H3/t20-/m0/s1 checkY
  • Key:WSEQXVZVJXJVFP-FQEVSTJZSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Escitalopram, sold under the brand names Lexapro and Cipralex, among others, is an antidepressant of the selective serotonin reuptake inhibitor (SSRI) class.[7] Escitalopram is mainly used to treat major depressive disorder and generalized anxiety disorder.[7] It is taken by mouth,[7] available commercially as an oxalate salt exclusively.

Common side effects include trouble sleeping, nausea, sexual problems, and feeling tired.

racemate), hence the name es-citalopram.[7]

Escitalopram was approved for medical use in the United States in 2002.[7] Escitalopram is rarely replaced by twice the dose of citalopram, though escitalopram is safer and more effective.[9] It is on the World Health Organization's List of Essential Medicines.[10] In 2021, it was the fifteenth most commonly prescribed medication in the United States, with more than 30 million prescriptions.[11][12]

Medical uses

Escitalopram has FDA approval for the treatment of

obsessive-compulsive disorder (OCD), and panic disorder with or without agoraphobia. In Australia it is approved for major depressive disorder.[13][14][15]

Depression

Escitalopram is among the most effective and well-tolerated antidepressants for the short-term (acute) treatment of major depressive disorder in adults.[16][17] It is also the safest one to give to children and adolescents.[18][19]

Controversy existed regarding the effectiveness of escitalopram compared with its predecessor, citalopram. The importance of this issue followed from the greater cost of escitalopram relative to the generic mixture of isomers of citalopram, prior to the expiration of the escitalopram patent in 2012, which led to charges of evergreening. Accordingly, this issue has been examined in at least 10 different systematic reviews and meta analyses. As of 2012, reviews had concluded (with caveats in some cases) that escitalopram is modestly superior to citalopram in efficacy and tolerability.[20][21][22][23]

Anxiety disorders

Escitalopram appears to be effective in treating generalized anxiety disorder, with relapse on escitalopram at 20% rather than placebo at 50%, which translates to a number needed to treat of 3.33.[24][25] Escitalopram appears effective in treating social anxiety disorder as well.[26]

Other

Escitalopram is effective in reducing the symptoms of premenstrual syndrome, whether taken continuously or in the luteal phase only.[27]

Side effects

Escitalopram, like other SSRIs, has been shown to affect sexual function, causing side effects such as decreased libido, delayed ejaculation, and anorgasmia.[28][29]

There is also evidence that SSRIs may cause an increase in

suicidality among the adults treated with escitalopram for psychiatric indications.[30][31][32] The authors of a related study note the general problem with statistical approaches: due to the rarity of suicidal events in clinical trials, it is hard to draw firm conclusions with a sample smaller than two million patients.[33]

liver impairment.[35][36] There are concerns of higher rates of QT prolongation and torsades de pointes compared with other SSRIs.[37][38] The US Food and Drug Administration and Health Canada did not similarly order restrictions on escitalopram dosage, only on its predecessor citalopram.[39]

Very common effects

Very common effects (>10% incidence) include:[40][41][42][5][43]

  • Headache (24%)
  • Nausea (18%)
  • Ejaculation disorder (9–14%)
  • Somnolence (4–13%)
  • Insomnia (7–12%)

Common (1–10% incidence)

Common effects (1–10% incidence) include:

Psychomotor effects

The most common effect is fatigue or somnolence, particularly in older adults,[44] although patients with pre-existing daytime sleepiness and fatigue may experience paradoxical improvement of these symptoms.[45] Escitalopram has not been shown to affect serial reaction time, logical reasoning, serial subtraction, multitask, or Mackworth Clock task performance.[46]

Discontinuation symptoms

Escitalopram discontinuation, particularly abruptly, may cause certain

brain zaps" by those affected. Frequent symptoms in one study were dizziness (44%), muscle tension (44%), chills (44%), confusion or trouble concentrating (40%), amnesia (28%), and crying (28%). Very slow tapering was recommended.[48] There have been spontaneous reports of discontinuation of Lexapro and other SSRIs and SNRIs, especially when abrupt, leading to dysphoric mood, irritability, agitation, anxiety, headache, lethargy, emotional lability, insomnia, and hypomania. Other symptoms such as panic attacks, hostility, aggressiveness, impulsivity, akathisia (psychomotor restlessness), mania, worsening of depression, and suicidal ideation can emerge when the dose is adjusted down.[49]

Sexual dysfunction

Some people experience persistent sexual side effects when taking SSRIs or after discontinuing them.[50] Symptoms of medication-induced sexual dysfunction from antidepressants include difficulty with orgasm, erection, or ejaculation.[50] Other symptoms may be genital anesthesia, anhedonia, decreased libido, vaginal lubrication issues, and nipple insensitivity in women. Rates are unknown, and there is no established treatment.[51]

Pregnancy

Antidepressant exposure (including escitalopram) is associated with shorter duration of pregnancy (by three days), increased risk of preterm delivery (by 55%), lower birth weight (by 75 g), and lower Apgar scores (by <0.4 points). Antidepressant exposure is not associated with an increased risk of spontaneous abortion.[52] There is a tentative association of SSRI use during pregnancy with heart problems in the baby.[53] The advantages of their use during pregnancy may thus not outweigh the possible negative effects on the baby.[53]

Overdose

Excessive doses of escitalopram usually cause relatively minor untoward effects, such as agitation and tachycardia. However, dyskinesia, hypertonia, and clonus may occur in some cases. Therapeutic blood levels of escitalopram are usually in the range of 20–80 μg/L but may reach 80–200 μg/L in the elderly, patients with hepatic dysfunction, those who are poor CYP2C19 metabolizers or following acute overdose. Monitoring of the drug in plasma or serum is generally accomplished using chromatographic methods. Chiral techniques are available to distinguish escitalopram from its racemate, citalopram.[36][54][55]

Pharmacology

Mechanism of action

Binding profile[56][57]
Site Ki (nM)
SERT 0.8–1.1
NET 7,800
DAT 27,400
5-HT1A >1,000
5-HT2A >1,000
5-HT2C
2,500
α1 3,900
α2 >1,000
D2 >1,000
H1 2,000
mACh 1,240
hERG 2,600 (IC50)

Escitalopram increases intrasynaptic levels of the neurotransmitter serotonin by blocking the reuptake of the neurotransmitter into the presynaptic neuron. Over time, this leads to a downregulation of pre-synaptic 5-HT1A receptors, which is associated with an improvement in passive stress tolerance, and delayed downstream increase in expression of brain-derived neurotrophic factor, which may contribute to a reduction in negative affective biases.[58][59]

Of the SSRIs currently available, escitalopram has the highest

selectivity for the serotonin transporter (SERT) compared to the norepinephrine transporter (NET), making the side-effect profile relatively mild in comparison to less-selective SSRIs.[60]

Escitalopram is a substrate of P-glycoprotein and hence P-glycoprotein inhibitors such as verapamil and quinidine may improve its blood brain barrier penetrability.[61] In a preclinical study in rats combining escitalopram with a P-glycoprotein inhibitor, its antidepressant-like effects were enhanced.[61]

Interactions

Escitalopram, similarly to other SSRIs, may increase bleed risk with

platelet aggregation via blocking serotonin transporters on platelets.[62] Escitalopram inhibits CYP2D6, and hence may increase plasma levels of a number of CYP2D6 substrates such as aripiprazole, risperidone, tramadol, codeine, etc. As escitalopram is only a weak inhibitor of CYP2D6, analgesia from tramadol may not be affected.[63] Escitalopram should be taken with caution when using St. John's wort, ginseng, dextromethorphan (DXM), linezolid, tramadol, and other serotonergic drugs due to the risk of serotonin syndrome.[64][65] Exposure to escitalopram is increased moderately, by about 50%, when it is taken with omeprazole. The authors of this study suggested that this increase is unlikely to be of clinical concern.[66]

Bupropion has been found to significantly increase citalopram plasma concentration and systemic exposure; as of April 2018 the interaction with escitalopram had not been studied, but some monographs warned of the potential interaction.[67]

Escitalopram can also prolong the QT interval, and hence it is not recommended in patients that are concurrently on other medications that also have the ability to prolong the QT interval. These drugs include

antiretrovirals (ritonavir, saquinavir, lopinavir).[35] As an SSRI, escitalopram should not be given concurrently with MAOIs.[60]

Chemistry

Escitalopram is the (S)-

racemate citalopram, which is responsible for its name: escitalopram.[7] [68]

History

Cipralex brand escitalopram 10mg package and tablet sheet. It is a reference escitalopram formulation, and was produced by Lundbeck.

Escitalopram was developed in cooperation between Lundbeck and Forest Laboratories. Its development was initiated in 1997, and the resulting new drug application was submitted to the US FDA in March 2001. The short time (3.5 years) it took to develop escitalopram can be attributed to the previous experience of Lundbeck and Forest with citalopram, which has similar pharmacology.[69]

Society and culture

Legal status

The FDA issued the approval of escitalopram for major depression in August 2002, and for generalized anxiety disorder in December 2003. In May 2006, the FDA approved a generic version of escitalopram by

Teva.[70] In July 2006, the U.S. District Court of Delaware decided in favor of Lundbeck regarding a patent infringement dispute and ruled the patent on escitalopram valid.[71]

In 2006, Forest Laboratories was granted an 828-day (2 years and 3 months) extension on its US patent for escitalopram.[72] This pushed the patent expiration date from 7 December 2009, to 14 September 2011. Together with the 6-month pediatric exclusivity, the final expiration date was 14 March 2012.

Allegations of illegal marketing

In 2004, separate civil suits alleging illegal marketing of citalopram and escitalopram for use by children and teenagers by Forest were initiated by two whistleblowers: a physician named Joseph Piacentile and a Forest salesman named Christopher Gobble.[73] In February 2009, the suits were joined. Eleven states and the District of Columbia filed notices of intent to intervene as plaintiffs in the action.

The suits alleged that Forest illegally engaged in off-label promotion of Lexapro for use in children; hid the results of a study showing lack of effectiveness in children; paid kickbacks to physicians to induce them to prescribe Lexapro to children; and conducted so-called "seeding studies" that were, in reality, marketing efforts to promote the drug's use by doctors.[74][75] Forest denied the allegations[76] but ultimately agreed to settle with the plaintiffs for over $313 million.[77]

Brand names

Escitalopram is sold under many brand names worldwide such as Cipralex, Lexapro, Lexam, Mozarin, Aciprex, Depralin, Ecytara, Elicea, Gatosil, Nexpram, Nexito, Nescital, Szetalo, Stalopam, Pramatis, Betesda, Scippa and Rexipra.[1][78]

See also

References

  1. ^ a b drugs.com Drugs.com international: Escitalopram Archived 19 June 2020 at the Wayback Machine Page accessed 25 April 2015
  2. FDA
    . Retrieved 22 October 2023.
  3. ^ "Prescription medicines: registration of new generic medicines and biosimilar medicines, 2017". Therapeutic Goods Administration (TGA). 21 June 2022. Retrieved 30 March 2024.
  4. ^ Anvisa (31 March 2023). "RDC Nº 784 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial" [Collegiate Board Resolution No. 784 - Lists of Narcotic, Psychotropic, Precursor, and Other Substances under Special Control] (in Brazilian Portuguese). Diário Oficial da União (published 4 April 2023). Archived from the original on 3 August 2023. Retrieved 3 August 2023.
  5. ^ a b "Lexapro- escitalopram tablet, film coated; Lexapro- escitalopram solution". DailyMed. 17 November 2023. Retrieved 31 December 2023.
  6. ^ Human Medicines Division (September 2022). "Active substance(s): escitalopram" (PDF). List of nationally authorised medicinal products. European Medicines Agency. Archived (PDF) from the original on 6 September 2022. Retrieved 6 September 2022.
  7. ^ a b c d e f g h i "X". The American Society of Health-System Pharmacists. Archived from the original on 29 December 2017. Retrieved 28 December 2017.
  8. ^ "Escitalopram (Lexapro) Use During Pregnancy". Drugs.com. Archived from the original on 31 December 2017. Retrieved 31 December 2017.
  9. ^ "Protocol for switching patients from escitalopram to citalopram". NHS. 2015. Archived from the original on 10 August 2020. Retrieved 13 February 2018.
  10. . WHO/MHP/HPS/EML/2021.02.
  11. ^ "The Top 300 of 2021". ClinCalc. Archived from the original on 15 January 2024. Retrieved 14 January 2024.
  12. ^ "Escitalopram - Drug Usage Statistics". ClinCalc. Retrieved 14 January 2024.
  13. from the original on 10 June 2020. Retrieved 15 March 2020.
  14. ^ "Lundbeck's Cipralex gets EU ok for OCD treatment". Reuters. 12 January 2007. Archived from the original on 10 June 2020. Retrieved 15 March 2020.
  15. ^ "Cipralex 10 mg film-coated tablets - Summary of Product Characteristics (SmPC) - (emc)". www.medicines.org.uk. Archived from the original on 10 June 2020. Retrieved 15 March 2020.
  16. .
  17. .
  18. .
  19. .
  20. .
  21. .
  22. .
  23. .
  24. .
  25. .
  26. .
  27. .
  28. .
  29. ^ "Lexapro prescribing information" (PDF). Archived (PDF) from the original on 15 August 2018. Retrieved 23 August 2017.
  30. ^ Levenson M, Holland C. "Antidepressants and Suicidality in Adults: Statistical Evaluation. (Presentation at Psychopharmacologic Drugs Advisory Committee; December 13, 2006)". Food and Drug Administration. Archived from the original on 27 September 2007. Retrieved 13 May 2007.
  31. ^ Stone MB, Jones ML (17 November 2006). "Clinical Review: Relationship Between Antidepressant Drugs and Suicidality in Adults" (PDF). Overview for 13 December Meeting of Pharmacological Drugs Advisory Committee (PDAC). FDA. pp. 11–74. Archived (PDF) from the original on 16 March 2007. Retrieved 22 September 2007.
  32. ^ Levenson M, Holland C (17 November 2006). "Statistical Evaluation of Suicidality in Adults Treated with Antidepressants" (PDF). Overview for 13 December Meeting of Pharmacological Drugs Advisory Committee (PDAC). FDA. pp. 75–140. Archived (PDF) from the original on 16 March 2007. Retrieved 22 September 2007.
  33. PMID 17453659
    .
  34. .
  35. ^ a b "Citalopram and escitalopram: QT interval prolongation—new maximum daily dose restrictions (including in elderly patients), contraindications, and warnings". Medicines and Healthcare products Regulatory Agency. December 2011. Archived from the original on 6 March 2013. Retrieved 5 March 2013.
  36. ^
    PMID 19556032
    .
  37. ^ "Towards better patient care: drugs to avoid in 2017". Archived from the original on 17 September 2018. Retrieved 17 September 2018.
  38. ^ "Drugs To Avoid 2017 PDF Download" (PDF). Archived (PDF) from the original on 4 December 2020. Retrieved 17 September 2018.
  39. PMID 23791140
    .
  40. ^ "Lexapro (escitalopram) dosing, indications, interactions, adverse effects, and more". Medscape. Archived from the original on 2 December 2013. Retrieved 27 November 2013.
  41. ^ "Cipralex 5, 10 and 20 mg film-coated tablets - Summary of Product Characteristics (SPC)". electronic Medicines Compendium. 2 October 2013. Archived from the original on 3 December 2013. Retrieved 27 November 2013.
  42. ^ "Escitalopram-Lupin Tablets (LUPIN AUSTRALIA PTY. LTD)" (PDF). TGA eBusiness Services. Lupin Australia Pty Ltd. 21 December 2011. Archived from the original on 29 March 2019. Retrieved 27 November 2013.
  43. PMID 27303087
    .
  44. .
  45. .
  46. .
  47. .
  48. .
  49. ^ "Lexapro (Escitalopram Oxalate) Drug Information: Warnings and Precautions - Prescribing Information at RxList". Archived from the original on 16 June 2008. Retrieved 9 August 2015.
  50. ^ .
  51. .
  52. .
  53. ^ .
  54. .
  55. .
  56. .
  57. .
  58. .
  59. .
  60. ^ a b Brunton L, Chabner B, Knollman B. Goodman and Gilman's The Pharmacological Basis of Therapeutics, Twelfth Edition. McGraw Hill Professional; 2010.
  61. ^
    PMID 23670590
    .
  62. ^ "UpToDate". www.uptodate.com. Archived from the original on 9 August 2022. Retrieved 10 August 2022.
  63. S2CID 29063004
    .
  64. .
  65. .
  66. .
  67. ^ "Drug interactions between bupropion and Lexapro". Drugs.com. Archived from the original on 23 April 2018. Retrieved 22 April 2018.
  68. ^ "Citalopram and escitalopram". Meyler's Side Effects of Drugs (6 ed.). Elsevier. 2016. p. 383.
  69. ^ "2000 Annual Report. p 28 and 33" (PDF). Lundbeck. 2000. Archived (PDF) from the original on 27 September 2007. Retrieved 7 April 2007.
  70. ^ Miranda H. "FDA OKs Generic Depression Drug – Generic Version of Lexapro Gets Green Light". WebMD. Archived from the original on 5 January 2007. Retrieved 10 October 2007.
  71. ^ Laforte ME (14 July 2006). "US court upholds Lexapro patent". FirstWord. Archived from the original on 30 October 2021. Retrieved 10 October 2007.
  72. ^ "Forest Laboratories Receives Patent Term Extension for Lexapro" (Press release). PRNewswire-FirstCall. 2 March 2006. Archived from the original on 15 April 2009. Retrieved 19 January 2009.
  73. ^ "Forest Laboratories: A Tale of Two Whistleblowers" Archived 28 February 2009 at the Wayback Machine article by Alison Frankel in The American Lawyer 27 February 2009
  74. ^ United States of America v. Forest Laboratories Archived 11 March 2009 at the Wayback Machine Full text of the federal complaint filed in the US District Court for the district of Massachusetts
  75. ^ "Drug Maker Is Accused of Fraud" Archived 11 November 2020 at the Wayback Machine article by Barry Meier and Benedict Carey in The New York Times 25 February 2009
  76. ^ "Forest Laboratories, Inc. Provides Statement in Response to Complaint Filed by U.S. Government" Archived 24 January 2013 at archive.today Forest press-release. 26 February 2009.
  77. ^ "Drug Maker Forest Pleads Guilty; To Pay More Than $313 Million to Resolve Criminal Charges and False Claims Act Allegations". www.justice.gov. 15 September 2010. Archived from the original on 30 November 2020. Retrieved 22 November 2020.
  78. ^ Gdziepolek.pl: Mozarin, zamienniki i podobne produkty Archived 17 October 2020 at the Wayback Machine Page accessed on 17 October 2020 (in Polish)

External links