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Fluvoxamine

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Not to be confused with Fluoxetine.
Fluvoxamine
Clinical data
Pregnancy
category
  • C
Routes of
administration		Oral
ATC code
Legal status
Legal status
Pharmacokinetic data
Bioavailability77%
MetabolismHepatic
Elimination half-life15.6 hours
ExcretionRenal
Identifiers
  • (E)-5-methoxy-1-[4-(trifluoromethyl)phenyl]pentan-1-one O-2-aminoethyl oxime
CAS Number
PubChem CID
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.125.476 Edit this at Wikidata
Chemical and physical data
FormulaC15H21F3N2O2
Molar mass318.335 g·mol−1
3D model (JSmol)
  • FC(F)(F)c1ccc(\C(=N\OCCN)CCCCOC)cc1
  • InChI=1S/C15H21F3N2O2/c1-21-10-3-2-4-14(20-22-11-9-19)12-5-7-13(8-6-12)15(16,17)18/h5-8H,2-4,9-11,19H2,1H3/b20-14+ checkY
  • Key:CJOFXWAVKWHTFT-XSFVSMFZSA-N checkY
  (verify)

Fluvoxamine (brand name Luvox) is an antidepressant which functions as a selective serotonin reuptake inhibitor (SSRI). Fluvoxamine was first approved by the U.S. Food and Drug Administration (FDA) in 1993 for the treatment of obsessive compulsive disorder (OCD).[1] Fluvoxamine CR (controlled release) is approved to treat social anxiety disorder.[2] Fluvoxamine is also prescribed to treat major depressive disorder (MDD) and anxiety disorders, such as generalized anxiety disorder (GAD), panic disorder, and post-traumatic stress disorder (PTSD).[3]

History

Fluvoxamine was developed by Solvay Pharmaceuticals and was the first non-TCA drug approved by the U.S. Food and Drug Administration (FDA) specifically for the treatment of OCD.[4] It was one of the first SSRI antidepressants to be launched (1984 in Switzerland), and following its FDA approval in 1993, it was launched in the U.S. in December 1994, Australia in February 1999 and Japan in June 1999.[5] At the end of 1995, more than 10 million patients worldwide had been treated with fluvoxamine.[6] Fluvoxamine was the first SSRI to be registered for the treatment of obsessive compulsive disorder in children by the FDA in 1997.[7] Fluvoxamine was the first drug approved for the treatment of social anxiety disorder in Japan in 2005.[8]

In 1999, fluvoxamine came under great public scrutiny after it was discovered that Eric Harris, one of the two teenage shooters involved in the Columbine High School massacre, had been taking the drug. Many immediately pointed fingers at fluvoxamine and its manufacturer Solvay Pharmaceuticals.[9] Sales fell, and Solvay withdrew the medication from the U.S. market in 2002.[10] In 2007, Solvay re-introduced Luvox to the U.S. market, which is now manufactured by Palo Alto, California-based Jazz Pharmaceuticals, Inc., with a generic version of Luvox available from IVAX Pharmaceuticals, Inc. On February 28, 2008, the FDA approved a controlled-release formulation of fluvoxamine for Solvay Pharmaceuticals, to be marketed as Luvox CR.[11][12]

Indications

Fluvoxamine is widely prescribed to treat major depressive disorder (MDD), and anxiety disorders such as obsessive compulsive disorder (OCD), generalized anxiety disorder (GAD), panic disorder, social phobia, and post-traumatic stress disorder (PTSD). Fluvoxamine is indicated for children and adolescents with OCD[13] and social anxiety disorder.[2]

Side effects

Side effects most commonly observed with fluvoxamine include nausea, vomiting, drowsiness, insomnia, dizziness, nervousness, feeling anxious, dry mouth, abdominal pain, constipation, diarrhea, heart burn, loss of appetite, muscle weakness, pins and needles, abnormal taste, headache, faster heart beat, sweating, weight gain, weight loss or unusual bruising. Other side effects which are observed more frequently in children include abnormal thoughts or behaviour, cough, increased period pain, nose bleeds, increased restlessness, infection and sinusitis.[14] Sexual side effects with fluvoxamine are less pronounced than with other SSRIs.[15]

Pharmacology

Fluvoxamine is a potent and selective serotonin reuptake inhibitor with approximately 100-fold affinity for the serotonin transporter over the norepinephrine transporter. It has negligible affinity for the dopamine transporter or any other receptor, with the sole exception of the σ1 receptor. It behaves as a potent agonist at this receptor and has the highest affinity of any SSRI for doing so. This may contribute to its antidepressant and anxiolytic effects inside the brain. Indeed, other SSRIs which also act as σ1 receptor agonists, such as sertraline and escitalopram (not verified but likely to be), display enhanced antidepressant efficacy.[16] suggesting that it may have particular benefits in the treatment of depressed patients who show features of anxiety/stress and for whom memory impairment is particularly undesirable (such as in depressed elderly patients, and also in treating psychotic depression).[17] In fact, the TCA opipramol, a σ1 receptor agonist without effects on the serotonin, dopamine, or norepinephrine systems, has considerable antidepressant and anxiolytic efficacy in its own right.

Pharmacokinetics

The oral bioavailability of fluvoxamine is 53%. The plasma protein binding is about 80%.[18]

Metabolism

Fluvoxamine is strongly metabolized in the liver, mostly by the processes of oxidative demethylation (producing fluvoxamine acid and its N-acetyl analog) and deamination (producing fluvoxethanol). Only fluvoxamine acid has been shown to have SERT inhibitor activity, roughly 1-2 orders of magnitude less potent than the parent compound.[19]

Radio-labeled administration of a dose of fluvoxamine produced nine identifiable metabolites, constituting 85% of the absorbed dosage (thus 15% of the fluvoxamine remained unchanged). This isolate of metabolites was empirically proven to contain 60% fluvoxamine acid and its N-acetyl analog, and 10% fluvoxethanol, with the other six metabolites making up 30%.[19]

Elimination

Fluvoxamine has the shortest serum half-life of all SSRIs, with a mean of 15.6 hours.[20]

Drug interactions

Fluvoxamine has a low potential for the drug interactions which are based on inhibition of enzyme Cytochrome P450 CYP2D6. Fluvoxamine shows the least interaction of the SSRIs, in regard to this specific enzyme.[21][22][23] Naturally the other SSRIs which are metabolized by CYP2D6 will have more CYP2D6-based interactions with TCAs, antiarrhythmics, B-blockers, phenytoin, opioids and neuroleptics.

Fluvoxamine does, however, inhibit cytochrome P450 enzyme CYP1A2, which metabolises agomelatine, caffeine, clozapine, haloperidol, phenacetin, tacrine, theophylline, and olanzapine. These substances can cause increased serum levels when administered together with fluvoxamine. Of major concern is the fact that the polycyclic aromatic hydrocarbons found in tobacco smoke are potent inducers of CYP1A2 so that smokers may require significant modification of medication dosage.[24] A recent warning has been published regarding potentially serious interaction with tizanidine, based on CYP1A2 metabolism.[25]

Fluvoxamine inhibits metabolism of diazepam and phenytoin via CYP2C19 and metabolism of aripiprazole, chlorpromazine, clozapine, haloperidol, olanzapine, perphenazine, risperidone, thioridazine and zuclopenthixol via CYP2D6 as well as of aripiprazole, clozapine, haloperidol, quetiapine and ziprasidone via CYP3A4.[26]

The plasma protein binding of fluvoxamine is about 77%. Drugs with low protein binding are less likely to displace other protein bound drugs, and therefore have a lower potential to cause protein binding-related drug interactions.

Fluvoxamine also inhibits CYP2C9.[19][27]

The drug was given visibility in the American television series The Sopranos produced by HBO, in the second season, episode 10. Dr. Jennifer Melfi, the psychiatrist treating the character named Tony Soprano, is prescribed Luvox by her own psychiatrist, to treat a strong inclination toward alcohol.

"Stuttering" John Melendez, formerly of The Howard Stern Show, had taken Luvox for a period of time before his departure from the show.

Synthesis

Luvox (fluvoxamine) 100 mg tablets (AU)

Fluvoxamine is one of only two SSRIs (along with alaproclate[28][29]) to have a monocyclic structure.

See also

References

  1. ^ "FDA Advisory Committee Recommends Luvox (Fluvoxamine) Tablets for Obsessive Compulsive Disorder," PRNewswire, 10/18/93
  2. ^ a b Stahl, S. Stahl's Essential Psychopharmacology: The Prescriber's Guide. Cambridge University Press. New York, NY. 2009. pp.215
  3. ^ Karen J. McClellan, David P. Figgitt (Drugs October 2000). "Fluvoxamine An Updated Review of its Use in the Management of Adults with Anxiety Disorders". Adis Drug Evaluation. 60 (4): 925–954. {{cite journal}}: Check date values in: |date= (help)
  4. ^ Pharmalot | BrainPhysics.com| Medications for OCD.
  5. ^ Solvay Pharmaceuticals Australia | Luvox.
  6. ^ Fluvoxamine Product Monograph. 1999. {{cite journal}}: Missing or empty |title= (help)
  7. ^ "Luvox Approved For Obsessive Compulsive Disorder in Children and Teens". Http://www.pslgroup.com/dg/2261a.htm. {{cite journal}}: External link in |journal= (help)
  8. ^ "Solvay's Fluvoxamine maleate is first drug approved for the treatment of social anxiety disorder in Japan". Http://www.solvaypress.com/pressreleases/0,,33713-2-83,00.htm. {{cite journal}}: External link in |journal= (help)
  9. ^ Pankratz, Howard (January 26, 2007). "Judge: Seal Columbine papers for 25 years". The Denver Post. Retrieved 2008-03-03.
  10. ^ "Solvay Pharmaceuticals, Inc. Withdraws LUVOX". Http://www.solvaypharmaceuticals-us.com/newsroom/pressreleases/0,,14517-2-0,00.htm. {{cite journal}}: External link in |journal= (help)
  11. ^ "Jazz Pharmaceuticals press release, February 28, 2008 – FDA APPROVES LUVOX CR (FLUVOXAMINE MALEATE) EXTENDED-RELEASE CAPSULES FOR THE TREATMENT OF SOCIAL ANXIETY DISORDER (SAD) AND OBSESSIVE COMPULSIVE DISORDER (OCD)". Archived from the original on 2008-05-26. Retrieved 2008-03-14.
  12. ^ "Luvox CR" (PDF). Retrieved 2008-02-21. {{cite web}}: Text "Prescribing Info" ignored (help)
  13. ^ "US-FDA Fluvoxamine Product Insert". 2005. {{cite journal}}: Cite journal requires |journal= (help); Unknown parameter |month= ignored (help)
  14. ^ LUVOX® Consumer Medicine Information | Better Health Channel
  15. ^ Hengeveld VW, Waldinger MD; Hengeveld, MW; Zwinderman, AH; Olivier, B; et al. (1998). "Effect of SSRI antidepressants on ***: a double blind, randomised, placebo-controlled study with fluoxetine, fluvoxamine, paroxetine and sertraline". Journal of Clinical Psychopharmacology. 18 (4): 274–281. doi:10.1097/00004714-199808000-00004. PMID 9690692. {{cite journal}}: Explicit use of et al. in: |last= (help)
  16. ^ Hashimoto K, Narita N; Hashimoto, K; Tomitaka, S; Minabe, Y; et al. (1996). "Interactions of selective reuptake inhibitors with subtypes of sigma receptor in rat brain". Eur J Pharmacol. 307 (1): 117–9. doi:10.1016/0014-2999(96)00254-3. PMID 8831113. {{cite journal}}: Explicit use of et al. in: |last= (help)
  17. ^ C.Sandner, Carrasco JL; Sandner, C (2005). "Clinical effects of pharmacological variations in selective serotonin reuptake inhibitors: an overview". International Journal of Clinical Practice. 59 (12): 1428–1434. doi:10.1111/j.1368-5031.2005.00681.x. PMID 16351675. {{cite journal}}: Unknown parameter |month= ignored (help)
  18. ^ Barr Laboratories Inc (2010). "Fluvoxamine Official FDA information, side effects and uses". Subsection: Fluvoxamine - Clinical Pharmacology -> Pharmacokinetics. Retrieved 2011-02-15. {{cite web}}: Unknown parameter |month= ignored (help)
  19. ^ a b c "Luvox Tablets (Fluvoxamine Maleate) Drug Information: Uses, Side Effects, Drug Interactions and Warnings at RxList". Retrieved 2009-02-17.
  20. ^ Center for Drug Evaluation and Research, (2000). Fluvoxamine Maleate Tablets. Application Number: 75901, Retrieved July 28, 2008, from http://www.fda.gov/cder/foi/anda/2000/75901_Fluvoxamine%20Maleate_Prntlbl.pdf
  21. ^ P., Baumann (1996). "Pharmacokinetic-pharmacodynamic relationship of the Selective serotonin reuptake inhibitors". Clinical Pharmacokinetics. 31 (6): 444–469. doi:10.2165/00003088-199631060-00004. PMID 8968657.
  22. ^ Gill HS, DeVane CL (1997). "Clinical Pharmacokinetics of Fluvoxamine: applications to dosage regime design". Journal of Clinical Psychiatry. 58 (Suppl 5): 7–14.
  23. ^ DeVane, CL (1998). "Translational pharmacokinetics: current issues with newer antidepressants". Depression and Anxiety. 8 (Suppl 1): 64–70. doi:10.1002/(SICI)1520-6394(1998)8:1+<64::AID-DA10>3.0.CO;2-S. PMID 9809216.
  24. ^ Kroom, Lisa A. (10-01-2007). "Drug Interactions With Smoking". Am J Health-Syst Pharm. 64 (18). Medscape: American Society of Health-System Pharmacists: 1917–1921. doi:10.2146/ajhp060414. PMID 17823102. Retrieved 2008-01-31. {{cite journal}}: Check date values in: |date= (help); Cite has empty unknown parameter: |coauthors= (help)
  25. ^ Waknine, Yael (April 13, 2007). "Prescribers Warned of Tizanidine Drug Interactions". Medscape News. Medscape. Retrieved 2008-02-01. {{cite web}}: Cite has empty unknown parameter: |coauthors= (help)
  26. ^ Bondy, Brigitta (2007). "Pharmacogenetics of Antipsychotics: Useful For the Clinician?". Curr Opin Psychiatry. 20 (1). Medscape: Lippincott Williams & Wilkins: 126–130. doi:10.1097/YCO.0b013e328017f69f. PMID 17278909. Retrieved 2008-02-01. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  27. ^ "Brain Elimination Half-Life of Fluvoxamine".
  28. ^ A Wilkinson, M Courtney, A Westlind-Danielsson, G Hallnemo and K E Akerman (December). "Alaproclate acts as a potent, reversible and noncompetitive antagonist of the NMDA receptor coupled ion flow". JPET. 271 (3): 1314–1319. {{cite journal}}: Check date values in: |date= and |year= / |date= mismatch (help)CS1 maint: multiple names: authors list (link)
  29. ^ K L Nicholson and R L Balster (23 April). "Evaluation of the phencyclidine-like discriminative stimulus effects of novel NMDA channel blockers in rats". Psychopharmacology. {{cite journal}}: Check date values in: |date= and |year= / |date= mismatch (help)
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