From Wikipedia, the free encyclopedia
Mr. Ibrahem/Ritonavir
Clinical data
Trade namesNorvir
AHFS/ Drugs.com Monograph
MedlinePlus a696029
License data
Pregnancy
category
  • AU: B3
Routes of
administration
By mouth
Legal status
Legal status
Pharmacokinetic data
Protein binding98-99%
MetabolismHepatic
Elimination half-life3-5 hours
Excretionmostly fecal
Identifiers
  • 1,3-thiazol-5-ylmethyl N-[(2S,3S,5S)-3-hydroxy-5-[(2S)-3-methyl-2-{[methyl({[2-(propan-2-yl)-1,3-thiazol-4-yl]methyl})carbamoyl]amino}butanamido]-1,6-diphenylhexan-2-yl]carbamate
Chemical and physical data
FormulaC37H48N6O5S2
Molar mass720.95 g·mol−1
3D model ( JSmol)
  • CC(C)c4nc(CN(C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](Cc1ccccc1)C[C@H](O)[C@H](Cc2ccccc2)NC(=O)OCc3cncs3)cs4
  • InChI=1S/C37H48N6O5S2/c1-24(2)33(42-36(46)43(5)20-29-22-49-35(40-29)25(3)4)34(45)39-28(16-26-12-8-6-9-13-26)18-32(44)31(17-27-14-10-7-11-15-27)41-37(47)48-21-30-19-38-23-50-30/h6-15,19,22-25,28,31-33,44H,16-18,20-21H2,1-5H3,(H,39,45)(H,41,47)(H,42,46)/t28-,31-,32-,33-/m0/s1 checkY
  • Key:NCDNCNXCDXHOMX-XGKFQTDJSA-N checkY
 ☒NcheckY  (what is this?)   (verify)

Ritonavir (RTV), sold under the trade name Norvir, is an antiretroviral medication used along with other medications to treat HIV/AIDS. [2] This combination treatment is known as highly active antiretroviral therapy (HAART). [2] Often a low dose is used with other protease inhibitors. [2] It may also be used in combination with other medications for hepatitis C. [3] It is taken by mouth. [2] The capsules of the medication do not work the same as the tablets. [2]

Common side effects include nausea, vomiting, loss of appetite, diarrhea, and numbness of the hands and feet. [2] Serious side effects include liver problems, pancreatitis, allergic reactions, and arrythmias. [2] Serious interactions may occur with a number of other medications including amiodarone and simvastatin. [2] At low doses it is considered to be acceptable for use during pregnancy. [4] Ritonavir is of the protease inhibitor class. [2] Typically, however, it is used to inhibit the enzyme that metabolizes other protease inhibitors. [5] This inhibition allows lower doses of these latter medication to be used. [5]

Ritonavir was patented in 1989 and came into medical use in 1996. [6] [7] It is on the World Health Organization's List of Essential Medicines. [8] Globally the wholesale cost in the developing world is between US$0.07 and $2.20 per day. [9] In the United States it costs about $9.20–55 per day depending on the dose. [2]

References

  1. ^ "WHOCC - ATC/DDD Index". www.whocc.no. Archived from the original on 6 November 2020. Retrieved 22 September 2020.
  2. ^ a b c d e f g h i j "Ritonavir". The American Society of Health-System Pharmacists. Archived from the original on 2015-10-17. Retrieved Oct 23, 2015.
  3. ^ "FDA approves Viekira Pak to treat hepatitis C". Food and Drug Administration. December 19, 2014. Archived from the original on October 31, 2015.
  4. ^ "Ritonavir Pregnancy and Breastfeeding Warnings". drugs.com. Archived from the original on 7 September 2015. Retrieved 23 October 2015.
  5. ^ a b British National Formulary 69 (69 ed.). Pharmaceutical Pr. March 31, 2015. p. 426. ISBN  9780857111562.
  6. ^ Hacker, Miles (2009). Pharmacology principles and practice. Amsterdam: Academic Press/Elsevier. p. 550. ISBN  9780080919225. Archived from the original on 2020-06-17. Retrieved 2017-09-10.
  7. ^ Fischer, Jnos; Ganellin, C. Robin (2006). Analogue-based Drug Discovery. John Wiley & Sons. p. 509. ISBN  9783527607495. Archived from the original on 2019-03-06. Retrieved 2019-03-02.
  8. ^ World Health Organization (2019). World Health Organization model list of essential medicines: 21st list 2019. Geneva: World Health Organization. hdl: 10665/325771. WHO/MVP/EMP/IAU/2019.06. License: CC BY-NC-SA 3.0 IGO.
  9. ^ "Ritonavir". International Drug Price Indicator Guide. Archived from the original on 10 May 2017. Retrieved 23 October 2015.
From Wikipedia, the free encyclopedia
Mr. Ibrahem/Ritonavir
Clinical data
Trade namesNorvir
AHFS/ Drugs.com Monograph
MedlinePlus a696029
License data
Pregnancy
category
  • AU: B3
Routes of
administration
By mouth
Legal status
Legal status
Pharmacokinetic data
Protein binding98-99%
MetabolismHepatic
Elimination half-life3-5 hours
Excretionmostly fecal
Identifiers
  • 1,3-thiazol-5-ylmethyl N-[(2S,3S,5S)-3-hydroxy-5-[(2S)-3-methyl-2-{[methyl({[2-(propan-2-yl)-1,3-thiazol-4-yl]methyl})carbamoyl]amino}butanamido]-1,6-diphenylhexan-2-yl]carbamate
Chemical and physical data
FormulaC37H48N6O5S2
Molar mass720.95 g·mol−1
3D model ( JSmol)
  • CC(C)c4nc(CN(C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](Cc1ccccc1)C[C@H](O)[C@H](Cc2ccccc2)NC(=O)OCc3cncs3)cs4
  • InChI=1S/C37H48N6O5S2/c1-24(2)33(42-36(46)43(5)20-29-22-49-35(40-29)25(3)4)34(45)39-28(16-26-12-8-6-9-13-26)18-32(44)31(17-27-14-10-7-11-15-27)41-37(47)48-21-30-19-38-23-50-30/h6-15,19,22-25,28,31-33,44H,16-18,20-21H2,1-5H3,(H,39,45)(H,41,47)(H,42,46)/t28-,31-,32-,33-/m0/s1 checkY
  • Key:NCDNCNXCDXHOMX-XGKFQTDJSA-N checkY
 ☒NcheckY  (what is this?)   (verify)

Ritonavir (RTV), sold under the trade name Norvir, is an antiretroviral medication used along with other medications to treat HIV/AIDS. [2] This combination treatment is known as highly active antiretroviral therapy (HAART). [2] Often a low dose is used with other protease inhibitors. [2] It may also be used in combination with other medications for hepatitis C. [3] It is taken by mouth. [2] The capsules of the medication do not work the same as the tablets. [2]

Common side effects include nausea, vomiting, loss of appetite, diarrhea, and numbness of the hands and feet. [2] Serious side effects include liver problems, pancreatitis, allergic reactions, and arrythmias. [2] Serious interactions may occur with a number of other medications including amiodarone and simvastatin. [2] At low doses it is considered to be acceptable for use during pregnancy. [4] Ritonavir is of the protease inhibitor class. [2] Typically, however, it is used to inhibit the enzyme that metabolizes other protease inhibitors. [5] This inhibition allows lower doses of these latter medication to be used. [5]

Ritonavir was patented in 1989 and came into medical use in 1996. [6] [7] It is on the World Health Organization's List of Essential Medicines. [8] Globally the wholesale cost in the developing world is between US$0.07 and $2.20 per day. [9] In the United States it costs about $9.20–55 per day depending on the dose. [2]

References

  1. ^ "WHOCC - ATC/DDD Index". www.whocc.no. Archived from the original on 6 November 2020. Retrieved 22 September 2020.
  2. ^ a b c d e f g h i j "Ritonavir". The American Society of Health-System Pharmacists. Archived from the original on 2015-10-17. Retrieved Oct 23, 2015.
  3. ^ "FDA approves Viekira Pak to treat hepatitis C". Food and Drug Administration. December 19, 2014. Archived from the original on October 31, 2015.
  4. ^ "Ritonavir Pregnancy and Breastfeeding Warnings". drugs.com. Archived from the original on 7 September 2015. Retrieved 23 October 2015.
  5. ^ a b British National Formulary 69 (69 ed.). Pharmaceutical Pr. March 31, 2015. p. 426. ISBN  9780857111562.
  6. ^ Hacker, Miles (2009). Pharmacology principles and practice. Amsterdam: Academic Press/Elsevier. p. 550. ISBN  9780080919225. Archived from the original on 2020-06-17. Retrieved 2017-09-10.
  7. ^ Fischer, Jnos; Ganellin, C. Robin (2006). Analogue-based Drug Discovery. John Wiley & Sons. p. 509. ISBN  9783527607495. Archived from the original on 2019-03-06. Retrieved 2019-03-02.
  8. ^ World Health Organization (2019). World Health Organization model list of essential medicines: 21st list 2019. Geneva: World Health Organization. hdl: 10665/325771. WHO/MVP/EMP/IAU/2019.06. License: CC BY-NC-SA 3.0 IGO.
  9. ^ "Ritonavir". International Drug Price Indicator Guide. Archived from the original on 10 May 2017. Retrieved 23 October 2015.

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