Dorzolamide

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Dorzolamide
Names
Trade namesTrusopt, others
  • (4S,6S)-4-(ethylamino)-6-methyl-7,7-dioxo-5,6-dihydro-4H-thieno[2,3-b]thiopyran-2-sulfonamide
Clinical data
Pregnancy
category
  • US: C (Risk not ruled out)
Routes of
use
Topical (eye drops)
Defined daily dose0.3 ml[1]
External links
AHFS/Drugs.comMonograph
MedlinePlusa602022
Legal
Legal status
Pharmacokinetics
Protein binding~33%
Elimination half-life4 months
Chemical and physical data
FormulaC10H16N2O4S3
Molar mass324.43 g·mol−1
3D model (JSmol)
  • CCNC1CC(C)S(=O)(=O)c2sc(cc12)S(=O)(=O)N
  • InChI=1S/C10H16N2O4S3/c1-3-12-8-4-6(2)18(13,14)10-7(8)5-9(17-10)19(11,15)16/h5-6,8,12H,3-4H2,1-2H3,(H2,11,15,16)/t6-,8-/m0/s1 checkY
  • Key:IAVUPMFITXYVAF-XPUUQOCRSA-N checkY


Dorzolamide, sold under the brand name Trusopt among others, is medications used to treat high pressure inside the eye including glaucoma.[2] It is used as an eye drop.[2] Effects begin within three hours and lasts for at least eight hours.[2] It is also available as the combination dorzolamide/timolol.[2]

Common side effects include eye discomfort, eye redness, taste changes, and blurry vision.[2] Serious side effects include Steven Johnson syndrome.[2] Those allergic to sulfonamides may be allergic to dorzolamide.[2][3] Use is not recommended in pregnancy or breastfeeding.[3] It is a carbonic anhydrase inhibitor and works by decreasing the production of aqueous humour.[2]

Dorzolamide was approved for medical use in the United States in 1994.[2] It is available as a generic medication.[3] A 5 milliliter bottle in the United Kingdom costs the NHS less than £2 as of 2019.[3] In the United States the wholesale cost of this amount is about US$7.10.[4] In 2017, it was the 281st most commonly prescribed medication in the United States, with more than one million prescriptions.[5][6]

Medical uses

Dorzolamide hydrochloride is used to lower excessive intraocular pressure in open-angle glaucoma and ocular hypertension.

Dosage

The defined daily dose is 0.3 ml.[1]

Side effects

(A) Bilateral eczematous swelling around the eyes after use of dorzolamide eyedrops. (B) Improved periorbital swelling after stopping.

Ocular stinging, burning, itching and bitter taste.[7] It causes shallowing of the anterior chamber and leads to transient myopia.

Pharmacodynamics

It lowers IOP by about 20%.[7] Carbonic Anhydrase can convert H2CO3 into HCO3 (bicarbonate) and H+. The H+ is then exchanged for sodium (Na) which allows you to make aqueous humor. By blocking carbonic anhydrase, the Na/H exchanger can't work, which will decrease Na in the cell and prevent aqueous humor production.

History

This drug, developed by Merck, was the first drug in human therapy (market introduction 1995) that resulted from structure-based drug design. It was developed to circumvent the systemic side effects of acetazolamide which has to be taken orally.[7]

Society and culture

Cost

A 5 milliliter bottle in the United Kingdom costs the NHS less than £2 as of 2019.[3] In the United States the wholesale cost of this amount is about US$7.10.[4] In 2017, it was the 281st most commonly prescribed medication in the United States, with more than one million prescriptions.[5][6]

References

  1. 1.0 1.1 "WHOCC - ATC/DDD Index". www.whocc.no. Archived from the original on 24 August 2019. Retrieved 9 September 2020.
  2. 2.0 2.1 2.2 2.3 2.4 2.5 2.6 2.7 2.8 "Dorzolamide Hydrochloride Monograph for Professionals". Drugs.com. American Society of Health-System Pharmacists. Archived from the original on 27 March 2019. Retrieved 26 March 2019.
  3. 3.0 3.1 3.2 3.3 3.4 British national formulary : BNF 76 (76 ed.). Pharmaceutical Press. 2018. p. 1148. ISBN 9780857113382.
  4. 4.0 4.1 "NADAC as of 2019-02-27". Centers for Medicare and Medicaid Services. Archived from the original on 2019-03-06. Retrieved 3 March 2019.
  5. 5.0 5.1 "The Top 300 of 2020". ClinCalc. Archived from the original on 12 February 2021. Retrieved 11 April 2020.
  6. 6.0 6.1 "Dorzolamide Hydrochloride - Drug Usage Statistics". ClinCalc. Archived from the original on 23 May 2020. Retrieved 11 April 2020.
  7. 7.0 7.1 7.2 KD Tripari MD. Essentials of Medical Pharmacology (5th ed.). Jaypee Brothers Medical Publishers(P) Ltd. p. 88. ISBN 81-8061-187-6.

Further reading

== External links ==

Identifiers: