Hydromorphone
| Subclass of | morphinan alkaloid |
|---|---|
| Get use | Medication |
| Stylized name | HYDROmorphone |
| Chemical formula | C₁₇H₁₉NO₃ |
| Canonical SMILES | CN1CCC23C4C1CC5=C2C(=C(C=C5)O)OC3C(=O)CC4 |
| Isomeric SMILES | CN1CC[C@]23[C@@H]4[C@H]1CC5=C2C(=C(C=C5)O)O[C@H]3C(=O)CC4 |
| Active ingredient in | Dilaudid, Exalgo |
| World Health Organisation international non-proprietary name | hydromorphone |
| Medical condition treated | pain, cough, substance abuse |
| Physically dey interact plus | Opioid receptor delta 1, opioid receptor kappa 1, opioid receptor mu 1 |
| Pregnancy category | Australian pregnancy category C, US pregnancy category C |
| Subject has role | opioid receptor agonist, opioid, narcotic |
Hydromorphone, dem sanso know as dihydromorphinone, wey dem sell under de brand name Dilaudid among odas, be a morphinan opioid dem use to treat moderate to severe pain.[1] Typically, long-term use only be recommended for pain secof cancer.[2] E fi be used by mouth anaa by injection into a vein, muscle, anaa under de skin.[1] Effects generally dey begin within half an hour den last for up to five hours.[1] A 2016 Cochrane review (dem update insyd 2021) find little difference in benefit between hydromorphone den oda opioids for cancer pain.[3]
Common side effects dey include dizziness, euphoria, sleepiness, nausea, itchiness, den constipation.[1] Serious side effects fi include abuse, low blood pressure, seizures, respiratory depression, den serotonin syndrome.[1] Rapidly dey decrease de dose fi result in opioid withdrawal.[1] Generally, ein use during pregnancy anaa breastfeeding no be recommended.[4] Hydromorphone dey exert ein effects by activating opioid receptors, mainly insyd de brain den spinal cord.[1] Hydromorphone 2 mg IV be equivalent to approximately 10 mg morphine IV.[2]
Dem patent hydromorphone insyd 1923.[5] Den nake hydromorphone from morphine.[6] Hydromorphone be a therapeutic alternative on de World Health Organization's List of Essential Medicines.[7] E be available as a generic medication.[1] Insyd 2022, na e be de 233rd most commonly prescribed medication insyd de United States, plus more dan 1 million prescriptions.[8][9]
References
[edit | edit source]- 1 2 3 4 5 6 7 8 "Hydromorphone Hydrochloride Monograph for Professionals". Drugs.com. American Society of Health-System Pharmacists. Retrieved 15 April 2019.
- 1 2 British national formulary: BNF 76 (76 ed.). Pharmaceutical Press. 2018. pp. 24, 456. ISBN 978-0-85711-338-2.
- ↑ Li Y, Ma J, Lu G, Dou Z, Knaggs R, Xia J, Zhao S, Dong S, Yang L (August 2021). "Hydromorphone for cancer pain". The Cochrane Database of Systematic Reviews. 2021 (8) CD011108. doi:10.1002/14651858.CD011108.pub3. PMC 8406835. PMID 34350974.
- ↑ "Hydromorphone Use During Pregnancy". Drugs.com. Retrieved 15 April 2019.
- ↑ Fischer J, Ganellin CR (2006). Analogue-based Drug Discovery. John Wiley & Sons. p. 526. ISBN 978-3-527-60749-5.
- ↑ Vardanyan R, Hruby V (2006). Synthesis of Essential Drugs. Elsevier. p. 25. ISBN 978-0-08-046212-7.
- ↑ World Health Organization (2025). The selection and use of essential medicines, 2025: WHO Model List of Essential Medicines, 24th list. Geneva: World Health Organization. hdl:10665/382243.
- ↑ "The Top 300 of 2022". ClinCalc. Archived from the original on 30 August 2024. Retrieved 30 August 2024.
- ↑ "Hydromorphone Drug Usage Statistics, United States, 2013 – 2022". ClinCalc. Retrieved 30 August 2024.
External links
[edit | edit source]- CS1:Vancouver names with accept markup
- Commons category link from Wikidata
- 4,5-Epoxymorphinans
- Euphoriants
- German inventions
- Ketones
- Mu-opioid receptor agonists
- Hydroxyarenes
- Semisynthetic opioids
- World Health Organization essential medicines
- Lethal injection components
- Recreational drug metabolites
- Human drug metabolites
- Translated from MDWiki