Raw research findings for this medication. Mostly single studies, not curated or confirmed robust.
Hydromorphone is a potent opioid, several times stronger than morphine, made from morphine. It acts on mu opioid receptors and is used for moderate to severe pain, after surgery, in cancer and in palliative care, by mouth, injection or pump. It is also the active product the body makes from hydrocodone. It is sold as Dilaudid, among other names.
Hydromorphone is cleared mainly by UGT2B7 and other UGT enzymes, not by CYP2D6, so it is not affected the way codeine and hydrocodone are; the CYP2D6 studies listed here mostly concern hydrocodone being turned into hydromorphone. Studies have also looked at the opioid receptor gene OPRM1, COMT and ABCB1 for how much hydromorphone people needed. There is no CPIC or DPWG guideline.
Every published finding on gene variants and Hydromorphone. Upload your DNA file to see which of these rows apply to you.
Studies of how quickly the body processes this medication.
Studies of how well it worked in people carrying a variant.
Studies of how much of the drug people needed or tolerated.
Studies that do not fall into the groups above.
Study findings and evidence levels: PharmGKB (CC BY-SA 4.0). Guidelines: CPIC and DPWG, as bundled in PharmCAT. Most studies were done mainly in people of European ancestry.
More drugs from the same category
Not a prescribing recommendation. This page is educational information about pharmacogenomic research and clinical guidelines - it is not medical or dosing advice, and not a prediction of how any medication will work for you. Never start, stop, or change a medication or dose based on it; talk to your doctor or pharmacist, who can order clinical-grade testing if appropriate.
Content updated September 2026.
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