Clinical data | |
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Trade names | Cymbalta, Ariclaim, Yentreve, others[1] |
AHFS/Drugs.com | Monograph |
MedlinePlus | a604030 |
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Routes of administration | By mouth |
Drug class | Serotonin–norepinephrine reuptake inhibitor |
ATC code | |
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Pharmacokinetic data | |
Bioavailability | ~ 50% (32% to 80%) |
Protein binding | ~ 95% |
Metabolism | Liver, two P450 isozymes, CYP2D6 and CYP1A2 |
Elimination half-life | 12 hours |
Excretion | 70% in urine, 20% in feces |
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ChEBI |
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PDB ligand | |
CompTox Dashboard (EPA) | |
ECHA InfoCard | 100.116.825 |
Chemical and physical data | |
Formula | C18H19NOS |
Molar mass | 297.42 g·mol−1 |
3D model (JSmol) | |
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Duloxetine, sold under the brand name Cymbalta among others,[1] is a medication used to treat major depressive disorder, generalized anxiety disorder, obsessive-compulsive disorder, fibromyalgia, neuropathic pain and central sensitization.[7][8] It is taken by mouth.[7]
Duloxetine is a serotonin–norepinephrine reuptake inhibitor (SNRI).[9] Similarly to SSRIs and other SNRIs, the precise mechanism for its antidepressant and anxiolytic effects is not known.[7]
Common side effects include dry mouth, nausea, feeling tired, dizziness, agitation, sexual problems, and increased sweating.[7] Severe side effects include an increased risk of suicide, serotonin syndrome, mania, and liver problems.[7] Antidepressant withdrawal syndrome may occur if stopped.[7] There are concerns that use during the later part of pregnancy can harm the developing fetus.[7]
Duloxetine was approved for medical use in the United States and in the European Union in 2004.[5][6][7] It is available as a generic medication.[9] In 2022, it was the 31st most commonly prescribed medication in the United States, with more than 18 million prescriptions.[10][11]
DailyMed-2020
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