Mirabegron
| Clinical data | |
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| Trade names | Myrbetriq, Betanis, Betmiga, others |
| Other names | YM-178 |
| AHFS/Drugs.com | Monograph |
| MedlinePlus | a612038 |
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| Routes of administration | By mouth |
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| Pharmacokinetic data | |
| Bioavailability | 29–35% |
| Protein binding | 71% |
| Metabolism | Liver via (direct) glucuronidation, amide hydrolysis, and minimal oxidative metabolism in vivo by CYP2D6 and CYP3A4. Some involvement of butylcholinesterase |
| Elimination half-life | 50 hours |
| Excretion | Urine (55%), faeces (34%) |
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| ECHA InfoCard | 100.226.392 |
| Chemical and physical data | |
| Formula | C21H24N4O2S |
| Molar mass | 396.51 g·mol−1 |
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Mirabegron, sold under the brand name Myrbetriq among others, is a medication used to treat overactive bladder. Its benefits are similar to antimuscarinic medication such as solifenacin or tolterodine. It is taken by mouth.
Common side effects include high blood pressure, headaches, and urinary tract infections. Other significant side effects include urinary retention, irregular heart rate, and angioedema. It works by activating the β3 adrenergic receptor in the bladder, resulting in its relaxation.
Mirabegron is the first clinically available beta-3 agonist with approval for use in adults with overactive bladder. Mirabegron was approved for medical use in the United States and in the European Union in 2012. In 2022, it was the 222nd most commonly prescribed medication in the United States, with more than 1 million prescriptions. It is available as a generic medication.
In the United Kingdom it is less preferred to antimuscarinic medication such as oxybutynin.