Clinical data | |
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Trade names | Amatine, Gutron, Orvaten, ProAmatine, others |
Other names | ST-1085; TS-701; 3,6-Dimethoxy-β-hydroxy-N-aminoethanonyl-2-phenylethylamine; 2-Amino-N-[2-(2,5-dimethoxyphenyl)-2-hydroxyethyl]acetamide; 1-2',5'-Dimethoxyphenyl-1)-2 glycinamidoethanol |
AHFS/Drugs.com | Monograph |
MedlinePlus | a616030 |
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Routes of administration | By mouth[1] |
Drug class | α1-Adrenergic receptor agonist; Antihypotensive agent; Vasopressor |
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Pharmacokinetic data | |
Bioavailability | 93% (as desglymidodrine)[3][4][1] |
Metabolism | Deglycination[3][1][4] |
Metabolites | • Desglymidodrine[3][1][4] |
Onset of action | ≤1 hour[3] |
Elimination half-life | Midodrine: 0.5 hours[4] Desglymidodrine: 2–4 hours[4][1] |
Duration of action | 2–6 hours[3][4] |
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ECHA InfoCard | 100.151.349 100.050.842, 100.151.349 |
Chemical and physical data | |
Formula | C12H18N2O4 |
Molar mass | 254.286 g·mol−1 |
3D model (JSmol) | |
Chirality | Racemic mixture |
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Midodrine, sold under the brand names ProAmatine and Orvaten among others, is a vasopressor or antihypotensive medication used to treat orthostatic hypotension (low blood pressure when standing) and urinary incontinence.[3][5][1] It is taken by mouth.[3][1]
Side effects of midodrine include hypertension (high blood pressure), paresthesia, itching, goosebumps, chills, urinary urgency, urinary retention, and urinary frequency.[3] Midodrine is a prodrug of its active metabolite desglymidodrine.[3][1] This metabolite acts as a selective agonist of the α1-adrenergic receptor.[3][1] This in turn results in vasoconstriction and increased blood pressure.[3][1]
Midodrine was discovered by 1971[6] and was introduced for medical use in the United States in 1996.[citation needed]
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