Midodrine: Difference between revisions

 
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*Supine hypertension
*Supine hypertension
*Acute renal disease, urinary retention
*Acute renal disease, urinary retention
*Pheochromocytoma
*[[Pheochromocytoma]]
*Thyrotoxicosis
*[[Thyrotoxicosis]]
*Caution with:
*Caution with:
**Concomitant beta-blockers or digoxin (reflex bradycardia)
**Concomitant [[beta-blockers]] or [[digoxin]] (reflex bradycardia)
**Concomitant use of drugs that increase BP (e.g. phenylephrine, levothyroxine, pseudoephedrine)
**Concomitant use of drugs that increase BP (e.g. [[phenylephrine]], [[levothyroxine]], [[pseudoephedrine]])
**Concomitant MAOIs or linezolid
**Concomitant MAOIs or [[linezolid]]
**DM
**DM
**Renal or hepatic impairment
**Renal or hepatic impairment

Latest revision as of 16:08, 12 January 2022

Administration

  • Type: Vasopressors, alpha-1 agonist
  • Dosage Forms:
  • Routes of Administration: PO
  • Common Trade Names: ProAmatine, Orvaten

Adult Dosing

  • 2.5-10mg PO q8h

Pediatric Dosing

Safety/efficacy not established

Special Populations

Pregnancy Rating

  • Category C

Lactation risk

  • Unknown if excreted in breastmilk

Renal Dosing

  • Adult: 2.5mg PO q8h, increase as tolerated

Hepatic Dosing

  • Adult: Use caution

Contraindications

Adverse Reactions

Serious

Common

  • Paresthesias
  • Piloerection, pruritus, rash, erythema multiforme, flushing
  • Hypertension
  • Urinary retention or urgency
  • Abdominal pain, nausea, xerostomia
  • Chills
  • Anxiety, insomnia, somnolence, weakness
  • Confusion, dizziness
  • Headache
  • Hyperesthesia

Pharmacology

  • Half-life: 3-4h
  • Metabolism: Enzymatic hydrolysis in systemic circulation
  • Excretion: Renal

Mechanism of Action

  • Selective alpha-1 adrenergic agonist

Comments

See Also

References