Midodrine: Difference between revisions
ClaireLewis (talk | contribs) (Created page with "==Administration== *Type: Vasopressor, alpha-1 agonist *Dosage Forms: *Routes of Administration: PO *Common Trade Names: ProAmatine, Orvaten ==Adult Dosing== *2.5-10mg PO...") |
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==Administration== | ==Administration== | ||
*Type: [[ | *Type: [[Vasopressors]], alpha-1 agonist | ||
*Dosage Forms: | *Dosage Forms: | ||
*Routes of Administration: PO | *Routes of Administration: PO | ||
| Line 29: | Line 29: | ||
*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 | ||
| Line 41: | Line 41: | ||
==Adverse Reactions== | ==Adverse Reactions== | ||
===Serious=== | ===Serious=== | ||
*Bradycardia | *[[Bradycardia]] | ||
* | *[[Elevated ICP]] | ||
===Common=== | ===Common=== | ||
*Paresthesias | *Paresthesias | ||
*Piloerection, pruritus, rash, erythema multiforme, flushing | *Piloerection, pruritus, rash, [[erythema multiforme]], flushing | ||
*Hypertension | *[[Hypertension]] | ||
*Urinary retention or urgency | *Urinary retention or urgency | ||
*Abdominal pain, nausea, xerostomia | *Abdominal pain, nausea, xerostomia | ||
| Line 53: | Line 53: | ||
*Anxiety, insomnia, somnolence, weakness | *Anxiety, insomnia, somnolence, weakness | ||
*Confusion, dizziness | *Confusion, dizziness | ||
*Headache | *[[Headache]] | ||
*Hyperesthesia | *Hyperesthesia | ||
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[[Category:Pharmacology]] | [[Category:Pharmacology]] | ||
[[Category:Cardiology]] | |||
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
- Allergy to class/drug
- Severe heart disease
- Supine hypertension
- Acute renal disease, urinary retention
- Pheochromocytoma
- Thyrotoxicosis
- Caution with:
- Concomitant beta-blockers or digoxin (reflex bradycardia)
- Concomitant use of drugs that increase BP (e.g. phenylephrine, levothyroxine, pseudoephedrine)
- Concomitant MAOIs or linezolid
- DM
- Renal or hepatic impairment
- Vision problems
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