Diferencia entre revisiones de «Verapamil»

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==Special Populations==
==Special Populations==
*[[Drug Ratings in Pregnancy|Pregnancy Rating]]:
*[[Drug Ratings in Pregnancy|Pregnancy Rating]]: Category C, verapapmil crosses the placenta and can cause adverse fetal effects such as heart block, hypotension, and bradycardia
*[[Lactation risk categories|Lactation risk]]:
*[[Lactation risk categories|Lactation risk]]: Present in breast milk with relative infant dose of <1% which is considered safe for the infant.
*Renal dosing: no adjustment
*Renal dosing: Can accumulate causing increased effects, monitor closely and consider lowering dose.
*Hepatic dosing: 20-50% of normal dose
*Hepatic dosing: 20-50% of normal dose


Línea 48: Línea 48:
*Reduces systemic vascular resistance, vasodiolates peripheral arteries
*Reduces systemic vascular resistance, vasodiolates peripheral arteries
==Comments==
==Comments==
==Indications by Condition==
''The following table is automatically generated from disease/condition pages across WikEM.''
{{#ask:[[Has DrugName::Verapamil]]
|?Has Indication=Indication
|?Has Dose=Dose
|?Has Context=Context
|?Has Route=Route
|?Has Population=Population
|format=table
|headers=plain
|mainlabel=-
|sort=Has Indication
|limit=50
}}


==See Also==
==See Also==
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<references/>
<references/>
[[Category:Pharmacology]]
[[Category:Pharmacology]]
[[Category:Cardiology]]

Revisión actual - 21:57 20 mar 2026

Administration

Adult Dosing

  • Atrial fibrillation, paroxysmal SVT
    • IV: 5-10mg (0.075-0.15 mg/kg), may give an initial 10mg IV after 30 minutes if inadequate response
    • PO: 240-48 mg daily in 3-4 divided doses
  • Angina, hypertension: 80-120mg PO 3 times per day

Pediatric Dosing

  • Afib/flutter, SVT
    • IV 0.1-0.2 (<1yo) or 0.1-0.3 (>1yo) mg/kg. Repeat after 30 minutes if inadequate response
    • PO: 4-10 mg/kg/day in 3 divided doses

Special Populations

  • Pregnancy Rating: Category C, verapapmil crosses the placenta and can cause adverse fetal effects such as heart block, hypotension, and bradycardia
  • Lactation risk: Present in breast milk with relative infant dose of <1% which is considered safe for the infant.
  • Renal dosing: Can accumulate causing increased effects, monitor closely and consider lowering dose.
  • Hepatic dosing: 20-50% of normal dose

Contraindications

Adverse Reactions

Serious

Common

Pharmacology

  • Half-life: 4-20 hours
  • Metabolism: Hepatic- P450 CYP3A4, CYP1A2, CYP2C8, CYP2C9 and CYP2C18
  • Excretion: Renal primarily. Not dialyzable

Mechanism of Action

  • Inhibits L-type (slow) calcium channels, blocking influx of calcium into myocardial cells
  • Reduces systemic vascular resistance, vasodiolates peripheral arteries

Comments

Indications by Condition

The following table is automatically generated from disease/condition pages across WikEM.

IndicationDoseContextRoutePopulation
Paroxysmal supraventricular tachycardia1-4 mg/kg PO q8h (pediatric, >12 months only)Calcium-channel blocker (pediatric >12 months)POPediatric

See Also

References