Betaxolol: Difference between revisions

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==Administration==
==Administration==
*Type: [[Beta blocker]]
*Type: [[Beta blocker]]
*Dosage Forms: 10, 20 mg
*Dosage Forms: 10 mg, 20 mg, 0.5% ophthalmic solution, 0.25% suspension
*Routes of Administration: Oral
*Routes of Administration: Oral, ophthalmic
*Common Trade Names: Kerlone
*Common Trade Names: Kerlone


==Adult Dosing==
==Adult Dosing==
*10-20 mg PO qd
*5-80 mg PO daily
**Start: 10 mg PO qd
*1-2 drops in affected eye BID
**Max: 40 mg/day
**Consider starting 5 mg PO qd in elderly pts
**Taper dose over 2 weeks to D/C


==Pediatric Dosing==
==Pediatric Dosing==
N/A
''Safety/efficacy of oral forms and 0.5% solution not established in peds''
*0.25% suspension: 1 drop in affected eye BID


==Special Populations==
==Special Populations==
*[[Drug Ratings in Pregnancy|Pregnancy Rating]]: C; Caution advised in 2nd and 3rd trimesters. Risk of intrauterine growth restriction and neonatal adverse effects including bradycardia and hypoglycemia.
*[[Drug Ratings in Pregnancy|Pregnancy Rating]]: C; Caution advised in 2nd and 3rd trimesters. Risk of intrauterine growth restriction and neonatal adverse effects including bradycardia and hypoglycemia.
*[[Lactation risk categories|Lactation risk]]: L3; Safety unknown
*[[Lactation risk categories|Lactation risk]]: L3; Safety unknown
 
*Severe renal impairment: Start at 5mg PO daily, increase by 5mg/day q2wk to max daily dose 20mg
===Renal Dosing===
*Hepatic dosing: no adjustment
*Adult: Severe impairment: Start 5 mg PO qd. May increase by 5 mg/day q 2 weeks to max 20 mg/day.
*Pediatric: N/A
 
===Hepatic Dosing===
*Adult: No adjustement
*Pediatric: N/A


==Contraindications==
==Contraindications==
*Allergy to class/drug
*Allergy to class/drug
*Sinus [[bradycardia]]
*Sinus [[bradycardia]], 2nd or 3rd degree [[AV block]], [[sick sinus syndrome]] (without pacemaker)
*2nd or 3rd degree [[AV block]]
*Decompensated [[heart failure]], [[cardiogenic shock]]
*Decompensated [[heart failure]]
*Untreated [[pheochromocytoma]]
*[[Cardiogenic shock]]
*[[Sick sinus syndrome]] w/o pacemaker
*[[Pheochromocytoma]], untreated
*Avoid abrupt withdrawal
*Avoid abrupt withdrawal


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===Serious===
===Serious===
*[[CHF]]
*[[CHF]]
*[[Bradycardia]], severe
*Severe [[bradycardia]], [[heart block]]
*[[Heart block]]
*[[Angina]] exacerbation, ventricular arrythmia, or [[MI]] with abrupt discontinuation
*[[Angina]] exacerbation with abrupt D/C
*[[MI]] if abrupt D/C
*Ventricular arrhythmia if abrupt D/C
*Bronchospasm
*Bronchospasm
*Hypersensitivity reaction
*Hypersensitivity reaction
*Raynaud's phenomenon
*[[Psoriasis]] exacerbation, [[lupus]] erythematosus, Raynaud's phenomenon
*[[Psoriasis]] exacerbation
*[[Lupus]] erythematosus
 
===Common===
===Common===
*[[Bradycardia]]
*[[Bradycardia]], [[chest pain]]
*[[Headache]]
*[[Headache]], [[dizziness]], [[fatigue]]
*[[Dyspepsia]]
*[[Dyspepsia]], [[diarrhea]]
*[[Dizziness]]
*[[Arthralgia]]
*[[Arthralgia]]
*[[Fatigue]]
*[[URI]], [[pharyngitis]]
*[[Lethargy]]
*[[URI]]
*[[Dyspnea]]
*[[Dyspnea]]
*[[Chest pain]]
*[[Pharyngitis]]
*[[Diarrhea]]


==Pharmacology==
==Pharmacology==
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==Mechanism of Action==
==Mechanism of Action==
Selectively antagonizes beta-1 adrenergic receptors.
*Selectively antagonizes beta-1 adrenergic receptors.


==Comments==
==Comments==


==See Also==
==See Also==
 
*[[Beta-blockers]]
==References==
==References==
<references/>
<references/>
[[Category:Pharmacology]]
[[Category:Pharmacology]]

Revision as of 02:20, 11 December 2016

Administration

  • Type: Beta blocker
  • Dosage Forms: 10 mg, 20 mg, 0.5% ophthalmic solution, 0.25% suspension
  • Routes of Administration: Oral, ophthalmic
  • Common Trade Names: Kerlone

Adult Dosing

  • 5-80 mg PO daily
  • 1-2 drops in affected eye BID

Pediatric Dosing

Safety/efficacy of oral forms and 0.5% solution not established in peds

  • 0.25% suspension: 1 drop in affected eye BID

Special Populations

  • Pregnancy Rating: C; Caution advised in 2nd and 3rd trimesters. Risk of intrauterine growth restriction and neonatal adverse effects including bradycardia and hypoglycemia.
  • Lactation risk: L3; Safety unknown
  • Severe renal impairment: Start at 5mg PO daily, increase by 5mg/day q2wk to max daily dose 20mg
  • Hepatic dosing: no adjustment

Contraindications

Adverse Reactions

Serious

Common

Pharmacology

  • Half-life: 14-22 hr
  • Metabolism: Liver extensively; CYP450: Unknown
  • Excretion: Urine > 80% (15% unchanged)

Mechanism of Action

  • Selectively antagonizes beta-1 adrenergic receptors.

Comments

See Also

References