Tamsulosin: Difference between revisions

(Created page with "==Administration== *Type: Alpha blocker *Dosage Forms: *Routes of Administration: oral *Common Trade Names: Flomax ==Adult Dosing== *0.4mg PO once daily ==Pediatric Dosing==...")
 
 
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==Administration==
==Administration==
*Type: Alpha blocker
*Type: α-blocker
*Dosage Forms:
*Dosage Forms:
*Routes of Administration: oral
*Routes of Administration: oral
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==Adult Dosing==
==Adult Dosing==
*0.4mg PO once daily
*0.4mg PO once daily or nightly
 
===[[Urolithiasis]]===
*0.4mg PO QHS until stone expulsion
 
==Pediatric Dosing==
==Pediatric Dosing==
''Safety/efficacy not established''
''Safety/efficacy not established''
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===Serious===
===Serious===
*Retinal detachment
*Retinal detachment
*Priapism
*[[Priapism]]
 
===Common===
===Common===
*Headache, dizziness, insomnia, somnolence
*Headache, dizziness, insomnia, somnolence
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==Mechanism of Action==
==Mechanism of Action==
*Alpha-1A antagonist--> smooth muscle relaxation in bladder neck, prostate, urethra--> increased urine flow rate
*α-1A antagonist→ smooth muscle relaxation in bladder neck, prostate, urethra→ increased urine flow rate
==Comments==
==Comments==


==See Also==
==See Also==
*[[EBQ:Alpha-blockers for ureteral stone expulsion]]
*[[EBQ:Alpha-blockers for ureteral stone expulsion]]
*[[Urolithiasis]]
==References==
==References==
<references/>
<references/>
[[Category:Pharmacology]]
[[Category:Pharmacology]]
[[Category:Urology]]

Latest revision as of 12:18, 6 March 2021

Administration

  • Type: α-blocker
  • Dosage Forms:
  • Routes of Administration: oral
  • Common Trade Names: Flomax

Adult Dosing

  • 0.4mg PO once daily or nightly

Urolithiasis

  • 0.4mg PO QHS until stone expulsion

Pediatric Dosing

Safety/efficacy not established

Special Populations

Renal Dosing

  • Adult: No adjustment for CrCl >10

Hepatic Dosing

  • Adult: No adjustment

Contraindications

  • Allergy to class/drug

Adverse Reactions

Serious

Common

  • Headache, dizziness, insomnia, somnolence
  • Abnormal ejaculation
  • Rhinitis
  • Back pain

Pharmacology

  • Half-life: 9-15h
  • Metabolism: CYP3A4 and CYP2D6
  • Excretion: Mostly renal

Mechanism of Action

  • α-1A antagonist→ smooth muscle relaxation in bladder neck, prostate, urethra→ increased urine flow rate

Comments

See Also

References