section name header

Pronunciation ⬇

DOR-nase AL -fa

Classifications ⬆ ⬇

Therapeutic Classification: cystic fibrosis therapy adjuncts

Pharmacologic Classification: pulmonary enzymes

Indications ⬆ ⬇

REMS


Action ⬆ ⬇

  • Breaks down excessive amounts of DNA found in the respiratory tract of patients with cystic fibrosis. Excessive DNA contributes to increased sputum viscosity and risk of infection.
Therapeutic effects:
  • Decreased infection rates and requirement for parenteral anti-infectives.
  • Improved pulmonary function.

Pharmacokinetics ⬆ ⬇

Absorption: Negligible absorption following inhalation.

Distribution: Action is primarily local.

Metabolism/Excretion: Unknown.

Half-Life: Unknown.

Time/Action Profile ⬆ ⬇

(effect on noted parameters)

ROUTEONSETPEAKDURATION
Inhalationwithin 15 min‡3 days–1 wk‡ weeks–months§48 hr

‡Significant concentrations in sputum.

‡Improvement in respiratory function.

§Decreased incidence of respiratory tract infections.

Contraind./Precautions ⬆ ⬇

Contraindicated in:

Use Cautiously in:

Adv. Reactions/Side Effects ⬆ ⬇

CV: chest pain

Derm: rash

EENT: rhinitis, sore throat, voice alteration, conjunctivitis, hoarseness

Resp: cough, dyspnea

Misc: fever

Interactions ⬆ ⬇

Drug-drug:

Route/Dosage ⬆ ⬇

Availability ⬆ ⬇

Assessment ⬆ ⬇

Implementation ⬆ ⬇

Patient/Family Teaching ⬆ ⬇

Evaluation/Desired Outcomes ⬆ ⬇

US Brand Names ⬆

Pulmozyme