section name header

Pronunciation

al-FEN-ta-nil audio

Indications

High Alert

Action

Therapeutic Effects:

Pharmacokinetics

Absorption: Following IV administration, absorption is essentially complete.

Distribution: Does not penetrate adipose tissue. Crosses placenta, enters breast milk.

Metabolism/Excretion: >95% metabolized by the liver.

Half-life: 60–130 min ( in children).

Contraind./Precautions

Contraindicated in:

Use Cautiously in:

Adv. Reactions/Side Effects

EENT: blurred vision.

CV: bradycardia, hypotension, tachycardia, arrhythmias, hypertension.

GI: nausea, vomiting.

MS: thoracic muscle rigidity, skeletal muscle rigidity.

Neuro: dizziness, sleepiness.

Resp: RESPIRATORY DEPRESSION (INCLUDING CENTRAL SLEEP APNEA AND SLEEP-RELATED HYPOXEMIA), apnea.

Interactions

Drug-Drug:

Drug-Natural Products:

Route/Dosage

see Calculator

Incremental Injection (Duration of Anesthesia <30 min) — Induction Period

Incremental Injection (Duration of Anesthesia <30 min) — Maintenance Period

Incremental Injection (Duration of Anesthesia 30–60 min) — Induction Period

Incremental Injection (Duration of Anesthesia 30–60 min) — Maintenance Period

Continuous Infusion (Duration of Anesthesia >45 min) — Induction

Continuous Infusion (Duration of Anesthesia >45 min) — Maintenance

Pediatric dose (unlabeled)

Anesthetic Induction (Duration of Anesthesia >45 min)

Monitored Anesthesia Care — Induction

Monitored Anesthesia Care — Maintenance

Implementation

US Brand Names

Alfenta

Contr. Subst. Schedule

Schedule II (C-II)

Classifications

Therapeutic Classification: analgesic adjuncts, opioid analgesics

Pharmacologic Classification: opioid agonists

Availability

(Generic available)

Time/Action Profile

(analgesia and respiratory depression)

ROUTEONSETPEAKDURATION
IVimmediate1–1.5 min5–10 min

in children.

Assessment

Lab Test Considerations: Toxicity and Overdose:

Pot. Nursing Diagnoses

Patient/Family Teaching

Evaluation/Desired Outcomes

Code

NDC Code*