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epinephrine racemic (AsthmaNefrin, S2)

 

Classes: Alpha/Beta Agonists

Dosing and uses of AsthmaNefrin, S2 (epinephrine racemic)

 

Adult dosage forms and strengths

solution for nebulization

  • 11.25mg/0.5mL (2.25% as 1.125% dextro-epinephrine and 1.125% levo-epinephrine)

 

Bronchial Asthma

Indicated for temporary relieve of symptoms associated with bronchial asthma (eg, shortness of breath, chest tightening, wheezing)

S2: 0.5 mL of 2.25% solution diluted in 3 mL NS via jet nebulizer q3-4hr PRn

Asthmanefrin: 1-3 inhalations of 0.5 mL of 2.25% solution via EZ Breathe Atomizer

 

Pediatric dosage forms and strengths

solution for nebulization

  • 11.25mg/0.5mL  (2.25% as 1.125% dextro-epinephrine and 1.125% levo-epinephrine)

 

Bronchial Asthma

Indicated for temporary relieve of symptoms associated with bronchial asthma (eg, shortness of breath, chest tightening, wheezing)

Asthmanefrin

  • <4 years: Safety and efficacy not established
  • ≥4 years: 1-3 inhalations of 0.5 mL of 2.25% solution via EZ Breathe Atomizer

S2

  • <4 years old: 0.05 mL/kg via jet nebulizer (diluted to 3 mL with NS) over 15 minutes; no more than q12hr; not to exceed 0.5 mL/dose
  • ≥4 years old: 0.5 mL of 2.25% solution via jet nebulizer (diluted to 3 mL with NS) over 15 minutes q3-4 hr PRN

Use low end of dosing range for younger infants

Should observe rapid response, can be repeated q2hr in older children but monitor HR with repeated dosing

 

Croup

<4 years: 0.05 mL/kg of 2.25% solution (S2) via jet nebulizer (diluted to 3 mL with NS) over 15 minutes q3-4 hr PRN; not to exceed 0.5 mL/dose

≥4 years old: 0.5 mL of 2.25% solution (S2) via jet nebulizer (diluted to 3 mL with NS) over 15 minutes q3-4 hr PRn

 

AsthmaNefrin, S2 (epinephrine racemic) adverse (side) effects

Frequency not defined

Tachycardia

Arrhythmias

Headache

Nausea

Sweating

Tremor

Restlessness

Rebound airway edema may occur

Angina

Autonomic hyperreflexia

Cardiac dysrhythmia

Ventricular fibrillation

Cerebral hemorrhage

Pulmonary edema

 

Warnings

Contraindications

Epiglottitis

Coadministration with MAOIs, or within 2 weeks after discontinuing an MAOI

 

Cautions

For oral inhalation only

Caution with heart disease, hypertension, thyroid disease, diabetes, or urinary retention caused by prostate enlargement

Instruct patient to seek immediate medical attention if symptoms not relieved within 20 minutes or become worse following administration

Do not use if product is brown in color or cloudy

Do not use if product is pinkish or darker than slightly yellow, or if it contains a precipitate

 

Pregnancy and lactation

Pregnancy category: C

Lactation: Excreted in breast milk

 

Pregnancy categories

A: Generally acceptable. Controlled studies in pregnant women show no evidence of fetal risk.

B: May be acceptable. Either animal studies show no risk but human studies not available or animal studies showed minor risks and human studies done and showed no risk.

C: Use with caution if benefits outweigh risks. Animal studies show risk and human studies not available or neither animal nor human studies done.

D: Use in LIFE-THREATENING emergencies when no safer drug available. Positive evidence of human fetal risk.

X: Do not use in pregnancy. Risks involved outweigh potential benefits. Safer alternatives exist.

NA: Information not available.

 

Pharmacology of AsthmaNefrin, S2 (epinephrine racemic)

Mechanism of action

Elicits agonistic action on alpha, beta-2, and beta-2 receptors resulting in bronchial smooth muscle relaxation, cardiac stimulation, vasodilation in skeletal muscle, and stimulation of glycogenolysis in the liver

 

Pharmacokinetics

Onset: 1-5 min

Duration: 1-3 hr

Metabolism: liver

Metabolites: metanephrine & 3-methoxy-4-hydroxymandelic acid (vanillylmandelic acid, VMA)

Excretion: unknown