Pulmicort Respules

— THERAPEUTIC CATEGORIES —
  • Asthma/COPD

Pulmicort Respules Generic Name & Formulations

General Description

Budesonide (micronized) 0.25mg/2mL, 0.5mg/2mL, 1mg/2mL; susp for inhalation.

Pharmacological Class

Steroid.

How Supplied

Flexhaler (90mcg/dose)—1 (60 inh); Flexhaler (180mcg/dose)—1 (120 inh); Respules—30

How Supplied

Pulmicort Respules is supplied in sealed aluminum foil envelopes containing one plastic strip of five single-dose Respules ampules together with patient instructions for use. There are 30 Respules ampules in a carton. Each single-dose Respules ampule contains 2 mL of sterile liquid suspension. 

Pulmicort Respules is available in 3 strengths, each containing 2 mL: 

  • 0.25 mg/2 mL

  • 0.5 mg/2 mL

  • 1 mg/2 mL

Storage

Pulmicort Respules should be stored upright at controlled room temperature 20-25°C (68-77°F) [see USP], and protected from light. When an envelope has been opened, the shelf life of the unused Respules ampules is 2 weeks when protected.

After opening the aluminum foil envelope, the unused Respules ampules should be returned to the aluminum foil envelope to protect them from light. Any opened Respules ampule must be used promptly. Gently shake the Respules ampule using a circular motion before use. Keep out of reach of children. Do not freeze.  

Generic Availability

Flexhaler (NO); Respules (YES)

Pulmicort Respules Indications

Indications

Maintenance treatment of asthma and as prophylactic therapy.

Pulmicort Respules Dosage and Administration

Adult

Use Flexhaler.

Children

Use jet nebulizer; do not mix with other drugs. 6–12months: not established (see full labeling). 12months–8yrs: Previously on bronchodilators alone: 0.5mg/day once daily or in 2 divided doses (if symptomatic and unresponsive to nonsteroidal therapy, may start at 0.25mg once daily). Previously on inhaled corticosteroids: 0.5mg/day once daily or in 2 divided doses; max 1mg/day. Previously on oral corticosteroids: 1mg/day once daily or in 2 divided doses. Rinse mouth and face (if face mask used) after use.

Pulmicort Respules Contraindications

Contraindications

Not for primary treatment of acute attack.

Pulmicort Respules Boxed Warnings

Not Applicable

Pulmicort Respules Warnings/Precautions

Warnings/Precautions

Maintain regular regimen. Infections. If exposed to chickenpox or measles, consider antiinfective prophylactic therapy. Adrenal insufficiency may occur when transferring patients from systemic corticosteroids to inhaled corticosteroids: see full labeling. Monitor for growth suppression in children. Post-op or during stress: monitor adrenal response. Monitor for hypercorticism and HPA axis suppression (if occur discontinue gradually). Transferring from oral corticosteroids: see full labeling. Pregnancy. Nursing mothers.

Warnings/Precautions

Local Effects

  • Localized infections with Candida albicans may occur in the mouth and pharynx in some patients.

  • If these infections develop, patients may require treatment with appropriate local or systemic antifungal therapy and/or discontinuation of treatment.

  • Rinse mouth after each inhalation. 

Deterioration of Disease and Acute Asthma Episodes

  • Pulmicort Flexhaler or Respules is not a bronchodilator and is not indicated for the rapid relief of acute bronchospasm or other acute episodes of asthma. 

  • During treatment, patients should contact their physician immediately if episodes of asthma are not responsive to their usual doses of bronchodilators. Treatment with oral corticosteroids may be needed during such episodes.

Hypersensitivity Reactions Including Anaphylaxis 

  • Discontinue treatment if hypersensitivity reactions occur, including anaphylaxis, rash, contact dermatitis, urticaria, angioedema, and bronchospasm.

Immunosuppression

  • If exposed to chicken pox, therapy with varicella zoster immune globulin (VZIG) or pooled intravenous immunoglobulin (IVIG), as appropriate, may be indicated.

  • If exposed to measles, prophylaxis with pooled intramuscular immunoglobulin (IG) may be indicated (see the respective package inserts for complete VZIG and IG prescribing information).

  • May consider treatment with antiviral agents if chicken pox develops.

  • Use caution in patients with active or quiescent tuberculosis infection of the respiratory tract, untreated systemic fungal, bacterial, viral or parasitic infections; or ocular herpes simplex. 

Transferring Patients from Systemic Corticosteroid Therapy

  • Use particular care when transferring patients from systemically active corticosteroids to inhaled corticosteroids because deaths due to adrenal insufficiency may occur.

  • The most susceptible patients are those who have been previously maintained on 20 mg or more per day of prednisone (or its equivalent).

  • A number of months are required for recovery of HPA-axis function after withdrawal from systemic corticosteroids. During this period of HPA-axis suppression, patients exposed to trauma, surgery, infection, or other conditions associated with severe electrolyte loss may exhibit signs and symptoms of adrenal insufficiency.

  • During periods of stress or a severe asthma attack, patients who have been withdrawn from systemic corticosteroids should be instructed to resume oral corticosteroids (in large doses) immediately and contact their physicians. These patients should carry a medical identification card.

  • If oral corticosteroids are required, patients should be weaned slowly from systemic corticosteroid use after transferring to Pulmicort Flexhaler or Respules. For these patients, use Pulmicort Flexhaler or Respules initially with their usual maintenance dose of systemic corticosteroid. Gradually withdraw systemic corticosteroid after approximately 1 week - do not exceed decrements of 25% of the prednisone dose or its equivalent. A slow rate of withdrawal is strongly recommended.

  • Monitor carefully lung function (FEV1 or AM PEF), beta-agonist use, and asthma symptoms during withdrawal of oral corticosteroids. Observe for signs and symptoms of adrenal insufficiency.

  • Transfer from systemic corticosteroid therapy to Pulmicort Flexhaler or Respules may unmask allergic or other immunologic conditions previously suppressed by the systemic corticosteroid therapy.

Hypercorticism and Adrenal Suppression  

  • Use particular care when observing patients post-operatively or during periods of stress for evidence of inadequate adrenal response

  • Systemic corticosteroid effects may occur, including hypercorticism, and adrenal suppression (including adrenal crisis), particularly when budesonide is administered at higher than recommended doses over prolonged periods of time. Reduce dose of Pulmicort Flexhaler or Respules slowly if these effects occur.

Reduction in Bone Mineral Density

  • Decreases in bone mineral density (BMD) have been observed with long-term administration of inhaled corticosteroids.

  • Monitor and treat appropriately in patients with major risk factors for decreased BMD, such as prolonged immobilization, family history of osteoporosis, poor nutrition, or chronic use of drugs that can reduce bone mass (e.g., anticonvulsants and corticosteroids).

Effects on Growth

  • May cause a reduction in growth velocity when administered to pediatric patients.

  • Monitor growth routinely if administered to pediatric patients. These systemic effects can be minimized by titrating each patient to their lowest effective dose.

Glaucoma and Cataracts

  • Monitor closely in patients with a change in vision or with a history of increased  intraocular pressure, glaucoma, and/or cataracts.

Paradoxical Bronchospasm and Upper Airway Symptoms 

  • Discontinue treatment and institute alternative therapy if paradoxical bronchospasm occurs, and treat immediately with a fast-acting inhaled bronchodilator.

Eosinophilic Conditions and Churg-Strauss Syndrome 

  • In rare cases, may present with systemic eosinophilic conditions.

  • Health care providers should be alert to eosinophilia, vasculitis rash, worsening pulmonary symptoms, cardiac complications, and/or neuropathy presenting in their patients.

Drug Interactions with Strong Cytochrome P450 3A4 Inhibitors

  • Use caution when considering using ketoconazole and other known strong CYP3A4 inhibitors (e.g., ritonavir, atazanavir, clarithromycin, indinavir, itraconazole, nefazodone, nelfinavir, saquinavir, telithromycin) with Pulmicort Flexhaler or Respules because may potentiate systemic exposure to budesonide. 

Pregnancy Considerations

Risk Summary

  • There are no adequate well-controlled studies of Pulmicort Flexhaler or Respules in pregnant women.

Clinical Considerations 

  • Disease-Associated Maternal and/or Embryo/Fetal risk: In women with poorly or moderately controlled asthma, there is an increased risk of several perinatal adverse outcomes such as preeclampsia in the mother and prematurity, low birth weight, and small for gestational age in the neonate.  

  • Labor or Delivery: There are no well-controlled human studies that have investigated the effects of Pulmicort Flexhaler or Respules during labor and delivery.

Nursing Mother Considerations

Risk Summary

  • Consider the developmental and health benefits of breastfeeding with the mother’s clinical need for Pulmicort Flexhaler or Respules and any potential adverse effects on the breastfed infant or from the underlying maternal condition.

Pediatric Considerations

Safety and efficacy in children 6 months to 12 months of age has been evaluated but not established.

Geriatric Considerations

No overall differences in safety were observed between these patients and younger patients.

Hepatic Impairment Considerations

Monitor closely in patients with hepatic disease.

Pulmicort Respules Pharmacokinetics

Absorption

In asthmatic children 4-6 years of age, the total absolute bioavailability (i.e., lung + oral) following administration of Pulmicort Respules via jet nebulizer was approximately 6% of the labeled dose.

In children, a peak plasma concentration of 2.6 nmol/L was obtained approximately 20 minutes after nebulization of a 1 mg dose. Systemic exposure, as measured by AUC and Cmax, is similar for young children and adults after inhalation of the same dose of Pulmicort Respules.  

Distribution

The volume of distribution of budesonide was approximately 3 L/kg. It was 85-90% bound to plasma proteins. Protein binding was constant over the concentration range (1-100 nmol/L) achieved with, and exceeding, recommended doses of Pulmicort Flexhaler. Budesonide showed little or no binding to corticosteroid binding globulin. Budesonide rapidly equilibrated with red blood cells in a concentration independent manner with a blood/plasma ratio of about 0.8.

Metabolism

In vitro studies with human liver homogenates have shown that budesonide is rapidly and extensively metabolized. Two major metabolites formed via cytochrome P450 (CYP) isoenzyme 3A4 (CYP3A4) catalyzed biotransformation have been isolated and identified as 16α-hydroxyprednisolone and 6β-hydroxybudesonide. The corticosteroid activity of each of these two metabolites is less than 1% of that of the parent compound. No qualitative difference between the in vitro and in vivo metabolic patterns has been detected. Negligible metabolic inactivation was observed in human lung and serum preparations. 

Elimination

Budesonide is primarily cleared by the liver. Budesonide is excreted in urine and feces in the form of metabolites. In adults, approximately 60% of an intravenous radiolabeled dose was recovered in the urine. No unchanged budesonide was detected in the urine. In asthmatic children 4-6 years of age, the terminal half-life of budesonide after nebulization is 2.3 hours, and the systemic clearance is 0.5 L/min, which is approximately 50% greater than in healthy adults after adjustment for differences in weight. 

Pulmicort Respules Interactions

Interactions

Caution with CYP3A4 inhibitors (eg, ketoconazole, itraconazole, atazanavir, ritonavir, indinavir, nefazodone, nelfinavir, saquinavir, clarithromycin, telithromycin).

Pulmicort Respules Adverse Reactions

Adverse Reactions

Pulmicort Flexhaler: nasopharyngitis, nasal congestion, pharyngitis, allergic rhinitis, viral upper respiratory tract infection, oral candidiasis, viral gastroenteritis, nausea, otitis media, bronchospasm (rare). Pulmicort Respules: Respiratory or other infection, GI upset, moniliasis, fatigue, cough, dysphonia, rash, epistaxis, hypersensitivity reactions (discontinue if occurs).

Pulmicort Respules Clinical Trials

Clinical Trials

  • The efficacy of Pulmicort Respules was evaluated in three 12-week, double-blind, placebo-controlled, parallel group, randomized US clinical trials. Each trial included 1018 pediatric patients 6 months to 8 years of age with persistent asthma of varying disease duration and severity. Patients were randomly assigned to receive Pulmicort Respules 0.15 mg, 0.5 mg, and 1 mg or placebo administered either once or twice daily. Pulmicort Respules were delivered via a Pari-LC-Jet Plus Nebulizer connected to a Pari Master compressor. The coprimary endpoints were nighttime and daytime asthma symptom scores (0-3 scale).

  • Results from the 3 clinical trials showed that treatment with Pulmicort Respules doses of 0.25 mg once daily, 0.25 mg twice daily, and 0.5 mg twice daily achieved statistically significant decreases in nighttime and daytime symptoms scores of asthma compared with placebo. The use of Pulmicort Respules 0.5 mg or 1 mg once daily achieved statistically significant decreases in either nighttime or daytime symptom scores, but not both. All doses of Pulmicort Respules also achieved statistically significant reductions in the need for bronchodilatory therapy.

  • While maximum benefit was not achieved for 4 to 6 weeks, a numerical reduction in nighttime and daytime symptom scores were observed for Pulmicort Respules within 2 to 8 days. These reductions were maintained throughout the 12 weeks.

Patients Not Receiving Inhaled Corticosteroid Therapy

  • The efficacy of Pulmicort Respules at doses of 0.25 mg, 0.5 mg, and 1 mg once daily was evaluated in 344 pediatric patients 12 months to 8 years of age with mild to moderate persistent asthma who were not well controlled by bronchodilators alone.

  • Treatment with Pulmicort Respules showed a statistically significant decrease in nighttime asthma symptoms scores compared with placebo; similar decreases were observed for daytime asthma symptom scores.

Patients Previously Maintained on Inhaled Corticosteroids

  • The efficacy of Pulmicort Respules at doses of 0.25 mg and 0.5 mg twice daily was evaluated in 133 pediatric asthma patients, 4 to 8 years of age, previously maintained on inhaled corticosteroids.

  • Treatment with Pulmicort Respules showed a statistically significant decrease in nighttime asthma symptoms scores compared with placebo; similar decreases were observed for daytime asthma symptom scores. 

  • Pulmicort Respules at a dose of 0.5 mg twice daily achieved statistically significant increases in FEV1 compared with placebo; and at doses of 0.25 mg and 0.5 mg twice daily, there were statistically significant increases in morning PEF compared with placebo.

Patients Receiving Once-Daily or Twice-Daily Dosing 

  • The efficacy of Pulmicort Respules at doses of 0.25 mg once daily, 0.25 mg twice daily, 0.5 mg twice daily, and 1 mg once daily, was evaluated in 469 pediatric patients 12 months to 8 years of age. The trial included approximately 70% who were not previously receiving inhaled corticosteroids.

  • Results showed that Pulmicort Respules at doses of 0.25 mg and 0.5 mg twice daily, and 1 mg once daily, achieved statistically significant decreases in nighttime asthma symptom scores compared with placebo; similar decreases were observed for daytime asthma symptom scores.

  • Compared with placebo, there were statistically significant increases in FEV1 for Pulmicort Respules at a dose of 0.5 mg twice daily, and statistically significant increases in morning PEF for Pulmicort at doses of 0.25 mg and 0.5 mg twice daily, and 1 mg once daily.

  • Evidence supports the efficacy for Pulmicort Respules to be administered on either a once-daily or twice-daily schedule. But the evidence is stronger for twice-daily dosing when all measures are considered together.

Pulmicort Respules Note

Not Applicable

Pulmicort Respules Patient Counseling

Patient Counseling

Administration with a Jet Nebulizer 

  • Advise patients to administer Pulmicort Respules with a jet nebulizer connected to a compressor with an adequate air flow, equipped with a mouthpiece or suitable face mask.

  • Do not use Ultrasonic nebulizers to administer Pulmicort Respules.

  • Administer Pulmicort Respules separately in the nebulizer.

Oral Candidiasis

  • Advise patients that localized infections with Candida albicans occurred in the mouth and pharynx in some patients.

  • Treat with appropriate local or systemic (i.e., oral) antifungal therapy while still continuing therapy with Pulmicort Respules if oropharyngeal candidiasis develops; at times, may need to temporarily interrupt Pulmicort Respules under close medical supervision.

  • Advise patients to rinse their mouth after inhalation.

Not for Acute Symptoms

  • Do not use to relieve acute asthma symptoms, and do not use extra doses for that purpose.

  • Use inhaled, short-acting beta2-agonist (i.e., albuterol) to treat acute symptoms.

  • Notify health care professional immediately if patients experience:

    • Decreasing effectiveness of inhaled, short-acting beta2- agonists 

    • Need for more inhalations than usual of inhaled, short-acting beta2-agonists

    • Significant decrease in lung function as outlined by the physician

  • Do not stop therapy with Pulmicort Respules without physician/provider guidance.

Hypersensitivity Including Anaphylaxis

  • Discontinue Pulmicort Respules if hypersensitivity reactions occur, including anaphylaxis, rash, contact dermatitis, urticaria, angioedema, and bronchospasm.

Immunosuppression

  • Warn patients who are on immunosuppressant doses of corticosteroids to avoid exposure to chickenpox or measles. If exposed, consult their physician without delay.

 Hypercorticism and Adrenal Suppression 

  • Advise patients that Pulmicort Respules may cause systemic corticosteroid effects of hypercorticism and adrenal suppression.

  • Slowly taper patients form systemic corticosteroids if transferring to Pulmicort Respules.

Reduction in Bone Mineral Density

  • Advise that the use of corticosteroids may pose increased risk for decreased BMD.

Reduced Growth Velocity 

  • May cause a reduction in growth velocity when given to pediatric patients.

Ocular Effects

  • Long-term use may increase the risk of cataracts or glaucoma. Consider regular eye examinations.

Use Daily 

  • Advise to use at regular intervals once or twice a day. Maximum benefit may not occur for 4 to 6 weeks or longer after starting treatment.