FDA label 3ddaa837-cd71-4acc-a667-467e2bde664c

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

SPL set ID
0e996cf8-6975-452a-a84c-ca1033a629b1
SPL ID
3ddaa837-cd71-4acc-a667-467e2bde664c
Version
2
Effective date
2019-11-01
Source export date
2026-09-28
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:40:27

Warnings cross-check#

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warnings

WARNINGS Particular care is needed in patients who are transferred from systemically active corticosteroids to AEROSPAN Inhalation Aerosol because deaths due to adrenal insufficiency have occurred in asthmatic patients during and after transfer from systemic corticosteroids to less systemically available inhaled corticosteroids. After withdrawal from systemic corticosteroids, a number of months are required for recovery of hypothalamic-pituitary-adrenal (HPA) function. Patients who have been previously maintained on 20 mg or more per day of prednisone (or its equivalent) may be most susceptible, particularly when their systemic corticosteroids have been almost completely withdrawn. During this period of HPA suppression, patients may exhibit signs and symptoms of adrenal insufficiency when exposed to trauma, surgery or infections (particularly gastroenteritis) or other conditions associated with severe electrolyte loss. Although AEROSPAN Inhalation Aerosol may provide control of asthmatic symptoms during these episodes, in recommended doses it supplies less than the physiologic amounts of glucocorticoid systemically and does NOT provide the mineralocorticoid activity that is necessary for coping with these emergencies. During periods of stress or a severe asthmatic attack, patients who have been withdrawn from systemic corticosteroids should be instructed to resume systemic steroids (in large doses) immediately and to contact their physician for further instruction. These patients should also be instructed to carry a warning card indicating that they may need supplementary systemic steroids during periods of stress or a severe asthma attack. Patients requiring oral corticosteroids should be weaned slowly from systemic corticosteroid use after transferring to AEROSPAN Inhalation Aerosol. Lung function (FEV 1 or AM PEF), beta-agonist use, and asthma symptoms should be carefully monitored during withdrawal of oral corticosteroids. In addition to monitoring asthma signs and symptoms, patients should be observed for signs and symptoms of adrenal insufficiency such as fatigue, lassitude, weakness, nausea and vomiting, and hypotension. Transfer of patients from systemic corticosteroid therapy to AEROSPAN Inhalation Aerosol may unmask allergic conditions previously suppressed by the systemic corticosteroid therapy, e.g. rhinitis, conjunctivitis, eczema, arthritis, and eosinophilic conditions. Patients who are on drugs that suppress the immune system are more susceptible to infections than healthy individuals. Chickenpox and measles, for example, can have a more serious or even fatal course in non-immune children or adults on corticosteroids. In such children or adults who have not had these diseases or been properly immunized, particular care should be taken to avoid exposure. How the dose, route, and duration of corticosteroid administration affects the risk of developing a disseminated infection is not known. The contribution of the underlying disease and/or prior corticosteroid treatment to the risk is also not known. If exposed to chickenpox, prophylaxis with varicella-zoster immune globulin (VZIG) 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.) If chickenpox develops, treatment with antiviral agents may be considered. AEROSPAN Inhalation Aerosol is not a bronchodilator and is not indicated for rapid relief of bronchospasm. As with other inhaled asthma medications, bronchospasm may occur with an immediate increase in wheezing after dosing. If bronchospasm occurs following dosing with AEROSPAN Inhalation Aerosol, it should be treated immediately with a fast-acting inhaled bronchodilator. Treatment with AEROSPAN Inhalation Aerosol should be discontinued and alternative therapy instituted. Patients should be instructed to contact their physician immediately when episodes of asthma that are not responsive to bronchodilators occur during the course of treatment with AEROSPAN Inhalation Aerosol. During such episodes, patients may require therapy with systemic corticosteroids.

Adverse reactions cross-check#

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Adverse reactions sections page 1 of 1 · 2 matching rows.

adverse reactions

ADVERSE REACTIONS The following table shows the adverse reactions that were reported in patients previously receiving bronchodilators and/or orally inhaled corticosteroids in two double-blind, placebo-controlled US clinical studies, in which 519 adult and pediatric patients age 4-78 years (279 males and 240 females) were treated with the AEROSPAN Inhalation Aerosol (80 mcg to 320 mcg twice daily for 12 weeks) or placebo. The mean duration of exposure was 76.7, 78.2, 80.5, and 69.4 days for AEROSPAN Inhalation Aerosol 80 mcg, 160 mcg, 320 mcg, and placebo, all dosed twice daily, respectively. The table includes all events (whether considered drug-related or non-drug-related by the investigators) that occurred at a rate of >3% in any AEROSPAN Inhalation Aerosol group and were more common than in the placebo group. In considering these data, the increased average duration of exposure for AEROSPAN Inhalation Aerosol patients should be taken into account, compared with placebo-treated patients. Adverse Events with >3% incidence reported in controlled clinical studies with AEROSPAN Inhalation Aerosol (% of patients) ADVERSE EVENT PLACEBO ( n = 220) AEROSPAN Inhalation Aerosol 80 MCG ( n = 189) 160 MCG ( n = 217) 320 MCG ( n = 113) BODY AS A WHOLE Headache 12.7 9.0 13.8 8.8 Fever 5.0 6.9 3.7 0.9 Allergic Reaction 2.3 4.2 4.6 4.4 Pain 3.6 2.6 4.6 1.8 Accidental Injury 2.3 3.7 3.7 3.5 Infection, Bacterial 0.9 3.7 0.9 0.9 Back Pain 2.3 0.5 3.2 1.8 DIGESTIVE SYSTEM Vomiting 4.1 4.2 4.6 0.0 Dyspepsia 1.4 2.1 3.2 3.5 RESPIRATORY SYSTEM Pharyngitis 13.2 17.5 16.6 16.8 Rhinitis 10.0 9.0 15.7 3.5 Cough Increased 7.7 8.5 5.5 1.8 Sinusitis 5.5 7.4 4.1 8.8 Epistaxis 0.9 3.2 0.9 0.0 SKIN AND APPENDAGES Rash 3.2 2.6 3.7 1.8 UROGENITAL SYSTEM Urinary Tract Infection 0.5 1.1 0.9 3.5 The following other adverse events occurred in patients in these clinical studies using AEROSPAN Inhalation Aerosol with an incidence of 1 to 3% and were more common in AEROSPAN Inhalation Aerosol than in the placebo group. Body As A Whole: abdominal pain, chest pain, infection, neck pain Digestive System: diarrhea, gastroenteritis, nausea, oral moniliasis Metabolic And Nutritional Disorders: edema Musculoskeletal System: myalgia Nervous System: dizziness, insomnia, migraine Respiratory System: bronchitis, laryngitis, voice alteration Skin And Appendages: erythema multiforme Special Senses: conjunctivitis, ear pain, taste perversion Urogenital System: dysmenorrhea, vaginitis Cases of growth suppression have been reported for orally inhaled corticosteroids (see PRECAUTIONS, Pediatric Use section.) ADVERSE EVENTS FROM OTHER SOURCES Two 52-week open label safety studies of AEROSPAN Inhalation Aerosol were conducted in 162 asthma patients 12 to 60 years of age and in 152 asthma patients 4 to 11 years of age. The adverse event profile exhibited in these studies was similar to that seen in the two 12-week studies. The following additional adverse events were derived from clinical studies conducted with flunisolide CFC inhalation aerosol with a frequency of ≥1% and not described above: Body as a Whole: flu, decreased appetite, chills, increased appetite, weight gain, malaise, peripheral edema, sweating, weakness Gastrointestinal System: upset stomach, heartburn, constipation, gas, abdominal fullness Cardiovascular System: palpitations, hypertension, tachycardia Nervous System: headache, irritability, shakiness, anxiety, depression, faintness, fatigue, hyperactivity, hypoactivity, moodiness, numbness, vertigo, Respiratory System: cold symptoms, nasal congestion, upper respiratory tract infection, chest congestion, hoarseness, runny nose, sinus congestion, sinus drainage, sinus infection, sneezing, sputum, wheezing, chest tightness, bronchospasm, dyspnea, head stuffiness, nasal irritation, pleurisy, pneumonia, sinus discomfort Skin and Appendages: eczema, pruritus, acne, urticaria Special Senses: loss of smell, loss of taste, ear infection, blurred vision, eye discomfort, eye infection Hemic and Lymph: capillary fragility, enlarged lymph nodes Mouth and Throat: sore throat, dry throat, glossitis, mouth irritation, phlegm, throat irritation

adverse reactions table

<table> <col width="118"/> <col width="117"/> <col width="118"/> <col width="118"/> <col width="111"/> <tbody> <tr> <td colspan="5" align="center"> <content styleCode="bold">Adverse Events with &gt;3% incidence reported in controlled </content> <content styleCode="bold">clinical </content> <content styleCode="bold">studies</content> <content styleCode="bold"> with AEROSPAN Inhalation Aerosol</content> <content styleCode="bold"> </content> <content styleCode="bold">(% of patients)</content> </td> </tr> <tr> <td align="center"> <content styleCode="bold">ADVERSE EVENT</content> </td> <td align="center"> <content styleCode="bold">PLACEBO</content> <content styleCode="bold">(</content> <content styleCode="bold">n</content> <content styleCode="bold"> = 220)</content> </td> <td colspan="3" align="center"> <content styleCode="bold">AEROSPAN </content>Inhalation Aerosol<content styleCode="bold"> </content> </td> </tr> <tr> <td/> <td align="center"/> <td align="center"> <content styleCode="bold">80 MCG</content> <content styleCode="bold">(</content> <content styleCode="bold">n</content> <content styleCode="bold"> = 189)</content> </td> <td align="center"> <content styleCode="bold">160 MCG</content> <content styleCode="bold">(</content> <content styleCode="bold">n</content> <content styleCode="bold"> = 217)</content> </td> <td align="center"> <content styleCode="bold">320 MCG</content> <content styleCode="bold">(</content> <content styleCode="bold">n</content> <content styleCode="bold"> = 113)</content> </td> </tr> <tr> <td styleCode="Toprule Lrule ">BODY AS A WHOLE</td> <td styleCode="Toprule "/> <td styleCode="Toprule "/> <td styleCode="Toprule "/> <td styleCode="Toprule "/> </tr> <tr> <td styleCode="Lrule " align="right"> Headache</td> <td align="right">12.7</td> <td align="right">9.0</td> <td align="right">13.8</td> <td align="right">8.8</td> </tr> <tr> <td styleCode="Lrule " align="right">Fever</td> <td align="right">5.0</td> <td align="right">6.9</td> <td align="right">3.7</td> <td align="right">0.9</td> </tr> <tr> <td styleCode="Lrule " align="right">Allergic Reaction</td> <td align="right">2.3</td> <td align="right">4.2</td> <td align="right">4.6</td> <td align="right">4.4</td> </tr> <tr> <td styleCode="Lrule " align="right"> Pain</td> <td align="right">3.6</td> <td align="right">2.6</td> <td align="right">4.6</td> <td align="right">1.8</td> </tr> <tr> <td styleCode="Lrule " align="right">Accidental Injury</td> <td align="right">2.3</td> <td align="right">3.7</td> <td align="right">3.7</td> <td align="right">3.5</td> </tr> <tr> <td styleCode="Lrule " align="right">Infection, Bacterial</td> <td align="right">0.9</td> <td align="right">3.7</td> <td align="right">0.9</td> <td align="right">0.9</td> </tr> <tr> <td styleCode="Lrule " align="right"> Back Pain</td> <td align="right">2.3</td> <td align="right">0.5</td> <td align="right">3.2</td> <td align="right">1.8</td> </tr> <tr> <td styleCode="Toprule Lrule ">DIGESTIVE SYSTEM</td> <td styleCode="Toprule "/> <td styleCode="Toprule "/> <td styleCode="Toprule "/> <td styleCode="Toprule "/> </tr> <tr> <td styleCode="Lrule " align="right"> Vomiting</td> <td align="right">4.1</td> <td align="right">4.2</td> <td align="right">4.6</td> <td align="right">0.0</td> </tr> <tr> <td styleCode="Lrule " align="right"> Dyspepsia</td> <td align="right">1.4</td> <td align="right">2.1</td> <td align="right">3.2</td> <td align="right">3.5</td> </tr> <tr> <td styleCode="Toprule Lrule ">RESPIRATORY SYSTEM</td> <td styleCode="Toprule "/> <td styleCode="Toprule "/> <td styleCode="Toprule "/> <td styleCode="Toprule "/> </tr> <tr> <td styleCode="Lrule " align="right"> Pharyngitis</td> <td align="right">13.2</td> <td align="right">17.5</td> <td align="right">16.6</td> <td align="right">16.8</td> </tr> <tr> <td styleCode="Lrule " align="right"> Rhinitis</td> <td align="right">10.0</td> <td align="right">9.0</td> <td align="right">15.7</td> <td align="right">3.5</td> </tr> <tr> <td styleCode="Lrule ">Cough Increased</td> <td align="right">7.7</td> <td align="right">8.5</td> <td align="right">5.5</td> <td align="right">1.8</td> </tr> <tr> <td styleCode="Lrule " align="right"> Sinusitis</td> <td align="right">5.5</td> <td align="right">7.4</td> <td align="right">4.1</td> <td align="right">8.8</td> </tr> <tr> <td styleCode="Lrule " align="right"> Epistaxis</td> <td align="right">0.9</td> <td align="right">3.2</td> <td align="right">0.9</td> <td align="right">0.0</td> </tr> <tr> <td styleCode="Toprule Lrule ">SKIN AND APPENDAGES</td> <td styleCode="Toprule "/> <td styleCode="Toprule "/> <td styleCode="Toprule "/> <td styleCode="Toprule "/> </tr> <tr> <td styleCode="Lrule " align="right"> Rash</td> <td align="right">3.2</td> <td align="right">2.6</td> <td align="right">3.7</td> <td align="right">1.8</td> </tr> <tr> <td styleCode="Toprule Lrule ">UROGENITAL SYSTEM</td> <td styleCode="Toprule "/> <td styleCode="Toprule "/> <td styleCode="Toprule "/> <td styleCode="Toprule Rrule "/> </tr> <tr> <td styleCode="Lrule " align="right"> Urinary Tract Infection </td> <td align="right">0.5</td> <td align="right">1.1</td> <td align="right">0.9</td> <td styleCode="Rrule " align="right">3.5</td> </tr> </tbody> </table>

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.