FDA label 076b1934-4c7a-4e53-b761-84c8f0ac8025

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
29f4b9a7-169e-4789-a27b-2e12274b6d80
SPL ID
076b1934-4c7a-4e53-b761-84c8f0ac8025
Version
1
Effective date
2012-03-23
Source export date
2026-10-12
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:36:06

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS Particular care is needed in patients who are transferred from systemically active corticosteroids to AEROBID Inhaler because deaths due to adrenal insufficiency have occurred in asthmatic patients during and after transfer from systemic corticosteroids to aerosol corticosteroids. After withdrawal from systemic corticosteroids, a number of months are required for recovery of hypothalamic-pituitary-adrenal (HPA) function. During this period of HPA suppression, patients may exhibit signs and symptoms of adrenal insufficiency when exposed to trauma, surgery or infections, particularly gastroenteritis. Although AEROBID Inhaler may provide control of asthmatic symptoms during these episodes, it does NOT provide the systemic steroid 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 During periods of stress or a severe asthmatic attack, patients who have been withdrawn from systemic corticosteroids should be instructed to resume systemic steroids (in large doses) immediately and to contact their physician for further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. To assess the risk of adrenal insufficiency in emergency situations, routine tests of adrenal cortical function, including measurement of early morning resting cortisol levels, should be performed periodically in all patients. An early morning resting cortisol level may be accepted as normal if it falls at or near the normal mean level. Localized infections with Candida albicans or Aspergillus niger have occurred in the mouth and pharynx and occasionally in the larynx. Positive cultures for oral Candida may be present in up to 34% of patients. Although the frequency of clinically apparent infection is considerably lower, these infections may require treatment with appropriate antifungal therapy or discontinuance of treatment with AEROBID Inhaler. AEROBID Inhaler is not to be regarded as a bronchodilator and is not indicated for relief of bronchospasm. 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. During such episodes, patients may require therapy with systemic corticosteroids. Theoretically, the use of inhaled corticosteroids with alternate day prednisone systemic treatment should be accompanied by more HPA suppression than a therapeutically equivalent regimen of either alone. Transfer of patients from systemic steroid therapy to AEROBID Inhaler may unmask allergic conditions previously suppressed by the systemic steroid therapy, e.g. rhinitis, conjunctivitis, and eczema. Persons who are on drugs which suppress the immune system are more susceptible to infections than healthy individuals. Chicken pox 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, 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 chicken pox, 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 chicken pox develops, treatment with antiviral agents may be considered.

Adverse reactions cross-check#

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

adverse reactions

ADVERSE REACTIONS Adverse events reported in controlled clinical trials and long-term open studies in 514 patients treated with AEROBID (flunisolide) are described below. Of those patients, 463 were treated for 3 months or longer, 407 for 6 months or longer, 287 for 1 year or longer, and 122 for 2 years or longer. Musculoskeletal reactions were reported in 35% of steroid-dependent patients in whom the dose of oral steroid was being tapered. This is a well-known effect of steroid withdrawal. Incidence 10% or greater: Gastrointestinal: diarrhea (10%), nausea and/or vomiting (25%), upset stomach (10%) General: flu (10%) Mouth and Throat: sore throat (20%) Nervous System: headache (25%) Respiratory: cold symptoms (15%), nasal congestion (15%), upper respiratory infection (25%) Special Senses: unpleasant taste (10%) Incidence 3-9% Cardiovascular: palpitations Gastrointestinal: abdominal pain, heartburn General: chest pain, decreased appetite, edema, fever Mouth and Throat: Candida infection Nervous System: dizziness, irritability, nervousness, shakiness Reproductive: menstrual disturbances Respiratory: chest congestion, cough*, hoarseness, rhinitis, runny nose, sinus congestion, sinus drainage, sinus infection, sinusitis, sneezing, sputum, wheezing 1 Skin: eczema, itching (pruritus), rash Special Senses: ear infection, loss of smell or taste Incidence 1-3% General: chills, increased appetite and weight gain, malaise, peripheral edema, sweating, weakness Cardiovascular: hypertension, tachycardia Gastrointestinal: constipation, dyspepsia, gas Hemic/Lymph: capillary fragility, enlarged lymph nodes Mouth and Throat: dry throat, glossitis, mouth irritation, pharyngitis, phlegm, throat irritation Nervous System: anxiety, depression, faintness, fatigue, hyperactivity, hypoactivity, insomnia, moodiness, numbness, vertigo Respiratory: bronchitis, chest tightness*, dyspnea, epistaxis, head stuffiness, laryngitis, nasal irritation, pleurisy, pneumonia, sinus discomfort Skin: acne, hives or urticaria Special Senses: blurred vision, earache, eye discomfort, eye infection Incidence less than 1%, judged by investigators as possibly or probably drug related: abdominal fullness, shortness of breath. 1 The incidences as shown of cough, wheezing, and chest tightness were judged by investigators to be possibly or probably drug related. In placebo-controlled trials, the overall incidences of these adverse events (regardless of investigators' judgement of drug relationship) were similar for drug and placebo-treated groups. They may be related to the vehicle or delivery system.

Reported adverse events (FAERS/openFDA)#

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