Interaksi Budesonid dan formoterol dan Flutikason

Budesonid dan formoterol dan Flutikason: kedua label peresepan menandai kombinasi ini dengan bahasa yang paling tegas, seperti kontraindikasi, peringatan kotak hitam, atau instruksi untuk menghindarinya.

Mayor

Jangan dikombinasikan tanpa arahan dokter yang meresepkan. Bahasa label di bawah ini adalah yang paling tegas yang digunakan FDA.

Apa kata label FDA

Dari label Budesonid dan formoterol (Budesonide and Formoterol Fumarate Dihydrate) · berlaku sejak 2026-04-24

Mayor

…intubation (endotracheal) 1 2 Asthma-related hospitalization (≥24-hour stay) 115 105 ICS = Inhaled Corticosteroid, LABA = Long-acting Beta2-adrenergic Agonist The pediatric safety trial included 6208 pediatric patients 4 to 11 years of age who received ICS/LABA (fluticasone propionate /salmeterol inhalation powder) or ICS (fluticasone propionate inhalation powder).

Peringatan dan perhatianmenyebut FlutikasonLihat label di DailyMed
Moderat

In this situation, the patient requires immediate re-evaluation with reassessment of the treatment regimen, giving special consideration to the possible need for replacing the current strength of budesonide and formoterol fumarate dihydrate with a higher strength, adding additional inhaled corticosteroid, or initiating systemic corticosteroids.

Peringatan dan perhatianberdasarkan golongan obatLihat label di DailyMed
Minor

…adolescent patients aged ≥12 years: one trial compared budesonide/formoterol (budesonide and formoterol fumarate dihydrate) to budesonide [see Clinical Studies (14.1) ] ; one trial compared fluticasone propionate/salmeterol inhalation powder to fluticasone propionate inhalation powder; and one trial compared mometasone furoate/formoterol to mometasone furoate.

Peringatan dan perhatianmenyebut FlutikasonLihat label di DailyMed
Minor

The fourth trial included pediatric patients 4 to 11 years of age and compared fluticasone propionate/salmeterol inhalation powder to fluticasone propionate inhalation powder.

Peringatan dan perhatianmenyebut FlutikasonLihat label di DailyMed

Dari label Flutikason (FLUTICASONE PROPIONATE DISKUS) · berlaku sejak 2026-05-14

Moderat

Lung function (mean forced expiratory volume in 1 second [FEV 1 ] or morning peak expiratory flow [AM PEF]), beta-agonist use, and asthma symptoms should be carefully monitored during withdrawal of oral corticosteroids.

Peringatan dan perhatianberdasarkan golongan obatLihat label di DailyMed
Minor

Acute Asthma Episodes Fluticasone Propionate DISKUS is not to be regarded as a bronchodilator and is not indicated for rapid relief of bronchospasm.

Peringatan dan perhatianberdasarkan golongan obatLihat label di DailyMed
Minor

Patients should be instructed to contact their physicians immediately when episodes of asthma that are not responsive to bronchodilators occur during the course of treatment with Fluticasone Propionate DISKUS.

Peringatan dan perhatianberdasarkan golongan obatLihat label di DailyMed
Minor

If bronchospasm occurs following dosing with Fluticasone Propionate DISKUS, it should be treated immediately with an inhaled, short-acting bronchodilator; Fluticasone Propionate DISKUS should be discontinued immediately; and alternative therapy should be instituted.

Peringatan dan perhatianberdasarkan golongan obatLihat label di DailyMed

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