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    HomeMedication GuideBudesonide Safety
    Corticosteroid

    Budesonide: What to Know Before You Take It

    Also sold as Pulmicort, Entocort

    What Budesonide Is Used For

    Use s Temporarily relieves these symptoms of hay fever or other upper respiratory allergies: • nasal congestion • runny nose • itchy nose • sneezing

    Warnings

    Warnings Do not use in children under 6 years of age if you have ever had an allergic reaction to any of the ingredients Ask a doctor before use if you have had recent nose ulcers or nose surgery have had a nose injury that has not healed are using a steroid medicine for asthma, allergies or skin rash have an eye infection have or had glaucoma or cataracts When using this product the growth rate of some children may be slower some symptoms may get better on the first day of treatment. It may take up to two weeks of daily use to feel the most symptom relief. do not share this bottle with anyone else as this may spread germs remember to tell your doctor about all the medicines you take, including this one Stop use and ask a doctor if you have, or come into contact with someone who has, chickenpox, measles or tuberculosis you have or develop symptoms of an infection such as persistent fever you have any change in vision you have severe or frequent nosebleeds If pregnant or breast-feeding , ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).

    Budesonide Drug Interactions (2)

    Check Budesonide against your full medication list in our free Interaction Checker

    Most-Reported Side Effects

    Based on 160,438 reports in the FDA Adverse Event Reporting System (FAERS). Reports do not prove the drug caused the effect.

    dyspnoea25,017asthma16,403drug ineffective13,220off label use11,974cough11,405fatigue8,990pneumonia8,520wheezing7,837headache7,746malaise6,865nausea6,741death6,056

    Explore full Budesonide safety data in our free FDA Safety Explorer

    FDA Recalls (8)

    Class IIOngoingMay 29, 2026

    Presence of Foreign Substance:This recall has been initiated in response to a product quality complaint reported for black/brown specs and particles within the ampoule solution

    Recalling firm: SUN PHARMACEUTICAL INDUSTRIES INC

    Class IIOngoingJun 30, 2025

    Lack of Assurance of Sterility: A market complaint was received for leakage and empty ampoule.

    Recalling firm: Cipla USA, Inc.

    Class IIOngoingMay 14, 2025

    Defective delivery system

    Recalling firm: AsttraZeneca Pharmaceuticals LP

    Class IIOngoingJan 8, 2024

    Failed Dissolution Specifications

    Recalling firm: Teva Pharmaceuticals USA, Inc

    Class IITerminatedSep 15, 2022

    Lack of Assurance of Sterility

    Recalling firm: CIPLA

    Class IITerminatedMar 15, 2021

    CGMP Deviations: Intermittent exposure to temperature excursion during storage.

    Recalling firm: Cardinal Health Inc.

    Class IIITerminatedJan 11, 2013

    Does Not Meet Monograph: Budesonide may be slightly above or below the specification range.

    Recalling firm: AstraZeneca LP

    Class IIITerminatedJan 11, 2013

    Does Not Meet Monograph: Budesonide may be slightly above or below the specification range.

    Recalling firm: AstraZeneca LP

    This information is educational — not medical advice.

    This page is provided for general educational purposes and summarizes publicly available data from sources such as the U.S. Food & Drug Administration. It is not a substitute for the judgment of a licensed clinician and should not be used to start, stop, or change any medication. It may be incomplete or out of date, and individual circumstances vary. Always talk with your prescriber or pharmacist about your specific medications and health conditions. If you think you may have a medical emergency, call 911.

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