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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does BUDESONIDE Cause Sepsis? 192 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 192 reports of Sepsis have been filed in association with BUDESONIDE (BREYNA). This represents 0.8% of all adverse event reports for BUDESONIDE.

192
Reports of Sepsis with BUDESONIDE
0.8%
of all BUDESONIDE reports
110
Deaths
98
Hospitalizations

How Dangerous Is Sepsis From BUDESONIDE?

Of the 192 reports, 110 (57.3%) resulted in death, 98 (51.0%) required hospitalization, and 43 (22.4%) were considered life-threatening.

Is Sepsis Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BUDESONIDE. However, 192 reports have been filed with the FAERS database.

What Other Side Effects Does BUDESONIDE Cause?

Asthma (4,544) Dyspnoea (4,441) Drug ineffective (4,384) Off label use (3,033) Wheezing (2,590) Cough (2,269) Therapeutic product effect incomplete (2,191) Loss of personal independence in daily activities (1,890) Condition aggravated (1,548) Fatigue (1,508)

What Other Drugs Cause Sepsis?

RITUXIMAB (4,043) CYCLOPHOSPHAMIDE (4,041) METHOTREXATE (3,933) ADALIMUMAB (3,169) DEXAMETHASONE (3,150) LENALIDOMIDE (2,956) VINCRISTINE (2,791) DOXORUBICIN (2,740) PREDNISONE (2,634) PREDNISOLONE (2,281)

Which BUDESONIDE Alternatives Have Lower Sepsis Risk?

BUDESONIDE vs BUDESONIDE\FORMOTEROL BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM BUDESONIDE vs BUMETANIDE BUDESONIDE vs BUPIVACAINE

Related Pages

BUDESONIDE Full Profile All Sepsis Reports All Drugs Causing Sepsis BUDESONIDE Demographics