Does BUDESONIDE\FORMOTEROL Cause Haemoptysis? 369 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 369 reports of Haemoptysis have been filed in association with BUDESONIDE\FORMOTEROL. This represents 1.0% of all adverse event reports for BUDESONIDE\FORMOTEROL.
369
Reports of Haemoptysis with BUDESONIDE\FORMOTEROL
1.0%
of all BUDESONIDE\FORMOTEROL reports
46
Deaths
218
Hospitalizations
How Dangerous Is Haemoptysis From BUDESONIDE\FORMOTEROL?
Of the 369 reports, 46 (12.5%) resulted in death, 218 (59.1%) required hospitalization, and 74 (20.1%) were considered life-threatening.
Is Haemoptysis Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUDESONIDE\FORMOTEROL. However, 369 reports have been filed with the FAERS database.
What Other Side Effects Does BUDESONIDE\FORMOTEROL Cause?
Dyspnoea (11,158)
Asthma (10,045)
Wheezing (5,632)
Cough (4,466)
Therapeutic product effect incomplete (4,392)
Drug ineffective (3,469)
Intentional product misuse (3,399)
Loss of personal independence in daily activities (3,397)
Off label use (3,269)
Device malfunction (2,771)
What Other Drugs Cause Haemoptysis?
RIVAROXABAN (1,961)
ASPIRIN (1,255)
APIXABAN (846)
TREPROSTINIL (838)
ALBUTEROL (652)
CLOPIDOGREL BISULFATE (643)
PREDNISONE (618)
WARFARIN (555)
ADALIMUMAB (472)
TIOTROPIUM (462)
Which BUDESONIDE\FORMOTEROL Alternatives Have Lower Haemoptysis Risk?
BUDESONIDE\FORMOTEROL vs BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE
BUDESONIDE\FORMOTEROL vs BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM
BUDESONIDE\FORMOTEROL vs BUMETANIDE
BUDESONIDE\FORMOTEROL vs BUPIVACAINE
BUDESONIDE\FORMOTEROL vs BUPIVACAINE\BUPIVACAINE ANHYDROUS