Does PULMICORT Cause Intentional product misuse? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Intentional product misuse have been filed in association with PULMICORT. This represents 10.3% of all adverse event reports for PULMICORT.
8
Reports of Intentional product misuse with PULMICORT
10.3%
of all PULMICORT reports
0
Deaths
1
Hospitalizations
How Dangerous Is Intentional product misuse From PULMICORT?
Of the 8 reports, 1 (12.5%) required hospitalization.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PULMICORT. However, 8 reports have been filed with the FAERS database.
What Other Side Effects Does PULMICORT Cause?
What Other Drugs Cause Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)