Does PULMICORT RESPULES Cause Intentional product misuse? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Intentional product misuse have been filed in association with PULMICORT RESPULES. This represents 28.2% of all adverse event reports for PULMICORT RESPULES.
11
Reports of Intentional product misuse with PULMICORT RESPULES
28.2%
of all PULMICORT RESPULES reports
0
Deaths
0
Hospitalizations
How Dangerous Is Intentional product misuse From PULMICORT RESPULES?
Of the 11 reports.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PULMICORT RESPULES. However, 11 reports have been filed with the FAERS database.
What Other Side Effects Does PULMICORT RESPULES Cause?
Off label use (21)
Asthma (7)
Dyspnoea (7)
Cough (5)
Drug dose omission (5)
Malaise (5)
Wheezing (5)
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)