Does RHINOCORT AQUA 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 RHINOCORT AQUA. This represents 22.5% of all adverse event reports for RHINOCORT AQUA.
11
Reports of Intentional product misuse with RHINOCORT AQUA
22.5%
of all RHINOCORT AQUA reports
0
Deaths
1
Hospitalizations
How Dangerous Is Intentional product misuse From RHINOCORT AQUA?
Of the 11 reports, 1 (9.1%) required hospitalization, and 1 (9.1%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RHINOCORT AQUA. However, 11 reports have been filed with the FAERS database.
What Other Side Effects Does RHINOCORT AQUA Cause?
Drug dose omission (14)
Off label use (12)
Nasal congestion (8)
Headache (7)
Malaise (7)
Sinusitis (7)
Cough (5)
Dizziness (5)
Sinus disorder (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)