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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 BECLOMETHASONE DIPROPIONATE Cause Product administration error? 25 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 25 reports of Product administration error have been filed in association with BECLOMETHASONE DIPROPIONATE (QVAR REDIHALER). This represents 0.5% of all adverse event reports for BECLOMETHASONE DIPROPIONATE.

25
Reports of Product administration error with BECLOMETHASONE DIPROPIONATE
0.5%
of all BECLOMETHASONE DIPROPIONATE reports
0
Deaths
22
Hospitalizations

How Dangerous Is Product administration error From BECLOMETHASONE DIPROPIONATE?

Of the 25 reports, 22 (88.0%) required hospitalization.

Is Product administration error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BECLOMETHASONE DIPROPIONATE. However, 25 reports have been filed with the FAERS database.

What Other Side Effects Does BECLOMETHASONE DIPROPIONATE Cause?

Asthma (911) Dyspnoea (855) Drug ineffective (770) Cough (489) Wheezing (420) Device malfunction (350)