Does BECLOMETHASONE DIPROPIONATE Cause Product storage error? 27 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 27 reports of Product storage error have been filed in association with BECLOMETHASONE DIPROPIONATE (QVAR REDIHALER). This represents 0.5% of all adverse event reports for BECLOMETHASONE DIPROPIONATE.
27
Reports of Product storage error with BECLOMETHASONE DIPROPIONATE
0.5%
of all BECLOMETHASONE DIPROPIONATE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product storage error From BECLOMETHASONE DIPROPIONATE?
Of the 27 reports.
Is Product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BECLOMETHASONE DIPROPIONATE. However, 27 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)
Malaise (229)
Therapeutic product effect incomplete (216)
Device issue (214)
Device delivery system issue (212)
What Other Drugs Cause Product storage error?
INSULIN GLARGINE (7,743)
EVOLOCUMAB (6,606)
ETANERCEPT (3,653)
DENOSUMAB (3,621)
ERENUMAB-AOOE (2,958)
DUPILUMAB (2,631)
ALBUTEROL (2,474)
ABATACEPT (2,101)
DARBEPOETIN ALFA (1,619)
INSULIN LISPRO (1,448)
Which BECLOMETHASONE DIPROPIONATE Alternatives Have Lower Product storage error Risk?
BECLOMETHASONE DIPROPIONATE vs BECLOMETHASONE DIPROPIONATE\FORMOTEROL
BECLOMETHASONE DIPROPIONATE vs BECLOMETHASONE\FORMOTEROL
BECLOMETHASONE DIPROPIONATE vs BEDAQUILINE
BECLOMETHASONE DIPROPIONATE vs BELANTAMAB MAFODOTIN
BECLOMETHASONE DIPROPIONATE vs BELANTAMAB MAFODOTIN-BLMF