Does BECLOMETHASONE DIPROPIONATE Cause Device defective? 43 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 43 reports of Device defective have been filed in association with BECLOMETHASONE DIPROPIONATE (QVAR REDIHALER). This represents 0.8% of all adverse event reports for BECLOMETHASONE DIPROPIONATE.
43
Reports of Device defective with BECLOMETHASONE DIPROPIONATE
0.8%
of all BECLOMETHASONE DIPROPIONATE reports
0
Deaths
3
Hospitalizations
How Dangerous Is Device defective From BECLOMETHASONE DIPROPIONATE?
Of the 43 reports, 3 (7.0%) required hospitalization.
Is Device defective Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BECLOMETHASONE DIPROPIONATE. However, 43 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 Device defective?
SOMATROPIN (1,719)
USTEKINUMAB (1,071)
SECUKINUMAB (666)
GUSELKUMAB (574)
GOLIMUMAB (539)
ABATACEPT (458)
ALBUTEROL (445)
TOCILIZUMAB (400)
INSULIN GLARGINE (397)
EXENATIDE (387)
Which BECLOMETHASONE DIPROPIONATE Alternatives Have Lower Device defective 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