Does BECLOMETHASONE DIPROPIONATE Cause Device issue? 214 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 214 reports of Device issue have been filed in association with BECLOMETHASONE DIPROPIONATE (QVAR REDIHALER). This represents 4.2% of all adverse event reports for BECLOMETHASONE DIPROPIONATE.
214
Reports of Device issue with BECLOMETHASONE DIPROPIONATE
4.2%
of all BECLOMETHASONE DIPROPIONATE reports
0
Deaths
4
Hospitalizations
How Dangerous Is Device issue From BECLOMETHASONE DIPROPIONATE?
Of the 214 reports, 4 (1.9%) required hospitalization.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BECLOMETHASONE DIPROPIONATE. However, 214 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 delivery system issue (212)
Drug hypersensitivity (197)
What Other Drugs Cause Device issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which BECLOMETHASONE DIPROPIONATE Alternatives Have Lower Device issue 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