Does DEVICE Cause Aphonia? 171 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 171 reports of Aphonia have been filed in association with DEVICE. This represents 1.3% of all adverse event reports for DEVICE.
171
Reports of Aphonia with DEVICE
1.3%
of all DEVICE reports
2
Deaths
8
Hospitalizations
How Dangerous Is Aphonia From DEVICE?
Of the 171 reports, 2 (1.2%) resulted in death, 8 (4.7%) required hospitalization, and 2 (1.2%) were considered life-threatening.
Is Aphonia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 171 reports have been filed with the FAERS database.
What Other Side Effects Does DEVICE Cause?
Blood glucose increased (2,114)
Device issue (1,417)
Product use issue (1,076)
Intercepted product preparation error (1,033)
Wrong technique in product usage process (935)
Device leakage (795)
Injection site pain (751)
Syringe issue (634)
Product quality issue (567)
Drug ineffective (488)
What Other Drugs Cause Aphonia?
AMIKACIN (465)
ADALIMUMAB (397)
OMALIZUMAB (338)
FLUTICASONE\SALMETEROL (300)
ETANERCEPT (278)
BUDESONIDE\FORMOTEROL (274)
DUPILUMAB (259)
TOFACITINIB (248)
TIOTROPIUM (227)
LENALIDOMIDE (207)
Which DEVICE Alternatives Have Lower Aphonia Risk?
DEVICE vs DEXAMETHASONE
DEVICE vs DEXAMETHASONE\DEXAMETHASONE
DEVICE vs DEXAMETHASONE\NEOMYCIN
DEVICE vs DEXAMETHASONE\NEOMYCIN\POLYMYXIN B
DEVICE vs DEXAMETHASONE\TOBRAMYCIN