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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 DEVICE Cause Dysphonia? 305 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 305 reports of Dysphonia have been filed in association with DEVICE. This represents 2.4% of all adverse event reports for DEVICE.

305
Reports of Dysphonia with DEVICE
2.4%
of all DEVICE reports
7
Deaths
28
Hospitalizations

How Dangerous Is Dysphonia From DEVICE?

Of the 305 reports, 7 (2.3%) resulted in death, 28 (9.2%) required hospitalization, and 2 (0.7%) were considered life-threatening.

Is Dysphonia Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 305 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 Dysphonia?

FLUTICASONE\SALMETEROL (1,729) CABOZANTINIB S-MALATE (1,229) ADALIMUMAB (1,216) BUDESONIDE\FORMOTEROL (1,204) FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (1,143) ALBUTEROL (1,114) LENVATINIB (1,021) FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE (943) LENALIDOMIDE (931) AMIKACIN (914)

Which DEVICE Alternatives Have Lower Dysphonia Risk?

DEVICE vs DEXAMETHASONE DEVICE vs DEXAMETHASONE\DEXAMETHASONE DEVICE vs DEXAMETHASONE\NEOMYCIN DEVICE vs DEXAMETHASONE\NEOMYCIN\POLYMYXIN B DEVICE vs DEXAMETHASONE\TOBRAMYCIN

Related Pages

DEVICE Full Profile All Dysphonia Reports All Drugs Causing Dysphonia DEVICE Demographics