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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 Dry mouth? 40 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 40 reports of Dry mouth have been filed in association with DEVICE. This represents 0.3% of all adverse event reports for DEVICE.

40
Reports of Dry mouth with DEVICE
0.3%
of all DEVICE reports
2
Deaths
8
Hospitalizations

How Dangerous Is Dry mouth From DEVICE?

Of the 40 reports, 2 (5.0%) resulted in death, 8 (20.0%) required hospitalization, and 3 (7.5%) were considered life-threatening.

Is Dry mouth Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 40 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 Dry mouth?

ADALIMUMAB (2,433) METHOTREXATE (2,356) RITUXIMAB (2,297) TOFACITINIB (2,267) ETANERCEPT (2,124) PREDNISONE (2,030) CETIRIZINE (1,988) SECUKINUMAB (1,893) TOCILIZUMAB (1,866) LEFLUNOMIDE (1,821)

Which DEVICE Alternatives Have Lower Dry mouth 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 Dry mouth Reports All Drugs Causing Dry mouth DEVICE Demographics