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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 Asthenopia? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Asthenopia have been filed in association with DEVICE. This represents 0.0% of all adverse event reports for DEVICE.

5
Reports of Asthenopia with DEVICE
0.0%
of all DEVICE reports
0
Deaths
1
Hospitalizations

How Dangerous Is Asthenopia From DEVICE?

Of the 5 reports, 1 (20.0%) required hospitalization.

Is Asthenopia Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 5 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 Asthenopia?

HYPROMELLOSE 2910 (346) POLYETHYLENE GLYCOL 400\PROPYLENE GLYCOL (299) DUPILUMAB (249) CENEGERMIN-BKBJ (124) CYCLOSPORINE (118) PROPYLENE GLYCOL (100) FINGOLIMOD (96) ONABOTULINUMTOXINA (85) MINERAL OIL\PETROLATUM (82) ADALIMUMAB (75)

Which DEVICE Alternatives Have Lower Asthenopia 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 Asthenopia Reports All Drugs Causing Asthenopia DEVICE Demographics