Alaway and Asthenopia

This page shows results related to Alaway and Asthenopia from the FDA Adverse Event Reporting System (AERS). The adverse event Asthenopia has been reported to the FDA a total of 4 times for Alaway.

Learn More About Alaway Adverse Events

Safety Comparison of Asthenopia in Alaway and Related Drugs

The Proportional Reporting Ratio (PRR) for Alaway and Asthenopia is 65. The chart below compares this proportional reporting ratio of Asthenopia for drugs used in similar therapies to Alaway. The higher the proportional reporting ratio is, the more likely a drug is associated with Asthenopia.


NOTE: The PRR metric is still in Beta testing by DrugCite and is intended for use by researchers only.

People Reporting Asthenopia Used Alaway For the Following Reasons

Of those reporting Asthenopia, why were they taking Alaway?

Seasonal Allergy
Allergy To Animal
Eye Pruritus

Scientific Publications on Asthenopia

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