Alaway and Nausea

This page shows results related to Alaway and Nausea from the FDA Adverse Event Reporting System (AERS). The adverse event Nausea has been reported to the FDA a total of 3 times for Alaway.

Learn More About Alaway Adverse Events

Safety Comparison of Nausea in Alaway and Related Drugs

The Proportional Reporting Ratio (PRR) for Alaway and Nausea is 0. The chart below compares this proportional reporting ratio of Nausea for drugs used in similar therapies to Alaway. The higher the proportional reporting ratio is, the more likely a drug is associated with Nausea.


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

People Reporting Nausea Used Alaway For the Following Reasons

Of those reporting Nausea, why were they taking Alaway?

Ocular Hyperaemia
Seasonal Allergy
Eye Pruritus

Scientific Publications on Nausea

Powered by Google