This page shows results related to Alaway and Dizziness from the FDA Adverse Event Reporting System (AERS). The adverse event Dizziness has been reported to the FDA a total of 5 times for Alaway.
Learn More About Alaway Adverse EventsThe Proportional Reporting Ratio (PRR) for Alaway and Dizziness is 1. The chart below compares this proportional reporting ratio of Dizziness for drugs used in similar therapies to Alaway. The higher the proportional reporting ratio is, the more likely a drug is associated with Dizziness.
| Dizziness | |
| Alaway | 1 |
NOTE: The PRR metric is still in Beta testing by DrugCite and is intended for use by researchers only.
Of those reporting Dizziness, why were they taking Alaway?
| Eye Allergy | 2 |
| Eye Pruritus | 2 |
| Ocular Hyperaemia | 1 |
Which medications reported to the FDA are most commonly associated with Dizziness?
| Vioxx | 5116 |
| Lyrica | 4661 |
| Forteo | 4274 |
| Byetta | 3038 |
| Humira | 2856 |
| Chantix | 2740 |
| Enbrel | 2608 |
| Tysabri | 2531 |
| Fosamax | 2486 |
| Paxil | 2370 |
| Digoxin | 2205 |
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