This page shows results related to Alaway and Condition Aggravated from the FDA Adverse Event Reporting System (AERS). The adverse event Condition Aggravated has been reported to the FDA a total of 36 times for Alaway.
Learn More About Alaway Adverse EventsThe Proportional Reporting Ratio (PRR) for Alaway and Condition Aggravated is 10. The chart below compares this proportional reporting ratio of Condition Aggravated for drugs used in similar therapies to Alaway. The higher the proportional reporting ratio is, the more likely a drug is associated with Condition Aggravated.
| Condition Aggravated | |
| Alaway | 10 |
NOTE: The PRR metric is still in Beta testing by DrugCite and is intended for use by researchers only.
Of those reporting Condition Aggravated, why were they taking Alaway?
| Eye Pruritus | 11 |
| Eye Allergy | 7 |
| Seasonal Allergy | 5 |
| Ocular Hyperaemia | 4 |
| Off Label Use | 4 |
| Eye Irritation | 3 |
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Which medications reported to the FDA are most commonly associated with Condition Aggravated?
| Avonex | 3144 |
| Enbrel | 2988 |
| Rebif | 1112 |
| Humira | 996 |
| Tracleer | 778 |
| Pristiq | 703 |
| Effexor Xr | 644 |
| Forteo | 643 |
| Remicade | 611 |
| Vioxx | 609 |
| Digoxin | 544 |
| Show More |
