This page shows results related to Alaway and Somnolence from the FDA Adverse Event Reporting System (AERS). The adverse event Somnolence has been reported to the FDA a total of 4 times for Alaway.
Learn More About Alaway Adverse EventsThe Proportional Reporting Ratio (PRR) for Alaway and Somnolence is 1. The chart below compares this proportional reporting ratio of Somnolence for drugs used in similar therapies to Alaway. The higher the proportional reporting ratio is, the more likely a drug is associated with Somnolence.
| Somnolence | |
| Alaway | 1 |
NOTE: The PRR metric is still in Beta testing by DrugCite and is intended for use by researchers only.
Of those reporting Somnolence, why were they taking Alaway?
| Eye Pruritus | 2 |
| Ocular Hyperaemia | 1 |
| Eye Allergy | 1 |
Which medications reported to the FDA are most commonly associated with Somnolence?
| Lyrica | 3618 |
| Seroquel | 1854 |
| Chantix | 1779 |
| Strattera | 995 |
| Neurontin | 989 |
| Cymbalta | 935 |
| Risperdal | 877 |
| Duragesic-100 | 799 |
| Paxil | 776 |
| Zyprexa | 774 |
| Oxycontin | 733 |
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