This page shows results related to Ativan and Disorientation from the FDA Adverse Event Reporting System (AERS). The adverse event Disorientation has been reported to the FDA a total of 24 times for Ativan.
Learn More About Ativan Adverse EventsThe Proportional Reporting Ratio (PRR) for Ativan and Disorientation is 2. The chart below compares this proportional reporting ratio of Disorientation for drugs used in similar therapies to Ativan. The higher the proportional reporting ratio is, the more likely a drug is associated with Disorientation.
| Disorientation | |
| Ativan | 2 |
NOTE: The PRR metric is still in Beta testing by DrugCite and is intended for use by researchers only.
Of those reporting Disorientation, why were they taking Ativan?
| Anxiety | 7 |
| Nausea | 2 |
| Agitation | 1 |
| Drug Abuser | 1 |
| Stress | 1 |
| Tremor | 1 |
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Which medications reported to the FDA are most commonly associated with Disorientation?
| Lyrica | 499 |
| Chantix | 411 |
| Vioxx | 303 |
| Lipitor | 276 |
| Cymbalta | 270 |
| Avonex | 268 |
| Seroquel | 252 |
| Paxil | 243 |
| Byetta | 227 |
| Humira | 219 |
| Exelon | 213 |
| Show More |
