Adverse events in clinical trials of pregabalin |
The most common adverse events are dizziness (24.3% of patients) and somnolence (15.1%) |
4% of patients withdraw from clinical trials due to dizziness |
1.9% due to somnolence |
The majority of instances of dizziness and somnolence emerge within the first 1 to 2 weeks of treatment |
The majority of instances of dizziness and somnolence resolve within 1 to 2 weeks |
Most adverse events are transient and resolve prior to the end of the study |
Most adverse events are mild or moderate in severity3,20
|
Patients with a lower baseline body mass index are more likely to gain weight12
|
Managing adverse events with pregabalin |
Carefully titrate pregabalin to the highest tolerable dose (a minimum of 150 mg/day6,27) |
The initial dose, and any dose increase, should be given at night |
To set expectations, potential AEs should be discussed with the patient ahead of treatment |