TABLE 3.
Adverse Events, No. | ||||||
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Totala | Emergency Departmentb | 24-hour Follow-Up | ||||
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Symptoms | Intranasal Ketorolac | Intravenous Ketorolac | Intranasal Ketorolac | Intravenous Ketorolac | Intranasal Ketorolac | Intravenous Ketorolac |
Nausea | 2 | 1 | 0 | 1 | 2 | 0 |
Dizziness | 1 | 1 | 0 | 0 | 1 | 1 |
Sleepiness | 0 | 1 | 0 | 1 | 0 | 0 |
Otherc | 2 | 3 | 2 | 3 | 0 | 0 |
Total | 5 | 6 | 2 | 5 | 3 | 1 |
For the intranasal ketorolac group, 4 patients reported 5 adverse events. For the intravenous ketorolac group, 6 patients reported 6 events. Adverse events documented were not present prior to initial assessment at 60 min after study medication administration.
Includes adverse events identified at 60 and 120 min after study medication administration.
Other includes “feeling cold”, “less focus, feel off”, transient extremity sensory complaints.