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. 2018 Mar 7;38(10):2454–2470. doi: 10.1523/JNEUROSCI.2496-17.2018

Table 4.

Adverse effects of remifentanil: Experiment 1a

SC T1
OS T1
SC T2
OS T2
Mean SEM Mean SEM Mean SEM Mean SEM
Headache 1.38 0.13 1.06 0.06 1.19 0.10 1.06 0.06
Dizziness 1.00 0 1.00 0 1.00 0 1.00 0
Nausea 1.00 0 1.00 0 1.06 0.06 1.06 0.06
Sedation 1.44 0.13 1.13 0.09 1.44 0.24 1.38 0.18
Blurred vision 1.00 0 1.00 0 1.00 0 1.00 0
Dry skin 1.00 0 1.00 0 1.13 0.09 1.00 0
Dry mouth 1.00 0 1.00 0 1.25 0.11 1.00 0
SC T3
OS T3
SC T4
OS T4
Mean SEM Mean SEM Mean SEM Mean SEM
Headache 1.06 0.06 1.06 0.06 1.06 0.06 1.06 0.06
Dizziness 1.06 0.06 1.00 0 1.13 0.09 1.13 0.09
Nausea 1.00 0 1.00 0 1.13 0.09 1.06 0.06
Sedation 1.75 0.31 1.50 0.20 1.75 0.21 2.00 0.39
Blurred vision 1.19 0.10 1.13 0.09 1.00 0 1.00 0
Dry skin 1.06 0.06 1.00 0 1.25 0.11 1.19 0.10
Dry mouth 1.00 0 1.00 0 1.13 0.09 2.56 1.30

aBefore and after each session, subjects also answered a 7 item questionnaire regarding adverse effects. Each adverse effect could be rated as “inexistent,” “very weak,” “weak,” “moderate,” “strong,” “very strong,” and “extremely strong” (scores 1–7). SC, Saline control group; OS, opioid suspension group; T1, before Session 1; T2, after Session 1; T3, before Session 2; T4, after Session 2.