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. Author manuscript; available in PMC: 2013 Jun 1.
Published in final edited form as: Behav Pharmacol. 2012 Jun;23(3):271–279. doi: 10.1097/FBP.0b013e3283536d6f

Table 3.

Peak participant ratings (mean ± SEM) of subjective drug effects as measured by the DEQ during the intermittent and daily dosing phases during the first and second session as a function of cumulative oxycodone dose. Participants rated their subjective drug liking by indicating on a scale from -4, corresponding to “Dislike very much,” to 4, corresponding to “Like very much.” Participants rated subjective drug strength and desire to take the dose again on a scale of 0–4, 0 corresponding to “No effects at all” and 4 corresponding to “Very strong effects.”

Dose (mg/70 kg) INTERMITTENT DAILY
Session 1 Session 2 Session 1 Session 2
LIKE 0 0.1 (0.1)* 0.5 (0.3)* 0.6 (0.3)* 0.1 (0.1)*
5 0.8 (0.4)# 1.4 (0.4) 1.1 (0.2) 0.6 (0.2)
20 1.3 (0.4) 2.1 (0.5) 1.6 (0.4) 1.3 (0.4)
STRONG 0 0.8 (0.4)* 0.8 (0.3)* 0.7 (0.2)* 0.8 (0.3)*
5 1.6 (0.8)#,† 2.2 (0.3) 2.1 (0.3)# 0.9 (0.3)
20 3.1 (0.2) 3.3 (0.2) 3.3 (0.2) 2.8 (0.3)
TAKE AGAIN 0 1.9 (0.5)# 1.3 (0.4)* 1.7 (0.4) 1.4 (0.3)
5 1.9 (0.5) 2.2 (0.5) 1.7 (0.4)# 1.4 (0.3)
20 1.8 (0.5) 2.1 (0.5) 2.0 (0.4) 1.3 (0.4)

Significant differences between placebo and oxycodone (cumulative doses of 5 and 20 mg/70kg) within a session are indicated by * (p ≤ 0.05). Within each phase, significant differences between sessions in placebo or oxycodone effects are indicated by # (p ≤ 0.05). Between phases, significant differences between corresponding sessions for placebo or oxycodone effects are indicated by (p ≤ 0.05).