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Table 3 Adverse events [n (%)] occurring in ≥ 10% of subjects in any treatment group

From: Pharmacokinetic profile of a 24-hour controlled-release OROS® formulation of hydromorphone in the presence and absence of food

Event

Treatment Regimen A (fasting; n= 28)

Treatment Regimen B (fed; n= 29)

Treatment Regimen C (fasting with naltrexone block; n= 27)

Nausea

6 (21.4)

9 (31.0)

7 (25.9)

Asthenia

6 (21.4)

8 (27.6)

7 (25.9)

Dizziness

8 (28.6)

5 (17.2)

3 (11.1)

Pruritus

2 (7.1)

4 (13.8)

9 (33.3)

Headache

6 (21.4)

3 (10.3)

4 (14.8)

Vomiting

2 (7.1)

3 (10.3)

5 (18.5)