“…The majority of adverse events involved the central nervous system and gastrointestinal system, with somnolence, dizziness, nausea, headache, constipation, sweating, vomiting and pruritus occurring in ‡5% of either treatment group. [34] Furthermore, 14 weeks' treatment with oxycodone/paracetamol IR 5 mg/325 mg was well tolerated by patients with chronic cancer-related pain, with side effects typical of opioids and not substantially different from those reported with comparator drugs (codeine, buprenorphine, pentazocine, dextropropoxyphene, all taken in combination with paracetamol). [28] Treatment with oxycodone/paracetamol IR was also well tolerated in fragile elderly female patients (n = 154; mean age 78 years) with pain associated with osteoarthritis.…”