Table 2.
Opioid Potencies and Special Featuresa
| Drug | Parenteral (mg equivalent) | Oral | Duration (h) | Special Features |
| Morphine | 10 | 30 mg | 4 | Morphine sulfate controlled release has 12-h duration |
| Codeine | 120 | 200 mg | 4 | Ceiling effect as dose increases, low lipophilic |
| Oxycodone | 4.5 | 30 mg | 4 | Oxycontin (10, 20, 40 mg slow release) every 12 h |
| Hydromorphone | 2 | 8 mg | 5 | Suppository 12 mg = 10 mg parenteral morphine |
| Levorphanol | 2 | 4 mg | 4 | Low nausea and vomiting, low lipophilic |
| Methadone | 5 | 10 mg | 2–12 | Cumulative effect, day 3–5 decrease respiration, equianalgesic ratio varies considerably |
| Meperidine | 100 | 300 mg | 3 | κ, proconvulsant metabolite, peristaltic slowing and sphincter of Oddi decrease |
| Fentanyl | 0.1 | 25 μg sublingual | 1 (patch 72 h) | 50-μg patch = 30 mg/d morphine intramuscular/intravenous |
| Sufentanil | Not recommended | 15 μg sublingual | 1 | High potency with low volume of fluid |
| Propoxyphene | Not available | 325 mg | 4 | High dose leads to psychosis |
| Pentazocine | 60 | 150 mg | 3 | δ, κ agonist-antagonist, nasal 1 mg every 1–2 h |
| Butorphanol | 2 | Not available, 3 mg (intramuscular), 2 mg (nasal) | Nasal 1 mg every1–2 h | μ, δ, κ agonist-antagonist |
| Buprenorphine | 0.3 | 4 mg | 4–6 | Partial agonist |
| Tramadol | Not available | 150 mg | 4 | μ agonist, decreased reuptake 5-hydroxytryptamine and norepinephrine P450 metabolism |
| Nalbuphine | 10 | Not available | 3 | Agonist-antagonist |
Adapted with permission from Stern et al.33