Vicodin
Vicodin
Generic Name
Vicodin
Mechanism
- Acetaminophen: Inhibits central prostaglandin synthesis (COX‑1/COX‑2) with limited peripheral activity, providing antipyretic and analgesic effects without significant anti‑inflammatory action.
- Hydrocodone: Acts as a potent μ‑opioid receptor agonist in the brainstem and spinal cord, producing analgesia, sedation, and euphoria. It undergoes metabolic conversion to hydromorphone via CYP2D6/CYP3A4, enhancing analgesic potency.
The synergistic combination reduces required opioid dose and exploits additive analgesic effects.
Pharmacokinetics
- Absorption: Rapid oral uptake; peak plasma concentrations in ~1‑2 h.
- Bioavailability: ~80 % for hydrocodone; ~75 % for acetaminophen.
- Distribution: Hydrocodone crosses the blood‑brain barrier; acetaminophen distributes widely, predominantly to the liver.
- Metabolism:
- *Hydrocodone*: CYP2D6 & CYP3A4 → hydromorphone, 4‑hydroxy‑hydrocodone.
- *Acetaminophen*: Glucuronidation & sulfation; small proportion to N‑acetyl‑p‑benzoquinone imine (NAPQI) via CYP2E1.
- Elimination:
- Hydrocodone half‑life: 4‑6 h (with dependence on CYP profile).
- Acetaminophen half‑life: 1.5‑3 h; hepatic clearance dominates.
- Drug–Drug Interactions: CYP3A4 inhibitors (e.g., ketoconazole) elevate hydrocodone levels; CYP2D6 polymorphisms alter hydromorphone formation.
Indications
- Post‑operative or procedural acute pain (moderate to severe).
- Moderate‑to‑severe musculoskeletal trauma.
- Chronic pain settings (requires careful monitoring for dependence).
Contraindications
- Contraindications:
- Severe hepatic disease or elevated hepatic enzymes.
- Known hypersensitivity to acetaminophen or hydrocodone.
- Concomitant use of other CNS depressants (opioids, benzodiazepines, alcohol).
- Warnings:
- Opioid‑related: Respiratory depression, sedation, risk of dependence, tolerance, and withdrawal.
- Hepatic: Potential acetaminophen‑induced hepatotoxicity; monitor liver function.
- CNS: Potential for overlapping neurologic side effects when combined with other analgesics.
Dosing
- Typical adult dosing: 5 mg hydrocodone + 300 mg acetaminophen (1 tablet) every 4–6 h as needed.
- Maximum: Not exceed 4 g of acetaminophen per 24 h (≈ 12 tablets).
- For stronger pain, 15 mg/975 mg combination may be prescribed, but again monitor acetaminophen limits.
- Special populations:
- *Renal impairment*: Reduce frequency; consider lower hydrocodone dose.
- *Hepatic impairment*: Avoid or use lower hydrocodone dose; strict acetaminophen limit.
- Administration route: Oral, typically standing tablets; may be chewed if swallowing difficult.
Adverse Effects
- Common:
- Nausea, vomiting, dizziness, pruritus, constipation, dry mouth.
- Somnolence and mild sedation.
- Serious:
- Respiratory depression (especially with concomitant CNS depressants).
- Hepatotoxicity (especially in high‑dose or prolonged use).
- Seizure activity in overdose.
- QTc interval prolongation (rare).
Monitoring
- Pain scores and functional status.
- Respiratory rate (RR) and oxygen saturation in patients at risk.
- Liver function tests (ALT/AST, bilirubin) at baseline and periodically when >2 weeks of therapy or high‑dose use.
- Kidney function (serum creatinine) for dosage adjustments.
- Signs of opioid misuse: requests for extra doses, early refill, or non‑medical use.
Clinical Pearls
- Limit acetaminophen to ≤4 g/day—the primary hepatotoxic risk point.
- Use the lowest effective opioid dose: Start with 5 mg hydrocodone; adjust based on analgesic response.
- Avoid combining with SSRIs/WX (e.g., fluoxetine, fluvoxamine) that inhibit CYP2D6, increasing hydrocodone levels.
- Naloxone availability: For patients with opioid‑related risks or existing overdose, naloxone kits should be accessible.
- Patient education: Emphasize a “take‑home” strategy to prevent diversion; instruct on storage and disposal.
- Consider abuse‑deterrent formulations (if available) or alternative analgesics in patients with substance‑use disorder history.
Key references:
1. Clinical Pharmacology, 2025; 2. FDA drug label for Hydrocodone/Acetaminophen.
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