Drug Guide
Acetaminophen
Classification
Therapeutic: Analgesic, Antipyretic
Pharmacological: Cyclooxygenase (COX) inhibitor (central action)
FDA Approved Indications
- Relief of mild to moderate pain
- Reduction of fever
Mechanism of Action
Acetaminophen exerts its analgesic and antipyretic effects primarily through central inhibition of COX enzymes in the brain, which reduces prostaglandin synthesis involved in pain and fever regulation.
Dosage and Administration
Adult: Regular strength: 325-1000 mg every 4-6 hours as needed, not to exceed 4 grams per day. Extended-release formulations vary; always follow package instructions.
Pediatric: Based on weight, typically 10-15 mg/kg/dose every 4-6 hours as needed. Max dose depends on weight and age, generally not exceeding 75 mg/kg/day.
Geriatric: Similar to adult dosing; assess renal and hepatic function, adjust if necessary.
Renal Impairment: Adjust dose; use with caution, monitoring hepatic function.
Hepatic Impairment: Use with caution; dose reduction may be necessary, especially in chronic use.
Pharmacokinetics
Absorption: Rapidly absorbed from gastrointestinal tract.
Distribution: Widely distributed, crosses blood-brain barrier.
Metabolism: Primarily hepatic via conjugation to inactive glucuronide and sulfate metabolites; minor pathway involves CYP enzymes to a toxic metabolite (NAPQI).
Excretion: Renally excreted as conjugates.
Half Life: Approximately 2-3 hours in healthy adults.
Contraindications
- Known hypersensitivity to acetaminophen.
- Severe hepatic impairment.
Precautions
- Use with caution in patients with hepatic disease or alcoholism.
- Monitor hepatic enzymes in prolonged therapy.
- Avoid concomitant use with other hepatotoxic drugs or alcohol.
Adverse Reactions - Common
- Hepatotoxicity (Rare but serious, dose-related)
- Rash (Uncommon)
- Other hypersensitivity reactions (e.g., angioedema, anaphylaxis) (Rare)
Adverse Reactions - Serious
- Acute liver failure (Rare, but potentially fatal)
- Anaphylaxis (Rare)
Drug-Drug Interactions
- Alcohol (increases hepatotoxicity risk)
- Warfarin (may enhance anticoagulant effect)
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor pain severity, temperature, baseline hepatic function.
Diagnoses:
- Risk for hepatotoxicity
- Ineffective pain management
Implementation: Administer with food or water if gastrointestinal upset occurs. Monitor hepatic enzymes during prolonged therapy.
Evaluation: Assess pain relief, reduction in fever, and absence of adverse effects.
Patient/Family Teaching
- Do not exceed recommended dose.
- Avoid alcohol consumption.
- Notify healthcare provider if symptoms of liver damage occur (e.g., jaundice, dark urine).
- Use properly measured dosing devices.
Special Considerations
Black Box Warnings:
- Severe hepatotoxicity risk with overdose or chronic use.
- Risk increases with alcohol use.
Genetic Factors: Genetic polymorphisms may influence metabolism, but routine testing is not standard.
Lab Test Interference: May interfere with certain blood tests, such as liver function tests.
Overdose Management
Signs/Symptoms: Nausea, vomiting, jaundice, confusion, hepatotoxicity signs.
Treatment: (Administer antidote) N-acetylcysteine ideally within 8-10 hours of overdose to prevent liver damage.
Storage and Handling
Storage: Store at room temperature, away from moisture and heat.
Stability: Stable when stored properly.