Paracetamol
Mechanism of Action
- Central analgesic effect via activation of descending serotonergic pathways.
- May inhibit prostaglandin (PG) synthesis or influence cannabinoid receptors.
Administration
- Oral (suspension, tablets, liquid), IV, and rectal (suppository).
Side Effects
- Common:
- Drowsiness and tiredness
- Rashes and itching
- Overdose:
- Liver damage/failure
- Abdominal pain, nausea, vomiting
- Seizures, coma, and death
Metabolism and Excretion
- Readily absorbed from the gastrointestinal tract (peak plasma in 10-60 minutes).
- Distributed into most body tissues.
- Metabolized extensively in the liver.
- Excreted in urine as inactive glucuronide and sulfate conjugates (less than 5% unchanged).
- Metabolites include a hydroxylated intermediate with hepatotoxic activity.
- Overdosage (more than 150mg/kg or 10g total ingested) can cause irreversible liver damage if untreated.
Contraindications
- Hypersensitivity to paracetamol or excipients.
- IV Paracetamol: Severe liver disease.
- Rectal Paracetamol: Avoid in neutropenic patients.