Naproxen

Second line non-steroidal anti-inflammatory drug (NSAID)

Mechanism of action:  A propionic acid derivative non-steroidal anti-inflammatory drug (NSAID).  It is a non-selective inhibitor of cyclooxygenases COX-1 and COX-2, thus results in a decrease in the synthesis of prostaglandins which are involved in pain and inflammatory processes.

Presentation:  tablet. Oral suspension & effervescent tablet not available in OUH.

Suggested dose:  250mg – 500mg twice a day for adults over 50kg with normal hepatic and renal function

Co-prescribe proton pump inhibitor (PPI) cover.

Oral absorption:  Very high bioavailability, peak plasma concentration at 0.5-3 hours

Protein binding:  99% protein bound, principally to albumin

Metabolism:  Naproxen is extensively metabolized in the liver by cytochrome P450 to 6-0-desmethyl naproxen.

Elimination:  Metabolites excreted in the urine, with very little of the drug excreted unchanged

Half-life:  12-17 hours

Significant interactions (see the BNF for more interactions):

  • Aspirin: NSAIDs competitively inhibit aspirin binding to platelets so antagonise the cardioprotective effect of low-dose aspirin
  • Lithium: NSAIDs increase the serum lithium level and reduce lithium clearance, risking acute lithium intoxication
  • Anti-hypertensives: NSAIDs compromise the efficacy of anti-hypertensive drugs such as ß-adrenergic blockers, angiotensin-converting enzyme inhibitors, angiotensin receptor blockers and diuretics.
  • Methotrexate: toxic interaction between naproxen and methotrexate

 

Further prescribing information (side effects, contraindications, interactions):

BNF-Naproxen

References

Davies NM, Anderson KE. Clinical pharmacokinetics of naproxen. Drug Disposition. 1997; 32(4):268-293.https://doi.org/10.2165/00003088-199732040-00002