Diclofenac is a non- steroidal anti-inflammatory drug (NSAID). It is commonly used for it's anti-inflammatory, analgesic, and antipyretic effects1.
Available as Diclofenac Sodium (slow acting) and Diclofenac Potassium (fast acting).
Diclofenac acts to suppress Prostaglandin production. Prostaglandins are a group of chemicals responsible for inflammation and pain.
Diclofenac inhibits Prostaglandin synthesis via the Cyclooxygenase (COX) 1 and 2 enzyme pathways1,2.
Common routes of administration in adults are Oral or Intravenous (IV) or Intramuscular (IM), in the following doses3:
Oral: 75–150 mg daily in 2–3 divided doses.
IV (pre-operatively in hospital settings): 75 mg, then 75 mg after 4–6 hours if required for a maximum of 2 days; maximum 150 mg per day.
IM: 75 mg 1–2 times a day for maximum 2 days
Other modes of Administration3:
Topical: Generally, found as 1% gel where 1g of gel contains 10mg of Diclofenac
Rectal: 75–150 mg daily in divided doses. For not more than 48 hours.
For more detailed information please visit the following websites:
https://bnf.nice.org.uk/drug/diclofenac-sodium.html and https://bnf.nice.org.uk/drug/diclofenac-potassium.html (Adults)
https://bnfc.nice.org.uk/drug/diclofenac-sodium.html (48) and https://bnfc.nice.org.uk/drug/diclofenac-potassium.html (49) (Children)
Toxicokinetics– The study of how the body responds to a Xenobiotic (substance found within the body that is not naturally occurring in the body)
The body’s response to Diclofenac is characterised by the following processes;
The main organs involved in these processes, making them susceptible to toxic events, are the Gastrointestinal Tract, Liver, Renal and Cardiovascular Systems.
Please click the links below.