Aceclofenac, a phenylacetic acid derivative, has antiinflammatory and analgesic properties. It is a potent inhibitor of cyclo-oxygenase which is involved in the production of prostaglandins.

Paracetamol is an analgesic and antipyretic drug that acts primarily in the CNS, increasing the pain threshold by inhibiting cyclooxygenase, enzymes involved in prostaglandin (PG) synthesis.

Celecoxib, a selective cyclooxygenase-2 (COX-2) inhibitor (prostaglandin synthesis inhibitor), is classified as a nonsteroidal anti-inflammatory drug (NSAID).

Diclofenac is an acetic acid nonsteroidal antiinflammatory drug (NSAID) with analgesic and antipyretic properties. The antiinflammatory effects of diclofenac are believed to be due to inhibition of both leukocyte migration and the enzyme cylooxygenase (COX-1 and COX-2), leading to the peripheral inhibition of prostaglandin synthesis.

Diclofenac is an acetic acid nonsteroidal antiinflammatory drug (NSAID) with analgesic and antipyretic properties. The antiinflammatory effects of diclofenac are believed to be due to inhibition of both leukocyte migration and the enzyme cylooxygenase (COX-1 and COX-2), leading to the peripheral inhibition of prostaglandin synthesis.
Paracetamol is an analgesic and antipyretic drug that acts primarily in the CNS, increasing the pain threshold by inhibiting cyclooxygenase, enzymes involved in prostaglandin (PG) synthesis.

Tramadol is a narcotic analgesic proposed for moderate to severe pain.

Paracetamol is an analgesic and antipyretic drug that acts primarily in the CNS, increasing the pain threshold by inhibiting cyclooxygenase, enzymes involved in prostaglandin (PG) synthesis.

Etoricoxib is a COX-2 selective inhibitor that reduces prostaglandins (PGs) generation from arachidonic acid.

Paracetamol is an analgesic and antipyretic drug that acts primarily in the CNS, increasing the pain threshold by inhibiting cyclooxygenase, enzymes involved in prostaglandin (PG) synthesis.

Tramadol is a narcotic analgesic proposed for moderate to severe pain.

Etoricoxib is a COX-2 selective inhibitor that reduces prostaglandins (PGs) generation from arachidonic acid.

Etoricoxib is a COX-2 selective inhibitor that reduces prostaglandins (PGs) generation from arachidonic acid.

Paracetamol is an analgesic and antipyretic drug that acts primarily in the CNS, increasing the pain threshold by inhibiting cyclooxygenase, enzymes involved in prostaglandin (PG) synthesis.

Ibuprofen, a propionic acid derivative, is a prototypical nonsteroidal anti-inflammatory agent (NSAIA) with analgesic and antipyretic properties.

A naturally occurring methylxanthine used as a pharmacological agent. Caffeine’s most notable pharmacological effect is as a central nervous system stimulant, also relaxes smooth muscle, stimulates cardiac muscle and stimulates diuresis.

Paracetamol is an analgesic and antipyretic drug that acts primarily in the CNS, increasing the pain threshold by inhibiting cyclooxygenase, enzymes involved in prostaglandin (PG) synthesis.

Diclofenac is an acetic acid nonsteroidal antiinflammatory drug (NSAID) with analgesic and antipyretic properties. The antiinflammatory effects of diclofenac are believed to be due to inhibition of both leukocyte migration and the enzyme cylooxygenase (COX-1 and COX-2), leading to the peripheral inhibition of prostaglandin synthesis.

A cyclooxygenase inhibiting, non-steroidal anti-inflammatory agent (NSAID). The antiinflammatory effect of Piroxicam may result from the reversible inhibition of cyclooxygenase, causing the peripheral inhibition of prostaglandin synthesis.

Diacerein is an anthraquinone derivative that acts via inhibition of interleukin-1β.