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    enzyme is responsible for converting precursor acids into prostaglandins.

    In the periphery NSAIDs work by decreasing the sensitivity of the nociceptor to painful stimuli induced by heat, trauma, or inflammation. In the central nervous system, they are thought to function as antihyperalgesics and block the increased transmission of repetitive incoming signals to higher centers. In effect, they modulate perception of pain caused by repetitive stimulation from the periphery.

    Differences Between NSAIDs

    NSAIDs vary in their potency, duration of action, and the way in which they are eliminated from the body. Another important difference is their

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    Nonsteroidal anti-inflammatory drugs (NSAIDs) are among the most commonly prescribed categories of drugs worldwide in the treatment of pain and inflammation in many conditions.

    NSAIDs are used primarily to treat inflammation, mild to moderate pain, and fever. Specific uses include the treatment of headaches, arthritis, sports injuries, and menstrual cramps. Aspirin is used to inhibit the clotting of blood and prevent strokes and heart attacks in individuals at high risk. NSAIDs also are included in many cold and allergy preparations. Two drugs in this category, ibuprofen and naproxen, also reduce fever.

    Uses

    NSAIDs are usually indicated for the treatment of acute or chronic conditions where pain and inflammation are present. These drugs also are effective in some neuropathic pain syndromes when used with other analgesics. NSAIDs are generally indicated for the symptomatic relief of the following conditions:

    • Rheumatoid arthritis
    • Osteoarthritis
    • Acute gout
    • Inflammatory arthropathies (e.g. ankylosing spondylitis, psoriatic arthritis, Reiter's syndrome)
    • Dysmenorrhoea (painful menstruation)
    • Headache and migraine
    • Postoperative pain
    • Mild-to-moderate pain due to inflammation and tissue injury
    • Back pain and sciatica.
    • Sprains, strains, and rheumatism.
    • Dental pain.
    • Pain from kidney stones (renal colic).
    • To reduce fever
    • Other painful conditions, especially where there is inflammation.

    Drugs In The Class

    There are several different types of NSAIDs:

    • Salicylates: aspirin (Ascriptin, Bayer, Ecotrin), diflunisal (Dolobid, Diflunisal Tablets), salsalate (Argesic SA, Disalcid, Salflex, Salsitab, Mono Gesic)
    • Arylalkanoic acids: diclofenac (Voltaren, Cataflam), indomethacin (Indocin)
    • 2-Arylpropionic acids (profens): ibuprofen (Motrin, Advil), ketoprofen (Orudis, Oruvail), naproxen (Naprosyn, Alleve), carprofen
    • Pyrroles: ketorolac (Toradol)
    • Enolic acids (oxicams): piroxicam (Feldene), meloxicam (Mobic)
    • Sulphonanilides: nimesulide
    • Napthylalkanones: nabumetone (Relafen)

    Mechanism Of Action

    NSAIDs work by suppressing the production of fatty acids called prostaglandins that cause inflammation and pain. They do this by blocking the action of an enzyme, cyclooxygenase (COX). This enzyme is responsible for converting precursor acids into prostaglandins.

    In the periphery NSAIDs work by decreasing the sensitivity of the nociceptor to painful stimuli induced by heat, trauma, or inflammation. In the central nervous system, they are thought to function as antihyperalgesics and block the increased transmission of repetitive incoming signals to higher centers. In effect, they modulate perception of pain caused by repetitive stimulation from the periphery.

    Differences Between NSAIDs

    NSAIDs vary in their potency, duration of action, and the way in which they are eliminated from the body. Another important difference is their

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    the treatment of acute or chronic conditions where pain and inflammation are present. These drugs also are effective in some neuropathic pain syndromes when used with other analgesics. NSAIDs are generally indicated for the symptomatic relief of the following conditions:

    • Rheumatoid arthritis
    • Osteoarthritis
    • Acute gout
    • Inflammatory arthropathies (e.g. ankylosing spondylitis, psoriatic arthritis, Reiter's syndrome)
    • Dysmenorrhoea (painful menstruation)
    • Headache and migraine
    • Postoperative pain
    • Mild-to-moderate pain due to inflammation and tissue injury
    • Back pain and sciatica.
    • Sprains, strains, and rheumatism.
    • Dental pain.
    • Pain from kidney stones (renal colic).
    • To reduce fever
    • Other painful conditions, especially where there is inflammation.

    Drugs In The Class

    There are several different types of NSAIDs:

    • Salicylates: aspirin (Ascriptin, Bayer, Ecotrin), diflunisal (Dolobid, Diflunisal Tablets), salsalate (Argesic SA, Disalcid, Salflex, Salsitab, Mono Gesic)
    • Arylalkanoic acids: diclofenac (Voltaren, Cataflam), indomethacin (Indocin)
    • 2-Arylpropionic acids (profens): ibuprofen (Motrin, Advil), ketoprofen (Orudis, Oruvail), naproxen (Naprosyn, Alleve), carprofen
    • Pyrroles: ketorolac (Toradol)
    • Enolic acids (oxicams): piroxicam (Feldene), meloxicam (Mobic)
    • Sulphonanilides: nimesulide
    • Napthylalkanones: nabumetone (Relafen)

    Mechanism Of Action

    NSAIDs work by suppressing the production of fatty acids called prostaglandins that cause inflammation and pain. They do this by blocking the action of an enzyme, cyclooxygenase (COX). This enzyme is responsible for converting precursor acids into prostaglandins.

    In the periphery NSAIDs work by decreasing the sensitivity of the nociceptor to painful stimuli induced by heat, trauma, or inflammation. In the central nervous system, they are thought to function as antihyperalgesics and block the increased transmission of repetitive incoming signals to higher centers. In effect, they modulate perception of pain caused by repetitive stimulation from the periphery.

    Differences Between NSAIDs

    NSAIDs vary in their potency, duration of action, and the way in which they are eliminated from the body. Another important difference is their

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  • Back pain and sciatica.
  • Sprains, strains, and rheumatism.
  • Dental pain.
  • Pain from kidney stones (renal colic).
  • To reduce fever
  • Other painful conditions, especially where there is inflammation.

  • Drugs In The Class

    There are several different types of NSAIDs:

    • Salicylates: aspirin (Ascriptin, Bayer, Ecotrin), diflunisal (Dolobid, Diflunisal Tablets), salsalate (Argesic SA, Disalcid, Salflex, Salsitab, Mono Gesic)
    • Arylalkanoic acids: diclofenac (Voltaren, Cataflam), indomethacin (Indocin)
    • 2-Arylpropionic acids (profens): ibuprofen (Motrin, Advil), ketoprofen (Orudis, Oruvail), naproxen (Naprosyn, Alleve), carprofen
    • Pyrroles: ketorolac (Toradol)
    • Enolic acids (oxicams): piroxicam (Feldene), meloxicam (Mobic)
    • Sulphonanilides: nimesulide
    • Napthylalkanones: nabumetone (Relafen)

    Mechanism Of Action

    NSAIDs work by suppressing the production of fatty acids called prostaglandins that cause inflammation and pain. They do this by blocking the action of an enzyme, cyclooxygenase (COX). This enzyme is responsible for converting precursor acids into prostaglandins.

    In the periphery NSAIDs work by decreasing the sensitivity of the nociceptor to painful stimuli induced by heat, trauma, or inflammation. In the central nervous system, they are thought to function as antihyperalgesics and block the increased transmission of repetitive incoming signals to higher centers. In effect, they modulate perception of pain caused by repetitive stimulation from the periphery.

    Differences Between NSAIDs

    NSAIDs vary in their potency, duration of action, and the way in which they are eliminated from the body. Another important difference is their

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  • 2-Arylpropionic acids (profens): ibuprofen (Motrin, Advil), ketoprofen (Orudis, Oruvail), naproxen (Naprosyn, Alleve), carprofen
  • Pyrroles: ketorolac (Toradol)
  • Enolic acids (oxicams): piroxicam (Feldene), meloxicam (Mobic)
  • Sulphonanilides: nimesulide
  • Napthylalkanones: nabumetone (Relafen)

  • Mechanism Of Action

    NSAIDs work by suppressing the production of fatty acids called prostaglandins that cause inflammation and pain. They do this by blocking the action of an enzyme, cyclooxygenase (COX). This enzyme is responsible for converting precursor acids into prostaglandins.

    In the periphery NSAIDs work by decreasing the sensitivity of the nociceptor to painful stimuli induced by heat, trauma, or inflammation. In the central nervous system, they are thought to function as antihyperalgesics and block the increased transmission of repetitive incoming signals to higher centers. In effect, they modulate perception of pain caused by repetitive stimulation from the periphery.

    Differences Between NSAIDs

    NSAIDs vary in their potency, duration of action, and the way in which they are eliminated from the body. Another important difference is their

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    enzyme is responsible for converting precursor acids into prostaglandins.

    In the periphery NSAIDs work by decreasing the sensitivity of the nociceptor to painful stimuli induced by heat, trauma, or inflammation. In the central nervous system, they are thought to function as antihyperalgesics and block the increased transmission of repetitive incoming signals to higher centers. In effect, they modulate perception of pain caused by repetitive stimulation from the periphery.

    Differences Between NSAIDs

    NSAIDs vary in their potency, duration of action, and the way in which they are eliminated from the body. Another important difference is their ability to cause ulcers and promote bleeding. The more an NSAID blocks Cox-1, the greater is its tendency to cause ulcers and promote bleeding.

    Choice of NSAID for chronic and disabling inflammatory joint diseases like rheumatoid arthritis and osteoarthritis is governed by age, diagnosis, degree of severity, relative gastrointestinal safety, tolerability, and relative efficacy in the given clinical situation. It is a common misconception that all NSAIDs are therapeutically equally efficacious and any one of them could be used for the given indication. Use of multiple NSAIDs should be discouraged. An agent with comparatively less gastrointestinal (GI) side effects like ibuprofen and diclofenac should be preferred in place of indomethacin, piroxicam, or naproxen, which are more gastrotoxic. In conditions where diagnosis is uncertain, the medicine should be empirically chosen and given for a week or so and if the response is adequate it should be continued until side effects mandate its withdrawal. Ankylosing spondylitis responds better to a particular NSAID like indomethacin. It is probably related to its stronger inhibition of prostaglandin synthesis.

    Aspirin is a unique NSAID, not only because of its many uses, but because it is the only NSAID that is able to inhibit the clotting of blood for a prolonged period (4 to 7 days). This prolonged effect of aspirin makes it an ideal drug for preventing the blood clots that cause heart attacks and strokes. Most other NSAIDs inhibit the clotting of blood for only a few hours.

    The major NSAIDs of potency comparable to opioids are diclofenac and ketorolac. Moderate postoperative pain, for example, may be managed using these agents. The overall analgesic effect of 30 mg of ketorolac is equivalent to that of 6 to 12 mg of morphine. Efficacy has been demonstrated for postsurgical pain including oral, orthopedic, gynecologic, and abdominal procedures. Efficacy for acute musculoskeletal pain has also been shown. Ketorolac causes ulcers more frequently than any other NSAID and is, therefore, not used for more than five days.

    Naproxen provides effective relief in acute traumatic injury and for acute pain associated with migraine, tension headache, postoperative pain, postpartum pain, pain consequent to various gynecologic procedures, and the pain of dysmenorrhea.

    Possible Side Effects

    NSAIDs are associated with a number of side effects. The two main adverse drug reactions, associated with NSAIDs relate to gastrointestinal effects and renal effects of the agents. These effects are dose-dependent, and in many cases severe enough to pose the risk of ulcer perforation, upper gastrointestinal bleeding,

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