MBBS · Pharmacology

Analgesics and NSAIDs

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Nonsteroidal anti-inflammatory drug — on-site reading

This reference extract addresses Nonsteroidal anti-inflammatory drug, a related subject. It does not cover every part of Analgesics and NSAIDs.. The article introduction is reproduced here, so you do not need to leave MedAtlas to read it. It may not match the latest official medical guidance.

Nonsteroidal anti-inflammatory drugs (NSAID) are members of a therapeutic drug class which reduces pain, decreases inflammation, decreases fever, and prevents blood clots. Side effects depend on the specific drug, its dose and duration of use, but largely include an increased risk of gastrointestinal ulcers and bleeds, heart attack, and kidney disease. Well-known nonsteroidal anti-inflammatory drugs include aspirin, ibuprofen, diclofenac, and naproxen, all of which are available over the counter (OTC). Paracetamol (acetaminophen) is generally not considered an NSAID because it has only minor anti-inflammatory activity.
The term nonsteroidal, common from around 1960, distinguishes these drugs from corticosteroids, another class of anti-inflammatory drugs, which during the 1950s had acquired a bad reputation due to overuse and side-effect problems after their introduction in 1948.
Nonsteroidal anti-inflammatory drugs work by inhibiting the activity of cyclooxygenase enzymes (the COX-1 and COX-2 isoenzymes). In cells, these enzymes are involved in the synthesis of key biological mediators, namely prostaglandins, which are involved in inflammation, and thromboxanes, which are involved in blood clotting.

There are two general types of NSAIDs available: non-selective and COX-2 selective. Most NSAIDs are non-selective, and inhibit the activity of both COX-1 and COX-2. These NSAIDs, while reducing inflammation, also inhibit platelet aggregation and increase the risk of gastrointestinal ulcers and bleeds. COX-2 selective inhibitors have fewer gastrointestinal side effects, but promote thrombosis, and some of these agents substantially increase the risk of heart attack. As a result, certain COX-2 selective inhibitors—such as rofecoxib—are no longer used due to the high risk of undiagnosed vascular disease. These differential effects are due to the different roles and tissue localisations of each COX isoenzyme. By inhibiting physiological COX activity, NSAIDs may cause deleterious effects on kidney function, and, perhaps as a result of water and sodium retention and decreases in renal blood flow, may lead to heart problems.

How this connects to Pharmacology

To study this topic responsibly, identify its normal structure or function, distinguish the main mechanism from its observable consequences, and ask which data can test a competing explanation. The subject foundations below outline these connections without pretending to be a specialist textbook chapter.

Text credit: Wikipedia contributors, “Nonsteroidal anti-inflammatory drug”, original article · authors & revision history · CC BY-SA 4.0. Unmodified opening extract, accessed 24 September 2026. This Wikipedia-derived section is provided under CC BY-SA 4.0; the independent MedAtlas notes and design are separate works.

On-site diagram

Analgesics and NSAIDs · visual study map

Scalable vector illustration. Labeled conceptual map, not a precise anatomical, histological or diagnostic image.
TOPIC LEARNING MAP · NOT AN ANATOMICAL PLATE01 · BackgroundNonsteroidal anti-inflammatory drugs(NSAID) are members of a therapeuticdrug class which reduces pain,…02 · Main conceptSide effects depend on the specificdrug, its dose and duration of use, butlargely include an increased…03 · Related processWell-known nonsteroidalanti-inflammatory drugs include aspirin,ibuprofen, diclofenac, and naproxen, allof…04 · Study connectionParacetamol (acetaminophen) is generallynot considered an NSAID because it hasonly minor anti-inflammatory…Analgesics and NSAIDsRead the full text below the visual · all reading is on this website

The wording in this learning map is adapted from the attributed Wikipedia background section below (CC BY-SA 4.0).

Study foundation 01

What the underlying subject studies

Pharmacology links a substance’s mechanism to the concentration reaching its target and the resulting physiological effect. Distinguish pharmacokinetics—how exposure changes—from pharmacodynamics—how a target responds.

Study foundation 02

How mechanisms and evidence connect

Benefits and harms depend on indication, route, dose, patient characteristics, organ function and interactions. A mechanism chart groups medicines for study but does not establish equivalence, superiority or an individual prescription.

Study foundation 03

How to develop a sound explanation

For each drug or drug class, identify the molecular target, intended effect, major limitations, common classes of adverse effects and how evidence and guidelines inform use. This library intentionally does not provide patient-specific doses or prescribing orders.

References and verification (optional)

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