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rdfs:label
비스테로이드성 항염증제 Nesteroidní antiflogistikum Нестероїдні протизапальні препарати NSAID's FANS Antiinflamatorio no esteroideo 非甾体抗炎药 Antiinflamatorio ez-esteroide Druga Frith-athlastach Neamhstéaróideach Anti-inflamatórios não esteroides 非ステロイド性抗炎症薬 Μη στεροειδή αντιφλεγμονώδη φάρμακα Nichtsteroidales Antirheumatikum Icke-steroida antiinflammatoriska läkemedel دواء لاستيرويدي مضاد للالتهاب Niesteroidowe leki przeciwzapalne Anti-inflammatoire non stéroïdien Obat antiinflamasi nonsteroid Antiinflamatori no esteroidal Nonsteroidal anti-inflammatory drug Нестероидные противовоспалительные препараты
rdfs:comment
Μη στεροειδή αντιφλεγμονώδη φάρμακα (ΜΣΑΦ) ( Nonsteroidal anti-inflammatory drugs ή NSAIDs) είναι μια κατηγορία φαρμάκων που μειώνει τον πόνο, ελαττώνει τον πυρετό, αποτρέπει τους θρόμβους αίματος και σε μεγαλύτερες δόσεις, μικραίνει φλεγμονές. Οι παρενέργειες εξαρτώνται από το συγκεκριμένο φάρμακο, αλλά περιλαμβάνει κυρίως αυξημένο κίνδυνο γαστρεντερικών ελκών και αιμορραγιών, έμφραγμα του μυοκαρδίου και νεφροπάθεια. 비스테로이드성 항염증제(영어: nonsteroidal anti-inflammatory drug , NSAID)는 진통 작용, 해열 작용, 항염증 작용이 있는 약이다. 손쉽게 사용할 수 있는 NSAIDs는 아스피린, 이부프로펜 및 나프록센이다. 대부분의 국가에서 일반의약품이므로 처방전 없이 구매가 가능하다. 아세트아미노펜은 신체의 항염증 활성이 미미하기 때문에 일반적으로 NSAID로 간주되지 않는다. Os anti-inflamatórios não esteroides (abreviadamente, AINEs ou NSAIDs, do inglês Non-steroidal anti-inflammatory drugs) são um grupo variado de fármacos que têm em comum a capacidade de controlar a inflamação, de analgesia (reduzir a dor), e de combater a febre. O termo foi criado em 1960 por Michael W. Whitehouse. Apesar de em sua maioria serem constituídos por ácidos orgânicos, sua estrutura química não é relacionada. Caracterizam-se por inibir a atividade de subtipos da ciclo-oxigenase, impedindo assim a síntese de eicosanoides pela via metabólica da cascata do ácido araquidónico.Fazem parte deste grupo medicamentos muito conhecidos, em parte por alguns já estarem disponíveis há muito tempo, por serem de venda livre (MNSRM), e pelo vasto número de situações em que são usados. Alguns nom Les anti-inflammatoires non stéroïdiens ou antiinflammatoires non stéroïdiens, souvent abrégés en AINS, sont des médicaments aux propriétés antalgiques, antipyrétiques et anti-inflammatoires. Ils réduisent la douleur, la fièvre et l'inflammation. Le terme « non stéroïdien » est utilisé pour les distinguer des glucocorticoïdes (appelés communément corticoïdes), qui (parmi un large éventail d'effets) ont une semblable action anti-inflammatoire (dépression des eicosanoïdes). Le terme a été introduit dans les années 1960 pour marquer la distinction avec la cortisone et ses dérivés. Els antiinflamatoris no esteroidals (o, més rarament no esteroideus) (AINE i, més rarament, AINES en plural) són substàncies químiques amb efecte antiinflamatori, analgèsic i antipirètic, efectes que són semblants als dels corticoides però sense les conseqüències secundàries. Són un grup variat i químicament heterogeni de fàrmacs que per la seva acció antiinflamatòria, analgèsica, i antipirètica redueixen els símptomes de la inflamació, el dolor i la febre respectivament. Actuen bloquejant la síntesi de prostaglandines. Tots exerceixen els seus efectes per acció de la inhibició de l'enzim . Els AINE contraresten l'efecte hipotensor del diürètics, betablocadors, IECA o fàrmacs com la o la perquè part de la seva acció hipotensora l'exerceixen aquestes substàncies a través de l'alliberament Is éard is Druga Frith-athlastach Neamhstéaróideach nó DFANSa (Béarla: NSAIDs) ann ná aicme drugaí a mhúchann pian sa duine. Niesteroidowe leki przeciwzapalne, niesterydowe leki przeciwzapalne, NLPZ, NSLPZ – szeroka, niejednorodna grupa leków przeciwzapalnych, przeciwbólowych i przeciwgorączkowych. Ich działanie polega na hamowaniu cyklooksygenazy prostaglandynowej (COX), co w 1971 wyjaśnił John Vane (Nobel 1982). W 1992 D. Simmonds wykazał, że istnieją co najmniej dwie izoformy cyklooksygenazy – obecna stale w organizmie COX-1 i wyzwalana w toku procesu zapalnego COX-2. Hamowanie tej drugiej jest istotne z klinicznego punktu widzenia, a blokowanie pierwszej może prowadzić do wystąpienia objawów ubocznych ze strony układu pokarmowego w leczeniu za pomocą NLPZ. Nazywane są niesteroidowymi ze względu na strukturę, odmienną od innych leków mających właściwości przeciwzapalne – kortykosteroidów. مضادات الالتهاب اللاستيرويدية هي أدوية ذات مفعول مسكن وخافض للحرارة في الجرعات العادية وتكون لها تأثيرات مضادة للالتهاب في الجرعات العالية. ويستخدم مصطلح «لاستيرويدي» لتمييزها عن الأدوية الستيرويدية التي لديها تأثيرات (من بين تأثيرات عديدة أخرى) كابتة للإيكوزانويد ومضادة للالتهاب. مضادات الالتهاب اللاستيرويدية تمتاز على غيرها من مسكنات الآلام بأنها غير مخدرة لذلك فهي لا تسبب الإدمان. ومن أكثر الأعضاء بروزاً في هذه المجموعة من الأدوية هو الأسبرين، الآيبوبروفين والنابروكسين وذلك يرجع جزئياً إلى أنهم أدوية بدون وصفة في العديد من البلدان. ولايعتبر الباراسيتامول عضواً في هذه المجموعة. Icke-steroida anti-inflammatoriska medel (NSAID från engelskans non-steroidal anti-inflammatory drug) är en grupp läkemedel med inflammationsdämpande, smärtlindrande och febernedsättande verkan. Kategorin icke-steroida antiinflammatoriska läkemedel infördes i slutet av 1950 för att klargöra skillnaden mellan dessa läkemedel och kortisonpreparat vilka också har antiinflammatorisk verkan. NSAID har ATC-kod M01A under namnet "icke-steroida antiinflammatoriska/antireumatiska medel (NSAID)". Antiinflamatorio ez-esteroidea (AIEE) hantura, sukarra eta mina tratatzeko erabilitako esteroidea ez den sendagaia da. AIEE talde honen barnean aurkitzen diren sendagaiak kimikoki oso desberdinak izan daitezkeen arren, denek ekintza mekanismo bera dute, entzimaren inhibizioa. Antiinflamatorio naturalak, organismoak berak jariatzen dituenak, kortikoideen deribatuak dira, jatorri esteroideko eta hanturaren aurkako ekintza handia duten substantziak, baina aldi berean eragin kaltegarri ugari dituztenak. AIEEak ordea, ez esteroideak direnez, albo ondorio gutxiago dituzte. Нестероидные противовоспалительные препараты (нестероидные противовоспалительные средства/агенты, НПВП, НПВС, НСПВП, NSAID) — группа лекарственных средств, обладающих обезболивающим, жаропонижающим и , уменьшают боль, лихорадку и воспаление. Использование в названии термина «нестероидные» подчёркивает их отличие от глюкокортикоидов, которые обладают не только противовоспалительным эффектом, но и другими, подчас нежелательными, свойствами стероидов. Наиболее известные представители НПВП: аспирин, ибупрофен, диклофенак. Obat anti-inflamasi nonsteroid (OAINS atau Nonsteroidal anti-inflammatory drugs (NSAIDs)) adalah kelas obat yang sama-sama memberikan efek analgesik (antinyeri) dan antipiretik (penurun panas), dan dalam dosis yang lebih tinggi berefek anti-inflamasi. Istilah "nonsteroid" membedakan obat ini dari anti-inflamasi lain yaitu "steroid", yang bekerja menekan produksi eikosanoid. Istilah ini pertama kali digunakan pada tahun 1960, digunakan untuk menjauhkan obat baru dari tragedi iatrogenik terkait steroid. Нестеро́їдні протизапальні́ препара́ти (НПЗП) — також відомі як нестероїдні протизапальні агенти / анальгетики (НПЗА), або нестероїдні протизапальні засоби (НПЗЗ) — це клас лікарських засобів, які забезпечують анальгетичний та антипіретичний (жарознижувальний) ефекти і, при застосуванні у вищих дозах, протизапальний ефект. Найвідомішими представниками цієї групи препаратів є ацетилсаліцилова кислота (аспірин), ібупрофен, диклофенак і напроксен, вони усі продаються в аптеках більшості країн. Nesteroidní antiflogistika (anglicky non-steroidal anti-inflammatory drugs), zkráceně NSA či NSAID, též nesteroidní antirevmatika a nesteroidní protizánětlivé léky, jsou léky s protibolestivým, protihorečnatým a protizánětlivým účinkem. Výraz "nesteroidní" se používá pro rozlišení těchto léků od steroidních léků s těmito účinky. Mezi protibolestivými léky jsou NSA neobvyklé tím, že nejsou narkotické. Los antiinflamatorios no esteroideos (abreviados AINE) son un grupo químicamente heterogéneo de fármacos diversos, principalmente antiinflamatorios,​ analgésicos y antipiréticos que reducen los síntomas de la inflamación, el dolor y la fiebre, respectivamente.​Todos ejercen sus efectos por acción de la inhibición de la enzima ciclooxigenasa.​Los antiinflamatorios naturales, segregados por el propio organismo, son los derivados de los corticoides, sustancias de origen esteroideo de potente acción antiinflamatoria, pero con importantes efectos secundarios.​ 非ステロイド性抗炎症薬(ひステロイドせいこうえんしょうやく、英語: Non-Steroidal Anti-Inflammatory Drug)は、抗炎症作用、鎮痛作用、解熱作用を有する薬剤の総称。頭文字を連ねて短縮表記されることも多く、NSAID(英語発音: [ˌen.es.eɪ.aɪ.ˈdiː] エヌ・エス・エイ・アイ・ディー))や(複数種類あるのでsつきで)NSAIDs(エヌセッズ、エヌセイズ)と表記し、カッコ内の発音をされる。疼痛、発熱、炎症の治療に用いられる。代表的なNSAIDにはアセチルサリチル酸(商品名アスピリン、バファリン)、イブプロフェン(商標名ブルフェン)、ロキソプロフェン(商品名ロキソニン)、ジクロフェナク(商品名ボルタレン)がある。また外用薬もある。 NSAIDsというのは先行するステロイド系抗炎症薬の副作用が問題視された後に登場したステロイドではない抗炎症薬。ところがこのNSAIDでも、NSAID潰瘍のような、死亡につながる可能性のある副作用は2000年前後にアメリカ合衆国で毎年3,200人、あるいは過剰推計ともされるが1万6,500人が死亡しているという2つの推計がある。COX-2への選択制を高め胃腸作用を減らしたNSAIDのいくつかでは心臓の副作用が増加した。 Non-steroidal 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. The term non-steroidal, common from around 1960, distinguishes these drugs from corticosteroids, which during the 1950s had acquired a bad reputation due to overuse and side-effect problems after their initial introduction in 1948. Ein nichtsteroidales Antirheumatikum (NSAR) – auch nichtsteroidales Antiphlogistikum (NSAP) oder NSAID (non-steroidal anti-inflammatory drug) – ist ein Schmerzmittel, das wegen seiner entzündungshemmenden (antiphlogistischen) Wirkung symptombezogen auch zur Rheumatherapie eingesetzt wird. Im Gegensatz dazu werden Glucocorticoide als steroidale Antirheumatika bezeichnet. Die Kategorie wurde in den späten 1950er Jahren eingeführt, um den Unterschied zu 'steroidalen Antirheumatika' mit ihren teils schweren Nebenwirkungen zu betonen. 非類固醇抗發炎藥(英語:Non-Steroidal Anti-Inflammatory Drug,縮寫:NSAID),也譯作非类固醇抗炎药,是一類具有解熱鎮痛效果的藥物,在施用较高劑量時也具有消炎作用。 “非類固醇”一詞用於將此類藥物與甾体藥物區分開,因類固醇類藥物也具有包括抑制花生酸生成、抗炎作用在內的諸多效果。“非類固醇抗發炎藥(非甾体抗炎药)”一詞首次使用於1960年,以將新藥與可能產生醫源性傷害的類固醇類藥物劃清界線。 非類固醇抗發炎藥中,屬阿斯匹靈、伊布洛芬、萘普生最為著名,在絕大多數國家都可作為非處方藥銷售。对乙酰氨基酚因其抗炎作用微弱,而通常不被歸為非類固醇抗發炎藥,它主要通過抑制分布在中樞神經系統的COX-2,以減少前列腺素的生成,從而緩解疼痛,但由於COX-2在周邊組織中數量較少,因此作用微弱。 大多數的非類固醇抗發炎藥抑制了環氧合酶-1(COX-1)以及環氧合酶-2(COX-2),進而減少前列腺素和血栓素的合成。一般認為,非類固醇抗發炎藥因為抑制環氧合酶-2會有解熱鎮痛、抗發炎的效果。部分非類固醇抗發炎藥,像是阿斯匹靈,也同時抑制了環氧合酶-1(COX-1),因而容易導致腸胃道出血和潰瘍。 FANS è l'acronimo dell'espressione farmaci anti-infiammatori non steroidei e individua una classe di farmaci dall'effetto antinfiammatorio, analgesico e antipiretico. Il termine non steroidei distingue questi farmaci dagli steroidi, che pur avendo una simile azione antinfiammatoria eicosanoide-deprimente, hanno una vasta gamma di altri effetti. Tale espressione fu introdotta negli anni sessanta del XX secolo per sottolineare la differenza rispetto ai tradizionali antinfiammatori steroidei impiegati in precedenza (cortisone e derivati), che avevano provocato gravissimi effetti avversi nel decennio precedente. NSAID's (afkorting van non-steroidal anti-inflammatory drugs, niet-steroïde anti-inflammatoire geneesmiddelen) zijn ontstekingsremmende geneesmiddelen die niet behoren tot de groep van de corticosteroïden. Een ander woord hiervoor is prostaglandinesynthetaseremmers. Voorbeelden van NSAID's zijn ibuprofen, diclofenac, meloxicam, naproxen, etofenamaat, celecoxib. Het acetylsalicylzuur (aspirine, Aspegic) wordt ook tot de NSAID's gerekend. Deze stof was er al een eeuw voordat de eigenlijke NSAID's werden ontwikkeld en heeft bovendien een werking op de bloedstolling.
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n19:200mg_ibuprofen_tablets.jpg?width=300
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M01A
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Film-coated 200 mg tablets of generic ibuprofen, a common non-steroidal anti-inflammatory drug
dbp:synonyms
* Cyclooxygenase inhibitor * Cyclooxygenase enzyme inhibitor * Non-steroidal anti-inflammatory agent/analgesic * Non-steroidal anti-inflammatory medicine
dbp:use
Pain, fever, inflammation, antithrombosis
dbo:abstract
مضادات الالتهاب اللاستيرويدية هي أدوية ذات مفعول مسكن وخافض للحرارة في الجرعات العادية وتكون لها تأثيرات مضادة للالتهاب في الجرعات العالية. ويستخدم مصطلح «لاستيرويدي» لتمييزها عن الأدوية الستيرويدية التي لديها تأثيرات (من بين تأثيرات عديدة أخرى) كابتة للإيكوزانويد ومضادة للالتهاب. مضادات الالتهاب اللاستيرويدية تمتاز على غيرها من مسكنات الآلام بأنها غير مخدرة لذلك فهي لا تسبب الإدمان. ومن أكثر الأعضاء بروزاً في هذه المجموعة من الأدوية هو الأسبرين، الآيبوبروفين والنابروكسين وذلك يرجع جزئياً إلى أنهم أدوية بدون وصفة في العديد من البلدان. ولايعتبر الباراسيتامول عضواً في هذه المجموعة. يقوم عمل هذا النوع من الأدوية على تثبيط عمل إنزيم يدعى: السايكلوأوكسيجنيز (بالإنجليزية: cyclooxygenase)‏ وهو الإنزيم المسؤول عن إنتاج البروستاجلاندين (بالإنجليزية: Prostaglandins)‏ والثرمبوأوكسوجنيز Thromboxane A2. البروستاجلاندين Prostaglandins هي مركبات ينتجها الجسم وتعمل وظائف هامة للجسم منها: الإحساس بالألم، تثبيط إفراز الحمض المعوي، تحفيز إفراز الغشاء المخاطي المعوي، مركبات وسطية في الالتهابات، الحمى أو ارتفاع حرارة الجسم.وبداية من عام 1829 عندما عُزل من لحاء الصفصاف الأبيض الذي كان يُستخدم كخافض للحرارة في الطب الشعبي، أصبحت مضادات الالتهاب اللاستيرويدية عاملاً رئيسياً في تسكين الألام (في الجرعات المنخفضة) وعلاج الالتهابات (في الجرعات العالية). وترجع شهرة مضادات الالتهاب اللاستيرويدية جزئياً - على عكس الأفيونات - إلى غياب التأثير المهدئ أو تثبيط التنفس لديها، كما أن احتمال تسبيبها للإدمان قليل جداً. ولكن لها مشاكلها أيضاً (انظر بالأسفل). وأصبحت بعض مضادات الالتهاب اللاستيرويدية، ومنها الإيبوبروفين والأسبرين، تُصنف كأدوية آمنة نسبياً وهي متاحة فوق الطاولة بدون وصفة طبية في بعض الدول. Los antiinflamatorios no esteroideos (abreviados AINE) son un grupo químicamente heterogéneo de fármacos diversos, principalmente antiinflamatorios,​ analgésicos y antipiréticos que reducen los síntomas de la inflamación, el dolor y la fiebre, respectivamente.​Todos ejercen sus efectos por acción de la inhibición de la enzima ciclooxigenasa.​Los antiinflamatorios naturales, segregados por el propio organismo, son los derivados de los corticoides, sustancias de origen esteroideo de potente acción antiinflamatoria, pero con importantes efectos secundarios.​ En oposición a los corticoides, el término "no esteroideo" se aplica a los AINE para recalcar su estructura química no esteroidea y la menor cantidad de efectos secundarios.​ El término fue acuñado en 1960 por .​ Como analgésicos, se caracterizan por el hecho de que no pertenecen a la clase de los narcóticos y actúan bloqueando la síntesis de prostaglandinas.​ Los antiinflamatorios no esteroideos disponibles en el mercado inhiben la actividad tanto de la (COX-1) como a la (COX-2) y, por lo tanto, la síntesis de prostaglandinas y tromboxanos. Se piensa que es la inhibición de la COX-2 la que en parte causa la acción antiinflamatoria, analgésica y antipirética de los AINE; sin embargo, aquellos que simultáneamente inhiben a la COX-1 tienen la capacidad de causar hemorragias digestivas y úlceras, en especial la aspirina.​Por lo tanto, se enfatizan las ventajas de los inhibidores selectivos para la COX-2. El AINE prototipo es la aspirina y le acompañan una gran variedad de ácidos orgánicos, incluyendo derivados del ácido propanoico (como el ibuprofeno y naproxen), derivados del ácido acético (como la indometacina) y (como el piroxicam), todos competidores con el ácido araquidónico por el sitio activo de la ciclooxigenasa. A partir del 2012, en los consensos internacionales el paracetamol se excluye de los AINE, por su poca/nula acción antiinflamatoria.​ 비스테로이드성 항염증제(영어: nonsteroidal anti-inflammatory drug , NSAID)는 진통 작용, 해열 작용, 항염증 작용이 있는 약이다. 손쉽게 사용할 수 있는 NSAIDs는 아스피린, 이부프로펜 및 나프록센이다. 대부분의 국가에서 일반의약품이므로 처방전 없이 구매가 가능하다. 아세트아미노펜은 신체의 항염증 활성이 미미하기 때문에 일반적으로 NSAID로 간주되지 않는다. Нестероидные противовоспалительные препараты (нестероидные противовоспалительные средства/агенты, НПВП, НПВС, НСПВП, NSAID) — группа лекарственных средств, обладающих обезболивающим, жаропонижающим и , уменьшают боль, лихорадку и воспаление. Использование в названии термина «нестероидные» подчёркивает их отличие от глюкокортикоидов, которые обладают не только противовоспалительным эффектом, но и другими, подчас нежелательными, свойствами стероидов. Наиболее известные представители НПВП: аспирин, ибупрофен, диклофенак. Μη στεροειδή αντιφλεγμονώδη φάρμακα (ΜΣΑΦ) ( Nonsteroidal anti-inflammatory drugs ή NSAIDs) είναι μια κατηγορία φαρμάκων που μειώνει τον πόνο, ελαττώνει τον πυρετό, αποτρέπει τους θρόμβους αίματος και σε μεγαλύτερες δόσεις, μικραίνει φλεγμονές. Οι παρενέργειες εξαρτώνται από το συγκεκριμένο φάρμακο, αλλά περιλαμβάνει κυρίως αυξημένο κίνδυνο γαστρεντερικών ελκών και αιμορραγιών, έμφραγμα του μυοκαρδίου και νεφροπάθεια. Ο όρος μη στεροειδή διακρίνει αυτά τα φάρμακα από τα στεροειδή, που αν και έχουν μια παρόμοια με εικοσανοειδή, αντιφλεγμονώδη δράση, έχουν πλατύ φάσμα άλλων επιπτώσεων. Πρωτοχρησιμοποιήθηκαν το 1960 και ο όρος χρησιμοποιείται στη διάκριση αυτών των φαρμάκων από τα στεροειδή, που είχαν στιγματιστεί ιδιαίτερα τότε λόγω της σύνδεσης με τη κατάχρηση των αναβολικών στεροειδών. Τα NSAIDs δουλεύουν με την καταστολή της δραστικότητας των ενζύμων της κυκλοοξυγενάσης (COX-1 και/ή COX-2]]). Στα κύτταρα, αυτά τα ένζυμα εμπλέκονται στη σύνθεση βασικών βιολογικών μεσολαβητών, συγκεκριμένα των προσταγλανδινών που εμπλέκονται στις φλεγμονές και στις θρομβοξάνες που υπεισέρχονται στην πήξη. Υπάρχουν δύο τύποι διαθέσιμων ΜΣΑΦ (NSAID): μη επιλεκτικά και επιλεκτικά COX-2. Τα περισσότερα ΜΣΑΦ είναι μη επιλεκτικά και καταστέλλουν τη δραστικότητα και των COX-1 και των COX-2. Αυτά τα ΜΣΑΦ, ενώ μειώνουν τη φλεγμονή, καταστέλλουν επίσης τη συσσωμάτωση αιμοπεταλίων (ιδιαίτερα η ασπιρίνη) και αυξάνουν τον κίνδυνο γαστρεντερικών ελκών/αιμορραγιών. Οι επιλεκτικοί αναστολείς COX-2 έχουν λιγότερες γαστρεντερικές παρενέργειες, αλλά προάγουν τη θρόμβωση και αυξάνουν σημαντικά τον κίνδυνο καρδιακής προσβολής. Ως αποτέλεσμα, οι επιλεκτικοί αναστολείς COX-2 αντενδείκνυνται λόγω του υψηλού κινδύνου αδιάγνωστων αγγειακών ασθενειών. Αυτά τα διαφοροποιημένα αποτελέσματα οφείλονται στους διαφορετικούς ρόλους και εντοπισμούς των ιστών κάθε ισοενζύμου COX. Καταστέλλοντας τη φυσιολογική δράση των COX, όλα τα ΜΣΑΦ αυξάνουν τον κίνδυνο νεφρικών ασθενειών και μέσω σχετικού μηχανισμού την καρδιακή προσβολή. Τα πιο σημαντικά ΜΣΑΦ είναι η ασπιρίνη, η ιβουπροφαίνη και η ναξοπρένη, που όλα τους είναι διαθέσιμα στις περισσότερες χώρες ως μη συνταγογραφούμενα φάρμακα. Η παρακεταμόλη δεν θεωρείται γενικά ως ΜΣΑΦ, επειδή έχει μόνο δευτερεύουσα αντιφλεγμονώδη δράση. Αντιμετωπίζει τον κίνδυνο κυρίως φράσσοντας τα COX-2 και εμποδίζοντας την επαναπρόσληψη του ενδοκανναβινοειδούς (endocannabinoid) σχεδόν αποκλειστικά στον εγκέφαλο και όχι στο υπόλοιπο σώμα. 非類固醇抗發炎藥(英語:Non-Steroidal Anti-Inflammatory Drug,縮寫:NSAID),也譯作非类固醇抗炎药,是一類具有解熱鎮痛效果的藥物,在施用较高劑量時也具有消炎作用。 “非類固醇”一詞用於將此類藥物與甾体藥物區分開,因類固醇類藥物也具有包括抑制花生酸生成、抗炎作用在內的諸多效果。“非類固醇抗發炎藥(非甾体抗炎药)”一詞首次使用於1960年,以將新藥與可能產生醫源性傷害的類固醇類藥物劃清界線。 非類固醇抗發炎藥中,屬阿斯匹靈、伊布洛芬、萘普生最為著名,在絕大多數國家都可作為非處方藥銷售。对乙酰氨基酚因其抗炎作用微弱,而通常不被歸為非類固醇抗發炎藥,它主要通過抑制分布在中樞神經系統的COX-2,以減少前列腺素的生成,從而緩解疼痛,但由於COX-2在周邊組織中數量較少,因此作用微弱。 大多數的非類固醇抗發炎藥抑制了環氧合酶-1(COX-1)以及環氧合酶-2(COX-2),進而減少前列腺素和血栓素的合成。一般認為,非類固醇抗發炎藥因為抑制環氧合酶-2會有解熱鎮痛、抗發炎的效果。部分非類固醇抗發炎藥,像是阿斯匹靈,也同時抑制了環氧合酶-1(COX-1),因而容易導致腸胃道出血和潰瘍。 非甾体表示非糖皮质激素。糖皮质激素是另一种抗炎药物。在1950年代,糖皮质激素损伤了许多患者,所以新的药物中不含糖皮质激素便成为一个非常重要的信息。于是“NSAID”这一概念于1960年被发明。 Non-steroidal 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. The term non-steroidal, common from around 1960, distinguishes these drugs from corticosteroids, which during the 1950s had acquired a bad reputation due to overuse and side-effect problems after their initial introduction in 1948. NSAIDs 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 older COX-2 selective inhibitors 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, all NSAIDs increase the risk of kidney disease and, through a related mechanism, heart attack. In addition, NSAIDs can blunt the production of erythropoietin, resulting in anaemia, since haemoglobin needs this hormone to be produced. The most prominent NSAIDs are aspirin, ibuprofen, and naproxen; all available over the counter (OTC) in most countries. Paracetamol (acetaminophen) is generally not considered an NSAID because it has only minor anti-inflammatory activity. Paracetamol treats pain mainly by blocking COX-2 and inhibiting endocannabinoid reuptake almost exclusively within the brain, and only minimally in the rest of the body. 非ステロイド性抗炎症薬(ひステロイドせいこうえんしょうやく、英語: Non-Steroidal Anti-Inflammatory Drug)は、抗炎症作用、鎮痛作用、解熱作用を有する薬剤の総称。頭文字を連ねて短縮表記されることも多く、NSAID(英語発音: [ˌen.es.eɪ.aɪ.ˈdiː] エヌ・エス・エイ・アイ・ディー))や(複数種類あるのでsつきで)NSAIDs(エヌセッズ、エヌセイズ)と表記し、カッコ内の発音をされる。疼痛、発熱、炎症の治療に用いられる。代表的なNSAIDにはアセチルサリチル酸(商品名アスピリン、バファリン)、イブプロフェン(商標名ブルフェン)、ロキソプロフェン(商品名ロキソニン)、ジクロフェナク(商品名ボルタレン)がある。また外用薬もある。 NSAIDsというのは先行するステロイド系抗炎症薬の副作用が問題視された後に登場したステロイドではない抗炎症薬。ところがこのNSAIDでも、NSAID潰瘍のような、死亡につながる可能性のある副作用は2000年前後にアメリカ合衆国で毎年3,200人、あるいは過剰推計ともされるが1万6,500人が死亡しているという2つの推計がある。COX-2への選択制を高め胃腸作用を減らしたNSAIDのいくつかでは心臓の副作用が増加した。 様々なNSAIDsは作用には大差がなく、異なるのは用量、服用方法である。NSAIDsの胃粘膜保護に関する試みで最も成功したのは、アセチル化とpHの調整、また、胃粘膜保護作用を持つ薬剤との併用である。胃酸分泌抑制効果のあるH2ブロッカー(例:ラフチジン(プロテカジン®)、ラニチジン(ザンタック®)や、ミソプロストール(サイトテック®)が、アメリカ合衆国では最も成功した薬剤である。例えば、ジクロフェナクとミソプロストールを合剤にしたオルソテックなどもあり、非常に効果的だが、高価である。日本では、バファリン®等の合剤がある。 一般医を受診する患者の25%は変形性関節症で、その半数から全ての例がNSAIDsを処方される。65歳以上の人口の80%にX線上有意な変形性関節症が存在するとされており、そのうち60%が疼痛などの症状を訴える。2001年には、アメリカ合衆国では7,000万錠のNSAIDsが処方され、300億錠が薬局で販売された。 FANS è l'acronimo dell'espressione farmaci anti-infiammatori non steroidei e individua una classe di farmaci dall'effetto antinfiammatorio, analgesico e antipiretico. Il termine non steroidei distingue questi farmaci dagli steroidi, che pur avendo una simile azione antinfiammatoria eicosanoide-deprimente, hanno una vasta gamma di altri effetti. Tale espressione fu introdotta negli anni sessanta del XX secolo per sottolineare la differenza rispetto ai tradizionali antinfiammatori steroidei impiegati in precedenza (cortisone e derivati), che avevano provocato gravissimi effetti avversi nel decennio precedente. Tali farmaci sono detti "analgesici periferici" e agiscono sul metabolismo dell'acido arachidonico e dell'acido eicosapentenoico, precursori di molecole coinvolte nel processo infiammatorio quali prostaglandine (PG), prostacicline (PC), trombossani (TX) e leucotrieni (LT). I FANS bloccano in maniera più o meno reversibile il sito di legame di un enzima, la cicloossigenasi, esistente in due isoforme: COX-1, prodotto costitutivamente e ubiquitario in condizioni fisiologiche e COX-2, sintetizzato in maniera inducibile e quasi assente se non in attiva fase infiammatoria. Sono disponibili due tipologie di FANS: selettivi e non selettivi per COX-2. I FANS non selettivi, pur riducendo l'infiammazione e l'aggregazione piastrinica (specialmente l'aspirina), aumentano il rischio di ulcere / sanguinamenti gastrointestinali. Gli inibitori selettivi della COX-2 hanno meno effetti gastrointestinali, ma promuovono la trombosi e aumentano sostanzialmente il rischio di infarto. Di conseguenza, gli inibitori selettivi della COX-2 sono generalmente controindicati a causa dell'alto rischio di malattia vascolare non diagnosticata. Questi effetti differenti tra le due tipologie di FANS sono dovuti ai diversi ruoli e localizzazioni tissutali di ciascun isoenzima COX. Inibendo l'attività fisiologica della COX, tutti i FANS aumentano il rischio di malattia renale e, attraverso un meccanismo correlato, infarto. Gli effetti collaterali dipendono dal farmaco specifico, ma includono in gran parte un aumento del rischio di ulcere e sanguinamenti gastrointestinali, infarto e malattie renali. Il motivo per cui è consigliabile assumerli a stomaco pieno per minimizzare la lesività verso le mucose del sistema gastrointestinale. Els antiinflamatoris no esteroidals (o, més rarament no esteroideus) (AINE i, més rarament, AINES en plural) són substàncies químiques amb efecte antiinflamatori, analgèsic i antipirètic, efectes que són semblants als dels corticoides però sense les conseqüències secundàries. Són un grup variat i químicament heterogeni de fàrmacs que per la seva acció antiinflamatòria, analgèsica, i antipirètica redueixen els símptomes de la inflamació, el dolor i la febre respectivament. Actuen bloquejant la síntesi de prostaglandines. Tots exerceixen els seus efectes per acció de la inhibició de l'enzim . Els AINE contraresten l'efecte hipotensor del diürètics, betablocadors, IECA o fàrmacs com la o la perquè part de la seva acció hipotensora l'exerceixen aquestes substàncies a través de l'alliberament de prostaglandines renals. Nesteroidní antiflogistika (anglicky non-steroidal anti-inflammatory drugs), zkráceně NSA či NSAID, též nesteroidní antirevmatika a nesteroidní protizánětlivé léky, jsou léky s protibolestivým, protihorečnatým a protizánětlivým účinkem. Výraz "nesteroidní" se používá pro rozlišení těchto léků od steroidních léků s těmito účinky. Mezi protibolestivými léky jsou NSA neobvyklé tím, že nejsou narkotické. Nejběžnějšími zástupci této skupiny léků jsou aspirin, ibuprofen, a naproxen, jež jsou volně prodejné, bez potřeby předpisu. (Paracetamol má též protihorečnaté a protibolestivé účinky, ale nemá protizánětlivé a není to NSA.) Is éard is Druga Frith-athlastach Neamhstéaróideach nó DFANSa (Béarla: NSAIDs) ann ná aicme drugaí a mhúchann pian sa duine. Les anti-inflammatoires non stéroïdiens ou antiinflammatoires non stéroïdiens, souvent abrégés en AINS, sont des médicaments aux propriétés antalgiques, antipyrétiques et anti-inflammatoires. Ils réduisent la douleur, la fièvre et l'inflammation. Le terme « non stéroïdien » est utilisé pour les distinguer des glucocorticoïdes (appelés communément corticoïdes), qui (parmi un large éventail d'effets) ont une semblable action anti-inflammatoire (dépression des eicosanoïdes). Le terme a été introduit dans les années 1960 pour marquer la distinction avec la cortisone et ses dérivés. Les deux plus connus sont l'aspirine (au dosage de 1 000 mg en une prise chez l'adulte) et l'ibuprofène. Le paracétamol n'est pas un AINS, ce qui autorise leur association dans la prise en charge de la douleur ou de la fièvre. Ein nichtsteroidales Antirheumatikum (NSAR) – auch nichtsteroidales Antiphlogistikum (NSAP) oder NSAID (non-steroidal anti-inflammatory drug) – ist ein Schmerzmittel, das wegen seiner entzündungshemmenden (antiphlogistischen) Wirkung symptombezogen auch zur Rheumatherapie eingesetzt wird. Im Gegensatz dazu werden Glucocorticoide als steroidale Antirheumatika bezeichnet. Die Kategorie wurde in den späten 1950er Jahren eingeführt, um den Unterschied zu 'steroidalen Antirheumatika' mit ihren teils schweren Nebenwirkungen zu betonen. Niesteroidowe leki przeciwzapalne, niesterydowe leki przeciwzapalne, NLPZ, NSLPZ – szeroka, niejednorodna grupa leków przeciwzapalnych, przeciwbólowych i przeciwgorączkowych. Ich działanie polega na hamowaniu cyklooksygenazy prostaglandynowej (COX), co w 1971 wyjaśnił John Vane (Nobel 1982). W 1992 D. Simmonds wykazał, że istnieją co najmniej dwie izoformy cyklooksygenazy – obecna stale w organizmie COX-1 i wyzwalana w toku procesu zapalnego COX-2. Hamowanie tej drugiej jest istotne z klinicznego punktu widzenia, a blokowanie pierwszej może prowadzić do wystąpienia objawów ubocznych ze strony układu pokarmowego w leczeniu za pomocą NLPZ. Nazywane są niesteroidowymi ze względu na strukturę, odmienną od innych leków mających właściwości przeciwzapalne – kortykosteroidów. NSAID's (afkorting van non-steroidal anti-inflammatory drugs, niet-steroïde anti-inflammatoire geneesmiddelen) zijn ontstekingsremmende geneesmiddelen die niet behoren tot de groep van de corticosteroïden. Een ander woord hiervoor is prostaglandinesynthetaseremmers. Voorbeelden van NSAID's zijn ibuprofen, diclofenac, meloxicam, naproxen, etofenamaat, celecoxib. Het acetylsalicylzuur (aspirine, Aspegic) wordt ook tot de NSAID's gerekend. Deze stof was er al een eeuw voordat de eigenlijke NSAID's werden ontwikkeld en heeft bovendien een werking op de bloedstolling. Obat anti-inflamasi nonsteroid (OAINS atau Nonsteroidal anti-inflammatory drugs (NSAIDs)) adalah kelas obat yang sama-sama memberikan efek analgesik (antinyeri) dan antipiretik (penurun panas), dan dalam dosis yang lebih tinggi berefek anti-inflamasi. Istilah "nonsteroid" membedakan obat ini dari anti-inflamasi lain yaitu "steroid", yang bekerja menekan produksi eikosanoid. Istilah ini pertama kali digunakan pada tahun 1960, digunakan untuk menjauhkan obat baru dari tragedi iatrogenik terkait steroid. Antiinflamatorio ez-esteroidea (AIEE) hantura, sukarra eta mina tratatzeko erabilitako esteroidea ez den sendagaia da. AIEE talde honen barnean aurkitzen diren sendagaiak kimikoki oso desberdinak izan daitezkeen arren, denek ekintza mekanismo bera dute, entzimaren inhibizioa. Antiinflamatorio naturalak, organismoak berak jariatzen dituenak, kortikoideen deribatuak dira, jatorri esteroideko eta hanturaren aurkako ekintza handia duten substantziak, baina aldi berean eragin kaltegarri ugari dituztenak. AIEEak ordea, ez esteroideak direnez, albo ondorio gutxiago dituzte. Antiinflamatorio ez esteroide gehienek ziklooxigenasa-1 (COX-1) eta ziklooxigenasa-2 (COX-2) inhibitzen dituzte, prostaglandina eta tronboxanoen sintesia oztopatuz. COX-2ren inhibizioa ekintza antiinflamatorio, analgesiko eta antipiretikoaren erantzulea da, baina COX-1ren inhibizioak digestio aparatuko odoljarioak eta ultzerak sortzen ditu. Horregatik, gaur egun badakigu COX-2 bakarrik inhibitzen duten sendagaiek abantaila handiak dituztela. Aspirina izan zen familia honetako lehenengo kidea, eta ondoren sortutakoen artean diklofenakoa, ibuprofenoa eta naproxenoa oso hedatuak izan dira. Berrienen artean piroxikama eta haren azpitaldekoak ditugu, eta azkena sortutakoak izenekoak dira, eta enparauak alegia. Azken hauen abantaila nagusia, lehen aipatu bezala, antiinflamatorio klasikoekin konparaturik, urdailean askoz albo-ondorio gutxiago eragitea da. Нестеро́їдні протизапальні́ препара́ти (НПЗП) — також відомі як нестероїдні протизапальні агенти / анальгетики (НПЗА), або нестероїдні протизапальні засоби (НПЗЗ) — це клас лікарських засобів, які забезпечують анальгетичний та антипіретичний (жарознижувальний) ефекти і, при застосуванні у вищих дозах, протизапальний ефект. Термін «нестероїдні» відрізняє ці препарати від стероїдів, які серед широкого кола інших ефектів, мають аналогічні ейкозаноїд-пригнічуючу і протизапальну дію. Як анальгетики, нестероїдні протизапальні засоби незвичайні тим, що вони не є наркотичними і можуть бути використані як альтернатива наркотикам, оскільки не призводять до звикання. Найвідомішими представниками цієї групи препаратів є ацетилсаліцилова кислота (аспірин), ібупрофен, диклофенак і напроксен, вони усі продаються в аптеках більшості країн. Os anti-inflamatórios não esteroides (abreviadamente, AINEs ou NSAIDs, do inglês Non-steroidal anti-inflammatory drugs) são um grupo variado de fármacos que têm em comum a capacidade de controlar a inflamação, de analgesia (reduzir a dor), e de combater a febre. O termo foi criado em 1960 por Michael W. Whitehouse. Apesar de em sua maioria serem constituídos por ácidos orgânicos, sua estrutura química não é relacionada. Caracterizam-se por inibir a atividade de subtipos da ciclo-oxigenase, impedindo assim a síntese de eicosanoides pela via metabólica da cascata do ácido araquidónico.Fazem parte deste grupo medicamentos muito conhecidos, em parte por alguns já estarem disponíveis há muito tempo, por serem de venda livre (MNSRM), e pelo vasto número de situações em que são usados. Alguns nomes sonantes incluem o ácido acetilsalicílico, ibuprofeno e naproxeno.O paracetamol, embora possua um mecanismo de ação semelhante e tenha efeito antipirético e analgésico, é praticamente desprovido de efeito anti-inflamatório. Icke-steroida anti-inflammatoriska medel (NSAID från engelskans non-steroidal anti-inflammatory drug) är en grupp läkemedel med inflammationsdämpande, smärtlindrande och febernedsättande verkan. Kategorin icke-steroida antiinflammatoriska läkemedel infördes i slutet av 1950 för att klargöra skillnaden mellan dessa läkemedel och kortisonpreparat vilka också har antiinflammatorisk verkan. NSAID har ATC-kod M01A under namnet "icke-steroida antiinflammatoriska/antireumatiska medel (NSAID)". Många värk- och febernedsättande läkemedel på apoteket finns i kategorin NSAID. Ett viktigt undantag är paracetamol som är den verksamma substansen i exempelvis Alvedon, Panodil med fler. Den smärtlindrande effekten av NSAID varierar. Enligt en systematisk forskningsöversikt från SBU är den smärtlindrande effekten av NSAID generellt mycket liten jämfört med placebo för äldre personer med vanliga långvariga smärttillstånd som artros, diabetesneuropati samt kotkompression. Samtidigt finns i denna grupp viss risk för ovanliga men allvarliga biverkningar.
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