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'''Non-steroidal anti-inflammatory agents''', also called '''non-steroidal anti-inflammatory drugs''' (NSAIDs) are defined as "anti-inflammatory agents that are not steroids. In addition to anti-inflammatory actions, they have analgesic, antipyretic, and platelet-inhibitory actions. They are used primarily in the treatment of chronic arthritic conditions and certain soft tissue disorders associated with pain and inflammation. They act by blocking the synthesis of prostaglandins by inhibiting [[cyclooxygenase]], which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins. Inhibition of prostaglandin synthesis accounts for their analgesic, antipyretic, and platelet-inhibitory actions; other mechanisms may contribute to their anti-inflammatory effects. Certain NSAIDs also may inhibit lipoxygenase enzymes or phospholipase C or may modulate T-cell function."<ref name="title-">{{cite web |url=http://www.nlm.nih.gov/cgi/mesh/2007/MB_cgi?term=Non-steroidal+anti-inflammatory+agents |title=Non-steroidalanti-inflammatory agents|author=National Library of Medicine |accessdate=2007-11-19 |format= |work=}}</ref>
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'''Non-steroidal anti-inflammatory agents''', also called '''non-steroidal anti-inflammatory drugs''' (NSAIDs) are defined as "anti-inflammatory agents that are not [[glucocorticoid|steroids]]. In addition to anti-inflammatory actions, they have analgesic, antipyretic, and platelet-inhibitory actions. They are used primarily in the treatment of chronic arthritic conditions and certain soft tissue disorders associated with [[pain]] and inflammation. They act by blocking the synthesis of [[prostaglandin]]s by inhibiting [[cyclooxygenase]]s, which convert arachidonic acid to cyclic endoperoxides, precursors of prostaglandins. Inhibition of prostaglandin synthesis accounts for their analgesic, antipyretic, and platelet-inhibitory actions; other mechanisms may contribute to their anti-inflammatory effects. Certain NSAIDs also may inhibit lipoxygenase enzymes or phospholipase C or may modulate T-cell function."<ref name="title-">{{cite web |url=http://www.nlm.nih.gov/cgi/mesh/2007/MB_cgi?term=Non-steroidal+anti-inflammatory+agents |title=Non-steroidal anti-inflammatory agents|author=National Library of Medicine |accessdate=2007-11-19 |format= |work=}}</ref>
 
The clinical characteristics of NSAISs have been reviewed.<ref>Chou R, Helfand M, Peterson K, Dana T. (2004). [http://derp.ohsu.edu/final/NSAIDS_Final_Report_Update%2032.pdfDrug Class Review of Cyclo-oxygenase (COX)-2 Inhibitors and Non-steroidal Anti-inflammatory Drugs (NSAIDS)]. [http://www.ohsu.edu/ohsuedu/research/policycenter/ Center for Evidence-based Policy]: [http://www.ohsu.edu/ohsuedu/research/policycenter/DERP/Drug Effectiveness Review Project (DERP)]</ref>
 
In general, they have been too toxic for [[veterinary medicine]], although there is now limited use in dogs and extremely limited use in cats. [[Meloxicam]], for example, is approved only for a single post-surgical dose in cats, but is used off-label in cancer treatment. One of the attractions of NSAIDs  here is that they appear to inhibit some cancers, such as [[squamous cell carcinoma]] that expresses [[cyclooxygenase 1]]. Nevertheless, they can cause sudden and life-threatening reactions, such as gastric bleeding.


==Classification==
==Classification==
===Non-selective inhibitors of clooxygenase===
===Non-selective inhibitors of cyclooxygenase===
These drugs inhibit both [[cyclooxygenase]] isozymes.
These drugs inhibit both [[cyclooxygenase]] isozymes. An example is [[aspirin]].


===Selective inhibitors of cyclooxygenase 2===
===Selective inhibitors of cyclooxygenase 2===
{{main|Cyclooxygenase 2 inhibitors}}
{{main|Cyclooxygenase 2 inhibitors}}
More selective inhibitors, which do not suppress COX-1 and thus are less likely to result in gastric irritation, seemed extremely promising until [[postmarketing surveillance]] indicate that they increase the risk of serious cardiac events. Only one remains on the market in the United States. There are reports, however, that COX-2 inhibitors can relieve pain that other NSAIDs do not.
===COX-inhibiting nitric oxide donator (CINOD)===
COX-inhibiting nitric oxide donators (CINODs or NO-NSAIDs), an example is [[nitronaproxen]], may have less [[drug toxicity]].<ref name="pmid17596112">{{cite journal| author=| title=Naproxcinod: AZD 3582, HCT 3012, naproxen nitroxybutylester, nitronaproxen, NO-naproxen. | journal=Drugs R D | year= 2007 | volume= 8 | issue= 4 | pages= 255-8 | pmid=17596112
| url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=clinical.uthscsa.edu/cite&email=badgett@uthscdsa.edu&retmode=ref&cmd=prlinks&id=17596112 }} <!--Formatted by http://sumsearch.uthscsa.edu/cite/--></ref>


==Adverse reactions==
==Adverse reactions==
===Gastrointestinal===
===Gastrointestinal===
NSAIDs may contribute to gastrointestinal ulceration including [[peptic ulcer disease]].
Non-steroidal anti-inflammatory agents should be avoided in [[geriatrics]] according to [[clinical practice guideline]]s.<ref name="urlThe American Geriatrics Society - Education - AGS Clinical Practice Guideline: Pharmacological Management of Persistent Pain in Older Persons">{{cite web |url=http://www.americangeriatrics.org/education/executive_summary.shtml |title=The American Geriatrics Society - Education - AGS Clinical Practice Guideline: Pharmacological Management of Persistent Pain in Older Persons |author= |authorlink= |coauthors= |date= |format= |work= |publisher= |pages= |language= |archiveurl= |archivedate= |quote= |accessdate=}}</ref>
 
====Dyspepsia====
Risk factors for developing dyspepsia with NSAIDs are:<ref name="pmid20955443">{{cite journal| author=Laine L, Curtis SP, Cryer B, Kaur A, Cannon CP| title=Risk factors for NSAID-associated upper GI clinical events in a long-term prospective study of 34 701 arthritis patients. | journal=Aliment Pharmacol Ther | year= 2010 | volume= 32 | issue= 10 | pages= 1240-8 | pmid=20955443 | doi=10.1111/j.1365-2036.2010.04465.x | pmc= | url= }} </ref>
* prior history of dyspepsia
* prior UGI complication
* age 65
 
====Peptic ulcer disease====
[[Clinical practice guideline]]s address the prevention of [[peptic ulcer disease]] among patients on NSAIDs.<ref name="pmid19240698">{{cite journal| author=Lanza FL, Chan FK, Quigley EM, Practice Parameters Committee of the American College of Gastroenterology| title=Guidelines for prevention of NSAID-related ulcer complications. | journal=Am J Gastroenterol | year= 2009 | volume= 104 | issue= 3 | pages= 728-38 | pmid=19240698
| url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=clinical.uthscsa.edu/cite&email=badgett@uthscdsa.edu&retmode=ref&cmd=prlinks&id=19240698 | doi=10.1038/ajg.2009.115 }}</ref>
 
NSAIDs may contribute to gastrointestinal ulceration including [[peptic ulcer disease]].<ref name="pmid1987872">{{cite journal |author=Griffin MR, Piper JM, Daugherty JR, Snowden M, Ray WA |title=Nonsteroidal anti-inflammatory drug use and increased risk for peptic ulcer disease in elderly persons |journal=Ann. Intern. Med. |volume=114 |issue=4 |pages=257–63 |year=1991 |month=February |pmid=1987872 |doi= |url= |issn=}}</ref><ref name="pmid7907735">{{cite journal |author=García Rodríguez LA, Jick H |title=Risk of upper gastrointestinal bleeding and perforation associated with individual non-steroidal anti-inflammatory drugs |journal=Lancet |volume=343 |issue=8900 |pages=769–72 |year=1994 |month=March |pmid=7907735 |doi= |url= |issn=}}</ref> A [[meta-analysis]] concluded "[[ibuprofen]] was associated with the lowest relative risk, followed by [[diclofenac]]. Azapropazone, tolmetin, ketoprofen, and [[piroxicam]] ranked highest for risk and [[indomethacin]], [[naproxen]], [[sulindac]], and [[aspirin]] occupied intermediate positions. Higher doses of ibuprofen were associated with relative risks similar to those withnaproxen and indomethacin."<ref name="pmid8664664">{{cite journal |author=Henry D, Lim LL, Garcia Rodriguez LA, ''et al'' |title=Variability in risk of gastrointestinal complications with individual non-steroidal anti-inflammatory drugs: results of a collaborative meta-analysis |journal=BMJ |volume=312 |issue=7046 |pages=1563–6 |year=1996 |month=June |pmid=8664664 |pmc=2351326 |doi= |url=http://bmj.com/cgi/pmidlookup?view=long&pmid=8664664 |issn=}}</ref>
 
The risk of [[peptic ulcer disease]] is higher if NSAIDs are combined with [[corticosteroid]]s.<ref name="pmid20955443">{{cite journal| author=Laine L, Curtis SP, Cryer B, Kaur A, Cannon CP| title=Risk factors for NSAID-associated upper GI clinical events in a long-term prospective study of 34 701 arthritis patients. | journal=Aliment Pharmacol Ther | year= 2010 | volume= 32 | issue= 10 | pages= 1240-8 | pmid=20955443 | doi=10.1111/j.1365-2036.2010.04465.x | pmc= | url= }} </ref><ref name="pmid2012355">{{cite journal |author=Piper JM, Ray WA, Daugherty JR, Griffin MR |title=Corticosteroid use and peptic ulcer disease: role of nonsteroidal anti-inflammatory drugs |journal=Ann. Intern. Med. |volume=114 |issue=9 |pages=735–40 |year=1991 |month=May |pmid=2012355 |doi= |url= |issn=}}</ref><ref name="pmid7907735">{{cite journal |author=García Rodríguez LA, Jick H |title=Risk of upper gastrointestinal bleeding and perforation associated with individual non-steroidal anti-inflammatory drugs |journal=Lancet |volume=343 |issue=8900 |pages=769–72 |year=1994 |month=March |pmid=7907735 |doi= |url= |issn=}}</ref>
 
Eradication of ''[[Helicobacter pylori]]'' may help prevent complications. [[Clinical practice guideline]]s state:<ref name="pmid19240698"/>
:"All patients regardless of risk status who are about to start long-term  traditional NSAID therapy should be considered for testing for ''H. pylori'' and treated, if positive."


===Renal===
===Renal===
NSAIDs may cause [[acute kidney injury]] due to acute tubular necrosis. This may rarely occur after just a few doses.<ref name="pmid17928602">{{cite journal |author=Rabb H, Colvin RB |title=Case records of the Massachusetts General Hospital. Case 31-2007. A 41-year-old man with abdominal pain and elevated serum creatinine |journal=N. Engl. J. Med. |volume=357 |issue=15 |pages=1531–41 |year=2007 |pmid=17928602 |doi=10.1056/NEJMcpc079024}}</ref>
NSAIDs may cause [[acute kidney injury]] due to acute tubular necrosis. Although this is usually interstitial nephritis, NSAIDS can also cause minimal-change disease in the glomerulus.<ref name="pmid17928602">{{cite journal |author=Rabb H, Colvin RB |title=Case records of the Massachusetts General Hospital. Case 31-2007. A 41-year-old man with abdominal pain and elevated serum creatinine |journal=N. Engl. J. Med. |volume=357 |issue=15 |pages=1531–41 |year=2007 |pmid=17928602 |doi=10.1056/NEJMcpc079024}}</ref>
 
Damage from NSAIDS may rarely occur after just a few doses.<ref name="pmid17928602">{{cite journal |author=Rabb H, Colvin RB |title=Case records of the Massachusetts General Hospital. Case 31-2007. A 41-year-old man with abdominal pain and elevated serum creatinine |journal=N. Engl. J. Med. |volume=357 |issue=15 |pages=1531–41 |year=2007 |pmid=17928602 |doi=10.1056/NEJMcpc079024}}</ref>
 
===Hypersensitivity===
Hypersensitivity may cause [[rhinitis]], [[asthma]], and [[urticaria]] or [[angioedema]].<ref name="pmid15613671">{{cite journal| author=Gollapudi RR, Teirstein PS, Stevenson DD, Simon RA| title=Aspirin sensitivity: implications for patients with coronary artery disease. | journal=JAMA | year= 2004 | volume= 292 | issue= 24 | pages= 3017-23 | pmid=15613671
| url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&retmode=ref&cmd=prlinks&id=15613671 | doi=10.1001/jama.292.24.3017 }}</ref><ref>{{OMIM|208550}}</ref>
 
===Vascular disease===
NSAIDs, especially [[diclofenac]], may cause recurrence of [[vascular disease]] among patients with prior [[myocardial infarction]]s.<ref name="pmid21555710">{{cite journal| author=Schjerning Olsen AM, Fosbøl EL, Lindhardsen J, Folke F, Charlot M, Selmer C et al.| title=Duration of treatment with nonsteroidal anti-inflammatory drugs and impact on risk of death and recurrent myocardial infarction in patients with prior myocardial infarction: a nationwide cohort study. | journal=Circulation | year= 2011 | volume= 123 | issue= 20 | pages= 2226-35 | pmid=21555710 | doi=10.1161/CIRCULATIONAHA.110.004671 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21555710  }} </ref>
 
==Effectiveness==
Some NSAIDs - diclofenac, [[ibuprofen]], ketoprofen, and piroxicam but not [[indomethacin]] and benzydamine - can be effective with [[topical administration]].<ref name="pmid20556778">{{cite journal| author=Massey T, Derry S, Moore RA, McQuay HJ| title=Topical NSAIDs for acute pain in adults. | journal=Cochrane Database Syst Rev | year= 2010 | volume= 6 | issue=  | pages= CD007402 | pmid=20556778
| url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=20556778 | doi=10.1002/14651858.CD007402.pub2 }} </ref>
 
===Combined with acetaminophen===
According to a [[systematic review]] sponsored by industry, combining  [[acetaminophen]] with  non-steroidal  anti-inflammatory agents  may help treatment of posteroperative pain.<ref name="pmid20142348">{{cite journal| author=Ong CK, Seymour RA,  Lirk P, Merry AF| title=Combining paracetamol (acetaminophen) with  nonsteroidal antiinflammatory drugs: a qualitative systematic review of  analgesic efficacy for acute postoperative pain. | journal=Anesth Analg |  year= 2010 | volume= 110 | issue= 4 | pages= 1170-9 | pmid=20142348
| url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=clinical.uthscsa.edu/cite&retmode=ref&cmd=prlinks&id=20142348  | doi=10.1213/ANE.0b013e3181cf9281 }}  </ref>
 
For [[lumbalgia]], [[acetaminophen]] one gram orally four times a day combined with [[diclofenac]], a non-steroidal anti-inflammatory agent, was not better than acetaminophen alone in a [[randomized controlled trial]].<ref name="pmid17993364">{{cite journal |author=Hancock MJ, Maher CG, Latimer J, ''et al'' |title=Assessment of diclofenac or spinal manipulative therapy, or both, in addition to recommended first-line treatment for acute low back pain: a randomised controlled trial |journal=Lancet |volume=370 |issue=9599 |pages=1638–43 |year=2007 |pmid=17993364 |doi=10.1016/S0140-6736(07)61686-9}}</ref>
 
For reducing [[fever]], acetaminophen combined with [[ibuprofen]] may be better than either drug alone according to a [[randomized controlled trial]].<ref name="pmid18765450">{{cite journal |author=Hay AD, Costelloe C, Redmond NM, ''et al'' |title=Paracetamol plus ibuprofen for the treatment of fever in children (PITCH): randomised controlled trial |journal=BMJ |volume=337 |issue= |pages=a1302 |year=2008 |pmid=18765450 |pmc=2528896 |doi= |url=http://bmj.com/cgi/pmidlookup?view=long&pmid=18765450 |issn=}}</ref>
 
===Aspirin resistance===
Aspirin resistance may reduce the abilitiy of aspirin to protect against [[coronary heart disease]].<ref name="pmid15738456">{{cite journal| author=Sanderson S, Emery J, Baglin T, Kinmonth AL| title=Narrative review: aspirin resistance and its clinical implications. | journal=Ann Intern Med | year= 2005 | volume= 142 | issue= 5 | pages= 370-80 | pmid=15738456
| url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&retmode=ref&cmd=prlinks&id=15738456 }} <!--Formatted by http://sumsearch.uthscsa.edu/cite/--></ref><ref>{{OMIM|608223}}</ref>


==References==
==References==
<references/>
<small>
<references>
 
</references>
</small>  
 


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Non-steroidal anti-inflammatory agents, also called non-steroidal anti-inflammatory drugs (NSAIDs) are defined as "anti-inflammatory agents that are not steroids. In addition to anti-inflammatory actions, they have analgesic, antipyretic, and platelet-inhibitory actions. They are used primarily in the treatment of chronic arthritic conditions and certain soft tissue disorders associated with pain and inflammation. They act by blocking the synthesis of prostaglandins by inhibiting cyclooxygenases, which convert arachidonic acid to cyclic endoperoxides, precursors of prostaglandins. Inhibition of prostaglandin synthesis accounts for their analgesic, antipyretic, and platelet-inhibitory actions; other mechanisms may contribute to their anti-inflammatory effects. Certain NSAIDs also may inhibit lipoxygenase enzymes or phospholipase C or may modulate T-cell function."[1]

The clinical characteristics of NSAISs have been reviewed.[2]

In general, they have been too toxic for veterinary medicine, although there is now limited use in dogs and extremely limited use in cats. Meloxicam, for example, is approved only for a single post-surgical dose in cats, but is used off-label in cancer treatment. One of the attractions of NSAIDs here is that they appear to inhibit some cancers, such as squamous cell carcinoma that expresses cyclooxygenase 1. Nevertheless, they can cause sudden and life-threatening reactions, such as gastric bleeding.

Classification

Non-selective inhibitors of cyclooxygenase

These drugs inhibit both cyclooxygenase isozymes. An example is aspirin.

Selective inhibitors of cyclooxygenase 2

For more information, see: Cyclooxygenase 2 inhibitors.

More selective inhibitors, which do not suppress COX-1 and thus are less likely to result in gastric irritation, seemed extremely promising until postmarketing surveillance indicate that they increase the risk of serious cardiac events. Only one remains on the market in the United States. There are reports, however, that COX-2 inhibitors can relieve pain that other NSAIDs do not.

COX-inhibiting nitric oxide donator (CINOD)

COX-inhibiting nitric oxide donators (CINODs or NO-NSAIDs), an example is nitronaproxen, may have less drug toxicity.[3]

Adverse reactions

Gastrointestinal

Non-steroidal anti-inflammatory agents should be avoided in geriatrics according to clinical practice guidelines.[4]

Dyspepsia

Risk factors for developing dyspepsia with NSAIDs are:[5]

  • prior history of dyspepsia
  • prior UGI complication
  • age 65

Peptic ulcer disease

Clinical practice guidelines address the prevention of peptic ulcer disease among patients on NSAIDs.[6]

NSAIDs may contribute to gastrointestinal ulceration including peptic ulcer disease.[7][8] A meta-analysis concluded "ibuprofen was associated with the lowest relative risk, followed by diclofenac. Azapropazone, tolmetin, ketoprofen, and piroxicam ranked highest for risk and indomethacin, naproxen, sulindac, and aspirin occupied intermediate positions. Higher doses of ibuprofen were associated with relative risks similar to those withnaproxen and indomethacin."[9]

The risk of peptic ulcer disease is higher if NSAIDs are combined with corticosteroids.[5][10][8]

Eradication of Helicobacter pylori may help prevent complications. Clinical practice guidelines state:[6]

"All patients regardless of risk status who are about to start long-term traditional NSAID therapy should be considered for testing for H. pylori and treated, if positive."

Renal

NSAIDs may cause acute kidney injury due to acute tubular necrosis. Although this is usually interstitial nephritis, NSAIDS can also cause minimal-change disease in the glomerulus.[11]

Damage from NSAIDS may rarely occur after just a few doses.[11]

Hypersensitivity

Hypersensitivity may cause rhinitis, asthma, and urticaria or angioedema.[12][13]

Vascular disease

NSAIDs, especially diclofenac, may cause recurrence of vascular disease among patients with prior myocardial infarctions.[14]

Effectiveness

Some NSAIDs - diclofenac, ibuprofen, ketoprofen, and piroxicam but not indomethacin and benzydamine - can be effective with topical administration.[15]

Combined with acetaminophen

According to a systematic review sponsored by industry, combining acetaminophen with non-steroidal anti-inflammatory agents may help treatment of posteroperative pain.[16]

For lumbalgia, acetaminophen one gram orally four times a day combined with diclofenac, a non-steroidal anti-inflammatory agent, was not better than acetaminophen alone in a randomized controlled trial.[17]

For reducing fever, acetaminophen combined with ibuprofen may be better than either drug alone according to a randomized controlled trial.[18]

Aspirin resistance

Aspirin resistance may reduce the abilitiy of aspirin to protect against coronary heart disease.[19][20]

References

  1. ↑ National Library of Medicine. Non-steroidal anti-inflammatory agents. Retrieved on 2007-11-19.
  2. ↑ Chou R, Helfand M, Peterson K, Dana T. (2004). Class Review of Cyclo-oxygenase (COX)-2 Inhibitors and Non-steroidal Anti-inflammatory Drugs (NSAIDS). Center for Evidence-based Policy: Effectiveness Review Project (DERP)
  3. ↑ (2007) "Naproxcinod: AZD 3582, HCT 3012, naproxen nitroxybutylester, nitronaproxen, NO-naproxen.". Drugs R D 8 (4): 255-8. PMID 17596112.
  4. ↑ The American Geriatrics Society - Education - AGS Clinical Practice Guideline: Pharmacological Management of Persistent Pain in Older Persons.
  5. ↑ 5.0 5.1 Laine L, Curtis SP, Cryer B, Kaur A, Cannon CP (2010). "Risk factors for NSAID-associated upper GI clinical events in a long-term prospective study of 34 701 arthritis patients.". Aliment Pharmacol Ther 32 (10): 1240-8. DOI:10.1111/j.1365-2036.2010.04465.x. PMID 20955443. Research Blogging.
  6. ↑ 6.0 6.1 Lanza FL, Chan FK, Quigley EM, Practice Parameters Committee of the American College of Gastroenterology (2009). "Guidelines for prevention of NSAID-related ulcer complications.". Am J Gastroenterol 104 (3): 728-38. DOI:10.1038/ajg.2009.115. PMID 19240698. Research Blogging.
  7. ↑ Griffin MR, Piper JM, Daugherty JR, Snowden M, Ray WA (February 1991). "Nonsteroidal anti-inflammatory drug use and increased risk for peptic ulcer disease in elderly persons". Ann. Intern. Med. 114 (4): 257–63. PMID 1987872. [e]
  8. ↑ 8.0 8.1 García Rodríguez LA, Jick H (March 1994). "Risk of upper gastrointestinal bleeding and perforation associated with individual non-steroidal anti-inflammatory drugs". Lancet 343 (8900): 769–72. PMID 7907735. [e]
  9. ↑ Henry D, Lim LL, Garcia Rodriguez LA, et al (June 1996). "Variability in risk of gastrointestinal complications with individual non-steroidal anti-inflammatory drugs: results of a collaborative meta-analysis". BMJ 312 (7046): 1563–6. PMID 8664664. PMC 2351326. [e]
  10. ↑ Piper JM, Ray WA, Daugherty JR, Griffin MR (May 1991). "Corticosteroid use and peptic ulcer disease: role of nonsteroidal anti-inflammatory drugs". Ann. Intern. Med. 114 (9): 735–40. PMID 2012355. [e]
  11. ↑ 11.0 11.1 Rabb H, Colvin RB (2007). "Case records of the Massachusetts General Hospital. Case 31-2007. A 41-year-old man with abdominal pain and elevated serum creatinine". N. Engl. J. Med. 357 (15): 1531–41. DOI:10.1056/NEJMcpc079024. PMID 17928602. Research Blogging.
  12. ↑ Gollapudi RR, Teirstein PS, Stevenson DD, Simon RA (2004). "Aspirin sensitivity: implications for patients with coronary artery disease.". JAMA 292 (24): 3017-23. DOI:10.1001/jama.292.24.3017. PMID 15613671. Research Blogging.
  13. ↑ Online Mendelian Inheritance in Man, OMIM®. Johns Hopkins University, Baltimore, MD. MIM Number: 208550. World Wide Web URL: http://omim.org/.
  14. ↑ Schjerning Olsen AM, Fosbøl EL, Lindhardsen J, Folke F, Charlot M, Selmer C et al. (2011). "Duration of treatment with nonsteroidal anti-inflammatory drugs and impact on risk of death and recurrent myocardial infarction in patients with prior myocardial infarction: a nationwide cohort study.". Circulation 123 (20): 2226-35. DOI:10.1161/CIRCULATIONAHA.110.004671. PMID 21555710. Research Blogging.
  15. ↑ Massey T, Derry S, Moore RA, McQuay HJ (2010). "Topical NSAIDs for acute pain in adults.". Cochrane Database Syst Rev 6: CD007402. DOI:10.1002/14651858.CD007402.pub2. PMID 20556778. Research Blogging.
  16. ↑ Ong CK, Seymour RA, Lirk P, Merry AF (2010). "Combining paracetamol (acetaminophen) with nonsteroidal antiinflammatory drugs: a qualitative systematic review of analgesic efficacy for acute postoperative pain.". Anesth Analg 110 (4): 1170-9. DOI:10.1213/ANE.0b013e3181cf9281. PMID 20142348. Research Blogging.
  17. ↑ Hancock MJ, Maher CG, Latimer J, et al (2007). "Assessment of diclofenac or spinal manipulative therapy, or both, in addition to recommended first-line treatment for acute low back pain: a randomised controlled trial". Lancet 370 (9599): 1638–43. DOI:10.1016/S0140-6736(07)61686-9. PMID 17993364. Research Blogging.
  18. ↑ Hay AD, Costelloe C, Redmond NM, et al (2008). "Paracetamol plus ibuprofen for the treatment of fever in children (PITCH): randomised controlled trial". BMJ 337: a1302. PMID 18765450. PMC 2528896. [e]
  19. ↑ Sanderson S, Emery J, Baglin T, Kinmonth AL (2005). "Narrative review: aspirin resistance and its clinical implications.". Ann Intern Med 142 (5): 370-80. PMID 15738456.
  20. ↑ Online Mendelian Inheritance in Man, OMIM®. Johns Hopkins University, Baltimore, MD. MIM Number: 608223. World Wide Web URL: http://omim.org/.

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