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Antacid

From Wikipedia, the free encyclopedia
Substance that relieves stomach problems
This article is about the medication used to relieve heartburn. For the acid produced by ants, known in many languages as "ant acid", seeFormic acid.
Not to be confused with acid suppression therapy withPPIs orH2RAs, which reduces acid production.

Calcium carbonate antacid tablets

Anantacid is a substance whichneutralizesstomach acidity and is used to relieveheartburn,indigestion, or an upset stomach.[1] Some antacids have been used in the treatment ofconstipation anddiarrhea.[2] Marketed antacids containsalts ofaluminium,calcium,magnesium, orsodium.[2] Some preparations contain a combination of twosalts, such asmagnesium carbonate andaluminium hydroxide (e.g.,hydrotalcite).[3]

Medical uses

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Antacids are availableover the counter and are taken by mouth to quickly relieve occasionalheartburn, the major symptom ofgastroesophageal reflux disease andindigestion. Treatment with antacids alone issymptomatic and only justified for minor symptoms.[4] Alternative uses for antacids include constipation, diarrhea, hyperphosphatemia, and urinary alkalization.[2] Some antacids are also used as anadjunct to pancreatic enzyme replacement therapy in the treatment ofpancreatic insufficiency.[5]

Non-particulate antacids (sodium citrate) increase gastricpH with little or no effect on gastric volume, and therefore may see some limited use in pre-operative procedures. Sodium citrate should be given within one hour of surgery to be the most effective.[6]

Side effects

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Conventional effervescent tablets contain a significant amount ofsodium and are associated with increased risk of adverse cardiovascular events according to a 2013 study.[7] Alternative sodium-free formulations containingmagnesium salts may cause diarrhea, whereas those containingcalcium oraluminium may causeconstipation.[8]: Table 2  Long-term use of antacids containingaluminium may increase the risk of developingosteoporosis.[9]In vitro studies have found a potential for acid rebound to occur due to antacid overuse, however the significance of this finding has been called into question.[10][11]

Properties of antacids

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When an excess amount of acid is produced in thestomach, the naturalmucous barrier that protects the lining of the stomach can degrade, leading topain andirritation.[12] There is also potential for the development ofacid reflux, which can cause pain and damage to theesophagus.[13] Antacids containalkaline ions thatchemically neutralize stomachgastric acid, reducing damage to the stomach lining andesophagus, and relieving pain.[1] Some antacids also inhibitpepsin, anenzyme that can damage theesophagus inacid reflux.[2][14]

Antacids do not directly inhibit acidsecretion, and thus are distinct from acid-reducing drugs likeH2-receptor antagonists orproton pump inhibitors.[4] Antacids do not kill the bacterium,Helicobacter pylori, which causes mostulcers.[4]

Types

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Antacids are mainly classified into two categories:

Interactions

[edit]
Structural depiction of tetracycline metal chelation, where 'M' is a metal such as those found in antacids

Antacids are known tointeract with severaloral medications, includingfluoroquinolone andtetracyclineantibiotics,iron,itraconazole, andprednisone.[16] Metalchelation is responsible for some of these interactions (e.g.fluoroquinolones,tetracyclines), leading to decreased absorption of the chelated drug. Some interactions may be due to thepH increase observed in thestomach following antacidingestion, leading to increased absorption of weak acids, and decreased absorption of weak bases.[17] Antacids also cause an increase inpH of theurine (alkalization), which may cause increasedblood concentrations of weak bases, and increasedexcretion of weak acids.[18]

A proposed method to mitigate the effects ofstomach acidity andchelation on drug absorption is to space out the administration of antacids with interactingmedications by at least two hours,[19] however this method has not been well studied for drugs affected byurine alkalization.[16]

There are concerns regarding interactions between delayed-release tablets and antacids, as antacids may increase the stomachpH to a point at which the coating of the delayed-release tablet will dissolve, leading to degradation of the drug if it ispH sensitive.[18]

Formulations

[edit]

Antacids may be formulated with otheractive ingredients such assimethicone to controlgas, oralginic acid to act as a physical barrier to acid.[20]

Liquids

[edit]
A bottle of liquid antacid containingbismuth subsalicylate as the active ingredient

Several liquid antacid preparations aremarketed. Common liquid preparations includemilk of magnesia and magnesium/aluminiumcombinations. A potential advantage of using a liquid preparation over a tablet is that liquids may provide quicker relief, however this may coincide with a shorter duration of action.[21]

Tablets

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Chewable tablets

[edit]

Chewable tablets are one of the most common forms of antacids, most frequently made fromcarbonate orhydroxidesalts, and are readily available over the counter. Upon reaching thestomach, the powdered antacid salts bind tohydronium (H+) ions, producingchloride salts, carbon dioxide, and water. This process reduces the concentration of H+ ions in the stomach, raising the pH and neutralizing the acid.[8]: Figure 1  Common carbonate salts available in tablet form include those of calcium, magnesium, aluminium, and sodium.[16]

Some common American brands areTums, Gaviscon chewable tablets, andMaalox chewable tablets.[22]

Effervescent tablets

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Effervescent tablets are tablets which are designed to dissolve inwater, and then releasecarbon dioxide.[23][24][25] Common ingredients includecitric acid andsodium bicarbonate, which react when in contact with water to producecarbon dioxide. Effervescent antacids may also containaspirin,[26]sodium carbonate, ortartaric acid.[27] Those containing aspirin may cause furthergastric irritation andulceration due toaspirin's effects on themucous membrane of thestomach.[28]

Brand names

[edit]

Somebrands includeAlka-Seltzer, Gaviscon,Tums, Gelusil andEno.[29][30][31]

References

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  1. ^abInternal Clinical Guidelines Team. (UK) (2014).Dyspepsia and Gastro-Oesophageal Reflux Disease: Investigation and Management of Dyspepsia, Symptoms Suggestive of Gastro-Oesophageal Reflux Disease, or Both. National Institute for Health and Care Excellence: Clinical Guidelines. London: National Institute for Health and Care Excellence (UK).PMID 25340236.
  2. ^abcdSalisbury BH, Terrell JM (2020)."Antacids".StatPearls. Treasure Island (FL): StatPearls Publishing.PMID 30252305.Archived from the original on 5 November 2021. Retrieved24 November 2020.
  3. ^"Aluminium hydroxide and magnesium carbonate Uses, Side Effects & Warnings".Drugs.com.Archived from the original on 20 May 2021. Retrieved24 November 2020.
  4. ^abc"Consumer Summary – Treatment Options for GERD or Acid Reflux Disease: A Review of the Research for Adults". U.S. Department of Health & Human Services. Agency for Healthcare Research and Quality. 23 September 2011. Archived fromthe original on 11 October 2014.
  5. ^Graham DY (June 1982). "Pancreatic enzyme replacement: the effect of antacids or cimetidine".Digestive Diseases and Sciences.27 (6):485–490.doi:10.1007/BF01296725.PMID 6282548.S2CID 10640940.
  6. ^Apfelbaum JL, Agarkar M, Connis RT, Coté CJ, Nickinovich DJ, Warner MA, et al. (American Society of Anesthesiologists Committee on Standards and Practice Parameters) (March 2017). "Practice Guidelines for Preoperative Fasting and the Use of Pharmacologic Agents to Reduce the Risk of Pulmonary Aspiration: Application to Healthy Patients Undergoing Elective Procedures: An Updated Report by the American Society of Anesthesiologists Task Force on Preoperative Fasting and the Use of Pharmacologic Agents to Reduce the Risk of Pulmonary Aspiration".Anesthesiology.126 (3):376–393.doi:10.1097/ALN.0000000000001452.PMID 28045707.
  7. ^George J, Majeed W, Mackenzie IS, Macdonald TM, Wei L (November 2013)."Association between cardiovascular events and sodium-containing effervescent, dispersible, and soluble drugs: nested case-control study".BMJ.347 f6954.doi:10.1136/bmj.f6954.PMC 3898660.PMID 24284017.
  8. ^abGarg V, Narang P, Taneja R (March 2022)."Antacids revisited: review on contemporary facts and relevance for self-management".The Journal of International Medical Research.50 (3) 03000605221086457.doi:10.1177/03000605221086457.PMC 8966100.PMID 35343261.
  9. ^"Taking Antacids".Medline Plus. U.S. Department of Health and Human Services, National Institutes of Health, U.S. National Library of Medicine. 7 November 2014.Archived from the original on 5 July 2016.
  10. ^Texter EC (February 1989). "A critical look at the clinical use of antacids in acid-peptic disease and gastric acid rebound".The American Journal of Gastroenterology.84 (2):97–108.PMID 2644821.
  11. ^Hade JE, Spiro HM (July 1992). "Calcium and acid rebound: a reappraisal".Journal of Clinical Gastroenterology.15 (1):37–44.doi:10.1097/00004836-199207000-00010.PMID 1500660.S2CID 10897187.
  12. ^McColl KE (October 2011). "The elegance of the gastric mucosal barrier: designed by nature for nature".Gut.61 (6):787–788.doi:10.1136/gutjnl-2011-301612.PMID 22147513.
  13. ^"When does long-term acid reflux become a serious issue?".Harvard Health. 1 June 2017. Retrieved14 August 2025.
  14. ^Bardhan KD, Strugala V, Dettmar PW (2012)."Reflux revisited: advancing the role of pepsin".International Journal of Otolaryngology.2012 646901.doi:10.1155/2012/646901.PMC 3216344.PMID 22242022.
  15. ^MrlabTest - Antacids. URL:https://www.mrlabtest.com/medication/antacids.htm. Accessed on: November 27, 2024.
  16. ^abcOgawa R, Echizen H (October 2011). "Clinically significant drug interactions with antacids: an update".Drugs.71 (14):1839–1864.doi:10.2165/11593990-000000000-00000.PMID 21942976.S2CID 36875514.
  17. ^Patel, Divya; Bertz, Richard; Ren, Song; Boulton, David W.; Någård, Mats (April 2020)."A Systematic Review of Gastric Acid-Reducing Agent-Mediated Drug-Drug Interactions with Orally Administered Medications".Clinical Pharmacokinetics.59 (4):447–462.doi:10.1007/s40262-019-00844-3.ISSN 1179-1926.PMC 7109143.PMID 31788764.
  18. ^abPatel D, Bertz R, Ren S, Boulton DW, Någård M (April 2020)."A Systematic Review of Gastric Acid-Reducing Agent-Mediated Drug-Drug Interactions with Orally Administered Medications".Clinical Pharmacokinetics.59 (4):447–462.doi:10.1007/s40262-019-00844-3.PMC 7109143.PMID 31788764.
  19. ^Australian Medicines Handbook 2022. Adelaide, SA: Australian Medicines Handbook Pty. 2022.ISBN 978-0-6485158-6-9.
  20. ^Thompson WG (12 September 2014)."Antacids".IFFGD Publication #520. International Foundation for Functional Gastrointestinal Disorders, Inc. (IFFGD). Archived fromthe original on 6 May 2016.
  21. ^Barnett CC, Richardson CT (November 1985). "In vivo and in vitro evaluation of magnesium-aluminium hydroxide antacid tablets and liquid".Digestive Diseases and Sciences.30 (11):1049–1052.doi:10.1007/BF01315602.PMID 4053915.S2CID 8133980.
  22. ^"Maalox Antacid Oral: Uses, Side Effects, Interactions, Pictures, Warnings & Dosing".WebMD.Archived from the original on 24 June 2022. Retrieved24 June 2022.
  23. ^Dubogrey I (2013)."Putting the Fizz into Formulation".European Pharmaceutical Contractor. No. Autumn. Archived fromthe original on 28 August 2021. Retrieved17 April 2017.
  24. ^"Tablets".British Pharmacopeia. 2003. Archived fromthe original on 3 January 2013.
  25. ^International Pharmacopoeia 2006. World Health Organization. 2006. pp. 966.ISBN 978-92-4-156301-7. Retrieved1 July 2013.
  26. ^"Alka Seltzer Directions of use, Sodium & Aspirin content – Alka Seltzer relief from Headaches, Migraine & Upset stomach".alkaseltzer.ie. Archived fromthe original on 29 April 2015. Retrieved17 April 2017.
  27. ^Blair GT, DeFraties JJ (2000). "Hydroxy Dicarboxylic Acids".Kirk-Othmer Encyclopedia of Chemical Technology.Kirk Othmer Encyclopedia of Chemical Technology. pp. 1–19.doi:10.1002/0471238961.0825041802120109.a01.ISBN 978-0-471-23896-6.
  28. ^Graham DY, Smith JL (March 1986). "Aspirin and the stomach".Annals of Internal Medicine.104 (3):390–398.doi:10.7326/0003-4819-104-3-390.PMID 3511824.
  29. ^"Which OTC Meds Treat Heartburn?".WebMD. 30 March 2023. Retrieved8 January 2024.
  30. ^"Eno – Summary of Product Characteristics at eMC".Electronic Medicines Compendium. Retrieved2 September 2016.Last updated 1 January 2016
  31. ^"Gelusil - Uses, Side Effects, and More". Retrieved27 February 2024.

External links

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  • The dictionary definition ofantacid at Wiktionary
Drugs for acid related disorders:Antacids (A02A)
Magnesium (increases motility)
Aluminium (decreases motility)
Calcium
Sodium
Combinations and complexes
of aluminium, calcium and magnesium
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