Wikipedia:WikiProject Chemicals/Chembox validation/VerifiedDataSandbox and Pyridostigmine: Difference between pages
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Saving copy of the {{drugbox}} taken from revid 457062639 of page Pyridostigmine for the Chem/Drugbox validation project (updated: 'DrugBank'). |
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{{Short description|Medication used to treat myasthenia gravis}} |
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{{ambox | text = This page contains a copy of the infobox ({{tl|drugbox}}) taken from revid [{{fullurl:Pyridostigmine|oldid=457062639}} 457062639] of page [[Pyridostigmine]] with values updated to verified values.}} |
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{{Distinguish|Physostigmine}} |
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{{Drugbox |
{{Drugbox |
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| Verifiedfields = changed |
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| IUPAC_name = 3-[(dimethylcarbamoyl)oxy]-1-methylpyridinium |
| IUPAC_name = 3-[(dimethylcarbamoyl)oxy]-1-methylpyridinium |
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| image = Pyridostigmine.svg |
| image = Pyridostigmine.svg |
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| image2 = Pyridostigmine ball-and-stick.png |
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<!--Clinical data--> |
<!-- Clinical data --> |
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| tradename = Mestinon |
| tradename = Mestinon, others |
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| Drugs.com = {{drugs.com|monograph|pyridostigmine-bromide}} |
| Drugs.com = {{drugs.com|monograph|pyridostigmine-bromide}} |
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| MedlinePlus = a682229 |
| MedlinePlus = a682229 |
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| pregnancy_AU = C |
| pregnancy_AU = C |
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| pregnancy_US = C |
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| legal_UK = POM |
| legal_UK = POM |
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| legal_US = Rx-only |
| legal_US = Rx-only |
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| routes_of_administration = Oral, [[Intravenous therapy|intravenous]] |
| routes_of_administration = [[Oral administration|By mouth]], [[Intravenous therapy|intravenous]] |
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| class = [[Acetylcholinesterase inhibitor]]; [[Parasympathomimetic drug|Parasympathomimetic]] |
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<!--Pharmacokinetic data--> |
<!-- Pharmacokinetic data --> |
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| bioavailability = 7.6 |
| bioavailability = 7.6 ± 2.4% |
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| protein_bound = |
| protein_bound = |
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| metabolism = |
| metabolism = |
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| elimination_half-life = 1.78 |
| elimination_half-life = 1.78 ± 0.24 hours |
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| excretion = [[ |
| excretion = [[kidney]] |
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<!--Identifiers--> |
<!-- Identifiers --> |
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| CASNo_Ref = {{cascite|correct|CAS}} |
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| CAS_number_Ref = {{cascite|correct|??}} |
| CAS_number_Ref = {{cascite|correct|??}} |
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| CAS_number = 155-97-5 |
| CAS_number = 155-97-5 |
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| ATC_prefix = N07 |
| ATC_prefix = N07 |
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| ATC_suffix = AA02 |
| ATC_suffix = AA02 |
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| ATC_supplemental = |
| ATC_supplemental = |
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| PubChem = 4991 |
| PubChem = 4991 |
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| DrugBank_Ref = {{drugbankcite|correct|drugbank}} |
| DrugBank_Ref = {{drugbankcite|correct|drugbank}} |
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| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
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| ChemSpiderID = 4817 |
| ChemSpiderID = 4817 |
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| UNII_Ref = {{fdacite| |
| UNII_Ref = {{fdacite|correct|FDA}} |
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| UNII = 19QM69HH21 |
| UNII = 19QM69HH21 |
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| KEGG_Ref = {{keggcite| |
| KEGG_Ref = {{keggcite|correct|kegg}} |
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| KEGG = |
| KEGG = C07410 |
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| ChEMBL_Ref = {{ebicite|correct|EBI}} |
| ChEMBL_Ref = {{ebicite|correct|EBI}} |
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| ChEMBL = 1115 |
| ChEMBL = 1115 |
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<!--Chemical data--> |
<!-- Chemical data --> |
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| C=9 | H=13 | N=2 | O=2 |
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| molecular_weight = 181.212 g/mol |
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| InChI = 1/C9H13N2O2/c1-10(2)9(12)13-8-5-4-6-11(3)7-8/h4-7H,1-3H3/q+1 |
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| InChIKey = RVOLLAQWKVFTGE-UHFFFAOYAK |
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| StdInChI_Ref = {{stdinchicite|correct|chemspider}} |
| StdInChI_Ref = {{stdinchicite|correct|chemspider}} |
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| StdInChI = 1S/C9H13N2O2/c1-10(2)9(12)13-8-5-4-6-11(3)7-8/h4-7H,1-3H3/q+1 |
| StdInChI = 1S/C9H13N2O2/c1-10(2)9(12)13-8-5-4-6-11(3)7-8/h4-7H,1-3H3/q+1 |
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| StdInChIKey = RVOLLAQWKVFTGE-UHFFFAOYSA-N |
| StdInChIKey = RVOLLAQWKVFTGE-UHFFFAOYSA-N |
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}} |
}} |
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<!-- Definition and medical uses --> |
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'''Pyridostigmine''' is a medication used to treat [[myasthenia gravis]]<ref name=WHO2008>{{cite book | title = WHO Model Formulary 2008 | year = 2009 | isbn = 9789241547659 | vauthors = ((World Health Organization)) | veditors = Stuart MC, Kouimtzi M, Hill SR | hdl = 10665/44053 | author-link = World Health Organization | publisher = World Health Organization |page=429 }}</ref> and underactive bladder.<ref>{{cite journal | vauthors = Moro C, Phelps C, Veer V, Clark J, Glasziou P, Tikkinen KA, Scott AM | title = The effectiveness of parasympathomimetics for treating underactive bladder: A systematic review and meta-analysis | journal = Neurourology and Urodynamics | date = November 2021 | volume = 41 | issue = 1 | pages = 127–139 | pmid = 34816481 | doi = 10.1002/nau.24839 | s2cid = 244530010 | url = https://research.bond.edu.au/en/publications/62295e6a-d035-4557-bb8d-12380be96c0c }}</ref> It is also used together with [[atropine]] to end the effects of [[neuromuscular blocking medication]] of the [[non-depolarizing]] type.<ref name=AHFS2016/> It is also used off-label to treat some forms of [[Postural orthostatic tachycardia syndrome]]. It is typically given [[Oral administration|by mouth]] but can also be used by injection.<ref name=AHFS2016/> The effects generally begin within 45 minutes and last up to 4 hours.<ref name=AHFS2016>{{cite web|title=Neostigmine Bromide|url=https://www.drugs.com/monograph/neostigmine-bromide.html|publisher=The American Society of Health-System Pharmacists|access-date=8 December 2016|url-status=live|archive-url=https://web.archive.org/web/20161221012812/https://www.drugs.com/monograph/neostigmine-bromide.html|archive-date=21 December 2016}}</ref> |
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<!-- Side effects and mechanisms --> |
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Common side effects include nausea, diarrhea, frequent urination, and abdominal pain.<ref name=AHFS2016/> More severe side effects include [[low blood pressure]], weakness, and [[allergic reactions]].<ref name=AHFS2016/> It is unclear if use in [[pregnancy]] is safe for the fetus.<ref name=AHFS2016/> Pyridostigmine is an [[acetylcholinesterase inhibitor]] in the [[cholinergic]] family of medications.<ref name=AHFS2016/> It works by blocking the action of [[acetylcholinesterase]] and therefore increases the levels of [[acetylcholine]].<ref name=AHFS2016/> |
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<!-- History and culture --> |
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Pyridostigmine was patented in 1945 and came into medical use in 1955.<ref name=Fis2006>{{cite book| vauthors = Fischer J, Ganellin CR |title=Analogue-based Drug Discovery|date=2006|publisher=John Wiley & Sons|isbn=9783527607495|page=540|url=https://books.google.com/books?id=FjKfqkaKkAAC&pg=PA540|language=en|url-status=live|archive-url=https://web.archive.org/web/20161220143859/https://books.google.ca/books?id=FjKfqkaKkAAC&pg=PA540|archive-date=2016-12-20}}</ref> It is on the [[WHO Model List of Essential Medicines|World Health Organization's List of Essential Medicines]].<ref name="WHO21st">{{cite book | vauthors = ((World Health Organization)) | title = World Health Organization model list of essential medicines: 21st list 2019 | year = 2019 | hdl = 10665/325771 | author-link = World Health Organization | publisher = World Health Organization | location = Geneva | id = WHO/MVP/EMP/IAU/2019.06. License: CC BY-NC-SA 3.0 IGO | hdl-access=free }}</ref> Pyridostigmine is available as a [[generic medication]].<ref name=AHFS2016/><ref>{{cite web | title=Competitive Generic Therapy Approvals | website=U.S. [[Food and Drug Administration]] (FDA) | date=3 March 2023 | url=https://www.fda.gov/drugs/generic-drugs/competitive-generic-therapy-approvals | access-date=6 March 2023}}</ref> |
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==Medical uses== |
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Pyridostigmine is used to treat muscle weakness in people with [[myasthenia gravis]] or forms of [[congenital myasthenic syndrome]] and to combat the effects of [[curare|curariform]] drug toxicity. Pyridostigmine bromide has been FDA approved for military use during combat situations as an agent to be given prior to exposure to the nerve agent [[Soman]] in order to increase survival. Used in particular during the first [[Gulf War]], pyridostigmine bromide has been implicated as a causal factor in [[Gulf War syndrome]].<ref name=Golomb>{{cite journal | vauthors = Golomb BA | title = Acetylcholinesterase inhibitors and Gulf War illnesses | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 105 | issue = 11 | pages = 4295–4300 | date = March 2008 | pmid = 18332428 | pmc = 2393741 | doi = 10.1073/pnas.0711986105 | doi-access = free | bibcode = 2008PNAS..105.4295G | jstor = 25461411}}</ref><ref name="Steenhuysen 2008">{{cite web | last=Steenhuysen | first=Julie | title=Gulf War illness linked to chemical exposure-study | work=[[Reuters]] | date=March 10, 2008 | url=https://www.reuters.com/article/idUSN10593482}}</ref> |
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With pyridostigmine classified as a type of [[parasympathomimetic drug|parasympathomimetic]], it can be used to treat underactive bladder.<ref>{{cite journal | vauthors = Moro C, Phelps C, Veer V, Clark J, Glasziou P, Tikkinen KA, Scott AM | title = The effectiveness of parasympathomimetics for treating underactive bladder: A systematic review and meta-analysis | journal = Neurourology and Urodynamics | date = November 2021 | volume = 41 | issue = 1 | pages = 127–139 | pmid = 34816481 | doi = 10.1002/nau.24839 | s2cid = 244530010 | url = https://research.bond.edu.au/en/publications/62295e6a-d035-4557-bb8d-12380be96c0c }}</ref> |
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Pyridostigmine sometimes is used to treat [[orthostatic hypotension]].<ref name="Gales-2007">{{cite journal | vauthors = Gales BJ, Gales MA | title = Pyridostigmine in the treatment of orthostatic intolerance | journal = The Annals of Pharmacotherapy | volume = 41 | issue = 2 | pages = 314–318 | date = February 2007 | pmid = 17284509 | doi = 10.1345/aph.1H458 | s2cid = 22855759 }}</ref> It may also be of benefit in chronic axonal [[polyneuropathy]].<ref name="Galassi-2011">{{cite journal | vauthors = Gales BJ, Gales MA | title = Pyridostigmine in the treatment of orthostatic intolerance | journal = The Annals of Pharmacotherapy | volume = 41 | issue = 2 | pages = 314–318 | date = February 2007 | pmid = 17284509 | doi = 10.1345/aph.1H458 | s2cid = 22855759 }}</ref> |
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It is also being prescribed [[off-label use|off-label]] for [[postural orthostatic tachycardia syndrome]] (POTS) as well as complications resulting from [[Ehlers–Danlos syndrome]].<ref name="Galassi-2011"/><ref>{{cite journal | vauthors = Kanjwal K, Karabin B, Sheikh M, Elmer L, Kanjwal Y, Saeed B, Grubb BP | title = Pyridostigmine in the treatment of postural orthostatic tachycardia: a single-center experience | journal = Pacing and Clinical Electrophysiology | volume = 34 | issue = 6 | pages = 750–755 | date = June 2011 | pmid = 21410722 | doi = 10.1111/j.1540-8159.2011.03047.x | s2cid = 20405336 }}</ref> |
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==Contraindications== |
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Pyridostigmine bromide is contraindicated in cases of mechanical intestinal or urinary obstruction and should be used with caution in patients with bronchial asthma.<ref name=autogenerated1>[http://www.mestinon.com Mestinon | Home<!-- Bot generated title -->] {{webarchive|url=https://web.archive.org/web/20080513104925/http://www.mestinon.com/ |date=2008-05-13 }}</ref><ref>[https://www.drugs.com/pro/mestinon.html Mestinon Official FDA information, side effects and uses<!-- Bot generated title -->] {{webarchive|url=https://web.archive.org/web/20080524034654/http://www.drugs.com/pro/mestinon.html |date=2008-05-24 }}</ref> |
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==Side effects== |
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Common side effects include:<ref name=autogenerated1 /> |
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* Sweating |
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* Diarrhea |
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* Nausea |
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* Vomiting |
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* Abdominal cramps |
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* Increased salivation |
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* Tearing |
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* Increased bronchial secretions |
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* Constricted pupils |
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* Facial flushing due to vasodilation |
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* Erectile dysfunction |
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Additional side effects include:<ref name=autogenerated1 /> |
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* Muscle twitching |
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* Muscle cramps and weakness |
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==Mechanism of action== |
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Pyridostigmine is an [[acetylcholinesterase inhibitor]]. It [[enzyme inhibitor|inhibit]]s [[acetylcholinesterase]] in the [[synaptic cleft]], thus slowing down the [[hydrolysis]] of [[acetylcholine]]. Like its predecessor [[neostigmine]], it is a quaternary [[carbamate]] inhibitor of cholinesterase that does not cross the [[blood–brain barrier]]. It carbamylates about 30% of peripheral cholinesterase enzyme, and the carbamylated enzyme eventually regenerates by natural hydrolysis and excess acetylcholine (ACh) levels revert to normal. |
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The ACh diffuses across the synaptic cleft and binds to receptors on the post synaptic membrane, causing an influx of [[sodium]] (Na<sup>+</sup>,) resulting in depolarization. If large enough, this depolarization results in an action potential. To prevent constant stimulation once the ACh is released, an enzyme called [[acetylcholinesterase]] is present in the endplate membrane close to the receptors on the post synaptic membrane, and quickly hydrolyses ACh. |
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==Names== |
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Pyridostigmine bromide is available under the trade name Mestinon ([[Valeant Pharmaceuticals International|Valeant Pharmaceuticals]]), Regonol and Gravitor (SUN Pharma). |
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==References== |
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{{Reflist}} |
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==External links== |
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* {{cite web | url = https://druginfo.nlm.nih.gov/drugportal/name/pyridostigmine | publisher = U.S. National Library of Medicine | work = Drug Information Portal | title = Pyridostigmine }} |
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{{Acetylcholine metabolism and transport modulators}} |
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{{Portal bar|Medicine}} |
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[[Category:Acetylcholinesterase inhibitors]] |
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[[Category:Aromatic carbamates]] |
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[[Category:Dimethylamino compounds]] |
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[[Category:Peripherally selective drugs]] |
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[[Category:Pyridinium compounds]] |
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[[Category:Wikipedia medicine articles ready to translate]] |
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[[Category:World Health Organization essential medicines]] |