Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

WHO Model List of Essential Medicines

This is a featured list. Click here for more information.
From Wikipedia, the free encyclopedia
Formulary by the World Health Organization
For the list for children, seeWHO Model List of Essential Medicines for Children.

TheWHO Model List of Essential Medicines (a.k.a.Essential Medicines List orEML[1]), published by theWorld Health Organization (WHO), contains the medications considered to be most effective and safe to meet the most important needs in ahealth system.[2] The list is frequently used by countries to help develop their own local lists ofessential medicines.[2] As of 2016[update], more than 155 countries have created national lists of essential medicines based on the World Health Organization's model list.[1] This includes bothdeveloped anddeveloping countries.[2][3]

The list is divided into core items and complementary items.[4] The core items are deemed to be the mostcost-effective options for key health problems and are usable with little additional health care resources.[4] The complementary items either require additional infrastructure such as specially trainedhealth care providers ordiagnostic equipment or have a lowercost–benefit ratio.[4] About 25% of items are in the complementary list.[5] Some medications are listed as both core and complementary.[6] While most medications on the list are available asgeneric products, being underpatent does not preclude inclusion.[7]

The first list was published in 1977 and included 208 medications.[8][2][9] The WHO updates the list every two years.[10] There are 306 medications in the 14th list in 2005,[11] 410 in the 19th list in 2015,[10] 433 in the 20th list in 2017,[12][13] 460 in the 21st list in 2019,[14][15][16] and 479 in the 22nd list in 2021.[17][18] Various national lists contain between 334 and 580 medications.[5][19] The Essential Medicines List (EML) was updated in September 2025 to its 24th edition.[20] The list contains recommendations for 523 medications.

A separate list for children up to twelve years of age, known as theWHO Model List of Essential Medicines for Children (EMLc), was created in 2007, and is in its 10th edition.[10][21][22][23][24] It was created to make sure that the needs of children were systematically considered such as availability of properformulations.[25][26] Everything in the children's list is also included in the main list.[27] The list and notes are based on the 19th to 24th edition of the main list.[4][12][14][17][28] Therapeutic alternatives with similar clinical performance are listed for some medicines and they may be considered for national essential medicines lists.[17][18] The 10th Essential Medicines List for Children was updated in September 2025.[24][29][30]

Note: Anα indicates a medicine is on the complementary list.[4][14][17]

Anaesthetics, preoperative medicines and medical gases

[edit]

General anaesthetics and oxygen

[edit]

Inhalational medicines

[edit]

Injectable medicines

[edit]

Local anaesthetics

[edit]

Complementary:

Preoperative medication and sedation for short-term procedures

[edit]

Medical gases

[edit]

Medicines for pain and palliative care

[edit]

Non-opioids and non-steroidal anti-inflammatory medicines (NSAIMs)

[edit]
A line drawing of a hexagon with two attachments
Askeletal model of the chemical structure of aspirin

Opioid analgesics

[edit]

Complementary:

Medicines for other common symptoms in palliative care

[edit]

Antiallergics and medicines used in anaphylaxis

[edit]

Antidotes and other substances used in poisonings

[edit]

Non-specific

[edit]

Specific

[edit]

Complementary:

Medicines for neurological disorders

[edit]

Medicines for central nervous system disorders

[edit]

Antiseizure medicines

[edit]

Complementary:

Medicines for multiple sclerosis

[edit]

Complementary:

Medicines for parkinsonism

[edit]

Medicines for cerebral palsy

[edit]

Medicines for headache disorders

[edit]
Medicines for acute migraine attacks
[edit]
Medicines for migraine prophylaxis
[edit]
Medicines for cluster headache
[edit]

Medicines for central nervous system infections

[edit]
Medicines for bacterial central nervous system infections
[edit]

Complementary:

Medicines for viral central nervous system infections
[edit]

Medicines for peripheral nervous system disorders

[edit]

Medicines for Guillain-Barré syndrome

[edit]

Complementary:

Medicines for myasthenia gravis

[edit]

Complementary:

Anti-infective medicines

[edit]

Anthelminthics

[edit]

Intestinal anthelminthics

[edit]
A hexagon joined to a polygon with two attachments to this double ringed structure
A skeletal model of the chemical structure of albendazole

Antifilarials

[edit]

Antischistosomals and other antinematode medicines

[edit]

Complementary:

Cysticidal medicines

[edit]

Complementary:

Antibacterials

[edit]

Access group antibiotics

[edit]

Watch group antibiotics

[edit]

Complementary:

Reserve group antibiotics

[edit]

Complementary:

Antileprosy medicines

[edit]

Antituberculosis medicines

[edit]
A small pile of white crystals
Pure crystals of ethambutol

Antifungal medicines

[edit]

Complementary:

Antiviral medicines

[edit]

Antiherpes medicines

[edit]

Antiretrovirals

[edit]
Nucleoside/nucleotide reverse transcriptase inhibitors
[edit]
Non-nucleoside reverse transcriptase inhibitors
[edit]
Protease inhibitors
[edit]
Integrase inhibitors
[edit]
Fixed-dose combinations of antiretroviral medicines
[edit]
Medicines for prevention of HIV-related opportunistic infections
[edit]
Other antivirals
[edit]

Complementary:

Antihepatitis medicines

[edit]
Medicines for hepatitis B
[edit]
Nucleoside/Nucleotide reverse transcriptase inhibitors
[edit]
Medicines for hepatitis C
[edit]
Pangenotypic direct-acting antiviral combinations
[edit]
Non-pangenotypic direct-acting antiviral combinations
[edit]
Other antivirals for hepatitis C
[edit]

Antiprotozoal medicines

[edit]

Antiamoebic and antigiardiasis medicines

[edit]

Antileishmaniasis medicines

[edit]

Antimalarial medicines

[edit]
Medicines for curative treatment
[edit]
Medicines for chemoprevention
[edit]
Medicines for chemoprophylaxis in travellers
[edit]

Antipneumocystosis and antitoxoplasmosis medicines

[edit]

Complementary:

Antitrypanosomal medicines

[edit]
African trypanosomiasis
[edit]
Medicines for the treatment of 1st stage African trypanosomiasis
[edit]
Medicines for the treatment of 2nd stage African trypanosomiasis
[edit]

Complementary:

American trypanosomiasis
[edit]

Medicines for ectoparasitic infections

[edit]

Medicines for Ebola virus disease

[edit]

Medicines for COVID-19

[edit]

No listings in this section.

Medicines for cystic fibrosis

[edit]

Complementary:

Immunomodulators and antineoplastics

[edit]

Immunomodulators for non-malignant disease

[edit]

Complementary:

Antineoplastics and supportive medicines

[edit]

Cytotoxic medicines

[edit]

Complementary:

Targeted therapies

[edit]

Complementary:

Immunomodulators

[edit]

Complementary:

Hormones and antihormones

[edit]

Complementary:

Supportive medicines

[edit]

Complementary:

Therapeutic foods

[edit]

Medicines affecting the blood

[edit]

Antianaemia medicines

[edit]

Complementary:

Medicines affecting coagulation

[edit]

Complementary:

Medicines for haemoglobinopathies

[edit]

Medicines for sickle-cell disease

[edit]

Complementary:

Medicines for thalassaemias

[edit]

Complementary:

Blood products, coagulation factors and plasma substitutes

[edit]

Blood and blood components

[edit]

Human immunoglobulins

[edit]

Complementary:

Coagulation factors

[edit]

Plasma substitutes

[edit]

Cardiovascular medicines

[edit]

Antianginal medicines

[edit]

Antiarrhythmic medicines

[edit]

Complementary:

Antihypertensive medicines

[edit]

Complementary:

Medicines used in heart failure

[edit]

Complementary:

Antithrombotic medicines

[edit]

Anti-platelet medicines

[edit]

Thrombolytic medicines

[edit]

Complementary:

Lipid-lowering agents

[edit]

Fixed-dose combinations for prevention of atherosclerotic cardiovascular disease

[edit]

Dermatological medicines

[edit]

Antifungal medicines

[edit]

Anti-infective medicines

[edit]

Anti-inflammatory and antipruritic medicines

[edit]

Medicines affecting skin differentiation and proliferation

[edit]

Complementary:

Scabicides and pediculicides

[edit]

Moisturizers

[edit]

Sunscreens, broad-spectrum

[edit]

Diagnostic agents

[edit]

Ophthalmic medicines

[edit]

Radiocontrast media

[edit]

Complementary:

Antiseptics and disinfectants

[edit]

Antiseptics

[edit]

Disinfectants

[edit]

Diuretics

[edit]

Complementary:

Gastrointestinal medicines

[edit]

Complementary:

Antiulcer medicines

[edit]

Antiemetic medicines

[edit]

Complementary:

Anti-inflammatory medicines

[edit]

Complementary:

Laxatives

[edit]

Medicines used in diarrhoea

[edit]

Oral rehydration

[edit]

Medicines for diarrhoea

[edit]

Medicines for endocrine disorders

[edit]

Adrenal hormones and synthetic substitutes

[edit]

Androgens

[edit]

Complementary:

Estrogens

[edit]

No listings in this section.

Progestogens

[edit]

Medicines for diabetes

[edit]

Insulins

[edit]

Hypoglycaemic agents

[edit]

Complementary:

Medicines for hypoglycaemia

[edit]

Complementary:

Thyroid hormones and antithyroid medicines

[edit]

Complementary:

Medicines for disorders of the pituitary hormone system

[edit]

Complementary:

Immunologicals

[edit]

Diagnostic agents

[edit]

Sera, immunoglobulins and monoclonal antibodies

[edit]

Vaccines

[edit]

Muscle relaxants (peripherally-acting) and cholinesterase inhibitors

[edit]

Complementary:

Ophthalmological preparations

[edit]

Anti-infective agents

[edit]

Anti-inflammatory agents

[edit]

Local anaesthetics

[edit]

Miotics and antiglaucoma medicines

[edit]

Mydriatics

[edit]

Complementary:

Anti-vascular endothelial growth factor (VEGF) preparations

[edit]

Complementary:

Medicines for reproductive health and perinatal care

[edit]

Contraceptives

[edit]

Oral hormonal contraceptives

[edit]

Injectable hormonal contraceptives

[edit]

Intrauterine devices

[edit]

Barrier methods

[edit]

Implantable contraceptives

[edit]

Intravaginal contraceptives

[edit]

Ovulation inducers

[edit]

Complementary:

Uterotonics

[edit]

Medicines for medical abortion

[edit]

Antioxytocics (tocolytics)

[edit]

Other medicines administered to the mother

[edit]

Medicines administered to the neonate

[edit]

Complementary:

Peritoneal dialysis solution

[edit]

Complementary:

Medicines for mental and behavioural disorders

[edit]

Medicines used in psychotic disorders

[edit]

Complementary:

Medicines used in mood disorders

[edit]

Medicines used in depressive disorders

[edit]

Medicines used in bipolar disorders

[edit]

Medicines for anxiety disorders

[edit]

Medicines used for obsessive compulsive disorders

[edit]

Medicines for disorders due to psychoactive substance use

[edit]

Medicines for alcohol use disorders

[edit]

Medicines for nicotine use disorders

[edit]

Medicines for opioid use disorders

[edit]

Complementary:

Medicines acting on the respiratory tract

[edit]

Antiasthmatic medicines and medicines for chronic obstructive pulmonary disease

[edit]

Solutions correcting water, electrolyte and acid-base disturbances

[edit]

Oral

[edit]

Parenteral

[edit]

Miscellaneous

[edit]

Vitamins and minerals

[edit]

Complementary:

Ear, nose and throat medicines

[edit]

Medicines for diseases of joints

[edit]

Medicines used to treat gout

[edit]

Disease-modifying anti-rheumatic drugs (DMARDs)

[edit]

Complementary:

Medicines for juvenile joint diseases

[edit]

Complementary:

Dental medicines and preparations

[edit]

Notes

[edit]

Anα indicates the medicine is on the complementary list for which specialized diagnostic or monitoring or training is needed. An item may also be listed as complementary on the basis of higher costs or a less attractivecost-benefit ratio.[4][14]

  1. ^Piped nitrous oxide is a major source of atmospheric pollution from healthcare facilities. Point-of-care cylinders are the preferred delivery system over centrally-supplied (piped) delivery systems
  2. ^Thiopental is an alternative
  3. ^For use in spinal anaesthesia during delivery, to prevent hypotension
  4. ^No more than 30% oxygen should be used to initiate resuscitation of neonates less than or equal to 32 weeks of gestation
  5. ^Not in children less than three months
  6. ^Not recommended for anti‐inflammatory use due to lack of proven benefit to that effect
  7. ^For the management of cancer pain
  8. ^Hydromorphone andoxycodone are alternatives
  9. ^For the management of cancer pain
  10. ^abMay be used for buccal administration when solution for oromucosal administration is not available
  11. ^abDolasetron,granisetron,palonosetron, andtropisetron are alternatives
  12. ^Cetirizine andfexofenadine are alternatives
  13. ^abcPrednisone is an alternative
  14. ^Alternative formulations of activated charcoal may be used if granules are not available
  15. ^For use as adjunctive therapy for treatment-resistant partial or generalized seizures
  16. ^Diazepam (injection) andmidazolam (injection) are alternatives
  17. ^For use in eclampsia and severe pre‐eclampsia and not for other convulsant disorders
  18. ^The presence of both 25 mg/5 mL and 30 mg/5 mL strengths on the same market would cause confusion in prescribing and dispensing and should be avoided
  19. ^abcValproic acid (sodium valproate) is not recommended in women and girls of childbearing potential owing to the high risk of birth defects and neurodevelopmental disorders in children exposed to valproic acid (sodium valproate) in the womb
  20. ^abcdefghijklmnIncluding quality-assuredbiosimilars
  21. ^Trihexyphenidyl is an alternative
  22. ^Benserazide is an alternative for carbidopa
  23. ^Naproxen is an alternative
  24. ^The presence of both 120 mg/5 mL and 125 mg/5mL strengths on the same market would cause confusion in prescribing and dispensing and should be avoided
  25. ^Eletriptan is an alternative
  26. ^Third-generation cephalosporin of choice for use in hospitalized neonates
  27. ^abDo not administer with calcium and avoid in infants with hyperbilirubinemia
  28. ^ab> 41 weeks corrected gestational age
  29. ^Only for the presumptive treatment of epidemic meningitis in children older than two years
  30. ^ab> three months
  31. ^abOralvalaciclovir is an alternative
  32. ^Moxidectin is an alternative
  33. ^Arpraziquantel is an alternative
  34. ^Oxamniquine is listed for use when praziquantel treatment fails
  35. ^> one month
  36. ^Only for the presumptive treatment of epidemic meningitis in children older than two years and in adults
  37. ^Alternatives are 4th level ATC chemical subgroup (J01CF Beta-lactamase resistant penicillins)
  38. ^Cloxacillin,dicloxacillin, andflucloxacillin are preferred for oral administration due to better bioavailability
  39. ^Use in children <8 years only for life-threatening infections when no alternative exists
  40. ^Procaine benzylpenicillin is not recommended as first-line treatment for neonatal sepsis except in settings with high neonatal mortality, when given by trained health workers in cases where hospital care is not achievable
  41. ^Third-generation cephalosporin of choice for use in hospitalized neonates
  42. ^Erythromycin is an alternative as second choice treatment for pharyngitis in children (EMLc only)
  43. ^For use in combination regimens for eradication ofH. pylori in adults
  44. ^Vancomycin powder for injection may also be used for oral administration
  45. ^Imipenem/cilastatin is an alternative for complicated intraabdominal infections and high-risk febrile neutropenia only. Meropenem is the preferred choice for acute bacterial meningitis in neonates
  46. ^Tedizolid phosphate is an alternative
  47. ^For use only in combination withmeropenem orimipenem/cilastatin
  48. ^Terizidone is an alternative
  49. ^Prothionamide is an alternative for multidrug-resistant tuberculosis
  50. ^Imipenem/cilastatin is an alternative
  51. ^For treatment of chronic pulmonaryaspergillosis,histoplasmosis,sporotrichosis,paracoccidioidomycosis, mycoses caused byT. marneffei andchromoblastomycosis; and prophylaxis of histoplasmosis and infections caused byT. marneffei in AIDS patients
  52. ^For treatment of chronic pulmonaryaspergillosis and acute invasive aspergillosis
  53. ^Anidulafungin andcaspofungin are alternatives
  54. ^Also indicated for pre-exposure prophylaxis
  55. ^> six weeks
  56. ^> three years
  57. ^≥ 4 weeks and ≥ 3 kg; ≥ 25 kg
  58. ^For use in pregnant women and in second-line regimens in accordance with WHO treatment guidelines
  59. ^abLamivudine is an alternative for emtricitabine
  60. ^Combination also indicated for pre-exposure prophylaxis
  61. ^For the treatment ofcytomegalovirus retinitis (CMVr)
  62. ^For severe illness due to confirmed or suspected influenza virus infection in critically ill hospitalized patients
  63. ^For the treatment of cytomegalovirus retinitis (CMVr)
  64. ^Pangenotypic when used in combination withsofosbuvir
  65. ^Pangenotypic when used in combination withsofosbuvir
  66. ^Pangenotypic when used in combination withdaclatasvir orravidasvir
  67. ^For the treatment of hepatitis C, in combination with direct acting anti-viral medicines
  68. ^Proposed for deletion in 2027
  69. ^> 25 kg
  70. ^Tinidazole is an alternative
  71. ^Liposomal amphotericin B has a better safety profile than the sodium deoxycholate formulation and should be prioritized for selection and use depending on local availability and cost
  72. ^abcFor use in the management of severe malaria
  73. ^For use only for the treatment ofPlasmodium vivax infection
  74. ^For use to reduce the transmission ofPlasmodium falciparum and for radical cure ofPlasmodium vivax andPlasmodium ovale infections
  75. ^For use only for prophylaxis ofPlasmodium vivax infection
  76. ^> 8 years
  77. ^For the treatment of 1st and 2nd stage human African trypanosomiasis due toTrypanosoma brucei gambiense infection
  78. ^abTo be used for the treatment ofTrypanosoma brucei gambiense infection
  79. ^To be used for the treatment of the initial phase ofTrypanosoma brucei rhodesiense infection
  80. ^Only to be used in combination witheflornithine, for the treatment ofTrypanosoma brucei gambiense infection
  81. ^abCertolizumab pegol,etanercept,golimumab, andinfliximab are alternatives, including quality-assuredbiosimilars
  82. ^Afatinib andgefitinib are alternatives
  83. ^Zanubrutinib is an alternative
  84. ^As monotherapy for deficient mismatch repair (dMMR ) / microsatellite instability-high (MSI-H) tumours
  85. ^Atezolizumab andcemiplimab are alternatives, including quality-assuredbiosimilars
  86. ^Nivolumab is an alternative, including quality-assuredbiosimilars
  87. ^Enzalutamide is an alternative
  88. ^Alternatives are 4th level ATC chemical subgroup (L02BG Aromatase inhibitors)
  89. ^Flutamide andnilutamide are alternatives
  90. ^Goserelin andtriptorelin are alternatives
  91. ^May also be used for oral administration
  92. ^Biscuit or paste of nutritional composition as determined by the UN joint statement on the community-based management of severe acute malnutrition andCodex alimentarius guidelines
  93. ^Periconceptual use for prevention of first occurrence of neural tube defects
  94. ^Epoetin alfa,beta andtheta;darbepoetin alfa;methoxy polyethylene glycol-epoetin beta; and their quality-assuredbiosimilars are alternatives
  95. ^Apixaban,edoxaban, andrivaroxaban are alternatives
  96. ^Alternatives aredalteparin andnadroparin, including their quality-assuredbiosimilars
  97. ^Acenocoumarol is an alternative
  98. ^abDeferiprone is an alternative
  99. ^Cryoprecipitate (not pathogen-reduced) is an alternative. Native cryoprecipitate should only be used in situations of life-threatening haemorrhage when pathogen-reduced cryoprecipitate is not available
  100. ^Polygeline, injectable solution, 3.5% is an alternative
  101. ^abcCarvedilol andmetoprolol are alternatives
  102. ^Alternatives are 4th level ATC chemical subgroup (C08CA Dihydropyridine derivatives)
  103. ^Atenolol,carvedilol, andmetoprolol are alternatives. Atenolol should not be used as a first-line agent in uncomplicated hypertension in patients > 60 years
  104. ^Alternatives are 4th level ATC chemical subgroup (C09AA ACE inhibitors, plain)
  105. ^Hydralazine is listed for use only in the acute management of severe pregnancy-induced hypertension. Its use in the treatment of essential hypertension is not recommended in view of the evidence of greater efficacy and safety of other medicines
  106. ^abcChlorothiazide,chlorthalidone, andindapamide are alternatives
  107. ^Alternatives are 4th level ATC chemical subgroup (C09AA ACE inhibitors, plain) (for lisinopril) and 4th level ATC chemical subgroup (C08CA Dihydropyridine derivatives) (for amlodipine)
  108. ^Alternatives are 4th level ATC chemical subgroup (C09AA ACE inhibitors, plain) (for lisinopril) and chlorthalidone, chlorothiazide, indapamide (for hydrochlorothiazide)
  109. ^abAlternatives are 4th level ATC chemical subgroup (C09CA Angiotensin II receptor blockers (ARBs), plain)
  110. ^Methyldopa is listed for use only in the management of pregnancy-induced hypertension. Its use in the treatment of essential hypertension is not recommended in view of the evidence of greater efficacy and safety of other medicines
  111. ^Alternatives are 4th level ATC chemical subgroup (C09AA ACE inhibitors, plain) (for perindopril); and 4th level ATC chemical subgroup (C08CA Dihydropyridine derivatives) (for amlodipine); and chlorthalidone, chlorothiazide, hydrochlorothiazide (for indapamide)
  112. ^Alternatives are 4th level ATC chemical subgroup (C09CA Angiotensin II receptor blockers (ARBs), plain) (for telmisartan); and 4th level ATC chemical subgroup (C08CA Dihydropyridine derivatives) (for amlodipine)
  113. ^Alternatives are 4th level ATC chemical subgroup (C09CA Angiotensin II receptor blockers (ARBs), plain) (for telmisartan); and chlorthalidone, chlorothiazide, indapamide (for hydrochlorothiazide)
  114. ^Alternatives are 4th level ATC chemical subgroup (C09CA Angiotensin II receptor blockers (ARBs), plain) (for valsartan); 4th level ATC chemical subgroup (C08CA Dihydropyridine derivatives) (for amlodipine); and chlorthalidone, chlorothiazide, indapamide (for hydrochlorothiazide)
  115. ^Alternatives are 4th level ATC chemical subgroup (C09AA ACE inhibitors, plain)
  116. ^Bumetanide andtorasemide are alternatives
  117. ^For use in high‐risk patients.Atorvastatin,fluvastatin,lovastatin, andpravastatin are alternatives
  118. ^abFluvastatin,lovastatin,pravastatin, andsimvastatin are alternatives for atorvastatin
  119. ^ab4th level ATC chemical subgroup (C09AA ACE inhibitors, plain) are alternatives for ramipril
  120. ^Atorvastatin,fluvastatin,lovastatin, andpravastatin are alternatives for simvastatin
  121. ^Bisoprolol,carvedilol, andmetoprolol are alternatives for atenolol
  122. ^Chlorthalidone,chlorothiazide, andindapamide are alternatives for hydrochlorothiazide
  123. ^4th level ATC chemical subgroup (C09AA ACE inhibitors, plain) are alternatives for perindopril
  124. ^4th level ATC chemical subgroup (C08CA Dihydropyridine derivatives) are alternatives for amlodipine
  125. ^Alternatives are 4th level ATC chemical subgroup (D01AC Imidazole and triazole derivatives) excluding combinations
  126. ^Alternatives are 4th level ATC chemical subgroup (D07AC Corticosteroids, potent (group III))
  127. ^Alternatives are 4th level ATC chemical subgroup (D07AA Corticosteroids, weak (group I))
  128. ^Calcitriol andtacalcitol are alternatives
  129. ^Podophyllotoxin is an alternative
  130. ^Certolizumab pegol,etanercept,infliximab, including quality-assuredbiosimilars, are alternatives
  131. ^Precipitated sulfur topical ointment is an alternative
  132. ^Atropine andcyclopentolate are alternatives
  133. ^Propanol is an alternative
  134. ^Iodine is an alternative
  135. ^Alternatives are 4th level ATC chemical subgroup (D08AE Phenol and derivatives)
  136. ^Bumetanide andtorasemide are alternatives
  137. ^Chlorothiazide andchlorthalidone are alternatives
  138. ^Alternatives are 4th level ATC chemical subgroup (A02BC Proton pump inhibitors) excluding combinations
  139. ^Alternatives are 4th level ATC chemical subgroup (A02BA H2-receptor antagonists) excluding combinations
  140. ^Mesalazine is an alternative
  141. ^Bisacodyl is an alternative
  142. ^In acute diarrhoea zinc sulfate should be used as an adjunct to oral rehydration salts
  143. ^Norethisterone is an alternative
  144. ^Insulin glargine,Insulin degludec, andinsulin detemir, including quality-assuredbiosimilars, are alternatives
  145. ^Insulin lispro,Insulin aspart, andinsulin glulisine, including quality-assuredbiosimilars, are alternatives
  146. ^Canagliflozin anddapagliflozin are alternatives
  147. ^Glibenclamide not suitable above 60 years. Alternatives are 4th level ATC chemical subgroup (A10BB Sulfonylureas)
  148. ^Dulaglutide,liraglutide, andtirzepatide, including quality-assuredbiosimilars, are alternatives
  149. ^abCarbimazole is an alternative depending on local availability
  150. ^For use when alternative first-line treatment is not appropriate or available; and in patients during the first trimester of pregnancy
  151. ^For use when alternative first-line treatment is not appropriate or available
  152. ^Bromocriptine is an alternative
  153. ^Exact type to be defined locally
  154. ^Atracurium is an alternative
  155. ^For infections due toChlamydia trachomatis orNeisseria gonorrhoeae
  156. ^Amikacin,kanamycin,netilmicin, andtobramycin are alternatives
  157. ^Alternatives are 4th level ATC chemical subgroup (S01AE Fluoroquinolones)
  158. ^Chlortetracycline andoxytetracycline are alternatives
  159. ^Alternatives are 4th level ATC chemical subgroup (S01HA Local anaesthetics) excluding cocaine and combinations
  160. ^Carbachol is an alternative
  161. ^Alternatives are 4th level ATC chemical subgroup (S01ED Beta blocking agents) excluding combinations
  162. ^Cyclopentolate hydrochloride orhomatropine hydrobromide are alternatives only for the EMLc
  163. ^For use in women actively breastfeeding at least 4 times per day
  164. ^Anastrozole is an alternative
  165. ^Methylergometrine is an alternative
  166. ^Only for use for induction of labour where appropriate facilities are available
  167. ^dinoprostone (prostaglandin E2) is an alternative
  168. ^Indometacin is an alternative
  169. ^Haloperidol decanonate andzuclopenthixol decanonate are alternatives
  170. ^Chlorpromazine is an alternative for the tablet
  171. ^Risperidone injection is an alternative
  172. ^Aripiprazole,olanzapine,paliperidone, andquetiapine are alternatives
  173. ^abcCitalopram,escitalopram,fluvoxamine,paroxetine, andsertraline are alternatives
  174. ^Aripiprazole,olanzapine, andpaliperidone are alternatives
  175. ^Lorazepam is an alternative
  176. ^For short-term emergency management of acute and severe anxiety symptoms only
  177. ^Buprenorphine is an alternative. The medicines should only be used within an established support programme
  178. ^Beclometasone,ciclesonide,flunisolide,fluticasone, andmometasone are alternatives
  179. ^Beclometasone/formoterol,budesonide/salmeterol,fluticasone/formoterol,fluticasone furoate/vilanterol, andmometasone/formoterol are alternatives
  180. ^Terbutaline is an alternative
  181. ^Aclidinium,glycopyrronium, andumeclidinium are alternatives
  182. ^Ergocalciferol is an alternative
  183. ^Colecalciferol is an alternative
  184. ^Ofloxacin is an alternative
  185. ^For use for rheumatic fever, juvenile arthritis, Kawasaki disease
  186. ^Triamcinolone acetonide is an alternative
  187. ^Of any type for use as dental sealant
  188. ^Of any type for use as dental filling material

References

[edit]
  1. ^ab"The WHO Essential Medicines List (EML): 30th anniversary". World Health Organization. Archived fromthe original on 27 May 2014. Retrieved26 June 2016.
  2. ^abcd"Essential medicines".World Health Organization. Archived fromthe original on 2 October 2008. Retrieved19 January 2017.
  3. ^Persaud N, Jiang M, Shaikh R, Bali A, Oronsaye E, Woods H, et al. (June 2019)."Comparison of essential medicines lists in 137 countries".Bull. World Health Organ.97 (6): 394–404C.doi:10.2471/BLT.18.222448.hdl:10665/325509.ISSN 0042-9686.PMC 6560372.PMID 31210677.
  4. ^abcdef"19th WHO Model List of Essential Medicines"(PDF). World Health Organization. April 2015. p. Annex 1. Retrieved17 January 2017.
  5. ^abBansal D, Purohit VK (January 2013)."Accessibility and use of essential medicines in health care: Current progress and challenges in India".Journal of Pharmacology & Pharmacotherapeutics.4 (1):13–18.doi:10.4103/0976-500X.107642.eISSN 0976-5018.ISSN 0976-500X.PMC 3643337.PMID 23662019.S2CID 207481731.
  6. ^World Health Organization (2003). The selection and use of essential medicines (Report).World Health Organization (WHO).hdl:10665/42826.ISBN 92-4-120920-8. WHO technical report series 920.
  7. ^Beall R (2016)."Patents and the WHO Model List of Essential Medicines (18th Edition): Clarifying the Debate on IP and Access"(PDF).World Intellectual Property Organization (WIPO). Retrieved3 May 2017.
  8. ^World Health Organization (1977).The selection of essential drugs: report of a WHO expert committee [meeting held in Geneva from 17 to 21 October 1977]. Geneva: World Health Organization.hdl:10665/41272.ISBN 92-4-120615-2. Technical report series; no. 615.
  9. ^Wirtz VJ, Hogerzeil HV, Gray AL, Bigdeli M, de Joncheere CP, Ewen MA, et al. (January 2017)."Essential medicines for universal health coverage".The Lancet.389 (10067):403–476.doi:10.1016/S0140-6736(16)31599-9.PMC 7159295.PMID 27832874.
  10. ^abc"WHO Model Lists of Essential Medicines".World Health Organization.The current versions are the 21st WHO Essential Medicines List (EML) and the 7th WHO Essential Medicines List for Children (EMLc) updated in June 2019.
  11. ^Prakash B, Nadig P, Nayak A (2016)."Rational Prescription for a Dermatologist".Indian Journal of Dermatology.61 (1):32–38.doi:10.4103/0019-5154.174017.PMC 4763692.PMID 26955092.
  12. ^abWorld Health Organization (2017).WHO model list of essential medicines, 20th list (March 2017, amended August 2017). Geneva.hdl:10665/273826.{{cite book}}: CS1 maint: location missing publisher (link)
  13. ^"Essential Medicines List and WHO Model Formulary".World Health Organization. Archived fromthe original on 3 August 2008. Retrieved5 May 2018.
  14. ^abcdWorld Health Organization (2019).World Health Organization model list of essential medicines: 21st list 2019. Geneva.hdl:10665/325771. WHO/MVP/EMP/IAU/2019.06. License: CC BY-NC-SA 3.0 IGO.{{cite book}}: CS1 maint: location missing publisher (link)
  15. ^World Health Organization (2019).Executive summary: the selection and use of essential medicines 2019: report of the 22nd WHO Expert Committee on the selection and use of essential medicines. Geneva.hdl:10665/325773. WHO/MVP/EMP/IAU/2019.05. License: CC BY-NC-SA 3.0 IGO.{{cite book}}: CS1 maint: location missing publisher (link)
  16. ^"Strengthening access to essential medicines".World Health Organization. Retrieved3 May 2020.
  17. ^abcdWorld Health Organization (2021).World Health Organization model list of essential medicines: 22nd list (2021). Geneva: World Health Organization.hdl:10665/345533. WHO/MHP/HPS/EML/2021.02.
  18. ^abWorld Health Organization (2021).Executive summary: the selection and use of essential medicines 2021: report of the 23rd WHO Expert Committee on the selection and use of essential medicines: virtual meeting, 21 June–2 July 2021. Geneva: World Health Organization.hdl:10665/345554. WHO/MHP/HPS/EML/2021.01.
  19. ^World Health Organization (2021).The selection and use of essential medicines: report of the WHO Expert Committee on Selection and Use of Essential Medicines, 2021 (including the 22nd WHO model list of essential medicines and the 8th WHO model list of essential medicines for children). Geneva: World Health Organization.hdl:10665/351172.ISBN 978-92-4-004114-1. WHO technical report series;1035. License: CC BY-NC-SA 3.0 IGO.
  20. ^World Health Organization (2025).The selection and use of essential medicines, 2025: WHO Model List of Essential Medicines, 24th list. Geneva: World Health Organization.doi:10.2471/B09474.hdl:10665/382243. License: CC BY-NC-SA 3.0 IGO.
  21. ^World Health Organization (2019).World Health Organization model list of essential medicines for children: 7th list 2019. Geneva.hdl:10665/325772. WHO/MVP/EMP/IAU/2019.07. License: CC BY-NC-SA 3.0 IGO.{{cite book}}: CS1 maint: location missing publisher (link)
  22. ^World Health Organization (2021).World Health Organization model list of essential medicines for children: 8th list (2021). Geneva: World Health Organization.hdl:10665/345534. WHO/MHP/HPS/EML/2021.03.
  23. ^World Health Organization (2023).The selection and use of essential medicines 2023: web annex B: World Health Organization model list of essential medicines for children: 9th list (2023). Geneva: World Health Organization.hdl:10665/371091. WHO/MHP/HPS/EML/2023.03.
  24. ^abWorld Health Organization (2025).The selection and use of essential medicines, 2025: WHO Model List of Essential Medicines for Children,10th list. Geneva: World Health Organization.doi:10.2471/B09475.hdl:10665/382242. License: CC BY-NC-SA 3.0 IGO.
  25. ^Rose K, Anker JN (2010).Guide to Paediatric Drug Development and Clinical Research. Karger Medical and Scientific Publishers. p. 42.ISBN 978-3-8055-9362-5.
  26. ^Seyberth HW, Rane A, Schwab M (2011).Pediatric Clinical Pharmacology. Springer Science & Business Media. p. 358.ISBN 978-3-642-20195-0.
  27. ^Hoppu K (June 2017). "Essential Medicines for Children".Clinical Pharmacology and Therapeutics.101 (6):718–720.doi:10.1002/cpt.661.PMID 28182281.S2CID 23873145.
  28. ^World Health Organization (2023).The selection and use of essential medicines 2023: web annex A: World Health Organization model list of essential medicines: 23rd list (2023). Geneva: World Health Organization.hdl:10665/371090. WHO/MHP/HPS/EML/2023.02.
  29. ^World Health Organization (2023).The selection and use of essential medicines 2023: executive summary of the report of the 24th WHO Expert Committee on Selection and Use of Essential Medicines, 24 28 April 2023. Geneva: World Health Organization.hdl:10665/371291. WHO/MHP/HPS/EML/2023.01.
  30. ^World Health Organization (2025).The selection and use of essential medicines 2025: report of the 25th WHO Expert Committee on Selection and Use of Essential Medicines: executive summary. Geneva: World Health Organization.doi:10.2471/B09544.hdl:10665/382350. License: CC BY-NC-SA 3.0 IGO.

Further reading

[edit]

External links

[edit]
Development
Classes
Administration
Vaccines
Bacterial
Viral
Protozoan
Helminthiasis
Other
Inventors/
researchers
Controversy
Related
Portals:
Retrieved from "https://en.wikipedia.org/w/index.php?title=WHO_Model_List_of_Essential_Medicines&oldid=1316043431"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp