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WHO Drug Information Vol. 17, No. 1, 2003
(2003; 77 pages) View the PDF document
Table of Contents
Open this folder and view contentsReports on Individual Drugs
Open this folder and view contentsVaccines and Biomedicines
Open this folder and view contentsCurrent Topics
Open this folder and view contentsSafety Issues
Open this folder and view contentsEssential Medicines
Open this folder and view contentsRegulatory and Safety Action
Open this folder and view contentsRecent Publications and Sources of Information
View the documentProposed International Nonproprietary Names: List 88
View the documentAnnex 1 - PROCEDURE FOR THE SELECTION OF RECOMMENDED INTERNATIONAL NONPROPRIETARY NAMES FOR PHARMACEUTICAL SUBSTANCES*
View the documentAnnex 2 - GENERAL PRINCIPLES FOR GUIDANCE IN DEVISING INTERNATIONAL NONPROPRIETARY NAMES FOR PHARMACEUTICAL SUBSTANCES*
View the documentAnnexe 1 - PROCEDURE A SUIVRE EN VUE DU CHOIX DE DENOMINATIONS COMMUNES INTERNATIONALES RECOMMANDEES POUR LES SUBSTANCES PHARMACEUTIQUES
View the documentAnnexe 2 - DIRECTIVES GENERALES POUR LA FORMATION DE DENOMINATIONS COMMUNES INTERNATIONALES APPLICABLES AUX SUBSTANCES PHARMACEUTIQUES*
View the documentAnexo 1 - PROCEDIMIENTO DE SELECCION DE DENOMINACIONES COMUNES INTERNACIONALES RECOMENDADAS PARA LAS SUSTANCIAS FARMACEUTICAS
View the documentAnexo 2 - PRINCIPIOS GENERALES DE ORIENTACION PARA FORMAR DENOMINACIONES COMUNES INTERNACIONALES PARA SUSTANCIAS FARMACEUTICAS*
 

Annex 2 - GENERAL PRINCIPLES FOR GUIDANCE IN DEVISING INTERNATIONAL NONPROPRIETARY NAMES FOR PHARMACEUTICAL SUBSTANCES*

* In its twentieth report (WHO Technical Report Series, No. 581, 1975), the WHO Expert Committee on Nonproprietary Names for Pharmaceutical Substances reviewed the general principles for devising, and the procedures for selecting, international nonproprietary names (INN) in the light of developments in pharmaceutical compounds in recent years. The most significant change has been the extension to the naming of synthetic chemical substances of the practice previously used for substances originating in or derived from natural products. This practice involves employing a characteristic "stem" indicative of a common property of the members of a group. The reasons for, and the implications of, the change are fully discussed.


1. International Nonproprietary Names (INN) should be distinctive in sound and spelling. They should not be inconveniently long and should not be liable to confusion with names in common use.

2. The INN for a substance belonging to a group of pharmacologically related substances should, where appropriate, show this relationship. Names that are likely to convey to a patient an anatomical, physiological, pathological or therapeutic suggestion should be avoided.

These primary principles are to be implemented by using the following secondary principles:

3. In devising the INN of the first substance in a new pharmacological group, consideration should be given to the possibility of devising suitable INN for related substances, belonging to the new group.

4. In devising INN for acids, one-word names are preferred; their salts should be named without modifying the acid name, e.g. "oxacillin" and "oxacillin sodium", "ibufenac" and "ibufenac sodium".

5. INN for substances which are used as salts should in general apply to the active base or the active acid. Names for different salts or esters of the same active substance should differ only in respect of the name of the inactive acid or the inactive base.

For quaternary ammonium substances, the cation and anion should be named appropriately as separate components of a quaternary substance and not in the amine-salt style.

6. The use of an isolated letter or number should be avoided; hyphenated construction is also undesirable.

7. To facilitate the translation and pronunciation of INN, "f" should be used instead of "ph", "t" instead of "th", "e" insteadof "ae" or "oe", and "i" instead of "y"; the use of the letters "h" and "k" should be avoided.

8. Provided that the names suggested are in accordance with these principles, names proposed by the person discovering or first developing and marketing a pharmaceutical preparation, or names already officially in use in any country, should receive preferential consideration.

9. Group relationship in INN (see Guiding Principle 2) should if possible be shown by using a common stem. The following list contains examples of stems for groups of substances, particularly for new groups. There are many other stems in active use.1 Where a stem is shown without any hyphens it may be used anywhere in the name.

1 A more extensive listing of stems is contained in the working document WHO/EDM/QSM 99.6 which is regularly updated and can be requested from the INN Programme, WHO, Geneva.


Latin

English

 

-acum

-ac

anti-inflammatory agents of the ibufenac group

-actidum

-actide

synthetic polypeptides with a corticotropin-like action

-adolum

-adol )

analgetics

-adol-

-adol-)

 

-astum

-ast

antiasthmatic, antiallergic substances not acting primarily as antihistaminics

-astinum

-astine

antihistaminics

-azepamum

-azepam

diazepam derivatives

-bactamum

-bactam

β-lactamase inhibitors

bol

bol

steroids, anabolic

-buzonum

-buzone

anti-inflammatory analgesics, phenylbutazone derivatives

-cain-

-cain

antifibrillant substances with local anaesthetic activity

-cainum

-caine

local anaesthetics

cef-

cef-

antibiotics, cefalosporanic acid derivatives

-cillinum

-cillin

antibiotics, derivatives of 6-aminopenicillanic acid

-conazolum

-conazole

systemic antifungal agents, miconazole derivatives

cort

cort

corticosteroids, except prednisolone derivatives

-dipinum

-dipine

calcium channel blockers, nifedipine derivatives

-fibratum

-fibrate

clofibrate derivatives

gest

gest

steroids, progestogens

gli

gli

sulfonamide hypoglycaemics

io

io-

iodine-containing contrast media

-ium

-ium

quaternary ammonium compounds

-metacinum

-metacin

anti-inflammatory substances, indometacin derivatives

-mycinum

-mycin

antibiotics, produced by Streptomyces strains

-nidazolum

-nidazole

antiprotozoal substances, metronidazole derivatives

-ololum

-olol

β-adrenoreceptor antagonists

-oxacinum

-oxacin

antibacterial agents, nalidixic acid derivatives

-pridum

-pride

sulpiride derivatives

-pril(at)um

pril(at)

angiotensin-converting enzyme inhibitors

-profenum

-profen

anti-inflammatory substances, ibuprofen derivatives

prost

prost

prostaglandins

-relinum

-relin

hypophyseal hormone release-stimulating peptides

-terolum

-terol

bronchodilators, phenethylamine derivatives

-tidinum

-tidine

histamine H2-receptor antagonists

-trexatum

-trexate

folic acid antagonists

-verinum

-verine

spasmolytics with a papaverine-like action

vin

vin )

vinca alkaloids

-vin-

-vin)

 

 

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Last updated: May 3, 2013