* 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) |
|