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Essential Drugs Monitor No. 017 (1988)
(1988)
Table of Contents
View the documentIntroduction
View the documentObjective
View the documentEthical criteria
View the documentApplicability and implementation of criteria
View the documentPromotion
View the documentAdvertising
View the documentMedical Representatives
View the documentFree samples of prescription drugs for promotional purposes
View the documentSymposia and other scientific meetings
View the documentPost-marketing scientific studies, surveillance and dissemination of information
View the documentPackaging and labelling
View the documentInformation for patients: package inserts, leaflets and booklets
View the documentPromotion of exported drugs
View the documentAppendix - Sample Drug Information Sheet
Open this folder and view contentsEDM-17 DRUG DISCUSSIONS AT THE 47TH WORLD HEALTH ASSEMBLY
Open this folder and view contentsRole of the Pharmacist
 

Appendix - Sample Drug Information Sheet

Drug information sheets Various types of information are needed by prescribers and consumers to ensure the safe and effective use of drugs. The following list is a sample that should be adjusted to meet the needs and abilities of the prescriber.

(1) International Nonproprietary Name (INN) of each active substance.

(2) Pharmacological data: a brief description of pharmacological effects and mechanism of action.

(3) Clinical Information:

(a) Indications: whenever appropriate, simple diagnostic criteria should be provided.

(b) Dosage regimen and relevant pharmacokinetic data:

* average and range for adults and children;

* dosing interval;

* average duration of treatment;

* special situations, e.g., renal, hepatic, cardiac, or nutritional insufficiencies that require either increased or reduced dosage.

(c) Contra-indications.

(d) Precautions and warnings (reference to pregnancy,lactation, etc.).

(e) Adverse effects (quantify by category, if possible). (f) Drug interactions (include only if clinically relevant; drugs used for self-medication should be included).

(g) Overdosage:

* brief clinical description of symptoms;

* non-drug treatment and supportive therapy;

* specific antidotes.

(4) Pharmaceutical information:

(a) Dosage forms.

(b) Strength of dosage form.

(c) Excipients.

(d) Storage conditions and shelf-life (expiry date).

(e) Pack sizes.

(f) Description of the product and package.

(g) Legal category (narcotic or other controlled drug, prescription or non-prescription. (h) Name and address of manufacturer(s) and importer(s).

Copies of the WHO Criteria for Medicinal Drug Promotion are available in English, French, Spanish, Russian, Chinese and Arabic from: World Health Organization, Distribution and Sales, 1211 Geneva 27, Switzerland. Price: Sw.fr.8.-/US$7.20 and in developing countries Sw.fr.5.60. If you have concerns about medicinal drug promotion in your country contact:

- the national drug regulatory authority;

- Medical Lobby for Appropriate Marketing (MaLAM);

- National/international consumer organizations;

- International Federation of Pharmaceutical Manufacturers' Association (IFPMA) and local industry associations, if you consider that the promotion conflicts with the international or any national industry code of marketing;

- Journal and newsletter editors/publishers;

- The Monitor, and enclose a copy of the offending advertisement

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Last updated: May 3, 2013