A Review on Marketing of OTC
Drugs
Md. Yaqub Khan*, Poonam Gupta, Dr. Dipendu Goswami, Bipin Bihari, Vikas Kumar Verma
Saroj Institute of Technology and Management, Ahimamau P.O. Arjunganj Sultanpur Road, Lucknow
*Corresponding Author E-mail: khanishaan16@yahoo.com
ABSTRACT
Purchase and use
of OTC drugs without full knowledge is not only a waste of resources for all
stakeholders but can be harmful for consumers. Creating awareness of rational
drug use is only possible through continued public education with a broad
vision of good health and wellbeing of the society. In developed economies, the
four As of marketing has been addressed fairly well but in India, the
accessibility and awareness is still on a lower side especially for allopathic
OTC drugs .In India, the import, manufacture, distribution and sale of drugs
and cosmetics are regulated by the Drugs and Cosmetics Act (DCA) and its
subordinate legislation, the Drugs and Cosmetics Rules (DCR).
KEYWORDS: Over the Counter (OTC) drugs, Pharmaceutical company, Continuous
pharmacist education (CPE), Corporate Social Opportunity (CSO), Food and drug
administration (FDA), Corporate social responsibility (CSR), ottom of pyramid (BOP)
INTRODUCTION:
OTC Drugs’ means
drugs legally allowed to be sold ‘Over The Counter’, i.e. without the
prescription of a Registered Medical Practitioner. In India, though the phrase has no legal
recognition, all the drugs that are not included in the list of ‘prescription
drugs’ are considered as non-prescription drugs (or OTC drugs). Prescription
Drugs are those that fall under two schedules of the Drug and Cosmetics Rules,
1945: Schedule H and Schedule X. Drugs falling under Schedule G require the
following mandatory text on the label: “Caution: It is dangerous to take this
preparation except under medical supervision” and hence are not advertised to
the public voluntarily by the industry. In India, the import, manufacture,
distribution and sale of drugs and cosmetics ares
regulated by the Drugs and Cosmetics Act (DCA) and its subordinate legislation,
the Drugs and Cosmetics Rules (DCR).
Over-the-counter (OTC) drugs are medicines
that may be sold directly to a consumer without a prescription from a healthcare
professional, as compared to prescription drugs, which may be sold only to
consumers possessing a valid prescription. In many countries, OTC drugs are
selected by a regulatory agency to ensure that they are
ingredients that are safe and effective when used without a physician's
care.
OTC drugs are usually regulated by active pharmaceutical ingredients
(APIs), not final products. By regulating APIs instead of specific drug
formulations, governments allow manufacturers freedom to formulate ingredients,
or combinations of ingredients, into proprietary mixtures. [1, 2]
REGULATION BY COUNTRY [3,
4]
CANADA:
An intermediate category—non-prescription items
that must be kept behind the counter, in a store room, or on a shelf readily
visible by the pharmacist, which includes weak codeine products, muscle
relaxants, and some antihistamines—exists.
UNITED STATES:
In the United States, the manufacture and sale of
OTC substances is regulated by the Food and Drug Administration. The FDA
requires that all "new drugs" obtain a New Drug Application ("NDA")
prior to entering interstate commerce, but the act exempts any drugs generally recognized as safe and
effective ("GRAS/E") from this requirement.
In order to deal with the vast number of OTC drugs
that were already on the market prior to the requirement that all drugs obtain
an NDA, the FDA created the OTC monograph system to review classes of drugs and
categorize them as GRAS/E after review by expert panels. This meant that
certain classes of OTC drugs would not be required to obtain an NDA and could
remain on the market if they conformed to the monograph guidelines for doses,
labeling, and warnings which are finalized in the Code of Federal Regulations .Thus, in the
United States an OTC drug product is allowed to be marketed either: (1)
pursuant to an FDA monograph; or (2)
pursuant to an NDA for products that do not fit within a specific monograph.
There is also the possibility that certain OTC drug products are marketed under
the grandfather provisions of the Federal Food, Drug, and Cosmetic Act,
but FDA has never formally acknowledged that any legitimate grandfather OTC
drug exists.
AYURVEDIC
MEDICINES [5]
OTC proprietary
drugs which are registered as ‘Ayurvedic Medicines’
(traditional Indian medicines containing natural / herbal ingredients) are also
regulated by the DCA and DCR. However, they do not require a drug licence and can therefore be sold by non-chemists. There is
no price control on ‘Ayurvedic medicines’. Some of
the top OTC brands in India such as Vicks VaproRub, Amrutanjan Balm, Zandu Balm, Iodex, Moov Pain Cream, Itch
Guard Cream, ENO Fruit Salt, Vicks Cough Drops, Halls Lozenges, etc., are
registered as ‘Ayurvedic Medicines’ because of their
plant-based natural active ingredients. Considering the above framework, key
categories with OTC potential in India would be:
• Vitamins and
minerals
• Cough and cold
• Gastrointestinals
• Analgesics
/Dermatological
RESTRICTED O.T.C.
SUBSTANCES:
An ill-defined third category of substances
comprises those products having over-the-counter status from the FDA, while being simultaneously subject to
other restrictions on sale. While these products are legally classified as OTC
drugs, they are typically stored behind the counter and are sold only in stores
that are registered with their state. Such items may be unavailable in
convenience or grocery stores that stock other non-restricted OTC medications.
For example, many U.S. drugstores have moved
products containing pseudoephedrine, an OTC product, into locations
where customers must ask a pharmacist for them. A prescription is not required;
the change has been made in an effort to reduce methamphetamine
production. Since the passage of the Illinois Methamphetamine Precursor
Control Act and the subsequent Federal Combat Methamphetamine Epidemic Act
of 2005, the purchase of pseudoephedrine
in the United States is restricted. Sellers of
pseudoephedrine must obtain and record the identity of the purchaser and
enforce quantity restrictions. [6]
ADVERTISING TO
THE GENERAL PUBLIC [7]
The Drug and
Magic Remedies (Objectionable Advertisement) Act mentions a list of ailments
for which no advertising is permitted. It also prohibits misleading
advertisements, which, directly or indirectly, give false impressions regarding
the true character of the drug; make false claims, or are otherwise false or
misleading in any particular respect. The DCGI’s office in collaboration with
OPPI has released a Voluntary Code on OTC Advertising, which is being followed
by all OPPI member companies. Currently, there is no specific law, which
prohibits the advertising of prescription drugs although industry practice is
not to advertise prescription-only drugs. The DCGI’s office is considering
coming out with a notification prohibiting the advertising of any drug, which
legally requires a doctor’s prescription for its purchase.
The following OTC
medicines advertising can be seen on TV in India:
• Digestives
• Antacids
• Antiflatulents
• Cold rubs
and analgesic balms/creams
•
Vitamins/tonics/health
supplements (especially herbals and Ayurvedic-registered)
• Medicated
skin treatment
• Analgesic/cold
tablets
• Antiseptic
creams/liquids
• Glucose
powders
• Cough
liquids
• Throat
lozenges
• Medicated
dressing (band-aids)
• Baby gripe
water.
•
Vasodilators
•
Anti-acne
Drugs
•
Non-Steroidal
Anti-Inflammatory Drugs
•
Smoking
Cessation Drugs
BENEFITS AND RISKS OF SWITCHING FROM PRESCRIPTION ONLY
TO O.T.C. [8]
POSSIBLE
BENEFITS:
·
Increased
access
·
Decreased
frequency of visits to physicians, leading to lower healthcare costs
·
s3.
Improved education of consumers
·
Increased
autonomy of patients
·
Decreased
cost to third party players
POSSIBLE RISKS:
·
Inaccurate
diagnosis
·
Delay
in obtaining needed therapy
·
Use of
suboptimal therapy
·
Drug
resistance
·
Increased
costs to patients
·
Failure
to follow label instructions (Adverse effects, Drug interactions)
7. Perceived loss
of control by physicians
DISTRIBUTION:
There is at
present no system of national chains of supermarkets or drugstores /
pharmacies, and small independent shops dominate retailing. However, a few
chains such as Apollo Pharmacy, Medicine Shoppe, and Good Health etc. are
entering the market, which will make inroads all over India in the near future.
Typically however, less than 5% of sales of FMCG manufacturers currently (in
2006) go through organized retailers. [9]
PRICING:
Price controls
are carried out on certain drugs by virtue of the Drugs (Prices Control) Order
1995 (DPCO), under the Essential Commodities Act (ECA). The DPCO is the
responsibility of the Ministry of Chemicals and Fertilizers and is supervised
by the National Pharmaceutical Pricing Authority (NPPA). It outlines the
classification of price-controlled products and methods of price fixation and
revision. The NPPA monitors the prices by fixing and revising prices of drugs.
Only a few OTC actives, e.g. acetylsalicylic acid and ephedrine and its salts,
fall under current DPCO price control. [10]
THE O.T.C.
MARKET:
Global OTC
pharmaceuticals grew with CAGR of 5.1% for the five year period spanning 2002-
06 to reach $88.7 billion. At a global level Parma giants are leveraging the
power of OTC to face the challenges they face today .Globalization, shrinking
new product pipeline, increasing cost of new drug discovery, shrinking PLC of
existing products, ever increasing demand by managed healthcare organizations,
public and government to cut down the prices of patent protected drugs,
stringent safety rules of FDA and entry of new players in the market are
putting tremendous pressure on all Parma companies especially the giants.
Pfizer Inc’s, world’s largest drug maker, recent decision to cut US sales force
by about 20% clearly express the pressure such giants face. [11]
MARKETING
AUTHORIZATION:
The major source
for pharmaceutical regulation is the Drugs and Cosmetics Act (DCA) and its
subordinate legislation, the Drugs and Cosmetics Rules (DCR). This legislation
applies to the whole of India and to all sorts of medicines (e.g. allopathic, ayurvedic, homeopathic, etc.) whether imported or made in
India. The legislation is enforced by the Central Government (Ministry of
Health and Family Affairs) in New Delhi, which is responsible for its overall
supervision. The office of the Drugs Controller General of India (DCGI) has
prime responsibility for approving all new molecules and unique new
formulations. However, power to provide manufacturing and selling licenses
which are the two main registrations required to manufacture and sell a drug –
belongs to each individual State government through its Food and Drug Administration
(FDA), who also carry out enforcement of DCA and DCR. Matters of new molecule
approval and standards, clinical trials, introduction of a new unique
formulation and import licenses are handled by the DCGI. [12]
THE CHANGING
CONSUMER:
The consumers are
changing world over. Today they are more informed, use more gadgets, lead a
fast life and thereby face higher stress. Environmental changes in the form of
ever increasing pollution, heavy road traffic leading to increasing commuting
time, stressful workplace environment and fast changing technology put
continuous pressure to adapt and adjust Changing lifestyle with smaller living
space, less exercise(sedentary jobs), taking junk food ,consuming addictive
products to stay awake on the job for longer hours and eating on the run put
more stress on the body which get expressed in the form of psychosomatic
disorders like frequent headache, allergy, common cold, constipation, backache,
acidity, chronic fatigue etc... Which they are trying to manage with Over The
Counter (OTC) drugs. This has lead to steady increase in self medication for
the past many years. The enfranchised customer of today feels more independent
and self reliant and is hesitant to adopt the orthodox model of expert
prescription, monitored medication and supervision throughout the treatment
period to manage common ailments. With increasing medico legal cases, [13]
US OTC
PHARMACEUTICALS MARKET:
Approval of
over-the-counter status for a drug requires an assessment by the Food and Drug
Administration (FDA) that the drug is safe and effective. Under current
regulations, a new drug can be exempted from prescription-only status by FDA
approval of a new-drug application supporting the use of the product on an
over-the-counter basis. Alternatively, a drug can be marketed over the counter
if its ingredients are included in previously published regulations defining
the requirements for over-the-counter status and if the labeling of the product
complies with these regulations. The standards also apply to drugs that have
already been approved for prescription-only sale and that are being considered
for a switch to over-the counter status. The Drug Price Competition and Patent
Term Restoration Act of 1984 potentially provides three additional years of marketing
exclusivity for the makers of drugs switched from prescription to
over-the-counter status if the FDA has required additional clinical trials
deemed essential to evaluate the switch. If a prescription drug is approved for
over-the-counter marketing, the drug may still be available by prescription for
certain indications or for use at doses not approved for over-the-counter
marketing. Can the patient recognize and diagnose in himself or herself the
condition specified in the proposed indication?
1.
When reading
a product label, can the patient extract the key information necessary to use
the drug properly?
2.
3. Will
the over-the-counter drug be effective when used as recommended?
3.
4. Is
the drug safe when used as instructed?
The US OTC
Pharmaceuticals market generated total revenues of $21.2 billion in 2006, this
representing a CAGR of 4.3%for the five year period spanning 2002-06.In
comparison, the Chinese and Japanese OTC Pharmaceuticals markets grew with
CAGRs of 7% and 2.9% over the same period, to reach respective values of $11.9
billion and $14.8billion in 2006.
[14]
TABLE 1:- UNITED STATES O.T.C. PHARMACEUTICALS MARKET
SEMENTATION: % SHARE, BY VALUE, 2006 [15]
CATEGORY |
%
SHARE |
Cough and cold preparation |
22.30 |
Vitamins and minerals |
18.70 |
Analgesics |
15.20 |
Medicated skin products |
12.60 |
Traditional medicines |
5.30 |
Other |
25.90 |
TABLE 2:- UNITED STATES O.T.C. PHARMACEUTICALS MARKET
SHARE: % SHARE, BY VALUE, 2004 [16]
COMPANY |
%
SHARE |
Pfizer Inc |
7.20 |
Wyeth |
6.00 |
Johnson and Johnson |
4.40 |
Other |
82.40 |
TABLE 3:- UNITED STATES O.T.C. PHARMACEUTICALS
DISTRIBUTION: % SHARE, BY VALUE, 2004 [17]
CHANNEL |
%
SHARE |
Pharmacies/ drugstores |
32.30 |
Mass merchandisers/ warehouse clubs |
20.80 |
Supermarkets/hypermarkets |
8.60 |
Other |
38.30 |
EUROPEAN
O.T.C. PHARMACEUTICALS MARKET
The European OTC
Pharmaceuticals market generated total revenues of $23.6 billion in 2006,this
representing a CAGR of 2.5%for the five year period spanning 2002-06.In
comparison, the Global and Asia-Pacific OTC Pharmaceuticals markets grew with
CAGR of 5.1% and 6.9 % over the same period, to reach respective values of
$88.7 billion and $39.1billion in 2006. [18]
TABLE 4:- EUROPE O.T.C. PHARMACEUTICALS MARKET
SEGMENTATION: % SHARE, BY VALUE, 2006 [19]
CATEGORY |
%
SHARE |
Cough and cold preparation |
18.70 |
Vitamins and minerals |
16.00 |
Analgesics |
15.00 |
Medicated skin products |
8.90 |
Traditional medicines |
16.70 |
Other |
24.60 |
INDIAN O.T.C.
PHARMACEUTICALS MARKET:
Indian market
faces the problem of ‘Deemed OTC market’ where in ethical drugs are also sold
without a prescription due to poor monitoring and control by FDA. Self
medication tendency is traditionally very high due to the high availability of
traditional medicines, the awareness and acceptance of which is very high among
the public. The Indian OTC pharmaceuticals market generated total revenues of
$2.5 billion in 2006,this representing a compound annual growth rate of 8.3%for
the five year period spanning 2002- 2006.In comparison ,the US and Chinese OTC
pharmaceuticals markets grew with CAGRs of 4.3% and 7% over the same period ,to
reach respective values of $21.2billion and $11.9billion in 2006. Traditional
medicines proved the most lucrative for the Indian OTC pharmaceuticals market
in 2006, generating total revenues of $679.3 million. In comparison, sales of
cough and cold preparations generated revenues of $492.6 million in 2006. [20]
TABLE 5:- INDIAN O.T.C. PHARMACEUTICALS MARKET
SEGMENTATION: % SHARE, BY VALUE, 2006 [21]
CATEGORY |
%
SHARE |
Cough and cold preparation |
19.80 |
Vitamins and minerals |
11.60 |
Analgesics |
11.40 |
Medicated skin products |
2.60 |
Traditional medicines |
27.30 |
Other |
27.30 |
TABLE 6:- INDIAN O.T.C.
PHARMACEUTICALS MARKET SHARE: % SHARE, BY VALUE, 2004[22]
COMPANY |
%
SHARE |
Pfizer Inc |
5.10 |
Sanofi-Aventis |
5.00 |
Johnson and Johnson |
4.80 |
Other |
85.10 |
TABLE 7:- INDIAN O.T.C.
PHARMACEUTICALS DISTRIBUTION: % SHARE, BY VALUE, 2004 [23]
CHANNEL |
%
SHARE |
Pharmacies/ drugstores |
73.60 |
Specialist retailers |
12.50 |
Supermarkets/hypermarkets |
12.60 |
Other |
1.40 |
MARKET DATA ON
O.T.C. MEDICINES:
India is currently ranked 11th in the global OTC market
in size, with an estimate that it will reach 9th position within five years.(Source :Nicholas Hall and
Company,India,DB6 2006) Currently the Indian OTC market (i.e. non-prescription
advertised medicines) is estimated to represent approximately Rs.104 Billion
growing at about 8-9% (Source :ORG-IMS). [24]
THE STUDY:
A pilot study was
done by the author to understand the awareness, attitude and usage of OTC drugs
among adults in the National Capital Region. A sample of 50 respondents was
selected using convenience and judgmental sampling which included people of
both sexes with different socio economic background. Data was collected using a
structured questionnaire. [25]
PHARMACY TRAINING AND ATTITUDES:
O.T.C. drugs
require no pharmacists’ consultation for selling. However, an active role and
responsibility of pharmacists in promoting self-medication is important.
[28]
DOCTORS TRAINING AND ATTITUDES:
A survey among
doctors on O.T.C. medicines brought out following interesting responses:-
Ø 72% of doctors were willing to give an
opinion on the O.T.C. medicines.
Ø 21% of doctors were willing to
recommend/prescribe an alternative.
Ø Only 7% of doctors found it against their
medical ethics to give advice on advertised brands.
In fact, if it is
well-known and trusted brand, then they have no problem if it moves into O.T.C.
domain and is directly marketed to consumers. [29]
TABLE 8:-
DEMOGRAPHIC PROFILE (TOTAL SAMPLE= 50 ADULTS) [26, 27]
S.NO. |
PARAMETER |
FREQUENCY |
% |
||
1 |
Gender |
Male |
25 |
50 |
|
|
|
Female |
25 |
50 |
|
|
|
Graduate |
25 |
50 |
|
2 |
Education |
Postgraduate |
25 |
50 |
|
3 |
Age group(Years) |
20-30 |
36 |
72 |
|
|
|
31-40 |
10 |
20 |
|
|
|
41-50 |
4 |
8 |
|
SUMMARY
OF RESPONSE |
|||||
S.NO. |
PARAMETER |
RESPONSE |
FREQUENCY |
% |
|
1 |
Safe to buy and use |
Yes |
46 |
92 |
|
|
|
No |
4 |
8 |
|
2 |
Common aliments |
Headache |
43 |
16 |
|
|
|
Common cold |
40 |
15 |
|
|
|
Fever |
38 |
15 |
|
|
|
Acidity |
33 |
13 |
|
|
|
Cough |
31 |
12 |
|
|
|
Body pain |
30 |
11 |
|
|
|
Stomach ache |
15 |
6 |
|
|
|
Diarrhea |
14 |
5 |
|
|
|
Allergy |
12 |
5 |
|
|
|
Flu |
6 |
2 |
|
3 |
Usage in children below 10 years |
Yes |
6 |
12 |
|
|
|
No |
44 |
88 |
|
4 |
Encourage others to take O.T.C. |
Yes |
16 |
32 |
|
|
|
No |
34 |
68 |
|
5 |
Seek more information from chemist |
Yes |
26 |
52 |
|
|
|
No |
24 |
48 |
|
6 |
Awareness of side effects |
Yes |
25 |
50 |
|
|
|
No |
25 |
50 |
|
7 |
Availability through Non-chemist outlets |
Yes |
22 |
44 |
|
|
|
No |
28 |
56 |
|
8 |
Maintain stock O.T.C. at home |
Yes |
44 |
88 |
|
CONSUMER ATTITUDES/RESEARCH [30]
Indian consumers
confidently self-treat a wide range of common ailments such as cough, cold,
fever, pain, sprains, heartburn and diarrhea. When suffering from a ailment,
consumer behavior is as follows:-
Ø Go to the pharmacist:45%
Ø Go to the doctor:24%
Ø Do nothing:9%
PRESCRIPTION
TO O.T.C. SWITCH [31]
Though not yet a
pill-popping country, India is inching the OTC way. Indian OTC healthcare is in
nascent stages and ranks 11th in the global OTC market. But, urban India is
catching up with the concept, thanks to the advent of technology, improving
literacy levels, increasing health awareness and high work stress levels. In
fact, Indian consumers, today, are confident about sharing healthcare
responsibility, especially in case of common ailments. Considering the changing
mindset and likely changes in regulatory framework, such as, OTC guidelines and
open distribution, it is reasonable to estimate that within the next ten years,
India will become a major contributor to the world of OTC market. However, the
big issue in OTC marketing is not the switch climate as currently even drugs,
which do not require a prescription, are promoted via the doctor because:-
a) Marketing
through medical representatives is less expensive than mass media advertised
marketing. This makes proprietary medicines higher priced than equivalent
ethically promoted drugs.
b) Practically
all prescription drugs can be purchased without prescription.
c) Doctor influence is strong in patient
purchase behavior.
d) Distribution
of OTC allopathic medicines is limited to drug licensed stores (mainly
pharmacies).
RESTRICTIONS CONCERNING IMPORTS:
Imports of
formulations into India are negligible given the price disadvantage arising
from imports tariffs and local manufacturing cost advantage. Further, the
product approval process for new molecules can be difficult and time-consuming.
Price controls are also an added negative factor. The Ministry of Health and
Family Welfare has published a Gazette Notification GSR no. 604 (E) dated
24.08.2001 amending the various provisions of the Drugs and Cosmetics Rules,
thereby introducing a new provision for the registration of the manufacturing
premises of foreign drug manufactures and individual drugs prior to their import
into the country. The notification also introduced a few other provisions, e.g.
enhanced import licence fees, increased validity
period of licence, deletion of exemption from
requirement of import licence for bulk drugs for
actual users, requirement of minimum 60% of residual shelf life for imported
drugs and provisions for import of small quantities of new drugs by government
hospitals for treatment of their patients, etc. Under these provisions, foreign
manufactures have to apply for a registration certificate for their
manufacturing firms in India can make the applications. [32]
TABLE 9: MOST FAVORED CATEGORY FOR O.T.C. [33]
VALID |
FREQUENCY |
PERCENT |
VALID
PERCENT |
CUMULATIVE
PERCENT |
Muscle pain |
21 |
21.0 |
21.0 |
21.0 |
Cuts and burns |
6 |
6.0 |
6.0 |
27.0 |
Diarrhea |
9 |
9.0 |
9.0 |
36.0 |
Constipation |
11 |
11.0 |
11.0 |
47.0 |
Cough and cold |
38 |
38.0 |
38.0 |
85.0 |
Skin problems |
15 |
15.0 |
15.0 |
100.0 |
Total |
100 |
100.0 |
100.0 |
|
TABLE 10: MAJOR SOURCES OF INFORMATION OF
O.T.C. MEDICINE [34]
SOURCES |
FREQUENCY |
PERCENT |
VALID PERCENT |
CUMULATIVE PERCENT |
TV advertisement
|
49 |
49 |
49 |
49 |
Newspaper and
magazine |
11 |
11 |
11 |
60 |
Friends |
14 |
14 |
14 |
74 |
Retail |
26 |
26 |
26 |
100 |
Total |
100 |
100 |
100 |
100 |
GO BEYOND
ACCESSIBILITY:
Any society will
be judged by its ability to provide universal healthcare for its people. This
does not merely entail the ability to treat diseases and ailments but also to
prevent their onset by means of suitable systems and measures. The rich at
least have access to information about health related issues. That is not the
case with the many lower income groups and poorer people. There is a total
absence of health awareness among these sections. And even if they want to,
many of them cannot afford a visit to a doctor, or afford regular medication
when it is urgently required. More often than not, they end up relying on
quacks, thus the need for empowering them through health education for self
management of common ailments to start of and finally
to prevent common ailments. The other reason being the less number of doctors
in rural areas. Of the 6.5 lakh qualifies doctors,
four fifth live in towns and cities. That leaves just 20% of the total medical
community to take care of 76% of country’s population. The BOP is engaged in
jobs which leave it confronted with constant insecurity about making ends meet
.This majority does not have economic surplus and has just enough for covering
its bare necessities. Investment in healthcare (read insurance) is an
impossible luxury. Advancement in the field of pharmaceutical research has
deepened our understanding of diseases and its preventive measures but it has
not percolated down. The information asymmetry is very high which escalate the
medical care cost by late detection which demands urgent and costly
interventions at tertiary care level. Diffusion of information will take time. [35]
THE KEY
PLAYERS IN THE PROPOSED NEW MODEL:
The new proposed
model of OTC drug marketing which is consumer education centric will involve
FMCG firms, advertising and media firms, nurses, NGOs and pharmacists as important
partners. To communicate to more than 50 crore
customers, pharma companies can take the assistance
of advertising agencies and media firms and can monitor and control this with
the help of the field force. Corporate hospitals can be of great help to pharma companies since most of them are already having
patient clubs which organize education programmes.Thus
hospitals and pharmacists can play the role of key partners in this initiative
by pharma companies. Patient clubs can also be
initiated with the help of pharmacists and this will give a superior role to
him as an educator and counselor. The assistance of Diagnostic labs and the
paramedical staff employed there can be sought. To address the issue of
accessibility the pharma companies can partner with FMCG
companies and organized retailers.
“Successful
companies ,brands, products and so on ,have one common denominator, namely that
they all succeed meeting not only the needs and wants of the customers ,but
also succeed meeting the needs and wants of the ultimate
consumer.”(Svensson,2001).The proposed new model can effectively address the
accessibility and awareness aspects which will in turn increase the acceptance
of OTC allopathic drugs and its rational use. [36]
CONCLUSION:
The study showed
a clear willingness among both doctors and consumers to accept more OTC
medicines. When asked for opinions on which categories were suitable for OTC,
both groups were receptive to more OTC treatments for Cough and cold, muscle
pain, cuts and burns, diarrhea, constipation and skin problems. Striking a good
balance between continued prescription heritage and high consumer familiarity
is one of the key factors in a successful Rx-to-OTC switch, as proven by brands
such as Benadryl. Reinforcing strong retail influence and continuous consumer
loyalty represents another successful OTC model. Marketers should consider the
value of each model on the basis of category of product switch, today’s retail
influence and the extent of consumer familiarity with the brand due to present
prescription status. Among various influencers, television followed by retail
was the strongest. Innovative integrated media strategy would be one of the
major reasons in the early success of OTC switches. In the OTC drug marketing,
the Customer and Consumer being the same, companies have to immediately address
the information needs more effectively and on a continuous basis. The
acceptability of OTC drugs will improve once the awareness level is enhanced.
When the knowledge of the traditional medicine is rooted in the culture, the
knowledge about allopathic OTC drugs has to be disseminated by manufacturing
company and ensure drastic reduction in the high information asymmetry existing
today Thus by educating public (consumer) on how to manage common ailments and
finally how to prevent them, the pharma companies can
achieve its real goal of health for all and improve the quality of people’s
life. The social benefit at a national level will be lesser work load on
general practitioners, lesser crowding in primary health centers (PHCs),
pharmacists who are more empowered to guide and counsel patients and more
confident public who are in a better position to take more informed choice of
the best available solution to treat their common ailments and prevent the
frequent occurrence of the same. This will increase productivity at work and
every one in society can make superior contribution towards nation building as
it strives to be a developed one.
[37, 38]
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Received on 06.04.2013 Accepted on 04.05.2013
© Asian Pharma
Press All Right Reserved
Asian J. Res. Pharm.
Sci. 2013; Vol. 3: Issue 2, Pg 72-78