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Clinical information in drug package inserts in India
by
Shivkar, YM
in
Drug-information, India, package inserts
/ Federal regulation
/ Industrialized nations
/ Labeling
/ Laws, regulations and rules
/ Management
/ Packaging
/ Patient package inserts
/ Patient safety
/ Patients
/ Pharmaceutical industry
/ Prescription drugs
2009
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Clinical information in drug package inserts in India
by
Shivkar, YM
in
Drug-information, India, package inserts
/ Federal regulation
/ Industrialized nations
/ Labeling
/ Laws, regulations and rules
/ Management
/ Packaging
/ Patient package inserts
/ Patient safety
/ Patients
/ Pharmaceutical industry
/ Prescription drugs
2009
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Do you wish to request the book?
Clinical information in drug package inserts in India
by
Shivkar, YM
in
Drug-information, India, package inserts
/ Federal regulation
/ Industrialized nations
/ Labeling
/ Laws, regulations and rules
/ Management
/ Packaging
/ Patient package inserts
/ Patient safety
/ Patients
/ Pharmaceutical industry
/ Prescription drugs
2009
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Journal Article
Clinical information in drug package inserts in India
2009
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Overview
Background: It is widely recognized that accurate and reliable product
information is essential for the safe and effective use of medications.
Pharmaceutical companies are the primary source of most drug
information, including package inserts. Package inserts are printed
leaflets accompanying marketed drug products and contain information
approved by the regulatory agencies. Studies on package inserts in
India, in 1996, had shown that crucial information was often missing
and they lacked uniformity. Aim: To assess the presentation and
completeness of clinically important information provided in the
currently available package inserts in India. Materials and Methods:
Package inserts accompanying allopathic drug products marketed by
pharmaceutical companies in India were collected. These package inserts
were analyzed for the content of clinically important information in
various sections. Statistical Analysis: The results were expressed as
absolute numbers and percentages. Results: Preliminary analyses
revealed that most package inserts did contain information under
headings, such as, therapeutic indications, contraindications,
undesirable effects, etc., listed in the Drugs and Cosmetics Rules
1945. The findings indicated considerable improvement in package
inserts since 1996. However, on critical evaluation it was revealed
that clinically important information was not well presented and was
often incomplete. Information with regard to pediatric and geriatric
use was present in only 44% and 13% of the package inserts,
respectively. Only five of the inserts had information on the most
frequent adverse drug reactions associated with the drug. Also,
information on interactions and overdosage was often missing.
Conclusion: Although the package inserts appear to have improved over
the past decade there is still a definite need to further refine the
clinical information contained, to minimize the risks to patients. This
could be brought about by self-regulation on the part of the industry
as well as by updating the relevant guidelines in line with those of
developed countries.
Publisher
Medknow Publications and Staff Society of Seth GS Medical College and KEM Hospital, Mumbai, India,Medknow Publications and Media Pvt. Ltd,Medknow Publications & Media Pvt. Ltd
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