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SOURCES OF DRUG
INFORMATION
ARBIND KUMAR
ASSISTANT PROFESSOR
IRT-PMC
Objectives:
1. To know what are the various sources of drug information.
2. To select the appropriate source depending on the information.
3. To discuss briefly the role of electronic media in medicine.
1. Pharmacopoeias:
It is an official code containing a
selected list of established drugs and
medicinal preparations with
descriptions of their physical
properties and tests for their identity,
purity and potency.
The different Pharmacopoeias are:
Indian pharmacopoeia, British
pharmacopoeia, European
pharmacopoeia, US pharmacopoeia
and International pharmacopoeia.
2. Drug formulary:
This includes notes on
drugs and preparations
used in the treatment
of diseases and
conditions and provide
information to Doctors,
Pharmacists, and
Nurses etc, to facilitate
the selection of suitable
treatment. This is a
pocket book meant for
rapid reference. E.g
National Formulary of
India.
3. Materia Medica:
It is a reference book
containing the origin,
constituents, actions,
indications and preparations
of drugs. It also gives the
doses and their mode of
administration. E.g.: Indian
Materia Medica by Dr. K. M.
Nadkarni and revised and
enlarged by A. K. Nadkarni.
4. Text books in Pharmacology:
• The textbook give standard information
about drugs and their rational
application in therapeutics. Students can
gather basic knowledge from textbooks.
Some pharmacology text books are
• a) Essentials of Medical Pharmacology-
6th edition KD Tripathi
• b) Pharmacology and
Pharmacotherapeutics - revised 21'
edition by RS Sathoskar, SD Bhandarkar
and Nirmala N. Rege
• c) Basic and Clinical Pharmacology — I
1th edition by Betram G Katzung
• d) Clinical Pharmacology - 9th edition
Bennet & MJ Brown
• e) Pharmacology 6th edition by Range &
Dale 5. Journals: These give details about
Clinical Trails involving new molecules
and recent developments in
Pharmacology.
6. Bulletins:
• This is an independent journal having articles
from various well known authors.
7. Monographs:
• This is a discourse on a
single topic/ it gives
details about a single
topic or about a
particular drug.
8. Patient Package Insert:
• Label should comply with the
requirements established under
"Good Manufacturing Practice"
and also with the official
National Labeling instructions.
Qus: Write down the relevant, specific information,
definition and its significance gathered from the patient
package insert provided.
Generic name:
It is officially accepted name. It is important as it
is followed world over—accepted by scientific
body.
Trade name:
Name given by manufacturer or company that
produces the drug
?????????
Composition:
• Represents chemical
ingredients. Helps to know the
active principle and the toxic
component.
Indications:
The conditions which demands the usage of the drug.
Used only for these conditions help to control
hazardous use
Dosage form, average Dose and the mode of
Administration:
• Helps to know the route of administration and extend of administration.
Quantity single unit And Total number /
Quantity In the pack Provided:
• Quantity per single unit, number per pack and quantity per pack.
Price -
• MRP not to exceed (Price is meant for patient compliance)
Contraindications:
Conditions where the drug should not be used. Helps to prevent
drug toxicity like do not use in eyes or do not use in those persons
hypersensitive to iodine or other ingredients of the preparation.
Side effects:
Helps to be aware of complication and to
mask the complication. Stop use if rash or
other allergic reaction develops.
Interactions:
To avoid complications and other adverse effects by interacting with
other drugs or chemicals
Warning:
• For maintaining potency of drug; or be
sold on retail only on prescription of
medical practitioner. Carcinogenic in mice
and hence unnecessary use should be
avoided
• Storage and special Instructions on handling: In
order to maintain the viability or potency of
drug store in cool place, shake well before use,
protect from light.
Shelf life/date of Expiry:
• The time for which the drug potency lasts or helps to prevent
harmful effects. Date of manufacture and expiry gives the shelf life of
the medication.
Batch number Assigned by the manufacturer:
• To identify the lot of drug preparation helps to localize the preparation
which has been found to have harmful effects.
Name of the Manufacturer:
•To contact in need of any information
regarding the medication.
Additional information:
• Includes details like Reg.No: License No: etc.

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Sources of drug information

  • 1. SOURCES OF DRUG INFORMATION ARBIND KUMAR ASSISTANT PROFESSOR IRT-PMC
  • 2. Objectives: 1. To know what are the various sources of drug information. 2. To select the appropriate source depending on the information. 3. To discuss briefly the role of electronic media in medicine.
  • 3. 1. Pharmacopoeias: It is an official code containing a selected list of established drugs and medicinal preparations with descriptions of their physical properties and tests for their identity, purity and potency. The different Pharmacopoeias are: Indian pharmacopoeia, British pharmacopoeia, European pharmacopoeia, US pharmacopoeia and International pharmacopoeia.
  • 4. 2. Drug formulary: This includes notes on drugs and preparations used in the treatment of diseases and conditions and provide information to Doctors, Pharmacists, and Nurses etc, to facilitate the selection of suitable treatment. This is a pocket book meant for rapid reference. E.g National Formulary of India.
  • 5. 3. Materia Medica: It is a reference book containing the origin, constituents, actions, indications and preparations of drugs. It also gives the doses and their mode of administration. E.g.: Indian Materia Medica by Dr. K. M. Nadkarni and revised and enlarged by A. K. Nadkarni.
  • 6. 4. Text books in Pharmacology: • The textbook give standard information about drugs and their rational application in therapeutics. Students can gather basic knowledge from textbooks. Some pharmacology text books are • a) Essentials of Medical Pharmacology- 6th edition KD Tripathi • b) Pharmacology and Pharmacotherapeutics - revised 21' edition by RS Sathoskar, SD Bhandarkar and Nirmala N. Rege • c) Basic and Clinical Pharmacology — I 1th edition by Betram G Katzung • d) Clinical Pharmacology - 9th edition Bennet & MJ Brown • e) Pharmacology 6th edition by Range & Dale 5. Journals: These give details about Clinical Trails involving new molecules and recent developments in Pharmacology.
  • 7. 6. Bulletins: • This is an independent journal having articles from various well known authors.
  • 8. 7. Monographs: • This is a discourse on a single topic/ it gives details about a single topic or about a particular drug.
  • 9. 8. Patient Package Insert: • Label should comply with the requirements established under "Good Manufacturing Practice" and also with the official National Labeling instructions.
  • 10. Qus: Write down the relevant, specific information, definition and its significance gathered from the patient package insert provided. Generic name: It is officially accepted name. It is important as it is followed world over—accepted by scientific body. Trade name: Name given by manufacturer or company that produces the drug
  • 12. Composition: • Represents chemical ingredients. Helps to know the active principle and the toxic component.
  • 13. Indications: The conditions which demands the usage of the drug. Used only for these conditions help to control hazardous use
  • 14. Dosage form, average Dose and the mode of Administration: • Helps to know the route of administration and extend of administration.
  • 15. Quantity single unit And Total number / Quantity In the pack Provided: • Quantity per single unit, number per pack and quantity per pack.
  • 16. Price - • MRP not to exceed (Price is meant for patient compliance)
  • 17. Contraindications: Conditions where the drug should not be used. Helps to prevent drug toxicity like do not use in eyes or do not use in those persons hypersensitive to iodine or other ingredients of the preparation.
  • 18. Side effects: Helps to be aware of complication and to mask the complication. Stop use if rash or other allergic reaction develops.
  • 19. Interactions: To avoid complications and other adverse effects by interacting with other drugs or chemicals
  • 20. Warning: • For maintaining potency of drug; or be sold on retail only on prescription of medical practitioner. Carcinogenic in mice and hence unnecessary use should be avoided
  • 21. • Storage and special Instructions on handling: In order to maintain the viability or potency of drug store in cool place, shake well before use, protect from light.
  • 22. Shelf life/date of Expiry: • The time for which the drug potency lasts or helps to prevent harmful effects. Date of manufacture and expiry gives the shelf life of the medication.
  • 23. Batch number Assigned by the manufacturer: • To identify the lot of drug preparation helps to localize the preparation which has been found to have harmful effects.
  • 24. Name of the Manufacturer: •To contact in need of any information regarding the medication.
  • 25. Additional information: • Includes details like Reg.No: License No: etc.

Notas del editor

  1. an official publication containing a list of medicinal drugs with their effects and directions for their use. a stock of medicinal drugs.
  2. A drug formulary is a list of prescription drugs, both generic and brand name, used by practitioners to identify drugs that offer the greatest overall value. A committee of physicians, nurse practitioners, and pharmacists maintain the formulary
  3. An example of a generic drug, one used for diabetes, is metformin. A brand name for metformin is Glucophage. (Brand names are usually capitalized while generic names are not.) A generic drug, one used for hypertension, is metoprolol, whereas a brand name for the same drug is 
  4. a sign or piece of information that indicates something. In medicine, a condition which makes a particular treatment or procedure advisable. CML (chronic myeloid leukemia) is an indication for the use of Gleevec (imatinib mesylate). 2. A sign or a circumstance which points to or shows the cause, pathology, treatment, or outcome of an attack of disease
  5. A contraindication is a specific situation in which a drug, procedure, or surgery should not be used because it may be harmful to the person. There are two types of contraindications: Relative contraindication means that caution should be used when two drugs or procedures are used together.
  6. Common Side Effects. Possibly the most common side effects of any prescription drug are gastrointestinal issues, including nausea, constipation and diarrhea, because most drugs go through the digestive system to be absorbed. Other common aftereffects include drowsiness, pain and skin reactions.