Skip to main content

Pharmaceutical Aspects of Drugs

  • Chapter
  • First Online:
Pharmacological Basis of Acute Care

Abstract

Drugs can be obtained from many sources such as plants, animals, minerals or microorganisms. However, most drugs are synthetically produced in the laboratory, as they can be produced on a larger scale, in a more cost effective manner and be of higher quality. It is important to know the sources of drugs as patients can develop hypersensitivity reactions to certain drug source. Some patients (based on their religious beliefs) also prefer not to use drugs obtained from bovine or porcine sources. Drug development and trials in animals and humans is a long and costly process. This process is essential to determine that the new drug is safe for human consumption. Drugs should be packaged in a manner that protects the active ingredient from deterioration due to external factors. Drugs should also be labeled with sufficient information to enable the determination of the exact content of the active ingredient, its storage conditions and manufacturing details.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 89.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 119.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 119.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Further Reading

  1. Adams CP, Brantner VV. Spending on new drug development. Health Econ. 2010;19(2):130–41.

    Article  PubMed  Google Scholar 

  2. Liljefors T, Krogsgaard-Larsen P, Madsen U, editors. Textbook of drug design and discovery, Third Edition (Forensic Science). 3rd ed. New York: Taylor & Francis; 2002.

    Google Scholar 

  3. Pharmaceutical Inspection Co-operation Scheme Secretariat. Guide to good manufacturing practice for medicinal products. Geneva 2009. Available from: http://www.tga.gov.au/pdf/manuf-pics-gmp-medicines-annexes.pdf. Last accessed 13th June 2014.

  4. World Health Organization. WHO Technical Report Series, No. 902, 2002, Annex 9, Guidelines on packaging for pharmaceutical Products. Geneva 2002.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Pauline Siew Mei Lai B.Pharm., Ph.D. .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2015 Springer International Publishing Switzerland

About this chapter

Cite this chapter

Lai, P.S.M. (2015). Pharmaceutical Aspects of Drugs. In: Chan, Y., Ng, K., Sim, D. (eds) Pharmacological Basis of Acute Care. Springer, Cham. https://doi.org/10.1007/978-3-319-10386-0_8

Download citation

  • DOI: https://doi.org/10.1007/978-3-319-10386-0_8

  • Published:

  • Publisher Name: Springer, Cham

  • Print ISBN: 978-3-319-10385-3

  • Online ISBN: 978-3-319-10386-0

  • eBook Packages: MedicineMedicine (R0)

Publish with us

Policies and ethics