Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

FDA Approved Drugs: Changes to Approved Drugs01:26

FDA Approved Drugs: Changes to Approved Drugs

Post-approval, manufacturers may modify an approved new or generic drug product. Such modifications can encompass alterations in the Active Pharmaceutical Ingredient (API), manufacturing process, formulation, batch size, manufacturing site, and container closure system (FDA Guidance for Industry, April 2004). Often, a drug product may undergo multiple changes.These modifications require careful evaluation to determine their potential impact on the drug product's identity, strength, quality,...
Formulation and Manufacturing Process: Physical Attributes of Generic Tablets and Capsules01:18

Formulation and Manufacturing Process: Physical Attributes of Generic Tablets and Capsules

Bioequivalence in generic drugs, such as tablets and capsules, refers to their pharmaceutical equivalence to the brand-name counterparts. However, for therapeutic equivalence, manufacturers must also consider physical attributes like size, shape, and weight (FDA Guidance for Industry, December 2003). Discrepancies in these aspects could impact patient compliance and cause medication errors. For instance, swallowing difficulties, often experienced with larger tablets or capsules, can lead to...
Pharmaceutical Alternatives: Polymorphic Form-Related and Particle Size-Related Therapeutic Nonequivalence01:27

Pharmaceutical Alternatives: Polymorphic Form-Related and Particle Size-Related Therapeutic Nonequivalence

Changes in polymorphic forms can significantly influence the bioavailability of poorly soluble drugs. Although the FDA defines pharmaceutical equivalence based on having the same active ingredient, dosage form, and route of administration, it does not automatically disqualify products with different polymorphic forms. This means two products with different polymorphs can still be deemed pharmaceutically equivalent. However, polymorphic differences can affect properties like wettability,...
Modified-Release Drug Delivery Systems: Influencing Factors01:20

Modified-Release Drug Delivery Systems: Influencing Factors

Modified-release drug delivery systems are designed to optimize the therapeutic effect of drugs by minimizing side effects, reducing the dosage required, and controlling drug release to align with pharmacokinetic and pharmacodynamic needs. The system depends on two key factors: the drug's release from the formulation and its movement through the body to the target site. Unlike conventional dosage forms, where absorption is the limiting step, the rate of drug release is the key determinant in...
Modified-Release Drug Delivery Systems: Overview01:19

Modified-Release Drug Delivery Systems: Overview

Modified-release dosage forms are designed to address the limitations of drugs with short biological half-lives. These forms maintain stable therapeutic drug concentrations over extended periods, reducing the need for frequent dosing. A consistent drug level helps minimize peak-trough fluctuations, which can reduce adverse effects, lower the risk of drug resistance, and improve overall treatment effectiveness.One common type of modified-release form is the extended-release (ER) formulation. ER...
Biopharmaceutical Factors Influencing Drug Product Design: Overview01:22

Biopharmaceutical Factors Influencing Drug Product Design: Overview

Rational drug product design integrates knowledge of the drug’s physicochemical properties, formulation components, manufacturing techniques, and intended route of administration. Each factor influences the drug’s performance, including how it is released, absorbed, and eliminated in the body.The physicochemical properties of a drug—such as solubility, stability, and particle size—affect its compatibility with excipients and the choice of dosage form. Excipients, though pharmacologically...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Patient- and Caregiver-Informed Considerations for the Design and Implementation of Generative AI-Supported Patient-Centered Clinical Decision Support: Qualitative Study.

Journal of medical Internet research·2026
Same author

Association of primary care telehealth with preventable healthcare utilization and care continuity among patients with chronic conditions.

NPJ digital medicine·2026
Same author

Reply to: Reassessing the evidence linking clinical leadership to AI deployment outcomes.

NPJ digital medicine·2026
Same author

Role of electronic health record in stigma experiences, trust, and care decisions by women with history of pregnancy and substance use disorder: a qualitative study of perceptions of clinical note language.

Journal of the American Medical Informatics Association : JAMIA·2026
Same author

A real-world feasibility evaluation of LLM-based clinical prediction: emergency department return visit admission across two academic medical centers.

Research square·2026
Same author

Outcomes of 72-hour emergency department return visits requiring hospital admission in older adults: a nationally representative analysis.

BMC geriatrics·2026

Related Experiment Video

Updated: May 19, 2026

Drug Repurposing Hypothesis Generation Using the "RE:fine Drugs" System
05:10

Drug Repurposing Hypothesis Generation Using the "RE:fine Drugs" System

Published on: December 11, 2016

Promoting generic medication prescribing by order interface redesign: small change, large impact.

Sameer Malhotra1, Jessica S Ancker, J Travis Gossey

  • 1Weill Medical College, Cornell University, New York, NY, USA. sam2032@med.cornell.edu

Studies in Health Technology and Informatics
|August 10, 2012
PubMed
Summary

Redesigning electronic health records to favor generic medications significantly boosted their prescription rates by 36.9%. This intervention streamlined the process, encouraging the use of cost-effective generic drugs.

More Related Videos

Improving IV Insulin Administration in a Community Hospital
12:08

Improving IV Insulin Administration in a Community Hospital

Published on: June 11, 2012

Related Experiment Videos

Last Updated: May 19, 2026

Drug Repurposing Hypothesis Generation Using the "RE:fine Drugs" System
05:10

Drug Repurposing Hypothesis Generation Using the "RE:fine Drugs" System

Published on: December 11, 2016

Improving IV Insulin Administration in a Community Hospital
12:08

Improving IV Insulin Administration in a Community Hospital

Published on: June 11, 2012

Area of Science:

  • Health Informatics
  • Pharmacoeconomics
  • Clinical Pharmacy

Background:

  • Rising healthcare expenditures are significantly influenced by prescription drug costs.
  • Electronic health records (EHRs) offer potential for optimizing prescribing patterns.
  • Generic medications present a cost-saving alternative to brand-name drugs.

Purpose of the Study:

  • To evaluate the impact of an EHR interface redesign on generic medication prescribing behavior.
  • To assess the effectiveness of automated generic substitution prompts in clinical practice.

Main Methods:

  • A before-and-after retrospective study was conducted.
  • The EHR order entry interface was modified to automatically substitute brand medications with generic equivalents.
  • Clinicians were required to actively select "dispense as written" to override the generic suggestion.

Main Results:

  • A net increase of 36.9% in generic medication prescriptions was observed post-redesign.
  • The interface change successfully shifted prescribing behavior towards generic options.
  • The "dispense as written" override was used minimally, indicating high acceptance of generic suggestions.

Conclusions:

  • Redesigning EHR interfaces can be an effective strategy to increase generic prescribing rates.
  • Automated prompts and simplified workflows can promote cost-effective medication choices.
  • This approach has the potential to reduce overall healthcare costs associated with prescription drugs.