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Related Concept Videos

Drug Regulation01:25

Drug Regulation

Drug regulation encompasses the management of drug usage by evaluating its safety and efficacy through assessments conducted by regulatory authorities. Regrettably, the history of drug regulation is marred by several catastrophic events. One such incident is the Elixir Sulfanilamide tragedy, in which the toxic compound diethyl glycol was included in a sweet-tasting medication, leading to numerous fatalities. This event prompted the enactment of the Food, Drug, and Cosmetic Act in 1938. Under...
Drug Classes and Categories01:25

Drug Classes and Categories

Drugs can be classified according to their chemical composition or their intended therapeutic application. For instance, anti-infective agents that possess the ability to eliminate pathogens or suppress their growth and reproduction can be grouped based on the organisms they target or their chemical structure. Furthermore, drugs can be divided into prescription, nonprescription, or controlled substances. Prescription medications, such as antibiotics, require oversight from a licensed healthcare...
Pharmacovigilance01:19

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Post-marketing surveillance is a critical component of pharmaceutical regulation, often uncovering unanticipated adverse drug reactions (ADRs) once a drug is widely used over an extended period.
This process, termed pharmacovigilance, aims to detect, evaluate, and minimize harmful effects related to medication use. The data collection for pharmacovigilance depends on spontaneous reporting systems, where healthcare professionals or patients voluntarily report suspected ADRs.
In some cases, there...
Prescription, Nonprescription and Orphan Drugs01:02

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Prescription drugs require a prescription from a medical practitioner and can only be obtained from a pharmacy. They have many applications, including treating pain, anxiety, and hypertension.
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Drug Control Governance: Regulatory Bodies and Their Impact01:03

Drug Control Governance: Regulatory Bodies and Their Impact

Drug control governance involves the oversight and regulation of pharmaceuticals to ensure their safety and efficacy while preventing illegal drug use and trafficking. Regulatory bodies, including the US Food and Drug Administration (FDA) and the European Union's European Medicines Agency (EMA), play a central role in this process. These agencies evaluate the safety and efficacy of drugs before they can be marketed. They fund clinical trials and assess the benefits and risks associated with a...
Pharmaceutical Poisoning: Potential Scenarios01:26

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Pharmaceutical poisoning can occur through various channels, impacting an estimated 2 million hospitalized patients in the U.S. annually with serious adverse drug responses. These scenarios encompass both therapeutic uses, such as drug toxicity, where even standard dosages can lead to severe central nervous system depression, and non-therapeutic exposures, including accidental ingestion by children, and environmental and occupational exposures.Unintentional poisonings often involve exploratory...

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Illicit Online Pharmacies: A Scoping Review.

Yam B Limbu1, Bruce A Huhmann2

  • 1Feliciano School of Business, Montclair State University, 1 Normal Ave., Montclair, NJ 07043, USA.

International Journal of Environmental Research and Public Health
|May 13, 2023
PubMed
Summary

Illicit online pharmacies (IOPs) are vastly understudied, with existing research focusing on specific drugs rather than the overall phenomenon. Further empirical research is urgently needed to address significant knowledge gaps.

Keywords:
illicit online pharmaciespatient safetypharmaceutical marketing and supply chainprescription drugpublic health awareness and educationscoping review

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Area of Science:

  • Pharmacology
  • Public Health
  • Information Science

Background:

  • Illicit online pharmacies (IOPs) pose significant risks to public health and patient safety.
  • The existing body of literature on IOPs is fragmented and requires a comprehensive review.

Purpose of the Study:

  • To conduct a scoping review of the literature on illicit online pharmacies.
  • To identify research gaps and propose an agenda for future research.

Main Methods:

  • A five-step framework by Arksey and O'Malley was employed for the scoping review.
  • Searches were conducted across multiple databases (PubMed, Web of Science, EMBASE, CINAHL, Science Direct, PsycInfo).
  • Forty-three peer-reviewed articles published in English were included.

Main Results:

  • Ten themes were identified, categorized into five clusters: patient risk, healthcare providers, marketing and supply chain, public health and society, and policy and regulation.
  • Research has increasingly focused on specific drugs rather than the overall IOP phenomenon.
  • Data collection predominantly used convenience sampling, online searches, content analysis, and surveys, with primarily descriptive data analysis.

Conclusions:

  • Illicit online pharmacies are significantly understudied.
  • There is an urgent need for more empirical and conclusive research on IOPs.
  • Future research should address regulation, enforcement, public health awareness, patient risks, and supply chain issues.