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Related Concept Videos

Pharmacovigilance01:19

Pharmacovigilance

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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.
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During the development of a new pharmaceutical, the manufacturer initially assigns a code name to the drug. Once approved, the drug receives a United States Adopted Name (USAN)—a generic, nonproprietary designation. Upon being listed in the United States Pharmacopeia, this nonproprietary name becomes the drug's official name. Additionally, the manufacturer assigns a proprietary name or trademark, which serves as the brand name under which the drug is marketed. It is worth noting that...
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The combined effects of drugs can result in various interactions, of which an important type is antagonism. Antagonism is a mechanism where one drug inhibits or counteracts the effects of another drug. Antagonism can occur through various means, including receptor binding, allosteric modulation, functional interaction, chemical reactions, and pharmacokinetic processes.
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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...
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Drug discovery is a multifaceted process involving extensive screening, testing, and optimization of lead compounds to identify potential new drugs for therapeutic use. It combines several approaches, including screening large numbers of natural products, chemical modification of known active molecules, identification of new drug targets, and rational design based on biological mechanisms and drug-receptor structure. These approaches are carried out in both academic research laboratories and...
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Comparing a Large Language Model with Previous Deep Learning Models on Named Entity Recognition of Adverse Drug

Théophile Tiffet1,2, Alexis Pikaar3, Béatrice Trombert-Paviot1,2

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Summary
This summary is machine-generated.

Fine-tuning deep learning models improved named entity recognition (NER) for adverse drug events more than few-shot learning with large language models. While convenient, few-shot learning

Keywords:
Deep learningGPTKnowledge discoveryLarge Language ModelNatural Language ProcessingPharmacovigilance

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Area of Science:

  • Computational linguistics
  • Biomedical informatics
  • Artificial intelligence

Background:

  • Deep learning models significantly enhance named entity recognition (NER) performance when fine-tuned on large datasets.
  • Large language models (LLMs) offer few-shot learning capabilities for new tasks via in-context learning with prompts.
  • Few-shot learning requires minimal examples, making it suitable for data-scarce scenarios.

Purpose of the Study:

  • To compare the performance of state-of-the-art deep learning models fine-tuned on PubMed abstracts against LLMs using few-shot learning for adverse drug event (ADE) NER.
  • To evaluate the efficacy of different machine learning approaches in identifying adverse drug events from biomedical text.

Main Methods:

  • Fine-tuning a state-of-the-art deep learning model (Hussain et al.) on a large corpus of PubMed abstracts for ADE NER.
  • Utilizing a large language model (ChatGPT-3.5) with few-shot learning for ADE NER, providing minimal examples and instructions.
  • Direct comparison of the F1-Scores achieved by both methodologies.

Main Results:

  • The fine-tuned deep learning model achieved a significantly higher F1-Score (97.6%) compared to the ChatGPT-3.5 model using few-shot learning (86.0%) for ADE NER.
  • Fine-tuning on extensive data yielded superior performance over few-shot learning in this specific NER task.
  • Few-shot learning demonstrated convenience but lower accuracy for ADE identification.

Conclusions:

  • Fine-tuning deep learning models with substantial data remains the superior approach for high-performance adverse drug event named entity recognition.
  • Few-shot learning with LLMs is a practical alternative when training data is limited, though performance is currently inferior.
  • Future research should explore advanced prompting techniques with newer LLMs like GPT-4 and investigate fine-tuning strategies for LLMs like GPT-3.5.