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Phenytoin is one of the most used antiepileptic drugs. Isoniazid, a first-line antitubercular drug, blocks the CYP2C19 enzyme, preventing phenytoin from being metabolised. Concomitant use of phenytoin and isoniazid predisposes to phenytoin toxicity.

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Background: A growing body of research is dedicated to developing new therapeutic agents for wound healing with fewer adverse effects. One of the proceedings being taken today in wound healing research is to identify promising biological materials that not only heal wounds but also vanish scarring. The effectiveness of nanofibers like polyvinyl alcohol (PVA), in improving wound healing can be related to their unique properties.

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Therapeutic drug monitoring (TDM), which involves measuring drug levels in patients' body fluids, is an important procedure in clinical practice. However, the analysis technique currently used, i.e.

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Article Synopsis
  • Antiseizure medications, like valproic acid (VPA), show different results in patients due to genetic factors, though there's limited research specifically on VPA compared to other drugs.
  • This study aimed to analyze how genetic variations influence the effectiveness, side effects, and serum levels of VPA in patients with genetic generalized epilepsies (GGE).
  • The results revealed that certain genetic variants are linked to treatment failure, increased serum levels, weight gain, and hair loss among GGE patients using VPA, suggesting a need for personalized medication approaches.
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Article Synopsis
  • Valproic acid (VPA) is an effective and cost-effective anti-seizure medication, but maintaining proper serum levels is critical due to its narrow therapeutic window.
  • A study at a hospital found that 63.2% of patients had subtherapeutic VPA levels (<50 mg/L), with factors such as male gender, previous phenytoin use, and lower dosages increasing this risk.
  • Findings highlight the need for careful monitoring and personalized treatment strategies to ensure effective VPA levels, with calls for further research on minimizing the risk of subtherapeutic levels.
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