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Related Concept Videos

Local Anesthetics: Adverse Effects01:12

Local Anesthetics: Adverse Effects

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While local anesthetics are generally safe and well-tolerated, they can occasionally cause adverse effects that vary in severity. Local anesthetics can induce toxicity at two distinct levels. They can either produce local effects through direct contact with the neural elements or be absorbed into the bloodstream from the injection site, leading to systemic effects.
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Insulin: Dosing Regimen and Adverse Effects01:16

Insulin: Dosing Regimen and Adverse Effects

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Insulin-replacement therapy usually includes both long-acting insulin (basal) and short-acting insulin (to cater to postprandial needs). In a diverse group of type 1 diabetes patients, the average daily insulin dose is typically 0.5-0.7 units/kg body weight. However, obese patients and pubertal adolescents may need more due to insulin resistance.
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Skeletal Muscle Relaxants: Adverse Effects01:21

Skeletal Muscle Relaxants: Adverse Effects

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Skeletal muscle relaxants are widely used for muscle paralysis and relieving pain following any muscle injury or stiffness. However, depending on the drug type, they can have adverse effects that range from mild to severe. Usually, nondepolarizing neuromuscular blockers have minimal side effects. For example, drugs like d-tubocurarine, cisatracurium, and rocuronium cause hypotension, whereas drugs like baclofen, when stopped abruptly, can lead to the recurrence of spastic conditions.
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Pharmacodynamics in Geriatric Patients: Effects of Age01:27

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Age-related pharmacokinetic changes are extensively documented, but understanding age-related pharmacodynamic alterations is relatively limited. This knowledge gap can be partly attributed to the complexity of developing appropriate measures of drug responses compared to bioanalytical methods for determining drug concentrations.Most information regarding age-related differences in human pharmacodynamics originates from cross-sectional studies. However, these studies assume that observed mean...
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Eukaryotic Transcription Inhibitors01:52

Eukaryotic Transcription Inhibitors

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Certain biochemical processes, such as embryonic development and cell growth regulation, depend on the repression of specific genes. DNA binding proteins known as eukaryotic transcription inhibitors regulate the repression of gene expression in eukaryotes. The presence of these inhibitors at the required location and time in the cell is triggered by the presence of hormones and additional signals from other cells.
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Buffer Effectiveness

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Buffer solutions do not have an unlimited capacity to keep the pH relatively constant . Instead, the ability of a buffer solution to resist changes in pH relies on the presence of appreciable amounts of its conjugate weak acid-base pair. When enough strong acid or base is added to substantially lower the concentration of either member of the buffer pair, the buffering action within the solution is compromised.
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Cutaneous Adverse Effects in Patients Treated with BTK Inhibitors.

Ewa Robak1, Tadeusz Robak2,3

  • 1Department of Dermatology, Medical University of Lodz, 90-647 Łódź, Poland.

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Summary

Bruton

Keywords:
BTK inhibitorsacalabrutinibbleedingibrutinibinfectionsmucosal symptomsneutrophilic dermatosespirtobrutinibrashskin toxicityzanubrutinib

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Area of Science:

  • Oncology
  • Dermatology
  • Pharmacology

Background:

  • Bruton's tyrosine kinase (BTK) inhibitors are vital for treating indolent lymphoid malignancies like CLL and MCL.
  • Common adverse events include cardiac issues, infections, and skin changes.
  • First-generation BTK inhibitors (e.g., ibrutinib) have a higher toxicity profile than newer agents.

Purpose of the Study:

  • To review the spectrum of skin symptoms associated with BTK inhibitor therapy.
  • To compare the dermatologic toxicity of ibrutinib with newer BTK inhibitors.
  • To summarize the clinical and pathological features of BTK inhibitor-induced skin reactions.

Main Methods:

  • A comprehensive literature search was conducted using PubMed, Web of Science, and Google Scholar.
  • English-language articles were prioritized.
  • References from selected articles were reviewed for additional relevant publications.

Main Results:

  • Skin manifestations are common BTK inhibitor side effects, particularly with ibrutinib.
  • Hemorrhage, bruising, and contusions are frequent skin toxicities.
  • Other dermatologic issues include rash, cellulitis, infections, abscesses, and edema.

Conclusions:

  • BTK inhibitors, while effective, are associated with various skin toxicities.
  • Second-generation and non-covalent BTK inhibitors appear to have a more favorable dermatologic safety profile than ibrutinib.
  • Understanding and managing these skin symptoms is crucial for patient care.