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Related Concept Videos

Renal Failure: Dose Adjustments01:11

Renal Failure: Dose Adjustments

In patients with renal impairment, drugs undergo significant changes in their pharmacokinetics, which require dosage adjustments to ensure safe and effective therapy.
Reduced renal clearance and elimination rate are common outcomes of renal impairment. These alterations lead to a prolonged elimination half-life and an altered apparent volume of distribution for drugs. As a result, dosage adjustments are typically necessary to maintain optimal drug levels in the body.
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In healthy individuals, serum creatinine levels remain stable due to a balance between its constant production—primarily from muscle metabolism—and renal excretion. Creatinine is freely filtered by the glomeruli, making it a valuable marker for estimating renal function. When the glomerular filtration rate (GFR) decreases, the kidneys can only eliminate less creatinine, causing serum levels to rise.Serum creatinine concentration is widely used to estimate creatinine clearance (Clcr), a...
Drug Toxicity: Dose-Dependent Reactions01:24

Drug Toxicity: Dose-Dependent Reactions

Drug toxicities can be stratified into pharmacological, pathological, or genotoxic based on their mechanisms. The incidence and severity of these toxicities generally increase with the drug's concentration in the body and exposure time.Pharmacological toxicity is evident when the therapeutic effects of drugs overshoot into adverse reactions in a predictable, dose-dependent manner. Central nervous system (CNS) depression from barbiturates is a classic example, with effects escalating from...
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Gentamicin, an aminoglycoside antibiotic, is commonly administered via intermittent intravenous infusion to treat severe infections. An intermittent one-hour infusion of gentamicin, administered at eight-hour intervals, allows for precise control of plasma drug concentrations, minimizing toxicity while ensuring therapeutic efficacy. Pharmacokinetic principles govern the dynamics of plasma concentrations and can be mathematically described using specific equations.The plasma drug concentration...
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Intermittent intravenous (IV) infusion is a method of drug administration where medications are delivered over short infusion periods followed by intervals of no drug delivery. This approach helps to prevent sustained high drug concentrations in the bloodstream, reducing the risk of adverse effects associated with prolonged exposure. Unlike continuous infusion, steady-state concentrations may not be achieved during a single dosing cycle but can be reached through repeated...
Time Course of Drug Effect01:14

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Published on: February 3, 2021

Carvedilol overdose with quantitative confirmation.

Nicole C Bouchard1, Jenice Forde, Robert S Hoffman

  • 1New York City Poison Control Center; and Columbia University Medical Center/New York-Presbyterian Hospital, New York, NY, USA. nb2233@columbia.edu

Basic & Clinical Pharmacology & Toxicology
|July 5, 2008
PubMed
Summary
This summary is machine-generated.

Massive carvedilol overdose in an elderly patient presented with bradycardia and hypotension. Despite unique pharmacology, clinical effects mimicked other beta-blocker overdoses, with recovery after glucagon and vasopressor support.

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Area of Science:

  • Pharmacology
  • Toxicology
  • Cardiology

Background:

  • Carvedilol, a non-selective beta-adrenoreceptor antagonist with alpha(1)-adrenoreceptor antagonism, possesses a unique profile.
  • Overdose cases are rare, with only one prior report of carvedilol overdose.

Observation:

  • An 84-year-old male ingested 375 mg (60 tablets of 6.25 mg) of carvedilol.
  • Presentation included severe bradycardia (45 bpm), hypotension (SBP 70 mmHg), and junctional rhythm.
  • Quantitative analysis confirmed a significantly elevated serum carvedilol concentration of 472 ng/ml.

Findings:

  • The patient was successfully treated with intravenous fluids, glucagon boluses, and dopamine infusion.
  • Recovery included normalization of heart rhythm to sinus rhythm and discontinuation of vasopressors within 14 hours.
  • Despite its dual receptor antagonism, carvedilol overdose manifestations were similar to other beta-adrenoreceptor antagonist overdoses.

Implications:

  • This case highlights the potential for severe toxicity with massive carvedilol ingestion.
  • Glucagon and vasopressors are effective in managing carvedilol-induced cardiovascular collapse.
  • The toxicodynamic profile of carvedilol overdose aligns with that of other beta-blockers, despite its unique alpha-blocking properties.