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Related Concept Videos

Renal Failure: Dose Adjustments01:11

Renal Failure: Dose Adjustments

556
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.
However, dosage adjustments...
556
Drug Accumulation During Multiple Dosing: Intermittent IV Infusions01:24

Drug Accumulation During Multiple Dosing: Intermittent IV Infusions

324
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...
324
Effect of Hepatic Disease on Pharmacokinetics: Dose Adjustments Due to Hepatic Impairment01:08

Effect of Hepatic Disease on Pharmacokinetics: Dose Adjustments Due to Hepatic Impairment

320
Hepatic impairment, characterized by decreased liver function, does not uniformly mandate adjustments in drug dosage. Whether dosage modifications are necessary depends on various factors related to the drug's metabolism and elimination pathways. If a drug is primarily excreted via the kidneys and bypasses significant hepatic processing, if it undergoes minimal metabolic transformation in the liver, or if it is volatile and primarily expelled through the lungs, dose adjustments may not be...
320
Drug toxicity: Drug–Drug Interaction01:30

Drug toxicity: Drug–Drug Interaction

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Drug–drug interactions can precipitate toxicity through multiple mechanisms. Absorption interactions alter how drugs enter the body, exemplified when ranitidine increases the absorption of basic drugs, while cholestyramine decreases the levels of propranolol. Protein binding interactions occur when drugs share the same binding sites on plasma proteins. Drugs like aspirin and warfarin, when bound in excess, can lead to increased free drug concentrations, enhancing the potential for...
208
Effect of Hepatic Disease on Pharmacokinetics: Active Drug, Metabolite and Fraction of Metabolized Drug01:14

Effect of Hepatic Disease on Pharmacokinetics: Active Drug, Metabolite and Fraction of Metabolized Drug

276
In pharmacotherapy, monitoring drug concentrations is paramount, especially for drugs whose therapeutic effects hinge on both the active compound and its metabolite. Hepatic impairment profoundly influences drug potency by altering liver function. If the drug is more potent than its metabolite, impaired liver function amplifies drug activity due to elevated drug concentration levels. Conversely, if the metabolite holds greater potency, diminished liver function diminishes drug activity by...
276
Effect of Hepatic Disease on Pharmacokinetics: Drug Dosing and Hepatic Blood Flow01:26

Effect of Hepatic Disease on Pharmacokinetics: Drug Dosing and Hepatic Blood Flow

309
Chronic liver disease significantly impacts drug metabolism due to alterations in hepatic blood flow and enzyme accessibility. This disruption affects the body's pharmacokinetics—the movement and processing of drugs within the system. Key enzymes crucial for metabolizing medications become less accessible, changing how drugs are processed and utilized. Furthermore, liver disease influences the synthesis of plasma proteins, such as albumin and globulins, which play critical roles in drug...
309

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System for Efficacy and Cytotoxicity Screening of Inhibitors Targeting Intracellular Mycobacterium tuberculosis
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Rifampicin-Induced Concomitant Renal Injury and Hepatitis.

Bharti Chogtu1, Vyshak Uddur Surendra2, Rahul Magazine3

  • 1Associate Professor, Department of Pharmacology, Kasturba Medical College, Manipal University , Manipal, Karnataka, India .

Journal of Clinical and Diagnostic Research : JCDR
|October 30, 2016
PubMed
Summary

Adverse drug reactions during Anti-Tubercular Therapy (ATT) can cause liver and kidney damage. This case highlights rifampicin as a suspected cause of drug-induced hepatitis and renal failure in tuberculosis patients.

Keywords:
Anti tubercular drugsLiver function testsSerum creatinineSerum urea

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Area of Science:

  • Nephrology
  • Hepatology
  • Infectious Diseases

Background:

  • Anti-Tubercular Therapy (ATT) is crucial for tuberculosis treatment but can lead to adverse drug reactions.
  • Drug-induced hepatitis and renal insufficiency are known complications of ATT, requiring prompt diagnosis.
  • Differential diagnoses include viral infections, pre-existing conditions, or drug toxicity.

Observation:

  • This case report details a patient experiencing ATT-induced renal failure and hepatitis.
  • Rifampicin, a first-line ATT drug, was identified as the suspected causative agent.
  • The patient's history included rifampicin re-exposure and alternate-day administration, factors linked to rifampicin-induced renal toxicity.

Findings:

  • Rifampicin is associated with various adverse drug reactions, including hepatitis, anemia, and interstitial nephritis.
  • Renal toxicity from rifampicin is often observed upon re-exposure or with alternate-day dosing.
  • This case underscores the potential for rifampicin to cause both hepatitis and renal failure concurrently.

Implications:

  • Prompt identification of drug-induced adverse events is critical for managing tuberculosis patients.
  • Suspected drugs, like rifampicin, should be identified to guide treatment adjustments and prevent life-threatening complications.
  • Understanding rifampicin's potential for hepatorenal toxicity is vital for optimizing ATT regimens and patient outcomes.