Pharmacology · MU Sofia

16. Pharmaceutical drug interactions (drug incompatibility). Drugs affecting clinical laboratory tests. Interactions of drugs with foods.

Covers physical, chemical and therapeutic drug incompatibility, with examples such as precipitation, adsorption, hydrolysis and antagonistic effects. Goes on to show how several drugs distort laboratory results across haematological, biochemical, endocrine, immunological and urine tests, then sets out drug-food interactions at each stage of absorption, metabolism, distribution and excretion. Ends with a set of recap questions.

Inside: 1 section · 3 labelled pictures · 10 flashcards · 4 min

Topic 15 of 93 in the MU Sofia syllabus for Pharmacology (Medicine, Year 3). The free AceMed note covers it in 1 section, about 505 words (4 min of reading), with 10 flashcards.

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  1. Pharmaceutical Drug Interactions & Effects on Clinical Lab Tests

Pharmaceutical Drug Interactions & Effects on Clinical Lab Tests

Drug incompatibility occurs when two or more drugs interact physically or chemically, leading to reduced efficacy, altered effects, or adverse reactions. This can happen when drugs are mixed together in a solution or administered simultaneously.

  1. 1. Types of Drug Incompatibility

1.1 Physical Incompatibility

  • Precipitation: Formation of solid particles when two drugs mix.
  • Example: Mixing calcium chloride with sodium bicarbonate causes precipitation.
  • Adsorption: Drug molecules stick to surfaces, reducing the effective dose.
  • Example: Insulin adsorbs to PVC tubing, reducing its availability.
  • Phase Separation: Emulsions separate into different layers.
  • Example: Mixing propofol (an emulsion) with other drugs can cause phase separation.

1.2 Chemical Incompatibility

  • pH Changes: Mixing drugs with different pH levels can lead to degradation.
  • Example: Acidic solutions mixed with alkaline drugs cause instability.
  • Oxidation-Reduction Reactions: Drugs that act as oxidizing/reducing agents degrade each other.
  • Example: Ascorbic acid (reducing agent) + iron salts → oxidation reaction.
  • Hydrolysis: Water-soluble drugs break down when mixed.
  • Example: Procaine (ester) undergoes hydrolysis in aqueous solutions.

1.3 Therapeutic Incompatibility

  • Antagonistic Effects: Drugs with opposing actions reduce each other's efficacy.
  • Example: Beta-blockers + beta-agonists cancel out their effects.
  • Synergistic Toxicity: Two drugs enhance each other’s toxicity.
  • Example: Aminoglycosides + loop diuretics → increased risk of ototoxicity.
  1. 2. Drugs Affecting Clinical Laboratory Tests

Some drugs interfere with clinical lab tests, leading to inaccurate results or misdiagnosis.

2.1 Hematological Tests

  • Heparin → falsely elevates aPTT (activated partial thromboplastin time).
  • Chemotherapy drugs → cause neutropenia, affecting WBC counts.

2.2 Biochemical Tests

  • Acetaminophen overdose → elevates liver enzymes (AST, ALT).
  • Statins → increase creatine kinase (CK), indicating muscle damage.

2.3 Endocrine Tests

  • Corticosteroids → suppress adrenal function, altering cortisol levels.
  • Oral contraceptives → increase thyroxine-binding globulin (TBG), affecting thyroid tests.

2.4 Immunological Tests

  • Immunosuppressants (e.g., cyclosporine) → affect immune function tests.
  • Biologics → interfere with cytokine assays.

2.5 Urinalysis

  • Rifampin → causes red/orange urine, leading to misinterpretation.
  • Metformin → interferes with urine glucose tests, causing false negatives.
  1. 3. Drug-Food Interactions

Food can significantly affect drug absorption, metabolism, distribution, and excretion, leading to changes in efficacy and safety.

3.1 Absorption

  • Grapefruit juice → inhibits CYP3A4, increasing statin levels → toxicity risk.
  • Dairy products (calcium) → bind to tetracyclines, reducing antibiotic absorption.

3.2 Metabolism

  • Cruciferous vegetables (e.g., broccoli, Brussels sprouts) → induce CYP enzymes, increasing metabolism of warfarin, reducing its effect.
  • High-protein diets → affect metabolism of CYP1A2 drugs like theophylline.

3.3 Distribution

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