adverse drug reactions
TRANSCRIPT
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Adverse Drug Reactions
Dr. Gyanendra Raj Joshi PharmD, RPh
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Terminologies
• Side effect • Toxicity • Secondary effects • Intolerance • Idiosyncrasy
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Adverse Drug Reaction
• WHO definition:– A response to a drug which is noxious, unintended
and occurs at doses used in man for prophylaxis, diagnosis or therapy.
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• UK Commission on Human Medicines:– An unwanted or harmful reaction experienced
after the administration of a drug or combination of drugs under normal conditions of use and suspected to be related to the drug.
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Predisposing factors
• Multiple drug therapy • Age • Gender • Concomitant disease • Race and genetic polymorphism
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Severity of ADR
• Minor • Moderate • Severe • Lethal
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Classification
• Type A ( Augmented)• Type B ( Bizarre)• Type C ( Chronic)• Type D ( Delayed )• Type E ( End of use )• Type F ( Therapeutic Failure )• Type G ( Genetic /Genomic)
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Type A reactions
• Exaggerated pharmacological response
• Excessive : Anticoagulants
• Unwanted : TCAs
• Withdrawal : Clonidine
• Delayed : Diethylstilbestrol
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Mechanisms of Type A reactions
1. Pharmaceutical causes :– Quantity of drug– Quality of drug – Release characters
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2. Pharmacokinetic causes :a. Absorption– Dosage– GI motility – First pass metabolism – Nature of gastric contents – Disease – Concomitant drugs
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b. Distribution:– Regional blood flow – Plasma protein binding – Tissue binding c. Elimination :– Reduced elimination – Increased elimination – Drug Metabolism – Drug Excretion
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3. Pharmacodynamic causes
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Mechanism of Type B Reactions
1. Pharmaceutical Causes :– Degradation products – Non-drug components (excipients )– Synthetic by- products
2. Pharmacokinetic Causes :– Bioactivation to reactive metabolites • Tacrine: hepatotoxicity• Clozapine : agranulocytosis • Halothane : hepatotoxicity
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3. Pharmacodynamic causes :a. Immunological b. Genetic c. Teratogenic
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Immunological mechanismsReaction Immunological mechanism Clinical manifestation Drugs
Type I IgE mediated •Anaphylaxis Penicillin
Type II Humoral (Antibody dependent Cytotoxic) IgG /IgM
•Hemolysis •Thrombocytopenia
Methyl Dopa
Type IIIArthus reaction
Humoral Immune Complex mediatedIgG/IgM
•Serum sickness•Acute Glomerulonephritis •SLE•Vasculitis
Streptokinase
Type IVDelayed
Cell mediated injuryT cells
•Skin eruptions •Steven Johnsons syndrome •Contact dermatitis •Delayed tuberculin test
Amoxicillin
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Genetic mechanisms
• G6PD deficiency • N-acetyltransferase activity
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Teratogenic mechanisms
• Fertilization and implantation (upto 17 days)• Organogenesis (18-55)• Growth and development (56 onwards )
• Thalidomide • Phenytoin• Warfarin• Valproic acid • Vit A derivatives • Tetracyclines
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Pregnancy category of drugs
• A• B• C• D• X
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Comparison between Type A and Type B
Basis Type A Type B
Pharmacologically predictable
Yes No
Dose dependent Yes No
Incidence High Low
Morbidity High Low
Mortality Low High
Management Dose adjustment Stop drug
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Detecting ADRs
• Causal attributes :– Time sequence – Withdrawal or reintroducing – Established pharmacology and toxicology
• Degrees of conviction:– Definite – Probable – Possible – Conditional – Doubtful
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Pharmacovigilance
• Science and activities relating to the detection , assessment , understanding and prevention of adverse effects or any other drug related problems.
• Activities :– Post marketing surveillance /ADR monitoring – Dissemination of ADR data – Changes in labeling
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Prevention of ADRs
• Avoid inappropriate use• Rational use of drugs • Past medication history • Past medical history• Drug interactions • Correct route and method • Lab tests
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