Lesson 5 and 6- Classification and Risk Factors of ADR's Flashcards

(18 cards)

1
Q

Type A (Augmented) Reaction

A
  • Characteristics: Dose-dependent, common, predictable, manageable with dose adjustment.
  • Examples: Bleeding (warfarin), hypoglycemia (antidiabetics), headache (nitrates).
  • Management: Reduce dose or discontinue therapy.
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2
Q

Type B (Bizarre) Reaction

A
  • Characteristics: Idiosyncratic, unpredictable, not dose-related, serious.
  • Examples: Anaphylaxis (penicillin), agranulocytosis (clozapine), hepatitis (halothane).
  • Management: Stop drug immediately; treat reaction (e.g., antihistamines, steroids).
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3
Q

Type C (Chronic) Reaction

A
  • Characteristics: Dose- and time-related, cumulative effects.
  • Examples: Osteoporosis (steroids), adrenal suppression (corticosteroids).
  • Management: Reduce dose or long-term withdrawal.
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4
Q

Type D (Delayed) Reaction

A
  • Characteristics: Lag time after drug use, irreversible.
  • Examples: Teratogenicity (anticonvulsants), tardive dyskinesia (antipsychotics).
  • Management: Avoid in high-risk populations (e.g., pregnancy).
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5
Q

Type E (Withdrawal) Reaction

A
  • Characteristics: Occurs after stopping therapy.
  • Examples: Myocardial ischemia (beta-blocker withdrawal), opioid withdrawal.
  • Management: Reintroduce drug and taper slowly.
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6
Q

Type F (Failure) Reaction

A
  • Characteristics: Due to drug interactions.
  • Examples: Digoxin toxicity (with furosemide), phenytoin toxicity (with fluconazole).
  • Management: Monitor interactions; adjust doses.
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7
Q

Type G (Genetic) Reaction

A
  • Characteristics: Pharmacokinetic/dynamic variability.
  • Examples: Antimicrobial resistance, contraceptive failure (enzyme inducers).
  • Management: Genetic screening; avoid specific drugs.
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8
Q

ADR Risk Factors in Children (Absorption)

A
  • Variable gastric emptying, reduced acid secretion, thin skin (↑ dermal absorption).
  • Implications: Higher bioavailability; systemic effects from topical drugs.
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9
Q

ADR Risk Factors in Elderly (Renal Excretion)

A
  • ↓ Renal blood flow, glomerular filtration rate, and tubular function.
  • Examples: Lithium toxicity, digoxin toxicity.
  • Management: Adjust doses based on renal function.
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10
Q

Dabigatran (Pradaxa)

A
  • Effect: Serious hemorrhages.
  • Mechanism: Thrombin inhibition (anticoagulant effect).
  • Management: Monitor renal function; avoid in renal impairment.
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11
Q

Clozapine

A
  • Effect: Agranulocytosis.
  • Mechanism: Idiosyncratic immune reaction.
  • Management: Regular blood monitoring; discontinue if neutropenia occurs.
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12
Q

Proton Pump Inhibitors (PPIs)

A
  • Effect: Hypomagnesemia.
  • Mechanism: Reduced intestinal magnesium absorption.
  • Management: Monitor Mg levels; supplement if needed.
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13
Q

Statins

A
  • Effect: Hyperglycemia/diabetes.
  • Mechanism: Insulin resistance.
  • Management: Monitor blood glucose; lifestyle modifications.
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14
Q

Tacrolimus

A
  • Effect: Graft rejection (brand switching).
  • Mechanism: Bioavailability variability between formulations.
  • Management: Prescribe and dispense the same brand.
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15
Q

Halothane

A
  • Effect: Hepatitis.
  • Mechanism: Immune-mediated liver injury.
  • Management: Avoid in patients with liver disease.
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16
Q

Corticosteroids

A
  • Effect: Adrenal suppression.
  • Mechanism: HPA axis inhibition.
  • Management: Taper doses gradually; avoid abrupt withdrawal.
17
Q

Metoclopramide (Children)

A
  • Effect: Extrapyramidal symptoms.
  • Mechanism: Immature blood-brain barrier.
  • Management: Avoid or use lower doses.
18
Q

Benzodiazepines (Elderly)

A
  • Effect: Falls, sedation.
  • Mechanism: ↑ CNS sensitivity, muscle relaxation.
  • Management: Use lowest effective dose; avoid long-term use.