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.
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).
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.
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).
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.
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.
7
Q
Type G (Genetic) Reaction
A
- Characteristics: Pharmacokinetic/dynamic variability.
- Examples: Antimicrobial resistance, contraceptive failure (enzyme inducers).
- Management: Genetic screening; avoid specific drugs.
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.
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.
10
Q
Dabigatran (Pradaxa)
A
- Effect: Serious hemorrhages.
- Mechanism: Thrombin inhibition (anticoagulant effect).
- Management: Monitor renal function; avoid in renal impairment.
11
Q
Clozapine
A
- Effect: Agranulocytosis.
- Mechanism: Idiosyncratic immune reaction.
- Management: Regular blood monitoring; discontinue if neutropenia occurs.
12
Q
Proton Pump Inhibitors (PPIs)
A
- Effect: Hypomagnesemia.
- Mechanism: Reduced intestinal magnesium absorption.
- Management: Monitor Mg levels; supplement if needed.
13
Q
Statins
A
- Effect: Hyperglycemia/diabetes.
- Mechanism: Insulin resistance.
- Management: Monitor blood glucose; lifestyle modifications.
14
Q
Tacrolimus
A
- Effect: Graft rejection (brand switching).
- Mechanism: Bioavailability variability between formulations.
- Management: Prescribe and dispense the same brand.
15
Q
Halothane
A
- Effect: Hepatitis.
- Mechanism: Immune-mediated liver injury.
- Management: Avoid in patients with liver disease.
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.