74, 75 Drug Interactions Flashcards
What is the difference of object drug and the precipitant drug?
Object drug is the drug being affected by the precipitant drug
Which of the following are examples of drugs with narrow therapeutic window? > steep dose response curve, increase risk of DDI
A. Digoxins (for heart failure) B. Warfarin (anticoagulants) C. Lithium D. Cytotoxic drugs for chemotherapy E. CNS drugs
All of the above
What is the difference between pharmacodynamic and pharmacokinetic interactions?
Pharmacodynamics = 1 drug potentiates/ reduces the therapeutic outcome of the other drug;
Pharmacokinetics = absorption, distribution, excretion, metabolism
Possible pharmaceutical interactions of diazepam? (anxiolytic)
With infusion fluid > precipitation to inactivate drug
phenytoin too
Possible pharmacokinetic interactions of diazepam? (metabolism)
with P450 inhibitor isoniazid 愛Sonia子 (antibiotic)
will cause increase in diazepam concentration, thus increase risk of overdose
Possible pharmaceutical interactions of thiopental (IV GA)?
Thiopental + Suxamethonium (NMBA) > precipitation
Possible pharmacodynamic interactions of naloxone?
Naloxone + opioids > reduce effectiveness of opioids (as an opioid mu receptor antagonist)
Possible pharmacodynamic + metabolic interactions of propranolol?
beta blocker propranolol + bronchodilators (b2 agonists) will reduce effectiveness of the bronchodilators
(metabolism: increase risk of overdose with cimetidine , P450 inhibitor)
Give examples of distribution wise drug interactions.
Precipitant drugs?
Object drugs? + consequence
Precipitant drugs:
- Salicylate (aspirin)
- valproate (anticonvulsant)
Object drugs
- Phenytoin (anticonvulsant) > headache, ataxia, confusion
- Warfarin (anticoagulant) > high risk of bleeding
e.g. aspirin displace warfarin
What type of drugs will have high chance of distribution drug interactions?
- Highly protein bound
2. Low volume of distribution (drugs stay in plasma, increase risk of reaching toxic concentration)
Interactions between aspirin and probenecid?
Probenecid increases plasma level of aspirin (+ indomethacin) by reducing its excretion. (competition for same transporter?)
- also increases plasma level of penicillin
Methotrexate drug interactions?
immunosuppression for arthritis patients
Methotrexate is partially bound to serum albumin, and toxicity may be increased because of displacement by other highly bound drugs, such as salicylates (aspirin) , phenytoin
> methotrexate toxicity
Drug interactions encountered by warfarin in albumin/P450?
Albumin: being displaced by aspirin, valproate >high risk of bleeding;
P450
- P450 inducers like phenobarbital, rifampicin, alcohol > reduce effectiveness of warfarin
- P450 inhibitors like cimetidine (H2 antagonist) increase risk of. overdose due to reduced metabolism
Cimetidine is a ? DDI?
P450 inhibitor, prolong other drug effects.
Phenobarbitone is a ? DDI?
P450 inducer, reduce effectiveness of other drugs.