L4: Principles of Pharmacology Flashcards
Digitalis
-contains cardiac glycoside (digoxin)
-inhibits Na/K ATPase and acts as cardiac inotrope
If 2 graphs, one has Rx effect close to Tx effect and the other has Rx effect farther from Tx effect, which drug would be better?
The drug with Rx and Tx farther apart is better.
-If had to double the dose, the Tx being farther apart would mean less chance of getting adverse/toxic effects
-Whereas the closer Tx line is, the more likely to experience negative effects
Pharmacokinetics
ADME
“What the body does to a drug”
Pharmacodynamics
“What a drug does to the body”
“Alternative” and “complementary” treatments
have been increasingly promoted but generally have not undergone validation with appropriately designed ___ and do not require ___ approval!
-RCTs
-FDA
Magic bullet
Drug that precisely targets a disease or a receptor
– Magic bullets would have a very wide therapeutic window
– But there are few magic bullets: antimicrobials that target bacterial cell walls (not found in humans/animals)
Specificity
- Drugs are almost never specific
-Drug with one and only one site of action is specific
-But even a drug with one main site of action may act at other receptors, especially at higher doses
Selectivity
- Drugs can be selective
-Drug mainly affects a particular target
-Drug mainly affects a particular tissue
Achieving Selectivity
Selectivity depends on several factors
* Chemical nature of drug
* Dose (keep it low)
* Route of administration (target a specific organ)
* Unpredictable differences between patients (e.g., due to genetics, age, co-existing diseases, other drugs)
Selectivity is especially important for ____ drugs
-chemotherapeutic (anticancer, antimicrobial)
Goal is to “kill” the target without harming the host
Risk-Benefit Ratio
Acceptable ratio depends on:
* Severity of the disease being treated (or prevented)
* Economics
* Societal factors
* Patient’s medical history and current/past drug use
Drug-related threats to quality of care
– Misuse: errors and defects in treatment
– Overuse: receiving treatment of no value
– Underuse: failing to receive needed treatment
- Drug safety initiatives often address only misuse – but overuse and underuse also need attention!
Drugs have many names
– Chemical name: scientific name, based on molecular structure
– Generic name: nonproprietary name, officially approved during drug development process
– Brand name: commercial name; aka trade name
Drugs in the same class often share a common suffix
-Cardio Examples
- -lol for β antagonists (e.g., propranolol)
- -osin for α1 antagonists (e.g., prazosin)
- -pril for ACE inhibitors (e.g., enalapril)
Generic version of a drug
– Copy of an approved brand name drug
* Manufactured and marketed after a brand name drug is off-patent
* Generally less expensive than brand name drug
* Same dose, route of administration, approved indications, safety, adverse effects, etc
– Required to meet bioequivalence standards defined by the FDA
* Chemical, manufacturing, and pharmacokinetic equivalence
* Therapeutic equivalence, which is generally but not always achieved by the generic version of a drug