Terms
Absorption
Distribution
Metabolism
Elimination (Kidneys)
100

The study of how various dosage forms influence the way in which a drug affects the body

What is Pharmaceutics?

100

Enteral (oral, Sublingual/Buccal, Suppositories; varying bioavailability) 

Parenteral (injection;100% bioavailable) 

Other (Eye drops, Inhalers, etc; varying bioavailability) 


What are the types of absorption routes? 

100

Occurs after the drug is absorbed into the bloodstream

What is distribution? 

100
The biochemical alteration of a drug (substrate = target drug) where it can be converted to an active or inactive metabolite 

What is metabolism? 

100

elimination of hydrophilic drugs from the body via the kidneys

What is elimination?

200

Determinant of how a drug dissolutes

What is dosage form? 

200
GI tract pH, co-administration with drugs/meals, pharmaceutics, P-Glycoproteins (Efflux Pumps), First Pass Effect

What are the influences of oral drug bioavailability? 

200

Non-polar Lipophilic drugs are easily distributed into fatty tissue and can cross BBB and placenta

Polar Hydrophilic typically remain in highly vascularized spaces and are easily eliminated via urine

What is permeability of cell membrane? 

200

Liver enzymes that target substrates that are lipophilic non-polar and covert them to hydrophilic polar form 

What are Cytochrome P-450 (CYP450)? 
200

Known as "The filter" 

Serum Creatinine (🫐0.6-1.2mg/dL 🎀0.5-1.1mg/dL) 

BUN (8-20mg/dL) 

Urine Output (>30ml/hr) 

Creatinine Clearance (CrCl) & Estimated Glomerular Filtration Rate (eGFR) = 90-120ml/min

What is the Glomerulus and normal lab values for kidney function?

300

The study of what the body does to the drug (ADME). 

Whats is Pharmacokinetics? 

300

- Age (Neonates and Elders have a high pH)

- Time of Day (pH is lowest when we wake up) 

- Presence of food 

- Tums/Medications

- Diseases/Conditions

What are influences of pH? 
300

Albumin is the most common blood protein; when drug is bound to this protein, it is a highly-bound drug/inactive so it stays in the bloodstream (Phenytoin is 🗝️)

Free drugs are active drugs that are not bound to albumin and can leave the bloodstream so they can reach extravascular tissue and intended target

What is Protein Binding? 

300

PS-PORCS 

Phenytoin, Smoking, Phenobarbital, Oxcarbazepine, Rifampin, Carbamazepine, St. John's Wort


What are components that induce metabolism? 

300

Elevated serum creatinine, and BUN with decreased CrCl, eGFR, and urine output

What are expected lab values due to kidney injury? 
400

The percentage of how much active drug reaches and is absorbed into the bloodstream

What is bioavailability? 

400

Grapefruit inhibits it's function and specifically does not fair well with Statins which results in rapid muscle breakdown (rhabdomyolysis) if taken together 

What influences P-Glycoproteins/Efflux Pumps? 
400

Competition leads to toxicity and albumin deficiency can lead to more free drug levels causing respiratory distress.

What are complications of Highly-Bound Drugs? 

400

PACMAN ♡ Grapefruit

Protease inhibitor (HIV), Azole antifungal (fluconazole, ketoconazole), Cimetidine (H2RAs), Macrolides (ACE, Azithromycin, Clarithromycin, Erythromycin), Amiodarone, Non-DHP Calcium Channel Blockers (diltiazem, verapamil), ♡, Grapefruit juice

What are inhibitors of CYP450? 
400

Follow expected values for women when treating transwomen and vice versa for transmen who have been on hormone therapy for > 6 months

What is transgender patient care?

500

Found in the GI tract/BBB and has the known function of eliminating xenobiotics (toxins,drugs) and preventing them from entering the bloodstream. AKA anti-absorption pump. 

What are P-Glycoproteins/Efflux Pumps? 

500
Only applies to oral drugs that are swallowed and metabolized by the liver before getting into the general blood circulation. 

What is the First Pass Effect? 

500

Rapid (⏩) occurs in heart, kidney, liver, brain

Slow (🐢) occurs in muscle, skin, fat 

Poor perfusion caused by disease/condition (heart disease, sepsis, PVD) 

What is circulation/blood supply? 

500

An inactive/less active form of a drug that is converted into its active form in the liver; meant to improve absorption/stability/distribution and allow better delivery to target tissues

What are Pro-drugs? 

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