Drugs
Drug induced disease states
Drug clearance
Metabolism
Antidotes, inhibitors and science stuff
100

This ultra short acting anesthetic is used for initial anesthesia.

Thiolpental

100

Kernicturus can occur in newborns due to this type of medication.

Sulfinamides

100

This is when a constant proportion of drug is cleared per unit time where the half life is constant.

First order elimination

100

This phase is metabolized by Cytochrome P450 enzymes.

Phase I metabolism

100

This drug is given as an antidote for tasty tasty antifreeze, because inhibition of Alcohol dehydrogenase prevents metabolism into toxic oxalate.

4-Methylprazole (Fomepizole)

200

Watch out clopidogrel takers, this PPI inhibits CYP2C19 which converts its it to the active form.

Omeprazole

200

Grey baby syndrome is a fatal adverse reaction because an infants inability to metabolize this drug...

Chloramphenicol

200

This is when a constant proportion of drug is cleared per unit time where the half life is NOT constant.

Zero order elimination.

200

When drugs undergo conjugation with exogenous molecules such as glucuronate, acetate, methyl, sulfate or glycine to form water soluble metabolites.

Phase II metabolism

200

When attempting to eat a whole bottle of tylenol, this drug provides the sulfide group needed to prevent death.

N-acetylcysteine (NAC, Acetadote, Mucomyst)

300

Used in colorectal cancer, this prodrug is metabolized into SN-38 to kill cancer cells. Patients with impaired UGT activity can experience sever leukopenia from it.

Irinotecan 

300

Not just a fancy dance, Torsades is QT prolongation that can be caused from too much of this drug for vaginal candidiasis. It's also "the poster child" for CYP inhibition.

Ketoconazole

300

These 3 drugs have a low extraction ratio.

Phenytoin, aspirin, ethanol

300

UGT, NAT, TPMT, GST and SULT are all enzymes involved with...

Phase II metabolism

300

Along with alcohol and grapefruit juice, these 3 drugs cause extensive CYP450 inhibition... 

1. Cimetidine

2.Ketoconazole

3. Erythromycin

400

These 3 thiopurines are immunosuppressants that are metabolized by TPMT. 

1. Azathioprine

2. 6-mercaptopurine

3. thioguanine

400

Rhabdomyolysis is a disease of rapid muscle degeneration. With This can happen when diminished OATP1B1 allows build up of this category of drugs...  

Statins

400

These 3 drugs can decrease the amount of other drugs in your system by inducing their metabolism.

1. St Johns Wort - Can reduce the amount of systemic HIV meds 

2. Rifampin - Tuberculosis treatment

3. Carbamazepine - used in epilepsy. Suicidal enzyme

400

The prodrug codeine is demethylated to morphine by CYP2D6, this is an example of...

Phase I metabolism

400

After the allergy drug Terfenadine was removed from the market fdue to fatal K+ channel block. This drug with similar structure, but no K+ channel effect was marketed.

Fexofenadine (allegra)

500

When taking codeine, people with this phenotype end up with morphine toxicity. 

Ultra rapid metabolizers

500

An HLA-B polymorphism can lead to toxic epidermal necrolysis or Steven Johnson's syndrome when taking this medication...

Abacavir

500

Hepatic clearance depends on these 3 things.

1.Bloodflow through the liver.

2. Fraction of free form of the drug

3. Intrinsic ability of hepatic enzymes to metabolize drug.

500

The drug Disulfiram is given to alcoholics to inhibit this enzyme... 

Aldehyde dehydrogenase

500

In the HMP-Shunt pathway, G6PD helps to metabolize these 3 drugs...

1. Primaquine - antimalarial 

2. Rasburicase - Treats increased uric acid in cancer

3. Sulfonamides