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Over 11 hours of high yield review. Separated into two parts: board prep and clinical prep.

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We tend to overcomplicate medicine. Tell me if this sounds familiar...

  • "There's so much to learn...where do I start?"
  • "Pharmacology is like learning a new language!"
  • "How am I supposed to get through all this material in such a short amount of time?"

Most students and new graduates feel this way; specifically with pharmacology. So, I wanted to share our number one tip to help get you ahead:

Realize there's only a limited amount of use cases per drug.

Let me explain.

It can be overwhelming to see hundreds of drugs and hundreds of diseases. Instead, let's change the way we view this. Let's take ACE inhibitors for example...

When are they indicated? Well, there are only 4 scenarios in which ACE inhibitors would be used:

  • Post MI
  • Systolic CHF
  • CKD/Diabetic nephropathy
  • Hypertension (first line if diabetic except in the African American population - no benefit noted)

That's it.

It can be easy to over complicate things. But if we realize that ACE inhibitors are the answer in only four situations, then things suddenly become manageable.

It's all about simplification. This is incredibly important as there are over 2,000 FDA approved medications on the market! I don't know about you, but that sounds like a lot of information to be responsible for.

The good news is there are only 400 classes of drugs (rough estimate).

400 is a lot nicer to look at, don't you think?

I have even better news...the boards only expect you to know about 150 classes of drugs.

Why is it important to break medications up like this? Well, because classes typically have the same mechanism of action, indications, adverse reactions, and contraindications (as we discussed with ACE inhibitors).

I say typically, because there are always exceptions. But, it is definitely easier to clump them into groups like this, and then review the exceptions afterwards.

Let's do another example with the second generation antipsychotics...

The second generation antipsychotics include: Aripiprazole, Clozapine, Olanzapine, Quetiapine, Risperidone, Paliperidone, Asenapine, Lurasidone, Brexpiprazole, Ziprazidone, and Iloperidone.

Instead of learning 11 medications, let's clump them into one class, and instead learn about that one class.

This makes things easy, because the second generation antipsychotics all have the same two indications:

  • Acute psychosis from any cause
  • To help manage chronic psychotic disorders

But, there is one exception we have to know: clozapine

What makes this different?

Well, it has the highest risk for agranulocytosis. For this reason, it's reserved for the management of resistant schizophrenia.

This is important for both board review and clinical practice.

Do you see how grouping medications together can simplify and accelerate the learning? We have enough to learn. The last thing we need to do is over complicate things.

What Our Clients Have to Say About Medgeeks

We'll be covering...

  • Cardiology
  • Endocrinology
  • Gastroenterology
  • Genitourinary
  • Neurology
  • Pulmonology
  • Psychiatry
  • Pain medication
  • The immune system
  • Antibiotics
  • Antivirals
  • Antifungals

Every Medication Listed Has...

  • Relevant human physiology explained
  • Mechanism of action
  • Contraindications
  • Adverse Reactions (the ones you must know)
  • Toxicity (if relevant)
  • When the drug is used
  • Clinical pearls on dosing, monitoring, and prescribing

Pharmacology = Variation of Human Physiology

How do you know which drug to choose?

A drug has an effect because it is altering the body's physiological state.

We are manipulating processes in order to achieve a desired effect.

So, if you understand the physiology, then you will dominate pharmacology.

Let's take a look at the adverse reactions of the second generation antipsychotics...

First off, how do they work? They inhibit serotonin at the 5-HT2a receptors and inhibit dopamine at the D2 receptors. They also affect the muscarinic and histamine receptors. They essentially have the same mechanism of action as the first generation antipsychotics, but have a higher affinity to serotonin receptors and rely less on the dopamine D2 receptors. Because of this, they are less likely to cause extrapyramidal side effects and tardive dyskinesia.

By understanding their physiology within the body, we can understand why they have the adverse effects they do.

Let's dig deeper into their specific adverse reactions...

  • From alpha-1 antagonism: hypotension

  • From muscarinic antagonism: dry mouth, constipation, blurred vision, and urinary retention

  • From the histamine antagonism: drowsiness

  • From dopamine inhibition: tardive dyskinesia and hyperprolactinemia (galactorrhea, amenorrhea and ED).

  • They can also cause metabolic syndrome, cardiomyopathies, sexual dysfunction, and cataracts.

See how this is nothing more than physiology? If you want to dig even deeper, then we hope to see you inside our pharmacology review course.

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