Extra Stuff Flashcards

1
Q

What Drugs belong to the 1st generation of Cephalosporins and what are they used for?

A
  1. Cephalexin - commonly prescribed for outpatient use

2. Cefazolin - Surgical Prophlylaxsis

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2
Q

What are second gernerations Cephalosporins used for?

A

Mild Gram (-) and Intraabdominal Infections

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3
Q

What drugs belong to the 3rd generation of Cephalosporins?

- what are they used for?

A
  1. Ceftriaxone - treatment of STDs, Pediatric Meningitis

2. Cefepime - pseudomonal Infections

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4
Q

What are 4th generation Cephalosporins used for?

A

Nosocomial Infections

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5
Q

T or F: Cephalosporins are acid stable so you can take them without food.

A

True

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6
Q

What are Monobactams used for?

A

Treatment of Gram (-) rods

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7
Q

T or F: Ampicillin works better on gram (-) bacteria because its amino groups allow it to pass through the LPS layer

A

True

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8
Q

T or F: Mitronidazole is given as a pro-drug

A

True

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9
Q

What does binding to CD3 prevent?

- what drug does this?

A
  • Prevents T cell activation

- Muranomab-OKT3 does this

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10
Q

What does Ab binding to CD80/86 prevent?

- what drug does this?

A
  • Prevents T cell co-stimulation so T cell never becomes completely active - apoptosis follows
  • Balatacept does this
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11
Q

What does Ab binding to CD25 do?

- what drug does this?

A
  • Prevents clonal expansion

- Basiliximab does this

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12
Q

T or F: since both sirolimus and tacrolimus work on FKBP12, they both act to some extent on calcineurin

A

False, they both act on FKBP12 but only tacrolimus works on calcineurin, sirolimus only works on mTOR

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13
Q

Which of the cell-cycle inhibitors is specific to B and T cells?
- explain.

A

Mycophenolate mofetil is specific to B and T cells because it interrupts the synthesis of Guanosine from IMP. B and T cells lack a GMP salvage pathway so depleting GMP synthesis is particularly toxic to these cells.

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14
Q

Which of the cell cycle drugs might be contraindicated with patients that have gout. why?

A
  • Contraindicated if they are taking Allopurinol
  • Allopurinol blocks the salvage pathways of Purines, this inhibits the side metabolic route of AZATHIOPRINE which shifts the dose response curve to the left because more 6-MP (mercaptopurine) is being produced
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15
Q

Which immunosuppressive drugs may vary in their bioavailability from patient to patient? why?

A
  • Sirolimus, Cyclosporine, Tacrolimus

- They are metabolized by CYP3A4

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16
Q

Why are so many drugs given during the maintenance phase of immunosuppressive therapy?

A

To prevent dose related toxicity (some drugs like sirolimus and cyclosporine are even synergistic)

17
Q

What are the 2 general effects of Ab treatment?

A
  • Block T Cell activation/Proliferation

- Activate complement and produced ADCC

18
Q

Azoles prevent conversion of what to what by what?

A

Lanosterol to Ergosterol via blockage of p450 (extensive side affects from azoles related to their ability to affect human p450 isoforms e.g. CYP3A4)

19
Q

What biochemical process causes the symptoms seen in an infusion reaction?

A

-Increases in PG synthesis

20
Q

Which of the Anti fungals is uniquely eliminated in the urine?

A

Fluconazole

21
Q

Which of the Anti-fungal drugs should you not use in the patients that a immunosuppressed? why?

A

Terbinafine because it causes transient lymphopenia and neutropenia (patients receiving this drug should have CBCs performed regularly)

22
Q

Why does treatment with azole drugs have to last so long?

A
  • its fungistatic, so ending treatment early would leave original cells in tact to reproduce when therapy was terminated
  • This is associated with high Relapse Rate