HIV Pharm High Yield Flashcards

1
Q

What is the phase II metabolic process for antiretroviral drug elimination that tends to result in fewer drug-drug interactions?

A

glucuronidation

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2
Q

can see a typically self-limiting decrease in this with the use of tenofovir?

A

bone density

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3
Q

what is an early adenosine analog noteworthy for its adverse effects due to mitochondrial toxicity?

A

didanosine

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4
Q

What HIV drugs were/are considered to be teratogenic?

A

efavirenz and dolutegravir

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5
Q

what HIV drug leads to renal toxicity and what syndrome is associated with this?

A

tenofovir; fanconi syndrome

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6
Q

which class of HIV drugs is resistant to HIV-2?

A

NNRTI

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7
Q

new pro drug of tenofovir that has a higher intracellular concentration and less renal and bone toxicity?

A

alafenamide

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8
Q

what class of HIV drugs induce CYP3A4?

A

NNRTI

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9
Q

what is an example of an HIV drug that causes hepatic steatosis?

A

zidovudine

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10
Q

example of an HIV INSTI that will likely decline in use with availability of bicregravir from the same company?

A

elvitegravir

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11
Q

what is a serious NRTI toxicity associated with early agents such as stavudine?

A

peripheral neuropathy

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12
Q

what is the NNRTI approved for use in treatment-experienced people infected with HIV since it still works after HIV mutations that cause resistance to nevirapine and efavirenz?

A

etravirine

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13
Q

among the toxicities associated with some NRTI that is thought to be due to inhibition of DNA polymerase gamma?

A

myopathy

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14
Q

what HIV drug is a sulfa drug?

A

darunavir

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15
Q

what is the toxicity associated with atazanavir?

A

unconjugated hyperbilirubinemia

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16
Q

an NNRTI that had early studies done on it that demonstrated the need for combination therapy

A

nevirapine

17
Q

early PI requiring 3x/day dosing, no longer used but still tested on for it’s unique ability to cause crystaluria/ renal stones

A

indianavir

18
Q

what is the newest 1x/day INSTI, only available in combination, well absorbed in comparison to other NSTI, high genetic barrier to resistance and very well tolerated?

A

bictegravir

19
Q

among early thymidine NRTI, notable for significant toxicities now associated with the drug class including CNS toxicities, fat wasting, and the ability to cause lactic acidosis and hepatic steatosis

A

stavudine

20
Q

when boosted, it is a first choice protease inhibitor for treatment naive patients due to its long half life and reduced side effects, but can cause sulfa drug hypersensitivity reactions?

A

darunavir

21
Q

newest/ best NNRTI with unique resistance mechanisms such that it works if resistance to efavirenz or rilpivirine and rilpivirine etravirine work if resistance to it; less significant drug-drug interaction and low incidence of typical side effects

A

doravirine

22
Q

HIV INSTI with 14 hr half life; widely recommended for initial ART because while resistance can develop due to integrase mutations, there is a high genetic barrier to this resistance

A

dolutegravir

23
Q

when boosted, a first-choice protease inhibitor for treatment naive HIV patients due to its long half life and reduced side effects

A

atazanavir

24
Q

early HIV target since mammalian cells lack this

A

reverse transcriptase

25
Q

the HIV drug class that is now the primary +1 addition to the NRTI backbone

A

INSTI

26
Q

common side effect of efavirenz, but typically subsides and rearely leads to discontinuations of the drug

A

CNS toxicity

27
Q

what hiv drugs cause renal insufficiency?

A

indinavir and tenofovir

28
Q

first HIV PI, it’s short half-life caused troublesome pill burden and it is among the agents well known for promoting irreversible lipodystrophy with long term use

A

saquinavir

29
Q

what is recommended every six months for HIV patients using TDF because of potential adverse effects?

A

urinalysis due to potential adverse effects on kidney

30
Q

what could happen when HIV drugs with activity against HBV are discontinued?

A

rebound of HBV

31
Q

chronic inflammation and/or reactivation of autoimmune disease as lymphocyte levels increase during ART

A

immune reconstrunction

32
Q

what is the NNRTI that is recommended for treatment naive patients, susceptible to mutations but not the one that quickly inactivate nevirapine and efacirenz- meaning they will will work

A

rilpivirine

33
Q

first generation INSTI, seems likely to be replaced

A

raltegravir

34
Q

what HIV drugs is HBV sensitive to?

A

tenofovir and emtricitabine and lamivudine

35
Q

what important drug is not sensitive to HBV?

A

abacavir

36
Q

why is resistance to PIs slow to develop and seldom a cause for treatment failure?

A

typically 4-5 mutations are required for HIV to develop resistance to PIs

37
Q

first generation NNRTI, has some typically self-limiting CNS side effects seldom requiring drug discontinuation

A

efavirenz

38
Q

ending of generic drug name that suggests the drug is an HIV PI?

A

-navir