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Exam (elaborations)

NR 566 Midterm Exam Questions with Verified Answers (Correct Update)

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NR 566 Midterm Exam Questions with Verified Answers (Correct Update)

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NR 566 Midterm Exam Questions with Verified Answers (Correct
Update)
Question 1: Aspergillosissystemic mycosis

Answer: Causative agent: Aspergillus spp. Drug of choice: Voriconazole Alternative Drugs:
Amphotericin B, isavuconzonium, itraconazole, posaconazole, caspofungin, micafungin

Question 2: Blastomycosis -systemic mycosis

Answer: Causative agent: Blastomyces dermatitidis Drug of choice: Amphotericin B OR itraconazole
Alternative Drugs: none

Question 3: Candidiasissystemic mycosis

Answer: Causative agent: Candida spp Drug of choice: Amphotericin B OR fluconazole, either one +/-
flucytosine Alternative Drugs: itraconazole, voriconazole, caspofungin

Question 4: Coccidiodomycosissystemic mycosis

Answer: Causative agent: coccidioides immitis Drug of choice: Amphotericin B OR fluconazole
Alternative Drugs: itraconazole, ketoconazole

Question 5: Cryptococcosissystemic mycosis

Answer: Causative agent: cryptococcus neoformans Drug of choice: Amphotericin B +/- flucytosine
Alternative Drugs: itraconazole Chronic suppression: Drug of choice: Fluconazole Alternative Drugs:
Amphotericin B

Question 6: Histoplasmosissystemic mycosis

Answer: Causative agent: histoplasma capsulatum Drug of choice: Amphotericin B OR itraconazole
Alternative Drugs: Fluconazole, ketoconazole Chronic suppression: Drug of choice: itraconazole
Alternative Drugs: Amphotericin B

Question 7: Mucormycosissystemic mycosis

Answer: Causative agent: Mucor Drug of choice: Amphotericin B Alternative Drugs: Isavuconazonium

Question 8: Paracoccidioidomycosissystemic mycosis

Answer: Causative agent: paracoccidioides brasiliensis Drug of choice: amphotericin B OR itraconazole
Alternative Drugs: Ketoconazole




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,Question 9: Sporotrichosissystemic mycosis

Answer: Causative agent: sporothrix schenckii Drug of choice: Amphotericin B OR itraconazole
Alternative Drugs: Fluconazole

Question 10: Itraconazole Drug interactions

Answer: PPIs, H2 inhibitors, antacidsmay have insuflcient stomach acid content for absorption. Take 1
hour prior or 2 hours after itraconazole. CYP3A4 inhibitorcan increase levels of other drugs such as
cisapride, pimozide, dofetilide, quinidine (increases the risk of ventricular dysrhythmias), cyclosporine,
digoxin, warfarin, sulfonylureas

Question 11: Therapeutic uses of caspofungin

Answer: Systemic Fungal infections- IV therapy of invasive aspergillosis in patients unresponsive or
intolerant to amphotericin B or itraconazole Systemic candida infectionsincluding Candice is and candid
-related peritonitis

Question 12: Acyclovir MOA

Answer: inhibits viral replication by suppressing the synthesis of viral DNA. must undergo activation.
critical step to activation is the conversion of acyclovirr to acyclovir-guanosine monophosphate (GMP)
by thymidine kinase. when formed, acyclovir-GMP is directly responsible for inhibiting DNA synthesis.
Selectively is based on the ability of the virus to activate the drug.

Question 13: acyclovir indications

Answer: mucocutaneous herpes simplex infections; varicella zoster infections; herpes simplex genitalis

Question 14: acyclovir route of administration considerations

Answer: IV, PO, topical PO bioavailability is low (15-30%) normal renal function: half life is 2.5 hours
anuric half life up to 20 hours. baseline renal function and dose reduction for renal impairment

Question 15: oseltamivir MOA inhibits

Answer: neuraminidase, a viral enzyme required for replication. this causes newly formed viral particles
from budding ott the cytoplasmic membrane of the host cells. Stops the viral spread.

Question 16: oseltamivir administration

Answer: PO suspension or capsule Treatment: twice a day prophylaxis once a day treatment: should be
started within 48 hours of treatment




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, Question 17: oseltamivir indications

Answer: prevention and treatment of influenza for patients 1 years old and older. can reduce symptom
severity, duration, and prevent complications. can be used in elderly and pregnancy after exposure to
illness and for treatment

Question 18: palivizumab indications

Answer: monoclonal antibody for preventing RSV infections in premature infants and young children
with chronic lung disease. binds to the surface protein on RSV and prevents replication. Dosing should
start before RSV season and continue until season end. IM injection, monthly, dosed by weight

Question 19: purpose of the annual flue vaccine

Answer: best protection against influenza due to virus constantly mutating. vaccines are changed yearly
as well. trivalent or quadrivalent vaccines available. provides protection against the three-four strains of
influenza deemed the most likely to cause disease in the upcoming season. jointly created by the CDC,
FDA, WHO

Question 20: flu vaccine contraindications

Answer: acute febrile illness, take once symptoms resolve precautions: severe egg allergy
Guillain-Barré syndrome (GBS) within 6 weeks following vaccine administration. pregnant women
should not receive the LIVE flu vaccine, okay to receive the inactivated vaccine severe allergic reaction
to influenza vaccine in the past

Question 21: Nucleoside/nucleotide reverse transcriptase inhibitors (NRTIs) drugs

Answer: Abacavir (prototype) Didanosine Emtricitabine Lamivudine Stavudine Tenofovir Zidovudine

Question 22: Nucleoside/nucleotide reverse transcriptase inhibitors (NRTIs) MOA

Answer: inhibit HIV replication by suppressing synthesis of viral DNA. undergoes intracellular
conversion to active (phosphate) form. active form acts as a substrate for reverse transcriptase. After
becoming incorporated into the growing DNA, they prevent reverse transcriptase from adding more
bases. DNA strand growth is blocked. leads to premature strand termination. activated NRTIs compete
with natural nucleoside triphosphate for finding to the active site of reverse transcriptase

Question 23: Nucleoside/nucleotide reverse transcriptase inhibitors (NRTIs) adverse effects

Answer: side ettects are associated with the mitochondrial toxicity. lactic acidosis: dysfunctional
mitochondria cannot breakdown lactic acid. S/S: N, malaise, fatigue, anorexia, hyperventilation
(BLACK BOX WARNING) hepatic steatosis and hepatomegaly: decreased breakdown of fatty acids by
the mitochondria leads to fatty deposits in the liver pancreatitis, and myopathies




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