Cumulative Pharm CIS Flashcards
acute on chronic bronchitis antibiotics use?
Yes; signs that suggest that: - increased sputum - increased SOB - purulent sputum
most likely adverse drug reaction of levofloxacin?
GI, such as mild nausea
they are renally excreted; with renal dysfunction they can build up in the CNS
What drug can cause myelosuppression?
linezolid
what drugs inhibit the final transpeptidation step in cell wall synthesis?
beta lactams
what drugs prevent initiation of protein synthesis?
aminogllycosides
what drugs form pores in the bacterial cell membrane?
polymyxins
what prevents access of aminoacyl tRNA to acceptor A site?
doxycycline
CAP – Empiric Antimicrobial Guidelines (outpatient)
Previously healthy
Macrolide PO (azithromycin, clarithromycin)
-OR-
Doxycycline PO
DRSP risk (comorbidities, age > 65 years, use of antimicrobials within 3 months)
Respiratory fluoroquinolone PO (levofloxacin, moxifloxacin)
-OR-
B-lactam PO [high dose amoxicillin or amoxicillin-clavulanate preferred (alternates: ceftriaxone, cefuroxime)] PLUS a macrolide PO
Protein Synthesis InhibitorsMechanisms of Action
Aminoglycosides (30S)
- Interferes with initiation
- Causes misreading & aberrant proteins
Tetracyclines (30S)
- Blocks aminoacyl tRNA acceptor site
Macrolides (50S)
- Inhibits translocation
Clindamycin (50S)
- Inhibits translocation
Linezolid (50S)
- Blocks formation of initiation complex
Inpatient, Non-Intensive Care Unit Recommendations
CAP
Respiratory FQ IV or PO (levofloxacin, moxifloxacin)
-OR-
B-lactam IV (ceftriaxone, cefotaxime, or ampicillin) PLUS macrolide IV (azithromycin)
multidrug resistant TB means
resistant to at least rifampin and isoniazid
a pt is having hepatotoxicity. Which standard TB drugs to we eliminate, and what do we replace with?
All but ethambutal need to be dropped
(PZA, rifampin, INH)
add a fluoroquinolone and an injectable agent like streptomycin
then we add the other drugs in one at a time every 2 weeks or so, PZA last, and extend drug therapy to 18-24 months
This drug class is preferred for HIV-infected treatment-naïve patients in combination with tenofovir/emtricitabine:
Integrase Strand Transfer Inhibitors (INSTIs)
P450 Induction by Rifamycins
Rifampin is a strong P450 inducer (1A2, 2C9, 2C19, 2D6, 3A4)
- Use with caution in patients with HIV who are taking protease inhibitors (PIs) and non-nucleoside reverse-transcriptase inhibitors (NNRTIs)
- Half-lives, and thus efficacy, of agents metabolized by CYP450s (e.g., PIs, NNRTIs) are reduced
- Other agents metabolized by P450s: isoniazid, digoxin, propranolol, warfarin, oral contraceptives, etc.
Rifampin is the most potent P450 inducer
Rifabutin is the least potent