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Vocabulary flashcards for antimicrobial drugs, their mechanisms, and uses.
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Penicillin
Inhibits cell wall synthesis, natural, -cidal, narrow spectrum, effective mainly against Gram-positive bacteria.
Cephalosporin
Inhibits cell wall synthesis, semisynthetic, -cidal, broad spectrum, four generations with varying spectrums.
Carbapenem
Inhibits cell wall synthesis, semisynthetic, -cidal, broad spectrum, used for resistant Gram-negative infections.
Vancomycin
Inhibits cell wall synthesis, natural, -cidal, narrow spectrum, used against MRSA, not absorbed orally.
Aminoglycosides
Inhibits protein synthesis (30S), natural/semisynthetic, -cidal, broad spectrum, nephrotoxic and ototoxic, used for serious infections.
Tetracycline
Inhibits protein synthesis (30S), natural, -static, broad spectrum, causes teeth discoloration in children.
Macrolides
Inhibits protein synthesis (50S), natural, -static, broad spectrum, alternative to penicillin for allergic patients.
Lincosamides
Inhibits protein synthesis (50S), semisynthetic, -static, narrow spectrum, Clindamycin is most common; risk of C. diff.
Chloramphenicol
Inhibits protein synthesis (50S), natural, -static, broad spectrum, rarely used due to toxicity.
Oxazolidinones
Inhibits protein synthesis (50S), synthetic, -static, narrow spectrum, used for resistant Gram-positive infections like MRSA.
Sulfonamides
Inhibits folic acid synthesis, synthetic, -static, broad spectrum, often combined with trimethoprim.
Trimethoprim
Inhibits folic acid synthesis, synthetic, -static, broad spectrum, combined with sulfonamides (Bactrim).
Fluoroquinolones
Inhibits DNA gyrase, synthetic, -cidal, broad spectrum, good for UTIs and respiratory infections.
Rifamycin
Inhibits RNA synthesis, natural, -cidal, broad spectrum, used for tuberculosis treatment.
Tamiflu
Antiviral, used for Influenza, Neuraminidase inhibitor, effective if taken within 48 hours of symptoms.
Xofluza
Antiviral, used for Influenza, Inhibits cap-dependent endonuclease, single dose treatment; newer than Tamiflu
Acyclovir
Antiviral, used for Herpes simplex virus (HSV), inhibits viral DNA polymerase, commonly used for HSV-1, HSV-2, and VZV.
Vidarabine
Antiviral, used for Herpes simplex virus (HSV), inhibits viral DNA synthesis, less used today; more toxic than acyclovir.
HAART
Antiviral, used for HIV/AIDS, combination therapy targeting reverse transcriptase, protease, integrase, highly active regimen slows progression of HIV.
PrEP
Antiviral, used for HIV prevention, blocks HIV entry via reverse transcriptase inhibitors, taken daily; used for high-risk individuals.
Ribavirin
Antiviral, used for Hepatitis C, RSV, inhibits viral RNA synthesis, used in combination therapy for Hepatitis C.
Epclusa
Antiviral, used for Hepatitis C, inhibits NS5A and NS5B viral proteins, direct-acting antiviral; well-tolerated.
Nystatin
Antifungal, used for candidiasis, binds to ergosterol and disrupts fungal membranes, topical use only; not absorbed systemically.
Amphotericin B
Antifungal, used for systemic fungal infections, binds to ergosterol forming membrane pores, can be nephrotoxic; used in severe infections.
5-flucytosine
Antifungal, used for cryptococcal meningitis, inhibits DNA and RNA synthesis in fungi, often combined with amphotericin B.
Echinocandins
Antifungal, used for aspergillosis, candidiasis, inhibits synthesis of β-glucan in cell wall, used for resistant fungal infections.
Chloroquine
Antiprotozoal, used for malaria, prevents heme detoxification in parasite, widespread resistance limits use.
Dapsone
Antiprotozoal, used for leprosy, inhibits folic acid synthesis in protozoa, also used as anti-inflammatory in some cases.