| Term 
 
        | MOA inhibits synthesis of mycolic acid by inhibiting enzymes. Complex w/NADH which inhibits the oxygen dependent pathway |  | Definition 
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        | 1st line for M. tub and is a bacerialstatic |  | Definition 
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        | Hepatotoxic and neurotoxic |  | Definition 
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        | Requires acetylaters to work and is water soluble |  | Definition 
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        | Blocks RNA synthesis by binding to DNA dependent RNA polymerase |  | Definition 
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        | 1st line for M. tub and is bactericidal |  | Definition 
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        | Term 
 
        | Adverse rxns include Hepatitis in elderly and alcoholics, GI problems, and proteinuria |  | Definition 
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        | Turns body fluids and shat red/orange |  | Definition 
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        | Resistance by pt mutations on proB gene of beta subunit |  | Definition 
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        | Term 
 
        | Similar to Rifampin with longer half life |  | Definition 
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        | Term 
 
        | Given to patients who are intolerant or resistant to Rifampin. Good for MAI or atypical Myco |  | Definition 
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        | MOA blocks arabio-galactin component of myco cell wall |  | Definition 
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        | 1st line for M. tub in combination/ bacteriostatic |  | Definition 
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        | Sides include visual disturbance and retinal damage |  | Definition 
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        | Term 
 
        | Similar MAO as Isoniazid/ only used for M. tub in short term situations |  | Definition 
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        | Term 
 
        | An M. tub enzyme converts this drug to active form |  | Definition 
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        | Cannot be used along with a protease inhibitors for HIV |  | Definition 
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        | Term 
 
        | Inhibits bacterial folic acid synthesis |  | Definition 
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        | Term 
 | Definition 
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        | Sides include Hemolysis dude to G-6-DPH, GI, rash |  | Definition 
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        | MAO is directly binding to DNA |  | Definition 
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        | Term 
 
        | Alternative to M. leprosy and causes skin discoloration |  | Definition 
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        | MAO forming pores or channels by interacting with ergosterol allowing ion leakage |  | Definition 
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        | Nephrotoxicity, lipid formulations bind to mammalian membranes much less readily. Therefore, they reduce drug induced renal impairments |  | Definition 
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        | For systemic fungal infections, meningitis, blader |  | Definition 
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        | MAO 5-FU inhibits thymidylate synthase, human cells don't react |  | Definition 
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        | Reversible bone marrow suppression and bacteria flora toxicity are sides |  | Definition 
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        | Term 
 
        | Bacteria become resistant at low doses |  | Definition 
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        | A base analogue but does not treat cancer |  | Definition 
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        | Term 
 
        | Ergosterol inhibits 14-alpha-methylsterols, disrupting phospholipid packaging |  | Definition 
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        | Sides include steroid problems and Hepatotoxic |  | Definition 
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        | Term 
 
        | Used as a topical cream for orapharyngeal and cutaneous fungal infections |  | Definition 
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        | Term 
 
        | Topical and Parental route with Sides of burning, skin problems, and itching used for fungal infections |  | Definition 
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        | Broad Spectrum Fungal fighter, suppressive therapy of histoplasmosis in HIV. Well used in AIDS patients. Crosses BBB during inflammation. |  | Definition 
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        | Term 
 
        | Increase plasma of phenytoin, zidovudine, cyclosporine, and warfarin |  | Definition 
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        | Crosses BBB with out inflammation and resistant to 1st pass metabolism |  | Definition 
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        | Increases Terfonadine, and can inhibit the conservation of other drugs |  | Definition 
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        | Sides include loss of libido, gynecomastia, and hepatitis |  | Definition 
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        | Not recommended in pregnant and nursing |  | Definition 
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        | Losses absorption when introduced to increased pH in the stomach or H2 inhibitor |  | Definition 
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        | Same Mechanism as Amphotericin B and looks like it. Treats candida of GI, mucosa, topical, skin, and vagina |  | Definition 
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        | Term 
 
        | Systemic skin, hair, and nails infected with microsporum, ipidermophytes, trichophytons |  | Definition 
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        | Inhibit enzyme gulcan synthase, required for fungal cell wall component b 1-3 D glucagon |  | Definition 
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        | Used for candidas esophageal and abdominal. Prophylaxis for Candida infections of hematopoietic stem cell transplantation |  | Definition 
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        | Term 
 
        | Mucosal and invasive candida, aspergillosis, and pneumocystis carinii.  Acceptible safety profile |  | Definition 
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        | Inhibitis fungal squalene monoozygenase |  | Definition 
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        | Term 
 
        | Used for Tinea capitis, aspergillosis, onychomycosis (ring worms). 1% cream |  | Definition 
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        | The main part of Mycobacterium cell wall, making them acid fast |  | Definition 
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        | Term 
 
        | What two drugs make multi drug resistant TB |  | Definition 
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        | Term 
 
        | XDR TB is resistant to Isoniazid and rifampin and also |  | Definition 
 
        | Any fluoroquinolone and at least one of the following (amikacin, kanamycin, or capreomycin) |  | 
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        | Term 
 | Definition 
 
        | No drugs currently available to treat strains |  | 
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        | If someone is diagnosed with TB patients are watched while taking medicine |  | Definition 
 
        | Direct Observation Therapy |  | 
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        | Best drug therapy for M. tub |  | Definition 
 
        | 6 months of one drug is better then two years of 4 drugs |  | 
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        | 20% of people may develop anti-DNA antibodies(lupus-like) while taking this |  | Definition 
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        | When TB forms grunulomas, especially caseous granulomas they can form: |  | Definition 
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        | Term 
 
        | Always used parenterally, very toxic, is a 1st line M. tub drug in other countries |  | Definition 
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        | Term 
 
        | When you use this drug for something like HIV with low CD4 counts for pneumocystosis jirovecii instead of for m. leprae its called |  | Definition 
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        | Two drugs which are affective against Atypical Myco |  | Definition 
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        | Cannot be given parenterally due to renal toxicity which distinguishes it from another similar drug |  | Definition 
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        | Term 
 
        | Inhibits fungal micro spindle (mitosis at metaphase) |  | Definition 
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