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The Clinical Guide to Supportive and Palliative Care for HIV/AIDS

The Clinical Guide to Supportive and Palliative Care for HIV/AIDS

The Clinical Guide to Supportive and Palliative Care for HIV/AIDS

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A <strong>Clinical</strong> <strong>Guide</strong> <strong>to</strong> <strong>Supportive</strong> <strong>and</strong> <strong>Palliative</strong> <strong>Care</strong> <strong>for</strong> <strong>HIV</strong>/<strong>AIDS</strong> • Chapter 27: Pharmacologic Interactions of <strong>Clinical</strong> SignificanceTable 27-7: <strong>HIV</strong>-related Drugs with Overlapping Toxicities* (continued)Drugs that cause hepa<strong>to</strong><strong>to</strong>xicitycontinued26 picasDrugs that cause rashwith or without pruritisDrugs that cause diarrheaDrugs that cause ocular <strong>to</strong>xicityDrugs <strong>to</strong> avoid in patientswith peripheral neuropathyKe<strong>to</strong>conazoleNevirapineNNRTIsPIsRifabutinRifampinAmprenavirAbacavirCotrimoxazoleDapsoneNNRTIsClindamycinDidanosineLopinavir/ri<strong>to</strong>navirNelfinavirRi<strong>to</strong>navirSaquinvirCidofovirEthambu<strong>to</strong>lIsoniazid (optic neuritis <strong>and</strong> optic atrophy)Lamivudine (uveitis in children)RifabutinSingle-ingredient DrugsDidanosineNitrofuran<strong>to</strong>in (oral)Nitrofuran<strong>to</strong>in macrocrystal (oral)Nitrofuran<strong>to</strong>in sodium injectionStavudineZalcitabineMultiple-ingredient DrugsDidanosine/calcium carbonate/magnesium salt (oral)Didanosine/magnesium salt/sodium citrate (oral)Nitrofuran<strong>to</strong>in/hexylresorcinols/cetrimonium (oral)Nitrofuran<strong>to</strong>in/nitrofuran<strong>to</strong>in macrocrystal (oral)Nitrofuran<strong>to</strong>in/pyridoxine HCL (oral)Nitrofuran<strong>to</strong>in/tetracaine (oral)Sulfadiazine/nitrofuran<strong>to</strong>in (oral)Sulfadiazine/nitrofuran<strong>to</strong>in/phenazopyridine (oral)Sulfamethizole/nitrofuran<strong>to</strong>in (oral)* Concomitant administration of agents not recommended; if unavoidable, close clinical moni<strong>to</strong>ring suggested.** Cotrimoxazole causes a 40% increase in the plasma concentrations of lamivudine <strong>and</strong> so may increase lamivudine <strong>to</strong>xicity such asheadaches, myalgia <strong>and</strong> neutropenia. Moni<strong>to</strong>r closely upon concomitant use.XXVIIU.S. Department of Health <strong>and</strong> Human Services • Health Resources <strong>and</strong> Services Administration • <strong>HIV</strong>/<strong>AIDS</strong> Bureau 563

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