2005
DOI: 10.1097/01.aids.0000189861.44311.ed
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Severe rhabdomyolysis during a hypersensitivity reaction to abacavir in a patient treated with ciprofibrate

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Cited by 20 publications
(8 citation statements)
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“…The mean peak CK reported for each of a variety of different causes and for patients with both single and multiple causes ranged from ∼10,000 to 25,000 in the largest series. [2,3]…”
Section: Discussionmentioning
confidence: 99%
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“…The mean peak CK reported for each of a variety of different causes and for patients with both single and multiple causes ranged from ∼10,000 to 25,000 in the largest series. [2,3]…”
Section: Discussionmentioning
confidence: 99%
“…Rhabdomyolysis is common in the HIV positive population, particularly in those with advanced disease. [3,5] Risk factors unique to this population includes HIV infection itself, opportunistic infections, co-infection with HCV, medication-related adverse effects (including pentamidine, trimethoprim-sulfamethoxazole, sulfadiazine, and antiretroviral agents, such as zidovudine, raltegravir and abacavir), drug–drug interactions, malignancy, alcohol and/or illicit drug abuse. [3,6,7] While infection is the most frequently encountered etiology of rhabdomyolysis among the HIV positive population, with sepsis being identified as major cause, Koubar et al demonstrated that 6% of cases of rhabdomyolysis in patients with HIV infection could be attributed to medications.…”
Section: Discussionmentioning
confidence: 99%
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“…HAART regimens can also interact through the cytochrome P450 system to increase the levels of other myotoxic medications including the commonly prescribed statins. There have been multiple reports of rhabdomyolysis in HIV-infected patients taking both HAART and statin therapy [68][69][70][71][72][73][74][75].…”
Section: Rhabdomyolysismentioning
confidence: 99%
“…[3] Recently, the ELISA titers of antibodies to BP180 NC16a were reported to fluctuate in parallel with the disease activity in HG patients. [5] The immunoblotting clearly showed positive reactivity at the 5 th , 12 th and 50 th day after delivery, which disappeared completely at the 120 th day after delivery. To further verify the ELISA results, we also performed immunoblotting of BP180 NC16a recombinant protein, which was a prototype method before the development of BP180 ELISA.…”
mentioning
confidence: 93%