SAFETY ALERT: RITONAVIR AND INTRA-ARTICULAR TRIMCINOLONE ACETONIDE INJECTION

June, 2010 – The Pharmacovigilance Program at the BC Centre for Excellence in HIV/AIDS has received four reports of suspected drug interaction between ritonavir and triamcinolone acetonide intra-articular injection leading to symptoms of corticosteroid excess (Cushingoid features) and adrenal suppression. The affected patients were HIV-infected adults whose antiretroviral therapy included a protease inhibitor boosted with ritonavir 100-200 mg daily. All patients received one or more injections of triamcinolone acetonide 40-80 mg into shoulder or knee joints. Adrenal suppression (morning serum cortisol <28 nmol/L, reference range 175-685 nmol/L) was diagnosed four to 14 weeks after the first triamcinolone acetonide injection.

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The BC-CfE Laboratory is streamlining reporting processes for certain tests in order to simplify distribution and record-keeping, and to ensure completeness of results. Beginning September 2, 2025, results for the ‘Resistance Analysis of HIV-1 Protease and Reverse Transcriptase’ (Protease-RT) and ‘HIV-1 Integrase Resistance Genotype’ tests will be combined into a single ‘HIV-1 Resistance Genotype Report’.
For more details and example reports, please click on the button below