BC-CfE Pharmacovigilance 2018 Annual Report
BC-CfE Pharmacovigilance 2018 Annual Report Read More »
This article was originally published as a Pharmacovigilance Initiative Safety Alert by the British Columbia Centre for Excellence in HIV/Aids on June 6, 2017. Patient safety concern Drug interactions between antiretroviral drugs and other medications can result in loss of therapeutic efficacy or drug toxicity. Selected proton pump inhibitors and inhaled corticosteroids recently became available
Guest Post: Antiretroviral Drug Interactions with Non-Prescription Medications Read More »
June 2017 – Drug interactions between antiretroviral drugs and other medications can result in loss of therapeutic efficacy or drug toxicity. Selected proton pump inhibitors and inhaled corticosteroids recently became available as non-prescription products in BC. These, and other non-prescription medications, can have clinically important interactions with certain antiretroviral drugs. This bulletin summarizes clinically important
SAFETY UPDATE: Antiretroviral drug interactions with non-prescription medications Read More »
September 17, 2012 – The Pharmacovigilance Program at the BC Centre for Excellence in HIV/AIDS has received reports of patients seeing nevirapine 400 mg XR (extended release) tablets or tablet fragments in their feces (stools). In BC, approximately 4% of patients treated with nevirapine XR have reported seeing tablet remnants in their stool. Nevirapine 400
SAFETY UPDATE: Nevirapine 400 mg XR (Viramune XR™) tablet remnants in feces Read More »
June 6, 2011 – The Pharmacovigilance Program at the BC Centre for Excellence in HIV/AIDS has reviewed the following incident: On May 11, 2011, Janssen Inc. issued an advisory that some bottles of darunavir (Prezista TM) 600 mg tablets in Lot # ALZ0J00 might have an uncharacteristic “musty” or “mouldy” odour caused by trace quantities
SAFETY ALERT: DARUNAVIR (PREZISTA TM) Read More »
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
SAFETY ALERT: RITONAVIR AND INTRA-ARTICULAR TRIMCINOLONE ACETONIDE INJECTION Read More »
July, 2009 – The Pharmacovigilance Initiative at the BC Centre for Excellence in HIV/AIDS received a report of an HLA-B*5701 positive patient who had tolerated long term abacavir therapy, discontinued antiretroviral drugs for several months, then developed a diffuse rash, respiratory distress and fever shortly after re-initiating an abacavir-containing regimen. The symptoms and rapid onset were
SAFETY WARNING: ABACAVIR USE IN HLA-B*5701 POSITIVE PATIENTS AND UNTESTED PATIENTS Read More »