Nearly half (49 percent) of all adolescents aged between 13 and 17 were up-to-date with their human papillomavirus (HPV) vaccines in 2017, according to new data from the Centers for Disease Control and Prevention (CDC). The organization’s latest Morbidity and Mortality Weekly Report (MMWR)...
Read More... Sep 11, 2018Human Immunodeficiency Virus (HIV) Infection
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A new treatment option is available for patients with multi-drug resistant (MDR) HIV following the US Food and Drug Administration’s (FDA) approval of Trogarzo (ibalizumab-uiyk). The medication, developed by TaiMed Biologics USA Corp, is a new form of antiretroviral medication indicated for...
Read More... Mar 09, 2018Last year was a record-breaking year for generic drug approvals in the United States. The US Food and Drug Administration (FDA) approved 1,027 generic drugs, 843 of which were full approvals, with tentative approvals making up the remainder. Tentative approvals are generic drugs considered ready...
Read More... Mar 02, 2018Over the course of 2017, the number of approvals granted by the US Food and Drug Administration (FDA) reached a 21-year high. More than 1,000 generic drugs were approved by the agency, according to FDA Commissioner Scott Gottlieb, MD, while first-time generic drug approvals numbered 74. Novel drug...
Read More... Jan 08, 2018Juluca (dolutegravir and rilpivirine), the first two-drug regimen for certain patients with HIV is now available in pharmacies across the United States. In November 2017, Viiv Healthcare, owned by pharmaceutical giant GlaxoSmithKline, gained US Food and Drug Administration (FDA) approval for...
Read More... Jan 04, 2018The US Food and Drug Administration (FDA) has approved the first once-daily, two-drug single pill treatment for certain patients with human immunodeficiency virus type 1 (HIV-1). Approval for Juluca (dolutegravir and rilpivirine) was granted to ViiV Healthcare, a global specialist in HIV owned by...
Read More... Nov 24, 2017A combination therapy used to reduce the chances of HIV infection in adult patients is safe for adolescents, a new study by the National Institutes of Health network suggests. Truvada (tenofovir, emtricitabine) is a single pill combination drug currently approved as a pre-exposure prophylaxis...
Read More... Sep 20, 2017The US Food & Drug Administration (FDA) has approved the first generic version of Truvada (emitricitabine/tenofovir disoproxil fumarate), a medication used in the treatment and prevention of HIV infection. Gilead Science's branded drug Truvada is a combination of the antiretroviral drugs...
Read More... Jun 15, 2017Login or Register to Share!
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