Efficacy and safety of the switch of Triumeq® to generic (abacavir + lamivudine) + Tivicay®: data at 48 weeks.
dc.contributor.author | Pérez-Stachowski, Javier | |
dc.contributor.author | Tortajada, Begoña | |
dc.contributor.author | Del Arco, Alfonso | |
dc.contributor.author | Márquez, Efrén | |
dc.contributor.author | De la Torre, Javier | |
dc.contributor.author | Nieto, Miriam | |
dc.contributor.author | García de Lomas, José María | |
dc.contributor.author | Prada, José Luis | |
dc.contributor.author | García-Alegría, Javier | |
dc.contributor.author | Olalla, Julián | |
dc.date.accessioned | 2025-01-07T14:50:19Z | |
dc.date.available | 2025-01-07T14:50:19Z | |
dc.date.issued | 2019-07-05 | |
dc.description.abstract | Introduction: Generic drugs are helpful to enhance the efficiency of the sanitary system. A generic coformulation of abacavir (ABC) and lamivudine (3TC) is available since 2016 in Spain. A report of our experience with its use is exposed. Methods: Patients between February 2017 and June 2017 who were taking Triumeq® were switched to the generic ABC + 3TC plus DTG. Efficacy, safety, reasons for discontinuation and costs savings were evaluated at 48 weeks. Results: Switch was made in 93 patients, with a median age of 47 years and a mean time of 12.33 years with HIV infection. Six patients (6.5%) discontinued the new ART, being toxicity of the central nervous system the most frequent reason. The effective saving derived from the change after 1 year of treatment was 151.127 €. Conclusions: The change from Triumeq® to a generic regimen of ABC + 3TC and another pill of DTG seems to be safe and efficient at 48 weeks. | |
dc.identifier.doi | 10.1080/23744235.2019.1637536 | |
dc.identifier.essn | 2374-4243 | |
dc.identifier.pmid | 31272264 | |
dc.identifier.unpaywallURL | https://europepmc.org/articles/pmc6180504?pdf=render | |
dc.identifier.uri | https://hdl.handle.net/10668/26684 | |
dc.issue.number | 9 | |
dc.journal.title | Infectious diseases (London, England) | |
dc.journal.titleabbreviation | Infect Dis (Lond) | |
dc.language.iso | en | |
dc.organization | SAS - Hospital Costa del Sol | |
dc.page.number | 691-693 | |
dc.pubmedtype | Journal Article | |
dc.rights | Attribution 4.0 International | |
dc.rights.accessRights | open access | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.subject | Dolutegravir | |
dc.subject | HIV | |
dc.subject | antiretroviral treatment | |
dc.subject | drugs | |
dc.subject | generic | |
dc.subject | switch | |
dc.subject.mesh | Anti-HIV Agents | |
dc.subject.mesh | Dideoxynucleosides | |
dc.subject.mesh | Drug Combinations | |
dc.subject.mesh | Drug Substitution | |
dc.subject.mesh | Drugs, Generic | |
dc.subject.mesh | Female | |
dc.subject.mesh | HIV Infections | |
dc.subject.mesh | Heterocyclic Compounds, 3-Ring | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Lamivudine | |
dc.subject.mesh | Male | |
dc.subject.mesh | Middle Aged | |
dc.subject.mesh | Retrospective Studies | |
dc.subject.mesh | Spain | |
dc.title | Efficacy and safety of the switch of Triumeq® to generic (abacavir + lamivudine) + Tivicay®: data at 48 weeks. | |
dc.type | research article | |
dc.type.hasVersion | VoR | |
dc.volume.number | 51 |