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1.
Chest ; 158(6): 2414-2424, 2020 12.
Artículo en Inglés | MEDLINE | ID: mdl-32805237

RESUMEN

Critical drug shortages have been widely documented during the coronavirus disease 2019 (COVID-19) pandemic, particularly for IV sedatives used to facilitate mechanical ventilation. Surges in volume of patients requiring mechanical ventilation coupled with prolonged ventilator days and the high sedative dosing requirements observed quickly led to the depletion of "just-in-time" inventories typically maintained by institutions. This manuscript describes drug shortages in the context of global, manufacturing, regional and institutional perspectives in times of a worldwide crisis such as a pandemic. We describe etiologic factors that lead to drug shortages including issues related to supply (eg, manufacturing difficulties, supply chain breakdowns) and variables that influence demand (eg, volatile prescribing practices, anecdotal or low-level data, hoarding). In addition, we describe methods to mitigate drug shortages as well as conservation strategies for sedatives, analgesics and neuromuscular blockers that could readily be applied at the bedside. The COVID-19 pandemic has accentuated the need for a coordinated, multi-pronged approach to optimize medication availability as individual or unilateral efforts are unlikely to be successful.


Asunto(s)
COVID-19/terapia , Industria Farmacéutica , Internacionalidad , Preparaciones Farmacéuticas/provisión & distribución , Antivirales/provisión & distribución , COVID-19/epidemiología , Cuidados Críticos , Desastres , Combinación de Medicamentos , Reposicionamiento de Medicamentos , Humanos , Hidroxicloroquina/provisión & distribución , Hipnóticos y Sedantes/provisión & distribución , Inventarios de Hospitales , Tiempo de Internación , Lopinavir/provisión & distribución , Respiración Artificial , Ritonavir/provisión & distribución , Reserva Estratégica , Capacidad de Reacción , Estados Unidos , United States Food and Drug Administration
2.
Cad Saude Publica ; 32(11): e00113815, 2016 Dec 01.
Artículo en Portugués, Inglés | MEDLINE | ID: mdl-27925025

RESUMEN

Since 1996, when antiretroviral (ARV) treatments started being guaranteed to people living with HIV in Brazil, the government has faced the challenge of ensuring sustainability of this policy within a context of incorporating patented medicines. This article sought to analyze the historical series of the price of lopinavir/ritonavir (LPV/r) in Brazil and in the international market also considering the initiatives to challenge patent barriers between 2001 and 2012. The methods used were mapping initiatives to challenge LPV/r patent barriers and the analysis of historical series of its price in Brazil and in the international market. Results show that, between 2001 and 2003, there were efforts to use compulsory licensing as a threat. From 2005 to 2007, initiatives by different satkeholders were identified: declaration of public interest, pre-grant opposition ("support to examination") and civil action. From 2006 to 2008, compulsory licensing initiatives in other countries resulted in a price reduction in Brazil. Between 2009 and 2012, there was a 30% reduction in the Brazilian purchasing price.


Asunto(s)
Fármacos Anti-VIH/economía , Costos de los Medicamentos/estadística & datos numéricos , Lopinavir/economía , Patentes como Asunto/legislación & jurisprudencia , Ritonavir/economía , Fármacos Anti-VIH/provisión & distribución , Brasil , Costos de los Medicamentos/legislación & jurisprudencia , Programas de Gobierno , Infecciones por VIH/tratamiento farmacológico , Humanos , Estudios Longitudinales , Lopinavir/provisión & distribución , Ritonavir/provisión & distribución
5.
Cad. Saúde Pública (Online) ; 32(11): e00113815, 2016. graf
Artículo en Portugués | LILACS | ID: biblio-828386

RESUMEN

Resumo: Desde 1996, com a consolidação da oferta do tratamento antirretroviral (ARV) às pessoas vivendo com HIV no Brasil, o governo tem como desafio assegurar a sustentabilidade desta oferta num contexto de incorporação de medicamentos patenteados. O artigo teve como objetivo analisar a série histórica do preço do lopinavir/ritonavir (LPV/r) no Brasil e no mercado internacional à luz de iniciativas de enfrentamento da barreira patentária no período de 2001 a 2012. A metodologia consistiu em mapeamento de iniciativas de enfrentamento da barreira patentária para o LPV/r e análise da série histórica do preço no Brasil e no mercado internacional. Os resultados encontrados apontam que, entre 2001 e 2003, identificaram-se esforços de ameaça de licença compulsória. De 2005 a 2007, identificaram-se iniciativas por diferentes atores: declaração de interesse público, subsídios ao exame e ação civil pública. De 2006 e 2008, iniciativas internacionais de licença compulsória resultaram na redução do preço no Brasil. Entre 2009 e 2012, observa-se uma redução do preço de aquisição pelo Brasil de 30%.


Resumen: Desde 1996, con la consolidación de la oferta de tratamiento antirretroviral (ARV) para las personas viviendo con VIH, el Gobierno de Brasil tiene el desafío de asegurar la sostenibilidad de dicha oferta en un contexto de incorporación de medicamentos patentados. El objetivo de este artículo es analizar la serie histórica del precio del lopinavir/ritonavir (LPV/r) en Brasil y en el mercado internacional, a la luz de iniciativas para enfrentar la barrera patentaria durante el período de 2001 a 2012. La metodología consistió en un mapeo de iniciativas para hacer frente a la barrera patentaria del LPV/r y el análisis de la serie histórica de sus precios de adquisición por el SUS y en el mercado internacional. Entre 2001 y 2003 se identificaron esfuerzos por obtener reducciones de precio de LPV/r, mediante la amenaza de expedición de licencia obligatoria. De 2005 a 2007, se identificaron varias iniciativas de diferentes actores, tales como, la expedición de declaración de interés público, preseentación de subsidios para el examen de solicitudes de patente de este medicamento y la interpesición de acción civil pública. Entre 2006 y 2008, la expedición de licencias obligatorias en el marco de iniciativas internacionales, propiciaron reducciones de precio de LPV/r en Brasil. La reducción promedio del precio de adquisición por parte SUS fue de 30% entre 2009 y 2012.


Abstract: Since 1996, when antiretroviral (ARV) treatments started being guaranteed to people living with HIV in Brazil, the government has faced the challenge of ensuring sustainability of this policy within a context of incorporating patented medicines. This article sought to analyze the historical series of the price of lopinavir/ritonavir (LPV/r) in Brazil and in the international market also considering the initiatives to challenge patent barriers between 2001 and 2012. The methods used were mapping initiatives to challenge LPV/r patent barriers and the analysis of historical series of its price in Brazil and in the international market. Results show that, between 2001 and 2003, there were efforts to use compulsory licensing as a threat. From 2005 to 2007, initiatives by different satkeholders were identified: declaration of public interest, pre-grant opposition ("support to examination") and civil action. From 2006 to 2008, compulsory licensing initiatives in other countries resulted in a price reduction in Brazil. Between 2009 and 2012, there was a 30% reduction in the Brazilian purchasing price.


Asunto(s)
Humanos , Patentes como Asunto/legislación & jurisprudencia , Costos de los Medicamentos/estadística & datos numéricos , Ritonavir/economía , Fármacos Anti-VIH/economía , Lopinavir/economía , Brasil , Infecciones por VIH/tratamiento farmacológico , Estudios Longitudinales , Costos de los Medicamentos/legislación & jurisprudencia , Ritonavir/provisión & distribución , Fármacos Anti-VIH/provisión & distribución , Lopinavir/provisión & distribución , Programas de Gobierno
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