Shivkumar Shete (36 results)
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Taschenbuch. Condition: Neu. Assessment of Adverse Drug Reactions in Respiratory Disease Patients | Screening the types of ADRs in Lung Disorders | Shivkumar Shete (u. a.) | Taschenbuch | 112 S. | Englisch | 2018 | LAP LAMBERT Academic Publishing | EAN 9786139831258 | Verantwortliche Person für die EU: BoD - Books on Demand, In…de Tarpen 42, 22848 Norderstedt, info[at]bod[dot]de | Anbieter: preigu.
Evaluación de las reacciones adversas a los medicamentos en pacientes con enfermedades respiratorias
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Language: English
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paperback. Condition: New. NEW. SHIPS FROM MULTIPLE LOCATIONS. book.
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Taschenbuch. Condition: Neu. Évaluation des effets indésirables des médicaments chez les patients atteints de maladies respiratoires | Dépistage des types d'EIM dans les maladies pulmonaires | Shivkumar Shete | Taschenbuch | Französisch | 2022 | Editions Notre Savoir | EAN 9786205428511 | Verantwortliche Person für die EU: preig…u GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu.
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Taschenbuch. Condition: Neu. Avaliação das Reacções Adversas dos Medicamentos em Doentes com Doenças Respiratórias | Rastreio dos tipos de ADRs em Perturbações Pulmonares | Shivkumar Shete | Taschenbuch | Portugiesisch | 2022 | Edições Nosso Conhecimento | EAN 9786205428535 | Verantwortliche Person für die EU: preigu GmbH & Co.…KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu.
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Taschenbuch. Condition: Neu. Valutazione delle reazioni avverse ai farmaci nei pazienti affetti da malattie respiratorie | Screening dei tipi di ADR nei disturbi polmonari | Shivkumar Shete | Taschenbuch | Italienisch | 2022 | Edizioni Sapienza | EAN 9786205428528 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lenger…icher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu.
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Taschenbuch. Condition: Neu. Bewertung von unerwünschten Arzneimittelwirkungen bei Patienten mit Atemwegserkrankungen | Screening der Arten von UAW bei Lungenkrankheiten | Shivkumar Shete | Taschenbuch | 84 S. | Deutsch | 2022 | Verlag Unser Wissen | EAN 9786205428481 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Le…ngericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu.
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Paperback. Condition: new. Paperback. Foundations in Clinical Pharmacy Practice is a concise textbook that combines theoretical knowledge with practical application in modern pharmacy practice. This book provides students, practitioners, and educators with essential knowledge and skills required for delivering patient-centered p…harmaceutical care across various healthcare settings. This textbook covers critical topics including evidence-based practice, medication therapy management, patient assessment techniques, management of diseases along with fundamental principles. This book serves as an indispensable resource for developing core competencies in clinical pharmacy practice with its systematic approach to clinical pharmacy practice, emphasis on patient safety, and focus on interprofessional collaboration. It equips pharmacy practitioners with core skills in patient assessment, medication therapy management, and evidence-based practice across ambulatory, acute, and specialty care. This item is printed on demand. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability.
Language: English
Published by LAP LAMBERT Academic Publishing Mai 2018, 2018
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Seller: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, GermanyBuchWeltWeit Ludwig Meier e.K.
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Taschenbuch. Condition: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -The WHO defines an 'Adverse drug reaction as any response to a drug which is noxious and unintended and which occurs or doses normally used in the man of prophylaxis diagnosis or therapy of disease or for the modification of physiol…ogic function'. Adverse drug reactions (ADRs) are types of adverse drug events (ADEs). ADEs include ADRs, medication errors and other drug-related problems. ADEs are the negative consequences' of drug misadventures. Henri Manasse defined drug misadventure as the iatrogenic hazard that is an inherent risk when drug therapy is indicated. The American Society of Health-System Pharmacists (ASHP) defines significant ADRs as an unexpected, unintended, undesired, or excessive response to a drug that includes 1.the Requires discontinuing the drug 2. Requires changing the drug therapy 3. Requires modifying the dose 4. Necessitates admission to the hospital 5. Prolongs stay in a health care facility 6. Necessitates supportive treatment 7. Significantly complicates diagnosis 8. Negatively affects prognosis or results in temporary or permanent harm, disability or death. 112 pp. Englisch.
Evaluación de las reacciones adversas a los medicamentos en pacientes con enfermedades respiratorias
Language: Spanish
Published by Ediciones Nuestro Conocimiento Dez 2022, 2022
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Seller: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, GermanyBuchWeltWeit Ludwig Meier e.K.
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Taschenbuch. Condition: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -La OMS define una 'reacción adversa a un medicamento como cualquier respuesta a un medicamento que sea nociva y no intencionada y que se produzca o dosis utilizadas normalmente en el hombre de profilaxis diagnóstico o terapia de la…enfermedad o para la modificación de la función fisiológica'. Las reacciones adversas a los medicamentos (RAM) son tipos de acontecimientos adversos a los medicamentos (ADE). Incluyen las reacciones adversas, los errores de medicación y otros problemas relacionados con los medicamentos. Los ADE son las 'consecuencias negativas' de los errores de medicación. Henri Manasse definió los contratiempos farmacológicos como el riesgo iatrogénico inherente a la indicación de un tratamiento farmacológico. La Sociedad Americana de Farmacéuticos del Sistema de Salud (ASHP) define las reacciones adversas significativas como una respuesta inesperada, no intencionada, no deseada o excesiva a un fármaco que incluye 1. Requiere interrumpir el fármaco 2. Requiere cambiar la terapia farmacológica Requiere cambiar el tratamiento farmacológico 3. Requiere modificar la dosis 4. Requiere ingreso hospitalario 5. Prolonga la estancia en un centro sanitario 6. Requiere tratamiento de apoyo 7. Complica significativamente el diagnóstico 8. Afecta negativamente al pronóstico o provoca daños temporales o permanentes, discapacidad o muerte. 80 pp. Spanisch.
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Condition: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Shete ShivkumarDr. Shivkumar, Pharm. D working as Assistant Professor at Sree Dattha Institute of Pharmacy, R.R Dist. He has 3 years of experience in teaching deals with Pharmacotherapeutics and has 5 I…nternational Journal Publicatio.
Language: English
Published by LAP LAMBERT Academic Publishing Mai 2018, 2018
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Seller: buchversandmimpf2000, Emtmannsberg, BAYE, Germanybuchversandmimpf2000
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Taschenbuch. Condition: Neu. This item is printed on demand - Print on Demand Titel. Neuware -The WHO defines an 'Adverse drug reaction as any response to a drug which is noxious and unintended and which occurs or doses normally used in the man of prophylaxis diagnosis or therapy of disease or for the modification of physiologic… function'. Adverse drug reactions (ADRs) are types of adverse drug events (ADEs). ADEs include ADRs, medication errors and other drug-related problems. ADEs are the negative consequences' of drug misadventures. Henri Manasse defined drug misadventure as the iatrogenic hazard that is an inherent risk when drug therapy is indicated. The American Society of Health-System Pharmacists (ASHP) defines significant ADRs as an unexpected, unintended, undesired, or excessive response to a drug that includes 1.the Requires discontinuing the drug 2. Requires changing the drug therapy 3. Requires modifying the dose 4. Necessitates admission to the hospital 5. Prolongs stay in a health care facility 6. Necessitates supportive treatment 7. Significantly complicates diagnosis 8. Negatively affects prognosis or results in temporary or permanent harm, disability or death.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 112 pp. Englisch.
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Seller: AHA-BUCH GmbH, Einbeck, GermanyAHA-BUCH GmbH
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Taschenbuch. Condition: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - The WHO defines an 'Adverse drug reaction as any response to a drug which is noxious and unintended and which occurs or doses normally used in the man of prophylaxis diagnosis or therapy of disease or for the modification of physiologic…function'. Adverse drug reactions (ADRs) are types of adverse drug events (ADEs). ADEs include ADRs, medication errors and other drug-related problems. ADEs are the negative consequences' of drug misadventures. Henri Manasse defined drug misadventure as the iatrogenic hazard that is an inherent risk when drug therapy is indicated. The American Society of Health-System Pharmacists (ASHP) defines significant ADRs as an unexpected, unintended, undesired, or excessive response to a drug that includes 1.the Requires discontinuing the drug 2. Requires changing the drug therapy 3. Requires modifying the dose 4. Necessitates admission to the hospital 5. Prolongs stay in a health care facility 6. Necessitates supportive treatment 7. Significantly complicates diagnosis 8. Negatively affects prognosis or results in temporary or permanent harm, disability or death.
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Seller: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, GermanyBuchWeltWeit Ludwig Meier e.K.
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Taschenbuch. Condition: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -L'OMS définit une 'réaction indésirable à un médicament comme toute réponse à un médicament qui est nocive et non intentionnelle et qui se produit ou des doses normalement utilisées dans l'homme de prophylaxie de diagnostic ou de th…érapie de la maladie ou pour la modification de la fonction physiologique'. Les effets indésirables des médicaments (EIM) sont des types d'événements indésirables des médicaments (EIM). Les EIM comprennent les EIM, les erreurs de médication et d'autres problèmes liés aux médicaments. Les EIM sont les 'conséquences négatives' des mésaventures médicamenteuses. Henri Manasse a défini la mésaventure médicamenteuse comme le danger iatrogène qui constitue un risque inhérent à l'indication d'un traitement médicamenteux. L'American Society of Health-System Pharmacists (ASHP) définit les EIM significatifs comme une réaction inattendue, non intentionnelle, non désirée ou excessive à un médicament qui comprend 1.la Nécessité d'interrompre le traitement médicamenteux 2. Nécessite de changer le traitement médicamenteux 3. Nécessite une modification de la dose 4. Nécessite une admission à l'hôpital 5. Prolonge le séjour dans un établissement de soins de santé 6. Nécessite un traitement de soutien 7. Complique considérablement le diagnostic 8. affecte négativement le pronostic ou entraîne un préjudice temporaire ou permanent, une invalidité ou un décès. 80 pp. Französisch.
Evaluación de las reacciones adversas a los medicamentos en pacientes con enfermedades respiratorias
Language: Spanish
Published by Ediciones Nuestro Conocimiento Dez 2022, 2022
- Softcover
- Print on Demand
Seller: buchversandmimpf2000, Emtmannsberg, BAYE, Germanybuchversandmimpf2000
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Taschenbuch. Condition: Neu. This item is printed on demand - Print on Demand Titel. Neuware -La OMS define una 'reacción adversa a un medicamento como cualquier respuesta a un medicamento que sea nociva y no intencionada y que se produzca o dosis utilizadas normalmente en el hombre de profilaxis diagnóstico o terapia de la enfe…rmedad o para la modificación de la función fisiológica'. Las reacciones adversas a los medicamentos (RAM) son tipos de acontecimientos adversos a los medicamentos (ADE). Incluyen las reacciones adversas, los errores de medicación y otros problemas relacionados con los medicamentos. Los ADE son las 'consecuencias negativas' de los errores de medicación. Henri Manasse definió los contratiempos farmacológicos como el riesgo iatrogénico inherente a la indicación de un tratamiento farmacológico. La Sociedad Americana de Farmacéuticos del Sistema de Salud (ASHP) define las reacciones adversas significativas como una respuesta inesperada, no intencionada, no deseada o excesiva a un fármaco que incluye 1. Requiere interrumpir el fármaco 2. Requiere cambiar la terapia farmacológica Requiere cambiar el tratamiento farmacológico 3. Requiere modificar la dosis 4. Requiere ingreso hospitalario 5. Prolonga la estancia en un centro sanitario 6. Requiere tratamiento de apoyo 7. Complica significativamente el diagnóstico 8. Afecta negativamente al pronóstico o provoca daños temporales o permanentes, discapacidad o muerte.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 80 pp. Spanisch.
Evaluación de las reacciones adversas a los medicamentos en pacientes con enfermedades respiratorias
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Seller: AHA-BUCH GmbH, Einbeck, GermanyAHA-BUCH GmbH
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Taschenbuch. Condition: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - La OMS define una 'reacción adversa a un medicamento como cualquier respuesta a un medicamento que sea nociva y no intencionada y que se produzca o dosis utilizadas normalmente en el hombre de profilaxis diagnóstico o terapia de la enfer…medad o para la modificación de la función fisiológica'. Las reacciones adversas a los medicamentos (RAM) son tipos de acontecimientos adversos a los medicamentos (ADE). Incluyen las reacciones adversas, los errores de medicación y otros problemas relacionados con los medicamentos. Los ADE son las 'consecuencias negativas' de los errores de medicación. Henri Manasse definió los contratiempos farmacológicos como el riesgo iatrogénico inherente a la indicación de un tratamiento farmacológico. La Sociedad Americana de Farmacéuticos del Sistema de Salud (ASHP) define las reacciones adversas significativas como una respuesta inesperada, no intencionada, no deseada o excesiva a un fármaco que incluye 1. Requiere interrumpir el fármaco 2. Requiere cambiar la terapia farmacológica Requiere cambiar el tratamiento farmacológico 3. Requiere modificar la dosis 4. Requiere ingreso hospitalario 5. Prolonga la estancia en un centro sanitario 6. Requiere tratamiento de apoyo 7. Complica significativamente el diagnóstico 8. Afecta negativamente al pronóstico o provoca daños temporales o permanentes, discapacidad o muerte.
Language: English
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Seller: Majestic Books, Hounslow, United KingdomMajestic Books
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Language: English
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Seller: Biblios, frankfurt am main, HESSE, GermanyBiblios
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Seller: buchversandmimpf2000, Emtmannsberg, BAYE, Germanybuchversandmimpf2000
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Taschenbuch. Condition: Neu. This item is printed on demand - Print on Demand Titel. Neuware -L'OMS définit une 'réaction indésirable à un médicament comme toute réponse à un médicament qui est nocive et non intentionnelle et qui se produit ou des doses normalement utilisées dans l'homme de prophylaxie de diagnostic ou de thérap…ie de la maladie ou pour la modification de la fonction physiologique'. Les effets indésirables des médicaments (EIM) sont des types d'événements indésirables des médicaments (EIM). Les EIM comprennent les EIM, les erreurs de médication et d'autres problèmes liés aux médicaments. Les EIM sont les 'conséquences négatives' des mésaventures médicamenteuses. Henri Manasse a défini la mésaventure médicamenteuse comme le danger iatrogène qui constitue un risque inhérent à l'indication d'un traitement médicamenteux. L'American Society of Health-System Pharmacists (ASHP) définit les EIM significatifs comme une réaction inattendue, non intentionnelle, non désirée ou excessive à un médicament qui comprend 1.la Nécessité d'interrompre le traitement médicamenteux 2. Nécessite de changer le traitement médicamenteux 3. Nécessite une modification de la dose 4. Nécessite une admission à l'hôpital 5. Prolonge le séjour dans un établissement de soins de santé 6. Nécessite un traitement de soutien 7. Complique considérablement le diagnostic 8. affecte négativement le pronostic ou entraîne un préjudice temporaire ou permanent, une invalidité ou un décès.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 80 pp. Französisch.
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Seller: AHA-BUCH GmbH, Einbeck, GermanyAHA-BUCH GmbH
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Taschenbuch. Condition: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - L'OMS définit une 'réaction indésirable à un médicament comme toute réponse à un médicament qui est nocive et non intentionnelle et qui se produit ou des doses normalement utilisées dans l'homme de prophylaxie de diagnostic ou de thérapi…e de la maladie ou pour la modification de la fonction physiologique'. Les effets indésirables des médicaments (EIM) sont des types d'événements indésirables des médicaments (EIM). Les EIM comprennent les EIM, les erreurs de médication et d'autres problèmes liés aux médicaments. Les EIM sont les 'conséquences négatives' des mésaventures médicamenteuses. Henri Manasse a défini la mésaventure médicamenteuse comme le danger iatrogène qui constitue un risque inhérent à l'indication d'un traitement médicamenteux. L'American Society of Health-System Pharmacists (ASHP) définit les EIM significatifs comme une réaction inattendue, non intentionnelle, non désirée ou excessive à un médicament qui comprend 1.la Nécessité d'interrompre le traitement médicamenteux 2. Nécessite de changer le traitement médicamenteux 3. Nécessite une modification de la dose 4. Nécessite une admission à l'hôpital 5. Prolonge le séjour dans un établissement de soins de santé 6. Nécessite un traitement de soutien 7. Complique considérablement le diagnostic 8. affecte négativement le pronostic ou entraîne un préjudice temporaire ou permanent, une invalidité ou un décès.
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Seller: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, GermanyBuchWeltWeit Ludwig Meier e.K.
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Taschenbuch. Condition: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -L'OMS definisce una 'reazione avversa ai farmaci come una qualsiasi risposta a un farmaco che sia nociva e non voluta e che si verifichi o a dosi normalmente utilizzate nell'uomo per la profilassi, la diagnosi o la terapia di una ma…lattia o per la modifica di una funzione fisiologica'. Le reazioni avverse ai farmaci (ADR) sono tipi di eventi avversi ai farmaci (ADE). Le ADE comprendono le ADR, gli errori terapeutici e altri problemi correlati ai farmaci. Le ADE sono le conseguenze negative delle disavventure farmacologiche. Henri Manasse ha definito l'evento avverso da farmaco come il rischio iatrogeno che è insito quando è indicata una terapia farmacologica. L'American Society of Health-System Pharmacists (ASHP) definisce le ADR significative come una risposta inattesa, non voluta, indesiderata o eccessiva a un farmaco che comprende 1. La necessità di sospendere il farmaco 2. La necessità di modificare la terapia farmacologica 3. La necessità di modificare la terapia. Richiede la modifica della terapia farmacologica 3. Richiede la modifica della dose 4. Necessita il ricovero in ospedale 5. Prolunga la permanenza in una struttura sanitaria 6. Richiede un trattamento di supporto. Necessità di un trattamento di supporto 7. Complica significativamente la diagnosi 8. Influisce negativamente sulla prognosi o provoca danni temporanei o permanenti, disabilità o morte. 76 pp. Italienisch.
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Taschenbuch. Condition: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Die WHO definiert eine 'unerwünschte Arzneimittelwirkung als jede Reaktion auf ein Arzneimittel, die schädlich und unbeabsichtigt ist und die bei der Prophylaxe, Diagnose oder Therapie von Krankheiten oder bei der Veränderung physio…logischer Funktionen auftritt'. Unerwünschte Arzneimittelwirkungen (UAW) sind Arten von unerwünschten Arzneimittelereignissen (UAE). Zu den UAW gehören unerwünschte Arzneimittelwirkungen, Medikationsfehler und andere arzneimittelbezogene Probleme. ADEs sind die negativen Folgen von Arzneimittelmissgeschicken. Henri Manasse definierte Arzneimittelmissgeschicke als iatrogene Gefahr, die ein inhärentes Risiko darstellt, wenn eine Arzneimitteltherapie angezeigt ist. Die American Society of Health-System Pharmacists (ASHP) definiert signifikante UAW als unerwartete, unbeabsichtigte, unerwünschte oder übermäßige Reaktion auf ein Arzneimittel, die 1. das Absetzen des Arzneimittels erforderlich macht 2. eine Änderung der Arzneimitteltherapie erforderlich macht 3. eine Änderung der Dosis erforderlich macht 4. eine Einweisung in ein Krankenhaus erforderlich macht 5. Verlängert den Aufenthalt in einer Einrichtung des Gesundheitswesens 6. Erfordert eine unterstützende Behandlung 7. Erschwert die Diagnose erheblich 8. Beeinträchtigt die Prognose oder führt zu vorübergehenden oder dauerhaften Schäden, Behinderungen oder zum Tod. 84 pp. Deutsch.
Language: Portuguese
Published by Edições Nosso Conhecimento Dez 2022, 2022
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Seller: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, GermanyBuchWeltWeit Ludwig Meier e.K.
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Taschenbuch. Condition: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -A OMS define uma 'reacção adversa ao medicamento como qualquer resposta a um medicamento nocivo e não intencional e que ocorre ou doses normalmente utilizadas no homem de diagnóstico de profilaxia ou terapia da doença ou para a modi…ficação da função fisiológica'. As reacções adversas aos medicamentos (RAMs) são tipos de eventos adversos aos medicamentos (EADs). Os EAMs incluem ADRs, erros de medicação e outros problemas relacionados com drogas. Os EAM são as 'consequências negativas' dos desventuramentos medicamentosos. Henri Manasse definiu os desventuramentos medicamentosos como o perigo iatrogénico que é um risco inerente quando a terapia medicamentosa é indicada. A Sociedade Americana de Farmacêuticos do Sistema de Saúde (ASHP) define ADRs significativas como uma resposta inesperada, não intencional, indesejada, ou excessiva a um fármaco que inclui 1.o Requer a descontinuidade do fármaco 2. Exige a alteração da terapia medicamentosa 3. Requer a modificação da dose 4. Necessita de internamento no hospital 5. Prolonga a permanência num estabelecimento de saúde 6. Necessita de tratamento de apoio 7. Complica significativamente o diagnóstico 8. Afecta negativamente o prognóstico ou resulta em danos temporários ou permanentes, incapacidade ou morte. 76 pp. Portugiesisch.
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Seller: moluna, Greven, Germanymoluna
Contact seller5-star sellerCondition: New
£ 34.93
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Condition: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Shete ShivkumarIl Dr. Shivkumar, Pharm. D lavora come professore assistente presso il Sree Dattha Institute of Pharmacy, R.R Dist. Ha 3 anni di esperienza nell insegnamento e si occupa di farmacoterapia… e ha 5 pubblicazioni su rivist.
- Softcover
- Print on Demand
Seller: moluna, Greven, Germanymoluna
Contact seller5-star sellerCondition: New
£ 43.71
£ 41.66 shippingShips from Germany to U.S.A.Quantity: Over 20 available
Condition: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Shete ShivkumarDr. Shivkumar, Pharm. D. arbeitet als Assistenzprofessor am Sree Dattha Institute of Pharmacy, R.R. Dist. Er hat 3 Jahre Erfahrung in der Lehre und beschaeftigt sich mit Pharmakotherapeut…ika und hat 5 internationale Fac.
