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Hasil Pencarian

Ditemukan 12 dokumen yang sesuai dengan query
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Elesenda May Gita
Abstrak :
Apoteker dalam penyelenggaraan pelayanan kefarmasian di apotek wajib mengikuti standar pelayanan kefarmasian yang tertera dalam Peraturan Menteri Kesehatan Nomor 73 Tahun 2016, yaitu salah satunya standar pengelolaan sediaan farmasi, alat kesehatan, dan bahan medis habis pakai (BMHP). Hal tersebut dilakukan agar menjamin ketersediaan sediaan farmasi, alat kesehatan, dan BMHP yang aman, bermutu, bermanfaat, dan terjangkau sehingga masyarakat terlindungi dari bahaya yang disebabkan oleh penggunaan sediaan farmasi, alat kesehatan, dan BMHP yang tidak memenuhi persyaratan mutu, keamanan, dan/atau kemanfaatan. Oleh karena itu, calon Apoteker harus memahami dan memiliki keterampilan pengelolaan perbekalan farmasi di apotek melalui analisis pengelolaan tersebut dalam pelaksanaan Praktik Kerja Profesi Apoteker (PKPA) di Apotek Roxy Galaxy. Pelaksanaan analisis dilakukan dengan metode bimbingan dalam beberapa tahap, yaitu orientasi, observasi, diskusi, simulasi, kerja mandiri, dan hasil pengamatan dibandingkan dengan Peraturan Menteri Kesehatan Nomor 73 Tahun 2016. Hasil yang diperoleh adalah pengelolaan sediaan farmasi, alat kesehatan, dan BMHP di Apotek Roxy Galaxy mencakup perencanaan, pengadaan, penerimaan, penyimpanan, pemusnahan, pengendalian, dan pencatatan dan pelaporan. Kegiatan pengelolaan tersebut menggunakan sistem informasi apotek yang terintegrasi secara terpusat dan telah banyak mengikuti ketentuan dalam peraturan perundang-undangan. ......Pharmacist in providing pharmaceutical care at pharmacy is required to comply with standard of pharmaceutical care that stated in the Minister of Health Regulation Number 73 year of 2016, one of which is standard of management for pharmaceutical preparations, medical devices, and consumable medical materials. Management activity is done for ensure the pharmaceutical supplies are safe, had a standard, useful, and affordable that leads the public to be protected from the hazard due to the pharmaceutical preparations, medical devices, and consumable medical materials which non compliance of the standard regulation. Therefore, the undergraduate pharmacist should have understand and have skills to manage pharmaceutical supplies at the pharmacy in the way of analyzing the management activity at pharmacy by Internship of Pharmacist Study Program at Apotek Roxy Galaxy. The analysis was carried out with the mentoring method by preceptor at Apotek Roxy Galaxy in several stages, namely orientation, observation, discussion, simulation, independent work. After that, result is compared to the Minister of Health Regulation Number 73 year of 2016. The results obtained is the management activities of pharmaceutical preparations, medical devices, and consumable medical materials at Apotek Roxy Galaxy are planning, procuring, receiving, storing, destroying, controlling, and recording and reporting. These management activities use a pharmacy information system that is centrally integrated and has followed the provisions of the laws and regulations
Depok: Fakultas Farmasi Universitas Indonesia, 2020
PR-Pdf
UI - Tugas Akhir  Universitas Indonesia Library
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Bauer, Larry A.
New York : McGraw Hil Medical, 2014
615.7 BAU a
Buku Teks  Universitas Indonesia Library
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Rafika Agusriana
Abstrak :
Penerapan kebijakan JKN untuk menjamin akses masyarakat terhadap obat dengan pengendalian biaya yang ketat berpotensi terhadap terjadinya kompromi kualitas dan keamanan obat.  Pembatasan harga obat dan adanya asimetris informasi terkait kualitas dan harga obat dapat mendorong moral hazard produsen memproduksi obat substandar dan palsu untuk mempertahankan keuntungan. Hasil analisis terhadap data sampling dan pengujian obat pada level kabupaten/kota menggunakan regresi logistik menunjukkan bahwa peluang suatu obat JKN tergolong tidak memenuhi syarat lebih rendah daripada peluang suatu obat non-JKN. Seiring dengan kenaikan harga satuan obat, peluang suatu obat tergolong tidak memenuhi syarat meningkat, hingga pada tingkat harga satuan tertentu yang tidak memungkinkan lagi obat substandar dan palsu dijual dengan harga kompetitif, peluang tersebut mulai menurun. Penelitian ini merekomendasikan implementasi penuh sistem JKN sebagai upaya mengatasi asimetris informasi harga dan kualitas obat, dengan memberlakukan diferensiasi harga sebagai suatu insentif bagi industri farmasi mempertahankan mutu dan ikut berkompetisi dalam penyediaan obat JKN. ......The implementation of National Health Insurance (NHIS; or Jaminan Kesehatan Nasional/JKN)s policy, increasing patient access to medicine while keeping its budget under tight control, has the potentiality to result in compromising the safety and efficacy of the medicine. Budget constraint and the existing asymmetry information in terms of quality and price of medicines could lead to a moral hazard situation where pharmaceutical companies may produce substandard and falsified medicines to secure their profit. The result of this research using logistic regression analysis of pharmaceutical sampling and testing on municipal/district level showed that despite previous assumptions, medicines included in JKN list are actually having lower probability of falsified or substandard compared to their counterparts, non-JKN medicines. In terms of the relation between price and quality of the medicines, the probability of falsified or substandard medicines increases up to a price level where for the poor qualified medicines does not have the ability to copy the original medicines while still making profit out of it. As a result, this research recommends full implementation of JKN to include all essential medicines into its list to avoid asymmetry information and maintain medicines quality. JKN also needs to have a price-differentiation policy which allows pharmaceutical companies to maintain quality of their medicines, even to innovate for a better one, while still maintaining a good profit and their ability to compete in the JKN era.
Depok: Fakultas Ekonomi dan Bisnis Universitas Indonesia, 2019
T52569
UI - Tesis Membership  Universitas Indonesia Library
cover
Gauwitz, Donna F
Boston: McGraw-Hill, Higher Education, 2005
615.6 GAU a
Buku Teks  Universitas Indonesia Library
cover
Seltzer, Meta Brown
Abstrak :
Covering the ratio and proportion method of drug calculations, "Drug Calculations: Ratio and Proportion Problems for Clinical Practice, 9th Edition" provides clear, step-by-step explanations and concise examples to ensure safety and accuracy. Unique to this book, a "proof" step in the answer key lets you double-check your calculation results to avoid medication errors. Safety is also addressed through the inclusion of Quality & Safety Education for Nurses (QSEN) information and with features such as Clinical Alerts and High Alert drug icons calling attention to situations in actual practice that have resulted in drug errors. Written by Meta Brown Seltzer and Joyce Mulholland, this text includes extensive hands-on practice with calculation problems, critical thinking exercises, worksheets, and assessment tests. And to boost your proficiency, a companion Evolve website adds more than 600 additional practice problems.
St Louis, Missouri: Elsevier , 2012
615.1 SEL d
Buku Teks  Universitas Indonesia Library
cover
Gatford, J.D.
London: Churchill Livingstone, 2011
615 GAT n
Buku Teks  Universitas Indonesia Library
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Dhyna Putri Aisyah
Abstrak :
ABSTRAK
Ringkasan penelitian ini membahas tentang kelalaian bidan dan asisten apoteker yang menyebabkan kematian berdasarkan analisis putusan No. 963 K/PID.SUS/2013 Tipe penelitian ini adalah deskriptif, karena penelitian ini menjelaskan permasalahan didasarkan pada teori atau ditinjau kaitannya antara teori dan praktek. Metode penelitian yang digunakan adalah yuridis normatif, yaitu dengan mengacu pada norma hukum yang terdapat pada peraturan Perundang-Undangan dan putusan pengadilan serta norma-norma yang berlaku dan mengikat masyarakat. Penelitian ini menjabarkan tanggung jawab dan kewenangan bidan dan asisten apoteker dalam menjalankan praktek dan dalam pemberian obat serta menganalisis putusan No. 963 K/PID.SUS/2013 Tanggung jawab dan kewenangan bidan dan asisten apoteker baik dalam menjalankan praktek dan dalam pemberian obat telah diatur dengan sangat baik dan merupakan bentuk jaminan keselamatan bagi pasien serta merupakan jaminan keamanan bagi tenaga kesehatan. Baiknya regulasi tersebut juga merupakan bentuk preventif terhadap timbulnya malpraktek atau kelalaian tenaga kesehatan dalam menjalankan tanggung jawab profesinya. Hasil penelitian ini adalah bahwa putusan pengadilan sudah tepat dan sesuai dengan aturan yang berlaku.
ABSTRACT
This summary will discuss about midwife and assistant pharmacist inadvertency on drug administration that had caused death based on health law Decision Number 536 PID.B.2010.PN.PDG. The type of this research is descriptive, meaning that the research will describe problems based on theory or by seeing the connection between the theory and the actual reality. The method used in this research is juridical normative, which means that the research is conducted according to the legal norm that is available in the legislation and court decision, also society rsquo s norms. This research explains midwife and pharmacist assistant rsquo s responsibilities and authorities on doing their duty and on drug administration, also gives a good analysis about court decision No. 963 K PID.SUS 2013 Both midwife and pharmacist assistant rsquo s responsibilities and authorities have been regulated so well so they become both form of safety assurance for patients, and form of security assurance for health workers. The good regulation also prevents malpractices on happening when health workers are doing their responsibilities. The result is that the court ruling is proper and is made based the rules applied.
2017
S68749
UI - Skripsi Membership  Universitas Indonesia Library
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Boyer, Mary Jo
Jakarta: Erlangga, 2013
615.14 BOY mt
Buku Teks  Universitas Indonesia Library
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Downie, George
London: Churchill Livingstone, 2010
615.14 DOW c
Buku Teks  Universitas Indonesia Library
cover
Abstrak :
Written by an international team from academia and the pharmaceutical industry, this book covers all aspects of the oral bioavailability of medicines. The focus is placed on methods for determining the parameters relevant to bioavailability. These range from modern physicochemical techniques via biological studies in vitro and in vivo right up to computer-aided predictions. The authors specifically address possibilities for optimizing bioavailability during the early screening stage for the active substance. Its clear structure and comprehensive coverage make this book equally suitable for researchers and lecturers in industry and teaching.
Weinheim, Germany: Wiley-VCH, 2003
e20385324
eBooks  Universitas Indonesia Library
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