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| 003 | ES-MaUEC | ||
| 005 | 20240611040132.0 | ||
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| 008 | 131209s2014 it | s |||| 0|eng d | ||
| 020 | _a9788847053137 | ||
| 024 | 7 |
_a10.1007/978-88-470-5313-7 _2doi |
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| 040 | _aES-MaUEC | ||
| 050 | 4 |
_aRM302.5 _b.T75 2014a EB |
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| 082 | 0 | 4 | _a610 |
| 100 | 1 |
_aTridente, Giuseppe _985977 _0Local _0http://id.loc.gov/authorities/names/n86068291 _1http://viaf.org/viaf/232989550 |
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| 245 | 1 | 0 |
_aAdverse Events with Biomedicines : _bPrevention Through Understanding _cby Giuseppe Tridente. |
| 264 | 1 |
_aMilano _bSpringer International Publishing _c2014 |
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| 300 | _a1 recurso en línea (XXX, 633 páginas) | ||
| 336 |
_aTexto (visual) _btxt _2rdacontent |
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| 337 |
_aelectrónico _bc _2rdamedia |
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| 338 |
_arecurso electrónico _bcr _2rdacarrier |
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| 505 | 0 | _aPart I General Aspects: 1 Introduction -- 2 Adverse drug events to biomedicines -- 3 Systemic syndromes caused by biomedicines -- Part II Monoclonal antibodies: 4 Monoclonal antibodies -- 5 Abciximab -- 6 Adalimumab -- 7 Alemtuzumab -- 8 Basiliximab -- 9 Belimumab -- 10 Bevacizumab -- 11 Brentuximab -- 12 Canakinumab -- 13 Catumaxomab -- 14.Âårtolizumab -- 15 Cetuximab -- 16 Daclizumab -- 17 Denosumab -- 18Âţulizumab -- 19 Edrecolomab -- 20 Efalizumab -- 21 Gemtuzumab -- 22 Golimumab -- 23 Ibritumomab -- 24 Infliximab -- 25 Ipilimumab -- 26 Muromonab -- 27 Natalizumab -- 28 Nimotuzumab -- 29 Ofatumumab -- 30 Omalizumab -- 31 Palivizumab -- 32 Panitumumab -- 33 Pertuzumab -- 34 Ranibizumab -- 35 Rituximab -- 36 Tocilizumab -- 37 Tositumomab -- 38 Trastuzumab -- 39 Ustekinumab -- Part III Fusion proteins: 40 Fusion proteins -- 41 Abatacept -- 42 Aflibercept -- 43 Alefacept -- 44 Belatacept -- 45 Etanercept -- 46 Rilonacept -- 47 Romiplostim -- Part IV CytokinesÂ{uA834}8 Cytokines -- 49 Interleukins -- 50 Denileukin-diftitox -- 51 Anakinra -- 52 Interferons -- 53 Hemopoietic stimulatory factors -- 54 Myelopoietic stimulatory factors -- 55 Thrombopoietic stimulatory factor -- 56 Pluripotent growth factors -- 57 Epidermal growth factors -- Part V Overview: 58 Biomedicines as adverse event inducers -- 59 Conclusions and perspectives. | |
| 520 | _aThis monograph gathers and evaluates data on adverse events (AEs) associated specifically with those “biomedicinesâ€{u0880}{u0B6F}noclonal antibodies, fusion proteins, and cytokines â€{u0D28}at have recently entered therapeutic use in humans. All AEs observed when using each member of this new drug class are covered, with a view to improving understanding of pathogenesis, facilitating prevention, monitoring, and control, and contributing to the development of better drugs that provide benefits while minimizing risk. Further aspects here examined include the role of drug mechanisms of action and immunogenicity in relation to AEs outcome and induction of systemic syndromes. Additional data on AEs in off-label treatments are also considered. Electronic data sheets, downloadable from the Springer Extra Materials platform, include more detailed safety data as well as additional basic information on product characteristics, pre- and post-marketing AEs classified according to frequency, and system/organ targeting. Data on excipients and selected information on drug interactions and associations are also provided. Adverse Events with Biomedicines: Prevention Through Understanding will serve as a detailed, practical guideline to this important new area, which demands the attention of clinicians, immunologists, oncologists, allergologists, public health professionals, and drug companies. | ||
| 650 | 7 |
_aMedicamentos _xEfectos secundarios _9168753 |
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_uhttps://go.openathens.net/redirector/universidadeuropea.es?url=https://link.springer.com/book/10.1007/978-88-470-5313-7 _zAcceso a este recurso digital (usuarios Universidad Europea de Madrid) |
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| 988 | 0 | 0 | _aEBOOK, EBSPRINGER, GOBI_sep2018 |
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