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1

The allergic reaction. 2nd ed. Braine-L'Alleud: UCB Pharmaceutical Sector, 1993.

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2

J, Waters William. Rhode Island Adverse Drug Reaction Reporting Project: Final report. Providence, RI: RI Dept. of Health, Office of Health Policy, 1988.

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3

Newman, Paula M. Development of an adverse drug reaction reporting program for Kingston General Hospital. [Toronto, Ont: s.n., 1989.

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4

Council for International Organizations of Medical Sciences. Harmonizing the use of adverse-drug-reaction terms: Definitions of terms and minimum requirements for their use. Geneva: CIOMS, 1996.

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5

Song, Hong-ji. Pujagyong monitʻŏring tŭng ŭiyakpʻum sipʻan hu kamsi chʻegye kyoyuk pʻŭrogŭraem kaebal =: Developing pharmacovigilance education program and adverse drug reaction reporting P.R. leaflet. [Seoul]: Sikpʻum Ŭiyakpʻum Anjŏnchʻŏng, 2007.

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6

Aronson, J. K., and J. C. C. Talbot. Stephens' detection and evaluation of adverse drug reactions: Principles and practice. 6th ed. Chichester, West Sussex, UK: John Wiley & Sons, 2011.

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7

Zaragoza Dörwald, Florencio, ed. Side Reactions in Organic Synthesis II. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527687800.

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8

Foundation), Centre for Medicines Research Workshop (1983 Ciba. Monitoring for adverse drug reactions. Lancaster: MTP Press, 1985.

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9

Uetrecht, Jack P. Adverse drug reactions. Heidelberg: Springer, 2010.

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10

Revised guidelines: Reporting of adverse drug reactions. Bethesda, Md: Dept. of Health & Human Services, Public Health Service, National Institutes of Health, National Cancer Institute, 1985.

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11

Pearce, Neil. Adverse reactions: The Fenoterol story. Auckland, N.Z: Auckland University Press, 2007.

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12

Adverse reactions: The Fenoterol story. Auckland, N.Z: Auckland University Press, 2007.

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13

Litt's D.E.R.M.: Drug eruptions & reactions manual. New York: Informa Healthcare, 2010.

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14

Marion, Giles M. Site remediation via dispersion by chemical reaction (DCR). [Hanover, N.H.]: US Army Corps of Engineers, Cold Regions Research & Engineering Laboratory, 1997.

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15

Curious, odd, rare, and abnormal reactions to medications. Fort Lee, NJ: Barricade Books, 2009.

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16

Atlas of drug reactions. New York: Churchill Livingstone, 1985.

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17

A, Routledge P., and Talbot J. C. C, eds. Detection of new adverse drug reactions. 4th ed. London: Macmillan Reference Ltd, 1998.

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18

Detection of new adverse drug reactions. 3rd ed. Basingstoke: Macmillan, 1992.

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19

Aronson, J. K. Side effects of drugs annual 31: A worldwide yearly survey of new data and trends in adverse drug reactions. Amsterdam: Elsevier Science, 2009.

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20

Seymour, R. A. Adverse drug reactions in dentistry. 2nd ed. Oxford: Oxford University Press, 1996.

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21

G, Walton J., ed. Adverse drug reactions in dentistry. Oxford: Oxford University Press, 1988.

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22

Meyler, Leopold. Meyler's side effects of drugs: An encyclopaedia of adverse reactions and interactions. Amsterdam: Elsevier, 1992.

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23

Meyler, Leopold. Meyler's side effects of drugs: An encyclopedia of adverse reactions and interactions. Amsterdam: Elsevier, 1988.

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24

Dukes, M. N. G. 1930- and Aronson J. K, eds. Meyler's side effects of drugs: An encyclopedia of adverse reactions and interactions. Amsterdam: Elsevier, 1996.

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25

C, Talbot J. C., ed. The detection of new adverse drug reactions. New York, N.Y: Stockton Press, 1985.

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26

Stephens, M. D. B. The detection of new adverse drug reactions. 2nd ed. London: Macmillan Press ; New York, NY : Stockton Press, 1988.

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27

C, Talbot J. C., ed. The detection of new adverse drug reactions. 2nd ed. Basingstoke: Macmillan, 1988.

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28

Side effects of drugs annual: A worldwide yearly survey of new data in adverse drug reactions. Amsterdam: Elsevier, 2011.

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29

Singh, M. Characterization of SiC (SCS-6) fiber reinforced reaction-formed silicon carbide matrix composites. [Washington, D.C: National Aeronautics and Space Administration, 1995.

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30

Phenylpropanolamine: A critical analysis of reported adverse reactions and overdosage. Fort Lee, N.J: J.K. Burgess, 1986.

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31

U, Wintroub Bruce, ed. Adverse cutaneous reactions to medication. Baltimore: Williams & Wilkins, 1996.

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32

Fraunfelder, Frederick T. Drug-induced ocular side effects. Edited by Randall Joan A. 4th ed. Baltimore: Williams & Wilkins, 1996.

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33

Litt's Drug Eruption & Reaction Manual 24E. CRC Press, 2017.

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34

Shear, Neil, and Jerome Z. Litt. Litt's Drug Eruption and Reaction Manual 24E. Taylor & Francis Group, 2017.

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35

Litt, Jerome Z., and Neil H. Shear. Litt's Drug Eruption and Reaction Manual, 23rd Edition. Taylor & Francis Group, 2017.

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36

Litt's Drug Eruption and Reaction Manual, 23rd Edition. Taylor & Francis Group, 2017.

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37

World Health Organization (WHO). Adverse Drug Reaction Terms - Definitions: Respiratory Disorders, Skin Disorders (Cioms Nonserial). World Health Organization, 1997.

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38

Institute, American Health Research. Prozac (Fluoxetine) Side Effects and Harmful Reactions: Index of New Information With Authors & Subjects (Fluoxetine -Side Effects & Harmful Reaction : ... of New Information With Authors and Subject). Abbe Pub Assn of Washington Dc, 1994.

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39

Institute, American Health Research. Prozac (Fluoxetine -Side Effects & Harmful Reaction : Index of New Information With Authors and Subject). Abbe Pub Assn of Washington Dc, 1994.

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40

On the influence of a fuel side heat-loss ("soot") layer on a planar diffusion flame. [Washington, DC: National Aeronautics and Space Administration, 1994.

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41

Adverse drug reactions: A practical guide to diagnosis and management. Chichester, West Sussex, England: Wiley, 1994.

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42

Henriksen, Niels Engholm, and Flemming Yssing Hansen. Bimolecular Reactions, Transition-State Theory. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198805014.003.0006.

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This chapter discusses an approximate approach—transition-state theory—to the calculation of rate constants for bimolecular reactions. A reaction coordinate is identified from a normal-mode coordinate analysis of the activated complex, that is, the supermolecule on the saddle-point of the potential energy surface. Motion along this coordinate is treated by classical mechanics and recrossings of the saddle point from the product to the reactant side are neglected, leading to the result of conventional transition-state theory expressed in terms of relevant partition functions. Various alternative derivations are presented. Corrections that incorporate quantum mechanical tunnelling along the reaction coordinate are described. Tunnelling through an Eckart barrier is discussed and the approximate Wigner tunnelling correction factor is derived in the limit of a small degree of tunnelling. It concludes with applications of transition-state theory to, for example, the F + H2 reaction, and comparisons with results based on quasi-classical mechanics as well as exact quantum mechanics.
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43

Molecules from Side Reactions. MDPI, 2021. http://dx.doi.org/10.3390/books978-3-0365-0005-8.

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44

Stephens, M. D. B., 1930-, Talbot J. C. C, and Waller Patrick, eds. Stephens' detection of new adverse drug reactions. 5th ed. Chichester: Wiley, 2004.

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45

(Editor), John Talbot, and Patrick Waller (Editor), eds. Stephens' Detection of New Adverse Drug Reactions. 5th ed. Wiley, 2004.

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46

Talbot, John, and Patrick Waller. Stephens' Detection of New Adverse Drug Reactions. Wiley & Sons, Incorporated, John, 2007.

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47

Talbot, John, and Patrick Waller. Stephens' Detection of New Adverse Drug Reactions. Wiley & Sons, Incorporated, John, 2004.

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48

Yang, Yi. Side Reactions in Peptide Synthesis. Elsevier Science & Technology Books, 2015.

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49

Side Reactions in Peptide Synthesis. Elsevier, 2016. http://dx.doi.org/10.1016/c2013-0-13700-2.

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50

Hopkins, Philip M. Adverse drug reactions in anaesthesia. Edited by Michel M. R. F. Struys. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199642045.003.0022.

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Adverse drug reactions are implicated in more than 40% of anaesthesia-related deaths. Undoubtedly, many more patients experience morbidity from adverse drug reactions. Widely cited definitions of adverse drug reactions encompass common side-effects but this chapter focuses on those that are unexpected reactions to drugs administered by anaesthetists and that occur at normal drug doses. The chapter includes a comprehensive account of malignant hyperthermia, which remains a major contributor to anaesthesia related to deaths. Malignant hyperthermia is a pharmacogenetic condition triggered by potent inhalational anaesthetics and possibly also suxamethonium. The genetic basis, pathophysiology, clinical presentations, and management of malignant hyperthermia are discussed. The chapter covers two other pharmacogenetic conditions: the acute porphyrias and butyrylcholinesterase (plasma cholinesterase) deficiency. Drug-induced anaphylaxis is another cause of perioperative morbidity and mortality. Recent data indicate that anaphylaxis during anaesthesia may be much more common than previously thought. The other type of adverse drug reaction covered in the chapter is serotonin syndrome. Perioperative serotonin syndrome is most likely to occur when patients who are already taking serotonergic drugs, such as selective serotonin reuptake inhibitor antidepressants or ‘triptan’ antimigraine treatments, are given a second drug with serotonergic properties, such as tramadol.
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