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1

Kiang, Tony K. L., Kyle John Wilby, and Mary H. H. Ensom. Clinical Pharmacokinetic and Pharmacodynamic Drug Interactions Associated with Antimalarials. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-10527-7.

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Kiang, Tony K. L., Kyle John Wilby, and Mary H. H. Ensom, eds. Pharmacokinetic and Pharmacodynamic Drug Interactions Associated with Antiretroviral Drugs. Singapore: Springer Singapore, 2016. http://dx.doi.org/10.1007/978-981-10-2113-8.

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3

Bartle, W. R., V. Braun, J. M. Dietschy, Y. Emori, M. Hagiwara, H. Hidaka, S. Imajoh, et al. Regulation of Plasma Low Density Lipoprotein Levels Biopharmacological Regulation of Protein Phosphorylation Calcium-Activated Neutral Protease Microbial Iron Transport Pharmacokinetic Drug Interactions. Berlin, Heidelberg: Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-72902-7.

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4

David, Rodrigues A., ed. Drug-drug interactions. New York: M. Dekker, 2002.

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5

David, Rodrigues A., ed. Drug-drug interactions. 2nd ed. New York: Informa Healthcare, 2008.

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6

Huang, L. Evaluation of the potential pharmacokinetic interaction between naproxen and zidovudine. [Ottawa: Ottawa General Hospital, 1991.

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7

Multiple chemical interactions. Chelsea, Mich: Lewis Publishers, 1991.

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8

Ritschel, W. A. Handbook of basic pharmacokinetics-- including clinical applications. 6th ed. Washington, D.C: American Pharmacists Association, 2004.

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9

Ritschel, W. A. Handbook of basic pharmacokinetics ... including clinical applications. 7th ed. Washington, D.C: American Pharmacists Association, 2009.

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10

Handbook of basic pharmacokinetics-- including clinical applications. 3rd ed. Hamilton, IL: Drug Intelligence Publications, 1986.

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11

Ritschel, W. A. Handbook of basic pharmacokinetics-- including clinical applications. 6th ed. Washington, D.C: American Pharmacists Association, 2004.

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12

Handbook of basic pharmacokinetics-- including clinical applications. 4th ed. Hamilton, IL: Drug Intelligence Publications, 1992.

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13

L, Kearns Gregory, ed. Handbook of basic pharmacokinetics-- including clinical applications. 5th ed. Washington, D.C: American Pharmaceutical Association, 1999.

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14

Handbook of essential pharmacokinetics, pharmacodynamics, and drug metabolism for industrial scientists. New York: Kluwer Academic/Plenum Publishers, 2001.

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15

Lyubimov, Alexander V. Encyclopedia of drug metabolism and interactions. Hoboken, N.J: Wiley, 2012.

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16

Garth, Powis, ed. Anticancer drugs: Reactive metabolism and drug interactions. Oxford, England: Pergamon Press, 1994.

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17

Kuhl, Herbert, ed. Pharmacokinetics of Oral Contraceptive Steroids and Drug Interaction: Salzburg, Austria, September 14-16, 1989. St. Louis, Missouri, USA: Mosby-Year Book, 1990.

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18

Cassileth, Barrie R. Herb-drug interactions in oncology. 2nd ed. Shelton, Conn: People's Medical Pub. House-USA, 2010.

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19

Lippincott Williams & Wilkins., ed. Alarming signs & symptoms. Ambler: Lippincott Williams & Wilkins, 2006.

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20

Ashraf, Mozayani, and Raymon Lionel P, eds. Handbook of drug interactions: A clinical and forensic guide. Totowa, N.J: Humana Press, 2004.

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21

Biochemical pharmacology. Hoboken, New Jersey: John Wiley & Sons, 2012.

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22

Dixit, Sameer M., and Kasipathy Kailasapathy. Antagonistic activity and interaction of probiotic bacteria with intestinal microbiota. Hauppauge, N.Y: Nova Science Publishers, 2012.

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23

Gayevyy, Mikhail, and Lyudmila Gayevaya. Pharmacotherapy with the basics of clinical pharmacology and herbal medicine. ru: INFRA-M Academic Publishing LLC., 2017. http://dx.doi.org/10.12737/23493.

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The textbook describes General and specific issues of clinical pharmacology and pharmacotherapy-basic information about diseases, principles of pharmacotherapy, pharmacokinetics, pharmacodynamics, indications for the appointment of a modern Arsenal of drugs, their doses, contraindications, effects and interactions. A special section is dedicated to herbal medicine. The discussion of this textbook was attended by teachers of the Department of pharmacology and related departments of the Pyatigorsk pharmaceutical, Volgograd and Kuban medical academies. Meets the requirements of the Federal state educational standard of higher education of the latest generation. For students of pharmaceutical and medical universities, interns, clinical residents, pharmacists and doctors of all specialties.
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24

Gabriele, Cruciani, ed. Molecular interaction fields: Applications in drug discovery and ADME prediction. Weinheim: Wiley-VCH, 2005.

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25

Olkkola, Klaus T., Hugo E. M. Vereecke, and Martin Luginbühl. Drug interactions in anaesthetic practice. Edited by Michel M. R. F. Struys. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199642045.003.0021.

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When two or more drugs are administered simultaneously, the pharmacological response may be greater or less than the sum of the effects of the individual drugs. One drug may antagonize or potentiate the effects of the other and there may be also qualitative differences in response. Although some drug interactions increase the toxicity or result in loss of therapeutic effect, others are beneficial. Indeed, modern anaesthetic techniques depend on beneficial drug interactions. A sound combination of drugs helps clinicians to increase both the efficacy and safety of drug treatment. Drugs may interact on a pharmaceutical, pharmacodynamic, or pharmacokinetic basis. Many pharmacodynamic interactions are predictable and can be avoided by the use of common sense. However, it is much more difficult to predict the likelihood of pharmacokinetic and pharmaceutical interactions despite good prior knowledge of pharmacokinetics and chemical properties of individual drugs. Pharmaceutical drug interactions usually occur before the drug is given to the patient and they are caused by chemical (such as acid–base, salt formation, oxidation–reduction, hydrolysis, or epimerization) or physical (such as adsorption/absorption or emulsion breaking) reactions. When drugs have a pharmacokinetic interaction, one drug alters the absorption, distribution, or the elimination of the other drug. Many pharmacokinetic drug interactions are due to inhibition or induction of cytochrome P450 enzymes. Pharmacodynamic drug interactions are caused by drugs having an effect on the same receptors or the same physiological system. This chapter gives anaesthetists an overview of clinically relevant perioperative drug interactions.
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26

Wijdicks, Eelco F. M., and Sarah L. Clark. Drug Delivery, Monitoring, and Interactions. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190684747.003.0001.

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This chapter outlines the typical pathway of an administered drug and the factors that affect it. The main components that determine a drug’s pharmacokinetics and pharmacodynamics are discussed. Issues important for the physician such as Pharmacokinetic parameters, drug administration routes, and principles of drug interactions are highlighted. Problems with inadvertently holding home or maintenance medications and other drug errors are outlined. Pharmacogenomics and its emerging clinical relevance is introduced.
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27

Pan, Wei-Jian. Pharmacokinetic/pharmacodynamic interactions between cocaine and alcohol. 1998.

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28

Kiang, Tony K. L., Kyle John Wilby, and Mary H. H. Ensom. Clinical Pharmacokinetic and Pharmacodynamic Drug Interactions Associated with Antimalarials. Springer International Publishing AG, 2014.

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29

Wilby, Kyle John, Tony K.L. K. L. Kiang, and Mary H. H. Ensom. Clinical Pharmacokinetic and Pharmacodynamic Drug Interactions Associated with Antimalarials. Adis, 2016.

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30

Kiang, Tony K. L., Kyle John Wilby, and Mary H. H. Ensom. Pharmacokinetic and Pharmacodynamic Drug Interactions Associated with Antiretroviral Drugs. Adis International, Limited, 2016.

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31

Kiang, Tony K. L., Kyle John Wilby, and Mary H. H. Ensom. Clinical Pharmacokinetic and Pharmacodynamic Drug Interactions Associated with Antimalarials. Springer, 2015.

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32

Kiang, Tony K. L., Kyle John Wilby, and Mary H. H. Ensom. Clinical Pharmacokinetic and Pharmacodynamic Drug Interactions Associated with Antimalarials. Springer International Publishing AG, 2014.

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33

Kiang, Tony K. L., Kyle John Wilby, and Mary H. H. Ensom. Pharmacokinetic and Pharmacodynamic Drug Interactions Associated with Antiretroviral Drugs. Adis, 2016.

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34

Kiang, Tony K. L., Kyle John Wilby, and Mary H. H. Ensom. Pharmacokinetic and Pharmacodynamic Drug Interactions Associated with Antiretroviral Drugs. Adis, 2018.

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35

Regulation of Plasma Low Density Lipoprotein Levels Biopharmacological Regulation of Protein Phosphorylation Calcium-Activated Neutral Protease ... Transport Pharmacokinetic Drug Interactions. Springer, 2012.

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36

Braun, V., W. R. Bartle, M. Hagiwara, J. M. Dietschy, and Y. Emori. Regulation of Plasma Low Density Lipoprotein Levels Biopharmacological Regulation of Protein Phosphorylation Calcium-Activated Neutral Protease Microbial Iron Transport Pharmacokinetic Drug Interactions. Springer, 2012.

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37

Schafer, Jason J., Elizabeth M. Sherman, Taylor K. Gill, and Jatandra Birney. Understanding and Managing Antineoplastic and Antiretroviral Therapy. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190493097.003.0029.

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The use of combination antiretroviral therapy in patients with malignancies is associated with improved HIV and cancer-related outcomes. Combining antiretroviral and antineoplastic therapy is often complicated by significant drug-drug interactions, drug-disease state monitoring interactions and overlapping toxicities. Definitive pharmacokinetic studies evaluating drug interactions between antineoplastics and antiretrovirals are uncommon and clinical judgment must often be used to determine the potential for significant interactions. Adjusting antiretroviral therapy in response to significant drug interactions or overlapping toxicities is often more feasible than modifying antineoplastic protocols.
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38

Emori, Yasufumi, Masatoshi Hagiwara, Volker Braun, William R. Bartle, and John M. Dietschy. Regulation of Plasma Low Density Lipoprotein Levels Biopharmacological Regulation of Protein Phosphorylation Calcium-Activated Neutral Protease Microbial Iron Transport Pharmacokinetic Drug Interactions. Springer London, Limited, 2012.

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39

Nageshwaran, Sathiji, David Ledingham, Heather C. Wilson, and Anthony Dickenson, eds. Drugs in Neurology. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199664368.001.0001.

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The Drugs in Neurology handbook succinctly brings together the most up-to-date management of adult neurological disorders and the evidence base for their drug treatment. Each neurological sub-specialty is covered within separate chapters, discussing disease classification, clinical features, suggested treatment pathways, and the evidence base behind modern treatment regimes. The latter half of the text contains an easily accessible A–Z drug compendium. Drug monographs include useful prescribing information, licensed and unlicensed uses, disease-specific mechanism(s) of action, contraindications, toxicity and side effects, use in special populations, efficacy (evidence-based), dosing and monitoring, pharmacokinetic data, and drug interactions.
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40

Björn, Lemmer, ed. Chronopharmacology: Cellular and biochemical interactions. New York: M. Dekker, 1989.

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41

Rodrigues, A. David. Drug-Drug Interactions. Taylor & Francis Group, 2001.

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42

Rodrigues, A. David. Drug-Drug Interactions. Taylor & Francis Group, 2019.

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43

Rodrigues, A. David. Drug-Drug Interactions. Taylor & Francis Group, 2019.

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44

Rodrigues, A. David. Drug-Drug Interactions. Taylor & Francis Group, 2019.

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45

Rodrigues, A. David. Drug-Drug Interactions. Taylor & Francis Group, 2019.

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46

Rodrigues, A. David. Drug-Drug Interactions. Taylor & Francis Group, 2019.

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47

Ritschel, Wolfgang A., and Gregory L. Kearns. Handbook of Basic Pharmacokinetics. 6th ed. APhA Publications, 2004.

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48

Rodrigues, A. David. Drug - Drug Interactions (Drugs and the Pharmaceutical Sciences). Informa Healthcare, 2001.

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49

Ramos, Fernando Jorge dos, Isabel Vitória Neves de Figueiredo Santos Pereira, and Maria Margarida Duarte Ramos Caramona. Food-Drug Interactions: Pharmacokinetics, Prevention and Potential Side Effects. Nova Science Publishers, Incorporated, 2018.

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50

Clinical manual of drug interaction principles for medical practice. Washington, DC: American Psychiatric Pub., 2009.

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