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  1. Buch ; Online ; E-Book: Precision medicine

    Cascorbi, Ingolf / Schwab, Matthias

    (Handbook of experimental pharmacology ; 280)

    2023  

    Verfasserangabe Ingolf Cascorbi, Matthias Schwab editors
    Serientitel Handbook of experimental pharmacology ; 280
    Überordnung
    Schlagwörter Pharmacology ; Internal medicine ; Cancer
    Sprache Englisch
    Umfang 1 Online-Ressource (x, 283 Seiten), Illustrationen, Diagramme
    Verlag Springer
    Erscheinungsort Cham
    Erscheinungsland Schweiz
    Dokumenttyp Buch ; Online ; E-Book
    Bemerkung Zugriff für angemeldete ZB MED-Nutzerinnen und -Nutzer
    HBZ-ID HT030370305
    ISBN 978-3-031-40047-6 ; 9783031400469 ; 3-031-40047-X ; 3031400461
    DOI 10.1007/978-3-031-40047-6
    Datenquelle ZB MED Katalog Medizin, Gesundheit, Ernährung, Umwelt, Agrar

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  2. Buch ; Online ; E-Book: Medikamenten-Pocket Schmerztherapie

    Cascorbi, Ingolf / Sorge, Jürgen / Strumpf, Michael

    2018  

    Verfasserangabe Ingolf Cascorbi, Jürgen Sorge, Michael Strumpf
    Schlagwörter Pain Medicine ; Family medicine
    Thema/Rubrik (Code) 616.0472
    Sprache Deutsch
    Umfang 1 Online-Ressource (VI, 120 Seiten)
    Ausgabenhinweis 2. überarbeitete Auflage
    Verlag Springer
    Erscheinungsort Berlin
    Erscheinungsland Deutschland
    Dokumenttyp Buch ; Online ; E-Book
    Bemerkung Zugriff für angemeldete ZB MED-Nutzerinnen und -Nutzer
    HBZ-ID HT019851360
    ISBN 978-3-662-57844-5 ; 9783662578438 ; 3-662-57844-1 ; 3662578433
    DOI 10.1007/978-3-662-57844-5
    Datenquelle ZB MED Katalog Medizin, Gesundheit, Ernährung, Umwelt, Agrar

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  3. Artikel ; Online: Clinical Pharmacology of Cannabinoid Therapeutics: Drug Interactions and Side Effects.

    Cascorbi, Ingolf

    Clinical pharmacology and therapeutics

    2023  Band 114, Heft 5, Seite(n) 943–946

    Mesh-Begriff(e) Humans ; Cannabinoids/adverse effects ; Drug-Related Side Effects and Adverse Reactions ; Drug Interactions ; Iatrogenic Disease ; Pharmacology ; Pharmacology, Clinical
    Chemische Substanzen Cannabinoids
    Sprache Englisch
    Erscheinungsdatum 2023-10-13
    Erscheinungsland United States
    Dokumenttyp Editorial
    ZDB-ID 123793-7
    ISSN 1532-6535 ; 0009-9236
    ISSN (online) 1532-6535
    ISSN 0009-9236
    DOI 10.1002/cpt.3037
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  4. Artikel ; Online: Why is There Still Debate About Recommending DPYD-Testing Before Fluoropyrimidine Treatment?

    Cascorbi, Ingolf

    Clinical pharmacology and therapeutics

    2023  Band 114, Heft 4, Seite(n) 733–737

    Sprache Englisch
    Erscheinungsdatum 2023-09-29
    Erscheinungsland United States
    Dokumenttyp Editorial ; Comment
    ZDB-ID 123793-7
    ISSN 1532-6535 ; 0009-9236
    ISSN (online) 1532-6535
    ISSN 0009-9236
    DOI 10.1002/cpt.3016
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  5. Artikel ; Online: Understanding the impact of ABCG2 polymorphisms on drug pharmacokinetics: focus on rosuvastatin and allopurinol.

    Kasten, Anne / Cascorbi, Ingolf

    Expert opinion on drug metabolism & toxicology

    2024  , Seite(n) 1–10

    Abstract: Introduction: In addition to the well-established understanding of the pharmacogenetics of drug-metabolizing enzymes, there is growing data on the effects of genetic variation in drug transporters, particularly ATP-binding cassette (ABC) transporters. ... ...

    Abstract Introduction: In addition to the well-established understanding of the pharmacogenetics of drug-metabolizing enzymes, there is growing data on the effects of genetic variation in drug transporters, particularly ATP-binding cassette (ABC) transporters. However, the evidence that these genetic variants can be used to predict drug effects and to adjust individual dosing to avoid adverse events is still limited.
    Areas covered: This review presents a summary of the current literature from the PubMed database as of February 2024 regarding the impact of genetic variants on ABCG2 function and their relevance to the clinical use of the HMG-CoA reductase inhibitor rosuvastatin and the xanthine oxidase inhibitor allopurinol.
    Expert opinion: Although there are pharmacogenetic guidelines for the ABCG2 missense variant Q141K, there is still some conflicting data regarding the clinical benefits of these recommendations. Some caution appears to be warranted in homozygous ABCG2 Q141K carriers when rosuvastatin is administered at higher doses and such information is already included in the drug label. The benefit of dose adaption to lower possible side effects needs to be evaluated in prospective clinical studies.
    Sprache Englisch
    Erscheinungsdatum 2024-06-04
    Erscheinungsland England
    Dokumenttyp Journal Article ; Review
    ZDB-ID 2214462-6
    ISSN 1744-7607 ; 1742-5255
    ISSN (online) 1744-7607
    ISSN 1742-5255
    DOI 10.1080/17425255.2024.2362184
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  6. Artikel ; Online: The Uncertainties of Metamizole Use.

    Cascorbi, Ingolf

    Clinical pharmacology and therapeutics

    2021  Band 109, Heft 6, Seite(n) 1373–1375

    Mesh-Begriff(e) Anti-Inflammatory Agents, Non-Steroidal/adverse effects ; Dipyrone/adverse effects ; Humans ; Uncertainty
    Chemische Substanzen Anti-Inflammatory Agents, Non-Steroidal ; Dipyrone (6429L0L52Y)
    Sprache Englisch
    Erscheinungsdatum 2021-05-26
    Erscheinungsland United States
    Dokumenttyp Editorial ; Comment
    ZDB-ID 123793-7
    ISSN 1532-6535 ; 0009-9236
    ISSN (online) 1532-6535
    ISSN 0009-9236
    DOI 10.1002/cpt.2258
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  7. Artikel: Polypharmazie – Interaktionen bei älteren Menschen

    Cascorbi, Ingolf

    Aktuelle Kardiologie

    2022  Band 11, Heft 06, Seite(n) 532–536

    Abstract: Thrombozytenaggregationshemmer und Antikoagulanzien sind wichtige Standardmedikationen in der Prophylaxe und Therapie kardiovaskulärer Erkrankungen. Die oft multiple Medikation und durch zusätzliche Begleiterkrankungen notwendige weitere ... ...

    Abstract Thrombozytenaggregationshemmer und Antikoagulanzien sind wichtige Standardmedikationen in der Prophylaxe und Therapie kardiovaskulärer Erkrankungen. Die oft multiple Medikation und durch zusätzliche Begleiterkrankungen notwendige weitere Medikation birgt besonders bei älteren Patienten ein hohes Risiko von Arzneimittelwechselwirkungen. Diese können das Blutungsrisiko oder im Fall des Wirkungsverlusts das Risiko thromboembolischer Ereignisse erhöhen. In diesem Artikel werden klinisch relevante Interaktionen von COX-Hemmern (COX: Cyclooxygenase) und Adenosinrezeptorantagonisten sowie von Vitamin-K-Antagonisten und direkten oralen Antikoagulanzien (DOAK) wie auch Strategien zur Vermeidung unerwünschter Wirkungen diskutiert.
    Schlagwörter P-Glycoprotein ; Blutungsereignis ; Thromboembolie ; Interaktionen ; Arzneistoffmetabolismus ; drug metabolism ; P-glycoprotein ; bleeding events ; thromboembolism ; interactions
    Sprache Deutsch
    Erscheinungsdatum 2022-12-01
    Verlag Georg Thieme Verlag KG
    Erscheinungsort Stuttgart ; New York
    Dokumenttyp Artikel
    ZDB-ID 2654127-0
    ISSN 2193-5211 ; 2193-5203
    ISSN (online) 2193-5211
    ISSN 2193-5203
    DOI 10.1055/a-1911-8015
    Datenquelle Thieme Verlag

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  8. Artikel: Molecular Mechanisms of Tyrosine Kinase Inhibitor Resistance in Chronic Myeloid Leukemia.

    Kaehler, Meike / Cascorbi, Ingolf

    Handbook of experimental pharmacology

    2023  Band 280, Seite(n) 65–83

    Abstract: The hematopoietic neoplasm chronic myeloid leukemia (CML) is a rare disease caused by chromosomal reciprocal translocation t(9;22)(q34:q11) with subsequent formation of the BCR-ABL1 fusion gene. This fusion gene encodes a constitutively active tyrosine ... ...

    Abstract The hematopoietic neoplasm chronic myeloid leukemia (CML) is a rare disease caused by chromosomal reciprocal translocation t(9;22)(q34:q11) with subsequent formation of the BCR-ABL1 fusion gene. This fusion gene encodes a constitutively active tyrosine kinase, which results in malignant transformation of the cells. Since 2001, CML can be effectively treated using tyrosine kinase inhibitors (TKIs) such as imatinib, which prevent phosphorylation of downstream targets by blockade of the BCR-ABL kinase. Due to its tremendous success, this treatment became the role model of targeted therapy in precision oncology. Here, we review the mechanisms of TKI resistance focusing on BCR-ABL1-dependent and -independent mechanisms. These include the genomics of the BCR-ABL1, TKI metabolism and transport and alternative signaling pathways.
    Mesh-Begriff(e) Humans ; Tyrosine Kinase Inhibitors ; Fusion Proteins, bcr-abl/genetics ; Fusion Proteins, bcr-abl/metabolism ; Drug Resistance, Neoplasm/genetics ; Precision Medicine ; Protein Kinase Inhibitors/pharmacology ; Protein Kinase Inhibitors/therapeutic use ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive/drug therapy ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive/genetics
    Chemische Substanzen Tyrosine Kinase Inhibitors ; Fusion Proteins, bcr-abl (EC 2.7.10.2) ; Protein Kinase Inhibitors
    Sprache Englisch
    Erscheinungsdatum 2023-03-07
    Erscheinungsland Germany
    Dokumenttyp Review ; Journal Article
    ISSN 0171-2004
    ISSN 0171-2004
    DOI 10.1007/164_2023_639
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  9. Artikel ; Online: Drug Interactions of Tetrahydrocannabinol and Cannabidiol in Cannabinoid Drugs.

    Herdegen, Thomas / Cascorbi, Ingolf

    Deutsches Arzteblatt international

    2023  Band 120, Heft 49, Seite(n) 833–840

    Abstract: Background: Cannabinoid drugs containing tetrahydrocannabinol (THC), or its structural analogues, as monotherapeutic agents or as extracts or botanical preparations with or without cannabidiol (CBD) are often prescribed to multimorbid patients who are ... ...

    Abstract Background: Cannabinoid drugs containing tetrahydrocannabinol (THC), or its structural analogues, as monotherapeutic agents or as extracts or botanical preparations with or without cannabidiol (CBD) are often prescribed to multimorbid patients who are taking multiple drugs. This raises the question of the risk of drug interactions.
    Methods: This review of the pharmacokinetics and pharmacodynamics of interactions with cannabinoid drugs and their potential effects is based on pertinent publications retrieved by a selective literature search.
    Results: As THC and CBD are largely metabolized in the liver, their bioavailability after oral or oral-mucosal administration is low (6-8% and 11-13%, respectively). The plasma concentrations of THC and its active metabolite 11-OH-THC can be increased by strong CYP3A4 inhibitors (verapamil, clarithromycin) and decreased by strong CYP3A4 inductors (rifampicin, carbamazepine). The clinical significance of these effects is unclear because of the variable plasma level and therapeutic spectrum of THC. The metabolism of CBD is less dependent on cytochrome P450 enzymes than that of THC. THC and CBD inhibit CYP2C and CYP3A4; the corresponding clinically relevant drug interactions probably are likely to arise only with THC doses above 30 mg/day and CBD doses above 300 mg/day.
    Conclusion: Potential drug interactions with THC and CBD are probably of little importance at low or moderate doses. Strong CYP inhibitors or inductors can intensify or weaken their effect. Slowly ramping up the dose of oral cannabinoid drugs can lessen their pharmacodynamic interactions, which can generally be well controlled. Administration by inhalation can worsen the interactions.
    Mesh-Begriff(e) Humans ; Cannabinoids ; Cannabidiol/pharmacokinetics ; Dronabinol/pharmacology ; Pharmaceutical Preparations ; Cytochrome P-450 CYP3A ; Drug Interactions
    Chemische Substanzen Cannabinoids ; Cannabidiol (19GBJ60SN5) ; Dronabinol (7J8897W37S) ; Pharmaceutical Preparations ; Cytochrome P-450 CYP3A (EC 1.14.14.1)
    Sprache Englisch
    Erscheinungsdatum 2023-10-24
    Erscheinungsland Germany
    Dokumenttyp Journal Article ; Review
    ZDB-ID 2406159-1
    ISSN 1866-0452 ; 1866-0452
    ISSN (online) 1866-0452
    ISSN 1866-0452
    DOI 10.3238/arztebl.m2023.0223
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  10. Artikel ; Online: Challenges in Neuropharmacology.

    Cascorbi, Ingolf

    Clinical pharmacology and therapeutics

    2019  Band 105, Heft 5, Seite(n) 1050–1053

    Mesh-Begriff(e) Drug Discovery/trends ; Humans ; Inventions ; Mental Disorders/drug therapy ; Mental Disorders/metabolism ; Molecular Biology/trends ; Nervous System Diseases/drug therapy ; Nervous System Diseases/metabolism ; Neuropharmacology/methods ; Neuropharmacology/trends ; Neuropsychiatry/trends ; Signal Transduction/drug effects
    Sprache Englisch
    Erscheinungsdatum 2019-04-15
    Erscheinungsland United States
    Dokumenttyp Editorial ; Introductory Journal Article
    ZDB-ID 123793-7
    ISSN 1532-6535 ; 0009-9236
    ISSN (online) 1532-6535
    ISSN 0009-9236
    DOI 10.1002/cpt.1407
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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