Oral Drugs Against COVID-19: Management of Drug Interactions With the Use of Nirmatrelvir/Ritonavir.

Background: Five-day oral therapies against early COVID-19 infection have recently been conditionally approved in Europe. In the drug combination nirmatrelvir + ritonavir (nirmatrelvir/r), the active agent, nirmatrelvir, is made bioavailable in clinically adequate amounts by the additional administr...

Descripción completa

Detalles Bibliográficos
Publicado en:Deutsches Ärzteblatt International Vol. 119; no. 15; pp. 263 - 273
Autores principales: Mikus, Gerd, Foerster, Kathrin I., Terstegen, Theresa, Vogt, Cathrin, Said, André, Schulz, Martin, Haefeli, Walter E.
Formato: Journal Article
Publicado: Deutscher Aerzte-Verlag GmbH 4/15/2022
Acceso en línea:Ver este registro en EBSCOhost
fields @attributes:
  recordID: 1
pdfLink:
plink: https://search.ebscohost.com/login.aspx?direct=true&db=ccm&AN=158071563&site=ehost-live
header:
  @attributes:
    shortDbName: ccm
    uiTerm: 158071563
    longDbName: CINAHL Complete
    uiTag: AN
  controlInfo:
    bkinfo:
    dissinfo:
    jinfo:
      jid:
        18660452
        5F0N
      jtl: Deutsches Ärzteblatt International
      issn: 18660452
      maglogo: N
    pubinfo:
      dt: 4/15/2022
      vid: 119
      iid: 15
      pid: 25312
      pub: Deutscher Aerzte-Verlag GmbH
    artinfo:
      ui:
        158071563
        10.3238/arztebl.m2022.0152
        158071563
      ppf: 263
      ppct: 10
      formats:
        fmt:
          @attributes:
            type: P
      tig:
        atl: Oral Drugs Against COVID-19: Management of Drug Interactions With the Use of Nirmatrelvir/Ritonavir.
      aug:
        au:
          Mikus, Gerd
          Foerster, Kathrin I.
          Terstegen, Theresa
          Vogt, Cathrin
          Said, André
          Schulz, Martin
          Haefeli, Walter E.
        affil: Department of Clinical Pharmacology and Pharmacoepidemiology, Heidelberg University Hospital, Heidelberg, Germany
      sug:
      ab: Background: Five-day oral therapies against early COVID-19 infection have recently been conditionally approved in Europe. In the drug combination nirmatrelvir + ritonavir (nirmatrelvir/r), the active agent, nirmatrelvir, is made bioavailable in clinically adequate amounts by the additional administration of a potent inhibitor of its first-pass metabolism by way of cytochrome P450 [CYP] 3A in the gut and liver. In view of the central role of CYP3A in the clearance of many different kinds of drugs, and the fact that many patients with COVID-19 are taking multiple drugs to treat other conditions, it is important to assess the potential for drug interactions when nirmatrelvir/r is given, and to minimize the risks associated with such interactions. Methods: We defined the interaction profile of ritonavir on the basis of information derived from two databases (Medline, GoogleScholar), three standard electronic texts on drug interactions, and manufacturer-supplied drug information. We compiled a list of drugs and their potentially relevant interactions, developed a risk minimization algorithm, and applied it to the substances in question. We also compiled a list of commonly prescribed drugs for which there is no risk of interaction with nirmatrelvir/r. Results: Out of 190 drugs and drug combinations, 57 do not need any special measures when given in combination with brief, low-dose ritonavir treatment, while 15 require dose modification or a therapeutic alternative, 8 can be temporarily discontinued, 9 contraindicate ritonavir use, and 102 should preferably be combined with a different treatment. Conclusion: We have proposed measures that are simple to carry out for the main types of drug that can interact with ritonavir. These measures can be implemented under quarantine conditions before starting a 5-day treatment with nirmatrelvir/r.
      pubtype: Academic Journal
      doctype: Journal Article
      ougenre: Article
    language: English
    refInfo:
    holdings:
      @attributes:
        islocal: N