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<front>
<journal-meta>
<journal-id journal-id-type="publisher">global-journal-of-science-frontier-research-g-bio-tech-genetics</journal-id>
<journal-title-group>
<journal-title>Global Journal of Science Frontier Research - G: Bio-Tech &amp; Genetics</journal-title>
</journal-title-group>
<issn publication-format="print">0975-5896</issn>
<issn publication-format="electronic">2249-4626</issn>
<publisher><publisher-name>Global Journals Publishing Group Incorporated</publisher-name></publisher>
<self-uri xlink:href="https://globaljournals.org/journal-seo-export/jats/52651.xml" />
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<article-meta>
<article-id pub-id-type="publisher-id">52651</article-id>
<title-group>
<article-title>Modulation of Warfarin Sodium into Warfarin Potassium for Patients with Hypertension</article-title>
<subtitle>History and Clinical Application of Warfarin</subtitle>
</title-group>
<contrib-group>
<contrib contrib-type="author"><name><surname>Akram</surname><given-names>Al-Baraa</given-names></name><xref ref-type="aff" rid="aff1" />
</contrib>
</contrib-group>
<aff id="aff1">UNITED KINGDOM</aff>
<pub-date publication-format="electronic" date-type="pub" iso-8601-date="2022-12-28">
<day>28</day>
<month>12</month>
<year>2022</year>
</pub-date>
<volume>22</volume>
<issue>G2</issue>
<fpage>1</fpage>
<lpage>14</lpage>
<abstract><p>Abstract not found</p></abstract>
<kwd-group kwd-group-type="author-generated">
<kwd>warfain</kwd>
<kwd>hypertension</kwd>
<kwd>international normalized ratio</kwd>
<kwd>therapeutic window</kwd>
<kwd>clinical trials</kwd>
<kwd>pharmaco-genomics</kwd>
<kwd>CYP2C9*3.</kwd>
</kwd-group>
<self-uri content-type="pdf" xlink:href="https://globaljournals.org/GJSFR_Volume22/1-Modulation-of-Warfarin.pdf" />
<self-uri content-type="html" xlink:href="https://globaljournals.org/scholarly-articles/modulation-of-warfarin-sodium-into-warfarin-potassium-for-patients-with-hypertension/" />
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<title>Full Text</title>
<p>Warfarin is an oral anticoagulant drug that has a prolonged duration of action with delayed onset of action; its chemical structure contains sodium atoms, which may be hazardous to hypertensive patients. To solve this problem, sodium atom can be substituted with potassium or lithium atom which can help the patient to relieve hypertension in addition to it essential role as an anticoagulant. Another advantage of this preparation is that it can be used as an antidote against digitalis toxicity, but the warfarin interactions with other drugs are still the same as a cytochrome P450 inhibitor. Warfarin reduces blood clotting by inactivating vitamin K epoxide reductase, which activates vitamin K1, the main component in the blood clotting process. Without sufficient vitamin K1 activation, clotting factors II, VII, IX and X have decreased clotting ability. The anticlotting protein C and protein S have also inhibited, but to a lesser degree. A few timesare required for the clotting process, and these effects can take about five days. Additionally, because this process requires enzymes like VKORC1, patients who take warfarin with polymorphism of these enzymes can require adjustment as genetic factors should be taken into consideration, thus may require lower doses.</p>
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