<?xml version="1.0" encoding="utf-8" standalone="yes"?><rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom"><channel><title>Diagnosis on A long dance with Rona</title><link>https://longcovid.blog/categories/diagnosis/</link><description>Recent content in Diagnosis on A long dance with Rona</description><generator>Hugo -- gohugo.io</generator><language>en-us</language><lastBuildDate>Fri, 13 Mar 2026 00:00:00 +0000</lastBuildDate><atom:link href="https://longcovid.blog/categories/diagnosis/index.xml" rel="self" type="application/rss+xml"/><item><title>Warning about CYP3A inhibition, Paxlovid, and Corticosteroids ⚠️</title><link>https://longcovid.blog/p/warning-about-cyp3a-inhibition-paxlovid-and-corticosteroids-%EF%B8%8F/</link><pubDate>Fri, 13 Mar 2026 00:00:00 +0000</pubDate><guid>https://longcovid.blog/p/warning-about-cyp3a-inhibition-paxlovid-and-corticosteroids-%EF%B8%8F/</guid><description>&lt;img src="https://longcovid.blog/p/warning-about-cyp3a-inhibition-paxlovid-and-corticosteroids-%EF%B8%8F/img/brtsunset.webp" alt="Featured image of post Warning about CYP3A inhibition, Paxlovid, and Corticosteroids ⚠️" /&gt;&lt;h3 id="tldr"&gt;TLDR
&lt;/h3&gt;&lt;p&gt;Probably shouldn&amp;rsquo;t have taken corticosteroids and Paxlovid; it can suppress the HPA axis and may cause secondary adrenal failure or secondary Cushing&amp;rsquo;s.&lt;/p&gt;
&lt;h3 id="a-few-light-bulbs-go-off"&gt;A few light bulbs go off
&lt;/h3&gt;&lt;p&gt;I had a few lightbulb moments recently. One specifically was seeing a cardiologist for a POTS test (which was negative with orthostatic testing). What triggered this is I was diagnosed with metabolic syndrome by my PCP and stage II hypertension despite still exercising, eating healthy, low stress, normal weight, and sleeping as best I can (it&amp;rsquo;s okay to good most nights with medication). This metabolic syndrome diagnosis came at 14 months in of long COVID.&lt;/p&gt;
&lt;p&gt;Cardio said I&amp;rsquo;m fine, but I need to get my blood pressure under control. Turns out it&amp;rsquo;s masked; if I take my own blood pressure at the doctor, it&amp;rsquo;s stage II; if a nurse or doctor pushes the button, it&amp;rsquo;s stage I hypertension. This is essentially the opposite of white coat syndrome and inherently more dangerous. I know I&amp;rsquo;ve had masked hypertension for a long time but was told otherwise. This has finally been charted for my doctors to ignore now going forward (yes, I&amp;rsquo;m bitter, and more on this shortly).&lt;/p&gt;
&lt;h3 id="cardiology-and-the-link"&gt;Cardiology and the link
&lt;/h3&gt;&lt;p&gt;A very long story short, I did labs for cardio. I told her you don&amp;rsquo;t need to; they&amp;rsquo;re going to be normal, but in the interest of pacifying both of us, I agreed. Well, they were, except for one thing still in the normal range but on the low side: cortisol. My morning fasting cortisol was just 7.1. The cardiologist said everything is in the normal range, just like &amp;lsquo;you&amp;rsquo; said.&lt;/p&gt;
&lt;table&gt;
 &lt;thead&gt;
 &lt;tr&gt;
 &lt;th&gt;&lt;strong&gt;Date&lt;/strong&gt;&lt;/th&gt;
 &lt;th&gt;&lt;strong&gt;Value&lt;/strong&gt;&lt;/th&gt;
 &lt;th&gt;&lt;strong&gt;Normal range&lt;/strong&gt;&lt;/th&gt;
 &lt;/tr&gt;
 &lt;/thead&gt;
 &lt;tbody&gt;
 &lt;tr&gt;
 &lt;td&gt;Feb 3, 2026&lt;/td&gt;
 &lt;td&gt;7.1mcg/dL&lt;/td&gt;
 &lt;td&gt;2.9 - 19.4 mcg/dL&lt;/td&gt;
 &lt;/tr&gt;
 &lt;tr&gt;
 &lt;td&gt;Dec 27, 2024&lt;/td&gt;
 &lt;td&gt;17.4mcg/dL&lt;/td&gt;
 &lt;td&gt;2.9 - 19.4 mcg/dL&lt;/td&gt;
 &lt;/tr&gt;
 &lt;/tbody&gt;
&lt;/table&gt;
&lt;p style="text-align:center; font-size:0.8em; margin-top:-1em;"&gt;Lab results pre and post covid.&lt;/p&gt;
&lt;p&gt;I started researching my charts over the past 15 months. One thing that stuck out was I was taking Paxlovid while on Flovent and then prescribed prednisone for my rebound covid. That right there should have never happened, and here is why: &lt;a class="link" href="https://pubmed.ncbi.nlm.nih.gov/18459946/" target="_blank" rel="noopener"
 &gt;https://pubmed.ncbi.nlm.nih.gov/18459946/&lt;/a&gt;&lt;/p&gt;
&lt;p&gt;I reached out to my inhaler and Xolair prescriber, Asthma and Allergy, and they said that never should have never happened either; it would have been flagged at the pharmacy, to say the least. The problem is, he was only prescribing my inhalers; Paxlovid and prednisone came from two different urgent care doctors—however, all of these people are in the same health care network and have access to my chart.&lt;/p&gt;
&lt;p&gt;I have been taking Symbicort throughout this. I got steroid injections in my neck for pain repeatedly last year. Furthermore, I was scheduled to get steroid injections again at the end of this month (I have since cancelled this).&lt;/p&gt;
&lt;h3 id="endocrinology"&gt;Endocrinology
&lt;/h3&gt;&lt;p&gt;Likewise, I reached out to my endocrinologist (whom I haven&amp;rsquo;t seen in 18 months) and told him my cortisol number and also my suspicions of HPA-axis suppression. Needless to say, I have had an urgent ACTH stimulation test scheduled for several weeks out 🙄&lt;/p&gt;
&lt;p&gt;I wanted to put this out there if someone is in a similar boat as me, and hopefully it can help point others in the right direction.&lt;/p&gt;
&lt;h3 id="next-steps"&gt;Next Steps
&lt;/h3&gt;&lt;p&gt;Ultimately, there is more at play here than just this, and I do have more to say beyond this, which will be coming soon. I have opted to reactivate a trip to the Mayo, as I&amp;rsquo;ve come across this and other things that were clearly missed. At this point, I am my own doctor as a patient and telling doctors what to do.&lt;/p&gt;</description></item></channel></rss>