Possibly it‘s acting so quickly because to increase the dose I was splitting one 30mg tablet in half to get to the 45mg new dose? Or maybe it just dissolves quickly… some up my other tablets that don’t effect BSL but do things I can feel work in 15 mins… but looking back on my graphs it (the sudden rise) is definetely there... the dose is a night 5 hour after dinner/novorapid and with no food since dinner15-20 minutes seems very quick for a tablet to increase blood sugar (unless it's a chewable one or dissolves in your mouth), but in answer to your question when I have to take a course of oral steroids, then I definitely need more insulin.
Probably not relevant, but I found I can get a 2mmol/l difference after changing packs of strips. Low batteries in the tester can also give a shift in readings. So perhaps you need to do the hokey cokey (eliminate as many other confounders that you can, then re introduce them and log results to see how the trends change and more importantly that reintroducing them causes the effect). Changing the Med once may be a fluke Repeated and it becomes believable This is a tenet of Science in that it nust be repeatable..Well I did the experiment again last night and convinced it’s the mirtazipine. I feel like I need the increased dose so will bring it up again next meeting. My experiment of n=1 and only 14 hours into it seems to show that it’s not a high that lasts just a few hours… my fasting BSL this morning was 2 mmol/L higher than it has been for the last 2 weeks. So many things to consider…
Absolutely. The confounding factors are quite tricky to account for sometimes, though. E.g. I can’t think of a way to account for sensor and CGM tolerable error except for statistically and that would require more data than I have or have the capacity to collect. I do know that both the CGM and finger pricks collaborated each other in this single test. I do plan on going back to the higher dose so there is a chance there to at least reproduce the result (or not). The only reason I ‘rushed’ to get back down to the lower dose is that I was doing field work that week and needed to be able to drive; with blurry vision and sustained high readings I didn’t feel comfortable driving. Now that I’m back working at home the blurry vision, even if it lasts awhile, isn’t so much of an issue (blurry in the distance, not close so it doesn’t effect my computer work, just driving). I have an appointment with the GP on Friday and will be telling him I’ll be doing some more tests. When I spoke to him last he said it (unstable BSL) wasn’t a known side effect for mirtazipine but I can find studies on Google Scholar saying different. I haven’t had time to properly read and assess the studies yet, though. Even if it turns out that they’re low quality studies, or studies not done on humans doesn’t mean that it doesn’t effect me in that way or it’s a very rare side effect. Or maybe it was all just coincidenceProbably not relevant, but I found I can get a 2mmol/l difference after changing packs of strips. Low batteries in the tester can also give a shift in readings. So perhaps you need to do the hokey cokey (eliminate as many other confounders that you can, then re introduce them and log results to see how the trends change and more importantly that reintroducing them causes the effect). Changing the Med once may be a fluke Repeated and it becomes believable This is a tenet of Science in that it nust be repeatable..
One of the reported side effects of Mirtazapine is increased pressure in the eyeball. similar to Glaucoma. Have you had a glaucoma test since starting this med? That may explain the visual problems. it does seem that the med can interefere with diabetes blood sugar control and make it less stable. These effects of the med are acknowledged by NHS UK and are listed on their website. Apparently it seems to lower blood sodium levels too.Absolutely. The confounding factors are quite tricky to account for sometimes, though. E.g. I can’t think of a way to account for sensor and CGM tolerable error except for statistically and that would require more data than I have or have the capacity to collect. I do know that both the CGM and finger pricks collaborated each other in this single test. I do plan on going back to the higher dose so there is a chance there to at least reproduce the result (or not). The only reason I ‘rushed’ to get back down to the lower dose is that I was doing field work that week and needed to be able to drive; with blurry vision and sustained high readings I didn’t feel comfortable driving. Now that I’m back working at home the blurry vision, even if it lasts awhile, isn’t so much of an issue (blurry in the distance, not close so it doesn’t effect my computer work, just driving). I have an appointment with the GP on Friday and will be telling him I’ll be doing some more tests. When I spoke to him last he said it (unstable BSL) wasn’t a known side effect for mirtazipine but I can find studies on Google Scholar saying different. I haven’t had time to properly read and assess the studies yet, though. Even if it turns out that they’re low quality studies, or studies not done on humans doesn’t mean that it doesn’t effect me in that way or it’s a very rare side effect. Or maybe it was all just coincidence
I had a complete eye examination in December 2022 and was on the 30mg of mirtazipine (not 45mg though)… have been on in for over 10 years. That’s interesting regarding the blood sodium levels as wellOne of the sude effets of the Mirtazipine is increas
One of the reported side effects of Mirtazapine is increased pressure in the eyeball. similar to Glaucoma. Have you had a glaucoma test since starting this med? That may explain the visual problems. it does seem that the med can interefere with diabetes blood sugar control and make it less stable. These effects of the med are acknowledged by NHS UK and are listed on their website. Apparently it seems to lower blood sodium levels too.
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