I very reluctantly started on prednisone and then found myself on it for longer than I wanted because another doctor had to run some tests to determine if I needed to triple my dose for some nerve pain. That was a two-month extension. I was at 10mg. I am now down to 3 mg and have never had break thru pain at night. I do take my prednisone after breakfast and before lunch. I have always taken it all at the same time. I wonder if my dosage timing has anything to do with not having break thru pain.
The half-life of prednisone is 3-4 hours. Meaning that half of it is out of your system in that time, then half of what remains is out of your system in another 3-4 hours. At the end of 8 hours you have approximately 25% of the dosage remaining. I use drugs.com as my subject matter expert resource.
I am experiencing fatigue daily but I discovered that prednisone can mess with your body's ability to convert T4 to T3 - these are the thyroid factors. Low T3, which is what I currently have, is hypothyroidism and one symptom is fatigue. My Endocrinologist is not treating it due the timeline to treat it is months and by then I will be off the prednisone. We will see it my body can recover on it's own. If not she will address it.
I am getting a bone scan this year to see how the prednisone robbed my bones. I am going to PT now to help rebuild some muscle strength I lost due to atrophy from my greatly reduced activity level due to PMR systemic pain.
Prednisone is not always your friend. It can be very naughty.
Just thought I would share in case it helps anyone.
Thank you. I have been on Prednisone for about a month, awaiting my appointment with a Rheumatologist.
I sort of figured out how to dose on my own (and with help from this forum and the internet). My doctor wanted me to take 30mg every other day. That left me in agony in the wee hours before my dose. I decided to take 10mg one day and 20 the next. Much better pain control. It's not quite enough though.
I understand why he dosed like that, my body would have a chance to produce its own cortisol.
Hoping the Rheumatologist figures out what I need RIGHT now. I'll worry about weaning off when the time comes.
I think I'll split the dose like you do. I need it to last longer.
Hoping this will pass for you soon.