I noticed my GP surgery have taken my prednisolone off my repeat medication list “because I’m supposed to be reducing it and it’s an acute drug “. I feel extremely vulnerable now as I’ve been on it for 15 years on top of all my other Lupus meds and obviously would have an adrenal crisis if it was stopped. It feels unsafe that it’s not listed as a repeat if anyone needed to check my list of meds in an acute situation. Does anyone know if there’s a new policy about it, or, alternatively, any guidelines saying this shouldn’t be done? I’m planning to tackle the practice pharmacist.
Prednisolone taken off repeats; “it’s an acute dr... - LUPUS UK
Prednisolone taken off repeats; “it’s an acute drug”, despite dose greater than 7.5mg for over 10 years
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BTW I was told by the medication team I would always be given it when I asked for more but as an acute drug .
But we who need it as a chronic drug CAN'T be told it is "an acute drug", But you are right - we are coming across this a great deal on the PMRGCAuk forum.
It really is concerning.
Worrying - thanks for letting me know I’m not alone, PMRpro. Has anyone tackled the issue in a particularly effective way?
We tell people to demand an audience with the practice manager and make a complaint. Though when they have spoken to the DOCTOR, the silliness has been overruled so far. Many practices are undergoing reviews by a pharmacist - who you would think was aware of adrenal insufficiency secondary to long term steroid use. But they probably DON'T study the back notes for all patients and possibly aren't aware that we aren't tapering relentlessly to zero but titrating the dose to find the lowest effective dose. What bothers me most is that a lot of patients are unaware of the risk of suddenly stopping steroids and may accept what they are told. Of course - a flood of adrenal crisis patients and even deaths might knock some sense into them ... As long as it isn't me or you ...
Same happened to me only last week. I just noticed by chance that it had been removed from my repeats. I’ve been on prednisone for 42 years. Unfortunately them days once you were put on them that was it. Now days I have to increase mine when I am having a flare then go back down to my base. I’m also on azathioprine to try and keep the preds low.
I was assured it wasn’t cut backs but feel it was. Fortunately it was reinstated shortly after without a reason as to why it was taken off in first place. If they’d only realised we don’t want to be on them but don’t have a choice 😟
HI have you spoke to your GP about your concerns and what the plan is going to be going forward?
EULAR recommendations are to eliminate it as a daily drug. Obviously the 7.5 mg needs to be tapered. You can get it in 1 mg tablets and taper i. Talk with your doctor about that.
If you are only taking hydroxychloroquine and you need the prednisone (for arthritis?) than you need to add a DMARD (methotrexate is one) as well as folic acid if it’s methotrexate that is added.