Comments on: Prednisone, Corticosteroids, and Lupus https://lupuscorner.com/prednisone-corticosteroids-and-lupus/ Health Info on Lupus Symptoms, Treatments & Research Sat, 18 Jul 2020 15:52:08 +0000 hourly 1 https://wordpress.org/?v=6.2.4 By: GG https://lupuscorner.com/prednisone-corticosteroids-and-lupus/#comment-33533 Sat, 18 Jul 2020 15:52:08 +0000 https://lupuscorner.com/?p=4515#comment-33533 FYI, my health insurance company put a requirement on all of their members to have authorization form from their doctor completed before they would pay for plaquinil. I called them as I already had an authorization months earlier because I’m allergic to talc and have to take the name brand drug, generic stopped making it years ago. If your insurance all of the sudden is denying a refill or prescription, call the insurance company ASAP.

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By: Cynthia R Tiniakos https://lupuscorner.com/prednisone-corticosteroids-and-lupus/#comment-33532 Sat, 18 Jul 2020 15:48:45 +0000 https://lupuscorner.com/?p=4515#comment-33532 I do not see a comment regarding the prednisone side effect that affected me. I developed Avascular Necrosis in my hips due to prednisone use for my Lupus. I had to have both hips replaced after they disintegrated due to blood flow loss

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By: Donna Osborne https://lupuscorner.com/prednisone-corticosteroids-and-lupus/#comment-31130 Sat, 04 Apr 2020 03:28:44 +0000 https://lupuscorner.com/?p=4515#comment-31130 My pharmacist had to use a work around to fill my plaquenil for 30 days. My insurance only wanted to fill for 14 days due to the COVID. They cannot do a 90 day fill at this time, and the doctor has to provide a diagnosis code, and no refills are authorized. Concerning steroids, they are a last resort for me, but if my pleurisy gets bad with a flare, then I will take it with a taper dose. It usually does the trick.

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By: Natasha Lyn Lehndorf https://lupuscorner.com/prednisone-corticosteroids-and-lupus/#comment-30954 Wed, 25 Mar 2020 21:53:53 +0000 https://lupuscorner.com/?p=4515#comment-30954 In reply to Cindy Dailey.

I too take Plaquenil for Lupus (SLE) and RA. I’ve received quite a bit of information from different places stating they are trying to prioritize the medication goes without delays for patients like us. One idea I have, which is what I did, is to ask the doctor for a 90 day supply ( 180 if given 2x daily) and get it refilled at any pharmacy.

https://www.hss.edu/conditions_hydroxychloroquine-plaquenil-chloroquine-shortage-covid-19-coronavirus.asp
^This article above mentioned: “- if your pharmacy can’t fill your prescription, you’re safe for at least several weeks or longer. If you can, get advance prescriptions now in case the drug does become hard to get later. Most patients can miss doses for a few weeks without developing a disease flare, so long as they can restart it again when the drug is available. “

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By: Cindy Dailey https://lupuscorner.com/prednisone-corticosteroids-and-lupus/#comment-30923 Tue, 24 Mar 2020 16:08:52 +0000 https://lupuscorner.com/?p=4515#comment-30923 my daughter takes plaquinel for her mixed connective tissue disease/lupus and associated related issues. She was able to get only a 1 month supply of her meds and told by the pharmacist that it may not be available 30 days from now. What are these people who need and have been on this medication for years supposed to do to make sure they can get their medications

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