Kevzara and Prednisone Tapering before and during Kevzara
I recently stated with Kevzara and I am interested in those who are currently on prednisone and Kevzara.
I would like to know...
1. What was your starting dosage of prednisone and how long have your been taking prednisone?
2. What was your daily dose of prednisone before Kevzara?
3. What was your prednisone tapering schedule before starting Kevzara?
4. What was your lowest dosage of prednisone before Kevzara and did you have difficulty dropping below that dose?
5. What is your tapering schedule now that you are on Kevzara?
6. How successful has this schedule been so far and have you had any flare ups?
7. What is your target date for stopping prednisone?
8. What changes have you noticed in your health, aches and energy level since starting Kevzara?
Please feel free to add any more information that might be helpful to those contemplating starting Kevzara or those currently on Kevzara
Thanks
Mike
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I have taken prednisone and methotrexate for 2.5 years and my disease appears to be chronic. My rheumatologist has mentioned Kevzara as an option and I am tired of the side effects of my present drugs. I am on Medicare A, B and D ( Aetna Silverscript for the D). I went on Medicare.gov and entered Kevzara as a medication that I take. Their calculation recommended staying on Silverscript and the monthly cost for Kevzara would be $280. Has anyone found a way to reduce this cost? The drug company offers co-pay assistance but I am not sure if people on straight Medicare and part D are eligible. Kevzara is not available as an infusion which would have better coverage.
Hi again, I am retired military and so I have Medicare and Tricare for Life. The copay for 4 doses (2 months) just went to $76 from $68. I am very fortunate in that regard. I think the manufacture Sanofi/Regeneron has a program to help with the copay. Could I suggest contacting them?
Best,John
Darcie, it is just wrong that because Kevzara is self administered as opposed to an infusion that D England and others are being held up by these 3d party plan managers. I would think that not having a provider administer a drug and not have to pay for an office visit would be a no brainer for the insurance companies.
I meant Dad Cue. Hate autocorrect
I am about to start Kevzara but would not have been able to since the cost to me would have been close to $2k every 28 days. I applied for patient assistance through the drug company and will be receiving the med at no cost to me. I am on Medicare and a good supplemental plan but the coverage was not good enough to pay for all of it. The process is fairly simple and it’s done through their website. I hope this helps you and that you are able to stay with the treatment especially since it seems to be working for you.
Nobody asked me when they crafted Medicare rules. I agree with you that it makes no sense.
The VA could have denied my rheumatologist’s request for Actemra since I wasn’t diagnosed with GCA. Actemra isn’t FDA approved for PMR.
The VA doesn’t have to abide by Medicare rules thankfully.
You can call me Mike if you wish.
I am not on Medicare. I have BCBS with Optum RX for my prescriptions. Kevzara is running about 4000 a month. My insurance covers about 2400/month with Kevzara covering about 1600/mo.
Just ridiculous that the Pharma can charge that much for a FDA approved drug. It is a 1cc injection every 2 weeks.
Just be careful-I assume you have the copay card? They pd for mine Oct, Nov, Jan but not December. I owe my pharmacy $1600. I am working with both but may I suggest to you that you call Kevzara monthly to check on your status so you don’t end up with a large bill like I have for reasons unknown. They are working on it.
They should. Check their website.
I do not have a co-pay card since I do not get it through my pharmacy. I have been approved for the drug through KevzaraConnect. They ship the medication to me every month. I will have to be re-approved again at the end of 2024. I pray I won’t need to take this drug beyond that. I haven’t even started this medication so I don’t even know if it will work for me.