Is it safe to get the Corona Virus (COVID-19) vaccine with PMR?

Posted by ncgal @ncgal, Nov 19, 2020

Just wondering if anyone has found out if it is okay to get the corona virus vaccine once it comes out. I'm 78, so past the 65+ age for early vaccinations, plus having the autoimmune diagnosis. I don't see my rheumatologist for another two months but guess I'll call him to find out if t comes to that. Just thought I'd see if anyone else has found out. I had no problem with the flu shot.

Interested in more discussions like this? Go to the Polymyalgia Rheumatica (PMR) Support Group.

@margaretva

Hi - I was diagnosed with PMR late last summer at age 58. Story similar to that of many here - took a while to diagnose, but prednisone took care of pain almost immediately. I started at 15 -20 mg and am now down to 6 - 6.5. I have been reading posts here since my husband found this group a month or so ago. Thank you all so much! It has really helped to know I am not alone. I am also going even more slowly on reducing pred thanks to the posts here.Ask rheum. today for 1 mg pred and he complied. I also am on methotrexate - rheumatol. is not sure it's helping, so he wants to start me on Humira - AFTER I have had my COVID shots. I am scheduled for 1st Moderna Wed. (April 7). Saw Rheumy to day - he said continue pred, but skip methotrexate the week of each COVID vaccine (I take it once a week). Re flu shot - I felt sick after the first one I took over 20 years ago and had not taken one since. Still got PMR. Rheumatol wanted me to take one this year - I did, with no problems. So thanks again for your shares, I'll keep you posted on how the COVID vaccines go.

Jump to this post

Hello @margaretva, Welcome to Mayo Clinic Connect. It's good to hear that you asked your rheumatologist for 1 mg prednisone tablets as it makes it easier to taper slower. You might want to ask for 2.5 mg prednisone tablets also as it makes it a little easier tapering until you get to the lower doses. Towards the end of my first round with PMR I found a good pill splitter and was splitting the 1 mg tablets going back and forth between 1 mg and 1/2 mg until I was finally able to stop taking prednisone and only have some minor aches in the morning.

You may find a few other discussions helpful also:
- Polymyalgia Rheumatica (PMR): Meet others & Share Your Story: https://connect.mayoclinic.org/discussion/polymyalgia-rheumatica-pmr-meet-others-share-your-story/
- PMR Anyone?: https://connect.mayoclinic.org/discussion/pmr-anyone/
- Resources / Polymyalgia Rheumatica (PMR): https://connect.mayoclinic.org/group/polymyalgia-rheumatica-pmr/
- Rheumatoid arthritis questions: https://connect.mayoclinic.org/discussion/rheumatoid-arthritis-questions/

You mentioned your rheumatologist also has you on methotrexate and is not sure it's helping so wants to start you on Humira. Do they think you also may have rheumatoid arthritis in addition to PMR?

REPLY
@johnbishop

Hello @margaretva, Welcome to Mayo Clinic Connect. It's good to hear that you asked your rheumatologist for 1 mg prednisone tablets as it makes it easier to taper slower. You might want to ask for 2.5 mg prednisone tablets also as it makes it a little easier tapering until you get to the lower doses. Towards the end of my first round with PMR I found a good pill splitter and was splitting the 1 mg tablets going back and forth between 1 mg and 1/2 mg until I was finally able to stop taking prednisone and only have some minor aches in the morning.

You may find a few other discussions helpful also:
- Polymyalgia Rheumatica (PMR): Meet others & Share Your Story: https://connect.mayoclinic.org/discussion/polymyalgia-rheumatica-pmr-meet-others-share-your-story/
- PMR Anyone?: https://connect.mayoclinic.org/discussion/pmr-anyone/
- Resources / Polymyalgia Rheumatica (PMR): https://connect.mayoclinic.org/group/polymyalgia-rheumatica-pmr/
- Rheumatoid arthritis questions: https://connect.mayoclinic.org/discussion/rheumatoid-arthritis-questions/

You mentioned your rheumatologist also has you on methotrexate and is not sure it's helping so wants to start you on Humira. Do they think you also may have rheumatoid arthritis in addition to PMR?

Jump to this post

Thanks for all your help as mentor, John. I have read all of the PMR threads on this site. COVID vaccine went fine. No ill effects - my arm would have been sore but for the 6 mg prednisone, I suspect. In answer to your question, my rheum has always felt I was too young for PMR, and says there's so much cross over with non-serol. RA that Humira is worth a try. I was happy last summer when my blood tests were negative for rheumatoid factor, but apparently that is not as good news as I thought at first! Thanks again

REPLY

I got my second Moderna shot 2 days ago. Was on 4-5 mg prednisone for both shots. No symptoms the first time. The second dose I had flu-like aches about 6 hours after the shot, but with 100mg ibuprophen I felt better.

REPLY

I had my Astra Zeneca vaccination yesterday evening and so far 24 hours down the track absolutely no side effects. Unfortunately my wife (has CLL) didn’t fare so well. Very sore arm, headache, couldn’t sleep last night and heart palpitations. The palpitations are subsiding now though but headache persists. Second dose in three months.

REPLY

Hi everyone. I was just diagnosed with PMR after 11wks of lumbar then hip, knee & eventual shoulder pain, stiffness & loss of range of motion. My symptoms occurred 2 days after my 2nd Pfizer COVID-19 Vaccine. I developed a 101.3 temp within 12 hrs. I was bedridden for 13 hrs and woke up feeling much better but had bilateral lumbar pain. Symptoms progressed to other body parts within 2 wks. R/O spine problems with negative MRI. C-Reactive Protein, Anemia & “text book” symptoms confirmed diagnosis. Started Prednisone 20mg and starting to definitely feel better. Wondering if anyone else developed this after the vaccines immune response? BTW I think the vaccine is a miracle and don’t want to cause any vaccine hesitation. This syndrome can occur after a flu or any vaccine.

REPLY

its very frustrating to hear one doctor tell me he does not think I have PMR and another tells me I do . I am taking Advil every day and do not get relief from the pain until early afternoon, I have also noticed my eyes become very sore. I have been resistant to go back on the prendnisone

REPLY
@cara7

its very frustrating to hear one doctor tell me he does not think I have PMR and another tells me I do . I am taking Advil every day and do not get relief from the pain until early afternoon, I have also noticed my eyes become very sore. I have been resistant to go back on the prendnisone

Jump to this post

Hello @cara7 and @marymv, Welcome to Mayo Clinic Connect, a welcoming online community where patients and caregivers share their experiences, find support and exchange information with others. You might want to join the following discussion and meet other members with PMR and learn what they have shared.

Polymyalgia Rheumatica (PMR): Meet others & Share Your Story: https://connect.mayoclinic.org/discussion/polymyalgia-rheumatica-pmr-meet-others-share-your-story/

PMR can difficult to diagnose. Here's some more information on PMR you might find helpful - Polymyalgia rheumatica - Diagnosis and treatment - Mayo Clinic: https://www.mayoclinic.org/diseases-conditions/polymyalgia-rheumatica/diagnosis-treatment/drc-20376545

@cara7 Have you seen a rheumatologist or thought about getting another opinion?
@marymv My PMR is currently in remission but the only bad side effect I had was the second day after my 2nd Pfizer shot. I had extreme fatigue that lasted all day.

REPLY
@johnbishop

Hello @cara7 and @marymv, Welcome to Mayo Clinic Connect, a welcoming online community where patients and caregivers share their experiences, find support and exchange information with others. You might want to join the following discussion and meet other members with PMR and learn what they have shared.

Polymyalgia Rheumatica (PMR): Meet others & Share Your Story: https://connect.mayoclinic.org/discussion/polymyalgia-rheumatica-pmr-meet-others-share-your-story/

PMR can difficult to diagnose. Here's some more information on PMR you might find helpful - Polymyalgia rheumatica - Diagnosis and treatment - Mayo Clinic: https://www.mayoclinic.org/diseases-conditions/polymyalgia-rheumatica/diagnosis-treatment/drc-20376545

@cara7 Have you seen a rheumatologist or thought about getting another opinion?
@marymv My PMR is currently in remission but the only bad side effect I had was the second day after my 2nd Pfizer shot. I had extreme fatigue that lasted all day.

Jump to this post

Thank you!

REPLY

Hi, i am a physician, internal medicine
,,3 and 4 years ago i got PMR about month after flu vaccine, ,,elevated sed rate,,normall C reactive protein
,,,Rhematologist put me on prednisone taper and slowly got better in about 2 to 3 months
,,for last 2 years i got flu vaccine without get PMR
,,however, i got Pfizer covid vaccines 1/21 and about 6 weeks later got what i am pretty sure was severe flare PMR in my right hip,,buttock with pain,,and best described weakness or "wobbly legs",,i could not walk without pain or jog
,,i started prednisone taper and about 3 weeks seem to be better now,
,,there is not much literature on PMR being triggered by vaccines,,,but sure seems in my case to be the culprit,
,,

REPLY
@marymv

Hi everyone. I was just diagnosed with PMR after 11wks of lumbar then hip, knee & eventual shoulder pain, stiffness & loss of range of motion. My symptoms occurred 2 days after my 2nd Pfizer COVID-19 Vaccine. I developed a 101.3 temp within 12 hrs. I was bedridden for 13 hrs and woke up feeling much better but had bilateral lumbar pain. Symptoms progressed to other body parts within 2 wks. R/O spine problems with negative MRI. C-Reactive Protein, Anemia & “text book” symptoms confirmed diagnosis. Started Prednisone 20mg and starting to definitely feel better. Wondering if anyone else developed this after the vaccines immune response? BTW I think the vaccine is a miracle and don’t want to cause any vaccine hesitation. This syndrome can occur after a flu or any vaccine.

Jump to this post

hi, see my comment above

REPLY
Please sign in or register to post a reply.