Smell - impaired is reported only by a few people who take Cortisone Acetate. We study 4,513 people who have side effects while taking Cortisone acetate from FDA and social media. Among them, 2 have Smell - impaired. Find out below who they are, when they have Smell - impaired and more.
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Cortisone acetate has active ingredients of cortisone acetate. It is often used in rheumatoid arthritis. (latest outcomes from Cortisone acetate 4,657 users)
Smell - impaired has been reported by people with ageusia, colostomy, nasopharyngitis, hyposmia, memory loss (latest reports from 6,722 Smell - impaired patients).
On Jul, 20, 2016
4,513 people reported to have side effects when taking Cortisone Acetate.
Among them, 2 people (0.04%) have Smell - Impaired
* Approximation only. Some reports may have incomplete information.
** Reports from social media are used.
How to use the study: print a copy of the study and bring it to your health teams to ensure drug risks and benefits are fully discussed and understood.
I have rheumatoid arthritis and have been on methotrexate for many years. I got a cortisone shot in my ankle joint and about 4 days later a red raised itchy & painful patch at the injection site. Looked like shingles that I have about 10 years ago. After some online research, I found that this happened to 36 out of over 5,000 RA patients on methotrexate (also with anemia). Guess I'm one of the 36. I'm watching it to make sure it doesn't spread and the Dr. told me to take benedryl. Has this happened to any of you and did it spread and how was yours treated. Thank you.
This is for my father. Shortly after starting methotrexate injections and cortisone for Rheumatoid arthritis my father started having language difficulties and now has dementia. He was diagnosed with Pick's disease. Could it be caused by these drugs? He is still taking them.
I have completely lost my sense of smell due to taking Zoloft. I have not taken it now for at least 3 months and still my sense of smell has not returned. I was wondering if anyone's sense of smell has returned, and how did it come back? I very much miss my sense of smell!
Recently dx with degenerative hip and given cortisone injection. Rheumatologist then said something about Crestor which I have been taking for yrs. he ordered blood tests and referred me back to pcp whom Iwill c tomorrow. What to ask pcp re interaction of meds?
Second day on Losartan, I got a sensation like toothpicks in my throat, which gave me a dry, hacking cough. Quit taking Losartan on day 5, but cough continues. By day 9, cough was moving to my chest. Today, on day 11, I've lost my sense of smell and sense of taste. Has anybody else had these ...
I have rheumatoid arthritis and have been on methotrexate for many years. I got a cortisone shot in my ankle joint and about 4 days later a red raised itchy & painful patch at the injection site. Looked like shingles that I have about 10 years ago. After some online research, I found that this ...
Hi: I'm a 58 y/o pt with dx of SLE,RA, SJOGRENS. I have been with a RA ans Sjogrens flare up for 2 1/2 yrs and in Rituxan for 1 1/2 yrs. Notice I have Anosmi since 5 months ago. I went to ENT and had a ct and they found nothing. Hope to read about this. Regards from S Florida, US
Hi, I am apparently not able to tolerate albuterol well; since using it a few times recently (for an asthma attack), I have totally lost my sense of smell. Sheesh... hoping to hear from you if this will correct itself. I'm self-employed & a grandma.
Hi, my name is Sheila, For starts l'm a chronic sinus suffer. In my middle 20's l had to have my sinuses drained. Which l feel now was a bad mistake. I'm now in my mid 60's and have been using nasal spray off and on. More on than off. About four years ago l had a pretty bad sinus infection and ...
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