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Review: could Cortisone acetate cause Smell - impaired?

Summary: Smell - impaired is reported only by a few people who take Cortisone acetate.

We study 3,299 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.

You are not alone: join a mobile support group for people who take Cortisone acetate and have Smell - impaired >>>

 

 

 

 

Cortisone acetate

Cortisone acetate has active ingredients of cortisone acetate. It is often used in pain. (latest outcomes from 3,398 Cortisone acetate users)

Smell - impaired

Smell - impaired has been reported by people with nasopharyngitis, high blood pressure, sinusitis, nasal congestion, asthma. (latest reports from 6,768 Smell - impaired patients)

On Feb, 27, 2015: 3,299 people reported to have side effects when taking Cortisone acetate. Among them, 2 people (0.06%) have Smell - Impaired.

Trend of Smell - impaired in Cortisone acetate reports

Time on Cortisone acetate when people have Smell - impaired * :

n/a

Gender of people who have Smell - impaired when taking Cortisone acetate * :

FemaleMale
Smell - impaired100.00%0.00%

Age of people who have Smell - impaired when taking Cortisone acetate * :

0-12-910-1920-2930-3940-4950-5960+
Smell - impaired0.00%0.00%0.00%0.00%0.00%0.00%0.00%100.00%

Severity of Smell - impaired when taking Cortisone acetate ** :

n/a

How people recovered from Smell - impaired ** :

n/a

Top conditions involved for these people * :

n/a

Top co-used drugs for these people * :

  1. Allopurinol (2 people, 100.00%)
  2. Rocaltrol (2 people, 100.00%)
  3. Esidrix (2 people, 100.00%)
  4. Diflucan (2 people, 100.00%)
  5. Lasix (2 people, 100.00%)

* 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.

Do you have Smell - Impaired while taking Cortisone Acetate?

You are not alone! Join a mobile support group:
- support group for people who take Cortisone acetate and have Smell - Impaired
- support group for people who take Cortisone acetate
- support group for people who have Smell - Impaired

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More questions for: Cortisone acetate, Smell - impaired

You may be interested at these reviews (Write a review):

  • Farxiga ? problems, stomach, smell, taste
    I have been on Farxiga for 2 months. First, I was on Farxiga 5mg, About 6 weeks ago changed to 10 mg, about same time I noticed my coffee smelled different and bad, kept on a week and asked my wife. Changed coffee brand twice. It got worse, began to taste it. For the last week I can smell it in my food, anything fresh out of microwave. Now I smell it in my bowel movement. I called Doctor earlier in week reported. He wants to wait about a week and call back if persists. I am a diabetic and first few days this helped. Doctor reduced my insulin and got me off glimepiride and my Sugar readings have been higher since such as 175-200. This is my only medicine change close to time period. Please respond with help or if you experience similar problems.
  • Traumatic anosmia, i cry every morning, still... (1 response)
    I have had 4 major surgeries including a radical craniotomy at which point I lost my sense of smell completely. I still come to tears each morning even when I am happy. It feels like my body has lost a very close friend and is reminded as soon as it wakes up with every breath I take through my nose, my body returns to mourning this great loss.

    I had hoped that over the past decade the tears would ease up and in some ways they have a little but it has taken a very long. I am 41, I lost my sense of smell at 26 years of age.



    I cannot quite put into words the great and unavoidable sadness I go through upon waking up; and the fact that I will never know what my man smells like, or my future niece or nephew, my GrandMother's house or mine.



    On several occasions I could not smell burning food on the stove or smoke in the house or when my hair caught on fire accidentally.

    It is my wish that one day, they may be able to transplant some olfactory ganglia and perhaps, some sense of smell will return.



    The emotional depression involved with this has been and will continue to be a significant part of my life. The body knows it has lost something great and no matter what I"m feeling like, upon awakening, it hits me, takes me and I become a sad wreck of tears.

    I feel for anyone else out there that goes through this and hope one day, we may smell the roses and anything else, again.

More reviews for: Cortisone acetate, Smell - impaired

Comments from related studies:

  • From this study (5 days ago):

  • Took Tamiflu for Type A Flu on January 21, 2015. Took two days of 5 days RX, made me sick to my stomach, stopped taking. Even since then, I have no sense of smell or taste.

    Reply

  • From this study (2 weeks ago):

  • after taking zicam my sense of smell has gone, my sister also has the symptoms and she has a brain tumor... I am going to get my head checked...

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  • From this study (1 month ago):

  • I have had 2 medial meniscus repair surgeries. over the past 7 years. I have needed cortisone injections faithfully at leas every 3 months or sooner. I am now experiencing knee pain and severe calf pain but am not due for an injection for another month.

    Reply

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