Review: could Fluocinonide cause Nail candida?
Summary: Nail candida is reported only by a few people who take Fluocinonide.
We study 729 people who have side effects while taking Fluocinonide from FDA and social media. Find out below who they are, when they have Nail candida and more.
You are not alone: join a mobile support group for people who take Fluocinonide and have Nail candida >>>
Fluocinonide has active ingredients of fluocinonide. It is often used in eczema. (latest outcomes from 741 Fluocinonide users)
Nail candida (fungal infection of nail) has been reported by people with dermatitis allergic, rheumatoid arthritis, secondary progressive multiple sclerosis, cellulitis. (latest reports from 17 Nail candida patients)
On Jan, 25, 2015: 729 people reported to have side effects when taking Fluocinonide. Among them, 1 people (0.14%) has Nail Candida.
Time on Fluocinonide when people have Nail candida * :
Gender of people who have Nail candida when taking Fluocinonide * :
|Nail candida||100.00%||0.00% |
Age of people who have Nail candida when taking Fluocinonide * :
Severity of Nail candida when taking Fluocinonide ** :
How people recovered from Nail candida ** :
Top conditions involved for these people * :n/a
Top co-used drugs for these people * :n/a
* 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 Nail Candida while taking Fluocinonide?
You are not alone! Join a mobile support group:
- support group for people who take Fluocinonide and have Nail Candida
- support group for people who take Fluocinonide
- support group for people who have Nail Candida
Drugs in real world that are associated with:
Could your condition cause:
More questions for: Fluocinonide, Nail candida
More reviews for: Fluocinonide, Nail candida
Comments from related studies:
From this study (11 months ago):
Been taking Vasotec since Dec 2013. !st noticed tongue burning after eating salty foods like popcorn and crackers. I stopped eating those foods. Now in March tongue is burning all the time even not eating salty foods.
I took Accupril for 20 years with no problems but the VA does not carry Accupril so they put me on Vasotec and I think it may be causing the burning tongue.
From this study (1 year ago):
Healed joint and soft tissue injuries (PID) return with increased pain and swelling. Pressure changes with position. Frequency and intensity of migraines increased with pressure symptoms. Genetic connective tissue disorder - Ehler Danlos Syndrome. Cardiac arrhythmia. History of rheumatic fever, pneumothorax, whooping cough, and severe allergic reactions.
From this study (2 years ago):
I have taken Zyrtec and citalopram for more than a year with no side-effects. After 1 cycle of prednisone, I had moderate insomnia and minor confusion and short-term memory loss. After the second cycle of prednison, and the addition of tramadol, fluocinonide, antivert, and ondansetron, the short term memory loss, insomnia, and confusion were markedly worse (severe).
Post a new comment OR Read more comments
NOTE: The study is based on active ingredients and brand name. Other drugs that have the same active ingredients (e.g. generic drugs) are NOT considered.
WARNING: Please DO NOT STOP MEDICATIONS without first consulting a physician since doing so could be hazardous to your health.
DISCLAIMER: All material available on eHealthMe.com is for informational purposes only, and is not a substitute for medical advice, diagnosis, or treatment provided by a qualified healthcare provider. All information is observation-only, and has not been supported by scientific studies or clinical trials unless otherwise stated. Different individuals may respond to medication in different ways. Every effort has been made to ensure that all information is accurate, up-to-date, and complete, but no guarantee is made to that effect. The use of the eHealthMe site and its content is at your own risk.
You may report adverse side effects to the FDA at http://www.fda.gov/medwatch/ or 1-800-FDA-1088 (1-800-332-1088).
If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.