Scleroderma and Atelectasis - from FDA reports
There is no Atelectasis reported by people with Scleroderma yet. We study people who have Atelectasis and Scleroderma from FDA. Find out below who they are, other conditions they have and drugs they take.
What to expect?
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On eHealthMe you can find out what patients like me (same gender, age) reported their drugs and conditions on FDA since 1977. Our tools are simple to use, anonymous and free. Start now >>>
On Mar, 27, 2017
No report is found.
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 Atelectasis and Scleroderma?
Scleroderma (hard skin) can be treated by Cellcept, Plaquenil, Hydroxychloroquine sulfate, Diltiazem hydrochloride, Methotrexate sodium (latest reports from 6,015 Scleroderma patients)
Atelectasis (partial or complete collapse of the lung) has been reported by people with multiple myeloma, osteoporosis, high blood pressure, pain, depression (latest reports from 12,169 Atelectasis patients).
Browse all symptoms of Sclerodermaa b c d e f g h i j k l m n o p q r s t u v w x y z
Could your drugs cause AtelectasisAtelectasis
Other conditions that could case AtelectasisAtelectasis
Can you answer these questions?
My osteopenia has gotten much worse and I am at risk for osteoperosis in my hips. I am 54 and have had scleroderma for 12 years. It is suggested that I take Evista. My question is, am I at risk for kick-starting the progression of my scleroderma by taking this drug?
Has anyone gained mobility with physical therapy? I have systemic diffused scleroderma & have contractures in shoulders, elbows & hands. I'm stating physical therapy this week. I cannot dress myself or anything else & hoping for relief.
I have Limited Scleroderma. My condition is worsening so I was put on Cellcept and I use Marijuana for my breakthrough pain as opposed to the prescribed Percocet. I just started taking the Cellcept today.Does anyone know of any kind of side effects this two drugs may cause together? I do take ...
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Hello, I'm 40 and was diagnosed with limited Scleroderma about 18 months ago. I suffer joint pain and cold hands/feet. I don't want to take chemo and turned that avenue of help down. Does anyone here have any leads to non-chemical help for joint pain?
I am a 28y.o. female diagnosed with Mixed Connective Tissue Disease. Right now, the myositis is in remission and my disease is 30% SLE and 70% Scleroderma. I came across some literature that discussed the use of oxandrolone in patients who had been on long term corticosteroid use. I had been on ...
Hello, my name is Alexandra and I've been struggling for four years now with different symptom and pain sometimes daily. I have not been diagnosed yet, I have been getting different opinions, finally got an appointment to see a neurologist. I just want to join the group and hear what others say ...