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 Aug, 21, 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.
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Do you have Atelectasis and Scleroderma?
Expand the study to include reports from both FDA and eHealthMeAtelectasis and Scleroderma from FDA and eHealthMe reports
Scleroderma (hard skin) can be treated by Cellcept, Plaquenil, Hydroxychloroquine sulfate, Methotrexate sodium, Diltiazem hydrochloride (latest reports from 6,531 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 12,496 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
What would happen?
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.
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I feel like I'm crying fiber optic pollen hairs! Am i the first to be pestered with the INEVITABLE porous EXPULSION OF EYE DISCHARGE. I know life's much more easy When We Pick Our Own Battles; but SERIOUSLY.
Hi there. I have had systemic scleroderma for nearly 20 years. Last week, I was diagnosed with an aortic aneurysm and atherosclerosis. I am only 55 coming down with something that usually occurs in the over 65 set. I have been searching for any information regarding the effects of my ...
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 ...