Sarcoidosis and Splenomegalic polycythemia - from FDA reports
There is no Splenomegalic Polycythemia reported by people with Sarcoidosis yet. We study people who have Splenomegalic Polycythemia and Sarcoidosis from FDA . Find out below who they are, other conditions they have and drugs they take.
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On Oct, 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 Splenomegalic polycythemia and Sarcoidosis?
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Expand the study to include reports from both FDA and eHealthMeSplenomegalic polycythemia and Sarcoidosis from FDA and eHealthMe reports
Sarcoidosis (an inflammatory disease that affects multiple organs in the body, but mostly the lungs and lymph glands) can be treated by Prednisone, Prednisolone, Methotrexate, Methotrexate sodium, Plaquenil (latest reports from 5,368 Sarcoidosis patients)
Splenomegalic polycythemia (a condition in which there is excessive production of red blood cells due to enlarged spleen) has been reported by people with idiopathic thrombocytopenic purpura, high blood pressure, osteoporosis, rheumatoid arthritis, depression (latest reports from 939 Splenomegalic polycythemia patients).
Browse all symptoms of Sarcoidosisa 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 Splenomegalic polycythemiaSplenomegalic polycythemia
Other conditions that could case Splenomegalic polycythemiaSplenomegalic polycythemia
What would happen?
Can you answer these questions?
I understand Natto can thin the blood to prevent stroke. However, I have polycythemia vera with a high platelet count. Since Natto has a lot of K2 and iron in it which I believe might increase the platelet count, does that mean that eating natto might not be good for people with polycythemia ...
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Hi,im Peter Pinili from Philippines i am newly diagnosed with polycythemia vera and i have psoriasis more than 40years. I like to join the group to know about the disease and how to deal with my condition. I hope i could find solution with my problems.
My husband has both PV and AS, I would like for us to join a support group for those who have both. He hasn't found where there are too many if any who have both PV and AS, so I thought it would be helpful to get other comments of those who have both. Thank you, Amanda
Hi! I am female, born 1956 in UK, live in Canada. I just had left and right hip replacements due to ankylosing spondylitis. I just got diagnosed with neurosarcoidosis. Anybody in a similar situation? Any suggestions, advice?