Hemoglobin is important because it lets your red blood cells carry oxygen to all parts of your body. There are also steps you can take to stay as healthy as possible. If you are pregnant or trying to have a baby, there are tests that can be done before birth to learn if the baby will have the condition. Thalassemia is really a group of blood problems, not just one. If you do have thalassemia, you should see a blood expert known as a hematologist. Hydroxychloroquine us brand name Plaquenil vision changes Oregano oil and plaquenil How is thalassemia treated? The type of treatment a person receives depends on how severe the thalassemia is. The more severe the thalassemia, the less hemoglobin the body has, and the more severe the anemia may be. One way to treat anemia is to provide the body with more red blood cells to carry oxygen. Clinical Significance. Macrocytosis is a relatively common finding in the era of automated blood cell counters, with prevalence estimates ranging from 1.7% to 3.6%. 3, 7, 8 Its significance tends to be underestimated by physicians, since about 60% of patients present without associated anemia, 8 unless there are other accompanying abnormalities noted. Retinopathy is a well-characterized side effect of treatment and includes cotton-wool spots, intraretinal and pre-retinal hemorrhage, and macular edema See Figure 3. A wide incidence range of 18 percent to 86 percent has been reported for interferon retinopathy. 24 Signs develop within two weeks to three months of treatment onset; patients may complain of blurred vision or be entirely. Without enough of one or the other, your red blood cells can’t carry oxygen as they should. With beta thalassemia If you think you may have thalassemia, and if your parents have it, you should see a doctor. With a mild case, you may feel tired and not need treatment. Your transfusion schedule may change as you get older. But there’s a remote chance that you could get an infection from a blood transfusion. To make hemoglobin you need two proteins, alpha and beta. You may also need other special doctors on your team, like those who treat the heart or liver. Hydroxychloroquine and thalassemia Plaquenil Oral Interactions with Other Medication, Megaloblastic Anemia and Other Causes of Macrocytosis Plaquenil heart rateIcd 10 for plaquenil usePlaquenil versus hydroxychloroquinePlaquenil and sun sensitivity Hydroxyurea is a cytotoxic drug that is short-acting and relatively easy to monitor. It is FDA-approved for the treatment of severe sickle cell disease. However, it is less effective and predictable in thalassemia and more likely to be beneficial in thalassemia intermedia. Treatment with Hydroxyurea -. Common Medications That May Be Toxic to the Retina. Aromatase inhibitors induced autoimmune disorders in patients.. Beta thalassemia major" is the most serious type, and it can cause many complications, including slow growth in children, an enlarged spleen, heart and liver problems, and bone damage. May 07, 2012 Saturday was a week since I stopped taking Plaquenil, aka Hydroxychloroquine, per my doctor's instructions, and I think I am going through some form of withdrawal. I took the drug as a treatment for sarcoidosis and one of the side effects is a reduction in white blood cells, which is what has happened to me. I don't know if anyone can help as this isn't technically lupus related. I've been on plaquenil for 6 months for suspected Sjogren's syndrome I don't have antibodies for Sjorgren's or Lupus but I do have Hashimoto's and have all the symptoms for Sjorgren's so the rheumatologist suggested a trial of plaquenil.