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  2. Pfizer withdraws sickle cell disease treatment on risk of ...

    www.aol.com/news/pfizer-withdraws-sickle-cell...

    (Reuters) -U.S. drugmaker Pfizer said on Wednesday it is withdrawing its sickle cell disease treatment Oxbryta from all markets where it is approved, citing risks of a painful complication and deaths.

  3. Sickle cell disease - Wikipedia

    en.wikipedia.org/wiki/Sickle_cell_disease

    Sickle cell disease (SCD), also simply called sickle cell, is a group of hemoglobin-related blood disorders typically inherited. [2] The most common type is known as sickle cell anemia. [2] It results in an abnormality in the oxygen-carrying protein haemoglobin found in red blood cells. [2] This leads to a rigid, sickle -like shape under ...

  4. New prescription drug price hikes hit Black patients hard - AOL

    www.aol.com/news/prescription-drug-price-hikes...

    One example she cites is the health care industry’s handling of sickle cell anemia, which 1 in 13 Black babies in the U.S. are born with, according to the Centers for Disease Control and Prevention.

  5. What Is Priapism & How Can Men Treat It? - AOL

    www.aol.com/priapism-men-treat-105700788.html

    Sickle cell test. A urologist might request this test for men with a higher risk of sickle cell disease. Duplex ultrasound. Sometimes called ultrasonography, this can measure blood flow in your ...

  6. Anemia - Wikipedia

    en.wikipedia.org/wiki/Anemia

    The types of anemia treated with drugs are iron-deficiency anemia, thalassemia, aplastic anemia, hemolytic anemia, sickle cell anemia, and pernicious anemia, the most important of them being deficiency and sickle cell anemia with together 60% of market share because of highest prevalence as well as higher treatment costs compared with other ...

  7. Spinal muscular atrophy - Wikipedia

    en.wikipedia.org/wiki/Spinal_muscular_atrophy

    1 in 10,000 people [2] Spinal muscular atrophy (SMA) is a rare neuromuscular disorder that results in the loss of motor neurons and progressive muscle wasting. [3][4][5] It is usually diagnosed in infancy or early childhood and if left untreated it is the most common genetic cause of infant death. [6] It may also appear later in life and then ...

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