FDA approves first treatment for congenital athymia
Congenital athymia is a rare condition in which babies are born without a thymus. As a result, the immune...
Congenital athymia is a rare condition in which babies are born without a thymus. As a result, the immune...
The Food and Drug Administration approves Boehringer Ingelheim’s Pradaxa (dabigatran etexilate) oral pellets to treat venous thromboembolism (VTE) in children aged 3...
FDA has authorized marketing for the first-of-its-kind device to assist upper limb rehabilitation of stroke patients.1 In 2017, a...
The U.S Food and Drug Administration (FDA) has approved the first clinical trial of CRISPR to correct sickle cell...
Chemotherapy can be lifesaving, but it can also damage bone marrow and cause blood cell counts to drop, sometimes...
The FDA has approved Qelbree (SPN-812), for children aged 6 to 17 years with attention deficit hyperactivity disorder (ADHD)....
The US FDA approved the use of Rydapt (midostaurin) in combination with chemotherapy for treating recently diagnosed adults with...
Breast implant-associated anaplastic large cell lymphoma (BIA-ALCL) is not breast cancer but a rare type of T-cell lymphoma that...
US Food and Drug Administration (FDA) has warned both patients and doctors alike about the use of balloon angioplasty...
Adult patients with recurrent epithelial ovarian, fallopian tube or primary peritoneal cancer who have responded completely or partially to...