Please provide your email address to receive an email when new articles are posted on . Women with vs. without cancer had similar serious adverse event risk after fertility preservation. Younger age, ...

Manufacturers to remove suicidal ideation warnings from Saxenda, Wegovy, and Zepbound labels following a large-scale FDA safety investigation.

Fred Hutchinson Cancer Center-led investigators found that higher patient-reported fatigue before cancer treatment aligned ...

In response to their prior inquiries, Medtronic Spine President Douglas King wrote letters to Minnesota Senators Al Franken and Amy Klobuchar, stating the adverse events that occurred during a study ...

BCMA-targeted therapies are transforming care for multiple myeloma patients. But these immunotherapies also come with various potentially dangerous side effects. A new study now looks at those risks ...

When the HSRO approves human-subjects research, the approval is based upon the information about how the research will be conducted and the risks and anticipated benefits to subjects that are known at ...

Channel 2 Action News has learned that the FDA is now alerting veterinarians about reports of health problems in dogs – including hundreds of deaths – tied to a drug for arthritis pain. The FDA ...

A new study has exposed "serious adverse events" linked to mifepristone, also known as the "abortion pill." Mifepristone is a "pregnancy blocker" that is used in combination with another medication, ...

Patient safety events, which are adverse events that could have been prevented, are altogether common in outpatient settings and speak to the need for improving safety in these settings, according to ...

Reports of these events, “until MoCRA, were only voluntary. So even if a serious adverse event was found, it was submitted to the agency on a voluntary basis,” Dr. Linda Katz, director of the FDA’s ...