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U.S. Requires New Warning on Antidepressants for Children

Antidepressants must now have a "black box" warning after researchers linked the drugs to increased suicidal thoughts and behaviors in children and adolescents, the Food and Drug Administration announced Friday.

FDA Blocks Over-the-Counter Sales of Morning-After Pill

The FDA, citing concerns about the morning-after-pill's use by young teenagers, rejected over-the-counter sales of the emergency contraception late Thursday, a move that contradicted the recommendation of the agency's advisory panel.

FDA Backs Stronger Warnings for Some Antidepressants

People on certain popular antidepressants should be monitored for signs of suicidal thoughts, the government warned Monday as it asked pharmaceutical companies to highlight a suicide warning on the labels of ten drugs.

Senate Approves McClellan As New Medicare Chief

The Senate approved FDA chief Mark McClellan's nomination to head Medicare on Friday, after the vote was delayed over concerns about his opposition to legalizing the importation of prescription drugs.

FDA Chief McClellan Testifies on Drug Importation Concerns

The Food and Drug Administration commissioner and White House nominee to run Medicare, Mark McClellan, reiterated his concerns about drug importation during a contentious Senate hearing Thursday.

FDA Approves New Cancer Treatment Drug

By PBS News Hour

The Food and Drug Administration on Thursday approved the first drug that attacks cancer by choking off its blood supply -- a treatment for advanced colon cancer called Avastin.

Illinois Residents Sue FDA As Debate Over Drug Importation Heats Up

The governor of Illinois Thursday backed a lawsuit against the U.S. Food and Drug Administration to overturn the ban on buying prescription drugs from Canada.

FDA Approves New Colon Cancer Drug

By PBS News Hour

The U.S. Food and Drug Administration approved the cancer drug Erbitux, which is at the center of the ImClone insider-trading scandal, for the treatment of colorectal cancer that has spread to other parts of the body.

FDA Maintains Ban on Silicone Breast Implants

By PBS News Hour

The Food and Drug Administration Thursday said it needed more evidence demonstrating the safety of silicone breast implants before it would reverse a 1992 ban on routine sales of the devices.

Morning-After Pill Should Be Sold on Drug Store Shelves, FDA Panel Says

The emergency contraception commonly referred to as the morning-after pill should be available on drug store shelves without the prescription that women currently need, a Food and Drug Administration advisory panel recommended Tuesday.