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To amend the Federal Food, Drug, and Cosmetic Act to require that the label of drugs with an increased risk of suicide or depression present such increased risk prominently, and for other purposes.

USA115th CongressHR-6717| House 
| Updated: 9/6/2018
Bobby L. Rush

Bobby L. Rush

Democratic Representative

Illinois

Energy and Commerce Committee

  • Introduced
  • In Committee
  • On Floor
  • Passed Chamber
  • Enacted
Depression Side Effect Labeling Awareness Act of 2018 This bill amends the Federal Food, Drug, and Cosmetic Act to require the label of a drug that has an increased risk of suicide or depression to prominently display such risk.
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Timeline
Sep 6, 2018
Introduced in House
Sep 6, 2018
Referred to the House Committee on Energy and Commerce.
  • September 6, 2018
    Introduced in House


  • September 6, 2018
    Referred to the House Committee on Energy and Commerce.

Health

Administrative law and regulatory proceduresConsumer affairsDepartment of Health and Human ServicesDrug safety, medical device, and laboratory regulationFood and Drug Administration (FDA)Mental health

To amend the Federal Food, Drug, and Cosmetic Act to require that the label of drugs with an increased risk of suicide or depression present such increased risk prominently, and for other purposes.

USA115th CongressHR-6717| House 
| Updated: 9/6/2018
Depression Side Effect Labeling Awareness Act of 2018 This bill amends the Federal Food, Drug, and Cosmetic Act to require the label of a drug that has an increased risk of suicide or depression to prominently display such risk.
View Full Text

Suggested Questions

Get AI-generated questions to help you understand this bill better

Timeline
Sep 6, 2018
Introduced in House
Sep 6, 2018
Referred to the House Committee on Energy and Commerce.
  • September 6, 2018
    Introduced in House


  • September 6, 2018
    Referred to the House Committee on Energy and Commerce.
Bobby L. Rush

Bobby L. Rush

Democratic Representative

Illinois

Energy and Commerce Committee

Health

  • Introduced
  • In Committee
  • On Floor
  • Passed Chamber
  • Enacted
Administrative law and regulatory proceduresConsumer affairsDepartment of Health and Human ServicesDrug safety, medical device, and laboratory regulationFood and Drug Administration (FDA)Mental health