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Bill > S326


NJ S326

NJ S326
Requires physicians and other prescribers to obtain electronic or written consent for certain medications with "black box warnings."


summary

Introduced
01/09/2024
In Committee
01/09/2024
Crossed Over
Passed
Dead

Introduced Session

2024-2025 Regular Session

Bill Summary

This bill requires physicians, physician assistants, advanced practice nurses, and other authorized prescribers to obtain informed electronic or written consent prior to prescribing psychotropic medications that are accompanied by a "black box warning," which consent is to include an electronic or a written acknowledgement that the patient or the patient's guardian received notification about the black box warning. The bill specifies that in cases where electronic or written consent cannot be obtained but oral consent is provided, the prescriber must make a notation in the patient's file indicating the date and circumstances of the informed consent. The United States Food and Drug Administration (FDA) requires pharmaceutical companies to place a "black box warning" on a drug label if medical studies indicate that the drug carries a significant risk of serious or life-threatening adverse effects. A "black box warning" is the strongest warning that the FDA requires. A physician, physician assistant, advanced practice nurse, or other authorized prescriber who violates the requirements established under the bill is subject to disciplinary action by the applicable State professional licensing board.

AI Summary

This bill requires physicians, physician assistants, advanced practice nurses, and other authorized prescribers to obtain informed electronic or written consent prior to prescribing psychotropic medications that have a "black box warning" from the United States Food and Drug Administration (FDA). A "black box warning" is the strongest warning the FDA requires on a drug label if medical studies indicate the drug carries a significant risk of serious or life-threatening adverse effects. The bill specifies that if electronic or written consent cannot be obtained, the prescriber must make a notation in the patient's file indicating the date and circumstances of the informed oral consent. Prescribers who violate the requirements are subject to disciplinary action by their state professional licensing board.

Committee Categories

Health and Social Services

Sponsors (1)

Last Action

Introduced in the Senate, Referred to Senate Health, Human Services and Senior Citizens Committee (on 01/09/2024)

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