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Adverse Event Reporting Information

Submit a Medical Inquiry

To report a medical adverse event, side effect, or product complaint, please call 1-855-844-3270.
Mon-Fri 8am – 8pm ET

You may also contact the U.S. Food and Drug Administration
MedWatch Adverse Event Reporting program:
Online: www.fda.gov/medwatch
Telephone: 1-800-FDA-1088

home / endocrinology / 2022

Therapeutic Area

2022

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Adverse Event Reporting Information

2022

Poster

Impact of mifepristone on liver function and liver steatosis in patients with Cushing syndrome

Annual Meeting of The Endocrine Society

2022

Poster

Favorable liver safety profile of the selective glucocorticoid receptor modulator relacorilant in healthy and hepatically impaired adults and in patients with Cushing syndrome

Annual Meeting of The Endocrine Society

2022

Poster

Favorable liver safety profile of the selective glucocorticoid receptor modulator relacorilant in healthy and hepatically impaired adults and in patients with Cushing syndrome

European Congress of Endocrinology

2022

Poster

Mifepristone use in hypercortisolism from an unknown source: a case study

American Association of Clinical Endocrinology

2022

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To report a medical adverse event, side effect, or product complaint, please call 1-855-844-3270.
Mon-Fri 8am – 8pm ET

You may also contact the U.S. Food and Drug Administration MedWatch Adverse Event Reporting program:
Online: www.fda.gov/medwatch
Telephone: 1-800-FDA-1088

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