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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

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Therapeutic Area

2016

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Adverse Event Reporting Information

2016

Poster

Immediate and sustained improvements in a cushing’s syndrome patient with primary macronodular adrenal hyperplasia treated with mifepristone

American Association of Clinical Endocrinology

2016

Poster

Prevention of secondary adrenal insufficiency with presurgical use of mifepristone in patients with autonomous cortisol-secreting adenomas

American Association of Clinical Endocrinology

2016

Poster

Short-Term Mifepristone Treatment Improved Preoperative Clinical Status in a High-Risk Patient With Unexpected Normalization of Liver Enzymes

Annual Meeting of The Endocrine Society

2016

Poster

Cushing’s Syndrome Misdiagnosed as Bipolar Depression

Annual Meeting of The Endocrine Society

2016

Poster

Persistent Acromegaly Controlled on Pegvisomant with Co-Existing Non-ACTH Dependent Cushing’s Syndrome (CS) Due to Bilateral Adrenal Adenomas with Dramatic Clinical Response to Mifepristone

Annual Meeting of The Endocrine Society

2016

Poster

No Incidence of Adrenal Insufficiency (AI) in Normo-cortisolemic Patients Treated With Mifepristone (MIFE): An Analysis of 5 Placebo-Controlled Clinical Trials

Annual Meeting of The Endocrine Society

2016

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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

Search