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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

2015

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Adverse Event Reporting Information

2015

Poster

Pre-surgical Use of Mifepristone for Ectopic Cushing’s in a High-Risk Bilateral Adrenalectomy Candidate

Annual Meeting of The Endocrine Society

2015

Poster

Mifepristone for the Successful Treatment of Cushing’s Syndrome After Multiple Failed Interventions

Annual Meeting of The Endocrine Society

2015

Poster

Marked Improvement in Liver Enzymes During Medical Therapy With Mifepristone for Cushing’s Syndrome

Annual Meeting of The Endocrine Society

2015

Poster

Treatment of Ectopic Cushing’s Syndrome With Mifepristone While Pending Tumor Localization

Annual Meeting of The Endocrine Society

2015

Poster

Mifepristone Re-established Glycemic Control in a Cushing’s Syndrome Patient That Relapsed After a 21-Month Interruption

American Association of Clinical Endocrinology

2015

Poster

Resistant Metabolic Abnormalities Prompting Cushing’s Syndrome Work-up and Treatment With Mifepristone

American Association of Clinical Endocrinology

2015

Poster

Improved Response to Octreotide LAR for Ectopic Cushing’s Syndrome During Mifepristone Therapy: a Case Study

American Association of Clinical Endocrinology

2015

Poster

Use of Mifepristone in an Ectopic Cushing’s Syndrome Patient Pending Tumor Localization

American Association of Clinical Endocrinology

2015

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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