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Medical Information for Patients and Caregivers

EMD Serono Products

Conception chances: Healthy 30-year-old woman - 20%, early 40s woman - 5%.

The United States Food and Drug Administration (FDA) requires human prescription drugs to have labels that contain essential scientific information for the safe and effective use of the drug. This includes Prescribing Information for healthcare providers, and FDA-approved labels for patients, which can be called Medication Guides, Patient Information, Patient Package Inserts, and/or Instructions for Use1

To report a side effect with an EMD Serono medication, please call 1-800-283-8088, ext. 5563.

To report any other problem with your EMD Serono medication, please call 1-800-283-8088, ext. 2020.

Patient assistance programs

References

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  1. FDA’s Labeling Resources for Human Prescription Drugs. https://www.fda.gov/drugs/laws-acts-and-rules/fdas-labeling-resourceshuman-prescription-drugs. Accessed 25 Nov 2024.

The information on this webpage is provided by EMD Serono Medical Affairs, who makes it their mission to provide unbiased medical information to healthcare providers, patients, and caregivers. Always seek the guidance of your healthcare provider. 

To report a side effect from your EMD Serono medication, please call 1-800-283-8088, ext. 5563. To report any other problems with your EMD Serono medication, please call 1-800-283-8088, ext. 2020. You may also report side effects to FDA at 1-800-FDA-1088.

EMD Serono is the Healthcare business of Merck KGaA, Darmstadt, Germany, in the United States and Canada.

US-MULE-00016 03/25

© 2025 Merck KGaA, Darmstadt, Germany or its affiliates. All rights reserved.

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