The following database was created at the recommendation of the National Marrow Donor Program’s Donor and Patient Safety Monitoring Committee, to facilitate communication of certain events within the NMDP network. This database contains information about events that have been reported by the NMDP to the FDA, HRSA, or the Principal Investigators of a research study. These events may have been reported pursuant to requirements related to one or more of these parties or may have been voluntarily reported at the NMDP Medical Director’s discretion. The reports included in the database were based on NMDP’s best understanding of the events at the time of their original reporting, are described here in accord with the original reporting of the event, and do not necessarily reflect any later information that was, is, or may have been available in relation to the reported event.
The database provides information of a general nature and is not intended to provide medical advice, medical diagnoses, or medical treatments, nor does it create a physician-patient relationship. The NMDP has taken reasonable measures to ensure that the information and data presented in this database are accurate and current. However, the NMDP makes no express or implied warranty regarding such information or data, and hereby expressly disclaims all legal liability and responsibility for the accuracy, completeness, or usefulness of any information contained in this database. The information is not a substitute for the medical judgment or advice of a qualified health care provider.
The information in this database is confidential and intended solely for the use of NMDP network centers. Neither access to the database nor information included in it may be shared with or provided to others. Use of the database is subject to all confidentiality and restrictions applicable under contract or law.
Adverse Events Results
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