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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does DATOPOTAMAB DERUXTECAN-DLNK Cause Disease progression? 49 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 49 reports of Disease progression have been filed in association with DATOPOTAMAB DERUXTECAN-DLNK. This represents 29.7% of all adverse event reports for DATOPOTAMAB DERUXTECAN-DLNK.

49
Reports of Disease progression with DATOPOTAMAB DERUXTECAN-DLNK
29.7%
of all DATOPOTAMAB DERUXTECAN-DLNK reports
25
Deaths
8
Hospitalizations

How Dangerous Is Disease progression From DATOPOTAMAB DERUXTECAN-DLNK?

Of the 49 reports, 25 (51.0%) resulted in death, 8 (16.3%) required hospitalization.

Is Disease progression Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DATOPOTAMAB DERUXTECAN-DLNK. However, 49 reports have been filed with the FAERS database.

What Other Side Effects Does DATOPOTAMAB DERUXTECAN-DLNK Cause?

Off label use (31) Stomatitis (27) No adverse event (22) Nausea (11) Prescribed underdose (9) Death (7)