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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 10-HYDROXYCAMPTOTHECIN Cause Device use issue? 20 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 20 reports of Device use issue have been filed in association with 10-HYDROXYCAMPTOTHECIN. This represents 60.6% of all adverse event reports for 10-HYDROXYCAMPTOTHECIN.

20
Reports of Device use issue with 10-HYDROXYCAMPTOTHECIN
60.6%
of all 10-HYDROXYCAMPTOTHECIN reports
4
Deaths
0
Hospitalizations

How Dangerous Is Device use issue From 10-HYDROXYCAMPTOTHECIN?

Of the 20 reports, 4 (20.0%) resulted in death.

Is Device use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for 10-HYDROXYCAMPTOTHECIN. However, 20 reports have been filed with the FAERS database.

What Other Side Effects Does 10-HYDROXYCAMPTOTHECIN Cause?

Off label use (20) Post embolisation syndrome (20)

What Other Drugs Cause Device use issue?

SOMATROPIN (2,571) LEVONORGESTREL (2,489) COPPER (1,318) BUDESONIDE\FORMOTEROL (1,236) EXENATIDE (992) BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (976) DUPILUMAB (528) ALIROCUMAB (471) INSULIN GLARGINE (469) BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM (459)

Related Pages

10-HYDROXYCAMPTOTHECIN Full Profile All Device use issue Reports All Drugs Causing Device use issue 10-HYDROXYCAMPTOTHECIN Demographics