Does ASFOTASE ALFA Cause Post procedural complication? 9 Reports in FDA Database

According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Post procedural complication have been filed in association with ASFOTASE ALFA (STRENSIQ). This represents 0.1% of all adverse event reports for ASFOTASE ALFA.

How Dangerous Is Post procedural complication From ASFOTASE ALFA?

Of the 9 reports, 3 (33.3%) required hospitalization.

Is Post procedural complication Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ASFOTASE ALFA. However, 9 reports have been filed with the FAERS database.

What Other Side Effects Does ASFOTASE ALFA Cause?