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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 MIGALASTAT Cause Product dose omission issue? 41 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 41 reports of Product dose omission issue have been filed in association with MIGALASTAT (Galafold). This represents 8.5% of all adverse event reports for MIGALASTAT.

41
Reports of Product dose omission issue with MIGALASTAT
8.5%
of all MIGALASTAT reports
0
Deaths
25
Hospitalizations

How Dangerous Is Product dose omission issue From MIGALASTAT?

Of the 41 reports, 25 (61.0%) required hospitalization.

Is Product dose omission issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for MIGALASTAT. However, 41 reports have been filed with the FAERS database.

What Other Side Effects Does MIGALASTAT Cause?

Renal impairment (34) Off label use (29) Death (26) Fatigue (26) Headache (25) Cerebrovascular accident (23) Nausea (20) Drug ineffective (19) Dyspnoea (19) Pain (19)

What Other Drugs Cause Product dose omission issue?

DUPILUMAB (18,189) USTEKINUMAB (9,405) GUSELKUMAB (9,267) LENALIDOMIDE (8,145) MEPOLIZUMAB (5,873) TOFACITINIB (5,646) VOXELOTOR (5,122) BELIMUMAB (4,671) SECUKINUMAB (4,572) APREMILAST (4,460)

Which MIGALASTAT Alternatives Have Lower Product dose omission issue Risk?

MIGALASTAT vs MIGLITOL MIGALASTAT vs MIGLUSTAT MIGALASTAT vs MILNACIPRAN MIGALASTAT vs MILRINONE MIGALASTAT vs MILTEFOSINE

Related Pages

MIGALASTAT Full Profile All Product dose omission issue Reports All Drugs Causing Product dose omission issue MIGALASTAT Demographics