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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.

LUMASIRAN for Primary hyperoxaluria: Side Effects & Safety Data

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There are 176 adverse event reports in the FDA FAERS database where LUMASIRAN was used for Primary hyperoxaluria.

Most Reported Side Effects for LUMASIRAN

Side Effect Reports % Deaths Hosp.
Renal transplant 38 13.6% 1 8
Nephrolithiasis 22 7.9% 0 4
Drug ineffective 15 5.4% 0 1
Hospitalisation 15 5.4% 0 15
Urine oxalate increased 14 5.0% 0 2
Acute kidney injury 11 3.9% 0 3
Liver transplant 11 3.9% 1 2
Laboratory test abnormal 9 3.2% 0 2
Product dose omission issue 9 3.2% 0 3
Death 8 2.9% 8 0
Dialysis 8 2.9% 0 0
Hyperoxalaemia 8 2.9% 0 0
Intentional dose omission 8 2.9% 0 6
Diarrhoea 7 2.5% 1 1
End stage renal disease 7 2.5% 0 0

Other Indications for LUMASIRAN

Product used for unknown indication (97)

Related Pages

LUMASIRAN Full Profile All Primary hyperoxaluria Drugs LUMASIRAN Demographics LUMASIRAN Timeline