Does LUMASIRAN Cause Intentional dose omission? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Intentional dose omission have been filed in association with LUMASIRAN (OXLUMO). This represents 2.9% of all adverse event reports for LUMASIRAN.
8
Reports of Intentional dose omission with LUMASIRAN
2.9%
of all LUMASIRAN reports
0
Deaths
6
Hospitalizations
How Dangerous Is Intentional dose omission From LUMASIRAN?
Of the 8 reports, 6 (75.0%) required hospitalization.
Is Intentional dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LUMASIRAN. However, 8 reports have been filed with the FAERS database.
What Other Side Effects Does LUMASIRAN Cause?
Renal transplant (38)
Nephrolithiasis (22)
Drug ineffective (15)
Hospitalisation (15)
Urine oxalate increased (14)
Acute kidney injury (11)
Liver transplant (11)
Laboratory test abnormal (9)
Product dose omission issue (9)
Death (8)
What Other Drugs Cause Intentional dose omission?
DUPILUMAB (2,269)
CERTOLIZUMAB PEGOL (1,253)
ADALIMUMAB (845)
TOFACITINIB (845)
INFLIXIMAB (815)
ABALOPARATIDE (623)
ETANERCEPT (615)
AMBRISENTAN (595)
SODIUM OXYBATE (580)
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (518)
Which LUMASIRAN Alternatives Have Lower Intentional dose omission Risk?
LUMASIRAN vs LUMATEPERONE
LUMASIRAN vs LUMIGAN
LUMASIRAN vs LUPRON DEPOT
LUMASIRAN vs LUPRON DEPOT-PED
LUMASIRAN vs LURASIDONE