Does LARONIDASE Cause Product dose omission? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Product dose omission have been filed in association with LARONIDASE (ALDURAZYME). This represents 0.5% of all adverse event reports for LARONIDASE.
16
Reports of Product dose omission with LARONIDASE
0.5%
of all LARONIDASE reports
2
Deaths
7
Hospitalizations
How Dangerous Is Product dose omission From LARONIDASE?
Of the 16 reports, 2 (12.5%) resulted in death, 7 (43.8%) required hospitalization.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LARONIDASE. However, 16 reports have been filed with the FAERS database.
What Other Side Effects Does LARONIDASE Cause?
Pyrexia (423)
Malaise (169)
Pneumonia (162)
Dyspnoea (157)
Vomiting (157)
Cough (154)
Fatigue (137)
Influenza (108)
Pain (107)
Inappropriate schedule of product administration (106)
What Other Drugs Cause Product dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which LARONIDASE Alternatives Have Lower Product dose omission Risk?
LARONIDASE vs LAROTRECTINIB
LARONIDASE vs LASILIX
LARONIDASE vs LASIX
LARONIDASE vs LASMIDITAN
LARONIDASE vs LATANOPROST