Does LARONIDASE Cause Product dose omission issue? 70 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 70 reports of Product dose omission issue have been filed in association with LARONIDASE (ALDURAZYME). This represents 2.3% of all adverse event reports for LARONIDASE.
70
Reports of Product dose omission issue with LARONIDASE
2.3%
of all LARONIDASE reports
2
Deaths
23
Hospitalizations
How Dangerous Is Product dose omission issue From LARONIDASE?
Of the 70 reports, 2 (2.9%) resulted in death, 23 (32.9%) 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 LARONIDASE. However, 70 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 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 LARONIDASE Alternatives Have Lower Product dose omission issue Risk?
LARONIDASE vs LAROTRECTINIB
LARONIDASE vs LASILIX
LARONIDASE vs LASIX
LARONIDASE vs LASMIDITAN
LARONIDASE vs LATANOPROST