Does VELAGLUCERASE ALFA Cause Product prescribing error? 21 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 21 reports of Product prescribing error have been filed in association with VELAGLUCERASE ALFA (VPRIV). This represents 1.2% of all adverse event reports for VELAGLUCERASE ALFA.
21
Reports of Product prescribing error with VELAGLUCERASE ALFA
1.2%
of all VELAGLUCERASE ALFA reports
0
Deaths
12
Hospitalizations
How Dangerous Is Product prescribing error From VELAGLUCERASE ALFA?
Of the 21 reports, 12 (57.1%) required hospitalization, and 1 (4.8%) were considered life-threatening.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VELAGLUCERASE ALFA. However, 21 reports have been filed with the FAERS database.
What Other Side Effects Does VELAGLUCERASE ALFA Cause?
Inappropriate schedule of product administration (197)
Product dose omission issue (188)
Covid-19 (163)
Fatigue (136)
Death (108)
Fall (104)
Pyrexia (101)
Malaise (98)
Weight increased (89)
Headache (88)
What Other Drugs Cause Product prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which VELAGLUCERASE ALFA Alternatives Have Lower Product prescribing error Risk?
VELAGLUCERASE ALFA vs VELCADE
VELAGLUCERASE ALFA vs VELETRI
VELAGLUCERASE ALFA vs VELIPARIB
VELAGLUCERASE ALFA vs VEMURAFENIB
VELAGLUCERASE ALFA vs VENETOCLAX