Does VELAGLUCERASE ALFA Cause Incorrect product administration duration? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Incorrect product administration duration have been filed in association with VELAGLUCERASE ALFA (VPRIV). This represents 0.3% of all adverse event reports for VELAGLUCERASE ALFA.
5
Reports of Incorrect product administration duration with VELAGLUCERASE ALFA
0.3%
of all VELAGLUCERASE ALFA reports
0
Deaths
2
Hospitalizations
How Dangerous Is Incorrect product administration duration From VELAGLUCERASE ALFA?
Of the 5 reports, 2 (40.0%) required hospitalization.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VELAGLUCERASE ALFA. However, 5 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which VELAGLUCERASE ALFA Alternatives Have Lower Incorrect product administration duration Risk?
VELAGLUCERASE ALFA vs VELCADE
VELAGLUCERASE ALFA vs VELETRI
VELAGLUCERASE ALFA vs VELIPARIB
VELAGLUCERASE ALFA vs VEMURAFENIB
VELAGLUCERASE ALFA vs VENETOCLAX