Does VELAGLUCERASE ALFA Cause Condition aggravated? 15 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 15 reports of Condition aggravated have been filed in association with VELAGLUCERASE ALFA (VPRIV). This represents 0.9% of all adverse event reports for VELAGLUCERASE ALFA.
15
Reports of Condition aggravated with VELAGLUCERASE ALFA
0.9%
of all VELAGLUCERASE ALFA reports
3
Deaths
7
Hospitalizations
How Dangerous Is Condition aggravated From VELAGLUCERASE ALFA?
Of the 15 reports, 3 (20.0%) resulted in death, 7 (46.7%) required hospitalization.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VELAGLUCERASE ALFA. However, 15 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which VELAGLUCERASE ALFA Alternatives Have Lower Condition aggravated Risk?
VELAGLUCERASE ALFA vs VELCADE
VELAGLUCERASE ALFA vs VELETRI
VELAGLUCERASE ALFA vs VELIPARIB
VELAGLUCERASE ALFA vs VEMURAFENIB
VELAGLUCERASE ALFA vs VENETOCLAX