Does AVACOPAN Cause Product dose omission in error? 15 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 15 reports of Product dose omission in error have been filed in association with AVACOPAN (TAVNEOS). This represents 0.3% of all adverse event reports for AVACOPAN.
15
Reports of Product dose omission in error with AVACOPAN
0.3%
of all AVACOPAN reports
0
Deaths
4
Hospitalizations
How Dangerous Is Product dose omission in error From AVACOPAN?
Of the 15 reports, 4 (26.7%) required hospitalization.
Is Product dose omission in error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AVACOPAN. However, 15 reports have been filed with the FAERS database.
What Other Side Effects Does AVACOPAN Cause?
Hospitalisation (520)
Off label use (264)
Death (254)
Fatigue (214)
Diarrhoea (211)
Nausea (200)
Headache (149)
Product dose omission issue (145)
Pneumonia (143)
Covid-19 (139)
What Other Drugs Cause Product dose omission in error?
DUPILUMAB (7,586)
TOFACITINIB (2,461)
LENALIDOMIDE (618)
PALBOCICLIB (592)
DIROXIMEL (481)
ABALOPARATIDE (457)
NIRAPARIB (428)
RUXOLITINIB (425)
TERIFLUNOMIDE (371)
DIMETHYL (308)
Which AVACOPAN Alternatives Have Lower Product dose omission in error Risk?
AVACOPAN vs AVALGLUCOSIDASE ALFA-NGPT
AVACOPAN vs AVANAFIL
AVACOPAN vs AVANDAMET
AVACOPAN vs AVANDIA
AVACOPAN vs AVAPRITINIB