Does AVACOPAN Cause Product dose omission issue? 145 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 145 reports of Product dose omission issue have been filed in association with AVACOPAN (TAVNEOS). This represents 3.3% of all adverse event reports for AVACOPAN.
145
Reports of Product dose omission issue with AVACOPAN
3.3%
of all AVACOPAN reports
1
Deaths
30
Hospitalizations
How Dangerous Is Product dose omission issue From AVACOPAN?
Of the 145 reports, 1 (0.7%) resulted in death, 30 (20.7%) 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 AVACOPAN. However, 145 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)
Pneumonia (143)
Covid-19 (139)
Drug ineffective (111)
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 AVACOPAN Alternatives Have Lower Product dose omission issue Risk?
AVACOPAN vs AVALGLUCOSIDASE ALFA-NGPT
AVACOPAN vs AVANAFIL
AVACOPAN vs AVANDAMET
AVACOPAN vs AVANDIA
AVACOPAN vs AVAPRITINIB