Does BELZUTIFAN Cause Product dose omission issue? 25 Reports in FDA Database
Boost Your Natural Energy & Metabolism
Mitolyn — 6 exotic plants to unlock your body's fat-burning power. 90-day guarantee.
According to the FDA Adverse Event Reporting System (FAERS), 25 reports of Product dose omission issue have been filed in association with BELZUTIFAN (WELIREG). This represents 2.5% of all adverse event reports for BELZUTIFAN.
25
Reports of Product dose omission issue with BELZUTIFAN
2.5%
of all BELZUTIFAN reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product dose omission issue From BELZUTIFAN?
Of the 25 reports, 3 (12.0%) required hospitalization, and 2 (8.0%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BELZUTIFAN. However, 25 reports have been filed with the FAERS database.
What Other Side Effects Does BELZUTIFAN Cause?
Anaemia (154)
Fatigue (88)
Hypoxia (85)
Diarrhoea (42)
Death (41)
Dyspnoea (40)
Haemoglobin decreased (36)
Malignant neoplasm progression (36)
Off label use (35)
Oxygen saturation decreased (30)
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 BELZUTIFAN Alternatives Have Lower Product dose omission issue Risk?
BELZUTIFAN vs BEMPEDOIC ACID
BELZUTIFAN vs BEMPEDOIC ACID\EZETIMIBE
BELZUTIFAN vs BEMPEGALDESLEUKIN
BELZUTIFAN vs BENADRYL
BELZUTIFAN vs BENAZEPRIL