Does BUROSUMAB-TWZA Cause Product dose omission issue? 475 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 475 reports of Product dose omission issue have been filed in association with BUROSUMAB-TWZA. This represents 9.2% of all adverse event reports for BUROSUMAB-TWZA.
475
Reports of Product dose omission issue with BUROSUMAB-TWZA
9.2%
of all BUROSUMAB-TWZA reports
1
Deaths
24
Hospitalizations
How Dangerous Is Product dose omission issue From BUROSUMAB-TWZA?
Of the 475 reports, 1 (0.2%) resulted in death, 24 (5.1%) 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 BUROSUMAB-TWZA. However, 475 reports have been filed with the FAERS database.
What Other Side Effects Does BUROSUMAB-TWZA Cause?
Inappropriate schedule of product administration (579)
Blood phosphorus decreased (509)
Arthralgia (285)
Pain (279)
Pain in extremity (272)
Headache (226)
Restless legs syndrome (217)
Incorrect dose administered (215)
Injection site pain (205)
Fatigue (189)
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 BUROSUMAB-TWZA Alternatives Have Lower Product dose omission issue Risk?
BUROSUMAB-TWZA vs BUSPIRONE
BUROSUMAB-TWZA vs BUSULFAN
BUROSUMAB-TWZA vs BUSULFEX
BUROSUMAB-TWZA vs BUTALBITAL
BUROSUMAB-TWZA vs BUTENAFINE