Does BUROSUMAB-TWZA Cause Product dose omission? 137 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 137 reports of Product dose omission have been filed in association with BUROSUMAB-TWZA. This represents 2.7% of all adverse event reports for BUROSUMAB-TWZA.
137
Reports of Product dose omission with BUROSUMAB-TWZA
2.7%
of all BUROSUMAB-TWZA reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product dose omission From BUROSUMAB-TWZA?
Of the 137 reports, 3 (2.2%) required hospitalization.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUROSUMAB-TWZA. However, 137 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)
Product dose omission issue (475)
Arthralgia (285)
Pain (279)
Pain in extremity (272)
Headache (226)
Restless legs syndrome (217)
Incorrect dose administered (215)
Injection site pain (205)
What Other Drugs Cause Product dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which BUROSUMAB-TWZA Alternatives Have Lower Product dose omission Risk?
BUROSUMAB-TWZA vs BUSPIRONE
BUROSUMAB-TWZA vs BUSULFAN
BUROSUMAB-TWZA vs BUSULFEX
BUROSUMAB-TWZA vs BUTALBITAL
BUROSUMAB-TWZA vs BUTENAFINE