Does ZOLEDRONIC ACID Cause Product dose omission issue? 86 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 86 reports of Product dose omission issue have been filed in association with ZOLEDRONIC ACID (Zoledronic acid). This represents 0.3% of all adverse event reports for ZOLEDRONIC ACID.
86
Reports of Product dose omission issue with ZOLEDRONIC ACID
0.3%
of all ZOLEDRONIC ACID reports
0
Deaths
26
Hospitalizations
How Dangerous Is Product dose omission issue From ZOLEDRONIC ACID?
Of the 86 reports, 26 (30.2%) required hospitalization, and 6 (7.0%) 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 ZOLEDRONIC ACID. However, 86 reports have been filed with the FAERS database.
What Other Side Effects Does ZOLEDRONIC ACID Cause?
Osteonecrosis of jaw (5,500)
Death (3,053)
Pain (2,925)
Arthralgia (2,541)
Pyrexia (2,455)
Fatigue (2,219)
Nausea (1,962)
Malaise (1,834)
Headache (1,739)
Asthenia (1,582)
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 ZOLEDRONIC ACID Alternatives Have Lower Product dose omission issue Risk?
ZOLEDRONIC ACID vs ZOLMITRIPTAN
ZOLEDRONIC ACID vs ZOLOFT
ZOLEDRONIC ACID vs ZOLPIDEM
ZOLEDRONIC ACID vs ZOLPIDEM\ZOLPIDEM
ZOLEDRONIC ACID vs ZOMETA