Does ZOLEDRONIC ACID Cause Product dose omission? 28 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 28 reports of Product dose omission have been filed in association with ZOLEDRONIC ACID (Zoledronic acid). This represents 0.1% of all adverse event reports for ZOLEDRONIC ACID.
28
Reports of Product dose omission with ZOLEDRONIC ACID
0.1%
of all ZOLEDRONIC ACID reports
0
Deaths
10
Hospitalizations
How Dangerous Is Product dose omission From ZOLEDRONIC ACID?
Of the 28 reports, 10 (35.7%) 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 ZOLEDRONIC ACID. However, 28 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?
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 ZOLEDRONIC ACID Alternatives Have Lower Product dose omission Risk?
ZOLEDRONIC ACID vs ZOLMITRIPTAN
ZOLEDRONIC ACID vs ZOLOFT
ZOLEDRONIC ACID vs ZOLPIDEM
ZOLEDRONIC ACID vs ZOLPIDEM\ZOLPIDEM
ZOLEDRONIC ACID vs ZOMETA