Does TAZEMETOSTAT HYDROBROMIDE Cause Intentional dose omission? 10 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Intentional dose omission have been filed in association with TAZEMETOSTAT HYDROBROMIDE (TAZVERIK). This represents 0.8% of all adverse event reports for TAZEMETOSTAT HYDROBROMIDE.
10
Reports of Intentional dose omission with TAZEMETOSTAT HYDROBROMIDE
0.8%
of all TAZEMETOSTAT HYDROBROMIDE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Intentional dose omission From TAZEMETOSTAT HYDROBROMIDE?
Of the 10 reports, 1 (10.0%) required hospitalization.
Is Intentional dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TAZEMETOSTAT HYDROBROMIDE. However, 10 reports have been filed with the FAERS database.
What Other Side Effects Does TAZEMETOSTAT HYDROBROMIDE Cause?
Off label use (298)
Fatigue (292)
Disease progression (267)
Nausea (207)
Product dose omission issue (183)
Death (106)
Diarrhoea (100)
Decreased appetite (81)
Asthenia (75)
Vomiting (75)
What Other Drugs Cause Intentional dose omission?
DUPILUMAB (2,269)
CERTOLIZUMAB PEGOL (1,253)
ADALIMUMAB (845)
TOFACITINIB (845)
INFLIXIMAB (815)
ABALOPARATIDE (623)
ETANERCEPT (615)
AMBRISENTAN (595)
SODIUM OXYBATE (580)
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (518)
Which TAZEMETOSTAT HYDROBROMIDE Alternatives Have Lower Intentional dose omission Risk?
TAZEMETOSTAT HYDROBROMIDE vs TAZOBACTAM
TAZEMETOSTAT HYDROBROMIDE vs TBO-FILGRASTIM
TAZEMETOSTAT HYDROBROMIDE vs TEBENTAFUSP-TEBN
TAZEMETOSTAT HYDROBROMIDE vs TECFIDERA
TAZEMETOSTAT HYDROBROMIDE vs TECHNETIUM TC-99M