Does VUTRISIRAN Cause Intentional dose omission? 80 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 80 reports of Intentional dose omission have been filed in association with VUTRISIRAN (AMVUTTRA). This represents 5.6% of all adverse event reports for VUTRISIRAN.
80
Reports of Intentional dose omission with VUTRISIRAN
5.6%
of all VUTRISIRAN reports
5
Deaths
68
Hospitalizations
How Dangerous Is Intentional dose omission From VUTRISIRAN?
Of the 80 reports, 5 (6.3%) resulted in death, 68 (85.0%) 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 VUTRISIRAN. However, 80 reports have been filed with the FAERS database.
What Other Side Effects Does VUTRISIRAN Cause?
Death (244)
Hospitalisation (143)
Therapy interrupted (66)
Fall (65)
Fatigue (56)
Product dose omission issue (45)
Pain in extremity (43)
Dyspnoea (42)
Gait disturbance (42)
Asthenia (37)
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 VUTRISIRAN Alternatives Have Lower Intentional dose omission Risk?
VUTRISIRAN vs VX-950
VUTRISIRAN vs VYVANSE
VUTRISIRAN vs WARFARIN
VUTRISIRAN vs WATER
VUTRISIRAN vs WELLBUTRIN