Does VUTRISIRAN Cause Fluid retention? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Fluid retention have been filed in association with VUTRISIRAN (AMVUTTRA). This represents 0.8% of all adverse event reports for VUTRISIRAN.
12
Reports of Fluid retention with VUTRISIRAN
0.8%
of all VUTRISIRAN reports
0
Deaths
10
Hospitalizations
How Dangerous Is Fluid retention From VUTRISIRAN?
Of the 12 reports, 10 (83.3%) required hospitalization.
Is Fluid retention Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VUTRISIRAN. However, 12 reports have been filed with the FAERS database.
What Other Side Effects Does VUTRISIRAN Cause?
Death (244)
Hospitalisation (143)
Intentional dose omission (80)
Therapy interrupted (66)
Fall (65)
Fatigue (56)
Product dose omission issue (45)
Pain in extremity (43)
Dyspnoea (42)
Gait disturbance (42)
What Other Drugs Cause Fluid retention?
AMBRISENTAN (3,927)
TREPROSTINIL (3,804)
MACITENTAN (2,861)
CALCIUM\DEXTROSE\MAGNESIUM\SODIUM\SODIUM (2,233)
SACUBITRIL\VALSARTAN (2,187)
ADALIMUMAB (1,193)
SELEXIPAG (1,044)
FUROSEMIDE (1,020)
LENALIDOMIDE (1,007)
EPOPROSTENOL (929)
Which VUTRISIRAN Alternatives Have Lower Fluid retention Risk?
VUTRISIRAN vs VX-950
VUTRISIRAN vs VYVANSE
VUTRISIRAN vs WARFARIN
VUTRISIRAN vs WATER
VUTRISIRAN vs WELLBUTRIN