Does TAFAMIDIS Cause Product dose omission in error? 36 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 36 reports of Product dose omission in error have been filed in association with TAFAMIDIS (Vyndamax). This represents 0.4% of all adverse event reports for TAFAMIDIS.
36
Reports of Product dose omission in error with TAFAMIDIS
0.4%
of all TAFAMIDIS reports
4
Deaths
9
Hospitalizations
How Dangerous Is Product dose omission in error From TAFAMIDIS?
Of the 36 reports, 4 (11.1%) resulted in death, 9 (25.0%) required hospitalization.
Is Product dose omission in error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TAFAMIDIS. However, 36 reports have been filed with the FAERS database.
What Other Side Effects Does TAFAMIDIS Cause?
Death (2,553)
Dyspnoea (608)
Off label use (571)
Cardiac failure (444)
Fatigue (438)
Fall (372)
Malaise (301)
Hypoacusis (298)
Atrial fibrillation (296)
Asthenia (256)
What Other Drugs Cause Product dose omission in error?
DUPILUMAB (7,586)
TOFACITINIB (2,461)
LENALIDOMIDE (618)
PALBOCICLIB (592)
DIROXIMEL (481)
ABALOPARATIDE (457)
NIRAPARIB (428)
RUXOLITINIB (425)
TERIFLUNOMIDE (371)
DIMETHYL (308)
Which TAFAMIDIS Alternatives Have Lower Product dose omission in error Risk?
TAFAMIDIS vs TAFAMIDIS MEGLUMINE
TAFAMIDIS vs TAFASITAMAB
TAFAMIDIS vs TAFASITAMAB-CXIX
TAFAMIDIS vs TAFINLAR
TAFAMIDIS vs TAFLUPROST