Does TAFAMIDIS Cause Intentional product use issue? 15 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 15 reports of Intentional product use issue have been filed in association with TAFAMIDIS (Vyndamax). This represents 0.2% of all adverse event reports for TAFAMIDIS.
15
Reports of Intentional product use issue with TAFAMIDIS
0.2%
of all TAFAMIDIS reports
3
Deaths
5
Hospitalizations
How Dangerous Is Intentional product use issue From TAFAMIDIS?
Of the 15 reports, 3 (20.0%) resulted in death, 5 (33.3%) required hospitalization.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TAFAMIDIS. However, 15 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which TAFAMIDIS Alternatives Have Lower Intentional product use issue Risk?
TAFAMIDIS vs TAFAMIDIS MEGLUMINE
TAFAMIDIS vs TAFASITAMAB
TAFAMIDIS vs TAFASITAMAB-CXIX
TAFAMIDIS vs TAFINLAR
TAFAMIDIS vs TAFLUPROST