Does TAFAMIDIS Cause Intentional product misuse? 44 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 44 reports of Intentional product misuse have been filed in association with TAFAMIDIS (Vyndamax). This represents 0.5% of all adverse event reports for TAFAMIDIS.
44
Reports of Intentional product misuse with TAFAMIDIS
0.5%
of all TAFAMIDIS reports
8
Deaths
14
Hospitalizations
How Dangerous Is Intentional product misuse From TAFAMIDIS?
Of the 44 reports, 8 (18.2%) resulted in death, 14 (31.8%) required hospitalization, and 2 (4.5%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TAFAMIDIS. However, 44 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 misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which TAFAMIDIS Alternatives Have Lower Intentional product misuse Risk?
TAFAMIDIS vs TAFAMIDIS MEGLUMINE
TAFAMIDIS vs TAFASITAMAB
TAFAMIDIS vs TAFASITAMAB-CXIX
TAFAMIDIS vs TAFINLAR
TAFAMIDIS vs TAFLUPROST