Does TAFAMIDIS Cause Poor quality product administered? 20 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 20 reports of Poor quality product administered have been filed in association with TAFAMIDIS (Vyndamax). This represents 0.2% of all adverse event reports for TAFAMIDIS.
20
Reports of Poor quality product administered with TAFAMIDIS
0.2%
of all TAFAMIDIS reports
5
Deaths
7
Hospitalizations
How Dangerous Is Poor quality product administered From TAFAMIDIS?
Of the 20 reports, 5 (25.0%) resulted in death, 7 (35.0%) required hospitalization.
Is Poor quality product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TAFAMIDIS. However, 20 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 Poor quality product administered?
ONABOTULINUMTOXINA (495)
ICOSAPENT ETHYL (452)
MINOXIDIL (428)
TUBERCULIN PURIFIED PROTEIN DERIVATIVE (376)
ADALIMUMAB (239)
TESTOSTERONE CYPIONATE (235)
SOMATROPIN (234)
POLYETHYLENE GLYCOL 3350 (223)
IBUPROFEN (222)
INSULIN GLARGINE (133)
Which TAFAMIDIS Alternatives Have Lower Poor quality product administered Risk?
TAFAMIDIS vs TAFAMIDIS MEGLUMINE
TAFAMIDIS vs TAFASITAMAB
TAFAMIDIS vs TAFASITAMAB-CXIX
TAFAMIDIS vs TAFINLAR
TAFAMIDIS vs TAFLUPROST