Does TAFAMIDIS Cause Wrong technique in product usage process? 28 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 28 reports of Wrong technique in product usage process have been filed in association with TAFAMIDIS (Vyndamax). This represents 0.3% of all adverse event reports for TAFAMIDIS.
28
Reports of Wrong technique in product usage process with TAFAMIDIS
0.3%
of all TAFAMIDIS reports
2
Deaths
9
Hospitalizations
How Dangerous Is Wrong technique in product usage process From TAFAMIDIS?
Of the 28 reports, 2 (7.1%) resulted in death, 9 (32.1%) required hospitalization, and 1 (3.6%) were considered life-threatening.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TAFAMIDIS. However, 28 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which TAFAMIDIS Alternatives Have Lower Wrong technique in product usage process Risk?
TAFAMIDIS vs TAFAMIDIS MEGLUMINE
TAFAMIDIS vs TAFASITAMAB
TAFAMIDIS vs TAFASITAMAB-CXIX
TAFAMIDIS vs TAFINLAR
TAFAMIDIS vs TAFLUPROST