Does EDOXABAN Cause Wrong technique in product usage process? 47 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 47 reports of Wrong technique in product usage process have been filed in association with EDOXABAN (SAVAYSA). This represents 0.6% of all adverse event reports for EDOXABAN.
47
Reports of Wrong technique in product usage process with EDOXABAN
0.6%
of all EDOXABAN reports
13
Deaths
35
Hospitalizations
How Dangerous Is Wrong technique in product usage process From EDOXABAN?
Of the 47 reports, 13 (27.7%) resulted in death, 35 (74.5%) required hospitalization, and 2 (4.3%) 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 EDOXABAN. However, 47 reports have been filed with the FAERS database.
What Other Side Effects Does EDOXABAN Cause?
Anaemia (663)
Cerebral infarction (419)
Gastrointestinal haemorrhage (378)
Renal impairment (359)
Cerebrovascular accident (337)
Dyspnoea (331)
General physical health deterioration (315)
Haematuria (312)
Fall (298)
Cardiac failure (272)
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 EDOXABAN Alternatives Have Lower Wrong technique in product usage process Risk?
EDOXABAN vs EDOXABAN TOSILATE
EDOXABAN vs EFALIZUMAB
EDOXABAN vs EFANESOCTOCOG ALFA
EDOXABAN vs EFAVIRENZ
EDOXABAN vs EFAVIRENZ\EMTRICITABINE\TENOFOVIR DISOPROXIL