Does DABIGATRAN ETEXILATE Cause Product administration error? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Product administration error have been filed in association with DABIGATRAN ETEXILATE (dabigatran etexilate). This represents 0.0% of all adverse event reports for DABIGATRAN ETEXILATE.
14
Reports of Product administration error with DABIGATRAN ETEXILATE
0.0%
of all DABIGATRAN ETEXILATE reports
4
Deaths
10
Hospitalizations
How Dangerous Is Product administration error From DABIGATRAN ETEXILATE?
Of the 14 reports, 4 (28.6%) resulted in death, 10 (71.4%) required hospitalization, and 2 (14.3%) were considered life-threatening.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DABIGATRAN ETEXILATE. However, 14 reports have been filed with the FAERS database.
What Other Side Effects Does DABIGATRAN ETEXILATE Cause?
Gastrointestinal haemorrhage (4,081)
Cerebrovascular accident (2,175)
Fall (1,786)
Ischaemic stroke (1,581)
Anaemia (1,412)
Haemorrhage (1,324)
Death (1,025)
Rectal haemorrhage (964)
Cerebral haemorrhage (946)
Upper gastrointestinal haemorrhage (861)
What Other Drugs Cause Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which DABIGATRAN ETEXILATE Alternatives Have Lower Product administration error Risk?
DABIGATRAN ETEXILATE vs DABRAFENIB
DABIGATRAN ETEXILATE vs DABRAFENIB\TRAMETINIB
DABIGATRAN ETEXILATE vs DACARBAZINE
DABIGATRAN ETEXILATE vs DACLATASVIR
DABIGATRAN ETEXILATE vs DACLIZUMAB