Does PRADAXA Cause Upper gastrointestinal haemorrhage? 119 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 119 reports of Upper gastrointestinal haemorrhage have been filed in association with PRADAXA. This represents 3.2% of all adverse event reports for PRADAXA.
119
Reports of Upper gastrointestinal haemorrhage with PRADAXA
3.2%
of all PRADAXA reports
28
Deaths
111
Hospitalizations
How Dangerous Is Upper gastrointestinal haemorrhage From PRADAXA?
Of the 119 reports, 28 (23.5%) resulted in death, 111 (93.3%) required hospitalization, and 4 (3.4%) were considered life-threatening.
Is Upper gastrointestinal haemorrhage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PRADAXA. However, 119 reports have been filed with the FAERS database.
What Other Side Effects Does PRADAXA Cause?
Gastrointestinal haemorrhage (907)
Anaemia (332)
Haemorrhage (311)
Haemorrhagic anaemia (286)
Cerebrovascular accident (218)
Coagulopathy (215)
Renal failure acute (193)
Lower gastrointestinal haemorrhage (135)
Fall (127)
Cerebral haemorrhage (125)
What Other Drugs Cause Upper gastrointestinal haemorrhage?
RIVAROXABAN (4,247)
ASPIRIN (3,411)
CLOPIDOGREL BISULFATE (1,265)
DABIGATRAN ETEXILATE (861)
IBUPROFEN (811)
APIXABAN (671)
WARFARIN (610)
NAPROXEN (445)
DICLOFENAC (305)
SERTRALINE (219)
Which PRADAXA Alternatives Have Lower Upper gastrointestinal haemorrhage Risk?
PRADAXA vs PRALATREXATE
PRADAXA vs PRALSETINIB
PRADAXA vs PRAMIPEXOLE
PRADAXA vs PRAMIPEXOLE\PRAMIPEXOLE
PRADAXA vs PRAMLINTIDE