Does PRADAXA Cause Activated partial thromboplastin time prolonged? 13 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Activated partial thromboplastin time prolonged have been filed in association with PRADAXA. This represents 0.4% of all adverse event reports for PRADAXA.
13
Reports of Activated partial thromboplastin time prolonged with PRADAXA
0.4%
of all PRADAXA reports
4
Deaths
8
Hospitalizations
How Dangerous Is Activated partial thromboplastin time prolonged From PRADAXA?
Of the 13 reports, 4 (30.8%) resulted in death, 8 (61.5%) required hospitalization, and 3 (23.1%) were considered life-threatening.
Is Activated partial thromboplastin time prolonged Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PRADAXA. However, 13 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 Activated partial thromboplastin time prolonged?
DABIGATRAN ETEXILATE (264)
HEPARIN (225)
RIVAROXABAN (163)
WARFARIN (146)
ACETAMINOPHEN (119)
ALLOPURINOL (110)
AMIODARONE (99)
METRONIDAZOLE (98)
SIMVASTATIN (94)
DARBEPOETIN ALFA (93)
Which PRADAXA Alternatives Have Lower Activated partial thromboplastin time prolonged Risk?
PRADAXA vs PRALATREXATE
PRADAXA vs PRALSETINIB
PRADAXA vs PRAMIPEXOLE
PRADAXA vs PRAMIPEXOLE\PRAMIPEXOLE
PRADAXA vs PRAMLINTIDE