Does AMBRISENTAN Cause International normalised ratio increased? 94 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 94 reports of International normalised ratio increased have been filed in association with AMBRISENTAN (AMBRISENTAN). This represents 0.1% of all adverse event reports for AMBRISENTAN.
94
Reports of International normalised ratio increased with AMBRISENTAN
0.1%
of all AMBRISENTAN reports
2
Deaths
54
Hospitalizations
How Dangerous Is International normalised ratio increased From AMBRISENTAN?
Of the 94 reports, 2 (2.1%) resulted in death, 54 (57.4%) required hospitalization, and 1 (1.1%) were considered life-threatening.
Is International normalised ratio increased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AMBRISENTAN. However, 94 reports have been filed with the FAERS database.
What Other Side Effects Does AMBRISENTAN Cause?
Dyspnoea (13,367)
Death (7,497)
Headache (7,325)
Pneumonia (4,693)
Dizziness (4,561)
Fatigue (4,436)
Diarrhoea (4,312)
Nausea (3,986)
Fluid retention (3,927)
Malaise (3,839)
What Other Drugs Cause International normalised ratio increased?
WARFARIN (5,622)
RIVAROXABAN (863)
ACETAMINOPHEN (533)
ASPIRIN (448)
APIXABAN (317)
CLOPIDOGREL BISULFATE (314)
FLUINDIONE (286)
AMIODARONE (277)
FUROSEMIDE (277)
DABIGATRAN ETEXILATE (223)
Which AMBRISENTAN Alternatives Have Lower International normalised ratio increased Risk?
AMBRISENTAN vs AMBROSIA ARTEMISIIFOLIA POLLEN
AMBRISENTAN vs AMBROXOL
AMBRISENTAN vs AMDINOCILLIN PIVOXIL
AMBRISENTAN vs AMG-510
AMBRISENTAN vs AMIFAMPRIDINE