Does ALTEPLASE Cause International normalised ratio increased? 29 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 29 reports of International normalised ratio increased have been filed in association with ALTEPLASE (Activase). This represents 0.2% of all adverse event reports for ALTEPLASE.
29
Reports of International normalised ratio increased with ALTEPLASE
0.2%
of all ALTEPLASE reports
5
Deaths
6
Hospitalizations
How Dangerous Is International normalised ratio increased From ALTEPLASE?
Of the 29 reports, 5 (17.2%) resulted in death, 6 (20.7%) required hospitalization, and 1 (3.4%) 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 ALTEPLASE. However, 29 reports have been filed with the FAERS database.
What Other Side Effects Does ALTEPLASE Cause?
No adverse event (2,456)
Off label use (1,752)
Gingival bleeding (1,018)
Cerebral haemorrhage (819)
Death (818)
Haemorrhage intracranial (615)
Angioedema (603)
Haemorrhage (536)
Drug ineffective (524)
Haemorrhagic transformation stroke (496)
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 ALTEPLASE Alternatives Have Lower International normalised ratio increased Risk?
ALTEPLASE vs ALTERNARIA ALTERNATA
ALTEPLASE vs ALTHIAZIDE
ALTEPLASE vs ALTHIAZIDE\SPIRONOLACTONE
ALTEPLASE vs ALUMINUM
ALTEPLASE vs ALUMINUM HYDROXIDE