Does ALTEPLASE Cause Condition aggravated? 63 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 63 reports of Condition aggravated have been filed in association with ALTEPLASE (Activase). This represents 0.5% of all adverse event reports for ALTEPLASE.
63
Reports of Condition aggravated with ALTEPLASE
0.5%
of all ALTEPLASE reports
26
Deaths
23
Hospitalizations
How Dangerous Is Condition aggravated From ALTEPLASE?
Of the 63 reports, 26 (41.3%) resulted in death, 23 (36.5%) required hospitalization, and 12 (19.0%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALTEPLASE. However, 63 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which ALTEPLASE Alternatives Have Lower Condition aggravated Risk?
ALTEPLASE vs ALTERNARIA ALTERNATA
ALTEPLASE vs ALTHIAZIDE
ALTEPLASE vs ALTHIAZIDE\SPIRONOLACTONE
ALTEPLASE vs ALUMINUM
ALTEPLASE vs ALUMINUM HYDROXIDE