Does ALTEPLASE Cause Product storage error? 371 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 371 reports of Product storage error have been filed in association with ALTEPLASE (Activase). This represents 2.9% of all adverse event reports for ALTEPLASE.
371
Reports of Product storage error with ALTEPLASE
2.9%
of all ALTEPLASE reports
1
Deaths
2
Hospitalizations
How Dangerous Is Product storage error From ALTEPLASE?
Of the 371 reports, 1 (0.3%) resulted in death, 2 (0.5%) required hospitalization, and 2 (0.5%) were considered life-threatening.
Is Product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALTEPLASE. However, 371 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 Product storage error?
INSULIN GLARGINE (7,743)
EVOLOCUMAB (6,606)
ETANERCEPT (3,653)
DENOSUMAB (3,621)
ERENUMAB-AOOE (2,958)
DUPILUMAB (2,631)
ALBUTEROL (2,474)
ABATACEPT (2,101)
DARBEPOETIN ALFA (1,619)
INSULIN LISPRO (1,448)
Which ALTEPLASE Alternatives Have Lower Product storage error Risk?
ALTEPLASE vs ALTERNARIA ALTERNATA
ALTEPLASE vs ALTHIAZIDE
ALTEPLASE vs ALTHIAZIDE\SPIRONOLACTONE
ALTEPLASE vs ALUMINUM
ALTEPLASE vs ALUMINUM HYDROXIDE