Does ALTEPLASE Cause Product preparation error? 65 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 65 reports of Product preparation error have been filed in association with ALTEPLASE (Activase). This represents 0.5% of all adverse event reports for ALTEPLASE.
65
Reports of Product preparation error with ALTEPLASE
0.5%
of all ALTEPLASE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product preparation error From ALTEPLASE?
Of the 65 reports.
Is Product preparation error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALTEPLASE. However, 65 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 preparation error?
ONABOTULINUMTOXINA (3,593)
EVOLOCUMAB (2,785)
DUPILUMAB (2,707)
BUPRENORPHINE\NALOXONE (777)
ABOBOTULINUMTOXINA (751)
ALBIGLUTIDE (691)
ALBUTEROL (520)
PEGFILGRASTIM (473)
ALIROCUMAB (402)
LEUPROLIDE (400)
Which ALTEPLASE Alternatives Have Lower Product preparation error Risk?
ALTEPLASE vs ALTERNARIA ALTERNATA
ALTEPLASE vs ALTHIAZIDE
ALTEPLASE vs ALTHIAZIDE\SPIRONOLACTONE
ALTEPLASE vs ALUMINUM
ALTEPLASE vs ALUMINUM HYDROXIDE