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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does ALTEPLASE Cause Product administration error? 16 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Product administration error have been filed in association with ALTEPLASE (Activase). This represents 0.1% of all adverse event reports for ALTEPLASE.

16
Reports of Product administration error with ALTEPLASE
0.1%
of all ALTEPLASE reports
1
Deaths
1
Hospitalizations

How Dangerous Is Product administration error From ALTEPLASE?

Of the 16 reports, 1 (6.3%) resulted in death, 1 (6.3%) required hospitalization, and 1 (6.3%) were considered life-threatening.

Is Product administration error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ALTEPLASE. However, 16 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 administration error?

HYDROXYPROGESTERONE CAPROATE (972) ACETAMINOPHEN (666) CENEGERMIN-BKBJ (613) LEUPROLIDE (595) EVOLOCUMAB (565) ADALIMUMAB (543) METHYLPHENIDATE (414) OLMESARTAN MEDOXOMIL (314) ASPIRIN (241) SECUKINUMAB (225)

Which ALTEPLASE Alternatives Have Lower Product administration error Risk?

ALTEPLASE vs ALTERNARIA ALTERNATA ALTEPLASE vs ALTHIAZIDE ALTEPLASE vs ALTHIAZIDE\SPIRONOLACTONE ALTEPLASE vs ALUMINUM ALTEPLASE vs ALUMINUM HYDROXIDE

Related Pages

ALTEPLASE Full Profile All Product administration error Reports All Drugs Causing Product administration error ALTEPLASE Demographics