Does TENECTEPLASE Cause Intercepted product storage error? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Intercepted product storage error have been filed in association with TENECTEPLASE (TNKase). This represents 0.5% of all adverse event reports for TENECTEPLASE.
7
Reports of Intercepted product storage error with TENECTEPLASE
0.5%
of all TENECTEPLASE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Intercepted product storage error From TENECTEPLASE?
Of the 7 reports.
Is Intercepted product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TENECTEPLASE. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does TENECTEPLASE Cause?
Off label use (430)
No adverse event (313)
Cerebral haemorrhage (132)
Angioedema (112)
Haemorrhage intracranial (74)
Haemorrhage (71)
Drug ineffective (68)
Death (60)
Haemorrhagic transformation stroke (49)
Cerebrovascular accident (45)
What Other Drugs Cause Intercepted product storage error?
TOCILIZUMAB (381)
DUPILUMAB (325)
OMALIZUMAB (256)
ALTEPLASE (227)
INSULIN GLARGINE (129)
DORNASE ALFA (115)
BEVACIZUMAB (113)
RITUXIMAB (105)
OCRELIZUMAB (88)
PERTUZUMAB (84)
Which TENECTEPLASE Alternatives Have Lower Intercepted product storage error Risk?
TENECTEPLASE vs TENELIGLIPTIN
TENECTEPLASE vs TENIPOSIDE
TENECTEPLASE vs TENOFOVIR
TENECTEPLASE vs TENOFOVIR ALAFENAMIDE
TENECTEPLASE vs TENOFOVIR DISOPROXIL