Does TIRZEPATIDE Cause Intercepted product storage error? 23 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 23 reports of Intercepted product storage error have been filed in association with TIRZEPATIDE (Zepbound). This represents 0.0% of all adverse event reports for TIRZEPATIDE.
23
Reports of Intercepted product storage error with TIRZEPATIDE
0.0%
of all TIRZEPATIDE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Intercepted product storage error From TIRZEPATIDE?
Of the 23 reports, 1 (4.3%) required hospitalization.
Is Intercepted product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TIRZEPATIDE. However, 23 reports have been filed with the FAERS database.
What Other Side Effects Does TIRZEPATIDE Cause?
Incorrect dose administered (23,301)
Injection site pain (10,989)
Nausea (10,018)
Off label use (7,007)
Extra dose administered (6,774)
Diarrhoea (5,463)
Vomiting (4,635)
Injection site haemorrhage (4,389)
Accidental underdose (3,897)
Injection site erythema (3,844)
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 TIRZEPATIDE Alternatives Have Lower Intercepted product storage error Risk?
TIRZEPATIDE vs TISAGENLECLEUCEL
TIRZEPATIDE vs TISLELIZUMAB
TIRZEPATIDE vs TISOTUMAB VEDOTIN
TIRZEPATIDE vs TISOTUMAB VEDOTIN-TFTV
TIRZEPATIDE vs TITANIUM DIOXIDE\ZINC