Does TIRZEPATIDE Cause Product storage error? 707 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 707 reports of Product storage error have been filed in association with TIRZEPATIDE (Zepbound). This represents 0.7% of all adverse event reports for TIRZEPATIDE.
707
Reports of Product storage error with TIRZEPATIDE
0.7%
of all TIRZEPATIDE reports
0
Deaths
13
Hospitalizations
How Dangerous Is Product storage error From TIRZEPATIDE?
Of the 707 reports, 13 (1.8%) required hospitalization, and 1 (0.1%) 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 TIRZEPATIDE. However, 707 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 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 TIRZEPATIDE Alternatives Have Lower Product storage error Risk?
TIRZEPATIDE vs TISAGENLECLEUCEL
TIRZEPATIDE vs TISLELIZUMAB
TIRZEPATIDE vs TISOTUMAB VEDOTIN
TIRZEPATIDE vs TISOTUMAB VEDOTIN-TFTV
TIRZEPATIDE vs TITANIUM DIOXIDE\ZINC