Does EXENATIDE Cause Product storage error? 114 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 114 reports of Product storage error have been filed in association with EXENATIDE (Exenatide). This represents 0.4% of all adverse event reports for EXENATIDE.
114
Reports of Product storage error with EXENATIDE
0.4%
of all EXENATIDE reports
0
Deaths
4
Hospitalizations
How Dangerous Is Product storage error From EXENATIDE?
Of the 114 reports, 4 (3.5%) required hospitalization.
Is Product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EXENATIDE. However, 114 reports have been filed with the FAERS database.
What Other Side Effects Does EXENATIDE Cause?
Injection site haemorrhage (5,527)
Device leakage (5,115)
Injection site pain (4,577)
Injection site mass (3,506)
Blood glucose increased (3,363)
Incorrect dose administered by device (3,332)
Device malfunction (3,273)
Wrong technique in device usage process (3,255)
Device issue (2,862)
Weight decreased (2,702)
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 EXENATIDE Alternatives Have Lower Product storage error Risk?
EXENATIDE vs EXFORGE
EXENATIDE vs EXJADE
EXENATIDE vs EXTAVIA
EXENATIDE vs EXTRANEAL
EXENATIDE vs EYLEA