Does EXENATIDE Cause Product packaging quantity issue? 154 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 154 reports of Product packaging quantity issue have been filed in association with EXENATIDE (Exenatide). This represents 0.5% of all adverse event reports for EXENATIDE.
154
Reports of Product packaging quantity issue with EXENATIDE
0.5%
of all EXENATIDE reports
0
Deaths
6
Hospitalizations
How Dangerous Is Product packaging quantity issue From EXENATIDE?
Of the 154 reports, 6 (3.9%) required hospitalization.
Is Product packaging quantity issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EXENATIDE. However, 154 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 packaging quantity issue?
LEUPROLIDE (523)
ALBUTEROL (431)
BUDESONIDE\FORMOTEROL (301)
FENTANYL (286)
BUPRENORPHINE (225)
CYCLOSPORINE (206)
ESTRADIOL (201)
BIMATOPROST (177)
RIVAROXABAN (174)
LIFITEGRAST (153)
Which EXENATIDE Alternatives Have Lower Product packaging quantity issue Risk?
EXENATIDE vs EXFORGE
EXENATIDE vs EXJADE
EXENATIDE vs EXTAVIA
EXENATIDE vs EXTRANEAL
EXENATIDE vs EYLEA