Does EXENATIDE Cause Product quality issue? 1,839 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,839 reports of Product quality issue have been filed in association with EXENATIDE (Exenatide). This represents 5.9% of all adverse event reports for EXENATIDE.
1,839
Reports of Product quality issue with EXENATIDE
5.9%
of all EXENATIDE reports
1
Deaths
80
Hospitalizations
How Dangerous Is Product quality issue From EXENATIDE?
Of the 1,839 reports, 1 (0.1%) resulted in death, 80 (4.4%) required hospitalization, and 7 (0.4%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EXENATIDE. However, 1,839 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 quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
METHYLPHENIDATE (1,728)
Which EXENATIDE Alternatives Have Lower Product quality issue Risk?
EXENATIDE vs EXFORGE
EXENATIDE vs EXJADE
EXENATIDE vs EXTAVIA
EXENATIDE vs EXTRANEAL
EXENATIDE vs EYLEA