Does EXENATIDE Cause Incorrect dose administered by device? 3,332 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 3,332 reports of Incorrect dose administered by device have been filed in association with EXENATIDE (Exenatide). This represents 10.7% of all adverse event reports for EXENATIDE.
3,332
Reports of Incorrect dose administered by device with EXENATIDE
10.7%
of all EXENATIDE reports
0
Deaths
75
Hospitalizations
How Dangerous Is Incorrect dose administered by device From EXENATIDE?
Of the 3,332 reports, 75 (2.3%) required hospitalization, and 1 (0.0%) were considered life-threatening.
Is Incorrect dose administered by device Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EXENATIDE. However, 3,332 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)
Device malfunction (3,273)
Wrong technique in device usage process (3,255)
Device issue (2,862)
Weight decreased (2,702)
Injection site extravasation (2,320)
What Other Drugs Cause Incorrect dose administered by device?
EVOLOCUMAB (2,840)
SOMATROPIN (2,486)
ALBUTEROL (1,236)
ETANERCEPT (1,032)
SECUKINUMAB (996)
ERENUMAB-AOOE (973)
BUDESONIDE\FORMOTEROL (753)
INSULIN GLARGINE (753)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (674)
PEGFILGRASTIM (487)
Which EXENATIDE Alternatives Have Lower Incorrect dose administered by device Risk?
EXENATIDE vs EXFORGE
EXENATIDE vs EXJADE
EXENATIDE vs EXTAVIA
EXENATIDE vs EXTRANEAL
EXENATIDE vs EYLEA