Does EXENATIDE Cause Wrong technique in product usage process? 1,053 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,053 reports of Wrong technique in product usage process have been filed in association with EXENATIDE (Exenatide). This represents 3.4% of all adverse event reports for EXENATIDE.
1,053
Reports of Wrong technique in product usage process with EXENATIDE
3.4%
of all EXENATIDE reports
1
Deaths
49
Hospitalizations
How Dangerous Is Wrong technique in product usage process From EXENATIDE?
Of the 1,053 reports, 1 (0.1%) resulted in death, 49 (4.7%) required hospitalization.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EXENATIDE. However, 1,053 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which EXENATIDE Alternatives Have Lower Wrong technique in product usage process Risk?
EXENATIDE vs EXFORGE
EXENATIDE vs EXJADE
EXENATIDE vs EXTAVIA
EXENATIDE vs EXTRANEAL
EXENATIDE vs EYLEA