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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does EXENATIDE Cause Intentional product misuse? 1,433 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 1,433 reports of Intentional product misuse have been filed in association with EXENATIDE (Exenatide). This represents 4.6% of all adverse event reports for EXENATIDE.

1,433
Reports of Intentional product misuse with EXENATIDE
4.6%
of all EXENATIDE reports
1
Deaths
87
Hospitalizations

How Dangerous Is Intentional product misuse From EXENATIDE?

Of the 1,433 reports, 1 (0.1%) resulted in death, 87 (6.1%) required hospitalization, and 5 (0.3%) were considered life-threatening.

Is Intentional product misuse Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for EXENATIDE. However, 1,433 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 Intentional product misuse?

ETANERCEPT (3,992) PREGABALIN (3,731) BUDESONIDE\FORMOTEROL (3,399) ACETAMINOPHEN (2,924) ESOMEPRAZOLE (2,852) MINOXIDIL (2,418) TOFACITINIB (2,331) CINACALCET (2,092) QUETIAPINE (1,855) ALPRAZOLAM (1,709)

Which EXENATIDE Alternatives Have Lower Intentional product misuse Risk?

EXENATIDE vs EXFORGE EXENATIDE vs EXJADE EXENATIDE vs EXTAVIA EXENATIDE vs EXTRANEAL EXENATIDE vs EYLEA

Related Pages

EXENATIDE Full Profile All Intentional product misuse Reports All Drugs Causing Intentional product misuse EXENATIDE Demographics