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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 LEUPROLIDE Cause Device use error? 9 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Device use error have been filed in association with LEUPROLIDE (Fensolvi). This represents 0.0% of all adverse event reports for LEUPROLIDE.

9
Reports of Device use error with LEUPROLIDE
0.0%
of all LEUPROLIDE reports
0
Deaths
0
Hospitalizations

How Dangerous Is Device use error From LEUPROLIDE?

Of the 9 reports.

Is Device use error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for LEUPROLIDE. However, 9 reports have been filed with the FAERS database.

What Other Side Effects Does LEUPROLIDE Cause?

Hot flush (9,146) Death (8,772) Intercepted product preparation error (8,621) Syringe issue (7,847) Device leakage (5,861) Wrong technique in product usage process (5,062) Fatigue (4,805) Injection site pain (4,678) Prostatic specific antigen increased (2,432) Asthenia (2,176)

What Other Drugs Cause Device use error?

PEGFILGRASTIM (6,001) ALBUTEROL (5,215) ALBIGLUTIDE (4,056) EVOLOCUMAB (4,002) SOMATROPIN (2,801) FLUTICASONE\SALMETEROL (1,749) FLUTICASONE (783) FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (766) ERENUMAB-AOOE (711) ETANERCEPT (665)

Which LEUPROLIDE Alternatives Have Lower Device use error Risk?

LEUPROLIDE vs LEVALBUTEROL LEUPROLIDE vs LEVAMISOLE LEUPROLIDE vs LEVAQUIN LEUPROLIDE vs LEVEMIR LEUPROLIDE vs LEVETIRACETAM

Related Pages

LEUPROLIDE Full Profile All Device use error Reports All Drugs Causing Device use error LEUPROLIDE Demographics