Does LEUPROLIDE Cause Intercepted product administration error? 307 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 307 reports of Intercepted product administration error have been filed in association with LEUPROLIDE (Fensolvi). This represents 0.4% of all adverse event reports for LEUPROLIDE.
307
Reports of Intercepted product administration error with LEUPROLIDE
0.4%
of all LEUPROLIDE reports
2
Deaths
0
Hospitalizations
How Dangerous Is Intercepted product administration error From LEUPROLIDE?
Of the 307 reports, 2 (0.7%) resulted in death.
Is Intercepted product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LEUPROLIDE. However, 307 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 Intercepted product administration error?
EVOLOCUMAB (2,508)
DENOSUMAB (1,209)
ERENUMAB-AOOE (1,015)
ETANERCEPT (574)
DARBEPOETIN ALFA (385)
PEGFILGRASTIM (356)
ERYTHROPOIETIN (301)
ROMOSOZUMAB-AQQG (115)
BENZYL ALCOHOL\ETANERCEPT (112)
CARFILZOMIB (102)
Which LEUPROLIDE Alternatives Have Lower Intercepted product administration error Risk?
LEUPROLIDE vs LEVALBUTEROL
LEUPROLIDE vs LEVAMISOLE
LEUPROLIDE vs LEVAQUIN
LEUPROLIDE vs LEVEMIR
LEUPROLIDE vs LEVETIRACETAM