Does LEUPROLIDE Cause Intercepted product preparation error? 8,621 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8,621 reports of Intercepted product preparation error have been filed in association with LEUPROLIDE (Fensolvi). This represents 12.2% of all adverse event reports for LEUPROLIDE.
8,621
Reports of Intercepted product preparation error with LEUPROLIDE
12.2%
of all LEUPROLIDE reports
5
Deaths
6
Hospitalizations
How Dangerous Is Intercepted product preparation error From LEUPROLIDE?
Of the 8,621 reports, 5 (0.1%) resulted in death, 6 (0.1%) required hospitalization.
Is Intercepted product preparation error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LEUPROLIDE. However, 8,621 reports have been filed with the FAERS database.
What Other Side Effects Does LEUPROLIDE Cause?
Hot flush (9,146)
Death (8,772)
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)
Off label use (2,060)
What Other Drugs Cause Intercepted product preparation error?
PEGFILGRASTIM (1,514)
DEVICE (1,033)
CARFILZOMIB (367)
BLINATUMOMAB (110)
BEVACIZUMAB-AWWB (54)
ROMIPLOSTIM (48)
TRASTUZUMAB-ANNS (42)
AFLIBERCEPT (39)
TOCILIZUMAB (26)
AVACINCAPTAD PEGOL (20)
Which LEUPROLIDE Alternatives Have Lower Intercepted product preparation error Risk?
LEUPROLIDE vs LEVALBUTEROL
LEUPROLIDE vs LEVAMISOLE
LEUPROLIDE vs LEVAQUIN
LEUPROLIDE vs LEVEMIR
LEUPROLIDE vs LEVETIRACETAM