Does LEUPROLIDE Cause Product preparation error? 400 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 400 reports of Product preparation error have been filed in association with LEUPROLIDE (Fensolvi). This represents 0.6% of all adverse event reports for LEUPROLIDE.
400
Reports of Product preparation error with LEUPROLIDE
0.6%
of all LEUPROLIDE reports
3
Deaths
2
Hospitalizations
How Dangerous Is Product preparation error From LEUPROLIDE?
Of the 400 reports, 3 (0.8%) resulted in death, 2 (0.5%) required hospitalization.
Is Product preparation error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LEUPROLIDE. However, 400 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 Product preparation error?
ONABOTULINUMTOXINA (3,593)
EVOLOCUMAB (2,785)
DUPILUMAB (2,707)
BUPRENORPHINE\NALOXONE (777)
ABOBOTULINUMTOXINA (751)
ALBIGLUTIDE (691)
ALBUTEROL (520)
PEGFILGRASTIM (473)
ALIROCUMAB (402)
SODIUM OXYBATE (222)
Which LEUPROLIDE Alternatives Have Lower Product preparation error Risk?
LEUPROLIDE vs LEVALBUTEROL
LEUPROLIDE vs LEVAMISOLE
LEUPROLIDE vs LEVAQUIN
LEUPROLIDE vs LEVEMIR
LEUPROLIDE vs LEVETIRACETAM