Does LEUPROLIDE Cause Wrong technique in product usage process? 5,062 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5,062 reports of Wrong technique in product usage process have been filed in association with LEUPROLIDE (Fensolvi). This represents 7.1% of all adverse event reports for LEUPROLIDE.
5,062
Reports of Wrong technique in product usage process with LEUPROLIDE
7.1%
of all LEUPROLIDE reports
6
Deaths
14
Hospitalizations
How Dangerous Is Wrong technique in product usage process From LEUPROLIDE?
Of the 5,062 reports, 6 (0.1%) resulted in death, 14 (0.3%) required hospitalization.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LEUPROLIDE. However, 5,062 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)
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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
DICLOFENAC (2,298)
Which LEUPROLIDE Alternatives Have Lower Wrong technique in product usage process Risk?
LEUPROLIDE vs LEVALBUTEROL
LEUPROLIDE vs LEVAMISOLE
LEUPROLIDE vs LEVAQUIN
LEUPROLIDE vs LEVEMIR
LEUPROLIDE vs LEVETIRACETAM