Does LEUPROLIDE Cause Product administration error? 595 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 595 reports of Product administration error have been filed in association with LEUPROLIDE (Fensolvi). This represents 0.8% of all adverse event reports for LEUPROLIDE.
595
Reports of Product administration error with LEUPROLIDE
0.8%
of all LEUPROLIDE reports
4
Deaths
7
Hospitalizations
How Dangerous Is Product administration error From LEUPROLIDE?
Of the 595 reports, 4 (0.7%) resulted in death, 7 (1.2%) required hospitalization.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LEUPROLIDE. However, 595 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 administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
HYDROCHLOROTHIAZIDE\OLMESARTAN MEDOXOMIL (222)
Which LEUPROLIDE Alternatives Have Lower Product administration error Risk?
LEUPROLIDE vs LEVALBUTEROL
LEUPROLIDE vs LEVAMISOLE
LEUPROLIDE vs LEVAQUIN
LEUPROLIDE vs LEVEMIR
LEUPROLIDE vs LEVETIRACETAM