Does LEUPROLIDE Cause Product storage error? 199 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 199 reports of Product storage error have been filed in association with LEUPROLIDE (Fensolvi). This represents 0.3% of all adverse event reports for LEUPROLIDE.
199
Reports of Product storage error with LEUPROLIDE
0.3%
of all LEUPROLIDE reports
3
Deaths
4
Hospitalizations
How Dangerous Is Product storage error From LEUPROLIDE?
Of the 199 reports, 3 (1.5%) resulted in death, 4 (2.0%) required hospitalization, and 3 (1.5%) were considered life-threatening.
Is Product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LEUPROLIDE. However, 199 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 storage error?
INSULIN GLARGINE (7,743)
EVOLOCUMAB (6,606)
ETANERCEPT (3,653)
DENOSUMAB (3,621)
ERENUMAB-AOOE (2,958)
DUPILUMAB (2,631)
ALBUTEROL (2,474)
ABATACEPT (2,101)
DARBEPOETIN ALFA (1,619)
INSULIN LISPRO (1,448)
Which LEUPROLIDE Alternatives Have Lower Product storage error Risk?
LEUPROLIDE vs LEVALBUTEROL
LEUPROLIDE vs LEVAMISOLE
LEUPROLIDE vs LEVAQUIN
LEUPROLIDE vs LEVEMIR
LEUPROLIDE vs LEVETIRACETAM