Does ENZALUTAMIDE Cause Product use complaint? 336 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 336 reports of Product use complaint have been filed in association with ENZALUTAMIDE (Xtandi). This represents 0.7% of all adverse event reports for ENZALUTAMIDE.
336
Reports of Product use complaint with ENZALUTAMIDE
0.7%
of all ENZALUTAMIDE reports
43
Deaths
60
Hospitalizations
How Dangerous Is Product use complaint From ENZALUTAMIDE?
Of the 336 reports, 43 (12.8%) resulted in death, 60 (17.9%) required hospitalization, and 2 (0.6%) were considered life-threatening.
Is Product use complaint Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ENZALUTAMIDE. However, 336 reports have been filed with the FAERS database.
What Other Side Effects Does ENZALUTAMIDE Cause?
Fatigue (8,891)
Death (6,680)
Malignant neoplasm progression (4,696)
Prostatic specific antigen increased (3,731)
Asthenia (3,589)
Drug ineffective (3,468)
Hot flush (3,144)
Decreased appetite (3,069)
Nausea (2,898)
Dizziness (2,776)
What Other Drugs Cause Product use complaint?
TROFINETIDE (472)
LIFITEGRAST (326)
VOXELOTOR (298)
CLASCOTERONE (285)
NIRMATRELVIR\RITONAVIR (248)
ABALOPARATIDE (224)
ESTRADIOL (208)
MOLNUPIRAVIR (206)
ACETAMINOPHEN (202)
DIMETHICONE\LOPERAMIDE (201)
Which ENZALUTAMIDE Alternatives Have Lower Product use complaint Risk?
ENZALUTAMIDE vs EPCORITAMAB
ENZALUTAMIDE vs EPCORITAMAB-BYSP
ENZALUTAMIDE vs EPERISONE
ENZALUTAMIDE vs EPHEDRINE
ENZALUTAMIDE vs EPINASTINE