Does ENZALUTAMIDE Cause Wrong technique in product usage process? 216 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 216 reports of Wrong technique in product usage process have been filed in association with ENZALUTAMIDE (Xtandi). This represents 0.4% of all adverse event reports for ENZALUTAMIDE.
216
Reports of Wrong technique in product usage process with ENZALUTAMIDE
0.4%
of all ENZALUTAMIDE reports
39
Deaths
53
Hospitalizations
How Dangerous Is Wrong technique in product usage process From ENZALUTAMIDE?
Of the 216 reports, 39 (18.1%) resulted in death, 53 (24.5%) required hospitalization, and 1 (0.5%) were considered life-threatening.
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 ENZALUTAMIDE. However, 216 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 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)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which ENZALUTAMIDE Alternatives Have Lower Wrong technique in product usage process Risk?
ENZALUTAMIDE vs EPCORITAMAB
ENZALUTAMIDE vs EPCORITAMAB-BYSP
ENZALUTAMIDE vs EPERISONE
ENZALUTAMIDE vs EPHEDRINE
ENZALUTAMIDE vs EPINASTINE