Does DEGARELIX Cause Intentional product use issue? 17 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 17 reports of Intentional product use issue have been filed in association with DEGARELIX (FIRMAGON). This represents 0.5% of all adverse event reports for DEGARELIX.
17
Reports of Intentional product use issue with DEGARELIX
0.5%
of all DEGARELIX reports
2
Deaths
11
Hospitalizations
How Dangerous Is Intentional product use issue From DEGARELIX?
Of the 17 reports, 2 (11.8%) resulted in death, 11 (64.7%) required hospitalization, and 1 (5.9%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEGARELIX. However, 17 reports have been filed with the FAERS database.
What Other Side Effects Does DEGARELIX Cause?
Injection site pain (296)
Injection site erythema (246)
Hot flush (199)
Fatigue (195)
Injection site swelling (183)
Product storage error (177)
Pyrexia (170)
Off label use (128)
Asthenia (123)
Death (120)
What Other Drugs Cause Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which DEGARELIX Alternatives Have Lower Intentional product use issue Risk?
DEGARELIX vs DELAFLOXACIN MEGLUMINE
DEGARELIX vs DELAMANID
DEGARELIX vs DELANDISTROGENE MOXEPARVOVEC-ROKL
DEGARELIX vs DELAVIRDINE
DEGARELIX vs DELORAZEPAM