Does TRIPTORELIN Cause Product reconstitution quality issue? 28 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 28 reports of Product reconstitution quality issue have been filed in association with TRIPTORELIN (TRIPTODUR). This represents 0.5% of all adverse event reports for TRIPTORELIN.
28
Reports of Product reconstitution quality issue with TRIPTORELIN
0.5%
of all TRIPTORELIN reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product reconstitution quality issue From TRIPTORELIN?
Of the 28 reports, 1 (3.6%) required hospitalization.
Is Product reconstitution quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TRIPTORELIN. However, 28 reports have been filed with the FAERS database.
What Other Side Effects Does TRIPTORELIN Cause?
Off label use (545)
Death (362)
Ovarian hyperstimulation syndrome (356)
Needle issue (242)
Disease progression (203)
Product dose omission issue (178)
Drug ineffective (175)
Weight increased (167)
Hot flush (153)
Headache (145)
What Other Drugs Cause Product reconstitution quality issue?
SOMATROPIN (149)
LEUPROLIDE (108)
RISPERIDONE (34)
SULFUR HEXAFLUORIDE (23)
ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT (20)
HUMAN C1-ESTERASE INHIBITOR (20)
AZACITIDINE (17)
ONABOTULINUMTOXINA (16)
NALTREXONE (15)
TEDUGLUTIDE (15)
Which TRIPTORELIN Alternatives Have Lower Product reconstitution quality issue Risk?
TRIPTORELIN vs TRISODIUM
TRIPTORELIN vs TROFINETIDE
TRIPTORELIN vs TROFOSFAMIDE
TRIPTORELIN vs TROPATEPINE
TRIPTORELIN vs TROPICAMIDE