Does TRIPTORELIN Cause Product administration error? 71 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 71 reports of Product administration error have been filed in association with TRIPTORELIN (TRIPTODUR). This represents 1.3% of all adverse event reports for TRIPTORELIN.
71
Reports of Product administration error with TRIPTORELIN
1.3%
of all TRIPTORELIN reports
0
Deaths
2
Hospitalizations
How Dangerous Is Product administration error From TRIPTORELIN?
Of the 71 reports, 2 (2.8%) required hospitalization.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TRIPTORELIN. However, 71 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 administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which TRIPTORELIN Alternatives Have Lower Product administration error Risk?
TRIPTORELIN vs TRISODIUM
TRIPTORELIN vs TROFINETIDE
TRIPTORELIN vs TROFOSFAMIDE
TRIPTORELIN vs TROPATEPINE
TRIPTORELIN vs TROPICAMIDE