Does HISTRELIN Cause Incorrect product administration duration? 64 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 64 reports of Incorrect product administration duration have been filed in association with HISTRELIN (SUPPRELIN LA). This represents 11.1% of all adverse event reports for HISTRELIN.
64
Reports of Incorrect product administration duration with HISTRELIN
11.1%
of all HISTRELIN reports
0
Deaths
2
Hospitalizations
How Dangerous Is Incorrect product administration duration From HISTRELIN?
Of the 64 reports, 2 (3.1%) required hospitalization.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for HISTRELIN. However, 64 reports have been filed with the FAERS database.
What Other Side Effects Does HISTRELIN Cause?
Drug ineffective (94)
Incorrect drug administration duration (65)
Procedural complication (54)
Device breakage (49)
Rash (36)
Off label use (35)
Implant site rash (25)
Device expulsion (22)
Weight increased (22)
Headache (21)
What Other Drugs Cause Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which HISTRELIN Alternatives Have Lower Incorrect product administration duration Risk?
HISTRELIN vs HIZENTRA
HISTRELIN vs HOLOXAN
HISTRELIN vs HOMATROPINE HYDROBROMIDE
HISTRELIN vs HOMATROPINE METHYLBROMIDE\HYDROCODONE
HISTRELIN vs HOMEOPATHICS