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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does HISTRELIN Cause Product quality issue? 8 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Product quality issue have been filed in association with HISTRELIN (SUPPRELIN LA). This represents 1.4% of all adverse event reports for HISTRELIN.

8
Reports of Product quality issue with HISTRELIN
1.4%
of all HISTRELIN reports
0
Deaths
0
Hospitalizations

How Dangerous Is Product quality issue From HISTRELIN?

Of the 8 reports.

Is Product quality issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for HISTRELIN. However, 8 reports have been filed with the FAERS database.

What Other Side Effects Does HISTRELIN Cause?

Drug ineffective (94) Incorrect drug administration duration (65) Incorrect product administration duration (64) Procedural complication (54) Device breakage (49) Rash (36) Off label use (35) Implant site rash (25) Device expulsion (22) Weight increased (22)

What Other Drugs Cause Product quality issue?

ETONOGESTREL (4,651) ALBUTEROL (4,466) TIOTROPIUM (3,821) MOMETASONE FUROATE (3,406) LIDOCAINE (3,126) FLUTICASONE\SALMETEROL (2,986) FORMOTEROL\MOMETASONE FUROATE (2,458) FENTANYL (2,450) NICOTINE (1,987) EXENATIDE (1,839)

Which HISTRELIN Alternatives Have Lower Product quality issue Risk?

HISTRELIN vs HIZENTRA HISTRELIN vs HOLOXAN HISTRELIN vs HOMATROPINE HYDROBROMIDE HISTRELIN vs HOMATROPINE METHYLBROMIDE\HYDROCODONE HISTRELIN vs HOMEOPATHICS

Related Pages

HISTRELIN Full Profile All Product quality issue Reports All Drugs Causing Product quality issue HISTRELIN Demographics