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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 PERGOLIDE Cause Product use in unapproved indication? 7 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Product use in unapproved indication have been filed in association with PERGOLIDE. This represents 10.5% of all adverse event reports for PERGOLIDE.

7
Reports of Product use in unapproved indication with PERGOLIDE
10.5%
of all PERGOLIDE reports
0
Deaths
0
Hospitalizations

How Dangerous Is Product use in unapproved indication From PERGOLIDE?

Of the 7 reports.

Is Product use in unapproved indication Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for PERGOLIDE. However, 7 reports have been filed with the FAERS database.

What Other Side Effects Does PERGOLIDE Cause?

Drug ineffective (17) Gambling disorder (15) Condition aggravated (12) Hypersomnia (12) Insomnia (12) Parkinson's disease psychosis (12) Drug abuse (11) Hypersexuality (11) Dopamine dysregulation syndrome (10) Anxiety (9)

What Other Drugs Cause Product use in unapproved indication?

DUPILUMAB (33,452) DICLOFENAC (12,197) METHOTREXATE (8,930) PREDNISONE (7,625) RITUXIMAB (7,519) MYCOPHENOLATE MOFETIL (5,910) ACETAMINOPHEN (5,819) CYCLOPHOSPHAMIDE (5,750) RISPERIDONE (5,551) TACROLIMUS (5,057)

Related Pages

PERGOLIDE Full Profile All Product use in unapproved indication Reports All Drugs Causing Product use in unapproved indication PERGOLIDE Demographics