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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 DIHYDROERGOTAMINE Cause Product use issue? 29 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 29 reports of Product use issue have been filed in association with DIHYDROERGOTAMINE (Dihydroergotamine Mesylate). This represents 2.7% of all adverse event reports for DIHYDROERGOTAMINE.

29
Reports of Product use issue with DIHYDROERGOTAMINE
2.7%
of all DIHYDROERGOTAMINE reports
0
Deaths
0
Hospitalizations

How Dangerous Is Product use issue From DIHYDROERGOTAMINE?

Of the 29 reports.

Is Product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DIHYDROERGOTAMINE. However, 29 reports have been filed with the FAERS database.

What Other Side Effects Does DIHYDROERGOTAMINE Cause?

Drug ineffective (565) Nausea (350) Off label use (343) Hyperhidrosis (314) Nightmare (313) Sedation (313) Product use in unapproved indication (252) Nephrolithiasis (230) Migraine (100) Treatment failure (99)

What Other Drugs Cause Product use issue?

INFLIXIMAB (12,752) DUPILUMAB (10,575) POLYETHYLENE GLYCOL 3350 (9,432) METHOTREXATE (8,185) DICLOFENAC (8,009) RITUXIMAB (6,948) ADALIMUMAB (6,379) ETANERCEPT (6,062) TOCILIZUMAB (5,944) ABATACEPT (5,915)

Which DIHYDROERGOTAMINE Alternatives Have Lower Product use issue Risk?

DIHYDROERGOTAMINE vs DILANTIN DIHYDROERGOTAMINE vs DILANTIN-125 DIHYDROERGOTAMINE vs DILAUDID DIHYDROERGOTAMINE vs DILTIAZEM DIHYDROERGOTAMINE vs DIMENHYDRINATE

Related Pages

DIHYDROERGOTAMINE Full Profile All Product use issue Reports All Drugs Causing Product use issue DIHYDROERGOTAMINE Demographics