Does DIHYDROERGOTAMINE Cause Off label use? 343 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 343 reports of Off label use have been filed in association with DIHYDROERGOTAMINE (Dihydroergotamine Mesylate). This represents 32.5% of all adverse event reports for DIHYDROERGOTAMINE.
343
Reports of Off label use with DIHYDROERGOTAMINE
32.5%
of all DIHYDROERGOTAMINE reports
0
Deaths
18
Hospitalizations
How Dangerous Is Off label use From DIHYDROERGOTAMINE?
Of the 343 reports, 18 (5.2%) required hospitalization.
Is Off label use Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DIHYDROERGOTAMINE. However, 343 reports have been filed with the FAERS database.
What Other Side Effects Does DIHYDROERGOTAMINE Cause?
Drug ineffective (565)
Nausea (350)
Hyperhidrosis (314)
Nightmare (313)
Sedation (313)
Product use in unapproved indication (252)
Nephrolithiasis (230)
Migraine (100)
Treatment failure (99)
Dyspnoea (94)
What Other Drugs Cause Off label use?
RITUXIMAB (39,751)
INFLIXIMAB (34,801)
DENOSUMAB (34,612)
METHOTREXATE (24,020)
VEDOLIZUMAB (21,017)
ETANERCEPT (20,178)
TOCILIZUMAB (18,256)
PREDNISONE (17,867)
LENALIDOMIDE (17,017)
ADALIMUMAB (16,417)
Which DIHYDROERGOTAMINE Alternatives Have Lower Off label use Risk?
DIHYDROERGOTAMINE vs DILANTIN
DIHYDROERGOTAMINE vs DILANTIN-125
DIHYDROERGOTAMINE vs DILAUDID
DIHYDROERGOTAMINE vs DILTIAZEM
DIHYDROERGOTAMINE vs DIMENHYDRINATE