Does DIHYDROERGOTAMINE Cause Intentional product misuse? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Intentional product misuse have been filed in association with DIHYDROERGOTAMINE (Dihydroergotamine Mesylate). This represents 0.8% of all adverse event reports for DIHYDROERGOTAMINE.
8
Reports of Intentional product misuse with DIHYDROERGOTAMINE
0.8%
of all DIHYDROERGOTAMINE reports
0
Deaths
7
Hospitalizations
How Dangerous Is Intentional product misuse From DIHYDROERGOTAMINE?
Of the 8 reports, 7 (87.5%) required hospitalization.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DIHYDROERGOTAMINE. However, 8 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 Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which DIHYDROERGOTAMINE Alternatives Have Lower Intentional product misuse Risk?
DIHYDROERGOTAMINE vs DILANTIN
DIHYDROERGOTAMINE vs DILANTIN-125
DIHYDROERGOTAMINE vs DILAUDID
DIHYDROERGOTAMINE vs DILTIAZEM
DIHYDROERGOTAMINE vs DIMENHYDRINATE