Does DIHYDROERGOTAMINE Cause Product substitution issue? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Product substitution issue have been filed in association with DIHYDROERGOTAMINE (Dihydroergotamine Mesylate). This represents 0.5% of all adverse event reports for DIHYDROERGOTAMINE.
5
Reports of Product substitution issue with DIHYDROERGOTAMINE
0.5%
of all DIHYDROERGOTAMINE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Product substitution issue From DIHYDROERGOTAMINE?
Of the 5 reports, 2 (40.0%) required hospitalization.
Is Product substitution issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DIHYDROERGOTAMINE. However, 5 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 substitution issue?
AMPHETAMINE ASPARTATE\AMPHETAMINE\DEXTROAMPHETAMINE SACCHARATE\DEXTROAMPHETAMINE (2,832)
BUPROPION (1,578)
METHYLPHENIDATE (1,408)
CLONAZEPAM (1,288)
LAMOTRIGINE (979)
ALBUTEROL (864)
LEVOTHYROXINE (803)
DULOXETINE (766)
ESTRADIOL (692)
SERTRALINE (636)
Which DIHYDROERGOTAMINE Alternatives Have Lower Product substitution issue Risk?
DIHYDROERGOTAMINE vs DILANTIN
DIHYDROERGOTAMINE vs DILANTIN-125
DIHYDROERGOTAMINE vs DILAUDID
DIHYDROERGOTAMINE vs DILTIAZEM
DIHYDROERGOTAMINE vs DIMENHYDRINATE