Does DIHYDROERGOTAMINE Cause Wrong technique in product usage process? 10 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Wrong technique in product usage process have been filed in association with DIHYDROERGOTAMINE (Dihydroergotamine Mesylate). This represents 1.0% of all adverse event reports for DIHYDROERGOTAMINE.
10
Reports of Wrong technique in product usage process with DIHYDROERGOTAMINE
1.0%
of all DIHYDROERGOTAMINE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Wrong technique in product usage process From DIHYDROERGOTAMINE?
Of the 10 reports.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DIHYDROERGOTAMINE. However, 10 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which DIHYDROERGOTAMINE Alternatives Have Lower Wrong technique in product usage process Risk?
DIHYDROERGOTAMINE vs DILANTIN
DIHYDROERGOTAMINE vs DILANTIN-125
DIHYDROERGOTAMINE vs DILAUDID
DIHYDROERGOTAMINE vs DILTIAZEM
DIHYDROERGOTAMINE vs DIMENHYDRINATE