Does MINOXIDIL Cause Wrong patient received product? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Wrong patient received product have been filed in association with MINOXIDIL (FLINKYE 5% Minoxidil Hair Growth). This represents 0.0% of all adverse event reports for MINOXIDIL.
6
Reports of Wrong patient received product with MINOXIDIL
0.0%
of all MINOXIDIL reports
0
Deaths
0
Hospitalizations
How Dangerous Is Wrong patient received product From MINOXIDIL?
Of the 6 reports.
Is Wrong patient received product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MINOXIDIL. However, 6 reports have been filed with the FAERS database.
What Other Side Effects Does MINOXIDIL Cause?
Drug ineffective (10,352)
Adverse drug reaction (8,530)
Alopecia (7,275)
Product use issue (5,249)
Off label use (4,913)
Application site pruritus (3,727)
Product use in unapproved indication (2,506)
Intentional product misuse (2,418)
Pruritus (2,414)
Overdose (2,361)
What Other Drugs Cause Wrong patient received product?
INSULIN LISPRO (334)
CLOZAPINE (198)
RISPERIDONE (176)
OXAZEPAM (152)
BISOPROLOL (150)
LEVETIRACETAM (126)
ACETAMINOPHEN (123)
METFORMIN (116)
INSULIN GLARGINE (114)
CLONAZEPAM (112)
Which MINOXIDIL Alternatives Have Lower Wrong patient received product Risk?
MINOXIDIL vs MIPOMERSEN
MINOXIDIL vs MIRABEGRON
MINOXIDIL vs MIRALAX
MINOXIDIL vs MIRCERA
MINOXIDIL vs MIRENA