Does MINOXIDIL Cause Product administration error? 36 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 36 reports of Product administration error have been filed in association with MINOXIDIL (FLINKYE 5% Minoxidil Hair Growth). This represents 0.1% of all adverse event reports for MINOXIDIL.
36
Reports of Product administration error with MINOXIDIL
0.1%
of all MINOXIDIL reports
0
Deaths
7
Hospitalizations
How Dangerous Is Product administration error From MINOXIDIL?
Of the 36 reports, 7 (19.4%) required hospitalization.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MINOXIDIL. However, 36 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 Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which MINOXIDIL Alternatives Have Lower Product administration error Risk?
MINOXIDIL vs MIPOMERSEN
MINOXIDIL vs MIRABEGRON
MINOXIDIL vs MIRALAX
MINOXIDIL vs MIRCERA
MINOXIDIL vs MIRENA