Does MINOXIDIL Cause Product use in unapproved indication? 2,506 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,506 reports of Product use in unapproved indication have been filed in association with MINOXIDIL (FLINKYE 5% Minoxidil Hair Growth). This represents 4.1% of all adverse event reports for MINOXIDIL.
2,506
Reports of Product use in unapproved indication with MINOXIDIL
4.1%
of all MINOXIDIL reports
0
Deaths
14
Hospitalizations
How Dangerous Is Product use in unapproved indication From MINOXIDIL?
Of the 2,506 reports, 14 (0.6%) required hospitalization, and 5 (0.2%) were considered life-threatening.
Is Product use in unapproved indication Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MINOXIDIL. However, 2,506 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)
Intentional product misuse (2,418)
Pruritus (2,414)
Overdose (2,361)
Hair texture abnormal (2,330)
What Other Drugs Cause Product use in unapproved indication?
DUPILUMAB (33,452)
DICLOFENAC (12,197)
METHOTREXATE (8,930)
PREDNISONE (7,625)
RITUXIMAB (7,519)
MYCOPHENOLATE MOFETIL (5,910)
ACETAMINOPHEN (5,819)
CYCLOPHOSPHAMIDE (5,750)
RISPERIDONE (5,551)
TACROLIMUS (5,057)
Which MINOXIDIL Alternatives Have Lower Product use in unapproved indication Risk?
MINOXIDIL vs MIPOMERSEN
MINOXIDIL vs MIRABEGRON
MINOXIDIL vs MIRALAX
MINOXIDIL vs MIRCERA
MINOXIDIL vs MIRENA