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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does MINOXIDIL Cause Intentional product use issue? 110 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 110 reports of Intentional product use issue have been filed in association with MINOXIDIL (FLINKYE 5% Minoxidil Hair Growth). This represents 0.2% of all adverse event reports for MINOXIDIL.

110
Reports of Intentional product use issue with MINOXIDIL
0.2%
of all MINOXIDIL reports
0
Deaths
3
Hospitalizations

How Dangerous Is Intentional product use issue From MINOXIDIL?

Of the 110 reports, 3 (2.7%) required hospitalization.

Is Intentional product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for MINOXIDIL. However, 110 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 Intentional product use issue?

INFLIXIMAB (11,028) RITUXIMAB (9,602) INFLIXIMAB-DYYB (7,549) TOCILIZUMAB (5,078) METHOTREXATE (4,087) PREDNISONE (3,961) ABATACEPT (3,693) ADALIMUMAB (3,557) NIVOLUMAB (3,297) LEFLUNOMIDE (3,280)

Which MINOXIDIL Alternatives Have Lower Intentional product use issue Risk?

MINOXIDIL vs MIPOMERSEN MINOXIDIL vs MIRABEGRON MINOXIDIL vs MIRALAX MINOXIDIL vs MIRCERA MINOXIDIL vs MIRENA

Related Pages

MINOXIDIL Full Profile All Intentional product use issue Reports All Drugs Causing Intentional product use issue MINOXIDIL Demographics