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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 Application site discharge? 45 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 45 reports of Application site discharge have been filed in association with MINOXIDIL (FLINKYE 5% Minoxidil Hair Growth). This represents 0.1% of all adverse event reports for MINOXIDIL.

45
Reports of Application site discharge with MINOXIDIL
0.1%
of all MINOXIDIL reports
0
Deaths
1
Hospitalizations

How Dangerous Is Application site discharge From MINOXIDIL?

Of the 45 reports, 1 (2.2%) required hospitalization.

Is Application site discharge Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for MINOXIDIL. However, 45 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 Application site discharge?

INGENOL MEBUTATE (188) BUPRENORPHINE (138) PRASTERONE (111) ESTRADIOL (72) BECAPLERMIN (52) MECHLORETHAMINE (45) PICATO (31) NICOTINE (20) IMIQUIMOD (14) DICLOFENAC (12)

Which MINOXIDIL Alternatives Have Lower Application site discharge Risk?

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

Related Pages

MINOXIDIL Full Profile All Application site discharge Reports All Drugs Causing Application site discharge MINOXIDIL Demographics