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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 Wrong product administered? 12 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Wrong product administered have been filed in association with MINOXIDIL (FLINKYE 5% Minoxidil Hair Growth). This represents 0.0% of all adverse event reports for MINOXIDIL.

12
Reports of Wrong product administered with MINOXIDIL
0.0%
of all MINOXIDIL reports
0
Deaths
3
Hospitalizations

How Dangerous Is Wrong product administered From MINOXIDIL?

Of the 12 reports, 3 (25.0%) required hospitalization.

Is Wrong product administered Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for MINOXIDIL. However, 12 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 product administered?

INSULIN LISPRO (337) INSULIN GLARGINE (226) RISPERIDONE (141) QUETIAPINE (137) ACETAMINOPHEN (133) INSULIN ASPART (112) CLOZAPINE (106) INSULIN HUMAN (104) TUBERCULIN PURIFIED PROTEIN DERIVATIVE (104) IBUPROFEN (102)

Which MINOXIDIL Alternatives Have Lower Wrong product administered Risk?

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

Related Pages

MINOXIDIL Full Profile All Wrong product administered Reports All Drugs Causing Wrong product administered MINOXIDIL Demographics