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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 Product container issue? 556 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 556 reports of Product container issue have been filed in association with MINOXIDIL (FLINKYE 5% Minoxidil Hair Growth). This represents 0.9% of all adverse event reports for MINOXIDIL.

556
Reports of Product container issue with MINOXIDIL
0.9%
of all MINOXIDIL reports
0
Deaths
0
Hospitalizations

How Dangerous Is Product container issue From MINOXIDIL?

Of the 556 reports.

Is Product container issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for MINOXIDIL. However, 556 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 container issue?

CYCLOSPORINE (910) MOMETASONE FUROATE (450) FORMOTEROL\MOMETASONE FUROATE (375) LIFITEGRAST (244) ALBUTEROL (192) LATANOPROST (158) CARBOXYMETHYLCELLULOSE\GLYCERIN (123) BRIMONIDINE (121) ACETAMINOPHEN (118) CALCIUM\DEXTROSE\MAGNESIUM\SODIUM\SODIUM (102)

Which MINOXIDIL Alternatives Have Lower Product container issue Risk?

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

Related Pages

MINOXIDIL Full Profile All Product container issue Reports All Drugs Causing Product container issue MINOXIDIL Demographics