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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 Poor quality product administered? 428 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 428 reports of Poor quality product administered have been filed in association with MINOXIDIL (FLINKYE 5% Minoxidil Hair Growth). This represents 0.7% of all adverse event reports for MINOXIDIL.

428
Reports of Poor quality product administered with MINOXIDIL
0.7%
of all MINOXIDIL reports
0
Deaths
0
Hospitalizations

How Dangerous Is Poor quality product administered From MINOXIDIL?

Of the 428 reports.

Is Poor quality product administered Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for MINOXIDIL. However, 428 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 Poor quality product administered?

ONABOTULINUMTOXINA (495) ICOSAPENT ETHYL (452) TUBERCULIN PURIFIED PROTEIN DERIVATIVE (376) ADALIMUMAB (239) TESTOSTERONE CYPIONATE (235) SOMATROPIN (234) POLYETHYLENE GLYCOL 3350 (223) IBUPROFEN (222) INSULIN GLARGINE (133) AMINOLEVULINIC ACID (124)

Which MINOXIDIL Alternatives Have Lower Poor quality product administered Risk?

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

Related Pages

MINOXIDIL Full Profile All Poor quality product administered Reports All Drugs Causing Poor quality product administered MINOXIDIL Demographics