Does MINOXIDIL Cause Intentional product misuse? 2,418 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,418 reports of Intentional product misuse have been filed in association with MINOXIDIL (FLINKYE 5% Minoxidil Hair Growth). This represents 4.0% of all adverse event reports for MINOXIDIL.
2,418
Reports of Intentional product misuse with MINOXIDIL
4.0%
of all MINOXIDIL reports
0
Deaths
11
Hospitalizations
How Dangerous Is Intentional product misuse From MINOXIDIL?
Of the 2,418 reports, 11 (0.5%) required hospitalization, and 2 (0.1%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MINOXIDIL. However, 2,418 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)
Pruritus (2,414)
Overdose (2,361)
Hair texture abnormal (2,330)
What Other Drugs Cause Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
TERIPARATIDE (1,503)
Which MINOXIDIL Alternatives Have Lower Intentional product misuse Risk?
MINOXIDIL vs MIPOMERSEN
MINOXIDIL vs MIRABEGRON
MINOXIDIL vs MIRALAX
MINOXIDIL vs MIRCERA
MINOXIDIL vs MIRENA