Does MINOXIDIL Cause Product formulation issue? 1,369 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,369 reports of Product formulation issue have been filed in association with MINOXIDIL (FLINKYE 5% Minoxidil Hair Growth). This represents 2.3% of all adverse event reports for MINOXIDIL.
1,369
Reports of Product formulation issue with MINOXIDIL
2.3%
of all MINOXIDIL reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product formulation issue From MINOXIDIL?
Of the 1,369 reports, 3 (0.2%) required hospitalization.
Is Product formulation issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MINOXIDIL. However, 1,369 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 formulation issue?
LEVOTHYROXINE (740)
AMPHETAMINE ASPARTATE\AMPHETAMINE\DEXTROAMPHETAMINE SACCHARATE\DEXTROAMPHETAMINE (174)
OMEPRAZOLE (99)
METHYLPHENIDATE (78)
OXYCODONE (73)
ACETAMINOPHEN\HYDROCODONE (62)
ACETAMINOPHEN\OXYCODONE (61)
ACETAMINOPHEN (59)
BUPROPION (59)
CLONAZEPAM (50)
Which MINOXIDIL Alternatives Have Lower Product formulation issue Risk?
MINOXIDIL vs MIPOMERSEN
MINOXIDIL vs MIRABEGRON
MINOXIDIL vs MIRALAX
MINOXIDIL vs MIRCERA
MINOXIDIL vs MIRENA