Does MINOXIDIL Cause Expired product administered? 982 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 982 reports of Expired product administered have been filed in association with MINOXIDIL (FLINKYE 5% Minoxidil Hair Growth). This represents 1.6% of all adverse event reports for MINOXIDIL.
982
Reports of Expired product administered with MINOXIDIL
1.6%
of all MINOXIDIL reports
0
Deaths
4
Hospitalizations
How Dangerous Is Expired product administered From MINOXIDIL?
Of the 982 reports, 4 (0.4%) required hospitalization, and 1 (0.1%) were considered life-threatening.
Is Expired product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MINOXIDIL. However, 982 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 Expired product administered?
POLYETHYLENE GLYCOL 3350 (1,637)
NAPROXEN (1,305)
ALBUTEROL (1,233)
LORATADINE (1,095)
ACETAMINOPHEN (797)
INSULIN LISPRO (770)
FLUTICASONE\SALMETEROL (753)
CETIRIZINE (714)
DICLOFENAC (714)
NICOTINE (704)
Which MINOXIDIL Alternatives Have Lower Expired product administered Risk?
MINOXIDIL vs MIPOMERSEN
MINOXIDIL vs MIRABEGRON
MINOXIDIL vs MIRALAX
MINOXIDIL vs MIRCERA
MINOXIDIL vs MIRENA