Does DUTASTERIDE Cause Product dispensing error? 37 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 37 reports of Product dispensing error have been filed in association with DUTASTERIDE (Dutasteride). This represents 0.9% of all adverse event reports for DUTASTERIDE.
37
Reports of Product dispensing error with DUTASTERIDE
0.9%
of all DUTASTERIDE reports
0
Deaths
34
Hospitalizations
How Dangerous Is Product dispensing error From DUTASTERIDE?
Of the 37 reports, 34 (91.9%) required hospitalization.
Is Product dispensing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DUTASTERIDE. However, 37 reports have been filed with the FAERS database.
What Other Side Effects Does DUTASTERIDE Cause?
Dyspnoea (502)
Asthma (329)
Wheezing (329)
Malaise (311)
Condition aggravated (300)
Sleep disorder due to a general medical condition (290)
Dizziness (288)
Fall (280)
Insomnia (276)
Fatigue (273)
What Other Drugs Cause Product dispensing error?
INSULIN GLARGINE (1,048)
FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE (692)
ADALIMUMAB (386)
SEMAGLUTIDE (379)
PREGABALIN (323)
NIRMATRELVIR\RITONAVIR (310)
ETANERCEPT (305)
SECUKINUMAB (300)
APIXABAN (299)
PALBOCICLIB (299)
Which DUTASTERIDE Alternatives Have Lower Product dispensing error Risk?
DUTASTERIDE vs DUTASTERIDE\TAMSULOSIN
DUTASTERIDE vs DUVELISIB
DUTASTERIDE vs DYDROGESTERONE
DUTASTERIDE vs EBASTINE
DUTASTERIDE vs ECALLANTIDE