Does DUTASTERIDE Cause Product prescribing error? 17 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 17 reports of Product prescribing error have been filed in association with DUTASTERIDE (Dutasteride). This represents 0.4% of all adverse event reports for DUTASTERIDE.
17
Reports of Product prescribing error with DUTASTERIDE
0.4%
of all DUTASTERIDE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product prescribing error From DUTASTERIDE?
Of the 17 reports.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DUTASTERIDE. However, 17 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 prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which DUTASTERIDE Alternatives Have Lower Product prescribing error Risk?
DUTASTERIDE vs DUTASTERIDE\TAMSULOSIN
DUTASTERIDE vs DUVELISIB
DUTASTERIDE vs DYDROGESTERONE
DUTASTERIDE vs EBASTINE
DUTASTERIDE vs ECALLANTIDE