Does DOCOSANOL Cause Product use in unapproved indication? 244 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 244 reports of Product use in unapproved indication have been filed in association with DOCOSANOL (Cold Sore Fever Blister Treatment). This represents 3.1% of all adverse event reports for DOCOSANOL.
244
Reports of Product use in unapproved indication with DOCOSANOL
3.1%
of all DOCOSANOL reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product use in unapproved indication From DOCOSANOL?
Of the 244 reports.
Is Product use in unapproved indication Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DOCOSANOL. However, 244 reports have been filed with the FAERS database.
What Other Side Effects Does DOCOSANOL Cause?
Drug ineffective (2,679)
Condition aggravated (1,523)
Oral herpes (1,459)
Incorrect drug administration duration (803)
Drug administration error (721)
Incorrect product administration duration (634)
Wrong technique in product usage process (548)
Inappropriate schedule of drug administration (489)
Inappropriate schedule of product administration (391)
Product complaint (374)
What Other Drugs Cause Product use in unapproved indication?
DUPILUMAB (33,452)
DICLOFENAC (12,197)
METHOTREXATE (8,930)
PREDNISONE (7,625)
RITUXIMAB (7,519)
MYCOPHENOLATE MOFETIL (5,910)
ACETAMINOPHEN (5,819)
CYCLOPHOSPHAMIDE (5,750)
RISPERIDONE (5,551)
TACROLIMUS (5,057)
Which DOCOSANOL Alternatives Have Lower Product use in unapproved indication Risk?
DOCOSANOL vs DOCUSATE
DOCOSANOL vs DOCUSATE\SENNOSIDES
DOCOSANOL vs DOCUSATE\SENNOSIDES A AND B
DOCOSANOL vs DOFETILIDE
DOCOSANOL vs DOLUTEGRAVIR