Does DOCOSANOL Cause Incorrect product administration duration? 634 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 634 reports of Incorrect product administration duration have been filed in association with DOCOSANOL (Cold Sore Fever Blister Treatment). This represents 8.1% of all adverse event reports for DOCOSANOL.
634
Reports of Incorrect product administration duration with DOCOSANOL
8.1%
of all DOCOSANOL reports
0
Deaths
0
Hospitalizations
How Dangerous Is Incorrect product administration duration From DOCOSANOL?
Of the 634 reports.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DOCOSANOL. However, 634 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)
Wrong technique in product usage process (548)
Inappropriate schedule of drug administration (489)
Inappropriate schedule of product administration (391)
Product complaint (374)
Lip swelling (373)
What Other Drugs Cause Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
ALENDRONATE (287)
Which DOCOSANOL Alternatives Have Lower Incorrect product administration duration Risk?
DOCOSANOL vs DOCUSATE
DOCOSANOL vs DOCUSATE\SENNOSIDES
DOCOSANOL vs DOCUSATE\SENNOSIDES A AND B
DOCOSANOL vs DOFETILIDE
DOCOSANOL vs DOLUTEGRAVIR