Does DOCUSATE Cause Incorrect product administration duration? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Incorrect product administration duration have been filed in association with DOCUSATE (SENNA-S). This represents 0.5% of all adverse event reports for DOCUSATE.
14
Reports of Incorrect product administration duration with DOCUSATE
0.5%
of all DOCUSATE reports
0
Deaths
3
Hospitalizations
How Dangerous Is Incorrect product administration duration From DOCUSATE?
Of the 14 reports, 3 (21.4%) required hospitalization.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DOCUSATE. However, 14 reports have been filed with the FAERS database.
What Other Side Effects Does DOCUSATE Cause?
Somnolence (514)
Gastrooesophageal reflux disease (419)
Pneumonia aspiration (341)
Coma (337)
Constipation (329)
Drug ineffective (288)
Dyspnoea (277)
Off label use (236)
Vomiting (207)
Pain (195)
What Other Drugs Cause Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which DOCUSATE Alternatives Have Lower Incorrect product administration duration Risk?
DOCUSATE vs DOCUSATE\SENNOSIDES
DOCUSATE vs DOCUSATE\SENNOSIDES A AND B
DOCUSATE vs DOFETILIDE
DOCUSATE vs DOLUTEGRAVIR
DOCUSATE vs DOLUTEGRAVIR\LAMIVUDINE