Does DOCUSATE Cause Wrong product administered? 36 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 36 reports of Wrong product administered have been filed in association with DOCUSATE (SENNA-S). This represents 1.4% of all adverse event reports for DOCUSATE.
36
Reports of Wrong product administered with DOCUSATE
1.4%
of all DOCUSATE reports
17
Deaths
19
Hospitalizations
How Dangerous Is Wrong product administered From DOCUSATE?
Of the 36 reports, 17 (47.2%) resulted in death, 19 (52.8%) required hospitalization.
Is Wrong product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DOCUSATE. However, 36 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 Wrong product administered?
INSULIN LISPRO (337)
INSULIN GLARGINE (226)
RISPERIDONE (141)
QUETIAPINE (137)
ACETAMINOPHEN (133)
INSULIN ASPART (112)
CLOZAPINE (106)
INSULIN HUMAN (104)
TUBERCULIN PURIFIED PROTEIN DERIVATIVE (104)
IBUPROFEN (102)
Which DOCUSATE Alternatives Have Lower Wrong product administered Risk?
DOCUSATE vs DOCUSATE\SENNOSIDES
DOCUSATE vs DOCUSATE\SENNOSIDES A AND B
DOCUSATE vs DOFETILIDE
DOCUSATE vs DOLUTEGRAVIR
DOCUSATE vs DOLUTEGRAVIR\LAMIVUDINE