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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does DOCUSATE Cause Device breakage? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Device breakage have been filed in association with DOCUSATE (SENNA-S). This represents 0.2% of all adverse event reports for DOCUSATE.

5
Reports of Device breakage with DOCUSATE
0.2%
of all DOCUSATE reports
0
Deaths
4
Hospitalizations

How Dangerous Is Device breakage From DOCUSATE?

Of the 5 reports, 4 (80.0%) required hospitalization, and 1 (20.0%) were considered life-threatening.

Is Device breakage Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DOCUSATE. However, 5 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 Device breakage?

COPPER (9,201) SOMATROPIN (7,761) ETONOGESTREL (4,140) LEVONORGESTREL (2,726) ETHINYL ESTRADIOL\ETONOGESTREL (741) CARBIDOPA\LEVODOPA (634) TREPROSTINIL (396) ADALIMUMAB (375) ALBUTEROL (256) EPOPROSTENOL (240)

Which DOCUSATE Alternatives Have Lower Device breakage Risk?

DOCUSATE vs DOCUSATE\SENNOSIDES DOCUSATE vs DOCUSATE\SENNOSIDES A AND B DOCUSATE vs DOFETILIDE DOCUSATE vs DOLUTEGRAVIR DOCUSATE vs DOLUTEGRAVIR\LAMIVUDINE

Related Pages

DOCUSATE Full Profile All Device breakage Reports All Drugs Causing Device breakage DOCUSATE Demographics