Does DOCUSATE Cause Haemoglobin decreased? 21 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 21 reports of Haemoglobin decreased have been filed in association with DOCUSATE (SENNA-S). This represents 0.8% of all adverse event reports for DOCUSATE.
21
Reports of Haemoglobin decreased with DOCUSATE
0.8%
of all DOCUSATE reports
0
Deaths
14
Hospitalizations
How Dangerous Is Haemoglobin decreased From DOCUSATE?
Of the 21 reports, 14 (66.7%) required hospitalization, and 9 (42.9%) were considered life-threatening.
Is Haemoglobin decreased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DOCUSATE. However, 21 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 Haemoglobin decreased?
LENALIDOMIDE (4,031)
RUXOLITINIB (3,297)
ECULIZUMAB (3,028)
ADALIMUMAB (2,459)
CLOZAPINE (2,396)
RITUXIMAB (1,803)
APIXABAN (1,779)
NIRAPARIB (1,759)
METHOTREXATE (1,754)
RIBAVIRIN (1,753)
Which DOCUSATE Alternatives Have Lower Haemoglobin decreased Risk?
DOCUSATE vs DOCUSATE\SENNOSIDES
DOCUSATE vs DOCUSATE\SENNOSIDES A AND B
DOCUSATE vs DOFETILIDE
DOCUSATE vs DOLUTEGRAVIR
DOCUSATE vs DOLUTEGRAVIR\LAMIVUDINE