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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 BISACODYL Cause Product dose omission issue? 85 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 85 reports of Product dose omission issue have been filed in association with BISACODYL (Gentle Laxative). This represents 2.5% of all adverse event reports for BISACODYL.

85
Reports of Product dose omission issue with BISACODYL
2.5%
of all BISACODYL reports
29
Deaths
80
Hospitalizations

How Dangerous Is Product dose omission issue From BISACODYL?

Of the 85 reports, 29 (34.1%) resulted in death, 80 (94.1%) required hospitalization, and 29 (34.1%) were considered life-threatening.

Is Product dose omission issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BISACODYL. However, 85 reports have been filed with the FAERS database.

What Other Side Effects Does BISACODYL Cause?

Drug ineffective (1,340) Constipation (966) Macular degeneration (764) Pain (691) Off label use (621) Nausea (524) Abdominal pain (473) Fall (448) Hypotension (445) Cognitive disorder (423)

What Other Drugs Cause Product dose omission issue?

DUPILUMAB (18,189) USTEKINUMAB (9,405) GUSELKUMAB (9,267) LENALIDOMIDE (8,145) MEPOLIZUMAB (5,873) TOFACITINIB (5,646) VOXELOTOR (5,122) BELIMUMAB (4,671) SECUKINUMAB (4,572) APREMILAST (4,460)

Which BISACODYL Alternatives Have Lower Product dose omission issue Risk?

BISACODYL vs BISACODYL OR DOCUSATE BISACODYL vs BISMUTH BISACODYL vs BISMUTH SUBCITRATE BISACODYL vs BISMUTH SUBCITRATE\METRONIDAZOLE\TETRACYCLINE BISACODYL vs BISMUTH SUBSALICYLATE

Related Pages

BISACODYL Full Profile All Product dose omission issue Reports All Drugs Causing Product dose omission issue BISACODYL Demographics