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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 Incorrect product administration duration? 11 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Incorrect product administration duration have been filed in association with BISACODYL (Gentle Laxative). This represents 0.3% of all adverse event reports for BISACODYL.

11
Reports of Incorrect product administration duration with BISACODYL
0.3%
of all BISACODYL reports
0
Deaths
1
Hospitalizations

How Dangerous Is Incorrect product administration duration From BISACODYL?

Of the 11 reports, 1 (9.1%) 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 BISACODYL. However, 11 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 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 BISACODYL Alternatives Have Lower Incorrect product administration duration 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 Incorrect product administration duration Reports All Drugs Causing Incorrect product administration duration BISACODYL Demographics