Does LACTULOSE 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 LACTULOSE (LACTULOSE). This represents 0.3% of all adverse event reports for LACTULOSE.
11
Reports of Incorrect product administration duration with LACTULOSE
0.3%
of all LACTULOSE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Incorrect product administration duration From LACTULOSE?
Of the 11 reports, and 11 (100.0%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LACTULOSE. However, 11 reports have been filed with the FAERS database.
What Other Side Effects Does LACTULOSE Cause?
Fall (833)
Constipation (818)
Hypotension (654)
Cognitive disorder (649)
Balance disorder (641)
Orthostatic hypotension (589)
Pain (587)
Sedation (581)
Toxicity to various agents (558)
Depressed level of consciousness (552)
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 LACTULOSE Alternatives Have Lower Incorrect product administration duration Risk?
LACTULOSE vs LAMICTAL
LACTULOSE vs LAMIVUDINE
LACTULOSE vs LAMIVUDINE\NEVIRAPINE\ZIDOVUDINE
LACTULOSE vs LAMIVUDINE\TENOFOVIR
LACTULOSE vs LAMIVUDINE\TENOFOVIR DISOPROXIL