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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 LACTULOSE Cause Condition aggravated? 104 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 104 reports of Condition aggravated have been filed in association with LACTULOSE (LACTULOSE). This represents 2.6% of all adverse event reports for LACTULOSE.

104
Reports of Condition aggravated with LACTULOSE
2.6%
of all LACTULOSE reports
28
Deaths
53
Hospitalizations

How Dangerous Is Condition aggravated From LACTULOSE?

Of the 104 reports, 28 (26.9%) resulted in death, 53 (51.0%) required hospitalization, and 4 (3.8%) were considered life-threatening.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for LACTULOSE. However, 104 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 Condition aggravated?

TOFACITINIB (16,925) INFLIXIMAB (16,616) DUPILUMAB (16,459) ETANERCEPT (15,897) METHOTREXATE (14,938) ADALIMUMAB (13,527) PREDNISONE (10,751) INFLIXIMAB-DYYB (10,275) HYDROXYCHLOROQUINE (8,848) RITUXIMAB (8,627)

Which LACTULOSE Alternatives Have Lower Condition aggravated Risk?

LACTULOSE vs LAMICTAL LACTULOSE vs LAMIVUDINE LACTULOSE vs LAMIVUDINE\NEVIRAPINE\ZIDOVUDINE LACTULOSE vs LAMIVUDINE\TENOFOVIR LACTULOSE vs LAMIVUDINE\TENOFOVIR DISOPROXIL

Related Pages

LACTULOSE Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated LACTULOSE Demographics