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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 LUBIPROSTONE Cause Dehydration? 40 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 40 reports of Dehydration have been filed in association with LUBIPROSTONE (Amitza). This represents 3.3% of all adverse event reports for LUBIPROSTONE.

40
Reports of Dehydration with LUBIPROSTONE
3.3%
of all LUBIPROSTONE reports
3
Deaths
27
Hospitalizations

How Dangerous Is Dehydration From LUBIPROSTONE?

Of the 40 reports, 3 (7.5%) resulted in death, 27 (67.5%) required hospitalization.

Is Dehydration Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for LUBIPROSTONE. However, 40 reports have been filed with the FAERS database.

What Other Side Effects Does LUBIPROSTONE Cause?

Diarrhoea (170) Drug ineffective (131) Nausea (110) Constipation (82) Vomiting (75) Dizziness (59) Abdominal distension (57) Dyspnoea (53) Headache (47) Abdominal pain (45)

What Other Drugs Cause Dehydration?

LENALIDOMIDE (3,469) ADALIMUMAB (3,233) CALCIUM\DEXTROSE\MAGNESIUM\SODIUM\SODIUM (3,168) FUROSEMIDE (2,195) SEMAGLUTIDE (1,816) METFORMIN (1,754) CAPECITABINE (1,599) LENVATINIB (1,526) TIRZEPATIDE (1,187) SACUBITRIL\VALSARTAN (1,171)

Which LUBIPROSTONE Alternatives Have Lower Dehydration Risk?

LUBIPROSTONE vs LUCENTIS LUBIPROSTONE vs LUCRIN DEPOT LUBIPROSTONE vs LUMASIRAN LUBIPROSTONE vs LUMATEPERONE LUBIPROSTONE vs LUMIGAN

Related Pages

LUBIPROSTONE Full Profile All Dehydration Reports All Drugs Causing Dehydration LUBIPROSTONE Demographics