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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 Gastrointestinal motility disorder? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Gastrointestinal motility disorder have been filed in association with LUBIPROSTONE (Amitza). This represents 0.4% of all adverse event reports for LUBIPROSTONE.

5
Reports of Gastrointestinal motility disorder with LUBIPROSTONE
0.4%
of all LUBIPROSTONE reports
0
Deaths
1
Hospitalizations

How Dangerous Is Gastrointestinal motility disorder From LUBIPROSTONE?

Of the 5 reports, 1 (20.0%) required hospitalization.

Is Gastrointestinal motility disorder Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for LUBIPROSTONE. However, 5 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 Gastrointestinal motility disorder?

ADALIMUMAB (207) LEVOTHYROXINE (191) LENALIDOMIDE (188) POLYETHYLENE GLYCOL 3350 (163) LINACLOTIDE (130) CABOZANTINIB S-MALATE (98) VEDOLIZUMAB (78) CARBIDOPA\LEVODOPA (70) SERTRALINE (65) INFLIXIMAB (61)

Which LUBIPROSTONE Alternatives Have Lower Gastrointestinal motility disorder Risk?

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

Related Pages

LUBIPROSTONE Full Profile All Gastrointestinal motility disorder Reports All Drugs Causing Gastrointestinal motility disorder LUBIPROSTONE Demographics