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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 Therapy non-responder? 11 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Therapy non-responder have been filed in association with LUBIPROSTONE (Amitza). This represents 0.9% of all adverse event reports for LUBIPROSTONE.

11
Reports of Therapy non-responder with LUBIPROSTONE
0.9%
of all LUBIPROSTONE reports
0
Deaths
0
Hospitalizations

How Dangerous Is Therapy non-responder From LUBIPROSTONE?

Of the 11 reports.

Is Therapy non-responder Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for LUBIPROSTONE. However, 11 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 Therapy non-responder?

ETANERCEPT (3,472) APREMILAST (3,360) METHOTREXATE (2,965) RITUXIMAB (2,731) ADALIMUMAB (2,595) PREDNISONE (2,563) TREPROSTINIL (2,289) INFLIXIMAB (2,122) TOCILIZUMAB (1,775) HYDROXYCHLOROQUINE (1,699)

Which LUBIPROSTONE Alternatives Have Lower Therapy non-responder Risk?

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

Related Pages

LUBIPROSTONE Full Profile All Therapy non-responder Reports All Drugs Causing Therapy non-responder LUBIPROSTONE Demographics