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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 Sepsis? 7 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Sepsis have been filed in association with LUBIPROSTONE (Amitza). This represents 0.6% of all adverse event reports for LUBIPROSTONE.

7
Reports of Sepsis with LUBIPROSTONE
0.6%
of all LUBIPROSTONE reports
3
Deaths
1
Hospitalizations

How Dangerous Is Sepsis From LUBIPROSTONE?

Of the 7 reports, 3 (42.9%) resulted in death, 1 (14.3%) required hospitalization, and 1 (14.3%) were considered life-threatening.

Is Sepsis Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for LUBIPROSTONE. However, 7 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 Sepsis?

RITUXIMAB (4,043) CYCLOPHOSPHAMIDE (4,041) METHOTREXATE (3,933) ADALIMUMAB (3,169) DEXAMETHASONE (3,150) LENALIDOMIDE (2,956) VINCRISTINE (2,791) DOXORUBICIN (2,740) PREDNISONE (2,634) PREDNISOLONE (2,281)

Which LUBIPROSTONE Alternatives Have Lower Sepsis Risk?

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

Related Pages

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