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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 Haemorrhage? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Haemorrhage have been filed in association with LUBIPROSTONE (Amitza). This represents 0.5% of all adverse event reports for LUBIPROSTONE.

6
Reports of Haemorrhage with LUBIPROSTONE
0.5%
of all LUBIPROSTONE reports
1
Deaths
1
Hospitalizations

How Dangerous Is Haemorrhage From LUBIPROSTONE?

Of the 6 reports, 1 (16.7%) resulted in death, 1 (16.7%) required hospitalization, and 1 (16.7%) were considered life-threatening.

Is Haemorrhage Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for LUBIPROSTONE. However, 6 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 Haemorrhage?

RIVAROXABAN (6,571) APIXABAN (4,770) EMICIZUMAB-KXWH (3,612) WARFARIN (2,930) ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT (2,925) ASPIRIN (2,878) ADALIMUMAB (2,681) IBRUTINIB (1,907) CLOPIDOGREL BISULFATE (1,762) INSULIN LISPRO (1,614)

Which LUBIPROSTONE Alternatives Have Lower Haemorrhage Risk?

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

Related Pages

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