Does LUBIPROSTONE Cause Hypokalaemia? 34 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 34 reports of Hypokalaemia have been filed in association with LUBIPROSTONE (Amitza). This represents 2.8% of all adverse event reports for LUBIPROSTONE.
34
Reports of Hypokalaemia with LUBIPROSTONE
2.8%
of all LUBIPROSTONE reports
3
Deaths
10
Hospitalizations
How Dangerous Is Hypokalaemia From LUBIPROSTONE?
Of the 34 reports, 3 (8.8%) resulted in death, 10 (29.4%) required hospitalization, and 2 (5.9%) were considered life-threatening.
Is Hypokalaemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LUBIPROSTONE. However, 34 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 Hypokalaemia?
FUROSEMIDE (2,503)
HYDROCHLOROTHIAZIDE (1,152)
CARBOPLATIN (1,118)
PREDNISONE (967)
DEXAMETHASONE (876)
CYCLOPHOSPHAMIDE (864)
OMEPRAZOLE (851)
RITUXIMAB (822)
AMLODIPINE (815)
PANTOPRAZOLE (811)
Which LUBIPROSTONE Alternatives Have Lower Hypokalaemia Risk?
LUBIPROSTONE vs LUCENTIS
LUBIPROSTONE vs LUCRIN DEPOT
LUBIPROSTONE vs LUMASIRAN
LUBIPROSTONE vs LUMATEPERONE
LUBIPROSTONE vs LUMIGAN