Does LUBIPROSTONE Cause Hypersensitivity? 15 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 15 reports of Hypersensitivity have been filed in association with LUBIPROSTONE (Amitza). This represents 1.2% of all adverse event reports for LUBIPROSTONE.
15
Reports of Hypersensitivity with LUBIPROSTONE
1.2%
of all LUBIPROSTONE reports
0
Deaths
3
Hospitalizations
How Dangerous Is Hypersensitivity From LUBIPROSTONE?
Of the 15 reports, 3 (20.0%) required hospitalization.
Is Hypersensitivity Listed in the Official Label?
Yes, Hypersensitivity is listed as a known adverse reaction in the official FDA drug label for LUBIPROSTONE.
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 Hypersensitivity?
ETANERCEPT (10,846)
ADALIMUMAB (10,641)
METHOTREXATE (9,799)
TOCILIZUMAB (9,076)
ABATACEPT (8,945)
INFLIXIMAB (8,519)
RITUXIMAB (8,408)
ADAPALENE (8,356)
LEFLUNOMIDE (7,926)
CERTOLIZUMAB PEGOL (7,353)
Which LUBIPROSTONE Alternatives Have Lower Hypersensitivity Risk?
LUBIPROSTONE vs LUCENTIS
LUBIPROSTONE vs LUCRIN DEPOT
LUBIPROSTONE vs LUMASIRAN
LUBIPROSTONE vs LUMATEPERONE
LUBIPROSTONE vs LUMIGAN