Does LUBIPROSTONE Cause Condition aggravated? 24 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 24 reports of Condition aggravated have been filed in association with LUBIPROSTONE (Amitza). This represents 2.0% of all adverse event reports for LUBIPROSTONE.
24
Reports of Condition aggravated with LUBIPROSTONE
2.0%
of all LUBIPROSTONE reports
3
Deaths
7
Hospitalizations
How Dangerous Is Condition aggravated From LUBIPROSTONE?
Of the 24 reports, 3 (12.5%) resulted in death, 7 (29.2%) required hospitalization.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LUBIPROSTONE. However, 24 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which LUBIPROSTONE Alternatives Have Lower Condition aggravated Risk?
LUBIPROSTONE vs LUCENTIS
LUBIPROSTONE vs LUCRIN DEPOT
LUBIPROSTONE vs LUMASIRAN
LUBIPROSTONE vs LUMATEPERONE
LUBIPROSTONE vs LUMIGAN