Does LUBIPROSTONE Cause Presyncope? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Presyncope have been filed in association with LUBIPROSTONE (Amitza). This represents 0.6% of all adverse event reports for LUBIPROSTONE.
7
Reports of Presyncope with LUBIPROSTONE
0.6%
of all LUBIPROSTONE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Presyncope From LUBIPROSTONE?
Of the 7 reports, 2 (28.6%) required hospitalization, and 1 (14.3%) were considered life-threatening.
Is Presyncope 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 Presyncope?
TREPROSTINIL (585)
BISOPROLOL (485)
LEVONORGESTREL (429)
ADALIMUMAB (420)
AMBRISENTAN (407)
ASPIRIN (370)
TAMSULOSIN (361)
FUROSEMIDE (348)
SERTRALINE (337)
ETANERCEPT (334)
Which LUBIPROSTONE Alternatives Have Lower Presyncope Risk?
LUBIPROSTONE vs LUCENTIS
LUBIPROSTONE vs LUCRIN DEPOT
LUBIPROSTONE vs LUMASIRAN
LUBIPROSTONE vs LUMATEPERONE
LUBIPROSTONE vs LUMIGAN