Does LUBIPROSTONE Cause Wrong technique in product usage process? 10 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Wrong technique in product usage process have been filed in association with LUBIPROSTONE (Amitza). This represents 0.8% of all adverse event reports for LUBIPROSTONE.
10
Reports of Wrong technique in product usage process with LUBIPROSTONE
0.8%
of all LUBIPROSTONE reports
4
Deaths
5
Hospitalizations
How Dangerous Is Wrong technique in product usage process From LUBIPROSTONE?
Of the 10 reports, 4 (40.0%) resulted in death, 5 (50.0%) required hospitalization.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LUBIPROSTONE. However, 10 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which LUBIPROSTONE Alternatives Have Lower Wrong technique in product usage process Risk?
LUBIPROSTONE vs LUCENTIS
LUBIPROSTONE vs LUCRIN DEPOT
LUBIPROSTONE vs LUMASIRAN
LUBIPROSTONE vs LUMATEPERONE
LUBIPROSTONE vs LUMIGAN