Does PLECANATIDE Cause Intentional product use issue? 13 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Intentional product use issue have been filed in association with PLECANATIDE (Trulance Immediate release). This represents 1.3% of all adverse event reports for PLECANATIDE.
13
Reports of Intentional product use issue with PLECANATIDE
1.3%
of all PLECANATIDE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Intentional product use issue From PLECANATIDE?
Of the 13 reports, 1 (7.7%) required hospitalization.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PLECANATIDE. However, 13 reports have been filed with the FAERS database.
What Other Side Effects Does PLECANATIDE Cause?
Diarrhoea (298)
Drug ineffective (100)
Constipation (92)
Abdominal distension (83)
Nausea (72)
Abdominal pain (71)
Abdominal pain upper (70)
Flatulence (58)
Product use in unapproved indication (51)
Muscle spasms (49)
What Other Drugs Cause Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which PLECANATIDE Alternatives Have Lower Intentional product use issue Risk?
PLECANATIDE vs PLERIXAFOR
PLECANATIDE vs PNEUMOCOCCAL 13-VALENT CONJUGATE VACCINE
PLECANATIDE vs PNEUMOCOCCAL 7-VALENT CONJUGATE VACCINE
PLECANATIDE vs PNEUMOCOCCAL VACCINE POLYVALENT
PLECANATIDE vs PNEUMOCOCCAL VACCINE, POLYVALENT 23