Does TENAPANOR Cause Product prescribing issue? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Product prescribing issue have been filed in association with TENAPANOR (IBSRELA). This represents 0.3% of all adverse event reports for TENAPANOR.
5
Reports of Product prescribing issue with TENAPANOR
0.3%
of all TENAPANOR reports
1
Deaths
0
Hospitalizations
How Dangerous Is Product prescribing issue From TENAPANOR?
Of the 5 reports, 1 (20.0%) resulted in death.
Is Product prescribing issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TENAPANOR. However, 5 reports have been filed with the FAERS database.
What Other Side Effects Does TENAPANOR Cause?
Diarrhoea (793)
Death (222)
Hospitalisation (138)
Inappropriate schedule of product administration (115)
Off label use (94)
Product use issue (72)
Nausea (59)
Abdominal distension (52)
Therapy interrupted (52)
Abdominal pain (50)
What Other Drugs Cause Product prescribing issue?
DUPILUMAB (1,715)
POLYETHYLENE GLYCOL 3350 (1,439)
LENALIDOMIDE (948)
OXYCODONE (646)
RIVAROXABAN (359)
ACETAMINOPHEN\OXYCODONE (347)
ETONOGESTREL (311)
ACETAMINOPHEN\HYDROCODONE (298)
CERTOLIZUMAB PEGOL (297)
CABOZANTINIB S-MALATE (294)
Which TENAPANOR Alternatives Have Lower Product prescribing issue Risk?
TENAPANOR vs TENECTEPLASE
TENAPANOR vs TENELIGLIPTIN
TENAPANOR vs TENIPOSIDE
TENAPANOR vs TENOFOVIR
TENAPANOR vs TENOFOVIR ALAFENAMIDE