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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does CROFELEMER Cause Product dose omission issue? 19 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 19 reports of Product dose omission issue have been filed in association with CROFELEMER (MYTESI). This represents 10.7% of all adverse event reports for CROFELEMER.

19
Reports of Product dose omission issue with CROFELEMER
10.7%
of all CROFELEMER reports
1
Deaths
4
Hospitalizations

How Dangerous Is Product dose omission issue From CROFELEMER?

Of the 19 reports, 1 (5.3%) resulted in death, 4 (21.1%) required hospitalization.

Is Product dose omission issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for CROFELEMER. However, 19 reports have been filed with the FAERS database.

What Other Side Effects Does CROFELEMER Cause?

Off label use (52) Drug ineffective (42) Diarrhoea (23) Death (19) Constipation (11) Fatigue (8) Flatulence (7) Abdominal discomfort (5) Back pain (5) Cough (5)

What Other Drugs Cause Product dose omission issue?

DUPILUMAB (18,189) USTEKINUMAB (9,405) GUSELKUMAB (9,267) LENALIDOMIDE (8,145) MEPOLIZUMAB (5,873) TOFACITINIB (5,646) VOXELOTOR (5,122) BELIMUMAB (4,671) SECUKINUMAB (4,572) APREMILAST (4,460)

Which CROFELEMER Alternatives Have Lower Product dose omission issue Risk?

CROFELEMER vs CROMOLYN CROFELEMER vs CROTALIDAE POLYVALENT IMMUNE FAB CROFELEMER vs CUBICIN CROFELEMER vs CUPRIC CROFELEMER vs CUPRIC ANHYDROUS

Related Pages

CROFELEMER Full Profile All Product dose omission issue Reports All Drugs Causing Product dose omission issue CROFELEMER Demographics