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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 DIETARY SUPPLEMENT\PROBIOTICS Cause Hepatic function abnormal? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Hepatic function abnormal have been filed in association with DIETARY SUPPLEMENT\PROBIOTICS. This represents 8.2% of all adverse event reports for DIETARY SUPPLEMENT\PROBIOTICS.

5
Reports of Hepatic function abnormal with DIETARY SUPPLEMENT\PROBIOTICS
8.2%
of all DIETARY SUPPLEMENT\PROBIOTICS reports
2
Deaths
5
Hospitalizations

How Dangerous Is Hepatic function abnormal From DIETARY SUPPLEMENT\PROBIOTICS?

Of the 5 reports, 2 (40.0%) resulted in death, 5 (100.0%) required hospitalization, and 2 (40.0%) were considered life-threatening.

Is Hepatic function abnormal Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DIETARY SUPPLEMENT\PROBIOTICS. However, 5 reports have been filed with the FAERS database.

What Other Side Effects Does DIETARY SUPPLEMENT\PROBIOTICS Cause?

Gastrointestinal pain (8) Pneumonia aspiration (8) Somnolence (8) Abdominal discomfort (7) Coma (7) Gastrooesophageal reflux disease (7) Anxiety (6) Generalised tonic-clonic seizure (5) Pyrexia (5)

What Other Drugs Cause Hepatic function abnormal?

NIVOLUMAB (1,131) PEMBROLIZUMAB (1,079) METHOTREXATE (1,054) CABOZANTINIB S-MALATE (912) CYCLOPHOSPHAMIDE (824) BEVACIZUMAB (769) PACLITAXEL (603) LENVATINIB (528) ATORVASTATIN (520) CYCLOSPORINE (508)

Related Pages

DIETARY SUPPLEMENT\PROBIOTICS Full Profile All Hepatic function abnormal Reports All Drugs Causing Hepatic function abnormal DIETARY SUPPLEMENT\PROBIOTICS Demographics