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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 CARPERITIDE Cause Hepatic function abnormal? 11 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Hepatic function abnormal have been filed in association with CARPERITIDE. This represents 13.6% of all adverse event reports for CARPERITIDE.

11
Reports of Hepatic function abnormal with CARPERITIDE
13.6%
of all CARPERITIDE reports
3
Deaths
9
Hospitalizations

How Dangerous Is Hepatic function abnormal From CARPERITIDE?

Of the 11 reports, 3 (27.3%) resulted in death, 9 (81.8%) required hospitalization, and 6 (54.5%) 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 CARPERITIDE. However, 11 reports have been filed with the FAERS database.

What Other Side Effects Does CARPERITIDE Cause?

Cardiac failure (15) Thrombotic microangiopathy (12) Drug ineffective (11) Renal impairment (10) Blood urea increased (9) Cardiac failure acute (9) Weight increased (9) Blood creatinine increased (8) Blood alkaline phosphatase increased (7) Cerebral infarction (7)

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

CARPERITIDE Full Profile All Hepatic function abnormal Reports All Drugs Causing Hepatic function abnormal CARPERITIDE Demographics