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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 TELMISARTAN Cause Hepatic function abnormal? 23 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 23 reports of Hepatic function abnormal have been filed in association with TELMISARTAN (telmisartan). This represents 0.4% of all adverse event reports for TELMISARTAN.

23
Reports of Hepatic function abnormal with TELMISARTAN
0.4%
of all TELMISARTAN reports
8
Deaths
15
Hospitalizations

How Dangerous Is Hepatic function abnormal From TELMISARTAN?

Of the 23 reports, 8 (34.8%) resulted in death, 15 (65.2%) required hospitalization, and 6 (26.1%) 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 TELMISARTAN. However, 23 reports have been filed with the FAERS database.

What Other Side Effects Does TELMISARTAN Cause?

Drug ineffective (685) Dizziness (569) Dyspnoea (556) Headache (508) Fall (500) Nausea (486) Hypertension (477) Blood pressure increased (473) Diarrhoea (467) Malaise (458)

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)

Which TELMISARTAN Alternatives Have Lower Hepatic function abnormal Risk?

TELMISARTAN vs TELOTRISTAT ETHYL TELMISARTAN vs TEMAZEPAM TELMISARTAN vs TEMODAR TELMISARTAN vs TEMOZOLOMIDE TELMISARTAN vs TEMSIROLIMUS

Related Pages

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