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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 REBOXETINE 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 REBOXETINE. This represents 2.7% of all adverse event reports for REBOXETINE.

5
Reports of Hepatic function abnormal with REBOXETINE
2.7%
of all REBOXETINE reports
0
Deaths
0
Hospitalizations

How Dangerous Is Hepatic function abnormal From REBOXETINE?

Of the 5 reports.

Is Hepatic function abnormal Listed in the Official Label?

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

What Other Side Effects Does REBOXETINE Cause?

Hyperhidrosis (21) Off label use (20) Weight increased (18) Tachycardia (17) Confusional state (16) Intentional overdose (16) Nausea (16) Drug ineffective (15) Drug interaction (15) Sleep disorder (15)

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 REBOXETINE Alternatives Have Lower Hepatic function abnormal Risk?

REBOXETINE vs RECLAST REBOXETINE vs RECOMBINANT VARICELLA ZOSTER VIRUS GLYCOPROTEIN E REBOXETINE vs REGADENOSON REBOXETINE vs REGORAFENIB REBOXETINE vs REGORAFENIB\REGORAFENIB

Related Pages

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