No black box warning on record for Kerendia

As of the latest FDA labeling reviewed, Kerendia (FINERENONE) does not carry a black box warning. Standard warnings and precautions still apply — see the full Kerendia medicine page for the complete safety profile.

Other warnings & precautions

5 WARNINGS AND PRECAUTIONS Hyperkalemia. Patients with decreased kidney function and higher baseline potassium levels are at increased risk. Monitor serum potassium levels and adjust dose as needed. ( 2.1 , 2.2 , 2.3 , 5.1 ) Worsening of Renal Function in Patients with Heart Failure. Measure eGFR and adjust dose as needed. ( 2.1 , 2.3 , 6.1 ) 5.1 Hyperkalemia Kerendia can cause hyperkalemia [see A

No black box warning on record for Kerendia

Other warnings & precautions

5 WARNINGS AND PRECAUTIONS Hyperkalemia. Patients with decreased kidney function and higher baseline potassium levels are at increased risk. Monitor serum potassium levels and adjust dose as needed. ( 2.1 , 2.2 , 2.3 , 5.1 ) Worsening of Renal Function in Patients with Heart Failure. Measure eGFR and adjust dose as needed. ( 2.1 , 2.3 , 6.1 ) 5.1 Hyperkalemia Kerendia can cause hyperkalemia [see A

Kerendia Black Box Warning

No black box warning on record for Kerendia

Other warnings & precautions

Kerendia Black Box Warning

No black box warning on record for Kerendia

Other warnings & precautions