Evkeeza Side Effects
Generic name: evinacumab
Medically reviewed by Drugs.com. Last updated on Jun 22, 2024.
Note: This document provides detailed information about Evkeeza Side Effects associated with evinacumab. Some dosage forms listed on this page may not apply specifically to the brand name Evkeeza.
Applies to evinacumab: intravenous solution.
Common side effects of Evkeeza
Some side effects of evinacumab may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects.
Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:
More common side effects
Less common side effects
- body aches or pain
- constipation
- ear congestion
- lack or loss of strength
- loss of voice
- pain in the arms or legs
- sneezing
- stomach pain
Serious side effects of Evkeeza
Along with its needed effects, evinacumab (the active ingredient contained in Evkeeza) may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.
Check with your doctor or nurse immediately if any of the following side effects occur while taking evinacumab:
Less common side effects
- chest tightness
- cough
- difficulty swallowing
- dizziness
- fast heartbeat
- hives, itching, skin rash
- puffiness or swelling of the eyelids or around the eyes, face, lips, or tongue
- trouble breathing
- unusual tiredness or weakness
For healthcare professionals
Applies to evinacumab: intravenous solution.
General adverse events
The more frequently reported adverse reactions have included nasopharyngitis, influenza-like illness, dizziness, rhinorrhea, and nausea.[Ref]
Hypersensitivity
- Uncommon (0.1% to 1%): Anaphylaxis
Anaphylaxis was reported in 1 patient receiving this drug during clinical trials and led to discontinuation of treatment.
Respiratory
- Very common (10% or more): Nasopharyngitis (16%)
- Common (1% to 10%): Rhinorrhea
- Frequency not reported: Upper respiratory tract infection, nasal congestion
Compared to placebo, upper respiratory tract infection and nasal congestion were reported at a higher incidence; incidence was less than 3% of patients.
Immunologic
- Frequency not reported: Influenza-like illness
Compared to placebo, influenza-like illness was reported at a higher incidence; incidence was less than 3% of patients.
Cardiovascular
- Frequency not reported: Diastolic blood pressure decreased, increased heart rate
During clinical trials, transient decreases in diastolic blood pressure and increases in heart rate occurred but did not require intervention and resolved post infusion.
Nervous system
- Common (1% to 10%): Dizziness
Gastrointestinal
- Common (1% to 10%): Nausea
- Frequency not reported: Constipation, abdominal pain
Compared to placebo, constipation and abdominal pain were reported at a higher incidence; incidence was less than 3% of patients.
Musculoskeletal
- Common (1% to 10%): Extremity pain
Other
- Common (1% to 10%): Asthenia
Local
- Common (1% to 10%): Infusion site reactions
Infusion site reactions including infusion site pruritus, pyrexia, muscular weakness, nausea, and nasal congestion were reported in 7% of patients (n=6) receiving this drug compared to 4% (n=2) of placebo patients.
References
1. (2021) "Product Information. Evkeeza (evinacumab)." Regeneron Pharmaceuticals Inc
Frequently asked questions
- What is the mechanism of action for Evkeeza (evinacumab-dgnb)?
- Is Evkeeza FDA approved as a high cholesterol treatment?
- Where can I find the Evkeeza FDA package insert?
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Further information
Evkeeza side effects can vary depending on the individual. Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
Note: Medication side effects may be underreported. If you are experiencing side effects that are not listed, submit a report to the FDA by following this guide.