Kisunla, illustration of injection vial form (not a photo of the actual pack)

Illustrative image.

Kisunla

Donanemab‑azbt

Prescription required

$15400.00

350mg · 11 × 1 vial · 3 months supply

BrandBranded medicine· By Eli lilly

$5133.33 per month

How long a supply?

1 month$5600.00 a month
3 months$5133.33 a month
Supplied from Israel

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Annual cost

$64400a year at this pack size

Prescription required

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FDA boxed warningAmyloid related imaging abnormalities

Monoclonal antibodies directed against aggregated forms of beta amyloid, including KISUNLA, can cause amyloid related imaging abnormalities (ARIA), characterized as ARIA with edema (ARIA-E) and ARIA with hemosiderin deposition (ARIA-H). Incidence and timing of ARIA vary among treatments. ARIA usually occurs early in treatment and is usually asymptomatic, although serious and life-threatening events can occur. ARIA can be fatal. Serious intracerebral hemorrhages >1 cm, some of which have been fatal, have been observed in patients treated with this class of medications. Because ARIA-E can cause focal neurologic deficits that can mimic an ischemic stroke, treating clinicians should consider whether such symptoms could be due to ARIA-E before giving thrombolytic therapy in a patient being treated with KISUNLA

ApoE ε4 Homozygotes

Consider the benefit of KISUNLA for the treatment of Alzheimer's disease and potential risk of serious adverse events associated with ARIA when deciding to initiate treatment with KISUNLA

Monoclonal antibodies directed against aggregated forms of beta amyloid, including KISUNLA, can cause amyloid related imaging abnormalities (ARIA), as ARIA with edema (ARIA-E) and ARIA with hemosiderin deposition (ARIA-H). ARIA is usually asymptomatic, although serious and life-threatening events can occur. ARIA can be fatal. Serious intracerebral hemorrhages >1 cm have occurred in patients treated with this class of medications. ARIA-E can cause focal neurologic deficits that can mimic ischemic stroke.

ApoE

ε4 Homozygotes

4 status should be performed prior to initiation of treatment to inform the risk of developing ARIA. Prior to testing, the risk of ARIA across genotypes and implications of genetic testing results should be discussed with patients.

Consider the benefit for the treatment of Alzheimer's disease and risk of ARIA when deciding to treat with KISUNLA.

Read this with the rest of the clinical information

About Kisunla

Overview

Kisunla (donanemab-azbt) is a monoclonal antibody medicine used to treat Alzheimer’s disease. Treatment should begin in people with mild cognitive impairment or mild dementia due to Alzheimer’s disease. It targets amyloid beta and reduces amyloid plaques in the brain.

What it treats

Alzheimer’s disease, with treatment started at the mild cognitive impairment or mild dementia stage.

Safety information

Side effects

Common side effects include headache and amyloid-related imaging abnormalities (ARIA): ARIA-E, microhemorrhages (small bleeds), and superficial siderosis. Serious reactions include ARIA, allergic reactions and infusion-related reactions. Contact your doctor if you suspect any of these reactions. Suspected ARIA requires medical assessment, which may include an MRI scan. Extra vigilance for ARIA is recommended during the first 24 weeks of treatment. Its risk is higher in people with two copies of the ApoE ε4 gene and in those with certain pre-existing MRI findings, including microhemorrhages or superficial siderosis.

FDA boxed warning

Amyloid related imaging abnormalities

Monoclonal antibodies directed against aggregated forms of beta amyloid, including KISUNLA, can cause amyloid related imaging abnormalities (ARIA), characterized as ARIA with edema (ARIA-E) and ARIA with hemosiderin deposition (ARIA-H). Incidence and timing of ARIA vary among treatments. ARIA usually occurs early in treatment and is usually asymptomatic, although serious and life-threatening events can occur. ARIA can be fatal. Serious intracerebral hemorrhages >1 cm, some of which have been fatal, have been observed in patients treated with this class of medications. Because ARIA-E can cause focal neurologic deficits that can mimic an ischemic stroke, treating clinicians should consider whether such symptoms could be due to ARIA-E before giving thrombolytic therapy in a patient being treated with KISUNLA

ApoE ε4 Homozygotes

Consider the benefit of KISUNLA for the treatment of Alzheimer's disease and potential risk of serious adverse events associated with ARIA when deciding to initiate treatment with KISUNLA

Monoclonal antibodies directed against aggregated forms of beta amyloid, including KISUNLA, can cause amyloid related imaging abnormalities (ARIA), as ARIA with edema (ARIA-E) and ARIA with hemosiderin deposition (ARIA-H). ARIA is usually asymptomatic, although serious and life-threatening events can occur. ARIA can be fatal. Serious intracerebral hemorrhages >1 cm have occurred in patients treated with this class of medications. ARIA-E can cause focal neurologic deficits that can mimic ischemic stroke.

ApoE

ε4 Homozygotes

4 status should be performed prior to initiation of treatment to inform the risk of developing ARIA. Prior to testing, the risk of ARIA across genotypes and implications of genetic testing results should be discussed with patients.

Consider the benefit for the treatment of Alzheimer's disease and risk of ARIA when deciding to treat with KISUNLA.

A boxed warning is the strongest warning the US Food and Drug Administration requires on a medicine label. Text is taken from the official label, with internal section references removed.

When to call your doctor

• Seek medical attention immediately for stroke-like symptoms. Kisunla can cause brain swelling that may mimic a stroke and can be life-threatening.

If symptoms are severe or getting worse quickly, seek emergency care rather than waiting.

Before taking this medicine

Kisunla must not be used in anyone with a known serious allergy to donanemab-azbt or any of its other ingredients. Serious allergic reactions, including anaphylaxis, have occurred. Kisunla requires careful monitoring for amyloid-related imaging abnormalities (ARIA), particularly during the first 24 weeks of treatment. The risk, including ARIA with symptoms, is higher in people with two copies of the ApoE ε4 gene than in those with one or no copies. Pre-existing small brain bleeds or superficial siderosis also increase the risk. Symptoms suggesting ARIA require clinical assessment, which may include an MRI scan. Infusion-related reactions may require the infusion to be slowed or stopped and appropriate treatment given. Medicines to help prevent reactions may be considered before later infusions.

Using Kisunla

Dosing

Dosing is set by your prescriber. Each health care professional may prescribe medication differently according to a patient's medical history and condition, so follow the directions on your prescription label and speak to your doctor or pharmacist before changing anything.

Storage

Store in the original carton below 25°C, protected from light, unless the pack states refrigeration. Do not freeze. Keep all medicines out of the sight and reach of children.

Clinical information on this page is summarised from the US FDA label KISUNLA (DONANEMAB-AZBT) INJECTION, SOLUTION [ELI LILLY AND COMPANY] (DailyMed, retrieved 19 September 2026).

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