Olumiant, illustration of tablet form (not a photo of the actual pack)

Illustrative image.

Olumiant

Baricitinib

Prescription required

$1980.00

4mg · 6 × 14 tablets · 3 months supply

BrandBranded medicine· By Lilly

$660.00 per month

Strength

How long a supply?

1 month$660.00 a month
Supplied from Turkey
3 months$660.00 a month
Supplied from Turkey
6 months$1655.30 a month
Supplied from Israel

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Annual cost

$8580a year at this pack size

Prescription required

Upload your prescription after ordering, or send it to our pharmacy team. We dispense only against a valid prescription.

2 mg

4mg

FDA boxed warningSerious infections, mortality, malignancy, major adverse cardiovascular events (mace), and thrombosis

Increased risk of serious bacterial, fungal, viral and opportunistic infections leading to hospitalization or death, including tuberculosis (TB). Interrupt treatment with OLUMIANT if serious infection occurs until the infection is controlled. OLUMIANT should not be given to patients with active tuberculosis. Test for latent TB before and during therapy, except for COVID-19; treat latent TB prior to use. Monitor all patients for active TB during treatment, even patients with initial negative, latent TB test.

Higher rate of all-cause mortality, including sudden cardiovascular death with another Janus kinase inhibitor (JAK) vs. TNF blockers in rheumatoid arthritis (RA) patients.

Malignancies have occurred in patients treated with OLUMIANT. Higher rate of lymphomas and lung cancers with another JAK inhibitor vs. TNF blockers in RA patients.

Higher rate of MACE (defined as cardiovascular death, myocardial infarction, and stroke) with another JAK inhibitor vs. TNF blockers in RA patients.

Thrombosis has occurred in patients treated with OLUMIANT. Increased incidence of pulmonary embolism, venous and arterial thrombosis with another JAK inhibitor vs. TNF blockers.

Read this with the rest of the clinical information

About Olumiant

Overview

Olumiant (baricitinib) is a prescription medicine supplied as film-coated tablets. It treats adults with moderately to severely active rheumatoid arthritis after an inadequate response to one or more TNF blockers, and adults with severe alopecia areata. It also treats COVID-19 in hospitalized adults who need supplemental oxygen, mechanical ventilation or extracorporeal membrane oxygenation (ECMO). It works by blocking Janus kinase (JAK) enzymes that carry signals involved in immune cell function and blood cell production.

What it treats

- Moderately to severely active rheumatoid arthritis in adults who have had an inadequate response to one or more TNF blockers. - COVID-19 in hospitalized adults requiring supplemental oxygen, non-invasive or invasive mechanical ventilation, or extracorporeal membrane oxygenation (ECMO). - Severe alopecia areata in adults.

Safety information

Side effects

Reported side effects vary by the condition being treated. Commonly reported effects include upper respiratory tract infections, nausea, headache, acne, tiredness, abdominal pain, weight gain, cold sores and shingles. Other reported effects include urinary tract and lower respiratory tract infections, infections around hair follicles, and genital yeast infections. Blood tests may show increased cholesterol or other blood fats, liver enzymes, creatine phosphokinase or platelet counts, or reduced red blood cells or certain white blood cells. Your doctor may monitor for these changes. Serious risks include serious infections, cancer and lymphoproliferative disorders, major cardiovascular events, blood clots in deep veins or the lungs, serious allergic reactions, and holes in the stomach or intestinal wall. The label also warns of a risk of death. Seek urgent medical attention if you suspect a serious reaction. Stop taking Olumiant if a serious allergic reaction occurs. Contact a doctor promptly about new abdominal symptoms. Low blood sugar can occur in people with diabetes. If you have diabetes, tell your healthcare provider if you develop symptoms of low blood sugar; closer blood glucose monitoring may be needed.

FDA boxed warning

Serious infections, mortality, malignancy, major adverse cardiovascular events (mace), and thrombosis

Increased risk of serious bacterial, fungal, viral and opportunistic infections leading to hospitalization or death, including tuberculosis (TB). Interrupt treatment with OLUMIANT if serious infection occurs until the infection is controlled. OLUMIANT should not be given to patients with active tuberculosis. Test for latent TB before and during therapy, except for COVID-19; treat latent TB prior to use. Monitor all patients for active TB during treatment, even patients with initial negative, latent TB test.

Higher rate of all-cause mortality, including sudden cardiovascular death with another Janus kinase inhibitor (JAK) vs. TNF blockers in rheumatoid arthritis (RA) patients.

Malignancies have occurred in patients treated with OLUMIANT. Higher rate of lymphomas and lung cancers with another JAK inhibitor vs. TNF blockers in RA patients.

Higher rate of MACE (defined as cardiovascular death, myocardial infarction, and stroke) with another JAK inhibitor vs. TNF blockers in RA patients.

Thrombosis has occurred in patients treated with OLUMIANT. Increased incidence of pulmonary embolism, venous and arterial thrombosis with another JAK inhibitor vs. TNF blockers.

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 immediate medical attention for a serious allergic reaction. - Contact your doctor promptly for new abdominal pain or other new abdominal symptoms. - If you have diabetes, notify your doctor if you develop signs or symptoms of low blood sugar.

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

Before taking this medicine

Olumiant is not recommended for people with rheumatoid arthritis or alopecia areata who have severe liver impairment or kidney function measured by an eGFR below 30 mL/min/1.73 m². For people with COVID-19, it is not recommended if eGFR is below 15 mL/min/1.73 m², or if they are on dialysis, have end-stage kidney disease or have acute kidney injury. It has not been studied in people with COVID-19 and severe liver impairment. Serious allergic reactions have been reported. Stop Olumiant if a serious allergic reaction occurs. People at increased risk of gastrointestinal perforation, a hole in the stomach or bowel, require monitoring, and new abdominal symptoms need prompt assessment. People with diabetes may need more frequent blood glucose checks and should tell their healthcare provider if symptoms of low blood sugar develop. Blood tests are needed to monitor lymphocytes, neutrophils, haemoglobin, liver enzymes and blood lipids. Avoid live vaccines during treatment. Based on animal studies, Olumiant may harm an unborn baby. Do not breastfeed during treatment.

Interactions

Tell your doctor if you take probenecid or another strong organic anion transporter 3 (OAT3) inhibitor. These medicines require your prescriber to reduce your Olumiant dose.

Using Olumiant

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 below 25°C in a dry place, in the original pack, away from direct light and moisture. Do not keep it in a bathroom. Keep all medicines out of the sight and reach of children.

Clinical information on this page is summarised from the US FDA label OLUMIANT (BARICITINIB) TABLET, FILM COATED [ELI LILLY AND COMPANY] (DailyMed, retrieved 19 September 2026).

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