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Humira
Adalimumab
$1800.00
20mg/0.2mL · 3 × 2 pre-filled syringe · 3 months supply
BrandBranded medicine· By Abbvie
$600.00 per month
Strength
How long a supply?
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Annual cost
$7800a year at this pack size
Prescription required
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20mg/0.2mL
40mg/0.4mL
80mg/0.8mL
FDA boxed warningSerious infections and malignancy
SERIOUS INFECTIONS
Discontinue YUSIMRY if a patient develops a serious infection or sepsis.
Reported infections include:
Active tuberculosis (TB), including reactivation of latent TB. Patients with TB have frequently presented with disseminated or extrapulmonary disease. Test patients for latent TB before YUSIMRY use and during therapy. Initiate treatment for latent TB prior to YUSIMRY use.
Invasive fungal infections, including histoplasmosis, coccidioidomycosis, candidiasis, aspergillosis, blastomycosis, and pneumocystosis. Patients with histoplasmosis or other invasive fungal infections may present with disseminated, rather than localized, disease. Antigen and antibody testing for histoplasmosis may be negative in some patients with active infection. Consider empiric anti-fungal therapy in patients at risk for invasive fungal infections who develop severe systemic illness.
Bacterial, viral and other infections due to opportunistic pathogens, including Legionella and Listeria.
Carefully consider the risks and benefits of treatment with YUSIMRY prior to initiating therapy in patients with chronic or recurrent infection.
Monitor patients closely for the development of signs and symptoms of infection during and after treatment with YUSIMRY, including the possible development of TB in patients who tested negative for latent TB infection prior to initiating therapy.
MALIGNANCY
Lymphoma and other malignancies, some fatal, have been reported in children and adolescent patients treated with TNF blockers including adalimumab products. Post-marketing cases of hepatosplenic T-cell lymphoma (HSTCL), a rare type of T-cell lymphoma, have been reported in patients treated with TNF blockers including adalimumab products. These cases have had a very aggressive disease course and have been fatal. The majority of reported TNF blocker cases have occurred in patients with Crohn's disease or ulcerative colitis and the majority were in adolescent and young adult males. Almost all these patients had received treatment with azathioprine or 6-mercaptopurine (6–MP) concomitantly with a TNF blocker at or prior to diagnosis. It is uncertain whether the occurrence of HSTCL is related to use of a TNF blocker or a TNF blocker in combination with these other immunosuppressants.
Perform test for latent TB; if positive, start treatment for TB prior to starting YUSIMRY.
Monitor all patients for active TB during treatment, even if initial latent TB test is negative.
Post-marketing cases of hepatosplenic T-cell lymphoma (HSTCL), a rare type of T-cell lymphoma, have occurred in adolescent and young adults with inflammatory bowel disease treated with TNF blockers including adalimumab products.
About Humira
Overview
Humira is a prescription medicine containing adalimumab, used to treat certain inflammatory autoimmune conditions. These include rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, plaque psoriasis, hidradenitis suppurativa, Crohn’s disease, ulcerative colitis, certain forms of juvenile arthritis and non-infectious uveitis. It works by blocking tumour necrosis factor (TNF), a protein involved in inflammation.
What it treats
- Moderately to severely active rheumatoid arthritis in adults. - Moderately to severely active polyarticular juvenile idiopathic arthritis in patients aged 2 years and older. - Active psoriatic arthritis in adults. - Active ankylosing spondylitis in adults. - Moderately to severely active Crohn’s disease in patients aged 6 years and older. - Moderately to severely active ulcerative colitis in adults. Effectiveness has not been established in patients who lost response to or could not tolerate TNF blockers. - Moderate to severe chronic plaque psoriasis in adults who are candidates for systemic therapy or phototherapy, when other systemic therapies are medically less appropriate. - Moderate to severe hidradenitis suppurativa in patients aged 12 years and older. - Non-infectious intermediate, posterior and panuveitis in patients aged 2 years and older.
Safety information
Side effects
Common side effects of adalimumab include infections such as upper respiratory infections and sinusitis, reactions at the injection site, headache and rash. Each was reported in more than 10% of patients. Serious side effects include severe infections, including invasive fungal infections; cancers; severe allergic reactions, including anaphylaxis; reactivation of hepatitis B; new or worsening diseases that damage the protective covering of nerves; low blood cell counts; new or worsening heart failure; and autoimmune conditions such as a lupus-like syndrome or autoimmune hepatitis. Cancers occurred more often in adalimumab-treated patients than in the comparison groups. Contact a doctor promptly if you develop an infection or suspect a serious side effect. Seek immediate medical attention for a severe allergic reaction or symptoms of low blood cell counts. Treatment should not begin during an active infection. People who carry hepatitis B need monitoring during treatment and for several months afterward.
FDA boxed warning
Serious infections and malignancy
SERIOUS INFECTIONS
Discontinue YUSIMRY if a patient develops a serious infection or sepsis.
Reported infections include:
Active tuberculosis (TB), including reactivation of latent TB. Patients with TB have frequently presented with disseminated or extrapulmonary disease. Test patients for latent TB before YUSIMRY use and during therapy. Initiate treatment for latent TB prior to YUSIMRY use.
Invasive fungal infections, including histoplasmosis, coccidioidomycosis, candidiasis, aspergillosis, blastomycosis, and pneumocystosis. Patients with histoplasmosis or other invasive fungal infections may present with disseminated, rather than localized, disease. Antigen and antibody testing for histoplasmosis may be negative in some patients with active infection. Consider empiric anti-fungal therapy in patients at risk for invasive fungal infections who develop severe systemic illness.
Bacterial, viral and other infections due to opportunistic pathogens, including Legionella and Listeria.
Carefully consider the risks and benefits of treatment with YUSIMRY prior to initiating therapy in patients with chronic or recurrent infection.
Monitor patients closely for the development of signs and symptoms of infection during and after treatment with YUSIMRY, including the possible development of TB in patients who tested negative for latent TB infection prior to initiating therapy.
MALIGNANCY
Lymphoma and other malignancies, some fatal, have been reported in children and adolescent patients treated with TNF blockers including adalimumab products. Post-marketing cases of hepatosplenic T-cell lymphoma (HSTCL), a rare type of T-cell lymphoma, have been reported in patients treated with TNF blockers including adalimumab products. These cases have had a very aggressive disease course and have been fatal. The majority of reported TNF blocker cases have occurred in patients with Crohn's disease or ulcerative colitis and the majority were in adolescent and young adult males. Almost all these patients had received treatment with azathioprine or 6-mercaptopurine (6–MP) concomitantly with a TNF blocker at or prior to diagnosis. It is uncertain whether the occurrence of HSTCL is related to use of a TNF blocker or a TNF blocker in combination with these other immunosuppressants.
Perform test for latent TB; if positive, start treatment for TB prior to starting YUSIMRY.
Monitor all patients for active TB during treatment, even if initial latent TB test is negative.
Post-marketing cases of hepatosplenic T-cell lymphoma (HSTCL), a rare type of T-cell lymphoma, have occurred in adolescent and young adults with inflammatory bowel disease treated with TNF blockers including adalimumab products.
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
If symptoms are severe or getting worse quickly, seek emergency care rather than waiting.
Before taking this medicine
Humira should not be used by people who are allergic to adalimumab or any of its ingredients, have active tuberculosis or another serious infection, or have moderate to severe heart failure. Treatment should not begin while an active infection is present, including a localised infection, until it is controlled. Extra caution is needed in people with recurrent infections, previous tuberculosis or exposure to it, hepatitis B infection, mild heart failure, a history of cancer, blood cell disorders, or a demyelinating condition such as multiple sclerosis. Adalimumab can increase the risk of serious infections and reactivate tuberculosis or hepatitis B. Screening for tuberculosis and hepatitis B is needed before treatment. Live vaccines should be avoided during treatment. Combining Humira with certain other biological medicines, including anakinra or abatacept, is not recommended because of the increased risk of serious infections.
Interactions
Tell your doctor if you take abatacept or anakinra, as combining either with adalimumab increases the risk of serious infection. Avoid live vaccines while using adalimumab, and check with your doctor before receiving any vaccine.
Using Humira
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 to protect it from light. Check the pack for whether it must be refrigerated before first use and how long it may be kept at room temperature afterwards. Keep all medicines out of the sight and reach of children.
Clinical information on this page is summarised from the US FDA label YUSIMRY (ADALIMUMAB-AQVH) INJECTION, SOLUTION [MEITHEAL PHARMACEUTICALS INC.] (DailyMed, retrieved 19 September 2026).
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