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Description

Actemra is a prescription medication used to treat several conditions. It helps adults with rheumatoid arthritis when other medications have not worked well.

Actemra also treats giant cell arteritis (a type of blood vessel inflammation) and slows lung damage in people with systemic sclerosis-associated interstitial lung disease.

For children aged two and older, it treats two types of arthritis (PJIA and SJIA) and helps manage severe reactions from certain cancer treatments. Actemra is also used for hospitalized adults with severe COVID-19 who need extra oxygen or a ventilator.

Common side effects include infections, headaches, high blood pressure, and reactions at the injection site. Actemra is available as an intravenous infusion or a subcutaneous injection.

Indications and Benefits of Actemra

Actemra is FDA-approved for the following conditions:

  • Rheumatoid Arthritis (RA)
  • Giant Cell Arteritis
  • Systemic Sclerosis-Associated Interstitial Lung Disease (SSc-ILD)
  • Polyarticular Juvenile Idiopathic Arthritis (PJIA)
  • Systemic Juvenile Idiopathic Arthritis (SJIA)
  • Cytokine Release Syndrome (CRS)
  • COVID-19 (hospitalized patients)

What Are the Benefits of Actemra?

  • Reduces inflammation and joint damage
  • Slows the progression of lung disease
  • Helps manage serious immune overreactions
  • Reduces the severity of symptoms in autoimmune diseases

How It Works

Actemra targets the immune system’s attack on the body, a problem in conditions like rheumatoid arthritis (RA).

It blocks interleukin-6 (IL-6), a substance involved in this harmful attack. By blocking IL-6, Actemra helps reduce inflammation and joint damage.

Dosage

Intravenous Infusion:

  • 80 mg/4 mL solution in a 20 mg/mL single-dose vial
  • 200 mg/10 mL solution in a 20 mg/mL single-dose vial
  • 400 mg/20 mL solution in a 20 mg/mL single-dose vial

Subcutaneous Injection:

  • 162 mg/0.9 mL solution in a single-dose prefilled syringe
  • 162 mg/0.9 mL solution in a single-dose prefilled ACTPen® autoinjector

Usage Guide

Actemra can be administered in two ways:

  • Intravenous (IV) infusion
  • Subcutaneous (SC) injection

Important Notes Before Starting Actemra

  • Do not use Actemra with other biologic disease-modifying antirheumatic drugs (DMARDs), such as TNF blockers or IL-1R antagonists, to avoid serious infections.
  • Before treatment, your doctor will do lab tests to check your:
    • White blood cell count (ANC)
    • Platelet count
    • Liver enzymes (ALT, AST)

Actemra Dosage Chart by Condition and Route

Condition Route Dosage Frequency Notes
Rheumatoid Arthritis (RA) Intravenous (IV) Start with 4 mg/kg, increase to 8 mg/kg Every 4 weeks Given by a healthcare provider; 60-minute infusion; max 800 mg
Subcutaneous (Injection at home) 162 mg Every other week if under 100 kg; Every week if 100 kg or more Rotate injection sites; dose can be adjusted based on labs
Giant Cell Arteritis (GCA) Intravenous (IV) 6 mg/kg Every 4 weeks Used with tapering steroids; max 600 mg per infusion
Subcutaneous 162 mg Every week or every other week Can be used alone after steroids are stopped
Systemic Sclerosis-Associated Interstitial Lung Disease (SSc-ILD) Subcutaneous only 162 mg Every week Use a prefilled syringe
Polyarticular Juvenile Idiopathic Arthritis (PJIA) Intravenous (IV) 10 mg/kg if under 30 kg

8 mg/kg if 30 kg or more

Every 4 weeks 60-minute infusion; dose based on weight
Subcutaneous 162 mg Every 3 weeks if under 30 kg

Every 2 weeks if 30 kg or more

Can be given at home with training
Systemic Juvenile Idiopathic Arthritis (SJIA) Intravenous (IV) 12 mg/kg if under 30 kg

8 mg/kg if 30 kg or more

Every 2 weeks 60-minute infusion
Subcutaneous 162 mg Every 2 weeks if under 30 kg

Every week, if 30 kg or more

Home injection with guidance
Cytokine Release Syndrome (CRS) Intravenous (IV) only 12 mg/kg if under 30 kg

8 mg/kg if 30 kg or more

Single dose (repeat every 8 hours if needed, up to 4 total doses) Max dose is 800 mg per infusion; subcutaneous use not approved

How to Administer Actemra

Actemra can be administered in two ways: as an intravenous (IV) infusion or as a subcutaneous (SC) injection.

The method of administration and frequency of dosage depends on the specific condition being treated.

  • Intravenous Infusion: Administered by a healthcare provider, this method involves injecting the medication into a vein over about one hour. The frequency of infusions varies:
    • For rheumatoid arthritis and giant cell arteritis: every 4 weeks.
    • For systemic juvenile idiopathic arthritis: every 2 weeks.
    • For cytokine release syndrome and COVID-19: typically a single dose, with a possible second dose if needed.
  • Subcutaneous Injection: This can be done at home after proper training. It involves injecting the medication under the skin. The dosing schedule includes:
    • Weekly or bi-weekly injections for rheumatoid arthritis, giant cell arteritis, and systemic sclerosis-associated interstitial lung disease.
    • For polyarticular and systemic juvenile idiopathic arthritis, the frequency depends on the patient’s weight and condition severity.

Always follow your healthcare provider’s instructions and keep all follow-up appointments to monitor your response to the treatment and adjust dosages as necessary.

Side Effects

Common Side Effects

  • Upper respiratory tract infections
  • Headache
  • High blood pressure
  • Injection site reactions

Serious but Rare Side Effects

  • Tiredness, vomiting, chills
  • Dark urine, yellow skin or eyes
  • Clay-colored stool
  • Stomach discomfort, skin rash
  • Appetite loss, fever, muscle aches
  • Shortness of breath, chest pain
  • Swelling (face, lips, tongue)
  • Dizziness or fainting
  • Abdominal pain or vomiting

Missed Dose

If you miss your weekly dose of Actemra and remember within 7 days, skip the missed dose and wait until your next scheduled dose. Do not take two doses to make up for the missed one. If you are not sure what to do, talk to your doctor or pharmacist.

Overdose

Overdosing with Actemra is not common, and there is little to no available information about it. In one case, a person with multiple myeloma accidentally got a high dose through an IV, but they didn’t have any bad reactions.

In another study, healthy individuals received single doses of Actemra up to a certain amount, and they mostly experienced low white blood cell counts, but these were not serious.

Warnings

Boxed Warning and Precautions for Actemra Patients on Actemra might get serious infections that could require hospitalization or even result in death.

Infections include:

  • Tuberculosis (test required before treatment)
  • Invasive fungal infections
  • Bacterial, viral, and opportunistic infections

General Precautions

  • Risk of serious infections
  • Gastrointestinal perforations
  • Liver injury (hepatotoxicity)
  • Blood abnormalities
  • Lipid abnormalities
  • Immunosuppression and potential cancer risk
  • Hypersensitivity reactions (including anaphylaxis)
  • Demyelinating disorders (e.g., multiple sclerosis)
  • Avoid live vaccines during treatment

Contraindications

Do not use Actemra if you have a known allergy to it. If you had a serious reaction to Actemra in the past, it is not safe to take it again. Inform your doctor if you have had allergic reactions to any medications before starting Actemra.

Interactions

  • methotrexate
  • non-steroidal anti-inflammatory drugs
  • corticosteroids
  • biological DMARDs such as TNF antagonists
  • CYP450 substrates
  • omeprazole
  • simvastatin
  • warfarin
  • cyclosporine
  • theophylline
  • oral contraceptives
  • lovastatin
  • atorvastatin
  • live vaccines

Storage Information

Store Actemra in the refrigerator at a temperature between 36 degrees Fahrenheit and 46 degrees Fahrenheit or 2 degrees Celsius and 8 degrees Celsius. Do not freeze the medication. Keep it in its original packaging to protect it from light.

If needed, Actemra can be stored at room temperature, up to 86 degrees Fahrenheit (30 degrees Celsius), for up to two weeks after it has been removed from the refrigerator.

Alternatives

If Actemra is not right for you, alternatives may include:

Cost & Discounts for Actemra in Canada

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Explore our Actemra (Tocilizumab) Offerings:

Strength Quantity Price (USD)
80mg/4mL 1 vial $287.00
2 vials $560.00
3 vials $810.00
162mg/0.9mL 4 pens $2499.00
8 pens $4960.00
12 pens $7410.00
200mg/10mL 1 vial $719.00
2 vials $1420.00
3 vials $2100.00
400mg/20mL 1 vial $1439.00
2 vials $2860.00
3 vials $4260.00

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FREQUENTLY ASKED QUESTIONS

Yes, Actemra may increase the risk of certain cancers by affecting how your immune system functions. It’s essential to consider this risk and discuss it with your healthcare provider.
Actemra treats several inflammatory conditions, mainly rheumatoid arthritis, where joints become swollen and painful. It also treats giant cell arteritis, causing blood vessels in the head and neck to inflame. Additionally, Actemra manages cytokine release syndrome after certain cancer treatments and is used for polyarticular and systemic juvenile idiopathic arthritis in children. It works by reducing inflammation.
Actemra injections for rheumatoid arthritis are typically given as an IV infusion once every 4 weeks. The dosage is based on your weight and is usually around 4 mg per kg. For instance, if you weigh 75 kg (about 165 lb), you’d receive 300 mg of Actemra every 4 weeks.
Actemra may lead to kidney problems in some cases. It’s important to inform your doctor about any existing kidney issues before starting Actemra treatment. They can monitor your kidney function regularly during treatment to detect any potential problems early on.
Actemra may lead to kidney problems in some cases. It’s important to inform your doctor about any existing kidney issues before starting Actemra treatment. They can monitor your kidney function regularly during treatment to detect any potential problems early on.
Actemra might cause fatigue as a side effect in some people. If you experience persistent tiredness while taking Actemra, it’s essential to inform your healthcare provider immediately. They can assess your symptoms and determine the appropriate course of action, which may include adjusting your treatment plan.
People with low neutrophil and platelet counts or high liver function test levels should not take Actemra. It’s important to talk to your healthcare provider to see if Actemra is right for you, based on your current health and medical history.
Actemra can be injected subcutaneously (under the skin) in the thigh, abdomen, or upper arm. It’s important to rotate the injection sites to avoid irritation or discomfort. Avoid injecting into areas that are bruised, tender, red, or hard. Always follow your healthcare provider’s instructions on the proper technique and site selection to ensure safe and effective administration.
There is currently no generic version of Actemra available. Actemra is a brand-name biologic drug containing tocilizumab, and traditional generics do not exist for biologics. While similar drugs, called biosimilars, might be developed in the future, they are not available yet. Biosimilars usually cost less than brand-name drugs, offering a more affordable option for patients.
The duration of Actemra treatment varies by condition. For rheumatoid arthritis (RA), it is often used long-term, as your doctor advises. For giant cell arteritis (GCA), Actemra is typically prescribed for up to one year. In cases of cytokine release syndrome (CRS), it is usually used for a short period, generally 1 to 2 weeks, until symptoms resolve. Always follow your doctor’s instructions on how long to use Actemra for your specific condition.
Actemra may affect your immune system, making you more susceptible to infections or worsening existing ones. Serious infections, such as tuberculosis (TB), and infections caused by bacteria, fungi, or viruses that can spread throughout the body, may occur while taking Actemra.

Disclaimer

Pharma Giant provides medical information to help you better understand medications and medical conditions. This content is for informational use only and does not replace advice from a licensed medical practitioner. Consult your doctor or pharmacist before starting or changing any medication. All our partners follow strict safety standards set by their country’s health authorities to make sure you receive safe and high-quality medications.