Skip to main content

Avsola Side Effects

Generic name: infliximab

Medically reviewed by Philip Thornton, DipPharm. Last updated on Jun 20, 2026.

Note: This document provides detailed information about Avsola side effects associated with infliximab. Some dosage forms listed on this page may not apply specifically to the brand name Avsola.

Applies to infliximab: intravenous powder for solution.

Important warnings

This medicine can cause some serious health issues

Intravenous route (powder for solution)

Increased risk of serious infections leading to hospitalization or death, including tuberculosis (TB), bacterial sepsis, invasive fungal infections (such as histoplasmosis) and infections due to other opportunistic pathogens.

Discontinue infliximab if a patient develops a serious infection.

Perform test for latent TB; if positive, start treatment for TB prior to starting infliximab.

Monitor all patients for active TB during treatment, even if initial latent TB test is negative.

Lymphoma and other malignancies, some fatal, have been reported in children and adolescent patients treated with tumor necrosis factor (TNF) blockers, including infliximab.

Postmarketing cases of fatal hepatosplenic T-cell lymphoma (HSTCL) have been reported in patients treated with TNF blockers including infliximab.

Almost all had received azathioprine or 6-mercaptopurine concomitantly with a TNF-blocker at or prior to diagnosis.

The majority of infliximab cases were reported in patients with Crohn’s disease or ulcerative colitis, most of whom were adolescent or young adult males.

Intravenous route (powder for solution)

Warning: Serious Infections and Malignancy Serious Infections Patients treated with infliximab products are at increased risk for developing serious infections that may lead to hospitalization or death.

Most patients who developed these infections were taking concomitant immunosuppressants such as methotrexate or corticosteroids.

Infliximab-dyyb should be discontinued if a patient develops a serious infection or sepsis.

Reported infections include: 1) Active tuberculosis, including reactivation of latent tuberculosis.

Patients with tuberculosis have frequently presented with disseminated or extrapulmonary disease.

Patients should be tested for latent tuberculosis before infliximab-dyyb use and during therapy.

Treatment for latent infection should be initiated prior to Infliximab-dyyb use.

Active tuberculosis, including reactivation of latent tuberculosis.

Patients with tuberculosis have frequently presented with disseminated or extrapulmonary disease.

Patients should be tested for latent tuberculosis before infliximab-dyyb use and during therapy.

Treatment for latent infection should be initiated prior to Infliximab-dyyb use. 2) 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.

Empiric anti-fungal therapy should be considered in patients at risk for invasive fungal infections who develop severe systemic illness. 3) Bacterial, viral and other infections due to opportunistic pathogens, including Legionella and Listeria.

The risks and benefits of treatment with infliximab-dyyb should be carefully considered prior to initiating therapy in patients with chronic or recurrent infection.

Patients should be closely monitored for the development of signs and symptoms of infection during and after treatment with infliximab-dyyb, including the possible development of tuberculosis in patients who tested negative for latent tuberculosis 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 infliximab products.

Postmarketing cases of hepatosplenic T-cell lymphoma (HSTCL), a rare type of T-cell lymphoma, have been reported in patients treated with TNF blockers including infliximab products.

These cases have had a very aggressive disease course and have been fatal.

Almost all patients had received treatment with azathioprine or 6-mercaptopurine concomitantly with a TNF blocker at or prior to diagnosis.

The majority of reported cases have occurred in patients with Crohn’s disease or ulcerative colitis and most were in adolescent and young adult males.

Intravenous route (powder for solution)

Increased risk of serious infections leading to hospitalization or death, including TB, bacterial sepsis, invasive fungal infections (such as histoplasmosis) and infections due to other opportunistic pathogens.

Discontinue infliximab-abda if a patient develops a serious infection.

Perform test for latent TB; if positive, start treatment for TB prior to starting infliximab-abda.

Monitor all patients for active TB during treatment, even if initial latent TB test is negative.

Lymphoma and other malignancies, some fatal, have been reported in children and adolescent patients treated with tumor necrosis factor (TNF) blockers, including infliximab.

Postmarketing cases of fatal hepatosplenic T-cell lymphoma (HSTCL) have been reported in patients treated with TNF blockers including infliximab products.

Almost all had received azathioprine or 6-mercaptopurine concomitantly with a TNF-blocker at or prior to diagnosis.

The majority of reported cases have occurred in patients with Crohn’s disease or ulcerative colitis, most of whom were adolescent or young adult males.

Intravenous route (powder for solution)

Increased risk of serious infections leading to hospitalization or death, including tuberculosis (TB), bacterial sepsis, invasive fungal infections (such as histoplasmosis) and infections due to other opportunistic pathogens.

Discontinue infliximab-qbtx if a patient develops a serious infection.

Perform test for latent TB; if positive, start treatment for TB prior to starting infliximab-qbtx.

Monitor all patients for active TB during treatment, even if initial latent TB test is negative.

Lymphoma and other malignancies, some fatal, have been reported in children and adolescent patients treated with tumor necrosis factor (TNF) blockers, including infliximab products.

Postmarketing cases of fatal hepatosplenic T-cell lymphoma (HSTCL) have been reported in patients treated with TNF blockers including infliximab products.

Almost all had received azathioprine or 6-mercaptopurine concomitantly with a TNF-blocker at or prior to diagnosis.

The majority of cases were reported in patients with Crohn disease or ulcerative colitis, most of whom were adolescent or young adult males.

Intravenous route (powder for solution)

Increased risk of serious infections leading to hospitalization or death, including TB, bacterial sepsis, invasive fungal infections (such as histoplasmosis) and infections due to other opportunistic pathogens.

Discontinue infliximab-axxq if a patient develops a serious infection.

Perform test for latent TB; if positive, start treatment for TB prior to starting infliximab-axxq.

Monitor all patients for active TB during treatment, even if initial latent TB test is negative.

Lymphoma and other malignancies, some fatal, have been reported in children and adolescent patients treated with tumor necrosis factor (TNF) blockers, including infliximab.

Postmarketing cases of fatal hepatosplenic T-cell lymphoma (HSTCL) have been reported in patients treated with TNF blockers including infliximab products.

Almost all had received azathioprine or 6-mercaptopurine concomitantly with a TNF-blocker at or prior to diagnosis.

The majority of reported cases have occurred in patients with Crohn’s disease or ulcerative colitis, most of whom were adolescent or young adult males.

Precautions

It is very important that your doctor check your or your child's progress closely and at regular visits to make sure that this medicine is working properly. Blood and urine tests may be needed to check for unwanted effects.

Infliximab may cause an infusion reaction, including a heart attack, stroke, changes in blood pressure, or heart rhythm problems (eg, arrhythmia), while you or your child are receiving it or right after the infusion ends. Check with your doctor or nurse right away if you have chest pain, fever, chills, itching, hives, rash, dizziness, fainting, lightheadedness, headache, joint pain, difficulty with swallowing, trouble breathing, or swelling of the face, tongue, and throat.

Your body's ability to fight an infection may be reduced while you or your child are using infliximab (the active ingredient contained in Avsola). It is very important that you call your doctor at the first sign of any infection. Check with your doctor right away if you or your child have a fever, chills, cough, flu-like symptoms, or unusual tiredness or weakness.

Serious skin reactions can occur while you or your child are receiving this medicine. Check with your doctor right away if you have blistering, peeling, or loosening of the skin, chills, cough, diarrhea, fever, itching, joint or muscle pain, red skin lesions, sore throat, sores, ulcers, or white spots in your mouth, or unusual tiredness or weakness.

This medicine may increase your or your child's risk of having a lupus-like syndrome or a liver disease called autoimmune hepatitis. Check with your doctor right away if you or your child have dark brown-colored urine, fever or chills, a general feeling of discomfort, illness, or weakness, joint pain, light-colored stools, nausea, vomiting, a rash on the cheeks or arms that gets worse under the sun, severe tiredness, upper right-sided stomach pain, or yellow eyes and skin.

A small number of people (including children and teenagers) who have used this medicine have developed certain types of cancer. This is more common in patients who have lung diseases (eg, emphysema, COPD) or are heavy smokers, and in psoriasis patients who have had phototherapy treatment for a long time. Phototherapy treatment is ultraviolet light or sunlight combined with oral medicine to make your skin sensitive to light. Some teenagers and young adults with Crohn disease or ulcerative colitis also developed a rare type of cancer called hepatosplenic T-cell lymphoma. Talk with your doctor if you have unusual bleeding, bruising, or weakness, swollen lymph nodes in the neck, underarms, or groin, unexplained weight loss, or red, scaly patches, or raised bumps with pus on the skin.

Receiving this medicine may increase your risk of getting skin cancer (eg, melanoma, Merkel cell carcinoma) or cervical cancer. If you have any changes or growths on your skin, abnormal vaginal bleeding or pelvic pain, tell your doctor right away.

While you are being treated with infliximab, do not have any immunizations (vaccines) without your doctor's approval. Live virus vaccines should not be given with infliximab. Your child's vaccinations must be current before receiving infliximab. Talk to your child's doctor if you have any questions about this.

Women: If you have a baby while receiving infliximab, make sure the baby's doctor knows that you are receiving this medicine. You will need to wait a few months before giving certain vaccines to your baby. Talk to the baby's doctor if you have questions.

You will need to have a skin test for tuberculosis before you start receiving this medicine. Tell your doctor if you or anyone in your home has ever had a positive reaction to a tuberculosis skin test.

It is important to have your heart checked closely if you receive infliximab. Call your doctor right away if you have trouble breathing, swelling in the ankles and feet, or a sudden weight gain.

Do not take other medicines unless they have been discussed with your doctor. This includes abatacept (Orencia®), anakinra (Kineret®), tocilizumab (Actemra®), or other medicines called biologics that are used to treat the same conditions as infliximab. Using these medicines together with infliximab may increase your chance of having serious unwanted effects.

Serious side effects of Avsola

Along with its needed effects, infliximab 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 infliximab:

More common side effects

  • black, tarry stools
  • bladder pain
  • bloody or cloudy urine
  • blurred vision
  • body aches or pain
  • chest pain
  • chills
  • cough
  • cough producing mucus
  • difficult, burning, or painful urination
  • difficulty breathing
  • dizziness
  • dryness or soreness of the throat
  • ear congestion
  • fever
  • frequent urge to urinate
  • headache
  • hoarseness
  • hives, itching, or rash
  • loss of voice
  • lower back or side pain
  • muscle pain
  • nervousness
  • pain or swelling in the arms or legs
  • pain or tenderness around the eyes and cheekbones
  • painful or difficult urination
  • pale skin
  • pounding in the ears
  • runny or stuffy nose
  • slow or fast heartbeat
  • sneezing
  • sore throat
  • sores, ulcers, or white spots on the lips or in the mouth
  • stomach pain
  • tender, swollen glands in the neck
  • tightness in the chest
  • trouble breathing
  • trouble swallowing
  • unusual bleeding or bruising
  • unusual tiredness or weakness
  • voice changes

Rare side effects

  • bleeding gums
  • blood in the stool
  • blue lips and fingernails
  • changes in skin color or tenderness of the foot or leg
  • chest discomfort
  • confusion
  • coughing that sometimes produces a pink frothy sputum
  • dark urine
  • decreased urination
  • dizziness, faintness, or lightheadedness when getting up suddenly from a lying or sitting position
  • dry mouth
  • fast or noisy breathing
  • feeling of discomfort
  • general feeling of illness
  • general tiredness and weakness
  • high fever
  • hives
  • increased sweating
  • irregular or pounding heartbeat
  • light-colored stools
  • muscle aches
  • nausea
  • pinpoint red spots on the skin
  • puffiness or swelling of the eyelids or around the eyes, face, lips, or tongue
  • rapid, shallow breathing
  • swelling of the joints
  • sunken eyes
  • thirst
  • upper right abdominal or stomach pain
  • vomiting
  • unusual weight loss
  • wrinkled skin
  • yellow skin and eyes

Incidence not known

  • back pain, sudden and severe
  • blistering, peeling, loosening of the skin
  • bloody nose
  • burning, tingling, numbness or pain in the hands, arms, feet, or legs
  • change in mental status
  • clay-colored stools
  • dark or bloody urine
  • diarrhea
  • difficulty with speaking
  • dilated neck veins
  • double vision
  • heavier menstrual periods
  • inability to move the arms, legs, or facial muscles
  • inability to speak
  • loss of appetite
  • muscle weakness, sudden and progressing
  • red, irritated eyes
  • red skin lesions, often with a purple center
  • seizures
  • sensation of pins and needles
  • slow or irregular breathing
  • slow speech
  • stabbing pain
  • temporary vision loss
  • vomiting of blood

Other side effects of Avsola

Some side effects of infliximab 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

  • belching
  • difficulty in moving
  • feeling of warmth
  • heartburn
  • indigestion
  • muscle stiffness
  • redness of the face, neck, arms, and occasionally, upper chest

Less common side effects

  • constipation, severe

For healthcare professionals

Applies to infliximab: intravenous powder for injection, subcutaneous kit.

General adverse events

One of the most-common reasons for discontinuation of treatment was infusion-related reactions (e.g., dyspnea, flushing, headache, rash)[Ref]

Immunologic

Respiratory

Other

Hypersensitivity

Nervous system

Gastrointestinal

Cardiovascular

Dermatologic

Oncologic

Hepatic

Hematologic

Musculoskeletal

Renal

Metabolic

Local

Genitourinary

Ocular

Psychiatric

References

1. (2001) "Product Information. Remicade (infliximab)." Centocor Inc

2. (2019) "Product Information. Inflectra (infliximab)." Pfizer U.S. Pharmaceuticals Group

3. (2019) "Product Information. Renflexis (infliximab)." Merck & Co., Inc

Does Avsola interact with my other drugs?

Frequently asked questions

Further information

Avsola 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.