Rituximab
Generic medicine reference
Not yet clinically reviewed
This entry was migrated from the earlier Pharmapedia app bundle and has not been reviewed by a named clinician on this site. It is provided for educational reference only — verify dosage and safety information against current, authoritative sources and a qualified healthcare professional before any clinical use.
Overview
Rituximab infusion is used to treat certain leukemias and lymphomas and some non-cancer conditions, such as rheumatoid arthritis, polyangiitis, and pemphigus vulgaris, depending on the brand. Brand names include Rituxan, Riabni, Ruxience, and Truxima. Rituximab is given by IV infusion (an infusion into a vein) by a healthcare provider.
Rituximab is not chemotherapy, it is a type of immunotherapy called a targeted cancer treatment.
Rituximab gained FDA approval on November 26, 1997, under the brand name Rituxan. Biosimilars to Rituxan followed, with:
Truxima (rituximab-abbs), approved on November 28, 2018 Ruxience (rituximab-pvvr), approved on July 23, 2019 Riabni (rituximab-arrx), approved on December 17, 2020.
Truxima, Ruxience, and Riabni are not approved for use in children or for pemphigus vulgaris . Only Rituxan can be used in children or for pemphigus vulgaris.
Indications
Rituximab infusion is used to treat certain leukemias and lymphomas and some non-cancer conditions, such as rheumatoid arthritis, polyangiitis, and pemphigus vulgaris, depending on the brand. Brand names include Rituxan, Riabni, Ruxience, and Truxima. Rituximab is given by IV infusion (an infusion into a vein) by a healthcare provider.
Rituximab is not chemotherapy, it is a type of immunotherapy called a targeted cancer treatment.
Rituximab gained FDA approval on November 26, 1997, under the brand name Rituxan. Biosimilars to Rituxan followed, with:
Truxima (rituximab-abbs), approved on November 28, 2018 Ruxience (rituximab-pvvr), approved on July 23, 2019 Riabni (rituximab-arrx), approved on December 17, 2020.
Truxima, Ruxience, and Riabni are not approved for use in children or for pemphigus vulgaris . Only Rituxan can be used in children or for pemphigus vulgaris.
Contraindications
Before you or your child receives rituximab, tell your healthcare provider about all of your or your child’s medical conditions, including if you or your child:
have had a severe reaction to rituximab, Rituxan, Riabni, Ruxience, Truxima, or any ingredients in the injection have a history of heart problems, irregular heartbeat, or chest pain have lung, liver, or kidney problems have an infection or a weakened immune system have or have had any severe infections, including: Hepatitis B virus (HBV) Parvovirus B19 Hepatitis C virus (HCV) Varicella zoster virus (chickenpox or shingles) Cytomegalovirus (CMV) West Nile Virus Herpes simplex virus (HSV). have had a recent vaccination or are scheduled to receive vaccinations. You or your child should not receive certain vaccines before or during treatment with rituximab. You should be up-to-date on any needed immunizations before starting treatment with rituximab. are pregnant or plan to become pregnant are breastfeeding or plan to breastfeed.
Side Effects
The most common side effects of rituximab are:
infusion-related reactions infections (may include fever, chills) body aches tiredness nausea.
In adults with GPA or MPA , the most common side effects of rituximab also include:
low white and red blood cells swelling diarrhea muscle spasms.
In children with B-cell NHL or B-AL who receive rituximab with chemotherapy, the most common side effects are:
decreased white blood cells with fever mouth sores inflammation of the upper intestine serious infection throughout the body and organs (sepsis) changes in liver function blood tests low level of potassium in the blood
Other side effects of rituximab are:
aching joints during or within hours of receiving an infusion more frequent upper respiratory tract infections.
These are not all of the possible side effects of rituximab. Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088.
Warnings
Rituximab carries a Boxed Warning for fatal infusion-related reactions, severe skin reactions, hepatitis B virus reactivation, and a rare brain condition called progressive multifocal leukoencephalopathy (PML).
Rituximab can cause the following serious side effects:
Infusion-related reactions . These are very common side effects of rituximab treatment. Serious infusion-related reactions can happen during your or your child’s infusion or within 24 hours after. Your healthcare provider should give you or your child medicines before your rituximab infusion to decrease the chance of having a severe infusion-related reaction. Tell your healthcare provider or get medical help right away if you or your child gets any of these symptoms during or after an infusion: hives (red itchy welts) or rash shortness of breath, difficulty breathing, or wheezing itching weakness swelling of your lips, tongue, throat, or face dizziness or feeling faint sudden cough palpitations (feel like your heart is racing or fluttering) chest pain. Severe skin and mouth reactions . Tell your healthcare provider or get medical help right away if you or your child gets any of these symptoms at any time during your treatment with rituximab: painful sores or ulcers on your skin, lips, or in your mouth blisters peeling skin rash pustules. Hepatitis B virus (HBV) reactivation . Before you or your child receives rituximab treatment, your healthcare provider will do blood tests to check for HBV infection. If you or your child has had hepatitis B or is a carrier of the hepatitis B virus, receiving rituximab could cause the virus to become an active infection again. Hepatitis B reactivation may cause serious liver problems, including liver failure and death. You or your child should not receive rituximab if you or your child has active hepatitis B liver disease. Your healthcare provider will monitor you or your child for hepatitis B infection during and for several months after you or your child stops receiving rituximab. Tell your healthcare provider immediately if you or your child gets worsening tiredness, or yellowing of your or your child’s skin or white part of your eyes, during treatment. Progressive Multifocal Leukoencephalopathy (PML) . PML is a rare, serious brain infection caused by a virus that can happen in people who receive rituximab. People with weakened immune systems can get PML. PML can result in death or severe disability. There is no known treatment, prevention, or cure for PML. Tell your healthcare provider right away if you or your child has any new or worsening symptoms or if anyone close to you notices these symptoms: confusion dizziness or loss of balance decreased strength or weakness on one side of your body difficulty walking or talking vision problems. Tumor Lysis Syndrome (TLS) . TLS is caused by the fast breakdown of cancer cells. TLS can cause you or your child to have: kidney failure and need dialysis treatment an abnormal heart rhythm.
TLS can happen within 12 to 24 hours after an infusion of rituximab. Your healthcare provider may do blood tests to check you or your child for TLS. Your healthcare provider may give you or your child medicine to help prevent TLS. Tell your healthcare provider right away if you or your child has any of the following signs or symptoms of TLS:
nausea diarrhea vomiting lack of energy. Serious infections. Serious infections can happen during and after treatment with rituximab, and can lead to death. Rituximab can increase your or your child’s risk of getting infections and can lower the ability of your or your child’s immune system to fight infections. Types of serious infections that can happen with rituximab include bacterial, fungal, and viral infections. After receiving rituximab, some people have developed low levels of certain antibodies in their blood for a long period (longer than 11 months). Some of these people with low antibody levels developed infections. People with serious infections should not receive rituximab. Tell your healthcare provider right away if you or your child has any symptoms of infection: fever cold symptoms, such as a runny nose or sore throat, that do not go away flu symptoms, such as cough, tiredness, and body aches earache or headache pain during urination cold sores in the mouth or throat cuts, scrapes, or incisions that are red, warm, swollen, or painful. Heart problems . Rituximab may cause chest pain, irregular heartbeats, and a heart attack. Your healthcare provider may monitor your or your child’s heart during and after treatment with rituximab if you or your child has symptoms or heart problems or has a history of heart problems. Tell your healthcare provider right away if you or your child has chest pain or irregular heartbeats during treatment with rituximab. Kidney problems , especially if you or your child is receiving rituximab for NHL. Rituximab can cause severe kidney problems that can lead to death. Your healthcare provider should do blood tests to check how well your or your child’s kidneys are working. Stomach and serious bowel problems that can sometimes lead to death. Bowel problems, including blockage or tears in the bowel, can happen if you or your child receives rituximab with chemotherapy medicines. Tell your healthcare provider right away if you or your child has any severe stomach-area (abdomen) pain or repeated vomiting during treatment with rituximab.
Your healthcare provider will stop treatment with rituximab if you have severe, serious, or life-threatening side effects.
Get emergency medical help if you have signs of an allergic reaction to rituximab, such as hives, difficulty breathing, swelling in your face or throat, or a severe skin reaction (symptoms may include fever, sore throat, burning eyes, skin pain, red or purple skin rash with blistering and peeling).
These are not all of the possible side effects of rituximab. Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088
High Risk Groups
Rituximab carries a Boxed Warning for fatal infusion-related reactions, severe skin reactions, hepatitis B virus reactivation, and a rare brain condition called progressive multifocal leukoencephalopathy (PML).
Rituximab can cause the following serious side effects:
Infusion-related reactions . These are very common side effects of rituximab treatment. Serious infusion-related reactions can happen during your or your child’s infusion or within 24 hours after. Your healthcare provider should give you or your child medicines before your rituximab infusion to decrease the chance of having a severe infusion-related reaction. Tell your healthcare provider or get medical help right away if you or your child gets any of these symptoms during or after an infusion: hives (red itchy welts) or rash shortness of breath, difficulty breathing, or wheezing itching weakness swelling of your lips, tongue, throat, or face dizziness or feeling faint sudden cough palpitations (feel like your heart is racing or fluttering) chest pain. Severe skin and mouth reactions . Tell your healthcare provider or get medical help right away if you or your child gets any of these symptoms at any time during your treatment with rituximab: painful sores or ulcers on your skin, lips, or in your mouth blisters peeling skin rash pustules. Hepatitis B virus (HBV) reactivation . Before you or your child receives rituximab treatment, your healthcare provider will do blood tests to check for HBV infection. If you or your child has had hepatitis B or is a carrier of the hepatitis B virus, receiving rituximab could cause the virus to become an active infection again. Hepatitis B reactivation may cause serious liver problems, including liver failure and death. You or your child should not receive rituximab if you or your child has active hepatitis B liver disease. Your healthcare provider will monitor you or your child for hepatitis B infection during and for several months after you or your child stops receiving rituximab. Tell your healthcare provider immediately if you or your child gets worsening tiredness, or yellowing of your or your child’s skin or white part of your eyes, during treatment. Progressive Multifocal Leukoencephalopathy (PML) . PML is a rare, serious brain infection caused by a virus that can happen in people who receive rituximab. People with weakened immune systems can get PML. PML can result in death or severe disability. There is no known treatment, prevention, or cure for PML. Tell your healthcare provider right away if you or your child has any new or worsening symptoms or if anyone close to you notices these symptoms: confusion dizziness or loss of balance decreased strength or weakness on one side of your body difficulty walking or talking vision problems. Tumor Lysis Syndrome (TLS) . TLS is caused by the fast breakdown of cancer cells. TLS can cause you or your child to have: kidney failure and need dialysis treatment an abnormal heart rhythm.
TLS can happen within 12 to 24 hours after an infusion of rituximab. Your healthcare provider may do blood tests to check you or your child for TLS. Your healthcare provider may give you or your child medicine to help prevent TLS. Tell your healthcare provider right away if you or your child has any of the following signs or symptoms of TLS:
nausea diarrhea vomiting lack of energy. Serious infections. Serious infections can happen during and after treatment with rituximab, and can lead to death. Rituximab can increase your or your child’s risk of getting infections and can lower the ability of your or your child’s immune system to fight infections. Types of serious infections that can happen with rituximab include bacterial, fungal, and viral infections. After receiving rituximab, some people have developed low levels of certain antibodies in their blood for a long period (longer than 11 months). Some of these people with low antibody levels developed infections. People with serious infections should not receive rituximab. Tell your healthcare provider right away if you or your child has any symptoms of infection: fever cold symptoms, such as a runny nose or sore throat, that do not go away flu symptoms, such as cough, tiredness, and body aches earache or headache pain during urination cold sores in the mouth or throat cuts, scrapes, or incisions that are red, warm, swollen, or painful. Heart problems . Rituximab may cause chest pain, irregular heartbeats, and a heart attack. Your healthcare provider may monitor your or your child’s heart during and after treatment with rituximab if you or your child has symptoms or heart problems or has a history of heart problems. Tell your healthcare provider right away if you or your child has chest pain or irregular heartbeats during treatment with rituximab. Kidney problems , especially if you or your child is receiving rituximab for NHL. Rituximab can cause severe kidney problems that can lead to death. Your healthcare provider should do blood tests to check how well your or your child’s kidneys are working. Stomach and serious bowel problems that can sometimes lead to death. Bowel problems, including blockage or tears in the bowel, can happen if you or your child receives rituximab with chemotherapy medicines. Tell your healthcare provider right away if you or your child has any severe stomach-area (abdomen) pain or repeated vomiting during treatment with rituximab.
Your healthcare provider will stop treatment with rituximab if you have severe, serious, or life-threatening side effects.
Get emergency medical help if you have signs of an allergic reaction to rituximab, such as hives, difficulty breathing, swelling in your face or throat, or a severe skin reaction (symptoms may include fever, sore throat, burning eyes, skin pain, red or purple skin rash with blistering and peeling).
These are not all of the possible side effects of rituximab. Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088
Adult Dosage
375 mg/m2 (380 (375)) As recommended. IV-Inf — Once weekly for 4 doses.
Child Dosage
No child dosage information is recorded for this medicine yet.
Neonatal Dosage
No neonatal dosage information is recorded for this medicine yet.
Drug Interactions
Tell your healthcare provider about all the medicines you or your child takes, including prescription and over-the-counter medicines, vitamins, and herbal supplements. Especially tell your healthcare provider if you or your child takes or has taken:
a Tumor Necrosis Factor (TNF) inhibitor medicine such as adalimumab, certolizumab, etanercept, or golimumab, infliximab a Disease Modifying Anti-Rheumatic Drug (DMARD) such as leflunomide, methotrexate, or sulfasalazine chemotherapy drugs, especially cisplatin.
If you are not sure if your or your child’s medicine is one listed above, ask your healthcare provider. This list is not complete. Other drugs may interact with rituximab, including prescription and over-the-counter medicines, vitamins , and herbal products . Not all possible drug interactions are listed here.
Storage
Inj Store . Do not Freeze. Protect from Sunlight and Heat.
Available Brands in Pakistan
7 active brands listed alphabetically.
MABTHERA
ActiveROCHE PAKISTAN LTD.
DML: MABTHERA
Inj
Ristova
ActiveROCHE PAKISTAN LTD.
DML: Ristova
Inj
RITUXIM
ActivePHARMEVO (PVT) LTD.
DML: RITUXIM
Inj
RUXIENCE
ActivePFIZER LABORATORIES LTD.
DML: RUXIENCE
Inf
TUXIMAB
ActiveSEARLE PAKISTAN (PVT.) LTD.
DML: TUXIMAB
Inj
XIMAB
ActiveHELIX PHARMA (PRIVATE) LIMITED
DML: XIMAB
Inj
ZYTUX
ActiveCCL Pharmaceuticals (Pvt.) Ltd. DML: 000052
DML: ZYTUX
Inj
