Rituximab - Monoclonal Antibodies - Antineoplastic Agents- (July 2000)
Drug Name:
Rituximab - Monoclonal Antibodies - Antineoplastic Agents- (July 2000)
List Of Brands:
Indication Type Description:
Drug Interaction:
Avoid live vaccines
Renal toxicity with cisplatin
Other monoclonal antibodies
DMARDs
Cardiotoxics
Antihypertensives
Indication:
Relapsed or chemoresistent stage III- IV folicullar lymphoma
New Drugs Approved by (DCI) Drug Controller GENERAL - India For Marketing
(Ref- IDMA Publication)
Name of Drug Indication Date of Approval
Rituximab Anti-cancer 10-07-2000
Patent Expiry Date of drugs (Ref - IDMA Publication)
Chemical Category Manufacturer/ US Patent
Ingredient- Marketer Expiration Date
Rituximab Biopharmaceuticals Genetech Inc 19-03-2013
Adverse Reaction:
Fever, chills Rigors, nausea Rash, urticaria
Pruritus Angioedema Asthenia Headache,throat irritation
Rhinitis, bronchospam Vomiting,
Myalgia, dizziness Hypotension Hypertension
Cough, flushing, chest tightness
Mylesuppression eg, lymphophaenia, leukopenia,
anaemia, thrombocytopenia Infusion reactions (may be fatal )
Decreased IgG mucocutaneous reactions (may be fatal )
Cardiac arrhythmias
Hepatic failure
Contra-Indications:
Discontinue if severe infusion or mucocutaneous reactions occur ( eg. hypoxia, pulmonary infiltrates
Acute respiratory stress disorder, MI ventricular fibrillation ,
cardiogenic shock , Steven-Johnson Syndrome,
toxic epidermal necrolysis Tumor lysis syndrome ( specialy with tumor burden )
Monitor for renal toxicity, fluid balance, elcetrolyte abnormalites ( correct if occurs )
Pre-existing cardiovascular disease- monitor during and after treatment
Tumor infiltration High circulating malignant cells
Hepatitis B reactivation with fulminant hepatitis may occur
Monitor for signs of active HBV infection, discontinue if occurs
History of recurring , chronic infection
Severely immunocopromised eg hypogamalobunaemia
Monitor CBC, platelet counts during treatment, then periodically
Elderly Pregnancy Lactation
Dosages/ Overdosage Etc:
Indication-
Relapsed or chemoresistent stage III- IV folicullar lymphoma
Dosage-
Given im infusion initially at the rate of 50mg/hr ,
May increase infusion rate in 50mg/increments every 30 minutes to a max of 400mg/hr if infusion reactions do not occur
Pregnancy and lactation:
Use contraindicated. Observe caution