Atgam Side Effects
Generic name: lymphocyte immune globulin, anti-thy (equine)
Medically reviewed by Drugs.com. Last updated on Jan 17, 2024.
Note: This document contains side effect information about lymphocyte immune globulin, anti-thy (equine). Some dosage forms listed on this page may not apply to the brand name Atgam.
Applies to lymphocyte immune globulin, anti-thy (equine): parenteral concentrate for injection.
Warning
- Should be used only by clinicians experienced in immunosuppressive therapy for the management of renal transplant or aplastic anemia patients.b
- Patients receiving antithymocyte globulin (equine) should be treated in facilities equipped and staffed with adequate laboratory and supportive medical resources.b
Side effects include:
Renal allotransplantation: Fever, chills, leukopenia, thrombocytopenia, dermatologic reactions (rash, pruritus, urticaria, wheal and flare).
Aplastic anemia: Fever, chills, skin reactions, arthralgia, headache, myalgia, nausea, chest pain, phlebitis, serum sickness.
For Healthcare Professionals
Applies to lymphocyte immune globulin, anti-thy (equine): intravenous solution.
Hypersensitivity
Uncommon (0.1% to 1%): Anaphylactic reaction[Ref]
Dermatologic
Very common (10% or more): Rash (26%)
Common (1% to 10%): Urticaria, pruritus, vomiting, diarrhea, abdominal pain upper
Uncommon (0.1% to 1%): Herpes simplex, allergic dermatitis, toxic epidermal necrolysis (TEN)
Postmarketing reports: Hyperhidrosis[Ref]
Musculoskeletal
Very common (10% or more): Arthralgia (17%)
Common (1% to 10%): Chest pain, back pain[Ref]
Gastrointestinal
Common (1% to 10%): Nausea
Uncommon (0.1% to 1%): Stomatitis
Postmarketing reports: Abdominal pain, GI hemorrhage, GI perforation, oral pain[Ref]
Cardiovascular
Common (1% to 10%): Thrombophlebitis, hypertension, hypotension, bradycardia, arteriovenous fistula thrombosis, tachycardia, iliac vein occlusion
Postmarketing reports: Congestive heart failure, deep vein thrombosis, vasculitis[Ref]
Hematologic
Very common (10% or more): Thrombocytopenia (22%), leukopenia (18%)
Postmarketing reports: Anemia, eosinophilia, granulocytopenia, hemolysis, hemolytic anemia, neutropenia, pancytopenia[Ref]
Respiratory
Common (1% to 10%): Dyspnea
Uncommon (0.1% to 1%): Pleural effusion, hiccups, laryngospasm, pulmonary edema
Postmarketing reports: Apnea, cough, epistaxis, oropharyngeal pain[Ref]
Nervous system
Common (1% to 10%): Headache, dizziness
Uncommon (0.1% to 1%): Convulsion, encephalitis, paresthesia
Postmarketing reports: Dyskinesia, Syncope, tremor[Ref]
Local
Common (1% to 10%): Infusion site pain
Postmarketing reports: Infusion site erythema, infusion site swelling[Ref]
Renal
Uncommon (0.1% to 1%): Renal function test abnormal, renal artery thrombosis
Postmarketing reports: Kidney rupture, renal failure acute[Ref]
Ocular
Uncommon (0.1% to 1%): Periorbital edema[Ref]
Metabolic
Uncommon (0.1% to 1%): Night sweats, hyperglycemia, proteinuria
Postmarketing reports: Flank pain, muscle rigidity, myalgia, pain in extremity[Ref]
Hepatic
Common (1% to 10%): Liver function test abnormal[Ref]
Immunologic
Common (1% to 10%): Infection
Uncommon (0.1% to 1%): Serum sickness
Postmarketing reports: Hepatitis viral, localized infection, systemic infection[Ref]
Psychiatric
Uncommon (0.1% to 1%): Agitation
Postmarketing reports: Confusion, disorientation[Ref]
Other
Very common (10% or more): Pyrexia (40%), chills (27%)
Common (1% to 10%): Edema, lymphadenopathy, asthenia, malaise, wound dehiscence
Postmarketing reports: Aplasia, pain[Ref]
More about Atgam (lymphocyte immune globulin, anti-thy (equine))
- Check interactions
- Compare alternatives
- Side effects
- Dosage information
- During pregnancy
- Drug class: selective immunosuppressants
- En español
Patient resources
Professional resources
Related treatment guides
References
1. Product Information. Atgam (lymphocyte immune globulin, anti-thy (equine)). Pfizer U.S. Pharmaceuticals Group. 2010.
Further information
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
Some side effects may not be reported. You may report them to the FDA.