Anakinra - Immunomodulators
Drug Name:
Anakinra - Immunomodulators
List Of Brands:
Indication Type Description:
Pharmacology/ Pharmacokinetics
Drug Interaction:
Reports not available
Indication:
Rheumatoid Arthiritis
Adverse Reaction:
Adverse reactions reported to have occurre in < 5% of patients treated for RA
Injection site reaction 70%
Worsening of RA 16%
Upper respiratory ttract infection 12%
Headache 10%
Nausea 8%
Sinusitis 7%
Diarrhea 7%
Arthalgia 6%
Flu like symptoms 5%
Abdominal pain 5%
Contra-Indications:
Known hypersensitivity to E.Coli -derived proteins, anakinra or any component
Warnings-
Infections- associated with an inceased incidence of serious infections . discontinue administration if patient develops serious infection. Do not initiate treatment in patients with active infection
Vaccinations- do not give live vaccines concurrently with anakinra
Hypersensitivity - hypersensitivity reactions with anakirna are rare.If severe hypersensitivity reactions develops, discontinue administration andinitiate appropriate therapy
Renal funtion impairment- the drug is exrcreted by the kidney , the risk of toxic reaction is greater in patients with impaired renal function
Pregnancy- no adequate and well controlled studies in pregnant women. Use during pregnancy only if clearly needed
Lactation- excercise caition if anakinra is administered to nursing mothers
Children- safety and efficacy not established in children
Elderly- use caution while administering to elderly patients
Dosages/ Overdosage Etc:
Indication-
Rheumatoid arthiritis
Dosage-
Recommended dose is 100mg/day administered daily by SC injection. Administer the dose at approximately at the same time every day
Patient Information:
1. Inform your doctor if signs or symtoms of adverse reactions occur.
2. Patients should be cautioned against the reuse of needles or syringes
Pharmacology/ Pharmacokinetics:
Pharmacolgy-
Anakinra is a recombinant , nonglycosylated form of human interluin-1 receptor antagonist
It acts by blocking the biologic activity of IL -1 by competively inhibiting IL -1 binding to the interleukin -1 type receptor IL- IRI .
Pregnancy and lactation:
Pregnancy-
No adequate and well controlled studies in pregnant women. Use during pregnancy only if clearly needed
Lactation-
Excercise caition if anakinra is administered to nursing mothers
Children-
Safety and efficacy not established in children
Elderly-
Use caution while administering to elderly patients