DrugInfoSys

Abacavir

Drug #1729

Abacavir is a neucloside reverse transcriptase inhibitor with antiretroviral activity against HIV. In contrast to earlier NRTIs, Abacavir is a guanosine analog. Abacavir is used in combination with other drugs to prevent viral replication in HIV infection. High-level resistance to it appears to require at least two to three concomitant mutations (e.g M184V, L 74V), for that reason it tends to develop slowly. Severe fatal hypersensitivity reactions may occur.

Primary Characteristics

Molecular Weight: 270.76 · Solubility in Water: insoluble · Solubility in Alcohol: null · Non-proprietary name: Olanzapine.

Molecular structure of Abacavir

Pharmacokinetics

Elimination: it is metabolised via 40% via liver, plasma half-life is 30-38 hr, renal excretion is 57%.

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Indications

Contraindications

Dosage

Abacavir's dosage details are as follows:

DoseSingle DoseFrequencyRouteInstructions
Adult Dosage
300 mg300 mgEvery 12hPO
300 mg300 mgEvery 24hPO
Paediatric Dosage (20kg)
No data.
Neonatal Dosage (3kg)
No data.

Drug Interactions

15 interactions
Moderate1 interaction

Always consult your physician for the change of dose regimen or an alternative drug of choice that may strictly be required.

Side Effects

Abacavir in overdosage may give rise to further complications which include Seizures , Extrapyramidal syndrome.

Abacavir produces potentially life-threatening effects which include Anaphylaxis , Lactic Acidosis , Lymphocytopenia, Hepatomegaly, Lactic acidosis. Careful monitoring is needed with proper medical management.

The signs and symptoms that are produced after acute overdosage of Abacavir are Tachycardia, Agitation, Agitation.

Abacavir is known to cause more or less tolerable side effects which are usually transient. These include Anorexia , Cough , Diarrhea, Dyspnea, Fatigue, Fever, GI disturbance, Headache, Hypersensitivity reactions, Lethargy, Nausea and vomiting, Pharyngitis, Rashes .

Warnings / Precautions

Abacavir should be avoided in moderate hepatic and renal impairment (unless essential), avoid in severe. HYPERSENSITIVITY REACTIONS: Life-threatening hypersensitivity reactions reported, characterised by fever or rash and possibly nausea, vomiting, diarrhoea, abdominal pain, lethargy, malaise, headache, myalgia, and renal failure; less frequently mouth ulceration, oedema, hypotension, dyspnoea,sore throat, cough paraesthesia, arthralgia, conjunctivitis, lymphadenopathy, lymphocytopenia and anaphylaxis (CSM has identified hypersensitivity reactions presenting as sore throat, influenza-like illness, cough and breathlessness); rarely myolysis; laboratory abnormalities may include raised liver function tests and creatine phosphokinase; symptoms usually appear in the first 6 weeks, but may occur at any time; monitor for symptoms every two weeks for two months; discontinue immediately if any symptom of hypersensitivity develops and do not rechallenge (risk of more severe hypersensitivity reaction); discontinue if hypersensitivity cannot be ruled out, even when other diagnoses possible, if rechallenge necessary it must be carried out in hospital setting; if abacavir is stopped for any reason other than hypersensitivity , exclude hypersensitivity reaction as the cause and rechallenge only if medical assistance is readily available; care needed with concomitant use of drugs which cause skin toxicity.COUNSELLING: Patients should be told the importance of regular dosing (intermittent therapy may increase the risk of sensitisation), how to recognise signs of hypersensitivity, and advised to seek immediate medical attention if symptoms develop or before re-starting ytreatment; patients should be advised to keep Allert card with them at all times. HEPATIC DISEASE:Potentially life-threatening lactic acidosis and severe hepatomegaly with steatosis reported therefore caution in liver disease , liver enzyme abnormalities, or risk factors for liver disease (perticularly in obese women); suspend or discontinue if deterioration in liver function tests, hepatic steatosis, prograssive hepatomegaly or unexplained lactic acidosis.

Interference in Pathology

Abacavir may interfere in the diagnosis of Raised creatine phosphokinase, Raised liver function tests, Liver enzyme abnormalities,or risk factors for liver disease (perticularly in obese women), Fasting blood glucose testing.

Available Brands

None recorded.

Storage Conditions

Abacavir should be stored film coated tTablet.

Drug Classification

  1. 1.6.5.2Antiretroviral drugs