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Active Pharma Ingredients / 25 Aug 2026

ANDUSOMERAN

Generic Name: ANDUSOMERAN

ABSTRACT -

Andusomeran is a nucleoside-modified messenger RNA vaccine active substance encoding a SARS-CoV-2 spike antigen for XBB.1.5-lineage COVID-19 vaccine formulations. The mRNA is formulated in lipid nanoparticles and is translated by host cells to trigger protective immune responses against COVID-19.

DOSAGE - 

  • Dosage should be determined according to the current national immunization schedule and product label.
  • Administration is by intramuscular injection by trained healthcare personnel.
  • Dose, age eligibility, booster timing, and variant formulation can change by country and season.
  • Patients should be observed after vaccination according to local guidance for immediate reactions.

SIDE EFFECTS–

  • Possible side effects include:
  • Injection-site pain, redness, or swelling
  • Fatigue
  • Headache
  • Myalgia
  • Chills
  • Fever
  • Lymphadenopathy
  • Nausea
  • Rare myocarditis or pericarditis, especially in younger males after mRNA vaccination

ALLRGIC REACTIONS–

  • Possible allergic reaction symptoms include:
  • Urticaria
  • Facial or throat swelling
  • Wheezing
  • Severe dizziness
  • Anaphylaxis
  • Important: Patients who develop an allergic reaction to Andusomeran should seek immediate medical attention and inform all future healthcare providers of the allergy.

DRUG INTERACTIONS–

  • Immunosuppressive therapy may reduce vaccine response.
  • Other vaccines may be co-administered only according to national guidance.
  • Anticoagulants or bleeding disorders require injection-site precautions.
  • Prior severe allergic reaction to vaccine components is a key contraindication or precaution.
  • Patients should inform healthcare providers about all prescription medicines, over-the-counter medicines, herbal products, vaccines, and supplements they are using.

PREAUTIONS–

  • Screen for prior anaphylaxis to vaccine ingredients and prior myocarditis/pericarditis after mRNA vaccination.
  • Defer vaccination during acute moderate or severe illness when advised.
  • Observe patients with allergy history for the recommended post-vaccination period.
  • Report serious adverse events through local vaccine-safety systems.

WARNINGS –

  • Severe allergic reactions require immediate emergency treatment.
  • Seek medical care for chest pain, shortness of breath, palpitations, or fainting after vaccination.
  • Use only formulations authorized for the patient age group and season.
  • Keep out of reach of children.

Have any questions? or Need help Contact us – 022 6163 6163 | support@medicus.com

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