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Drug Details

ANATERA 100mg/ml solution for injection

• Drug Class Description
  Pharmacotherapeutic group: DIAGNOSTIC AGENTS, Colouring agents ATC code: S01JA01 Fluorescein sodium is a fluorochrome used in medicine as a diagnostic stain. Fluorescein is used to make the blood vessels of the ocular fundus visible (angiography of the retina and choroid).
• Generic Name
  fluorescein sodium
• Presentation
  Solution for injection Clear, red-orange solution
• Description
  Anatera 100 mg/ml solution for injection
• Indications
  

  This medicinal product is for diagnostic use only. For fluorescein angiography of the ocular fundus.

• Adult Dosage
  

  Use in adults, including the elderly:

  5 ml of Anatera 100 mg/ml solution for injection rapidly into the antecubital vein after taking precautions to avoid extravasation. In cases when highly sensitive imaging systems e.g., scanning laser ophthalmoscope are used, the dose of this product should be reduced to 2 ml of Anatera 100 mg/ml solution for injection.

  Use in pediatric patients:

  Anatera 100 mg/ml solution for injection has not been studied in children and dose-adaptation data are not available. Therefore, Anatera 100 mg/ml solution for injection should not be used in patients below 18 years as efficacy and safety in this group have not been established.

  Use in patients with renal insufficiency (glomerular filtration rate below 20 ml/min):

  Limited experience in renally impaired subjects (glomerular filtration rate below 20 ml/min) suggests that, in general, no dose adjustment is required although a longer excretion rate in patients with renal impairment is possible.

  Dialysed patients: Reduce dose to 2.5 ml (half a vial)

   

  Method of administration and fluorescence angiography

  Anatera 100 mg/ml solution for injection should be used exclusively by qualified physicians with technical expertise in performing and interpreting fluorescence angiography.

  This product should only be administered intravenously.

  Flush intravenous cannulas with sterile sodium chloride solution (0.9%) before and after medicinal products are injected to avoid physical incompatibility reactions. The injection should be administered rapidly (1 ml per second is normally recommended) into the antecubital vein, after taking precautions to avoid extravasation using a 23 gauge butterfly needle for injection. Luminescence usually appears in the retina and choroidal vessels in 7 to 14 seconds.

• Child Dosage
  

  Use in adults, including the elderly:

  5 ml of Anatera 100 mg/ml solution for injection rapidly into the antecubital vein after taking precautions to avoid extravasation. In cases when highly sensitive imaging systems e.g., scanning laser ophthalmoscope are used, the dose of this product should be reduced to 2 ml of Anatera 100 mg/ml solution for injection.

  Use in pediatric patients:

  Anatera 100 mg/ml solution for injection has not been studied in children and dose-adaptation data are not available. Therefore, Anatera 100 mg/ml solution for injection should not be used in patients below 18 years as efficacy and safety in this group have not been established.

  Use in patients with renal insufficiency (glomerular filtration rate below 20 ml/min):

  Limited experience in renally impaired subjects (glomerular filtration rate below 20 ml/min) suggests that, in general, no dose adjustment is required although a longer excretion rate in patients with renal impairment is possible.

  Dialysed patients: Reduce dose to 2.5 ml (half a vial)

   

  Method of administration and fluorescence angiography

  Anatera 100 mg/ml solution for injection should be used exclusively by qualified physicians with technical expertise in performing and interpreting fluorescence angiography.

  This product should only be administered intravenously.

  Flush intravenous cannulas with sterile sodium chloride solution (0.9%) before and after medicinal products are injected to avoid physical incompatibility reactions. The injection should be administered rapidly (1 ml per second is normally recommended) into the antecubital vein, after taking precautions to avoid extravasation using a 23 gauge butterfly needle for injection. Luminescence usually appears in the retina and choroidal vessels in 7 to 14 seconds.

• Elderly Dosage
  

  Use in adults, including the elderly:

  5 ml of Anatera 100 mg/ml solution for injection rapidly into the antecubital vein after taking precautions to avoid extravasation. In cases when highly sensitive imaging systems e.g., scanning laser ophthalmoscope are used, the dose of this product should be reduced to 2 ml of Anatera 100 mg/ml solution for injection.

  Use in pediatric patients:

  Anatera 100 mg/ml solution for injection has not been studied in children and dose-adaptation data are not available. Therefore, Anatera 100 mg/ml solution for injection should not be used in patients below 18 years as efficacy and safety in this group have not been established.

  Use in patients with renal insufficiency (glomerular filtration rate below 20 ml/min):

  Limited experience in renally impaired subjects (glomerular filtration rate below 20 ml/min) suggests that, in general, no dose adjustment is required although a longer excretion rate in patients with renal impairment is possible.

  Dialysed patients: Reduce dose to 2.5 ml (half a vial)

   

  Method of administration and fluorescence angiography

  Anatera 100 mg/ml solution for injection should be used exclusively by qualified physicians with technical expertise in performing and interpreting fluorescence angiography.

  This product should only be administered intravenously.

  Flush intravenous cannulas with sterile sodium chloride solution (0.9%) before and after medicinal products are injected to avoid physical incompatibility reactions. The injection should be administered rapidly (1 ml per second is normally recommended) into the antecubital vein, after taking precautions to avoid extravasation using a 23 gauge butterfly needle for injection. Luminescence usually appears in the retina and choroidal vessels in 7 to 14 seconds.

• Contra Indications
  

  Hypersensitivity to the active substance or to any of the excipients.

  Anatera 100 mg/ml solution for injection should not be injected intrathecally or intra-arterial.

• Special Precautions
  

  Fluorescein sodium can induce serious intolerance reactions.

  Detailed questioning of each patient must be carried out before the angiography to search for any history of cardiopulmonary disease or allergy or concomitant medications (such as beta-blocking agents, including eye-drops solutions). If the examination appears to be really necessary for a patient treated with beta-blocking agents (including eye-drops solutions), this examination should be performed under the supervision of a physician experienced in intensive care (resuscitation). Beta-blocking agents could reduce the vascular compensation reactions to anaphylactic shock and reduce the effectiveness of adrenaline in the case of cardiovascular collapse. Before any fluorescein sodium injection, the physician should seek information about concomitant treatment with a beta-blocking agent.

   

  In the event of serious intolerance reactions during a first angiography, the benefit of an additional fluorescein angiography should be balanced with the risk of severe hypersensitivity reactions (with fatal outcome in some cases).

  These reactions of intolerance are always unpredictable but they are more frequent in patients who have previously experienced an adverse reaction after fluorescein injection (symptoms other than nausea and vomiting) or in patients with history of allergy such as food or drug induced urticaria, asthma, eczema, allergic rhinitis. Intradermal skin tests are not reliable in predicting these intolerance reactions and so their use can be dangerous. A specialized allergy consultation should be undertaken to make this diagnosis.

  Premedication can be undertaken. However, the risk of occurrence of severe adverse drug reactions still remains. Premedication includes mainly oral antihistaminic H1 drugs, followed by corticosteroids, before injection of fluorescein. Given the low incidence of these adverse reactions, such pre-medication is not recommended for all patients.

  The risk of hypersensitivity reactions with fluorescein sodium requires:

  − Close monitoring of the patient by the ophthalmologist performing the examination, throughout the examination and for at least 30 minutes after;

  − Maintaining the infusion line for at least 5 minutes, to treat a possible severe adverse reaction without delay;

  −?To have at one's disposal appropriate material for emergency resuscitation which is based at first on the installation of a 2nd intravenous line, allowing the restoration of the plasma volume (aqueous solution polyionic or colloidal substitute of plasma) and the intravenous injection of adrenaline at the recommended dosage.

   

  Note:

  Extravasation should be avoided due to the high pH of fluorescein solution which can result in severe local tissue damage (severe pain in the arm for several hours, sloughing of the skin; superficial phlebitis). When extravasation occurs, the injection should be immediately discontinued.

  If an X-ray procedure is conducted within 36 hours of injection (maximum duration of fluorescein elimination from the body), the resultant high visibility of the excretory organs in the X-ray image may lead to misinterpretation.

  This medicinal product contains up to 3.15 mmol (72.45 mg) sodium per dose. This should be taken into consideration by patients on a controlled sodium diet.

• Interactions
  

  Fluorescein is a relatively inert dye and specific drug interaction studies have not been reported. There are few case reports on potential interactions with organic anion transporters and interference with certain laboratory tests. Compounds that inhibit or compete with the active transport of organic anions (e.g., probenicid) may affect the systemic profile of fluorescein.

  The concomitant use of Anatera 100 mg/ml solution for injection with beta-blocking agents (including eye-drops solutions) may rarely provoke severe anaphylactic reactions.

  Concomitant intravenous injection of other solutions or the mixing of Anatera 100 mg/ml solution for injection with other solutions should be avoided as the possibility of interactions cannot be excluded.

  It is possible that fluorescein may influence certain blood and urine values for 3 to 4 days after application.

• Adverse Drug Reactions
  

  The most frequently reported treatment related undesirable effects were nausea, vomiting, syncope and pruritis. More severe adverse reactions have been reported shortly after fluorescein injection such as angioedema, respiratory disorders (bronchospasm, laryngeal oedema, respiratory failure), anaphylactic shock, hypotension, respiratory arrest and cardiac arrest.

  Additionally, a yellowish discoloration of the skin could appear but usually disappears within 6 to 12 hours. Urine, which may also exhibit a bright yellow colouration, returns to its normal colour after 24 to 36 hours.

  The following undesirable effects were assessed to be treatment-related and are classified according to the following convention: very common (1/10), common (>1/100 to <1/10), uncommon (>1/1000 to 1/100), rare (>1/10,000 to 1/1000), or very rare (1/10,000). Within each frequency grouping, undesirable effects are presented in decreasing order of seriousness.

   

  Immune system disorders:

  Uncommon: hypersensitivity

  Rare: anaphylactic reaction

  Very Rare: anaphylactic shock

   

  Nervous system disorders:

  Common: syncope

  Uncommon: paresthesia, dizziness, headache

  Very Rare: convulsion

  Not Known: vertebrobasilar insufficiency

   

  Cardiac disorders:

  Rare: cardiac arrest

  Very Rare: angina pectoris, bradycardia, tachycardia

   

  Vascular disorders:

  Uncommon: thrombophlebitis

  Rare: hypotension, shock

  Very Rare: hypertension, vasospasm, vasodilation, pallor, hot flush

   

  Respiratory, thoracic and mediastinal disorders:

  Uncommon: cough, throat tightness

  Rare: bronchospasm

  Very Rare: respiratory arrest, pulmonary oedema, asthma, laryngeal oedema, dyspnoea, nasal oedema, sneezing

   

  Gastrointestinal disorders:

  Very Common: nausea

  Common: abdominal discomfort, vomiting

  Uncommon: abdominal pain

   

  Skin and subcutaneous tissue disorders:

  Common: pruritus

  Uncommon: urticaria

   

  General disorders and administration site conditions:

  Common: extravasation

  Uncommon: dysphasia, pain, feeling hot