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Fluorescite: Uses, Side Effects and Dosage

Strength:
10 %

Patient Medication Information: uses, side effects, how to take - Fluorescite

What the medication is used for:

FLUORESCITE is a diagnostic aid used by your doctor as part of certain eye exams.

What it does:

FLUORESCITE contains fluorescein sodium, which acts by lighting up your eye (fluorescence) to allow your doctor to see the blood moving through the small blood vessels at the back of your eye(s).

When it should not be used:

FLUORESCITE should not be used if you are allergic to fluorescein sodium or any other of the ingredients in FLUORESCITE (see What the important nonmedicinal ingredients are).

FLUORESCITE is injected into a vein and must not be injected into an artery or intrathecally (i.e. into any space surrounded by a sheath or membrane, such as the spine or brain).

What the medicinal ingredient is:

Fluorescein sodium (fluorescein 100 mg/mL)

What the important nonmedicinal ingredients are: Hydrochloric acid and/or sodium hydroxide (to adjust pH), purified water

What dosage forms it comes in:

FLUORESCITE comes as a solution for intravenous injection in a 5 mL bottle.

  • Are taking many different drugs at the same type.
  • Are pregnant or planning to become pregnant.

These are all important factors your doctor needs to know about when deciding whether to use FLUORESCITE.

Low Salt Diet

Before FLUORESCITE is used, tell your doctor if you are on a low salt diet. FLUORESCITE can contain a lot of salt.

Breastfeeding

Tell your doctor if you are or planning to breastfeed. Stop breastfeeding for at least 1 week after FLUORESCITE is used. Breast milk should be pumped and discarded.

Driving and Using Machines

If you experience blurry vision after FLUORESCITE is used, wait until your vision is back to normal before driving or using machines.

Tell your doctor about all the medicines you are taking, recently took or are planning to take.

Drugs that may interact with FLUORESCITE include:

  • Beta-blocking agents (e.g. propranolol, atenolol, sotalol).
  • Antiarrhythmics (for irregular heartbeat, e.g. quinidine, digoxin).
  • Probenecid (gout medicine).

If you are scheduled for any laboratory tests, tell your doctor that you were given FLUORESCITE as it may affect your test results.

Usual dose:

Your doctor will decide how much to give to you or your child and will administer FLUORESCITE by injection into a vein.

Overdose:

Your doctor should carefully decide how much FLUORESCITE to give you to avoid an overdose.

BEFORE FLUORESCITE is used, tell to your doctor if you:

  • Have ever had any side effects (other than nausea or vomiting) after FLUORESCITE was used.
  • Have a history of allergies, including those to foods or other drugs.
  • Have asthma.
  • Have or have had heart disease.
  • Have diabetes.

ABOUT THIS MEDICATION

WARNINGS AND PRECAUTIONS

Serious Warnings and Precautions

Your doctor must weigh the benefit of using FLUORESCITE as a diagnostic agent with the risk of a serious allergic reaction (see Side Effects and What to Do About Them).

If you feel you have been given too much FLUORESCITE, contact your attending healthcare practitioner, hospital emergency department or regional Poison Control Centre immediately, even if there are no symptoms.

INTERACTIONS WITH THIS MEDICATION

PROPER USE OF THIS MEDICATION

IMPORTANT: PLEASE READ

Like all medicines, FLUORESCITE may cause side effects, but not everyone gets them.

Side effects that can occur at the injection site may include: general pain and soreness or accidental leakage of FLUORESCITE into surrounding areas, which may cause intense pain, local reaction and other effects, such as a dull aching pain in the injected arm. If this occurs, contact your healthcare professional immediately for medical attention.

Your skin may also become yellowish in colour and your urine may become bright. These effects should go away on their own after a few days.

Other side effects include: stomach pain/discomfort, nausea, vomiting, diarrhea, feeling hot or cold, dizziness, bad taste in the mouth, fainting, a tingling or numb sensation, headache, tremors, cough, shortness of breath, sneezing, throat irritation, rash or itchy skin, excess sweating and low or high blood pressure.

SERIOUS SIDE EFFECTS, HOW OFTEN THEY HAPPEN AND WHAT TO DO ABOUT THEM

Tell your doctor if you experience any of the following side effects:

  • Allergic reaction (includes itching, hives, difficulty breathing, swelling in the throat, chest tightness and itching or tingling around the lips or tongue).
  • Severe shock or fits (convulsions).
  • Swelling in the vein.
  • Irregular heartbeat or cardiac arrest (i.e. heart stops beating).

Your doctor will watch you closely for any signs of these serious side effects, for at least 30 minutes after treatment, and give you immediate medical treatment if you need it.

This is not a complete list of side effects.

You may also report any suspected side effects to Alcon Canada Inc. directly at: 1-800-613-2245.

This document plus the full product information, prepared for health professionals can be found at: www.alcon.ca or by contacting the sponsor, Alcon Canada Inc., at: 1-800-613-2245

©2018, 2020, 2025Alcon Inc.

The healthcare professional will store FLUORESCITE between 2oC to 30oC.

HOW TO STORE IT

SIDE EFFECTS AND WHAT TO DO ABOUT THEM

MORE INFORMATION

REPORTING SUSPECTED SIDE EFFECTS

You can report any suspected adverse reactions associated with the use of health products to the Canada Vigilance Program by one of the following 3 ways:

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  • Report online at www.healthcanada.gc.ca/medeffect
  • Call toll-free at 1-866-234-2345
  • Complete a Canada Vigilance Reporting Form and:

    • Fax toll-free to 1-866-678-6789, or
    • Mail to: Canada Vigilance Program Health Canada

      Postal Locator 0701D Ottawa, Ontario

      K1A 0K9

Postage paid labels, Canada Vigilance Reporting Form and the adverse reaction reporting guidelines are available on the MedEffect™ Canada Web site at www.healthcanada.gc.ca/medeffect.

NOTE: Should you require information related to the management of side effects, contact your health professional. The Canada Vigilance Program does not provide medical advice.

About this document

Source: Health Canada – Drug Product Database (DPD) and product monographs · DIN (Drug Identification Number): 00505005

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The information on this site does not replace the advice of a doctor or pharmacist.

Drug information for Fluorescite

DIN 00505005
Schedule(s) ETHICAL
Active ingredient(s) Fluorescein (fluorescein sodium) 10 %
Dosage form(s) Solution
Route(s) of administration Intravenous
Company ALCON CANADA INC
Current status Marketed
Current status date May 30, 2019

Source: Health Canada – Drug Product Database (DPD) and product monographs, data as of November 1, 2026. Data from the Health Canada Drug Product Database, as published there. Not a substitute for the advice of a doctor or pharmacist.