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Information on this page was last modified on : 2021/04/28 3:22:04 PM

Visudyne Injection 1 Vial

Visudyne Injection contains Verteporfin | belongs to Photosensitizer

How it works

Visudyne Injection 1 Vial is activated by light, it closes up the leaking blood vessels.

Side effects

Major & minor side effects for Visudyne Injection 1 Vial

  • Blurred vision
  • Dizziness
  • Eye pain
  • Fainting
  • Pale skin rare
  • Irregular heartbeat
  • Discoloration of skin
  • Unusual tiredness or weakness
  • Headache

Uses of Visudyne Injection 1 Vial

What is it prescribed for?

  • Neovascular (Wet) Age-Related Macular Degeneration (AMD)

    This medicine is used for the treatment of a wet type of age-related macular degeneration, an eye disease that impairs central vision making difficult to read, drive, or perform other daily activities.

Concerns

Frequently asked questions

  • Onset of action

    The amount of time required for this medicine to show its action is not clinically established.

  • Duration of Effect

    The amount of time for which this medicine remains active in the body is not clinically established.

  • Safe with Alchohol?

    Use of ethanol is not recommended along with Visudyne Injection 1 Vial because it can alter the desired effects of Visudyne Injection 1 Vial .

  • Is it habit forming?

    No habit-forming tendencies were reported.

  • Usage in pregnancy?

    This medicine is not recommended for use in pregnant women unless necessary. The risks and benefits should be discussed with the doctor before receiving this medicine.

  • Usage while breast-feeding?

    This medicine is not recommended for use in breastfeeding women unless necessary. The risks and benefits should be discussed with the doctor before receiving this medicine.

When not to use?

  • Allergy

    This medicine is not recommended for use in patients with a known allergy to Visudyne Injection 1 Vial or any other inactive ingredients present along with it.

  • Porphyria

    This medicine is not recommended for use in patients with a condition called porphyria which is a rare disorder resulting in the accumulation of porphyrin in the body.

Warnings

Warnings for special population
  • Pregnancy

    This medicine is not recommended for use in pregnant women unless necessary. The risks and benefits should be discussed with the doctor before receiving this medicine.

  • Breast-feeding

    This medicine is not recommended for use in breastfeeding women unless necessary. The risks and benefits should be discussed with the doctor before receiving this medicine.

General Warnings
  • Liver impairment

    This medicine should be used with caution in patients suffering from liver diseases due to the increased risk of severe adverse effects. Close monitoring of liver function tests is necessary while receiving this medicine. Appropriate dose adjustments or replacement with a suitable alternative may be required in some cases based on the clinical condition.

  • Light exposure

    It is advised not to get exposed to sunlight or bright indoor lights for 2 to 5 days after the therapy with this medicine due to the risk of adverse effects.

  • Kidney impairment

    This medicine should be used with caution in patients with kidney diseases due to the increased risk of severe adverse effects. Close monitoring of kidney function tests, appropriate dose adjustments, or replacement with a suitable alternative may be required in some cases based on the clinical condition.

  • Use in children

    This medicine is not recommended for use in patients below 18 years of age since the safety and efficacy of use are not clinically established.

  • Visual disturbances

    This medicine may cause temporary visual disturbances in some patients on therapy. It is advised that you do not perform any activities that require high mental alertness like driving a vehicle or operating machinery if you experience any such symptoms.

Dosage

  • Missed Dose

    Since this medicine is usually administered by a qualified healthcare professional in the clinical/hospital setting, the likelihood of a missed dose is very low.

  • Overdose

    Since this medicine is administered in the hospital setting by a qualified healthcare professional, the likelihood of an overdose is very less. However, emergency medical treatment will be initiated by the doctor if an overdose is suspected.

Interactions

Interaction with Medicines
  • Amitriptyline
  • Acetazolamide
  • Ranibizumab

General Instructions

This medicine is usually administered in the clinical/hospital setting under the supervision of a qualified healthcare professional. Follow all the instructions given by your doctor. Inform the doctor if you have a known allergy to this medicine. Report all your current medicines as well as your medical conditions to the doctor before receiving this medicine.

Other details

  • Usage does not depend on food timings
  • To be taken as instructed by doctor
  • Effect on sleep is not established

References

Additional Information:

How to use Visudyne Injection 1 Vial

Administration should be done under the supervision of expert medical practitioners only.
IV: The full infusion volume is administered IV over 10 min at a rate of 3 mL/min, using an appropriate syringe pump and in-line filter. Following injection with verteporfin, care should be taken to avoid exposure of skin or eyes to direct sunlight or bright indoor light for 5 days.
Stability: Store verteporfin between 20°C-25°C (68°-77°F).

What happens if I miss a dose of Visudyne Injection 1 Vial?

See literature.

One of the following licensed pharmacy from the nearest location will deliver Visudyne Injection 1 Vial. The details of the licensed pharmacy shall be shared once you request the drugs and the respective pharmacy accepts your request based on valid prescription and availability.

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