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Luveris TM

You should seek medical advice in relation to medicines and use only as directed by a healthcare professional. Always read the label. If symptoms persist see your healthcare professional.

Active ingredients: lutropin alfa

Brand name

(ARTG)

: LUVERIS lutropin alfa (rch) 75IU powder for injection vial with diluent vial

Download the Consumer Medicine Information Leaflet

Download consumer medicine information leaflet (pdf) from the Therapeutic Goods Administration (TGA) website

What this medicine is used for

(ARTG)

LUVERIS in association with a recombinant follicle stimulating hormone (FSH) preparation is indicated for the stimulation of follicular development in women with severe LH and FSH deficiency.

How to use this medicine

(ARTG)

This medicine is a pack that contains more than one component.

Component :

  • Injection, solution
  • Subcutaneous
  • CLEAR, COLOURLESS SOLUTION

Component :

  • Injection, powder for
  • Subcutaneous
  • WHITE LYOPHILISED PELLET

Storage conditions

(ARTG)

  • Store below 25 degrees Celsius
  • Protect from Light
  • Shelf lifetime is 3 Years.

Do I need a prescription ?

(ARTG)

These medicine packs are available from a pharmacist and requires a prescription. It is Schedule 4 : Prescription Only Medicine.

  • 1 vial of active powder - 75IU with 1 vial of diluent pack
  • 10 vials of active powder - 75IU with 10 vials of diluent pack
  • 3 vials of active powder - 75IU with 3 vials of diluent pack

Pregnant or planning a pregnancy ?

(AHT)

For the active ingredient lutropin alfa

You should seek advice from your doctor or pharmacist about taking this medicine. They can help you balance the risks and the benefits of this medicine during pregnancy.

Reporting side effects

You can help ensure medicines are safe by reporting the side effects you experience.

You can report side effects to your doctor, or directly at www.tga.gov.au/reporting-problems

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