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Pramipexole ER (Apo) 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: pramipexole

Brand name

(ARTG)

: APO-PRAMIPEXOLE ER pramipexole dihydrochloride monohydrate 1.5 mg modified release tablet blister pack

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)

For the treatment of signs and symptoms of idiopathic Parkinson's disease. It may be used as monotherapy or in combination with levodopa.

How to use this medicine

(ARTG)

This medicine contains one component only.

Component :

  • Tablet, modified release
  • Oral
  • White or nearly white, cylindrical and biconvex tablets marked with 105 on one side.

Storage conditions

(ARTG)

  • Store below 25 degrees Celsius
  • Store in Original Container
  • Shelf lifetime is 36 Months.

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.

  • 10 pack
  • 30 pack

Pregnant or planning a pregnancy ?

(AHT)

For the active ingredient pramipexole

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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