Bupredermal 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: buprenorphine
Brand name
(ARTG)
: BUPREDERMAL buprenorphine 30 micrograms/hour transdermal drug delivery system sachetDownload 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)
BUPREDERMAL patches are indicated for the management of severe pain where: other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain, and the pain is opioid-responsive, and requires daily, continuous, long-term treatment. BUPREDERMAL patches are not indicated for use in chronic non-cancer pain other than in exceptional circumstances. BUPREDERMAL patches are not indicated as an as-needed (PRN) analgesia.
How to use this medicine
(ARTG)
This medicine contains one component only.
Component :
- Drug delivery system, transdermal
- Transdermal
- Beige coloured rectangular patch with rounded corners on an aluminised rigid removable protective layer. The trade name and the strength is printed on the patch.
Storage conditions
(ARTG)
- Store below 25 degrees Celsius
- Shelf lifetime is 3 Years.
Do I need a prescription ?
(ARTG)
These medicines require authorisation for prescription from your doctor. It is Schedule 8 : Controlled Drug.
- 2 patches pack
- 4 patches pack
Is this medicine subsidised ?
(PBS)
This medicine was verified as being available on the PBS (Pharmaceutical Benefits Scheme) on November, 1 2024. To learn more about this subsidy, visit the Pharmaceutical Benefits Scheme (PBS) website.
Pregnant or planning a pregnancy ?
(AHT)
For the active ingredient buprenorphine
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
Brand name
(ARTG)
: BUPREDERMAL buprenorphine 30 micrograms/hour transdermal drug delivery system sachetDownload 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)
BUPREDERMAL patches are indicated for the management of severe pain where: other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain, and the pain is opioid-responsive, and requires daily, continuous, long-term treatment. BUPREDERMAL patches are not indicated for use in chronic non-cancer pain other than in exceptional circumstances. BUPREDERMAL patches are not indicated as an as-needed (PRN) analgesia.
How to use this medicine
(ARTG)
This medicine contains one component only.
Component :
- Drug delivery system, transdermal
- Transdermal
- Beige coloured rectangular patch with rounded corners on an aluminised rigid removable protective layer. The trade name and the strength is printed on the patch.
Storage conditions
(ARTG)
- Store below 25 degrees Celsius
- Shelf lifetime is 3 Years.
Do I need a prescription ?
(ARTG)
These medicines require authorisation for prescription from your doctor. It is Schedule 8 : Controlled Drug.
- 2 patches pack
- 4 patches pack
Pregnant or planning a pregnancy ?
(AHT)
For the active ingredient buprenorphine
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
Brand name
(ARTG)
: BUPREDERMAL buprenorphine 25 micrograms/hour transdermal drug delivery system sachetDownload 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)
BUPREDERMAL patches are indicated for the management of severe pain where: other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain, and the pain is opioid-responsive, and requires daily, continuous, long-term treatment. BUPREDERMAL patches are not indicated for use in chronic non-cancer pain other than in exceptional circumstances. BUPREDERMAL patches are not indicated as an as-needed (PRN) analgesia.
How to use this medicine
(ARTG)
This medicine contains one component only.
Component :
- Drug delivery system, transdermal
- Transdermal
- Beige coloured rectangular patch with rounded corners on an aluminised rigid removable protective layer. The trade name and the strength is printed on the patch.
Storage conditions
(ARTG)
- Store below 25 degrees Celsius
- Shelf lifetime is 3 Years.
Do I need a prescription ?
(ARTG)
These medicines require authorisation for prescription from your doctor. It is Schedule 8 : Controlled Drug.
- 2 patches pack
- 4 patches pack
Is this medicine subsidised ?
(PBS)
This medicine was verified as being available on the PBS (Pharmaceutical Benefits Scheme) on November, 1 2024. To learn more about this subsidy, visit the Pharmaceutical Benefits Scheme (PBS) website.
Pregnant or planning a pregnancy ?
(AHT)
For the active ingredient buprenorphine
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
Brand name
(ARTG)
: BUPREDERMAL buprenorphine 25 micrograms/hour transdermal drug delivery system sachetDownload 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)
BUPREDERMAL patches are indicated for the management of severe pain where: other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain, and the pain is opioid-responsive, and requires daily, continuous, long-term treatment. BUPREDERMAL patches are not indicated for use in chronic non-cancer pain other than in exceptional circumstances. BUPREDERMAL patches are not indicated as an as-needed (PRN) analgesia.
How to use this medicine
(ARTG)
This medicine contains one component only.
Component :
- Drug delivery system, transdermal
- Transdermal
- Beige coloured rectangular patch with rounded corners on an aluminised rigid removable protective layer. The trade name and the strength is printed on the patch.
Storage conditions
(ARTG)
- Store below 25 degrees Celsius
- Shelf lifetime is 3 Years.
Do I need a prescription ?
(ARTG)
These medicines require authorisation for prescription from your doctor. It is Schedule 8 : Controlled Drug.
- 2 patches pack
- 4 patches pack
Pregnant or planning a pregnancy ?
(AHT)
For the active ingredient buprenorphine
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
Brand name
(ARTG)
: BUPREDERMAL buprenorphine 40 micrograms/hour transdermal drug delivery system sachetDownload 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)
BUPREDERMAL patches are indicated for the management of severe pain where: other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain, and the pain is opioid-responsive, and requires daily, continuous, long-term treatment. BUPREDERMAL patches are not indicated for use in chronic non-cancer pain other than in exceptional circumstances. BUPREDERMAL patches are not indicated as an as-needed (PRN) analgesia.
How to use this medicine
(ARTG)
This medicine contains one component only.
Component :
- Drug delivery system, transdermal
- Transdermal
- Beige coloured rectangular patch with rounded corners on an aluminised rigid removable protective layer. The trade name and the strength is printed on the patch.
Storage conditions
(ARTG)
- Store below 25 degrees Celsius
- Shelf lifetime is 3 Years.
Do I need a prescription ?
(ARTG)
These medicines require authorisation for prescription from your doctor. It is Schedule 8 : Controlled Drug.
- 2 patches pack
- 4 patches pack
Is this medicine subsidised ?
(PBS)
This medicine was verified as being available on the PBS (Pharmaceutical Benefits Scheme) on November, 1 2024. To learn more about this subsidy, visit the Pharmaceutical Benefits Scheme (PBS) website.
Pregnant or planning a pregnancy ?
(AHT)
For the active ingredient buprenorphine
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
Brand name
(ARTG)
: BUPREDERMAL buprenorphine 40 micrograms/hour transdermal drug delivery system sachetDownload 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)
BUPREDERMAL patches are indicated for the management of severe pain where: other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain, and the pain is opioid-responsive, and requires daily, continuous, long-term treatment. BUPREDERMAL patches are not indicated for use in chronic non-cancer pain other than in exceptional circumstances. BUPREDERMAL patches are not indicated as an as-needed (PRN) analgesia.
How to use this medicine
(ARTG)
This medicine contains one component only.
Component :
- Drug delivery system, transdermal
- Transdermal
- Beige coloured rectangular patch with rounded corners on an aluminised rigid removable protective layer. The trade name and the strength is printed on the patch.
Storage conditions
(ARTG)
- Store below 25 degrees Celsius
- Shelf lifetime is 3 Years.
Do I need a prescription ?
(ARTG)
These medicines require authorisation for prescription from your doctor. It is Schedule 8 : Controlled Drug.
- 2 patches pack
- 4 patches pack
Pregnant or planning a pregnancy ?
(AHT)
For the active ingredient buprenorphine
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
Brand name
(ARTG)
: BUPREDERMAL buprenorphine 20 micrograms/hour transdermal drug delivery system sachetDownload 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)
BUPREDERMAL patches are indicated for the management of severe pain where: other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain, and the pain is opioid-responsive, and requires daily, continuous, long-term treatment. BUPREDERMAL patches are not indicated for use in chronic non-cancer pain other than in exceptional circumstances. BUPREDERMAL patches are not indicated as an as-needed (PRN) analgesia.
How to use this medicine
(ARTG)
This medicine contains one component only.
Component :
- Drug delivery system, transdermal
- Transdermal
- Beige coloured square patch with rounded corners on a aluminised rigid removable protective layer.The trade name and the strength are printed on the patch.
Storage conditions
(ARTG)
- Store below 25 degrees Celsius
- Shelf lifetime is 3 Years.
Do I need a prescription ?
(ARTG)
These medicines require authorisation for prescription from your doctor. It is Schedule 8 : Controlled Drug.
- 1 Sachet pack
- 2 Sachet pack
- 4 Sachets pack
Pregnant or planning a pregnancy ?
(AHT)
For the active ingredient buprenorphine
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
Brand name
(ARTG)
: BUPREDERMAL buprenorphine 20 micrograms/hour transdermal drug delivery system sachetDownload 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)
BUPREDERMAL patches are indicated for the management of severe pain where: other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain, and the pain is opioid-responsive, and requires daily, continuous, long-term treatment. BUPREDERMAL patches are not indicated for use in chronic non-cancer pain other than in exceptional circumstances. BUPREDERMAL patches are not indicated as an as-needed (PRN) analgesia.
How to use this medicine
(ARTG)
This medicine contains one component only.
Component :
- Drug delivery system, transdermal
- Transdermal
- Beige coloured square patch with rounded corners on a aluminised rigid removable protective layer.The trade name and the strength are printed on the patch.
Storage conditions
(ARTG)
- Store below 25 degrees Celsius
- Shelf lifetime is 3 Years.
Do I need a prescription ?
(ARTG)
These medicines require authorisation for prescription from your doctor. It is Schedule 8 : Controlled Drug.
- 1 Sachet pack
- 2 Sachet pack
- 4 Sachets pack
Is this medicine subsidised ?
(PBS)
This medicine was verified as being available on the PBS (Pharmaceutical Benefits Scheme) on November, 1 2024. To learn more about this subsidy, visit the Pharmaceutical Benefits Scheme (PBS) website.
Pregnant or planning a pregnancy ?
(AHT)
For the active ingredient buprenorphine
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
Brand name
(ARTG)
: BUPREDERMAL buprenorphine 20 micrograms/hour transdermal drug delivery system sachetDownload 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)
BUPREDERMAL patches are indicated for the management of severe pain where: other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain, and the pain is opioid-responsive, and requires daily, continuous, long-term treatment. BUPREDERMAL patches are not indicated for use in chronic non-cancer pain other than in exceptional circumstances. BUPREDERMAL patches are not indicated as an as-needed (PRN) analgesia.
How to use this medicine
(ARTG)
This medicine contains one component only.
Component :
- Drug delivery system, transdermal
- Transdermal
- Beige coloured square patch with rounded corners on a aluminised rigid removable protective layer.The trade name and the strength are printed on the patch.
Storage conditions
(ARTG)
- Store below 25 degrees Celsius
- Shelf lifetime is 3 Years.
Do I need a prescription ?
(ARTG)
These medicines require authorisation for prescription from your doctor. It is Schedule 8 : Controlled Drug.
- 1 Sachet pack
- 2 Sachet pack
- 4 Sachets pack
Pregnant or planning a pregnancy ?
(AHT)
For the active ingredient buprenorphine
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
Brand name
(ARTG)
: BUPREDERMAL buprenorphine 15 micrograms/hour transdermal drug delivery system sachetDownload 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)
BUPREDERMAL patches are indicated for the management of severe pain where: other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain, and the pain is opioid-responsive, and requires daily, continuous, long-term treatment. BUPREDERMAL patches are not indicated for use in chronic non-cancer pain other than in exceptional circumstances. BUPREDERMAL patches are not indicated as an as-needed (PRN) analgesia.
How to use this medicine
(ARTG)
This medicine contains one component only.
Component :
- Drug delivery system, transdermal
- Transdermal
- Beige coloured rectangular patch with rounded corners on an aluminised rigid removable protective layer. The trade name and the strength is printed on the patch.
Storage conditions
(ARTG)
- Store below 25 degrees Celsius
- Shelf lifetime is 3 Years.
Do I need a prescription ?
(ARTG)
These medicines require authorisation for prescription from your doctor. It is Schedule 8 : Controlled Drug.
- 2 patches pack
- 4 patches pack
Is this medicine subsidised ?
(PBS)
This medicine was verified as being available on the PBS (Pharmaceutical Benefits Scheme) on November, 1 2024. To learn more about this subsidy, visit the Pharmaceutical Benefits Scheme (PBS) website.
Pregnant or planning a pregnancy ?
(AHT)
For the active ingredient buprenorphine
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
Brand name
(ARTG)
: BUPREDERMAL buprenorphine 15 micrograms/hour transdermal drug delivery system sachetDownload 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)
BUPREDERMAL patches are indicated for the management of severe pain where: other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain, and the pain is opioid-responsive, and requires daily, continuous, long-term treatment. BUPREDERMAL patches are not indicated for use in chronic non-cancer pain other than in exceptional circumstances. BUPREDERMAL patches are not indicated as an as-needed (PRN) analgesia.
How to use this medicine
(ARTG)
This medicine contains one component only.
Component :
- Drug delivery system, transdermal
- Transdermal
- Beige coloured rectangular patch with rounded corners on an aluminised rigid removable protective layer. The trade name and the strength is printed on the patch.
Storage conditions
(ARTG)
- Store below 25 degrees Celsius
- Shelf lifetime is 3 Years.
Do I need a prescription ?
(ARTG)
These medicines require authorisation for prescription from your doctor. It is Schedule 8 : Controlled Drug.
- 2 patches pack
- 4 patches pack
Pregnant or planning a pregnancy ?
(AHT)
For the active ingredient buprenorphine
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
Brand name
(ARTG)
: BUPREDERMAL buprenorphine 10 micrograms/hour transdermal drug delivery system sachetDownload 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)
BUPREDERMAL patches are indicated for the management of severe pain where: other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain, and the pain is opioid-responsive, and requires daily, continuous, long-term treatment. BUPREDERMAL patches are not indicated for use in chronic non-cancer pain other than in exceptional circumstances. BUPREDERMAL patches are not indicated as an as-needed (PRN) analgesia.
How to use this medicine
(ARTG)
This medicine contains one component only.
Component :
- Drug delivery system, transdermal
- Transdermal
- Beige coloured rectangular patch with rounded corners on a aluminised rigid removable protective layer.The trade name and the strength are printed on the patch.
Storage conditions
(ARTG)
- Store below 25 degrees Celsius
- Shelf lifetime is 3 Years.
Do I need a prescription ?
(ARTG)
These medicines require authorisation for prescription from your doctor. It is Schedule 8 : Controlled Drug.
- 1 Sachet pack
- 2 Sachet pack
- 4 Sachets pack
Pregnant or planning a pregnancy ?
(AHT)
For the active ingredient buprenorphine
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
Brand name
(ARTG)
: BUPREDERMAL buprenorphine 10 micrograms/hour transdermal drug delivery system sachetDownload 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)
BUPREDERMAL patches are indicated for the management of severe pain where: other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain, and the pain is opioid-responsive, and requires daily, continuous, long-term treatment. BUPREDERMAL patches are not indicated for use in chronic non-cancer pain other than in exceptional circumstances. BUPREDERMAL patches are not indicated as an as-needed (PRN) analgesia.
How to use this medicine
(ARTG)
This medicine contains one component only.
Component :
- Drug delivery system, transdermal
- Transdermal
- Beige coloured rectangular patch with rounded corners on a aluminised rigid removable protective layer.The trade name and the strength are printed on the patch.
Storage conditions
(ARTG)
- Store below 25 degrees Celsius
- Shelf lifetime is 3 Years.
Do I need a prescription ?
(ARTG)
These medicines require authorisation for prescription from your doctor. It is Schedule 8 : Controlled Drug.
- 1 Sachet pack
- 2 Sachet pack
- 4 Sachets pack
Is this medicine subsidised ?
(PBS)
This medicine was verified as being available on the PBS (Pharmaceutical Benefits Scheme) on November, 1 2024. To learn more about this subsidy, visit the Pharmaceutical Benefits Scheme (PBS) website.
Pregnant or planning a pregnancy ?
(AHT)
For the active ingredient buprenorphine
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
Brand name
(ARTG)
: BUPREDERMAL buprenorphine 10 micrograms/hour transdermal drug delivery system sachetDownload 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)
BUPREDERMAL patches are indicated for the management of severe pain where: other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain, and the pain is opioid-responsive, and requires daily, continuous, long-term treatment. BUPREDERMAL patches are not indicated for use in chronic non-cancer pain other than in exceptional circumstances. BUPREDERMAL patches are not indicated as an as-needed (PRN) analgesia.
How to use this medicine
(ARTG)
This medicine contains one component only.
Component :
- Drug delivery system, transdermal
- Transdermal
- Beige coloured rectangular patch with rounded corners on a aluminised rigid removable protective layer.The trade name and the strength are printed on the patch.
Storage conditions
(ARTG)
- Store below 25 degrees Celsius
- Shelf lifetime is 3 Years.
Do I need a prescription ?
(ARTG)
These medicines require authorisation for prescription from your doctor. It is Schedule 8 : Controlled Drug.
- 1 Sachet pack
- 2 Sachet pack
- 4 Sachets pack
Pregnant or planning a pregnancy ?
(AHT)
For the active ingredient buprenorphine
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
Brand name
(ARTG)
: BUPREDERMAL buprenorphine 5 micrograms/hour transdermal drug delivery system sachetDownload 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)
BUPREDERMAL patches are indicated for the management of severe pain where: other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain, and the pain is opioid-responsive, and requires daily, continuous, long-term treatment. BUPREDERMAL patches are not indicated for use in chronic non-cancer pain other than in exceptional circumstances. BUPREDERMAL patches are not indicated as an as-needed (PRN) analgesia.
How to use this medicine
(ARTG)
This medicine contains one component only.
Component :
- Drug delivery system, transdermal
- Transdermal
- Beige coloured square patch with rounded corners on a aluminised rigid removable protective layer.The trade name and the strength are printed on the patch.
Storage conditions
(ARTG)
- Store below 25 degrees Celsius
- Shelf lifetime is 2 Years.
Do I need a prescription ?
(ARTG)
These medicines require authorisation for prescription from your doctor. It is Schedule 8 : Controlled Drug.
- 1 Sachet pack
- 2 Sachet pack
- 4 Sachets pack
Pregnant or planning a pregnancy ?
(AHT)
For the active ingredient buprenorphine
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
Brand name
(ARTG)
: BUPREDERMAL buprenorphine 5 micrograms/hour transdermal drug delivery system sachetDownload 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)
BUPREDERMAL patches are indicated for the management of severe pain where: other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain, and the pain is opioid-responsive, and requires daily, continuous, long-term treatment. BUPREDERMAL patches are not indicated for use in chronic non-cancer pain other than in exceptional circumstances. BUPREDERMAL patches are not indicated as an as-needed (PRN) analgesia.
How to use this medicine
(ARTG)
This medicine contains one component only.
Component :
- Drug delivery system, transdermal
- Transdermal
- Beige coloured square patch with rounded corners on a aluminised rigid removable protective layer.The trade name and the strength are printed on the patch.
Storage conditions
(ARTG)
- Store below 25 degrees Celsius
- Shelf lifetime is 2 Years.
Do I need a prescription ?
(ARTG)
These medicines require authorisation for prescription from your doctor. It is Schedule 8 : Controlled Drug.
- 1 Sachet pack
- 2 Sachet pack
- 4 Sachets pack
Is this medicine subsidised ?
(PBS)
This medicine was verified as being available on the PBS (Pharmaceutical Benefits Scheme) on November, 1 2024. To learn more about this subsidy, visit the Pharmaceutical Benefits Scheme (PBS) website.
Pregnant or planning a pregnancy ?
(AHT)
For the active ingredient buprenorphine
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
Brand name
(ARTG)
: BUPREDERMAL buprenorphine 5 micrograms/hour transdermal drug delivery system sachetDownload 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)
BUPREDERMAL patches are indicated for the management of severe pain where: other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain, and the pain is opioid-responsive, and requires daily, continuous, long-term treatment. BUPREDERMAL patches are not indicated for use in chronic non-cancer pain other than in exceptional circumstances. BUPREDERMAL patches are not indicated as an as-needed (PRN) analgesia.
How to use this medicine
(ARTG)
This medicine contains one component only.
Component :
- Drug delivery system, transdermal
- Transdermal
- Beige coloured square patch with rounded corners on a aluminised rigid removable protective layer.The trade name and the strength are printed on the patch.
Storage conditions
(ARTG)
- Store below 25 degrees Celsius
- Shelf lifetime is 2 Years.
Do I need a prescription ?
(ARTG)
These medicines require authorisation for prescription from your doctor. It is Schedule 8 : Controlled Drug.
- 1 Sachet pack
- 2 Sachet pack
- 4 Sachets pack
Pregnant or planning a pregnancy ?
(AHT)
For the active ingredient buprenorphine
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