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Bupreplast Patch

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Prescription Required

Marketer

Zuventus Healthcare Ltd

Salt Composition

Buprenorphine (5mg)

Overview Bupreplast Patch

Bupreplast patches effectively manage moderate to severe pain and opioid addiction. They alleviate withdrawal symptoms associated with opioid cessation. Your physician will provide detailed application instructions; adhere to them closely for optimal results. Dosage and treatment length vary based on your condition and response. Consistent use is crucial; discontinue only as directed by your doctor. Common side effects include constipation, dizziness, drowsiness, headache, and nausea. These may be more frequent initially or after dosage increases, typically subsiding with continued use. Persistent or severe side effects necessitate patch removal and immediate medical consultation. Inform your doctor of any pre-existing health conditions or medications you are taking before commencing treatment, as interactions are possible. Pregnant or breastfeeding individuals should seek medical advice prior to use.

Primary Ingredients of Bupreplast Patch

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Uses of Bupreplast Patch

Moderate to severe pain necessitates opioid analgesia (morphine).

Major Benefits of Bupreplast Patch:

Apply this medication according to your doctor's prescribed dosage and schedule. Always verify the instructions on the packaging prior to application. Ensure the application area is clean and completely dry. Peel away the patch's protective covering. Avoid touching the adhesive surface. Apply the patch firmly to the skin, adhesive side down, ensuring even contact.

Common Side effects of Bupreplast Patch:

  • Headache
  • Back pain
  • Drowsiness
  • Vomiting
  • Insomnia (difficulty in sleeping)
  • Dizziness
  • Abdominal pain
  • Weakness
  • Sweating
  • Constipation
  • Withdrawal syndrome
  • Infection
  • Vertigo
  • Inflammation of the nose
  • Chills
  • Flu-like symptoms
  • Nausea

How to use Bupreplast Patch:

Apply this medication precisely as your physician directs, adhering to both the prescribed dosage and duration. Always verify the product information on the packaging prior to application. Ensure the application area is clean and completely dry. Peel away the patch's protective covering, avoiding contact with the adhesive surface. Then, apply the patch firmly to the skin with the adhesive side in contact with the skin.

How Bupreplast Patch works:

The Bupreplast Patch, a partial opioid agonist, mitigates opioid withdrawal symptoms by mimicking the actions of opioid medications. Simultaneously, it alleviates pain through its interaction with specialized brain receptors, modifying pain perception and response.

SAFETY ADVICE

AlcoholAlcoholNone

No known drug interactions.

PregnancyPregnancyCONSULT YOUR DOCTOR

Using the Bupreplast Patch during pregnancy may pose risks. While human research is scant, animal studies indicate potential harm to the unborn child. A physician will assess the advantages against possible dangers prior to any prescription. Seek medical advice.

Breast feedingBreast feedingCONSULT YOUR DOCTOR

Using the Bupreplast Patch while breastfeeding is likely inadvisable. Available human data indicates potential transfer of the medication into breast milk, posing a possible risk to the infant.

DrivingDrivingNone

No known drug interactions.

KidneyKidneyCAUTION

For patients with significant kidney impairment, Buprenorphine patches require careful administration. Dosage modification of the Buprenorphine patch may be necessary; physician consultation is advised.

LiverLiverCAUTION

Patients with severe liver disease should use the Bupreplast Patch cautiously. Dosage modification of the Bupreplast Patch might be necessary. A physician's consultation is advised. An alternative pain reliever offering greater dosing flexibility may be considered for individuals with significant hepatic dysfunction.

What if you forget to take Bupreplast Patch :

NA

Facts to Know About Bupreplast Patch

LabelValue
Chemical Category Phenanthrene Derivatives
Developing Habits .
Treatment Category Neuroscience Central Nervous System

FAQs on Bupreplast Patch

Buprenorphine patches are prescribed for severe pain unresponsive to other analgesics or where those analgesics are poorly tolerated. This medication is unsuitable for mild or intermittent pain, or for pain requiring only occasional treatment. It's also indicated for opioid use disorder.
Apply the Buprenorphine patch to clean, dry, rash-free skin on your upper chest, back, arm, or side. Use only water to cleanse the application area; avoid soaps, oils, or gels. Dispose of used patches safely and away from children and pets. Skin varies; follow your doctor's instructions for placement.
Use only undamaged patches. Apply only one patch at a time, unless otherwise directed by your doctor. Avoid applying the patch to irritated or damaged skin. Keep the patch out of a child's reach. Don't let children see you apply the patch, and never call it a bandage.
To prevent overdose and potential death, avoid heat sources while wearing the patch. This includes heating pads, electric blankets, tanning beds, saunas, direct sunlight, hot baths, and strenuous exercise. Heat accelerates skin absorption of the medication.
Avoid layering patches; each patch must adhere directly to your skin. Always consult your doctor if you have any questions about using this medication.
Should you have difficulty applying the patch, avoid using bandages or tape. Consult your doctor or pharmacist.
Buprenorphine patches allow showering and swimming, but limit immersion time. Always check the patch's secure placement and thoroughly dry the surrounding skin afterward. If the patch falls off, apply a new one to a different location and return the old patch to its original packaging. Follow your doctor's instructions for use.
This medication can significantly lower blood pressure, potentially causing dizziness when standing up, especially if you're also taking anti-hypertensive drugs. Consult your doctor; your dosage may need adjustment.
Get immediate medical attention if you experience shallow breathing, chest pain, rapid heart rate, seizures, dizziness (feeling faint), blisters, swelling, or severe skin irritation at the patch site, nausea, vomiting, appetite loss, or liver issues such as upper abdominal pain, dark urine, pale stools, or jaundice (yellowing of skin or eyes).
Using Buprenorphine patches during pregnancy may cause your baby to become dependent on the medication, leading to potentially life-threatening withdrawal symptoms after birth. Newborns experiencing such withdrawal may require several weeks of medical care.
Buprenorphine patches may transfer into breast milk, potentially causing respiratory distress or life-threatening complications in infants. Consult your doctor thoroughly regarding these risks.
Store Bupreplast Patches at room temperature, away from heat, moisture, and sunlight, in a secure location out of children's reach. Dispose of any unused portions safely.
Buprenorphine patches, opioid partial agonist-antagonist analgesics, are controlled substances with addictive potential. Discuss alternative pain management options with your doctor if addiction develops.
Buprenorphine patches effectively block the effects of opiates.
Bupreplast Patches are not associated with depression. Report any depressive symptoms to your doctor.
Bupreplast Patch
765
MRP 885
13% off