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Buprocare 0.2mg Tablet

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Prescription Required

Marketer

Gentech Healthcare Pvt Ltd

Salt Composition

Buprenorphine (0.2mg)

Overview Buprocare 0.2mg Tablet

Opioid withdrawal symptoms are managed with Buprocare 0.2mg tablets, effective in treating morphine dependence. This medication aids in mitigating withdrawal effects from other opioids, forming a component of a comprehensive treatment strategy incorporating counseling and lifestyle adjustments. Prescribed only to patients aged 16 and older, Buprocare 0.2mg tablets possess addictive potential and must be administered precisely as directed by a physician. Treatment may include psychosocial support. Consumption is independent of food intake; consistent daily use, as advised by your doctor, is crucial to maintain efficacy. Missed doses diminish effectiveness. Potential side effects include weakness, withdrawal symptoms, anxiety, restlessness, vertigo, headache, somnolence, diarrhea, nausea, emesis, and abdominal discomfort. Persistent or worsening side effects necessitate medical consultation. Your physician can offer strategies for symptom management or reduction. Prior to commencing Buprocare 0.2mg tablets, disclose any existing medical conditions or medications to your doctor to ensure safety. This includes informing your doctor if you are pregnant or breastfeeding.

Uses of Buprocare 0.2mg Tablet

Moderate to severe pain managed with morphine, a potent opioid.

Major Benefits of Buprocare 0.2mg Tablet:

Administer this medication precisely as your physician directs, adhering to both the prescribed dosage and treatment schedule. Ingest the tablet whole; avoid chewing, crushing, or fracturing it. Buprocare 0.2mg Tablets can be consumed with or without food; however, consistent daily timing is recommended.

Common Side effects of Buprocare 0.2mg Tablet:

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

How to use Buprocare 0.2mg Tablet:

Administer this medication precisely as your physician directs, adhering to both the prescribed dosage and treatment duration. Ingest the tablet whole; avoid chewing, crushing, or breaking it. Buprocare 0.2mg Tablets can be consumed with or without food, although consistent timing is recommended.

How Buprocare 0.2mg Tablet works:

Suboxone 0.2mg tablets function as a partial opioid agonist, mitigating withdrawal symptoms in individuals discontinuing opioid use by mimicking the effects of these medications.

SAFETY ADVICE

AlcoholAlcoholUNSAFE

Consuming alcohol while taking Buprocare 0.2mg tablets is unsafe.

PregnancyPregnancyCONSULT YOUR DOCTOR

The use of Buprocare 0.2mg Tablet during pregnancy may pose risks. While human research is scant, animal studies indicate potential harm to the fetus. A physician will assess the potential benefits against the risks prior to prescribing. Patient consultation with their doctor is advised.

Breast feedingBreast feedingCONSULT YOUR DOCTOR

The use of Buprocare 0.2mg tablets while breastfeeding is likely unsafe. Available human data indicates potential transfer of the medication into breast milk, posing a possible risk to the infant.

DrivingDrivingUNSAFE

Taking Buprocare 0.2mg tablets may cause drowsiness, blurred vision, and dizziness. Refrain from driving if you experience these side effects.

KidneyKidneyCAUTION

Patients with severe kidney impairment should exercise caution when using Buprocare 0.2mg tablets. Dosage modification may be necessary; physician consultation is recommended.

LiverLiverCAUTION

Patients with liver impairment should use 0.2mg Buprocare tablets cautiously, potentially requiring dosage modification. Consult a physician before use. Buprocare 0.2mg tablets are contraindicated in individuals with severe hepatic dysfunction.

What if you forget to take Buprocare 0.2mg Tablet :

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Facts to Know About Buprocare 0.2mg Tablet

LabelValue
Chemical Type Phenanthrene Derivatives
Developing Habits Affirmative.
Type of Treatment Neuroscience of the Central Nervous System
Action Class Partial Opioid Agonists

FAQs on Buprocare 0.2mg Tablet

Buprocare 0.2mg tablets treat severe pain unresponsive to other analgesics or poorly tolerated analgesics. This medication isn't suitable for mild, intermittent, or occasional pain, nor is it for "as needed" pain relief. It also treats opioid use disorder.
This medication may require dosage adjustment or be unsuitable for individuals with liver disease, a history of substance abuse, psychiatric disorders, head injury, seizures, certain gastrointestinal or respiratory conditions, or for older adults. Consult your doctor if you have any concerns.
To prevent withdrawal symptoms such as restlessness, nasal and eye discharge, muscle aches, and insomnia, gradually reduce your Buprocare 0.2mg Tablet dosage rather than stopping abruptly. Consult your doctor for guidance on tapering your medication.
Get immediate medical help if you experience agitation, hallucinations, fever, sweating, chills, rapid heart rate, muscle rigidity, twitching, incoordination, nausea, vomiting, or diarrhea.
You'll start feeling the effects of this medication soon after taking a single dose.
This medication can cause drowsiness or dizziness, impairing your ability to drive or use machinery. Refrain from alcohol consumption, and seek medical advice if you have any concerns.
This medication can significantly lower blood pressure, potentially causing dizziness when standing up after sitting, particularly if you're also taking antihypertensive drugs. Consult your doctor; your dosage may need adjusting.
Prolonged use of this medication can lead to physical and psychological dependence, potentially resulting in withdrawal symptoms upon cessation.
Taking Buprocare 0.2mg Tablet during pregnancy may lead to fetal dependence on the medication, resulting in potentially life-threatening withdrawal symptoms after birth. Newborns experiencing such withdrawal may require several weeks of medical care.
Buprocare 0.2mg tablets may transfer to breast milk, potentially causing drowsiness or breathing difficulties in infants. Consult your doctor thoroughly regarding the risks.
Store Buprocare 0.2mg Tablets at room temperature, away from heat, moisture, and direct sunlight. Keep them in a secure, child-resistant location. Dispose of any remaining medication safely.
Buprocare 0.2mg tablets are opioid partial agonist-antagonist analgesics. As a controlled substance with addictive potential, alternative pain relief should be discussed with your doctor if addiction occurs.
Buprocare 0.2mg tablets can block the effects of opiates.
Buprocare 0.2mg tablets are not associated with depression. Report any depressive symptoms to your doctor.
Buprocare 0.2mg Tablet
41
MRP 50
18% off