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BUPROCARE 2MG TABLET

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Prescription Required

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Gentech Healthcare Pvt Ltd

Salt Composition

Buprenorphine (2mg)

Overview BUPROCARE 2MG TABLET

Buprenorphine 2mg tablets (BUPROCARE) are indicated for managing opioid (e.g., morphine) addiction. This medication mitigates withdrawal symptoms associated with opioid cessation. Successful treatment often incorporates comprehensive support, including therapy and lifestyle adjustments. Prescription is limited to patients aged 16 and older. As a potentially habit-forming medication, strict adherence to the physician's instructions is crucial. Treatment may involve additional social and psychological interventions. It can be administered with or without food. Consistent daily use, as directed by your doctor, is essential for efficacy; missed doses reduce effectiveness. Common adverse reactions include fatigue, opioid withdrawal symptoms, unease, jitteriness, lightheadedness, cephalgia, somnolence, bowel looseness, nausea, emesis, and stomach discomfort. Persistent or worsening side effects warrant immediate medical attention; your doctor can offer management strategies. Prior to commencing treatment, disclose any pre-existing health issues or medications to your physician to ensure safety. This is especially important for pregnant and breastfeeding individuals, who must seek medical counsel before use.

Uses of BUPROCARE 2MG TABLET

Morphine addiction; Treatment of significant to intense pain

Major Benefits of BUPROCARE 2MG TABLET:

Administer this medication precisely as directed by your physician, adhering to the prescribed dosage and treatment period. Ingest the 2mg BUPROCARE tablet whole; avoid chewing, crushing, or fracturing. Consumption with or without food is acceptable; however, consistent timing is recommended.

Common Side effects of BUPROCARE 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 2MG TABLET:

Consume this medication precisely as your physician directs, adhering to the prescribed dosage and schedule. Ingest the 2mg BUPROCARE tablet whole; avoid chewing, crushing, or fracturing it. While it can be taken with or without food, consistent timing is recommended for optimal efficacy.

How BUPROCARE 2MG TABLET works:

Suboxone 2mg tablets function as a partial opioid agonist, mitigating withdrawal symptoms in individuals ceasing opioid use by mimicking the effects of opioids.

SAFETY ADVICE

AlcoholAlcoholUNSAFE

Combining BUPROCARE 2MG TABLETS with alcohol is dangerous.

PregnancyPregnancyCONSULT YOUR DOCTOR

Using BUPROCARE 2MG TABLETS during pregnancy may pose risks. While human data is scarce, animal studies indicate potential harm to a developing fetus. A physician will assess the benefits against potential risks prior to prescription. Seek medical advice.

Breast feedingBreast feedingCONSULT YOUR DOCTOR

The use of BUPROCARE 2MG TABLETS while breastfeeding is likely inadvisable. Available human data indicates potential transfer of the medication into breast milk, posing a possible risk to the infant.

DrivingDrivingUNSAFE

Taking a BUPROCARE 2MG TABLET may cause drowsiness, blurred vision, or dizziness. Refrain from driving if you experience these effects.

KidneyKidneyCAUTION

Patients with severe kidney impairment should use BUPROCARE 2MG TABLETS cautiously; dosage modification may be necessary. Physician consultation is advised.

LiverLiverCAUTION

Caution is advised when administering Buprocare 2mg tablets to individuals with hepatic impairment; dosage modification may be necessary. Physician consultation is recommended. Buprocare 2mg tablets are contraindicated in patients exhibiting severe liver dysfunction.

What if you forget to take BUPROCARE 2MG TABLET :

NA

Facts to Know About BUPROCARE 2MG TABLET

LabelValue
Chemical Type Phenanthrene Derivatives
Developing Habits Affirmative.
Treatment Category Neuroscience Central Nervous System
Actions Partial Opioid Agonists

FAQs on BUPROCARE 2MG TABLET

BUPROCARE 2MG TABLETS treat severe pain unresponsive to other analgesics or when those analgesics are poorly tolerated. This medication isn't for minor or intermittent pain, or for pain relief "as needed." 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 the elderly. Consult your doctor if you have any concerns.
To prevent withdrawal symptoms (such as restlessness, runny nose and eyes, muscle aches, and insomnia), gradually reduce your BUPROCARE 2MG TABLET dosage instead of stopping abruptly. Your doctor can provide personalized guidance on this process.
Get immediate medical help if you experience agitation, hallucinations, fever, sweating, shivering, rapid heart rate, muscle rigidity, twitching, incoordination, nausea, vomiting, or diarrhea.
You'll start to feel 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 contact your doctor if you have any concerns.
This medication can significantly lower your blood pressure, potentially causing dizziness when standing up after sitting, particularly if you also take anti-hypertensive drugs. Discuss this with your doctor, who may adjust your dosage.
Prolonged use of this medication carries a risk of addiction, psychological dependence, and subsequent withdrawal symptoms.
Taking BUPROCARE 2MG TABLET during pregnancy may lead to your baby developing a dependence on the medication. This can result in life-threatening withdrawal symptoms after birth, potentially requiring several weeks of medical care for the newborn.
BUPROCARE 2MG TABLETS may transfer to breast milk, potentially causing drowsiness or breathing difficulties in nursing infants. Consult your doctor thoroughly regarding all potential risks.
Store BUPROCARE 2MG TABLETS at room temperature, away from heat, moisture, and sunlight, in a secure, child-resistant location. Dispose of any remaining medication safely.
BUPROCARE 2MG TABLETS are opioid partial agonist-antagonist analgesics. As a controlled substance with addictive potential, alternative pain management should be discussed with your doctor if addiction occurs.
Yes. BUPROCARE 2MG TABLETS can block the effects of opiates.
BUPROCARE 2MG TABLETS are not associated with depression. Report any depressive symptoms to your doctor.
BUPROCARE 2MG TABLET
349
MRP 425
17% off