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BUPROCARE 0.4MG TABLET

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Prescription Required

Marketer

Gentech Healthcare Pvt Ltd

Salt Composition

Buprenorphine (0.4mg)

Overview BUPROCARE 0.4MG TABLET

BUPROCARE 0.4MG tablets are indicated for managing opioid (morphine) addiction. They alleviate withdrawal symptoms associated with opioid cessation. This medication forms part of a comprehensive treatment plan incorporating counseling and lifestyle adjustments. BUPROCARE 0.4MG tablets are exclusively prescribed to patients aged 16 and older. Potential for dependence necessitates strict adherence to the physician's instructions. Treatment may encompass psychosocial support services. Administration is independent of food intake. Consistent daily use, as directed by your doctor, is crucial; missed doses diminish efficacy. Frequently reported side effects include fatigue, opioid withdrawal symptoms, unease, jitters, lightheadedness, cephalalgia, somnolence, bowel looseness, queasiness, emesis, and stomach discomfort. Persistent or worsening side effects warrant immediate medical consultation. Your physician can offer strategies for mitigation or symptom reduction. Prior to commencing treatment, inform your doctor of any pre-existing health conditions or medications currently in use to ensure suitability. Pregnant or lactating individuals must seek medical advice before using this medication.

Uses of BUPROCARE 0.4MG TABLET

Morphine addiction; management of significant to intense pain

Major Benefits of BUPROCARE 0.4MG TABLET:

Administer this medication precisely as your physician directs, adhering to both the prescribed dosage and treatment length. Ingest the BUPROCARE 0.4MG TABLET whole; avoid chewing, crushing, or fracturing it. Consumption may coincide with meals or be independent of them, however, maintaining a consistent daily intake time is recommended.

Common Side effects of BUPROCARE 0.4MG 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 0.4MG TABLET:

Administer BUPROCARE 0.4MG TABLETS precisely as prescribed by your physician, adhering to both the dosage and treatment schedule. Ingest the tablet whole; avoid chewing, crushing, or fracturing. This medication can be consumed with or without food, though consistent timing is recommended.

How BUPROCARE 0.4MG TABLET works:

Suboxone 0.4mg tablets function as a partial opioid agonist, mitigating withdrawal symptoms in individuals discontinuing opioid use by mimicking the effects of such medications.

SAFETY ADVICE

AlcoholAlcoholUNSAFE

Combining BUPROCARE 0.4MG TABLETS with alcohol is strongly discouraged due to safety concerns.

PregnancyPregnancyCONSULT YOUR DOCTOR

Using BUPROCARE 0.4MG TABLETS during pregnancy may pose risks. While human data is scarce, animal research indicates potential harm to the fetus. A physician will assess the advantages against possible risks prior to prescription. Seek medical advice.

Breast feedingBreast feedingCONSULT YOUR DOCTOR

The use of BUPROCARE 0.4MG TABLETS while breastfeeding is likely inadvisable. Available human data indicates a potential for the medication to transfer to breast milk, posing a risk to the infant.

DrivingDrivingUNSAFE

Taking BUPROCARE 0.4MG TABLETS may cause drowsiness, blurred vision, or dizziness. Refrain from driving if you experience these effects.

KidneyKidneyCAUTION

Patients with severe kidney impairment should use 0.4mg BUPROCARE tablets cautiously. A dose modification of BUPROCARE 0.4mg tablets may be necessary; physician consultation is recommended.

LiverLiverCAUTION

Patients with liver impairment should use 0.4mg BUPROCARE tablets cautiously, potentially requiring dose modification. Physician consultation is advised. BUPROCARE 0.4mg tablets are contraindicated in patients with severe hepatic dysfunction.

What if you forget to take BUPROCARE 0.4MG TABLET :

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Facts to Know About BUPROCARE 0.4MG TABLET

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

FAQs on BUPROCARE 0.4MG TABLET

BUPROCARE 0.4MG TABLETS treat severe pain unresponsive to other medications or where those medications are poorly tolerated. This medication isn't for minor or intermittent pain, or for pain relief on an as-needed basis. 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.
Gradually reduce your BUPROCARE 0.4MG TABLET dosage to avoid withdrawal symptoms like restlessness, nasal and eye discharge, muscle aches, and insomnia. Never stop abruptly; consult your doctor for guidance on tapering the medication.
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 feeling the effects of this medication soon after the first 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 blood pressure, potentially causing dizziness upon standing, particularly if you're also taking antihypertensive drugs. Consult your doctor; your dosage may need adjustment.
Prolonged use of this medication carries a risk of addiction, psychological dependence, and withdrawal symptoms.
Taking BUPROCARE 0.4MG TABLETS during pregnancy may lead to your baby's dependence on the medication. This dependence can cause potentially life-threatening withdrawal symptoms in your newborn. Newborns experiencing such withdrawal may require several weeks of medical care.
BUPROCARE 0.4MG TABLETS may transfer to breast milk, potentially causing drowsiness or breathing difficulties in infants. Consult your doctor thoroughly regarding the associated risks.
Store BUPROCARE 0.4MG TABLETS at room temperature, away from heat, moisture, and sunlight, in a secure, child-resistant location. Dispose of any unused medication safely.
BUPROCARE 0.4MG 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 arises.
BUPROCARE 0.4MG TABLETS are an opiate blocker.
BUPROCARE 0.4MG TABLETS are not associated with depression. Report any depressive symptoms to your doctor.
BUPROCARE 0.4MG TABLET
86
MRP 100
14% off