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Pramirol SR 2.1 Tablet

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Prescription Required

Marketer

Intas Pharmaceuticals Ltd

Salt Composition

Pramipexole (2.1mg)

Overview Pramirol SR 2.1 Tablet

Pramipexole extended-release 2.1 mg tablets manage Parkinson's disease symptoms and restless legs syndrome (characterized by an irresistible urge to move legs due to unpleasant sensations). This medication reduces excessive tremors by regulating movement. Administer Pramipexole with food, consistently at the same time daily for optimal blood levels. Follow your physician's dosage instructions precisely; if a dose is missed, take it immediately upon recollection. Complete the prescribed course, even with symptom improvement; never discontinue abruptly without consulting your doctor. Potential side effects include nausea, dry mouth, tiredness, visual disturbances, constipation, and swelling in the extremities. Drowsiness and dizziness are also possible; avoid driving or tasks requiring alertness until effects are known. Report any unusual mood shifts, heightened libido, compulsive gambling, or excessive spending to your doctor immediately, as these can be serious.

Primary Ingredients of Pramirol SR 2.1 Tablet

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Uses of Pramirol SR 2.1 Tablet

Tremors and involuntary movements | Uncomfortable leg sensations and urge to move

Major Benefits of Pramirol SR 2.1 Tablet:

Follow your doctor's instructions or consult the product label for proper administration. Ingest Pramirol SR 2.1 Tablet with a meal.

Common Side effects of Pramirol SR 2.1 Tablet:

  • Dizziness
  • Sleepiness
  • Nausea
  • Dryness in mouth
  • Fatigue
  • Hallucination
  • Constipation
  • Peripheral edema
  • Muscle spasm

How to use Pramirol SR 2.1 Tablet:

Follow your physician's instructions or consult the product label for proper administration. Ingest Pramirol SR 2.1 Tablet with a meal.

How Pramirol SR 2.1 Tablet works:

Pramirol SR 2.1 tablets function by replicating the effects of dopamine, a neurotransmitter crucial for regulating motor control within the brain.

SAFETY ADVICE

AlcoholAlcoholUNSAFE

Concurrent use of Pramirol SR 2.1 Tablet and alcohol may result in heightened sleepiness.

PregnancyPregnancyCONSULT YOUR DOCTOR

The use of Pramirol SR 2.1 Tablets during pregnancy may pose risks. While human data is scarce, animal research indicates potential harm to the fetus. A physician will assess the potential benefits against possible risks prior to prescribing. Physician consultation is advised.

Breast feedingBreast feedingCONSULT YOUR DOCTOR

Employing Pramirol SR 2.1 Tablet while breastfeeding is likely inadvisable. Available evidence from human studies indicates potential transfer of the medication into breast milk, posing a risk to the infant. This medication's suppression of serum prolactin could negatively impact lactation.

DrivingDrivingUNSAFE

Driving ability may be impaired by Pramirol SR 2.1 Tablet, a medication that can induce hallucinations—perceptual disturbances involving sights, sounds, or sensations not present in reality.

KidneyKidneyCAUTION

Patients with kidney impairment should exercise caution when using Pramirol SR 2.1 Tablets. Dosage modification may be necessary; physician consultation is advised.

LiverLiverSAFE IF PRESCRIBED

Pramirol SR 2.1 Tablets appear to pose minimal risk for individuals with hepatic impairment. Existing evidence indicates dose modification may be unnecessary, however, medical consultation is advised.

What if you forget to take Pramirol SR 2.1 Tablet :

Omit any missed Pramirol SR 2.1 Tablet dose and resume your usual medication regimen. Avoid taking a double dose.

Facts to Know About Pramirol SR 2.1 Tablet

LabelValue
Chemical Category Benzothiazole-based compound
Developing Habits No.
Treatment Category Neuroscience of the Central Nervous System
Active Class Dopamine-stimulating medications

FAQs on Pramirol SR 2.1 Tablet

Pramirol SR 2.1 Tablet may cause weight loss, often related to reduced appetite. Weight gain is a less frequent side effect. Consult your doctor or a nutritionist if you have weight concerns.
Pramirol SR 2.1 Tablets can cause drowsiness, including sudden sleep episodes. Avoid driving or operating heavy machinery if affected, and consult your doctor.
Restless legs syndrome (RLS) involves uncomfortable leg sensations and an overwhelming urge to move them, particularly at night or while resting. Pramirol SR 2.1 Tablet, a dopamine agonist, alleviates RLS symptoms by stimulating brain dopamine receptors crucial for movement control.
Pramirol SR 2.1 Tablets don't relax muscles; instead, they enhance movement and muscle control in Parkinson's disease by acting as a dopamine agonist on dopamine receptors.
Never stop taking Pramirol SR 2.1 Tablets without consulting your doctor. Abruptly stopping this medication can lead to neuroleptic malignant syndrome, characterized by muscle rigidity, reduced movement, fever, unstable blood pressure, rapid heart rate, confusion, and decreased consciousness.
Follow your doctor's instructions for taking Pramirol SR 2.1 Tablets. Your dosage will depend on your condition. Ideally, take it 2-3 hours before sleep. Swallow the tablets whole with water; food may lessen nausea, but isn't required.
Pramirol SR 2.1 Tablet may cause serious side effects including hallucinations, confusion, aggression, agitation, unusual thoughts, vision changes, involuntary movements, and uncontrolled postural changes (like neck bending, forward bending, or tilting). You may also experience dark urine, muscle pain, stiffness, weakness, or tenderness. Seek immediate medical attention if any of these occur.
Pramirol SR 2.1 Tablets may trigger impulse control problems, leading to unusual cravings or urges and potentially harmful behaviors such as compulsive gambling, overeating, or excessive spending. It may also increase libido or cause preoccupation with sexual thoughts and feelings.
Pramirol SR 2.1 Tablet
483
MRP 559
13% off