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Pramirol SR 0.52 Tablet

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Prescription Required

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Intas Pharmaceuticals Ltd

Salt Composition

Pramipexole (0.52mg)

Overview Pramirol SR 0.52 Tablet

Pramipexole extended-release 0.52 mg tablets treat Parkinson's disease and restless legs syndrome (characterized by an irresistible urge to move legs, often due to unpleasant sensations). This medication reduces excessive tremors by moderating body movements. Administer Pramipexole with food, consistently at the same time daily to ensure steady blood levels. Follow your doctor's prescribed dosage and duration. If a dose is missed, take it immediately upon recall; never skip doses, and complete the entire course of therapy. Discontinuing this medication abruptly is unsafe; consult your physician before stopping treatment. Potential side effects include nausea, dry mouth, tiredness, visual disturbances, bowel irregularity, and fluid retention in the extremities. Drowsiness and dizziness are also possible; avoid driving or activities requiring concentration until the medication's 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 0.52 Tablet

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Uses of Pramirol SR 0.52 Tablet

Parkinson's disease and restless legs syndrome

Major Benefits of Pramirol SR 0.52 Tablet:

Follow your physician's instructions or consult the product information leaflet for guidance prior to administration. Ingest Pramirol SR 0.52mg tablets with a meal.

Common Side effects of Pramirol SR 0.52 Tablet:

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

How to use Pramirol SR 0.52 Tablet:

Follow your doctor's instructions or the product label for proper administration. Consume Pramirol SR 0.52mg tablets with a meal.

How Pramirol SR 0.52 Tablet works:

Pramirol SR 0.52 mg tablets function by replicating the effects of dopamine, a neurotransmitter crucial for regulating brain motor functions.

SAFETY ADVICE

AlcoholAlcoholUNSAFE

Concomitant use of Pramirol SR 0.52 mg tablets and alcohol may lead to increased sleepiness.

PregnancyPregnancyCONSULT YOUR DOCTOR

Using Pramirol SR 0.52 Tablet during pregnancy may pose risks. While human research is scarce, animal studies indicate potential harm to a fetus. A physician will assess the advantages against possible risks prior to prescribing. Seek medical advice.

Breast feedingBreast feedingCONSULT YOUR DOCTOR

Breastfeeding while taking Pramirol SR 0.52 Tablet is likely inadvisable. Available data suggests potential transfer of the medication into breast milk, posing a risk to the infant. The medication's prolactin-suppressing effect may also negatively impact lactation.

DrivingDrivingUNSAFE

Driving ability may be impaired by Pramirol SR 0.52 Tablet, a medication that can induce hallucinations – perceiving nonexistent sights, sounds, or sensations.

KidneyKidneyCAUTION

Exercise caution when administering Pramirol SR 0.52 Tablets to individuals with impaired renal function. Dosage modification may be necessary. Physician consultation is recommended.

LiverLiverSAFE IF PRESCRIBED

Pramirol SR 0.52 mg tablets appear to pose minimal risk for individuals with hepatic impairment. Existing evidence indicates dose modification may be unnecessary; however, physician consultation is recommended.

What if you forget to take Pramirol SR 0.52 Tablet :

Omit any missed Pramirol SR 0.52 mg tablet and resume your regular dosing regimen. Avoid taking a double dose.

Facts to Know About Pramirol SR 0.52 Tablet

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

FAQs on Pramirol SR 0.52 Tablet

Pramirol SR 0.52 Tablets may cause weight loss, often related to reduced appetite. Weight gain is a less frequent side effect. Consult your doctor or a registered dietitian if you have weight concerns.
Pramirol SR 0.52 mg tablets can cause drowsiness, including sudden sleep episodes. Avoid driving or operating machinery if affected, and consult your doctor.
Restless legs syndrome (RLS) involves uncomfortable legs and an overwhelming urge to move them, particularly at night or while resting. Pramirol SR 0.52 Tablet, a dopamine agonist, stimulates brain dopamine receptors that regulate movement, thus alleviating RLS symptoms.
Pramirol SR 0.52 Tablet doesn't relax muscles; instead, it improves movement and muscle control in Parkinson's disease by acting as a dopamine agonist on dopamine receptors.
Discontinue Pramirol SR 0.52 Tablets only under your doctor's guidance. Abrupt cessation may lead to neuroleptic malignant syndrome, characterized by muscle rigidity, fever, unstable blood pressure, rapid heart rate, altered mental status (confusion, decreased consciousness), and impaired movement.
Follow your doctor's instructions for taking Pramirol SR 0.52 Tablet. Dosage depends on your condition. For best results, take it 2-3 hours before sleep. Swallow the tablet whole with water; food may help prevent nausea.
Pramirol SR 0.52 Tablet may cause serious side effects, including hallucinations, confusion, aggression, agitation, unusual thoughts, vision changes, uncontrolled body movements, and involuntary postural changes (e.g., neck bending, forward bending, tilting). Other potential side effects are dark urine, muscle pain, stiffness, weakness, and tenderness. Seek immediate medical attention if any of these occur.
Pramirol SR 0.52 Tablets may trigger impulse control problems, leading to unusual cravings or urges you wouldn't normally experience. This can manifest as difficulty resisting harmful behaviors such as compulsive gambling, overeating, or excessive spending. Additionally, it may increase sex drive or cause preoccupation with sexual thoughts and feelings.
Pramirol SR 0.52 Tablet
195
MRP 226
13% off