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Pramirol SR 0.26 Tablet

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Prescription Required

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Intas Pharmaceuticals Ltd

Salt Composition

Pramipexole (0.26mg)

Overview Pramirol SR 0.26 Tablet

Pramipexole extended-release 0.26 mg tablets treat Parkinson's disease and restless legs syndrome, characterized by an irresistible urge to move legs due to unpleasant sensations. This medication reduces excessive tremors by controlling body movements. Ingest Pramipexole SR 0.26 mg tablets with food, consistently at the same time daily for optimal blood levels. Follow your doctor's prescribed dosage and duration; if a dose is missed, take it immediately upon recollection. Complete the full course of treatment, even with symptom improvement; never discontinue abruptly without consulting your physician. Potential side effects include nausea, dry mouth, tiredness, visual or auditory disturbances, constipation, and swelling in the extremities. Dizziness and drowsiness may occur, so avoid activities requiring alertness 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 0.26 Tablet

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Uses of Pramirol SR 0.26 Tablet

Restless legs syndrome and Parkinson's disease

Major Benefits of Pramirol SR 0.26 Tablet:

Follow your physician's instructions or consult the product label for usage guidelines. Ingest the Pramirol SR 0.26 Tablet with a meal.

Common Side effects of Pramirol SR 0.26 Tablet:

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

How to use Pramirol SR 0.26 Tablet:

Follow your physician's instructions or consult the product label for proper administration. Consume Pramirol SR 0.26 Tablet with a meal.

How Pramirol SR 0.26 Tablet works:

Pramirol SR 0.26 mg tablets function by replicating the effects of dopamine, a neurotransmitter crucial for regulating motor control within the brain.

SAFETY ADVICE

AlcoholAlcoholUNSAFE

Combining Pramirol SR 0.26 mg tablets and alcohol can lead to significant sleepiness.

PregnancyPregnancyCONSULT YOUR DOCTOR

Use of Pramirol SR 0.26 Tablet during pregnancy may pose risks. While human data is scarce, animal research indicates potential harm to a developing fetus. A physician will assess the potential advantages against any risks prior to prescribing. Seek medical advice.

Breast feedingBreast feedingCONSULT YOUR DOCTOR

Using Pramirol SR 0.26 Tablet while breastfeeding is likely inadvisable. Studies in humans indicate potential transfer of the medication into breast milk, posing a risk to the infant. This medication's effect of reducing prolactin levels might negatively impact lactation.

DrivingDrivingUNSAFE

Driving ability may be impaired by Pramirol SR 0.26 Tablet side effects, including potential hallucinations (perceptual distortions such as seeing, hearing, or feeling nonexistent things).

KidneyKidneyCAUTION

Patients with kidney impairment should use Pramirol SR 0.26mg tablets cautiously; dosage modification may be necessary. Physician consultation is advised.

LiverLiverSAFE IF PRESCRIBED

Pramirol SR 0.26mg 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 0.26 Tablet :

Omit any missed Pramirol SR 0.26 Tablet dose and resume your usual regimen. Avoid taking a double dose.

Facts to Know About Pramirol SR 0.26 Tablet

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

FAQs on Pramirol SR 0.26 Tablet

Pramirol SR 0.26 Tablets 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 0.26 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 0.26 Tablet, a dopamine agonist, stimulates brain dopamine receptors to regulate movement, thus alleviating RLS symptoms.
Pramirol SR 0.26 Tablet isn't a muscle relaxant; instead, it aids movement and muscle control in Parkinson's disease by acting as a dopamine agonist on dopamine receptors.
Always consult your doctor before stopping Pramirol SR 0.26 Tablet. Abruptly ceasing treatment may lead to neuroleptic malignant syndrome, characterized by muscle rigidity, reduced movement, fever, fluctuating blood pressure, rapid heart rate, confusion, and altered consciousness.
Follow your doctor's instructions when taking Pramirol SR 0.26 Tablets. Dosage depends on your condition. For best results, take the tablets 2-3 hours before sleep, swallowing them whole with water. While you can take them with or without food, eating beforehand may lessen nausea.
Pramirol SR 0.26 Tablet can have serious side effects, including hallucinations, confusion, aggression, agitation, unusual thoughts, vision changes, uncontrolled body movements, and postural instability (e.g., forward head bending, stooping, or sideways tilting). You may also experience dark, red, or cola-colored urine, muscle pain, stiffness, or weakness. Seek immediate medical attention if any of these occur.
Pramirol SR 0.26 Tablets may trigger impulse control disorders, leading to unusual cravings and behaviors you wouldn't normally exhibit. This can manifest as difficulty resisting harmful impulses, such as compulsive gambling, overeating, or excessive spending. Increased libido and preoccupation with sexual thoughts or feelings may also occur.
Pramirol SR 0.26 Tablet
114
MRP 132
13% off