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Pramirol SR 3.15 Tablet

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Prescription Required

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Intas Pharmaceuticals Ltd

Salt Composition

Pramipexole (3.15mg)

Overview Pramirol SR 3.15 Tablet

Pramipexole extended-release 3.15mg tablets manage Parkinson's disease and restless legs syndrome (characterized by an irresistible urge to move legs, often due to unpleasant sensations). This medication reduces tremor by moderating body movements. Administer Pramipexole 3.15mg 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 remembering. Complete the entire course of treatment, even if symptoms improve, and never discontinue use abruptly without consulting your physician. 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 mentally demanding tasks until the effects are known. Report any unusual shifts in mood, hypersexuality, compulsive gambling, or excessive spending to your doctor, as these can be serious.

Primary Ingredients of Pramirol SR 3.15 Tablet

No text was provided to rewrite.

Uses of Pramirol SR 3.15 Tablet

Parkinson's disease and restless legs syndrome

Major Benefits of Pramirol SR 3.15 Tablet:

Follow your doctor's instructions or refer to the product label for usage guidance. Consume Pramirol SR 3.15 Tablet with a meal.

Common Side effects of Pramirol SR 3.15 Tablet:

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

How to use Pramirol SR 3.15 Tablet:

Follow your physician's instructions or consult the product information leaflet for dosage details. Ingestion of Pramirol SR 3.15mg Tablets should coincide with meals.

How Pramirol SR 3.15 Tablet works:

Pramirol SR 3.15mg 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 3.15mg tablets and alcohol may result in increased sleepiness.

PregnancyPregnancyCONSULT YOUR DOCTOR

Extended-release pramipexole (3.15 mg) tablets may pose risks during pregnancy. While human data is scarce, animal research indicates potential harm to a developing fetus. A physician will assess the potential advantages against the risks before prescribing. Seek medical advice.

Breast feedingBreast feedingCONSULT YOUR DOCTOR

The use of Pramirol SR 3.15 Tablet while breastfeeding is likely unsafe. Available human data indicates potential transfer of the drug into breast milk, posing a risk to the infant. This medication's prolactin-suppressing effect may negatively impact lactation.

DrivingDrivingUNSAFE

Driving ability may be impaired by Pramirol SR 3.15 Tablet, a medication that can induce hallucinations—perceptual disturbances involving sights, sounds, or sensations lacking external stimuli.

KidneyKidneyCAUTION

Exercise caution when administering Pramirol SR 3.15 Tablets to individuals with impaired renal function. Dosage modification for Pramirol SR 3.15 Tablets might be necessary. Physician consultation is advised.

LiverLiverSAFE IF PRESCRIBED

The use of Pramirol SR 3.15 Tablet in individuals with hepatic impairment is likely safe. Existing evidence indicates dose modification may be unnecessary; however, physician consultation is recommended.

What if you forget to take Pramirol SR 3.15 Tablet :

Omit any missed Pramirol SR 3.15 Tablet dose and resume your usual dosing regimen. Avoid taking a double dose.

Facts to Know About Pramirol SR 3.15 Tablet

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

FAQs on Pramirol SR 3.15 Tablet

Pramirol SR 3.15 Tablet may cause weight loss, often related to reduced appetite. Weight gain is less common. Consult your doctor or a nutritionist about any weight concerns.
Pramirol SR 3.15 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 leg sensations and an overwhelming urge to move them, particularly at night or while resting. Pramirol SR 3.15 Tablet, a dopamine agonist, alleviates RLS symptoms by stimulating brain dopamine receptors crucial for movement control.
Pramirol SR 3.15 Tablet isn't a muscle relaxant; instead, it improves movement and muscle control in Parkinson's disease by acting as a dopamine agonist on dopamine receptors.
Consult your doctor before stopping Pramirol SR 3.15 Tablet. Abruptly stopping this medication may lead to neuroleptic malignant syndrome, characterized by muscle rigidity, loss of muscle movement, fever, unstable blood pressure, rapid heart rate, confusion, and decreased consciousness.
Follow your doctor's instructions for taking Pramirol SR 3.15 Tablets. Dosage depends on your condition. For best results, take the tablets 2-3 hours before bed, swallowing them whole with water. Food may help prevent nausea, but it's not required.
Pramirol SR 3.15 Tablet may cause serious side effects such as hallucinations (seeing or hearing things that aren't there), confusion, aggression, agitation, unusual thoughts, vision changes, uncontrolled movements, and posture changes (like uncontrollable bending forward or tilting). It can also cause dark urine, muscle pain, stiffness, weakness, or tenderness. Seek immediate medical attention if any of these occur.
Pramirol SR 3.15 Tablets may lead to impulse control problems, such as unusual urges or cravings prompting behaviors you wouldn't normally engage in. This can include difficulty resisting harmful activities like compulsive gambling, overeating, or excessive spending. Increased sex drive or preoccupation with sexual thoughts and feelings may also occur.
Pramirol SR 3.15 Tablet
583
MRP 675
13% off