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Pramirise 0.25mg Tablet

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Arinna Lifescience Pvt Ltd

Salt Composition

Pramipexole (0.25mg)

Overview Pramirise 0.25mg Tablet

Pramiprexole 0.25mg tablets are indicated for Parkinson's disease and restless legs syndrome (characterized by an irresistible urge to move one's legs, often due to unpleasant sensations). This medication mitigates tremors by reducing motor activity. Administer Pramiprexole 0.25mg with food, maintaining a consistent daily intake schedule for optimal therapeutic levels. Follow your physician's prescribed dosage and duration; if a dose is missed, take it immediately upon recollection. Complete the entire course of treatment, even if symptoms improve. Discontinuation should only occur under medical supervision. Potential side effects include nausea, xerostomia, lethargy, visual disturbances, bowel irregularity, and peripheral swelling. Drowsiness and vertigo are also possible; avoid activities requiring alertness until the medication's effects are known. Report any unusual mood shifts, hypersexuality, compulsive gambling, or impulsive spending to your doctor promptly due to their potential severity.

Primary Ingredients of Pramirise 0.25mg Tablet

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Uses of Pramirise 0.25mg Tablet

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

Major Benefits of Pramirise 0.25mg Tablet:

Consume this medication precisely as your physician directs, adhering to both the prescribed dosage and treatment length. Ingest the tablet whole; avoid chewing, crushing, or fracturing it. The Pramirise 0.25mg Tablet should be administered with a meal.

Common Side effects of Pramirise 0.25mg Tablet:

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

How to use Pramirise 0.25mg Tablet:

Consume this medication precisely as directed by your physician, adhering to the prescribed dosage and timeframe. Ingest the tablet whole; avoid chewing, crushing, or fracturing it. The Pramirise 0.25mg Tablet should be administered with a meal.

How Pramirise 0.25mg Tablet works:

Pramipexole 0.25mg tablets function by imitating the effects of dopamine, a neurotransmitter crucial for regulating motor control within the brain.

SAFETY ADVICE

AlcoholAlcoholUNSAFE

Taking Pramirise 0.25mg tablets with alcohol can lead to significant sleepiness.

PregnancyPregnancyCONSULT YOUR DOCTOR

The use of Pramirise 0.25mg tablets 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

Use of the 0.25mg Pramirise tablet while breastfeeding is likely unsafe. Available data from humans indicates potential transfer to breast milk, posing a risk to the infant. This medication reduces prolactin levels, potentially disrupting lactation.

DrivingDrivingUNSAFE

Driving ability may be impaired by side effects of Pramirise 0.25mg Tablet, including hallucinations—the perception of nonexistent sights, sounds, or sensations.

KidneyKidneyCAUTION

Patients with kidney impairment should use Pramirise 0.25mg tablets cautiously; dosage modification may be necessary. Physician consultation is advised.

LiverLiverSAFE IF PRESCRIBED

Pramipexole 0.25mg tablets appear safe for use in individuals with hepatic impairment. Existing evidence indicates dose modification may not be necessary; however, physician consultation is advised.

What if you forget to take Pramirise 0.25mg Tablet :

Omit any missed Pramirise 0.25mg Tablet dose and resume your regular medication regimen. Avoid taking a double dose.

Facts to Know About Pramirise 0.25mg Tablet

LabelValue
Chemical Type Benzothiazole-based compound
Developing Habits No.
Treatment Category Neuroscience, Central Nervous System
Actions Dopamine-stimulating drugs

FAQs on Pramirise 0.25mg Tablet

Pramirise 0.25mg Tablets may cause weight loss, often related to reduced appetite. Weight gain is less common. Consult your doctor or a nutritionist about any weight concerns.
Pramirise 0.25mg 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 irresistible urge to move them, particularly at night or while resting. Pramipexole 0.25mg tablets are dopamine agonists that stimulate brain dopamine receptors, regulating movement and thus alleviating RLS symptoms.
Pramipexole 0.25mg 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.
Do not discontinue Pramirise 0.25mg Tablet without consulting your doctor. Abrupt cessation may 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 Pramirise 0.25mg tablets. Dosage depends on your condition. For best results, take it 2-3 hours before sleep. Swallow the tablets whole with water; while you can take them with or without food, taking them with food may lessen nausea.
Pramirise 0.25mg Tablet may cause serious side effects including hallucinations, confusion, aggression, agitation, unusual thoughts, vision changes, uncontrolled movements, and postural instability (e.g., neck bending, forward bending, or tilting). You may also experience dark or reddish urine, muscle pain, stiffness, or weakness. Seek immediate medical attention if any of these occur.
Pramirise 0.25mg Tablets may lead to impulse control problems, including unusual urges and cravings. This can manifest as difficulty resisting harmful behaviors such as compulsive gambling, overeating, or excessive spending. Increased sex drive and preoccupation with sexual thoughts or feelings may also occur.
Pramirise 0.25mg Tablet
78
MRP 90
13% off