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Pramirol SR 1.05 Tablet

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Prescription Required

Marketer

Intas Pharmaceuticals Ltd

Salt Composition

Pramipexole (1.05mg)

Overview Pramirol SR 1.05 Tablet

Pramipexole extended-release 1.05 mg tablets manage Parkinson's disease symptoms and restless legs syndrome, characterized by an irresistible urge to move legs often due to unpleasant sensations. This medication reduces excessive tremor by moderating body movements. Administer Pramipexole ER 1.05 mg with food, consistently at the same time daily for stable blood levels. Follow your physician's prescribed dosage and duration; if a dose is missed, take it immediately upon recall. Complete the full course of treatment, even with symptom improvement; never abruptly discontinue use without consulting your doctor. Potential side effects include nausea, dry mouth, tiredness, visual disturbances, constipation, and swelling in the extremities. Drowsiness and dizziness are possible; avoid driving or tasks requiring alertness until the drug's effects are known. Report any unusual shifts in mood, hypersexuality, compulsive gambling, or excessive spending to your doctor promptly, as these can be serious.

Uses of Pramirol SR 1.05 Tablet

Tremors and involuntary movements | Uncontrollable leg urges

Major Benefits of Pramirol SR 1.05 Tablet:

Follow your physician's instructions or refer to the product label for usage guidance. Administer Pramirol SR 1.05 Tablet with food.

Common Side effects of Pramirol SR 1.05 Tablet:

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

How to use Pramirol SR 1.05 Tablet:

Follow your doctor's instructions or consult the product labeling for guidance prior to administration. Ingest Pramirol SR 1.05 Tablet with a meal.

How Pramirol SR 1.05 Tablet works:

Pramirol SR 1.05 mg 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 1.05 mg tablets and alcohol can lead to increased sleepiness.

PregnancyPregnancyCONSULT YOUR DOCTOR

The use of Pramirol SR 1.05 Tablet during pregnancy may pose risks. While human data is scarce, animal research indicates potential harm to the fetus. A physician will assess the advantages against possible risks prior to prescription. Seek medical advice.

Breast feedingBreast feedingCONSULT YOUR DOCTOR

Using Pramirol SR 1.05 Tablet while breastfeeding is likely inadvisable. Studies in humans indicate potential transfer to breast milk, posing a risk to the infant. This medication's prolactin-suppressing effect could negatively impact lactation.

DrivingDrivingUNSAFE

Driving ability may be impaired by Pramirol SR 1.05 Tablet side effects, including hallucinations – experiencing sensations or perceptions without external stimuli.

KidneyKidneyCAUTION

Patients with kidney impairment should exercise caution when using Pramirol SR 1.05 mg tablets, as dose modification may be necessary. Physician consultation is recommended.

LiverLiverSAFE IF PRESCRIBED

Pramirol SR 1.05 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 1.05 Tablet :

Omit any missed Pramirol SR 1.05 Tablet dose and resume your usual medication regimen. Avoid taking a double dose.

Facts to Know About Pramirol SR 1.05 Tablet

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

FAQs on Pramirol SR 1.05 Tablet

Pramirol SR 1.05 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 1.05 Tablets can cause drowsiness, including sudden sleep episodes. Avoid driving or operating heavy machinery, and report this to your doctor.
Restless legs syndrome (RLS) is characterized by uncomfortable leg sensations and an overwhelming urge to move them, particularly at night or while resting. Pramirol SR 1.05 Tablet, a dopamine agonist, alleviates RLS symptoms by stimulating brain dopamine receptors crucial for movement control.
Pramirol SR 1.05 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.
Always consult your doctor before stopping Pramirol SR 1.05 Tablet. Abruptly ceasing treatment may lead to neuroleptic malignant syndrome, characterized by muscle rigidity, loss of muscle control, fever, fluctuating blood pressure, rapid heart rate, confusion, and reduced consciousness.
Follow your doctor's instructions for taking Pramirol SR 1.05 Tablet. Dosage depends on your condition. Ideally, take it 2-3 hours before sleep. Swallow the tablet whole with water; food may help prevent nausea.
Pramirol SR 1.05 Tablet may cause serious side effects such as hallucinations (seeing or hearing things that aren't there), confusion, aggression, agitation, unusual thoughts, vision changes, involuntary movements, and uncontrollable posture changes (e.g., neck bending, stooping, tilting). Dark, red, or cola-colored urine, muscle pain, stiffness, or weakness are also possible. Contact your doctor immediately if any of these occur.
Pramirol SR 1.05 Tablets may lead to impulse control problems, including unusual urges or cravings you wouldn't normally experience. This can manifest as difficulty resisting harmful behaviors like compulsive gambling, overeating, or excessive spending. Increased sex drive or preoccupation with sexual thoughts and feelings may also occur.
Pramirol SR 1.05 Tablet
312
MRP 362
13% off