Pramirol 0.125 Tablet
Marketer
Intas Pharmaceuticals Ltd
Salt Composition
Pramipexole (0.125mg)
Overview Pramirol 0.125 Tablet
Pramipexole 0.125mg 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 Pramipexole 0.125mg with food, consistently at the same time daily for optimal blood levels. Follow your physician's prescribed dosage and regimen; if a dose is missed, take it immediately upon recollection. Complete the entire course of treatment, even with symptom improvement; discontinuation requires prior consultation with your doctor. Potential side effects include nausea, xerostomia, lethargy, visual or auditory disturbances, constipation, and peripheral swelling. Drowsiness and dizziness are also possible; avoid activities demanding 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.
Primary Ingredients of Pramirol 0.125 Tablet
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Uses of Pramirol 0.125 Tablet
Parkinson's disease and restless legs syndrome
Major Benefits of Pramirol 0.125 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. It's recommended to take the Pramirol 0.125mg tablet with a meal.
Common Side effects of Pramirol 0.125 Tablet:
- Dizziness
- Sleepiness
- Nausea
- Dryness in mouth
- Fatigue
- Hallucination
- Constipation
- Peripheral edema
- Muscle spasm
How to use Pramirol 0.125 Tablet:
Consume this medication precisely as prescribed by your physician, adhering to both the dosage and treatment schedule. Ingest the tablet whole; avoid chewing, crushing, or fracturing it. The Pramirol 0.125mg tablet should be administered with a meal.
How Pramirol 0.125 Tablet works:
Pramirol 0.125 mg tablets function by acting as a dopamine agonist, replacing the activity of this crucial neurotransmitter for regulating brain motor functions.
SAFETY ADVICE
AlcoholUNSAFE
Taking Pramirol 0.125 mg tablets with alcohol can lead to significant sleepiness.
PregnancyCONSULT YOUR DOCTOR
The use of Pramirol 0.125mg tablets during pregnancy may pose risks. While human data is scarce, animal research indicates potential harm to a fetus. A physician will assess the advantages against possible risks prior to prescribing this medication. Patient consultation with their doctor is advised.
Breast feedingCONSULT YOUR DOCTOR
The use of Pramirol 0.125 Tablet while breastfeeding is likely unsafe. Available human data indicates potential transfer to breast milk, posing a risk to the infant. Pramirol 0.125 Tablet's prolactin-suppressing action could negatively impact lactation.
DrivingUNSAFE
Taking Pramirol 0.125mg tablets might induce adverse reactions impairing driving ability. These tablets can cause hallucinations – perceiving nonexistent sights, sounds, or sensations – potentially affecting driving safety.
KidneyCAUTION
Patients with impaired kidney function should use Pramirol 0.125mg tablets cautiously; dosage modification may be necessary. Physician consultation is advised.
LiverSAFE IF PRESCRIBED
Pramirol 0.125mg 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 0.125 Tablet :
Omit any missed Pramirol 0.125 Tablet and resume your usual dosing regimen. Avoid taking a double dose.
Facts to Know About Pramirol 0.125 Tablet
| Label | Value |
|---|---|
| Chemical Type | Benzothiazole compound |
| Developing Habits | No. |
| Treatment Category | Neuroscience (CNS) |
| Actions | Dopamine-stimulating medications |
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