Pramipexole is a non-ergot dopamine receptor agonist, primarily indicated for the treatment of Parkinson's disease and moderate-to-severe primary restless legs syndrome (RLS). Due to its unique pharmacological effects and strict medication requirements, patients must pay special attention to the legitimacy of purchase channels, identification of genuine vs. counterfeit drugs, and relevant contraindications when purchasing this medication.

How to Purchase Pramipexole

Overseas Purchase

Patients may choose to consult and purchase Pramipexole at hospital pharmacies or authorized pharmacies in countries/regions where the drug has been approved for marketing.

Since drug prices may be affected by factors such as regional differences and exchange rate fluctuations, patients need to make a budget and plan in advance before purchasing.

Purchase via Medical Service Institutions

Patients may consult domestic overseas medical service institutions that cooperate with international pharmacies or pharmaceutical companies.

These institutions usually provide legal import channels and can offer professional consultation and guidance.

Precautions for Purchasing Pramipexole

Strictly Follow Medical Advice

Dose Titration: Pramipexole requires gradual dose titration to reduce side effects.

Patients with Renal Impairment: Dosage adjustment is necessary based on creatinine clearance (e.g., patients with moderate renal impairment need a dose reduction).

Be Alert to Drug Interactions

Dopamine Antagonists (e.g., antipsychotic drugs) may reduce the efficacy of pramipexole.

Cimetidine may increase the plasma concentration of pramipexole, requiring dosage adjustment.

Alcohol or other sedatives may exacerbate the side effect of drowsiness.

Contraindications and High-Risk Populations

Patients with Severe Mental Illness: Pramipexole may worsen hallucinations or psychiatric symptoms.

Patients with Hypotension or Cardiovascular Diseases: Monitoring for orthostatic hypotension is required.

Pregnant and Lactating Women: The safety of pramipexole has not been fully established, so the benefits and risks must be carefully weighed.

How to Identify Genuine vs. Counterfeit Pramipexole

Inspect Details of Outer Packaging

Approval Information: The packaging of genuine pramipexole should clearly indicate "Initial U.S. Approval: 1997" and the latest revision date.

Specification Labeling: Pramipexole tablets are available in multiple strengths ranging from 0.125 mg to 1.5 mg. They appear as white, round or oval tablets, engraved with "BI" and corresponding numbers (e.g., 0.25 mg tablets are engraved with "BI BI" and "84 84").

Verify Drug Characteristics

Tablet Appearance: Genuine tablets should be free of damage, discoloration, or unusual odor. For example, 0.5 mg tablets are white and oval, with engraved markings on both sides.

Completeness of Package Insert: The accompanying prescribing information must include comprehensive content on indications, administration methods, and warnings.