Neuracalm is an advanced pharmaceutical formulation combining 75mg pregabalin and 500mcg methylcobalamin. Specifically designed to address diabetic peripheral neuropathic pain, this medication offers a sophisticated approach to managing complex neurological symptoms and improving patient quality of life.
Uses
Neuracalm provides targeted therapeutic support for patients experiencing diabetic neuropathy. Under medical supervision, the medication effectively manages chronic nerve pain, helps restore neurological function, improves sleep patterns, and supports cognitive performance compromised by persistent pain conditions.
Benefits
- Dual-action relief targeting neuropathic pain pathways
- Assists in the regeneration of damaged peripheral nerve fibers
- Ameliorates comorbid anxiety and depression associated with chronic pain
- Protects nerve cell membrane integrity to promote healing
- Improves overall quality of life for patients with diabetic neuropathy
How It Works
The medication operates through a sophisticated dual-mechanism approach. Pregabalin modulates calcium channels in the nervous system, reducing neurotransmitter release associated with pain signaling. Methylcobalamin, a specialized vitamin B12 form, simultaneously supports nerve health and regeneration, creating a comprehensive treatment strategy.
Duration of Action
Neuracalm demonstrates a progressive therapeutic response. Initial effects typically emerge within several days, with full clinical benefits potentially manifesting after consistent 4-6 week treatment periods. Individual response may vary based on specific patient characteristics and underlying health conditions.
Dosage
Standard Neuracalm administration involves 1 tablet twice daily, preferably consumed immediately following meals. Strict adherence to physician-prescribed instructions is crucial for optimal therapeutic outcomes. Patients should maintain consistent medication scheduling and promptly communicate any observed side effects.
Side Effects
Potential side effects include dizziness, sleepiness, headache, appetite changes, cognitive disturbances, balance issues, visual complications, gastrointestinal discomfort, muscle challenges, and metabolic variations. Patients experiencing persistent or severe symptoms should immediately consult their healthcare provider.
Warning
Exercise vigilant monitoring during Neuracalm treatment. Immediately report any concerning symptoms such as self-harm ideation, visual disturbances, respiratory changes, or sudden headaches. Discontinuation must always occur under professional medical guidance to prevent potential withdrawal complications.
Pregnancy and Breastfeeding
Current research presents limited conclusive data regarding Neuracalm’s safety during pregnancy and lactation. Women who are pregnant, considering pregnancy, or currently breastfeeding must obtain comprehensive medical consultation before initiating this medication.
Interactions
- Potential interactions with medications causing drowsiness or dizziness
- Possible interactions with angiotensin-converting enzyme (ACE) inhibitors
- Potential impact on blood sugar levels in diabetic patients
- Possible interactions with specific pain medications and antidepressants
- Enhanced sedative effects when combined with alcohol consumption
Important Information
Proper storage is critical: maintain Neuracalm tablets below 25°C, protecting from direct sunlight and moisture. Keep medication securely away from children’s access. The medication may influence cognitive and reactive capabilities, necessitating caution during activities requiring full alertness. Regular medical follow-ups remain essential for monitoring treatment progress and potential medication adjustments.
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Customer questions & answers
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What is the chemical name
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A
Hi Precious,
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Neuracalm tablets contain a combination of Pregabalin and Methylcobalamin.
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