Mirovan is indicated for the treatment of:
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Mirovan contains mirogabalin, a medicine used to relieve pain caused by nerve damage. It is primarily prescribed for different forms of neuropathic pain, including pain associated with diabetes and pain that persists after shingles.
Adult Dose:
The usual starting dose is 5 mg twice daily. Depending on the patient's response and tolerability, the dose may be increased by 5 mg at intervals of at least 1 week, up to a maximum of 15 mg twice daily. Depending on age and symptoms, the appropriate maintenance dose may range between 10 mg and 15 mg twice daily.
Children & Adolescents:
The safety and effectiveness of mirogabalin in children and adolescents have not been established.
Mirogabalin belongs to the gamma-amino acid and related compound class. It selectively binds to the α2δ subunit of voltage-gated calcium channels (VGCCs) in the nervous system.
By reducing calcium entry into nerve cells, mirogabalin decreases the release of certain neurotransmitters from presynaptic nerve endings. This reduces excessive neuronal activity and helps relieve pain associated with nerve damage.
After oral administration, mirogabalin is rapidly absorbed, reaching peak blood concentrations in approximately 0.5–1.5 hours. About 25% is bound to plasma proteins. The medicine is distributed throughout the body and is eliminated predominantly through the kidneys, largely in unchanged form. A smaller proportion undergoes hepatic metabolism. Its reported elimination half-life is approximately 2–4.9 hours.
Other possible reactions include:
Because mirogabalin is primarily eliminated through the kidneys, dose adjustment may be required in patients with reduced renal function.
Dose selection should be individualized according to renal function and medical advice.
Patients with renal or hepatic impairment require appropriate assessment and dose adjustment rather than routine use at standard doses.
A single 15 mg dose has not been associated with significant additional adverse reactions in patients with mild to moderate hepatic impairment. There is limited information regarding its use in patients with severe hepatic impairment, so medical supervision is recommended.
Pregnancy:
Mirovan should be used during pregnancy only when the expected therapeutic benefit is considered to outweigh the potential risk to the fetus. Animal studies have indicated placental transfer.
Breastfeeding:
Animal studies have reported transfer of mirogabalin into milk. A healthcare professional should assess the benefits of treatment against the benefits of breastfeeding before deciding whether to continue or discontinue breastfeeding.
⚠️Disclaimer:
At ePharma, we’re committed to providing accurate and accessible health information. However, all content is intended for informational purposes only and should not replace medical advice from a qualified physician. Please consult your healthcare provider for personalized guidance. We aim to support, not substitute, the doctor-patient relationship.