Product image of Misabri Pr (Pregabalin) supplied by GNH India

Misabri Pr

Active Ingredient:
Pregabalin
Origin:
EU

Misabri Pr (Pregabalin)

Pregabalin, the active ingredient in Misabri Pr, is an anticonvulsant presented as an oral tablet for oral use. It treats neuropathic pain, partial onset seizures and generalized anxiety disorder in adult patients.

GNH India supplies Misabri Pr as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Cnx Therapeutics Limited

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Indications & Clinical Uses

Pregabalin is used across several neurological and psychiatric conditions where abnormal neuronal excitability is a key factor.

  • Neuropathic pain: reduces pain intensity in diabetic peripheral neuropathy and post‑herpetic neuralgia.
  • Partial onset seizures: provides adjunctive control of seizures in epilepsy.
  • Generalized anxiety disorder: alleviates anxiety symptoms in adult patients.

How It Works

  • Pregabalin binds selectively to the α2‑δ subunit of voltage‑gated calcium channels in the central nervous system. This binding reduces calcium influx into presynaptic neurons, which in turn decreases the release of excitatory neurotransmitters such as glutamate, norepinephrine, and substance P, dampening neuronal hyper‑excitability associated with pain, seizures, and anxiety.

Side Effects

Pregabalin may cause a range of adverse reactions, from mild to severe.

Common Side Effects

  • Dizziness: sensation of light‑headedness or unsteadiness.
  • Somnolence: increased sleepiness or fatigue.
  • Peripheral edema: swelling of the lower extremities.
  • Weight gain: gradual increase in body weight.
  • Blurred vision: temporary visual disturbances.
  • Dry mouth: reduced salivary flow.

Serious or Rare Side Effects

  • Angioedema: rapid swelling of face, lips, tongue, or throat.
  • Severe hypersensitivity reactions: rash, fever, or organ involvement.
  • Suicidal thoughts or behavior: emergence of depressive symptoms.
  • Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Respiratory depression: especially when combined with other CNS depressants.
  • Blood dyscrasias: rare cases of agranulocytosis or thrombocytopenia.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate several safety considerations.

  • Renal impairment: adjust dose based on creatinine clearance.
  • Elderly patients: start at lower doses due to increased sensitivity.
  • History of substance misuse: monitor for signs of dependence.
  • Suicidal ideation: assess risk regularly during treatment.
  • Pregnancy and lactation: use only if potential benefit justifies potential risk.
  • Store at room temperature: keep in original container, protect from moisture and direct sunlight.

Avoid Interactions

Pregabalin can interact with other medicines, altering its safety or effectiveness.

Major Interactions (Avoid)

  • Opioids: combined use may cause profound sedation or respiratory depression.
  • Benzodiazepines: increased risk of CNS depression and impaired coordination.
  • Alcohol: additive sedative effects leading to excessive drowsiness.
  • ACE inhibitors: may heighten risk of angioedema.
  • Anticholinergic agents: can exacerbate cognitive impairment.

Moderate Interactions (Monitor Closely)

  • Diuretics: may raise pregabalin plasma concentrations.
  • NSAIDs: concurrent use can increase risk of renal dysfunction.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole): may elevate pregabalin levels.
  • CYP3A4 inducers (e.g., carbamazepine): may reduce therapeutic effect.
  • Antihistamines: may enhance dizziness or somnolence.

Frequently Asked Questions

Misabri Pr contains pregabalin, which is prescribed for neuropathic pain such as diabetic peripheral neuropathy, as an adjunctive therapy for partial onset seizures in epilepsy, and for the management of generalized anxiety disorder in adult patients.

Pregabalin binds to the α2‑δ subunit of voltage‑gated calcium channels in the central nervous system, reducing calcium influx and consequently decreasing the release of excitatory neurotransmitters. This action helps to calm neuronal over‑activity that underlies pain, seizures, and anxiety.

The specific dose of Misabri Pr is determined by the prescribing clinician based on the individual’s medical condition, age, renal function, and response to therapy. Dosage adjustments are made according to clinical guidelines and patient needs.

Pregabalin is classified as a pregnancy category where safety data are limited. It should only be used during pregnancy or lactation if the potential benefit to the mother outweighs any possible risk to the fetus or infant. Consultation with a healthcare professional is essential.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details, and any necessary import documentation.

Pregabalin, the active ingredient in Misabri Pr, is a first‑line agent for neuropathic pain and is often compared with gabapentin, duloxetine, or tricyclic antidepressants. It generally offers rapid onset of pain relief and a predictable pharmacokinetic profile, though individual response and tolerability may vary.

Misabri Pr should be stored at room temperature, below 25 °C, in its original packaging to protect it from moisture and light. Keep the product out of reach of children and do not use it after the expiration date.

Misabri Pr is taken orally, usually with or without food, as directed by the prescriber. The tablets should be swallowed whole with a glass of water and not crushed or chewed unless specifically instructed.

Serious risks include the potential for angioedema, severe hypersensitivity reactions, suicidal thoughts or behaviors, respiratory depression when combined with other CNS depressants, and rare blood disorders. Patients should be monitored closely for any of these events.

Misabri Pr is contraindicated in patients with known hypersensitivity to pregabalin or any of the tablet’s excipients. Caution is advised for individuals with severe renal impairment, uncontrolled psychiatric conditions, or a history of substance misuse.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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