Product image of Kartesada (Pregabalin) supplied by GNH India

Kartesada

Active Ingredient:
Pregabalin
Origin:
EU

Kartesada (Pregabalin)

Pregabalin, the active ingredient in Kartesada, is a gabapentinoid presented as an oral tablet for oral use. It is indicated for the management of partial onset seizures, diabetic peripheral neuropathic pain, postherpetic neuralgia, fibromyalgia, and generalized anxiety disorder in adult patients.

GNH India supplies Kartesada as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, with distribution channels across the EU and other regulated markets. Our quality‑assured product meets EU pharmacopeial standards and is manufactured under GMP conditions.

Manufacturer / TM Owner

Neuraxpharm Bohemia S.R.O.

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Indications & Clinical Uses

  • Pregabalin is used to treat several neurological and pain‑related conditions by modulating calcium channel activity.
  • Partial onset seizures: reduces seizure frequency in patients with focal epilepsy.
  • Diabetic peripheral neuropathic pain: alleviates chronic pain associated with diabetic neuropathy.
  • Postherpetic neuralgia: decreases pain intensity following shingles.
  • Fibromyalgia: improves pain and sleep quality in affected individuals.
  • Generalized anxiety disorder: lessens anxiety symptoms in adult patients.

How It Works

  • Pregabalin binds with high affinity 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. The resulting modulation of neuronal excitability underlies its anticonvulsant, analgesic and anxiolytic effects.

Side Effects

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

Common Side Effects

  • Dizziness
  • Somnolence
  • Peripheral edema
  • Weight gain

Serious or Rare Side Effects

  • Angioedema
  • Suicidal thoughts or behaviors

Precautions & Warnings

  • When prescribing Kartesada, clinicians should consider several safety factors.
  • Renal impairment: dose may need adjustment in patients with reduced kidney function.
  • Elderly patients: monitor for increased sedation and falls.
  • History of substance misuse: use with caution due to potential for dependence.
  • Concomitant CNS depressants: may enhance sedation and respiratory depression.
  • Pregnancy and lactation: risk unknown; avoid unless clearly needed.
  • Store at ambient temperature: keep in original container, protect from moisture and light.

Avoid Interactions

Pregabalin can interact with other medicines, requiring attention to avoid adverse outcomes.

Major Interactions (Avoid)

  • Opioids: combined use can cause profound respiratory depression.
  • Alcohol: may increase CNS depression.
  • ACE inhibitors: may increase risk of angioedema.

Moderate Interactions (Monitor Closely)

  • Diuretics: may enhance peripheral edema.
  • Anticholinergics: may worsen dry mouth.
  • Other antiepileptics: may require dose adjustments.

Frequently Asked Questions

Kartesada, containing pregabalin, is prescribed for partial onset seizures, diabetic peripheral neuropathic pain, postherpetic neuralgia, fibromyalgia, and generalized anxiety disorder. These indications reflect its ability to reduce neuronal excitability and modulate pain pathways in adult patients.

Pregabalin binds to the α2‑δ subunit of voltage‑gated calcium channels in the central nervous system. This binding limits calcium entry into presynaptic neurons, decreasing the release of excitatory neurotransmitters such as glutamate, norepinephrine, and substance P, which underlies its anticonvulsant, analgesic, and anxiolytic actions.

The appropriate dose of Kartesada is individualized by the prescribing healthcare professional based on the specific indication, patient age, renal function, and response to therapy. No fixed regimen is provided here; clinicians adjust dosing to achieve optimal therapeutic effect while minimizing adverse reactions.

Safety data for pregabalin in pregnancy and lactation are limited, and the product carries an unknown pregnancy category. It should only be used when the potential benefit justifies the potential risk to the fetus or infant, and the decision must be made by a qualified prescriber.

To request Kartesada, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including any cold‑chain requirements), and necessary import documentation.

Both pregabalin (Kartesada) and gabapentin belong to the gabapentinoid class and share a similar mechanism of binding to the α2‑δ calcium‑channel subunit. Pregabalin generally has higher bioavailability and a more predictable pharmacokinetic profile, allowing for simpler dosing schedules, whereas gabapentin may require more frequent dosing.

Kartesada should be stored at ambient temperature, below 25 °C, in its original packaging to protect it from moisture and light. Keep the container tightly closed and out of reach of children. Do not store in bathrooms or near heat sources.

Kartesada is taken orally, usually with a glass of water. The tablet should be swallowed whole and not chewed or crushed unless specifically instructed by a healthcare professional. Administration can be with or without food, depending on the prescriber’s guidance.

Serious risks include angioedema (swelling of the face, lips, tongue, or throat) and the emergence of suicidal thoughts or behaviors. Patients should be monitored closely for signs of severe allergic reactions or mood changes, and any concerning symptoms should prompt immediate medical evaluation.

Kartesada is contraindicated in patients with known hypersensitivity to pregabalin or any of the tablet’s excipients. Caution is also advised for individuals with severe renal impairment, uncontrolled heart failure, or a history of substance misuse, as these conditions may increase the risk of adverse effects.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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