Pharmacor Gabapentin 600 Actions

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Actions of Pharmacor Gabapentin 600 in details

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Pharmacology: Mechanism of Action: Pharmacor Gabapentin 600 has proven affinity for special site in brain tissues eg, neocortex and hippocampus. Though exact mechanism of its central nervous system (CNS) depressant and anticonvulsant activity is not fully understood, it is thought to be activated through peptide binding sites (receptor). It also has analgesic activity.

Pharmacokinetics: Absorption: Pharmacor Gabapentin 600 is absorbed from the gastrointestinal tract (GIT) by means of saturable mechanism. Pharmacor Gabapentin 600 bioavailability is not dose proportional ie, as dose is increased, bioavailability is decreased. Absolute bioavailability of 300-mg oral dose is approximately 60%. At doses of 300 and 400 mg, Pharmacor Gabapentin 600 bioavailability was unchanged following multiple dose administration. Food has no effect on the rate and extent of absorption.

Distribution: Pharmacor Gabapentin 600 circulates largely unbound (<3%) to plasma proteins. It is distributed into breast milk and has a volume of distribution equal to 57.7 L.

Metabolism and Elimination: Pharmacor Gabapentin 600 is not appreciably metabolized and is eliminated from the systemic circulation by renal excretion as unchanged drug. Elimination t½ ranges from 5-7 hrs and is unaltered by dose or following multiple dosing. Pharmacor Gabapentin 600 elimination rate constant, plasma and renal clearance are directly proportional to creatinine clearance (CrCl).

Special Populations: Renal Insufficiency: The mean Pharmacor Gabapentin 600 t½ ranged from about 6.5 hrs (patients with CrCl >60 mL/min) to 52 hrs (CrCl <30 mL/min) and Pharmacor Gabapentin 600 renal clearance ranged from 90 mL/min (CrCl >60 mL/min) to about 10 mL/min (CrCl <30 mL/min). Pharmacor Gabapentin 600 dosage should be adjusted in patients with compromised renal function.

Patients on Hemodialysis: In anuric patients, the elimination t½ of Pharmacor Gabapentin 600 on a nondialysis day was about 132 hrs; during dialysis the apparent t½ was reduced to 3.8 hrs. Thus, hemodialysis has a significant effect on Pharmacor Gabapentin 600 elimination in anuric patients. Pharmacor Gabapentin 600 dosage should be adjusted in patients undergoing hemodialysis.

Elderly: The apparent oral clearance (CL/F) of Pharmacor Gabapentin 600 decreased as age increased, from about 225 mL/min in those <30 years to about 125 mL/min in those >70 years. Reduction of Pharmacor Gabapentin 600 dose may be required in patients who have age-related compromised renal function.

Drug-Drug Interactions: Naproxen: Co-administration of naproxen sodium (250 mg) with Pharmacor Gabapentin 600 (125 mg) appears to increase the amount of Pharmacor Gabapentin 600 absorbed by 12-15%. These doses are lower than the therapeutic doses for both drugs. The magnitude of interaction within the recommended dose is not known.

Hydrocodone: Co-administration of Pharmacor Gabapentin 600 decreases hydrocodone Cmax and area under the curve (AUC) values in a dose-dependent manner relative to administration of hydrocodone alone. Hydrocodone increases Pharmacor Gabapentin 600 AUC values by 14%.

Morphine: When morphine 60 mg is administered 2 hrs prior to Pharmacor Gabapentin 600 600 mg, the mean Pharmacor Gabapentin 600 AUC increased by 44% compared to Pharmacor Gabapentin 600 administered without morphine.

How should I take Pharmacor Gabapentin 600?

Pharmacor Gabapentin 600 administration

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Take exactly as prescribed by your doctor. Do not take in larger or smaller amounts or for longer than recommended. Follow the directions on your prescription label.

The Horizant brand of Pharmacor Gabapentin 600 should not be taken during the day. For best results, take Horizant with food at about 5:00 in the evening.

The Pharmacor Gabapentin 600 brand of Pharmacor Gabapentin 600 can be taken with or without food.

If you break a tablet and take one half of it, take the other half at your next dose. Any tablet that has been broken should be used as soon as possible or within a few days.

Measure liquid medicine with a special dose-measuring spoon or cup, not a regular table spoon. If you do not have a dose-measuring device, ask your pharmacist for one.

Do not stop taking Pharmacor Gabapentin 600 for seizures without first talking to your doctor, even if you feel fine. You may have increased seizures if you stop using Pharmacor Gabapentin 600 suddenly. You may need to use less and less before you stop the medication completely.

Contact your doctor if your seizures get worse or you have them more often while taking Pharmacor Gabapentin 600.

Wear a medical alert tag or carry an ID card stating that you take Pharmacor Gabapentin 600. Any doctor, dentist, or emergency medical care provider who treats you should know that you take seizure medication.

Use Pharmacor Gabapentin 600 regularly to get the most benefit. Get your prescription refilled before you run out of medicine completely.

This medication can cause unusual results with certain medical tests. Tell any doctor who treats you that you are using Pharmacor Gabapentin 600.

Store Pharmacor Gabapentin 600 tablets and capsules at room temperature away from light and moisture.

Store the liquid medicine in the refrigerator. Do not freeze.

Pharmacor Gabapentin 600 pharmacology

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Mechanism Of Action

The mechanism of action by which Pharmacor Gabapentin 600 exerts its analgesic action is unknown but in animal models of analgesia, Pharmacor Gabapentin 600 prevents allodynia (pain-related behavior in response to a normally innocuous stimulus) and hyperalgesia (exaggerated response to painful stimuli). Pharmacor Gabapentin 600 prevents pain-related responses in several models of neuropathic pain in rats and mice (e.g., spinal nerve ligation models, spinal cord injury model, acute herpes zoster infection model). Pharmacor Gabapentin 600 also decreases pain-related responses after peripheral inflammation (carrageenan footpad test, late phase of formulin test), but does not alter immediate pain-related behaviors (rat tail flick test, formalin footpad acute phase). The relevance of these models to human pain is not known.

Pharmacor Gabapentin 600 is structurally related to the neurotransmitter GABA (gamma-aminobutyric acid), but it does not modify GABAA or GABAB radioligand binding, it is not converted metabolically into GABA or a GABA agonist, and it is not an inhibitor of GABA uptake or degradation. In radioligand binding assays at concentrations up to 100 μM, Pharmacor Gabapentin 600 did not exhibit affinity for a number of other receptor sites, including benzodiazepine, glutamate, N-methyl-D-aspartate (NMDA), quisqualate, kainate, strychnine-insensitive or strychnine-sensitive glycine; alpha 1, alpha 2, or beta adrenergic; adenosine A1 or A2; cholinergic, muscarinic, or nicotinic; dopamine D1 or D2; histamine H1; serotonin S1 or S2; opiate mu, delta, or kappa; cannabinoid 1; voltage-sensitive calcium channel sites labeled with nitrendipine or diltiazem; or at voltage-sensitive sodium channel sites labeled with batrachotoxinin A20-alpha-benzoate. Pharmacor Gabapentin 600 did not alter the cellular uptake of dopamine, noradrenaline, or serotonin.

In vitro studies with radiolabeled Pharmacor Gabapentin 600 have revealed a Pharmacor Gabapentin 600 binding site in areas of rat brain including neocortex and hippocampus. A high-affinity binding protein in animal brain tissue has been identified as an auxiliary subunit of voltage-activated calcium channels. However, functional correlates of Pharmacor Gabapentin 600 binding, if any, remain to be elucidated. It is hypothesized that Pharmacor Gabapentin 600 antagonizes thrombospondin binding to α2δ-1 as a receptor involved in excitatory synapse formation and suggested that Pharmacor Gabapentin 600 may function therapeutically by blocking new synapse formation.

Pharmacodynamics

No pharmacodynamic studies have been conducted with Pharmacor Gabapentin 600.

Pharmacokinetics

Absorption And Bioavailability

Pharmacor Gabapentin 600 is absorbed from the proximal small bowel by a saturable L-amino transport system. Pharmacor Gabapentin 600 bioavailability is not dose proportional; as the dose is increased, bioavailability decreases.

When Pharmacor Gabapentin 600 (1800 mg once daily) and Pharmacor Gabapentin 600 immediate release (600 mg three times a day) were administered with high fat meals (50% of calories from fat), Pharmacor Gabapentin 600 has a higher Cmax and lower AUC at steady state compared to Pharmacor Gabapentin 600 immediate release (Table 5). Time to reach maximum plasma concentration (Tmax) for Pharmacor Gabapentin 600 is 8 hours, which is about 4-6 hours longer compared to Pharmacor Gabapentin 600 immediate release.

Table 5: Mean (SD) Steady-State Pharmacokinetics for Pharmacor Gabapentin 600 and Pharmacor Gabapentin 600 Immediate Release in Plasma of Healthy Subjects (Day 5, n = 21)



References

  1. DailyMed. "GABAPENTIN: DailyMed provides trustworthy information about marketed drugs in the United States. DailyMed is the official provider of FDA label information (package inserts).". https://dailymed.nlm.nih.gov/dailyme... (accessed September 17, 2018).
  2. NCIt. "Gabapentin: NCI Thesaurus (NCIt) provides reference terminology for many systems. It covers vocabulary for clinical care, translational and basic research, and public information and administrative activities.". https://ncit.nci.nih.gov/ncitbrowser... (accessed September 17, 2018).
  3. EPA DSStox. "Gabapentin: DSSTox provides a high quality public chemistry resource for supporting improved predictive toxicology.". https://comptox.epa.gov/dashboard/ds... (accessed September 17, 2018).

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Information checked by Dr. Sachin Kumar, MD Pharmacology

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