Nuropentin

Nuropentin Uses, Dosage, Side Effects, Food Interaction and all others data.

Nuropentin is an anti-convulsant. It is a structural analog of gamma-amino-butyric-acid (GABA). All pharmacological actions following administration of Nuropentin are due to the activity of parent compound. Nuropentin binds with the alpha-2-delta subunit of voltage gated L-type Calcium channel, and inhibits branched chain amino acid transferase & probably inhibits neurotransmitter release of excitatory amino acid.

Nuropentin is an anti-convulsant medication that inhibits the release of excitatory neurotransmitters, allowing for its use against pathologic neurotransmission such as that seen in neuropathic pain and seizure disorders. It has a wide therapeutic index, with doses in excess of 8000 mg/kg failing to cause a fatal reaction in rats.

Nuropentin is ineffective in absence seizures and should be used in caution in patients with mixed seizure disorders involving absence seizures. Nuropentin has been associated with drug reaction with eosinophilia and systemic symptoms (DRESS), otherwise known as multi-organ hypersensitivity. This reaction can prove fatal and early symptoms such as fever, lymphadenopathy, and rash should be promptly investigated.

Trade Name Nuropentin
Availability Prescription only
Generic Gabapentin
Gabapentin Other Names Gabapentin, Gabapentina, Gabapentine, Gabapentino, Gabapentinum
Related Drugs clonazepam, lamotrigine, pregabalin, Lyrica, topiramate, levetiracetam, lidocaine topical, Neurontin, Lidoderm, capsaicin topical
Type Capsule
Formula C9H17NO2
Weight Average: 171.2368
Monoisotopic: 171.125928793
Protein binding

Less than 3% of an orally administered dose of gabapentin is bound to plasma proteins.

Groups Approved, Investigational
Therapeutic Class Adjunct anti-epileptic drugs
Manufacturer Zee Laboratories Ltd
Available Country India
Last Updated: September 19, 2023 at 7:00 am
Nuropentin
Nuropentin

Uses

Nuropentin is used for-

  • Epilepsy
  • Neuropathic pain (e.g. postherpetic neuralgia) and other pain conditions
  • Bipolar disorder
  • Headache syndrome
  • Spasticity in multiple sclerosis and spinal cord diseases

Others indication are:

  • Alcohol withdrawal
  • Schizoaffective disorder
  • Post-traumatic stress disorder
  • Agitation and behavioural disturbances
  • associated with dementia
  • Lesch-Nyhan syndrome
  • Essential tremor
  • Restless legs syndrome
  • Brachioradial pruritus
  • Hemichorea/hemiballismus
  • Hot Flashes

Nuropentin is also used to associated treatment for these conditions: Partial-Onset Seizures, Peripheral Neuropathic Pain, Postherpetic Neuralgia

How Nuropentin works

The precise mechanism through which gabapentin exerts its therapeutic effects is unclear. The primary mode of action appears to be at the auxillary α2δ-1 subunit of voltage-gated calcium channels (though a low affinity for the α2δ-2 subunit has also been reported). The major function of these subunits is to facilitate the movement of pore-forming α1 subunits of calcium channels from the endoplasmic reticulum to the cell membrane of pre-synaptic neurons. There is evidence that chronic pain states can cause an increase in the expression of α2δ subunits and that these changes correlate with hyperalgesia. Nuropentin appears to inhibit the action of α2δ-1 subunits, thus decreasing the density of pre-synaptic voltage-gated calcium channels and subsequent release of excitatory neurotransmitters. It is likely that this inhibition is also responsible for the anti-epileptic action of gabapentin.

There is some evidence that gabapentin also acts on adenosine receptors and voltage-gated potassium channels, though the clinical relevance of its action at these sites is unclear.

Dosage

Nuropentin dosage

Neuropathic pain: 300 mg on day-1, then 300 mg twice on day-2, then 300 mg thrice on day-3, then increase the dose according to response in steps of 300 mg daily to maximum 1800 mg daily in three divided doses.

Partial seizure/epilepsy: 300 mg on day-1, then 300 mg twice on day-2, then 300 mg thrice on day-3, then increase the dose according to response in steps of 300 mg daily to maximum 2400 mg daily in three divided doses.

In case of children:

  • For 3-12 years: 10 to 15 mg/kg, Incase of titration 25-35 mg/kg daily in 3 divided doses.
  • Maintenance dose is 900 mg daily (body weight 26-36 Kg) or 1.2 gm daily (body weight 37-50 Kg).

Nuropentin can be taken orally with or without food.

Side Effects

Generally Nuropentin is well tolerated but a few side effects like fatigue, dizziness , ataxia, weight gain, peripheral edema, dry mouth and somnolence, may occur. Rarely it may cause fulminate hepatic failure, or aplasticanemia.

Toxicity

The oral TDLo of gabapentin in humans is 2.86 mg/kg and the LD50 in rats has been found to be >8000 mg/kg. Symptoms of overdose are consistent with the drug's adverse effect profile and involve CNS depression (e.g. dizziness, drowsiness, slurred speech, lethargy, loss of consciousness) and gastrointestinal symptoms such as diarrhea. Management of overdose should involve symptomatic and supportive treatment. Nuropentin can be removed by hemodialysis - this may be of benefit in some patients, such as those with impaired renal function.

Multi-drug overdoses involving gabapentin, particularly in combination with other CNS depressants such as opioids, can result in coma and death - this possibility should be considered when managing overdosage.

Precaution

Patients should be instructed to take Nuropentin only as prescribed. While using Nuropentin patients should be instructed either not to drive a car or to operate other complex machinery until they have gained sufficient experiences about Nuropentin whether or not it affects their mental and/or motor performance adversely.

Interaction

Antacids may reduce the bioavailability of Nuropentin by up to 20%. Cimetidine may alter its reanal excretion. Nuropentin does not interact with other anti-epileptic drug or with oral contraceptive preparations.

Food Interaction

  • Avoid alcohol. Nuropentin possesses CNS depressant activity that may be potentiated by co-administration with alcohol.
  • Take with or without food. Co-administration with food slightly alters pharmacokinetics, but not to a clinically significant extent.

[Moderate] GENERALLY AVOID: Alcohol may potentiate some of the pharmacologic effects of CNS-active agents.

Use in combination may result in additive central nervous system depression and
MANAGEMENT: Patients receiving CNS-active agents should be warned of this interaction and advised to avoid or limit consumption of alcohol.

Ambulatory patients should be counseled to avoid hazardous activities requiring complete mental alertness and motor coordination until they know how these agents affect them, and to notify their physician if they experience excessive or prolonged CNS effects that interfere with their normal activities.

Volume of Distribution

The apparent volume of distribution of gabapentin after IV administration is 58±6 L. The drug is found in the CSF in concentrations approximately 9-20% of the corresponding plasma concentrations and is secreted into breast milk in concentrations similar to that seen in plasma.

Elimination Route

Absorption of gabapentin is thought to occur solely via facilitated transport by the LAT1 transporter within the intestines. As this process is saturable, the oral bioavailability of gabapentin is inversely proportional to the administered dose - the oral bioavailability of a 900mg/day regimen is approximately 60%, whereas a 4800mg/day regimen results in only 27% bioavailability. The Tmax of gabapentin has been estimated to be 2-3 hours. Food has no appreciable effect on gabapentin absorption.

Half Life

The elimination t1/2 of gabapentin in patients with normal renal function is 5-7 hours. In patients with reduced renal function, the elimination t1/2 may be prolonged - in patients with a creatinine clearance of 16,17

Clearance

Both the plasma clearance and renal clearance of gabapentin are directly proportional to the patient's creatinine clearance due to its primarily renal elimination.

Elimination Route

Nuropentin is eliminated solely in the urine as unchanged drug. Cimetidine, an inhibitor of renal tubular secretion, reduces clearance by approximately 12%, suggesting that some degree of tubular secretion is involved in the renal elimination of gabapentin.

Pregnancy & Breastfeeding use

Pregnancy: Nuropentin is a pregnancy category C drug; it should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.

Lactation: Nuropentin may be secreted through the breast milk like many other drugs , so it should be used in women who are nursing, only if the benefits clearly outweigh the risks.

Contraindication

Nuropentin is contraindicated in patients who have known hypersensitivity to the drug.

Special Warning

Use in Children: Safety and effectiveness of Nuropentin in the management of neuropathic pain in pediatric patients have not been established. Safety and effectiveness of Nuropentin in the management of seizures in pediatric patients below the age of 3 years have not been established.

Renal impaired patient: In case of renal impaired patient Nuropentin doses must be reduced :

  • CrCl >60 ml/min: 1200 mg/daily in 3 divided doses
  • CrCl 30-60 ml/min: 600 mg/daily in 2 divided doses
  • CrCl 15-30 ml/min: 300 mg/daily single dose
  • CrCl <15 ml/min: 150 mg/daily single dose or 300 mg/every alternate day
  • Heamodialysis: maximum 300 mg after each dialysis Nuropentin can be taken orally with or without food.

Storage Condition

Tablets should be stored below 25° C and protected from light & moisture

Innovators Monograph

You find simplified version here Nuropentin

FAQ

What is Nuropentin used to treat?

Nuropentin is used to treat epilepsy. It's also taken for nerve pain. Nerve pain can be caused by different illnesses, including diabetes and shingles, or it can happen after an injury.

Is Nuropentin considered a painkiller?

Nuropentin is a prescription painkiller belonging to its own drug class, Gabapentinoids. It is considered an anti-convulsant, and is most commonly used to treat epilepsy, restless leg syndrome, hot flashes, and neuropathic pain.

What is the most common side effect of Nuropentin?

The most common side effects are Drowsiness, dizziness, loss of coordination, tiredness, blurred/double vision, unusual eye movements, or shaking (tremor). 

How does Nuropentin make my feel?

Nuropentin can produce feelings of relaxation, calmness and euphoria. Some users have reported that the high from snorted Nuropentin can be similar to taking a stimulant. It can also enhance the euphoric effects of other drugs, like heroin and other opioids, and is likely to increase the risks when taken in this way.

Why is Nuropentin bad?

Nuropentin may interact with certain types of substances and cause negative side effects. For example, mixing alcohol and gabapentin can cause people to feel dizzy or tired. Despite the risk of bad side effects of using Nuropentin, it can be more dangerous to stop using it. Nuropentin use can cause physical dependence.

Can I drink coffee with Nuropentin?

In addition, Nuropentin can interact with caffeine and diminish its anticonvulsant effects (mice studies).

Does Nuropentin help to sleep?

Nuropentin enhances slow-wave sleep in patients with primary insomnia. It also improves sleep quality by elevating sleep efficiency and decreasing spontaneous arousal. Nuropentin may be beneficial in the treatment of primary insomnia.

Is Nuropentin a muscle relaxer?

Nuropentin is an anticonvulsive medication that originally saw use as a muscle relaxer and anti-spasmodic medication, but later it was discovered it had the potential of the medication as anticonvulsive medication and as an adjunct to more potent anticonvulsants.

How long does Nuropentin take to work?

Peak concentrations of Nuropentin (immediate-release) occur within 2 to 3 hours. Although Nuropentin may improve sleep problems due to nerve pain within a week, it may take up to two weeks for symptom relief from nerve pain to occur.

Who should not take Nuropentin?

The following conditions are contraindicated with this Nuropentin. Check with your physician if you have any of the following Conditions:

  • suicidal thoughts
  • depression
  • myasthenia gravis, a skeletal muscle disorder
  • decreased lung function
  • chronic obstructive pulmonary disease
  • chronic kidney disease
  • kidney disease with likely reduction in kidney function

What vitamins should not be taken with Nuropentin?

Avoid taking aluminum or magnesium containing products (such as antacids) for 2 hours before your Nuropentin. If you notice any signs of seizures, including abnormal auras or motor movements, contact your healthcare professional (e.g. doctor or pharmacist).

Should I eat before taking Nuropentin?

You can take Nuropentin with or without food. But wait at least two hours after taking an antacid that contains magnesium, calcium or aluminum before taking your gabapentin dose.

Is Nuropentin safe for seniors?

Nuropentin is an effective treatment for chronic neuropathic pain but may cause dizziness, drowsiness, and confusion in some older adults.

Does Nuropentin help with anxiety?

Nuropentin is considered an off-Nuropentin drug used to treat anxiety. Nuropentin has shown to help people with sleeping better, as insomnia is a symptom of anxiety.

How safe is Nuropentin?

Nuropentin is a fairly safe medication when people take it according to a doctor's instructions. However, some people may experience side effects. Common side effects that generally do not require medical attention include: blurred vision.

What happens when I stop Nuropentin?

Symptoms of Nuropentin withdrawal may include nausea, dizziness, headaches, insomnia, and anxiety. The safest way to stop using Nuropentin is to taper off the medication under the supervision of a doctor.

Does Nuropentin help with depression?

There is no clear evidence for Nuropentin therapy in depression, PTSD prevention, OCD, or other types of substance abuse.

Does Nuropentin raise my blood pressure?

High blood pressure is not a common side effect from Nuropentin. However, if a patient is abruptly withdrawn from Nuropentin and they are using it to control nerve pain, the pain can abruptly return. Severe pain in and of itself can drive up blood pressure.

What drugs should not be taken with Nuropentin?

Nuropentin can interact with losartan, ethacrynic acid, caffeine, phenytoin, mefloquine, magnesium oxide, cimetidine, naproxen, sevelamer and morphine. Nuropentin use is contraindicated in patients with myasthenia gravis or myoclonus.

How does Nuropentin work?

Nuropentin appears to work by altering electrical activity in the brain and influencing the activity of chemicals called neurotransmitters, which send messages between nerve cells.

How long does it take for Nuropentin to work?

You should notice that your pain starts to improve over one to two weeks after starting Nuropentin, but it may take longer in some people. However, some feel benefit straight away. Your treatment will be reviewed when you next see the doctor or nurse.

How long does Nuropentin last?

The half-life of Nuropentin in most people will range from five to seven hours.

How long does Nuropentin stay in our system?

The detectability of Nuropentin will range from five to seven hours for most blood tests. It is undetectable in saliva swab tests. Hair tests might be able to specifically detect the presence of Nuropentin for up to 90 days; however, it would be highly unusual for a hair test to be used to detect Nuropentin.

What are the risks of taking Nuropentin?

Nuropentin may cause 

  • abnormal eye movements that are continuous, uncontrolled, back-and-forth, or rolling.
  • clumsiness or unsteadiness.
  • constipation.
  • diarrhea.
  • difficulty speaking.
  • drowsiness or tiredness.
  • dry mouth.
  • nausea.

What are the long term effects of taking Nuropentin?

People with preexisting kidney disease may experience potentially fatal toxicity when taking Nuropentin. Nuropentin may cause other long-term effects, including memory loss, weakened muscles, and respiratory failure.

Why is Nuropentin bad?

Nuropentin may interact with certain types of substances and cause negative side effects. For example, mixing alcohol and Nuropentin can cause people to feel dizzy or tired. Despite the risk of bad side effects of using Nuropentin, it can be more dangerous to stop using it. Nuropentin use can cause physical dependence.

How to I stop taking Nuropentin?

The timeline to reduce Nuropentin depends on the individual and the current dose of the medication. Your doctor will develop a plan to slowly take you off the medication. This could be lowering the dose over a week or over several weeks.

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