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Generic Neurontin

Gabapentin 300/400mg

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Active ingredient: Gabapentin

Category: Analgesics, Anticonvulsants

Generic Neurontin is used for treating seizures associated with epilepsy. It may also be used for treating nerve pain associated with herpes zoster (shingles) infection (postherpetic neuralgia).

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Product Information

Neurontin

Gabapentin capsule

What is this medicine?

GABAPENTIN is effective in helping to control partial seizures (convulsions) in adults with epilepsy. Gabapentin is also used to help relieve certain types of nerve pain, and may be prescribed for other nervous system disorders.

What should I tell my health care provider before I take this medicine?

They need to know if you have any of these conditions:

  • depression
  • kidney disease
  • suicidal thoughts, plans, or attempt; a previous suicide attempt by you or a family member
  • an unusual or allergic reaction to gabapentin, other medicines, foods, dyes, or preservatives
  • pregnant or trying to get pregnant
  • breast-feeding

How should I take this medicine?

Take gabapentin by mouth. Swallow the capsules with a drink of water. If gabapentin upsets your stomach, take it with food or milk. Take your doses at regular intervals. Do not take your medicine more often than directed.

Contact your pediatrician or health care professional regarding the use of this medicine in children. Special care may be needed.

Overdosage: If you think you have taken too much of this medicine contact a poison control center or emergency room at once.

NOTE: This medicine is only for you. Do not share this medicine with others.

What if I miss a dose?

If you miss a dose, take it as soon as you can. If it is almost time for your next dose, take only that dose. Do not take double or extra doses.

What may interact with this medicine?

  • antacids
  • hydrocodone
  • morphine
  • naproxen
  • sevelamer

Tell your prescriber or health care professional about all other medicines you are taking, including non-prescription medicines, nutritional supplements, or herbal products. Also tell your prescriber or health care professional if you are a frequent user of drinks with caffeine or alcohol, if you smoke, or if you use illegal drugs. These may affect the way your medicine works. Check with your health care professional before stopping or starting any of your medicines.

What should I watch for while taking this medicine?

Visit your prescriber or health care professional for a regular check on your progress. You may want to keep a personal record at home of how you feel your condition is responding to gabapentin treatment. You may want to share this information with your prescriber or health care professional at each visit.

Wear a Medic Alert bracelet or necklace if you are taking gabapentin for seizures. Carry an identification card with information about your condition, medications, and prescriber or health care professional. You should contact your prescriber or health care professional if your seizures get worse or if you have any new types of seizures. Do not stop taking gabapentin or any of your seizure medicines unless instructed by your prescriber or health care professional. Stopping your medicine suddenly can increase your seizures or their severity.

You may get drowsy, dizzy, or have blurred vision. Do not drive, use machinery, or do anything that needs mental alertness until you know how gabapentin affects you. To reduce dizzy or fainting spells, do not sit or stand up quickly, especially if you are an older patient. Alcohol can increase drowsiness and dizziness. Avoid alcoholic drinks.

The use of this medicine may increase the chance of suicidal thoughts or actions. Pay special attention to how you are responding while on this medicine. Any worsening of mood, or thoughts of suicide or dying should be reported to your health care professional right away.

If you are going to have surgery, tell your prescriber or health care professional that you are taking gabapentin.

What side effects may I notice from this medicine?

Side effects that you should report to your prescriber or health care professional as soon as possible:

  • difficulty breathing or tightening of the throat
  • swelling of lips or tongue
  • rash
  • worsening of mood, thoughts or actions of suicide or dying
  • fever
  • hyperactivity
  • hostile or aggressive behavior
  • mood changes or changes in behavior
  • difficulty concentrating

Side effects that usually do not require medical attention (report to your prescriber or health care professional if they continue or are bothersome):

  • constipation
  • difficulty walking or controlling muscle movements
  • dizziness, drowsiness
  • dry mouth
  • back pain, joint aches and pains
  • indigestion, gas or heartburn
  • loss of appetite
  • nausea
  • pain, burning or tingling in the hands or feet
  • restlessness
  • sexual difficulty (impotence)
  • skin itching
  • slurred speech
  • sore gums
  • tremor
  • weight gain

Where can I keep my medicine?

Keep out of reach of children in a container that small children cannot open.

Store at room temperature between 15 and 30 degrees C (59 and 86 degrees F). Throw away any unused medicine after the expiration date.

FAQ about NEURONTIN Medications:

Should I have a prescription to order from you?

Some products available in our pharmacy require a valid perscription. If the law of your country or territory requires you to obtain perscription for any of the products which you plan to purchase you will be asked by our customer support representative to send it after you complete the order.

I can purchase NEURONTIN with no prescription?

Yes, our online drugstore sell pharmacy without prescription, and you can buy online NEURONTIN with no doctor prescriptions.

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Popular painkiller to be withdrawn

Twenty years after doctors were warned that a painkiller taken by 1.7m people a year was linked to suicides and accidental deaths, the government announced yesterday it was to be withdrawn.

Co-proxamol, also known by the trade names Distalgesic, Cosalgesic and Dolgesic, is involved in between 300 and 400 deaths every year. About a fifth of those are accidental, sometimes involving alcohol.

There has been concern about the dangers of the drug in overdose for decades. In 1985, after a review by the government’s Committee on the Safety of Medicines, the warnings to doctors and patients were strengthened.

In 2003, a research paper in the British Medical Journal made it clear that the drug was a problem. “Self poisoning with co-proxamol is particularly dangerous and contributes substantially to drug related suicides. Restricting availability of co-proxamol could have an important role in suicide prevention,” wrote Keith Hawton, a professor of psychiatry at the Centre for Suicide Research of Oxford University, and colleagues. The study found it was implicated in nearly one in five deaths from overdose.

The drugs licensing body, the Medicines and Healthcare Products Regulatory Agency, said yesterday that the 20-year-old warnings to doctors and in the patient leaflets had not had the desired effect. It announced that the painkiller would be phased out over 18 months, to allow time for patients to see their doctors and switch to an alternative.

“Whilst the risks of co-proxamol are well known to health professionals, the latest evidence is that the measures to strengthen the labelling … have been ineffective in reducing the high fatality rate involving both intentional and accidental overdose,” said Alasdair Breckenridge, the MHRA chairman.

The painkiller uses a combination of paracetamol and a minor opioid called dextropropoxyphene, and can only be prescribed by doctors. Patients take it for mild to moderate pain in a number of conditions, including arthritis. Reviews have shown, however, that it is no more effective than paracetamol alone.

The National Institute of Mental Health in England has adopted a suicide-reduction strategy which hopes to cut the number of deaths by overdose. The institute believes that reducing access to the means of suicide is important. In 1998, action was taken over paracetamol. The law was changed to limit pack sizes to 16 tablets in general stores and 32 in pharmacies.

The CSM said there was no need for patients to stop taking co-proxamol immediately. “Co-proxamol will be phased out of the market place gradually to give patients time to discuss their treatment with their doctor and change to a suitable alternative,” said the committee’s chairman, Gordon Duff.

“There is no need for panic or concern, and if patients have been taking co-proxamol continuously for a long time they should not stop without consulting their doctor.”

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