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Doloneuron (Gabapentin)
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Doloneuron

Doloneuron is a medicine used to relieve the pain caused by nerve damage (neuropathic pain) due to various conditions like diabetes, shingles (herpes zoster infection), spinal cord injury, etc. It is also used to treat certain types of seizures (fits) in combination with other medicines.

Other names for this medication:
Agemax, Cobanerve, Coblamix, Doloneuron, Gabacent, Gabacord, Gabaneuron, Gabanez, Gabatop, Gabina, Gabion, Gabpam, Gabtin, Gabufast, Gabwell, Gapen, Gapin, Gentin, Juvigen, Mecotin, Metgaba, Methylife, Methyneuron, Micknerve, Mycolin, Nervicin, Nervine, Nervoptin, Nerwin, Nerwita, Neuroage, Neurocob, Neuronti, Neuropin, Neurotec, Nulex, Nurokind, Nuromark, Nuropentin, Sologab, Zecoba, Zepentine

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Also known as: Gabapentin

Description

Doloneuron (gabapentin) is an anti-epileptic drug, also called an anticonvulsant. It affects chemicals and nerves in the body that are involved in the cause of seizures and some types of pain.

Doloneuron is used in adults to treat neuropathic pain (nerve pain) caused by herpes virus or shingles (herpes zoster).

Doloneuron is also used to treat seizures in adults and children who are at least 3 years old.

Use only the brand and form of gabapentin your doctor has prescribed. Check your medicine each time you get a refill to make sure you receive the correct form.

Dosage

Generic Doloneuron is available in tablets, liquid form and capsules(300 mg, 400 mg). The dosage of Generic Doloneuron depends on the type of your disease and health state. Take Generic Doloneuron tablets, liquid form and capsules orally at the same time every day with water. Generic Doloneuron can be used together with other seizures medicines. Take Generic Doloneuron 3 times a day with or without food. If you want to achieve most effective results do not stop taking Generic Doloneuron suddenly.

Overdose

Seek emergency medical attention or call the Poison Help line at 1-800-222-1222.

Storage

Store at room temperature between 15 and 30 degrees C (59 and 86 degrees F) away from moisture and heat. Throw away any unused medicine after the expiration date. Keep out of reach of children in a container that small children cannot open.

Side effects

The most common side effects associated with Doloneuron are:

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Side effect occurrence does not only depend on medication you are taking, but also on your overall health and other factors.

Contraindications

Do not take Generic Doloneuron if you are allergic to Generic Doloneuron components. Do not take Generic Doloneuron if you are pregnant, planning to become pregnant. Avoid breast-feeding. Be careful with Generic Doloneuron if you are taking morphine (such as MSIR, Avinza, Kadian), hydrocodone (in Vicodin, in Hydrocet), naproxen (such as Anaprox, Aleve, Naprosyn). Generic Doloneuron can be used together with other seizures medicines. Be very careful with Generic Doloneuron if you suffer from or have a history of heart, kidney or liver disease. Be careful with Generic Doloneuron if you are going to have a surgery. Children should be very careful with Generic Doloneuron because it can cause changes in behavior. If you experience drowsiness and dizziness while taking Generic Doloneuron you should avoid any activities such as driving or operating machinery. Avoid alcohol. It can be dangerous to stop Generic Doloneuron taking suddenly.

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CF cord-blood PLs had patterns similar to those of CF siblings and to normal newborns, but the pattern for CF did not shift toward adult patterns during infancy as did patterns for normal infants. These data suggested that Prog may promote the maturation of SDCs and enhance their ability to interact with T cells so as to change the course of autoimmune diseases. The corticospinal system is the principal motor system for controlling movements that require the greatest skill and flexibility. Changes in fatigue, actual mobility and perceived functioning seem not to be influenced by changes in physical fitness. The effects of intrathecally administered adrenoceptor agonists on the responses to CRD were examined in conscious rats. From day 14 on after the CaWO4 deposition, tungsten-positive lymph node macrophages showed a massive accumulation of ferritin. Comparative attitudes to verbal and written medication information among hospital outpatients.

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The aim of this study is to evaluate the biodistribution pattern and normal variants of 18F-DOPA in a cohort of patients with neuroendocrine tumours using semiquantitative analysis (maximum standardized uptake value). Pretreatment of N87 cells with the anti-MHC class II IgM antibody RFD1 resulted in a reduction in global caspase activation at 24 h of H pylori infection. efbaA and gelE virulence factors have been detected in all strains. We sought to investigate the effect of acutely elevating leptin to concentrations observed in obese individuals on muscle and adipose tissue metabolism and muscle signaling in healthy lean males. Abnormal B-cell function in rats with non-insulin-dependent diabetes induced by neonatal streptozotocin: effect of in vivo insulin, phlorizin, or vanadate treatments. Seven patients with erosive esophagitis and reflux esophagitis were examined. KNL-2 and CENP-A localize to centromeres throughout the cell cycle in an interdependent manner and coordinately direct chromosome condensation, kinetochore assembly, and chromosome segregation. Plasma alkalinization for acute organophosphorus poisoning--is it a reality in the developing world?.

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The toxicity of nanomaterials depends on the basic interaction of the chemistry of the material with the molecular pathways in an organism. To determine whether healthy adult nasal carriers of Staphylococcus aureus can disperse S. OEP was obtained by ethanol extraction and its four fractions by sequential liquid-liquid extraction. We investigated if ethynylestradiol (EE)-induced cholestasis is associated with scratching in rats and if nalfurafine, a kappa opioid receptor agonist with antipruritic effects in human uremic pruritus, would antagonize such scratching. But in the research setting, baseline scanning is useful to make subsequent scanning more valuable, and it reduces false-positive results. Performance of long-stay schizophrenics on matched verbal and visuospatial recall tasks. During March 2006, a series of statewide conferences was held to discuss home care outcomes, with a special emphasis on strategies for retaining home care nurses. Giant stellate cells embedded in crude fibrillar connective tissue matrix were often found there. In conclusion, the results suggest that rats and mice are a more appropriate model for human toluene ototoxicity.

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These combined data support the involvement of miR-185 and its down-stream pathways in schizophrenia. Angiography in 2 patients and pathologic examination of arteries in 1 patient disclosed no occlusion in the vertebrobasilar system. Clinical parameters fail to predict patients with a long-lasting rate-QT mismatch. Case-control study between extrapleural pneumonectomy and radical pleurectomy/decortication for pathological N2 malignant pleural mesothelioma. Surgical correction of upper extremity deformities in arthrogrypotics. An enhancement of prepulse inhibition was observed after stimulation of the ventral tegmental area and co-administration of SCH 23390 into the nucleus accumbens. Emerging drug resistance thwarts progress in chemotherapy, resulting in increased morbidity, mortality and healthcare costs. Subsequent reloading restores reduced bone formation and suppresses increased bone resorption. There are limited data on the incidence of seizures and utility of brain imaging and electroencephalogram (EEG) to predict outcome of children with acute liver failure (ALF).

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The effect of Xylometazoline on the blood flow, the pulse amplitude and the gas exchange in the antral mucosa of the maxillary sinus was studied in five healthy subjects. Optic neuropathy is a serious complication of endocrine ophthalmopathy (EOP). Taken together, these results imply that inbreeding depression is not a necessary consequence of limited dispersal and consanguineous matings in B. The principal outcome was the change in the number of damaged joints between visits, both clinically and radiologically. The mixed lymphocyte response at the 6th week after birth tended to be slightly lower than the control levels, but the cytotoxic T-cell response and the antibody-forming response were the same as the control levels.

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