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Gabagamma (Gabapentin)
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Gabapentin

Gabagamma comes as a capsule, a tablet, an extended-release (long-acting) tablet, and an oral solution (liquid) to take by mouth. Gabagamma capsules, tablets, and oral solution are usually taken with a full glass of water (8 ounces [240 milliliters]), with or without food, three times a day.

These medications should be taken at evenly spaced times throughout the day and night; no more than 12 hours should pass between doses. The extended-release tablet (Horizant) is taken with food once daily at about 5 PM. Follow the directions on your prescription label carefully, and ask your doctor or pharmacist to explain any part you do not understand. Take Gabagamma exactly as directed. Do not take more or less of it or take it more often than prescribed by your doctor.

Gabagamma extended-release tablets cannot be substituted for another type of Gabagamma product. Be sure that you receive only the type of Gabagamma that was prescribed by your doctor. Ask your pharmacist if you have any questions about the type of Gabagamma you were given.

Swallow the extended-release tablets whole; do not cut, chew, or crush them.

If your doctor tells you to take one-half of a regular tablet as part of your dose, carefully split the tablet along the score mark. Use the other half-tablet as part of your next dose. Properly dispose of any half-tablets that you have not used within several days of breaking them.

If you are taking Gabagamma to control seizures or PHN, your doctor will probably start you on a low dose of Gabagamma and gradually increase your dose as needed to treat your condition. If you are taking Gabagamma to treat PHN, tell your doctor if your symptoms do not improve during your treatment.

Gabagamma may help to control your condition but will not cure it. Continue to take Gabagamma even if you feel well. Do not stop taking Gabagamma without talking to your doctor, even if you experience side effects such as unusual changes in behavior or mood. If you suddenly stop taking Gabagamma tablets, capsules, or oral solution, you may experience withdrawal symptoms such as anxiety, difficulty falling asleep or staying asleep, nausea, pain, and sweating. If you are taking Gabagamma to treat seizures and you suddenly stop taking the medication, you may experience seizures more often. Your doctor may decrease your dose gradually over at least a week.

Your doctor or pharmacist will give you the manufacturer's patient information sheet (Medication Guide) when you begin treatment with Gabagamma and each time you refill your prescription. Read the information carefully and ask your doctor or pharmacist if you have any questions. You can also visit the Food and Drug Administration (FDA) website (http://www.fda.gov/Drugs) or the manufacturer's website to obtain the Medication Guide.

Other names for this medication:
Gabapentin, Neurontin, Algia, Alpentin, Bapex, Blugat, Dineurin, Edion, Epleptin, Gabagamma, Gabalept, Gabanet, Gabaneural, Gabantin, Gabapen, Gabapentina, Gabapentine, Gabapin, Gabaran, Gabatal, Gabateva, Gabatin, Gabatine, Gabator, Gabax, Gabex, Gabexal, Gabictal, Gabiton, Gaboton, Gabrion, Gabtin, Galepsi, Ganin, Gantin, Gapridol, Gatilox, Gordius, Kaptin, Neurexal, Neuril, Neuropen, Neuros, Neurotin, Nupentin, Pendine, Progresse, Ritmenal, Tebantin,

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The goal of this article is to review the importance of considering malaria in the differential diagnosis of the febrile returned traveler and to discuss the role of exchange transfusion in the management of severe Plasmodium falciparum malaria. Although hypercalcemia was controlled, both patients died shortly thereafter. All but three fractures healed (pathologic fracture with multiple myeloma in one case, impaired bone healing in two cases).

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Volatile composition of six horsetails: prospects and perspectives. Guinea pigs immunized with HCV-1 genotype 1a E1E2p7, E1E2 or E2 generated high titer anti-glycoprotein antibody responses that neutralized the infectivity of HCVpp and HCVcc expressing gps of the same genotype as the immunizing antigen.

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In leukocytes of healthy persons the rate of ornithine decarboxylase activity depended on belonging of the cells to myeloid or lymphoid forms: the enzyme activity was higher in lymphocytes as compared with granulocytes. One hundred consecutive patients with LUTS attending the prostate assessment clinic anonymously completed a locally developed, qualitatively validated questionnaire and sexual health inventory for men. A number of electrophysiologically active chemicals were identified from headspace extracts of M. Comparative development and evaluation of topical gel and cream formulations of psoralen. The objective was to determine whether the side of deafness affected lateralization and magnitude of evoked blood oxygen level-dependent responses across different auditory cortical fields (ACFs).

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T-cell therapy using a bank of EBV-specific cytotoxic T cells: lessons from a phase I/II feasibility and safety study. Special tips like the examination of the stomach filled with liquid are required particularly in targeted questions. The amyloidogenic potential and behavioral correlates of stress.

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Ang-2 could potentially identify a patient population that might have a better PFS when under anti-angiogenic treatment, like the tyrosine kinase inhibitor sunitinib. We found a dramatic elevation in Beclin 1 levels in the penumbra of rats challenged by cerebral ischemia. Early and mid-term outcomes of trans-sternal and video-assisted thoracoscopic surgery for thymoma.

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Clinical features and prognostic factors for liver cancer from a referral center in northern Thailand. Organ transplant recipients were included, as they are prone to severe gout that is difficult to manage, and because treatment to prevent graft rejection might influence the immune response to pegloticase. cDNA microarray technology was utilized to examine gene expression in normal buspirone mb3 555 prescription human KC (NHKC) following 20 mJcm(-2) UVB irradiation. Participants completed self-report measures of alcohol-related problems and intrapersonal, interpersonal, and familial predictors of drinking.

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