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Maxolon (Metoclopramide)
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Maxolon

Maxolon is a prescription medicine used to treat nausea, vomiting, indigestion, and heartburn. It prevents the feeling of fullness during or shortly after a meal and help reduce symptoms caused by the flow of the stomach contents back into the food pipe.

Other names for this medication:
Actinorm, Apomatine, Cepar, Cerinorm, Clomet, Donmet, Emenil, Emenorm, Fenomet, Gastonorm, Maxeron, Megatech, Metadrate, Metanorm, Metcon, Metochlopramide, Metocin, Metoclop, Metoclopramide, Metocontin, Metomit, Metopar, Metozolv, Metpar, Migrosh, Molmet, Nausifar, Norvin, Pacimol, Paramet, Paranorm, Perilan, Peripan, Promet, Propamid, Pymet, Rivnorm, Tomid, Vominorm, Vomitrac, Vomitran, Vomonil, Zerinorm

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Hydrea, Tricor, Lioresal, Glyburide, Ditropan, Remeron, Tofranil, Buspar, Rocaltrol, Relasmin, Spasomonyl, Lizocas, Skizoril, Omson, Prograf, Hiikold, Clopicard, Pantabol,

Also known as: Metoclopramide

Description

Maxolon is a muscle relaxant that is prescribed after an injury makes muscles tense or lock up. The generic term for this drug is carisoprodol, and it may come in a pill compounded with aspirin, codeine or caffeine.

Unfortunately, this drug has become a frequently-abused drug. It is a drug that also creates a tolerance in the user, meaning that more and more of the drug must be abused to get the effect the drug user intended. It can also result in addiction. More than two million people in the US have abused Maxolon at some point in their lives.

When abused, Maxolon creates pain relief, sedation, sleepiness and muscle relaxation. In the body, the drug breaks down in part to form meprobamate, itself a drug that is sold to reduce anxiety. The brand names of meprobamate are Miltown and Equanil.

Dosage

This section provides information on the proper use of a number of products that contain lamotrigine. It may not be specific to Maxolon CD. Please read with care.

Take this medicine only as directed by your doctor to help your condition as much as possible and to decrease the chance of unwanted effects. Do not take more of it, do not take it more often, and do not take it for a longer time than your doctor ordered.

This medicine should come with a Medication Guide. Read and follow these instructions carefully. Ask your doctor if you have any questions.

Lamotrigine may be taken with or without food or on a full or empty stomach. However, if your doctor tells you to take the medicine a certain way, take it exactly as directed.

If you are taking the chewable dispersible tablets or tablets for suspension, they may be swallowed whole, chewed, and swallowed, or dispersed in a small amount of liquid and swallowed. If the tablets are chewed, they should be followed with a small amount of water or diluted fruit juice to aid in swallowing. To break up these tablets, add them in enough water or diluted fruit juice to cover the tablets (about a teaspoonful). Wait until the tablets are completely dispersed (about 1 minute), then swirl the solution and swallow it immediately.

If you are taking the disintegrating tablet, make sure your hands are dry before you handle the tablet. Do not open the blister pack that contains the tablet until you are ready to take it. Remove the tablet from the blister pack by peeling back the foil, then taking the tablet out. Do not push the tablet through the foil. Place the tablet into your tongue and move it around in your mouth. It should melt quickly. After the tablet has melted, swallow or take a sip of water.

Swallow the extended-release tablets whole. Do not break, crush, or chew it.

Use only the brand of this medicine that your doctor prescribed. Different brands and dosage forms may not work the same way.

This medicine can be used with other seizure medicines. Keep using all of your seizure medicines unless your doctor tells you to stop.

The dose of this medicine will be different for different patients. Follow your doctor's orders or the directions on the label. The following information includes only the average doses of this medicine. If your dose is different, do not change it unless your doctor tells you to do so.

The amount of medicine that you take depends on the strength of the medicine. Also, the number of doses you take each day, the time allowed between doses, and the length of time you take the medicine depend on the medical problem for which you are using the medicine.

For oral dosage forms (chewable dispersible tablets, disintegrating tablets, tablets for suspension, or tablets): For treatment of bipolar disorder: Adults not taking valproic acid (Depakote®) and not taking carbamazepine (Tegretol®), phenobarbital (Luminal®), phenytoin (Dilantin®), or primidone (Mysoline®)—At first, 25 milligrams (mg) of lamotrigine once a day for 2 weeks, then 50 mg once a day for 2 weeks. After this, your doctor may gradually increase your dose as needed. However, the dose is usually not more than 200 mg a day. Adults taking valproic acid (Depakote®)—At first, 25 mg of lamotrigine once every other day for 2 weeks, then 25 mg once a day for 2 weeks. After this, your doctor may gradually increase your dose as needed. However, the dose is usually not more than 100 mg a day. Adults not taking valproic acid (Depakote®) but taking carbamazepine (Tegretol®), phenobarbital (Luminal®), phenytoin (Dilantin®), or primidone (Mysoline®)—At first, 50 mg of lamotrigine once a day for 2 weeks, then a total of 100 mg divided into 2 smaller doses each day for 2 weeks. After this, your doctor may gradually increase your dose as needed. However, the dose is usually not more than 400 mg a day. Adults who are discontinuing valproic acid (Depakote®) or discontinuing carbamazepine (Tegretol®), phenobarbital (Luminal®), phenytoin (Dilantin®), or primidone (Mysoline®)—Dose will be determined by your doctor. Children—Use and dose must be determined by your doctor. For treatment of epilepsy: Adults not taking valproic acid (Depakote®) but taking carbamazepine (Tegretol®), phenobarbital (Luminal®), phenytoin (Dilantin®), or primidone (Mysoline®)—At first, 50 milligrams (mg) of lamotrigine once a day for 2 weeks, then a total of 100 mg divided into 2 smaller doses each day for 2 weeks. After this, your doctor may gradually increase your dose as needed. However, the dose is usually not more than 500 mg a day. Adults not taking valproic acid (Depakote®), carbamazepine (Tegretol®), phenobarbital (Luminal®), phenytoin (Dilantin®), or primidone (Mysoline®)—At first, 25 mg of lamotrigine once a day for 2 weeks, then 50 mg once a day for 2 weeks. After this, your doctor may gradually increase your dose as needed. However, the dose is usually not more than 375 mg a day. Adults taking valproic acid (Depakote®)—At first, 25 mg of lamotrigine once every other day for 2 weeks, then 25 mg once a day for 2 weeks. After this, your doctor may gradually increase your dose as needed. However, the dose is usually not more than 400 mg a day. Adults who are discontinuing valproic acid (Depakote®) or discontinuing carbamazepine (Tegretol®), phenobarbital (Luminal®), phenytoin (Dilantin®), or primidone (Mysoline®)—Dose will be determined by your doctor. Children 2 to 12 years of age: Children not taking valproic acid (Depakote®) but taking carbamazepine (Tegretol®), phenobarbital (Luminal®), phenytoin (Dilantin®), or primidone (Mysoline®)— At first, 0.6 milligrams per kilogram (mg/kg) of body weight of lamotrigine divided into 2 smaller doses each day for 2 weeks, then 1.2 mg/kg of body weight divided into 2 smaller doses each day for 2 weeks. After this, your doctor may gradually increase your dose as needed. However, the dose is usually not more than 400 mg a day. Children not taking valproic acid (Depakote®), carbamazepine (Tegretol®), phenobarbital (Luminal®), phenytoin (Dilantin®), or primidone (Mysoline®)— At first, 0.3 mg/kg of body weight of lamotrigine given in one dose or two smaller doses each day for 2 weeks, then 0.6 mg/kg of body weight divided into 2 smaller doses each day for 2 weeks. After this, your doctor may gradually increase your dose as needed. However, the dose is usually not more than 300 mg a day. Children taking valproic acid (Depakote®)— At first, 0.15 mg/kg of body weight of lamotrigine given in one dose or two smaller doses each day for 2 weeks, then 0.3 mg/kg of body weight given in one dose or two smaller doses each day for 2 weeks. After this, your doctor may gradually increase your dose as needed. However, the dose is usually not more than 200 mg a day. Children younger than 2 years of age—Use and dose must be determined by your doctor. For oral dosage form (extended-release tablets): For seizures: Adults and children older than 13 years of age not taking valproic acid (Depakote®) but taking carbamazepine (Tegretol®), phenobarbital (Luminal®), phenytoin (Dilantin®), or primidone (Mysoline®)—At first, 50 milligrams (mg) of lamotrigine once a day for 2 weeks, then 100 mg once a day for 2 weeks. After this, your doctor may gradually increase your dose as needed. However, the dose is usually not more than 600 mg a day. Adults and children older than 13 years of age not taking valproic acid (Depakote®), carbamazepine (Tegretol®), phenobarbital (Luminal®), phenytoin (Dilantin®), or primidone (Mysoline®)—At first, 25 mg of lamotrigine once a day for 2 weeks, then 50 mg once a day for 2 weeks. After this, your doctor may gradually increase your dose as needed. However, the dose is usually not more than 400 mg a day. Adults and children older than 13 years of age taking valproic acid (Depakote®)—At first, 25 mg of lamotrigine once every other day for 2 weeks, then 25 mg once a day for 2 weeks. After this, your doctor may gradually increase your dose as needed. However, the dose is usually not more than 250 mg a day. Children younger than 13 years of age—Use and dose must be determined by your doctor.

Overdose

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

An overdose of dexamethasone is not expected to produce life threatening symptoms. Long term use of high doses can lead to thinning skin, easy bruising, changes in body fat (especially in your face, neck, back, and waist), increased acne or facial hair, menstrual problems, impotence, or loss of interest in sex.

Storage

Store at room temperature between 15 and 30 degrees C (59 and 86 degrees F) away from moisture, light and heat. Do not freeze. Throw away any unused medicine after the expiration date. Keep out of the reach of children.

Side effects

The most common side effects associated with Maxolon 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

You should not take Maxolon if you are allergic to capecitabine or fluorouracil, or if you have:

severe kidney disease.

To make sure Maxolon is safe for you, tell your doctor if you have ever had:

a metabolic disorder called DPD (dihydropyrimidine dehydrogenase) deficiency; liver or kidney disease; heart problems; or if you use a blood thinner and you have routine "INR" or prothrombin time tests.

Capecitabine can harm an unborn baby if the mother or the father is using Maxolon .

If you are a woman, you may need a pregnancy test to make sure you are not pregnant. Use birth control while using Maxolon and for at least 6 months after your last dose. If you are a man, use birth control if your sex partner is able to get pregnant. Keep using birth control for at least 3 months after your last dose. Tell your doctor right away if a pregnancy occurs.

Pregnancy may be less likely to occur while the mother or the father is using this medicine. Both men and women should still use birth control to prevent pregnancy because the medicine can harm an unborn baby.

Do not breastfeed while using Maxolon, and for at least 2 weeks after your last dose.

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Neuropsychiatric symptoms and expenditure on complementary and alternative medicine. This has been supported in a number of systematic reviews and meta-analyses. a set of coordinates with associated uncertainties, are recorded and not a continuous intensity distribution. We conducted a clinical trial-based cost-effectiveness analysis comparing UC, PDS and CDS for management of acute bronchitis. Mechanistic studies supported by DFT calculations suggest that the oxygen atom of N2O is transferred to the metal center by insertion into the Rh-H bond of a rhodium amino hydride species, generating a rhodium hydroxy complex as a key intermediate. Cord blood (CB) is a valuable source of hematopoietic stem cells (HSCs). This contributes to the imbalance between structural and neuromotor factors ultimately leading to UA collapse during sleep.

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The purpose of this realist review was to examine PHN interventions and their outcomes during the period preceding the Affordable Care Act (1990-2010), to determine what types of interventions demonstrated effectiveness, and whether these were related to target population or setting. We pooled motrin kids dosage data from sixteen studies from the Breast Cancer Association Consortium (BCAC), and employed two independent studies for replications. This meta-analysis reviewed raw data from prospective studies on 1345 patients with known or suspected non-muscle-invasive bladder cancer (NMIBC). The distribution of this mosquito in Florida and the United States is currently unknown, and recognition of the adult female is likely hampered by morphological similarities to Ae. This study analysed M/F in island populations available from a World Health Organization dataset. On each day the enamel on the mesial sides of the cusps was about twice as thick as on the distal sides. Although the morbidity of SCEC is very low, few studies of patients with SCEC have been conducted in China, there are no sufficient studies of SCEC conducted and reported in the existing published works, and the choices of treatment remain controversial.

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Evidence for neuropeptide Y synthesis in the rat anterior pituitary and the influence of thyroid hormone status: comparison with vasoactive intestinal peptide, substance P, and neurotensin. In preschoolers, children of migrant parents have lower HRQOL than children of non-migrant parents. Recent studies have shown that a widely distributed class of glial cells, termed NG2-glia, engages in rapid signaling with surrounding neurons through direct synaptic contacts in the developing and mature central nervous system (CNS). Face transplantation requires more time and patient numbers and a clearer definition of inclusion and exclusion criteria before standard of care assessment can be made. It has also been documented that the blood pressure decrease persists during 1-year continued administration. Lithotripsy was made in renal failure caused by two-sided block in 6 cases, in acute pyelonephritis in 29 cases in which lithotripsy was performed after preliminary stenting, sanation and elimination of suppuration. Ageing and environmental factors, such as smoking, modulate the individual genetic risk profile. ALS-L1023 reduced mRNA expression of angiogenic factors (VEGF-A and FGF-2) and MMPs (MMP-2 and MMP-9) in differentiated cells. This muscle tone seems to be produced mostly by a vago-vagal reflex loop initiated by the tonic discharge of tracheo-bronchial and/or alveolar receptors connected to thin sensory vagal fibres (non-myelinated or C-fibres).

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The identification of a mutation in this Pelizaeus-Merzbacher family should facilitate the molecular classification and diagnosis of these X chromosome-linked human dysmyelinating disorders. Neonatal and 8-week-old rats were inoculated with Mycoplasma pulmonis. Co-injection of GR231118 and MK-801showed that GR231118 suppressed the antidepressant effect of MK-801. The empirical study is based on Swedish register data, with a focus on 60-year olds in Sweden, linking them to their adult children, siblings and parents as well as in-laws. LVSI, parametrial invasion, and depth of cervical stromal invasion were identified as independent clinicopathological risk factors for pelvic LNM.

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Moreover, the effectiveness of adjuvant chemo- and/or radiotherapy remains controversial. In the present study, we demonstrate the application of this technology for visualization of cardiovascular structures in developing mouse embryos using Lugol solution (aqueous potassium iodide plus iodine). Although studies show that many cell signaling pathways, genes and cell factors are involved in the progression and development of NAFLD related HCC, the exact mechanism underling the pathogenesis of NAFLD-HCC remains poorly understand. After calibration, the model was validated with additional experimental results. Two groups of patients with bucket-handle tears of the meniscus were treated by open operation (27) and by closed operation (29 inderal 10 mg tablet side effects ). It is also common for surgeons to analyze results before and after a change in technique to determine whether the change led to better results.

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This would be a contribution to solve open questions on the clinical relevance of the low-frequency masking phenomenon. We present proton and phosphorus NMR data, which contribute to explain why the 5-methylcytidine (m5C) differently affects the conformational transitions of CGUAm5CG (Bloch et al., FEBS Letters 219, 464 (1987)) and CGm5CGCG (Ceolin et al., J. Composite pre-heating significantly reduces shrinkage force formation of high-viscosity bulk-fill and conventional resin composites, while maintaining or increasing the degree of monomer conversion, dependent upon the specific composite material used. However, the dose and administration route used is associated with cardiovascular side effects such as hypotension and bradycardia in humans and mice, which could preclude its potential use as adjunctive treatment in HCM. Self-assembly of biogenic gold nanoparticles and their use to enhance drug delivery into cells. Organization of a midline proliferative cluster in the embryonic brain of the grasshopper. A number of key effector molecules such as parasite protein ligands for receptor-engagement during invasion as well as proteases and perforin-like proteins that mediate egress have been identified. Tumor-induced pressure in the bone microenvironment causes osteocytes to promote the growth of prostate cancer bone metastases.

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