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Apomatine (Metoclopramide)

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Apomatine injection is used to treat severe diabetic gastroparesis. The injection is also used to prevent nausea and vomiting caused by chemotherapy or surgery, or to aid in certain medical procedures involving the stomach or intestines.

Other names for this medication:
Acimet, Actinorm, Cepar, Copar, Cosmet, Elinorm, Emenorm, Gastrinorm, Maxeron, Metanorm, Metcon, Metochlopramide, Metoclop, Metoclopramide, Metopar, Metoz, Metozolv, Molmet, Nausifar, Norvin, Nutec, Perilan, Peronorm, Propamid, Pymet, Regurg, Sigmet, Tomid, Vagonorm, Vominorm, Vomitrac, Vomitran, Vomonil

Similar Products:
Lasix, Mircette, Aricept, Colospa, Avelox, Addyi, Cycrin

Also known as: Metoclopramide


{name} (amlodipine) is a calcium channel blocker that dilates (widens) blood vessels and improves blood flow.

{name} is used to treat chest pain (angina) and other conditions caused by coronary artery disease.

{name} is also used to treat high blood pressure (hypertension). Lowering blood pressure may lower your risk of a stroke or heart attack.

Amlodipine is for use in adults and children who are at least 6 years old.


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

Take this medicine only as directed by your doctor. 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. Your dose may need to be changed several times in order to find out what works best for you.

In addition to the use of this medicine, treatment for your high blood pressure may include weight control and changes in the types of food you eat, especially foods high in sodium (salt). Your doctor will tell you which of these are most important for you. You should first check with your doctor before changing your diet.

Many patients who have high blood pressure will not notice any signs of the problem. In fact, many patients feel normal. It is very important that you take your medicine exactly as directed and that you keep your appointments with your doctor even if you feel well.

Remember that this medicine will not cure your high blood pressure, but it does help control it. You must continue to take it as directed if you expect to lower your blood pressure and keep it down. You may have to take high blood pressure medicine for the rest of your life. If high blood pressure is not treated, it can cause serious problems such as heart failure, blood vessel disease, strokes, or kidney disease.

Swallow the extended-release capsule and tablet whole. Do not crush, break, or chew them.

If you cannot swallow the extended-release capsule:

You may open it and sprinkle the contents over a small amount (teaspoonful) of soft food (including applesauce, pudding, or yogurt). Swallow the mixture within 60 minutes. Do not store for later use. You may also use a nasogastric tube to give the medicine. Mix the contents of the opened capsule with water into a syringe. Gently shake the mixture for about 10 seconds, then flush it through the tube. Rinse the tube with water until all of the medicine is washed out.

Take the tablet or extended-release tablet with a meal or just after you eat. You may break the extended-release tablet into two pieces, but swallow the two pieces whole and do not crush or chew them.

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 acute heart attack or heart failure: For oral dosage form (extended-release capsules): Adults—At first, 25 milligrams (mg) once a day for 2 weeks. Your doctor may adjust your dose as needed. However, the dose is usually not more than 200 mg per day. Children—Use and dose must be determined by your doctor. For oral dosage form (extended-release tablets): Adults—At first, 25 milligrams (mg) once a day for 2 weeks. In patients with severe heart failure, the starting dose is 12.5 mg once a day. Your doctor may adjust your dose as needed. Children—Use and dose must be determined by your doctor. For oral dosage form (tablets): Adults—At first, 50 milligrams (mg) every 6 hours for 2 days. Then, 100 mg 2 times a day. The medicine will be started in the hospital. Children—Use and dose must be determined by your doctor. For chest pain: For oral dosage form (extended-release capsules): Adults—At first, 100 milligrams (mg) once a day. Your doctor may adjust your dose as needed. However, the dose is usually not more than 400 mg per day. Children—Use and dose must be determined by your doctor. For oral dosage form (extended-release tablets): Adults—At first, 100 milligrams (mg) once a day. Your doctor may adjust your dose as needed. However, the dose is usually not more than 400 mg per day. Children—Use and dose must be determined by your doctor. For oral dosage form (tablets): Adults—At first, 100 milligrams (mg) per day, given in two divided doses. Your doctor may adjust your dose as needed. However, the dose is usually not more than 400 mg per day. Children—Use and dose must be determined by your doctor. For high blood pressure: For oral dosage form (extended-release capsules): Adults—At first, 25 to 100 milligrams (mg) once a day. Your doctor may adjust your dose as needed. However, the dose is usually not more than 400 mg per day. Children 6 years of age and older—Dose is based on body weight and must be determined by your doctor. The dose is usually 1 milligram (mg) per kilogram (kg) of body weight once a day. The first dose should not be more than 50 mg once a day. Your doctor may adjust your dose as needed. Children younger than 6 years of age—Use and dose must be determined by your doctor. For oral dosage form (extended-release tablets): Adults—At first, 25 to 100 milligrams (mg) once a day. Your doctor may adjust your dose as needed. However, the dose is usually not more than 400 mg per day. Children 6 years of age and older—Dose is based on body weight and must be determined by your doctor. The dose is usually 1 milligram (mg) per kilogram (kg) of body weight per day, given as a single dose. The first dose should not be more than 50 mg per day. Children younger than 6 years of age—Use and dose must be determined by your doctor. For oral dosage form (tablets): Adults—At first, 100 milligrams (mg) per day, given as a single dose or in divided doses. Your doctor may adjust your dose as needed. However, the dose is usually not more than 450 mg per day. Children—Use and dose must be determined by your doctor. .


If you overdose Generic Apomatine and you don't feel good you should visit your doctor or health care provider immediately.


Keep out of the reach of children.

Do not keep outdated medicine or medicine no longer needed.

Ask your healthcare professional how you should dispose of any medicine you do not use.

Store the medicine in a closed container at room temperature, away from heat, moisture, and direct light. Keep from freezing.

Do not store the oral liquid in the refrigerator or freezer. Throw away any unused liquid after 3 months of first opening the bottle.

Detailed Apomatine dosage information

Side effects

The most common side effects associated with Apomatine 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.


Do not take Apomatine if you are allergic to Apomatine components or to aspirin. Do not take Apomatine if you are pregnant, planning to become pregnant, or are breast-feeding. Apomatine can't be given to patients who experience bypass surgery. Apomatine can't be given to children under 2 years. Do not use Apomatine in case of suffering from peptic ulcer or bleeding from the gut, inflammatory bowel disease or peripheral arterial disease. Try to be careful with Apomatine in case of using such medication as lithium (Eskalith, Lithobid); ACE inhibitor (quinapril (Accupril), captopril (Capoten), enalapril (Vasotec), fosinopril (Monopril), moexipril (Univasc), perindopril (Aceon), benazepril (Lotensin), trandolapril (Mavik), naproxen (Naprosyn, Aleve), ibuprofen (Motrin, Advil); lisinopril (such as Zestril, Prinivil), ramipril (Altace); aspirin or other NSAIDs (ketoprofen (Orudis), indomethacin (Indocin), diclofenac (Voltaren), etodolac (Lodine); steroids (prednisone); cyclosporine (Sandimmune, Gengraf, Neoral); blood thinner (warfarin (Coumadin)); glyburide (DiaBeta, Micronase); methotrexate (such as Trexall, Rheumatrex), diuretics (such as furosemide (Lasix). Try to be careful with Apomatine in case of having heart, liver or kidney disease; stomach disorders; nose polyps; high blood pressure; asthma; diverticulosis; congestive heart failure; bowel problems; bleeding; blood clot; stroke. Apomatine can be dangerous for elderly people. Use Apomatine with great care in case you want to undergo an operation (dental or any other). Avoid machine driving. Avoid drinking alcohol and smoking. It can be dangerous to stop Apomatine taking suddenly.

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Unlike BMP2, NELL1 protein does not activate the Smad signaling cascade. Could higher NPP offset anticipated C losses resulting from increased disturbances?. Minor gender differences were not considered clinically relevant. A fourth type of material, not seen in conventionally prepared human basophils, was also often observed in the granules. In view of these results, it is concluded that the TRH-test provides reliable information after iodine exposure. Multiple cyclic nucleotide phosphodiesterases (PDEs) degrade cAMP in cardiomyocytes but the role of PDEs in controlling cAMP signaling during pathological cardiac hypertrophy is poorly defined. The interaction of either membrane-bound or soluble forms of IL-1RAcP and IL-33Ralpha-chain depends on the presence of IL-33, as demonstrated by coimmunoprecipitation assays. Children with impaired glucose tolerance seem to be at increased risk for later cardiovascular diseases. Two problems encountered at VAT-LA are accessing the pleural space and fibrinous intrapleural septa. This work should facilitate the studies on population genetic diversity, and molecular evolution in Gobioidei fishes.

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Prostaglandin F2 alpha induces unsynchronized intracellular calcium oscillations in monolayers of gap junctionally coupled NRK fibroblasts. To aid the design of targeted adherence interventions, we investigated the factors associated with noncompletion of isoniazid (INH) therapy for LTBI. It may be important for individuals to receive medical attention if their identical twin presents with vasospastic angina. Functional analysis methodology focuses on the identification of variables that influence the occurrence of problem behavior and has become a hallmark of contemporary approaches to behavioral assessment. Our results revealed an important role of Foxo3A in the differentiation process of MSC toward chondrogenic fate, both in early and late stages. The Akaike Information Criterion was also considered to ascertain the best-fit equation. Radiologically there were pronounced reticular changes in both lungs affecting mostly the middle and lower zones. Interaction of diet and drugs in the regulation of brain 5-hydroxyindoles and the response to painful electric shock. Comparison of individual responses to slow ramps with predictions based on linear theory indicated the presence of abrupt departures from linearity for both primary and secondary endings.

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Neither format nor age had a significant effect on brain oxygenation. Our review of the literature indicated that there is currently no standardized approach to measuring the symptom status of persons living with RA. Bone marrow stromal cell lines having high potential for osteoclast-supporting activity express PPARgamma1 and show high potential for differentiation into adipocytes. A rate-limiting delay of 2-5 min occurred between BMP activation and Smad1 activity. However, higher throughput methods are needed to identify targets of AGL15. The piezoelectric material is polarized in z-axis direction and the material properties change gradually with the thickness of the layer.

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Here we report a comparison of the general morphology of the mandibular, propharyngeal and postpharyngeal glands between the three castes of the black ant Lasius niger. Comparison of the effects of human chorionic gonadotropin and luteininzing hormone on phosphofructokinase activity in isolated rat ovaries. Patient demographic information, length of stay, cost of treatments, interventions and diagnostic testing, and types of cancer were analyzed. The docking and per residue interaction studies were carried out to elucidate the interaction energies of amino acid residues with pyruvate. Patient characteristics and dose rate were obtained to test the model structure. We consider a two-competitor/one-prey model in which both competitors exhibit a general functional response and one of the competitors exhibits a density-dependent mortality rate. Determination of phloroglucinol in human plasma by high-performance liquid chromatography-mass spectrometry. One of the three cases of exposure involved infected and prominent hardware with purulence. One hundred and fifty-six couples undergoing an IVF/ICSI procedure.

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The bleaching agent increased microleakage of composite restorations in non-vital bleaching, whereas microleakage was not found to be increased by calcium hydroxide. In particolar, speech sounds presented in noisy background evoke bioelectric responses in neural populations located in the right cerebral hemisphere, that otherwise would not be activated. For the world does not yet censure those who tread the paths of dreams. To account for a possible effect of heterozygous mutations, assessing imprinting of all candidate genes by studying the expression pattern of heterozygous SNPs in testis biopsies of five unrelated men. Immuno-electron microscopy showed that two-thirds of the promastigote MSP is distributed along the cell surface. Compared with controls, women with aPL had greater functional and structural arterial abnormalities, which were associated with lower activity of paraoxonase. Variants of one of these hybridomas, DO-11.10, were isolated that had lost the ability to respond to antigen plus MHC.

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