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Actinorm (Metoclopramide)

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Actinorm is a prokinetic. It works on the region in the brain that controls vomiting. It also acts on the upper digestive tract to increase the movement of the stomach and intestines, allowing food to move more easily through the stomach.

Other names for this medication:
Acimet, Actinorm, Apomatine, Cepar, Cerinorm, Clomet, Copar, Cosmet, Elinorm, Emenil, Emenorm, Fenomet, Gastonorm, Gastrinorm, Maxeron, Megatech, Metadrate, Metanorm, Metochlopramide, Metoclop, Metomit, Metopar, Metoz, Metvo, Motil, Nausifar, Norvin, Nutec, Pacimol, Paramet, Paranorm, Perilan, Perinorm, Peripan, Peronorm, Promet, Propamid, Pymet, Reglan, Regurg, Rivnorm, Sigmet, Tomid, Vagonorm, Vominil, Vominorm, Vomitex, Vomitrac, Vomitran

Similar Products:
Avelox, Cordarone, Decadron, Avodart, Periactin, Loxitane, Rogaine, Duricef, Lioresal, Arimidex, Nubeta, Cetup, Desogen, Meglipride, Divalrate, Acidosh, Dutoprol, Prelonb, Larotid,

Also known as: Metoclopramide


Actinorm is a prescription medication used to treat bacterial infections of the lungs, urinary tract, ears, throat, and infections that cause gonorrhea. Actinorm belongs to a group of drugs called cephalosporin antibiotics, which work to stop the growth of bacteria in the body.

This medication is available in tablet, chewable tablet, capsule, and oral (by mouth) suspension forms and is taken once or twice daily, with or without food.

Common side effects of Actinorm include rash, diarrhea, nausea, and upset stomach.


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

You will receive your first dose of this medicine in the hospital. Your doctor will watch you closely after you take this medicine to make sure you do not have any serious side effects.

Take this medicine exactly 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. Do not miss any doses. It may also take 1 to 3 weeks before your body responds to this medicine.

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

You may take this medicine with or without food, but take it the same way each time.

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 form (tablets): For ventricular arrhythmias: Adults—At first, 800 to 1600 milligrams (mg) per day taken in divided doses. Your doctor may adjust your dose as needed and tolerated. Children—Use and dose must be determined by your doctor.


If you overdose Actinorm and you don't feel good you should visit your doctor or health care provider immediately. Symptoms of Actinorm overdosage: breathing problems, blue-colored lips or fingernails, weakness, lack of coordination, shaking, convulsions, vision problems, skin redness, watery eyes or mouth.


Store at room temperature below 30 degrees C (86 degrees F) away from moisture and heat. Do not store it in the bathroom or near a sink. Do not leave it in the car or on window sills. Keep out of the reach of children in a container that small children cannot open.

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The most common side effects associated with Actinorm 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.


You should not take Actinorm ER if you are allergic to it, or if you have:

severe asthma or breathing problems; a stomach or bowel obstruction (including paralytic ileus); if you have recently used alcohol, sedatives, tranquilizers, or narcotic medications; or if you have used an MAO inhibitor in the past 14 days (such as isocarboxazid, linezolid, methylene blue injection, phenelzine, or tranylcypromine).

Actinorm ER should not be given to a child younger than 12 years old. Actinorm ER should not be given to anyone younger than 18 years old.

Do not give Actinorm ER to anyone younger than 18 years old who recently had surgery to remove the tonsils or adenoids.

Seizures have occurred in some people taking Actinorm ER. Your seizure risk may be higher if you have ever had:

a head injury, epilepsy or other seizure disorder; drug or alcohol addiction; or a metabolic disorder.

Tell your doctor if you have ever had:

breathing problems, sleep apnea; liver or kidney disease; urination problems; problems with your gallbladder, pancreas, or thyroid; a stomach disorder; or mental illness, or suicide attempt.

If you use Actinorm ER during pregnancy, your baby could be born with life-threatening withdrawal symptoms, and may need medical treatment for several weeks.

Ask a doctor before using Actinorm ER if you are breastfeeding. Tell your doctor if you notice severe drowsiness or slow breathing in the nursing baby.

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In vivo treatment of human leukemia in a scid mouse model with c-myb antisense oligodeoxynucleotides. Histology, however, plays an important role in the differential diagnosis. Modified bone block distraction arthrodesis of the hallux metatarsophalangeal joint. Molecular and antigenic characterisation of ribosomal phosphoprotein P0 from Babesia bovis. Development in molecular genetic manipulation of solventogenic clostridia. These did not colocalize with fluorescent probes for mitochondria, lysosomes or the Golgi apparati. Opinions on optimal therapy vary across disciplines and between countries. The aim of this study was to examine the role of HMGI(Y) proteins in adipocytic cell growth and differentiation.

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Cardiovascular risk profile assessment in glucose-intolerant Asian individuals--an evaluation of the World Health Organization two-step strategy: the DECODA Study (Diabetes Epidemiology: Collaborative Analysis of Diagnostic Criteria in Asia). Magnetopneumography as a tool for the study of dust retention in the lungs. Both supported and unsupported bifurcated endograft limbs develop flow-restricting lesions, including kinks, stenoses, and occlusions, which can be identified during or after surgery. Delayed Awareness of the History of Barium Examination: Perforated Barium Appendicitis. Overall, 603 patients with MB-mural coronary arteries (MB-MCAs) diagnosed by angiography initially were enrolled in this observational study during May 2004 to May 2009. Excision of rhinophyma with a laser scanner handpiece--a modified technique.

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