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Maxolon (Metoclopramide)
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Maxolon

Maxolon helps you recover more comfortably from cancer treatments such as radiation therapy or chemotherapy. It is also effective at preventing nausea and vomiting after an operation (in adults only). The dose will depend on what you are being treated for but always take Maxolon as it is prescribed.

Other names for this medication:
Actinorm, Apomatine, Cepar, Cerinorm, Clomet, Cosmet, Donmet, Emenil, Fenomet, Gastonorm, Gastrinorm, Maxeron, Maxinorm, Megatech, Metadrate, Metajex, Metanorm, Metcon, Metocin, Metomit, Metoz, Metozolv, Metpar, Migrosh, Molmet, Motil, Naushi, Nausifar, Norvin, Nutec, Perilan, Perinorm, Peronorm, Promet, Pymet, Reglan, Regurg, Rivnorm, Vagonorm, Vominil, Vomitrac, Vomitran

Similar Products:
Imovane, Cycrin, Pamelor, Cytoxan, Feldene, Indocin, Diovan, Pocef, Cetcold, Aplatin, Codistar, Linzomax, Victadol,

Also known as: Metoclopramide

Description

Generic Maxolon is a medication of cephalosporin antibiotic group. Generic Maxolon is used to treat nose, throat, urinary tract, and skin infections that are caused by specific bacteria. Generic Maxolon prevents bacteria to grow in the organism. Brand name of Generic Maxolon is Maxolon. Generic name of Generic Maxolon is Cefadroxil Monohydrate.

Dosage

The dosage schemes below are meant as general recommendations. For optimal therapeutic effect, the dosages are to be adapted to the nature and severity of the disorder. In irregular cycles due to endogenous progesterone deficiency Generic Maxolon 5 to 10 mg is recommended especially in irregular cycles due to shortened luteal phase (ie pre-menopause). Treatment should be repeated for several cycles. In secondary amenorrhoea Administration of Generic Maxolon in combination with an estrogen is usually recommended as in these conditions endogenous progesterone deficiency is nearly always accompanied by estrogen deficiency. 0,05 mg ethinylestradiol is administered each day from the 1st to the 25th day of the cycle, and 5 mg Generic Maxolon is added twice daily from the 11th to the 25th day. Five days after the subsequent withdrawal bleeding, the same is repeated to imitate a natural cycle. In dysfunctional uterine bleeding The symptomatic treatment is aimed at stopping the bleeding and including a subsequent withdrawal bleeding. To stop bleeding: Generic Maxolon 10 mg together with 0,10 mg ethinylestradiol twice daily for 5 to 7 days. To prevent heavy bleedings: Generic Maxolon 5 mg twice daily from day 11 to day 25 of the cycle, if necessary, combined with an estrogen during the first half of the cycle. In post-menopausal complaints If for the symptomatic treatment of post-menopausal complaints estrogens are used (hormone replacement therapy A?A?A? HRT), Generic Maxolon 10 mg is used to counteract the effects of unopposed estrogens on the endometrium. A subsequent withdrawal bleeding is induced. On continuous estrogen therapy: Generic Maxolon 10 mg twice daily during the first 12 to 14 days of each calendar month. On cyclic estrogen therapy: Generic Maxolon 10 mg twice daily during the last 12 to 14 days of the treatment. If you want to achieve most effective results do not stop taking Generic Maxolon suddenly.

Overdose

Seek emergency medical attention or call the Poison Help line at 1-800-222-1222. An overdose of diazepam can be fatal if you take it with alcohol, opioid medicine, or other drugs that cause drowsiness or slow your breathing.

Overdose symptoms may include extreme drowsiness, loss of balance or coordination, limp or weak muscles, slow breathing, or coma.

Storage

Store at room temperature between 20 and 25 degrees C (68 and 77 degrees F) away from moisture and heat. 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

Prescribing Maxolon Tablets in the absence of a proven or strongly suspected bacterial infection or a prophylactic indication is unlikely to provide benefit to the patient and increases the risk of the development of drug-resistant bacteria.

Since Maxolon is principally excreted by the liver, caution should be exercised when Maxolon is administered to patients with impaired hepatic function.

Exacerbation of symptoms of myasthenia gravis and new onset of symptoms of myasthenic syndrome has been reported in patients receiving Maxolon therapy.

There have been reports of infantile hypertrophic pyloric stenosis (IHPS) occurring in infants following Maxolon therapy. In one cohort of 157 newborns who were given Maxolon for pertussis prophylaxis, seven neonates (5%) developed symptoms of non-bilious vomiting or irritability with feeding and were subsequently diagnosed as having IHPS requiring surgical pyloromyotomy. A possible dose-response effect was described with an absolute risk of IHPS of 5.1% for infants who took Maxolon for 8 to 14 days and 10% for infants who took Maxolon for 15 to 21 days.5 Since Maxolon may be used in the treatment of conditions in infants which are associated with significant mortality or morbidity (such as pertussis or neonatal Chlamydia trachomatis infections), the benefit of Maxolon therapy needs to be weighed against the potential risk of developing IHPS. Parents should be informed to contact their physician if vomiting or irritability with feeding occurs.

Prolonged or repeated use of Maxolon may result in an overgrowth of nonsusceptible bacteria or fungi. If superinfection occurs, Maxolon should be discontinued and appropriate therapy instituted.

When indicated, incision and drainage or other surgical procedures should be performed in conjunction with antibiotic therapy.

Observational studies in humans have reported cardiovascular malformations after exposure to drug products containing Maxolon during early pregnancy.

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