Wholesale Metoclopramide Injection with GMP/BP/USP Supplier, Service

[Drug name]
General name: metoclopramide Injection
Trade name: metoclopramide Injection
English name: Metoclopramide Injection

[Composition and traits]
Main ingredients: The main ingredients of this product are metoclopramide.
Character: This product is a colorless and clear liquid.

[indication]
1. Chemotherapy, radiotherapy, surgery, brain injury, sequelae of brain trauma, sea and air operations, and vomiting caused by drugs.
2. Symptomatic treatment of nausea and vomiting in acute gastroenteritis, biliary tract pancreas, uremia and other diseases.
3. Before diagnostic duodenal intubation is helpful for smooth intubation; gastrointestinal barium X-ray examination can reduce nausea and vomiting and promote the passage of barium.

[Specifications and Packaging]
Single-dose specification: 10MG: 2ML
Packaging specification: 10 pieces

[usage and dosage]
Intramuscular or i. v.
1. Adults, 10-20mg at a time, with a daily dose not exceeding 0.5mg / kg.
2 Children, 0.1mg / kg once under 6 years and 2. 5 – 5mg once aged 6 – 14.
3. In the case of renal insufficiency, the dose is halved.

[untoward effect]
1. The more common adverse reactions are: drowsiness, restlessness, fatigue and weakness.
2. Rare reactions include: breast swelling, nausea, constipation, rash, diarrhea, sleep disturbance, dizziness, severe thirst, headache, and easy excitement.
3. Milk was increased during the medication, due to the stimulation of prolactin.

[taboo]
1. The following conditions are prohibited: allergic to procaine or procainine. The frequency and severity of seizures can be increased by medication. Gastrointestinal bleeding, mechanical intestinal obstruction or perforation, can be used to increase the gastrointestinal power, disease aggravation. Pheochromocytoma can be hypertensive crisis.
2. Use with caution in the following conditions: liver failure, lost the ability to bind the protein. Renal failure, that is, severe chronic renal failure, increases the risk of extrapyramidal reaction, and the dosage should be reduced.

[matters need attention]
1. Invalid for vomiting caused by motion sickness.
2. Aldosterone and serum prolactin concentrations can be increased by the use of metoclopramide.
3. The dose must be reduced at least by 60% in patients with severe renal insufficiency, who are prone to extrapyramidal symptoms.
4. Intravenous injection of metoclopomide should be slow. After 1-2 minutes of injection, rapid administration can cause restless movement and then enter drowsiness.
5. Because this product can reduce the oral bioavailability of cimetidine, if the two drugs must be used together, the interval should be at least 1 hour.
6. This product becomes yellow or yellow brown in light, the toxicity increases.

[condition of storage]
Keep sealed below 25℃.

[term of validity]
36 Months

Product Description

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Frequently Asked Questions
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All products are manufactured in compliance with international standards, including GMP (Good Manufacturing Practice), BP (British Pharmacopoeia), and USP (United States Pharmacopeia) specifications to ensure safety and efficacy.
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Are these products available for international distribution?
Yes, our range of GMP-certified products is designed to meet international regulatory requirements for distribution across various global markets.

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