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Constipation, diarrhea, stomach pain, upset stomach, or throwing up. Irritation where ranitidine injection is given. These are not all of the side effects that may occur. If you have questions about side effects, call your doctor. Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-332-1088.
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Ranitidine comes as a tablet, an effervescent tablet, effervescent granules, and a syrup to take by mouth. It is usually taken once a day at bedtime or two to four times a day. Over-the-counter ranitidine comes as a tablet to take by mouth. It is usually taken once or twice a day. To prevent symptoms, it is taken 30 to 60 minutes before eating.
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Side Effects. Headache, constipation, or diarrhea may occur. Pain, redness, burning, or stinging may occur at the injection site. If any of these effects last or get worse, tell your doctor or.
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easy bruising or bleeding; or. problems with your skin or hair. Common ranitidine side effects may include: nausea, vomiting, stomach pain; or. diarrhea, constipation. This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
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Ranitidine is clearly comparable or superior to most other antiulcer agents in the treatment and prevention of a variety of gastrointestinal disorders associated with gastric acid secretion. With its favourable efficacy and tolerability profiles, ranitidine must be considered a first-line agent when suppression of gastric acid secretion is.
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Ranitidine injection comes as a solution (liquid) to be mixed with another fluid and injected intravenously (into a vein) over 5 to 20 minutes. Ranitidine may also be injected into a muscle. It is usually given every 6 to 8 hours, but may also be given as a constant infusion over 24 hours.
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The molecular formula is C 13 H 22 N 4 O 3 SโขHCl, representing a molecular weight of 350.87. Ranitidine hydrochloride, USP is a white to pale yellow, granular substance that is soluble in water. Ranitidine injection, USP is a clear, colorless to yellow, nonpyrogenic liquid. The yellow color of the liquid tends to intensify without adversely.
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Dosis rumatan adalah 2-4 mg/kg per oral sekali sehari, tidak boleh melebihi 150 mg/hari. Jika digunakan secara injeksi, dosis yang disarankan adalah 2-4 mg/kg/hari intravena, dibagi dalam 3-4 dosis. Dosis maksimal adalah 50 mg/dosis atau 200 mg/hari. [3] Esofagitis Erosif.
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Usual dose: 2 to 4 mg/kg IV, divided and given every 6 to 8 hours OR as a continuous infusion. Maximum dose: 50 mg/dose. 16 years and older: ORAL: Treatment dose: 150 mg orally 2 times a day OR 300 mg orally once a day after the evening meal or at bedtime. Maintenance dose: 150 mg orally once a day at bedtime.
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Introduction. Ranitidine is a histamine H2-receptor antagonist that acts by antagonizing histamine at gastric H2-receptor sites. Ranitidine inhibits both basal gastric secretion and gastric acid secretion induced by histamine, pentagastrin, and other secretagogues. 1,2 Ranitidine is used for many different indications including gastroesophageal reflux disease and the prophylaxis of stress.
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Generic Name Ranitidine DrugBank Accession Number DB00863 Background. Ranitidine is a commonly used drug, classified as a histamine H2-receptor antagonist, and belongs to the same drug class as cimetidine and famotidine.This drug helps to prevent and treat gastric-acid associated conditions, including ulcers, because of its ability to decrease gastric acid secretion. 2,11 Ranitidine is often.
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Tablet, injeksi, sirup. Ranitidine untuk ibu hamil dan menyusui. Kategori B: Penelitian pada reproduksi hewan tidak memperlihatkan adanya risiko terhadap janin. Akan tetapi, tidak ada penelitian pada wanita hamil sehingga belum diketahui pasti keamanannya bagi ibu hamil.
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Injeksi: 50mg/2mL. Melansir dari MIMS, berikut ini pembagian dosis ranitidine sesuai kondisi yang ditangani. 1. Ulkus duodenal dan lambung ringan. Dewasa. Oral: 150 mg dua kali sehari, atau 300 mg sekali sebelum tidur selama 4 minggu. Parenteral: 50 mg, injeksi intravena (IV) atau intramuskular (IM), selama 2 menit.
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Ranitidine hydrochloride USP is a white to pale yellow, crystalline powder that is very soluble in water. Ranitidine injection USP is a clear, colorless to yellow, nonpyrogenic liquid. The yellow color of the liquid tends to intensify without adversely affecting potency. The pH of the injection solution is 6.7 to 7.3.
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Penggunaan ranitidine bisa dilakukan melalui beberapa cara seperti oral, injeksi ke otot atau vena. Obat yang termasuk dalam antagonis reseptor histamin H2 ini bekerja dengan memblokir histamin yaitu suatu komponen nitrogen organik yang mengatur fungsi fisiologi dalam usus dan bertindak sebagai neurotransmiter untuk otak, sumsum tulang belakang.
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