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Ranee (Ranitidine)
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Ranee

Ranee belongs to a group of drugs called histamine-2 blockers. It works by reducing the amount of acid your stomach produces. Ranee has been used to treat ulcers in the stomach and intestines.

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Also known as: Ranitidine

Description

Ranee (ranitidine) belongs to a group of drugs called histamine-2 blockers. It works by reducing the amount of acid your stomach produces.

Ranee has been used to treat and prevent ulcers in the stomach and intestines. It also was used to treat conditions in which the stomach produces too much acid, such as Zollinger-Ellison syndrome..

Ranee was also used to treat gastroesophageal reflux disease (GERD) and other conditions in which acid backs up from the stomach into the esophagus, causing heartburn.

A cancer-causing impurity found in many ranitidine medications may increase to unacceptable levels over time and when ranitidine is stored at high temperatures. As a result, the FDA has asked all makers of ranitidine to withdraw this medicine from the market in the United States.

Dosage

Generic Ranee is available in tablets (150 mg, 300 mg), capsules, syrup. Before swallowing, fizzy tablets of 25 ml should be dissolved in 1 teaspoon of water. Before drinking Generic Ranee granules should be mixed with 6 to 8 ounces of water. The treatment can take more than 8 weeks. Keep Generic Ranee away from children and do not share it with other people. Take Generic Ranee tablets orally with water. Do not crush or chew it. If you want to achieve most effective results do not stop taking Generic Ranee suddenly.

Overdose

Seek emergency medical attention or call the Poison Help line at 1-800-222-1222.

Overdose symptoms may include lack of coordination, feeling light-headed, or fainting.

Storage

Store at room temperature between 2 and 30 degrees C (36 and 86 degrees F) away from moisture, light and heat. Keep container tightly closed. 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 Ranee 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

If you have been taking prescription-strength Ranee: Before you stop taking the medicine, ask your doctor about safer treatment options.

If you have been taking over-the-counter (OTC) Ranee: Stop taking the medicine, and ask your doctor or pharmacist about other approved OTC stomach acid reducers.

Heartburn can mimic early symptoms of a heart attack. Get emergency medical help if you have chest pain that spreads to your jaw or shoulder and you feel anxious or light-headed.

Before using any OTC medicine to reduce stomach acid, ask a doctor or pharmacist if the medicine is safe for you if you have other medical conditions or allergies.

Ask a doctor before using any OTC stomach acid medicine if you are pregnant or breastfeeding.

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Functional studies in cells and zebrafish embryos and in silico modeling indicate that MIB1 functions as a dimer, which is disrupted by the human mutations. A comparison of lens development in normal mice and in mice with hereditary cataracts. The IL-1beta, IL-2 and TNF-alpha levels of the peripheral blood and cervical mucous of the two groups were measured by the Ria testing before and after the treatment, and the mycoplasma culture (-) of 32 infertile women as set for control. When recombinant adenoviruses are infused directly into the circulation, transgene expression is almost completely restricted to the liver. A novel optical method was used for quantitative characterization and continuous measurement of both the adhesion and spreading of mammalian cells on inorganic surfaces. Based on this assay, a linear range of 0.2-20 U mL(-1) is achieved with high sensitivity and selectivity. The autocorrelation used to compute the discrete FTES formed the basis to define repeating bases in terms of conditional probabilities. Transduction of stimulated primary human peripheral blood cells, which consisted mainly of T cells, was about fivefold more efficient than transduction of B cells. Clinical association was judged possible in 3 patients: one infant girl with no signs of encephalitis developed brain atrophy, one had an Aicardi Type 1 syndrome and one 2 1/2-year-old boy had an acute encephalitis with insufficient serological support for CMV but was 12 months later PCR positive for CMV. The production of cephalosporin C by Acremonium chrysogenum is improved by the intracellular expression of a bacterial hemoglobin.

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