Dexlansoprazole is classified as a proton pump inhibitor (PPI) and belongs to the group of antiulcer medicines.
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Consuming a large amount of alcohol can increase acidity and cause acid reflux, leading to heartburn. This can decrease the effectiveness of the medication and worsen your underlying condition.
DDR 60mg Capsule is likely safe to use during pregnancy. While animal studies have shown no or low adverse effects on the fetus, there is limited human data. Consulting your doctor is recommended.
There is not enough information from human or animal studies to determine the safety of DDR 60mg Capsules during breastfeeding. It's advisable to consult your doctor if you have concerns.
DDR 60mg Capsule does not interact with your ability to drive, so no dose adjustment is needed.
This medication does not affect kidney function, and no dose adjustment is required for patients with renal impairment.
Patients with mild to moderate liver disease do not require dose adjustment. However, it is not advisable for patients with severe liver disease.
This medication is one of the proton pump inhibitors that work by reducing the level of acid in the stomach. Hence, the medicine is used to treat gastroesophageal reflux disease (GERD) which causes heartburn and heals the damage done to the esophagus by the acid.
Abdominal pain, Diarrhea, Flatulence, Nausea, Vomiting, Upper respiratory tract infection, Headache
DDR 60mg Capsule is a medication that reduces the production of stomach acid. It is prescribed to treat various stomach and intestinal conditions caused by excessive acid production, including heartburn, acid reflux, peptic ulcer disease, and other stomach conditions. It is also used to prevent acidity and stomach ulcers that may result from long-term use of painkillers.
Dexlansoprazole, the active ingredient in DDR 60mg Capsule, belongs to a class of drugs known as proton pump inhibitors (PPIs). It works by specifically blocking (H + / K +) ATPase in gastric parietal cells, which inhibits the secretion of gastric acid. By targeting the proton pump, dexlansoprazole prevents the final step of acid production. It is the enantiomer of lansoprazole, which is a racemic mixture of R and the enantiomer. Dexlansoprazole is available in a dual delayed-release (DDR) formulation in an oral capsule. This capsule contains two types of enteric-coated granules with different pH-dependent dissolution profiles. This results in two different peak plasma concentration-time profiles for dexlansoprazole: the first peak occurs 1 to 2 hours after administration, followed by the second peak within 4 to 5 hours. When taken orally, the Cmax and AUC values of dexlansoprazole increase approximately in proportion to the dose. Dexlansoprazole is metabolized extensively in the liver and is eliminated in the urine.
The dosage recommendations for Dexlansoprazole in adults and children are as follows:
Adult Dose:
Erosive Esophagitis (Healing):
Erosive Esophagitis (Maintenance):
Gastroesophageal Reflux Disease (GERD):
Hepatic Impairment:
Child Dose:
DDR 60mg Capsule can be taken without consideration of diet, and it should be swallowed whole. However, you can also take it one hour before a meal, preferably in the morning. DDR 60mg Capsule is well-tolerated and provides long-term relief. It's important to avoid eating late at night or just before bedtime. If you experience watery diarrhea, a fever, or persistent stomach pain, inform your doctor. Also, let your doctor know if you don't feel better after taking the medication for 14 days, as this may indicate an underlying issue. Long-term use of DDR 60mg may lead to weakened bones and a deficiency of minerals like magnesium. Your doctor may recommend calcium and magnesium supplements to reduce the risk. If you experience decreased urination, swelling, lower back pain, nausea, fatigue, rash, or fever, contact your doctor immediately, as these could be signs of a kidney problem.
Drug-Drug Interactions:
It's important to inform your healthcare provider of all the medications you are taking, including over-the-counter drugs and supplements. This can help prevent potential interactions.
Drug-Food Interactions:
Smoking: Smoking can contribute to the development of stomach ulcers and may reduce the effectiveness of Dexlansoprazole in healing and preventing ulcers. Quitting smoking is often recommended.
Alcohol: Alcohol intake can increase the production of stomach acid, potentially leading to increased acidity and heartburn. It's advisable to avoid alcohol consumption while taking Dexlansoprazole
Drug-Disease Interactions:
Dexlansoprazole an interacts with various medical conditions:
Clostridium difficile-associated diarrhea: There is a potential risk of developing this type of diarrhea while taking Dexlansoprazole.
Bone Fractures: Long-term use of Dexlansoprazole may be associated with an increased risk of bone fractures, particularly in the hip, wrist, or spine. It's important to discuss this risk with your healthcare provider and consider measures to maintain bone health.
Severe Liver Disease: Caution is advised when using Dexlansoprazole, especially in individuals with a history of severe liver disease. Dose adjustments may be necessary.
Low Bone Mineral Density (Osteopenia): People with reduced bone mineral density may be at a higher risk of bone fractures when taking Dexlansoprazole.
Low Levels of Magnesium in the Blood: Dexlansoprazole may lead to hypomagnesemia (low magnesium levels). It's important to be aware of the symptoms of magnesium deficiency, such as muscle spasms, irregular heartbeat, and seizures. Your healthcare provider may recommend magnesium supplements.
Hypersensitivity.
Pregnancy: There have been no specific studies conducted on the use of dexlansoprazole in pregnant women to determine its effects. Dexlansoprazole is the R-enantiomer of lansoprazole, and available observational studies of lansoprazole use during pregnancy have not shown an association with adverse pregnancy-related outcomes. In animal studies, where lansoprazole (the precursor to dexlansoprazole) was given to rats during organogenesis through lactation at a dose equivalent to 1.8 times the maximum recommended human dexlansoprazole dose, it led to reductions in femur weight, femur length, crown-rump length, and growth plate thickness (in males only) on postnatal day 21. These effects were associated with a decrease in body weight gain. Pregnant women should be advised of the potential risk to the fetus.
Lactation: There is no information available regarding the presence of dexlansoprazole in human milk, its effects on breastfed infants, or its impact on milk production. However, it's known that lansoprazole and its metabolites are present in rat milk. When considering the use of dexlansoprazole, it's important to weigh the developmental and health benefits of breastfeeding against the mother's clinical need for therapy and the potential adverse effects on the breastfed child, both from the therapy and the underlying maternal condition. If you are pregnant or breastfeeding and considering the use of dexlansoprazole, it's advisable to consult with your healthcare provider to discuss the potential risks and benefits.
It is also crucial to avoid alcohol consumption while taking DDR 60mg Capsules. Additionally, this medication should be used with caution if you have liver or kidney conditions, and you should contact your doctor if you experience certain side effects like nausea, abdominal pain, flatulence, diarrhea, or vomiting. If you are pregnant or breastfeeding, consult your doctor before taking DDR 60mg Capsule.
It should be stored below 30°C in a dry place, protected from light, and out of reach of children.
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