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HomeHEALTH Monas 10 Tablet, 1 Strip [Montelukast 10 mg]
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Monocast 5 Tablet, 1 Strip [Montelukast 5 mg] ৳ 80

Monas 10 Tablet, 1 Strip [Montelukast 10 mg]

৳ 240

Product details of Monas 10 Tablet, 1 Strip [Montelukast 10 mg]
  • Quantity number indicates 15 tablets in one strip.
  • 1pcs tablets/strip
  • Indicated for: Prophylaxis and chronic treatment of Asthma & for the symptomatic relief of Allergic Rhinitis
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Categories: HEALTH, HEALTHCARE, MEDICINES, PRESCRIPTION Tags: Monas, Monas 10 Tablet, Table Monas 10
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Description

Indications

Montelukast is a leukotriene receptor antagonist indicated for:

  • Prophylaxis and chronic treatment of asthma in patients 12 months of age and older.
  • Acute prevention of Exercise-Induced Bronchoconstriction (EIB) in patients 6 years of age and older.
  • Relief of symptoms of Allergic Rhinitis (AR): Seasonal Allergic Rhinitis (SAR) in patients 2 years of age and older, and perennial allergic rhinitis (PAR) in patients 6 months of age and older.
Therapeutic Class
Leukotriene receptor antagonists

Pharmacology

The cysteinyl leukotrienes (LTC4, LTD4, LTE4) are products of arachidonic acid metabolism and are released from various cells, including mast cells and eosinophils. These eicosanoids bind to cysteinyl leukotriene receptors (CysLT) found in the human airway. Montelukast is an orally active compound that binds with high affinity and selectivity to the CysLT1 receptor. Montelukast inhibits physiologic actions of LTD4 at the CysLT1 receptor without any agonist activity.

Dosage & Administration

By indications-

  • Asthma: Once daily in the evening for patients 12 months and older.
  • Acute prevention of exercise-induced bronchoconstriction: One tablet at least 2 hours before exercise for patients 6 years of age and older.
  • Seasonal allergic rhinitis: Once daily for patients 2 years and older.
  • Perennial allergic rhinitis: Once daily for patients 6 months and older.

By age-

  • 15 years and older: One 10-mg tablet.
  • 6 to 14 years: One 5-mg tablet.
  • 2 to 5 years: One 4-mg.

Interaction

Montelukast may be administered with other therapies routinely used in the prophylaxis and chronic treatment of asthma. In drug-interactions studies, the recommended clinical dose of montelukast did not have clinically important effects on the following medicinal products: theophylline, prednisone, prednisolone, oral contraceptives, terfenadine, digoxin and warfarin. Caution should be exercised, particularly in children, when montelukast is co-administered with phenytoin, phenobarbital and rifampicin.

Contraindications

Hypersensitivity to any component of this product.

Side Effects

Montelukast appears to be well tolerated. In clinical trials, the most common adverse effect reported was headache, occurring in approximately 18% of patients. Rash, dyspepsia, dizziness, and abdominal pain were all reported in less than 2% of patients. Elevated liver transaminases have been reported with montelukast use, but not at a greater incidence than with placebo. A small percentage of pediatric patients have experienced diarrhea, sinusitis and otitis media during montelukast clinical trials.

Pregnancy & Lactation

Montelukast is classified as pregnancy category B. The drug has been shown to cross the placenta of pregnant rats and rabbits, but there have been no reports of its use in pregnant women. Montelukast is also known to be excreted into breast-milk, but only limited information is available on the significance of this finding. Caution should be used prior to initiating montelukast therapy in nursing mothers.

Precautions & Warnings

Montelukast is not indicated for use in the reversal of bronchospasm in acute asthma attacks, including status asthmaticus. Patients should be advised to have appropriate rescue medication available.

Storage Conditions

Store below 25° C at a cool and dry place, away from light and moisture. Keep out of reach of children.
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Shipping & Delivery

Delivery System

Product Delivery & Replace Conditions:

  • Please check your products in front of riders or courier service agents.
  • Product will be replaced if it has any defect by its manufacturer.
  • If product quality or quantity problem found then customer can return/cancel their order on delivery time with presence of delivery person.
  • Products must be with the tags intact and in their original packaging, in an unwashed and undamaged condition.
  • Replacement for products is subject to inspection and checking by sevenone QC Team.
  • Replacement cannot be possible if the product is burnt, damaged by short circuit, damaged due to neglect, improper usage, or broken by customer.
  • Innerwear and product of clearance sale cannot be replaced.

Delivery Time:

If your delivery address is within Dhaka city, products will be delivered by within 2-5 business days. If it is outside Dhaka, it will take 5-7 business days.

Note: Product delivery duration may vary due to product availability in stock.

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Finix 20 Tablet, 1 Strip [Rabeprazole Sodium 20mg]

৳ 140

Rabeprazole Sodium is an antiulcerant drug in the class of Proton Pump Inhibitors. Rabeprazole Sodium is a substituted benzimidazole which suppresses gastric acid secretion by inhibiting the gastric H+/K+-ATPase enzyme at the secretory surface of the gastric parietal cell. It is an enteric coated tablet, because of its coated formulation it is highly stable in stomach and because of higher pKa value of Rabeprazole Sodium it provides faster onset of action. It blocks the final step of gastric acid secretion. After oral administration of 20 mg, Rabeprazole is absorbed and can be detected in plasma by 1 hour. The effects of food on the absorption of Rabeprazole have not been evaluated. Rabeprazole is 96.3% bound to human plasma proteins. Rabeprazole is primarily metabolized in the liver by Cytochrome P-450 3A (Sulphone metabolite) and 2C19 (Desmethyl Rabeprazole). Following a single 20 mg oral dose of Rabeprazole, approximately 90% of the drug is eliminated in the urine.The remainder of the dose is excreted in the feaces.

Dosage & Administration Healing of Erosive or Ulcerative Gastroesophageal Reflux Disease (GERD): 20 mg to be taken once daily for 4 to 8 weeks. For those patients who have not healed after 8 weeks of treatment, an additional 8 week course may be considered. Maintenance of Healing of Erosive or Ulcerative Gastroesophageal Reflux Disease (GERD Maintenance): The recommended adult oral dose is 20 mg once daily. Treatment of Symptomatic Gastroesophageal Reflux Disease (GERD):The recommended adult oral dose is 20 mg once daily for 4 weeks. If symptoms do not resolve completely after 4 weeks, an additional course of treatment may be considered. Healing of Duodenal Ulcers:The recommended adult oral dose is 20 mg once daily after the morning meal for a period up to four weeks. Most patients with duodenal ulcer heal within four weeks. A few patients may require additional therapy to achieve healing. Helicobacter pylori Eradication: To Reduce the Risk of Duodenal Ulcer Recurrence- Rabeprazole Sodium 20 mg Twice Daily for 7 Days Amoxicillin 1000 mg Twice Daily for 7 Days Clarithromycin 500 mg Twice Daily for 7 Days All three medications should be taken twice daily with the morning and evening meals. It is important that patients comply with the full 7-day regimen. Treatment of Pathological Hypersecretory Conditions Including Zollinger-Ellison Syndrome: The dosage of Rabeprazole Sodium in patients with pathologic hypersecretory conditions varies with the individual patient. The recommended adult oral starting dose is 60 mg once a day. Doses should be adjusted to individual patient needs and should continue for as long as clinically indicated. Some patients may require divided doses. Doses up to 100 mg QD and 60 mg BID have been administered. Some patients with Zollinger-Ellision syndrome have been treated continuously with Rabeprazole Sodium for up to one year. Interaction Rabeprazole is metabolized by the Cytochrome P-450 (CYP-450) drug metabolizing enzyme system. Rabeprazole does not have clinically significant interactions with other drugs metabolized by the CYP-450 system,such as Warfarin and Theophylline given as single oral dose, Diazepam as a single intravenous dose, and Phenytoin given as a single intravenous dose. In normal subjects, co-administration of Rabeprazole 20 mg QD resulted in an approximately 30% decrease in the bioavailability of Ketoconazole and increase in the AUC and Cmax for digoxin of 90% and 29% respectively. Contraindications Rabeprazole Sodium is contraindicated in patient with known hypersensitivity to Rabeprazole or to any component in the product. Side Effects Rabeprazole Sodium may sometimes cause headache, diarrhoea, abdominal pain, vomiting, constipation, dry mouth, increased or decreased appetite, muscle pain, drowsiness and dizziness. Pregnancy & Lactation Rabeprazole is FDA Pregnancy Category B. No data is available on administration of Rabeprazole to pregnant women. However this drug should be used during pregnancy, only if clearly needed. There are no data on the excretion of Rabeprazole into the breast milk. A decision should be made whether to discontinue nursing or to discontinue the drug, taking into account the benefit of the drug to the mother. Precautions Administration of Rabeprazole Sodium to patients with mild to moderate liver impairment resulted in increased exposure and decreased elimination. Caution should be exercised in patients with severe hepatic impairment. Overdose Effects There has been no experience with large overdoses with Rabeprazole. No specific antidote for Rabeprazole is known. Rabeprazole is extensively protein bound and is not readily dialyzable. In the event of overdosage, treatment should be symptomatic and supportive. Use in Special Population

Use in pediatric patients: The safety and effectiveness of Rabeprazole in pediatric patients have not been established. Storage Conditions Store below 25°C, protected from light and moisture. Keep all medicines out of the reach of the children.

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Ace Tablet, 1 Strip [Paracetamol 500mg]

৳ 8
Ace® Paracetamol Non-narcotic analgesics (Non Narcotic Analgesic) Indication: Fever, headache, toothache, earache, bodyache, myalgia, dysmenorrhoea, neuralgia, and sprains. Colic pain, back pain, chronic pain of cancer, inflammatory pain, and post-vaccination pain and fever of children. Rheumatism and osteoarthritic pain & stiffness of joints in fingers, hips, knees, wrists, elbows, feet, ankles and top & bottom of the spine. Dosage & Administration:

Tablet: Adults 1-2 tablets every 4 to 6 hours up to a maximum of 4g (8 tablets) daily. Children (6-12 years) 1/2 to 1 tablet 3 to 4 times daily. Syrup and Suspension: Children (3 months to below 1 year) 1/2 to 1 teaspoonful 3 to 4 times daily. Children (1-5 years) 1-2 teaspoonful 3 to 4 times daily. Children (6-12 years) 2-4 teaspoonful 3 to 4 times daily. Adults: 4-8 teaspoonful 3 to 4 times daily. Paediatric Drops: Children (0-3 months): 0.5 ml. Children (4 to 11 months) 1.0 ml. Children (1 to 2 years) 1.5 ml. Dose can be repeated, every 4 hours.

Suppository: Suppository should be administered rectaly. Children below (5 years) 125-250 mg, 4 times daily. Show more Preparation: Ace® Tablet: Each box contains 500 tablets in blister pack. Ace® XR Tablet: Each box contains 100 tablets in blister pack. Ace® Syrup (60 ml): 60 ml syrup in sealed cap PET bottle (with measuring cup). Ace® Syrup (100 ml): 100 ml syrup in sealed cap PET bottle (with measuring cup). Ace® Suspension: 60 ml suspension in sealed cap PET bottle. Ace® Paediatric drops (30 ml): 30 ml paediatric drop in sealed cap PET bottle (with dropper). Ace® 125 Suppository: Each box contains 20 suppositories in blister pack. Ace® 250 Suppository: Each box contains 20 suppositories in blister pack. Ace® 500 Suppository: Each box contains 20 suppositories in blister pack.
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Fexo 120 Tablet, 1 Strip [Fexofenadine HCl 120mg]

৳ 80
COMPOSITION

FexoTM 60: Each film coated tablet contains Fexofenadine Hydrochloride USP 60 mg. FFexoTM 120: Each film coated tablet contains Fexofenadine Hydrochloride USP 120 mg. FexoTM 180: Each film coated tablet contains Fexofenadine Hydrochloride USP 180 mg. FexoTM Suspension: Each 5 ml suspension contains Fexofenadine Hydrochloride USP 30 mg. PHARMACOLOGY Fexofenadine Hydrochloride is an antihistamine with selective peripheral H1-receptor antagonist activity. Fexofenadine is rapidly absorbed after oral doses with peak plasma concentrations being reached in 2-3 hours. It is about 60% to 70% bound to plasma proteins. About 5% of the total doses is metabolized, mostly by the intestinal mucosa, with only 0.5% to 1.5% of the dose undergoing hepatic biotransformation by the cyto-chrome P450 system. Elimination half-life of 14 hours has been reported although this may be prolonged in patients with renal impairment. Excretion is mainly in the faeces with only 10% being present in the urine. Fexofenadine does not appear to cross the blood-brain barrier.

INDICATION Seasonal Allergic Rhinitis: FexoTM tablets are indicated for the relief of symptoms associated with seasonal allergic rhinitis in adults and children 6 years of age and older. FexoTM Oral Suspension is indicated for the relief of symptoms associated with seasonal allergic rhinitis in children 2 to 11 years of age. Symptoms to treat effectively: sneezing, rhinorrhea, itchy nose/palate/throat, itchy/watery/red eyes. Chronic Idiopathic Urticaria: FexoTM tablets are indicated for treatment of uncomplicated skin manifestations of chronic idiopathic urticaria in adults and children 6 years of age and older. FexoTM Oral Suspension is indicated for treatment of uncomplicated skin manifestations of chronic idiopathic urticaria in children 6 months to 11 years of age. Fexofenadine Hydrochloride significantly reduces pruritus and the number of wheals. USE IN PREGNANCY AND LACTATION There are no adequate and well controlled studies in pregnant women. Fexofenadine should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus. It is not known whether Fexofenadine is excreted in human milk or not. Caution should be exercised when Fexofenadine is administered to a nursing woman. DRUG INTERACTION Plasma concentrations of Fexofenadine have been increased when given with Erythromycin or Ketoconazole. Antacid containing Aluminium and Magnesium Hydroxide reduces the absorption of Fexofenadine. Fruit juices including grapesfruit may reduce the bioavailability of Fexofenadine and use together should be avoided. CONTRAINDICATION Fexofenadine is contraindicated in patients with known hypersensitivity to any of the ingredients. DOSAGE AND ADMINISTRATION In case of decreased renal function, care should be taken in dose selection and it may be useful to monitor renal function. STORAGE CONDITION Tablet: Store at a cool and dry place, protected from light & moisture. Suspension: Store at a cool and dry place, protected from light. Keep out of the reach of children.

HOW SUPPLIED FexoTM 60: Each box contains 5 x 10 tablets in blister pack. FexoTM 120: Each box contains 5 x 10 tablets in blister pack. FexoTM 180: Each box contains 3 x 10 tablets in blister pack. FexoTM Susupension: Each bottle contains 50 ml suspension and calibrated dropper & measuring cup.

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Panther Dotted Condom, 4’s Combo pack

৳ 60

Panther

Panther is the best selling condom brand of SMC. Introduced in 1986, it is the most popular condom brand in Bangladesh.

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Alvasin-225l-Syrup

৳ 300
50pcs Tablet CALRIP (MARWAREEDI). General tonic, nervine tonic & uterotonic.
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Losectil 20mg Capsule, 1 strip [Omeprazole]

৳ 50
Indications Omeprazole is indicated for the treatment of- Gastric and duodenal ulcer NSAID-associated duodenal and gastric ulcer As prophylaxis in patients with a history of NSAID-associated duodenal and gastric ulcer Gastro-esophageal reflux disease Long-term management of acid reflux disease Acid-related dyspepsia Severe ulcerating reflux esophagitis Prophylaxis of acid aspiration during general anesthesia Zollinger-Ellison syndrome Helicobacter pylori-induced peptic ulcer. Therapeutic Class Proton Pump Inhibitor Pharmacology Omeprazole, a substituted benzimidazole, is an inhibitor of gastric acid secretion. It inhibits gastric acid secretion by blocking hydrogen-potassium-adenosine triphosphatase (H+/K+ ATPase) enzyme system in the gastric parietal cell. After oral administration, the onset of the antisecretory effect occurs within one hour, with the maximum effect occurring within two hours and inhibition of secretion lasts up to 72 hours. When the drug is discontinued, secretory activity returns gradually, over 3 to 5 days. Dosage Oral- Benign gastric and duodenal ulcer: 20 mg once daily for 4 weeks in duodenal ulceration, 8 weeks in gastric ulceration; in severe or recurrent cases, dose to be increased to 40 mg daily; maintenance dose for recurrent duodenal ulcer, 20 mg once daily; in prevention of relapse in duodenal ulcer, 10-20 mg daily. NSAID-associated duodenal or gastric ulcer: 20 mg once daily for 4 weeks, continued for further 4 weeks, if not fully healed. 20 mg once daily is used as prophylaxis in patients with a history of NSAID-associated duodenal or gastric ulcers. Gastro-esophageal reflux disease: 20 mg once daily for 4 weeks, continued for further 4-8 weeks, if not fully healed; 40 mg once daily has been given for 8 weeks in gastro-esophageal reflux disease, refractory to other treatment; maintenance dose is 20 mg once daily. Long-term management of acid reflux disease: 10-20 mg daily. Acid-related dyspepsia: 10-20 mg once daily for 2-4 weeks. Prophylaxis of acid aspiration: 40 mg on the preceding evening, then 40 mg 2-6 hours before surgery. Zollinger-Ellison syndrome: Initially 60 mg once daily; usual range 20-120 mg daily (If daily dose is more than 80 mg, 2 divided dose should be used). Helicobacter pylori eradication regimen in peptic ulcer disease: Omeprazole is recommended at a dose of 20 mg twice daily in association with antimicrobial agents as detailed below: Amoxicillin 500 mg and Metronidazole 400 mg both three times a day for one week, or Clarithromycin 250 mg and Metronidazole 400 mg both twice a day for one week, or Amoxicillin 1 g and Clarithromycin 500 mg both twice a day for one week. Paeditaric use in severe ulcerating reflux esophagitis (Child>1 year): If body-weight 10-20 kg, 10-20 -mg once daily for 4-12 weeks; if body-weight over 20 kg, 20-40 mg once daily for 4-12 weeks. IV Injection- Prophylaxis of acid aspiration: Omeprazole 40 mg to be given slowly (over a period of 5 minutes) as an intravenous injection, one hour before surgery. Duodenal ulcer, gastric ulcer or reflux oesophagitis: In patients with duodenal ulcer, gastric ulcer or reflux oesophagitis where oral medication is inappropriate, Omeprazole IV 40 mg once daily is recommended. Zollinger- Ellison syndrome (ZES): In patients with Zollinger-Ellison Syndrome the recommended initial dose of Omeprazole given intravenously is 60 mg daily. Higher daily doses may be required and the dose should be adjusted individually. When doses exceed 60 mg daily, the dose should be divided & given twice daily. Administration Direction for use of IV Injection: Omeprazole lyophilized powder and water for injection is for intravenous administration only and must not be given by any other route. Omeprazole IV injection should be given as a slow intravenous injection. The solution for IV injection is obtained by adding 10 ml water for injection to the vial containing powder. After reconstitution the injection should be given slowly over a period of at least 2 to 5 minutes at a maximum rate of 4 ml/minute. Use only freshly prepared solution. The solution should be used within 4 hours of reconstitution. Direction for use of IV Infusion: Omeprazole IV infusion should be given as an intravenous infusion over a period of 20-30 minutes or more. The contents of one vial must be dissolved in 100 ml saline for infusion or 100 ml 5% Dextrose for infusion. The solution should be used within 12 hours when Omeprazole is dissolved in saline and within 6 hours when dissolved in 5% Dextrose. The reconstituted solution should not be mixed or co-administered in the same infusion set with any other drug. Interaction Omeprazole can prolong the elimination of diazepam, warfarin and phenytoin. So, reduction of warfarin or phenytoin dose may be necessary when Omeprazole is added to the treatment. There is no evidence of an interaction of Omeprazole with theophylline, propranolol or antacids. Contraindications Omeprazole is contraindicated in patients with known hypersensitivity to any of the components of the formulation. Side Effects Omeprazole is generally well tolerated. Nausea, abdominal colic, paresthesia, dizziness and headache have been stated to be generally mild and transient and not requiring a reduction in dosage. Pregnancy & Lactation US FDA pregnancy category of Omeprazole is C. However, results from three prospective epidemiological studies indicate no adverse effects of Omeprazole on pregnancy or on the health of the fetus/newborn child. There is no information available on the passage of Omeprazole into breast milk or its effects on the neonate. Breast-feeding should, therefore, be discontinued, if the use of Omeprazole is considered essential. Precautions & Warnings When gastric ulcer is suspected, the possibility of gastric malignancy should be excluded before treatment with Omeprazole is instituted, as treatment may alleviate the symptoms and delay diagnosis. Storage Conditions Keep in a dry place away from light and heat. Keep out of the reach of children.
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Voligel Cream, 1 Tube [Diaclofenac Sodium 50gm]

৳ 97

Product details of Voligel Cream, 1 Tube [Diaclofenac Sodium 50gm]

  • Quantity number indicates 1 tube.
  • 1 tube containing 50gm cream.
  • Indicated for:Rheumatoid arthritis, Osteoarthritis, Joint and Muscular Pain
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Entacyd Plus Suspension 200ml, 1 Bottle [Aluminium Hydroxide + Magnesium Hydroxide + Simethicone]

৳ 80

COMPOSITION Tablet: Each tablet containsDried Aluminium Hydroxide Gel BP 425.53 mg (Al2O3, 47% minimum) Magnesium Hydroxide BP 400 mg Simethicone USP 30 mg Suspension: Each 5 ml contains - Aluminium Oxide 200 mg (Equivalent amount of Aluminium Hydroxide Gel USP) Magnesium Hydroxide 400 mg (Equivalent amount of Magnesium Hydroxide Paste USP) Simethicone USP 30 mg

PHARMACOLOGY Entacyd® Plus is the mixture of non-systemic acid neutralizing substances and antiflatulent. This preparation offers reliability as well as long action. Aluminium Hydroxide and Magnesium Hydroxide induce the relief of ulcer by neutralizing gastric acid secreted from parietal cells of the stomach. The clinical use of simethicone is based on its antifoam properties. Simethicone spreads on the surface of aqueous liquids, forming a film of low surface tension and causing collapse of foam bubbles. Simethicone repeatedly allows mucous surrounded gas bubbles in the GI tract to coalesce and be expelled. Entacyd® plus is used in the treatment of flatulence and meteorism for the elimination of gas, air or foam from the gastro-intestinal tract prior to radiography and for the relief of abdominal distension and dyspepsia. Simethicone is physiologically inert; it does not appeared to be absorbed from the GI tract to interfere with gastric secretion or absorption of nutrients. Following oral administration, the drug is excreted unchanged in the feces. INDICATION Entacyd® Plus is indicated for symptomatic relief of hyperacidity associated with the peptic ulcer, gastritis, peptic oesophagitis, gastric hyperacidity, heartburn, sour stomach or hiatus hernia. It is effective in the prevention of stress ulceration and GI bleeding. It acts as an antiflatulent to alleviate the symptoms of gas including post operative gas pain. Entacyd® Plus rapidly Aluminium Hydroxide, Magnesium Hydroxide, Simethicone Antacid, Antiulcerants Entacyd® Plus ALIMENTARY PREPARATIONS relieves acid pain, disperses gastric foam and facilitates eructation of gas and air. DOSAGE AND ADMINISTRATION Tablet: 1-2 tablets 1-3 hours after meal and at bed time or as directed by the physician. Suspension: 1-2 teaspoonful 1-3 hours after meal and at bedtime or as directed by the physician. CONTRAINDICATION AND PRECAUTION

Entacyd® Plus should not be administered in patients with renal failure or hypophosphataemia or in those who are severely debilitated. It is also contraindicated in alkalosis and hypermagnesaemia, where abdominal distention may be due to partial or complete intestinal obstruction. Entacyd® Plus should be used with caution in patients with kidney disease.

SIDE EFFECT Gastrointestinal side effects are uncommon. Occasionally, if excessive amount is consumed, diarrhea, constipation or regurgitation may occur. DRUG INTERACTION All antacids may increase or decrease the rate and/or extent of absorption of concomitantly administered oral drugs. Antacids decrease the bioavailability of theophyline, tetracycline, quinolone antibiotics, isoniazide, ketoconazole, ethambutol, some antimuscarinic drugs, benzodiazepines, phenothiazines, ranitidine, indomethacine, nitrofurantoin, fluoride, phosphate, propanolol, atenolol, digoxins, vitamins etc. Antacids increase the bioavailability of some drugs; e.g. sulphonamides, levodopa, valproic acid, enteric coated aspirin etc. USE IN PREGNANCY It is advised to avoid antacid preparations in the first trimester of pregnancy. STORAGE CONDITION Store in cool and dry place, out of reach of children. HOW SUPPLIED Entacyd® Plus tablet: Box containing 20 x 10 tablets in blister pack. Entacyd® Plus suspension: Bottle containing 200 ml suspension.
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