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HomeHEALTHCARE Icturn-225ml-Syrup
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Package 5 ৳ 130
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Icturn-225ml-Syrup

৳ 300

50pcs Tablet CALRIP (MARWAREEDI). General tonic, nervine tonic & uterotonic.

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Description

Calrip is a well known unani medicine. It acts as general tonic & nervine tonic. Calrip is also effective in leucorrhoea, menstrual irregularity, dysmenorrhoea and metritis. Indications:

» General debility
» Nervous debility
» Leucorrhoea
» Menstrual irregularity
» Dysmenorrhoea
» Metritis

Dosage & Administration: 1-2 tablet(s) twice daily with milk or as prescribed by the physician. Contraindication: There is no known contraindication. Side effect: No significant side effect has been observed in proper dosage. Precaution: Keep out of reach of the children. Storage: Store at cool and dry place, protect from light.

Presentation: Box containing 50 tablets in blister pack.

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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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Bicozin® Vitamin B Complex and Zinc Vitamin B and B-complex (Vitamins and Minerals) Indication: Treatment and prevention of B-vitamins and Zinc deficiencies.

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Fexo 120 Tablet, 1 Strip [Fexofenadine HCl 120mg]

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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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Napa Tablet, 1 Strip [Paracetamol 500mg]

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Napa® Paracetamol Tablet/Extra Tablet/Syrup/Suspension/ Suppository/Paediatric Drops Description: Napa (Paracetamol) is a fast acting and safe analgesic with marked antipyretic property. It is specially suitable for patients who, for any reason, can not tolerate aspirin or other analgesics.IndicationsAll conditions requiring relief from pain and fever such as neuritis, neuralgia, headache, earache, toothache, pain due to rheumatic disorder, cold, influenza, dysmenorrhoea, post-vaccination pain and fever of children etc. Napa suppositories are used for rapid symptomatic management of pain and fever. It is given as rectal suppository for mild to moderate pain and for pyrexia. Dosage and Administration Tablet/Extra Tablet: Adults: 1-2 tablets 3-4 times daily; Syrup/Suspension: Adults: 4-8 Measuring spoonful 3-4 times daily; Children: 6-12 years: 2- 4 measuring spoonful 3-4 times daily, 1-5 years: 1-2 Measuring spoonful 3-4 times daily, Up to 1 year: 1/2 -1 Measuring spoonful 3-4 times daily. Paediatric drops: Neonates & Children: 0-3 months: 0.5 ml, 4-11 months: 1ml, 12-23 months: 1.5 ml, 2-3 years: 2 ml, 4-5 years: 3ml four times daily or as directed by physicians. Suppositories: Children: 1-5 years: 125- 250 mg, 6-12 years: 250-500 mg, up to 4 times daily. Contraindications Paracetamol is contraindicated in patients with severe renal function impairment and hepatic disease (Viral Hepatitis). Precautions Paracetamol should be given with caution to patients with impaired kidney or liver function. Paracetamol should be given with care to patients taking other drugs that affect the liver. Side Effects Side effects of paracetamol are usually mild, though haematological reactions including thrombocytopenia, leucopenia, pancytopenia, neutropenia, and agranulocytosis have been reported. Pancreatitis, skin rashes, and other allergic reactions occur occasionally. Use in Special Population Pregnancy and lactation: Pregnant or nursing mother seek the advice of a health professional before using this product. Commercial Packs

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Napa Syrup 60ml, 1 Bottle [Paracetamol 120 mg/ 5 ml]

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Product details of Napa Syrup 60ml, 1 Bottle [Paracetamol 120 mg/ 5 ml]

  • Quantity number indicates 1 Bottle
  • 1 PET bottle contains 60ml syrup.
  • Indications:
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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:

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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. 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Monocast 5 Tablet, 1 Strip [Montelukast 5 mg]

৳ 80

Product details of Monocast 5 Tablet, 1 Strip [Montelukast 5 mg]

  • Quantity number indicates 1 strip.
  • 1 strip contains 10 tablets..
  • Indications:
  • -Treatment of asthma
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