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HomeHEALTH Voligel Cream, 1 Tube [Diaclofenac Sodium 50gm]
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Acifix Tablet, 1 Strip [Rabeprazole sodium 20mg] ৳ 70
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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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Categories: HEALTH, HEALTHCARE, MEDICINES, PRESCRIPTION Tags: Voligel, Voligel Cream
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Description

Voligel® gel Description:

Diclofenac Diethylamine is systemically absorbed through the skin; it inhibits the enzyme cyclooxygenase, thus reducing the formation of PGE2. Moreover, it also increases the uptake of Arachidonic acid into the cellullar pool. Oleum Lini contains predominantly Essential Fatty Acids i.e. µ Linolenic acid. On percutaneous absorbtion, µ- Linolenic acid gets converted to Elcosapentanoic acid (EPA). EPA is acted upon by cyclo-oxygahase enzyme to produce prostaglandin E3 which is a weak inflammatory agent. Presence of EPA prevents the action of cyclo-oxygenase on Archidonic acid which reduces its coversion to PGE2 (a highly inflammatory agent). Presence of PGE3 itself modulates the inflammatory response through a feedback mechanism. Menthol is a vasodiator. It dilates the blood vessels, produces a feeling of coolness and produces analgesia. Methyl salicylate is a known anti-inflammatory agent.

Indications

Indicated for the quick relief from pain, swelling and inflalmmation due to musculo-skeletal disorders such as sprains, Strains, tendinitis, bursitis, hands, neck & shoulder pain, sciatica, muscle stiffness, joint pain, back ache and lumbago.

Dosage:

Approximately one inch band of Cream should be applied to the affected site three to four times daily with rubbing till the film disappears.

Side effects:

Usually well tolerated. Extremely low frequency of hypersensitivity reactions.Contraindications:

Known hypersensitivity to any part of the preparation.

Precaution:

For external use only.

Avoid contact with the eyes. Stop use and ask a doctor if condition worsens or does not improve within 7 days. Keep out of the reach of children. If swallowed, get medical help or contact a poison control center right away.

Pharmaceutical Precautions

Store in a cool and dry place, protected from light.Commercial PackBox containing 50 gm tube. Each 100 gm Gel contains Diclofenac Diethylamine BP 1.16 gm (eq. to Diclofenac Sodium 1 gm).

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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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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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Napa Extend Tablet, 1 strip [Paracetamol 665 mg]

৳ 15

What Napa Extend is and what it is used for?

Napa® Extend is the preparation of Paracetamol 665 mg extended release formulation. It is formulated by dual granulation technology. There are two types’ granules in each tablet 31% (206 mg) is in immediate release form for immediate action and 69% (459 mg) in sustain release form for continuous pain relief for 8 hours. Paracetamol 665 mg Extended Release tablet is effective for the relief of persistent pain associated with osteoarthritis and muscle aches and pains such as backache. Paracetamol 665 mg Extended Release tablet also provides effective, temporary relief of pain and discomfort associated with headache, tension headache, period pain, toothache and pain after dental procedures, and cold & flu. Reduces fever.   Before you take Napa Extend Do not take this medicine and tell your doctor if: Hypersensitivity to Paracetamol or to any of the excipients.   Take special care with Napa Extend Check with your doctor before taking this medicine if: Paracetamol should be administered with caution to patients with hepatic or renal Dysfunction.   Taking other medicines Anticoagulant dosage may require reduction if paracetamol medication is prolonged. Paracetamol absorption from immediate release preparations is increased by drugs which increase gastric emptying, eg metoclopramide, and decreased by drugs which decrease gastric emptying, eg propantheline, antidepressants with anticholinergic properties, narcotic analgesics.   Pregnancy and Lactation Pregnancy category: B This drug should not be used during pregnancy unless the benefit outweighs the risk.A decision should be made to discontinue breastfeeding or to not administer the drug, taking into account the importance of the drug to the mother.   Warnings & Precaution Hypersensitivity Reactions: Serious hypersensitivity reactions, including anaphylactic-type reactions, some of which have been life-threatening and fatal, have been reported in patients receiving Ferric Carboxymaltose. Patients may present with shock, clinically significant hypotension, loss of consciousness, and/or collapse.   How to take Napa Extend Paracetamol 665 mg Extended Release tablet are to be administered orally, with or without food. Adults and children over 12 years. Two tablets, swallowed whole, every 6 to 8 hours (maximum of 6 tablets in any 24 hours). The tablets must not be crushed.   If you forget to take Napa Extend If you forget to take a dose, take it as soon as you remember it. If it is almost time for your next dose, do not take the missed dose. Take the next dose on time.   If you stop taking Napa Extend Do not stop taking this medicine without talking to your doctor. You should not stop taking Napa Extend just because you feel better. This is because the problem may come back or get worse again.   If you have any further questions on the use of this product, ask your doctor or pharmacist.   Possible side effects (Adverse effect/Side effect as short form) Like all medicines, Napa Extend can cause side effects, although not everybody gets them. Reports of adverse reactions are rare. Although the following adverse reactions have been reported, a causal relationship to the administration of paracetamol has been neither confirmed nor refuted: dyspepsia, nausea, allergic and haematological reactions.   How to store Napa Extend (Storage condition)?

Store in a cool and dry place and keep away from children.

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Ambrox Syrup 100ml, 1 Bottle [Ambroxol Hydrochloride 15mg/5ml]

৳ 50

Product details of Ambrox Syrup 100ml, 1 Bottle [Ambroxol Hydrochloride 15mg/5ml]

  • Quantity number indicates 1 Bottle
  • 1 bottle contains 100 ml syrup
  • Indicated for: **Productive cough, Acute and chronic inflammatory disorders-acute and chronic bronchitis, laryngitis, Pharyngitis, sinusitis and rhinitis associated with viscid mucus **Asthmatic bronchitis, bronchial asthma with thick expectoration, Bronchiectasis, Chronic pneumonia
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Icturn-225ml-Syrup

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

৳ 60

Product details of Seclo 20 Capsule, 1 Strip [Omeprazole 20mg]

  • Quantity number indicates strip.
  • 10 pieces of capsule/strip.
  • Indication:**Seclo capsule and tablet is indicated for gastroesophageal reflux disease including reflux esophagitis, acid reflux disease, duodenal and benign gastric ulcers, Helicobacter pylori eradication regimens in peptic ulcer disease, prophylaxis of acid aspiration, Zollinger-Ellison Syndrome (ZES) and for the treatment of NSAID-associated gastric ulcers, duodenal ulcers or gastroduodenal erosions.
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Napa Syrup 60ml, 1 Bottle [Paracetamol 120 mg/ 5 ml]

৳ 21

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:
  • Relief from pain and fever such as neuritis, neuralgia, headache, earache,pyrexia,toothache,rheumatic disorder cold, influenza, dysmenorrhoea etc
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Alatrol Tablet, 1 Strip [Cetirizine Dihydrochloride 10mg]

৳ 30
Alatrol® Cetirizine Hydrochloride BP COMPOSITION Alatrol® Tablet:
Each film coated tablet contains Cetirizine Hydrochloride BP 10 mg . Alatrol® Syrup: Each 5 ml syrup contains Cetirizine Hydrochloride BP 5 mg. Alatrol® Paediatric Drops: Each ml contains Cetirizine Hydrochloride BP 2.5 mg.
INDICATION
Alatrol® is indicated for the relief of symptoms associated with seasonal allergic rhinitis due to allergen. Symptoms treated effectively include sneezing, rhinorrhea, pruritus, ocular pruritus, tearing and redness of the eyes. Alatrol® is indicated for the relief of symptoms associated with perennial allergic rhinitis due to allergens. Symptoms treated effectively include sneezing, rhinorrhea, post-nasal discharge, nasal pruritus, ocular pruritus and tearing. Alatrol® is indicated for the treatment of the uncomplicated skin manifestations of chronic idiopathic urticaria. It is also used in allergen induced asthma.
DOSAGE AND ADMINISTRATION
Alatrol® is administered with or without food. Adults and Children 6 years and older: Alatrol® Tablet: 1 tablet daily. Alatrol® Syrup: 10 ml (2 teaspoons full) once daily or 5 ml (1 teaspoon full) twice daily. In patients with decreased renal function (Creatinine clearance 11-31 ml/min), patients on hemodialysis (Creatinine clearance less than 7 ml/min) and in hepatically impaired patients, a dose of 1/2 tablet or 5 ml (1 teaspoon full) once daily is recommended. Children 2-6 years: Alatrol® Syrup: 5 ml (1 teaspoon full) once daily or 2.5 ml (half teaspoon full) twice daily. Children 6 months to less than two years: Alatrol® Syrup: 2.5 ml (half teaspoon full) once daily. The dose in children 12-23 months of age can be increased to a maximum dose as 2.5 ml (half teaspoon full) every 12 hours. Alatrol® Paediatric Drops: 1 ml, once daily. The dose in children 12-23 months of age can be increased to a maximum dose as 1 ml, every 12 hours.
DOSAGE IN RENAL AND HEPATIC IMPAIRMENT: Dosing adjustment is necessary in patients with moderate or severe renal impairment, hepatic impairment and patients on dialysis. SIDE EFFECT Cetirizine seems to cause an incidence of sedation similar to that observed with placebo and with other non-sedating antihistamines such as astemizole and terfenadine and causes a lower incidence of sedation than that with ketotifen, clemastine, pheniramine, chlorpheniramine or mequitazine. Cetirizine does not cause anticholinergic effects. USE IN PREGNANCY AND LACTATION:

Pregnancy category B. Cetirizine should be used in pregnancy only if clearly needed. Cetirizine has been reported to be excreted in human milk and thus, use of Cetirizine in lactating mother is not recommended. STORAGE CONDITION: Protect from direct light exposure. Store in dry place at a temperature not exceeding 300 C. Keep out of the reach of children. HOW SUPPLIED Alatrol® Tablet: Each box contains 100’s tablets. Alatrol® Syrup: Each bottle contains 60 ml syrup and a measuring cup. Alatrol® Paediatric Drops: Each bottle contains 15 ml paediatric drops and a calibrated dropper.

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Alvasin-225l-Syrup

৳ 300
50pcs Tablet CALRIP (MARWAREEDI). General tonic, nervine tonic & uterotonic.
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