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HomeMEDICINES Adovas Syrup 100ml, 1 Bottle [Adhatoda vasica]
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Adovas Syrup 100ml, 1 Bottle [Adhatoda vasica]

৳ 65

Product details of Adovas Syrup 100ml, 1 Bottle [Adhatoda vasica]

  • Quantity number indicates 1 bottle.
  • 100 ml Syrup in PET bottle
  • Indicated for:Adovas® is a sugar free, non sedating herbal cough syrup. It liquefies phlegm. It is effective for all kinds of common cold and cough such as, dry irritable cough, allergic cough, smokers cough and cough associated with bronchitis. It soothens the throat irritation and relieves hoarseness.

Adovas Syrup contains extracts of Adhatoda Vasica 0.68 gm, Piper longum0.14 gm, 0.05gm, Glycyrrhiza glabra 6.80 mg, 6.80 mg, Piper Nigrum 6.80 mg, Terminalia chebula73.00 mg, Saussurea lappa 6.80 mg, Syzygium aromaticum 6.80 mg, Eletteria cardamomum 6.80 mg, Cinnamomum zeylanicum 6.80 mg, Cinnamomum tamala6.80 mg, Pistacia integerrima 6.80 mg and Myrica nagi 6.80 mg.DescriptionAdovas ® syrup is a sugar free preparation of right combination of herbs which is tolerated, safe and non-sedating with potent anti-allergic properties. Adovas ® syrup constipation and dryness of mouth.Adhatodo vasica Piper longum(P ipul): Relieves allergic cough, cough with asthma, chronic congestion and hoarseness.Glycyrrhiza glabra (Jashthi madhu): Relieves irritation of throat. Modulates the agent.Terminalia chebula (Haritaki): It has laxative, tonic and alter ative properties. It helps in smooth evacuation and removing toxins and fat from the body. It is used to prevent aging and impart longevity, immunity and body’s resistance against disease; it has Saussurea lappa (K ur): The essential oil of the roots has strong antiseptic, disinfectant in the treatment of bronchial asthma. (Shunthi): Reported to contain an antihistaminic factor . Shown to Piper nigrumproperties.Syzygium aromaticum (Labanga): Useful in coughs and other respiratory disorders. It improves the breath and is a remedy for sore throat, headaches and coryza. It has Elettaria cardamomum (Elach): It is used as an aromatic stimulant, carminative. Volatile components of cardamom exhibit antimicrobial activity. It is also reported to Cinnamomum zeylanicum(Darchini): It is a good anti-infective agent and is useful in relieving cough due to its soothing action. The oil fr om the bark shows potent antibacter ial and antifungal activity.Cinnamomum tamala (Tejpata): It Is a tonic, digestive, carminative, uterine stimulant.Pistacia integrrima (K akra sr ingi): It is known to help in cough, asthma & anorexia. It giv es strength to mucous membrane.Myrica nagi(K atphal): It cures dyspnoea, cough & throat ir ritation. It is a stimulant, alter ative, expectorant and tonic.

Tulshi extract and other ingredients: Tulshi extract and some other ingredients ar e Indicationir ritable cough, allergic & smoker’s cough. It soothes the throat irritation and relieves hoarseness. Sugar free preparation is suitable for diabetic patients.

Dosage & Administration:Children under 1 2 years: 1-2 teaspoonful (5-1 0 ml) 3 time a day. Adult: 3 teaspoonful (15 ml) 2-3 times a day. In acute cough war m water can be added for better result.

Herbal medicine is clinically proven as safe & well tolerated. In the recommended
Contraindication:
There is no evidence available on contraindication but it may happen in patients who ar e hypersensitive to any of its ingredients.
Use in Pregnancy:The safety of Adovas ® syrup in pregnancy has not been studied. Theref ore, it should than the risks to fetus.

Storage:Keep away from light and moisture, keep below 300 C temperatures in cool and dry place. Keep the medicine out of reach of children. How Supplied Adovas 100 mI Syrup: Each PET bottle contains 100 ml syrup. Adovas 200 ml Syrup: Each PET bottle contains 200 ml syrup.Herbal Cough Syrup2000012175Alc ohol & sugar free.

Specifications of Adovas Syrup 100ml, 1 Bottle [Adhatoda vasica]

  • Brand
    Square Pharmaceuticals Ltd
  • Generic Name
    Adhatoda vasica
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Adovas Syrup 100ml
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  • Product will be replaced if it has any defect by its manufacturer.
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  • 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.

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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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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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Voligel Cream, 1 Tube [Diaclofenac Sodium 50gm]

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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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Alatrol Tablet, 1 Strip [Cetirizine Dihydrochloride 10mg]

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Alatrol® Cetirizine Hydrochloride BP COMPOSITION Alatrol® Tablet:
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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.
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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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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.

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Acifix Tablet, 1 Strip [Rabeprazole sodium 20mg]

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Product details of Acifix Tablet, 1 Strip [Rabeprazole sodium 20mg]

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Tufnil 200mg Tablet, 1 strip [Tolfenamic Acid]

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Product details of Tufnil 200mg Tablet, 1 strip [Tolfenamic Acid]

  • Quantity number indicates 1 strip. 10 pieces of tablets/strip. Indication: Tolfenamic acid is used specifically for relieving the pain of migraine headaches and also recommended for use as an analgesic in post-operative pain, and fever.
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Maxpro 20 Capsule, 1 Strip [Esomeprazole Magnesium]

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Pharmacology

Esomeprazole is a PPI that suppresses gastric acid secretion by inhibiting H+/K+ ATPase in the gastric parietal cell. It is the S-isomer of omeprazole. Dosage

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Healing of erosive esophagitis: 20 mg or 40 mg once daily for 4 to 8 Weeks. For those patients who have not healed after 4-8 weeks of treatment, an additional 4-8 weeks course of Esomeprazole may be considered.  

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Napa Rapid, 1 Strip [Paracetamol 500 mg.]

৳ 9
Description:

Napa® Rapid caplet is an advanced formulation of Paracetamol that contains Actizorb® technology. It dissolves up to five times faster than standard Paracetamol tablets. Napa® Rapid caplet 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.

  Indications: All conditions requiring relief from pain and fever such as neuritis, neuralgia, headache, earache, toothache, pain due to rheumatic disorder, cold, influenza, dysmenorrhoea, migraine, backache, pain due to arthritis etc.   Dosage and Administration: Adults and children (aged 12 years and over): Take 1 to 2 caplets every four to six hours as needed. Do not take more than 8 caplets in 24 hours. Children (7 to 11 years): Take ½-1 caplet every four to six hours as needed. Do not take more than 4 caplets in 24 hours. Not recommended in children under 7 years.   Pregnancy and Lactation: Epidemiological studies in human pregnancy have shown no ill effects due to paracetamol used in the recommended dosage, but patients should follow the advice of the doctor regarding its use. Paracetamol is excreted in breast milk but not in a clinically significant amount. Available published data do not contraindicate breast feeding.   Contraindications: Paracetamol is contraindicated in patients with severe renal function impairment and hepatic disease (Viral Hepatitis). Precautions: Paracetamol should be given with care 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, including thrombocytopenia, leukopenia, breathing problem. Pancreatitis, skin rashes, and other allergic reactions occur occasionally.   Overdosage: Symptoms of Paracetamol overdose in the first 24 hours are pallor, nausea, vomiting, anorexia and abdominal pain. Liver damage may become apparent 12 to 48 hours after ingestion. Abnormalities of glucose metabolism and metabolic acidosis may occur.   Pharmaceutical Precautions: Keep in a cool & dry place. Protect from light. Keep out of the reach of children.   Commercial Pack:

Napa® Rapid Caplet: Box containing 270 caplets in 9x30’s blister strips. Each caplet contains Paracetamol BP 500 mg

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