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Alatrol® Cetirizine Hydrochloride BP COMPOSITION Alatrol® Tablet:
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.
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.
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 PRECAUTIONEntacyd® 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.
Ceevit® VITAMINS
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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