Angricold powder for solution for oral administration (lemon) in bags 5g №10

Name:
Angricold powder for priming d / in. priming (lemon) in pack. 5 g in pack No. 10
Description:
Almost white to yellow powder with lemon or black currant aroma. After dissolving in warm water, a yellow solution with a lemon or blackcurrant flavor is formed. The main active ingredient Paracetamol + phenylephrine + ascorbic acid Release form powder Dosage 5 g Special instructions The risk of predominantly mental dependence appears only at doses exceeding the recommended ones and with long-term treatment. To avoid the risk of overdose, make sure that other medicines taken by the patient do not contain paracetamol. For adults weighing more than 50 kg, the total dose of paracetamol should not exceed 4 g per day. Indications for use Short-term treatment of colds, rhinitis, rhinopharyngitis, influenza-like conditions in adults and children from 12 years of age and older, accompanied by: clear nasal discharge and lacrimation; sneezing headache and/or fever. Method of administration and doses For oral administration. Pour the contents of 1 sachet into a glass, pour hot water, stir until dissolved. Adults: one sachet every 4-6 hours. Do not exceed 4 sachets in 24 hours. Do not take the drug more often than after 4 hours. Children over 12 years old: one sachet every 6 hours. Do not exceed 3 sachets in 24 hours. It is not recommended to use more than 5 days as an anesthetic and more than 3 days as an antipyretic without consulting a doctor. If symptoms persist, see a doctor. Do not exceed the indicated dose. Use during pregnancy and lactation The drug is contraindicated during pregnancy. Paracetamol – category A (FDA classification): drugs that have been taken by a large number of pregnant women and women of childbearing age without any proven increase in the incidence of malformations or other direct or indirect harmful effects on the fetus. Paracetamol crosses the placental barrier. Animal studies with paracetamol did not reveal any risk to pregnancy or fetal development. Precautionary measures In case of ongoing febrile syndrome against the background of the use of the drug for more than 3 days and pain syndrome – more than 5 days, you should consult a doctor. A doctor should be consulted if symptoms: Do not improve within 5 days. Accompanied by a fever that lasts more than 3 days. Include sore throat that does not go away for more than 3 days, accompanied by fever, headache, rash, nausea and vomiting. The simultaneous use of other medicinal products containing paracetamol should be avoided. When using the drug, it is not recommended to drink alcoholic beverages, since ethyl alcohol while taking paracetamol can cause liver dysfunction. Always consult your doctor before taking this medicinal product in patients with the following conditions: Hypertension Cardiovascular disease Diabetes Hyperthyroidism Increased intraocular pressure (i.e. glaucoma) Pheochromocytoma Enlarged prostate Vascular obliterans (i.e. Raynaud’s phenomenon) Epilepsy Bronchitis Bronchiectasia Bronchial asthma Diseases liver and kidneys. Caution should be exercised in patients with renal impairment and in patients with hepatic insufficiency, due to the fact that this drug contains paracetamol, which increases the risk of paracetamol-related liver damage. Patients who have been diagnosed with liver or kidney failure should consult a doctor before taking this medicine. Phenylephrine may contribute to false positive doping control results in athletes. Keep out of sight and reach of children. Children Children under 12 years of age should not take this medicine. Interactions with other drugs Drug interactions with paracetamol are usually minor, but increase when concomitant drugs such as anticoagulants (warfarin and coumarin) and anticonvulsants with a low therapeutic index. Simultaneous use of paracetamol with NSAIDs may increase their nephrotoxicity. Pharmacodynamic interactions may occur with other pain relievers such as caffeine, opiates; barbiturates reduce the antipyretic effect. The half-life of chloramphenicol is increased. Probenecid, cholestyramine inhibit the metabolism of paracetamol. Treatment of tuberculosis with rifampicin and isoniazid increases the hepatotoxicity of paracetamol. Antiepileptic drugs (phenobarbital, phenytoin, carbamazepine) do not increase the risk of hepatotoxicity. Contraindications hypersensitivity to any component of the drug; severe violations of the liver and kidneys; hyperthyroidism (thyrotoxicosis); diabetes mellitus and hereditary disorders of sugar absorption; deficiency of glucose-6-phosphate dehydrogenase; diseases of the blood system; heart disease (coronary heart disease, aortic stenosis, severe atherosclerosis, myocardial infarction, arrhythmias, decompensated heart failure); arterial hypertension; taking tricyclic antidepressants, beta-blockers, MAO inhibitors, incl. up to 14 days after cancellation; sympathomimetics (such as appetite suppressants, amphetamine-like psychostimulants); taking other paracetamol-containing products and products to relieve the symptoms of colds, flu and nasal congestion; prostate adenoma; pheochromocytoma; occlusive vascular disease (Raynaud’s syndrome); angle-closure glaucoma; age up to 12 years; during pregnancy and lactation. Composition Each sachet contains: Active ingredients: paracetamol – 325.0 mg, phenylephrine hydrochloride – 10 mg, ascorbic acid – 60 mg; excipients: mannitol, anhydrous lactose, anhydrous citric acid, sodium citrate, sodium chloride, sucralose, disodium edetate, lemon or blackcurrant flavor, quinoline yellow supra dye (E 104). OverdoseSymptoms caused by paracetamol: Liver damage is possible in adults who have taken 10 g or more of paracetamol. Taking 5 g or more of paracetamol can lead to liver damage if the patient has the risk factors listed below. Risk factors If the patient: a) is on long-term treatment with carbamazepine, phenobarbital, phenytoin, primidone, rifampicin, St. John’s wort and other drugs that induce liver enzymes. Or b) regularly consumes ethanol in excess of the recommended amounts. Or c) exhausted, for example, cystic fibrosis, HIV infection, hunger. Symptoms Symptoms of an overdose of paracetamol in the first 24 hours include: pallor, nausea, vomiting, loss of appetite and abdominal pain. Liver damage may appear 12 to 48 hours after ingestion. Glucose metabolism disorders and metabolic acidosis may occur. In severe poisoning, liver failure can progress to encephalopathy, bleeding, hypoglycemia, cerebral edema, and death. Acute renal failure with acute necrosis, low back pain, hematuria, and proteinuria may develop even in the absence of severe liver damage. There have been reports of cardiac arrhythmias and pancreatitis. Treatment Immediate measures are of great importance in the treatment of paracetamol overdose. Despite the absence of significant early symptoms, patients should be referred urgently to the hospital to see a doctor. Symptoms may be limited to nausea or vomiting and may not be consistent with the severity of the overdose or the risk of organ damage. Management should be in accordance with established treatment guidelines. Treatment with activated charcoal should be considered if the overdose was within 1 hour. Plasma concentrations of paracetamol should be measured every 4 hours after ingestion. Treatment with N-acetylcysteine can be used within 24 hours after taking paracetamol, however, the maximum protective effect is achieved up to 8 hours after taking the drug. The effectiveness of the antidote drops sharply after this time. If necessary, the patient N-acetylcysteine should be administered intravenously, in accordance with the established dosing schedule. If vomiting is not a problem, oral methionine may be a suitable alternative for remote areas outside of the hospital. Phenylephrine Symptoms Symptoms of overdose include increased blood pressure and associated with hypertension reflex bradycardia and arrhythmia. Treatment Elevated blood pressure should be treated with an alpha receptor antagonist such as intravenous phentolamine. A decrease in blood pressure leads to a reflex increase in heart rate, if necessary, this condition can be alleviated by the administration of atropine. Side effectsThe frequency of possible side effects listed below is defined as follows: Very often (?1/10) Often (?1/100 to <1/10) Uncommon (?1/1000 to <1/100) 10000 to <1/1000) Very rare (< 1/10000) Not known (cannot be estimated from available data) Storage conditions At temperatures not exceeding 25 °C. Keep out of the reach of children. Buy Angricold powder for oral solution (lemon) in bags 5g No. 10 Price for Angricold powder for oral solution (lemon) in bags 5g No. 10 for oral administration (lemon) in packages 5g №10