Vicks Anti-Influenza Complex, lemon 5 pcs

A combination drug, the effect of which is due to the composition of its constituent components.

Indications

Symptoms of colds and flu (headache, sore throat, pain in the body and extremities, stuffy nose, cough with difficult discharge of viscous sputum, fever).

Active ingredient

Paracetamol, Phenylephrine

Composition

Associates:

sucrose – 2000 mg,

citric acid – 330 mg,

tartaric acid – 330 mg,

/p>

sodium cyclamate – 200 mg,

sodium citrate – 500 mg,

aspartame – 6 mg,

ascorbic acid – 100 mg,

potassium acesulfame – 17 mg,

lemon flavoring 8476 – 50 mg,

lemon juice flavoring – 120 mg,

menthol flavoring – 100 mg,

quinoline yellow dye – 1 mg.

How to take, the dosage

Adults and children over 12 years: 1 sachet.

Special Instructions

It is recommended that the drug be taken in the shortest possible course and in the lowest effective dose necessary to eliminate symptoms.

Contraindications

Impaired liver function; severe chronic renal failure; arterial hypertension; hyperthyroidism; diabetes mellitus; phenylketonuria; CHD (acute myocardial infarction, coronary artery atherosclerosis); aortic stenosis; tachyarrhythmia; Gastric and duodenal ulcer in acute stage; prostatic hyperplasia; closed-angle glaucoma; porphyria; pheochromocytoma; age less than 12 years; pregnancy, lactation; concurrent use of beta-adrenoblockers, tricyclic antidepressants, MAO inhibitors (includingincluding within 14 days after their withdrawal); concomitant use of other sympathomimetic drugs; concomitant use of other drugs containing paracetamol; sucrose/isomaltase deficiency, fructose intolerance, glucose-galactose malabsorption syndrome; hypersensitivity to guaifenesin, paracetamol, phenylephrine or other drug components.

Side effects

The incidence of adverse reactions is rated as follows: very common (≥1/10), common (≥1/100 to <1/10), infrequent (≥1/1000 to <1/100), rare (≥1/10 000 to <1/1000), very rare (<1/10 000), frequency unknown (no data available to estimate).

Overdose

Paracetamol

Hepatic damage is possible in adults who have taken 10 grams or more of paracetamol. Taking 5 grams or more of paracetamol can affect the liver if the following risk factors are present: prolonged treatment with carbamazepine phenobarbitone phenytoin primidone rifampicin St. John’s wort or other drugs which activate liver enzymes alcohol abuse glutanione deficiency (eg poor diet) cystic fibrosis HIV infection fasting cachexia.

Symptoms of paracetamol overdose in the first 24 hours: pale skin nausea vomiting anorexia and abdominal pain.

Elevated activity of “hepatic” transaminases increased prothrombin time.

Liver damage may appear 12-48 hours after intake, so it is necessary to see a doctor even if there are no symptoms. Impaired glucose metabolism and metabolic acidosis are possible. In severe poisoning liver failure may progress with complications such as encephalopathy hemorrhage hypoglycemia cerebral edema and death. Acute renal failure with acute tubular necrosis (defined by lumbar hematuria pain and proteinuria) can develop even in the absence of severe liver damage. There have been reports of abnormal heart rhythm and pancreatitis.

Phenylephrine

Phenylephrine overdose symptoms include irritability headache increased blood pressure and associated reflex bradycardia and heart rhythm disturbances.

If the above symptoms of overdose occur, a physician should be consulted.

Guaifenesin

Small to moderate overdose may cause dizziness gastrointestinal upset (nausea vomiting and diarrhea). Very high overdose may cause agitation, confusion, and respiratory depression. Treatment

Gastric lavage activated charcoal acetylcysteine (paracetamol antidote) symptomatic therapy.

In case of paracetamol overdose, immediate treatment is necessary. Despite the lack of significant early symptoms, patients should be rushed to the hospital for immediate medical evaluation. Symptoms may be limited to nausea or vomiting and not consistent with the severity of the overdose or risk of organ damage. Liver damage can occur 12 to 48 hours after ingestion of paracetamol, so you should see a doctor even if there are no symptoms.

The treatment of activated charcoal and gastric lavage should be considered if the excessive dose was taken less than 1 hour ago. Plasma concentrations of paracetamol should be measured 4 hours or more after ingestion (earlier concentrations are unreliable).

The treatment with N-acetylcysteine can be given up to 2 hours after paracetamol ingestion; however, the maximum protective effect is achieved about 8 hours after taking the drug. The effectiveness of the antidote gradually decreases after this time. If necessary, intravenous N-acetylcysteine is administered according to the established regimen. Outside the hospital, oral methionine may be administered if there is no vomiting. Patients presenting with severe hepatic dysfunction should be referred to a specialist in poisoning within 24 hours after taking the drug.

In case of hypertensive effects of phenylephrine overdose, intravenous alpha-adrenoreceptor blockers such as phentolamine may be used. Decrease in blood pressure will be reflexively accompanied by an increase in heart rate, but if necessary this effect can be increased by administration of atropine.

Pregnancy use

Do not use the drug during pregnancy and while breast-feeding.