Rinzasip with vitamin C powder for preparing a solution of black currant sachet 5 g 5 pcs
Condition: New product
1000 Items
Rating:
Be the first to write a review!
More info
Active ingredients
Caffeine + Paracetamol + Phenylephrine + Pheniramine
Release form
Powder
Composition
Paracetamol 750 mg, ascorbic acid (Vit. C) 200 mg, caffeine 30 mg, pheniramine maleate 20 mg, phenylephrine hydrochloride 10 mg. Additional substances: citric acid - 200 mg, sodium saccharinate - 40 mg, sodium citrate - 500 mg, sucrose - 2915 mg, dye azorubine (E122) - 4 mg, fruit flavoring (tutti-frutti) - 166.7 mg, raspberry flavor - 66.7 mg, blackcurrant flavor - 66.7 mg.
Pharmacological effect
Combined medication, has antipyretic, analgesic, alpha-adrenostimulating, vasoconstrictor and antihistamine action, eliminates cold symptoms. Paracetamol is a non-narcotic analgesic; blocks cyclooxygenase, mainly in the central nervous system, affecting the centers of pain and thermoregulation; It has an analgesic and antipyretic effect. Phenylephrine is an alpha adrenomimetic with a moderate vasoconstrictor effect. Reduces swelling and hyperemia of the mucous membranes of the upper respiratory tract and paranasal sinuses. Pheniramine is a blocker of H1-histamine receptors. It has antiallergic effect: eliminates itchy eyes, nose and throat, swelling and hyperemia of the mucous membranes of the nasal cavity, nasopharynx and paranasal sinuses, reduces exudative manifestations. Caffeine has a stimulating effect on the central nervous system, enhances the effect of analgesics, eliminates sleepiness and fatigue, increases mental performance, reduces fatigue and drowsiness. Ascorbic acid (vitamin C) is involved in the regulation of redox processes, carbohydrate metabolism, coagulation Mosti blood, tissue regeneration, in the synthesis of steroid hormones; reduces the permeability of blood vessels and increases the body's resistance to the effects of various adverse environmental factors.
Pharmacokinetics
Data on the pharmacokinetics of the drug Rinzasip; with vitamin C is not provided.
Indications
- symptomatic treatment of colds, flu, acute respiratory viral infections (febrile syndrome, pain syndrome, rhinorrhea).
Contraindications
- simultaneous intake of other drugs containing substances that are part of the drug; - simultaneous reception of tricyclic antidepressants,MAO inhibitors, beta-blockers; - pregnancy; - lactation period; - children's age (up to 15 years); - sucrase / isomaltase deficiency, fructose intolerance, glucose-galactose malabsorption; - hypersensitivity to paracetamol and other components of the preparation .
Precautionary measures
Do not exceed the recommended dose. With caution: pronounced atherosclerosis of the coronary arteries, arterial hypertension, thyrotoxicosis, pheochromocytoma, diabetes mellitus, bronchial asthma, chronic obstructive pulmonary disease, glucose-6-phosphate dehydrogenase deficiency, blood diseases, congenital hyperbilirubyroses, congenital anemia, and heart failure, deficiencies, glucose-6-phosphate dehydrogenase, blood diseases, congenital hyperbilirubyroses, and hemorrhages, congenital hyperbilirubyiniums, and hemorrhagic deficiencies, glucose-6-phosphate dehydrogenase, blood diseases, congenital hyperbilirubyinia, and blood diseases, congenital hyperbilirubyinia, and hemorrhagic deficiencies, deficiency of glucose-6-phosphate dehydrogenase, blood diseases, congenital hyperbilirubyrinia, and hemorrhagic diseases, congenital hyperbilirubyrinia, and hemorrhagic deficiencies. and Rotor), hepatic and / or renal failure, angle-closure glaucoma, prostatic hyperplasia.
Use during pregnancy and lactation
The drug is contraindicated for use during pregnancy and lactation.
Dosage and administration
Adults and children over 15 years old are prescribed 1 sachet 3-4 times / day with intervals between doses of 4-6 hours. The maximum daily dose is 4 sachets. The course of treatment without consultation with a doctor is not more than 5 days. Before use, the contents of 1 sachet should be poured into a glass, filled with hot water, mixed until completely dissolved and drunk (if desired, you can add sugar or honey).
Side effects
Allergic reactions: skin rash, pruritus, urticaria, angioedema. From the nervous system: dizziness, sleep disturbance, hyperexcitability. From the cardiovascular system: increased blood pressure, tachycardia. From the digestive system: nausea, vomiting, epigastric pain areas, dryness of the oral mucosa, hepatotoxic action. From the sense organs: mydriasis, accommodation paresis, increased intraocular pressure. From the blood-forming organs: anemia, thrombocytopenia, agranulo toxicity, hemolytic anemia, aplastic anemia, methemoglobinemia, pancytopenia. From the urinary system: urinary retention, nephrotoxicity (papillary necrosis). Other: bronchospasm.
Overdose
Symptoms (mainly caused by paracetamol): pallor of the skin, anorexia, nausea, vomiting; hepatonecrosis; increased activity of hepatic transaminases, an increase in prothrombin time. Treatment: gastric lavage, the appointment of activated carbon, the introduction of methionine (within 8-9 hours after overdose) and N-acetylcysteine (within 8-9 hours after overdose), symptomatic therapy.
Interaction with other drugs
Enhances the effects of MAO inhibitors, sedatives, ethanol. Anti-depressants, anti-Parkinsonian drugs, antipsychotics, phenothiazine derivatives - increase the risk of urinary retention, dry mouth, constipation. Glucocorticosteroids increase the risk of developing glaucoma. Paracetamol reduces the effectiveness of uricohydrophytic drugs. , furazolidone can cause hypertensive crisis, agitation, hyperpyrexia. Tricyclic antidepressants increase adrenomime cal effects of phenylephrine, co-administration of halothane increases the risk of ventricular aritmii.Pri while the appointment of the drug with barbiturates, phenytoin, carbamazepine, rifampicin and other inducers of microsomal liver enzymes increased risk of hepatotoxic action of paracetamol.
special instructions
The patient should be warned that in the absence of a therapeutic effect (hyperthermia for more than 3 days and pain syndrome for more than 5 days), one should consult a doctor. The preparation contains sucrose, which should be taken into account by patients with diabetes mellitus and hypocaloric diet. A single dose of the drug contains from 2915.0 mg to 3136.0 mg of sucrose, which corresponds to 0.24-0.26 XE. The patient should be informed that if the drug has become unusable or the expiration date has expired, then it should not be thrown into the wastewater or the street. It is necessary to put the drug in the bag and put it in the trash. These measures will help to protect the environment. Impact on the ability to drive motor vehicles and control mechanisms. During the period of taking the drug, it is necessary to refrain from driving and practicing other potentially hazardous activities that require increased concentration and psychomotor reactions.