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Tachipirina 100 mg oral drops solution 30 ml

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tachipirina 100 mg oral drops solution 30 ml

< A Href = ""> aifa illustrative leaflet

pharmacotherapeutic category:
< Span Style = "Font-Size: 12pt;"> analgesic and antipyretic.

Active principles:
Syrup; 5 ml of paracetamol syrup 120 mg.
oral drops, solution: 1 ml of solution contains paracetamol 100 mg. excipients:
syrup: saccharose, sodium citrate, sodium saccarina, methyl ssibenzoate paraidro, potassium sorbato, macrogol 6000, monohydrate citric acid, strawberry aroma, mandarin aroma, purified water.
oral drops: propylene glycol, macrogol 6000, sorbitol, sodium saccharin, vanilla citrus aroma, propyle Gallato, caramello (E150A), sodium editato, water de purata. < /p>

As antipyretic: symptomatic treatment of febrile affections such as influence, exanthematic diseases, acute affections of the respiratory tract, etc.
as analgesic: headache, neuralgie, mylgie and on three painful medium entities, of various origins. font-size: 12pt; "> contraindications/eff.secondar: span>
hypersensitivity to paracetamol or ad any of the excipients.
patients with severe hemolytic anemia (this contraindication does not refer to oral 500mg formulations).
severe insufficiency and cell phone (this contraindication does not refer to the oral 500 mg oral formulazi). Size: 12pt; "> dosage:
< Span Style = "Font-Size: 12pt;"> for children it is essential to respect the dosage defined in fu nation of their body weight, and then choose the proper formulation.

The ages approximately according to body weight are indicated as an information.
below three months, in case of jaundice, it is appropriate to reduce the single dose orally.
In adults, the maximum orally oral oral is 3000 mg of paracetamol per day.
the doctor must evaluate the need for treatments for 3 consecutive.
the dosage scheme of Tachipirina in relation to the body weight and the way of administration is the following. "> syrup of 120 mg/5 ml to the package is annexed a glass-dostor with the level of level notches corresponding to the capacity of 5 ml, 7.5 ml, 10 ml, 15 ml and 20 ml.
children of weight between 7 and 10 kg (approximately approximately between 6 and 18 months): 5 ml at a time (corresponding to 120 mg of paracetamol), to be repeated without if necessary after 6 hours, exceed 4 administrations per day.
children of weight between 11 and 12 kg (approximately between 18 and 24 months): 5 ml at the Volt A (corresponding to 120 mg of paracetamol), to be repeated without exceeding the 6 administrations per day.
Children of weight between 13 and 20 kg (approximately between 2 and 7 year): 7.5 - 10 ml at a time (corresponding to 180 and 240 mg of paracetamol), to be repeated if after necessary 6 hours, Without super rare the 4 administrations per day.
children of weight between 21 and 25 kg (approximately between 6 and 10 years): 10 ml at a time (corresponding to 240 mg of paracetamol), repeat from if necessary I give some 4 hours, without exceeding 6 administrations per day.
children of PE Eso between 26 and 40 kg (approximately between 8 and 13 year): 15 - 20 ml at a time (corresponding to 360 and 480 mg of paracetamol respectively), to be repeated if necessary after 6 hours, without super are the 4 administrations per day.
children of weight between 41 and 50 kg (approximately between 12 and 15 years): 20 ml at a time (corresponding to 480 mg of paracetamol), to be repeated Without if necessary I give 4 hours, exceed 6 administrations per day.
boys from PEo greater than 50 kg (approximately over 15 years): 20 ml all time (corresponding to 480 mg of paracetamol), to be repeated if necessary after 4 hours, without exceeding 6 administrations per day .
adu LTI: 20 ml at a time (corresponding to 480 mg), to be repeated if necessary after 4 hours, without exceeding 6 administrations per day.
the syrup with a dosage adjustment to facilitate the atmosphere of the dose of the product in the function of body weight. Size: 12pt; "> drops or wings, 100 mg/ml solution: a drop of oral drops corresponds to 3, 1 mg.
children of weight between 3.2 and 6 kg (approximately TR A The birth and 6 months): 14-20 drops at a time (correspondent gives ethically to 43.4 and 62 mg of paracetamol), to be repeated If necessary after 6 hours, without exceeding 4 administrations per day.
children of weight between 7 and 10 kg (approximately between 6 and 18 mes i): 35-40 drops at a time (corresponding to 108.5 and 1 24 mg of paracetamol respectively), to be repeated if necessary After 6 hours, without pearing the 4 administrations per day.
children of weight between 1 1 and 12 kg (approximately between 18 and 24 months): 35-40 drops per vaulted (corresponding to 108, 5 and 124 mg of Paracetamo Lo), to be repeated if necessary after 4 hours, without exceeding 6 tops of tractions per day.
renal failure: in case of insufficiency King Nale severe (creatinine clearance of less than 10 ml/min), the inter valle among the administrations must be at least 8 hours.

syrup and oral drops, solution: no special precaution for conservation.

in rare cases of allergies reactions that the administration must be suspended and a suitable treatment must be established.
use cautiously in case of chronic alcoholism, excessive intake of alcohol (3 op iu 'alcoholic beverages per day), anorexia, bulimia or cachexia, chronic maln (low reserves of liver glutathione) dehydration, hypovolemia.
Paracetamol should be administered with caution to patients with mild to moderate hepatocellular insufficiency (including Gilbert syndrome), severe hepatic failure (Child-Paugh & GT; 9), acute hepatitis, in concomitant treatment with drugs that alter they alter The hepatic function, deficiency of glucose-6-phosphate dehydrogenase, to nemia hemolytic.
doses for administration in subjects with insufficiency must be filed only if necessary and under the direct controll or doctor.
In case of protracted use it is advisable to monitor the liver and renal funz and the blood crashes.
During treatment with P Aracetamolo before any other drug check that does not contain the same active ingredient, since the paracetamol is taken in high doses, serious adverse reactions can be verified.
invite the patient to contact the doctor before associating any other drug.
tachipirina drops, solution contains.
sorbitol: u would be caution in patients suffering from rare hereditary problems of fruit inlerance.
propylene glycol that can cause symptoms to imili to those caused by alcohol.
the syrup contains sucrose: u would be caution in patients with rare hereditary problems of fructose illegics, by malabsorption of-galattose, obey insufficiency of sucrase-isomaltase; this is also taken into account for use in diabetic patients and in patients who follow hypocaloric tedy regimes.
methyl parahydroxybenzoate that can cause allergic reactions (also delayed). Font style = "vertical-align: inherit;"> interactions:
the oral absorption of paracetamol depends on the speed of gastric emptying.
therefore, the concomitant administration of drugs that slow down (e.g.
anticholinergic, opioids) or increase ano (e.g.
procinetics) the speed of gastric emptying can concern a habitability biodysp ' of the product.
Concomitant administration of Colestira Mina reduces the absorption of paracetamol.
contemporary intake to paracetamol and chloramfeniculus can induce an increase in the emivit to chloramfenicolo, with the risk of raising its toxicity.
the concomitant use of paracetamol (4 g per day for at least 4 days) with oral ncoagulants can
in these cases it must be conducted in a more frequent monitoring of the values ​​of INR during the concomitant use and after its interruption.
use with extreme caution and under strict control during chronic treatment with drugs that can induction of liver lives or in case of exposure to substances that can true this effect (for example rifampicin, cimetidine, anti -epileptics such as glutimmide , phenobarbital, carbamazepine).
The same applies to the cases of ethitism and in patients treated with Zidovudine.
the top action of paracetamol can interfere with the determination of the Cemia agency (media the method of phosphotong acid) and with that of blood sugar (through the method of function-oxidase-peroxidase).

unwanted effects:
pathologies of the emolinfopoietic system: trombocytopenia, leukopenia, in nemia, agranulocytosis.
disorders of the immune system: reactions of the persensilitities (urticaria, edema of the larynx, angioedema, shock ana filactic).
Pathology of the nervous system: dizziness.
Gastro intestinal pathologies: gastrointestinal reaction.
hepatobiliary pathologies: abnormal hepatic onalitas, hepatitis.
pathologies of the skin and subcutaneous tissue: Erythema Multiform, Stevens Johnson syndrome, Epidermal ISI Necrol, rash.
Renal and urinary pathologies: acute renal icing insuff, interstitial nephritis, hematuria, anuria.

pregnancy and breastfeeding:
despite clinical studies in pregnant or breastfeeding patients did not highlight Particular contraindications to the use of paracetamol or nor undesirable effects against the mother or child or, it is recommended to administer the product only in cases of effective need and under the direct control of the doctor.

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