Tachipirina Flashtab 16 Tablets 500 mg

€8.90
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Minsan
034329058
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WARNINGS
Do not exceed the recommended dose. Prolonged use of the product, other than medical supervision, can be harmful. This product should only be used if strictly necessary. Doses higher than those recommended carry a risk of very serious liver damage. Treatment with an antidote should be performed as soon as possible. To avoid the risk of overdose, patients should be advised to avoid concomitant use of other medicines containing paracetamol. This medicine contains aspartame, a source of phenylalanine, equivalent to 0.2 mg per tablet and, therefore, is contraindicated in subjects with phenylketonuria. Paracetamol should be used with caution in case of: adults weighing less than 50 kg; mild to moderate hepatocellular insufficiency (note: paracetamol is contraindicated in cases of severe hepatocellular insufficiency); chronic alcoholism; chronic malnutrition (low reserves of hepatic glutathione); dehydration; severe renal insufficiency (creatinine clearance <= 10 ml / min). In case of high fever, or signs of secondary infection, or persistence of symptoms beyond 3 days, a re-evaluation of the treatment should be carried out. During prolonged treatment with analgesic drugs, carried out with doses higher than those provided in the package leaflet, headache may occur that should not be treated with higher doses of the drug. In general, the habitual use of analgesics, especially the combination of different analgesic drugs, can lead to permanent renal lesions with the risk of renal failure (analgesic nephropathy). If this situation occurs or if its onset is suspected, it is necessary to consult the doctor and stop the treatment. The diagnosis of "analgesic overuse headache" should be considered in those patients who suffer from frequent or daily headaches despite (or due to) the regular use of headache medications.
PHARMACOTHERAPEUTIC CATEGORY
Analgesics and antipyretics, anilides.
STORAGE
This medicine does not require any special storage conditions.
CONTRAINDICATIONS / SECONDARY EFFECT
Hypersensitivity 'to paracetamol or to any of the listed excipients. Phenylketonuria (due to the presence of aspartame). Severe hepatocellular insufficiency.
NAME
TACHIPIRINA FLASHTAB 500 MG GOLD DISPERSIBLE TABLETS
EXCIPIENTS
Coated paracetamol crystals: basic butylated methacrylate copolymer; 30% polyacrylate dispersion; silica, colloidal hydrophobic. Tablet: mannitol (granules, powder), crospovidone, aspartame (E951), currant flavor, magnesium stearate.
SIDE EFFECTS
Hepatobiliary disorders. Rare (> = 1/10000 to <1/1000): hepatic transaminase levels increased. Disorders of the immune system. Very rare (<1/10000), not known: hypersensitivity reaction '(from simple skin rash or urticaria, up to anaphylactic shock requiring treatment interruption). Disorders of the blood and lymphatic system. Very rare, not known: thrombocytopenia, leukopenia, neutropenia (sporadic reports).
PREGNANCY AND BREASTFEEDING
Epidemiological data on the use of therapeutic oral doses of paracetamol show no adverse effects on pregnancy or on the health of the fetus / newborn. Prospective data on pregnancies exposed to overdoses did not show an increase in the risk of malformations. Reproduction studies performed with oral administration did not show any malformation or fetotoxic effects. Consequently, in normal conditions of use, paracetamol can 'be used during pregnancy after an assessment of the risk-benefit ratio. During pregnancy, paracetamol should not be taken for long periods, in high doses or in combination with other medicines, since the safety of use in these cases has not been established. After oral administration, paracetamol is excreted in breast milk in small quantities. No undesirable effects have been reported in breastfed infants. Therapeutic doses of this medicine can be taken during breastfeeding.
INDICATIONS
Symptomatic treatment of mild to moderate pain and / or fever.
INTERACTIONS
Probenecid causes at least a 2-fold reduction in paracetamol clearance through inhibition of its conjugation with glucuronic acid. In case of concomitant treatment with probenecid a dose reduction of paracetamol should be considered. Salicylamide may prolong the elimination half-life of paracetamol. Paracetamol should be used with caution in case of concomitant intake of enzyme inducers (such as carbamazepine, phenobarbital, phenytoin, primidone, rifampicin, St. John's wort or St. John's wort) or potentially hepatotoxic substances. Metoclopramide and domperidone: accelerate the absorption of paracetamol. Cholestyramine: reduces the absorption of paracetamol. The concomitant use of paracetamol (4 g per day for at least 4 days) with oral anticoagulants can induce slight variations in the INR values with a consequent increase in the risk of bleeding. In these cases, more frequent monitoring of INR values should be performed during concomitant use and after its discontinuation. Interactions with clinical tests: the administration of paracetamol can alter the dosage of uric acid in the blood, obtained with the phosphotungstic acid method, and the dosage of glycaemia obtained with the glucose oxidase-peroxidase method.
DOSAGE
This medicine is for adults only. The maximum recommended dosage is 3000 mg of paracetamol per day, corresponding to 6 tablets per day. The usual dosage is 1 tablet of 500 mg, to be repeated if necessary after not less than four hours. In the case of severe pain or high fever, 2 tablets of 500 mg to be repeated if necessary after not less than four hours. Do not exceed 6 tablets of 500 mg in 24 hours. Maximum recommended dosage: the total dose of paracetamol should not exceed 3 g per day for adults. Frequency of administration: In adults, administration should be performed at intervals of at least 4 hours. Renal insufficiency: in case of severe renal insufficiency, the interval between 2 administrations should be at least 8 hours. Method of administration: oral route. The tablet should be sucked and not chewed. It can be dispersed in half a glass of water.
ACTIVE PRINCIPLES
Each orodispersible tablet contains 500 mg paracetamol (as coated paracetamol crystals).
Angelini
034329058
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Tachipirina Flashtab 16...

€8.90