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Tachifludec adults 10 orange taste sachets for the treatment of flu symptoms

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tachifludc 10 sachets taste orange for the treatment of the symptoms of the influence

illustrative leaflet aifa

what is tachifludc

tachifludec is an analgesic based on paracetamol and phenylefrin hydrochloride.

active ingredients:

Each sachet contains: Paracetamol 600 mg, Ascorbic acid 40 mg and phenylefrine hydrochloride 10 mg (equal to phenylefrin 8.2 mg).

< Font style = "vertical-align: inherit;"> excipients:

saccharose, anhydrous citric acid, sodium citrate, corn starch, cyclated sodium, sodium sucrine, colloidal silice anhydra, red orange aroma, sunset yellow (and 110 ).


short-term treatment of colds and flu symptoms, Including mild/moderate entity pain and fever, when associated with nasal congestion

< Font Style = "Vertical-Align: inherit;"> CONTRAINDICATIONS/EFF. SECOND:

children and adolescents under the age of 18.

Hypersensitivity to the active ingredients or to any of the excipients.

patients who take non-beta-blockers.

patients taking tricyclic antidepressants and those who take or have taken in the 2 weeks inhibitors of the monoamine oxidase.

patients with bronchial, feocrocitoma, closed angle glaucoma, or who simultaneously take other medicines me appetite and psychostimulating deco dell similar to similaritamines.

patients affected by liver or renal insufficiency, diabetes, hyperthyroidism, hypertension and cardiovascular diseases. = "vertical-align: inherit;"> paracetamol products are contraindicated in patients with manifest insufficiency of -6-phosphate dehydrogenase and in those with severe hemolytic anemia.
< /p>

severe hepocellular insufficiency.


adults: 1 sachet every 4-6 hours and up to a maximum of 3 sachets in the 24 hours.

the medicine must not be used for more than 3 consecutive days without a lower drug for children and teenagers under the age of 18: the job of the drug is not recommended in children in age to 1 years.

way of administration: dissolve the content of a sachet in a glass of cold water ao cold and sweeten at will.

once the medicine is dissolved from a place to an opalescent solution of orange color, without foreign particles e with orange flavor

conservation :

Ratura less than 25 degrees c.

Store in the original container to protect the product from humidity.


Patients should be notified not to take other medicines with lieutenant paracetamol while the drug elevates as paracetamol can react serious adverse.

avoid alcohol consumption during treatment.

the danger of overdose is in fact greater in patients with liver problems.
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invite the patient to contact the doctor before associating warfarin or any other drug.

the use of the product is not recommended if the patient is in treatment with anti-inflammatory. < /font>

consult the doctor before using the product in patients with enlargement of the prostate gland or occlusive vascular diseases (e.g. Raynaud of Raynaud) do not exceed the recommended dose and not administer for over 3 consecutive days without spending the doctor.

< Font style = "vertical-align: inherit;"> the medicine contains 5.9 mmoli (135.8 mg) of sodium per sachet: to be taken into consideration in patients with reduced renal function or which follow a low sodium diet; sucrose: patients suffering from rare hereditary problems of fructose intolerance, by malabsorption of insufficiency of Sucrasi-Isomaltase do not have to take this medicine. < /font>

patients with diabetes should take into consideration the content of sucrose inside the product when they take more than 2 sachets per day (Saccarosio & GT; 5G); yellow azo dyes TR am statement 110 that can react (allergic.


paracetamol: the hepatotoxic effect of paracetamol can be unnitted from the intake of other drugs active on the liver, such as the vudine zido and the isoniazide that can produce An inhibition of the SMO metabols of paracetamol.

The administration of probenecid before Paracetamol reduces the clearance of paracetamol and the urinary elimination of the Paracetamol sulfate and paracetamol-glucoronide, and increases the half-life of the paracetamol itself.

use with e Street caution and under strict control during chronic treatment with drugs that may contain the induction of liver monoxygnais or in the event of an expo sion to which substances may have this effect (for example, Rifampi China, Cimetidine, anti -epileptics such as glutetimmide, Fenobarbital, Bamazepine car ).

the paracetamol increases L 'half-life of chloramfenicolo.

the Product taken in high doses can enhance the effect of the cumarinic anticulants (Warfarin) Meclframide and Domperidone can lie the absorption of paracetamol while it is reduced respectively or rit arded by cholestiramine and anticholinergic.

fe nilefrine: the phenylefrin can antag izzare the effect of Bet A-Biloccanti and Antihypertensive drugs (including, Guanetidine, res erpine and methildopa) and can enhance the action of the inhibitors of the m Onaminooxidase.

the contemporary use of phenylefrin with tricyclic pressy pains or cute mimetics can increase the r Ischio of cardiovascular effects.

Fenilefrine can interact with digoxin and with cardiac glycosids by increasing the risk of arrhythmia or heart attack, and with alkaloid (ergotamine and methyl giving) and menting the risk of ergotic.

ascorbic acid: ascorbic acid can increase the absorption of iron and estrogen.

the ASC orbic acid is metabolized, and can be added to bones in patients of hyperpoxaluria and kidney stones through the crystallization of the Calcium oxalate in tendon patients to form calcium of calcium interference with some laboratory tests The paracetamol action can interfere with the determination of the UCO (through the method of phosphotun acid) and with that of blood sugar (through the method of Ossidase-peroxidase function).

Ascorbic acid can interfere in the measurement of the tumical and urinary hema parameters (e.g. vati, glucose, bilirubin, hemoglobin).

indulgeted effects:

below These are the side effects organized according to the classification for Systems and organs.

frequency is so defined: very common (& gt; = 1/10), common (from & gt; = 1/100 a & lt; 1/10), not co mune (from & gt ; = 1/1000 A & LT; 1/100), Rare (Da & GT; = 1/10,000 A & LT; 1/1000), very rar or (& lt; 1/10,000), not known (the frequency cannot be defined on the basis of the available data).

Pathology of the emolinphopoietic system.

Rar to: agranulocytosis, leukopenia, trombocytopenia; not known: anemia.

dyst urbi of the immune system.

rare: allergic reactions, hypersensitivity reactions, anaphylaxis; not known: anaphylactic shock.

disorders of metabolism and nutrition.

common: anorexia.

psychiatric disorders.

very rare: insomnia, nervousness, anxiety, restlessness, confusio ne, irritability.

pathology of the nervous system.

very rare: tremor, dizziness, headache.

pathology of the eye.

does not notice: mydriasis, acute angle acute glaucoma.

cardiac pathology.

< Font style = "vertical-align: inherit;"> rare: tachycardia, palpitations.

< Font style = "vertical-align: inherit;"> vascular pathologies.

not known.


Respiratory, thoracic and mediastinic pathologies.

rare: bronchospasm; not known: edema della larynx.

gastrointestinal pathologies.

common: nausea, vomiting; not known: diarrhea, gastrointestinal pathology.

hepatobiliary pathologies.

rare: abnormal liver function; not known: liver pathology, hepatitis.

pathologies of the skin and subcutaneous tissue.

rare: rash, angioedema; not known: epidermal toxic necrolysis, stevens-johnson syndrome, multifaceted erythema or polymorphic.

kidney and urinary disorders.

< p> very rare: tubulinterse nefrite (after prolonged use of paracetamol with high doses); not known: renal failure aggravat a, hematuria, anuria, retention of urine.

> report an adverse reaction suspected through the Italian drug agency.

pregnancy and breastfeeding:


< Font style = "vertical-align: inherit;"> epidemiological studies in pregnant women have shown that there are no contraindications in the use of paracetamol when used in doses, but the Administration of the preparation in pregnancy and in the breastfeeding must take place under direct control or of the doctor.

phenylefrine: the data relating to the use of phenylephrine in pregnancy are limited.

the vasoconstriction of the uterine vessels and the reduction of the blood flow at the level of the uterus associated with the use of phenylephrine can dare to place fetal hypoxia.

the use of phenylephrine in pregnancy must to be avoided since they are needed in ascorbic acid formations. Align: Inherit; "> There are no controlled data relating to pregnancy Font style = "vertical-align: inherit;"> the use of ascorbic acid in pregnancy is recommended only when the benefit exceeds the risk.

paracetamol: par acetamol is excreed in breast milk but in clinically non-significant quantities.

data available not to contraindic the employment during breastfeeding. < /font>

phenylefrine: they are not available from ATI relating to the excretion of the phenylephrine in breast milk nor no information reported relating to the effects of phenylephrine on breastfeed children. -Align: inherit; "> in the absence of available data, the use of phenylephrine must be avoided during breastfeeding.

acid ascorbi co: the ac: Ido Ascorbico is excreted in breast milk.

The effects on breastfed children are not known. vertical-align: inherit; "> in summary the use is not rich in pregnancy and breastfeeding.

there is no evidence in non-clinical studies that seem to be the effects of paracetamol on male and female wounds at the commonly used doses in the clinic.

the effect has not been studied of the phenylephrine on male fertility and female.

there are sufficient evidence that underline the importance Ascorbic acid at different levels in the reproductive process.

however, definitive data are not available in man on the potential c linte of vitamin C.

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