Coldrex Junior Hot Drink bags, 10 pc. (cetamol, Phenylephrine, Ascorbic acid)
Special Price
$22.95
Regular Price
$27.00
In stock
SKU
newyork464171
Latin name
STALORAL BIRCH dopplefflp8 solution for use POLLEN ALLERGEN a drug. It is used in children 6-12 years old to eliminate flu symptoms and colds, such as:
fever
headache
chills
joint and muscle pain
nasal congestion
pain in the sinuses and throat. *
* Instructions for medical use, RU P N015713 / 01 Buy Coldrex Junior Hot Drink bags, 10 pc. (cetamol, Phenylephrine, Ascorbic acid) in newyork free shipping. Fast international shipping USA, AU, EU, UK and others.
STALORAL BIRCH dopplefflp8 solution for use POLLEN ALLERGEN a drug. It is used in children 6-12 years old to eliminate flu symptoms and colds, such as:
fever
headache
chills
joint and muscle pain
nasal congestion
pain in the sinuses and throat. *
* Instructions for medical use, RU P N015713 / 01 Buy Coldrex Junior Hot Drink bags, 10 pc. (cetamol, Phenylephrine, Ascorbic acid) in newyork free shipping. Fast international shipping USA, AU, EU, UK and others.
Latin name
STALORAL BIRCH dopplefflp8 solution for use POLLEN ALLERGEN a drug. It is used in children 6-12 years old to eliminate flu symptoms and colds, such as:
fever
headache
chills
joint and muscle pain
nasal congestion
pain in the sinuses and throat. *
* Instructions for medical use, RU P N015713 / 01
Description
Powder for solution for oral administration (for children) heterogeneous, white to pale yellow, with a lemon smell
dissolves in 125 ml of hot water with the formation of a cloudy solution from yellow to yellow-green, which does not have the surface of the foam, with the smell of lemon
, a slight precipitate is possible.
Release form
3 g per laminate bag: paper / polyethylene / aluminum foil / polyethylene.
10 sachets along with instructions for use are placed in a cardboard box.
ФармакологичРскоРдРйствимbr>
Комбинированн й прРпарат для симптоматичРского лРчРния остр х рРспираторн х заболРваний.
ПарацРтамол оказ ваРт жаропонижающРР, анальгРзирующРРдРйствиР.
ФРнилэфрина гидрохлорид - симпатомимРтик, сужаРт сосуд слизистой оболочки носа и околоносов х пазух, вслРдствиРчРго умРньшаРтся отРк и облРгчаРтся носовоРд ханиР.
Аскорбиновая кислота восполняРт пов шРнную потрРбность в витаминРС при простудн х заболРваниях и гриппР.
Indications
To eliminate the symptoms of acute respiratory infections and flu in children aged 6-12 years, including: - elevated body temperature
- headache
- chills
- pain in joints and muscles
- nasal congestion
- pain in the sinuses of the nose and throat.
Contraindications
- hypersensitivity to the components of the drug
- severe liver disease
- severe kidney disease
- hematopoietic system
- thyrotoxicosis
- arterial hypertension, acute myocardial infarction, acute heart disease tachyarrhythmias)
- prostatic hyperplasia
- angle-closure glaucoma
- diabetes mellitus
- genetic lack of glucose-6-phosphate dehydrogenase
- deficiency of sucrose / isomaltase, intolerance to fructose, glucose malactose, the preparation includes sucrose
- the simultaneous administration of tricyclic antidepressants, beta-blockers, MAO inhibitors and the period up to 14 days after their withdrawal
- children under 6 years of age.
If your child has one of the following diseases / conditions / risk factors, be sure to consult your doctor before taking the drug:
Benign hyperbilirubinemia.
Impaired liver and kidney function of mild to moderate severity.
Diseases of the prostate and problems with urination.
Cardiovascular disease, including high blood pressure, obliterating vascular disease (Raynaud's syndrome).
Glaucoma (excluding angle-closure glaucoma).
Pheochromocytoma.
The presence of severe infections, including sepsis, because taking the drug may increase the risk of metabolic acidosis.
Patients with glutathione deficiency (in particular, extremely malnourished patients suffering from anorexia, chronic alcoholism or patients with a low body mass index).
Use during pregnancy and lactation
The drug is intended for adolescents
Composition
Paracetamol 300 mg,
phenylephrine hydrochloride 5 mg,
ascorbic acid 20 mg.
Excipients:
sodium saccharinate,
sodium cyclamate,
citric acid,
sodium citrate,
corn starch,
sucrose,
lemon flavor (610399E),
dye silica curcumin.
Dosage and administration
For oral administration.
Do not exceed the indicated dose!
Use the lowest dose necessary to achieve the effect within the shortest possible time of treatment!
The minimum interval between doses of Coldrex Junior should be at least 4 hours.
Pour the contents of 1 sachet into a mug, pour about 125 ml of hot water, stir until dissolved. If necessary, add cold water and sugar.
Children 6 to 12 years of age: 1 sachet every 4 to 6 hours, but not more than 4 sachets per day. The maximum daily dose should not exceed 4 sachets. The maximum duration of the drug without consulting a doctor is no more than 3 days.
Do not take concomitantly with other paracetamol-containing agents, decongestants and agents to alleviate the symptoms of the common cold and flu, as well as ethanol-containing agents and drinks.
If symptoms of the disease persist while taking the drug, consult a doctor.
Side effects
Determination of the frequency of side effects: very often ( 1/10), often ( 1/100 and <1/10), infrequently ( 1/1000 and <1/100), rarely ( 1 / 10 000 and <1/1000), very rarely ( 1/100 000 and <1/10 000).
At recommended doses, the drug is usually well tolerated.
Paracetamol rarely has a side effect.
With prolonged use in excess of the recommended dose, hepatotoxic and nephrotoxic effects may be observed.
From the hemopoietic system: very rarely - thrombocytopenia.
Allergic reactions: rarely - skin rash, urticaria, allergic dermatitis very rarely - anaphylaxis, hypersensitivity reactions, incl. angioedema, Stevens-Johnson syndrome.
From the respiratory system: very rarely - bronchospasm in patients sensitive to acetylsalicylic acid and other NSAIDs.
From the digestive system: very rarely - nausea, vomiting, impaired liver function.
From the side of the central nervous system: very rarely - dizziness, headache, insomnia.
From the sensory organs: rarely - mydriasis, an acute attack of glaucoma in most cases in patients with angle-closure glaucoma.
From the cardiovascular system: rarely - tachycardia, palpitations, increased blood pressure.
From the urinary system: very rarely - dysuria, urinary retention in patients with obstruction of the outlet of the bladder with prostatic hypertrophy.
In the event of any adverse reactions, the patient should consult a doctor.
Drug Interaction
Paracetamol
Enhances the effects of MAO inhibitors, sedatives, ethanol.
The risk of hepatotoxic action of paracetamol increases with the concomitant use of barbiturates, phenytoin, phenobarbital, carbamazepine, rifampicin, isoniazid, zidovudine and other inducers of liver microsomal enzymes.
With long-term regular use of paracetamol, the anticoagulant effect of warfarin and other coumarins may be increased, with the risk of bleeding increasing. Single administration of paracetamol has no significant effect.
Metoclopramide increases the rate of absorption of paracetamol and reduces the time to reach its Cmax in blood plasma. Similarly, domperidone can increase the rate of absorption of paracetamol.
Paracetamol may increase T1 / 2 chloramphenicol.
Paracetamol is able to reduce the bioavailability of lamotrigine, while reducing the effectiveness of lamotrigine due to the induction of its metabolism in the liver.
The absorption of paracetamol may be reduced when used with cholestyramine, but the absorption is negligible if cholestyramine is taken an hour later.
Regular administration of paracetamol with zidovudine can cause neutropenia and increase the risk of liver damage.
Probenecid affects the metabolism of paracetamol. Patients using probenecid concomitantly should reduce the dose of paracetamol.
The hepatotoxicity of paracetamol is exacerbated by prolonged excessive use of ethanol (alcohol).
Paracetamol can affect the results of a uric acid test using a phosphovalframate precipitating reagent.
Pheniramine
The effects of other substances on the CNS (eg MAO inhibitors, tricyclic antidepressants, alcohol, antiparkinsonian drugs, barbiturates, tranquilizers and narcotics) may be increased. Pheniramine can inhibit the action of anticoagulants.
Phenylephrine
Teraflu® for influenza and cold is contraindicated in patients receiving or receiving MAO inhibitors within the last 2 weeks. Phenylephrine can potentiate the effects of MAO inhibitors and cause hypertensive crises.
Concomitant administration of phenylephrine with other sympathomimetic drugs or tricyclic antidepressants (eg, amitriptyline) may increase the risk of adverse reactions by the cardiovascular system.
Phenylephrine may reduce the effectiveness of beta-blockers and other antihypertensive drugs (eg, debrizochina, guanethidine, reserpine, methyldopa). It is possible to increase the risk of hypertension and other side effects from the cardiovascular system.
Co-administration of phenylephrine with digoxin and cardiac glycosides may increase the risk of heart rhythm disturbance or myocardial infarction.
Concomitant use of phenylephrine with ergot alkaloids (ergotamine and methysergide) may increase the risk of ergotism Episodic intake of a single dose of the drug has no significant effect on the effect of indirect anticoagulants.
Inducers of enzymes of microsomal oxidation in the liver (barbiturates, diphenin, carbamazepine, rifampicin, zidovudine, phenytoin, ethanol, flumecinol, phenylbutazone and tricyclic antidepressants) increase the risk of hepatotoxic action.
Microsomal oxidation inhibitors (cimetidine) reduce the risk of hepatotoxic action.
Paracetamol reduces the effectiveness of diuretics.
Metoclopramide and domperidone increase, and cholestyramine reduces the absorption rate of paracetamol.
Paracetamol enhances the effects of MAO inhibitors, sedatives, ethanol.
Phenylephrine, when taken with MAO inhibitors, can lead to increased blood pressure.
Phenylephrine reduces the effectiveness of beta-blockers and antihypertensive drugs, increases the risk of hypertension and disorders of the cardiovascular system.
Tricyclic antidepressants increase the sympathomimetic effect of phenylephrine, and may increase the risk of side effects from the cardiovascular system.
Co-administration of halothane with phenylephrine increases the risk of ventricular arrhythmia.
Phenylephrine reduces the hypotensive effect of guanethidine, which in turn enhances the alpha-adrenostimulating activity of phenylephrine.
Antidepressants, antiparkinsonian agents, antipsychotics, phenothiazine derivatives increase the risk of urinary retention, dry mouth, constipation.
Co-administration of ACS with phenylephrine increases the risk of glaucoma.
When used with digoxin and cardiac glycosides, the risk of developing heart rhythm or heart attack may be increased.
Ascorbic acid, when used concurrently with iron preparations, thanks to its restorative properties, converts trivalent iron into divalent, which helps to improve its absorption.
When used concurrently, ascorbic acid increases iron excretion in patients receiving deferoxamine.
When administered concurrently with barbiturates, primidone increases urinary excretion of ascorbic acid.
High-dose ascorbic acid can lower urinary pH, which, when used simultaneously, reduces tubular reabsorption of amphetamine and tricyclic antidepressants.
Acetylsalicylic acid reduces the absorption of ascorbic acid by about a third when used simultaneously.
When used with warfarin, the effects of warfarin may be reduced.
When used with tetracycline, urinary excretion of ascorbic acid is increased.
overdose
In the event of an overdose of Caldrex® Junior (even if you are feeling well), the risk of delayed signs of serious liver damage should be considered.
Symptoms caused by paracetamol: for 24 hours - pale skin, decreased appetite, nausea, vomiting, abdominal pain. After 12-48 h, signs of impaired liver function, signs of impaired glucose metabolism and metabolic acidosis may occur.
In the case of severe poisoning, severe hepatic failure may develop up to hepatic encephalopathy, coma and death.
Acute renal failure with acute tubal necrosis, which is diagnosed by severe lumbar pain, hematuria and proteinuria, can develop without severe liver dysfunction. There have been reports of cardiac arrhythmias and pancreatitis with an overdose of paracetamol.
In the early period, symptoms may be limited only by nausea and vomiting and may not reflect the severity of the overdose or the degree of risk of damage to the internal organs.
Treatment: Within the first hour after the presumed overdose, it is advisable to administer activated charcoal inside. 4 or more hours after the presumed overdose, a determination of the plasma concentration of paracetamol is required (earlier determination of the paracetamol concentration may be unreliable).
A specific antidote for paracetamol poisoning is acetylcysteine. Acetylcysteine treatment can be performed up to 24 h after administration of paracetamol, however, the maximum hepatoprotective effect can be obtained within the first 8 h after overdose. After that, the effectiveness of the antidote drops sharply. If necessary, acetylcysteine can be given in / in.
In the absence of vomiting, the alternative (in the absence of the possibility of rapid inpatient care) is the appointment of methionine inside. Treatment of patients with severe liver dysfunction 24 hours after taking acetaminophen should be carried out in conjunction with specialists of the toxicology center or specialized department of diseases however, the maximum hepatoprotective effect may be obtained within the first 8 h after overdose. After that, the effectiveness of the antidote drops sharply. If necessary, acetylcysteine can be given in / in.
In the absence of vomiting, the alternative (in the absence of the possibility of rapid inpatient care) is the appointment of methionine inside. Treatment of patients with severe liver dysfunction 24 hours after taking acetaminophen should be carried out in conjunction with specialists of the toxicology center or specialized department of diseases however, the maximum hepatoprotective effect may be obtained within the first 8 h after overdose. After that, the effectiveness of the antidote drops sharply. If necessary, acetylcysteine can be given in / in.
In the absence of vomiting, the alternative (in the absence of the possibility of rapid inpatient care) is the appointment of methionine inside. Treatment of patients with severe liver dysfunction 24 hours after taking acetaminophen should be carried out in conjunction with specialists of the toxicology center or specialized department of diseases an alternative (in the absence of rapid inpatient care) is the appointment of methionine inside. Treatment of patients with severe liver dysfunction 24 hours after taking acetaminophen should be carried out in conjunction with specialists of the toxicology center or specialized department of diseases an alternative (in the absence of rapid inpatient care) is the appointment of methionine inside. Treatment of patients with severe liver dysfunction 24 hours after taking acetaminophen should be carried out in conjunction with specialists of the toxicology center or specialized department of diseasesroast.
Symptoms caused by phenylephrine: irritability, headache, dizziness, insomnia, increased blood pressure, nausea, vomiting, increased excitability, reflex bradycardia. In severe cases of overdose development of hallucinations, confusion, convulsions, arrhythmias is possible.
Treatment: symptomatic therapy with severe hypertension using alpha-blockers such as phentolamine.
Symptoms caused by ascorbic acid: ascorbic acid in high doses (more than 3000 mg) can cause temporary osmotic diarrhea and gastrointestinal disorders such as nausea, stomach discomfort.
The manifestations of ascorbic acid overdose can be categorized as those caused by severe liver damage as a result of paracetamol overdose.
Treatment: symptomatic, forced diuresis.
Storage conditions
The drug should be stored out of the reach of children at a temperature not exceeding 25 ° C.
Expiration
3 years. Do not use after the expiry date stated on the package
Deystvuyuschee substances
Paracetamol, phenylephrine, ascorbic acid
Terms of sale from pharmacies
fpf8fp8pf88fp8 pff8pf8pf8pf8pf8pf8pf8pf8pf8pf8
Over-the-counter
GlaxoSmithKline, UK
Coldrex Junior Hot Drink bags, 10 pc. (cetamol, Phenylephrine, Ascorbic acid) florida in pharmacy online. Cheap price, instruction, side effects, dosage. Coldrex Junior Hot Drink bags, 10 pc. - Sale. PayPal accept. Free shipping florida. Fast international shipping.
STALORAL BIRCH dopplefflp8 solution for use POLLEN ALLERGEN a drug. It is used in children 6-12 years old to eliminate flu symptoms and colds, such as:
fever
headache
chills
joint and muscle pain
nasal congestion
pain in the sinuses and throat. *
* Instructions for medical use, RU P N015713 / 01
Description
Powder for solution for oral administration (for children) heterogeneous, white to pale yellow, with a lemon smell
dissolves in 125 ml of hot water with the formation of a cloudy solution from yellow to yellow-green, which does not have the surface of the foam, with the smell of lemon
, a slight precipitate is possible.
Release form
3 g per laminate bag: paper / polyethylene / aluminum foil / polyethylene.
10 sachets along with instructions for use are placed in a cardboard box.
ФармакологичРскоРдРйствимbr>
Комбинированн й прРпарат для симптоматичРского лРчРния остр х рРспираторн х заболРваний.
ПарацРтамол оказ ваРт жаропонижающРР, анальгРзирующРРдРйствиР.
ФРнилэфрина гидрохлорид - симпатомимРтик, сужаРт сосуд слизистой оболочки носа и околоносов х пазух, вслРдствиРчРго умРньшаРтся отРк и облРгчаРтся носовоРд ханиР.
Аскорбиновая кислота восполняРт пов шРнную потрРбность в витаминРС при простудн х заболРваниях и гриппР.
Indications
To eliminate the symptoms of acute respiratory infections and flu in children aged 6-12 years, including: - elevated body temperature
- headache
- chills
- pain in joints and muscles
- nasal congestion
- pain in the sinuses of the nose and throat.
Contraindications
- hypersensitivity to the components of the drug
- severe liver disease
- severe kidney disease
- hematopoietic system
- thyrotoxicosis
- arterial hypertension, acute myocardial infarction, acute heart disease tachyarrhythmias)
- prostatic hyperplasia
- angle-closure glaucoma
- diabetes mellitus
- genetic lack of glucose-6-phosphate dehydrogenase
- deficiency of sucrose / isomaltase, intolerance to fructose, glucose malactose, the preparation includes sucrose
- the simultaneous administration of tricyclic antidepressants, beta-blockers, MAO inhibitors and the period up to 14 days after their withdrawal
- children under 6 years of age.
If your child has one of the following diseases / conditions / risk factors, be sure to consult your doctor before taking the drug:
Benign hyperbilirubinemia.
Impaired liver and kidney function of mild to moderate severity.
Diseases of the prostate and problems with urination.
Cardiovascular disease, including high blood pressure, obliterating vascular disease (Raynaud's syndrome).
Glaucoma (excluding angle-closure glaucoma).
Pheochromocytoma.
The presence of severe infections, including sepsis, because taking the drug may increase the risk of metabolic acidosis.
Patients with glutathione deficiency (in particular, extremely malnourished patients suffering from anorexia, chronic alcoholism or patients with a low body mass index).
Use during pregnancy and lactation
The drug is intended for adolescents
Composition
Paracetamol 300 mg,
phenylephrine hydrochloride 5 mg,
ascorbic acid 20 mg.
Excipients:
sodium saccharinate,
sodium cyclamate,
citric acid,
sodium citrate,
corn starch,
sucrose,
lemon flavor (610399E),
dye silica curcumin.
Dosage and administration
For oral administration.
Do not exceed the indicated dose!
Use the lowest dose necessary to achieve the effect within the shortest possible time of treatment!
The minimum interval between doses of Coldrex Junior should be at least 4 hours.
Pour the contents of 1 sachet into a mug, pour about 125 ml of hot water, stir until dissolved. If necessary, add cold water and sugar.
Children 6 to 12 years of age: 1 sachet every 4 to 6 hours, but not more than 4 sachets per day. The maximum daily dose should not exceed 4 sachets. The maximum duration of the drug without consulting a doctor is no more than 3 days.
Do not take concomitantly with other paracetamol-containing agents, decongestants and agents to alleviate the symptoms of the common cold and flu, as well as ethanol-containing agents and drinks.
If symptoms of the disease persist while taking the drug, consult a doctor.
Side effects
Determination of the frequency of side effects: very often ( 1/10), often ( 1/100 and <1/10), infrequently ( 1/1000 and <1/100), rarely ( 1 / 10 000 and <1/1000), very rarely ( 1/100 000 and <1/10 000).
At recommended doses, the drug is usually well tolerated.
Paracetamol rarely has a side effect.
With prolonged use in excess of the recommended dose, hepatotoxic and nephrotoxic effects may be observed.
From the hemopoietic system: very rarely - thrombocytopenia.
Allergic reactions: rarely - skin rash, urticaria, allergic dermatitis very rarely - anaphylaxis, hypersensitivity reactions, incl. angioedema, Stevens-Johnson syndrome.
From the respiratory system: very rarely - bronchospasm in patients sensitive to acetylsalicylic acid and other NSAIDs.
From the digestive system: very rarely - nausea, vomiting, impaired liver function.
From the side of the central nervous system: very rarely - dizziness, headache, insomnia.
From the sensory organs: rarely - mydriasis, an acute attack of glaucoma in most cases in patients with angle-closure glaucoma.
From the cardiovascular system: rarely - tachycardia, palpitations, increased blood pressure.
From the urinary system: very rarely - dysuria, urinary retention in patients with obstruction of the outlet of the bladder with prostatic hypertrophy.
In the event of any adverse reactions, the patient should consult a doctor.
Drug Interaction
Paracetamol
Enhances the effects of MAO inhibitors, sedatives, ethanol.
The risk of hepatotoxic action of paracetamol increases with the concomitant use of barbiturates, phenytoin, phenobarbital, carbamazepine, rifampicin, isoniazid, zidovudine and other inducers of liver microsomal enzymes.
With long-term regular use of paracetamol, the anticoagulant effect of warfarin and other coumarins may be increased, with the risk of bleeding increasing. Single administration of paracetamol has no significant effect.
Metoclopramide increases the rate of absorption of paracetamol and reduces the time to reach its Cmax in blood plasma. Similarly, domperidone can increase the rate of absorption of paracetamol.
Paracetamol may increase T1 / 2 chloramphenicol.
Paracetamol is able to reduce the bioavailability of lamotrigine, while reducing the effectiveness of lamotrigine due to the induction of its metabolism in the liver.
The absorption of paracetamol may be reduced when used with cholestyramine, but the absorption is negligible if cholestyramine is taken an hour later.
Regular administration of paracetamol with zidovudine can cause neutropenia and increase the risk of liver damage.
Probenecid affects the metabolism of paracetamol. Patients using probenecid concomitantly should reduce the dose of paracetamol.
The hepatotoxicity of paracetamol is exacerbated by prolonged excessive use of ethanol (alcohol).
Paracetamol can affect the results of a uric acid test using a phosphovalframate precipitating reagent.
Pheniramine
The effects of other substances on the CNS (eg MAO inhibitors, tricyclic antidepressants, alcohol, antiparkinsonian drugs, barbiturates, tranquilizers and narcotics) may be increased. Pheniramine can inhibit the action of anticoagulants.
Phenylephrine
Teraflu® for influenza and cold is contraindicated in patients receiving or receiving MAO inhibitors within the last 2 weeks. Phenylephrine can potentiate the effects of MAO inhibitors and cause hypertensive crises.
Concomitant administration of phenylephrine with other sympathomimetic drugs or tricyclic antidepressants (eg, amitriptyline) may increase the risk of adverse reactions by the cardiovascular system.
Phenylephrine may reduce the effectiveness of beta-blockers and other antihypertensive drugs (eg, debrizochina, guanethidine, reserpine, methyldopa). It is possible to increase the risk of hypertension and other side effects from the cardiovascular system.
Co-administration of phenylephrine with digoxin and cardiac glycosides may increase the risk of heart rhythm disturbance or myocardial infarction.
Concomitant use of phenylephrine with ergot alkaloids (ergotamine and methysergide) may increase the risk of ergotism Episodic intake of a single dose of the drug has no significant effect on the effect of indirect anticoagulants.
Inducers of enzymes of microsomal oxidation in the liver (barbiturates, diphenin, carbamazepine, rifampicin, zidovudine, phenytoin, ethanol, flumecinol, phenylbutazone and tricyclic antidepressants) increase the risk of hepatotoxic action.
Microsomal oxidation inhibitors (cimetidine) reduce the risk of hepatotoxic action.
Paracetamol reduces the effectiveness of diuretics.
Metoclopramide and domperidone increase, and cholestyramine reduces the absorption rate of paracetamol.
Paracetamol enhances the effects of MAO inhibitors, sedatives, ethanol.
Phenylephrine, when taken with MAO inhibitors, can lead to increased blood pressure.
Phenylephrine reduces the effectiveness of beta-blockers and antihypertensive drugs, increases the risk of hypertension and disorders of the cardiovascular system.
Tricyclic antidepressants increase the sympathomimetic effect of phenylephrine, and may increase the risk of side effects from the cardiovascular system.
Co-administration of halothane with phenylephrine increases the risk of ventricular arrhythmia.
Phenylephrine reduces the hypotensive effect of guanethidine, which in turn enhances the alpha-adrenostimulating activity of phenylephrine.
Antidepressants, antiparkinsonian agents, antipsychotics, phenothiazine derivatives increase the risk of urinary retention, dry mouth, constipation.
Co-administration of ACS with phenylephrine increases the risk of glaucoma.
When used with digoxin and cardiac glycosides, the risk of developing heart rhythm or heart attack may be increased.
Ascorbic acid, when used concurrently with iron preparations, thanks to its restorative properties, converts trivalent iron into divalent, which helps to improve its absorption.
When used concurrently, ascorbic acid increases iron excretion in patients receiving deferoxamine.
When administered concurrently with barbiturates, primidone increases urinary excretion of ascorbic acid.
High-dose ascorbic acid can lower urinary pH, which, when used simultaneously, reduces tubular reabsorption of amphetamine and tricyclic antidepressants.
Acetylsalicylic acid reduces the absorption of ascorbic acid by about a third when used simultaneously.
When used with warfarin, the effects of warfarin may be reduced.
When used with tetracycline, urinary excretion of ascorbic acid is increased.
overdose
In the event of an overdose of Caldrex® Junior (even if you are feeling well), the risk of delayed signs of serious liver damage should be considered.
Symptoms caused by paracetamol: for 24 hours - pale skin, decreased appetite, nausea, vomiting, abdominal pain. After 12-48 h, signs of impaired liver function, signs of impaired glucose metabolism and metabolic acidosis may occur.
In the case of severe poisoning, severe hepatic failure may develop up to hepatic encephalopathy, coma and death.
Acute renal failure with acute tubal necrosis, which is diagnosed by severe lumbar pain, hematuria and proteinuria, can develop without severe liver dysfunction. There have been reports of cardiac arrhythmias and pancreatitis with an overdose of paracetamol.
In the early period, symptoms may be limited only by nausea and vomiting and may not reflect the severity of the overdose or the degree of risk of damage to the internal organs.
Treatment: Within the first hour after the presumed overdose, it is advisable to administer activated charcoal inside. 4 or more hours after the presumed overdose, a determination of the plasma concentration of paracetamol is required (earlier determination of the paracetamol concentration may be unreliable).
A specific antidote for paracetamol poisoning is acetylcysteine. Acetylcysteine treatment can be performed up to 24 h after administration of paracetamol, however, the maximum hepatoprotective effect can be obtained within the first 8 h after overdose. After that, the effectiveness of the antidote drops sharply. If necessary, acetylcysteine can be given in / in.
In the absence of vomiting, the alternative (in the absence of the possibility of rapid inpatient care) is the appointment of methionine inside. Treatment of patients with severe liver dysfunction 24 hours after taking acetaminophen should be carried out in conjunction with specialists of the toxicology center or specialized department of diseases however, the maximum hepatoprotective effect may be obtained within the first 8 h after overdose. After that, the effectiveness of the antidote drops sharply. If necessary, acetylcysteine can be given in / in.
In the absence of vomiting, the alternative (in the absence of the possibility of rapid inpatient care) is the appointment of methionine inside. Treatment of patients with severe liver dysfunction 24 hours after taking acetaminophen should be carried out in conjunction with specialists of the toxicology center or specialized department of diseases however, the maximum hepatoprotective effect may be obtained within the first 8 h after overdose. After that, the effectiveness of the antidote drops sharply. If necessary, acetylcysteine can be given in / in.
In the absence of vomiting, the alternative (in the absence of the possibility of rapid inpatient care) is the appointment of methionine inside. Treatment of patients with severe liver dysfunction 24 hours after taking acetaminophen should be carried out in conjunction with specialists of the toxicology center or specialized department of diseases an alternative (in the absence of rapid inpatient care) is the appointment of methionine inside. Treatment of patients with severe liver dysfunction 24 hours after taking acetaminophen should be carried out in conjunction with specialists of the toxicology center or specialized department of diseases an alternative (in the absence of rapid inpatient care) is the appointment of methionine inside. Treatment of patients with severe liver dysfunction 24 hours after taking acetaminophen should be carried out in conjunction with specialists of the toxicology center or specialized department of diseasesroast.
Symptoms caused by phenylephrine: irritability, headache, dizziness, insomnia, increased blood pressure, nausea, vomiting, increased excitability, reflex bradycardia. In severe cases of overdose development of hallucinations, confusion, convulsions, arrhythmias is possible.
Treatment: symptomatic therapy with severe hypertension using alpha-blockers such as phentolamine.
Symptoms caused by ascorbic acid: ascorbic acid in high doses (more than 3000 mg) can cause temporary osmotic diarrhea and gastrointestinal disorders such as nausea, stomach discomfort.
The manifestations of ascorbic acid overdose can be categorized as those caused by severe liver damage as a result of paracetamol overdose.
Treatment: symptomatic, forced diuresis.
Storage conditions
The drug should be stored out of the reach of children at a temperature not exceeding 25 ° C.
Expiration
3 years. Do not use after the expiry date stated on the package
Deystvuyuschee substances
Paracetamol, phenylephrine, ascorbic acid
Terms of sale from pharmacies
fpf8fp8pf88fp8 pff8pf8pf8pf8pf8pf8pf8pf8pf8pf8
Over-the-counter
GlaxoSmithKline, UK
Coldrex Junior Hot Drink bags, 10 pc. (cetamol, Phenylephrine, Ascorbic acid) florida in pharmacy online. Cheap price, instruction, side effects, dosage. Coldrex Junior Hot Drink bags, 10 pc. - Sale. PayPal accept. Free shipping florida. Fast international shipping.
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