Combigripp Hot Sip with raspberry flavor 10 sachets — Made in India — Free Delivery
(Combigripp Hot Sip)
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Description Combigripp Hot Sip with raspberry flavor 10 sachets — Made in India — Free Delivery
Product description
Powder for oral solution with raspberry flavor in a sachet Combigripp Hot Sip is indicated in the treatment of symptoms arising from acute respiratory viral infections, influenza, allergic rhinitis (fever, runny nose, swelling of the nasal mucosa, body aches, headache).
Structure
Active ingredients: paracetamol, cetirizine dihydrochloride, phenylephrine hydrochloride;
1 sachet of 5 g paracetamol 500 mg, cetirizine hydrochloride 10 mg, phenylephrine hydrochloride 10 mg;
Excipients:
Combigripp Hot Sip with lemon flavored silicon colloidal dioxide, aspartame (E 951), mannitol (E 421), xanthan gum, tartrazine (E 102), lemon flavor, sucrose;
Combigripp Hot Sip with raspberry flavor: colloidal silicon dioxide, aspartame (E 951), mannitol (E 421), xanthan gum, erythrosine (E 127), raspberry flavor, sucrose.
Contraindications
Hypersensitivity to active substances, hydroxyzine, any piperazine derivatives in history, or to other components of the preparation.
Severe violations of the liver and kidneys.
Congenital hyperbilirubinemia.
Gilbert's syndrome.
Deficiency of glucose-6-phosphate dehydrogenase.
Alcoholism, blood diseases (including severe anemia, leukopenia), arterial hypertension.
Cardiovascular diseases.
Diabetes mellitus glaucoma.
Hypertrophy of the prostate gland pheochromocytoma.
Application to patients who are treated with MAO inhibitors and within 2 weeks after discontinuation of such therapy.
Mode of application
Dissolve the content of 1 sachet in a glass of hot water (but not boiling water) and drink.
For adults and children over 12 years of age, use 1 sachet every 4-6 hours (as needed to relieve symptoms) up to 4 times a day. The intervals between doses should be at least 4 hours. A single dose should not exceed 1 sachet.
The duration of treatment is no more than 7 days.
Application features
Pregnant
Not applicable.
Children
Do not use in children under 12 years of age.
Drivers
In the event of side effects such as dizziness, it is recommended to avoid driving and operating machinery.
Overdose
Paracetamol. The risk of overdose is increased in patients with liver disease and in those who abuse alcohol. Paracetamol overdose can cause liver failure, necessitate liver transplantation, or lead to death.
Liver damage is possible in adults who have taken more than 10 g of paracetamol, and in children who have taken more than 150 mg / kg of body weight. The use of 5 g or more of paracetamol can lead to liver damage in patients with risk factors (long-term treatment with carbamazepine, phenobarbital, phenytoin, primidone, rifampicin, St. John's wort or other preparations that induce liver enzymes; regular intake of excessive amounts of ethanol; glutathione cachexia (digestive disorders , cystic fibrosis, HIV infection, hunger, cachexia).
Side effects
From the blood and lymphatic system: thrombocytopenia, agranulocytosis, anemia, sulfhemoglobinemia and methemoglobinemia (cyanosis, shortness of breath, heart pain), hemolytic anemia, bruising or bleeding.
From the nervous system: headache, dizziness, paresthesia, convulsions, dysgeusia, dyskinesia, dystonia, fainting, tremor, amnesia, memory impairment.
From the side of the organ of vision: violation of accommodation, blurred vision, involuntary movements of the eyeball.
On the part of the hearing and balance organs: vertigo.
From the side of the cardiovascular system: tachycardia, palpitations, arrhythmias, arterial hypertension.
From the respiratory system: bronchospasm in patients sensitive to acetylsalicylic acid and other NSAIDs, pharyngitis.
From the digestive tract: abdominal pain, dry mouth, nausea, diarrhea, epigastric pain, vomiting.
On the part of the kidneys and urinary system: dysuria, enuresis, urinary retention.
From the endocrine system: hypoglycemia, up to hypoglycemic coma.
From the side of nutrition and metabolism: increased appetite.
From the digestive system: impaired liver function (increased levels of bilirubin and liver enzymes: transatransaminases, alkaline phosphatase, γ-glutamyl transferase), usually without the development of jaundice.
On the part of the immune system, skin and subcutaneous tissue: hypersensitivity reactions, including anaphylaxis, anaphylactic shock, itching, rashes on the skin and mucous membranes (including erythematous and generalized rash), hyperemia, urticaria, angioedema, local preparation-induced rash erythema (including Stevens-Johnson syndrome), toxic epidermal necrolysis (Lyell's syndrome), edema.
From the side of the psyche: drowsiness, anxiety, aggressiveness, confusion, depression, hallucinations, insomnia, tics, suicidal thoughts.
General disorders: increased fatigue, asthenia, malaise, edema.
Examination: weight gain.
Interaction
The rate of absorption of paracetamol may increase with simultaneous use with metoclopramide and domperidone and decrease with cholestyramine. The anticoagulant effect of warfarin and other coumarins may increase with an increased risk of bleeding with simultaneous long-term regular daily use of paracetamol. With short-term use in accordance with the recommended regimen, these interactions have no clinical significance. Anticonvulsants (including phenytoin, barbiturates, carbamazepine), which stimulate the activity of microsomal liver enzymes, can increase the toxic effect of paracetamol on the liver due to an increase in the conversion of the preparation to hepatotoxic metabolites. The simultaneous use of high doses of paracetamol with isoniazid increases the risk of developing hepatotoxic syndrome. Do not use concomitantly with alcohol.
Storage conditions
Store in original packaging at a temperature not exceeding 25 ° C.
Keep out of the reach of children.
Shelf life is 2 years.
Tags: CombiGrip
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