Robitussin Expectorans, 100 mg/5 ml, syrup
Guaifenesin
This medicine should always be taken exactly as described in the patient leaflet or as directed by a doctor or pharmacist.
Robitussin Expectorans contains the active substance guaifenesin. It increases the production of mucus in the bronchi and thins the accumulated secretion, helping to cough it up. Robitussin Expectorans is indicated for use in coughs with excessive amounts of difficult-to-cough-up secretions in the bronchi in adults and children over 6 years of age. If after 7 days in adults (3 days in children) there is no improvement or the patient feels worse, they should consult a doctor.
Patients should inform their doctor or pharmacist about all medicines they are currently taking or have recently taken, as well as any medicines they plan to take.
While taking Robitussin Expectorans, patients should avoid alcoholic beverages and medicines containing alcohol.
If the patient is pregnant or breastfeeding, thinks they may be pregnant, or plans to have a child, they should consult their doctor or pharmacist before taking this medicine. This medicine should not be taken during pregnancy and breastfeeding without consulting a doctor. This medicine contains 228 mg of alcohol (ethanol) in 10 ml of syrup.
The medicine may affect the ability to drive and use machines. Patients who drive or use machines should take into account that the medicine contains alcohol. Robitussin Expectorans contains sodium benzoate, sorbitol, maltitol, ethanol, propylene glycol, glucose, fructose, sodium
The medicine contains 12.0 mg of sodium benzoate in 10 ml of syrup, which is equivalent to 1.2 mg/ml.
The medicine contains 2.1 g of sorbitol in 10 ml of syrup, which is equivalent to 209.4 mg/ml.
Sorbitol is a source of fructose. If the patient has previously been diagnosed with intolerance to some sugars or has been diagnosed with hereditary fructose intolerance, a rare genetic disorder in which the patient's body does not break down fructose, they should consult their doctor before taking the medicine or giving it to their child. Sorbitol may cause gastrointestinal discomfort and may have a mild laxative effect. The medicine contains maltitol. If the patient has previously been diagnosed with intolerance to some sugars, they should consult their doctor before taking the medicine. This medicine contains 228 mg of alcohol (ethanol) in 10 ml of syrup, which is equivalent to 23 mg/ml (2.06% v/v). The amount of alcohol in 10 ml of syrup is equivalent to 6 ml of beer or 3 ml of wine. The amount of alcohol in this medicine is unlikely to have an effect on adults and adolescents, and its effect on children is unlikely to be noticeable. However, it may cause some effect in younger children, such as drowsiness. The alcohol in this medicine may alter the effect of other medicines. If the patient is taking other medicines, they should consult their doctor or pharmacist. If the patient is pregnant or breastfeeding, they should consult their doctor or pharmacist before taking this medicine. If the patient is addicted to alcohol, they should consult their doctor or pharmacist before taking this medicine. The medicine contains 22.2 mg of sodium (the main component of common salt) in 10 ml of syrup. This is equivalent to 1.1% of the maximum recommended daily intake of sodium in the diet for adults. The medicine contains 15.8 mg of propylene glycol in 10 ml of syrup. The medicine contains 0.03 mg of fructose in 5 ml of syrup. The medicine contains 1.0 mg of glucose in 10 ml of syrup. If the patient has previously been diagnosed with intolerance to some sugars, they should consult their doctor before taking the medicine. This should be taken into account in patients with diabetes.
This medicine should always be taken exactly as described in the patient leaflet or as directed by a doctor or pharmacist. In case of doubt, patients should consult their doctor or pharmacist. Recommended dose: Adults and adolescents over 12 years: 10 ml of syrup 4 times a day. Children from 6 to 12 years: 5 ml of syrup 4 times a day. Before taking the medicine, patients should consult their doctor. Oral administration. Robitussin Expectorans is contraindicated in children under 6 years of age (see "When not to take Robitussin Expectorans"). Do not take higher doses than recommended. Patients should stop taking Robitussin Expectorans and consult their doctor if their cough persists for more than 7 days in adults (3 days in children), recurs, or is accompanied by fever, rash, or persistent headache. These may be symptoms of a serious illness.
In case of overdose, patients should stop taking the medicine and consult their doctor. After an overdose, nausea and vomiting may occur.
Patients should not take a double dose to make up for a missed dose. If patients have any further doubts about taking this medicine, they should consult their doctor or pharmacist.
Like all medicines, Robitussin Expectorans can cause side effects, although not everybody gets them. While taking Robitussin Expectorans, the following side effects may occur: Rare(may affect up to 1 in 1000 people): hypersensitivity, nausea, vomiting. Frequency not known(cannot be estimated from the available data): dizziness, headache, dyspnea, rash, urticaria, anaphylactic reactions (severe allergic reactions causing difficulty breathing and usually a significant drop in blood pressure), angioedema (a severe allergic reaction with swelling of the skin and/or mucous membranes, e.g., in the face, throat, limbs, joints), diarrhea, stomach pain.
If patients experience any side effects, including any possible side effects not listed in the leaflet, they should inform their doctor or pharmacist. Side effects can be reported directly to the Department for Monitoring of Adverse Reactions to Medicinal Products of the Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products: Al. Jerozolimskie 181C, 02-222 Warsaw, tel.: +48 22 49 21 301, fax: +48 22 49 21 309, website: https://smz.ezdrowie.gov.pl. Side effects can also be reported to the marketing authorization holder. By reporting side effects, patients can help provide more information on the safety of the medicine.
The medicine should be stored out of sight and reach of children. Do not use this medicine after the expiry date stated on the label or carton after "Expiry date". The expiry date refers to the last day of the month stated. Store in a temperature below 25°C, in the original packaging. The shelf life of the medicine after first opening is 6 months. Do not use this medicine if the cap is damaged. Medicines should not be disposed of via wastewater or household waste. Patients should ask their pharmacist how to dispose of medicines they no longer use. This will help protect the environment.
Robitussin Expectorans is a brown syrup with a cherry flavor and aroma. The bottle is made of orange glass with a PE/PP cap and a PP measuring cup.
Haleon Poland Sp. z o.o.
ul. Rzymowskiego 53
02-697 Warsaw
tel. 800 702 849
Doppel Farmaceutici S.r.l.
Via Martiri delle Foibe 1
29016 Cortemaggiore (Piacenza)
Italy
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