Package Leaflet: Information for the User
Ilvico Coated Tablets
paracetamol / caffeine / brompheniramine maleate
Read the entire package leaflet carefully before starting to take this medication, as it contains important information for you.
Follow the administration instructions for the medication contained in this package leaflet or as indicated by your doctor or pharmacist exactly.
Contents of the Package Leaflet:
Ilvico belongs to the group of combination medications for colds.
It is indicated for symptomatic relief in flu-like and catarrhal processes that occur with fever, mild or moderate pain, and nasal secretion.
You should consult a doctor if your symptoms worsen or do not improve after 5 days.
Warnings and Precautions
Consult your doctor or pharmacist before starting to take Ilvico.
During treatment with Ilvico, inform your doctor immediately if
If you have severe diseases, such as severe renal insufficiency or sepsis (when bacteria and their toxins circulate in the blood, causing organ damage), or if you have malnutrition, chronic alcoholism, or are also taking flucloxacillin (an antibiotic). A serious disease called metabolic acidosis (a blood and fluid anomaly) has been reported in patients in these situations when using paracetamol at regular doses for a prolonged period or when taking paracetamol with flucloxacillin. The symptoms of metabolic acidosis may include: severe breathing difficulties with deep and rapid breathing, drowsiness, feeling unwell (nausea) and vomiting.
Taking Ilvico with other medications
Inform your doctor or pharmacist if you are using, have recently used, or may need to use any other medication. As many other medications can affect liver function and increase the risk of liver toxicity.
In particular, if you are using any of the following medications, it may be necessary to modify the dose of some of them or even interrupt treatment:
Interference with analytical tests
If you are going to have any analytical tests (including blood, urine, etc.), inform your doctor that you are taking this medication, as it may alter the results.
Taking Ilvico with food and beverages
Coffee, tea, chocolate, or cola drinks are sources of caffeine. Therefore, it is recommended to moderate the consumption of these products while taking Ilvico. Taking up to 400 mg of caffeine per day in healthy adults is considered safe, so it is important that you consider the total caffeine content in other foods or products while taking this medication.
Taking Ilvico by patients who regularly consume alcohol (three or more alcoholic beverages - beer, wine, liquor... - per day) may cause liver damage.
Concomitant consumption of Ilvico with alcoholic beverages may increase its side effects.
Taking this medication with food does not affect its efficacy.
Use in children
Do not administer to children under 12 years of age.
Use in adults over 65 years
Talk to your doctor before taking brompheniramine, as it is more likely to cause confusion, and you may need to take a lower daily dose. Elderly people are more likely to experience side effects. Consult your doctor before taking this medication.
Pregnancy and breastfeeding
If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before using this medication.
Pregnant or breastfeeding women cannot take this medication. Its use will only be considered in case of medical recommendation and under strict supervision, if the benefits outweigh the risks.
Driving and using machines
This medication may cause drowsiness, dizziness, or blurred vision, especially if you drink alcoholic beverages while taking this medication. If the medication causes these effects, do not drive or operate hazardous tools or machines while taking it.
Ilvico contains sodium carboxymethylcellulose (type A)
This medication contains less than 1 mmol of sodium (23 mg) per tablet, which is essentially 'sodium-free'.
Follow the administration instructions for the medication contained in this package leaflet or as indicated by your doctor or pharmacist exactly. In case of doubt, consult your doctor or pharmacist again.
The recommended dose is:
2 tablets (650 mg of paracetamol) every 8 hours. Do not take more than 6 tablets in 24 hours. Do not take more than 3 g of paracetamol every 24 hours (see "Warnings and Precautions" in section 2).
Adolescents from 12 years of age
1 tablet every 6 or 8 hours. Do not take more than 4 tablets in 24 hours.
Children under 12 years of age
Cannot take this medication.
This medication is taken orally.
Tablets should be taken with a little water.
Suspend treatment once symptoms have disappeared.
If symptoms worsen or persist for more than 5 days of treatment, you should consult a doctor.
If you take more Ilvico than you should
If you have taken an overdose, go to a medical center immediately, even if you do not notice symptoms, as they often do not appear until 3 days after taking the overdose, even in cases of severe poisoning. Taking too much paracetamol can cause severe liver damage.
The symptoms of overdose may be: excitement, discomfort, diarrhea, abdominal pain, convulsions, dizziness, nausea, vomiting, loss of appetite, yellowing of the skin and eyes (jaundice), drowsiness, disorientation, and sweating.
Treatment of overdose is most effective if started within 4 hours of taking the medication.
Patients taking barbiturics or chronic alcoholics may be more susceptible to paracetamol overdose toxicity.
In case of overdose or accidental ingestion, go to a medical center immediately or call the Toxicology Information Service (phone 91 562 04 20), indicating the medication and the amount ingested.
Like all medications, this medication can cause side effects, although not everyone experiences them.
Side effects are uncommon with paracetamol.
Stop taking the product and contact your doctor immediately if you notice:
Very rare cases of severe skin reactions have been reported. If a skin reaction occurs, discontinue use and seek medical help immediately.
You should discontinue treatment immediately if you experience dizziness or palpitations (abnormally strong heartbeats).
The following side effects have been observed for which the exact frequency cannot be established: pupil dilation, dry eyes, constipation, alterations in intellectual ability, abdominal pain, fatigue, loss of coordination, confusion, vomiting, or digestion problems. Some children may become hyperactive after taking this medication.
Frequent disorders (observed in 1 to 10 people out of 100):
Rare disorders (observed in 1 to 10 people out of 10,000):
Discomfort.
Convulsions and tremors.
Very rare disorders (observed in less than 1 in 10,000 people):
Very rare cases of severe skin reactions have been reported. If a skin reaction occurs, discontinue use and seek medical help immediately.
Other side effects related to caffeine have been observed, for which the exact frequency cannot be established. The most commonly observed effects were: insomnia, restlessness, nervousness, irritability, excitement, and disorientation. Nausea, vomiting, and stomach irritation have also been observed.
You should discontinue treatment immediately if you feel dizzy or experience palpitations (abnormally strong heartbeats).
Frequency not known (cannot be estimated from available data): A serious disease called metabolic acidosis (a blood and fluid anomaly) in patients with severe disease using paracetamol (see section 2).
Reporting side effects:
If you experience any side effects, consult your doctor or pharmacist, even if they are possible side effects not listed in this package leaflet. You can also report them directly through the Spanish Medication Surveillance System for Human Use: http://www.notificaram.es. By reporting side effects, you can contribute to providing more information on the safety of this medication.
Do not store above 30 °C.
Keep this medication out of sight and reach of children.
Do not use this medication after the expiration date shown on the packaging after CAD. The expiration date is the last day of the month indicated.
Medications should not be disposed of through wastewater or household waste. Deposit the packaging and medications you no longer need at the SIGRE collection point in your pharmacy. If in doubt, ask your pharmacist how to dispose of the packaging and medications you no longer need. This will help protect the environment.
The active ingredients are paracetamol 325 mg, caffeine 30 mg, and brompheniramine maleate 3 mg.
The other components are microcrystalline cellulose, sodium carboxymethylcellulose (type A) (derived from potato starch), crospovidone, hypromellose, cellulose powder, magnesium stearate, glycerol (E-422), colloidal anhydrous silica, titanium dioxide (E171), macrogol, talc.
Appearance of the product and package contents
Ilvico are white, coated tablets, presented in blisters, packaged in boxes of 20 tablets.
Marketing authorization holder
Laboratorios Vicks, S.L.
Avda. Bruselas, 24
28108 Alcobendas (Madrid) Spain
Manufacturer
P&G Health Austria GmbH & Co. OG
Hösslgasse 20
9800 Spittal an der Drau
Austria
Local representative
Procter & Gamble España, S.L.U.
Avda. Bruselas, 24
28108 Alcobendas (Madrid) Spain
Date of the last revision of this package leaflet:January 2025
Detailed information about this medication is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) (http://www.aemps.gob.es/).