Paracetamol Stada Juice 200 mg / 5 ml, 100 ml

Upute za korištenje Paracetamol Stada Juice 200 mg / 5 ml, 100 ml

Important notes (compulsory information):

Paracetamol Stada Juice 200 mg / 5 ml Solution for taking Applications: For symptomatic treatment of light to moderately strong pain such as headache, toothache, control pain and / or fever.

For risks and side effects, read the package leaflet and ask your doctor or pharmacist.


LEAFLET: INFORMATION FOR THE USER

Paracetamol Stada Juice 200 mg / 5 ml solution to take
Active substance: Paracetamol

Read all of the use information carefully before you start taking this medicine because it contains important information. Always take this medicine as described in this document information or Just as your doctor's instructions or pharmacist.

• Lift the use information. You might want to read it again.
• Ask your pharmacist if you need more information or advice.
• If you notice side effects, contact your doctor or pharmacist. This also applies to side effects that are not specified in this information information.
• If you do not feel better or even worse after 3 days, contact your doctor.

What is in this use information

1. What is Paracetamol STADA And what is it used for?
2. What should you take before taking Paracetamol STADA NOTE?
3. What is Paracetamol STADA To take?
4. WHAT SIDE EFFECTS ARE POSSIBLE?
5. What is Paracetamol STADA To keep?
6. Content of the pack and further information

1. What is Paracetamol STADA And what is it used for?
Paracetamol Stada is an analgesic, fever-lowering medicine (analgesic and antipyretics). Paracetamol Stada is used:

• to symptomatic treatment of light to moderately strong pain such as headaches, toothache, control pain and / or
• Fever.

2. What should you take before taking Paracetamol STADA NOTE?
Paracetamol Stada may not be taken:

• if they are allergic to paracetamol, sodium metabisulfite or one of the other ingredients of this medicine mentioned in Section 6

Warnings and Precautions:
Please talk to your doctor or pharmacist before taking Paracetamol Stada:

• if they are chronically alcoholic
• if you suffer from an impairment of liver function (Lieberitis, Gilbert syndrome)
• for preheat kidney.

If your symptoms will aggravate or no improvement after 3 days, or at high fever, you must consult a doctor. In order to prevent the risk of overdose, it should be ensured that other medicines that are applied at the same time do not contain any paracetamol. With prolonged high-dose, non-intended use of painkillers, headaches may occur, which must not be treated by increased doses of the medicine. Generally, the habitual intake of painkillers, especially when combining multiple analgesic active ingredients for permanent kidney damage with the risk of renal failure (AnalgeTika Nephropathy) lead. At abrupt settling after prolonged high dose, non-intended use of painkillers, headaches as well as fatigue, muscle pain, nervousness and vegetative symptoms can occur. The settling symptoms sounds within a few days. Until then, the re-acceptance of painkillers should be omitted and the re-taking is not without a medical advice. You are allowed paracetamol Stada not ohapply a medical or dental council for a long time or in higher doses.

Application of Paracetamol Stada together with other medicines:
Inform your doctor or pharmacist if you apply other medicines, recently applied other medicines or intend to apply other medicines.

Interactions are possible with the following medicines:

• Medicines against gout like sampleecide. With simultaneous intake of SampleCid, the dose of Paracetamol Stada should be reduced as the degradation of Paracetamol Stada can be slowed down.
• Medicines against nausea (metoclopramide and domperidone). These can accelerate the recording and effect of the effect of paracetamol STADA.
• Medicines for reducing elevated blood fat levels (Colestyramine). These medicines can reduce the recording and thus the effectiveness of Paracetamol Stada.
• Medicines in HIV infections (Zidovudin). The tendency to reduce white blood cells (neutropenia) is reinforced. Paracetamol Stada should therefore only be taken after medical advice simultaneously with Zidovudin.
• Medicines that lead to a slowdown in gastric emptying. With simultaneous use of these medicines with Paracetamol STADA, the recording and the effect entry of paracetamol may be delayed.
• Sleeps, such as phenobarbital, drugs for the treatment of epilepsy, such as phenytoin, carbamazepine, drugs for the treatment of tuberculosis (rifampicin), other possibly the liver medicinal products: may occur while taking these medicines with paracetamol STADA to liver damage.

Impact of taking Paracetamol STADA on laboratory tests:
The urinary acidity, as well as blood sugar determination can be influenced.

Taking Paracetamol Stada along with food, drinks and alcohol:
Paracetamol Stada must not be taken or administered together with alcohol.

Pregnancy and breast feeding period:
If you are pregnant or breastfeeding, or if you suspect to be pregnant or intend to become pregnant, ask your doctor or pharmacist for advice before applying this medicine.

Pregnancy:
Paracetamol Stada should only be taken after strict beyond the benefit risk ratio during pregnancy. You should not occupy paracetamol STADA during pregnancy for a long time, high doses or in combination with other medicines, as the safety of the application is not occupied for these cases.

Latving:
Paracetamol goes into breast milk. Since adverse consequences for the infant have not yet become known, interruption of breastfeeding is usually not required.

Driving and ability to operate machines:
Paracetamol Stada has no influence on the ability to drive and use machines. Nevertheless, after taking a painkiller is always caution.

Paracetamol Stada contains sorbitol and propylene glycol:
This medicine contains sorbitol. Please take Paracetamol Stada only after consultation with your doctor if you are known to suffer from any intolerance to certain sugars.

5 ml of solution for taking 2,275 g of sorbitol (a source for 0.569 g fructose, corresponding to approx. 0.19 bread units (BE). Sorbitol can have a slightly laxative effect. Propylene glycol can cause symptoms as after alcohol enjoyment.

3. What is Paracetamol STADA To take?

Always take this medicine exactly as described in this document information or just according to the agreement made with your doctor or pharmacist. Ask your doctor or pharmacist if you are not sure. Unless otherwise prescribed by the doctor, the recommended dose is: Paracetamol is dosed depending on body weight and age, usually with 10 to 15 mg per kg body weight of the child as a single dose, up to a maximum of 60 mg per kg body weight of the child as a dental dose of the child. The respective dosage interval is directed after the symptoms and the maximum daily dose. However, the distance between the individual revenue should not fall below 6 hours. The maximum daily dose (24 hours) must not be exceeded. With complaints that last longer than 3 days, a doctor should be visited. The dosage depends on the information below:

• Body weight 7 to 9 kg (children: 6 to 12 months): single dose 2.5 ml (corresponding to 100 mg paracetamol), max. Daily dose 10 ml (corresponding to 400 mg paracetamol)
• Body weight 10 to 12 kg (children: 1 to 2 years): single dose 3.75 ml (corresponding to 150 mg paracetamol), max. Daily dose 15 ml (corresponding to 600 mg paracetamol)
• Body weight 13 to 18 kg (children: 2 to 5 years): single dose 5 ml (corresponding to 200 mg paracetamol), max. Daily dose 20 ml (corresponding to 800 mg paracetamol)
• Body weight 19 to 25 kg (children: 5 to 8 years): single dose 7.5 ml (corresponding to 300 mg paracetamol), max. Daily dose 30 ml (corresponding to 1200 mg paracetamol)
• Body weight 26 to 32 kg (children: 8 to 11 years): Single dose 10 ml (corresponding to 400 mg paracetamol), max. Daily dose 40 ml (corresponding to 1600 mg paracetamol)
• Body weight 33 to 43 kg (children: 11 to 12 years): Single dose 12.5 ml (i.e., 10 ml + 2.5 ml) (corresponding to 500 mg of paracetamol), max. Daily dose 50 ml (corresponding to 2000 mg paracetamol)

For children or patients with a body weight of 33 to 43 kg (Age about 11 to 12 years) other dosage forms may be better suited.

Special patient groups:

• Liver Facilities and Lightweight Restriction of Kidney Function: In patients with liver or kidney function disorders and Gilbert syndrome, the dose must be reduced or the dose interval must be extended.
• Heavy renal insufficiency: in heavy renal insufficiency (Creatinine Clearance < 10 ml per min) must be adhered to a dose interval of at least 8 hours.
• Older patients: No special dose adjustment is required.
• Children and adolescents with little body weight: An application of paracetamol STADA in children under 6 months or Under 7 kg body weight is not recommended because the dose thickness is not suitable for these patient groups. However, suitable dose strengths are suitable for these patient groups Dosage forms available.

Type of application:
The bottle must be shaken vigorously before use. For precise dosing, the pack is a measuring cup with the division 1.25 ml, 2.5 ml, 3.75 ml, 5 ml, 7.5 ml and 10 ml. Paracetamol Stada is ready to use and, if necessary, mixed with food and beverages. The ingestion after meals can lead to a delayed effect entry.

Note:
To open, press the shutter down and simultaneously turn it into the direction of the arrow. After use, tighten closure again.

Duration of application:
Do not use Paracetamol Stada without a medical or dental council no longer than 3 days.

If you take a larger amount of Paracetamol Stada than you should:
The total dose of Paracetamol may not exceed 4000 mg paracetamol daily for adults and adolescents from 12 years or from 43 kg of body weight, 60 mg / kg / day for children. In an overdose, complaints occur within 24 hours of complaints that include nausea, vomiting, loss of appetite, paleness and abdominal pain. If a larger amount of Paracetamol Stada was taken than recommended, call the nearest doctor to help!

If you forget to take Paracetamol Stada:
Do not take the double amount when you forget the previous taking.

If you have further questions about the application of this medicine, contact your doctor and pharmacist.

4. Which side effects are possible?

Like all medicines, this medicine can also have side effects, but they do not have to occur each other. In the evaluation of side effects usually the following frequency information is basedsets:

The frequency information on side effects is based on the following categories:
Very often:	more than 1 treated from 10
Frequently:	1 to 10 treated from 100
Occasionally:	1 to 10 treated from 1 000
Rarely:	1 to 10 treated from 10 000
Very rare:	less than 1 treated from 10 000
Not known:	Frequency on the basis of the available data does not estimate.

Rarely:

• easy increase in liver enzymes (serum transamination)
• Very rare
• Changes in the blood count as a reduction in platelets (Thrombocytopenia) or a strong reduction of certain white blood cells (agranulocytosis).
• allergic reactions such as simple rash or nettle rash (urticaria) to a shock reaction.
• For sensitive persons, a narrowing of the respiratory tract (analgesics asthma) can be triggered very rarely.
• Very rarely, cases of heavy skin reactions were reported.

In the case of an allergic shock reaction, you immediately call the nearest doctor to help. Paracetamol Stada contains sodium metabisulfite, which rarely can cause hypersensitivity reactions and bronchial cramps (bronchospasms.

Message of side effects:
If you notice side effects, contact your doctor or pharmacist. This also applies to side effects that are not specified in this information information. You can also view side effects directly:

Federal Institute for Pharmaceuticals and Medical Products
Dept. Pharmacovigilance
Kurt-Georg-Kiesinger-Allee 3
D-53175 Bonn
Website: www.bfarm.de

By reporting side effects, you can help to provide more information about the security of this medicine.

5. What is Paracetamol STADA To keep?

Keep this medicine inaccessible to children. You may not use this medicine after the expiration date specified on the carton and on the label "usable until". The expiration date refers to the last day of the specified month. Do not store at +8 ° C. Do not store or freeze in the fridge. After opening the container 12 months durable. Do not dispose drugs in the wastewater or household waste. Ask your pharmacist how to dispose of the medicine if you do not use it anymore. You help to protect our environment.

6. Content of the pack and further information

What Paracetamol Stada contains:
The active ingredient is: paracetamol. 5 ml solution for taking 200 mg paracetamol. The other ingredients are sodium metabisulfite (pH. EUR.), Propylene glycol, saccharin sodium 2H2O, sorbitol solution 70% (not crystallizing) (Ph. EUR.), Purified water, raspberry aroma, cream aroma.

Like Paracetamol Stada looks and content of the pack:
Colorless to slightly yellowish, clear solution, smell and taste after raspberries, sweet tasting. Paracetamol Stada is available in packs with 100 ml solution for taking.

Pharmaceutic entrepreneur:
Stadapharm GmbH
Stadastraße 2-18
61118 Bad Vilbel
Telephone: 06101 603-0
Fax: 06101 603-259
Internet: www.stada.de

Manufacturer:
STADA Arzneimittel AG
Stadastraße 2-18
61118 Bad Vilbel

This information information was last revised in May 2014.

Source: Information of the leaflet
Status: 12/2014