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Paracetamol 10 Mg/Ml Solution For Infusion

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PACKAGE LEAFLET: INFORMATION FOR THE USER


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Paracetamol 10 mg/ml, solution for infusion

Paracetamol


Read all of this leaflet carefully before you are given this medicine because it contains important information for you.

•    Keep this leaflet. You may need to read it again.

•    If you have any further questions, ask your doctor or pharmacist.

•    If you get any side effects talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet.


What is in this leaflet:

1.    What Paracetamol is and what it is used for

2.    What you need to know before is administered to you

3.    How Paracetamol is administered to you

4.    Possible side effects

5.    How to store Paracetamol

6.    Contents of the pack and other information


1 What Paracetamol is and what it is used for


Paracetamol contains the active substance paracetamol, an analgesic (it relieves pain) and an antipyretic (it lowers fever).

This medicine is given by intravenous infusion directly into a vein. It is used for

•    short-term treatment of moderate pain, especially following surgery

•    short-term treatment of fever.


What you need to know before is administered to you


Do not use Paracetamol

•    if you are allergic to paracetamol or to any of the other ingredients of this medicine (listed in section 6)

•    if you are allergic to propacetamol (another analgesic and related to paracetamol)

•    if you suffer from severe liver disease

Warnings and precautions

•    Do not exceed the recommended dose. Doses higher than those recommended entail the risk of very serious liver damage. Symptoms of liver damage are not usually seen until 2 days, and up to a maximum of 4-6 days, after administration

•    Take care not to exceed the maximum dose of paracetamol if you are using other medicines containing paracetamol (see section 2 “Other medicines and Paracetamol”)

•    Dosage adjustment may be necessary in the following cases:

-    liver or kidney disease

-    alcohol abuse

-    nutrition problems (malnutrition)

-    dehydration

Inform your doctor before treatment, if any of the above mentioned conditions apply to you.

Use a suitable analgesic for oral use (via the mouth) as soon as this is possible.

Other medicines and Paracetamol

Please tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines.

This medicine contains paracetamol. This must be taken into account if you are using other medicines containing paracetamol, in order not to exceed the recommended daily dose (see section 3 “How Paracetamol is administered to you”). Inform your doctor if you are taking other medicines containing paracetamol.

It is very important to tell your doctor if you are taking any of the following medicines. These medicines and Paracetamol can


interfere with each other:

•    Probenecid (medicine used to treat gout): a lower dose of paracetamol may be needed

•    Salicylamide (anti-inflammatory drug)

•    Anticoagulants taken via the mouth (such as warfarin, acenocoumarol). It may be necessary to control the effect of the anticoagulant.

Paracetamol with food, drink and alcohol

Limit the use of alcohol during treatment with this medicine.

Pregnancy and breast-feeding

Inform your doctor if you are pregnant. Paracetamol may be used during pregnancy. However, in this case the doctor must evaluate if the treatment is advisable.

Paracetamol may be used during breast-feeding.

If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine.

Driving and using machines

Paracetamol has no influence on the ability to drive and use machines.

Important information about some of the ingredients of Paracetamol

This medicinal product contains less than 1 mmol sodium (23 mg) per 100 ml, i.e. essentially 'sodium free'.


3 How Paracetamol is administered to you


The 100 ml vial or 100 ml bag is restricted to adults, adolescents and children weighing more than 33 Kg.

Dosage

Dosing based on patient weight (please see the dosing table here below)


Patient

weight

Dose per administration

Volume

per

admin

istration

Maximum volume of Paracetamol (10mg/mL) per administration based on upper weight limits of group (mL)***

Maxi

mum

Daily

Dose**

> 33 kg to s50kg

15 mg/kg

1.5mL/kg

75 mL

60mg/kg not exceeding 3g


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>50kg with additional risk factors for hepatotoxicity

1g

100mL

100mL

3g

> 50 kg and no additional riskfactorsfor hepatotoxicity

1g

100mL

100mL

4g


(platelets, white blood cells) can occur, possibly leading to bleeding from the nose or gums. Should this occur, please inform your doctor.

Cases of skin redness, flushing, itching and abnormally rapid heart rate have been reported.

As with all injectable medicinal products the patient may experience local reactions (such as pain and burning sensation) at the injection site.

If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet.


**Maximum daily dose: The maximum daily dose as presented in the table above is for patients that are not receiving other paracetamol containing products and should be adjusted accordingly taking such products into account.

***Patients weighing less will require smaller volumes.

The minimum interval between each administration must be at least 4 hours.

The minimum interval between each administration in patients with severe renal insufficiency must be at least 6 hours.

No more than 4 doses to be given in 24 hours.

Method of administration:


5 How to store Paracetamol


RISK OF MEDICATION ERRORS Take care to avoid dosing errors due to confusion between milligram (mg) and milliliter (mL), which could result in accidental overdose and death.


Keep out of the sight and reach of children.

Do not use this medicine after the expiry date which is stated on the vial and carton after EXP. The expiry date refers to the last day of that month.

Do not store above 30°C. Keep the vial in the original carton, in order to protect from light. Do not refrigerate or freeze.

Shelf life after first opening: Use immediately after opening

Before administration, the product should be inspected visually. Do not use Paracetamol if you notice any particulate matter and discolouration. These are visible signs of deterioration.

Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to dispose of medicines you no longer use. These measures will help protect the environment.


For the vials, a 0.8 mm needle (21 gauge needle) has to be used and the stopper vertically perforated at the spot specifically indicated.

Intravenous use. This medicine is given as a slow infusion (drip) into a vein over 15 minutes. Close monitoring is needed before the end of the infusion.

For single use only.

Any unused solution should be discarded.

If you have the impression that the effect of your medicine is too strong or too weak, talk to your doctor.

If you are given more Paracetamol than you should

Because of the risk of irreversible liver damage, immediately contact your doctor even if you feel well if too much Paracetamol has been administered to you. In overdose cases, symptoms generally appear within the first 24 hours. These symptoms comprise of nausea (feeling sick), vomiting, anorexia, a pale appearance to the skin and abdominal pain.

If you have any further questions on the use of this medicine ask your doctor or pharmacist.


6 Contents of the pack and other information


4 Possible side effects


Like all medicines, this medicine can cause side effects, although not everybody gets them.

Rare side effects: may affect up to 1 in 1,000 people

The following may occur:

•    a drop in blood pressure

•    changes in laboratory test results:

-    abnormally high levels of liver enzymes found during blood checks. Regular blood checks may be required

•    feeling generally unwell and run down.

Very rare side effects: may affect upto 1 in 10,000 people

The following may occur:

•    a serious skin rash or allergic reaction. Stop the treatment immediately and inform your doctor. In isolated cases, other changes in laboratory test results have been observed which have necessitated regular blood checks:

-    abnormally low levels of some types of blood cells


What Paracetamol contains

•    The active substance is paracetamol. One ml contains 10 mg paracetamol. Each vial (100 ml) contains 1000 mg paracetamol.

•    The other ingredients are mannitol, disodium phosphate dihydrate, cysteine hydrochloride monohydrate, sodium hydroxide (4%) (for pH-adjustment), hydrochloric acid (37%) (for pH-adjustment) and water for injections.

What Paracetamol looks like and contents of the pack

Paracetamol is a solution for infusion.

It is a clear, slightly yellowish solution which is contained in a colourless glass vial with a rubber stopper and sealed with an aluminium cap.

The vials are packed in carton boxes. Each box contains 1 or 10 vials.

Not all pack sizes may be marketed.

Marketing Authorisation Holder

Sandoz Ltd, Frimley Business Park, Frimley, Camberley, Surrey, GU16 7SR, United Kingdom.

Manufacturer

SM Farmaceutici SRL, Zona industriale, 85050TITO -POTENZA, Italy or

Neogen Developments N.V., Square Marie Curie, 50,

1070Anderlecht, Belgium or

Salutas Pharma GmbH, Otto-von-Guericke-Allee 1,

39179 Barleben, Germany.

This leaflet was last revised in 12/2013.


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