Heparin sodium 10 IU/ml I.V. flush solution

Heparin Sodium Ph. Eur. 10 IU/ml

For the full list of excipients, see section 6.1.

Solution for injection.

To maintain the patency of in-dwelling intravenous lines.

Not recommended for therapeutic use.

Method of administration

For injection into the catheter/cannula.

For routine use, 1-5 ml (10-50 IU heparin) should be administered into the catheter/cannula every 4 to 8 hours or as required.

Hypersensitivity to the active substance or to any of the other excipients listed insection 6.1.

Current or history of heparin-induced thrombocytopenia.

Concomitant use of intravenous diclofenac.

Heparin Sodium 10 IU/ml i.v. flush solution should be used with caution in patients with hypersensitivity to low molecular weight heparin.

Rigorous aseptic technique should be observed at all times in its use.

As there is a risk of antibody-mediated heparin-induced thrombocytopenia, platelet counts should be measured in patients receiving regular and repeated use of heparin flush solutions for longer than 5 days and the treatment should be stopped immediately in those who develop thrombocytopenia or paradoxical thrombosis andheparin should immediately be eliminated from all flushes and ports.

Repeated flushing of a catheter device with heparin may result in a systemic anticoagulant effect.

When an indwelling device is used for repeated withdrawal of blood samples for laboratory analyses and the presence of heparin or saline is likely to interfere with or alter the results of the tests, the in situ heparin flush solution should be cleared from the device by aspirating and discarding a volume of solution equivalent to that of the indwelling venipuncture device before the desired blood sample is taken.

Pregnancy

The safety of Heparin Sodium 10 I.U/ml Flushing Solution in pregnancy is not established, but the dose of heparin used would not be expected to constitute a hazard.

Breast-feeding

Heparin is not excreted in breast milk.

Heparin has no or negligible influence on the ability to drive or use machines.

Used as directed, it is extremely unlikely that the low levels of heparin reaching the blood will have any systemic effect, however, there have been rare reports of immune-mediated thrombocytopenia and thrombosis in patients receiving heparin flushes. Pulmonary embolism has been reported as thromboembolic complications of heparin-induced thrombocytopenia.

Hypersensitivity reactions to heparin are rare. They include urticaria, conjunctivitis, rhinitis, asthma, cyanosis, tachypnoea, feeling of oppression, fever, chills, angioneurotic oedema and anaphylactic shock.

Reporting of suspected adverse reactions

Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via the Yellow Card Scheme at: www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store.

An overdose is unlikely to occur. Bleeding is the main sign of overdose with heparin. As heparin is eliminated quickly, discontinuation of heparinis sufficient in case of minor haemorrhages. In case of severe haemorrhages heparin may be neutralised with protamine sulphate injected slowly intravenously. One mg of protamine sulphate neutralises approximately 100 IU of heparin. Nevertheless, the required protamine sulphate dose varies according to the time of heparin administration and the dose administered.

Heparin is a naturally occurring anticoagulant which prevents the coagulation of blood in-vivo and in-vitro. The dose used to flush indwelling devices is unlikely to produce blood levels of heparin having any systemic effect.

Not applicable

There are no preclinical data of relevance to the prescriber which are additional to that already included in other sections.

Sodium chloride

Water for Injections

This product is compatible with normal saline. Heparin has been reported to be incompatible in aqueous solution with certain substances, e.g. some antibiotics, hydrocortisone, phenothiazines, narcotic analgesics and antihistamines

Heparin and reteplase are incompatible when combined in solution.

Amikacin sulfate, gentamicin sulfate, netilmicin sulfate, pethidine hydrochloride, promethazine hydrochloride and tobramycin sulfate.

If reteplase and heparin are to be given through the same line this, together with any Y-lines, must be thoroughly flushed with a 0.9% saline or a 5% glucose solution prior to and following the reteplase injection.

2 years.

From a microbiological point of view, unless the method of opening precludes the risk of microbial contamination, the product should be used immediately.

If not used immediately, in-use storage times and conditions are the responsibility of the user.

Do not store above 25°C.

10 x 5 ml ampoules

10 x 10 ml ampoules

Ph Eur Type 1 glass ampoules.

Any portion of the contents not used at once should be discarded.

Kent Pharma UK Limited

The Bower,

4 Roundwood Avenue,

Stockley Park, Heathrow,

United Kingdom.

UB11 1AF

PL 51463/0033

8 March 1984/21 May 1995.

06/11/2020