HAEMACCEL

Posology Haemaccel should be administered intravenously in a volume approximately equal to the estimated blood loss. 6. for Special precautions for disposal and other Handling.

Infusion rate:

The rate of infusion is determined by the condition of the patient. Normally, 500 ml will be infused in not less than 60 minutes but in emergencies Haemaccel can be rapidly infused. Losses of up to 25 % of the blood volume can be replaced by Haemaccel alone.

Hypovolaemic shock: 500 -1,000 ml Haemaccel should be infused intravenously initially. Up to 1,500 ml blood loss can be replaced entirely by Haemaccel. For between 1,500 ml and 4,000 ml blood loss, fluid replacement should be with equal volumes of Haemaccel and blood given separately (see Pharmaceutical Precautions).

For losses over 4,000 ml, the separate infusion should be in the ratio of two parts blood to one part Haemaccel. The Haematocrit should not be allowed to fall below 25 %.

Burns:

It is suggested that at least 1 ml Haemaccel be infused per kg of body weight. g. if a 70 kg person has burns covering 10 % of body surface, then the dosage of Haemaccel should be at least 1 (ml) x 70 (kg) x 10 (%) = 700 ml/24 hours.

e. about 2,000 ml per 24 hours. In severe burns additional protein and vitamin therapy may be required. The volume of colloid and crystalloid given should be varied according to the clinical response of the patient, the urine volume, its specific gravity and osmolality etc.

Plasma exchange:

Haemaccel should be given either alone or in combination with other replacement fluids in a volume adequate to replace the plasma removed. Up to 2 litres have been given as sole replacement fluid. Method of administration Intravenous infusion.

During or after the infusion of volume-expanding solutions, transient urticarial skin reactions (wheals), hypotension, tachycardia, bradycardia, nausea/vomiting, dyspnoea, increases in temperature and/or shivering may occasionally occur.

Rare cases of severe hypersensitivity reactions including shock have been observed. Treatment will depend on the nature and severity of the reaction. Mild reactions: administer corticosteroids and antihistamines. v. c. injection) should immediately be given.

Administration of adrenalin should be repeated every 15 minutes until improvement occurs. Circulatory collapse requires volume replacement, preferably monitored by a central venous pressure line. Large volumes of electrolyte solution may be necessary because, in severe anaphylactic shock, plasma loss may constitute up to 40 % of the plasma volume.

v. injection of an H1 antagonist such as 10 - 20 mg chlorpheniramine may be given. Histamine release has been shown to be a cause of anaphylactic side-effects associated with infusions of Haemaccel. g. anaesthetics, muscle relaxants, analgesics, ganglia blockers and anticholinergic drugs).

Due to the calcium content of Haemaccel, the serum calcium concentrations may be found to be slightly elevated for a temporary period especially when large amounts of Haemaccel are administered by rapid infusion. So far, no reports have been received of cases involving clinical signs of hypercalcaemia resulting from an infusion of Haemaccel.

The infusion of Haemaccel may result in a temporary increase in the erythrocyte sedimentation rate. 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. uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store.

In the following cases, Haemaccel is indicated to a restricted extent only; if the physician considers the infusion necessary, it should be given taking special precautions. g. increased stroke volume, elevated blood pressure), or an increase in interstitial fluid volume, or haemodilution could represent a special risk for the patient.

Examples of such conditions are: congestive heart failure, hypertension, oesophageal varices, pulmonary oedema, haemorrhagic diathesis, renal and post-renal anuria. g. allergic persons and patients with a history of histamine response; also patients who in the previous 7 days have received a drug which releases histamine).

In the latter cases, Haemaccelmay be given only after taking appropriate prophylactic steps. Reactions caused by histamine release can be avoided by the prophylactic use of H1 and H2 receptor antagonists. Inappropriate rapid administration of Haemaccel, especially to normovolaemic patients may cause the release of vasoactive substances.

The exact mechanism of this histamine release has not been clearly defined. 20g potassium chloride per 500ml. 1847mmol sodium in each 500ml vial. This should be taken into consideration by patients on a controlled sodium diet. 005mmol potassium in each 500ml vial.

This should be taken into consideration by patients on a controlled potassium diet.

Haemaccel is contra-indicated in patients with a known hypersensitivity to constituents of the preparation and/or patients with existing anaphylactoid reactions.