Patient leaflets and SmPCs, drug interaction checker, official dosages and NHS pharmacy opening hours — all in one place.
Patient leaflets and SmPCs, drug interaction checker, official dosages and NHS pharmacy opening hours — all in one place.
The electronic medicines compendium (emc) no longer publishes a Summary of Product Characteristics for this product, which usually means it is no longer marketed in the UK. The patient leaflet below is kept for reference, but the product may not be available.
If you were prescribed this medicine, other products containing Cyclizine lactate may still be available. Do not stop your treatment — ask your pharmacist or GP what to use instead.
for Cyclizine Lactate Injection contains the active substance cyclizine lactate, which belongs to a group of medicines called antihistamines which can be used to help stop you feeling sick (nausea) or being sick (vomiting). Cyclizine lactate injection may be used by adults. Cyclizine lactate injection may be used if you suffer from travel or motion sickness; nausea caused by cancer treatment (radiotherapy) or other medicines; or if you have had an operation, as general anaesthetics can sometimes cause sickness. Cyclizine lactate injection can also be used to treat sickness caused by some inner ear problems such as Meniere's disease.
Cyclizine Lactate Injection Do not use this medicine:
if you are allergic to cyclizine lactate or any of the other ingredients of this medicine (listed in section 6) if you have allergic reactions which include mild symptoms such as itching and/or rash. More severe symptoms include swelling of the face, lips, tongue and/or throat with difficulty in swallowing or breathing. if you have been drinking alcohol. The anti-vomiting properties of Cyclizine lactate injection may increase the toxicity of alcohol.
Warning and precautions Talk to your doctor or nurse before you are given Cyclizine lactate injection if you:
to you You will be given Cyclizine lactate Injection under supervision and your doctor will decide on a dose which is right for you. Cyclizine lactate Injection can be given as a slow injection into a vein (intravenously) or by injection into a muscle (intramuscularly). The recommended dose for adults is:
If you receive more Cyclizine lactate Injection than you should As this medicine is given to you by a doctor, it is very unlikely that an overdose will happen. Should an overdose occur, the doctor will treat any symptoms that follow. Symptoms of overdose include dry mouth, nose and throat, blurred vision, fast or irregular heartbeat, difficulty passing urine, drowsiness, dizziness, lack of balance and coordination, weakness, excitability, disorientation, impaired judgement, hallucinations, muscle spasm, involuntary movements, convulsions, high temperature and difficulty breathing. 4. Possible side effects Like all medicines, this medicine can cause side effects, although not everybody gets them. If you notice:
may include:
Cyclizine lactate Injection Keep this medicine out of the sight and reach of children. Cyclizine lactate Injection will be stored by the hospital pharmacy before it is given to you. They will follow the instructions below. For single use only. Discard any unused product Do not freeze Cyclizine lactate Injection should be stored in a safe place below 25°C and protected from light. The injection should not be used if there are any particles floating in it or after the "EXP" date on the carton and label. 6. Content of the pack and other information What Cyclizine lactate Injection contains Cyclizine lactate Injection comes as a 1 ml ampoule containing 50 mg of the active ingredient, cyclizine lactate, dissolved in sterile water. The injection also contains the inactive ingredient, (S)-lactic acid.
What Cyclizine lactate Injection looks like and contents of the pack Cyclizine lactate Injection is a Clear, colorless to slightly yellow solution. Each pack contains 5 or 10 ampoules. Not all pack sizes may be marketed.
Marketing Authorisation Holder and Manufacturer
Brown & Burk UK Ltd 5 Marryat Close Hounslow Middlesex TW4 5DQ United Kingdom This leaflet was last revised in 02/2026.
Cyclizine 50 mg/ml solution for injection comes as injection containing 50mg/ml. Always follow the dose your doctor or pharmacist has given you, and read the leaflet that comes with the medicine.
The active substance in Cyclizine 50 mg/ml solution for injection is cyclizine lactate.
Medicines with the same active substance, strength and form include: Valoid 50 mg/ml Injection, Cyclizine Lactate 50 mg/ml Injection, Cyclizine Lactate 50 mg/ml Injection – PL 35104/0021. In total there are 6 equivalent products. They are interchangeable only if your prescriber or pharmacist says so.
This leaflet reproduces the patient information leaflet approved for Cyclizine 50 mg/ml solution for injection, as published on the electronic medicines compendium (emc). The version printed inside your medicine’s packaging is the one that applies to you.
Whether a medicine is available over the counter or on prescription only depends on its licence. Check the leaflet, or ask your pharmacist — they can tell you straight away.
The text above reproduces the patient information leaflet approved for this medicine, restructured for easier reading.
Cyclizine lactate is indicated in adults for the prevention and treatment of nausea and vomiting including:-
• Motion sickness when the oral route cannot be used.
• Nausea and vomiting caused by narcotic analgesics and by general anaesthetics in the post-operative period.
• Vomiting associated with radiotherapy especially for breast cancer since Cyclizine does not elevate prolactin levels.
• Cyclizine lactate injection, by the intravenous route, is also indicated pre-operatively in patients undergoing emergency surgery inorder to reduce the hazard of regurgitation and aspiration of gastric contents during induction of general anaesthesia.
Cyclizine lactate may be of value in relieving vomiting and attacks of vertigo associated with Menière's disease and other forms of vestibular disturbance when the oral route cannot be used.
Posology
For the prevention of postoperative nausea and vomiting, administer the first dose by slow intravenous injection 20 minutes before the anticipated end of surgery.
Adults
50 mg intramuscularly or intravenously up to three times daily.
When used intravenously, cyclizine lactate should be injected slowly into the bloodstream, with only minimal withdrawal of blood into the syringe.
For the prevention of postoperative nausea and vomiting, administer the first dose by slow intravenous injection 20 minutes before the anticipated end of surgery.
Cyclizine given intravenously, in half the recommended dose, increases the lower oesophageal sphincter tone and thereby reduces the hazard of regurgitation and aspiration of gastric contents if given to patients, undergoing emergency surgery, before induction of general anaesthesia.
Elderly
There have been no specific studies of cyclizine lactate in the elderly. Experience has indicated that normal adult dosage is appropriate.
Paediatric population
Not licensed for use in children.
Method of Administration:
Intramuscularly or intravenously.
Hypersensitivity to the active substance or to any of the excipients listed in section 6.1.
Cyclizine lactate is contraindicated in the presence of acute alcohol intoxication. The anti-emetic properties of cyclizine may increase the toxicity of alcohol.
As with other anticholinergic agents, cyclizine lactate may precipitate incipient glaucoma and it should be used with caution and appropriate monitoring in patients with glaucoma, urinary retention, obstructive disease of the gastrointestinal tract, hepatic disease, pheochromocytoma, hypertension, epilepsy and in males with possible prostatic hypertrophy. Cyclizine lactate injection may have a hypotensive effect.
Cyclizine should be used with caution in patients with severe heart failure or acute myocardial infarction. In such patients, cyclizine may cause a fall in cardiac output associated with increases in heart rate, mean arterial pressure and pulmonary wedge pressure.
Cyclizine should be avoided in porphyria.
There have been reports of abuse of cyclizine, either oral or intravenous, for its euphoric or hallucinatory effects. The concomitant misuse of cyclizine lactate with large amounts of alcohol is particularly dangerous, since the antiemetic effect of cyclizine may increase the toxicity of alcohol (see also Section 4.5).
Case reports of paralysis have been received in patients using intravenous cyclizine. Some of the patients mentioned in these case reports had an underlying neuromuscular disorder. Thus intravenous cyclizine should be used with caution in all patients and with particular care in patients with underlying neuromuscular disorders.
Cyclizine lactate may have additive effects with alcohol and other central nervous system depressants e.g. hypnotics, tranquillisers, anaesthetics, antipsychotics, barbiturates.
Cyclizine lactate enhances the soporific effect of pethidine.
Cyclizine lactate may counteract the haemodynamic benefits of opioid analgesics.
Because of its anticholinergic activity, cyclizine may enhance the side-effects of other anticholinergic drugs, and may have an additive antimuscarinic action with other antimuscarinic drugs, such as atropine and some antidepressants (both tricyclics and MAOIs).
Cyclizine lactate may mask the warning signs of damage caused by ototoxic drugs such as aminoglycoside antibacterials.
Pregnancy
In the absence of any definitive human data, the use of cyclizine lactate in pregnancy is not advised.
Breast-feeding
Cyclizine is excreted in human milk, however, the amount has not been quantified.
Fertility
In a study involving prolonged administration of cyclizine to male and female rats, there was no evidence of impaired fertility after continuous treatment for 90-100 days at dose levels of approximately 15 and 25 mg/kg/day. There is no experience of the effect of cyclizine lactate on human fertility.
Studies designed to detect drowsiness did not reveal sedation in healthy adults who took a single oral therapeutic dose (50 mg) of cyclizine, sedation of short duration was reported by subjects receiving intravenous cyclizine.
Patients should not drive or operate machinery until they have determined their own response.
Although there are no data available, patients should be cautioned that cyclizine lactate may have additive effects with alcohol and other central nervous system depressants, e.g. hypnotics and tranquillisers.
Adverse reactions are ranked under heading of frequency, the most frequent first, using the following convention: Very common: (≥1/10); Common (≥1/100 to <1/10); Uncommon (≥1/1,000 to <1/100); Rare (≥1/10,000 to <1/1,000); Very rare(<1/10,000); Not known: cannot be estimated from the available data.
The following undesirable effects have been reported with a frequency of Not known.
System Organ Class
Frequency
Adverse Reactions
Blood and lymphatic system disorders
Not known
Agranulocytosis, leucopenia, haemolytic anaemia, thrombocytopenia.
Cardiac disorders
Not known
Tachycardia palpitations, arrhythmias (see section 4.4)
Ear and labyrinth disorders
Not known
Tinnitus.
There have been rare case reports of patients experiencing depressed levels of consciousness/loss of consciousness.
Eye disorders
Not known
Blurred vision, oculogyric crisis
Gastrointestinal system disorders
Not known
Dryness of the mouth, nose and throat, constipation, increased gastric reflux, nausea, vomiting, diarrhoea, stomach pain, loss of appetite.
General disorders and administration site conditions
Not known
Asthenia
Injection site reactions including vein tracking, erythema, pain, thrombophlebitis and blisters. A sensation of heaviness, chills and pruritus have been reported rarely.
Anaphylaxis has been recorded following intravenous administration of cyclizine co-administered with propanidid in the same syringe.
Hepatobiliary disorders
Not known
Hepatic dysfunction (see section 4.4), hypersensitivity hepatitis, cholestatic jaundice and cholestatic hepatitis have occurred in association with cyclizine.
Immune system disorders
Not known
Hypersensitivity reactions, including anaphylaxis have occurred.
Musculoskeletal and connective tissue disorders
Not known
Twitching, muscle spasms
Nervous system disorders
Not known
Effects on the central nervous system have been reported with cyclizine these include somnolence, drowsiness, incoordination, headache, dystonia, dyskinesia, extrapyramidal motor disturbances, restless legs syndrome, tremor, convulsions, dizziness, decreased consciousness, transient speech disorders, paraesthesia, paralysis* and generalised chorea.
Psychiatric disorders
Not known
Disorientation, restlessness or agitation, nervousness, euphoria, insomnia and auditory and visual hallucinations have been reported, particularly when dosage recommendations have been exceeded.
Renal and urinary disorders
Not known
Urinary retention
Respiratory, thoracic and mediastinal disorders
Not known
Bronchospasm, apnoea
Skin and subcutaneous tissue disorders
Not known
Urticaria, pruritus, drug rash, angioedema, allergic skin reactions, fixed drug eruption, photosensitivity
Vascular disorders
Not known
Hypertension, hypotension
* Case reports of paralysis have been received in patients using intravenous cyclizine. Some of the patients mentioned in these case reports had an underlying neuromuscular disorder (see section 4.4).
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.
Symptoms
Symptoms of acute toxicity from cyclizine arise from peripheral anticholinergic effects and effects on the central nervous system.
Peripheral anticholinergic symptoms include, dry mouth, nose and throat, blurred vision, tachycardia and urinary retention. Central nervous system effects include drowsiness, dizziness, incoordination, ataxia, weakness, hyperexcitability, disorientation, impaired judgement, hallucinations, hyperkinesia, extrapyramidal motor disturbances, convulsions, hyperpyrexia and respiratory depression.
An oral dose of 5 mg/kg is likely to be associated with at least one of the clinical symptoms stated above. Younger children are more susceptible to convulsions. The incidence of convulsions, in children less than 5 years, is about 60% when the oral dose ingested exceeds 40 mg/kg.
Management
In the management of acute overdosage with cyclizine lactate, gastric lavage and supportive measures for respiration and circulation should be performed if necessary. Convulsions should be controlled in the usual way with parenteral anticonvulsant therapy.
Ask anything about Cyclizine 50 mg/ml solution for injection. The assistant answers only from this leaflet — if the leaflet does not cover it, it will say so. It does not give medical advice.
Answers come from the patient leaflet published on the electronic medicines compendium (emc). They are not medical advice. Ask a pharmacist or your GP if you are unsure. For urgent help call NHS 111, or 999 in an emergency.
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