- Approval Id
- 71019adb96e2d38d
- Drug Approval Emc Name
- Phenergan Elixir
- Drug Name
- Phenergan Elixir
- Company Name
- Opella Healthcare UK Limited
- Company Address
- 410, Thames Valley Park Drive, Reading, Berkshire, RG6 1PT, UK
- Company Telephone
- +44 (0)118 354 3000
- Company Medical Info Direct Line
- +44 (0)800 035 2525
- Company Medical Info Email
- uk-medicalinformation@sanofi.com
- Atc Code
- R06AD02
- Legal Category
- Pharmacy
- Authorisation Holder
- Opella Healthcare UK Limited, trading as Sanofi
410 Thames Valley Park Drive,
Reading,
Berkshire,
RG6 1PT,
United Kingdom.
- Authorisation Number
- PL 53886/0057
- Authorisation Date
- Date of first authorisation: 28 February 1973
Date of latest renewal: 12 June 2003
- Instruction Authorisation Holder
- Opella Healthcare UK Limited, trading as Sanofi
410 Thames Valley Park Drive,
Reading,
Berkshire,
RG6 1PT,
United Kingdom.
- Instruction Authorisation Number
- PL 53886/0057
- Instruction Authorisation Date
- Date of first authorisation: 28 February 1973
Date of latest renewal: 12 June 2003
- Instruction Composition
- Each 5ml of solution contains 5 mg of the active substance promethazine hydrochloride.
Excipient(s) with known effect:
Each 5 ml of solution contains 36.65 mg sodium, 1.457 mg potassium, and 5 mg sodium benzoate (see section 4.4).
Also contains maltitol, sodium sulphite anhydrous (E221) and sodium metabisulphite (E223).
For the full list of excipients see section 6.1.
- Instruction Dosage Form
- Oral Solution
Clear, golden, syrupy liquid.
- Instruction Clinical Particulars
- 4.1 Therapeutic indications
• As symptomatic treatment for allergic conditions of the upper respiratory tract and skin including allergic rhinitis, urticaria and anaphylactic reactions to drugs and foreign proteins.
• As an antiemetic.
For short term use:
• Treatment of insomnia in adults.
• As a paediatric sedative.4.2 Posology and method of administration
Paediatric population
Not for use in children under the age of 6 years (see section 4.3).
\*As an antihistamine in allergy:\*
| | |
| --- | --- |
| Children 6 – 10 years | Either 10 – 25 mg as a single dose. Or 5 – 10 mg twice a day. Maximum daily dose 25 mg. |
| Children over 10 years and adults (including elderly) | Initially 10 mg twice a day. Increasing to a maximum of 20 mg three times a day as required. |
\*As an antiemetic:\*
| | |
| --- | --- |
| Children 6 – 10 years | 10 mg to be taken the night before the journey. To be repeated after 6 – 8 hours as required. |
| Children over 10 years and adults (including elderly) | 25 mg to be taken the night before the journey. To be repeated after 6 – 8 hours as required. |
\*As a paediatric sedative for short term use and for short term treatment of insomnia in adults:\*
| | |
| --- | --- |
| Children 6 – 10 years | 20 mg or 25 mg as a single night time dose. |
| Children over 10 years and adults (including elderly) | 25 mg or 50 mg as a single night time dose. The use of Phenergan tablets to provide these doses is recommended. |
Method of administration
For oral administration.4.3 Contraindications
• Phenergan should not be given to patients with a known hypersensitivity to promethazine, other phenothiazines, or to any other ingredients in the formulation of Phenergan Elixir.
• Phenergan should not be used in patients in coma or suffering from CNS depression of any cause.
• Phenergan is contraindicated for use in children less than 6 years of age (see Section 4.4).
• Phenergan should be avoided in patients taking monoamine oxidase inhibitors up to 14 days previously.4.4 Special warnings and precautions for use
Hypersensitivity reactions including anaphylaxis, urticaria and angioedema have been reported with Phenergan Elixir use. In case of allergic reaction, treatment with Phenergan Elixir must be discontinued and appropriate symptomatic treatment initiated (see Section 4.8).
Phenergan Elixir should be avoided in patients with liver or renal dysfunction, Parkinson's disease, hypothyroidism, cardiac failure, pheochromocytoma, myasthenia gravis, or prostate hypertrophy, or in patients with a history of narrow angle glaucoma or agranulocytosis.
Caution must be exercised when using H1-antihistamines such as Phenergan Elixir due to the risk of sedation. Combined use with other sedative medicinal products is not recommended (see section 4.5).
Phenergan Elixir should not be used for longer than 7 days without seeking medical advice.
Caution should be used in patients with:
• Asthma, bronchitis or bronchiectasis. Phenergan may thicken or dry lung secretions and impair expectoration.
• Severe coronary artery disease
• Epilepsy
• Bladder neck or pyloro-duodenal obstruction
Otoxicity
Promethazine may mask the warning signs of ototoxicity caused by ototoxic drugs e.g. salicylates.
It may also delay the early diagnosis of intestinal obstruction or raised intracranial pressure through the suppression of vomiting.
QT prolongation
Phenothiazine derivatives may potentiate QT interval prolongation which increases the risk of onset of serious ventricular arrhythmias of the torsade de pointes type, which is potentially fatal (sudden death). QT prolongation is exacerbated, in particular, in the presence of bradycardia, hypokalemia, and acquired (i.e. drug induced) QT prolongation. If the clinical situation permits, medical and laboratory evaluations should be performed to rule out possible risk factors before initiating treatment with a phenothiazine derivative and as deemed necessary during treatment (see section 4.8).
Photosensitivity reactions
Due to the risk of photosensitivity, exposure to strong sunlight or ultraviolet light should be avoided during or shortly after treatment.
Paediatric population
Promethazine must not be used in children less than six years of age due to the potential for fatal respiratory depression, psychiatric and CNS events (see section 4.3 and section 4.8).
The use of promethazine should be avoided in children and adolescents with signs and symptoms suggestive of Reye's Syndrome.
Excipients with known effect
\*Sugar as hydrogenated glucose syrup (maltitol liquid):\* Patients with rare hereditary problems of fructose intolerance should not take this medicine. If you have diabetes, you should be aware that Phenergan Elixir contains carbohydrates, which the body will convert into small amounts of sugar. The maximum 25 ml single dose of Phenergan Elixir is equivalent to approximately 5 g of sugar, or one teaspoon of sugar/sugar lump. Taking this amount of Phenergan Elixir is unlikely to affect the control of your diabetes or require you to increase your diabetes medication.
\*Sodium:\* This medicinal product contains 36.65 mg sodium per 5 ml, equivalent to 1.83% of the WHO recommended daily intake of 2 g sodium for an adult. This should be taken into account if you are on a controlled sodium diet.
\*Sulphites\*: These are preservatives used in Phenergan Elixir, which may rarely cause severe hypersensitivity reaction , characterised by circulatory collapse with CNS depression and bronchospasm in certain susceptible individuals with allergic tendencies.
\*Benzoic acid:\* Phenergan Elixir contains 5mg sodium benzoate in each 5ml dose, which is equivalent to 1mg/ml. Sodium benzoate may increase bilirubinemia in newborn babies (up to 4 weeks old).
Alcohol and alcohol-containing medicines should be avoided while on this medicine (see section 4.5).
Phenothiazines may be additive with, or may potentiate the action of, other CNS depressants such as opiates or other analgesics, barbiturates or other sedatives, general anesthetics, or alcohol.
The occurrence of unexplained infections or fever may be evidence of blood dyscrasia (see section 4.8), and requires immediate hematological investigation.
All patients should be advised that, if they experience fever, sore throat or any other infection, they should inform their physician immediately and undergo a complete blood count. Treatment should be discontinued if any marked changes (hyperleucocytosis, granulocytopenia) are observed in the blood count.4.5 Interaction with other medicinal products and other forms of interaction
Phenergan will enhance the action of any anticholinergic agent, tricyclic antidepressant, sedative or hypnotic.
Alcohol should be avoided during treatment. Combination with alcohol enhances the sedative effects of H1 antihistamines.
Phenergan may interfere with immunological urine pregnancy tests to produce false-positive or false-negative results.
Phenergan should be discontinued at least 72 hours before the start of skin tests as it may inhibit the cutaneous histamine response thus producing false-negative results.
Special caution is required when promethazine is used concurrently with drugs known to cause QT prolongation (such as antiarrhythmics, antimicrobials, antidepressants, antipsychotics) to avoid exacerbation of risk of QT prolongation.
Cytochrome P450 2D6 Metabolism: Some phenothiazines are moderate inhibitors of CYP2D6. There is a possible pharmacokinetic interaction between inhibitors of CYP2D6, such as phenothiazines, and CYP2D6 substrates. Co administration of promethazine with amitriptyline/amitriptylinoxide, a CYP2D6 substrate, may lead to an increase in the plasma levels of amitriptyline/amitriptylinoxide. Monitor patients for dose-dependent adverse reactions associated with amitriptyline/amitriptylinoxide.
Phenergan should be avoided in patients taking monamine oxidase inhibitors within the previous 14 days, and monamine oxidase inhibitors should be avoided while using Phenergan.
Seizure threshold-lowering drugs: Concomitant use of seizure-inducing drugs or seizure threshold-lowering drugs should be carefully considered due to the severity of the risk for the patient (see section 4.4).
Gastro-intestinal agents that are not absorbed (magnesium, aluminium and calcium salts, oxides and hydroxides): Reduced gastro-intestinal absorption of phenothiazines may occur. Such gastro-intestinal agents should not be taken at the same time as phenothiazines (at least 2 hours apart, if possible).
Drugs with anticholinergic properties: Concomitant use of Phenergan with drugs with anticholinergic properties enhances the anticholinergic effect.4.6 Fertility, pregnancy and lactation
Pregnancy
The use of Phenergan Elixir is not recommended during pregnancy and in women of childbearing potential not using contraception, unless the potential benefits outweigh the potential risks.When promethazine has been given in high doses during late pregnancy, promethazine has caused prolonged neurological disturbances in the infant.
Advise patients to inform their healthcare provider of a known or suspected pregnancy. Advise patients to avoid becoming pregnant while receiving this medicine. Advise female patients of reproductive potential to use effective contraception.
There are no available animal studies regarding reproductive toxicity.
Breast-feeding
Phenergan Elixir is excreted in breast milk (see section 5.2). There are risks of neonatal irritability and excitement. Phenergan Elixir is not recommended for use in breast-feeding.
Fertility
There are no relevant fertility data in animals.4.7 Effects on ability to drive and use machines
Because the duration of action may be up to 12 hours, patients should be advised that if they feel drowsy, dizzy and have blurred vision, they should not drive or operate heavy machinery.4.8 Undesirable effects
The following CIOMS frequency rating is used: \*Very common (≥ 1/10); common (≥ 1/100 to <1/10); uncommon (≥ 1/1000 to <1/100); rare (≥ 1/10 00 to <1/1000); very rare (<1/10 000), not known (cannot be estimated from the available data).\*
Immune system disorders
Frequency not known: Allergic reactions, including anaphylactic reaction, urticaria, angioedema.
Skin and subcutaneous tissue disorders
Frequency not known: Rash, photosensitivity reaction.
Nervous system disorders
Very common: Sedation or somnolence
Frequency not known: Dizziness, headaches, extrapyramidal effects, restless legs syndrome, muscle spasms and tic-like movements of the head and face.
Frequency not known: Dystonia, including oculogyric crisis, usually transitory are commoner in children and young adults, and usually occur within the first 4 days of treatment or after dosage increases.
Frequency not known: Anticholinergic effects such as ileus paralytic, risk of urinary retention, dry mouth, constipation, accommodation disorder. The elderly are particularly susceptible to the anticholinergic effects and confusion due to promethazine.
Frequency Not known: children less than 6 years of age also experienced psychomotor hyperactivity.
Psychiatric disorders
Frequency not known: Agitation, confusional state, anxiety.
Frequency not known: Infants, newborns and premature are susceptible to the anticholinergic effects of promethazine, while other children may display paradoxical hyperexcitability, restlessness, nightmares, disorientation
Frequency Not known: children less than 6 years of age also experienced aggression and hallucination.
Eye disorders
Frequency not known: Blurred vision
Gastrointestinal disorders
Frequency not known: Epigastric irritation/discomfort, dry mouth
Renal and urinary disorders
Frequency not known: Urinary retention
Metabolism and nutrition disorders
Frequency not known: Decreased appetite
Cardiac disorders
Frequency not known: Palpitations, arrhythmias (including QT prolongation and torsade de pointes)
Vascular disorders
Frequency not known: Hypotension
Respiratory, thoracic and mediastinal disorders
Frequency not known: Respiratory depression (see Section 4.4), nasal congestion
Hepatobiliary disorders
Frequency not known: Jaundice cholestatic
Blood and lymphatic system disorders
Frequency not known: Blood dyscrasias including haemolytic anaemia, agranulocytosis, leukopenia, eosinophilia, thrombocytopenia (including thrombocytopenic purpura).
General disorders and administration site conditions
Frequency not known: Tiredness
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 Yellow Card Scheme at: www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store.4.9 Overdose
Symptoms
Symptoms of severe overdosage are variable. They are characterised in children by various combinations of excitation, ataxia, incoordination, athetosis and hallucinations, intellectual disability and cognition deficit in children less than 6 years of age while adults may become drowsy and lapse into coma. Convulsions may occur in both adults and children; coma or excitement may precede their occurrence. Tachycardia may develop. Cardiorespiratory depression is uncommon. High doses (supratherapeutic doses) can cause ventricular arrhythmias including QT prolongation and torsade de pointes (see section 4.8).
Management
If the patient is seen soon enough after ingestion, it should be possible to induce vomiting with ipecacuanha despite the antiemetic effect of promethazine; alternatively, gastric lavage may be used.
Treatment is otherwise supportive with attention to maintenance of adequate respiratory and circulatory status. Convulsions should be treated with diazepam or another suitable anticonvulsant.
In the event of overdose of Phenergan, take all appropriate measures immediately.
- Instruction Pharmacology
- 5.1 Pharmacodynamic properties
Pharmacotherapeutic group: Antihistamines for systemic use; Phenothiazine derivatives, ATC code: R06AD02
Potent, long acting, antihistamine with additional anti-emetic central sedative and anti-cholinergic properties.5.2 Pharmacokinetic properties
Promethazine is distributed widely in the body. It enters the brain and crosses the placenta. Promethazine is slowly excreted via urine and bile. Phenothiazines pass into the milk at low concentrations.5.3 Preclinical safety data
No additional preclinical data of relevance to the prescriber.
- Instruction Pharmaceutical Particulars
- 6.1 List of excipients
Maltitol liquid
Citric acid monohydrate (E330)
Sodium citrate (E331)
Ascorbic acid (E300)
Sodium sulphite anhydrous (E221)
Sodium metabisulphite (E223)
Sodium benzoate (E211)
Orange juice flavour 510844E
Caramel (E150)
Acesulfame potassium (E950)
Purified water6.2 Incompatibilities
None stated.6.3 Shelf life
2 years when unopened.
1 month when opened.6.4 Special precautions for storage
Store below 25° C. Keep the bottle in the outer carton in order to protect from light.6.5 Nature and contents of container
Amber glass type III bottle containing 100 ml. Closed by a child-proof cap with a seal containing polyvinylidene chloride seal.6.6 Special precautions for disposal and other handling
No special requirements.
- Instruction Content
- ## Composition
Each 5ml of solution contains 5 mg of the active substance promethazine hydrochloride.
Excipient(s) with known effect:
Each 5 ml of solution contains 36.65 mg sodium, 1.457 mg potassium, and 5 mg sodium benzoate (see section 4.4).
Also contains maltitol, sodium sulphite anhydrous (E221) and sodium metabisulphite (E223).
For the full list of excipients see section 6.1.
## Pharmaceutical Form
Oral Solution
Clear, golden, syrupy liquid.
## Clinical Particulars
4.1 Therapeutic indications
• As symptomatic treatment for allergic conditions of the upper respiratory tract and skin including allergic rhinitis, urticaria and anaphylactic reactions to drugs and foreign proteins.
• As an antiemetic.
For short term use:
• Treatment of insomnia in adults.
• As a paediatric sedative.4.2 Posology and method of administration
Paediatric population
Not for use in children under the age of 6 years (see section 4.3).
\*As an antihistamine in allergy:\*
| | |
| --- | --- |
| Children 6 – 10 years | Either 10 – 25 mg as a single dose. Or 5 – 10 mg twice a day. Maximum daily dose 25 mg. |
| Children over 10 years and adults (including elderly) | Initially 10 mg twice a day. Increasing to a maximum of 20 mg three times a day as required. |
\*As an antiemetic:\*
| | |
| --- | --- |
| Children 6 – 10 years | 10 mg to be taken the night before the journey. To be repeated after 6 – 8 hours as required. |
| Children over 10 years and adults (including elderly) | 25 mg to be taken the night before the journey. To be repeated after 6 – 8 hours as required. |
\*As a paediatric sedative for short term use and for short term treatment of insomnia in adults:\*
| | |
| --- | --- |
| Children 6 – 10 years | 20 mg or 25 mg as a single night time dose. |
| Children over 10 years and adults (including elderly) | 25 mg or 50 mg as a single night time dose. The use of Phenergan tablets to provide these doses is recommended. |
Method of administration
For oral administration.4.3 Contraindications
• Phenergan should not be given to patients with a known hypersensitivity to promethazine, other phenothiazines, or to any other ingredients in the formulation of Phenergan Elixir.
• Phenergan should not be used in patients in coma or suffering from CNS depression of any cause.
• Phenergan is contraindicated for use in children less than 6 years of age (see Section 4.4).
• Phenergan should be avoided in patients taking monoamine oxidase inhibitors up to 14 days previously.4.4 Special warnings and precautions for use
Hypersensitivity reactions including anaphylaxis, urticaria and angioedema have been reported with Phenergan Elixir use. In case of allergic reaction, treatment with Phenergan Elixir must be discontinued and appropriate symptomatic treatment initiated (see Section 4.8).
Phenergan Elixir should be avoided in patients with liver or renal dysfunction, Parkinson's disease, hypothyroidism, cardiac failure, pheochromocytoma, myasthenia gravis, or prostate hypertrophy, or in patients with a history of narrow angle glaucoma or agranulocytosis.
Caution must be exercised when using H1-antihistamines such as Phenergan Elixir due to the risk of sedation. Combined use with other sedative medicinal products is not recommended (see section 4.5).
Phenergan Elixir should not be used for longer than 7 days without seeking medical advice.
Caution should be used in patients with:
• Asthma, bronchitis or bronchiectasis. Phenergan may thicken or dry lung secretions and impair expectoration.
• Severe coronary artery disease
• Epilepsy
• Bladder neck or pyloro-duodenal obstruction
Otoxicity
Promethazine may mask the warning signs of ototoxicity caused by ototoxic drugs e.g. salicylates.
It may also delay the early diagnosis of intestinal obstruction or raised intracranial pressure through the suppression of vomiting.
QT prolongation
Phenothiazine derivatives may potentiate QT interval prolongation which increases the risk of onset of serious ventricular arrhythmias of the torsade de pointes type, which is potentially fatal (sudden death). QT prolongation is exacerbated, in particular, in the presence of bradycardia, hypokalemia, and acquired (i.e. drug induced) QT prolongation. If the clinical situation permits, medical and laboratory evaluations should be performed to rule out possible risk factors before initiating treatment with a phenothiazine derivative and as deemed necessary during treatment (see section 4.8).
Photosensitivity reactions
Due to the risk of photosensitivity, exposure to strong sunlight or ultraviolet light should be avoided during or shortly after treatment.
Paediatric population
Promethazine must not be used in children less than six years of age due to the potential for fatal respiratory depression, psychiatric and CNS events (see section 4.3 and section 4.8).
The use of promethazine should be avoided in children and adolescents with signs and symptoms suggestive of Reye's Syndrome.
Excipients with known effect
\*Sugar as hydrogenated glucose syrup (maltitol liquid):\* Patients with rare hereditary problems of fructose intolerance should not take this medicine. If you have diabetes, you should be aware that Phenergan Elixir contains carbohydrates, which the body will convert into small amounts of sugar. The maximum 25 ml single dose of Phenergan Elixir is equivalent to approximately 5 g of sugar, or one teaspoon of sugar/sugar lump. Taking this amount of Phenergan Elixir is unlikely to affect the control of your diabetes or require you to increase your diabetes medication.
\*Sodium:\* This medicinal product contains 36.65 mg sodium per 5 ml, equivalent to 1.83% of the WHO recommended daily intake of 2 g sodium for an adult. This should be taken into account if you are on a controlled sodium diet.
\*Sulphites\*: These are preservatives used in Phenergan Elixir, which may rarely cause severe hypersensitivity reaction , characterised by circulatory collapse with CNS depression and bronchospasm in certain susceptible individuals with allergic tendencies.
\*Benzoic acid:\* Phenergan Elixir contains 5mg sodium benzoate in each 5ml dose, which is equivalent to 1mg/ml. Sodium benzoate may increase bilirubinemia in newborn babies (up to 4 weeks old).
Alcohol and alcohol-containing medicines should be avoided while on this medicine (see section 4.5).
Phenothiazines may be additive with, or may potentiate the action of, other CNS depressants such as opiates or other analgesics, barbiturates or other sedatives, general anesthetics, or alcohol.
The occurrence of unexplained infections or fever may be evidence of blood dyscrasia (see section 4.8), and requires immediate hematological investigation.
All patients should be advised that, if they experience fever, sore throat or any other infection, they should inform their physician immediately and undergo a complete blood count. Treatment should be discontinued if any marked changes (hyperleucocytosis, granulocytopenia) are observed in the blood count.4.5 Interaction with other medicinal products and other forms of interaction
Phenergan will enhance the action of any anticholinergic agent, tricyclic antidepressant, sedative or hypnotic.
Alcohol should be avoided during treatment. Combination with alcohol enhances the sedative effects of H1 antihistamines.
Phenergan may interfere with immunological urine pregnancy tests to produce false-positive or false-negative results.
Phenergan should be discontinued at least 72 hours before the start of skin tests as it may inhibit the cutaneous histamine response thus producing false-negative results.
Special caution is required when promethazine is used concurrently with drugs known to cause QT prolongation (such as antiarrhythmics, antimicrobials, antidepressants, antipsychotics) to avoid exacerbation of risk of QT prolongation.
Cytochrome P450 2D6 Metabolism: Some phenothiazines are moderate inhibitors of CYP2D6. There is a possible pharmacokinetic interaction between inhibitors of CYP2D6, such as phenothiazines, and CYP2D6 substrates. Co administration of promethazine with amitriptyline/amitriptylinoxide, a CYP2D6 substrate, may lead to an increase in the plasma levels of amitriptyline/amitriptylinoxide. Monitor patients for dose-dependent adverse reactions associated with amitriptyline/amitriptylinoxide.
Phenergan should be avoided in patients taking monamine oxidase inhibitors within the previous 14 days, and monamine oxidase inhibitors should be avoided while using Phenergan.
Seizure threshold-lowering drugs: Concomitant use of seizure-inducing drugs or seizure threshold-lowering drugs should be carefully considered due to the severity of the risk for the patient (see section 4.4).
Gastro-intestinal agents that are not absorbed (magnesium, aluminium and calcium salts, oxides and hydroxides): Reduced gastro-intestinal absorption of phenothiazines may occur. Such gastro-intestinal agents should not be taken at the same time as phenothiazines (at least 2 hours apart, if possible).
Drugs with anticholinergic properties: Concomitant use of Phenergan with drugs with anticholinergic properties enhances the anticholinergic effect.4.6 Fertility, pregnancy and lactation
Pregnancy
The use of Phenergan Elixir is not recommended during pregnancy and in women of childbearing potential not using contraception, unless the potential benefits outweigh the potential risks.When promethazine has been given in high doses during late pregnancy, promethazine has caused prolonged neurological disturbances in the infant.
Advise patients to inform their healthcare provider of a known or suspected pregnancy. Advise patients to avoid becoming pregnant while receiving this medicine. Advise female patients of reproductive potential to use effective contraception.
There are no available animal studies regarding reproductive toxicity.
Breast-feeding
Phenergan Elixir is excreted in breast milk (see section 5.2). There are risks of neonatal irritability and excitement. Phenergan Elixir is not recommended for use in breast-feeding.
Fertility
There are no relevant fertility data in animals.4.7 Effects on ability to drive and use machines
Because the duration of action may be up to 12 hours, patients should be advised that if they feel drowsy, dizzy and have blurred vision, they should not drive or operate heavy machinery.4.8 Undesirable effects
The following CIOMS frequency rating is used: \*Very common (≥ 1/10); common (≥ 1/100 to <1/10); uncommon (≥ 1/1000 to <1/100); rare (≥ 1/10 00 to <1/1000); very rare (<1/10 000), not known (cannot be estimated from the available data).\*
Immune system disorders
Frequency not known: Allergic reactions, including anaphylactic reaction, urticaria, angioedema.
Skin and subcutaneous tissue disorders
Frequency not known: Rash, photosensitivity reaction.
Nervous system disorders
Very common: Sedation or somnolence
Frequency not known: Dizziness, headaches, extrapyramidal effects, restless legs syndrome, muscle spasms and tic-like movements of the head and face.
Frequency not known: Dystonia, including oculogyric crisis, usually transitory are commoner in children and young adults, and usually occur within the first 4 days of treatment or after dosage increases.
Frequency not known: Anticholinergic effects such as ileus paralytic, risk of urinary retention, dry mouth, constipation, accommodation disorder. The elderly are particularly susceptible to the anticholinergic effects and confusion due to promethazine.
Frequency Not known: children less than 6 years of age also experienced psychomotor hyperactivity.
Psychiatric disorders
Frequency not known: Agitation, confusional state, anxiety.
Frequency not known: Infants, newborns and premature are susceptible to the anticholinergic effects of promethazine, while other children may display paradoxical hyperexcitability, restlessness, nightmares, disorientation
Frequency Not known: children less than 6 years of age also experienced aggression and hallucination.
Eye disorders
Frequency not known: Blurred vision
Gastrointestinal disorders
Frequency not known: Epigastric irritation/discomfort, dry mouth
Renal and urinary disorders
Frequency not known: Urinary retention
Metabolism and nutrition disorders
Frequency not known: Decreased appetite
Cardiac disorders
Frequency not known: Palpitations, arrhythmias (including QT prolongation and torsade de pointes)
Vascular disorders
Frequency not known: Hypotension
Respiratory, thoracic and mediastinal disorders
Frequency not known: Respiratory depression (see Section 4.4), nasal congestion
Hepatobiliary disorders
Frequency not known: Jaundice cholestatic
Blood and lymphatic system disorders
Frequency not known: Blood dyscrasias including haemolytic anaemia, agranulocytosis, leukopenia, eosinophilia, thrombocytopenia (including thrombocytopenic purpura).
General disorders and administration site conditions
Frequency not known: Tiredness
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 Yellow Card Scheme at: www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store.4.9 Overdose
Symptoms
Symptoms of severe overdosage are variable. They are characterised in children by various combinations of excitation, ataxia, incoordination, athetosis and hallucinations, intellectual disability and cognition deficit in children less than 6 years of age while adults may become drowsy and lapse into coma. Convulsions may occur in both adults and children; coma or excitement may precede their occurrence. Tachycardia may develop. Cardiorespiratory depression is uncommon. High doses (supratherapeutic doses) can cause ventricular arrhythmias including QT prolongation and torsade de pointes (see section 4.8).
Management
If the patient is seen soon enough after ingestion, it should be possible to induce vomiting with ipecacuanha despite the antiemetic effect of promethazine; alternatively, gastric lavage may be used.
Treatment is otherwise supportive with attention to maintenance of adequate respiratory and circulatory status. Convulsions should be treated with diazepam or another suitable anticonvulsant.
In the event of overdose of Phenergan, take all appropriate measures immediately.
## Pharmacological Properties
5.1 Pharmacodynamic properties
Pharmacotherapeutic group: Antihistamines for systemic use; Phenothiazine derivatives, ATC code: R06AD02
Potent, long acting, antihistamine with additional anti-emetic central sedative and anti-cholinergic properties.5.2 Pharmacokinetic properties
Promethazine is distributed widely in the body. It enters the brain and crosses the placenta. Promethazine is slowly excreted via urine and bile. Phenothiazines pass into the milk at low concentrations.5.3 Preclinical safety data
No additional preclinical data of relevance to the prescriber.
## Pharmaceutical Particulars
6.1 List of excipients
Maltitol liquid
Citric acid monohydrate (E330)
Sodium citrate (E331)
Ascorbic acid (E300)
Sodium sulphite anhydrous (E221)
Sodium metabisulphite (E223)
Sodium benzoate (E211)
Orange juice flavour 510844E
Caramel (E150)
Acesulfame potassium (E950)
Purified water6.2 Incompatibilities
None stated.6.3 Shelf life
2 years when unopened.
1 month when opened.6.4 Special precautions for storage
Store below 25° C. Keep the bottle in the outer carton in order to protect from light.6.5 Nature and contents of container
Amber glass type III bottle containing 100 ml. Closed by a child-proof cap with a seal containing polyvinylidene chloride seal.6.6 Special precautions for disposal and other handling
No special requirements.
