UNICOUGH 14mg / 135mg / 1.1mg in 5ml Oral Solution
|Each 5ml contains:Diphenhydramine Hydrochloride Ammonium ChlorideLevomenthol
|| 14.00 mg 135.00 mg 1.10 mg
For full list of excipients, see section 6.1
Appearance: smooth brown solution
For the oral symptomatic relief of common coughs (such as dry and/or tickly, or troublesome cough) associated with upper respiratory tract congestion and aids restful sleep.
One to two 5ml spoonfuls to be taken every 4 hours
To aid sleep the patient may start with two 5ml spoonfuls at bedtime followed by two 5ml spoonfuls every 6 hours.
Not suitable for children under 12 years.
Do not take more than 4 doses (1 dose = two 5ml spoonfuls) in 24 hours.
Do not exceed the stated dose.
Method of Administration
• Hypersensitivity to any of the ingredients
• Children below 12 years of age
• Patients on monoamine oxidase inhibitor therapy within previous 14 days (see Section 4.5)
Do not combine with other treatments for coughs and colds.
Unicough Oral Solution should be used with caution in patients with the following conditions : prostatic hypertrophy, urinary retention, susceptibility to 'closed angle' glaucoma and hepatic disease.
Unicough Oral Solution may cause drowsiness.
Seek medical advice when suffering from chronic or persistent cough and when also suffering from asthma, and acute asthmatic attack or where cough is accompanied by excessive secretions
Keep out of the reach and sight of children.
Parahydroxybenzoates may cause allergic reactions (possible delayed).
Sucrose: Patients with rare hereditary problems of fructose intolerance, glucose-galactose malabsorption or sucrose-isomaltase insufficiency should not take this medicine.
• Additive CNS depressant effects with alcohol and other CNS depressants including barbiturates, hypnotics, opiod analgesics, anxiolytic sedatives and anti-psychotics.
• Additive anti-muscarinic effects with other drugs of similar properties such as atropine and some anti-depressants.
• Not to be taken in patients taking monoamine oxidase inhibitors (MAOIs) or within 14 of stopping treatment as there is a risk of serotonin syndrome.
• Diphenhydramine can inhibit the oxidative metabolism of some drugs.
• Diphenhydramine may enhance the effects of ephedrine.
• Diphenhydramine may mask the response of the skin to allergenic skin tests and also the ototoxic symptoms associated with certain antibiotics.
In view of the potential risks versus small benefits, it is recommended that Unicough Oral Solution should not be used during pregnancy particularly as the safety of Unicough Oral Solution in human pregnancy is not established.
In view of the potential risks versus small benefits, it is recommended that Unicough Oral Solution should not be used during lactation particularly as the safety of Unicough Oral Solution during lactation is not established.
Unicough Oral Solution may cause drowsiness. Do not drive or operate machinery. Avoid alcoholic drink.
The overall percentage of treated patients expected to experience adverse reactions is unknown.
Common side effects include:
CNS effects such as nervous drowsiness (usually diminishes within a few days), paradoxical stimulation, nervous headache, nervous psychomotor impairment.
Anti-muscarinic effects such as urinary retention, dry mouth, blurred vision, gastrointestinal disturbances and thickened respiratory tract secretions.
Rare side effects include:
Hypotension, extrapyramidal effects, dizziness, confusion, depression, sleep disturbances, tremor, convulsions, palpitation, arrhythmia, hypersensitivity reactions, blood disorders and liver dysfunction.
| Organ system Class
|| Common ADRs, >1/100, < 1/10
|| Uncommon ADRs, >1/1,000, <1/100
|| Rare ADRs >1/10,000, <1/1000
| Blood Lymphatic System Disorder
|| Blood Disorders NOS
| Cardiac Disorder
|| Palpitation, arrhythmia
| Eye Disorders
|| Blurred vision
| Gastrointestinal Disorder
|| Dry mouth, gastrointestinal disturbance
| General Disorder
|| Paradoxical drug reaction
| Hepatobiliary Disorder
|| Liver Disorder
| Immune System Disorders
| Nervous System Disorders
|| Psychomotor skills impairment, drowsiness, headache
|| Tremor, convulsions, extrapyramidal disorder, dizziness
| Psychiatric Disorders
|| Confusion, depression, sleep disturbances
| Renal and Urinary Disorder
|| Urinary retention
| Respiratory Disorder
|| Increased upper airway secretion
| Vascular Disorders
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 Website: www.mhra.gov.uk/yellowcard
Symptoms of overdosage include those due to diphenhydramine or menthol (drowsiness, dizziness, ataxia, anti-cholinergic effects, pyrexia, headaches, convulsions, hallucinations, excitement and respiratory depression).
Treatment consists of gastric lavage and aspiration. Administration of activated charcoal may help. Other symptomatic and supportive measures should be provided.
Pharmacotherapeutic group: Antihistamines for systemic use
ATC Code: R06AA52Diphenhydramine
possesses antitussive, antihistaminic, and anticholinergic properties and suppresses the urge to cough. It also dries up secretions in the nose and chest. Experiments have shown that the antitussive effect is discrete from its sedative effect. Taken at night will assist sleepingAmmonium Chloride
"Traditional" Expectorant. Menthol
Subjective relief of upper respiratory congestion, it has mild local anaesthetic and cooling effect.
Unicough oral solution is a thick demulcent, which in the buccal cavity and throat forms a soothing film over the mucous membrane. This brings it into contact with the sensitive nerve endings of the throat lining.
Is a histamine receptor antagonist. Main site of metabolic transformation is the liver. Oral availability - 50%, Plasma bound - 80%, Half life - 4 hours
Effectively absorbed from GI tract. Ammonium Ion converted to urea by the liver.
Acid ion released gives mild metabolic acidosis.
After absorption menthol is excreted in the urine and bile as a glucuronide.
There are no preclinical data of relevance, within are additional to those already included in other sections of the SmPC.
Sucrose, Cocoa flavour, Glycerol, Propylene Glycol, Sodium Citrate, Nipastat (methylparahydroxybenzoate E218, ethylparahydroxybenzoate E215, propylparahydroxybenzoate E216, butylparahydroxybenzoate), Purified Water.
150ml amber glass bottle
300ml amber glass bottle
Measuring red spoon PPH 578N
Cap Red PP28 TE CR with EPE/PE/AL/PET Wad
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